Optically active devices Field of the Invention The present invention relates to novel ophthalmic devices comprising polymerized compounds comprising a photoactive chromophore, said polymerized compounds, and special monomer compounds being particularly suitable for compositions and ophthalmic devices. The present invention is also directed to a process of changing the optical properties of said ophthalmic device or a precursor article for an ophthalmic device. Background of the Invention Cataract is a general term for an affection of the eye that leads to a loss of vision and in the extreme to blindness by clouding of the normally clear lens of the eye. It is the major cause of blindness in the world, affecting more than 100 million people. Due to the fact that its major cause is age and the population’s average age is increasing, it is expected that the number of cataracts will continue to increase substantially in the future. Effective treatment of cataract is only possible by surgical intervention, whereby the natural lens of the eye is removed through an incision in the cornea and replaced with an ophthalmic device, often also referred to as “intraocular lens". In preparation of surgery current state-of-the-art surgical methods employ eye mapping so as to approximate the refractive power best suited to the respective patient. Even though cataract surgery is one of the most widely used and safest surgical procedures it is not without specific post-surgery problems. It frequently happens that the refractive power of the implanted intraocular lens (IOL) is insufficient for restoring good vision. Such problems may, for example, be caused by changes in eye geometry as consequence of the surgery as well as irregular wound healing and positioning errors that result in the ophthalmic device not having the optimal optical properties. As a result the patient will still require corrective vision aids, e.g. glasses, to be able to see correctly. In some cases the resulting refractive power of the implanted ophthalmic device is so far removed from the required refractive power that further surgery will be required. Particularly for aged persons this is not desirable because the body’s capability for healing is reduced with increasing age. Furthermore, there is the risk of attracting endophthalmitis, an inflammation of the eye, which can even lead to a complete loss of vision or worse, loss of the eye. There is therefore a need in the health sector for optically active ophthalmic devices, and particularly for artificial intraocular lenses, that would allow for non-invasive adjustment of refractive power after implantation of the lens, thereby preferably further reducing the need for post-surgery vision aids. Some developments in this sense have already been made, as for example evidenced by WO 2007033831, WO 2009074520, US 20100324165, WO 2017032442, WO 2017032443, WO 2017032444, WO 2018149850, WO 2018149852, WO 2018149853, WO 2018149855, WO 2018149856, WO 2018149857, WO2019121642. M. Schraub et al, European Polymer Journal 51 (2014) 21-27 describe the photochemistry of 3-phenyl-coumarin containing polymethacrylates. When a chromophore undergoes cycloaddition there is a change in both density and polarizability. Refractive index is a function of density and polarizability according to the Lorentz-Lorenz equation (Equation 1), where M is the molar mass, ρ is the density, N is the number density of molecules, and α is the polarizability. The conversion of a carbon- carbon double bond to carbon-carbon single bond results in a reduction of volume of 22 cm ³ /mole (Patel, M.P. et al., Biomaterials, 1987, 8, 53-56). Equation 1. This alone would lead to an increase in refractive index due to cycloaddition. However, by taking advantage of the nonlinear decrease in refractivity caused by breaking of conjugated systems, large negative refractive index changes can be seen for certain chromophores, in far excess of the positive refractive index change of volume reduction. However, large conjugated chromophores also show large optical dispersion. Optical dispersion is characterized by Abbe number, V _D , defined by Equation 2. Equation 2. High optical dispersion is characterized by low Abbe number and is detrimental in optical applications where more than one wavelength of light passes through the material such as ophthalmic devices e.g. lenses. The higher the Abbe number is, the lower the chromatic aberration. S. Helmstetter et al, J Polym Res, 2016, 23:249, describes quinolinone-based cross- linked homo- as well as copolymers showing refractive indices at 589 nm ranging from 1.60 up to 1.68 and Abbe numbers of 19 to 25. It is further reported that the higher the refractive index of a lens material is, the thinner the intraocular lens becomes but in most cases this is accompanied by an increase in glass transition temperature and a decrease of the Abbe number. It is reported that the optimal balance between high refractive index, low glass transition temperature, and high Abbe number is the chemical challenge in polymer synthesis for IOL manufacture and that state-of-the-art foldable but not adjustable hydrophobic IOLs have refractive indices up to 1.55, glass transition temperatures of about 14 to 15°C and Abbe numbers up to 37. Takadate et al, Chem. Pharm. Bull, 1982, 30,(11), 4120-4125 describe the synthesis and properties of 4-diazomethyl-7-methoxycoumarin as a fluorescent labeling reagent for alcohols and carboxylic acids for use in high-performance liquid chromatography. Bach et al., JACS, 2002, 124, 27, 7982-7990 describe enantioselective intra- and intermolecular [2+2] photocycloaddition reactions of 4-alkenyloxy-quinolones mediated by a chiral lactam host. Nam et al., Bioorganic & Medicinal Chemistry Letters, 2002, 12, 17, 2345-2348 describe preliminary structure-antiangiogenic activity relationships of 4-senecioyloxymethyl-6,7- dimethoxycoumarin by replacement of the lactone functionality with e.g.4- methoxycinnamoyl. Chen-Xu Jiao et al, Sensors and Actuators, 2003, B 94, 176-183 describes 4-allyloxy-7- aminocoumarin as a fluorescent carrier for optical sensor preparation. Lee et al., Yakhak Hoeji, 2006, 50, 5, 338-344 describe the synthesis of 6,7-dimethoxy substituted coumarin analogues and their antitumor activity such as 3-methyl-but-2-enoic acid 6,7-dimethoxy-2-oxo-2H-chromen-4-ylmethyl ester or 2-methyl-acrylic acid 6,7- dimethoxy-2-oxo-2H-chromen-4-ylmethyl ester. Babin et al., Angew. Chem. Int. Ed., 2009, 48, 18, 3329-3332 describe a two-photon- sensitive block copolymer nanocarrier comprising polymerized [7-(diethylamino)coumarin- 4-yl]methyl methacrylate. M.M. Maturi et al, Chemistry – A European Journal 2013, 19 (23), 7461-7472 describes an intramolecular [2+2] photocycloaddition of 3- and 4-(but-3-enyl)oxyquinolones. Gumbley et al., Chem. Mater., 2014, 26, 3, 1450-1456 describe the synthesis of photolabile polymers comprising dialkylaminocoumarin side chains. Hu et al., Chem. Mater., 2017, 29, 2951-2960 describe photolabile polyelectrolyte multilayers which comprise commercially available photoinert polyanions and photolabile polycations where one photolabile polycation is based on dialkylaminocoumarin. Enrico Rampazzo et al, J. Mater. Chem., 2005, 15, 2687-2696 describe a surface modification of silica nanoparticles for the realization of self-organized fluorescence chemosensors for transition metal ions. It is reportet that silica nanoparticles, in particular, are suitable for the realization of fluorescence chemosensors as they are transparent to light, photophysically inert and their surface can be easily modified by reaction with alkoxysilane derivatives. EP0155177 describes unsaturated cyclic amido-substituted ether compounds which can be used in crosslinking agents, adhesives, paints and raw materials for hygroscopic resins. N-{4-[(2-oxo-2H-chromen-4-yl)oxy]butyl}prop-2-enamide is disclosed on page 59. This compound has a high melting point of 141.5 to 142.5°C and is therefore less suitable as a component in ophthalmic compositions. US2647133 describes 7-amino substituted coumarines useful for the whitening of silk, wool and synthetic fibers. US2844539 describes 7-diethylaminocoumarines in a water-soluble brightener composition. US3008969 describes a ring-closure method which permits the synthesis of 7- aminocoumarins and describes specific 7-carbethoxyamino-coumarins. WO9713762 describes the preparation of benzopyranones as fungicides. WO2007147775 describes a process for preparing aromatic compounds via catalyzed- benzannulation. WO2009074520 and WO2009074521 describe acrylic ophthalmologic compositions and their use. KR2008054564 describes coumarin derivatives to inhibit secretion of beta- hexosaminidase and reduce passive skin anaphylaxis, so that the compounds are useful for preventing and treating inflammation and allergic diseases. WO2010049044 describes a liquid-crystal medium comprising coumarin derivatives. WO2012097858 describes polymerizable compounds and the use thereof in liquid-crystal displays. WO2012070024 describes derivatized coumarin-based pharmaceutical compositions characterized in that they inhibit the activity of tumor-related CAIX and CAXII to a greater degree than they inhibit the activity of CAI and CAII. US20120225448 describes substrates with photo-controllable cell adhesion properties for the method and the device to sort and analyze cells. US20130334461 describes a polymerizable liquid crystal composition containing coumarin derivatives. CN103204837 describes the preparation of photodegradable crosslinking agents. KR2014047208 describes a polymer composition for contact lens comprising natural compounds or prepolymer containing natural compounds such as eugenol, safrole or myristicin. CN103755888 describes 2-methyl-2-propenoic acid [7-(didodecylamino)-2-oxo-2H-1- benzopyran-4-yl]methyl ester and a preparation method for its amphiphilic polymer as well as magnetic hollow nano drug carrier with core-shell structure containing the amphiphilic polymer. WO2015175963 describes pressure sensitive adhesive polymers comprising adhesive polymers crosslinked with a crosslinker that includes a coumarin photoresponsive group. CN107621751 describes a polymer resin containing an alkaline coumarin structure and a photoresist composition thereof. CN110407986 describes a preparation method of pH and temperature responsive double- shell hollow microspheres by using 3-allyl-coumarins as fluorescent dye. CN111333774 (pub.2020) describes an antibacterial hydrogel based on a coumarin skeleton which comprises 4-hydroxymethyl-7-hydroxycoumarin or its derivatives. However, there is still a need to provide alternative or improved ophthalmic devices e.g. contact lenses or lenses to be implanted by state of the art surgical methods, especially cataract surgical methods, and there is still a need to provide special compounds for the manufacture of ophthalmic devices e.g. of intraocular lenses to be implanted by state of the art surgical methods, particularly by state of the art micro-incision cataract surgical methods. Preferably, high refractive index-change materials with high Abbe numbers are needed to fulfill the above mentioned needs. Consequently, it is an objective of the present application to provide for alternative or improved ophthalmic devices and suitable compounds for the manufacture of such ophthalmic devices. It is also an objective of the present application to provide for compounds, the optical properties of which may be changed, preferably by non-invasive techniques. It is a further objective of the present application to provide alternative compounds or compounds having advantages over currently known compounds, preferably in combination with being suitable for ophthalmic devices. Advantages for polymers or copolymers comprising polymerized monomers of formula (I) according to the invention are shown in the experimental section. The polymers or copolymers as well as the ophthalmic device comprising said material according to the invention preferably show a significant polarizability change or refractive index change after irradiation. In addition, the said polymers or copolymers ensure a much higher Abbe number compared to prior art materials. Advantages for polymers or copolymers comprising polymerized monomers of formula (I) according to the invention are further good flexibilities and low glass transition temperatures. Based on this advantage of the polymers or copolymers of the invention, the ophthalmic device comprising said materials has an intrinsically lower chromatic aberration. Summary of the Invention The present inventors have now found that the above objects may be attained either individually or in any combination by ophthalmic devices and the compounds of the present application. The invention relates to an ophthalmic device or a precursor article for an ophthalmic device comprising at least one polymerized compound of formula (I), wherein X-W is O-C(=O), O-C(=S), O-SO ₂ , SO ₂ -O, SO ₂ -C(=S), S-C(=O), S-C(=S), NR _B - C(=O) or NR _B -C(=S); R _B is at each occurrence independently H, a linear or branched alkyl group having 1 to 6 C atoms or a linear or branched partially or fully fluorinated alkyl group having 1 to 10 C atoms; R ₃ is H, R# or F; R ₄ is at each occurrence independently H, F, Cl, SF ₅ , CN or [Y ₁ ] _m1 - R ₅ ; R ₅ is a linear or branched alkyl group having 1 to 6 C atoms or a linear or branched partially or fully fluorinated alkyl group having 1 to 10 C atoms, a cycloalkyl group having 3 to 6 C atoms or a heterocycloalkyl group having 4 to 6 ring atoms; Y is O, S, SO, SO ₂ , Se, NR ₀ or a bond; Y ₁ is O, S or NR _B ; m1 is 0 or 1; R ₀ is at each occurrence independently selected from the group consisting of a linear or branched alkyl group having 1 to 4 C atoms; R# is a linear or branched alkyl group having 1 to 6 C atoms or a linear or branched partially or fully fluorinated alkyl group having 1 to 6 C atoms; R ₁ is a trialkoxysilyl group or a dialkoxyalkylsilyl group where the alkyl and/or alkoxy groups are each independently linear or branched having 1 to 6 C atoms, or a silyl group of formula (1), (2) or (3) or a polymerizable group of formula (4), where alkyl means at each occurrence independently of each other a linear or branched alkyl group having 1 to 6 C atoms and each asterisk “*” denotes at each occurrence independently of each other a linkage to the rest of one or more compounds of formula (I) via the linker -R ₂ -Y-; and wherein X ₁₁ is selected from the group consisting of O, S, O-SO ₂ , SO ₂ -O, C(=O), OC(=O), C(=O)O, S(C=O) and (C=O)S, R ₆ , R ₇ , R ₈ are at each occurrence independently of each other selected from the group consisting of H, F, a linear or branched, non-fluorinated, partially or completely fluorinated alkyl group having 1 to 20 C atoms and aryl with 6 to 14 C atoms and c is 0 or 1; -R ₂ - is –(C(R) ₂ ) _o –, or –(C(R) ₂ ) _p –X ₈ –(C(R) ₂ ) _q –(X ₉ ) _s –(C(R) ₂ ) _r –(X ₁₀ ) _t -(C(R) ₂ ) _u -; R is at each occurrence independently selected from the group consisting of H, F, a linear or branched alkyl group having 1 to 4 C atoms or a linear or branched partially or fully fluorinated alkyl group having 1 to 4 C atoms; o is selected from the group consisting of 0 to 20, X ₈ , X _9, X ₁₀ are at each occurrence independently O, S, SO ₂ , or NR _B , s, t is 0 or 1, p, q are at each occurrence independently selected from the group consisting of 1 to 10, r, u are at each occurrence independently selected from the group consisting of 0 to 10, wherein the overall number of atoms for –(C(R) ₂ ) _p – X ₈ –(C(R) ₂ ) _q –(X ₉ ) _s –(C(R) ₂ ) _r –(X ₁₀ ) _t -(C(R) ₂ ) _u - is up to 20 atoms. The invention relates further to a process of forming an ophthalmic device or a precursor article for an ophthalmic device as described before or preferably described below, said process comprising the steps of - providing a composition comprising at least one compound of formula (I) as described before or preferably described below and/or an oligomer or polymer derived from a compound of formula (I) as described below or preferably described below and having at least one reactive group left for polymerization and optionally further monomers different from compounds of formula (I) and/or crosslinking agents and/or UV absorbers and/or radical initiators; - subsequently forming the ophthalmic device or precursor article of said composition. The invention relates further to a process of changing the optical properties of an ophthalmic device or a precursor article for an ophthalmic device as described before or preferably described below said process comprising the steps of - providing an ophthalmic device or a precursor article with the process as described before or preferably described below, and - subsequently exposing said ophthalmic device or precursor article to irradiation having a wavelength of at least 200 nm and at most 1500 nm. The invention relates further to an ophthalmic device or precursor article for an ophthalmic device obtainable by said process. The invention relates further to compounds of formula (I), wherein X-W is O-C(=O), O-C(=S), O-SO ₂ , SO ₂ -O, SO ₂ -C(=S), S-C(=O), S-C(=S), NR _B - C(=O) or NR _B -C(=S); R _B is at each occurrence independently H, a linear or branched alkyl group having 1 to 6 C atoms or a linear or branched partially or fully fluorinated alkyl group having 1 to 10 C atoms; R ₃ is H or F; R ₄ is at each occurrence independently H, F, Cl, SF ₅ , CN or [Y ₁ ] _m1 -R ₅ ; R ₅ is a linear or branched alkyl group having 1 to 6 C atoms or a linear or branched partially or fully fluorinated alkyl group having 1 to 10 C atoms, a cycloalkyl group having 3 to 6 C atoms or a heterocycloalkyl group having 4 to 6 ring atoms; Y is O, S, SO,SO ₂ , Se, NR ₀ or a bond; Y ₁ is O, S or NR _B ; m1 is 0 or 1; R ₀ is at each occurrence independently selected from the group consisting of a linear or branched alkyl group having 1 to 4 C atoms; R ₁ is a trialkoxysilyl group or a dialkoxyalkylsilyl group where the alkyl and/or alkoxy groups are each independently linear or branched having 1 to 6 C atoms, or a silyl group of formula (1), (2) or (3) or a polymerizable group of formula (4), where alkyl means at each occurrence independently of each other a linear or branched alkyl group having 1 to 6 C atoms and each asterisk “*” denotes at each occurrence independently of each other a linkage to the rest of one or more compounds of formula (I) via the linker -R ₂ -Y-; and wherein X ₁₁ is selected from the group consisting of O, S, O-SO ₂ , SO ₂ -O, C(=O), OC(=O), C(=O)O, S(C=O) and (C=O)S, R ₆ , R ₇ , R ₈ are at each occurrence independently of each other selected from the group consisting of H, F, a linear or branched, non-fluorinated, partially or completely fluorinated alkyl group having 1 to 20 C atoms and aryl with 6 to 14 C atoms and c is 1; -R ₂ - is –(C(R) ₂ ) _o –, or –(C(R) ₂ ) _p –X ₈ –(C(R) ₂ ) _q –(X ₉ ) _s –(C(R) ₂ ) _r –(X ₁₀ ) _t -(C(R) ₂ ) _u -; R is at each occurrence independently selected from the group consisting of H, F, a linear or branched alkyl group having 1 to 4 C atoms or a linear or branched partially or fully fluorinated alkyl group having 1 to 4 C atoms; o is selected from the group consisting of 0 to 20, X ₈ , X _9, X ₁₀ are at each occurrence independently O, S, SO ₂ , or NR _B , s, t is 0 or 1, p, q are at each occurrence independently selected from the group consisting of 1 to 10, r, u are at each occurrence independently selected from the group consisting of 0 to 10, wherein the overall number of atoms for –(C(R) ₂ ) _p – X ₈ –(C(R) ₂ ) _q –(X ₉ ) _s –(C(R) ₂ ) _r –(X ₁₀ ) _t -(C(R) ₂ ) _u - is up to 20 atoms; provided that in case of X-W is O-C(=O) and Y ₁ is NR _B , X ₁₁ is not O-C(=O), provided that in case of X-W is O-C(=O), Y is a bond, o is 1, m1 is 1, Y ₁ is O and c is 1, X ₁₁ is not O-C(=O), and provided that in case of X-W is O-C(=O), R ₁ is not a trialkoxysilyl group or a dialkoxyalkylsilyl group where the alkyl and/or alkoxy groups are each independently linear or branched having 1 to 6 C atoms, or a silyl group of formula (1), (2) or (3),

The invention relates further to oligomers, polymers or copolymers comprising at least one polymerized compound of formula (I) as described before or preferably described below, provided that in case of X-W is O-C(=O) and Y ₁ is NR _B , X ₁₁ is not O-C(=O); provided that in case of X-W is O-C(=O), Y is a bond, o is 1, m1 is 1, Y ₁ is O and c is 1, X ₁₁ is not O-C(=O); and provided that in case of X-W is O-C(=O), R ₁ is not a trialkoxysilyl group or a dialkoxyalkylsilyl group where the alkyl and/or alkoxy groups are each independently linear or branched having 1 to 6 C atoms, or a silyl group of formula (1), (2) or (3), The invention relates further to compositions for polymerization comprising at least one compound of formula (I) as described before or preferably described below, provided that in case of X-W is O-C(=O) and Y ₁ is NR _B , X ₁₁ is not O-C(=O); provided that in case of X-W is O-C(=O), Y is a bond, o is 1, m1 is 1, Y ₁ is O and c is 1, X ₁₁ is not O-C(=O); and provided that in case of X-W is O-C(=O), R ₁ is not a trialkoxysilyl group or a dialkoxyalkylsilyl group where the alkyl and/or alkoxy groups are each independently linear or branched having 1 to 6 C atoms, or a silyl group of formula (1), (2) or (3), and/or an oligomer or polymer derived from said compounds of formula (I) and having at least one reactive group left for polymerization and a crosslinking agent and/or a UV absorber and/or a radical initiator and optionally further monomers different from said compounds of formula (I). Detailed Description of the Invention Compounds of formula (I) as described before or preferably described below can be preferably used as monomers for the preparation of a precursor article such as a blank which may be transformed to an ophthalmic device such as an eye-implant or specifically an intraocular lens or can be preferably used for the preparation of the ophthalmic device as such as described before or preferably described below. The compounds of formula (I) and all preferred embodiments of compounds of formula (I) including any monomeric units according to the present invention include all stereoisomers or racemic mixtures. The compounds of formula (I) provide several advantages over prior art materials for the preparation of ophthalmic devices or precursor articles for an ophthalmic device according to the invention. Moreover, the addition of the substituent Y-R ₂ - R1 in 3-position or 4-position of the central chromophore in the compounds of formula (I) or oligomers, polymers and copolymers comprising polymerized compounds of formula (I) has a significant impact on the optical properties over prior art compounds as described before. One way chosen in prior art to increase the polarizability was by extending the aromatic system of the photoactive unit. However, the Abbe number usually tends to lower with an increase of the aromatic system as described before. The inventors found that making use of the substitution in 3-position or 4-position by the substituent Y-R ₂ -R ₁ as described still enables a high polarizability of the double bond and maintains high Abbe numbers. Polymers/copolymers that are foldable at room temperature generally exhibit glass transition temperatures (T _g ) lower than room temperature (ca.21 °C). They are easily deformable at this temperature without causing physical damage to the polymer, for example by inducing creep, stress or fissures. For polymers in intraocular lenses, T _g ’s of less than or equal to 15 °C are preferred. Polymers/copolymers used in ophthalmic device manufacturing, preferably in intraocular lens manufacturing, have preferably relatively high refractive indices, which enable the fabrication of thinner ophthalmic devices such as intraocular lenses. Preferably, the polymer used in an ophthalmic device, preferably an intraocular lens, will have a refractive index greater than about 1.5 and presently most preferably greater than about 1.55. Polymers/copolymers used in ophthalmic device manufacturing, preferably in intraocular lens manufacturing, have preferably relatively high Abbe numbers. Preferably, the polymer/copolymer used in an ophthalmic device, preferably an intraocular lens, will have an Abbe number greater than 35 and presently most preferably greater than or equal to 37. In case an asterisk ("*") is used within the description of the present invention, it denotes a linkage to an adjacent unit or group or, in case of a polymer, to an adjacent repeating unit or any other group whenever it is not specifically defined. A linear or branched alkyl group having 1 to 10 C atoms denotes an alkyl group having 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 C atoms, for example methyl, ethyl, iso-propyl, n-propyl, iso- butyl, n-butyl, tert-butyl, n-pentyl, 1-, 2- or 3-methylbutyl, 1,1-, 1,2- or 2,2-dimethylpropyl, 1-ethylpropyl, n-hexyl, n-heptyl, n-octyl, ethylhexyl, n-nonyl or n-decyl. A linear or branched alkyl group having 1 to 20 C atoms include all examples for a linear or branched alkyl group having 1 to 10 C atoms including any alkyl group having 11, 12, 13, 14, 15, 16, 17, 18, 19 and 20 C atoms such as n-undecyl, n-dodecyl, n-tridecyl, n-tetradecyl, n- pentadecyl, n-hexadecyl, n-heptadecyl, n-octadecyl, n-nonadecyl and n-eicosyl. The term partially fluorinated alkyl group denotes that at least one H atom of the alkyl group is replaced by F. A preferred partially halogenated alkyl group is CH ₂ CF ₃ . The term completely fluorinated alkyl group denotes that all H atoms of the alkyl group are replaced by F. A preferred completely fluorinated alkyl group is trifluoromethyl or pentafluoroethyl. The term halogenated or preferably fluorinated corresponds additionally to other groups such as a halogenated cycloalkyl group, a halogenated alkoxy group or a halogenated thioalkyl group. A cycloalkyl group having 3 to 6 C atoms includes cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl. Preferably, the cycloalkyl group is cyclopentyl or cyclohexyl. A heterocycloalkyl group having 4 to 6 C ring atoms is a cycloalkyl group having 4 to 6 C atoms, where at least one of said C atoms is a heteroatom selected from N, O or S. In case of a heterocycloalkyl group having 4 to 6 ring atoms comprising a nitrogen, said heterocycloalkyl group may be linked to the remainder of the molecule via said N atom. In case said heterocycloalkyl group is bonded via a C-Atom, the N atom is further substituted with R ₀ as defined before or as preferably defined below. A linear or branched alkoxy group having 1 to 20 C atoms denotes an O-alkyl group having 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19 or 20 C atoms, for example methoxy, ethoxy, iso-propoxy, n-propoxy, iso-butoxy, n-butoxy, tert-butoxy, n- pentyloxy, 1-, 2- or 3-methylbutyloxy, 1,1-, 1,2- or 2,2-dimethylpropoxy, 1-ethylpropoxy, n- hexyloxy, n-heptyloxy, n-octyloxy, ethylhexyloxy, n-nonyloxy, n-decyloxy, n-undecyloxy, n- dodecyloxy, n-tridecyloxy, n-tetradecyloxy, n-pentadecyloxy, n-hexadecyloxy, n- heptadecyloxy, n-octadecyloxy, n-nonadecyloxy and n-eicosyloxy which may be partially or completely fluorinated. A preferred completely fluorinated alkoxy group is trifluoromethoxy or pentafluoroethoxy. A linear or branched thioalkyl group having 1 to 20 C atoms denotes a S-alkyl group having 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19 or 20 C atoms, for example thiomethyl, 1-thioethyl, 1-thio-iso-propyl, 1-thio-n-propoyl, 1-thio-iso-butyl, 1-thio- n-butyl, 1-thio-tert-butyl, 1-thio-n-pentyl, 1-thio-1-, -2- or -3-methylbutyl, 1-thio-1,1-, -1,2- or -2,2-dimethylpropyl, 1-thio-1-ethylpropyl, 1-thio-n-hexyl, 1-thio-n-heptyl, 1-thio-n-octyl, 1- thio-ethylhexyl, 1-thio-n-nonyl, 1-thio-n-decyl, 1-thio-n-undecyl, 1-thio-n-dodecyl, 1-thio-n- tridecyl, 1-thio-n-tetradecyl, 1-thio-n-pentadecyl, 1-thio-n-hexadecyl, 1-thio-n-heptadecyl, 1-thio-n-octadecyl, 1-thio-n-nonadecyl and 1-thio-n-eicosyl which may be partially or completely halogenated or preferably may be partially or completely fluorinated. A preferred completely fluorinated thioether group is trifluoromethyl thioether. Preferred alkyl and alkoxy radicals have 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 C atoms. An aryl group in the context of this invention contains 6 to 40 ring atoms and a heteroaryl group in the context of this invention contains 5 to 40 ring atoms comprising at least one heteroatom. The heteroatoms are preferably selected from N, O and/or S. An aryl group or heteroaryl group is understood here to mean either a simple aromatic cycle, i.e. phenyl, or a simple heteroaromatic cycle, for example pyridinyl, pyrimidinyl, thiophenyl, etc., or a fused (annelated) aryl or heteroaryl group, for example naphthyl, anthracenyl, phenanthrenyl, quinolinyl or isoquinolinyl. An aryl group or heteroaryl group is preferably derived from benzene, naphthalene, anthracene, phenanthrene, pyrene, benzanthracene, chrysene, perylene, fluoranthene, naphthacene, pentacene, benzopyrene, biphenyl, biphenylene, terphenyl, triphenylene, fluorene, spirobifluorene, dihydrophenanthrene, dihydropyrene, tetrahydropyrene, cis- or trans-indenofluorene, cis- or trans-indenocarbazole, cis- or trans-indolocarbazole, truxene, isotruxene, spirotruxene, spiroisotruxene, furan, benzofuran, isobenzofuran, dibenzofuran, thiophene, benzothiophene, isobenzothiophene, dibenzothiophene, pyrrole, indole, isoindole, carbazole, pyridine, quinoline, isoquinoline, acridine, phenanthridine, benzo-5,6- quinoline, benzo-6,7-quinoline, benzo-7,8-quinoline, phenothiazine, phenoxazine, pyrazole, indazole, imidazole, benzimidazole, naphthimidazole, phenanthrimidazole, pyridimidazole, pyrazinimidazole, quinoxalinimidazole, oxazole, benzoxazole, naphthoxazole, anthroxazole, phenanthroxazole, isoxazole, 1,2-thiazole, 1,3-thiazole, benzothiazole, pyridazine, hexaazatriphenylene, benzopyridazine, pyrimidine, benzopyrimidine, quinoxaline, 1,5-diazaanthracene, 2,7-diazapyrene, 2,3-diazapyrene, 1,6-diazapyrene, 1,8-diazapyrene, 4,5-diazapyrene, 4,5,9,10-tetraazaperylene, pyrazine, phenazine, phenoxazine, phenothiazine, fluorubine, naphthyridine, azacarbazole, benzocarboline, phenanthroline, 1,2,3-triazole, 1,2,4-triazole, benzotriazole, 1,2,3- oxadiazole, 1,2,4-oxadiazole, 1,2,5-oxadiazole, 1,3,4-oxadiazole, 1,2,3-thiadiazole, 1,2,4- thiadiazole, 1,2,5-thiadiazole, 1,3,4-thiadiazole, 1,3,5-triazine, 1,2,4-triazine, 1,2,3-triazine, tetrazole, 1,2,4,5-tetrazine, 1,2,3,4-tetrazine, 1,2,3,5-tetrazine, purine, pteridine, indolizine and benzothiadiazole. A polymerizable group is a group which can be subject to or can undergo polymerization thus forming an oligomer or a polymer. Polymerization is the process of taking individual monomers and chaining them together to make longer units. These longer units are called polymers. The compounds of formula (I) as described before and preferably described below are suitable monomers for the preparation of an ophthalmic device or a precursor article for an ophthalmic device. Within the gist of the invention, the polymerizable group R ₁ once oligomerized or polymerized thus forms or is part of the backbone of the oligomer, polymer or copolymer comprising polymerized compounds of formula (I). Suitable polymerizable groups are defined to be a trialkoxysilyl group or a dialkoxyalkylsilyl group where the alkyl and/or alkoxy groups are each independently linear or branched having 1 to 6 C atoms, or a silyl group of formula (1), (2) or (3) or a polymerizable group of formula (4), where alkyl means at each occurrence independently of each other a linear or branched alkyl group having 1 to 6 C atoms and each asterisk “*” denotes at each occurrence independently of each other a linkage to the rest of one or more compounds of formula (I) via the linker -R ₂ -Y-; and wherein X ₁₁ is selected from the group consisting of O, S, O-SO ₂ , SO ₂ -O, C(=O), OC(=O), C(=O)O, S(C=O) and (C=O)S, R ₆ , R ₇ , R ₈ are at each occurrence independently of each other selected from the group consisting of H, F, a linear or branched, non-fluorinated, partially or completely fluorinated alkyl group having 1 to 20 C atoms and aryl with 6 to 14 C atoms and c is 0 or 1. Particularly preferred polymerizable groups are described below. Aryl with 6 to 14 C atoms is an aryl group preferably selected from the group consisting of phenyl, naphthyl or anthryl, particularly preferably phenyl. In one preferred embodiment, the compounds of formula (I) acting as monomers for the preparation of the ophthalmic device or precursor article of the ophthalmic device as described before or for the preparation of an oligomer, polymer or copolymer according to the invention or as compound according to the invention contain the linker Y-R ₂ -R ₁ in 4- position of the photoactive ring system which can be described according to formula (Ia), wherein X-W, Y, R ₁ , -R ₂ -, R ₃ and R ₄ have a meaning as described before or preferably described below. The invention is therefore additionally directed to an ophthalmic device or a precursor article for an ophthalmic device comprising at least one polymerized compound of formula (Ia), , wherein X-W, Y, R ₁ , -R ₂ -, R ₃ and R ₄ have a meaning as described before or preferably described before or below. This embodiment is particularly preferred. In another preferred embodiment, the compounds of formula (I) acting as monomers for the preparation of the ophthalmic device or precursor article of the ophthalmic device as described before or for the preparation of an oligomer, polymer or copolymer according to the invention or as compound according to the invention contain the linker Y-R ₂ -R ₁ in 3- position of the photoactive ring system which can be described according to formula (Ib), wherein X-W, Y, R ₁ , -R ₂ -, R ₃ and R ₄ have a meaning as described before or preferably described below. The invention is therefore additionally directed to an ophthalmic device or a precursor article for an ophthalmic device comprising at least one polymerized compound of formula (Ib), wherein X-W, Y, R ₁ , -R ₂ -, R ₃ and R ₄ have a meaning as described before or preferably described before or below. The invention is therefore additionally directed to compounds of formula (Ia) or (Ib), wherein X-W, Y, R ₁ , -R ₂ -, R ₃ and R ₄ have a meaning as described before or preferably described before or below; provided that in case of X-W is O-C(=O) and Y ₁ is NR _B , X ₁₁ is not O-C(=O); provided that in case of X-W is O-C(=O), Y is a bond, o is 1, m1 is 1, Y ₁ is O and c is 1, X ₁₁ is not O- C(=O); and provided that in case of X-W is O-C(=O), R ₁ is not a trialkoxysilyl group or a dialkoxyalkylsilyl group where the alkyl and/or alkoxy groups are each independently linear or branched having 1 to 6 C atoms, or a silyl group of formula (1), (2) or (3), In compounds of formulae (I), (Ia) or (Ib) acting as monomers for the preparation of the ophthalmic device or precursor article of the ophthalmic device as described before or for the preparation of an oligomer, polymer or copolymer according to the invention or as compound according to the invention, the symbol X-W is O-C(=O), O-C(=S), O-SO ₂ , SO ₂ - O, SO ₂ -C(=S), S-C(=O), S-C(=S), NR _B -C(=O) or NR _B -C(=S) where R _B has a meaning as described before or preferably described below. Preferably, X-W is O-C(=O), O-SO ₂ , SO ₂ -O, SO ₂ -C(=S), S-C(=O) or NR _B -C(=O) where R _B has a meaning as described before or preferably described below. Particularly preferably, X-W is O-C(=O), O-SO ₂ , SO ₂ -O, S- C(=O) or NR _B -C(=O) where R _B has a meaning as described before or preferably described below. Very particularly preferably, X-W is O-C(=O), S-C(=O) or NR _B -C(=O) where R _B has a meaning as described before or preferably described below. Within NR _B -C(=O), R _B is preferably a linear or branched alkyl group having 1 to 6 C atoms or a linear or branched partially or fully fluorinated alkyl group having 1 to 10 C atoms. Within NR _B -C(=O), RB is particularly preferably a linear or branched alkyl group having 1 to 6 C atoms, preferably methyl, ethyl, n-propyl or n-butyl. The invention is therefore additionally directed to an ophthalmic device or a precursor article for an ophthalmic device comprising at least one polymerized compound of formulae (I), (Ia) or (Ib) wherein X-W is O-C(=O), O-SO ₂ , SO ₂ -O, SO ₂ -C(=S), S-C(=O) or NR _B -C(=O) and where RB has a meaning as described before. The invention is therefore additionally directed to compounds of formulae (I), (Ia) or (Ib) wherein X-W is O-C(=O), O-SO ₂ , SO ₂ -O, SO ₂ -C(=S), S-C(=O) or NR _B -C(=O) and where R _B has a meaning as described before and where the given disclaimers have to be used as disclosed. As described before within the ophthalmic device or precursor article, compounds of formulae (I), (Ia), (Ib), and any oligomers, polymers or copolymers derived therefrom according to the invention, the substituent R ₃ is H, R# or F, preferably H or F, particularly preferably H. Within R ₃ , R# is a linear or branched alkyl group having 1 to 6 C atoms or a linear or branched partially or fully fluorinated alkyl group having 1 to 6 C atoms. Preferably, R# is a linear or branched alkyl group having 1 to 6 C atoms. Particularly preferably, R# is methyl, ethyl, n-propyl, i-propyl, n-butyl or 2-methyl-propan-3-yl. As described before within the inventive compounds of formulae (I), (Ia) or (Ib), and any oligomers, polymers or copolymers derived therefrom according to the invention, the substituent R ₃ is H or F, preferably H. As described before within the ophthalmic device, precursor article, compounds of formulae (I), (Ia), (Ib), preferred compounds of formulae (I), (Ia), (Ib) and any oligomers, polymers or copolymers derived therefrom according to the invention, the substituent R ₄ is at each occurrence independently preferably H, F or [Y ₁ ] _m1 -R ₅ , where Y ₁ , m1 and R ₅ have a meaning as described before or as preferably described below. Y ₁ is defined as O, S or NR _B , where R _B has a meaning as described before. Within Y ₁ , R _B is preferably a linear or branched alkyl group having 1 to 6 C atoms or a linear or branched partially or fully fluorinated alkyl group having 1 to 10 C atoms. Within Y ₁ , R _B is particularly preferably a linear or branched alkyl group having 1 to 6 C atoms, preferably methyl or ethyl. As described before within the ophthalmic device, precursor article, compounds of formulae (I), (Ia), (Ib), preferred compounds of formulae (I), (Ia), (Ib) and any oligomers, polymers or copolymers derived therefrom according to the invention, preferably at most two substituents R ₄ are different from H and have a meaning as described before or preferably described below. As described before within the ophthalmic device, precursor article, compounds of formulae (I), (Ia), (Ib), preferred compounds of formulae (I), (Ia), (Ib) and any oligomers, polymers or copolymers derived therefrom according to the invention, preferably at most one substituent R ₄ is different from H and have a meaning as described before or preferably described below. As described before within the ophthalmic device, precursor article, compounds of formulae (I), (Ia), (Ib), preferred compounds of formulae (I), (Ia), (Ib) and any oligomers, polymers or copolymers derived therefrom according to the invention, preferably all substituents R ₄ are H. In case R ₄ is different from H, it is preferably selected from F, Cl, R ₅ , or Y ₁ -R ₅ where Y ₁ and R ₅ have a meaning as described before or preferably described below. Y ₁ is preferably O or S. In case R ₄ is O-R ₅ and S-R ₅ , R ₅ is preferably a linear or branched alkyl group having 1 to 6 C atoms or a linear or branched partially or fully fluorinated alkyl group having 1 to 10 C atoms, a cycloalkyl group having 3 to 6 C atoms. In case R ₄ is NR _B R ₅ , R ₅ is preferably identical to R _B and has a meaning as described or preferably described for R _B before. In case R ₄ is NR _B R ₅ , R _B and R ₅ are particularly preferably methyl or ethyl. In case R ₄ is different from H and is R ₅ , R ₅ is preferably a linear or branched alkyl group having 1 to 6 C atoms or a linear or branched partially or fully fluorinated alkyl group having 1 to 10 C atoms, a cycloalkyl group having 3 to 6 C atoms or a heterocycloalkyl group having 4 to 6 ring atoms. In case R ₄ is different from H and is R ₅ , R ₅ is preferably methyl, ethyl, isopropyl, n-propyl, trifluoromethyl, pentafluoroethyl or trifluoroethyl or a heterocycloalkyl group having 4 to 6 ring atoms where the heterocycloalkyl group has a meaning as defined before. Preferred heterocycloalkyl groups are In case R ₄ is different from H, it is preferably selected from F, Cl, methyl, ethyl, isopropyl, n-propyl, trifluoromethyl, trifluoroethyl, pentafluoroethyl, methoxy, trifluoromethoxy, thiomethyl, thiocyclopentyl, thiocyclohexyl, dimethylamino, diethylamino, trifluoromethoxy, pentafluoroethoxy, As described before within the ophthalmic device, precursor article, compounds of formulae (I), (Ia) or (Ib), preferred compounds of formulae (I), (Ia) or (Ib) and any oligomers, polymers or copolymers derived therefrom according to the invention, Y is O, S, SO, SO ₂ , Se, NR ₀ or a bond and R ₀ is a linear or branched alkyl group having 1 to 4 C atoms. As described before within the ophthalmic device, precursor article, compounds of formulae (I), (Ia) or (Ib), preferred compounds of formulae (I), (Ia) or (Ib) and any oligomers, polymers or copolymers derived therefrom according to the invention, Y is preferably O, S, SO, NR ₀ or a bond and R ₀ is a linear or branched alkyl group having 1 to 4 C atoms. As described before within the ophthalmic device, precursor article, compounds of formulae (I), (Ia) or (Ib), preferred compounds of formulae (I), (Ia) or (Ib) and any oligomers, polymers or copolymers derived therefrom according to the invention, Y is preferably O, S or NR ₀ and R ₀ is a linear or branched alkyl group having 1 to 4 C atoms. R ₀ is preferably methyl or ethyl. As described before within the ophthalmic device, precursor article, compounds of formulae (I), (Ia) or (Ib), preferred compounds of formulae (I), (Ia) or (Ib) and any oligomers, polymers or copolymers derived therefrom according to the invention, Y is preferably O or NR ₀ and R ₀ is a linear or branched alkyl group having 1 to 4 C atoms. R ₀ is preferably methyl or ethyl. According to the invention, compounds of formulae (I), (Ia) or (Ib) with substituents as described before or preferably described before have a polymerizable group as described before or preferably described before or below and have one linking element Y-R ₂ where Y has a meaning as described before. According to the invention, the linking element -R ₂ - is –(C(R) ₂ ) _o –, or –(C(R) ₂ ) _p –X ₈ – (C(R) ₂ ) _q –(X ₉ ) _s –(C(R) ₂ ) _r –(X ₁₀ ) _t -(C(R) ₂ ) _u -, R is at each occurrence independently selected from the group consisting of H, F, a linear or branched alkyl group having 1 to 4 C atoms or a linear or branched partially or fully fluorinated alkyl group having 1 to 4 C atoms and o is 0 to 20, X ₈ , X ₉ and X ₁₀ are at each occurrence O, S, SO ₂ , or NR _B , s and t are at each occurrence independently 0 or 1, p and q are at each occurrence independently selected from the group consisting of 1 to 10, r and u are at each occurrence independently selected from the group consisting of 0 to 10, wherein the overall number of atoms for – (C(R) ₂ ) _p –X ₈ –(C(R) ₂ ) _q –(X ₉ ) _s –(C(R) ₂ ) _r –(X ₁₀ ) _t -(C(R) ₂ ) _u -, is up to 20 C atoms. R _B in NR _B within -R ₂ - is at each occurrence independently selected from the group consisting of a linear or branched alkyl group having 1 to 4 C atoms and a linear or branched partially or fully fluorinated alkyl group having 1 to 4 C atoms. R _B within -R ₂ - is independently at each occurrence and preferably methyl, ethyl or trifluoromethyl. R _B within -R ₂ - is independently at each occurrence particularly preferably methyl. R within -R ₂ - is at each occurrence independently preferably H, a linear or branched alkyl group having 1 to 4 C atoms and a linear or branched partially or fully fluorinated alkyl group having 1 to 4 C atoms. R within -R ₂ - is at each occurrence independently particularly preferably H, ethyl, n-propyl or trifluoromethyl. R within -R ₂ - is at each occurrence independently particularly preferably H. In another preferred embodiment of the invention, o is preferably selected from the group consisting of 0, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 and 13 within the compounds of formulae (I), (Ia) and (Ib) acting as monomers for the preparation of the ophthalmic device or precursor article of the ophthalmic device as described before or for the preparation of an oligomer, polymer or copolymer according to the invention or within the compounds according to the invention. Preferably, o is selected from the group consisting of 3, 5, 6, 7 and 11. Particularly preferably, o is selected from the group consisting of 5, 6 and 7, where 6 is especially preferred. With regards to the compounds according to the invention, the described disclaimers have to be considered for the definition of o. In another preferred embodiment of the invention, s, t, X ₈ , X ₉ , X ₁₀ , p, q, r and u within the compounds of formulae (I), (Ia) and (Ib) acting as monomers for the preparation of the ophthalmic device or precursor article of the ophthalmic device as described before or for the preparation of an oligomer, polymer or copolymer according to the invention or within the compounds according to the invention have the following preferred meaning: Preferably, s is 1. Preferably, s is 0. Preferably t is 0 or 1. Preferably, s and t are 0. Preferably, X ₈ , X ₉ and X ₁₀ are O, S or SO ₂ . Particularly preferably, X ₈ , X ₉ and X ₁₀ are O. Particularly preferably, X ₈ , X ₉ and X ₁₀ are S. Particularly preferably, X ₈ , X ₉ and X ₁₀ are SO ₂ . Particularly preferably, X ₈ , and X ₁₀ are O and X ₉ is S. Particularly preferably, X ₈ , and X ₁₀ are S and X ₉ is O. Preferably, p and q are each independently 1, 3, 3, 4, 5 or 6, particularly preferably 2 or 3, very particularly preferably 2. Preferably, r and u are each independently 0, 1, 2 or 3, particularly preferably 0 or 2, very particularly preferably 0. In case o is 0, -R ₂ - is a bond. According to the invention, suitable examples for -R ₂ - are -(CH ₂ )-, -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -, - (CH ₂ ) ₄ -, -(CH ₂ ) ₅ -, -(CH ₂ ) ₆ -, -(CH ₂ ) ₇ -, -(CH ₂ ) ₈ -, -(CH ₂ ) ₉ -, -(CH ₂ ) ₁₀ -, -(CH ₂ ) ₁₁ -, -(CH ₂ ) ₁₂ -, - (CH ₂ ) ₁₃ -, -(CH ₂ ) ₁₄ -, -(CH ₂ ) ₁₅ -, -(CH ₂ ) ₁₆ -, -(CH ₂ ) ₁₇ -, -(CH ₂ ) ₁₈ -, -(CH ₂ ) ₁₉ -, -(CH ₂ ) ₂₀ - , -(CHCH ₃ )-, -(CHCH ₃ ) ₂ -, -(CHCH ₃ ) ₃ -, -(CHCH ₃ ) ₄ -, -(CHCH ₃ ) ₅ -, -(CHCH ₃ ) ₆ -, -(CHCH ₃ ) ₇ -, -(CHCH ₃ ) ₈ -, -(CHCH ₃ ) ₉ -, -(CHCH ₃ ) ₁₀ -, -(CHCH ₃ ) ₁₁ -, -(CHCH ₃ ) ₁₂ -, -(CHCH ₃ ) ₁₃ -, - (CHCH ₃ ) ₁₄ -, -(CHCH ₃ ) ₁₅ -, -(CHCH ₃ ) ₁₆ -, -(CHCH ₃ ) ₁₇ -, -(CHCH ₃ ) ₁₈ -, -(CHCH ₃ ) ₁₉ -, - (CHCH ₃ ) ₂₀ -, -(C(CH ₃ ) ₂ )-, -(C(CH ₃ ) ₂ ) ₂ -, -(C(CH ₃ ) ₂ ) ₃ -, -(C(CH ₃ ) ₂ ) ₄ -, -(C(CH ₃ ) ₂ ) ₅ - , -(C(CH ₃ ) ₂ ) ₆ -, -(C(CH ₃ ) ₂ ) ₇ -, -(C(CH ₃ ) ₂ ) ₈ -, -(C(CH ₃ ) ₂ ) ₉ -, -(C(CH ₃ ) ₂ ) ₁₀ -, -(C(CH ₃ ) ₂ ) ₁₁ - , -(C(CH ₃ ) ₂ ) ₁₂ -, -(C(CH ₃ ) ₂ ) ₁₃ -, -(C(CH ₃ ) ₂ ) ₁₄ -, -(C(CH ₃ ) ₂ ) ₁₅ -, -(C(CH ₃ ) ₂ ) ₁₆ -, -(C(CH ₃ ) ₂ ) ₁₇ -, -(C(CH ₃ ) ₂ ) ₁₈ -, -(C(CH ₃ ) ₂ ) ₁₉ -, -(C(CH ₃ ) ₂ ) ₂₀ -, -(CHC ₂ H ₅ )-, -(CHC ₂ H ₅ ) ₂ -, -(CHC ₂ H ₅ ) ₃ -, - (CHC ₂ H ₅ ) ₄ -, -(CHC ₂ H ₅ ) ₅ -, -(CHC ₂ H ₅ ) ₆ -, -(CHC ₂ H ₅ ) ₇ -, -(CHC ₂ H ₅ ) ₈ -, -(CHC ₂ H ₅ ) ₉ -, - (CHC ₂ H ₅ ) ₁₀ -, -(CHC ₂ H ₅ ) ₁₁ -, -(CHC ₂ H ₅ ) ₁₂ -, -(CHC ₂ H ₅ ) ₁₃ -, -(CHC ₂ H ₅ ) ₁₄ -, -(CHC ₂ H ₅ ) ₁₅ -, - (CHC ₂ H ₅ ) ₁₆ -, -(CHC ₂ H ₅ ) ₁₇ -, -(CHC ₂ H ₅ ) ₁₈ -, -(CHC ₂ H ₅ ) ₁₉ -, -(CHC ₂ H ₅ ) ₂₀ -, -(CH ₂ )- (CHCH ₃ )-(CH ₂ )-, -(CH ₂ )-(CHCH ₃ )-(CH ₂ ) ₂ -, -(CH ₂ )-(CHCH ₃ )-(CH ₂ ) ₃ -, -(CH ₂ )-(CHCH ₃ )- (CH ₂ ) ₁₁ -, -(CH ₂ ) ₂ -(CHCH ₃ )-(CH ₂ )-, -(CH ₂ ) ₃ -(CHCH ₃ )-(CH ₂ )-, -(CH ₂ ) ₁₁ -(CHCH ₃ )-(CH ₂ )-, - (CH(C ₃ H ₇ )-(CH ₂ ) ₂ -, -(CH(C ₃ H ₇ )-(CH ₂ ) ₃ -, -(CH(C ₃ H ₇ )-(CH ₂ ) ₄ -, -(CH(C ₃ H ₇ )-(CH ₂ ) ₅ -, - (CH(C ₃ H ₇ )-(CH ₂ ) ₆ -, -(CH(C ₃ H ₇ )-(CH ₂ ) ₇ -, -(CH(C ₂ H ₅ )-(CH ₂ ) ₂ -, -(CH(C ₂ H ₅ )-(CH ₂ ) ₃ -, - (CH(C ₂ H ₅ )-(CH ₂ ) ₄ -, -(CH(C ₂ H ₅ )-(CH ₂ ) ₅ -, -(CH(C ₂ H ₅ )-(CH ₂ ) ₆ -, -(CH(C ₂ H ₅ )-(CH ₂ ) ₇ -, - (CH ₂ ) ₂ -O-(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -O-(CH ₂ ) ₃ -, -(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -O-(CH ₂ ) ₃ -O- (CH ₂ ) ₃ -, -(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -O-(CH ₂ ) ₆ -, -(CH ₂ ) ₆ -O-(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -O- (CH ₂ ) ₈ -, -(CH ₂ ) ₈ -O-(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -S-(CH ₂ ) ₃ -, -(CH ₂ ) ₂ -S- (CH ₂ ) ₂ -S-(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -S-(CH ₂ ) ₃ -S-(CH ₂ ) ₃ -, -(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -S-(CH ₂ ) ₆ -, -(CH ₂ ) ₆ -S- (CH ₂ ) ₂ -S-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -S-(CH ₂ ) ₈ -, -(CH ₂ ) ₈ -S-(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ - SO ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₄ -SO ₂ -(CH ₂ ) ₄ -, -(CH ₂ ) ₃ -SO ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₂ -SO ₂ - (CH ₂ ) ₂ -, -(CH ₂ ) ₃ -SO ₂ -(CH ₂ ) ₃ -SO ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₆ -, -(CH ₂ ) ₆ - SO ₂ -(CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₈ -, -(CH ₂ ) ₈ -SO ₂ -(CH ₂ ) ₂ -SO ₂ - (CH ₂ ) ₂ -, -(CH ₂ )-S-(CH ₂ ) ₂ -O-(CH ₂ )-, -(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -S- (CH ₂ ) ₂ -, -(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₂ -, -(CH ₂ )-SO ₂ -(CH ₂ ) ₂ -O-(CH ₂ )-, -(CH ₂ )-SO ₂ - (CH ₂ ) ₂ -S-(CH ₂ )-, -(CH ₂ )-O-(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -O-(CH ₂ )-, -(CH ₂ )-S-(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -S- (CH ₂ )-, -(CH ₂ )-SO ₂ -(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -SO ₂ -(CH ₂ )-, -(CH ₂ )-S-(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -S-(CH ₂ )-, - (CH ₂ )-SO ₂ -(CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₂ -SO ₂ -(CH ₂ )-, -(CH ₂ )-O-(CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₂ -O-(CH ₂ )-, - (CH ₂ ) ₂ -S-(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ - (NCH ₃ )-(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -(NCH ₃ )-(CH ₂ ) ₃ -, -(CH ₂ ) ₂ -(NCH ₃ )-(CH ₂ ) ₂ -(NCH ₃ )-(CH ₂ ) ₂ -, - (CH ₂ ) ₃ -(NCH ₃ )-(CH ₂ ) ₃ -(NCH ₃ )-(CH ₂ ) ₃ -, -(CH ₂ ) ₂ -(NCH ₃ )-(CH ₂ ) ₂ -(NCH ₃ )-(CH ₂ ) ₆ -, -(CH ₂ ) ₆ - (NCH ₃ )-(CH ₂ ) ₂ -(NCH ₃ )-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -(NCH ₃ )-(CH ₂ ) ₂ -(NCH ₃ )-(CH ₂ ) ₈ - and-(CH ₂ ) ₈ - (NCH ₃ )-(CH ₂ ) ₂ -(NCH ₃ )-(CH ₂ ) ₂ -; -(CF ₂ )-(CH ₂ )-, -(CH ₂ )-(CF ₂ )-, -(CH ₂ )-(CF ₂ )-(CH ₂ )-, -(CH ₂ )-(CF ₂ )-(CH ₂ ) ₂ -, -(CH ₂ )-(CF ₂ )- (CH ₂ ) ₃ -, -(CH ₂ )-(CF ₂ )-(CH ₂ ) ₄ -, -(CH ₂ )-(CF ₂ )-(CH ₂ ) ₅ -, -(CH ₂ )-(CF ₂ )-(CH ₂ ) ₆ -, -(CH ₂ )-(CF ₂ )- (CH ₂ ) ₇ -, -(CH ₂ )-(CF ₂ )-(CH ₂ ) ₈ -, -(CH ₂ )-(CF ₂ )-(CH ₂ ) ₉ -, -(CH ₂ )-(CF ₂ )-(CH ₂ ) ₁₀ -, -(CH ₂ ) ₂ - (CF ₂ )-(CH ₂ )-, -(CH ₂ ) ₃ -(CF ₂ )-(CH ₂ )-, -(CH ₂ ) ₄ -(CF ₂ )-(CH ₂ )-, -(CH ₂ ) ₅ -(CF ₂ )-(CH ₂ )-, -(CH ₂ ) ₆ - (CF ₂ )-(CH ₂ )-, -(CH ₂ ) ₇ -(CF ₂ )-(CH ₂ )-, -(CH ₂ ) ₈ -(CF ₂ )-(CH ₂ )-, -(CH ₂ ) ₉ -(CF ₂ )-(CH ₂ )-, - (CH ₂ ) ₁₀ -(CF ₂ )-(CH ₂ )-, -(CH ₂ ) ₂ -(CF ₂ )-(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -(CF ₂ )-(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -(CF ₂ )- (CH ₂ ) ₄ -, -(CH ₂ ) ₅ -(CF ₂ )-(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -(CF ₂ )-(CH ₂ )-, -(CH ₂ ) ₂ -(CF ₂ )-(CH ₂ ) ₃ -, -(CH ₂ ) ₂ - (CF ₂ )-(CH ₂ ) ₄ -, -(CH ₂ ) ₂ -(CF ₂ )-(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -(CF ₂ )-(CH ₂ ) ₆ -, -(CH ₂ ) ₂ -(CF ₂ )-(CH ₂ ) ₇ -, - (CH ₂ ) ₂ -(CF ₂ )-(CH ₂ ) ₈ -, -(CH ₂ ) ₂ -(CF ₂ )-(CH ₂ ) ₉ -, -(CH ₂ ) ₃ -(CF ₂ )-(CH ₂ )-, -(CH ₂ ) ₃ -(CF ₂ )- (CH ₂ ) ₂ -, -(CH ₂ ) ₃ -(CF ₂ )-(CH ₂ ) ₄ -, -(CH ₂ ) ₃ -(CF ₂ )-(CH ₂ ) ₅ -, -(CH ₂ ) ₃ -(CF ₂ )-(CH ₂ ) ₆ -, -(CH ₂ ) ₃ - (CF ₂ )-(CH ₂ ) ₇ -, -(CH ₂ ) ₃ -(CF ₂ )-(CH ₂ ) ₈ -, -(CH ₂ ) ₄ -(CF ₂ )-(CH ₂ )-, -(CH ₂ ) ₄ -(CF ₂ )-(CH ₂ ) ₂ -, - (CH ₂ ) ₄ -(CF ₂ )-(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -(CF ₂ )-(CH ₂ ) ₅ -, -(CH ₂ ) ₄ -(CF ₂ )-(CH ₂ ) ₆ -, -(CH ₂ ) ₄ -(CF ₂ )- (CH ₂ ) ₇ -, -(CH ₂ ) ₅ -(CF ₂ )-(CH ₂ )-, -(CH ₂ ) ₅ -(CF ₂ )-(CH ₂ ) ₂ -, -(CH ₂ ) ₅ -(CF ₂ )-(CH ₂ ) ₃ -, -(CH ₂ ) ₅ - (CF ₂ )-(CH ₂ ) ₄ -, -(CH ₂ ) ₅ -(CF ₂ )-(CH ₂ ) ₆ -, -(CH ₂ ) ₆ -(CF ₂ )-(CH ₂ )-, -(CH ₂ ) ₆ -(CF ₂ )-(CH ₂ ) ₂ -, - (CH ₂ ) ₆ -(CF ₂ )-(CH ₂ ) ₃ -, -(CH ₂ ) ₆ -(CF ₂ )-(CH ₂ ) ₄ -, -(CH ₂ ) ₆ -(CF ₂ )-(CH ₂ ) ₅ -, -(CFH)-(CH ₂ )-, -(CH ₂ )-(CFH)-, -(CH ₂ )-(CFH)-(CH ₂ )-, -(CH ₂ )-(CFH)-(CH ₂ ) ₂ -, -(CH ₂ )-(CFH)- (CH ₂ ) ₃ -, -(CH ₂ )-(CFH)-(CH ₂ ) ₄ -, -(CH ₂ )-(CFH)-(CH ₂ ) ₅ -, -(CH ₂ )-(CFH)-(CH ₂ ) ₆ -, -(CH ₂ )- (CFH)-(CH ₂ ) ₇ -, -(CH ₂ )-(CFH)-(CH ₂ ) ₈ -, -(CH ₂ )-(CFH)-(CH ₂ ) ₉ -, -(CH ₂ )-(CFH)-(CH ₂ ) ₁₀ -, - (CH ₂ ) ₂ -(CFH)-(CH ₂ )-, -(CH ₂ ) ₃ -(CFH)-(CH ₂ )-, -(CH ₂ ) ₄ -(CFH)-(CH ₂ )-, -(CH ₂ ) ₅ -(CFH)-(CH ₂ )- , -(CH ₂ ) ₆ -(CFH)-(CH ₂ )-, -(CH ₂ ) ₇ -(CFH)-(CH ₂ )-, -(CH ₂ ) ₈ -(CFH)-(CH ₂ )-, -(CH ₂ ) ₉ -(CFH)- (CH ₂ )-, -(CH ₂ ) ₁₀ -(CFH)-(CH ₂ )-, -(CH ₂ ) ₂ -(CFH)-(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -(CFH)-(CH ₂ ) ₃ -, -(CH ₂ ) ₄ - (CFH)-(CH ₂ ) ₄ -, -(CH ₂ ) ₅ -(CFH)-(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -(CFH)-(CH ₂ )-, -(CH ₂ ) ₂ -(CFH)-(CH ₂ ) ₃ -, - (CH ₂ ) ₂ -(CFH)-(CH ₂ ) ₄ -, -(CH ₂ ) ₂ -(CFH)-(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -(CFH)-(CH ₂ ) ₆ -, -(CH ₂ ) ₂ -(CFH)- (CH ₂ ) ₇ -, -(CH ₂ ) ₂ -(CFH)-(CH ₂ ) ₈ -, -(CH ₂ ) ₂ -(CFH)-(CH ₂ ) ₉ -, -(CH ₂ ) ₃ -(CFH)-(CH ₂ )-, -(CH ₂ ) ₃ - (CFH)-(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -(CFH)-(CH ₂ ) ₄ -, -(CH ₂ ) ₃ -(CFH)-(CH ₂ ) ₅ -, -(CH ₂ ) ₃ -(CFH)-(CH ₂ ) ₆ -, - (CH ₂ ) ₃ -(CFH)-(CH ₂ ) ₇ -, -(CH ₂ ) ₃ -(CFH)-(CH ₂ ) ₈ -, -(CH ₂ ) ₄ -(CFH)-(CH ₂ )-, -(CH ₂ ) ₄ -(CFH)- (CH ₂ ) ₂ -, -(CH ₂ ) ₄ -(CFH)-(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -(CFH)-(CH ₂ ) ₅ -, -(CH ₂ ) ₄ -(CFH)-(CH ₂ ) ₆ -, -(CH ₂ ) ₄ - (CFH)-(CH ₂ ) ₇ -, -(CH ₂ ) ₅ -(CFH)-(CH ₂ )-, -(CH ₂ ) ₅ -(CFH)-(CH ₂ ) ₂ -, -(CH ₂ ) ₅ -(CFH)-(CH ₂ ) ₃ -, - (CH ₂ ) ₅ -(CFH)-(CH ₂ ) ₄ -, -(CH ₂ ) ₅ -(CFH)-(CH ₂ ) ₆ -, -(CH ₂ ) ₆ -(CFH)-(CH ₂ )-, -(CH ₂ ) ₆ -(CFH)- (CH ₂ ) ₂ -, -(CH ₂ ) ₆ -(CFH)-(CH ₂ ) ₃ -, -(CH ₂ ) ₆ -(CFH)-(CH ₂ ) ₄ -, -(CH ₂ ) ₆ -(CFH)-(CH ₂ ) ₅ -, -(CF ₂ ) ₂ -(CH ₂ )-, -(CH ₂ )-(CF ₂ ) ₂ -, -(CH ₂ )-(CF ₂ ) ₂ -(CH ₂ )-, -(CH ₂ )-(CF ₂ ) ₂ -(CH ₂ ) ₂ -, -(CH ₂ )- (CF ₂ ) ₂ -(CH ₂ ) ₃ -, -(CH ₂ )-(CF ₂ ) ₂ -(CH ₂ ) ₄ -, -(CH ₂ )-(CF ₂ ) ₂ -(CH ₂ ) ₅ -, -(CH ₂ )-(CF ₂ ) ₂ -(CH ₂ ) ₆ -, - (CH ₂ )-(CF ₂ ) ₂ -(CH ₂ ) ₇ -, -(CH ₂ )-(CF ₂ ) ₂ -(CH ₂ ) ₈ -, -(CH ₂ )-(CF ₂ ) ₂ -(CH ₂ ) ₉ -, -(CH ₂ ) ₂ -(CF ₂ ) ₂ - (CH ₂ )-, -(CH ₂ ) ₃ -(CF ₂ ) ₂ -(CH ₂ )-, -(CH ₂ ) ₄ -(CF ₂ ) ₂ -(CH ₂ )-, -(CH ₂ ) ₅ -(CF ₂ ) ₂ -(CH ₂ )-, -(CH ₂ ) ₆ - (CF ₂ ) ₂ -(CH ₂ )-, -(CH ₂ ) ₇ -(CF ₂ ) ₂ -(CH ₂ )-, -(CH ₂ ) ₈ -(CF ₂ ) ₂ -(CH ₂ )-, -(CH ₂ ) ₉ -(CF ₂ ) ₂ -(CH ₂ )-, - (CH ₂ ) ₂ -(CF ₂ ) ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -(CF ₂ ) ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -(CF ₂ ) ₂ -(CH ₂ ) ₄ -, -(CH ₂ ) ₅ -(CF ₂ ) ₂ - (CH ₂ ) ₅ -, -(CH ₂ ) ₂ -(CF ₂ ) ₂ -(CH ₂ )-,-(CH ₂ ) ₂ -(CF ₂ ) ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₂ -(CF ₂ ) ₂ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ - (CF ₂ ) ₂ -(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -(CF ₂ ) ₂ -(CH ₂ ) ₆ -, -(CH ₂ ) ₂ -(CF ₂ ) ₂ -(CH ₂ ) ₇ -, -(CH ₂ ) ₂ -(CF ₂ ) ₂ -(CH ₂ ) ₈ -, -(CH ₂ ) ₃ -(CF ₂ ) ₂ -(CH ₂ )-, -(CH ₂ ) ₃ -(CF ₂ ) ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -(CF ₂ ) ₂ -(CH ₂ ) ₄ -, -(CH ₂ ) ₃ -(CF ₂ ) ₂ - (CH ₂ ) ₅ -, -(CH ₂ ) ₃ -(CF ₂ ) ₂ -(CH ₂ ) ₆ -, -(CH ₂ ) ₃ -(CF ₂ ) ₂ -(CH ₂ ) ₇ -, -(CH ₂ ) ₄ -(CF ₂ ) ₂ -(CH ₂ )-, -(CH ₂ ) ₄ - (CF ₂ ) ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₄ -(CF ₂ ) ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -(CF ₂ ) ₂ -(CH ₂ ) ₅ -, -(CH ₂ ) ₄ -(CF ₂ ) ₂ -(CH ₂ ) ₆ -, -(CH ₂ ) ₅ -(CF ₂ ) ₂ -(CH ₂ )-, -(CH ₂ ) ₅ -(CF ₂ ) ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₅ -(CF ₂ ) ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₅ -(CF ₂ ) ₂ - (CH ₂ ) ₄ -, -(CH ₂ ) ₆ -(CF ₂ ) ₂ -(CH ₂ )-, -(CH ₂ ) ₆ -(CF ₂ ) ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₆ -(CF ₂ ) ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₆ - (CF ₂ ) ₂ -(CH ₂ ) ₄ -, -(CFH) ₂ -(CH ₂ )-, -(CH ₂ )-(CFH) ₂ -, -(CH ₂ )-(CFH) ₂ -(CH ₂ )-, -(CH ₂ )-(CFH) ₂ -(CH ₂ ) ₂ -, -(CH ₂ )- (CFH) ₂ -(CH ₂ ) ₃ -, -(CH ₂ )-(CFH) ₂ -(CH ₂ ) ₄ -, -(CH ₂ )-(CFH) ₂ -(CH ₂ ) ₅ -, -(CH ₂ )-(CFH) ₂ -(CH ₂ ) ₆ -, - (CH ₂ )-(CFH) ₂ -(CH ₂ ) ₇ -, -(CH ₂ )-(CFH) ₂ -(CH ₂ ) ₈ -, -(CH ₂ )-(CFH) ₂ -(CH ₂ ) ₉ -, -(CH ₂ ) ₂ -(CFH) ₂ - (CH ₂ )-, -(CH ₂ ) ₃ -(CFH) ₂ -(CH ₂ )-, -(CH ₂ ) ₄ -(CFH) ₂ -(CH ₂ )-, -(CH ₂ ) ₅ -(CFH) ₂ -(CH ₂ )-, -(CH ₂ ) ₆ - (CFH) ₂ -(CH ₂ )-, -(CH ₂ ) ₇ -(CFH) ₂ -(CH ₂ )-, -(CH ₂ ) ₈ -(CFH) ₂ -(CH ₂ )-, -(CH ₂ ) ₉ -(CFH) ₂ -(CH ₂ )-, - (CH ₂ ) ₂ -(CFH) ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -(CFH) ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -(CFH) ₂ -(CH ₂ ) ₄ -, -(CH ₂ ) ₅ - (CFH) ₂ -(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -(CFH) ₂ -(CH ₂ )-,-(CH ₂ ) ₂ -(CFH) ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₂ -(CFH) ₂ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ -(CFH) ₂ -(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -(CFH) ₂ -(CH ₂ ) ₆ -, -(CH ₂ ) ₂ -(CFH) ₂ -(CH ₂ ) ₇ -, -(CH ₂ ) ₂ - (CFH) ₂ -(CH ₂ ) ₈ -, -(CH ₂ ) ₃ -(CFH) ₂ -(CH ₂ )-, -(CH ₂ ) ₃ -(CFH) ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -(CFH) ₂ -(CH ₂ ) ₄ - , -(CH ₂ ) ₃ -(CFH) ₂ -(CH ₂ ) ₅ -, -(CH ₂ ) ₃ -(CFH) ₂ -(CH ₂ ) ₆ -, -(CH ₂ ) ₃ -(CFH) ₂ -(CH ₂ ) ₇ -, -(CH ₂ ) ₄ - (CFH) ₂ -(CH ₂ )-, -(CH ₂ ) ₄ -(CFH) ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₄ -(CFH) ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -(CFH) ₂ -(CH ₂ ) ₅ - , -(CH ₂ ) ₄ -(CFH) ₂ -(CH ₂ ) ₆ -, -(CH ₂ ) ₅ -(CFH) ₂ -(CH ₂ )-, -(CH ₂ ) ₅ -(CFH) ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₅ - (CFH) ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₅ -(CFH) ₂ -(CH ₂ ) ₄ -, -(CH ₂ ) ₆ -(CFH) ₂ -(CH ₂ )-, -(CH ₂ ) ₆ -(CFH) ₂ -(CH ₂ ) ₂ - , -(CH ₂ ) ₆ -(CFH) ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₆ -(CFH) ₂ -(CH ₂ ) ₄ -, -(CF ₂ ) ₃ -(CH ₂ )-, -(CH ₂ )-(CF ₂ ) ₃ -, -(CH ₂ )-(CF ₂ ) ₃ -(CH ₂ )-, -(CH ₂ )-(CF ₂ ) ₃ -(CH ₂ ) ₂ -, -(CH ₂ )- (CF ₂ ) ₃ -(CH ₂ ) ₃ -, -(CH ₂ )-(CF ₂ ) ₃ -(CH ₂ ) ₄ -, -(CH ₂ )-(CF ₂ ) ₃ -(CH ₂ ) ₅ -, -(CH ₂ )-(CF ₂ ) ₃ -(CH ₂ ) ₆ -, - (CH ₂ )-(CF ₂ ) ₃ -(CH ₂ ) ₇ -, -(CH ₂ )-(CF ₂ ) ₃ -(CH ₂ ) ₈ -, -(CH ₂ ) ₂ -(CF ₂ ) ₃ -(CH ₂ )-, -(CH ₂ ) ₃ -(CF ₂ ) ₃ -(CH ₂ )- , -(CH ₂ ) ₄ -(CF ₂ ) ₃ -(CH ₂ )-, -(CH ₂ ) ₅ -(CF ₂ ) ₃ -(CH ₂ )-, -(CH ₂ ) ₆ -(CF ₂ ) ₃ -(CH ₂ )-, -(CH ₂ ) ₇ -(CF ₂ ) ₃ - (CH ₂ )-, -(CH ₂ ) ₈ -(CF ₂ ) ₃ -(CH ₂ )-, -(CH ₂ ) ₂ -(CF ₂ ) ₃ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -(CF ₂ ) ₃ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ - (CF ₂ ) ₃ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ -(CF ₂ ) ₃ -(CH ₂ )-,-(CH ₂ ) ₂ -(CF ₂ ) ₃ -(CH ₂ ) ₃ -, -(CH ₂ ) ₂ -(CF ₂ ) ₃ -(CH ₂ ) ₄ -, - (CH ₂ ) ₂ -(CF ₂ ) ₃ -(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -(CF ₂ ) ₃ -(CH ₂ ) ₆ -, -(CH ₂ ) ₂ -(CF ₂ ) ₃ -(CH ₂ ) ₇ -, -(CH ₂ ) ₃ -(CF ₂ ) ₃ - (CH ₂ )-, -(CH ₂ ) ₃ -(CF ₂ ) ₃ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -(CF ₂ ) ₃ -(CH ₂ ) ₄ -, -(CH ₂ ) ₃ -(CF ₂ ) ₃ -(CH ₂ ) ₅ -, -(CH ₂ ) ₃ - (CF ₂ ) ₃ -(CH ₂ ) ₆ -, -(CH ₂ ) ₄ -(CF ₂ ) ₃ -(CH ₂ )-, -(CH ₂ ) ₄ -(CF ₂ ) ₃ -(CH ₂ ) ₂ -, -(CH ₂ ) ₄ -(CF ₂ ) ₃ -(CH ₂ ) ₃ -, - (CH ₂ ) ₄ -(CF ₂ ) ₃ -(CH ₂ ) ₅ -, -(CH ₂ ) ₅ -(CF ₂ ) ₃ -(CH ₂ )-, -(CH ₂ ) ₅ -(CF ₂ ) ₃ -(CH ₂ ) ₂ -, -(CH ₂ ) ₅ -(CF ₂ ) ₃ - (CH ₂ ) ₃ -, -(CH ₂ ) ₅ -(CF ₂ ) ₃ -(CH ₂ ) ₄ -, (CH ₂ ) ₆ -(CF ₂ ) ₃ -(CH ₂ )-, -(CH ₂ ) ₆ -(CF ₂ ) ₃ -(CH ₂ ) ₂ -, -(CH ₂ ) ₆ - (CF ₂ ) ₃ -(CH ₂ ) ₃ -, -(CF ₂ ) ₄ -(CH ₂ )-, -(CH ₂ )-(CF ₂ ) ₄ -, -(CH ₂ )-(CF ₂ ) ₄ -(CH ₂ )-, -(CH ₂ )-(CF ₂ ) ₄ -(CH ₂ ) ₂ -, -(CH ₂ )- (CF ₂ ) ₄ -(CH ₂ ) ₃ -, -(CH ₂ )-(CF ₂ ) ₄ -(CH ₂ ) ₄ -, -(CH ₂ )-(CF ₂ ) ₄ -(CH ₂ ) ₅ -, -(CH ₂ )-(CF ₂ ) ₄ -(CH ₂ ) ₆ -, - (CH ₂ )-(CF ₂ ) ₄ -(CH ₂ ) ₇ -, -(CH ₂ )-(CF ₂ ) ₄ -(CH ₂ ) ₈ -, -(CH ₂ )-(CF ₂ ) ₄ -(CH ₂ ) ₉ -, -(CH ₂ )-(CF ₂ ) ₄ - (CH ₂ ) ₁₀ -, -(CH ₂ ) ₂ -(CF ₂ ) ₄ -(CH ₂ )-, -(CH ₂ ) ₃ -(CF ₂ ) ₄ -(CH ₂ )-, -(CH ₂ ) ₄ -(CF ₂ ) ₄ -(CH ₂ )-, -(CH ₂ ) ₅ - (CF ₂ ) ₄ -(CH ₂ )-, -(CH ₂ ) ₆ -(CF ₂ ) ₄ -(CH ₂ )-, -(CH ₂ ) ₇ -(CF ₂ ) ₄ -(CH ₂ )-, -(CH ₂ ) ₂ -(CF ₂ ) ₄ -(CH ₂ ) ₂ -, - (CH ₂ ) ₃ -(CF ₂ ) ₄ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -(CF ₂ ) ₄ -(CH ₂ ) ₄ -, -(CH ₂ ) ₅ -(CF ₂ ) ₄ -(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -(CF ₂ ) ₄ - (CH ₂ ) ₃ -, -(CH ₂ ) ₂ -(CF ₂ ) ₄ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ -(CF ₂ ) ₄ -(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -(CF ₂ ) ₄ -(CH ₂ ) ₆ -, - (CH ₂ ) ₃ -(CF ₂ ) ₄ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -(CF ₂ ) ₄ -(CH ₂ ) ₄ -, -(CH ₂ ) ₄ -(CF ₂ ) ₄ -(CH ₂ ) ₂ -, -(CH ₂ ) ₄ -(CF ₂ ) ₄ - (CH ₂ ) ₃ -, -(CH ₂ ) ₅ -(CF ₂ ) ₄ -(CH ₂ ) ₂ -, -(CH ₂ ) ₅ -(CF ₂ ) ₄ -(CH ₂ ) ₃ -, -(CH ₂ ) ₆ -(CF ₂ ) ₄ -(CH ₂ ) ₂ -, -(CF ₂ ) ₅ -(CH ₂ )-, -(CH ₂ )-(CF ₂ ) ₅ -, -(CH ₂ )-(CF ₂ ) ₅ -(CH ₂ )-, -(CH ₂ )-(CF ₂ ) ₅ -(CH ₂ ) ₂ -, -(CH ₂ )- (CF ₂ ) ₅ -(CH ₂ ) ₃ -, -(CH ₂ )-(CF ₂ ) ₅ -(CH ₂ ) ₄ -, -(CH ₂ )-(CF ₂ ) ₅ -(CH ₂ ) ₅ -, -(CH ₂ )-(CF ₂ ) ₅ -(CH ₂ ) ₆ -, - (CH ₂ ) ₂ -(CF ₂ ) ₅ -(CH ₂ )-, -(CH ₂ ) ₃ -(CF ₂ ) ₅ -(CH ₂ )-, -(CH ₂ ) ₄ -(CF ₂ ) ₅ -(CH ₂ )-, -(CH ₂ ) ₅ -(CF ₂ ) ₅ - (CH ₂ )-, -(CH ₂ ) ₆ -(CF ₂ ) ₅ -(CH ₂ )-, -(CH ₂ ) ₂ -(CF ₂ ) ₅ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -(CF ₂ ) ₅ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ - (CF ₂ ) ₅ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ -(CF ₂ ) ₅ -(CH ₂ ) ₃ -, -(CH ₂ ) ₂ -(CF ₂ ) ₅ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ -(CF ₂ ) ₅ -(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -(CF ₂ ) ₅ -(CH ₂ ) ₆ -, -(CH ₂ ) ₃ -(CF ₂ ) ₅ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -(CF ₂ ) ₅ -(CH ₂ ) ₄ -, -(CH ₂ ) ₄ -(CF ₂ ) ₅ - (CH ₂ ) ₂ -, -(CH ₂ ) ₄ -(CF ₂ ) ₅ -(CH ₂ ) ₃ -, -(CH ₂ ) ₅ -(CF ₂ ) ₅ -(CH ₂ ) ₂ -, -(CHCF ₃ )-(CH ₂ )-, -(CH ₂ )-(CHCF ₃ )-, -(CH ₂ )-(CHCF ₃ )-(CH ₂ )-, -(CH ₂ )-(CHCF ₃ )-(CH ₂ ) ₂ -, - (CH ₂ )-(CHCF ₃ )-(CH ₂ ) ₃ -, -(CHC ₂ H ₅ )-(CH ₂ )-(CHCF ₃ )-(CH ₂ ) ₃ -, -(CH ₂ )-(CHCF ₃ )-(CH ₂ ) ₄ -, - (CH ₂ )-(CHCF ₃ )-(CH ₂ ) ₅ -, -(CH ₂ )-(CHCF ₃ )-(CH ₂ ) ₆ -, -(CH ₂ )-(CHCF ₃ )-(CH ₂ ) ₇ -, -(CH ₂ )- (CHCF ₃ )-(CH ₂ ) ₈ -, -(CH ₂ )-(CHCF ₃ )-(CH ₂ ) ₉ -, -(CH ₂ )-(CHCF ₃ )-(CH ₂ ) ₁₀ -, -(CH ₂ ) ₂ -(CHCF ₃ )- (CH ₂ )-, -(CH ₂ ) ₃ -(CHCF ₃ )-(CH ₂ )-, -(CH ₂ ) ₄ -(CHCF ₃ )-(CH ₂ )-, -(CH ₂ ) ₅ -(CHCF ₃ )-(CH ₂ )-, - (CH ₂ ) ₆ -(CHCF ₃ )-(CH ₂ )-, -(CH ₂ ) ₇ -(CHCF ₃ )-(CH ₂ )-, -(CH ₂ ) ₈ -(CHCF ₃ )-(CH ₂ )-, -(CH ₂ ) ₉ - (CHCF ₃ )-(CH ₂ )-, -(CH ₂ ) ₁₀ -(CHCF ₃ )-(CH ₂ )-, -(CH ₂ ) ₂ -(CHCF ₃ )-(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -(CHCF ₃ )- (CH ₂ ) ₃ -, -(CH ₂ ) ₄ -(CHCF ₃ )-(CH ₂ ) ₄ -, -(CH ₂ ) ₅ -(CHCF ₃ )-(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -(CHCF ₃ )-(CH ₂ ) ₃ -, - (CH ₂ ) ₂ -(CHCF ₃ )-(CH ₂ ) ₄ -, -(CH ₂ ) ₂ -(CHCF ₃ )-(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -(CHCF ₃ )-(CH ₂ ) ₆ -, -(CH ₂ ) ₂ - (CHCF ₃ )-(CH ₂ ) ₇ -, -(CH ₂ ) ₂ -(CHCF ₃ )-(CH ₂ ) ₈ -, -(CH ₂ ) ₂ -(CHCF ₃ )-(CH ₂ ) ₉ -, -(CH ₂ ) ₃ -(CHCF ₃ )- (CH ₂ ) ₂ -, -(CH ₂ ) ₃ -(CHCF ₃ )-(CH ₂ ) ₄ -, -(CH ₂ ) ₃ -(CHCF ₃ )-(CH ₂ ) ₅ -, -(CH ₂ ) ₃ -(CHCF ₃ )-(CH ₂ ) ₆ -, - (CH ₂ ) ₃ -(CHCF ₃ )-(CH ₂ ) ₇ -, -(CH ₂ ) ₃ -(CHCF ₃ )-(CH ₂ ) ₈ -, -(CH ₂ ) ₄ -(CHCF ₃ )-(CH ₂ ) ₂ -, -(CH ₂ ) ₄ - (CHCF ₃ )-(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -(CHCF ₃ )-(CH ₂ ) ₅ -, -(CH ₂ ) ₄ -(CHCF ₃ )-(CH ₂ ) ₆ -, -(CH ₂ ) ₄ -(CHCF ₃ )- (CH ₂ ) ₇ -, -(CH ₂ ) ₅ -(CHCF ₃ )-(CH ₂ ) ₂ -, -(CH ₂ ) ₅ -(CHCF ₃ )-(CH ₂ ) ₃ -, -(CH ₂ ) ₅ -(CHCF ₃ )-(CH ₂ ) ₄ -, - (CH ₂ ) ₅ -(CHCF ₃ )-(CH ₂ ) ₆ -, -(CH ₂ ) ₆ -(CHCF ₃ )-(CH ₂ ) ₂ -, -(CH ₂ ) ₆ -(CHCF ₃ )-(CH ₂ ) ₃ -, -(CH ₂ ) ₆ - (CHCF ₃ )-(CH ₂ ) ₄ -, -(CH ₂ ) ₆ -(CHCF ₃ )-(CH ₂ ) ₅ -, -(CHCF ₃ ) ₂ -(CH ₂ )-, -(CH ₂ )-(CHCF ₃ ) ₂ -, -(CH ₂ )-(CHCF ₃ ) ₂ -(CH ₂ )-, -(CH ₂ )-(CHCF ₃ ) ₂ -(CH ₂ ) ₂ -, -(CH ₂ )-(CHCF ₃ ) ₂ -(CH ₂ ) ₃ -, -(CH ₂ )-(CHCF ₃ ) ₂ -(CH ₂ ) ₄ -, -(CH ₂ )-(CHCF ₃ ) ₂ -(CH ₂ ) ₅ -, -(CH ₂ )- (CHCF ₃ ) ₂ -(CH ₂ ) ₆ -, -(CH ₂ )-(CHCF ₃ ) ₂ -(CH ₂ ) ₇ -, -(CH ₂ )-(CHCF ₃ ) ₂ -(CH ₂ ) ₈ -, -(CH ₂ )- (CHCF ₃ ) ₂ -(CH ₂ ) ₉ -, -(CH ₂ ) ₂ -(CHCF ₃ ) ₂ -(CH ₂ )-, -(CH ₂ ) ₃ -(CHCF ₃ ) ₂ -(CH ₂ )-, -(CH ₂ ) ₄ - (CHCF ₃ ) ₂ -(CH ₂ )-, -(CH ₂ ) ₅ -(CHCF ₃ ) ₂ -(CH ₂ )-, -(CH ₂ ) ₆ -(CHCF ₃ ) ₂ -(CH ₂ )-, -(CH ₂ ) ₇ - (CHCF ₃ ) ₂ -(CH ₂ )-, -(CH ₂ ) ₈ -(CHCF ₃ ) ₂ -(CH ₂ )-, -(CH ₂ ) ₉ -(CHCF ₃ ) ₂ -(CH ₂ )-, -(CH ₂ ) ₂ - (CHCF ₃ ) ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -(CHCF ₃ ) ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -(CHCF ₃ ) ₂ -(CH ₂ ) ₄ -, -(CH ₂ ) ₅ - (CHCF ₃ ) ₂ -(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -(CHCF ₃ ) ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₂ -(CHCF ₃ ) ₂ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ - (CHCF ₃ ) ₂ -(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -(CHCF ₃ ) ₂ -(CH ₂ ) ₆ -, -(CH ₂ ) ₂ -(CHCF ₃ ) ₂ -(CH ₂ ) ₇ -, -(CH ₂ ) ₂ - (CHCF ₃ ) ₂ -(CH ₂ ) ₈ -, -(CH ₂ ) ₃ -(CHCF ₃ ) ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -(CHCF ₃ ) ₂ -(CH ₂ ) ₄ -, -(CH ₂ ) ₃ - (CHCF ₃ ) ₂ -(CH ₂ ) ₅ -, -(CH ₂ ) ₃ -(CHCF ₃ ) ₂ -(CH ₂ ) ₆ -, -(CH ₂ ) ₃ -(CHCF ₃ ) ₂ -(CH ₂ ) ₇ -, -(CH ₂ ) ₄ - (CHCF ₃ ) ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₄ -(CHCF ₃ ) ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -(CHCF ₃ ) ₂ -(CH ₂ ) ₅ -, -(CH ₂ ) ₄ - (CHCF ₃ ) ₂ -(CH ₂ ) ₆ -, -(CH ₂ ) ₅ -(CHCF ₃ ) ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₅ -(CHCF ₃ ) ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₅ - (CHCF ₃ ) ₂ -(CH ₂ ) ₄ -, -(CH ₂ ) ₆ -(CHCF ₃ ) ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₆ -(CHCF ₃ ) ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₆ - (CHCF ₃ ) ₂ -(CH ₂ ) ₄ -, -(CHCF ₃ ) ₃ -(CH ₂ )-, -(CH ₂ )-(CHCF ₃ ) ₃ -, -(CH ₂ )-(CHCF ₃ ) ₃ -(CH ₂ )-, -(CH ₂ )-(CHCF ₃ ) ₃ -(CH ₂ ) ₂ -, -(CH ₂ )-(CHCF ₃ ) ₃ -(CH ₂ ) ₃ -, -(CH ₂ )-(CHCF ₃ ) ₃ -(CH ₂ ) ₄ -, -(CH ₂ )-(CHCF ₃ ) ₃ -(CH ₂ ) ₅ -, -(CH ₂ )- (CHCF ₃ ) ₃ -(CH ₂ ) ₆ -, -(CH ₂ )-(CHCF ₃ ) ₃ -(CH ₂ ) ₇ -, -(CH ₂ )-(CHCF ₃ ) ₃ -(CH ₂ ) ₈ -, -(CH ₂ ) ₂ - (CHCF ₃ ) ₃ -(CH ₂ )-, -(CH ₂ ) ₃ -(CHCF ₃ ) ₃ -(CH ₂ )-, -(CH ₂ ) ₄ -(CHCF ₃ ) ₃ -(CH ₂ )-, -(CH ₂ ) ₅ - (CHCF ₃ ) ₃ -(CH ₂ )-, -(CH ₂ ) ₆ -(CHCF ₃ ) ₃ -(CH ₂ )-, -(CH ₂ ) ₇ -(CHCF ₃ ) ₃ -(CH ₂ )-, -(CH ₂ ) ₈ - (CHCF ₃ ) ₃ -(CH ₂ )-, -(CH ₂ ) ₂ -(CHCF ₃ ) ₃ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -(CHCF ₃ ) ₃ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ - (CHCF ₃ ) ₃ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ -(CHCF ₃ ) ₃ -(CH ₂ ) ₃ -, -(CH ₂ ) ₂ -(CHCF ₃ ) ₃ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ - (CHCF ₃ ) ₃ -(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -(CHCF ₃ ) ₃ -(CH ₂ ) ₆ -, -(CH ₂ ) ₂ -(CHCF ₃ ) ₃ -(CH ₂ ) ₇ -, -(CH ₂ ) ₃ - (CHCF ₃ ) ₃ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -(CHCF ₃ ) ₃ -(CH ₂ ) ₄ -, -(CH ₂ ) ₃ -(CHCF ₃ ) ₃ -(CH ₂ ) ₅ -, -(CH ₂ ) ₃ - (CHCF ₃ ) ₃ -(CH ₂ ) ₆ -, -(CH ₂ ) ₄ -(CHCF ₃ ) ₃ -(CH ₂ ) ₂ -, -(CH ₂ ) ₄ -(CHCF ₃ ) ₃ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ - (CHCF ₃ ) ₃ -(CH ₂ ) ₅ -, -(CH ₂ ) ₅ -(CHCF ₃ ) ₃ -(CH ₂ ) ₂ -, -(CH ₂ ) ₅ -(CHCF ₃ ) ₃ -(CH ₂ ) ₃ -, -(CH ₂ ) ₅ - (CHCF ₃ ) ₃ -(CH ₂ ) ₄ -, -(CH ₂ ) ₆ -(CHCF ₃ ) ₃ -(CH ₂ ) ₂ -, -(CH ₂ ) ₆ -(CHCF ₃ ) ₃ -(CH ₂ ) ₃ -, -(CHCF ₃ ) ₄ -(CH ₂ )-, -(CH ₂ )-(CHCF ₃ ) ₄ -, -(CH ₂ )-(CHCF ₃ ) ₄ -(CH ₂ )-, -(CH ₂ )-(CHCF ₃ ) ₄ -(CH ₂ ) ₂ -, -(CH ₂ )-(CHCF ₃ ) ₄ -(CH ₂ ) ₃ -, -(CH ₂ )-(CHCF ₃ ) ₄ -(CH ₂ ) ₄ -, -(CH ₂ )-(CHCF ₃ ) ₄ -(CH ₂ ) ₅ -, -(CH ₂ )- (CHCF ₃ ) ₄ -(CH ₂ ) ₆ -, -(CH ₂ )-(CHCF ₃ ) ₄ -(CH ₂ ) ₇ -, -(CH ₂ )-(CHCF ₃ ) ₄ -(CH ₂ ) ₈ -, -(CH ₂ )- (CHCF ₃ ) ₄ -(CH ₂ ) ₉ -, -(CH ₂ )-(CHCF ₃ ) ₄ -(CH ₂ ) ₁₀ -, -(CH ₂ ) ₂ -(CHCF ₃ ) ₄ -(CH ₂ )-, -(CH ₂ ) ₃ - (CHCF ₃ ) ₄ -(CH ₂ )-, -(CH ₂ ) ₄ -(CHCF ₃ ) ₄ -(CH ₂ )-, -(CH ₂ ) ₅ -(CHCF ₃ ) ₄ -(CH ₂ )-, -(CH ₂ ) ₆ - (CHCF ₃ ) ₄ -(CH ₂ )-, -(CH ₂ ) ₇ -(CHCF ₃ ) ₄ -(CH ₂ )-, -(CH ₂ ) ₂ -(CHCF ₃ ) ₄ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ - (CHCF ₃ ) ₄ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -(CHCF ₃ ) ₄ -(CH ₂ ) ₄ -, -(CH ₂ ) ₅ -(CHCF ₃ ) ₄ -(CH ₂ ) ₅ -, -(CH ₂ ) ₂ - (CHCF ₃ ) ₄ -(CH ₂ ) ₃ -, -(CH ₂ ) ₂ -(CHCF ₃ ) ₄ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ -(CHCF ₃ ) ₄ -(CH ₂ ) ₅ -, -(CH ₂ ) ₂ - (CHCF ₃ ) ₄ -(CH ₂ ) ₆ -, -(CH ₂ ) ₃ -(CHCF ₃ ) ₄ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -(CHCF ₃ ) ₄ -(CH ₂ ) ₄ -, -(CH ₂ ) ₄ - (CHCF ₃ ) ₄ -(CH ₂ ) ₂ -, -(CH ₂ ) ₄ -(CHCF ₃ ) ₄ -(CH ₂ ) ₃ -, -(CH ₂ ) ₅ -(CHCF ₃ ) ₄ -(CH ₂ ) ₂ -, -(CH ₂ ) ₅ - (CHCF ₃ ) ₄ -(CH ₂ ) ₃ -, -(CH ₂ ) ₆ -(CHCF ₃ ) ₄ -(CH ₂ ) ₂ -, -(CHCF ₃ ) ₅ -(CH ₂ )-, -(CH ₂ )-(CHCF ₃ ) ₅ -, -(CH ₂ )-(CHCF ₃ ) ₅ -(CH ₂ )-, -(CH ₂ )-(CHCF ₃ ) ₅ -(CH ₂ ) ₂ -, -(CH ₂ )-(CHCF ₃ ) ₅ -(CH ₂ ) ₃ -, -(CH ₂ )-(CHCF ₃ ) ₅ -(CH ₂ ) ₄ -, -(CH ₂ )-(CHCF ₃ ) ₅ -(CH ₂ ) ₅ -, -(CH ₂ )- (CHCF ₃ ) ₅ -(CH ₂ ) ₆ -, -(CH ₂ ) ₂ -(CHCF ₃ ) ₅ -(CH ₂ )-, -(CH ₂ ) ₃ -(CHCF ₃ ) ₅ -(CH ₂ )-, -(CH ₂ ) ₄ - (CHCF ₃ ) ₅ -(CH ₂ )-, -(CH ₂ ) ₅ -(CHCF ₃ ) ₅ -(CH ₂ )-, -(CH ₂ ) ₆ -(CHCF ₃ ) ₅ -(CH ₂ )-, -(CH ₂ ) ₂ - (CHCF ₃ ) ₅ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -(CHCF ₃ ) ₅ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -(CHCF ₃ ) ₅ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ - (CHCF ₃ ) ₅ -(CH ₂ ) ₃ -, -(CH ₂ ) ₂ -(CHCF ₃ ) ₅ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ -(CHCF ₃ ) ₅ -(CH ₂ ) ₅ -, -(CH ₂ ) ₂ - (CHCF ₃ ) ₅ -(CH ₂ ) ₆ -, -(CH ₂ ) ₃ -(CHCF ₃ ) ₅ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -(CHCF ₃ ) ₅ -(CH ₂ ) ₄ -, -(CH ₂ ) ₄ - (CHCF ₃ ) ₅ -(CH ₂ ) ₂ -, -(CH ₂ ) ₄ -(CHCF ₃ ) ₅ -(CH ₂ ) ₃ -, -(CH ₂ ) ₅ -(CHCF ₃ ) ₅ -(CH ₂ ) ₂ -, -[C(CH ₃ )CF ₃ ]-(CH ₂ )-, -(CH ₂ )-[C(CH ₃ )CF ₃ ]-, -(CH ₂ )-[C(CH ₃ )CF ₃ ]-(CH ₂ )-, -(CH ₂ )- [C(CH ₃ )CF ₃ ]-(CH ₂ ) ₂ -, -(CH ₂ )-[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₃ -, -(CH ₂ )-[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₄ -, -(CH ₂ )- [C(CH ₃ )CF ₃ ]-(CH ₂ ) ₅ -, -(CH ₂ )-[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₆ -, -(CH ₂ )-[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₇ -, -(CH ₂ )- [C(CH ₃ )CF ₃ ]-(CH ₂ ) ₈ -, -(CH ₂ )-[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₉ -, -(CH ₂ )-[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₁₀ -, - (CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ]-(CH ₂ )-, -(CH ₂ ) ₃ -[C(CH ₃ )CF ₃ ]-(CH ₂ )-, -(CH ₂ ) ₄ -[C(CH ₃ )CF ₃ ]-(CH ₂ )-, - (CH ₂ ) ₅ -[C(CH ₃ )CF ₃ ]-(CH ₂ )-, -(CH ₂ ) ₆ -[C(CH ₃ )CF ₃ ]-(CH ₂ )-, -(CH ₂ ) ₇ -[C(CH ₃ )CF ₃ ]-(CH ₂ )-, - (CH ₂ ) ₈ -[C(CH ₃ )CF ₃ ]-(CH ₂ )-, -(CH ₂ ) ₉ -[C(CH ₃ )CF ₃ ]-(CH ₂ )-, -(CH ₂ ) ₁₀ -[C(CH ₃ )CF ₃ ]-(CH ₂ )-, - (CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₄ - , -(CH ₂ ) ₅ -[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₃ -, -(CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ]- (CH ₂ ) ₄ -, -(CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₆ -, -(CH ₂ ) ₂ - [C(CH ₃ )CF ₃ ]-(CH ₂ ) ₇ -, -(CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₈ -, -(CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₉ -, - (CH ₂ ) ₃ -[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₄ -, -(CH ₂ ) ₃ -[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₅ - , -(CH ₂ ) ₃ -[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₆ -, -(CH ₂ ) ₃ -[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₇ -, -(CH ₂ ) ₃ -[C(CH ₃ )CF ₃ ]- (CH ₂ ) ₈ -, -(CH ₂ ) ₄ -[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₂ -, -(CH ₂ ) ₄ -[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₃ -, -(CH ₂ ) ₄ - [C(CH ₃ )CF ₃ ]-(CH ₂ ) ₅ -, -(CH ₂ ) ₄ -[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₆ -, -(CH ₂ ) ₄ -[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₇ -, - (CH ₂ ) ₅ -[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₂ -, -(CH ₂ ) ₅ -[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₃ -, -(CH ₂ ) ₅ -[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₄ - , -(CH ₂ ) ₅ -[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₆ -, -(CH ₂ ) ₆ -[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₂ -, -(CH ₂ ) ₆ -[C(CH ₃ )CF ₃ ]- (CH ₂ ) ₃ -, -(CH ₂ ) ₆ -[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₄ -, -(CH ₂ ) ₆ -[C(CH ₃ )CF ₃ ]-(CH ₂ ) ₅ -, -[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ )-, -(CH ₂ )-[C(CH ₃ )CF ₃ ] ₂ -, -(CH ₂ )-[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ )-, -(CH ₂ )- [C(CH ₃ )CF ₃ ] ₂ -(CH ₂ ) ₂ -, -(CH ₂ )-[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ ) ₃ -, -(CH ₂ )-[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ ) ₄ -, - (CH ₂ )-[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ ) ₅ -, -(CH ₂ )-[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ ) ₆ -, -(CH ₂ )-[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ ) ₇ - , -(CH ₂ )-[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ ) ₈ -, -(CH ₂ )-[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ ) ₉ -, -(CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ] ₂ - (CH ₂ )-, -(CH ₂ ) ₃ -[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ )-, -(CH ₂ ) ₄ -[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ )-, -(CH ₂ ) ₅ - [C(CH ₃ )CF ₃ ] ₂ -(CH ₂ )-, -(CH ₂ ) ₆ -[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ )-, -(CH ₂ ) ₇ -[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ )-, - (CH ₂ ) ₈ -[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ )-, -(CH ₂ ) ₉ -[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ )-, -(CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ] ₂ - (CH ₂ ) ₂ -, -(CH ₂ ) ₃ -[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ ) ₄ -, -(CH ₂ ) ₅ - [C(CH ₃ )CF ₃ ] ₂ -(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ ) ₄ -, - (CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ ) ₆ -, -(CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ] ₂ - (CH ₂ ) ₇ -, -(CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ ) ₈ -, -(CH ₂ ) ₃ -[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ - [C(CH ₃ )CF ₃ ] ₂ -(CH ₂ ) ₄ -, -(CH ₂ ) ₃ -[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ ) ₅ -, -(CH ₂ ) ₃ -[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ ) ₆ -, - (CH ₂ ) ₃ -[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ ) ₇ -, -(CH ₂ ) ₄ -[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₄ -[C(CH ₃ )CF ₃ ] ₂ - (CH ₂ ) ₃ -, -(CH ₂ ) ₄ -[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ ) ₅ -, -(CH ₂ ) ₄ -[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ ) ₆ -, -(CH ₂ ) ₅ - [C(CH ₃ )CF ₃ ] ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₅ -[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₅ -[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ ) ₄ -, - (CH ₂ ) ₆ -[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₆ -[C(CH ₃ )CF ₃ ] ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₆ -[C(CH ₃ )CF ₃ ] ₂ - (CH ₂ ) ₄ -, -[C(CH ₃ )CF ₃ ] ₃ -(CH ₂ )-, -(CH ₂ )-[C(CH ₃ )CF ₃ ] ₃ -, -(CH ₂ )-[C(CH ₃ )CF ₃ ] ₃ -(CH ₂ )-, -(CH ₂ )- [C(CH ₃ )CF ₃ ] ₃ -(CH ₂ ) ₂ -, -(CH ₂ )-[C(CH ₃ )CF ₃ ] ₃ -(CH ₂ ) ₃ -, -(CH ₂ )-[C(CH ₃ )CF ₃ ] ₃ -(CH ₂ ) ₄ -, - (CH ₂ )-[C(CH ₃ )CF ₃ ] ₃ -(CH ₂ ) ₅ -, -(CH ₂ )-[C(CH ₃ )CF ₃ ] ₃ -(CH ₂ ) ₆ -, -(CH ₂ )-[C(CH ₃ )CF ₃ ] ₃ -(CH ₂ ) ₇ - , -(CH ₂ )-[C(CH ₃ )CF ₃ ] ₃ -(CH ₂ ) ₈ -, -(CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ] ₃ -(CH ₂ )-, -(CH ₂ ) ₃ -[C(CH ₃ )CF ₃ ] ₃ - (CH ₂ )-, -(CH ₂ ) ₄ -[C(CH ₃ )CF ₃ ] ₃ -(CH ₂ )-, -(CH ₂ ) ₅ -[C(CH ₃ )CF ₃ ] ₃ -(CH ₂ )-, -(CH ₂ ) ₆ - [C(CH ₃ )CF ₃ ] ₃ -(CH ₂ )-, -(CH ₂ ) ₇ -[C(CH ₃ )CF ₃ ] ₃ -(CH ₂ )-, -(CH ₂ ) ₈ -[C(CH ₃ )CF ₃ ] ₃ -(CH ₂ )-, - (CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ] ₃ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -[C(CH ₃ )CF ₃ ] ₃ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -[C(CH ₃ )CF ₃ ] ₃ - (CH ₂ ) ₄ -, -(CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ] ₃ -(CH ₂ ) ₃ -, -(CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ] ₃ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ - [C(CH ₃ )CF ₃ ] ₃ -(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ] ₃ -(CH ₂ ) ₆ -, -(CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ] ₃ -(CH ₂ ) ₇ -, - (CH ₂ ) ₃ -[C(CH ₃ )CF ₃ ] ₃ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -[C(CH ₃ )CF ₃ ] ₃ -(CH ₂ ) ₄ -, -(CH ₂ ) ₃ -[C(CH ₃ )CF ₃ ] ₃ - (CH ₂ ) ₅ -, -(CH ₂ ) ₃ -[C(CH ₃ )CF ₃ ] ₃ -(CH ₂ ) ₆ -, -(CH ₂ ) ₄ -[C(CH ₃ )CF ₃ ] ₃ -(CH ₂ ) ₂ -, -(CH ₂ ) ₄ - [C(CH ₃ )CF ₃ ] ₃ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -[C(CH ₃ )CF ₃ ] ₃ -(CH ₂ ) ₅ -, -(CH ₂ ) ₅ -[C(CH ₃ )CF ₃ ] ₃ -(CH ₂ ) ₂ -, - (CH ₂ ) ₅ -[C(CH ₃ )CF ₃ ] ₃ -(CH ₂ ) ₃ -, -(CH ₂ ) ₅ -[C(CH ₃ )CF ₃ ] ₃ -(CH ₂ ) ₄ -, -(CH ₂ ) ₆ -[C(CH ₃ )CF ₃ ] ₃ - (CH ₂ ) ₂ -, -(CH ₂ ) ₆ -[C(CH ₃ )CF ₃ ] ₃ -(CH ₂ ) ₃ -, -[C(CH ₃ )CF ₃ ] ₄ -(CH ₂ )-, -(CH ₂ )-[C(CH ₃ )CF ₃ ] ₄ -, -(CH ₂ )-[C(CH ₃ )CF ₃ ] ₄ -(CH ₂ )-, -(CH ₂ )- [C(CH ₃ )CF ₃ ] ₄ -(CH ₂ ) ₂ -, -(CH ₂ )-[C(CH ₃ )CF ₃ ] ₄ -(CH ₂ ) ₃ -, -(CH ₂ )-[C(CH ₃ )CF ₃ ] ₄ -(CH ₂ ) ₄ -, - (CH ₂ )-[C(CH ₃ )CF ₃ ] ₄ -(CH ₂ ) ₅ -, -(CH ₂ )-[C(CH ₃ )CF ₃ ] ₄ -(CH ₂ ) ₆ -, -(CH ₂ )-[C(CH ₃ )CF ₃ ] ₄ -(CH ₂ ) ₇ - , -(CH ₂ )-[C(CH ₃ )CF ₃ ] ₄ -(CH ₂ ) ₈ -, -(CH ₂ )-[C(CH ₃ )CF ₃ ] ₄ -(CH ₂ ) ₉ -, -(CH ₂ )-[C(CH ₃ )CF ₃ ] ₄ - (CH ₂ ) ₁₀ -, -(CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ] ₄ -(CH ₂ )-, -(CH ₂ ) ₃ -[C(CH ₃ )CF ₃ ] ₄ -(CH ₂ )-, -(CH ₂ ) ₄ - [C(CH ₃ )CF ₃ ] ₄ -(CH ₂ )-, -(CH ₂ ) ₅ -[C(CH ₃ )CF ₃ ] ₄ -(CH ₂ )-, -(CH ₂ ) ₆ -[C(CH ₃ )CF ₃ ] ₄ -(CH ₂ )-, - (CH ₂ ) ₇ -[C(CH ₃ )CF ₃ ] ₄ -(CH ₂ )-, -(CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ] ₄ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -[C(CH ₃ )CF ₃ ] ₄ - (CH ₂ ) ₃ -, -(CH ₂ ) ₄ -[C(CH ₃ )CF ₃ ] ₄ -(CH ₂ ) ₄ -, -(CH ₂ ) ₅ -[C(CH ₃ )CF ₃ ] ₄ -(CH ₂ ) ₅ -, -(CH ₂ ) ₂ - [C(CH ₃ )CF ₃ ] ₄ -(CH ₂ ) ₃ -, -(CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ] ₄ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ] ₄ -(CH ₂ ) ₅ -, - (CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ] ₄ -(CH ₂ ) ₆ -, -(CH ₂ ) ₃ -[C(CH ₃ )CF ₃ ] ₄ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -[C(CH ₃ )CF ₃ ] ₄ - (CH ₂ ) ₄ -, -(CH ₂ ) ₄ -[C(CH ₃ )CF ₃ ] ₄ -(CH ₂ ) ₂ -, -(CH ₂ ) ₄ -[C(CH ₃ )CF ₃ ] ₄ -(CH ₂ ) ₃ -, -(CH ₂ ) ₅ - [C(CH ₃ )CF ₃ ] ₄ -(CH ₂ ) ₂ -, -(CH ₂ ) ₅ -[C(CH ₃ )CF ₃ ] ₄ -(CH ₂ ) ₃ -, -(CH ₂ ) ₆ -[C(CH ₃ )CF ₃ ] ₄ -(CH ₂ ) ₂ -, -[C(CH ₃ )CF ₃ ] ₅ -(CH ₂ )-, -(CH ₂ )-[C(CH ₃ )CF ₃ ] ₅ -, -(CH ₂ )-[C(CH ₃ )CF ₃ ] ₅ -(CH ₂ )-, -(CH ₂ )- [C(CH ₃ )CF ₃ ] ₅ -(CH ₂ ) ₂ -, -(CH ₂ )-[C(CH ₃ )CF ₃ ] ₅ -(CH ₂ ) ₃ -, -(CH ₂ )-[C(CH ₃ )CF ₃ ] ₅ -(CH ₂ ) ₄ -, - (CH ₂ )-[C(CH ₃ )CF ₃ ] ₅ -(CH ₂ ) ₅ -, -(CH ₂ )-[C(CH ₃ )CF ₃ ] ₅ -(CH ₂ ) ₆ -, -(CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ] ₅ -(CH ₂ )- , -(CH ₂ ) ₃ -[C(CH ₃ )CF ₃ ] ₅ -(CH ₂ )-, -(CH ₂ ) ₄ -[C(CH ₃ )CF ₃ ] ₅ -(CH ₂ )-, -(CH ₂ ) ₅ -[C(CH ₃ )CF ₃ ] ₅ - (CH ₂ )-, -(CH ₂ ) ₆ -[C(CH ₃ )CF ₃ ] ₅ -(CH ₂ )-, -(CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ] ₅ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ - [C(CH ₃ )CF ₃ ] ₅ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -[C(CH ₃ )CF ₃ ] ₅ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ] ₅ -(CH ₂ ) ₃ -, - (CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ] ₅ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ] ₅ -(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -[C(CH ₃ )CF ₃ ] ₅ - (CH ₂ ) ₆ -, -(CH ₂ ) ₃ -[C(CH ₃ )CF ₃ ] ₅ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -[C(CH ₃ )CF ₃ ] ₅ -(CH ₂ ) ₄ -, -(CH ₂ ) ₄ - [C(CH ₃ )CF ₃ ] ₅ -(CH ₂ ) ₂ -, -(CH ₂ ) ₄ -[C(CH ₃ )CF ₃ ] ₅ -(CH ₂ ) ₃ -, -(CH ₂ ) ₅ -[C(CH ₃ )CF ₃ ] ₅ -(CH ₂ ) ₂ -, -[CH(CH ₂ CF ₃ )]-(CH ₂ )-, -(CH ₂ )-[CH(CH ₂ CF ₃ )]-, -(CH ₂ )-[CH(CH ₂ CF ₃ )]-(CH ₂ )-, -(CH ₂ )- [CH(CH ₂ CF ₃ )]-(CH ₂ ) ₂ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )] -(CH ₂ ) ₃ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )]-(CH ₂ ) ₄ -, - (CH ₂ )-[CH(CH ₂ CF ₃ )]-(CH ₂ ) ₅ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )]-(CH ₂ ) ₆ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )]- (CH ₂ ) ₇ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )]-(CH ₂ ) ₈ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )]-(CH ₂ ) ₉ -, -(CH ₂ )- [CH(CH ₂ CF ₃ )]-(CH ₂ ) ₁₀ -, -(CH ₂ ) ₂ -[CH(CH ₂ CF ₃ )]-(CH ₂ )-, -(CH ₂ ) ₃ -[CH(CH ₂ CF ₃ )]-(CH ₂ )-, - (CH ₂ ) ₄ -[CH(CH ₂ CF ₃ )]-(CH ₂ )-, -(CH ₂ ) ₅ -[CH(CH ₂ CF ₃ )]-(CH ₂ )-, -(CH ₂ ) ₆ -[CH(CH ₂ CF ₃ )]- (CH ₂ )-, -(CH ₂ ) ₇ -[CH(CH ₂ CF ₃ )]-(CH ₂ )-, -(CH ₂ ) ₈ -[CH(CH ₂ CF ₃ )]-(CH ₂ )-, -(CH ₂ ) ₉ - [CH(CH ₂ CF ₃ )]-(CH ₂ )-, -(CH ₂ ) ₁₀ -[CH(CH ₂ CF ₃ )]-(CH ₂ )-, -(CH ₂ ) ₂ -[CH(CH ₂ CF ₃ )]-(CH ₂ ) ₂ -, - (CH ₂ ) ₃ -[CH(CH ₂ CF ₃ )]-(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -[CH(CH ₂ CF ₃ )]-(CH ₂ ) ₄ -, -(CH ₂ ) ₅ -[CH(CH ₂ CF ₃ )]- (CH ₂ ) ₅ -, -(CH ₂ ) ₂ -[CH(CH ₂ CF ₃ )]-(CH ₂ ) ₃ -, -(CH ₂ ) ₂ -[CH(CH ₂ CF ₃ )]-(CH ₂ ) ₄ -, -(CH ₂ ) ₂ - [CH(CH ₂ CF ₃ )]-(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -[CH(CH ₂ CF ₃ )]-(CH ₂ ) ₆ -, -(CH ₂ ) ₂ -[CH(CH ₂ CF ₃ )]-(CH ₂ ) ₇ -, - (CH ₂ ) ₂ -[CH(CH ₂ CF ₃ )]-(CH ₂ ) ₈ -, -(CH ₂ ) ₂ -[CH(CH ₂ CF ₃ )]-(CH ₂ ) ₉ -, -(CH ₂ ) ₃ -[CH(CH ₂ CF ₃ )]- (CH ₂ ) ₂ -, -(CH ₂ ) ₃ -[CH(CH ₂ CF ₃ )]-(CH ₂ ) ₄ -, -(CH ₂ ) ₃ -[CH(CH ₂ CF ₃ )]-(CH ₂ ) ₅ -, -(CH ₂ ) ₃ - [CH(CH ₂ CF ₃ )]-(CH ₂ ) ₆ -, -(CH ₂ ) ₃ -[CH(CH ₂ CF ₃ )]-(CH ₂ ) ₇ -, -(CH ₂ ) ₃ -[CH(CH ₂ CF ₃ )]-(CH ₂ ) ₈ -, - (CH ₂ ) ₄ -[CH(CH ₂ CF ₃ )]-(CH ₂ ) ₂ -, -(CH ₂ ) ₄ -[CH(CH ₂ CF ₃ )]-(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -[CH(CH ₂ CF ₃ )]- (CH ₂ ) ₅ -, -(CH ₂ ) ₄ -[CH(CH ₂ CF ₃ )]-(CH ₂ ) ₆ -, -(CH ₂ ) ₄ -[CH(CH ₂ CF ₃ )]-(CH ₂ ) ₇ -, -(CH ₂ ) ₅ - [CH(CH ₂ CF ₃ )]-(CH ₂ ) ₂ -, -(CH ₂ ) ₅ -[CH(CH ₂ CF ₃ )]-(CH ₂ ) ₃ -, -(CH ₂ ) ₅ -[CH(CH ₂ CF ₃ )]-(CH ₂ ) ₄ -, - (CH ₂ ) ₅ -[CH(CH ₂ CF ₃ )]-(CH ₂ ) ₆ -, -(CH ₂ ) ₆ -[CH(CH ₂ CF ₃ )]-(CH ₂ ) ₂ -, -(CH ₂ ) ₆ -[CH(CH ₂ CF ₃ )]- (CH ₂ ) ₃ -, -(CH ₂ ) ₆ -[CH(CH ₂ CF ₃ )]-(CH ₂ ) ₄ -, -(CH ₂ ) ₆ -[CH(CH ₂ CF ₃ )]-(CH ₂ ) ₅ -, -[CH(CH ₂ CF ₃ )] ₂ -(CH ₂ )-, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₂ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₂ -(CH ₂ )-, -(CH ₂ )- [CH(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₂ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₃ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₄ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₅ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₆ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₂ - (CH ₂ ) ₇ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₈ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₉ -, -(CH ₂ ) ₂ - [CH(CH ₂ CF ₃ )] ₂ -(CH ₂ )-, -(CH ₂ ) ₃ -[CH(CH ₂ CF ₃ )] ₂ -(CH ₂ )-, -(CH ₂ ) ₄ -[CH(CH ₂ CF ₃ )] ₂ -(CH ₂ )-, - (CH ₂ ) ₅ -[CH(CH ₂ CF ₃ )] ₂ -(CH ₂ )-, -(CH ₂ ) ₆ -[CH(CH ₂ CF ₃ )] ₂ -(CH ₂ )-, -(CH ₂ ) ₇ -[CH(CH ₂ CF ₃ )] ₂ - (CH ₂ )-, -(CH ₂ ) ₈ -[CH(CH ₂ CF ₃ )] ₂ -(CH ₂ )-, -(CH ₂ ) ₉ -[CH(CH ₂ CF ₃ )] ₂ -(CH ₂ )-, -(CH ₂ ) ₂ - [CH(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -[CH(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -[CH(CH ₂ CF ₃ )] ₂ - (CH ₂ ) ₄ -, -(CH ₂ ) ₅ -[CH(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -[CH(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₂ - [CH(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ -[CH(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -[CH(CH ₂ CF ₃ )] ₂ - (CH ₂ ) ₆ -, -(CH ₂ ) ₂ -[CH(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₇ -, -(CH ₂ ) ₂ -[CH(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₈ -, -(CH ₂ ) ₃ - [CH(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -[CH(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₄ -, -(CH ₂ ) ₃ -[CH(CH ₂ CF ₃ )] ₂ - (CH ₂ ) ₅ -, -(CH ₂ ) ₃ -[CH(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₆ -, -(CH ₂ ) ₃ -[CH(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₇ -, -(CH ₂ ) ₄ - [CH(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₄ -[CH(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -[CH(CH ₂ CF ₃ )] ₂ - (CH ₂ ) ₅ -, -(CH ₂ ) ₄ -[CH(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₆ -, -(CH ₂ ) ₅ -[CH(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₅ - [CH(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₅ -[CH(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₄ -, -(CH ₂ ) ₆ -[CH(CH ₂ CF ₃ )] ₂ - (CH ₂ ) ₂ -, -(CH ₂ ) ₆ -[CH(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₆ -[CH(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₄ -, -[CH(CH ₂ CF ₃ )] ₃ -(CH ₂ )-, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₃ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₃ -(CH ₂ )-, -(CH ₂ )- [CH(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₂ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₃ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₄ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₅ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₆ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₃ - (CH ₂ ) ₇ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₈ -, -(CH ₂ ) ₂ -[CH(CH ₂ CF ₃ )] ₃ -(CH ₂ )-, -(CH ₂ ) ₃ - [CH(CH ₂ CF ₃ )] ₃ -(CH ₂ )-, -(CH ₂ ) ₄ -[CH(CH ₂ CF ₃ )] ₃ -(CH ₂ )-, -(CH ₂ ) ₅ -[CH(CH ₂ CF ₃ )] ₃ -(CH ₂ )-, - (CH ₂ ) ₆ -[CH(CH ₂ CF ₃ )] ₃ -(CH ₂ )-, -(CH ₂ ) ₇ -[CH(CH ₂ CF ₃ )] ₃ -(CH ₂ )-, -(CH ₂ ) ₈ -[CH(CH ₂ CF ₃ )] ₃ - (CH ₂ )-, -(CH ₂ ) ₂ -[CH(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -[CH(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ - [CH(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ -[CH(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₃ -, -(CH ₂ ) ₂ -[CH(CH ₂ CF ₃ )] ₃ - (CH ₂ ) ₄ -, -(CH ₂ ) ₂ -[CH(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -[CH(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₆ -, -(CH ₂ ) ₂ - [CH(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₇ -, -(CH ₂ ) ₃ -[CH(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -[CH(CH ₂ CF ₃ )] ₃ - (CH ₂ ) ₄ -, -(CH ₂ ) ₃ -[CH(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₅ -, -(CH ₂ ) ₃ -[CH(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₆ -, -(CH ₂ ) ₄ - [CH(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₂ -, -(CH ₂ ) ₄ -[CH(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -[CH(CH ₂ CF ₃ )] ₃ - (CH ₂ ) ₅ -, -(CH ₂ ) ₅ -[CH(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₂ -, -(CH ₂ ) ₅ -[CH(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₃ -, -(CH ₂ ) ₅ - [CH(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₄ -, -(CH ₂ ) ₆ -[CH(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₂ -, -(CH ₂ ) ₆ -[CH(CH ₂ CF ₃ )] ₃ - (CH ₂ ) ₃ -, -[CH(CH ₂ CF ₃ )] ₄ -(CH ₂ )-, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₄ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₄ -(CH ₂ )-, -(CH ₂ )- [CH(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₂ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₃ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₄ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₅ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₆ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₄ - (CH ₂ ) ₇ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₈ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₉ -, -(CH ₂ )- [CH(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₁₀ -, -(CH ₂ ) ₂ -[CH(CH ₂ CF ₃ )] ₄ -(CH ₂ )-, -(CH ₂ ) ₃ -[CH(CH ₂ CF ₃ )] ₄ -(CH ₂ )-, -(CH ₂ ) ₄ -[CH(CH ₂ CF ₃ )] ₄ -(CH ₂ )-, -(CH ₂ ) ₅ -[CH(CH ₂ CF ₃ )] ₄ -(CH ₂ )-, -(CH ₂ ) ₆ -[CH(CH ₂ CF ₃ )] ₄ - (CH ₂ )-, -(CH ₂ ) ₇ -[CH(CH ₂ CF ₃ )] ₄ -(CH ₂ )-, -(CH ₂ ) ₂ -[CH(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ - [CH(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -[CH(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₄ -, -(CH ₂ ) ₅ -[CH(CH ₂ CF ₃ )] ₄ - (CH ₂ ) ₅ -, -(CH ₂ ) ₂ -[CH(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₃ -, -(CH ₂ ) ₂ -[CH(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ - [CH(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -[CH(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₆ -, -(CH ₂ ) ₃ -[CH(CH ₂ CF ₃ )] ₄ - (CH ₂ ) ₂ -, -(CH ₂ ) ₃ -[CH(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₄ -, -(CH ₂ ) ₄ -[CH(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₂ -, -(CH ₂ ) ₄ - [CH(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₃ -, -(CH ₂ ) ₅ -[CH(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₂ -, -(CH ₂ ) ₅ -[CH(CH ₂ CF ₃ )] ₄ - (CH ₂ ) ₃ -, -(CH ₂ ) ₆ -[CH(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₂ -, -[CH(CH ₂ CF ₃ )] ₅ -(CH ₂ )-, -(CH ₂ )-[CH(CH ₂ CF ₃ ) ₅ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₅ -(CH ₂ )-, -(CH ₂ )- [CH(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₂ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₃ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₄ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₅ -, -(CH ₂ )-[CH(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₆ -, -(CH ₂ ) ₂ -[CH(CH ₂ CF ₃ )] ₅ - (CH ₂ )-, -(CH ₂ ) ₃ -[CH(CH ₂ CF ₃ )] ₅ -(CH ₂ )-, -(CH ₂ ) ₄ -[CH(CH ₂ CF ₃ )] ₅ -(CH ₂ )-, -(CH ₂ ) ₅ - [CH(CH ₂ CF ₃ )] ₅ -(CH ₂ )-, -(CH ₂ ) ₆ -[CH(CH ₂ CF ₃ )] ₅ -(CH ₂ )-, -(CH ₂ ) ₂ -[CH(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -[CH(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -[CH(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ - [CH(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₃ -, -(CH ₂ ) ₂ -[CH(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ -[CH(CH ₂ CF ₃ )] ₅ - (CH ₂ ) ₅ -, -(CH ₂ ) ₂ -[CH(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₆ -, -(CH ₂ ) ₃ -[CH(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ - [CH(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₄ -, -(CH ₂ ) ₄ -[CH(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₂ -, -(CH ₂ ) ₄ -[CH(CH ₂ CF ₃ )] ₅ - (CH ₂ ) ₃ -, -(CH ₂ ) ₅ -[CH(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₂ -, -[C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ )-, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )]-, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ )-, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₂ -, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₃ -, -(CH ₂ )- [C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₄ -, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₅ -, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )]- (CH ₂ ) ₆ -, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₇ -, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₈ -, -(CH ₂ )- [C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₉ -, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₁₀ -, -(CH ₂ ) ₂ - [C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ )-, -(CH ₂ ) ₃ -[C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ )-, -(CH ₂ ) ₄ -[C(CH ₃ )(CH ₂ CF ₃ )]- (CH ₂ )-, -(CH ₂ ) ₅ -[C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ )-, -(CH ₂ ) ₆ -[C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ )-, -(CH ₂ ) ₇ - [C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ )-, -(CH ₂ ) ₈ -[C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ )-, -(CH ₂ ) ₉ -[C(CH ₃ )(CH ₂ CF ₃ )]- (CH ₂ )-, -(CH ₂ ) ₁₀ -[C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ )-, -(CH ₂ ) ₂ -[C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₂ -, -(CH ₂ ) ₃ - [C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -[C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₄ -, -(CH ₂ ) ₅ - [C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -[C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₃ -, -(CH ₂ ) ₂ - [C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₄ -, -(CH ₂ ) ₂ -[C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₅ -, -(CH ₂ ) ₂ - [C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₆ -, -(CH ₂ ) ₂ -[C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₇ -, -(CH ₂ ) ₂ - [C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₈ -, -(CH ₂ ) ₂ -[C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₉ -, -(CH ₂ ) ₃ - [C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -[C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₄ -, -(CH ₂ ) ₃ - [C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₅ -, -(CH ₂ ) ₃ -[C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₆ -, -(CH ₂ ) ₃ - [C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₇ -, -(CH ₂ ) ₃ -[C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₈ -, -(CH ₂ ) ₄ - [C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₂ -, -(CH ₂ ) ₄ -[C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₃ -, -(CH ₂ ) ₄ - [C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₅ -, -(CH ₂ ) ₄ -[C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₆ -, -(CH ₂ ) ₄ - [C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₇ -, -(CH ₂ ) ₅ -[C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₂ -, -(CH ₂ ) ₅ - [C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₃ -, -(CH ₂ ) ₅ -[C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₄ -, -(CH ₂ ) ₅ - [C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₆ -, -(CH ₂ ) ₆ -[C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₂ -, -(CH ₂ ) ₆ - [C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₃ -, -(CH ₂ ) ₆ -[C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₄ -, -(CH ₂ ) ₆ - [C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ ) ₅ -, -[C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ )-, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )] ₂ -, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )] ₂ - (CH ₂ )-, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₂ -, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₃ -, -(CH ₂ )- [C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₄ -, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₅ -, -(CH ₂ )- [C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₆ -, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₇ -, -(CH ₂ )- [C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₈ -, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₉ -, -(CH ₂ ) ₂ - [C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ )-, -(CH ₂ ) ₃ -[C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ )-, -(CH ₂ ) ₄ - [C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ )-, -(CH ₂ ) ₅ -[C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ )-, -(CH ₂ ) ₆ - [C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ )-, -(CH ₂ ) ₇ -[C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ )-, -(CH ₂ ) ₈ - [C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ )-, -(CH ₂ ) ₉ -[C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ )-, -(CH ₂ ) ₂ - [C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -[C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ - [C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₄ -, -(CH ₂ ) ₅ -[C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₅ -, -(CH ₂ ) ₂ - [C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₂ -[C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ - [C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -[C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₆ -, -(CH ₂ ) ₂ - [C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₇ -, -(CH ₂ ) ₂ -[C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₈ -, -(CH ₂ ) ₃ - [C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -[C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₄ -, -(CH ₂ ) ₃ - [C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₅ -, -(CH ₂ ) ₃ -[C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₆ -, -(CH ₂ ) ₃ - [C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₇ -, -(CH ₂ ) ₄ -[C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₄ - [C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -[C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₅ -, -(CH ₂ ) ₄ - [C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₆ -, -(CH ₂ ) ₅ -[C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₅ - [C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₅ -[C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₄ -, -(CH ₂ ) ₆ - [C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₆ -[C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₆ - [C(CH ₃ )(CH ₂ CF ₃ )] ₂ -(CH ₂ ) ₄ -, -[C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ )-, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )] ₃ -, -(CH ₂ )- [C(CH ₃ )(CH ₂ CF ₃ )] ₃ - (CH ₂ )-, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₂ -, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₃ -, -(CH ₂ )- [C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₄ -, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₅ -, -(CH ₂ )- [C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₆ -, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₇ -, -(CH ₂ )- [C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₈ -, -(CH ₂ ) ₂ -[C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ )-, -(CH ₂ ) ₃ - [C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ )-, -(CH ₂ ) ₄ -[C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ )-, -(CH ₂ ) ₅ - [C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ )-, -(CH ₂ ) ₆ -[C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ )-, -(CH ₂ ) ₇ - [C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ )-, -(CH ₂ ) ₈ -[C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ )-, -(CH ₂ ) ₂ - [C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -[C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ - [C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ -[C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₃ -, -(CH ₂ ) ₂ - [C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ -[C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₅ -, -(CH ₂ ) ₂ - [C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₆ -, -(CH ₂ ) ₂ -[C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₇ -, -(CH ₂ ) ₃ - [C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -[C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₄ -, -(CH ₂ ) ₃ - [C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₅ -, -(CH ₂ ) ₃ -[C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₆ -, -(CH ₂ ) ₄ - [C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₂ -, -(CH ₂ ) ₄ -[C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ - [C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₅ -, -(CH ₂ ) ₅ -[C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₂ -, -(CH ₂ ) ₅ - [C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₃ -, -(CH ₂ ) ₅ -[C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₄ -, -(CH ₂ ) ₆ - [C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₂ -, -(CH ₂ ) ₆ -[C(CH ₃ )(CH ₂ CF ₃ )] ₃ -(CH ₂ ) ₃ -, -[C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ )-, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )] ₄ -, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )] ₄ - (CH ₂ )-, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₂ -, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₃ -, -(CH ₂ )- [C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₄ -, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₅ -, -(CH ₂ )- [C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₆ -, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₇ -, -(CH ₂ )- [C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₈ -, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₉ -, -(CH ₂ )- [C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₁₀ -, -(CH ₂ ) ₂ -[C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ )-, -(CH ₂ ) ₃ - [C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ )-, -(CH ₂ ) ₄ -[C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ )-, -(CH ₂ ) ₅ - [C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ )-, -(CH ₂ ) ₆ -[C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ )-, -(CH ₂ ) ₇ - [C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ )-, -(CH ₂ ) ₂ -[C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ - [C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -[C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₄ -, -(CH ₂ ) ₅ - [C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -[C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₃ -, -(CH ₂ ) ₂ - [C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ -[C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₅ -, -(CH ₂ ) ₂ - [C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₆ -, -(CH ₂ ) ₃ -[C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ - [C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₄ -, -(CH ₂ ) ₄ -[C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₂ -, -(CH ₂ ) ₄ - [C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₃ -, -(CH ₂ ) ₅ -[C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₂ -, -(CH ₂ ) ₅ - [C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₃ -, -(CH ₂ ) ₆ -[C(CH ₃ )(CH ₂ CF ₃ )] ₄ -(CH ₂ ) ₂ -, -[C(CH ₃ )(CH ₂ CF ₃ )] ₅ -(CH ₂ )-, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )] ₅ -, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )] ₅ - (CH ₂ )-, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₂ -, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₃ -, -(CH ₂ )- [C(CH ₃ )(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₄ -, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₅ -, -(CH ₂ )- [C(CH ₃ )(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₆ -, -(CH ₂ ) ₂ -[C(CH ₃ )(CH ₂ CF ₃ )] ₅ -(CH ₂ )-, -(CH ₂ ) ₃ - [C(CH ₃ )(CH ₂ CF ₃ )] ₅ -(CH ₂ )-, -(CH ₂ ) ₄ -[C(CH ₃ )(CH ₂ CF ₃ )] ₅ -(CH ₂ )-, -(CH ₂ ) ₅ - [C(CH ₃ )(CH ₂ CF ₃ )] ₅ -(CH ₂ )-, -(CH ₂ ) ₆ -[C(CH ₃ )(CH ₂ CF ₃ )] ₅ -(CH ₂ )-, -(CH ₂ ) ₂ - [C(CH ₃ )(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -[C(CH ₃ )(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ - [C(CH ₃ )(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ -[C(CH ₃ )(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₃ -, -(CH ₂ ) ₂ - [C(CH ₃ )(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ -[C(CH ₃ )(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₅ -, -(CH ₂ ) ₂ - [C(CH ₃ )(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₆ -, -(CH ₂ ) ₃ -[C(CH ₃ )(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ - [C(CH ₃ )(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₄ -, -(CH ₂ ) ₄ -[C(CH ₃ )(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₂ -, -(CH ₂ ) ₄ - [C(CH ₃ )(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₃ -, -(CH ₂ ) ₅ -[C(CH ₃ )(CH ₂ CF ₃ )] ₅ -(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -(CF ₂ )-O-(CH ₂ )-O-(CF ₂ )-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -(CF ₂ )- O-(CH ₂ ) ₂ -O-(CF ₂ )-(CH ₂ ) ₂ , -(CH ₂ )-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ )-, -(CH ₂ ) ₂ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₂ -, -(CH ₂ ) ₃ - (CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₄ -, -(CH ₂ )-(CF ₂ )-O- (CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₂ -, -(CH ₂ )-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₃ -, -(CH ₂ )-(CF ₂ )-O-(CF ₂ )-O- (CF ₂ )-(CH ₂ ) ₄ -, -(CH ₂ )-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₅ -, -(CH ₂ )-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )- (CH ₂ ) ₆ -, -(CH ₂ )-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₇ -, -(CH ₂ ) ₂ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ )- , -(CH ₂ ) ₃ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ )-, -(CH ₂ ) ₄ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ )-, -(CH ₂ ) ₅ - (CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ )-, -(CH ₂ ) ₆ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ )-, -(CH ₂ ) ₇ -(CF ₂ )-O- (CF ₂ )-O-(CF ₂ )-(CH ₂ )-, -(CH ₂ ) ₂ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₃ -, -(CH ₂ ) ₂ -(CF ₂ )-O-(CF ₂ )-O- (CF ₂ )-(CH ₂ ) ₄ -, -(CH ₂ ) ₂ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )- (CH ₂ ) ₆ -, -(CH ₂ ) ₃ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₂ -, -(CH ₂ ) ₄ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₂ - , -(CH ₂ ) ₅ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₂ -, -(CH ₂ ) ₆ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₂ - , -(CH ₂ ) ₃ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₄ -, -(CH ₂ ) ₄ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₃ - , -(CH ₂ ) ₃ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₅ -, -(CH ₂ ) ₅ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₃ -, -(CH ₂ )-(CF ₂ )-O-(CF ₂ ) ₂ -O-(CF ₂ )-(CH ₂ )-, -(CH ₂ ) ₂ -(CF ₂ )-O-(CF ₂ ) ₂ -O-(CF ₂ )-(CH ₂ ) ₂ - , -(CH ₂ ) ₃ -(CF ₂ )-O-(CF ₂ ) ₂ -O-(CF ₂ )-(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -(CF ₂ )-O-(CF ₂ ) ₂ -O-(CF ₂ )-(CH ₂ ) ₄ - , -(CH ₂ )-(CF ₂ )-O-(CF ₂ ) ₂ -O-(CF ₂ )-(CH ₂ ) ₂ -, -(CH ₂ )-(CF ₂ )-O-(CF ₂ ) ₂ -O-(CF ₂ )-(CH ₂ ) ₃ - , -(CH ₂ )-(CF ₂ )-O-(CF ₂ ) ₂ -O-(CF ₂ )-(CH ₂ ) ₄ -, -(CH ₂ )-(CF ₂ )-O-(CF ₂ ) ₂ -O-(CF ₂ )-(CH ₂ ) ₅ - , -(CH ₂ )-(CF ₂ )-O-(CF ₂ ) ₂ -O-(CF ₂ )-(CH ₂ ) ₆ -, -(CH ₂ )-(CF ₂ )-O-(CF ₂ ) ₂ -O-(CF ₂ )-(CH ₂ ) ₇ - , -(CH ₂ ) ₂ -(CF ₂ )-O-(CF ₂ ) ₂ -O-(CF ₂ )-(CH ₂ )-, -(CH ₂ ) ₃ -(CF ₂ )-O-(CF ₂ ) ₂ -O-(CF ₂ )-(CH ₂ )- , -(CH ₂ ) ₄ -(CF ₂ )-O-(CF ₂ ) ₂ -O-(CF ₂ )-(CH ₂ )-, -(CH ₂ ) ₅ -(CF ₂ )-O-(CF ₂ ) ₂ -O-(CF ₂ )-(CH ₂ )- , -(CH ₂ ) ₆ -(CF ₂ )-O-(CF ₂ ) ₂ -O-(CF ₂ )-(CH ₂ )-, -(CH ₂ ) ₇ -(CF ₂ )-O-(CF ₂ ) ₂ -O-(CF ₂ )-(CH ₂ )- , -(CH ₂ ) ₂ -(CF ₂ )-O-(CF ₂ ) ₂ -O-(CF ₂ )-(CH ₂ ) ₃ -, -(CH ₂ ) ₂ -(CF ₂ )-O-(CF ₂ ) ₂ -O-(CF ₂ )-(CH ₂ ) ₄ - , -(CH ₂ ) ₂ -(CF ₂ )-O-(CF ₂ ) ₂ -O-(CF ₂ )-(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -(CF ₂ )-O-(CF ₂ ) ₂ -O-(CF ₂ )-(CH ₂ ) ₆ - , -(CH ₂ ) ₃ -(CF ₂ )-O-(CF ₂ ) ₂ -O-(CF ₂ )-(CH ₂ ) ₂ -, -(CH ₂ ) ₄ -(CF ₂ )-O-(CF ₂ ) ₂ -O-(CF ₂ )-(CH ₂ ) ₂ - , -(CH ₂ ) ₅ -(CF ₂ )-O-(CF ₂ ) ₂ -O-(CF ₂ )-(CH ₂ ) ₂ -, -(CH ₂ ) ₆ -(CF ₂ )-O-(CF ₂ ) ₂ -O-(CF ₂ )-(CH ₂ ) ₂ - , -(CH ₂ ) ₃ -(CF ₂ )-O-(CF ₂ ) ₂ -O-(CF ₂ )-(CH ₂ ) ₄ -, -(CH ₂ ) ₄ -(CF ₂ )-O-(CF ₂ ) ₂ -O-(CF ₂ )-(CH ₂ ) ₃ - , -(CH ₂ ) ₃ -(CF ₂ )-O-(CF ₂ ) ₂ -O-(CF ₂ )-(CH ₂ ) ₅ -, -(CH ₂ ) ₅ -(CF ₂ )-O-(CF ₂ ) ₂ -O-(CF ₂ )-(CH ₂ ) ₃ -, -(CH ₂ )-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ )-, -(CH ₂ ) ₂ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₂ - , -(CH ₂ ) ₃ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₄ - , -(CH ₂ )-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₂ -, -(CH ₂ )-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₃ - , -(CH ₂ )-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₃ -, -(CH ₂ )-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₄ - , -(CH ₂ )-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₅ -, -(CH ₂ )-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₆ - , -(CH ₂ )-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₇ -, -(CH ₂ ) ₂ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ )- , -(CH ₂ ) ₃ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ )-, -(CH ₂ ) ₄ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ )- , -(CH ₂ ) ₅ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ )-, -(CH ₂ ) ₆ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ )- , -(CH ₂ ) ₇ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ )-, -(CH ₂ ) ₂ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₃ - , -(CH ₂ ) ₂ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₅ - , -(CH ₂ ) ₂ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₆ -, -(CH ₂ ) ₃ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₂ - , -(CH ₂ ) ₄ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₅ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₂ - , -(CH ₂ ) ₆ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₄ - , -(CH ₂ ) ₄ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₃ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₅ - , -(CH ₂ ) ₅ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₃ -, -(CH ₂ )-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ )-, -(CH ₂ ) ₂ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )- (CH ₂ ) ₂ -, -(CH ₂ ) ₃ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -(CF ₂ )-O-(CF ₂ )-O- (CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₄ -, -(CH ₂ )-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₂ -, -(CH ₂ )-(CF ₂ )-O- (CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₃ -, -(CH ₂ )-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₄ -, -(CH ₂ )- (CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₅ -, -(CH ₂ )-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₆ - , -(CH ₂ )-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₇ -, -(CH ₂ ) ₂ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-O- (CF ₂ )-(CH ₂ )-, -(CH ₂ ) ₃ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ )-, -(CH ₂ ) ₄ -(CF ₂ )-O-(CF ₂ )-O- (CF ₂ )-O-(CF ₂ )-(CH ₂ )-, -(CH ₂ ) ₅ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ )-, -(CH ₂ ) ₆ -(CF ₂ )-O- (CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ )-, -(CH ₂ ) ₇ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ )-, -(CH ₂ ) ₂ - (CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₃ -, -(CH ₂ ) ₂ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₄ - , -(CH ₂ ) ₂ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-O- (CF ₂ )-(CH ₂ ) ₆ -, -(CH ₂ ) ₃ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₂ -, -(CH ₂ ) ₄ -(CF ₂ )-O-(CF ₂ )- O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₂ -, -(CH ₂ ) ₅ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₂ -, -(CH ₂ ) ₆ - (CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₄ - , -(CH ₂ ) ₄ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₃ -, -(CH ₂ ) ₃ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-O- (CF ₂ )-(CH ₂ ) ₅ -, -(CH ₂ ) ₅ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₃ -, -(CH ₂ )-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ )-, -(CH ₂ ) ₂ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O- (CF ₂ ) ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -(CF ₂ ) ₂ -O- (CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₄ -, -(CH ₂ )-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₂ - , -(CH ₂ )-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₃ -, -(CH ₂ )-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ - O-(CF ₂ ) ₂ -(CH ₂ ) ₄ -, -(CH ₂ )-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₅ -, -(CH ₂ )-(CF ₂ ) ₂ -O- (CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₆ -, -(CH ₂ )-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₇ - , -(CH ₂ ) ₂ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ )-, -(CH ₂ ) ₃ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ - O-(CF ₂ ) ₂ -(CH ₂ )-, -(CH ₂ ) ₄ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ )-, -(CH ₂ ) ₅ -(CF ₂ ) ₂ -O- (CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ )-, -(CH ₂ ) ₆ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ )- , -(CH ₂ ) ₇ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ )-, -(CH ₂ ) ₂ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ - O-(CF ₂ ) ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₂ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ -(CF ₂ ) ₂ - O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₅ -, -(CH ₂ ) ₂ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ - (CH ₂ ) ₆ -, -(CH ₂ ) ₃ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₄ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ - O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₅ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₂ - , -(CH ₂ ) ₆ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O- (CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₄ -, -(CH ₂ ) ₄ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₃ -, -(CH ₂ ) ₃ - (CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -(CH ₂ ) ₅ -, -(CH ₂ ) ₅ -(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O-(CF ₂ ) ₂ -O- (CF ₂ ) ₂ -(CH ₂ ) ₃ -. Preferred examples for -R ₂ - are -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -, -(CH ₂ ) ₅ -, -(CH ₂ ) ₆ -, -(CH ₂ ) ₇ -, -(CH ₂ ) ₈ -, -(CH ₂ ) ₉ -, -(CH ₂ ) ₁₀ -, -(CH ₂ ) ₁₁ -, -(CH ₂ ) ₁₂ -, -(CH ₂ ) ₁₃ -, -(CH(C ₃ H ₇ )-(CH ₂ ) ₂ -, -(CH(C ₂ H ₅ )- (CH ₂ ) ₃ -, -(CH(C ₂ H ₅ )-(CH ₂ ) ₄ -, -(CH(C ₂ H ₅ )-(CH ₂ ) ₇ -, -(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -SO ₂ - (CH ₂ ) ₂ -, -(CH ₂ ) ₄ -SO ₂ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -O-(CH ₂ ) ₃ -, -(CH ₂ ) ₃ -S-(CH ₂ ) ₃ -, -(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -, - (CH ₂ ) ₂ -O-(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₂ -O- (CH ₂ ) ₂ -, -(CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ - O-(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -SO ₂ - (CH ₂ ) ₂ -O-(CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -SO ₂ - (CH ₂ ) ₂ -S-(CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -O- (CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -(CF ₂ )-(CH ₂ ) ₃ -, -(CH ₂ )-(CF ₂ ) ₃ -(CH ₂ )-, -(CH ₂ ) ₂ - (CF ₂ ) ₄ -(CH ₂ ) ₂ -, -(CH ₂ )-[CH(CF ₃ )]-(CH ₂ )-, -(CH ₂ )-[C(CH ₃ )CF ₃ ]-(CH ₂ )-, -(CH ₂ )- [CH(CH ₂ CF ₃ )]-(CH ₂ )-, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ )-, -(CHC ₂ H ₅ )-(CH ₂ )-(CHCF ₃ )- (CH ₂ ) ₃ -, -(CH ₂ ) ₃ -(CHCF ₃ )-(CH ₂ ) ₃ -,-(CH ₂ ) ₂ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₂ - and -(CH ₂ )- (CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ )- according to the invention. Particularly preferred examples for -R ₂ - are -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -, -(CH ₂ ) ₅ -, -(CH ₂ ) ₆ -, - (CH ₂ ) ₇ -, -(CH ₂ ) ₈ -, -(CH ₂ ) ₉ -, -(CH ₂ ) ₁₀ -, -(CH ₂ ) ₁₁ -, -(CH ₂ ) ₁₂ -, -(CH ₂ ) ₁₃ -, -(CH(C ₃ H ₇ )- (CH ₂ ) ₂ -, -(CH(C ₂ H ₅ )-(CH ₂ ) ₃ -, -(CH(C ₂ H ₅ )-(CH ₂ ) ₄ -, -(CH(C ₂ H ₅ )-(CH ₂ ) ₇ -, -(CH ₂ ) ₂ -O- (CH ₂ ) ₂ -, -(CH ₂ ) ₃ -O-(CH ₂ ) ₃ -, -(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -S- (CH ₂ ) ₃ -, -(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₄ -SO ₂ -(CH ₂ ) ₄ -, - (CH ₂ ) ₂ -S-(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -, -(CH ₂ ) ₃ - (CF ₂ )-(CH ₂ ) ₃ -, -(CHC ₂ H ₅ )-(CH ₂ )-(CHCF ₃ )-(CH ₂ ) ₃ -, -(CH ₂ ) ₃ -(CHCF ₃ )-(CH ₂ ) ₃ - according to the invention. Compounds of formulae (I), (Ia) and (Ib) with substituents as described before or preferably described before having a polymerizable group as described before or preferably described before or below are preferred in case the substituent -R ₂ - within the at least one linking element Y-R ₂ - corresponds to –(C(R) ₂ ) _o –, wherein R and o has a meaning as described or preferably described before. Accordingly, monomers of formulae (I), (Ia) and (Ib) for the preparation of an ophthalmic device or precursor article for an ophthalmic device as described before with substituents as described before or preferably described before having a polymerizable group as described before or preferably described before or below are preferred in case the substituent -R ₂ - within the at least one linking element Y-R ₂ - corresponds to –(C(R) ₂ ) _o –, wherein R and o has a meaning as described or preferably described before. Such ophthalmic devices and precursor articles prepared by using these monomers are especially preferred. Particularly preferred examples for -R ₂ - are -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -, -(CH ₂ ) ₅ -, -(CH ₂ ) ₆ -, - (CH ₂ ) ₇ -, -(CH ₂ ) ₈ -, -(CH ₂ ) ₉ -, -(CH ₂ ) ₁₀ -, -(CH ₂ ) ₁₁ -, -(CH ₂ )12-, -(CH ₂ ) ₁₃ -, -(CH(C ₃ H ₇ )- (CH ₂ ) ₂ -, -(CH(C ₂ H ₅ )-(CH ₂ ) ₃ -, -(CH(C ₂ H ₅ )-(CH ₂ ) ₄ - and -(CH(C ₂ H ₅ )-(CH ₂ ) ₇ - according to the invention. Very particularly preferably, -R ₂ - is -(CH ₂ ) ₅ -, -(CH ₂ ) ₆ - or -(CH ₂ ) ₇ - according to the invention. Therefore, the invention is furthermore directed to an ophthalmic device or precursor article for an ophthalmic device comprising polymerized compounds of formulae (I), (Ia) or (Ib) as described before or preferably described before wherein -R ₂ - is at each occurrence independently –(C(R) ₂ ) _o –, wherein R and o have a meaning as described or preferably described before. The invention therefore relates to compounds of formulae (I), (Ia) or (Ib) as described before or preferably described before wherein -R ₂ - is at each occurrence independently – (C(R) ₂ ) _o –, wherein R and o have a meaning as described or preferably described before and the disclosed disclaimers are considered. The substituent Y-R ₂ - within formulae (I), (Ia) and (Ib) is selected from the group consisting of O-R ₂ -, S-R ₂ -, SO-R ₂ -, SO ₂ -R ₂ -, Se-R ₂ -, NR ₀ -R ₂ - and -R ₂ - where Y is a bond and wherein -R ₂ - has a meaning as described before or preferably or particularly preferably described before. The substituent Y-R ₂ - is preferably selected from the group consisting of O-R ₂ -, S-R ₂ -, SO-R ₂ -, NR ₀ -R ₂ - and -R ₂ - where Y is a bond and wherein -R ₂ - has a meaning as described before or preferably or particularly preferably described before. The substituent Y-R ₂ - is preferably selected from the group consisting of O-R ₂ -, S-R ₂ - and NR ₀ -R ₂ - and -R ₂ - where Y is a bond and wherein -R ₂ - has a meaning as described before or preferably or particularly preferably described before. The substituent Y-R ₂ - is preferably selected from the group consisting of O-R ₂ - and NR ₀ - R ₂ - and wherein -R ₂ - has a meaning as described before or preferably or particularly preferably described before. The substituent Y-R ₂ - is preferably selected from the group consisting of S-R ₂ - and -R ₂ - has a meaning as described before or preferably or particularly preferably described before. The substituent Y-R ₂ -R ₁ within formulae (I), (Ia) and (Ib) is selected from the group consisting of O-R ₂ -R ₁ , S-R ₂ -R ₁ , SO-R ₂ -R ₁ , SO ₂ -R ₂ -R ₁ , Se-R ₂ -R ₁ , NR ₀ -R ₂ -R ₁ and -R ₂ - R ₁ , or very preferably selected from the group consisting of O-R ₂ -R ₁ , S-R ₂ -R ₁ and NR ₀ - R ₂ -R ₁ , wherein -R ₂ - has a meaning as described before or preferably or particularly preferably described before and wherein R ₁ is preferably trimethoxysilyl, triethoxysilyl, dimethoxymethylsilyl, diethoxymethylsilyl or a polymerizable group according to formula (4), wherein X ₁₁ is selected from the group consisting of O, S, O-SO ₂ , SO ₂ -O, C(=O), OC(=O), C(=O)O, S(C=O) and (C=O)S, R ₆ , R ₇ , R ₈ are at each occurrence independently of each other selected from the group consisting of H, F, a linear or branched, non-fluorinated, partially or completely fluorinated alkyl group having 1 to 20 C atoms and aryl with 6 to 14 C atoms and c is 0 or 1. In another preferred embodiment of the invention, c, X ₁₁ , R ₆ , R ₇ and R ₈ within the compounds of formulae (I), (Ia) and (Ib) acting as monomers for the preparation of the ophthalmic device or precursor article of the ophthalmic device as described before or for the preparation of an oligomer, polymer or copolymer according to the invention or within the compounds according to the invention have the following preferred meaning: Preferably, R ₆ and R ₇ are H. Preferably, c is 1. Preferably, R ₈ is H, methyl, ethyl or phenyl. Particularly preferably, R ₈ is H or methyl. Preferably, X ₁₁ is C(=O), OC(=O), C(=O)O or SC(=O). Particularly preferably, X ₁₁ is C(=O)O. Preferred alkenyl groups of formula (4) as polymerizable groups R ₁ according to the invention are therefore represented by any one selected from the group consisting of formulae (4-1), (4-2), (4-3), (4-4), (4-5), (4-6), (4-7), (4-8), (4-9), (4-10), (4-11) and (4-12):

Particularly preferred alkenyl groups of formula (4) as polymerizable groups R ₁ according to the invention are represented by any one selected from the group consisting of formulae (4-1), (4-2), (4-3), (4-5), (4-6), (4-8), (4-9), (4-11) and (4-12) as described before. Particularly preferred alkenyl groups of formula (4) as polymerizable groups R ₁ according to the invention are represented by any one selected from the group consisting of formulae (4-1), (4-2), (4-3), (4-5), (4-6), (4-11) and (4-12) as described before. The alkenyl group represented by formula (4-1) is called methacrylate. The alkenyl group represented by formula (4-2) is called acrylate. The preferred groups R ₁ are preferably combined with preferred groups of the linking element -R ₂ - and/or the linking element Y-R ₂ -. Combinations are excluded where two O atoms or one O atom and one S atom are directly bonded to each other as known for a skilled artisan in the field of organic chemistry. Particularly preferably, the compounds of formulae (I), (Ia) and (Ib) comprise a polymerizable group R ₁ which is represented by formulae (4-1), (4-2), (4-5), (4-6), (4-8), (4-9), (4-11) and (4-12). Particularly preferably, the compounds of formulae (I), (Ia) and (Ib) comprise a polymerizable group R ₁ which is represented by formulae (4-1), (4-2), (4-5), (4-6), (4-11) and (4-12). Very particularly preferably, the compounds of formulae (I), (Ia) and (Ib) comprise a polymerizable group R ₁ which is a methacryl or an acryl group represented by formula (4- 1) and (4-2). The invention therefore relates further to an ophthalmic device or a precursor article for an ophthalmic device comprising polymerized compounds of formulae (I), (Ia) and/or (Ib) as described before or preferably described before wherein R ₁ is at each occurrence independently an acryl or methacryl group. The invention therefore relates further to compounds of formulae (I), (Ia) and/or (Ib) as described before or preferably described before wherein R ₁ is at each occurrence independently an acryl or methacryl group. With regards to the compounds according to the invention, the described disclaimers have to be considered. Examples for compounds/monomers of formulae (I), (Ia) and/or (Ib) are the following compounds (A-001) to (A-188) as shown in table 1. Table 1: Parts of the compounds of the present application may be synthesized by methods well known to the skilled person. Preferably, all syntheses are carried out under an inert atmosphere using dried solvents. An exemplary reaction sequence is shown in Scheme 1 for the compounds of formula (I) where X-W is O-C(=O), Y is O and all further symbols and indices have a meaning as described before and the polymerizable group R ₁ is as shown in scheme 1. Scheme 1: A representative synthesis for compound A-014 is described in Scheme 1-1. Scheme 1-1: The first type of reaction is a nucleophilic bromination reaction. The second type of reaction is a Williamson ether synthesis. An exemplary reaction sequence is shown in Scheme 2 for the compounds of formula (I) where X-W is O-C(=O), Y is S and all further symbols and indices have a meaning as described before and the polymerizable group R ₁ is as shown in scheme 2. DMAP means 4-N,N-dimethylaminopyridine. TBABr means tetrabutylammonium bromide. Scheme 2: The first type of reaction is a nucleophilic bromination reaction. The second type of reaction is a Williamson ether synthesis. The third type of reaction is an esterification reaction. A representative synthesis for compound A-102 is described in Scheme 2-2. Scheme 2-2: An exemplary reaction sequence is shown in Scheme 3 for the compounds of formula (I) where X-W is NR _B -C(=O), RB is methyl, Y is S and all further symbols and indices have a meaning as described before and the polymerizable group R ₁ is as shown in scheme 3. Scheme 3: The first type of reaction is a nucleophilic bromination reaction. The second type of reaction is a Williamson ether synthesis. The third type of reaction is an esterification reaction. A representative synthesis for compound A-040 is described in Scheme 3-3. Scheme 3-3: An exemplary reaction sequence is shown in Scheme 4 for the compounds of formula (I) where X-W is O-C(=O), Y is NR ₀ , R ₀ is methyl and all further symbols and indices have a meaning as described before and the polymerizable group R ₁ is as shown in scheme 4. Scheme 4: The first type of reaction is a nucleophilic bromination reaction. The second type of reaction is a nucleophilic substitution amine synthesis. The third type of reaction is an esterification reaction. A representative synthesis for compound A-017 is described in Scheme 4-4. Scheme 4-4: As described before, the compounds/monomers of formulae (I), (Ia) and (Ib) as described before or preferably described before contain a polymerizable group and are predestinated as monomers for an oligomerization or a polymerization. The resulting oligomers, polymers or copolymers are advantageous materials being at least part of the ophthalmic device or precursor article for an ophthalmic device or building the material for the ophthalmic device or precursor article for the ophthalmic device according to the invention. The term "polymer" generally means a molecule of high relative molecular mass, the structure of which essentially comprises the multiple repetition of units derived, actually or conceptually, from molecules of low relative molecular mass (PAC, 1996, 68, 2291). The term “polymer” includes homopolymers and copolymers if not mentioned otherwise within the description. The term "oligomer" generally means a molecule of intermediate relative molecular mass, the structure of which essentially comprises a small plurality of units derived, actually or conceptually, from molecules of lower relative molecular mass (PAC, 1996, 68, 2291). In a preferred sense according to the present invention a polymer means a compound having ≥ 30 repeating units, and an oligomer means a compound with > 1 and < 30 repeating units. Above and below, in formulae showing a polymer, an oligomer, a compound of formulae (I), (Ia) or (Ib) or a monomeric unit or a polymer formed from a compound of formulae (I), (Ia) or (Ib), an asterisk ("*") denotes a linkage to the adjacent repeating unit in the polymer chain or oligomer chain or to a terminal end group whenever it is not specifically defined elsewhere. Suitable terminal end groups are known to the skilled artisan and depend on the polymerization method used. The terms "repeating unit" and "monomeric unit" mean the constitutional repeating unit (CRU), which is the smallest constitutional unit the repetition of which constitutes a regular macromolecule, a regular oligomer molecule, a regular block or a regular chain (PAC, 1996, 68, 2291). Unless stated otherwise, the molecular weight is given as the number average molecular weight M _n or weight average molecular weight M _W , which is determined by gel permeation chromatography (GPC) against polystyrene standards in eluent solvents such as tetrahydrofuran, trichloromethane (TCM, chloroform), chlorobenzene or 1,2,4-trichloro- benzene. Unless stated otherwise, tetrahydrofuran is used as solvent. The degree of polymerization (n) means the number average degree of polymerization given as n = M _n /M _U , wherein M _U is the molecular weight of the single repeating unit as described in J. M. G. Cowie, Polymers: Chemistry & Physics of Modern Materials, Blackie, Glasgow, 1991. In the polymers or copolymers according to the present invention as described below or within the ophthalmic device or precursor material for an ophthalmic device according to the invention, the total number of repeating units n is preferably ≥ 30, very preferably ≥ 100, most preferably ≥ 200, and preferably up to 5000, very preferably up to 3000, most preferably up to 2000, including any combination of the aforementioned lower and upper limits of n. The invention is therefore further directed to an oligomer, polymer or copolymer comprising at least one polymerized compound of formula (I) , wherein X-W is O-C(=O), O-C(=S), O-SO ₂ , SO ₂ -O, SO ₂ -C(=S), S-C(=O), S-C(=S), NR _B - C(=O) or NR _B -C(=S); RB is at each occurrence independently H, a linear or branched alkyl group having 1 to 6 C atoms or a linear or branched partially or fully fluorinated alkyl group having 1 to 10 C atoms; R ₃ is H or F; R ₄ is at each occurrence independently H, F, Cl, SF ₅ , CN or [Y ₁ ] _m1 -R ₅ ; R ₅ is a linear or branched alkyl group having 1 to 6 C atoms or a linear or branched partially or fully fluorinated alkyl group having 1 to 10 C atoms, a cycloalkyl group having 3 to 6 C atoms or a heterocycloalkyl group having 4 to 6 ring atoms; Y is O, S, SO, SO ₂ , Se, NR ₀ or a bond; Y ₁ is O, S or NR _B ; m1 is 0 or 1; R ₀ is at each occurrence independently selected from the group consisting of a linear or branched alkyl group having 1 to 4 C atoms; R ₁ is a trialkoxysilyl group or a dialkoxyalkylsilyl group where the alkyl and/or alkoxy groups are each independently linear or branched having 1 to 6 C atoms, or a silyl group of formula (1), (2) or (3) or a polymerizable group of formula (4), where alkyl means at each occurrence independently of each other a linear or branched alkyl group having 1 to 6 C atoms and each asterisk “*” denotes at each occurrence independently of each other a linkage to the rest of one or more compounds of formula (I) via the linker -R ₂ -Y-; and wherein X ₁₁ is selected from the group consisting of O, S, O-SO ₂ , SO ₂ -O, C(=O), OC(=O), C(=O)O, S(C=O) and (C=O)S, R ₆ , R ₇ , R ₈ are at each occurrence independently of each other selected from the group consisting of H, F, a linear or branched, non-fluorinated, partially or completely fluorinated alkyl group having 1 to 20 C atoms and aryl with 6 to 14 C atoms and c is 1; -R ₂ - is –(C(R) ₂ )o–, or –(C(R) ₂ ) _p –X ₈ –(C(R) ₂ ) _q –(X ₉ )s–(C(R) ₂ )r–(X ₁₀ )t-(C(R) ₂ )u-; R is at each occurrence independently selected from the group consisting of H, F, a linear or branched alkyl group having 1 to 4 C atoms or a linear or branched partially or fully fluorinated alkyl group having 1 to 4 C atoms; o is selected from the group consisting of 0 to 20, X ₈ , X ₉ , X ₁₀ are at each occurrence independently O, S, SO ₂ , or NR _B , s, t is 0 or 1, p, q are at each occurrence independently selected from the group consisting of 1 to 10, r, u are at each occurrence independently selected from the group consisting of 0 to 10, wherein the overall number of atoms for –(C(R) ₂ ) _p –X ₈ –(C(R) ₂ ) _q – (X ₉ ) _s –(C(R) ₂ ) _r –(X ₁₀ ) _t -(C(R) ₂ ) _u - is up to 20 atoms; and provided that in case of X-W is O-C(=O) and Y ₁ is NR _B , X ₁₁ is not O-C(=O), provided that in case of X-W is O-C(=O), Y is a bond, o is 1, m1 is 1, Y ₁ is O and c is 1, X ₁₁ is not O-C(=O); and provided that in case of X-W is O-C(=O), R ₁ is not a trialkoxysilyl group or a dialkoxyalkylsilyl group where the alkyl and/or alkoxy groups are each independently linear or branched having 1 to 6 C atoms, or a silyl group of formula (1), (2) or (3), or the invention is therefore further directed to an oligomer, polymer or copolymer comprising at least one polymerized compound of formulae (Ia) or (Ib) with substituents as described before or preferably described before. The polymers within the ophthalmic device or precursor material for an ophthalmic device according to the invention and/or the polymers of the present invention include homopolymers, statistical copolymers, random copolymers, alternating copolymers and block copolymers, and combinations of the aforementioned. Throughout the description and claims of this specification, the words “comprise” and “contain” and variations of the words, for example “comprising” and “comprises”, mean “including but not limited to”, and are not intended to (and do not) exclude other components. Preferably, the polymers within the ophthalmic device or precursor material for an ophthalmic device according to the invention and/or the oligomers, polymers or copolymers according to the invention comprise a constitutional unit M ⁰ based on formulae (I), (Ia) or (Ib), where the polymerizable group R ₁ on each occurrence is polymerized and forms the regioregular, alternated, regiorandom, statistical, block or random oligomer or polymer backbone or is part of the copolymer backbone and where all the symbols and indices used within the formulae (I), (Ia) and (Ib) have a meaning as described before or preferably described before. Preferably the polymerizable group R ₁ forms the regioregular, alternated, regiorandom, statistical, block or random homopolymer or copolymer backbone or is part of the polymer backbone where R ₁ has a meaning as described or preferably described before. The invention is furthermore directed to an ophthalmic device or a precursor article for an ophthalmic device as described before or preferably described below comprising an oligomer, polymer or copolymer comprising a constitutional unit M ⁰ based on formulae (I), (Ia) or (Ib) as described before or preferably described before where R ₁ on each occurrence is polymerized and forms the regioregular, alternated, regiorandom, statistical, block or random oligomer or polymer backbone or is part of the copolymer backbone. Preferably, such polymerized groups R ₁ are of formulae (1-p), (2-p), (3-p) or (4-p) , where the asterisk “*” within formulae (1-p) to (4-p) denotes a linkage to the adjacent repeating unit in the polymer chain or oligomer chain or to a terminal end group, the asterisk “**” within formulae (1-p) to (4-p) denotes the linkage to the remainder of formula (I) as described before or preferably described before and R ₆ , R ₇ , R ₈ , X ₁₁ and c have a meaning as described before or preferably described before. The invention is furthermore directed to an ophthalmic device or a precursor article for an ophthalmic device as described before or preferably described below where said polymerized group R ₁ is of formulae (1-p), (2-p), (3-p) or (4-p) as described before. The invention is furthermore directed to an oligomer, polymer or copolymer as described before or preferably described below where said polymerized group R ₁ is of formulae (1- p), (2-p), (3-p) or (4-p) as described before. Particularly preferably, such polymers within the ophthalmic device or precursor material for an ophthalmic device according to the invention and/or such oligomers, polymers or copolymers according to the invention comprise a constitutional unit M ⁰ of formulae (M ⁰ - Ia) or (M ⁰ -Ib), wherein R ₁ , -R ₂ -, X-W, Y, R ₃ , R ₄ , R ₆ , R ₇ , R ₈ , X ₁₁ and c have a meaning as described before or preferably described before and where the asterisk “*” denotes at each occurrence a linkage to the adjacent repeating unit in the polymer chain or oligomer chain or a linkage to a terminal end group. Combinations are excluded where two O atoms or an O atom and a S atom are directly linked to each other as known for a skilled artisan in the field of organic chemistry. The invention is furthermore directed to an ophthalmic device or a precursor article for an ophthalmic device as described before or preferably described below wherein the constitutional unit M ⁰ is of formulae (M ⁰ -Ia) or (M ⁰ -Ib) as described before and where the asterisk “*” denotes at each occurrence a linkage to the adjacent repeating unit in the polymer chain or oligomer chain or a linkage to a terminal end group. Preferably, such polymers within the ophthalmic device or precursor material for an ophthalmic device according to the invention and/or oligomers, polymers or copolymers according to the invention comprise a constitutional unit (M ⁰ -Ia) or (M ⁰ -Ib) as described before, wherein -R ₂ - is selected from -(CH ₂ ) ₃ -, -(CH ₂ ) ₄ -, -(CH ₂ ) ₅ -, -(CH ₂ ) ₆ -, -(CH ₂ ) ₇ -, -(CH ₂ ) ₈ -, -(CH ₂ ) ₉ -, - (CH ₂ ) ₁₀ -, -(CH ₂ ) ₁₁ -, -(CH ₂ ) ₁₂ -, -(CH ₂ ) ₁₃ -, -(CH(C ₃ H ₇ )-(CH ₂ ) ₂ -, -(CH(C ₂ H ₅ )-(CH ₂ ) ₃ -, - (CH(C ₂ H ₅ )-(CH ₂ ) ₄ -, -(CH(C ₂ H ₅ )-(CH ₂ ) ₇ -, -(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₂ -, - (CH ₂ ) ₄ -SO ₂ -(CH ₂ ) ₄ -, -(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -O-(CH ₂ ) ₃ -, -(CH ₂ ) ₃ -S-(CH ₂ ) ₃ -, -(CH ₂ ) ₂ - S-(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ - O-(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -, - (CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -O-(CH ₂ ) ₂ - S-(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₂ -O- (CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -S-(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₂ -S- (CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₂ -SO ₂ -(CH ₂ ) ₂ -, -(CH ₂ ) ₂ -O-(CH ₂ ) ₂ - SO ₂ -(CH ₂ ) ₂ -O-(CH ₂ ) ₂ -, -(CH ₂ ) ₃ -(CF ₂ )-(CH ₂ ) ₃ -, -(CH ₂ )-(CF ₂ ) ₃ -(CH ₂ )-, -(CH ₂ ) ₂ -(CF ₂ ) ₄ - (CH ₂ ) ₂ -, -(CH ₂ )-[CH(CF ₃ )]-(CH ₂ )-, -(CH ₂ )-[C(CH ₃ )CF ₃ ]-(CH ₂ )-, -(CH ₂ )-[CH(CH ₂ CF ₃ )]- (CH ₂ )-, -(CH ₂ )-[C(CH ₃ )(CH ₂ CF ₃ )]-(CH ₂ )-, -(CHC ₂ H ₅ )-(CH ₂ )-(CHCF ₃ )-(CH ₂ ) ₃ -, -(CH ₂ ) ₃ - (CHCF ₃ )-(CH ₂ ) ₃ -,-(CH ₂ ) ₂ -(CF ₂ )-O-(CF ₂ )-O-(CF ₂ )-(CH ₂ ) ₂ - and -(CH ₂ )-(CF ₂ )-O-(CF ₂ )-O- (CF ₂ )-O-(CF ₂ )-(CH ₂ )- or has a meaning as preferably described before. The copolymer within the ophthalmic device or precursor material for an ophthalmic device according to the invention or the copolymer according to the invention may be an oligomer or polymer comprising one or more polymerized compounds of formulae (I), (Ia) or (Ib) as described before or preferably described before or one or more constitutional units M ⁰ of formulae (M ⁰ -Ia) and/or (M ⁰ -Ib) as described before or preferably described before or one or more constitutional units (M ⁰ -001) to (M ⁰ -188) as described below, which may be the same or different from one another, and one or more constitutional units M ² , which may be the same or different from one another. Said one or more constitutional units M ² are chemically different from the units M ⁰ . Preferably, said one or more constitutional units M ² are derived by polymerization of one or more monomers selected from the group consisting of styrene, ethoxyethyl methacrylate (EOEMA), methyl methacrylate (MMA), methyl acrylate, n-alkyl acrylates (the n-alkyl group comprising 2-20 C-atoms), n-alkyl methacrylates (the n-alkyl group comprising 2-20 C-atoms), i-alkyl acrylates (the i-alkyl group comprising 3-20 C-atoms), i-alkyl methacrylates (the i-alkyl group comprising 3-20 C-atoms), ethoxyethoxy ethylacrylate (EEEA), n-hydroxalkyl acrylate (the n-alkyl group comprising 2 to 10 C-atoms), n-hydroxalkyl methacrylate (the n-alkyl group comprising 2 to 10 C-atoms), tetrahydrofuryl methacrylate (THFMA), glycidylmethacrylate (GMA), 16-hydroxyhexadecyl acrylate, 16-hydroxyhexadecyl methacrylate, 18-hydroxyoctadecyl acrylate, 18-hydroxyoctadecyl methacrylate, 2- phenoxyethyl acrylate (EGPEA), heptafluorobutyl acrylate, heptafluorobutyl methacrylate, hexafluorobutyl acrylate, hexafluorobutyl methacrylate, hexafluoroisopropyl acrylate, hexafluoroisopropyle methacrylate, octafluoropentyl acrylate, octafluoropentyl methacrylate, petanfluoropropyl acrylate, pentafluoropropyl methacrylate, tetrafluoropropyl methacrylate, trifluoroethyl acrylate, trifluoroethyl methacrylate, trimethyl- cyclohexyl acrylate, trimethylcyclohexyl methacrylate, 2-(4-bromophenyl)ethyl methacrylate, 4-phenylbutyl methacrylate, 4-methylphenyl methacrylate, phenyl methacrylate, 4-methylphenyl acrylate, benzyl acrylate, benzyl methacrylate, 2-benzyloxy- ethyl methacrylate, 3-benzyloxypropyl methacrylate, phenylethyl acrylate, phenylethyl methacrylate, 3-phenylpropyl methacrylate, 2-phenoxyethyl acrylate, 2-benzyloxyethyl acrylate, 3-phenylpropyl acrylate, 4-methylbenzyl acrylate, phenyl acrylate, 2-(phenyl- thio)ethyl methacrylate, 4-phenylbutyl acrylate, 5-phenylpentyl acrylate, 3-benzyloxypropyl acrylate, 2-(phenylthio)propyl acrylate, 2-(phenylthio)ethyl acrylate, 4-phenylbutyl acrylate, 4-methylbenzyl methacrylate, 2-(2-methylphenyl)ethyl acrylate, 2-(2-methylphenyl)ethyl methacrylate, 2-(3-methylphenyl)ethyl acrylate, 2-(3-methylphenyl)ethyl methacrylate, 2- (4-methylphenyl)ethyl acrylate, 2-(4-methylphenyl)ethyl methacrylate, 2-(4-propyl- phenyl)ethyl acrylate, 2-(4-propylphenyl)ethyl methacrylate, 2-(4-(1-methyl- ethyl)phenyl)ethyl acrylate, 2-(4-(1-methylethyl)phenyl)ethyl methacrylate, 2-(4- methoxyphenyl)ethyl methacrylate, 2-(4-methoxyphenyl)ethyl acrylate, 2-(4- cyclohexylphenyl)ethyl acrylate, 2-(4-cyclohexylphenyl)ethyl methacrylate, 2-(4- chlorophenyl)ethyl methacrylate, 2-(4-chlorophenyl)ethyl acrylate, 2-(3-chlorophenyl)ethyl methacrylate, 2-(3-chlorophenyl)ethyl acrylate, 2-(2-chlorophenyl)ethyl methacrylate, 2-(2- chlorophenyl)ethyl acrylate, 2-(4-bromophenyl)ethyl acrylate, 2-(4-phenylphenyl)ethyl methacrylate, 2-(4-phenylphenyl)ethyl acrylate, 2-(3-phenylphenyl)ethyl methacrylate, 2- (3-phenylphenyl)ethyl acrylate, 2-(4-benzylphenyl)ethyl methacrylate, 2-(4- benzylphenyl)ethyl acrylate, 2-(phenylthio)ethyl acrylate, 3-benzyloxypropyl acrylate, 2-[2- (benzyloxy)ethoxy]ethyl acrylate, 2-[2-(benzyloxy)ethoxy]ethyl methacrylate, pentafluorophenyl methacrylate, heptadecafluorodecyl methacrylate, dodecafluoroheptyl methacrylate, heptadecafluorodecyl acrylate, pentafluorophenyl acrylate. The invention therefore relates further to an ophthalmic device or a precursor article for the ophthalmic device as described or preferably described before comprising beside of the at least one polymerized compound of formulae (I), (Ia) or (Ib) or the constitutional unit M ⁰ of formulae (M ⁰ -Ia) and/or (M ⁰ -Ib) as described before or preferably described before or one or more constitutional units (M ⁰ -001) to (M ⁰ -188) as described one or more constitutional units M ² derived by polymerization of one or more co-monomers selected from the group consisting of styrene, ethoxyethyl methacrylate (EOEMA), methyl methacrylate (MMA), methyl acrylate, n-alkyl acrylates (the n-alkyl group comprising 2-20 C-atoms), n-alkyl methacrylates (the n-alkyl group comprising 2-20 C-atoms), i-alkyl acrylates (the i-alkyl group comprising 3-20 C-atoms), i-alkyl methacrylates (the i-alkyl group comprising 3-20 C-atoms), ethoxyethoxy ethylacrylate (EEEA), n-hydroxalkyl acrylate (the n-alkyl group comprising 2 to 10 C-atoms), n-hydroxalkyl methacrylate (the n-alkyl group comprising 2 to 10 C-atoms), tetrahydrofuryl methacrylate (THFMA), glycidyl methacrylate (GMA), 16-hydroxyhexadecyl acrylate, 16-hydroxyhexadecyl methacrylate, 18-hydroxyoctadecyl acrylate, 18-hydroxyoctadecyl methacrylate, 2-phenoxyethyl acrylate (EGPEA), heptafluorobutyl acrylate, heptafluorobutyl methacrylate, hexafluorobutyl acrylate, hexafluorobutyl methacrylate, hexafluoroisopropyl acrylate, hexafluoroisopropyle methacrylate, octafluoropentyl acrylate, octafluoropentyl methacrylate, petanfluoropropyl acrylate, pentafluoropropyl methacrylate, tetrafluoropropyl methacrylate, trifluoroethyl acrylate, trifluoroethyl methacrylate, trimethylcyclohexyl acrylate, trimethylcyclohexyl methacrylate, 2-(4-bromophenyl)ethyl methacrylate, 4-phenylbutyl methacrylate, 4- methylphenyl methacrylate, phenyl methacrylate, 4-methylphenyl acrylate, benzyl acry- late, benzyl methacrylate, 2-benzyloxyethyl methacrylate, 3-benzyloxypropyl methacrylate, phenylethyl acrylate, phenylethyl methacrylate, 3-phenylpropyl methacrylate, 2-phenoxyethyl acrylate, 2-benzyloxyethyl acrylate, 3-phenylpropyl acrylate, 4-methylbenzyl acrylate, phenyl acrylate, 2-(phenylthio)ethyl methacrylate, 4-phenylbutyl acrylate, 5-phenylpentyl acrylate, 3-benzyloxypropyl acrylate, 2-(phenylthio)propyl acrylate, 2-(phenylthio)ethyl acrylate, 4-phenylbutyl acrylate, 4-methylbenzyl methacrylate, 2-(2-methylphenyl)ethyl acrylate, 2-(2-methylphenyl)ethyl methacrylate, 2-(3-methyl- phenyl)ethyl acrylate, 2-(3-methylphenyl)ethyl methacrylate, 2-(4-methylphenyl)ethyl acrylate, 2-(4-methylphenyl)ethyl methacrylate, 2-(4-propylphenyl)ethyl acrylate, 2-(4- propylphenyl)ethyl methacrylate, 2-(4-(1-methylethyl)phenyl)ethyl acrylate, 2-(4-(1- methylethyl)phenyl)ethyl methacrylate, 2-(4-methoxyphenyl)ethyl methacrylate, 2-(4- methoxyphenyl)ethyl acrylate, 2-(4-cyclohexylphenyl)ethyl acrylate, 2-(4- cyclohexylphenyl)ethyl methacrylate, 2-(4-chlorophenyl)ethyl methacrylate, 2-(4- chlorophenyl)ethyl acrylate, 2-(3-chlorophenyl)ethyl methacrylate, 2-(3-chlorophenyl)ethyl acrylate, 2-(2-chlorophenyl)ethyl methacrylate, 2-(2-chlorophenyl)ethyl acrylate, 2-(4- bromophenyl)ethyl acrylate, 2-(4-phenylphenyl)ethyl methacrylate, 2-(4- phenylphenyl)ethyl acrylate, 2-(3-phenylphenyl)ethyl methacrylate, 2-(3- phenylphenyl)ethyl acrylate, 2-(4-benzylphenyl)ethyl methacrylate, 2-(4- benzylphenyl)ethyl acrylate, 2-(phenylthio)ethyl acrylate, 3-benzyloxypropyl acrylate, 2-[2- (benzyloxy)ethoxy]ethyl acrylate, 2-[2-(benzyloxy)ethoxy]ethyl methacrylate, pentafluorophenyl methacrylate, heptadecafluorodecyl methacrylate, dodecafluoroheptyl methacrylate, heptadecafluorodecyl acrylate, pentafluorophenyl acrylate. The term constitutional units M ² derived by polymerization of one or more co-monomers may comprise compounds having the function of a cross-linker, blue absorber or UV absorber as further described below. By using n-alkyl acrylates as co-monomer beside the compounds of formulae (I), (Ia) or (Ib), the n-alkyl group has preferably 2 to 10 C-atoms, particularly preferably 2 to 5 C- atoms and very particularly preferably 4 C-atoms. By using n-alkyl methacrylates as co-monomer beside the compounds of formulae (I), (Ia) or (Ib), the n-alkyl group has preferably 2 to 10 C-atoms, particularly preferably 2 to 5 C- atoms and very particularly preferably 4 C-atoms. By using i-alkyl acrylates as co-monomer beside the compounds of formulae (I), (Ia) or (Ib), the i-alkyl group has preferably 3 to 10 C-atoms, particularly preferably 5 to 10 C- atoms and very particularly preferably 10 C-atoms. By using i-alkyl methacrylates as co-monomer beside the compounds of formulae (I), (Ia) or (Ib), the i-alkyl group has preferably 3 to 10 C-atoms, particularly preferably 5 to 10 C- atoms and very particularly preferably 10 C-atoms. By using n-hydroxyalkyl acrylates as further monomer beside the compounds of formulae (I), (Ia) or (Ib), the n-hydroxyalkyl group has preferably 2 to 8 C-atoms, particularly preferably 2 to 5 C-atoms, more preferably 2 to 4 C-atoms, and very particularly preferably 2 or 4 C-atoms. By using n-hydroxyalkyl methacrylates as further monomer beside the compounds of formulae (I), (Ia) or (Ib), the n-hydroxyalkyl group has preferably 2 to 8 C-atoms, particularly preferably 2 to 5 C-atoms, more preferably 2 to 4 C-atoms, and very particularly preferably 2 or 4 C-atoms. Particularly preferably, the at least one further co-monomer beside of crosslinkers and/or UV absorbers as described below is selected from methyl methacrylate, n-alkyl acrylates (the n-alkyl group comprising 2-20 C-atoms), fluorinated n-alkyl acrylates (the n-alkyl group comprising 2-20 C-atoms), n-alkyl methacrylates (the n-alkyl group comprising 2-20 C-atoms), fluorinated n-alkyl methacrylates (the n-alkyl group comprising 2-20 C-atoms), i- alkyl acrylates (the i-alkyl group comprising 3-20 C-atoms), fluorinated i-alkyl acrylates (the i-alkyl group comprising 3-20 C-atoms), i-alkyl methacrylates (the i-alkyl group comprising 3-20 C-atoms), fluorinated i-alkyl methacrylates, n-hydroxyalkyl acrylates (the n-alkyl group comprising 2-10 C-atoms), n-hydroxyalkyl methacrylates (the n-alkyl group comprising 2-10 C-atoms) or a mixture thereof. Particularly preferably, the at least one further co-monomer beside of crosslinkers and/or UV absorbers as described below is selected from methyl methacrylate, 2-hydroxyethyl methacrylate, 2-hydroxyethyl acrylate, 3-hydroxypropyl methacrylate, 3-hydroxypropyl acrylate, 4-hydroxybutyl methacrylate, 4-hydroxybutyl acrylate, 5-hydroxypentyl methacrylate, 5-hydroxypentyl acrylate, 8-methylnonyl methacrylate, n-butyl-acrylate, n- butyl methacrylate, ethyl methacrylate, 2-ethyl hexylmethacrylate, 2,2,3,3,4,4,5,5- octafluoropentyl acrylate or a mixture thereof. Both hydrophobic, soft acrylate polymers and siloxane polymers, which are known for use for the production of intraocular lenses, exhibit glistening. The tendency towards glistening is more pronounced in the first-mentioned polymers. According to A. Miyata and S. Yaguchi, J Cataract Refract Surg 2004; 30:1768–1772, glistening is a phase-separation phenomenon that occurs in the case of temperature variations as soon as the polymer is located in an aqueous environment, as is the case in the human eye. The water content of the polymer increases with the temperature. In the case of a temperature drop, the water absorption capacity of the polymer falls, causing phase separation. The polymer phase here has a different refractive index to the water phase, causing the water phase in the form of vacuoles to be perceived as glistening. The degree of glistening is crucially determined by the temperature dependence of the water content of the polymer. The greater the temperature dependence, the more severe the glistening- induced visual impairment of the patient can be. The water content of a polymer can be increased by addition of a hydrophilic component during the polymerisation. A hydrophilic component is a monomer whose uncrosslinked homopolymer is water-soluble or swellable in water. Examples are described before and below. For the division of intraocular lenses into hydrophilic and hydrophobic lenses, Bozukova et al indicate their water content as the division criterion. If this water content is less than 10 - 20% by weight, it is a hydrophobic intraocular lens; if this water content is greater than 10 - 20% by weight, it is a hydrophilic intraocular lens (literature: Bozukova D, Pagnoulle C, Jêrome R, Jêrome C, (2010) Polymers in modern ophthalmic implants -Historical background and recent advances, Material Science and Engineering R 69:63-83). The water absorption of a material is the more appropriate decision criterion with respect to hydrophilicity and hydrophobicity for the polymers prepared in the context of this invention with respect to their area of application. For division of monomers into hydrophilic and hydrophobic monomers, it is useful in the context of this invention and the application aims thereof to use a division described by Bozukova et al: if a monomer gives a homopolymer which is either completely water-soluble or has a water absorption of greater than 10% by weight, this exhibits a hydrophilic property and is classified as hydrophilic monomer for the purposes of this invention. The hydrophilic property is caused by functional groups in the monomer which are capable of binding water molecules. The property can be confirmed in the swollen state by the presence of non-freezable water. The non-freezable water here is based on the fact that functional groups in the polymer bind water per se and this water is therefore not capable of forming ice crystals, irrespective of the temperature. Unaffected by this, a polymer of this type may also contain freezable water which forms ice crystals, but this is not utilised for the division into hydrophilic and hydrophobic monomers. Examples of functional groups which are capable of binding non-freezable water are, inter alia, hydroxyl groups, amino groups, ammonium groups, carboxyl groups, sulfone groups, sulfate groups, ether bridges or amide groups. The presence of functional groups of this type in a monomer is thus an indicator of a hydrophilic monomer. Therefore, if a monomer satisfies one or more of the said criteria water solubility of the resultant homopolymer, water absorption of the resultant homopolymer greater than 10% by weight and/or presence of non-freezable water in the resultant homopolymer, this is a "hydrophilic monomer" for the purposes of the invention. If a monomer does not satisfy any of the said criteria, this is referred to as "non-hydrophilic monomer" for the purposes of the invention. By using a hydrophilic co-monomer, thus building a constitutional unit M ² , as described before beside of the at least one compound of formulae (I), (Ia) or (Ib) as described before or preferably described before, the resulting copolymer to be used in the ophthalmic device according to the invention or to be used in the precursor material for an ophthalmic device according to the invention exhibits little glistening or no glistening and is sufficiently hydrophobic at the same time so that calcification cannot occur. This is a further advantage for the ophthalmic device according to the invention. The invention therefore relates further to an ophthalmic device or a precursor article for the ophthalmic device as described or preferably described before comprising beside of the at least one polymerized compound of formulae (I), (Ia) or (Ib) or the constitutional unit M ⁰ of formulae (M ⁰ -Ia) and/or (M ⁰ -Ib) as described before or preferably described before or one or more constitutional units (M ⁰ -001) to (M ⁰ -188) as described below at least one further polymerized hydrophilic monomer as described before, preferably selected from the group consisting of n-hydroxalkyl acrylate (the n-alkyl group comprising 2 to 10 C- atoms), n-hydroxalkyl methacrylate (the n-alkyl group comprising 2 to 10 C-atoms), glycidyl methacrylate (GMA), N-vinylpyrrolidone and 2-phenoxyethyl acrylate (EGPEA). The invention therefore relates further to an ophthalmic device or a precursor article for the ophthalmic device as described or preferably described before comprising beside of the at least one polymerized compound of formulae (I), (Ia) or (Ib) or the constitutional unit M ⁰ of formulae (M ⁰ -Ia) and/or (M ⁰ -Ib) as described before or preferably described before or one or more constitutional units (M ⁰ -001) to (M ⁰ -188) as described below at least one further polymerized hydrophilic monomer as described before, preferably selected from the group consisting of n-hydroxalkyl acrylate (the n-alkyl group comprising 2 to 10 C- atoms), n-hydroxalkyl methacrylate (the n-alkyl group comprising 2 to 10 C-atoms), glycidyl methacrylate (GMA), N-vinylpyrrolidone and 2-phenoxyethyl acrylate (EGPEA). Particularly preferably, such copolymer is comprised in the ophthalmic device or precursor article for an ophthalmic device according to the invention. Alternatively the oligomer or polymer, preferably the polymer, according to the invention is a homopolymer, i.e. an oligomer or polymer, preferably a polymer, comprising one or more constitutional units M ⁰ of formula (M ⁰ -Ia) or (M ⁰ -Ib) as described before or preferably described before or (M ⁰ -001) to (M ⁰ -188) as described below and wherein all constitutional units M ⁰ are the same. Exemplary homopolymeric compounds based on compounds of formulae (I), (Ia) and/or (Ib) are the following compounds (P-001) to (P-188) as shown in table 2. Table 2:

The letter n gives the degree of polymerization as explained before. Exemplary constitutional units M ⁰ based on compounds of formulae (I), (Ia) and/or (Ib) or constitutional units M ⁰ of formulae (M ⁰ -Ia) or (M ⁰ -Ib) are the following compounds (M ⁰ - 001) to (M ⁰ -188) as shown in table 2-1. Table 2-1:

Preferably a copolymer within the ophthalmic device or precursor material for an ophthalmic device according to the invention or the copolymer according to the invention as described before or preferably described before comprises the one or more constitutional units M ⁰ as described before with substituents as described before or preferably described before in a molar ratio m1 and the one or more constitutional units M ² as described before or preferably described before in a molar ratio m2, wherein the ratio m1 : m2 is at least 0.01 and at most 100. Particularly preferably, such copolymer is comprised in the ophthalmic device or precursor article for an ophthalmic device according to the invention. Preferably a copolymer within the ophthalmic device or precursor material for an ophthalmic device according to the invention or the copolymer according to the invention as described before or preferably described before comprises the one or more constitutional units M ⁰ as described before with substituents as described before or preferably described before in a concentration of at least 12 wt% to 70 wt%, preferably in a concentration of at least 15 wt% to 60 wt% or at least 18 wt% to 55 wt%, or at least 20 wt% to 45 wt%. Particularly preferably, such copolymer is comprised in the ophthalmic device or precursor article for an ophthalmic device according to the invention. The invention therefore relates further to an ophthalmic device or a precursor article for the ophthalmic device as described or preferably described before wherein the total amount of photoactive chromophores of the polymerized compounds of formulae (I), (Ia) or (Ib) or the total amount of constitutional unit M ⁰ of formulae (M ⁰ -Ia) and/or (M ⁰ -Ib) as described before or preferably described before or the total amount of the constitutional units (M ⁰ -001) to (M ⁰ -188) as described below is at least 12 wt% to 70 wt%, preferably at least 15 wt% to 60 wt%, particularly preferably at least 18 wt% to 55 wt%, very particularly preferably at least 20 wt% to 45 wt%. The invention therefore relates further to an ophthalmic device or a precursor article for the ophthalmic device as described or preferably described before wherein the total amount of photoactive chromophores of the polymerized compounds of formulae (I), (Ia) or (Ib) or the total amount of constitutional unit M ⁰ of formulae (M ⁰ -Ia) and/or (M ⁰ -Ib) as described before or preferably described before or the total amount of the constitutional units (M ⁰ -001) to (M ⁰ -188) as described below is at least 12 wt% to 70 wt%, preferably at least 15 wt% to 60 wt%, particularly preferably at least 18 wt% to 55 wt%, very particularly preferably at least 20 wt% to 45 wt% and where the total amount of polymerized hydrophilic monomer as described before or preferably described before is at least 1 wt% to 80 wt%, preferably 5 wt% to 55 wt%, particularly preferably 8 wt% to 40 wt%, very particularly preferably 10 to 30 wt%. The oligomers, polymers or copolymers, preferably polymers or copolymers, within the ophthalmic device or precursor material for an ophthalmic device according to the invention or the oligomers, polymers or copolymer according to the invention as described before or preferably described may be cross-linked. Particularly preferably, such polymer or copolymer is comprised in the ophthalmic device or precursor article for an ophthalmic device according to the invention. The oligomers, polymers or copolymers within the ophthalmic device or precursor material for an ophthalmic device according to the invention or the oligomer, polymer or copolymer according to the invention of the present invention may be made by any suitable method. It is, however, preferred that the present oligomers, polymers and copolymers are made by radical polymerization, wherein the polymerization reaction is started by means of a suitable radical polymerization initiator. For the purposes of the present invention the type of radical polymerization initiator is not particularly limited and may be any suitable radical generating compound. Such compounds are well known to the skilled person. Suitable polymerization initiators may be selected from thermal initiators or photoinitiators, i.e. compounds that generate radicals by exposure to heat or irradiation with light of a suitable wavelength. Examples of suitable thermal polymerization initiators may be selected from the groups of compounds comprising one or more peroxide groups, i.e. compounds comprising a group –O–O–, and/or compounds comprising one or more azo groups, i.e. compounds comprising a group –N≡N–. Suitable polymerization initiators comprising one or more peroxide groups may, for example, be selected from the groups consisting of t-butyl(peroxy-2-ethyl-hexanoate), di- (tert-butylcyclohexyl)peroxydicarbonate and benzoylperoxide. Suitable polymerization initiators comprising one or more azo groups may, for example, be selected from the group consisting of 1,1’-azobis(cyclohexancarbonitrile) and 2,2’azobis(cyclohexanecarbonitrile) (AIBN). Suitable examples of a photoinitiator are dimethylaminobenzoate /camphorquinone, diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide (TPO) or phenylbis(2,4,6- trimethylbenzoyl)phosphine oxide (BAPO). If a photoinitiator is used as polymerization initiator, it is preferred that the wavelength required to decompose said photoinitiator is different from the wavelength needed to irradiate the compound of the present application so as to change its optical properties. Preferably, the radical initiators are used in an amount of at least 0.0001 eq and of at most 0.1 eq of the main monomer. Such radical initiators could be thermal initiators, e.g. azobisisobutyronitrile (AIBN) or photochemical initiators like dimethylaminobenzoate/camphorquinone, diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide (TPO) or phenylbis(2,4,6-trimethylbenzoyl)phosphine oxide (BAPO). Preferred ophthalmic devices are optically active ophthalmic devices. Examples of such ophthalmic devices or eye-implants include lenses, keratoprostheses, and corneal inlays or rings. More preferably, said ophthalmic device or eye-implant is a lens article. Most preferably, such ophthalmic device is a lens. The type of lens is not restricted and may comprise a contact lens or an intraocular lens. Most preferably, such ophthalmic device is an intraocular lens, which may, for example, be a posterior chamber intraocular lens or an anterior chamber intraocular lens. A blank of this invention may be produced as a step in the manufacturing process used to create an ophthalmic device as described before, preferably an intraocular lens. For example, without limitation, a manufacturing process may include the steps of polymer synthesis, polymer sheet casting, blank cutting, optic lathe cutting, optic milling, haptic milling or attachment, polishing, solvent extraction, sterilization and packaging while the term polymer is used as described before or preferably described before. The present ophthalmic devices or precursor articles for an ophthalmic device according to the invention as described before or preferably described before may be formed by a process comprising the steps of - providing a composition comprising at least one compound of formulae (I), (Ia) or (Ib) or the compounds (A-001) to (A-188) as described herein or preferably described herein and/or an oligomer or polymer as described herein or preferably described herein but having at least one reactive group left for polymerization and optionally further monomers different from compounds of formulae (I), (Ia) and (Ib) or the compounds (A- 001) to (A-188) as described herein or preferably described herein and/or crosslinking agents and/or UV absorbers and/or radical initiators; and - subsequently forming the ophthalmic device or precursor article of said composition. The present invention is also directed to a composition for polymerization comprising a compound of formula (I) wherein X-W is O-C(=O), O-C(=S), O-SO ₂ , SO ₂ -O, SO ₂ -C(=S), S-C(=O), S-C(=S), NR _B - C(=O) or NR _B -C(=S); R _B is at each occurrence independently H, a linear or branched alkyl group having 1 to 6 C atoms or a linear or branched partially or fully fluorinated alkyl group having 1 to 10 C atoms; R ₃ is H or F; R ₄ is at each occurrence independently H, F, Cl, SF ₅ , CN or [Y ₁ ] _m1 -R ₅ ; R ₅ is a linear or branched alkyl group having 1 to 6 C atoms or a linear or branched partially or fully fluorinated alkyl group having 1 to 10 C atoms, a cycloalkyl group having 3 to 6 C atoms or a heterocycloalkyl group having 4 to 6 ring atoms; Y is O, S, SO, SO ₂ , Se, NR ₀ or a bond; Y ₁ is O, S or NR _B ; m1 is 0 or 1; R ₀ is at each occurrence independently selected from the group consisting of a linear or branched alkyl group having 1 to 4 C atoms; R ₁ is a trialkoxysilyl group or a dialkoxyalkylsilyl group where the alkyl and/or alkoxy groups are each independently linear or branched having 1 to 6 C atoms, or a silyl group of formula (1), (2) or (3) or a polymerizable group of formula (4), , , where alkyl means at each occurrence independently of each other a linear or branched alkyl group having 1 to 6 C atoms and each asterisk “*” denotes at each occurrence independently of each other a linkage to the rest of one or more compounds of formula (I) via the linker -R ₂ -Y-; and wherein X ₁₁ is selected from the group consisting of O, S, O-SO ₂ , SO ₂ -O, C(=O), OC(=O), C(=O)O, S(C=O) and (C=O)S, R ₆ , R ₇ , R ₈ are at each occurrence independently of each other selected from the group consisting of H, F, a linear or branched, non-fluorinated, partially or completely fluorinated alkyl group having 1 to 20 C atoms and aryl with 6 to 14 C atoms and c is 1; -R ₂ - is –(C(R) ₂ ) _o –, or –(C(R) ₂ ) _p –X ₈ –(C(R) ₂ ) _q –(X ₉ ) _s –(C(R) ₂ ) _r –(X ₁₀ ) _t -(C(R) ₂ ) _u -; R is at each occurrence independently selected from the group consisting of H, F, a linear or branched alkyl group having 1 to 4 C atoms or a linear or branched partially or fully fluorinated alkyl group having 1 to 4 C atoms; o is selected from the group consisting of 0 to 20, X ₈ , X ₉ , X ₁₀ are at each occurrence independently O, S, SO ₂ , or NR _B , s, t is 0 or 1, p, q are at each occurrence independently selected from the group consisting of 1 to 10, r, u are at each occurrence independently selected from the group consisting of 0 to 10, wherein the overall number of atoms for –(C(R) ₂ ) _p –X ₈ –(C(R) ₂ ) _q –(X ₉ ) _s – (C(R) ₂ ) _r –(X ₁₀ ) _t -(C(R) ₂ ) _u - is up to 20 atoms; provided that in case of X-W is O-C(=O) and Y ₁ is NR _B , X ₁₁ is not O-C(=O), provided that in case of X-W is O-C(=O), Y is a bond, o is 1, m1 is 1, Y ₁ is O and c is 1, X ₁₁ is not O-C(=O); and provided that in case of X-W is O-C(=O), R ₁ is not a trialkoxysilyl group or a dialkoxyalkylsilyl group where the alkyl and/or alkoxy groups are each independently linear or branched having 1 to 6 C atoms, or a silyl group of formula (1), (2) or (3), , or a compound of formulae (Ia) or (Ib) with substituents as described before or preferably described before and a crosslinking agent and/or a UV absorber and/or a radical initiator and optionally further monomers different from compounds of formulae (I), (Ia) or (Ib). Depending upon the intended manufacturing process of the ophthalmic device or precursor article of said ophthalmic device such composition for polymerization as described or preferably described before may comprise further different components. Such further components may, for example, be selected from the group consisting of UV absorbers, antioxidants and cross-linkers. Cross-linkers (crosslinkers) may also be referred to as crosslinking agents. The present application is also directed to a composition for polymerization comprising at least one compound of formulae (I), (Ia) or (Ib) or compounds (A-001) to (A-188) as described or preferably described before and/or an oligomer or polymer as described before or preferably described before but having at least one reactive group left for polymerization and/or a crosslinking agent and/or a UV absorber and/or a radical initiator and optionally further monomers different from compounds of formulae (I), (Ia) and (Ib) or the compounds (A-001) to (A-188). A composition comprising at least one compound of formulae (I), (Ia) or (Ib) or compounds (A-001) to (A-188) as described or preferably described before or at least an oligomer or polymer comprising polymerized compounds of formulae (I), (Ia) or (Ib) or compounds (A- 001) to (A-188) as described or preferably described before is primarily used for the synthesis of block copolymers with the condition that the oligomer or polymer has at least one reactive group left which may react with the monomers. The described compositions may include or comprise, essentially consist of or consist of the said requisite or optional constituents. All compounds or components which can be used in the compositions are either known and commercially available or can by synthesized by known processes or as described herein. The components of the composition for polymerization as described before are combined in such amounts that at least 12 wt% to 70 wt%, preferably at least 15 wt% to 60 wt%, particularly preferably at least 18 wt% to 55 wt%, or very particularly preferably at least 20 wt% to 45 wt% of photoactive chromophores of polymerized formulae (I), (Ia) or (Ib) are comprised in the resulting oligomers, polymers or copolymers. The components of the composition for polymerization as described before are preferably combined in such amounts that at least 12 wt% to 70 wt%, preferably at least 15 wt% to 60 wt%, particularly preferably at least 18 wt% to 55 wt%, or very particularly preferably at least 20 wt% to 45 wt% of photoactive chromophores of polymerized formulae (I), (Ia) or (Ib) are comprised in the resulting oligomers, polymers or copolymers and that at least 1 wt% to 80 wt%, preferably 5 wt% to 55 wt%, particularly preferably 8 wt% to 40 wt%, very particularly preferably 10 to 30 wt% of polymerized hydrophilic monomer as described before or preferably described before is comprised in the resulting oligomers, polymers or copolymers. Besides one or more compounds of the formulae (I), (Ia) or (Ib), as described above or preferably described or the compounds (A-001) to (A-188) and the hydrophilic monomers, as described above, in the said molar ratios, the composition according to the invention may comprise at least one further non-hydrophilic co-monomer which does not conform to the formula (I) and optionally at least one blue absorber. Said non-hydrophilic monomers are preferably selected from styrene, methyl methacrylate (MMA), methyl acrylate, n-alkyl acrylates (the n-alkyl group comprising 2-20 C-atoms), n- alkyl methacrylates (the n-alkyl group comprising 2-20 C-atoms), i-alkyl acrylates (the i- alkyl group comprising 3-20 C-atoms), i-alkyl methacrylates (the i-alkyl group comprising 3-20 C-atoms), tetrahydrofuryl methacrylate (THFMA), heptafluorobutyl acrylate, heptafluorobutyl methacrylate, hexafluorobutyl acrylate, hexafluorobutyl methacrylate, hexafluoroisopropyl acrylate, hexafluoroisopropyle methacrylate, octafluoropentyl acrylate, octafluoropentyl methacrylate, petanfluoropropyl acrylate, pentafluoropropyl methacrylate, tetrafluoropropyl methacrylate, trifluoroethyl acrylate, trifluoroethyl methacrylate, trimethyl- cyclohexyl acrylate, trimethylcyclohexyl methacrylate, 2-(4-bromophenyl)ethyl methacrylate, 4-phenylbutyl methacrylate, 4-methylphenyl methacrylate, phenyl methacrylate, 4-methylphenyl acrylate, benzyl acrylate, benzyl methacrylate, 2-benzyloxy- ethyl methacrylate, 3-benzyloxypropyl methacrylate, phenylethyl acrylate, phenylethyl methacrylate, 3-phenylpropyl methacrylate, 2-phenoxyethyl acrylate, 2-benzyloxyethyl acrylate, 3-phenylpropyl acrylate, 4-methylbenzyl acrylate, phenyl acrylate, 2-(phenyl- thio)ethyl methacrylate, 4-phenylbutyl acrylate, 5-phenylpentyl acrylate, 3-benzyloxypropyl acrylate, 2-(phenylthio)propyl acrylate, 2-(phenylthio)ethyl acrylate, 4-phenylbutyl acrylate, 4-methylbenzyl methacrylate, 2-(2-methylphenyl)ethyl acrylate, 2-(2-methylphenyl)ethyl methacrylate, 2-(3-methylphenyl)ethyl acrylate, 2-(3-methylphenyl)ethyl methacrylate, 2- (4-methylphenyl)ethyl acrylate, 2-(4-methylphenyl)ethyl methacrylate, 2-(4-propyl- phenyl)ethyl acrylate, 2-(4-propylphenyl)ethyl methacrylate, 2-(4-(1-methyl- ethyl)phenyl)ethyl acrylate, 2-(4-(1-methylethyl)phenyl)ethyl methacrylate, 2-(4- methoxyphenyl)ethyl methacrylate, 2-(4-methoxyphenyl)ethyl acrylate, 2-(4- cyclohexylphenyl)ethyl acrylate, 2-(4-cyclohexylphenyl)ethyl methacrylate, 2-(4- chlorophenyl)ethyl methacrylate, 2-(4-chlorophenyl)ethyl acrylate, 2-(3-chlorophenyl)ethyl methacrylate, 2-(3-chlorophenyl)ethyl acrylate, 2-(2-chlorophenyl)ethyl methacrylate, 2-(2- chlorophenyl)ethyl acrylate, 2-(4-bromophenyl)ethyl acrylate, 2-(4-phenylphenyl)ethyl methacrylate, 2-(4-phenylphenyl)ethyl acrylate, 2-(3-phenylphenyl)ethyl methacrylate, 2- (3-phenylphenyl)ethyl acrylate, 2-(4-benzylphenyl)ethyl methacrylate, 2-(4- benzylphenyl)ethyl acrylate, 2-(phenylthio)ethyl acrylate, 3-benzyloxypropyl acrylate, 2-[2- (benzyloxy)ethoxy]ethyl acrylate, 2-[2-(benzyloxy)ethoxy]ethyl methacrylate, pentafluorophenyl methacrylate, heptadecafluorodecyl methacrylate, dodecafluoroheptyl methacrylate, heptadecafluorodecyl acrylate, pentafluorophenyl acrylate. Suitable blue absorbers are substances which exhibit absorption in the blue wavelength region of visible light. A blue absorber which is likewise an acrylate or a methacrylate and is available as further monomer during the polymerisation is preferably selected. Suitable blue absorbers are known from the literature, for example from WO 2012/167124. A particularly preferred blue absorber is N-2-[3-(2'-methylphenylazo)-4-hydroxyphenylethyl]- ethylmethacrylamide. They can be added to the composition as described in order that the polymerised composition is also able to filter short-wave visible light in addition to the UV light in order thus to protect the retina better if the material is used for the production of an ophthalmological product. The UV absorber that may be used in the composition for polymerization as described before is not particularly limited and can easily be selected from those generally known to the skilled person. Generally suitable UV absorbers are characterized by being unsaturated compounds, preferably compounds comprising one or more selected from group consisting of olefinic groups, aryl groups and heteroaryl groups; these groups may be present in any combination. Suitable UV-absorber for use in the composition for polymerization as described before may, for example, be selected from those comprising a group selected from benzotriazole, benzophenone and triazine. Suitable UV-absorbers are, for example, disclosed in U.S. Pat. Nos.5,290,892; 5,331,073 and 5,693,095. Suitable UV-absorber are 2-(3-(t-butyl)-4-hydroxy-5-(5-methoxy-2- benzotriazolyl)phenoxy)ethyl methacrylate, 3-(3-(t-butyl)-4-hydroxy-5-(5-methoxy-2- benzotriazolyl)phenoxy)propyl methacrylate, 3-(3-t-butyl-5-(5-chlorobenzotriazol-2-yl)-4- hydroxyphenyl)propyl methacrylate, 3-(3-(tert-butyl)-4-hydroxy-5-(5-methoxy-2H- benzo[d][1,2,3]triazol-2-yl)phenoxy)propylmethacrylate, 2-(2-hydroxy-5-vinylphenyl)-2H- benzotriazol, allyl-2-hydroxybenzophenon, 2-allyl-6-(2H-benzotriazol-2-yl)-p-cresol, 4- methacryloxy-2-hydroxybenzophenon, 2-(2'-hydroxy-3'-methallyl-5'- methylphenyl)benzotriazol, 2-hydroxy-4-methacryloyloxybenzophenon, 4-acryloylethoxy- 2-hydroxybenzophenon, 2-[3-(2H-benzotriazol-2-yl)-4-hydroxyphenyl]ethylmethacrylat e, 2- (2'-hydroxy-5'-methacrylamidophenyl)-5-methoxybenzotriazol, 2-(2'-hydroxy-5'- methacrylamidophenyl)-5-chlorobenzotriazol, 2-(2'-hydroxy-5'- methacryloxypropylphenyl)benzotriazol, 2-(2'-hydroxy-5'-methacryloylpropyl-3'-tert-butyl- phenyl)-5-methoxy-2H-benzotriazol, 2-(3-(tert-butyl)-4-hydroxy-5-(5-methoxy-2H- benzo[d][1,2,3]triazol-2-yl)phenoxy)ethylmethacrylat, 2-[3'-tert-butyl-2'-hydroxy-5'-(3''- methacryloyloxypropyl)phenyl]-5-chlorbenzotriazol, 2-{2'-hydroxy-3'-tert-butyl-5'-[3'- methacryloyloxypropoxy]phenyl}-5-methoxy-2H-benzotriazol, 2-[3'tert-butyl-5'-(3''- dimethylvinylsilylpropoxy)-2'-hydroxyphenyl]-5-methoxybenzot riazol, 2-(tert-butyl)-6-(5- chloro-2H-benzo[d][1,2,3]triazol-2-yl)-4-vinylphenol, 2-(2H-1,2,3-benzotriazol-2-yl)-4- methyl-6-(2-methylprop-2-enyl)phenol, 2-(3-acetyl-2-aminophenoxy)ethyl methacrylat, 2- (4-benzoyl-3-hydroxyphenoxy)ethyl acrylate, 3-[3-(2H-1,2,3-benzotriazol-2-yl)-5-tert-butyl- 4-hydroxyphenyl]propyl methacrylate or a combination of this compounds. Preferred UV-Absorber are selected from the group of 2-[3'-2'H-benzotriazol- 2'-yl)-4'- hydroxyphenyl]ethyl methacrylate (BTPEM), 2-(3-(t-butyl)-4-hydroxy-5-(5-methoxy-2- benzotriazolyl)phenoxy)ethyl methacrylate, 3-(3-(t-butyl)-4-hydroxy-5-(5-methoxy-2- benzotriazolyl)phenoxy)propyl methacrylate, 3-(3-t-Butyl-5-(5-chlorobenzotriazol-2-yl)-4- hydroxyphenyl)propyl methacrylate, 3-[3-(2H-1,2,3-benzotriazol-2-yl)-5-tert-butyl-4- hydroxyphenyl]propyl methacrylate which may be polymerized together with the monomers as described or preferably described before. A crosslinker is a monomer containing at least two polymerisable groups. The crosslinker preferably has two polymerisable groups. The crosslinker may optionally also contain functional groups which are capable of coordinating water, such as, for example, OH or NH ₂ groups. Crosslinkers functionalised in this way are likewise suitable hydrophilic monomers in the sense of the invention and are preferably employed in combination with the hydrophilic co-monomers described above and below. Suitable cross-linker may be used to impart elastomeric properties to the present composition and the ophthalmic devices or precursor articles produced therewith. Typically any suitable di- or tri-functional monomer may be used as crosslinker. Such monomers are generally well known to the skilled person and may be selected from the group of para-divinylbenzene, allyl acrylate, ethylene glycol divinyl ether, divinyl sulfone, allyl methacrylate, N,N'-methylene-bis-acrylamide, ethylene glycol diacrylate, ethyleneglycoldimethacrylate (EGDMA), N,N'-methylene-bis-methacrylamide, 1,3- propanediol diacrylate, 2,3-propanediol diacrylate, 1,4-butanediol diacrylate, 1,3- butanediol diacrylate, 1,5-pentanediol diacrylate, 1,6-hexanediol diacrylate, 1,7- heptanediol diacrylate, 1,8-octanediol diacrylate, 1,9-nonanediol diacrylate, 1,10- decanediol diacrylate, 1,11-undecanediol diacrylate, 1,12-dodecanediol diacrylate, 1,13- tridecanediol diacrylate, 1,14-tetradecanediol diacrylate, 1,15-pentadecanediol diacrylate, 1,16-hexadecanediol diacrylate, 1,17-heptadecanediol diacrylate, 1,18-octadecanediol diacrylate, 1,19-nonadecanediol diacrylate, 1,20-eicosanediol diacrylate, 1,21- heneicosanediol diacrylate, 1,22-docosanediol diacrylate, 1,23-tricosanediol diacrylate, 1,24-tetracosanediol diacrylate, ethylene glycol dimethacrylate, N,N'-dihydroxyethylene- bisacrylamide, thiodiethylene glycol diacrylate, 1,3-propanediol dimethacrylate, 2,3- propanediol dimethacrylate, 1,3-butanediol dimethacrylate, 1,4-butanediol dimethacrylate, 1,5-pentanediol dimethacrylate, 1,6-hexanediol dimethacrylate, 1,7-heptanediol dimethacrylate, 1,8-octanediol dimethacrylate, 1,9-nonanediol dimethacrylate, 1,10- decanediol dimethacrylate, 1,11-undecanediol dimethacrylate, 1,12-dodecanediol dimethacrylate, 1,13-tridecanediol dimethacrylate, 1,14-tetradecanediol dimethacrylate, 1,15-pentadecanediol dimethacrylate, 1,16-hexadecanediol dimethacrylate, 1,17-hepta- decanediol dimethacrylate, 1,18-octadecanediol dimethacrylate, 1,19-nonadecanediol dimethacrylate, 1,20-eicosanediol dimethacrylate, 1,21-heneicosanediol dimethacrylate, 1,22-docosanediol dimethacrylate, 1,23-tricosanediol dimethacrylate, 1,24-tetracosanediol dimethacrylate, 2-(acryloyloxy)ethyl methacrylate, 2-(acryloyloxy)propyl methacrylate, 3- (acryloyloxy)propyl methacrylate, 4-(acryloyloxy)butyl methacrylate, 5-(acryloyloxy)pentyl methacrylate, 6-(acryloyloxy)hexyl methacrylate, 7-(acryloyloxy)heptyl methacrylate, 8- (acryloyloxy)octyl methacrylate, 9-(acryloyloxy)nonyl methacrylate, 10-(acryloyloxy)decyl methacrylate, 11-(acryloyloxy)undecyl methacrylate, 12-(acryloyloxy)dodecyl methacry- late, 13-(acryloyloxy)tridecyl methacrylate, 14-(acryloyloxy)tetradecyl methacrylate, 15- (acryloyloxy)pentadecyl methacrylate, 16-(acryloyloxy)hexadecyl methacrylate, 17- (acryloyloxy)heptadecyl methacrylate, 18-(acryloyloxy)octadecyl methacrylate, 19- (acryloyloxy)nonadecyl methacrylate, 20-(acryloyloxy)eicosanyl methacrylate, 21- (acryloyloxy)heneicosanyl methacrylate, 22-(acryloyloxy)docosanyl methacrylate, 23- (acryloyloxy)tricosanyl methacrylate, 24-(acryloyloxy)tetracosanyl methacrylate, neopentyl glycol diacrylate, di(ethylene glycol) diacrylate, N,N'-hexamethylenebisacrylamide, thiodiethylene glycol diacrylate, thiodiethylene glycol dimethacrylate, neopentyl glycol dimethacrylate, diethylene glycol dimethacrylate, diallyl phthalate, triallyl cyanurate, glyceryl 1,3-dimethacrylate, N,N'-hexamethylenebismethacrylamide, tri(ethylene glycol) diacrylate, tri(ethylene glycol) dimethacrylate (e.g. M _n 286) tetra(ethylene glycol) diacrylate, tetra(ethylene glycol) dimethacrylate, penta(ethylene glycol) diacrylate, penta(ethylene glycol) dimethacrylate, hexa(ethylene glycol) diacrylate, hexa(ethylene glycol) dimethacrylate, poly(ethylene glycol) diacrylate (e.g. M _n 250 to 750), poly(ethyleneglycol) dimethacrylate (e.g. M _n 250 to 750). Preferred crosslinkers are ethylene glycol dimethacrylate, 1,3-propanediol diacrylate, 2,3- propanediol diacrylate, 1,4-butanediol diacrylate, 1,3-butanediol diacrylate, 1,5- pentanediol diacrylate, 1,6-hexanediol diacrylate, 1,7-heptanediol diacrylate, 1,8- octanediol diacrylate, 1,9-nonanediol diacrylate, 1,10-decanediol diacrylate, 1,11- undecanediol diacrylate, 1,12-dodecanediol diacrylate, 1,13-tridecanediol diacrylate, 1,14- tetradecanediol diacrylate, 1,15-pentadecanediol diacrylate, 1,16-hexadecanediol diacrylate, 1,17-heptadecanediol diacrylate, 1,18-octadecanediol diacrylate, 1,19-nona- decanediol diacrylate, 1,20-eicosanediol diacrylate, 1,21-heneicosanediol diacrylate, 1,22- docosanediol diacrylate, 1,23-tricosanediol diacrylate, 1,24-tetracosanediol diacrylate, 1,3- propanediol dimethacrylate, 2,3-propanediol dimethacrylate, 1,3-butanediol dimethacrylate, 1,4-butanediol dimethacrylate, 1,5-pentanediol dimethacrylate, 1,6- hexanediol dimethacrylate, 1,7-heptanediol dimethacrylate, 1,8-octanediol dimethacrylate, 1,9-nonanediol dimethacrylate, 1,10-decanediol dimethacrylate, 1,11-undecanediol dimethacrylate, 1,12-dodecanediol dimethacrylate, 1,13-tridecanediol dimethacrylate, 1,14-tetradecanediol dimethacrylate, 1,15-pentadecanediol dimethacrylate, 1,16- hexadecanediol dimethacrylate, 1,17-heptadecanediol dimethacrylate, 1,18- octadecanediol dimethacrylate, 1,19-nonadecanediol dimethacrylate, 1,20-eicosanediol dimethacrylate, 1,21-heneicosanediol dimethacrylate, 1,22-docosanediol dimethacrylate, 1,23-tricosanediol dimethacrylate, 1,24-tetracosanediol dimethacrylate, glyceryl 1,3- dimethacrylate and diallyl phthalate. Particularly preferred crosslinkers are ethylene glycol dimethacrylate (EGDMA), poly(ethyleneglycol) diacrylate (e.g. M _n 250 to 750), poly(ethyleneglycol) dimethacrylate (e.g. M _n 250 to 750), tri(ethyleneglycol) dimethacrylate (M _n 286), alkylene dimethacrylate (the alkylene group is linear or branched and comprises 2 to 18 C-atoms), alkylene diacrylate (the alkylene group is linear or branched and comprises 2 to 18 C-atoms), glyceryl 1,3-dimethacrylate and diallyl phthalate. By using alkylene dimethacrylate as crosslinker, the alkylene group is preferably linear and comprises 2 to 18 C-atoms, preferably 14 to 18 C-atoms. By using alkylene acrylate as crosslinker, the alkylene group is preferably linear and comprises 2 to 18 C-atoms, preferably 14 to 18 C-atoms. Glyceryl 1,3- dimethacrylate (GDMA), ethylene glycol dimethacrylate (EGDMA), penta(ethylene glycol) dimethacrylate, hexa(ethylene glycol) dimethacrylate, polyethyleneglycol diacrylate (e.g. M _n 250 to 750), polyethyleneglycol dimethacrylate (e.g. M _n 250 to 750) are particularly preferred. triethyleneglycol dimethacrylate (M _n 286), alkylene dimethacrylate or alkylene diacrylate. Ethylene glycol dimethacrylate (EGDMA), polyethyleneglycol diacrylate (e.g. M _n 250 to 750), polyethyleneglycol dimethacrylate (e.g. M _n 250 to 750) are particularly preferred. triethyleneglycol dimethacrylate (M _n 286), alkylene dimethacrylate or alkylene diacrylate or a combination of these compounds is very particularly preferably selected in accordance with the invention Suitable antioxidants are phenyl acrylate derivatives bearing a hindered phenol moiety. A preferred antioxidant is The compounds of formulae (I), (Ia) or (Ib) or the compounds (A-001) to (A-188) as described or preferably described before and their oligomers, polymers or copolymers as described before or preferably described before comprising one or more constitutional units M ⁰ of formulae (M ⁰ -Ia) or (M ⁰ -Ib) or one or more constitutional units (M ⁰ -001) to (M ⁰ - 188) as described before or preferably described before are particularly well suited for use in optically active devices e.g. ophthalmic devices as described before. The compounds of formulae (I), (Ia) or (Ib) or the compounds (A-001) to (A-188) as described or preferably described before and their oligomers, polymers or copolymers as described before or preferably described before comprising one or more constitutional units M ⁰ of formulae (M ⁰ -Ia) or (M ⁰ -Ib) or one or more constitutional units (M ⁰ -001) to (M ⁰ - 188) as described before or preferably described before are particularly sensitive to two- photon or multiphoton absorption. Hence the ophthalmic device and the precursor article for the ophthalmic device are sensitive to two-photon or multiphoton absorption. The system for two-photon or multi-photon irradiating of the ophthalmic device according to the invention, preferably of an intraocular lens preferably arranged within an eye of a patient is not restricted. Some examples are described below. Hence the present invention is also directed to precursor articles wherein said precursor article is a blank which may be transformed into optically active ophthalmic devices comprising at least one oligomer, polymer or copolymer as described before or preferably comprising one or more constitutional units M ⁰ of formulae (M ⁰ -Ia) or (M ⁰ -Ib) or one or more constitutional units (M ⁰ -001) to (M ⁰ -188) as described before or preferably described before. The type of intraocular lens is not limited in any way. It may, for example, be a pseudo- phakic intraocular lens or a phakic intraocular lens. The former type replaces the eye’s natural, crystalline lens, usually to replace a cataractous lens that has been removed. The latter type is used to supplement an existing lens and functions as a permanent corrective lens, which is implanted in the anterior or posterior chamber to correct refractive errors of the eye. It may, for example, comprise one or more optic and one or more haptic components, wherein the one or more optic components serve as lens and the one or more haptic components are attached to the one or more optic components and hold the one or more optic components in place in the eye. The present intraocular lens may be of a one-piece design or of multi-piece design, depending on whether the one or more optic components and the one or more haptic components are formed from a single piece of material (one-piece design) or are made separately and then combined (multi-piece design). The present intraocular lens is also designed in such a way that it allows to be, for example, rolled up or folded small enough so that it fits through an incision in the eye, said incision being as small as possible, for example, at most 3 mm in length. Additionally, intraocular lenses in accordance with the present invention allow for the non- invasive adjustment of the optical properties, particularly the polarizability or the refractive power, after implantation of the lens into the eye, thus reducing the need for post-surgery vision aids or reducing or totally avoiding follow-up surgery. In order to change the optical properties and particularly the polarizability or refractive power of the ophthalmic device according to the invention e.g. an intraocular lens it is exposed to irradiation having a wavelength of at least 200 nm and of at most 1500 nm. Said irradiation is not limited and may be a based on a single-photon or two- or multi- photon process. Hence, the present invention is also directed to a process of changing the optical properties of an ophthalmic device or a precursor article for an ophthalmic device as defined or preferably defined herein, said process comprising the steps of - providing an ophthalmic device or a precursor article for an ophthalmic device as defined herein; and - subsequently exposing said ophthalmic device or precursor article to irradiation having a wavelength of at least 200 nm and at most 1500 nm. Preferably, said irradiation has a wavelength of at least 250 nm or 300 nm, more preferably of at least 350 nm, even more preferably of at least 400 nm, still even more preferably of at least 450 nm, and most preferably of at least 500 nm. Preferably, said irradiation has a wavelength of at most 1400 nm or 1300 nm or 1200 nm or 1100 nm or 1000 nm, more preferably of at most 950 nm or 900 nm, even more preferably of at most 850 nm, still even more preferably of at most 800 nm and most preferably of at most 750 nm. Hence, the present invention is also directed to an ophthalmic device or precursor article for an ophthalmic device obtainable by said irradiation process as described before or preferably described before and below. Alternatively, you may describe the change of refractive power as a modification of the index of refraction of said ophthalmic device as described before or preferably described before. Alternatively, you may describe the change of refractive power as a modification of the index of refraction of said intraocular lens as described before or preferably described before. Irradiation within the focal volume results in refractive optical structures characterized by a change in refractive index relative to the index of refraction of the bulk of said ophthalmic device or alternatively the non-irradiated portion of said ophthalmic device. Irradiation within the focal volume results in refractive optical structures characterized by a change in refractive index relative to the index of refraction of the bulk of said ophthalmic device or intraocular lens or alternatively the non-irradiated portion of said ophthalmic device or intraocular lens. The change in polarizability or refractive index can in other words be used to form patterned desired refractive structures in the optical ophthalmic device as described or preferably described before, preferably in the intraocular lens as described or preferably described before. Hence, the present invention is also directed to an ophthalmic device obtainable by said irradiation process as described before or preferably described before and below having refractive optical structures characterized by a change in refractive index relative to the index of refraction of the bulk of said ophthalmic device or alternatively the non-irradiated portion of said ophthalmic device. It is preferred to provide refractive structures that exhibit a change in refractive index, and exhibit little or no scattering loss in such a way that ablation or removal of the optical ophthalmic device, preferably the intraocular lens article, is not observed in the irradiated region. In such processes, the irradiated regions of the ophthalmic device as described before or preferably described before can take the form of two- or three-dimensional, area or volume filled refractive structures that can provide spherical, aspherical, toroidal, or cylindrical correction. In fact, any optical structure can be formed to yield power correction in both physical directions. Moreover, the optical structures can be stacked vertically or written in separate planes in the ophthalmic device as described before or preferably described before to act as a single lens element. The invention is therefore further related to a method for locally adjusting a polarizability and/or a refractive index of an ophthalmic device according to the invention, preferably an intraocular lens, preferably arranged within an eye of a patient. The method relates in particular to fabrication of optical profiles by adjusting polarizability through two- or multi- photon processes in a non-destructive manner. Said two- or multi-photon processes allow for different optical profiles compared to single-photon processes and can be advantageously used for the manufacture of the ophthalmic devices according to the invention containing optical profiles. The system to be used for said two- or multi-photon process advantageously allows for post-operative and non-invasive adjustment of optical properties/profiles of an implanted intraocular lens (IOL) to remove visual impairments such as refractive errors. Furthermore, when manufacturing the ophthalmic device according to the invention, the system advantageously allows for a gentle preparation of the ophthalmic device so as to in particular allow for refractive structures that can provide spherical, aspherical, toroidal, or cylindrical correction and/or maintaining flexibility of the ophthalmic device once preparation of the ophthalmic device is completed. The polarizability of the ophthalmic device is modified based on a two-photon (or generally multi-photon) process which allows adjustment of optical properties/profiles of said ophthalmic device or which allows adjustment of optical properties in different planes of the ophthalmic device. Furthermore, the modification of polarizability based on a two-photon or multi-photon process allows for improved maintaining of flexibility of the ophthalmic device when treated with wavelength of 400 nm to 550 nm. Therefore, the invention further relates to a process for adjusting a polarizability of an ophthalmic device according to the invention based on a two- or multi-photon absorption process, the process comprising the steps of: providing said ophthalmic device as described before or preferably described before; and adjusting the polarizability of said ophthalmic device through irradiation of said ophthalmic device by using a system, said system comprising: one or more irradiation sources for two-photon or multi-photon irradiating a said ophthalmic device with an irradiation beam focused with an optic and of a first wavelength and/or a second wavelength different from the first wavelength, a scanner coupled to the one or more irradiation sources and configured to scan a said irradiation beam across said ophthalmic device, and an input unit coupled to the one or more irradiation sources and the scanner, wherein the input unit is configured to input data for treating said ophthalmic device by scanning a said irradiation beam across said ophthalmic device based on the input data, and wherein the first wavelength is between 551 nm and 800 nm for locally decreasing, based on said treating of said ophthalmic device, a polarizability of said ophthalmic device, and wherein the second wavelength is between 400 nm and 550 nm for locally increasing, based on said treating of said ophthalmic device, the polarizability of said ophthalmic device and thereupon changing the polymeric optical material of said ophthalmic device, preferably with significant differences in the UV/Vis spectrum with respect to the non-irradiated polymeric optical material of the ophthalmic device. Ultraviolet–visible spectroscopy or ultraviolet–visible spectrophotometry (UV–Vis or UV/Vis) is known to a person skilled in the art. It refers to absorption spectroscopy or reflectance spectroscopy in part of the ultraviolet and the full, adjacent visible spectral regions. Suitable UV/Vis spectrometers are commercially available. The choice of the UV/Vis spectrometer is not critical for the comparison of the UV/Vis spectrum of the initial ophthalmic device and the UV/Vis spectrum of said irradiated ophthalmic device to be made according to the present invention. As long as both measurements are made under comparable conditions so that the results can be compared which is known to the person skilled in the art. A suitable spectrometer is the UV/Vis spectrometer Lambda 900 from Perkin Elmer. The polarizability may hereby be locally changed particularly precisely. The invention is furthermore related to a method for correcting vision in a patient by modifying the refractive index of an intraocular lens within the eye of said patient comprising identifying and measuring the degree of vision correction of the patient; determining the position and type of refractive structures to be written into said intraocular lens to correct the patient’s vision; and subsequently exposing said intraocular lens to two-photon or multi-photon irradiation having a wavelength between 551 nm and 800 nm to locally decrease the polarizability of the intraocular lens or exposing said intraocular lens or subsequently exposing said intraocular lens to two-photon or multi-photon irradiation having a wavelength between 400 nm and 550 nm to locally increase the polarizability of the intraocular lens. In the present application, input data are all kinds of data used for creating the treatment plan which is defined as the translation of the ophthalmic need into control commands for the writing process of the ophthalmic device according to the invention. During the writing process the optical pattern is written by irradiation in said ophthalmic device. The term “control commands” refers to commands directly controlling the process of writing as defined before. A control command may control e.g. the movement of the scanner. The term “scanner” used within the description is not part of the input unit according to the invention. The „scanner“ as described herein is a component of the system to be used in the process for adjusting a polarizability of an ophthalmic device according to the invention which controls the movement of the irradiation beam. The ophthalmic need refers to the desired optical profile which has to be created in the ophthalmic device through the system as described. The optical profile is the needed change defined by the surgeon according to the patient’s examination results before or after the ophthalmic device, preferably the intraocular lens is implanted; for example but not limiting to a spherical full diopter change, a toric profile, an EDOF profile or a bi-, tri- or multifocal profile. Alternatively, the optical profile is the optical property adjustment of the ophthalmic device. The optical pattern is the necessary change of polarizability resulting in change of refractive index in every voxel of the ophthalmic device. The term “optic” as used herein as a part of the system to be used in the process for adjusting a polarizability of an ophthalmic device according to the invention includes all optical equipment necessary to control the spatial distribution of the irradiation source (focus) on the ophthalmic device. Critical parameters of the focus include the lateral focus size (or beam waist) and the focus length (or Rayleigh range). The optic comprises all elements along the optical beam path that determine the focus, such as beam expanders, aperture stops, shutter and in particular the focusing optics, such as a microscope objective or a single aspherical lens. Multi-photon excitation occurs only in the vicinity of the focal point and preferably by employing ultra-short laser pulses. The average power is limited by the sample damage threshold such threshold being part of the input data as defined before. Criteria for the selection and optimization of system parameters: One ultimate purpose is to generate localized refractive-index modification of IOLs post- implantation as prescribed by the physician to improve the visual acuity of the patient. A crucial criterion for the procedure of refractive-index modification is the total treatment time required to obtain the desired result. It is generally recognized that such procedure should not take more than a few minutes in order to be recognized as viable. The systems capable of localized refractive-index modifications of the state of the art do not include an approach to obtain practical treatment times for IOL applications. Discussion of system tradeoffs and limitations: For a practical high-performing system capable of adjusting ophthalmic devices in general or specifically IOLs after implantation it is recognized that its subcomponents have to be treated as a system and must therefore be optimized Jointly as many interdependencies and tradeoffs between the subcomponents exist. The subcomponents include the irradiation source, the optic, the scanner and treatment plan. A key requirement of any system/parameter optimization is to stay within safe limits for the ophthalmic device material in case of the treatment or the material and the eye with its components (e.g. retina) in case of the treatment of an ophthalmic device being an IOL. Such requirements build the basis for input data as described before. In particular, two main damage mechanisms for radiation from an irradiation source, preferably a pulsed laser source can be distinguished: Single-pulse damage (dielectric breakdown and avalanche breakdown), and thermal damage, where the temperature of the lens material and/or the eye is heated up subsequently for repeated pulses to the same volume. For example: the average power of a pulsed irradiation source relates to the heating and therefore to the potential damage of the lens material and/or the eye. Therefore, while keeping the average power of the irradiation source below the threshold of overheating the lens material and/or eye, pulse energy and pulse repetition rate are inversely related product of pulse energy and number of pulses per second (= inverse of repetition rate) is equal to the average power. Average power is defined as pulse energy multiplied by number of pulses per second) and is characterized by Watt (W). Irradiance is equal to flux density) (W/cm ² ). Radiant exposure is equal to fluence) (J/cm ² ). One overall objective is to minimize the treatment time for an IOL adjustment after implantation. In theory, higher and higher pulse energies with more frequent pulses (= higher repetition rate) could be applied, however, above an average power of typically 1 Watt, overheating starts creating unsafe conditions for IOL material and retina. Therefore, in order to stay within safe operating limits, while completing a treatment of the full IOL volume in a few minutes, one can define a preferred radiant exposure. The preferred radiant exposure is ≤ 5 kJ/cm², particular preferably < 1kJ/cm² and very particular preferably <0.3 kJ/cm². This described radiant exposure applies additionally to the processes and methods according to the invention as further described below. For the case a treatment plan is too extensive and would exceed the limits of laser safety concerning overheating, it is possible to interrupt the treatment to allow a cool down of all by the treatment affected ophthalmic device material and tissues. After the cool-down the locating system can compare the treated voxel in the ophthalmic device with the optical pattern and the treatment can be continued. The process of adjustment of optical properties/profiles of said ophthalmic device according to the invention through the system and with requirements as described before will be done according to a treatment plan as described before. According to a treatment plan, profiles for e.g. toric, spheric, multifocal or EDOF (extended depth of focus) can be written into the ophthalmic device according to the invention. An algorithm may be utilized to write in profiles for e.g. toric, spheric, multifocal or EDOF (extended depth of focus) profiles. By combining the information of the desired optical profile together with the input data, the needed optical pattern and the control commands for irradiation source, optics and scanner of the system as described before can be calculated. Further input data are for example lens data as such as the needed laser-energy for a certain refractive index change per voxel of said ophthalmic device material, and further patient data as the exact position and orientation of the ophthalmic device in the patient’s eye being part of the treatment plan data. The control commands can be updated and modified during the writing process by in- process input data such as temperature data of the patient’s eye by e.g. IR-temperature measurements, in-process positioning data of the irradiation beam, the ophthalmic device or the eye acquired for example by OCT (optical coherence tomography) and/or refractive data acquired from Scheimpflug images. In a further embodiment of input data, the input data comprises lens data of said ophthalmic device preferably of said intraocular lens and/or treatment plan data relating to a treatment plan for said treating of said ophthalmic device. For example, the lens data may comprise data relating to one or more of the polarizability and/or refractive index of the ophthalmic device as a function of the location of a respective volume or part of the ophthalmic device, shape, diopter, cylinder and sphere and/or its individual aberrations in said dimensions. The polarizability may therefore be increased or decreased at a particular location or volume in one or more planes of the ophthalmic device depending on the current polarizability (or refractive index) and the polarizability (or refractive index) to be obtained via the treatment. The treatment plan calculation may, in some examples, generate control commands resulting in one or more of treatment plan data comprising: scan strategy control command data of a scan strategy (for example a scanning pattern and/or a scanning sequence and/or a scanning speed and/or a scanning duration of the scanning pattern and/or a scanning duration of the scanning sequence and/or a pulse duration of a pulse of the irradiation beam of the first and/or second wavelength (for example, nanosecond or picosecond or femtosecond pulses) and/or an irradiation beam profile of the irradiation beam of the first and/or second wavelength and/or a radiation (photon) density and/or a radiation intensity and/or a radiation power and/or radiation wavelength) for said scanning of the irradiation beam of the first and/or second wavelength across the ophthalmic device, in-process input data such as temperature data of a current and/or predicted temperature of the ophthalmic device during said exposure, refractive index/polarizability data of a refractive index/polarizability of the ophthalmic device to be obtained based on said exposure, the refractive index/polarizability to be obtained in particular relating to a mapping of the refractive index/polarizability to be obtained to a specific location/coordinates of the ophthalmic device, rhexis dimension data of a dimension of a rhexis, and input data such as eye data relating to a dimension and/or a shape of the eye of the patient, positioning data relating to a position and/or orientation of the ophthalmic device relative to the eye, and registration data relating to an identification of the patient and/or the specific eye of the patient. Preferably, the scan strategy control command data of a scan strategy are a scanning pattern and/or a scanning speed and/or a pulse duration of a pulse and/or radiation intensity as described further below. The parameters of the irradiation beam(s) may then be adjusted according to the lens data and/or the treatment plan data as defined herein in order to precisely (locally) change the polarizability/refractive index of the ophthalmic device, where desired. Preferably, the parameters of the irradiation beam(s) are adjusted according to the lens data and/or the treatment plan data as described before or preferably described herein. The skilled artisan is well aware in this regard that optimum irradiation focus conditions are reached when the depth-of-field (Rayleigh range) of the irradiation beam is matched to the desired thickness of the optical structure to be written into the ophthalmic device. The skilled artisan is well aware in this regard that optimum irradiation focus conditions are reached when the depth-of-field (Rayleigh range) of the irradiation beam is matched adapted to the local thickness of the ophthalmic device. In a further embodiment, the lens data comprises data relating to a radiation absorption property (for example an absorption and/or light attenuation coefficient, which may be dependent from the wavelength of light) of a said ophthalmic device, and wherein the system is configured to adjust the first wavelength and/or the second wave-length for said ophthalmic device to locally change the polarizability based on a multi-photon absorption process. For example, based on the material used for the ophthalmic device, a particular wavelength or wavelength ranges may be input for a precise local change of the polarizability of the ophthalmic device. The one or more irradiation sources as part of the system to be used in the process for adjusting a polarizability of an ophthalmic device according to the invention may comprise one or more pulsed lasers which may be utilized to generate nano-second pulses, preferably pico-second pulses and more preferably femto-second pulses. Preferably, one irradiation source is used. Particular preferably, the one or more irradiation sources comprise one or more pulsed lasers which are used to generate femto-second pulses. Particular preferably, one pulsed laser is used to generate femto-second pulses is used as irradiation for the system according to the invention or for the processes and methods according to the invention. In one embodiment, the one or more irradiation sources comprise a laser which is tunable to emit a laser beam having the first and second wavelengths, respectively. This may be particularly advantageous as a single laser may be used to (locally) increase or decrease the polarizability/refractive index of the ophthalmic device or intraocular lens, as desired. Different pulsed laser types are suitable for said irradiation sources within the system to be used in the process for adjusting a polarizability of an ophthalmic device according to the invention. MHz laser as well as kHz laser are suitable and have their particular merits. While a MHz laser system, for example, operates at lower pulse energy, the focused laser spots can be kept at µm-scale (<1 µm to several µm) and thus be used for precise local index modifications in all three dimensions, for example, to generate diffractive structures. A preferred MHz-irradiation source is an 80 MHz laser with a pulse energy ranging from 0.1 to 10 nJ. A kHz-laser on the other hand operates at higher pulse energy of typically 0.1 to 10 µJ and thus requires a larger spot size of, for example, 10 to 100 µm in order to not damage the lens material. A larger laser spot size, however, implies a large depth of field (= long Rayleigh range) that can be equal to or even exceed the thickness of the ophthalmic device material. For such long Rayleigh ranges, it might not be possible to modify the refractive index layer by layer in the IOL but only uniformly along a line around the focus. A preferred kHz-irradiation source is a laser with a repetition rate of 100 to 500 kHz. The average power of the irradiation source as described before or preferably described before is preferably between 300 and 600 mW, particular preferably between 400 and 500 mW. The irradiation source as part of the system to be used in the process for adjusting a polarizability of an ophthalmic device according to the invention preferably comprises a tunable laser that can provide a variable wavelength in the range of approximately 680- 1080 nm, such as a Ti:Sapphire laser (for example Chameleon Ultra II by Coherent, Santa Clara, CA, USA). The system may also comprise an optical parametric oscillator (for example frequency doubled Chameleon Compact OPO-Vis by Coherent, Santa Clara, CA, USA). The irradiation source as part of the system to be used in the process for adjusting a polarizability of an ophthalmic device according to the invention particularly preferably comprises a femtosecond pump laser along with an optical parametric amplifier. Said pump laser emits irradiation >10 Watt average power at 1030 nm in <350 fs pulses with a repetition rate of 0.1 to 700 kHz. The radiation of said pump laser is directed to an optical parametric amplifier, where the pump laser output is frequency-doubled and optically mixed, resulting in a final tunable output in a wavelength range of 551 nm to 800 nm. A preferred repetition rate is between 50 and 600 kHz. A particular preferred repetition rate is between 100 and 500 kHz. The irradiation source as part of the system to be used in the process for adjusting a polarizability of an ophthalmic device according to the invention particularly preferably comprises a femto-second pump laser >10 Watt average power at 1030 nm in combination with an optical parametric amplifier, which is emitting irradiation pulses <350 fs at a repetition rate of 1 to 700 kHz. The radiation of said pump laser is directed to an optical parametric amplifier with one or multiple second-harmonic stages, resulting in a final optical output in a wavelength range of 400 nm to 550 nm. A preferred repetition rate is between 50 and 600 kHz. A particular preferred repetition rate is between 100 and 500 kHz. The laser types as described before or preferably described before generate a collimated optical beam of a few millimeter in diameter, which is then directed to optics and scanner. The optical beam quality (measured in units of M²) is ideally between 1.0 and 1.5, more ideally between 1.0 and 1.3. The first wavelength of the irradiation beam within the system to be used in the process for adjusting a polarizability of an ophthalmic device according to the invention is between 551 nm and 800 nm, preferably between 551 nm and 700 nm, in order to (locally) decrease the polarizability (and hence the refractive index) of the IOL. The second wavelength of the irradiation beam within the system to be used in the process for adjusting a polarizability of an ophthalmic device according to the invention is between 400 nm and 550 nm, preferably between 500 nm and 550 nm, in order to (locally) increase the polarizability (and hence the refractive index) of the IOL. The polarizability may hereby be locally changed particularly precisely. Optics within the system to be used in the process for adjusting a polarizability of an ophthalmic device according to the invention: The main function of the optics is to focus the irradiation beam, which is emitted from the irradiation source and controlled by the scanner, onto the ophthalmic device. Key considerations as described before are spot size and depth of focus in order to minimize treatment time while staying within limits given by laser safety requirements and material damage as described before as part of common input data. The most important characteristics of the optic is given by its numerical aperture (NA), along with its effective focal length (EFL) and the diameter of the irradiation beam at the entry aperture of the focusing optics. Additionally, all optical elements within the system to be used in the process for adjusting a polarizability of an ophthalmic device according to the invention should be selected for diffraction- or near-diffraction-limited properties, in order to not substantially degrade the optical beam quality. Different ophthalmic needs will require different spot sizes as the spot size determines the obtainable spatial resolution. Ideally, the spot size is between 1 and 100 µm, more ideally between 50 and 100 µm in order to minimize treatment time while also keeping the potential for material damage low. Scanner within the system to be used in the process for adjusting a polarizability of an ophthalmic device according to the invention: The scanner to be used within the system to be used in the process for adjusting a polarizability of an ophthalmic device according to the invention may comprise a Galvano- scanner, a piezo scanner, a rotational scanner or an acousto optic modulator or it may be digital such as a spatial light modulator, a digital micromirror device or stereolithography apparatus. Preferably, the scanner as part of the inventive system according to the description is selected from a Galvano-scanner, a piezo scanner, a rotational scanner, an acousto optic modulator, a spatial light modulator, a digital micromirror device or stereolithography apparatus. A preferred Galvano-scanner is a single Pivot-Point- Scanner. Preferably, the scanner is configured to operate at a scanning speed of more than 50 mm/s. This may allow for keeping the treatment time short. As a general rule, the treatment time should not exceed several minutes and is preferably less than 10 minutes, preferably less than 5 minutes, particularly preferably less than 3 minutes per treatment session. The treatment area may be defined as the ophthalmic devices volume and size. Typically, the optic of said ophthalmic device or intraocular lens is 5 mm to 7 mm in diameter and typically between 0.2 mm and 2.0 mm thick. The optimum radiation exposure is <1 kJ/cm² and more ideally <0.3 kJ/cm² to keep the overall irradiation exposure low and treatment time short, while addressing the full volume of the ophthalmic device. Particularly preferably, random scan patterns or interleaved scanning lines are used to spread out the irradiation energy of the irradiation beam. The scanning can be performed with three modes. In the bottom-up scanning, the laser may travel from spot-to-spot with a specific dwell time on each spot (“bottom-up, spot-to- spot”). Alternatively, in the bottom-up scanning, the laser may dwell on spots that overlap with one another (“bottom-up, spot overlay”). Alternatively, the laser can travel with a fixed velocity without dwelling on any spots (“fly by, constant velocity”). In one embodiment of a scan pattern, the IOL is scanned with the irradiation source as described before or preferably described before by shining through the pupil. The IOL, contained in the capsular bag at the time of scanning, is previously inserted through an incision in the cornea using conventional operation procedures. In this embodiment, the full volume of the IOL is scanned and the scanning is performed in a bottom-up manner (i.e. parts of the IOL which are further away from the cornea are scanned first), this way the optical profile is created in order to avoid unnecessary changes in refractive index in the light path. As described before a key consideration when selecting the scanning program is to minimize local heating of the ophthalmic device and/or the eye of the patient and therefore various variables are used in the scanning program. Taking into account anatomical features such as Rhexis and pupil size as well as optical features such as numerical aperture and laser pulse characteristics, a laser program is created with a specific scanning speed and sequence. The relation between lens coordinate and eye coordinate system are, in this example, automatically taken into account. The parameters for the scanning program and/or treatment plan are preferably the first and second wavelengths, the scanning speed and sequence, the positioning (e.g. in Cartesian coordinates) of the lens relative to the eye, the scan strategy, the refractive index change which is to be obtained (optical pattern), the numerical aperture of the objective, the Rhexis, the optical diameter (in some examples approximately 6 mm) of the pupil and/or the lens, the pulse duration (shape, intensity and x-y positioning) of the laser beam, laser safety when operating the laser, and centration with respect to the positioning of the lens and the eye. The photons generated in the laser are in one embodiment of the system to be used in the process for adjusting a polarizability of an ophthalmic device according to the invention preferably guided through mirrors (e.g. as optic 1) to a e.g. a beam expander, which prepares the beam for the subsequent scanner and focusing optic. After passing through the beam expander, the photons are directed toward the scanner (e.g. Galvano-scanner or piezo scanner or rotational scanner or acousto optic modulator or digitally with a spatial light modulator or digital micromirror device or stereolithography apparatus). After having gone through the scanner, the laser beam travels through another optic such as a divider mirror. In this embodiment, the divider mirror splits up the beam into the main imaging beam for the ophthalmic device irradiation and a beam for monitoring beam properties as well as for positioning feedback. After the divider mirror, the optical beam is focused onto the ophthalmic device by imaging group or focusing optic. In one embodiment, the imaging group comprise a microscope objective to obtain high numerical apertures (for µm-level spatial resolution) or low-NA optics to allow higher pulse energy of µJ-level. The system as described before or preferably described before may further comprise a microscope objective coupled to the scanner for focusing, by the microscope objective, a said irradiation beam onto said ophthalmic device, wherein the microscope objective has a numerical aperture of between 0.1 and 0.8, preferably between 0.2 and 0.5, and more preferably between 0.2 and 0.4. Providing a microscope objective having such numerical aperture may allow for high irradiation beam quality in particular in terms of focusing and resolution characteristics of the beam used for treating the intraocular lens. The microscope objective comprises of a typical lens configuration to allow for e.g. correction of chromatic aberration. The microscope objective is preferably linked to an eye interface system, typically a suction system that keeps the eye of the patient in a fixed position as further described below. In a further embodiment of an objective to be used within the system as described before, the objective is an Olympus LUCPLFLN objective in order to focus the irradiation beam onto the ophthalmic device. An alternative focusing optic/imaging group is configured with a single aspherical lens with an effective focal length preferably within 50 to 150 mm and a numerical aperture of preferably 0.025 to 0.1. The system as described before or preferably described before may further comprise a positioning system for determining a position of a said focus of said irradiation beam within a said eye of a said patient, wherein the positioning system is coupled to the scanner and wherein the scanning, by the scanner, of said irradiation beam across said intraocular lens is based on the position of said focus of said irradiation beam within the eye. The positioning system may comprise a locating system such as an optical coherence tomography system, a confocal microscope or a Scheimpflug camera. The positioning system may be directly or indirectly coupled to the scanner. In some examples in which a confocal microscope is used, the confocal microscope may be directly coupled to the scanner. The locating system as described before is used to provide topographic data of the eye to the positioning system for determination of the position of the laser focus in dependence of the eye and said intraocular lens. For confocal microscopy, a partially transparent mirror is used to allow for video imaging. The system as described before or preferably described before is preferably configured further to determine a location and/or orientation of said intraocular lens relative to the eye and the outlet of the irradiation beam, and wherein the scanning, by the scanner, of said irradiation beam across said intraocular lens is based on the location and/or orientation of said intraocular lens relative to the eye. This may be particularly advantageous since the position of the intraocular lens may not be centered relative to the eye, which misalignment may be taken into account when treating the intraocular lens with the irradiation beam(s). With respect to the position of the IOL, at least 2 coordinate systems may be considered relevant: coordinates-system of the eye and coordinates-system of the lens within the eye, as both may not be centered with respect to each other. With respect to the position of the IOL, at least 2 coordinate systems may be considered relevant: x,y,z coordinates of the eye and x,y,z coordinates of the lens within the eye, as both may not be centered with respect to each other. In one embodiment, the locating system creates input data. These input data contain for example data concerning lens position and/or orientation of the ophthalmic device within the eye and relative to the laser beam outlet, and/or an optical power mapping of the eye and/or the ophthalmic device. These data are used for the calculation of the optical pattern or a continuation of a treatment. Additionally, it is possible that the locating system creates input data during the writing process. These in-process input data contain for example data concerning lens position and/or orientation of the ophthalmic device within the eye and relative to the laser beam outlet, and/or an optical power mapping of the eye and/or the ophthalmic device. These data are used for in-process modification of the control commands used to generate the optical pattern. The system as described before or preferably described before may further comprise a temperature management unit coupled to one or both of (i) the one or more irradiation sources and (ii) the scanner, wherein the temperature management unit is configured to determine, based on an irradiation beam property of a said irradiation beam and an ophthalmic device property of a said ophthalmic device, a temperature of a part of said ophthalmic device during said treating of said ophthalmic device by said scanning, and wherein the system is configured to control, based on said determination of the temperature, one or both of (i) the one or more irradiation sources and (ii) the scanner. This may allow for ensuring that the eye and/or the ophthalmic device may not be detrimentally affected based on the treatment with an irradiation beam. Additionally, the temperature management unit is preferably configured to predict said temperature during said treating of said ophthalmic device, and wherein said input data comprises the predicted temperature. This may allow for taking preventative measures to ensure that the eye and/or the ophthalmic device may not be detrimentally affected based on the treatment with an irradiation beam. Alternatively, the temperature management unit is an infrared camera logging the temperature of the eye and correlating the measured data with common data bearing calibration data to calculate the real temperature in the eye. In another embodiment, the temperature dependence of refractive index is used for temperature controlling. In these examples, the system comprises a refractive power mapping device. Based on the deviation of the measured refractive power map and the progress of the writing predicted refractive power map, temperatures in the lens can be calculated in process. In another embodiment, the temperature dependence of the emission spectrum is used for temperature controlling. In these examples, the system comprises a UV–Vis spectrometer. Based on the deviation of the measured emission peak wavelength and/or peak width, temperatures in the focal spot can be calculated in process. The system as described before or preferably described before may further comprise an eye interface system configured to keep a said eye of a said patient in a fixed position. The eye interface system may comprise a suction system for fixing the position of the eye of the patient during treatment. The patient may be “docked” to the system in a lie flat or upright position. The system as described before or preferably described before may further comprise a wireless or wired receiver and/or transceiver for one or more of (i) sending control commands to the one or more irradiation sources, (ii) sending control commands to the scanner, and (iii) inputting the control command data needed for creating the optical pattern into the scanner. The one or more irradiation sources and/or the scanner may therefore be controlled remotely. Additionally or alternatively, the data relating to one or both of the lens data and the treatment plan data may be stored externally from the system and may be provided to the system as and when desired. In some examples, it may be preferable to provide a wired receiver or transceiver at least for controlling the one or more irradiation sources and/or for controlling the scanner in order to reduce (or avoid) any delay when sending a control signal to the one or more irradiation sources and/or the scanner In another example, the receiver/transceiver sends treatment plan data and lens data to a central computing unit which calculates the optical pattern and sends this as input data back to the receiver which provides it to the system. The system as described before or preferably described before may further comprise a device for locally measuring the refractive power of said ophthalmic device during said treating of the ophthalmic device. Adjustments to one or more of the irradiation source(s), the scanner and the input data may hereby be made during the treatment process. The system as described before or preferably described before may further comprise a refractometer for locally measuring the refractive index of said ophthalmic device during said treating of the ophthalmic device. Adjustments to one or more of the irradiation source(s), the scanner and the input data may hereby be made during the treatment process. Further components of the system providing the photons are optionally a cover in which all the equipment is built in, a power unit to provide the system and all sub-systems with sufficient energy, and sub-systems like a suction system and/or chiller. In addition to the above mentioned components, controller, firmware and a graphics user interface (GUI) as well as treatment algorithms may be provided. To connect to the system, connectivity may be established via Bluetooth, Wi-Fi or other ports like RS-232. The invention further relates to a method for locally adjusting a polarizability of an intraocular lens according to the invention arranged within an eye of a patient, wherein the treatment plan data comprises one or more of: scan strategy control command data of a scan strategy (for example a scanning pattern and/or a scanning sequence and/or a scanning speed and/or a scanning duration of the scanning pattern and/or a scanning duration of the scanning sequence and/or a pulse duration of a pulse of the irradiation beam of the first and/or second wavelength and/or an irradiation beam profile of a said irradiation beam and/or a radiation (photon) density and/or a radiation intensity and/or a radiation power and/or radiation wavelength) for said scanning of a said irradiation beam across the intraocular lens, temperature data of a current and/or predicted temperature of the intraocular lens during said exposure, refractive index data of a refractive index of the intraocular lens to be obtained based on said exposure, the refractive index to be obtained in particular relating to a mapping of the refractive index to be obtained to a specific location/coordinates of the intraocular lens, rhexis dimension data of a dimension of a rhexis, eye data relating to a dimension and/or a shape of the eye of the patient, positioning data relating to a position and/or orientation of the intraocular lens relative to the eye, and registration data relating to an identification of the patient and/or the specific eye of the patient. The invention further relates to a method for locally adjusting a polarizability of an intraocular lens according to the invention arranged within an eye of a patient, wherein said exposing of the intraocular lens to a said irradiation beam comprises exposing a first volume of the intraocular lens prior to exposing a second volume of the intraocular lens, wherein the first volume is further away from the cornea of the eye of the patient than the second volume. In the above-stated clauses, an initial step of the methods may be to provide a said intraocular lens. In examples, in which said exposing of the intraocular lens to a said irradiation beam comprises exposing a first volume and/or plane and/or location of the intraocular lens prior to exposing a second volume and/or plane and/or location of the intraocular lens, wherein the first volume and/or plane and/or location is further away from the cornea of the eye of the patient than the second volume and/or plane and/or location, volumes and/or planes and/or locations irradiated at later time points in the irradiation sequence may be closer to the cornea than volumes and/or planes and/or locations irradiated at earlier time points. A said volume may hereby relate to one or more planes of the intraocular lens. The invention is furthermore related to a method for correcting vision in a patient by modifying the refractive index of an intraocular lens according to the invention within the eye of said patient comprising identifying and measuring the degree of vision correction of the patient; determining the position and type of refractive structures to be written into said intraocular lens to correct the patient’s vision; and subsequently exposing said intraocular lens to two-photon or multi-photon irradiation having a wavelength between 551 nm and 800 nm to locally decrease the polarizability of the intraocular lens and/or subsequently exposing said intraocular lens to two-photon or multi-photon irradiation having a wavelength between 400 nm and 550 nm to locally increase the polarizability of the intraocular lens, preferably by using the system and/or the process as described before for exposing said intraocular lens to said irradiation. As outlined above, the change of polarizability results in a change of refractive index. It should be pointed out that variations of the embodiments described in the present invention are covered by the scope of this invention. Any feature disclosed in the present invention may, unless this is explicitly ruled out, be exchanged for alternative features which serve the same purpose or an equivalent or similar purpose. Thus, any feature disclosed in the present invention, unless stated otherwise, should be considered as an example of a generic series or as an equivalent or similar feature. All features of the present invention may be combined with one another in any manner, unless particular features and/or steps are mutually exclusive. This is especially true of preferred features of the present invention. Equally, features of non-essential combinations may be used separately (and not in combination). It should also be pointed out that many of the features, and especially those of the preferred embodiments of the present invention, are themselves inventive and should not be regarded merely as some of the embodiments of the present invention. For these features, independent protection may be sought in addition to or as an alternative to any currently claimed invention. The technical teaching disclosed with the present invention may be abstracted and combined with other examples. No doubt many other effective alternatives will occur to the skilled person. It will be understood that the invention is not limited to the described embodiments and encompasses modifications apparent to those skilled in the art and lying within the scope of the claims appended hereto. Examples The following examples are intended to show the advantages of the present compounds in a non-limiting way. Unless indicated otherwise, all syntheses are carried out under an inert atmosphere using dried (i.e. water-free) solvents. Solvents and reagents are purchased from commercial suppliers. DCM is used to denote dichloromethane. DMF is used to denote dimethylformamide. EE or EtOAc is used to denote ethyl acetate. THF is used to denote tetrahydrofuran. RT means room temperature. Cyhex is used to denote cyclohexane. Melting points are measured with a TA Instruments Q2000 differential scanning calorimeter during heating in the first heating run with 20 K/min from -100 °C to 200 °C in a hermetic aluminum pans. Copolymer-properties can be investigated on blanks, prepared by bulk polymerization of the monomers. Co-monomers, cross-linkers and initiators therefore can be purchased from commercial sources. All chemicals are of highest purity available and can be used as received. Synthesis of precursor materials: Example 1a: 4-Hydroxycoumarin (30 g, 185.02 mmol) in toluene (0.4 L) is heated under a N ₂ atmosphere at 100 °C. Bu ₄ NBr (85.39 g, 264.88 mmol) is then added and the mixture is heated to become a solution. P ₂ O ₅ (46.3 g, 319.66 mmol) is added and the mixture is heated for 3 h. The hot upper organic layer is transferred to a separation funnel and the lower layer is extracted with boiling toluene (3 × 50 mL). The combined toluene layers are washed with aqueous 5% NaHCO ₃ (2 × 50 mL), water (50 mL), and brine (50 mL), dried (anhydrous Na ₂ SO ₄ ), and concentrated under vacuum to give compound 4-bromo-2H- chromen-2-one (20.4 g, 49%). 1H NMR (500 MHz, CDCl ₃ ) δ 7.81 (dd, J = 8.0, 1.5 Hz, 1H), 7.57 (ddd, J = 8.5, 7.4, 1.5 Hz, 1H), 7.36 – 7.28 (m, 2H), 6.83 (s, 1H). Analogously, other derivatives are prepared in the same manner 1H NMR (500 MHz, CDCl ₃ ) δ 7.73 (d, J = 8.9 Hz, 1H), 6.91 (dd, J = 8.9, 2.4 Hz, 1H), 6.81 (d, J = 2.4 Hz, 1H), 6.68 (s, 1H), 3.90 (s, 3H). 1H NMR (500 MHz, CDCl ₃ ) δ 7.68 (d, J = 8.3 Hz, 1H), 7.22 – 7.16 (m, 2H), 6.76 (s, 1H), 3.38 – 3.26 (m, 1H), 2.12 – 1.99 (m, 2H), 1.80 (d, J = 4.6 Hz, 2H), 1.67 (dt, J = 12.5, 4.4 Hz, 2H), 1.52 – 1.26 (m, 6H). 1H NMR (500 MHz, CDCl ₃ ) δ 8.00 (dd, J = 8.1, 1.5 Hz, 1H), 7.63 (ddd, J = 8.6, 7.2, 1.5 Hz, 1H), 7.42 – 7.36 (m, 1H), 7.32 (ddd, J = 8.2, 7.2, 1.0 Hz, 1H), 7.15 (s, 1H), 3.71 (s, 3H). Bis(2,4,6-trichlorophenyl) malonate (2.04 g, 4.41 mmol, 1.0 equiv.) and N,N-dialkyl- aminophenol (0.73g, 4.41 mmol, 1 equiv.) is dissolved in toluene and the resulting reaction mixture is heated at reflux for 4 h. The desired 7-(diethylamino)-4-hydroxy-2H- chromen-2-one gradually precipitated and is collected by filtration, washed twice with Et2O and dried under vacuum to obtain 7-(diethylamino)-4-hydroxy-2H-chromen-2-one (0.7g, 68%) as a grey solid. 1H NMR (500 MHz, DMSO-d ₆ ) δ 11.89 (s, 1H), 7.54 (d, J = 8.9 Hz, 1H), 6.66 (dd, J = 9.0, 2.5 Hz, 1H), 6.45 (d, J = 2.4 Hz, 1H), 5.24 (s, 1H), 3.41 (q, J = 7.1 Hz, 4H), 1.11 (t, J = 7.0 Hz, 6H). A suspension of malonic acid (0.122 mol, 13 g) and thiophenol (0.122 mol, 12.5 mL) is treated successively with AlCl ₃ (0.366 mol, 48.7 g) and POCl ₃ (0.366 mol, 34.85 mL), stirred, heated at 70°C for 30 h, and treated with ice (500 g) and EtOAc (500 mL). The organic layer is extracted and washed with H ₂ O (3 × 100 mL) and extracted with NaOH solution (10%, 3 × 300 mL). The aqueous phase is acidified with HCl solution (10%) until a precipitate formed (pH = 4). The precipitate is dissolved in EtOAc (20 mL) and washed with distilled H2O (20 mL). The organic layer is filtered through filter paper and evaporated to dryness. The solid is recrystallized from EtOH (45 mL) to afford malonic acid dithiophenyl ester as a gray powder (5.36 g, 19%). 1H NMR (500 MHz, CDCl ₃ ) δ 7.47 – 7.41 (m, 10H), 3.96 (s, 2H). 1,3-bis(phenylsulfanyl)propane-1,3-dione (20 mmol, 5.76 g) is treated with AlCl ₃ (60 mmol, 8.15 g) and NaCl (40 mmol, 2.34 g), thoroughly mixed, heated at 195°C for 25 min, cooled, and treated with HCl solution (1%, 100 mL) and EtOAc (100 mL). The organic layer is separated. The product is extracted with NaCl solution (10%, 100 mL). The aqueous solution is separated and acidified to pH = 4. The resulting precipitate is filtered off and rinsed with distilled H ₂ O (2 × 20 mL) to afford 4-hydroxy-2H-thiochromen-2-one as yellow to beige solid (1.85 g, 73%). 1H NMR (500 MHz, DMSO-d ₆ ) δ 12.01 (s, 1H), 8.14 (d, J = 8.1 Hz, 1H), 7.70 – 7.54 (m, 2H), 7.49 (t, J = 7.1 Hz, 1H), 6.06 (s, 1H). 4-Hydroxycoumarin (5.13 g, 31.64 mmol) and Lawesson’s reagent (12.80 g, 31.64 mmol) are dissolved in anhydrous toluene (285 mL) and heated under reflux for 4 h. The dark brown solution is evaporated under reduced pressure to give a darkbrown to orange solid, which is filtered, washed with ethanol and dried to yield 4-sulfanyl-2H-chromene-2-thion (2.34g, 38%). 1H NMR (500 MHz, CDCl ₃ ) δ 7.69 – 7.65 (m, 2H), 7.50 (dd, J = 8.4, 1.2 Hz, 1H), 7.41 – 7.37 (m, 1H), 7.34 (s, 1H). An oven-dried carousel reaction tube containing a stirrer bar is charged with 4-bromo-2H- chromen-2-one (1.75g, 7.78 mmol), Bis(dibenzylideneacetone)-palladium(0) (89.43mg, 0.156 mmol) and N-Phenyl-2-(di-tert.-butylphosphino)indole 0.137g, 0.39 mmol). After degassing three times with nitrogen, allylalcohol (0.582ml, 8.55 mmol), N-methyldicyclohexylamine (1.9ml, 8.55 mmol) and 30ml DMF are added sequentially. The reaction mixture is stirred at 100 °C for 1 h. After cooling down to room temperature, EtOAc is added and the mixture is washed with H ₂ O to remove the DMF, dried over Na ₂ SO4, and concentrated in vacuo. The crude product is then purified by flash chromatography on silica gel using a mixture of ethyl acetate and hexane as eluant. The desired 3-(2-oxo-2H-chromen-4-yl)propanal is obtained in 71% yield (1.12g). 1H NMR (500 MHz, CDCl ₃ ) δ 9.90 (s, 1H), 7.63 (dd, J = 8.0, 1.5 Hz, 1H), 7.55 (ddd, J = 8.6, 7.3, 1.5 Hz, 1H), 7.36 (dd, J = 8.3, 1.2 Hz, 1H), 7.32 (td, J = 7.7, 1.2 Hz, 1H), 6.28 (s, 1H), 3.21 – 3.07 (m, 2H), 2.93 (t, J = 7.5 Hz, 2H). 3-(2-oxo-2H-chromen-4-yl)propanal (1.12 g, 5.54 mmol) is suspended in methanol (11.9 mL, 290 mmol) and cooled to 0 °C. Sodium borohydride (272 mg, 7.20 mmol) is added portion wise which results in small gas evolution. The brown reaction mixture is stirred at 0 °C for 3 h until TLC indicates full conversion. The reaction mixture is neutralized by addition of 1M HCl before it is extracted with EtOAc (3x20 mL). Combined organics are washed with brine and dried over Na ₂ SO ₄ . The crude product is purified by column chromatography on silica using Cyhex/EtOAc 20% to 70%.4-(3-hydroxypropyl)-2H- chromen-2-one (1.12 g, 5.53 mmol, 99%) is isolated as yellow oil. 1H NMR (500 MHz, CDCl ₃ ) δ 7.69 (d, J = 7.9 Hz, 1H), 7.53 (t, J = 7.8 Hz, 1H), 7.36 (d, J = 8.3 Hz, 1H), 7.30 (t, J = 7.6 Hz, 1H), 6.32 (s, 1H), 3.80 (t, J = 6.0 Hz, 2H), 2.97 – 2.84 (m, 2H), 2.03 – 1.80 (m, 2H), 1.42 (s, 1H). Example 1aa: 4-Fluoro-2-hydroxyacethophenone (64.88 mmol; 10.0 g) is suspended in toluene (2.595,08 mmol; 40.0 eq.; 274,83 ml) and cooled to 0 °C. Sodium hydride (60% dispersion in mineral oil) (324.38 mmol; 5.0 eq.; 12.97 g) is added portionwise and the reaction mixture is stirred for 15 min. Then diethyl carbonate (140.78 mmol; 2.17 eq.; 16,97 ml) is added to the reaction mixture and is stirred at 0 °C for 15 min. before it is heated to 110 °C for 22 h. The reaction mixture is cooled to r.t. and H ₂ O is added slowly, the phases are separated and the organic phase is washed with H ₂ O. The aqueous phase is acidified to pH = 1 by addition of 2M HCl and the resulting precipitate is collected by filtration. The solid crude product is dried in vacuo and yield 8.74g of 7-fluoro-4-hydroxy-2H-chromen-2- one (48,52 mmol; 75 % of theory) as a white solid. 1H NMR (500 MHz, DMSO-d ₆ ) δ 7.86 (dd, J = 8.8, 6.4 Hz, 1H), 7.28 (dd, J = 9.8, 2.5 Hz, 1H), 7.18 (td, J = 8.7, 2.5 Hz, 1H), 5.43 (d, J = 2.5 Hz, 1H), 3.39 (br s, 1H). 1 ⁹ F NMR (471 MHz, DMSO-d ₆ ) δ -106.9 (s, 1F). Analogously, other derivatives are prepared in the same manner: 1H NMR (500 MHz, DMSO) δ 7.57 – 7.49 (m, 2H), 7.44 (ddd, J = 8.6, 4.5, 1.1 Hz, 1H), 5.64 (s, 1H), 3.35 (s, 1H). 1 ⁹ F NMR (471 MHz, DMSO-d ₆ ) δ -118.9 (m, 1F). Example 1ab: 7-fluoro-4-hydroxy-2H-chromen-2-one (11.10 mmol; 1.0 eq.; 2.00 g) is dissolved in Phosphorus(V)oxychloride (194.30 mmol; 17.50 eq.; 18.29 ml). Triethylamine (16.65 mmol; 1,50 eq.; 2.33 ml) is added dropwise and the reaction mixture is stirred at 100 °C for 2.5 h before TLC is done showing full conversion of the starting material. The reaction mixture is added to ice water before it is 3x extracted with CHCl ₃ . The combined organic extracts are washed with 2x NaHCO ₃ and brine; dried over Na ₂ SO ₄ and the crude product is purified by column chromatography on silica using Cyclohexane/EtOAc.1.75g 4-chloro- 7-fluoro-2H-chromen-2-one (8,81 mmol; 79% of theory) is isolated as an orange solid. 1H NMR (500 MHz, CDCl ₃ ) δ 7.92 – 7.84 (m, 1H), 7.15 – 7.07 (m, 2H), 6.57 (s, 1H). Analogously, other derivatives are prepared in the same manner:

1H NMR (500 MHz, CDCl ₃ ) δ 7.57 (dd, J = 8.3, 2.7 Hz, 1H), 7.40 – 7.30 (m, 2H), 6.67 (s, 1H). Example 1b: 4-Bromo-2H-chromen-2-one (4.00 g, 17.8 mmol) is dissolved in N,N-dimethylformamide (34.6 mL, 444 mmol) before 6-mercapto-1-hexanol (2.61 mL, 18.7 mmol) followed by potassiumcarbonat (6.20 g, 44.4 mmol) are added. The resulting reaction mixture is stirred at r.t. for 16 h before TLC show complete conversion. The reaction mixture is neutralized by addition of 1M HCl before it is extracted with EtOAc (3x100 mL). Combined organics are washed with NaHCO ₃ solution, H ₂ O and brine and dried over Na ₂ SO ₄ . The crude product (4.9 g, 17.8 mmol) is isolated as yellow crystals and could be used for next step without further purification. 1H NMR (500 MHz, CDCl ₃ ) δ 7.77 (dd, J = 8.0, 1.5 Hz, 1H), 7.57 (ddd, J = 8.6, 7.3, 1.5 Hz, 1H), 7.36 (dd, J = 8.4, 1.1 Hz, 1H), 7.32 – 7.28 (m, 1H), 6.17 (s, 1H), 3.70 (q, J = 6.2 Hz, 2H), 3.05 (t, J = 7.4 Hz, 2H), 1.86 (p, J = 7.4 Hz, 2H), 1.71 – 1.53 (m, 4H), 1.52 – 1.42 (m, 2H), 1.35 (t, J = 5.1 Hz, 1H). Analogously, other derivatives are prepared in the same manner: R1 means reactant, R2 means reactant 2, [P] means product.

1H NMR (500 MHz, CDCl ₃ ) δ 7.71 (dd, J = 8.1, 1.5 Hz, 1H), 7.48 (ddd, J = 8.5, 7.2, 1.5 Hz, 1H), 7.33 (dd, J = 8.3, 1.2 Hz, 1H), 7.23 (ddd, J = 8.3, 7.2, 1.3 Hz, 1H), 5.65 (s, 1H), 3.74 (q, J = 5.6 Hz, 2H), 3.55 – 3.42 (m, 2H), 3.02 (s, 3H), 2.03 – 1.95 (m, 2H), 1.50 – 1.41 (m, 1H). 1H NMR (500 MHz, CDCl ₃ ) δ 7.75 (dd, J = 8.0, 1.5 Hz, 1H), 7.55 (ddd, J = 8.6, 7.3, 1.5 Hz, 1H), 7.34 (dd, J = 8.4, 1.3 Hz, 1H), 7.28 (ddd, J = 8.3, 7.3, 1.2 Hz, 1H), 6.23 (s, 1H), 3.85 (t, J = 5.9 Hz, 2H), 3.18 (t, J = 7.2 Hz, 2H), 2.07 (tt, J = 7.2, 5.9 Hz, 2H), 1.65 – 1.56 (m, 1H). 1H NMR (500 MHz, CDCl ₃ ) δ 7.63 (d, J = 8.8 Hz, 1H), 6.84 (dd, J = 8.8, 2.5 Hz, 1H), 6.80 (d, J = 2.5 Hz, 1H), 6.01 (s, 1H), 3.87 (s, 3H), 3.73 – 3.60 (m, 2H), 3.01 (t, J = 7.4 Hz, 2H), 1.82 (p, J = 7.4 Hz, 2H), 1.68 – 1.50 (m, 4H), 1.48 – 1.41 (m, 2H), 1.33 – 1.29 (m, 1H). 1H NMR (500 MHz, CDCl ₃ ) δ 7.59 (d, J = 8.4 Hz, 1H), 7.21 (d, J = 1.8 Hz, 1H), 7.15 (dd, J = 8.4, 1.8 Hz, 1H), 6.07 (s, 1H), 3.67 (td, J = 6.5, 2.7 Hz, 2H), 3.40 – 3.22 (m, 1H), 3.01 (t, J = 7.4 Hz, 2H), 2.12 – 1.99 (m, 2H), 1.81 (q, J = 7.5 Hz, 4H), 1.71 – 1.49 (m, 6H), 1.49 – 1.15 (m, 9H). 1H NMR (500 MHz, CDCl ₃ ) δ 7.90 (dd, J = 8.1, 1.4 Hz, 1H), 7.58 (ddd, J = 8.6, 7.2, 1.4 Hz, 1H), 7.36 (d, J = 8.5 Hz, 1H), 7.27 – 7.16 (m, 1H), 6.51 (s, 1H), 3.69 (s, 3H), 3.66 (q, J = 6.2 Hz, 2H), 3.01 (t, J = 7.4 Hz, 2H), 1.81 (p, J = 7.4 Hz, 2H), 1.66 – 1.40 (m, 8H). 1H NMR (500 MHz, CDCl ₃ ) δ 7.78 (dd, J = 8.1, 1.5 Hz, 1H), 7.54 (ddd, J = 8.5, 7.2, 1.5 Hz, 1H), 7.32 (d, J = 8.3 Hz, 1H), 7.26 (s, 1H), 6.36 (s, 1H), 3.84 (q, J = 5.6 Hz, 2H), 3.66 (p, J = 6.6 Hz, 1H), 2.10 – 1.94 (m, 2H), 1.88 – 1.70 (m, 2H), 1.58 – 1.47 (m, 2H), 0.97 (t, J = 7.3 Hz, 3H). 1H NMR (500 MHz, CDCl ₃ ) δ 7.63 – 7.57 (m, 1H), 6.83 – 6.77 (m, 2H), 5.52 (s, 1H), 3.86 (s, 3H), 3.73 (q, J = 5.5 Hz, 2H), 3.50 – 3.44 (m, 2H), 3.00 (s, 3H), 2.02 – 1.95 (m, 2H), 1.48 (t, J = 4.8 Hz, 1H). 1H NMR (500 MHz, CDCl ₃ ) δ 7.73 (dd, J = 8.8, 5.8 Hz, 1H), 7.07 – 6.97 (m, 2H), 6.09 (s, 1H), 3.67 (t, J = 6.4 Hz, 2H), 3.07 – 2.95 (m, 2H), 1.83 (p, J = 7.4 Hz, 2H), 1.65 – 1.41 (m, 6H). 1H NMR (500 MHz, CDCl ₃ ) δ 7.43 (dd, J = 8.8, 2.8 Hz, 1H), 7.32 (dd, J = 9.1, 4.7 Hz, 1H), 7.26 (s, 1H), 6.18 (s, 1H), 3.67 (dt, J = 12.5, 6.5 Hz, 2H), 3.04 (t, J = 7.4 Hz, 2H), 1.84 (p, J = 7.4 Hz, 2H), 1.65 – 1.33 (m, 6H). 1H NMR (500 MHz, CDCl ₃ ) δ 7.72 (d, J = 2.4 Hz, 1H), 7.49 (dd, J = 8.8, 2.4 Hz, 1H), 7.27 (d, J = 8.8 Hz, 1H), 6.17 (s, 1H), 3.68 (t, J = 6.5 Hz, 2H), 3.03 (t, J = 7.3 Hz, 2H), 1.83 (p, J = 7.4 Hz, 2H), 1.61 (dq, J = 8.3, 6.8 Hz, 2H), 1.57 – 1.52 (m, 2H), 1.50 – 1.43 (m, 2H). Example 1c: 4-[(6-hydroxyhexyl)sulfanyl]-2H-chromen-2-one (2.00 g, 7.18 mmol) is suspended in phosphoric acid (0.08 mL, 1.44 mmol) and water (10 mL). Hydrogen peroxide (1.50 mL, 14.7 mmol) is slowly added and the resulting reaction mixture is heated to 100 °C over 18 h before it is added to aqueous NaHCO ₃ -solution and extracted with EtOAc (3×). Combined organic phases are washed with brine and dried over Na ₂ SO ₄ . Purification via column chromatography on silica using Cyhex/EtOAc as eluent is performed to give 4-(6- hydroxyhexanesulfinyl)-2H-chromen-2-one (1.23 g, 4.18 mmol, 58%) as pale yellow solid. 1H NMR (500 MHz, CDCl ₃ ) δ 7.63 (ddd, J = 8.6, 7.3, 1.5 Hz, 1H), 7.45 (dd, J = 8.4, 1.0 Hz, 1H), 7.41 (dd, J = 7.9, 1.5 Hz, 1H), 7.36 – 7.29 (m, 1H), 7.06 (s, 1H), 3.64 (td, J = 6.5, 3.1 Hz, 2H), 3.13 (ddd, J = 13.4, 9.8, 6.3 Hz, 1H), 2.87 (ddd, J = 13.5, 9.6, 5.1 Hz, 1H), 1.97 (dtd, J = 12.3, 9.3, 4.8 Hz, 1H), 1.75 (dtt, J = 14.8, 10.0, 5.2 Hz, 1H), 1.62 – 1.35 (m, 6H), 1.28 (s, 1H). Example 1d: To a solution of 4-Hydroxycoumarin (1.00 g; 6.17 mmol) in N,N-Dimethylformamide (anhydrous) (5.25 ml; 67.84 mmol), Potassium carbonate (2.56 g; 18.50 mmol) and 6- Bromohexan-1-ol (988.04 µl; 7.40 mmol) are added. The reaction mixture is heated to 110 °C overnight, then quenched with HCl (1M) and exacted with 2-methyl-THF. Afterwards, the organic layer is dried over anhydrous Na ₂ SO ₄ and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography using ethyl acetate/cyclohexane (1/1,) to get 4-[(6-Hydroxyhexyl)oxy]-coumarin (1.23 g; 4.7 mmol; 76%). 1H NMR (500 MHz, DMSO-d ₆ ) δ 7.80 (dd, J = 7.9, 1.6 Hz, 1H), 7.65 (ddd, J = 8.6, 7.3, 1.7 Hz, 1H), 7.41 – 7.34 (m, 2H), 5.88 (s, 1H), 4.35 (t, J = 5.1 Hz, 1H), 4.20 (t, J = 6.4 Hz, 2H), 3.40 (td, J = 6.4, 5.1 Hz, 2H), 1.86 – 1.78 (m, 2H), 1.50 – 1.42 (m, 4H), 1.41 – 1.35 (m, 2H). Analogously, other derivatives are prepared in the same manner: R1 means reactant, R2 means reactant 2, [P] means product. 1H NMR (500 MHz, DMSO-d ₆ ) δ 7.81 (dd, J = 7.9, 1.5 Hz, 1H), 7.66 (ddd, J = 8.6, 7.3, 1.6 Hz, 1H), 7.41 – 7.34 (m, 2H), 5.89 (s, 1H), 4.40 (t, J = 5.1 Hz, 1H), 4.21 (t, J = 6.3 Hz, 2H), 3.43 (q, J = 5.6 Hz, 2H), 1.83 (dq, J = 10.5, 6.5 Hz, 2H), 1.50 (dq, J = 6.7, 3.4 Hz, 4H). 1H NMR (500 MHz, CDCl ₃ ) δ 7.80 (dd, J = 7.9, 1.6 Hz, 1H), 7.54 (ddd, J = 8.6, 7.3, 1.6 Hz, 1H), 7.31 (dd, J = 8.4, 1.1 Hz, 1H), 7.29 (t, J = 7.5 Hz, 1H), 5.71 (s, 1H), 4.29 (t, J = 6.1 Hz, 2H), 3.91 (td, J = 6.0, 5.0 Hz, 2H), 2.17 (p, J = 6.1 Hz, 2H), 1.63 (t, J = 5.0 Hz, 1H). 1 ³ C NMR (126 MHz, CDCl ₃ ) δ 165.7, 163.1, 153.5, 132.5, 124.0, 123.1, 117.0, 115.9, 90.8, 66.3, 59.2, 31.5. 1H NMR (500 MHz, DMSO-d ₆ ) δ 7.80 (dd, J = 7.9, 1.6 Hz, 1H), 7.66 (ddd, J = 8.6, 7.2, 1.6 Hz, 1H), 7.42 – 7.33 (m, 2H), 5.89 (s, 1H), 4.31 (t, J = 5.1 Hz, 1H), 4.21 (t, J = 6.4 Hz, 2H), 3.36 (td, J = 6.6, 5.0 Hz, 2H), 1.86 – 1.77 (m, 2H), 1.49-1.32 (m, 4H), 1.31-1.21 (m, 12H). 1H NMR (500 MHz, DMSO) δ 7.89 (dd, J = 8.0, 1.6 Hz, 1H), 7.65 (ddd, J = 8.7, 7.1, 1.6 Hz, 1H), 7.51 (d, J = 8.4 Hz, 1H), 7.28 (q, J = 7.5, 7.0 Hz, 1H), 6.02 (s, 1H), 4.35 (t, J = 5.2 Hz, 1H), 4.12 (t, J = 6.4 Hz, 2H), 3.56 (s, 3H), 3.45 – 3.35 (m, 2H), 1.86 – 1.77 (m, 2H), 1.54 – 1.30 (m, 6H). ¹ H NMR (500 MHz, DMSO-d ₆ ) δ 7.70 (d, J = 8.8 Hz, 1H), 6.98 (d, J = 2.4 Hz, 1H), 6.95 (dd, J = 8.7 Hz, 2.4 Hz, 1H), 5.72 (s, 1H), 4.35 (t, J = 5.1 Hz, 1H), 4.18 (t, J = 6.4 Hz, 2H), 3.85 (s, 3H), 3.43 – 3.36 (m, 2H), 1.85 – 1.76 (m, 2H), 1.45 (pd, J = 6.8, 3.5 Hz, 4H), 1.41 – 1.32 (m, 2H). 1H NMR (500 MHz, CDCl ₃ ) δ 7.65 (dd, J = 7.9, 1.6 Hz, 1H), 7.49 (ddd, J = 8.6, 7.3, 1.6 Hz, 1H), 7.34 (dd, J = 8.4, 1.1 Hz, 1H), 7.31 – 7.27 (m, 1H), 4.06 (t, J = 6.4 Hz, 2H), 3.79 – 3.64 (m, 2H), 2.49 (d, J = 7.3 Hz, 2H), 2.11 – 2.00 (m, 1H), 1.98 – 1.88 (m, 2H), 1.75 – 1.60 (m, 4H), 1.27 (t, J = 5.2 Hz, 1H), 0.95 (d, J = 6.7 Hz, 6H). 1H NMR (500 MHz, CDCl ₃ ) δ 7.67 (d, J = 8.3 Hz, 1H), 7.21 (d, J = 1.6 Hz, 1H), 7.15 (dd, J = 8.3, 1.7 Hz, 1H), 5.60 (s, 1H), 4.20 – 4.05 (m, 2H), 3.71 (q, J = 5.9 Hz, 2H), 3.29 (ddd, J = 14.1, 8.5, 3.8 Hz, 1H), 2.04 (d, J = 4.8 Hz, 2H), 1.94 (p, J = 6.6 Hz, 2H), 1.85 – 1.75 (m, 2H), 1.71 – 1.57 (m, 5H), 1.50 – 1.28 (m, 5H). 1H NMR (500 MHz, CDCl ₃ ) δ 7.56 (d, J = 9.1 Hz, 1H), 6.59 – 6.53 (m, 1H), 6.46 (d, J = 2.5 Hz, 1H), 6.10 (s, 1H), 5.55 (s, 1H), 5.39 (s, 1H), 4.17 (t, J = 6.6 Hz, 2H), 4.09 (t, J = 6.4 Hz, 2H), 3.40 (q, J = 7.1 Hz, 4H), 1.94 (s, 3H), 1.89 (t, J = 7.1 Hz, 2H), 1.73 (t, J = 7.2 Hz, 2H), 1.49 (d, J = 7.1 Hz, 2H), 1.20 (t, J = 7.1 Hz, 6H), 1.13 (s, 2H). m. p. (DSC): not observed ¹ H NMR (500 MHz, CDCl ₃ ) δ 8.14 (d, J = 7.9 Hz 1H), 7.54 – 7.47 (m, 1H), 7.46 – 7.36 (m, 2H), 6.09 (s, 1H), 6.06 (s, 1H), 5.57 – 5.48 (m, 1H), 4.18 (t, J = 6.6 Hz, 2H), 4.11 (t, J = 6.3 Hz, 2H), 1.95 (d, J = 5.1 Hz, 5H), 1.75 (p, J = 6.8 Hz, 2H), 1.59 (p, J = 7.4 Hz, 2H), 1.54 – 1.47 (m, 2H). m. p. (DSC): -44 °C 1H NMR (500 MHz, CDCl ₃ ) δ 7.76 (dd, J = 8.0, 1.5 Hz, 1H), 7.59 (ddd, J = 8.6, 7.2, 1.5 Hz, 1H), 7.47 (dd, J = 8.3, 1.1 Hz, 1H), 7.36 – 7.29 (m, 1H), 7.09 (s, 1H), 6.10 (d, J = 4.5 Hz, 1H), 5.55 (dt, J = 3.1, 1.6 Hz, 1H), 4.16 (t, J = 6.5 Hz, 2H), 3.06 (t, J = 7.3 Hz, 2H), 1.94 (q, J = 1.4 Hz, 3H), 1.83 (p, J = 7.3 Hz, 2H), 1.72 (dt, J = 14.2, 6.9 Hz, 2H), 1.60 – 1.55 (m, 2H), 1.51 – 1.45 (m, 2H). 1 ³ C NMR (126 MHz, CDCl ₃ ) δ 194.3, 167.6, 154.6, 151.0, 136.6, 132.7, 125.5, 125.5, 125.3, 123.9, 121.1, 119.6, 117.3, 77.2, 64.6, 31.0, 28.7, 28.6, 27.7, 25.7, 18.5. m. p. (DSC): 64 °C 1H NMR (500 MHz, CDCl ₃ ) δ 7.71 (d, J = 8.8 Hz, 1H), 6.84 (dd, J = 8.8, 2.4 Hz, 1H), 6.80 (d, J = 2.4 Hz, 1H), 5.85 (ddt, J = 16.9, 10.3, 6.6 Hz, 1H), 5.54 (s, 1H), 5.13 – 5.02 (m, 2H), 4.12 (t, J = 6.3 Hz, 2H), 3.87 (s, 3H), 2.29 (q, J = 7.1 Hz, 2H), 2.00 (p, J = 6.7 Hz, 2H). 1H NMR (500 MHz, CDCl ₃ ) δ 7.56 (d, J = 9.0 Hz, 1H), 6.55 (dd, J = 9.0, 2.5 Hz, 1H), 6.46 (d, J = 2.4 Hz, 1H), 5.39 (s, 1H), 4.08 (t, J = 6.4 Hz, 2H), 3.67 (q, J = 5.7 Hz, 2H), 3.40 (q, J = 7.1 Hz, 4H), 1.92 – 1.83 (m, 2H), 1.62 (h, J = 6.8 Hz, 3H), 1.57 – 1.43 (m, 3H), 1.36 (d, J = 5.0 Hz, 1H), 1.19 (t, J = 7.1 Hz, 6H). (A-181) 1H NMR (500 MHz, CDCl ₃ ) δ 7.80 (dd, J = 8.7, 6.1 Hz, 1H), 7.02 (qd, J = 8.7, 2.5 Hz, 2H), 6.09 (dd, J = 1.6, 1.0 Hz, 1H), 5.62 (s, 1H), 5.55 (t, J = 1.7 Hz, 1H), 4.18 (t, J = 6.6 Hz, 2H), 4.13 (t, J = 6.4 Hz, 2H), 1.97 – 1.84 (m, 5H), 1.74 (p, J = 6.8 Hz, 2H), 1.61 – 1.42 (m, 4H). 1 ⁹ F NMR (471 MHz, CDCl ₃ ) δ -104.95 – 105.00 (m, 1F). m. p. (DSC): 51.7 °C (A-182) 1H NMR (500 MHz, CDCl ₃ ) δ 7.47 (dd, J = 8.3, 2.9 Hz, 1H), 7.32 – 7.22 (m, 2H), 6.10 (dd, J = 1.8, 1.0 Hz, 1H), 5.70 (s, 1H), 5.55 (t, J = 1.6 Hz, 1H), 4.18 (t, J = 6.6 Hz, 2H), 4.14 (t, J = 6.4 Hz, 2H), 1.99 – 1.88 (m, 5H), 1.75 (dt, J = 14.7, 6.7 Hz, 2H), 1.60 – 1.46 (m, 4H). 1 ⁹ F NMR (471 MHz, CDCl ₃ ) δ -117.44 (d, J = 7.6 Hz, 1F). m. p. (DSC): 55.4 °C (A-188) 1H NMR (500 MHz, CDCl ₃ ) δ 7.76 (d, J = 2.5 Hz, 1H), 7.49 (dd, J = 8.8, 2.5 Hz, 1H), 7.32 – 7.18 (m, 1H), 6.10 (dq, J = 1.9, 1.0 Hz, 1H), 5.68 (s, 1H), 5.55 (p, J = 1.6 Hz, 1H), 4.18 (t, J = 6.6 Hz, 2H), 4.13 (t, J = 6.4 Hz, 2H), 2.01 – 1.82 (m, 5H), 1.75 (p, J = 6.8 Hz, 2H), 1.61 – 1.44 (m, 4H). m. p. (DSC): 76.7 °C Example 2: 4-[(5-Hydroxypentyl)oxy]-2H-chromen-2-on (0.8gg, 3.22 mmol, 1.00 eq.) is dissolved in THF (15 mL) and triethylamine (1.79 mL, 12.89 mmol, 4.00 eq.) and acryloyl chloride (0.324 mL, 3.87 mmol, 1.2 eq.) is added at 0 °C. After stirring at r.t. overnight the suspension is filtered. The solvent of the filtrate is evaporated, and the crude product is cleaned by column chromatography (5-20% ethyl acetate/cyclohexane). The synthesis yield 0.75 g 5-[(2-oxo-2H-chromen-4-yl)oxy]pentyl prop-2-enoat (2.48 mmol, 77% of theory). ¹ H NMR (500 MHz, CDCl ₃ δ 7.81 (dd, J = 7.9, 1.5 Hz, 1H), 7.55 (ddd, J = 8.7, 7.3, 1.6 Hz, 1H), 7.32 (d, J = 8.3 Hz, 1H), 7.27 (t, J = 7.6 Hz, 1H), 6.41 (dd, J = 17.3, 1.4 Hz, 1H), 6.13 (dd, J = 17.4, 10.4 Hz, 1H), 5.83 (dd, J = 10.4, 1.4 Hz, 1H), 5.67 (s, 1H), 4.22 (t, J = 6.5 Hz, 2H), 4.15 (t, J = 6.3 Hz, 2H), 1.97 (p, J = 6.6 Hz, 2H), 1.80 (p, J = 6.8 Hz, 2H), 1.63 (tt, J = 9.9, 6.2 Hz, 2H). m. p. (DSC): 72-77 °C. Analogously, other derivatives are prepared in the same manner:

1H NMR (500 MHz, CDCl ₃ ) δ 7.64 (dd, J = 8.0, 1.6 Hz, 1H), 7.59 (ddd, J = 8.6, 7.3, 1.6 Hz, 2H), 7.39 (d, J = 8.3 Hz, 1H), 7.31 (t, J = 7.6 Hz, 1H), 6.75 (d, J = 17.2 Hz, 1H), 6.57 (s, 1H), 6.40 (dd, J = 17.3, 10.5 Hz, 1H), 6.20 (d, J = 10.5 Hz, 1H). m. p. (DSC): 84 °C. 1H NMR (500 MHz, CDCl ₃ ) δ 7.81 (dd, J = 8.0, 1.6 Hz, 1H), 7.58 – 7.51 (m, 1H), 7.30 (dd, J = 15.2, 8.0 Hz, 2H), 6.40 (d, J = 17.3 Hz, 1H), 6.f12 (dd, J = 17.3, 10.4 Hz, 1H), 5.82 (d, J = 10.5 Hz, 1H), 5.67 (s, 1H), 4.19 (t, J = 6.6 Hz, 2H), 4.14 (t, J = 6.3 Hz, 2H), 1.93 (p, J = 6.6 Hz, 2H), 1.75 (h, J = 8.1, 6.9 Hz, 2H), 1.58 (p, J = 7.3 Hz, 2H), 1.50 (td, J = 8.6, 8.0, 3.6 Hz, 2H). m. p. (DSC): 59.6 °C. 1H NMR (500 MHz, CDCl ₃ ) δ 7.90 (dd, J = 8.1, 1.4 Hz, 1H), 7.58 (ddd, J = 8.6, 7.2, 1.5 Hz, 1H), 7.36 (dd, J = 8.6, 1.1 Hz, 1H), 7.28 – 7.21 (m, 1H), 6.50 (s, 1H), 6.40 (dd, J = 17.3, 1.5 Hz, 1H), 6.12 (dd, J = 17.3, 10.4 Hz, 1H), 5.82 (dd, J = 10.4, 1.5 Hz, 1H), 4.17 (t, J = 6.6 Hz, 2H), 3.70 (s, 3H), 3.01 (t, J = 7.4 Hz, 2H), 1.81 (p, J = 7.4 Hz, 2H), 1.75 – 1.66 (m, 2H), 1.60 – 1.50 (m, 2H), 1.50 – 1.40 (m, 2H). m. p. (DSC): 73 °C 1H NMR (500 MHz, CDCl ₃ ) δ 7.56 (d, J = 9.0 Hz, 1H), 6.56 (dd, J = 9.0, 2.5 Hz, 1H), 6.46 (d, J = 2.5 Hz, 1H), 6.40 (dd, J = 17.3, 1.5 Hz, 1H), 6.12 (dd, J = 17.4, 10.4 Hz, 1H), 5.82 (dd, J = 10.4, 1.5 Hz, 1H), 5.39 (s, 1H), 4.18 (t, J = 6.6 Hz, 2H), 4.08 (t, J = 6.4 Hz, 2H), 3.40 (q, J = 7.1 Hz, 4H), 1.97 – 1.81 (m, 2H), 1.73 (p, J = 6.9 Hz, 2H), 1.58 – 1.44 (m, 4H), 1.20 (t, J = 7.1 Hz, 6H). 1H NMR (500 MHz, CDCl ₃ ) δ 7.75 (dd, J = 8.0, 1.5 Hz, 1H), 7.54 (ddd, J = 8.5, 7.3, 1.5 Hz, 1H), 7.33 (dd, J = 8.4, 1.2 Hz, 1H), 7.31 – 7.24 (m, 1H), 6.40 (dd, J = 17.3, 1.4 Hz, 1H), 6.20 – 6.03 (m, 2H), 5.82 (dd, J = 10.4, 1.4 Hz, 1H), 4.18 (t, J = 6.6 Hz, 2H), 3.03 (t, J = 7.3 Hz, 2H), 1.83 (p, J = 7.4 Hz, 2H), 1.76 – 1.67 (m, 2H), 1.59 – 1.51 (m, 2H), 1.51 – 1.41 (m, 2H). m. p. (DSC): 44.5 °C Example 3: 4-(3-Hydroxypropoxy)-2H-chromen-2-one (4.46 g, 20.52 mmol, 1.00 eq.) is dissolved in DCM (71 mL) and triethylamine (11.34 mL, 81.01 mmol, 4.00 eq.). (Dimethylamino)pyridine (0.25 g, 2.03 mmol, 0.10 eq.) and methacrylic anhydride (3.41 ml, 21.27 mmol, 1.05 eq.) are added at 0 °C. After stirring at r.t. overnight, the reaction mixture is quenched with 1M aq. HCl solution and extracted with DCM three times. Combined organic extracts are washed with NaHCO ₃ solution and brine and are dried over Na ₂ SO ₄ . The solvent of the filtrate is evaporated and the crude product is cleaned by column chromatography (10-30% ethyl acetate/cyclohexane). The synthesis yield 3.05 g 3-[(2-oxo-2H-chromen-4- yl)oxy]propyl 2-methylprop-2-enoate (10.27 mmol, 51% of theory). ¹ H NMR (500 MHz, CDCl ₃ ) δ 7.81 (dd, J = 7.9, 1.6 Hz, 1H), 7.55 (ddd, J = 8.7, 7.2, 1.6 Hz, 1H), 7.32 (dd, J = 8.4, 1.0 Hz, 1H), 7.29 – 7.24 (m, 1H), 6.11 (d, J = 1.2 Hz, 1H), 5.69 (s, 1H), 5.59 (d, J = 1.6 Hz, 1H), 4.40 (t, J = 6.1 Hz, 2H), 4.25 (t, J = 6.1 Hz, 2H), 2.38 – 2.19 (m, 2H), 1.94 (t, J = 1.3 Hz, 3H). m. p. (DSC): 97 °C. Analogously, other derivatives are prepared in the same manner: ¹ H NMR (500 MHz, CDCl ₃ ) δ 7.80 (dd, J = 7.9, 1.6 Hz, 1H), 7.55 (ddd, J = 8.7, 7.2, 1.6 Hz, 1H), 7.32 (dd, J = 8.3, 1.1 Hz, 1H), 7.27 (t, J = 7.6 Hz, 1H), 6.10 (t, J = 1.4 Hz, 1H), 5.67 (s, 1H), 5.56 (t, J = 1.6 Hz, 1H), 4.21 (t, J = 6.5 Hz, 2H), 4.15 (t, J = 6.2 Hz, 2H), 2.00 – 1.93 (m, 5H), 1.84 – 1.77 (m, 2H), 1.68 – 1.61 (m, 2H). m. p. (DSC): 75 °C 1H NMR (500 MHz, CDCl ₃ ) δ 7.96 (dd, J = 8.0, 1.6 Hz, 1H), 7.57 (ddd, J = 8.6, 7.1, 1.6 Hz, 1H), 7.32 (d, J = 8.4 Hz, 1H), 7.25 – 7.18 (m, 1H), 6.08 (t, J = 1.3 Hz, 1H), 6.00 (s, 1H), 5.53 (p, J = 1.7 Hz, 1H), 4.16 (t, J = 6.6 Hz, 2H), 4.08 (t, J = 6.3 Hz, 2H), 3.66 (s, 3H), 1.95 – 1.86 (m, 5H), 1.73 (p, J = 6.8 Hz, 2H), 1.62 – 1.53 (m, 2H), 1.49 (qd, J = 7.5, 4.1 Hz, 2H). m. p. (DSC): T _g -41 °C 1H NMR (500 MHz, CDCl ₃ ) δ 7.68 (d, J = 8.8 Hz, 1H), 6.81 (dd, J = 8.8, 2.5 Hz, 1H), 6.77 (d, J = 2.4 Hz, 1H), 6.08 (t, J = 1.3 Hz, 1H), 5.56 – 5.50 (m, 2H), 4.16 (t, J = 6.6 Hz, 2H), 4.10 (t, J = 6.4 Hz, 2H), 3.85 (s, 3H), 1.94 – 1.85 (m, 5H), 1.72 (p, J = 6.8 Hz, 2H), 1.58 – 1.45 (m, 4H). m. p. (DSC): 88 °C 1H NMR (500 MHz, CDCl ₃ ) δ 7.79 (dd, J = 7.9, 1.6 Hz, 1H), 7.52 (ddd, J = 8.6, 7.3, 1.6 Hz, 1H), 7.33 – 7.28 (m, 1H), 7.24 (d, J = 7.0 Hz, 1H), 6.06 (t, J = 1.3 Hz, 1H), 5.64 (s, 1H), 5.52 (t, J = 1.7 Hz, 1H), 4.13 (dt, J = 20.0, 6.4 Hz, 4H), 1.93 – 1.87 (m, 5H), 1.71 (p, J = 6.8 Hz, 2H), 1.58 – 1.52 (m, 2H), 1.50 – 1.43 (m, 2H). m. p. (DSC): 52 °C. 1H NMR (500 MHz, CDCl ₃ ) δ 7.74 (dd, J = 8.0, 1.5 Hz, 1H), 7.55 (ddd, J = 8.6, 7.3, 1.5 Hz, 1H), 7.34 (dd, J = 8.4, 1.2 Hz, 1H), 7.31 – 7.27 (m, 1H), 6.17 (s, 1H), 6.16 (s, 1H), 5.62 (t, J = 1.6 Hz, 1H), 4.33 (d, J = 6.0 Hz, 2H), 3.14 (t, J = 7.2 Hz, 2H), 2.21 (ddd, J = 13.2, 7.2, 6.0 Hz, 2H), 1.98 (t, J = 1.2 Hz, 3H). m. p. (DSC): 72 °C. 1H NMR (500 MHz, CDCl ₃ ) δ 7.75 (dd, J = 8.0, 1.5 Hz, 1H), 7.54 (ddd, J = 8.6, 7.3, 1.5 Hz, 1H), 7.33 (dd, J = 8.4, 1.1 Hz, 1H), 7.29 – 7.20 (m, 1H), 6.14 (s, 1H), 6.10 (dd, J = 1.7, 1.0 Hz, 1H), 5.55 (t, J = 1.6 Hz, 1H), 4.16 (t, J = 6.6 Hz, 2H), 3.03 (t, J = 7.3 Hz, 2H), 1.94 (t, J = 1.3 Hz, 3H), 1.83 (p, J = 7.4 Hz, 2H), 1.77 – 1.66 (m, 2H), 1.63 – 1.53 (m, 2H), 1.53 – 1.41 (m, 2H). m. p. (DSC): 45°C. 1H NMR (500 MHz, CDCl ₃ ) δ 7.63 (d, J = 8.9 Hz, 1H), 6.84 (dd, J = 8.9, 2.6 Hz, 1H), 6.80 (d, J = 2.5 Hz, 1H), 6.12 – 6.06 (m, 1H), 6.00 (s, 1H), 5.55 (t, J = 1.7 Hz, 1H), 4.16 (t, J = 6.6 Hz, 2H), 3.87 (s, 3H), 3.01 (t, J = 7.3 Hz, 2H), 1.94 (d, J = 1.3 Hz, 3H), 1.82 (p, J = 7.4 Hz, 2H), 1.71 (p, J = 6.8 Hz, 2H), 1.60 – 1.50 (m, 2H), 1.50 – 1.39 (m, 2H). m. p. (DSC): 109 °C 1H NMR (500 MHz, CDCl ₃ ) δ 7.65 (dd, J = 8.1, 1.5 Hz, 1H), 7.49 (ddd, J = 8.6, 7.2, 1.5 Hz, 1H), 7.34 (dd, J = 8.3, 1.2 Hz, 1H), 7.25 – 7.17 (m, 1H), 6.03 (d, J = 1.6 Hz, 1H), 5.66 (s, 1H), 5.54 (t, J = 1.6 Hz, 1H), 4.22 (t, J = 6.1 Hz, 2H), 3.50 – 3.41 (m, 2H), 3.01 (s, 3H), 2.22 – 2.09 (m, 2H), 1.90 (t, J = 1.2 Hz, 3H). m. p. (DSC): Tg -37 °C. 1H NMR (500 MHz, CDCl ₃ ) δ 7.82 (dd, J = 8.0, 1.6 Hz, 1H), 7.55 (ddd, J = 8.6, 7.2, 1.6 Hz, 1H), 7.32 (dd, J = 8.4, 1.1 Hz, 1H), 7.26 (s, 1H), 6.11 – 6.07 (m, 1H), 5.67 (s, 1H), 5.54 (p, J = 1.6 Hz, 1H), 4.13 (td, J = 6.6, 4.7 Hz, 4H), 1.94 (t, J = 1.3 Hz, 3H), 1.90 (dd, J = 8.5, 6.5 Hz, 2H), 1.71 – 1.62 (m, 2H), 1.55 – 1.46 (m, 2H), 1.41 – 1.28 (m, 12H). m. p. (DSC): 59 °C. 1H NMR (500 MHz, CDCl ₃ ) δ 7.63 (ddd, J = 8.6, 7.3, 1.6 Hz, 1H), 7.46 (dd, J = 8.4, 1.1 Hz, 1H), 7.41 (dd, J = 7.9, 1.6 Hz, 1H), 7.33 (td, J = 7.7, 1.2 Hz, 1H), 7.06 (s, 1H), 6.14 – 5.98 (m, 1H), 5.65 – 5.46 (m, 1H), 4.13 (t, J = 6.5 Hz, 2H), 3.12 (ddd, J = 13.4, 9.9, 6.3 Hz, 1H), 2.87 (ddd, J = 13.3, 9.7, 5.0 Hz, 1H), 2.04 – 1.95 (m, 1H), 1.93 (s, 3H), 1.78 – 1.64 (m, 3H), 1.60 – 1.38 (m, 4H). m. p. (DSC): not observed 1H NMR (500 MHz, CDCl ₃ ) δ 7.64 (dd, J = 7.9, 1.6 Hz, 1H), 7.50 (ddd, J = 8.7, 7.3, 1.6 Hz, 1H), 7.34 (dd, J = 8.3, 1.1 Hz, 1H), 7.31 – 7.26 (m, 1H), 6.11 (d, J = 1.3 Hz, 1H), 5.56 (t, J = 1.6 Hz, 1H), 4.22 (t, J = 6.5 Hz, 2H), 4.06 (t, J = 6.4 Hz, 2H), 2.49 (d, J = 7.3 Hz, 2H), 2.05 (dq, J = 13.7, 6.8 Hz, 1H), 1.98 – 1.90 (m, 5H), 1.81 (dt, J = 14.2, 6.7 Hz, 2H), 1.72 – 1.61 (m, 2H), 0.94 (d, J = 6.6 Hz, 6H). m. p. (DSC): Tg -54 °C. 1H NMR (500 MHz, CDCl ₃ ) δ 7.65 (d, J = 8.3 Hz, 1H), 7.21 (d, J = 1.7 Hz, 1H), 7.15 (dd, J = 8.3, 1.7 Hz, 1H), 6.10 (s, 1H), 5.60 (s, 1H), 5.56 (s, 1H), 4.20 (t, J = 6.5 Hz, 2H), 4.13 (t, J = 6.3 Hz, 2H), 3.29 (tt, J = 10.5, 3.7 Hz, 1H), 2.08 – 2.01 (m, 2H), 1.99 – 1.91 (m, 5H), 1.79 (p, J = 6.4 Hz, 4H), 1.63 (qt, J = 13.1, 5.4 Hz, 3H), 1.50 – 1.24 (m, 5H). m. p. (DSC): 56 °C. 1H NMR (500 MHz, CDCl ₃ ) δ 7.59 (d, J = 8.4 Hz, 1H), 7.21 (d, J = 1.8 Hz, 1H), 7.15 (dd, J = 8.4, 1.8 Hz, 1H), 6.10 (d, J = 0.8 Hz, 1H), 6.06 (s, 1H), 5.55 (t, J = 1.6 Hz, 1H), 4.16 (t, J = 6.6 Hz, 2H), 3.39 – 3.22 (m, 1H), 3.01 (t, J = 7.3 Hz, 2H), 2.17 – 1.98 (m, 2H), 1.94 (t, J = 1.3 Hz, 3H), 1.87 – 1.76 (m, 4H), 1.76 – 1.62 (m, 3H), 1.54 (d, J = 5.9 Hz, 2H), 1.50 – 1.23 (m, 7H). m. p. (DSC): 80 °C. 1H NMR (500 MHz, CDCl ₃ ) δ 7.91 (dd, J = 8.1, 1.4 Hz, 1H), 7.58 (ddd, J = 8.5, 7.2, 1.4 Hz, 1H), 7.37 (d, J = 8.5 Hz, 1H), 7.28 – 7.21 (m, 1H), 6.50 (s, 1H), 6.16 – 6.02 (m, 1H), 5.55 (s, 1H), 4.15 (t, J = 6.6 Hz, 2H), 3.70 (s, 3H), 3.01 (t, J = 7.3 Hz, 2H), 1.94 (t, J = 1.3 Hz, 3H), 1.81 (p, J = 7.4 Hz, 2H), 1.71 (p, J = 6.8 Hz, 2H), 1.63 – 1.51 (m, 2H), 1.46 (td, J = 8.1, 5.6 Hz, 2H). m. p. (DSC): 45 °C. 1H NMR (500 MHz, CDCl ₃ ) δ 7.63 (dd, J = 7.9, 1.5 Hz, 1H), 7.54 (ddd, J = 8.6, 7.2, 1.5 Hz, 1H), 7.36 (dd, J = 8.3, 1.2 Hz, 1H), 7.30 (td, J = 7.6, 1.2 Hz, 1H), 6.32 (d, J = 1.2 Hz, 1H), 6.11 (t, J = 1.3 Hz, 1H), 5.60 (p, J = 1.6 Hz, 1H), 4.29 (t, J = 6.2 Hz, 2H), 2.90 (ddd, J = 9.1, 6.1, 1.1 Hz, 2H), 2.16 – 2.07 (m, 2H), 1.96 (t, J = 1.3 Hz, 3H). m. p. (DSC): 50 °C 1H NMR (500 MHz, CDCl ₃ ) δ 7.77 (dd, J = 8.1, 1.5 Hz, 1H), 7.54 (ddd, J = 8.6, 7.2, 1.5 Hz, 1H), 7.33 (dd, J = 8.4, 1.2 Hz, 1H), 7.29 – 7.26 (m, 1H), 6.22 (s, 1H), 6.16 (t, J = 1.2 Hz, 1H), 5.62 (p, J = 1.6 Hz, 1H), 4.38 (dt, J = 11.9, 6.1 Hz, 1H), 4.27 (ddd, J = 11.8, 6.9, 5.6 Hz, 1H), 3.54 (p, J = 6.6 Hz, 1H), 2.17 (qt, J = 14.8, 7.4 Hz, 2H), 1.97 (t, J = 1.3 Hz, 3H), 1.89 – 1.72 (m, 2H), 1.60 – 1.49 (m, 2H), 0.97 (t, J = 7.3 Hz, 3H). m. p. (DSC): 73 °C. 1H NMR (500 MHz, CDCl ₃ ) δ 7.54 (d, J = 8.9 Hz, 1H), 6.83 – 6.75 (m, 2H), 6.04 (s, 1H), 5.57 – 5.51 (m, 2H), 4.21 (t, J = 6.1 Hz, 2H), 3.86 (s, 3H), 3.43 (t, J = 7.5 Hz, 2H), 2.99 (s, 3H), 2.17 – 2.09 (m, 2H), 1.93 – 1.89 (m, 3H). m. p. (DSC): not observed 1H NMR (500 MHz, CDCl ₃ ) δ 7.81 (dd, J = 7.9, 1.6 Hz, 1H), 7.55 (ddd, J = 8.7, 7.2, 1.6 Hz, 1H), 7.32 (dd, J = 8.4, 1.1 Hz, 1H), 7.29 – 7.25 (m, 1H), 6.11 (t, J = 1.3 Hz, 1H), 5.69 (s, 1H), 5.59 (p, J = 1.6 Hz, 1H), 4.40 (t, J = 6.1 Hz, 2H), 4.25 (t, J = 6.1 Hz, 2H), 2.31 (p, J = 6.1 Hz, 2H), 1.94 (t, J = 1.4 Hz, 3H). m. p. (DSC): 97 °C 1H NMR (500 MHz, CDCl ₃ ) δ 7.73 (dd, J = 8.8, 5.8 Hz, 1H), 7.09 – 6.96 (m, 2H), 6.10 (dt, J = 2.0, 1.1 Hz, 1H), 6.09 (s, 1H), 5.55 (t, J = 1.6 Hz, 1H), 4.16 (t, J = 6.6 Hz, 2H), 3.02 (t, J = 7.3 Hz, 2H), 1.94 (t, J = 1.3 Hz, 3H), 1.83 (p, J = 7.4 Hz, 2H), 1.72 (dt, J = 14.6, 6.7 Hz, 2H), 1.61 – 1.51 (m, 2H), 1.47 (dddd, J = 14.4, 9.0, 6.5, 3.3 Hz, 2H). 1 ⁹ F NMR (471 MHz, CDCl ₃ ) δ -105.19 (d, J = 7.8 Hz, 1F). m. p. (DSC): 76.5 °C ¹ H NMR (500 MHz, CDCl ₃ ) δ 7.37 (dd, J = 8.8, 2.8 Hz, 1H), 7.25 (dd, J = 9.1, 4.7 Hz, 1H), 7.23 – 7.17 (m, 1H), 6.11 (s, 1H), 6.04 (t, J = 1.4 Hz, 1H), 5.50 (t, J = 1.6 Hz, 1H), 4.11 (t, J = 6.6 Hz, 2H), 2.98 (t, J = 7.3 Hz, 2H), 1.89 (t, J = 1.3 Hz, 3H), 1.77 (p, J = 7.4 Hz, 2H), 1.70 – 1.62 (m, 2H), 1.50 (dq, J = 9.3, 6.8 Hz, 2H), 1.45 – 1.36 (m, 2H). 1 ⁹ F NMR (471 MHz, CDCl ₃ ) δ -110.48 – -120.36 (m, 1F). m. p. (DSC): 70.6 °C 1H NMR (500 MHz, CDCl ₃ ) δ 7.74 (dd, J = 8.0, 1.5 Hz, 1H), 7.55 (ddd, J = 8.5, 7.2, 1.5 Hz, 1H), 7.34 (dd, J = 8.4, 1.2 Hz, 1H), 7.28 (ddd, J = 8.4, 7.3, 1.2 Hz, 1H), 6.15 (s, 1H), 6.11 (dt, J = 1.9, 0.9 Hz, 1H), 5.57 (t, J = 1.6 Hz, 1H), 4.27 – 4.15 (m, 2H), 3.08 (t, J = 6.8 Hz, 2H), 1.98 – 1.86 (m, 7H). m. p. (DSC): 91.5 °C 1H NMR (500 MHz, CDCl ₃ ) δ 7.71 (d, J = 2.4 Hz, 1H), 7.49 (dd, J = 8.8, 2.4 Hz, 1H), 7.27 (d, J = 8.8 Hz, 1H), 6.16 (s, 1H), 6.10 (dq, J = 2.0, 1.0 Hz, 1H), 5.64 – 5.44 (m, 1H), 4.16 (t, J = 6.5 Hz, 2H), 3.03 (t, J = 7.3 Hz, 2H), 1.95 (dd, J = 1.6, 1.0 Hz, 3H), 1.83 (p, J = 7.3 Hz, 2H), 1.72 (dq, J = 7.8, 6.6 Hz, 2H), 1.60 – 1.51 (m, 2H), 1.47 (dddd, J = 14.6, 9.1, 6.5, 3.4 Hz, 2H). m. p. (DSC): 87.8 °C Examples of application: Example 4 – General polymerization procedure to produce bulk copolymer For production of bulk polymer blanks, the monomers are melted under vacuum and additional components in respective amounts are added as indicated in table 3 below. Exemplarily for application example 4-1, a composition of 5-[(2-oxo-2H-chromen-4- yl)oxy]pentyl 2-methylprop-2-enoate (A-002) (0.096 g, 0.3 mmol, 40.6 mol%), iso-decyl methacrylate (0.096 g, 0.403 mmol, 54.8 mol%) and poly(ethylene glycol) diacrylate (M _n 250) (0.007 g, 0.027 mmol, 3.7 mol%) as crosslinker is well mixed under stirring using gentle heat and degassed by three freeze pump- thaw cycles. Appropriate amounts (0.02 – 0.12 equiv.) of a radical initiator (e. g.1,1'-(3,3,5-trimethylcyclohexylidene)bis[2-(1,1- dimethylethyl)-peroxide [Luperox® 231], 2-[(E)-2-(1-cyano-1-methylethyl)diazen-1-yl]-2- methylpropanenitrile) or tert-Butyl peroxide are added. The compositions shown in table 3 are manufactured in the same way as described for application example 4-1. A heating bath for the stirring is used, where necessary. Polymerization: Two glass plates are coated with a polyethylene terephthalate sheet and a 1 mm thick cell is created between the polyethylene terephthalate sheets using a silicone rubber gasket. The coated faces of the glass sheets are clipped together using spring clips with a syringe needle being placed between the gasket and the polyethylene terephthalate sheets. The cavity is then filled with the above manufactured compositions through the needle using a gastight syringe. Once the cavity is filled the syringe needle is removed, a final clip is used to seal the mould and the assembly is placed in an oven. The polymerization temperature is between 60 °C and 180 °C and the individual polymerization conditions are choosen for the respective initiators. The moulds are allowed to cool to room temperature before the polymer plate is removed from the mould. Refractive index change is induced by irradiation at 275-340 nm. The refractive indices (n) of the polymer films and blanks at 589 nm are measured on Schmidt+Haensch ATR-L before and after irradiation. The refractive index n _D , _{35 °C} is measured before irradiation. The difference of refractive indices before and after irradiation is Δn. The following table shows the refractive indices n _{D, 35 °C} as well as the change in refractive index after irradiation (Δn). The phase transition temperatures are determined with a TA Instruments Q2000 differential scanning calorimeter during heating in the second heating run with 20 K/min from -100 °C to 200 °C in a hermetic aluminum pans. Ref-[1] and Ref-[2] are examples of monomers embraced by the general disclosure of WO17032443 A1 and exemplified in EP3337793.

Table 3: Compositions – Amount of components is given in mol-%, the amount of the respective chosen radical initiator adds to 100 mol%:

n-BuAc = n-butylacrylate; EGDMA = ethylene glycol dimethacrylate; HEMA = 2- hydroxyethyl methacrylate; EtMAc = ethyl methacrylate. a polyethyleneglycol dimethacrylate (M _n 750) is used instead of EGDMA. b 8-methylnonyl methacrylate is used instead of n-butylacrylate. c polyethyleneglycol diacrylate (M _n 250) is used instead of EGDMA. e methyl methacrylate is used instead of EtMAc. f n-butyl methacrylate is used instead of EtMAc. g triethyleneglycol dimethacrylate (M _n 286) is used instead of EGDMA. h 4-hydroxybutyl acrylate is used instead of HEMA. i 2-(4-benzoyl-3-hydroxyphenoxy)ethyl acrylate is used instead of ethylmethacrylate. J methyl methacrylate is used instead of ethyl methacrylate. Table 4: Polymer properties (refractive index n _{D, 35 °C} and Abbe number ν ₀ ) and refractive index change after irradiation

The results of the application examples 4-1 to 4-45 show a significant refractive index change after irradiation and high Abbe numbers. The refractive index change versus Abbe numbers of the application examples 4-1 to 4-45 compared to application examples for prior art reference compounds Ref-[1] and Ref-[2] is visualized in Figure 1. Figure 1 clearly shows the advantage of the described polymers over prior art references.