Liquid-crystal Medium

The present invention relates to a liquid-crystal medium, to components for high-frequency technology comprising said medium, especially microwave components for high-frequency devices, such as devices for shifting the phase of microwaves, tunable filters, tunable metamaterial structures and electronic beam steering antennas (e.g. phased array antennas.

Liquid-crystalline media have been used for many years in electro-optical displays (liquid crystal displays: LCDs) in order to display information. More recently, liquid-crystalline media have also been proposed for use in components for microwave technology, such as, for example, in

DE 10 2004 029 429 A and in JP 2005-120208 (A).

DE 10 2004 029 429 A describes the use of liquid-crystal media in micro- wave technology, inter alia in phase shifters. Therein, liquid-crystalline

20

media with respect to their properties in the corresponding frequency range have been discussed and liquid-crystalline media based on mixtures of mostly aromatic nitriles and isothiocyanates have been shown.

Isothiocyanates derived from thieno[3,2-b]thiophene are proposed for the

25 use in liquid-crystal light modulators in CN 106518890 A. In

EP 2 982 730 A1 , LC mixtures are shown that consist of isothiocyanate compounds. However, these compositions are all still afflicted with several disadvantages as for example high dielectric loss or inadequate phase go shift or inadequate material quality, resulting in limited performance in devices operating in the microwave regime. Further it is required to improve these media with respect to their general physical properties, such as, the clearing point, the phase range, especially their storage stability at low temperatures, and their viscosities, in particular their 35

rotational viscosity. There is still a demand for devices for high frequency-technology comprising LC media with improved performance.

For these applications, liquid-crystalline media having particular, hitherto 5

rather unusual and uncommon properties or combinations of properties are required. One aspect of the present invention is to provide LC media with properties that enable improved devices for microwave technology. It has been recognised that the dielectric loss in the microwave region can 10 be reduced and the material quality (h, also known as“figure of merit” (FoM) i.e., a high tunability and a low dielectric loss) can be improved. Besides these requirements the focus must increasingly be directed to improved response times especially for those devices using planar -1 ₅ structures such as e.g. phase shifters and leaky antennas.

In addition, it has been recognised that an improvement in the low- temperature behaviour of the components results in an improvement in the operating properties at low temperatures and also in the shelf life.

²⁰ Especially upon cooling, the formation of smectic phases or crystallisation is undesired and may even lead to the destruction of a device. The existence of a nematic phase without formation of smectic phases or crystallisation at low temperatures and over a period of time sufficient for 25 the operation of a device is referred to as low temperature stability (LTS).

Therefore, there is a considerable demand for liquid-crystalline media hav ing suitable properties for corresponding practical applications.

30

Surprisingly, it has been found that it is possible to achieve components for high-frequency technology with improved performance by using liquid- crystalline media that comprise a thienothiophene derivative of formula S below. The present invention relates to a liquid crystal medium for use in a component operable in the microwave region of the electromagnetic spectrum, characterised in that the medium comprises one, two or more compounds of formula S

in which

R ^s denotes H, alkyl or alkoxy having 1 to 12 C atoms, or alkenyl, alkenyloxy or alkoxyalkyl having 2 to 12 C atoms, in which one or more CFte-groups may be

more H atoms may be replaced by F,

on each occurrence, independently of one another,

denote

in which R ^L , on each occurrence identically or differently, denotes H, Cl or straight chain, branched or cyclic alkyl having 1 to 6 C atoms,

L ^S1 , L ^S2 identically or differently, denote H, Cl or F,

R ^S1 , R ^S2 , identically or differently, denote H, alkyl or alkenyl,

having up to 6 C atoms, or cyclopropyl, cyclobutyl, cyclopentenyl, or cyclopentyl,

R™, R ^Th2 identically or differently, denote H, alkyl or alkenyl or alkoxy, having up to 6 C atoms, or cyclopropyl, cyclobutyl, cyclopentenyl or cyclopentyl,

Z ^S1 , Z ^S2 , Z ^S3 identically or differently, denote -CH=CH-, -CH=CF-,

-CF=CFI-, -CF=CF-, -CºC-, or a single bond, a, b identically or differently, are 0 or 1 , and optionally, one or more compounds of formula IC IC

in which

R ¹ denotes H, alkyl or alkoxy having 1 to 15 C atoms, or alkenyl, alkenyloxy or alkoxyalkyl having 2 to 15 C atoms, in which one or more CH2-groups may be

, on each occurrence, independently of one another, denote

in which R ^L , on each occurrence identically or differently, denotes H, Cl or straight chain, branched or cyclic alkyl having 1 to 6 C atoms.

A first aspect of the present invention relates to LC media comprising a compound of formula S and a compound of formula IC. The present invention further relates to a compound of formula S as defined above, with the proviso that the compounds of formula S ^* are excluded:

in which

R ^s denotes alkyl, alkenyl or alkoxy having up to 9 C atoms,

Z ^S2 denotes -CH=CH-, -CH=CF-, -CF=CH-, -CF=CF-, -CºC-, or a single bond,

R ^S1 , R ^S2 identically or differently, denote H or F, and

L ^S1 , L ^S2 identically or differently, denote H or F.

Another aspect of the present invention relates to liquid crystal media comprising one or more compounds of formula S wherein compounds of formula S ^* defined above are excluded.

The present invention further relates to a component operable in the microwave region of the electromagnetic spectrum comprising the liquid crystal medium according to the invention.

Components for high frequency technology that make use of a liquid- crystalline medium as a switchable dielectric which comprises one or more compounds of formula S are distinguished by fast switching times, a broad operating temperature range, high tunability and low dielectric loss. A further object of the present invention are devices for microwave technology comprising said components.

Preferred components are phase shifters, varactors, wireless and radio wave antenna arrays, matching circuits, adaptive filters and others.

The media according to the present invention are distinguished by a particularly high birefringence, furthermore a high clearing temperature, excellent low-temperature stability and broad nematic phase range. As a result, devices according to the invention containing the media are operable under extreme temperature conditions. The media are further distinguished by high values of the dielectric anisotropy and a low rotational viscosities. As a result, the threshold voltage, i.e. the minimum voltage at which a device is switchable, is very low. A low operating voltage and low threshold voltage is desired in order to enable a device having improved switching characteristics and high energy efficiency. Low rotational viscosities enable fast switching of the devices according to the invention.

The media according to the present invention are distinguished by low dielectric loss and high tunability, resulting in a high material quality (h).

The compounds of formula S are distinguished by an advantageously high birefringence, high solubility in liquid crystalline media, high tunability and low dielectric loss.

These properties as a whole make the media particularly suitable for use in components and devices for high-frequency technology and

applications in the microwave range, in particular devices for shifting the phase of microwaves, tunable filters, tunable metamaterial structures, and electronic beam steering antennas (e.g. phased array antennas). Herein, halogen is F, Cl, Br or I, preferably F or Cl, particularly preferably F.

Herein, an alkyl radical and/or an alkoxy radical, can be straight-chain or branched. It is preferably straight-chain, has 2, 3, 4, 5, 6 or 7 carbon atoms and accordingly is preferably ethyl, propyl, butyl, pentyl, hexyl, heptyl, ethoxy, propoxy, butoxy, pentoxy, hexoxy or heptoxy, furthermore methyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, methoxy, octoxy, nonoxy, decoxy, undecoxy, dodecoxy, tridecoxy or tetradecoxy. Branched alkyl is preferably isopropyl, isobutyl, sec.-butyl, tert.-butyl, 2,2-dimethylpropyl, 3-methylbutyl, 1 -methylbutyl, 1 - ethylpropyl, 1 ,2-dimethylpropy, 2-methylbutyl. Cyclic alkyl is preferably cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl, all of which can be substituted by one or more, preferably one, alkyl group, preferably by methyl or ethyl.

Herein, an alkenyl radical may have from 2 to 15 carbon atoms, which may be straight-chain or branched. It is preferably straight-chain and has from 2 to 7 carbon atoms. Accordingly, it is preferably vinyl, prop-1 - or -2-enyl, but-1 -, -2- or -3-enyl, pent-1 -, -2-, -3- or -4-enyl, hex-1 -, -2-, -3-, -4- or -5- enyl, or hept-1 -, -2-, -3-, -4-, -5- or -6-enyl.

Herein, oxaalkyl is preferably straight-chain 2-oxapropyl (=

methoxymethyl), 2-oxabutyl (= ethoxymethyl) or 3-oxabutyl (=

methoxyethyl), 2-, 3- or 4-oxapentyl, 2-, 3-, 4- or 5-oxahexyl, or 2-, 3-, 4-,

5- or 6-oxaheptyl.

Herein, in an alkyl radical having from 1 to 15 carbon atoms in which one CH2 group has been replaced by -O- and one has been replaced by -CO-, these are preferably adjacent. This thus contains an acyloxy group -CO-O- or an oxycarbonyl group -0-CO-. This is preferably straight-chain and has from 2 to 6 carbon atoms.

Herein, alkyl radical having from 1 to 15 carbon atoms in which one CH2 group has been replaced by unsubstituted or substituted -CH=CH- and an adjacent CH2 group has been replaced by CO or CO-O or O-CO, where this may be straight-chain or branched is preferably straight-chain and has from 4 to 13 carbon atoms.

Herein, an alkyl radical having from 1 to 15 carbon atoms or an alkenyl radical having from 2 to 15 carbon atoms, each of which is at least monosubstituted by halogen (F, Cl, Br, I) are preferably straight-chain and halogen is preferably -F or -Cl. In the case of polysubstitution, halogen is preferably -F. The resultant radicals also include perfluorinated radicals, such as -CF3. In the case of monosubstitution, the fluorine or chlorine substituent can be in any desired position.

Herein, an alkyl or alkoxy radical having 1 to 15 C atoms, preferably 1 to 5, particularly preferably 1 , where one or more CH2 groups, preferably one, in these radicals may each be replaced, independently of one another, by or is preferably cyclopropyl, cyclobutyl, cyclopentyl or cyclopent-1 -enyl, or cyclopropylmethyl.

In case R ^F denotes a halogenated, preferably fluorinated alkyl-, alkoxy-, alkenyl or alkenyloxy it can be branched or unbranched. Preferably it is unbranched and has 1 , 2, 3, 4, 5, 6 or 7 C atoms, in case of alkenyl 2, 3, 4, 5, 6 or 7 C atoms. It can be partially fluorinated or perfluorinated, preferably perfluorinated. R ^T preferably denotes CN, NCS, Cl, F, -(CH )n-CH=CF2, -(CH ₂ ) _n -CH=CHF, -(CH ₂ ) _n -CH=CI ₂ , -CnF _2n+i , -(CF ₂ ) _n -CF ₂ H, -(CH ₂ ) _n -CF ₃ , -(CH ₂ ) _n - CHF ₂ , -(CH ₂ ) _n CH ₂ F, -CH=CF ₂ , -0(CH ₂ ) _n -CH=CF ₂ , -0(CH ₂ ) _n CHCI ₂ , - OCnF _2n+i , -0(CF ₂ ) _n -CF ₂ H, -0(CH ₂ ) _n CF ₃ , -0(CH ₂ ) _n -CHF ₂ , -0(CF) _n CH ₂ F, - OCF=CF ₂ , -SCnF _2n+i , -S(CF) _n -CF ₃ , wherein n is an integer from 0 to 7.

Preferably, the compounds of formula S are selected from the group of compounds of the formulae S-1 to S-24:



 in which R ^S3 denotes F or has the meaning of R ^L defined above and the other occurring groups have the meanings given above for formula S and preferably R ^s denotes alkyl or alkenyl having 2 to 6 C atoms, in which one or more CFte-groups may be replaced by

R™ and

R ^Th2 identically or differently, denote FI or alkyl having 1 to 6 C atoms, preferably FI,

R ^S3 denotes H, F or alkyl, having up to 6 C atoms, or cyclopropyl, preferably H, F or ethyl, very preferably H, L ^S1 and L ^S2 identically or differently, denote FI or F, preferably F.

The compounds of the general formula S are prepared by methods known per se, as described in the literature (for example in the standard works, such as Flouben-Weyl, Methoden der organischen Chemie [Methods of

Organic Chemistry], Georg-Thieme-Verlag, Stuttgart), to be precise under reaction conditions which are known and are suitable for the said reactions. Use can be made here of variants which are known per se, but are not mentioned here in greater detail.

The compounds of formula S are prepared for example according to or in analogy to the procedures described in CN 106518890 A. A general approach towards this class of compound is also given in

EP 0144013 A, further examples of thienothiophene derived mesogenic compounds are described in KR20160001773 A. If desired, the starting materials can also be formed in situ by not isolating them from the reaction mixture, but instead immediately converting them further into the compounds of the general formula S.

Preferred synthetic pathways towards compounds according to the invention are shown in the schemes below and are further illustrated by means of the working examples. The syntheses can be adapted to the particular desired compounds of the general formula S by choice of suitable starting materials.

Versatile building blocks are compounds 1 , 2, 3 and 4 shown below, which can be prepared as described in Weihua Tang et al., J. Mater. Chem., 2010, 20, 1497-1505; KR20100092592 (A), JP 2012167068 A and

WO 2011/1 19870 A1 , and in which R has the meanings given above for R ^s and may also denote alkylcyclohexyl or alkylcyclohexenyl and R‘ denotes H or SiMe3 or an equivalent protecting group known in the art.

According to CN 106518890 A, the compounds of formula 1 can be used for the preparation of compounds of formula S1 by Suzuki cross coupling, and the compounds of formula 3 have been used for the preparation of compounds of formula S2 by Sonogashira coupling, with suitably substituted 4-bromo or iodoanilines. Similarly, by using a cyclic alkyl radical R, e.g. alkylcyclohexyl, the compounds of formulae S10 and S1 1 , respectively, can be made using the same chemistry. Likewise, by using p- aminobiphenyl bromides and iodides such as e.g. compounds of the following formula

where Y is H or F, known from EP 1 126006 A2, it is possible to synthesise compounds for example of formulae S4, S8 and S9. Likewise, from alkynes such as

described in Arakawa, Yuki et al., RSC Advances (2016), 6(95), 92845- 92851 , compounds of the type S6 are prepared.

The building block 4 shown above enables the synthesis of aryl- substituted compounds of formulae S5 and S7, exemplified by the synthesis shown in the following scheme, by for example first reacting the position carrying the bromine atom to give intermediate 5, where R’ is optionally a protecting group, followed by a Sonogashira coupling:

The starting materials for the synthesis of compounds with a -CF=CF- bridge are commercially available or can be synthesised according to known procedures. Preferably, these compounds are synthesised analogously to the procedures disclosed in WO 2012/069133 A1 and WO 2018/077765 A1.

The compounds of formula S according to the present invention are preferably prepared from the precursors of formula SP below,

in which the groups and parameters have the meanings defined above for formula S. The invention relates to a compound of formula SP with the proviso that if a and b are both 0, Z ^S2 denotes -CH=CH-, -CH=CF-, -CF=CH-, or -CF=CF-.

The invention further relates to a process for the preparation of a compound of formula S by reaction of a compound of formula SP with a reagent selected from the group of thiophosgene, thiocarbonyldiimidazol, carbon disulfide, carbonochloridothioic acid-O-phenyl ester, N,N,N',N'- tetramethyl-thioperoxydicarbonic diamide, carbonothioic acid-O, O-di-2- pyridinyl ester, chloro ethyl formate, 1 ,1 '-carbonothioylbis-2(1 H)- pyridinone, and the like; for a review cf. Braverman, S.; Cherkinsky, M.; Birsa, M. L, Science of Synthesis, (2005) 18, 190.

The compounds of formula IC are preferably selected from the group of the compounds of the formulae ICa to ICd , particularly preferably of formula ICb:

in which R ¹ has the meaning indicated above for formula I and preferably denotes alkyl having 1 to 7 C atoms or alkenyl having 2 to 7 C atoms.

In a preferred embodiment of the present invention the medium comprises one or more compounds selected from the group of compounds of formulae I, II and III,

in which

denotes H, alkyl or alkoxy having 1 to 15, preferably 3 to 10 C atoms, or alkenyl, alkenyloxy or alkoxyalkyl having 2 to 15, preferably 3 to 10, C atoms, in which one or more CH2-

preferably alkyl or alkenyl, n is 0, 1 or 2, to on each occurrence, independently of one another, denote in which R ^L , on each occurrence, identically or differently, denotes H or alkyl having 1 to 6 C atoms, preferably H, methyl or ethyl, particularly preferably H, and wherein

and in case n = 2, alternatively denotes and preferably one denotes and the other denotes independently of one another, denote

denotes R ² denotes H, alkyl or alkoxy having 1 to 15, preferably 3 to 10 C atoms, or alkenyl, alkenyloxy or alkoxyalkyl hav ing 2 to 15, preferably 3 to 10, C atoms, in which one or

preferably alkyl or alkenyl,

_Z 21 denotes trans- CH=CH-, frans-CF=CF- or -C=C-,

preferably -CºC- or trans-C FI =C H -, and independently of one another, denote

in which R ^L , on each occurrence, identically or differently, denotes H or alkyl having 1 to 6 C atoms, preferably H, methyl or ethyl, particularly preferably H, and wherein preferably independently of one another, denote

more preferably

Ft ³ denotes H, alkyl or alkoxy having 1 to 1 5, preferably 3 to 10 C atoms, or alkenyl, alkenyloxy or alkoxyalkyl hav ing 2 to 1 5, preferably 3 to 1 0, C atoms, in which one or more CFte-groups may be replaced by

preferably alkyl or alkenyl, one of Z ³¹ and Z ³² , preferably Z ³² , denotes trans- CH=CH-, frans-CF=CF- or -CºC- and the other one, independently thereof, denotes -CºC-, trans- CH=CH-, frans-CF=CF- or a single bond, preferably one of them, preferably Z ³² denotes -CºC- or frans-CH=CH- and the other denotes a single bond, and independently of one another, denote

in which R ^L , on each occurrence, identically or differently, denotes H or alkyl having 1 to 6 C atoms, preferably H, methyl or ethyl, particularly preferably H, and wherein

independently of one another, denote

more preferably

In the compounds of formulae I, II and III R ^L preferably denotes H.

In another preferred embodiment, in the compounds of formulae I, II and III, one or two groups R ^L , preferably one group R ^L is different from H.

In a preferred embodiment of the present invention, the compounds of formula I are selected from the group of compounds of the formulae 1-1 to I-4:

in which

L ¹ , L ² and L ³ on each occurrence, identically or differently, denote H or F, and the other groups have the respective meanings indicated above for formula I and preferably

R ¹ denotes alkyl having 1 to 7 C atoms or alkenyl having 2 to 7

C atoms.

The media preferably comprise one or more compounds of formula 1-1 , which are preferably selected from the group of the compounds of the formulae 1-1 a to 1-1 f, preferably of formula 1-1 b or 1-1 f:

in which R ¹ has the meaning indicated above for formula I and preferably denotes alkyl having 1 to 7 C atoms or alkenyl having 2 to 7 C atoms.

The media preferably comprise one or more compounds of formula I-2, which are preferably selected from the group of the compounds of the formulae l-2a to l-2e, preferably of formula l-2c:

in which R ¹ has the meaning indicated above for formula I and preferably denotes alkyl having 1 to 7 C atoms or alkenyl having 2 to 7 C atoms.

The media preferably comprise one or more compounds of formula I-3, which are preferably selected from the group of the compounds of the formulae l-3a to l-3d, particularly preferably of formula l-3b:

in which R ¹ has the meaning indicated above for formula I and preferably denotes alkyl having 1 to 7 C atoms or alkenyl having 2 to 7 C atoms. The media preferably comprise one or more compounds of formula I-4, which are preferably selected from the group of the compounds of the formulae l-4a to l-4d, particularly preferably of formula l-4b: in which R ¹ has the meaning indicated above for formula I and preferably denotes alkyl having 1 to 7 C atoms or alkenyl having 2 to 7 C atoms.

The media preferably comprise one or more compounds of formula II, which are preferably selected from the group of the compounds of the formulae 11-1 to II-3, preferably selected from the group of the compounds of the formulae 11-1 and II-2:

in which the parameters have the meanings given under formula II above and preferably

R ² denotes H, alkyl or alkoxy having 1 to 7 C atoms or alkenyl having 2 to 7 C atoms, and one of

and the other, independently denotes

preferably and preferably

R ² denotes Cnhten+i or CH2=CH-(CH2)z, and n denotes an integer in the range from 0 to 15, preferably in the range from 1 to 7 and particularly preferably 1 to 5, and z denotes 0, 1 , 2, 3 or 4, preferably 0 or 2.

The compounds of formula 11-1 are preferably selected from the group of the compounds of the formulae 11-1 a to 11-1 e:

R ² has the meaning indicated above and preferably denotes Cnhten+i or CH2=CH-(CH2)z, and n independently of one another, denote an integer in the range from 0 to 1 5, preferably in the range from 1 to 7 and particularly preferably 1 to 5, and z denotes 0, 1 , 2, 3 or 4, preferably 0 or 2.

The compounds of formula II-2 are preferably selected from the group of the compounds of the formulae ll-2a and ll-2b:

in which R ² has the meaning indicated above and preferably denotes Cnhten+i or CH2=CH-(CH2)z, n denotes an integer in the range from 0 to 15, preferably in the range from 1 to 7 and particularly preferably 1 to 5, and z denotes 0, 1 , 2, 3 or 4, preferably 0 or 2.

The compounds of formula II-3 are preferably selected from the group of the compounds of the of formulae ll-3a to ll-3d:

in which

R ² has the meaning indicated above and preferably

denotes Cnhten+i or CH2=CH-(CH2)z, n denotes an integer in the range from 0 to 15, preferably in the range from 1 to 7 and particularly preferably 1 to 5, and z denotes 0, 1 , 2, 3 or 4, preferably 0 or 2.

The compounds of formula III are preferably selected from the group of the compounds of the formulae III-1 to III-6, more preferably of the formulae selected from the group of the compounds of the formulae MI-1 , MI-2, MI-3 and MI-4, and particularly preferably of formula MI-1 :

MI-4 A ³¹ )— ( A ³² ) - Z ³² -( A ³³ )— NCS

MI-5

R ³ _( _A ³¹ >— _Z ³ A ³² )— ( A ³³ )— NCS

in which

Z ³¹ and Z ³² independently of one another denote frans-CH=CH- or trans- CF=CF-, preferably trans- CH=CH-, and in formula III-6 alternatively one of Z ³¹ and Z ³² may denote -CºC- and the other parameters have the meaning given above under formula III, and preferably

Ft ³ denotes H, alkyl or alkoxy having 1 to 7 C atoms or alkenyl having 2 to 7 C atoms, and one of

and the others, independently of one another, denote more preferably and preferably

R ³ denotes Cnhten+i or CH2=CH-(CH2)z, n denotes an integer in the range from 0 to 15, preferably in the range from 1 to 7 and particularly preferably 1 to 5, and z denotes 0, 1 , 2, 3 or 4, preferably 0 or 2.

The compounds of formula III-1 are preferably selected from the group of the compounds of the formulae III-1 a to MI-1 e, more preferably selected from the group of the compounds of the formulae III-1 a and III-1 b, particularly preferably of formula MI-1 b,:

R ³ has the meaning indicated above and preferably

denotes Cnhten+i or CH2=CH-(CH2)z, n denotes an integer in the range from 0 to 15, preferably in the range from 1 to 7 and particularly preferably 1 to 5, and z denotes 0, 1 , 2, 3 or 4, preferably 0 or 2.

The compounds of formula III-2 are preferably compounds of formula lll-2a to III- 2h, very preferably lll-2b and/or lll-2h:

in which

R ³ has the meaning indicated above and preferably denotes

CnH _2n+i or CH ₂ =CH-(CH ₂ )Z, n denotes an integer in the range from 0 to 15, preferably in the range from 1 to 7 and particularly preferably 1 to 5, and z denotes 0, 1 , 2, 3 or 4, preferably 0 or 2.

The compounds of formula III-5 are preferably selected from the compounds of formula lll-5a:

R ³ has the meaning indicated above for formula III-5 and preferably denotes Cnhten+i , in which n denotes an integer in the range from 0 to 7, preferably in the range from 1 to 5.

In a preferred embodiment, the media according to the invention comprise one or more compounds selected from the group of compounds of the formulae IIA-1 -1 to IIA-1 -12, very preferably IIA-1 -1 or llA-1 -2:

in which

R ¹ denotes alkyl or alkenyl having up to 7 C atoms, preferably ethyl, n-propyl, n-butyl or n-pentyl, n-hexyl,

R ^L on each occurrence, the same or differently, denotes alkyl or alkenyl having 1 to 5 C atoms, or cycloalkyl or cycloalkenyl each having 3 to 6 C atoms,

preferably methyl, ethyl, n-propyl, n-butyl, isopropyl, cyclopropyl, cyclobutyl, cyclopentyl or cyclopent-1 -enyl, very preferably ethyl.

In a preferred embodiment, the medium according to the present invention comprises one or more compounds of formula MIC in which

R ^c denotes H, alkyl or alkoxy having 1 to 1 2 C atoms, or alkenyl, alkenyloxy or alkoxyalkyl having 2 to 1 2 C atoms, in which one or more CFte-groups may be replaced by

L ^C1 , L ^C2 identically or differently, denote H, Cl or F,

R ^C1 , R ^C2 identically or differently, denote H or alkyl having 1 to 6 C atoms, or cyclopropyl, cyclobutyl or cyclopentyl,

R ^C3 , R ^C4 ,

R ^C5 and R ^C6 identically or differently, denote H, Cl, F or alkyl having 1 to

6 C atoms, or cyclopropyl, cyclobutyl or cyclopentyl.

Preferably, the compounds of formula C are selected from the group of compounds of the formulae IIIC-1 to IIIC-1 2

R ^c has one of the meanings indicated above for formula C and preferably denotes alkyl or alkenyl having 2 to 6 C atoms, in which one or more CH2-groups may be replaced by or

In a preferred embodiment, the medium according to the invention comprises one or more compounds of formula T

T

in which

R ^T denotes halogen, CN, NCS, R ^F , R ^F -0- or R ^F -S-, wherein R ^F denotes fluorinated alkyl or fluorinated alkenyl having up to 12 C atoms,

on each occurrence, independently of one another, denote

L ¹ and L ² identically or differently, denote Cl, F, alkyl having 1 to 6 C atoms or cyclopropyl, cyclobutyl or cyclopentyl, preferably F, and t is 0, 1 or 2, preferably 1. Preferably, the one or more compounds of formula T are selected from the group of compounds of the formulae T-1 and T-2,

in which have the meanings given above for formula T, and n is 1 , 2, 3, 4, 5 ,6 or 7, preferably 1 , 2, 3 or 4, particularly preferably 1 .

In a particularly preferred embodiment of the present invention the media comprise one or more compounds of formula T-1 .

Preferred compounds of formula T-1 are selected from the group of compounds of the following sub-formulae:

in which n is 1 , 2, 3 or 4, preferably 1.

In another particularly preferred embodiment of the present invention the media comprise one or more compounds of formula T-2.

Preferred compounds of formula T-2 are selected from the group of compounds of the following sub-formulae:

in which n is 1 , 2, 3 or 4, preferably 1.

Additionally, the liquid-crystalline media according to the present invention in a certain embodiment, which may be the same or different from the previous preferred embodiments preferably comprise one or more compounds of formula IV,

particularly preferably

L ⁴ denotes alkyl having 1 to 6 C atoms, cycloalkyl having 3 to 6 C atoms or cycloalkenyl having 4 to 6 C atoms, preferably CH ₃ , C2H5, n-C ₃ H ₇ (-(CH ₂ ) ₂ CH ₃ ), /-C ₃ H ₇ (-CFI(CFI ₃ ) ₂ ), cyclopropyl, cyclobutyl, cyclohexyl, cyclopent-1 -enyl or cyclohex-1 -enyl, and particularly preferably CFI ₃ , C ₂ Fl5, cyclopropyl or cyclobutyl,

X ⁴ denotes H, alkyl having 1 to 3 C atoms or halogen, preferably H, F or Cl, and particularly preferably H or F and very particularly preferably F,

R ⁴¹ to R ⁴⁴ , independently of one another, denote alkyl or alkoxy, each having 1 to 1 5 C atoms, alkenyl, alkenyloxy or alkoxyalkyl, each having 2 to 15 C atoms, or cycloalkyl, alkylcycloalkyl, cycloalkenyl, alkylcycloalkenyl, alkylcycloalkylalkyl or alkylcycloalkenylalkyl, each having up to 1 5 C atoms, and alternatively one of R ⁴³ and R ⁴⁴ or both also denote H, preferably

R ⁴¹ and R ⁴² , independently of one another, denote alkyl or alkoxy, each having 1 to 7 C atoms, or alkenyl, alkenyloxy or alkoxyalkyl, each having 2 to 7 C atoms, particularly preferably

R ⁴¹ denotes alkyl having 1 to 7 C atoms or alkenyl,

alkenyloxy or alkoxyalkyl, each having 2 to 7 C atoms, and particularly preferably

R ⁴² denotes alkyl or alkoxy, each having 1 to 7 C atoms, and preferably

R ⁴³ and R ⁴⁴ denote H, alkyl having 1 to 5 C atoms, cycloalkyl or cycloalkenyl having 3 to 7 C atoms, alkylcyclohexyl or cyclohexylalkyl, each having 4 to 1 2 C atoms, or alkylcyclohexylalkyl having 5 to 1 5 C atoms, particularly preferably cyclopropyl, cyclobutyl or cyclohexyl, and very particularly preferably at least one of R ⁴³ and R ⁴⁴ denotes n-alkyl, particularly preferably methyl, ethyl or n-propyl, and the other denotes H or n-alkyl, particularly preferably H, methyl, ethyl or n-propyl.

In a preferred embodiment of the present application, the liquid-crystal medium additionally comprises one or more compounds selected from the group of compounds of the formulae V, VI, VII, VIII and IX:

in which

L ⁵¹ denotes R ⁵¹ or X ⁵¹ ,

L ⁵² denotes R ⁵² or X ⁵² ,

R ⁵¹ and R ⁵² , independently of one another, denote H, alkyl or alkoxy having 1 to 15, preferably 3 to 10, C atoms or alkenyl, alkenyloxy or alkoxyalkyl having 2 to 1 5, preferably 3 to 1 0, C atoms, preferably alkyl or alkenyl,

X ⁵¹ and X ⁵² , independently of one another, denote H, F, Cl, -CN,

SFs, fluorinated alkyl or fluorinated alkoxy having 1 to 7 C atoms or fluorinated alkenyl, fluorinated alkenyloxy or fluorinated alkoxyalkyl having 2 to 7 C atoms, preferably fluorinated alkoxy, fluorinated alkenyloxy, F or Cl, and independently of one another, denote

l_61 denotes R ⁶¹ and, in the case where Z ⁶¹ and/or Z ⁶² denote frans-CH=CH- or trans- CF=CF-, alternatively also denotes X ⁶¹ ,

L ⁶² denotes R ⁶² and, in the case where Z ⁶¹ and/or Z ⁶² denote frans-CH=CH- or frans-CF=CF-, alternatively also denotes X ⁶² , R ⁶¹ and R ⁶² , independently of one another, denote H, alkyl or alkoxy having 1 to 15, preferably 3 to 10, C atoms or alkenyl, alkenyloxy or alkoxyalkyl having 2 to 1 5, preferably 3 to 1 0, C atoms, preferably alkyl or alkenyl,

X ⁶¹ and X ⁶² , independently of one another, denote F or Cl, -CN, SFs, fluorinated alkyl or alkoxy having 1 to 7 C atoms or fluorinated alkenyl, alkenyloxy or alkoxyalkyl having 2 to 7 C atoms, one of

Z ⁶¹ and Z ⁶² denotes trans- CFI=CFI-, frans-CF=CF- or -CºC- and the other, independently thereof, denotes trans- CFI=CFI-, frans-CF=CF- or a single bond, preferably one of them denotes -CºC- or trans- CFI=CFI- and the other denotes a single bond, and

preferably and

x denotes 0 or 1 ,

L ⁷¹ denotes R ⁷¹ or X ⁷¹ ,

L ⁷² denotes R ⁷² or X ⁷² ,

R ⁷¹ and R ⁷² , independently of one another, denote H, alkyl or alkoxy having 1 to 15, preferably 3 to 10, C atoms or alkenyl, alkenyloxy or alkoxyalkyl having 2 to 1 5, preferably 3 to 1 0, C atoms, preferably alkyl or alkenyl,

X ⁷¹ and X ⁷² , independently of one another, denote H, F, Cl, - CN, -NCS, -SFs, fluorinated alkyl or fluorinated alkoxy having 1 to 7 C atoms or fluorinated alkenyl, or fluorinated alkenyloxy or fluorinated alkoxyalkyl having 2 to 7 C atoms, preferably fluorinated alkoxy, fluorinated alkenyloxy, F or Cl, and

Z ⁷¹ to Z ⁷³ , independently of one another, denote trans- CFI=CFI-, trans- CF=CF-, -CºC- or a single bond, preferably one or more of them denote a single bond, particularly preferably all denote a single bond and to independently of one another, denote

R ⁸¹ and R ⁸² , independently of one another, denote H, alkyl or alkoxy having 1 to 15, preferably 3 to 10, C atoms or alkenyl, alkenyloxy or alkoxyalkyl having 2 to 1 5, preferably 3 to 1 0, C atoms, preferably alkyl or alkenyl, one of

Z ⁸¹ and Z ⁸² denotes trans- CH=CH-, frans-CF=CF- or -CºC- and the other, independently thereof, denotes trans- CFI=CFI-, frans-CF=CF- or a single bond, preferably one of them denotes -C=C- or trans- CH=CH- and the other denotes a single bond, and

independently of one another, denote

l_91 denotes R ⁹¹ or X ⁹¹ ,

|_92 denotes R ⁹² or X ⁹² ,

R ⁹¹ and R ⁹² , independently of one another, denote H, alkyl or alkoxy having 1 to 15, preferably 3 to 10, C atoms or alkenyl, alkenyloxy or alkoxyalkyl having 2 to 1 5, preferably 3 to 1 0, C atoms, preferably alkyl or alkenyl,

X ⁹¹ and X ⁹² , independently of one another, denote H, F, Cl, - CN, -NCS, -SFs, fluorinated alkyl or fluorinated alkoxy having 1 to 7 C atoms or fluorinated alkenyl, or fluorinated alkenyloxy or fluorinated alkoxyalkyl having

2 to 7 C atoms, preferably fluorinated alkoxy, fluorinated alkenyloxy, F or Cl, and

Z ⁹¹ to Z ⁹³ , independently of one another, denote trans- CH=CH-, trans- CF=CF-, -CºC- or a single bond, preferably one or more of them denotes a single bond, and particularly preferably all denote a single bond,

independently of one another, denote

In a preferred embodiment of the present invention, the liquid-crystal medium comprises one or more compounds of the formula V, preferably selected from the group of the compounds of the formulae V-1 to V-3, preferably of the formulae V-1 and/or V-2 and/or V-3, preferably of the formulae V-1 and V-2:

in which the parameters have the respective meanings indicated above for formula V and preferably

R ⁵¹ denotes alkyl having 1 to 7 C atoms or alkenyl having 2 to 7 C atoms,

R52 denotes alkyl having 1 to 7 C atoms or alkenyl having 2 to 7 C atoms or alkoxy having 1 to 7 C atoms,

X ⁵¹ and X ⁵² , independently of one another, denote F,

Cl, -OCF3, -CF3, -CN or -SF5, preferably F, Cl, -OCF3 or -CN.

The compounds of the formula V-1 are preferably selected from the group of the compounds of the formulae V-1 a to V-1 d, preferably V-1 c and V-1 d :

in which the parameters have the respective meanings indicated above for formula V-1 and in which

Y ⁵¹ and Y ⁵² , in each case independently of one another, denote H or

F, and preferably

Ft ⁵¹ denotes alkyl or alkenyl, and

X51 denotes F, Cl or -OCF3.

The compounds of the formula V-2 are preferably selected from the group of the compounds of the formulae V-2a to V-2e and/or from the group of the compounds of the formulae V-2f and V-2g:

where in each case the compounds of the formula V- 2a are excluded from the compounds of the formulae V-2b and V- 2c, the compounds of the for mula V-2b are excluded from the compounds of the formula V- 2c and the compounds of the formula V- 2e are excluded from the compounds of the formula V-2f, and

in which the parameters have the respective meanings indicated above for formula V-1 and in which Y ⁵¹ and Y ⁵² , in each case independently of one another, denote H or F, and preferably

Y ⁵¹ and Y ⁵² denotes H and the other denotes H or F, preferably like wise denotes H.

The compounds of the formula V-3 are preferably compounds of the for mula V-3a:

in which the parameters have the respective meanings indicated above for formula V-1 and in which preferably

X51 denotes F, Cl, preferably F,

X ⁵² denotes F, Cl or -OCF3, preferably -OCF3.

The compounds of the formula V-1 a are preferably selected from the group of the compounds of the formulae V-1 a-1 and V-1 a-2:

in which R ⁵¹ has the meaning indicated above and preferably denotes Cnhten+i , in which n denotes an integer in the range from 0 to 7, preferably in the range from 1 to 5 and particularly preferably 3 or 7. The compounds of the formula V-1 b are preferably compounds of the for mula V-1 b-1 :

in which

R ⁵¹ has the meaning indicated above and preferably

denotes Cnhten+i , in which n denotes an integer in the range from 0 to 15, preferably in the range from 1 to 7 and particularly preferably 1 to 5.

The compounds of the formula V-1 c are preferably selected from the group of the compounds of the formulae V-1 c-1 to V-1 c-4, particularly preferably selected from the group of the compounds of the formulae V-1 c-1 and V-1 c-2: in which

R ⁵¹ has the meaning indicated above and preferably

denotes Cnhten+i , in which n denotes an integer in the range from 0 to 15, preferably in the range from 1 to 7 and particularly preferably 1 to 5.

The compounds of the formula V-1 d are preferably selected from the group of the compounds of the formulae V-1 d-1 and V-1 d-2, particularly preferably the compound of the formula V-1 d-2:

in which

R ⁵¹ has the meaning indicated above and preferably

denotes Cnhten+i , in which n denotes an integer in the range from 0 to 15, preferably in the range from 1 to 7 and particularly preferably 1 to 5.

The compounds of the formula V-2a are preferably selected from the group of the compounds of the formulae V-2a-1 and V-2a-2, particularly preferably the compounds of the formula V-2a-1 :

F

R 51 f/ XU/ XU/ % R 52 V-2a-1

V-2a-2 in which

R ⁵¹ has the meaning indicated above and preferably

denotes Cnhten+i or CH2=CH-(CH2)z, and

R52 has the meaning indicated above and preferably

denotes Cmhtem+i or O-Cmhtem+i or (CH2)z-CH=CH2, and in which n and m, independently of one another, denote an integer in the range from 0 to 1 5, preferably in the range from 1 to 7 and particularly preferably 1 to 5, and z denotes 0, 1 , 2, 3 or 4, preferably 0 or 2.

Preferred combinations of (R ⁵¹ and R ⁵² ), in particular in the case of formula

V-2a-1 , are (CnH2n _+i and CmH2m ₊ i), (CnH2n _+i and 0-CmH2m ₊ i), (CH2=CH-

(CH ₂ )Z and CmH2m+i), (CH2=CH-(CH2)z and O-Cmhtem+i) and (Cnhten+i and (CH2)Z-CH=CH ).

Preferred compounds of the formula V-2b are the compounds of the for mula V-2b-1 :

V-2b-1 in which

R ⁵¹ has the meaning indicated above and preferably

denotes Cnhten+i or CH2=CH-(CH2)z, and

R52 has the meaning indicated above and preferably

denotes Cmhtem+i or O-Cmhtem+i or (CH2)z-CH=CH2, and in which n and m, independently of one another, denote an integer in the range from 0 to 1 5, preferably in the range from 1 to 7 and particularly preferably 1 to 5, and z denotes 0, 1 , 2, 3 or 4, preferably 0 or 2.

The preferred combination of (R ⁵¹ and R ⁵² ) here is, in particular, (Cnhten+i and CmH2m+i).

Preferred compounds of the formula V- 2c are the compounds of the for mula V-2c-1 :

in which

R ⁵¹ has the meaning indicated above and preferably

denotes Cnhten+i or CH2=CH-(CH2)z, and R ⁵² has the meaning indicated above and preferably

denotes Cmhtem+i or O-Cmhtem+i or (CH2)z-CH=CH2, and in which n and m, independently of one another, denote an integer in the range from 0 to 15, preferably in the range from 1 to 7 and particularly preferably 1 to 5, and z denotes 0, 1 , 2, 3 or 4, preferably 0 or 2.

The preferred combination of ( R ⁵¹ and R ⁵² ) here is, in particular, (Cnhten+i and CmH2m+i).

Preferred compounds of the formula V-2d are the compounds of the for mula V-2d-1 : in which

R ⁵¹ has the meaning indicated above and preferably

denotes Cnhten+i or CH2=CH-(CH2)z, and

R ⁵² has the meaning indicated above and preferably

denotes Cmhtem+i or O-Cmhtem+i or (CH2)z-CH=CH2, and in which n and m, independently of one another, denote an integer in the range from 0 to 1 5, preferably in the range from 1 to 7 and particularly preferably 1 to 5, and z denotes 0, 1 , 2, 3 or 4, preferably 0 or 2.

The preferred combination of (R ⁵¹ and R ⁵² ) here is, in particular, (Cnhten+i and CmH2m+i).

Preferred compounds of the formula V- 2e are the compounds of the for mula V-2e-1 :

in which R ⁵¹ has the meaning indicated above and preferably denotes Cnhten+i or CH2=CH-(CH2)z, and

R ⁵² has the meaning indicated above and preferably

denotes Cmhtem+i or O-Cmhtem+i or (CH2)z-CH=CH2, and in which n and m, independently of one another, denote an integer in the range from 0 to 1 5, preferably in the range from 1 to 7 and particularly preferably 1 to 5, and z denotes 0, 1 , 2, 3 or 4, preferably 0 or 2.

The preferred combination of (R ⁵¹ and R ⁵² ) here is, in particular, (Cnhten _+i and 0-CmH2m+i).

Preferred compounds of the formula V-2f are the compounds of the for mula V-2M :

V-2M in which

R ⁵¹ has the meaning indicated above and preferably

denotes Cnhten+i or CH2=CH-(CH2)z, and

R ⁵² has the meaning indicated above and preferably

denotes Cmhtem+i or O-Cmhtem+i or (CH2)z-CH=CH2, and in which n and m, independently of one another, denote an integer in the range from 0 to 15, preferably in the range from 1 to 7 and particularly preferably 1 to 5, and z denotes 0, 1 , 2, 3 or 4, preferably 0 or 2.

The preferred combinations of (R ⁵¹ and R ⁵² ) here are, in particular,

(CnH2n _+i and CmH2m _+i ) and (Cnhten _+i and O-Cmhtem _+i ), particularly prefera- bly (CnH2n+1 and CmH2m _+l ).

Preferred compounds of the formula V- 2g are the compounds of the for mula V-2g-1 :

^F \ ^F

_R Y L _R V-2g-1

in which

R ⁵¹ has the meaning indicated above and preferably

denotes Cnhten+i or CH2=CH-(CH2)z, and

R ⁵² has the meaning indicated above and preferably

denotes Cmhtem+i or O-Cmhtem+i or (CH2)z-CH=CH2, and in which n and m, independently of one another, denote an integer in the range from 0 to 15, preferably in the range from 1 to 7 and particularly preferably 1 to 5, and z denotes 0, 1 , 2, 3 or 4, preferably 0 or 2. The preferred combinations of (R ⁵¹ and R ⁵² ) here are, in particular, (CnH2n+i and CmH2m+i ) and (Cnhten+i and O-Cmhtem+i ), particularly prefera bly (CnH2n+1 and 0-CmH2m+l ).

The compounds of the formula VI are preferably selected from the group of the compounds of the formulae VI-1 to VI-5:

in which

Z ⁶¹ and Z ⁶² denote frans-CH=CH- or trans- CF=CF-, preferably

trans- CH=CH-, and the other occurring groups and parameters have the meaning given above under formula VI,

and preferably

R ⁶¹ and R ⁶² , independently of one another, denote H, alkyl or alkoxy having 1 to 7 C atoms or alkenyl having 2 to 7 C atoms, X ⁶² denotes F, Cl, -OCF3 or -CN,

The compounds of the formula VI-1 are preferably selected from the group of the compounds of the formulae VI-1 a and VI-1 b, more preferably selected from compounds of the formula VI-1 a:

in which

R ⁶¹ has the meaning indicated above and preferably

denotes CnFten+i or CFl2=CFI-(CFl2)z, and

R ⁶² has the meaning indicated above and preferably

denotes CmFl2m+i or 0-CmFl2m+i or (CFl2)z-CFI=CFl2, and in which n and m, independently of one another, denote an integer in the range from 0 to 1 5, preferably in the range from 1 to 7 and particularly preferably 1 to 5, and z denotes 0, 1 , 2, 3 or 4, preferably 0 or 2.

The preferred combinations of (R ⁶¹ and R ⁶² ) here are, in particular, (CnH2n _+i and CmFl2m _+i ) and (CnFten _+i and 0-CmFl2m _+i ), in the case of for- mula VI-1 a particularly preferably (Cnhten+i and Cmhtem+i ) and in the case of formula VI-1 b particularly preferably (Cnhten+i and O-Cmhtem+i ).

The compounds of the formula VI-2 are preferably selected from the compounds of the formula Vl-2a to Vl-2c:

in which the parameters have the meaning given above under formula VI- 2 and preferably

R ⁶¹ has the meaning indicated above and preferably

denotes Cnhten+i , in which n denotes an integer in the range from 0 to 7, preferably in the range from 1 to 5, and X ⁶² denotes -F, -Cl, -OCF3, or -CN.

The compounds of the formula VI-3 are preferably selected from compounds of the formulae Vl-3a to Vl-3c:

in which the parameters have the meaning given above under formula VI-3 and preferably

R ⁶¹ has the meaning indicated above and preferably

denotes CnFten+i , in which n denotes an integer in the range from 0 to 7, preferably in the range from 1 to 5, and

X ⁶² denotes F, Cl, OCF ₃ , or -CN. The compounds of the formula VI-5 are preferably selected from the compounds of the formula Vl-5b:

in which the parameters have the meaning given above under formula VI-5 and preferably

Ft ⁶¹ has the meaning indicated above and preferably

denotes CnFten _+i , in which n denotes an integer in the range from 0 to 7, preferably in the range from 1 to 5, and

X ⁶² denotes -F, -Cl, -OCF3, or -CN, particularly preferably - OCF3. The compounds of the formula VII are preferably selected from the group of the compounds of the formulae VII-1 to VII-6:

where the compounds of the formula VII-5 are excluded from the com pounds of the formula VII-6, and in which the parameters have the respective meanings indicated above for formula VII,

Y ⁷¹ , Y ⁷² , Y ⁷³ independently from one another, denote FI or F, and preferably

R ⁷¹ denotes alkyl or alkoxy, each having 1 to 7 C atoms, or alkenyl having 2 to 7 C atoms,

R ⁷² denotes alkyl or alkoxy, each having 1 to 7 C atoms, or alkenyl having 2 to 7 C atoms,

X ⁷² denotes F, Cl, NCS or -OCF3, preferably F or NCS, and particularly preferably R ⁷¹ has the meaning indicated above and preferably

denotes CnFten _+i or CFl2=CFI-(CFl2)z, and

R ⁷² has the meaning indicated above and preferably

denotes CmFl2m+i or 0-CmFl2m _+i or (CFl2)z-CFI=CFl2, and in which n and m, independently of one another, denote an integer in the range from 0 to 1 5, preferably in the range from 1 to 7 and particularly preferably 1 to 5, and z denotes 0, 1 , 2, 3 or 4, preferably 0 or 2.

The compounds of the formula VI 1-1 are preferably selected from the group of the compounds of the formulae VII-1 a to VII-1 d: in which X ⁷² has the meaning given above for formula VII-2 and

R ⁷¹ has the meaning indicated above and preferably

denotes CnFten+i , in which n denotes 1 to 7, preferably 2 to 6, particularly preferably

2, 3 or 5, and z denotes 0, 1 , 2, 3 or 4, preferably 0 or 2, and

X ⁷² preferably denotes F. The compounds of the formula VI 1-2 are preferably selected from the group of the compounds of the formulae Vll-2a and Vll-2b, particularly preferably of the formula Vll-2a:

in which

R ⁷¹ has the meaning indicated above and preferably

denotes Cnhten+i or CH2=CH-(CH2)z, and

R ⁷² has the meaning indicated above and preferably

denotes Cmhtem+i or O-Cmhtem+i or (CH2)z-CH=CH2, and in which n and m, independently of one another, denote an integer in the range from 0 to 15, preferably in the range from 1 to 7 and particularly preferably 1 to 5, and z denotes 0, 1 , 2, 3 or 4, preferably 0 or 2.

The preferred combinations of (R ⁷¹ and R ⁷² ) here are, in particular, (CnH2n _+i and Cmhtem _+i ) and (Cnhten _+i and O-Cmhtem _+i ), particularly prefera bly (CnH2n+1 and CmH2m+l).

The compounds of the formula VII-3 are preferably compounds of the for mula Vll-3a: in which

R ⁷¹ has the meaning indicated above and preferably

denotes Cnhten+i or CH2=CH-(CH2)z, and

R ⁷² has the meaning indicated above and preferably

denotes Cmhtem+i or O-Cmhtem+i or (CH2)z-CH=CH2, and in which n and m, independently of one another, denote an integer in the range from 0 to 1 5, preferably in the range from 1 to 7 and particularly preferably 1 to 5, and z denotes 0, 1 , 2, 3 or 4, preferably 0 or 2.

The preferred combinations of (R ⁷¹ and R ⁷² ) here are, in particular, (CnH2n+i and Cmhtem+i ) and (CnH2n+i and 0-CmH2m+i ), particularly prefera bly (CnH2n+1 and CmH2m+l ).

The compounds of the formula VII-4 are preferably compounds of the formula Vll-4a:

in which has the meaning indicated above and preferably denotes Cnhten+i or CH2=CH-(CH2)z, and has the meaning indicated above and preferably denotes Cmhtem+i or O-Cmhtem+i or (CH2)z-CH=CH2, and in which n and m, independently of one another, denote an integer in the range from 0 to 15, preferably in the range from 1 to 7 and particularly preferably 1 to 5, and z denotes 0, 1 , 2, 3 or 4, preferably 0 or 2.

The preferred combinations of (R ⁷¹ and R ⁷² ) here are, in particular, (CnH2n _+i and Cmhtem ₊ i) and (Cnhten _+i and O-Cmhtem ₊ i), particularly prefera bly (CnH2n+1 and CmH2m+l).

The compounds of the formula VII-5 are preferably selected from the group of the compounds of the formulae Vll-5a and Vll-5b, more preferably of the formula Vll-5a:

in which has the meaning indicated above and preferably denotes Cnhten+i or CH2=CH-(CH2)z, and has the meaning indicated above and preferably denotes Cmhtem+i or O-Cmhtem+i or (CH2)z-CH=CH2, and in which n and m, independently of one another, denote an integer in the range from 0 to 15, preferably in the range from 1 to 7 and particularly preferably 1 to 5, and z denotes 0, 1 , 2, 3 or 4, preferably 0 or 2.

The preferred combinations of (R ⁷¹ and R ⁷² ) here are, in particular, (CnH2n _+i and Cmhtem ₊ i) and (Cnhten _+i and O-Cmhtem ₊ i), particularly prefera bly (CnH2n+1 and CmH2m+l).

The compounds of the formula VII-6 are preferably selected from the group of the compounds of the formulae Vll-6a and Vll-6b:

in which has the meaning indicated above and preferably denotes Cnhten+i or CH2=CH-(CH2)z, and has the meaning indicated above and preferably denotes Cmhtem+i or O-Cmhtem+i or (CH2)z-CH=CH2, and in which n and m, independently of one another, denote an integer in the range from 0 to 15, preferably in the range from 1 to 7 and particularly preferably 1 to 5, and z denotes 0, 1 , 2, 3 or 4, preferably 0 or 2.

The preferred combinations of (R ⁷¹ and R ⁷² ) here are, in particular, (CnH2n+i and CmH2m+i ) and (Cnhten+i and O-Cmhtem+i ), particularly prefera- bly (CnH2n+1 and CmH2m+l ).

The compounds of the formula VII-7 are preferably selected from the group of the compounds of the formulae Vll-7a and Vll-7b:

in which R ⁷¹ has the meaning indicated above and preferably denotes Cnhten+i or CH2=CH-(CH2)z,

X ⁷² denotes F, -OCF3 or -NCS, n denotes an integer in the range from 0 to 15, preferably in the range from 1 to 7 and particularly preferably 1 to 5, and, z denotes 0, 1 , 2, 3 or 4, preferably 0 or 2.

The compounds of the formula VIII are preferably selected from the group of the compounds of the formulae VIII-1 to VIII-3, more preferably these compounds of the formula VIII predominantly consist, even more prefera bly essentially consist and very particularly preferably completely consist thereof:

in which one of

Y ⁸¹ and Y ⁸² denotes H and the other denotes H or F, and R ⁸¹ has the meaning indicated above and preferably denotes Cnhten+i or CH2=CH-(CH2)z, and

R ⁸² has the meaning indicated above and preferably

denotes Cmhtem+i or O-Cmhtem+i or (CH2)z-CH=CH2, and in which n and m, independently of one another, denote an integer in the range from 0 to 15, preferably in the range from 1 to 7 and particularly preferably 1 to 5, and z denotes 0, 1 , 2, 3 or 4, preferably 0 or 2.

The preferred combinations of (R ⁸¹ and R ⁸² ) here are, in particular, (CnH2n _+i and Cmhtem _+i ) and (Cnhten _+i and O-Cmhtem _+i ), particularly preferably (CnH2n+1 and CmH2m+l).

The compounds of the formula VI 11-1 are preferably selected from the group of the compounds of the formulae VIII-1 a to VIII-1 c:

in which R ⁸¹ has the meaning indicated above and preferably denotes Cnhten+i or CH2=CH-(CH2)z, and

R ⁸² has the meaning indicated above and preferably

denotes Cmhtem+i or O-Cmhtem+i or (CH2)z-CH=CH2, and in which n and m, independently of one another, denote an integer in the range from 0 to 1 5, preferably in the range from 1 to 7 and particularly preferably 1 to 5, and z denotes 0, 1 , 2, 3 or 4, preferably 0 or 2.

The preferred combinations of (R ⁸¹ and R ⁸² ) here are, in particular, (CnH2n _+i and Cmhtem ₊ i) and (Cnhten _+i and O-Cmhtem ₊ i), particularly prefera bly (CnH2n+1 and CmH2m+l).

The compounds of the formula VIII-2 are preferably compounds of the for mula VII l-2a:

in which

R ⁸¹ has the meaning indicated above and preferably

denotes Cnhten+i or CH2=CH-(CH2)z, and R ⁸² has the meaning indicated above and preferably denotes Cmhtem+i or O-Cmhtem+i or (CH2)z-CH=CH2, and in which n and m, independently of one another, denote an integer in the range from 0 to 15, preferably in the range from 1 to 7 and particularly preferably 1 to 5, and z denotes 0, 1 , 2, 3 or 4, preferably 0 or 2.

The preferred combinations of (R ⁸¹ and R ⁸² ) here are, in particular,

(CnH2n+i and Cmhtem+i), (CnH2n+i and 0-CmH2m+i) and (CH2=CH-(CH2)Z and CmH2m ₊ i), particularly preferably (Cnhten _+i and Cmhtem ₊ i).

The compounds of the formula VIII-3 are preferably compounds of the for mula Vlll-3a:

Vlll-3a in which

R ⁸¹ has the meaning indicated above and preferably

denotes Cnhten+i or CH2=CH-(CH2)z, and R ⁸² has the meaning indicated above and preferably

denotes Cmhtem+i or O-Cmhtem+i or (CH2)z-CH=CH2, and in which n and m, independently of one another, denote an integer in the range from 0 to 15, preferably in the range from 1 to 7 and particularly preferably 1 to 5, and z denotes 0, 1 , 2, 3 or 4, preferably 0 or 2.

The preferred combinations of (R ⁸¹ and R ⁸² ) here are, in particular, (CnH2n+1 and CmH2m+l ) and (CnH2n+1 and 0-CmH2m+l ).

The compounds of the formula IX are preferably selected from the group of the compounds of the formulae IX-1 to IX-3:

in which the parameters have the respective meaning indicated above under formula IX and preferably one of denotes and

in which

Ft ⁹¹ has the meaning indicated above and preferably

denotes Cnhten+i or CH2=CH-(CH2)z, and

R92 has the meaning indicated above and preferably

denotes Cmhtem+i or O-Cmhtem+i or (CH2)z-CH=CH2, and in which n and m, independently of one another, denote an integer in the range from 0 to 15, preferably in the range from 1 to 7 and particularly preferably 1 to 5, and z denotes 0, 1 , 2, 3 or 4, preferably 0 or 2.

The preferred combinations of (R ⁹¹ and R ⁹² ) here are, in particular,

(CnH2n+1 and CmH2m+l ) and (CnH2n+1 and 0-CmH2m+l ).

The compounds of the formula IX-1 are preferably selected from the group of the compounds of the formulae IX-1 a to IX-1 e:

in which the parameters have the meaning given above and preferably

R ⁹¹ has the meaning indicated above and preferably

denotes CnFten+i , and n denotes an integer in the range from 0 to 15, preferably in the range from 1 to 7 and particularly preferably 1 to 5, and

X ⁹² preferably denotes F or Cl. The compounds of the formula IX-2 are preferably selected from the group of the compounds of the formulae IX-2a and IX-2b:

IX-2a in which

R ⁹¹ has the meaning indicated above and preferably

denotes Cnhten+i or CH2=CH-(CH2)z, and

R ⁹² has the meaning indicated above and preferably

denotes Cmhtem+i or O-Cmhtem+i or (CH2)z-CH=CH2, and in which n and m, independently of one another, denote an integer in the range from 0 to 15, preferably in the range from 1 to 7 and particularly preferably 1 to 5, and z denotes 0, 1 , 2, 3 or 4, preferably 0 or 2.

The preferred combination of (R ⁹¹ and R ⁹² ) here is, in particular, (Cnhten+i and CmH2m+i).

The compounds of the formula IX-3 are preferably compounds of the for mulae IX-3a and IX-3b:

in which

R ⁹¹ has the meaning indicated above and preferably

denotes CnH2n+i or CH2=CH-(CH2)z, and

R ⁹² has the meaning indicated above and preferably

denotes CmH2m+i or 0-CmH2m+i or (CH2)z-CH=CH2, and in which n and m, independently of one another, denote an integer in the range from 0 to 15, preferably in the range from 1 to 7 and particularly preferably 1 to 5, and z denotes 0, 1 , 2, 3 or 4, preferably 0 or 2.

The preferred combinations of (R ⁹¹ and R ⁹² ) here are, in particular,

(CnH2n+i and CmH2m+i ) and (CnH2n+i and 0-CmH2m+i ), particularly prefera bly (CnH2n+1 and 0-CmH2m+l ).

The media according to the present invention comprise one or more chiral dopants. Preferably these chiral dopants have an absolute value of the helical twisting power (HTP) in the range of from 1 pm ¹ to 150 pm ¹ , preferably in the range of from 10 pm ¹ to 100 pm ¹ . In case the media comprise two or more chiral dopants, these may have opposite signs of their HTP-values. This condition is preferred for some specific

embodiments, as it allows to compensate the chirality of the respective compounds to some degree and, thus, may be used to compensate various temperature dependent properties of the resulting media in the devices. Generally, however, it is preferred that most, preferably all of the chiral compounds present in the media according to the present invention have the same sign of their HTP-values. Preferably the chiral dopants present in the media according to the instant application are mesogenic compounds and most preferably they exhibit a mesophase on their own. In a preferred embodiment of the present invention, the medium comprises two or more chiral compounds which all have the same algebraic sign of the HTP.

The temperature dependence of the HTP of the individual compounds may be high or low. The temperature dependence of the pitch of the medium can be compensated by mixing compounds having different temperature dependencies of the HTP in corresponding ratios.

For the optically active component, a multitude of chiral dopants, some of which are commercially available, is available to the person skilled in the art, such as, for example, cholesteryl nonanoate, R- and S-81 1 , R- and S- 1011 , R- and S-2011 , R- and S-3011 , R- and S-4011 , or CB15 (all Merck KGaA, Darmstadt). Particularly suitable dopants are compounds which contain one or more chiral groups and one or more mesogenic groups, or one or more aromatic or alicyclic groups which form a mesogenic group with the chiral group.

Suitable chiral groups are, for example, chiral branched hydrocarbon radicals, chiral ethane diols, binaphthols or dioxolanes, furthermore mono- or polyvalent chiral groups selected from the group consisting of sugar derivatives, sugar alcohols, sugar acids, lactic acids, chiral substituted glycols, steroid derivatives, terpene derivatives, amino acids or sequences of a few, preferably 1 -5, amino acids.

Preferred chiral groups are sugar derivatives, such as glucose, mannose, galactose, fructose, arabinose and dextrose, sugar alcohols, such as, for example, sorbitol, mannitol, iditol, galactitol or anhydro derivatives thereof, in particular dianhydrohexitols, such as dianhydrosorbide (1 , 4:3,6- dianhydro-D-sorbide, isosorbide), dianhydromannitol (isosorbitol) or dianhydroiditol (isoiditol), sugar acids, such as, for example, gluconic acid, gulonic acid and ketogulonic acid, chiral substituted glycol radicals, such as, for example, mono- or oligoethylene or propylene glycols, in which one or more CH ₂ groups are substituted by alkyl or alkoxy, amino acids, such as, for example, alanine, valine, phenylglycine or phenylalanine, or sequences of from 1 to 5 of these amino acids, steroid derivatives, such as, for example, cholesteryl or cholic acid radicals, terpene derivatives, such as, for example, menthyl, neomenthyl, campheyl, pineyl, terpineyl, isolongifolyl, fenchyl, carreyl, myrthenyl, nopyl, geraniyl, linaloyl, neryl, citronellyl or dihydrocitronellyl.

The media according to the present invention preferably comprise chiral dopants which are selected from the group of known chiral dopants.

Suitable chiral groups and mesogenic chiral compounds are described, for example, in DE 34 25 503, DE 35 34 777, DE 35 34 778, DE 35 34 779 and DE 35 34 780, DE 43 42 280, EP 01 038 941 and DE 195 41 820. Examples are also compounds listed in Table F below.

Chiral compounds preferably used according to the present invention are selected from the group consisting of the formulae shown below.

Particular preference is given to chiral dopants selected from the group consisting of compounds of the following formulae A-l to A-lll and Ch:

A-Ch

in which

Ra ⁱ 1 , R ^a12 and R ^b12 , independently of one another, denote alkyl having 1 to

15 C atoms, in which, in addition, one or more non-adjacent CH2 groups may each be replaced, independently of one another, by -C(R ^Z )=C(R ^Z )-, -CºC-, -0-, -S-, -CO-, -CO-O-, -O- CO- or -O-CO-O- in such a way that O and/or S atoms are not linked directly to one another, and in which, in addition, one or more H atoms may be replaced by F, Cl, Br, I or CN, preferably alkyl, more preferably n-alkyl, with the proviso that R ^a12 is different from R ^b12

R ^a21 and R ^a22 , independently of one another, denote alkyl having 1 to 15 C atoms, in which, in addition, one or more non-adjacent CH2 groups may each be replaced, independently of one another, by -C(R ^Z )=C(R ^Z )-, -OC-, -0-, -S-, -CO-, -CO-O-, -O-CO- or - O-CO-O- in such a way that O and/or S atoms are not linked directly to one another, and in which, in addition, one or more H atoms may be replaced by F, Cl, Br, I or CN, preferably both are alkyl, more preferably n-alkyl,

Ra ³ⁱ , R ^a31 and R ^b32 , independently of one another, denote straight-chain or branched alkyl having 1 to 15 C atoms, in which, in addition, one or more non-adjacent CFI2 groups may each be replaced, independently of one another, by -C(R ^Z )=C(R ^Z )- , -CºC-, -0-, -S-, -C0-, -C0-0-, -O-CO- or -O-CO-O- in such a way that O and/or S atoms are not linked directly to one another, and in which, in addition, one or more FI atoms may be replaced by F, Cl, Br, I or CN, preferably alkyl, more preferably n-alkyl, with the proviso that R ^a32 is different from R ^b32 ,

R ^z denotes H, CH3, F, Cl, or CN, preferably H or F,

R ⁸ has one of the meanings of R ^{a1 1} given above, preferably alkyl, more preferably n-alkyl having 1 to 1 5 C atoms,

Z ⁸ denotes -C(0)0-, -CFI2O-, -CF2O- or a single bond,

preferably -C(0)0-,

A ¹¹ is defined as A ¹² below, or alternatively denotes

in which L ¹¹ , on each occurrence, independently of one another, denotes halogen, CN, or alkyl, alkenyl, alkoxy or alkenyloxy having up to 1 2 C atoms and in which one or more H atoms are optionally replaced with halogen, preferably Me, Et, Cl or F, particularly preferably F.

A ²¹ denotes

A ²² has the meanings given for A ¹²

A ³¹ has the meanings given for A ¹¹ ,

alternatively denotes

A ³² has the meanings given for A ¹² . n2 on each occurrence, identically or differently, is 0, 1 or 2, and n3 is 1 , 2 or 3.

Particular preference is given to dopants selected from the group consisting of the compounds of the following formulae:

A-l-1 in which

m is, on each occurrence, identically or differently, an integer from

1 to 9 and

n is, on each occurrence, identically or differently, an integer from

2 to 9.

Particularly preferred compounds of formula A are compounds of formula A IM.

Further preferred dopants are derivatives of the isosorbide, isomannitol or isoiditol of the following formula A-IV:

A-IV

(dianhydrosorbitol),

(dianhydromannitol), or (dianhydroiditol), preferably dianhydrosorbitol, and chiral ethane diols, such as, for example, diphenylethanediol

(hydrobenzoin), in particular mesogenic hydrobenzoin derivatives of the following formula A-V:

A-V

including the (S,S) enantiomers, which are not shown, in which

are each, independently of one another, 1 ,4-phenylene,

which may also be mono-, di- or trisubstituted by L, or 1 ,4- cyclohexylene,

L is H, F, Cl, CN or optionally halogenated alkyl, alkoxy,

alkylcarbonyl, alkoxycarbonyl or alkoxycarbonyloxy having 1 -7 carbon atoms, c is 0 or 1 ,

Z° is -COO-, -OCO-, -CH2CH2- or a single bond, and R° is alkyl, alkoxy, alkylcarbonyl, alkoxycarbonyl or alkylcarbonyl- oxy having 1 -12 carbon atoms.

Examples of compounds of formula A-IV are: 1

2 3 4 5 6 7

8

The compounds of the formula A-IV are described in WO 98/00428. The

compounds of the formula A-V are described in GB-A-2,328,207.

Very particularly preferred dopants are chiral binaphthyl derivatives, as

described in WO 02/94805, chiral binaphthol acetal derivatives, as

described in WO 02/34739, chiral TADDOL derivatives, as described in

WO 02/06265, and chiral dopants having at least one fluorinated bridging group and a terminal or central chiral group, as described in WO 02/06196 and WO 02/06195.

Particular preference is given to chiral compounds of the formula A-VI

in which

X ¹ , X ² , Y ¹ and Y ² are each, independently of one another, F, Cl, Br, I, CN,

SCN, SFs, straight-chain or branched alkyl having from 1 to 25 carbon atoms, which may be monosubstituted or

polysubstituted by F, Cl, Br, I or CN and in which, in addition, one or more non-adjacent CFI2 groups may each, independently of one another, be replaced by -0-, -S-, -NH-,

NR ⁰ -, -CO-, -COO-, -OCO-, -OCOO-, -S-CO-, -CO-S-, -CH=CH- or -CºC- in such a way that O and/or S atoms are not bonded directly to one another, a polymerisable group or cycloalkyl or aryl having up to 20 carbon atoms, which may optionally be monosubstituted or polysubstituted by halogen, preferably F, or by a polymerisable group, x ¹ and x ² are each, independently of one another, 0, 1 or 2, y ¹ and y ² are each, independently of one another, 0, 1 , 2, 3 or 4,

B ¹ and B ² are each, independently of one another, an aromatic or partially or fully saturated aliphatic six-membered ring in which one or more CH groups may be replaced by N atoms and one or more non-adjacent CH ₂ groups may be replaced by O and/or S,

W ¹ and W ² are each, independently of one another, -Z ¹ -A ¹ -(Z ² -A ² ) _m -R, and one of the two is alternatively R ¹ or A ³ , but both are not simultaneously H, or

U ¹ and U ² are each, independently of one another, CH2, O, S, CO or CS, V ¹ and V ² are each, independently of one another, (CH2)n, in which from one to four non-adjacent CH ₂ groups may be replaced by O and/or S, and one of V ¹ and V ² and, in the case where both are a single bond, Z ¹ and Z ² are each, independently of one

another, -0-, -S-, -CO-, -COO-, -OCO-, -0-C00-, -CO- NR ⁰ -, -NR°-CO-, -O-CH2-, -CH2-O-, -S-CH2-, -CH2-S-, -CF2- 0-, -O-CF2-, -CF2-S-, -S-CF2-, -CH2-CH2-, -CF2-CH2-, -CH2- CF2-, -CF2-

CF2-, -CH=N-, -N=CH-, -N=N-, -CH=CH-, -CF=CH-, -CH=CF-, - CF=CF-, -CºC-, a combination of two of these groups, where no two O and/or S and/or N atoms are bonded directly to one another, preferably -CFI=CFI-COO-, or -COO-CFI=CFI-, or a single bond,

A ¹ , A ² and A ³ are each, independently of one another, 1 ,4-phenylene, in which one or two non-adjacent CFI groups may be replaced by N, 1 ,4-cyclohexylene, in which one or two non-adjacent OHI ₂ groups may be replaced by O and/or S, 1 ,3-dioxolane-4,5-diyl,

1.4-cyclohexenylene, 1 ,4-bicyclo[2.2.2]octylene, piperidine-1 ,4- diyl, naphthalene-2, 6-diyl, decahydronaphthalene-2,6-diyl or

1.2.3.4-tetrahydronaphthalene-2,6-diyl, where each of these groups may be monosubstituted or polysubstituted by L, and in addition A ¹ is a single bond,

L is a halogen atom, preferably F, CN, NO2, alkyl, alkoxy,

alkylcarbonyl, alkoxycarbonyl or alkoxycarbonyloxy having 1 -7 carbon atoms, in which one or more FI atoms may be replaced by F or Cl, m is in each case, independently, 0, 1 , 2 or 3, and

R and R ¹ are each, independently of one another, FI, F, Cl, Br, I, CN,

SCN, SF5, straight-chain or branched alkyl having from 1 or 3 to

25 carbon atoms respectively, which may optionally be mono substituted or polysubstituted by F, Cl, Br, I or CN, and in which one or more non-adjacent CFI2 groups may be replaced by -0-, -S-, -NH-, -NR ⁰ -, -CO-, -COO-, -OCO-, -O-COO-, -S- CO-, -CO-S-, -CFI=CFI- or -CºC-, where no two O and/or S atoms are bonded directly to one another, or a polymerisable group.

Particular preference is given to chiral binaphthyl derivatives of the formula A-VI-1

A-VI-1 in particular those selected from the following formulae A-VI-1 a to A-VI-1 c:

in which ring B and Z° are as defined for the formula A-IV, and

R° as defined for formula A-IV or H or alkyl having from 1 to 4

carbon atoms, and b is 0, 1 or 2, and Z° is, in particular, -0C(0)- or a single bond.

The concentration of the one or more chiral dopant(s), in the LC medium is preferably in the range from 0.001 % to 20 %, preferably from 0.05 % to 5 %, more preferably from 0.1 % to 2 %, and, most preferably from 0.5 % to 1.5 %. These preferred concentration ranges apply in particular to the chiral dopant S-401 1 or R-401 1 (both from Merck KGaA) and for chiral dopants having the same or a similar HTP. For Chiral dopants having either a higher or a lower absolute value of the HTP compared to S-4011 these preferred concentrations have to be decreased, respectively increased proportionally according to the ratio of their HTP values relatively to that of S-401 1. The pitch p of the LC media or host mixtures according to the invention is preferably in the range of from 5 to 50 pm, more preferably from 8 to 30 pm and particularly preferably from 10 to 20 pm. Preferably, the media according to the invention, comprise a stabilizer selected from the group of compounds of the formulae ST-1 to ST-18.

ST-1

ST-2 ST-10

ST-15 in which

RST denotes H, an alkyl or alkoxy radical having 1 to 15 C atoms, where, in addition, one or more CH2 groups in these radicals may each be replaced, independently of one another,

0-, -CO-O-, -O-CO- in such a way that O atoms are not linked directly to one another, and in which, in addition, one or more FI atoms may be replaced by halogen,

 Z ^ST each, independently of one another, denote -C0-0-, -O-

CO-, -CF2O-, -OCF2-, -CH2O-, -OCH2-, -CH2- , -CH2CH2-, -(CH )4-, -CH=CH-CH O- , -C2F4-, -CH2CF2-, -CF2CH2-, -CF=CF-, -CH=CF-, -CF=CH-, -CFI=CFI-, -CºC- or a single bond,

L ¹ and L ² each, independently of one another, denote F, Cl, CF3 or

CHF2,

P denotes 1 or 2, q denotes 1 , 2, 3, 4, 5, 6, 7, 8, 9 or 10.

Of the compounds of the formula ST, special preference is given to the compounds of the formulae

in which n = 1 , 2, 3, 4, 5, 6 or 7, preferably n = 3

In the compounds of the formulae ST-3a and ST-3b, n preferably denotes 3. In the compounds of the formula ST-2a, n preferably denotes 7.

Very particularly preferred mixtures according to the invention comprise one or more stabilisers from the group of the compounds of the formulae ST-2a-1 , ST-3a-1 , ST-3b-1 , ST-8-1 , ST-9-1 and ST-12:

-1

The compounds of the formulae ST-1 to ST-18 are preferably each present in the liquid-crystal mixtures according to the invention in amounts of 0.005 - 0.5%, based on the mixture.

If the mixtures according to the invention comprise two or more

compounds from the group of the compounds of the formulae ST-1 to ST- 18, the concentration correspondingly increases to 0.01 - 1 % in the case of two compounds, based on the mixtures. However, the total proportion of the compounds of the formulae ST-1 to ST-18, based on the mixture according to the invention, should not exceed 2%.

The compounds according to the present invention can be synthesized by or in analogy to known methods described in the literature (for example in the standard works such as Houben-Weyl, Methoden der Organischen Chemie [Methods of Organic Chemistry], Georg-Thieme-Verlag, Stuttgart), under reaction conditions which are known and suitable for said reactions. Use may also be made here of variants which are known per se, but are not mentioned here. In particular, they can be prepared as described in or in analogy to the following reaction schemes. Further methods for preparing the inventive compounds can be taken from the examples.

The compounds of formula S are preferably synthesized following or in analogy to the procedures described in CN 106518890 A.

Other mesogenic compounds which are not explicitly mentioned above can optionally and advantageously also be used in the media in

accordance with the present invention. Such compounds are known to the person skilled in the art.

Preferably, the total concentration of the one or more compounds of formula S in the medium is in the range of from 1 % to 50%, preferably from 5% to 40% and particularly preferably from 10% to 20%.

In another embodiment of the present invention, the medium comprises one or more compounds of formula S and one or more compounds of formula IC, where the total concentration of the one or more compounds of formula IC is in the range of from 5 % to 50 %, more preferably from 10 % to 40 %, and particularly preferably from 15 % to 35 %. In a preferred embodiment of the present invention, the liquid-crystalline media preferably comprise in total 5 % to 35 %, preferably 10 % to 32 % and particularly preferably 20 % to 30 % of compounds of formula T.

5

In a preferred embodiment of the present invention, the liquid-crystalline medium comprises in total 30 % or less, preferably 15 % or less and particularly preferably 10 % or less compounds of formula T.

10

In a preferred embodiment of the present invention, the liquid-crystalline medium comprises in total 30 % or more, preferably 40 % or more and particularly preferably 50 % or more compounds of formula I and/or IC,

_{1 5} preferably selected from the group of compounds of the 1-1 , I-2 and IC, particularly preferably selected from the compounds of the formulae I-2 and IC.

Preferably, the proportion of the compounds if formula 1-1 in the medium is

20

20% or less, more preferably 15% or less, particularly preferably 10% or less and very particularly preferably 5% or less.

In a preferred embodiment, the medium comprises one or more

25 compounds of formula I-2 in a total concentration in the range of from 5 % to 25 %, more preferably from 7 % to 25 %, and particularly preferably from 10 % to 20 %.

In another preferred embodiment, the medium comprises one or more ou

compounds of formula I-2 in a total concentration of 10% or less, preferable of 5% or less and particularly preferably of 2% or less.

In a preferred embodiment, the total concentration of the compounds of 35

formula IC in the media according to the present invention is in the range of from 5 % to 50 %, more preferably from 10 % to 40 %, and particularly preferably from 15 % to 35 %.

In a preferred embodiment, the total concentration of the compounds of formula IC in the media according to the present invention is 20 % or more, more preferably 25 % or more and particularly preferably 30 % or more. In a preferred embodiment of the present invention the medium comprises one or more compounds of formula II and/or IIA-1 , preferably 11-1 and/or II- 1 -A1 , in a total concentration of 5 % to 35 %, more preferably 10 % to 30 %, particularly preferably 15 % to 25 %.

Preferably, the medium comprises one or more the compounds of the formula P(2)TU-n-S.

Preferably, the medium comprises one or more the compounds of the formula 11-1.

Preferably, the medium comprises either one or more the compounds of the formula P(2)TU-n-S or one or more compounds of the formula 11-1.

In a preferred embodiment of the present invention the medium comprises one or more compounds of formula 11-1 in an total concentration of 25% or less, more preferably 20% or less, particularly preferably 15% or less, very particularly preferably 10% or less.

In a preferred embodiment of the present invention the medium comprises one or more compounds of formula III, preferably III-1 , in a total concentration of 2 % to 30 %, more preferably 5 % to 25 %, particularly preferably 10 % to 20 %. Further preferred embodiments of the present invention, taken alone or in combination with one another, are as follows, wherein some compounds are abbreviated using the acronyms given in Table C:

- The medium comprises one or more compounds of formula S and one or more compounds of formula 1C

- The medium comprises one or more compounds of formula T-1 ;

- The medium comprises one or more compounds of formula T-2;

- The medium comprises one or more compounds of formula T-1 and T-2;

- The medium comprises one or more compounds of formula T-1 and/or T-2 and one or more compounds of formula I and/or IC and/or II and/or III;

- The medium comprises one or more compounds of formula III-1 ;

- The medium comprises two or more compounds of formula T-1 ;

- The medium comprises two or more compounds of formula T-2;

- The medium comprises the compound PPU-TO-S;

- The medium comprises one or more compounds of formula S and one or more compounds of formula III-1 , preferably in a total concentration in the range of from 5 to 40%, more preferably from 10 to 35%, particularly preferably from 18 to 30%;

- The medium comprises one or more compounds of formula S and one or more compounds of formula IC, preferably in a total concentration in the range of from 20 to 65%, more preferably from 30 to 60%, particularly preferably from 45 to 55%;

- The medium comprises one or more compounds of formula ICb,

preferably the compounds CPU-2-S and/or CPU-4-S;

- The medium comprises one or more compounds of formula ICb and formula 11-1 b, preferably the compounds CPU-2-S and/or CPU-4-S and PTU-3-S and/or PTU-4-S and/or PTU-5-S;

- The medium comprises one or more compounds of formula PPTU-n-S in an total concentration in the range of from 5 to 15 %; - The medium comprises one or more compounds of formula PPTU-n-S and PGTU-n-S in an total concentration in the range of from 10 to

20 %;

- The medium comprises one or more compounds of formula ST-3, preferably ST-3a and/or ST-3b, particularly preferably ST-3b-1 , in a total concentration in the range of from 0.01 to 1 %, preferably from 0.05 to 0.5%, particularly from 0.10 to 0.15%. The liquid-crystal media in accordance with the present invention prefera bly have a clearing point of 90Ό or more, more pre ferably 100Ό or more, more preferably 1 10Ό or more, more preferably 120° C or more, more preferably 130Ό or more, particularly preferably 1 40Ό or more and very particularly preferably 150Ό or more.

The liquid-crystal media in accordance with the present invention prefera bly have a clearing point of 210Ό or less, more pr eferably 200Ό or less, particularly preferably 190Ό or less, and very par ticularly preferably 180Ό or less.

The nematic phase of the media according to the invention preferably extends at least from 0Ό or less to 9013 or more. It is advantageous for the media according to the invention to exhibit even broader nematic phase ranges, preferably at least from -10Ό or les s to 120Ό or more, very preferably at least from -20Ό or less to 140° C or more and in particular at least from -30Ό or less to 150Ό or more, very particularly preferably at least from -40Ό or less to 170Ό or more.

The De of the liquid-crystal medium according to the present invention, at

1 kHz and 20Ό, is preferably 5 or more, more prefe rably 10 or more and very preferably 12 or more. The birefringence (Dh) of the liquid-crystal media according to the present invention, at 589 nm (Na ^D ) and 20Ό, is preferably in the range of from

0.250 to 0.900, more preferably from 0.300 to 0.850, and very particularly preferably in the range from 0.350 to 0.800 or less.

The birefringence (Dh) of the liquid-crystal media according to the present invention, at 589 nm (Na ^D ) and 20Ό, is preferably 0.250 or more, more preferably 0.300 or more, and particularly preferably 0.35 or more.

The compounds of the formulae I to III in each case include dielectrically positive compounds having a dielectric anisotropy of greater than 3, dielectrically neutral compounds having a dielectric anisotropy of less than 3 and greater than -1.5 and dielectrically negative compounds having a dielectric anisotropy of -1.5 or less.

The compounds of the formulae I, II and III are preferably dielectrically positive.

Herein, the expression dielectrically positive describes compounds or components where De > 3.0, dielectrically neutral describes those where -1.5 < De < 3.0 and dielectrically negative describes those where

De < -1.5. De is determined at a frequency of 1 kHz and at 20Ό. The dielectric anisotropy of the respective compound is determined from the results of a solution of 10 % of the respective individual compound in a nematic host mixture. If the solubility of the respective compound in the host mixture is less than 10 %, the concentration is reduced to 5 %. The capacitances of the test mixtures are determined both in a cell having homeotropic alignment and in a cell having homogeneous alignment. The cell thickness of both types of cells is approximately 20 pm. The voltage applied is a rectangular wave having a frequency of 1 kHz and an effective value of typically 0.5 V to 1.0 V, but it is always selected to be below the capacitive threshold of the respective test mixture.

De is defined as (e| I - e±), while 8ave. is (e| I + 2 e±) / 3.

The host mixture used for dielectrically positive compounds is mixture ZLI-4792 and that used for dielectrically neutral and dielectrically negative compounds is mixture ZLI-3086, both from Merck KGaA, Germany. The absolute values of the dielectric constants of the compounds are deter mined from the change in the respective values of the host mixture on addition of the compounds of interest. The values are extrapolated to a concentration of the compounds of interest of 100 %.

Components having a nematic phase at the measurement temperature of 20Ό are measured as such, all others are treated I ike compounds.

The expression threshold voltage in the present application refers to the optical threshold and is quoted for 10 % relative contrast (Vio), and the expression saturation voltage refers to the optical saturation and is quoted for 90 % relative contrast (V90), in both cases unless expressly stated otherwise. The capacitive threshold voltage (Vo), also called the Freeder- icks threshold (VFC), is only used if expressly mentioned.

The parameter ranges indicated in this application all include the limit values, unless expressly stated otherwise.

The different upper and lower limit values indicated for various ranges of properties in combination with one another give rise to additional preferred ranges.

Herein, the following conditions and definitions apply, unless expressly stated otherwise. All concentrations are quoted in per cent by weight and relate to the respective mixture as a whole, all temperatures are quoted in degrees Celsius and all temperature differences are quoted in differential degrees. All physical properties are determined in accordance with "Merck

Liquid Crystals, Physical Properties of Liquid Crystals", Status Nov. 1997,

Merck KGaA, Germany, and are quoted for a temperature of 20Ό, unless expressly stated otherwise. The optical anisotropy (Dh) is determined at a wavelength of 589.3 nm. The dielectric anisotropy (De) is determined at a frequency of 1 kHz. The threshold voltages, as well as all other electro- optical properties, are determined using test cells produced at Merck KGaA, Germany. The test cells for the determination of De have a cell thickness of approximately 20 pm. The electrode is a circular ITO electrode having an area of 1.13 cm ² and a guard ring. The orientation layers are SE-121 1 from Nissan Chemicals, Japan, for homeotropic orientation (e| I) and polyimide AL-1054 from Japan Synthetic Rubber, Japan, for homogeneous orientation (e±). The capacitances are deter mined using a Solatron 1260 frequency response analyser using a sine wave with a voltage of 0.3 Vrms. The light used in the electro-optical meas urements is white light. A set-up using a commercially available DMS instrument from Autronic-Melchers, Germany, is used here. The character istic voltages have been determined under perpendicular observation. The threshold (Vio), mid-grey (Vso) and saturation (V90) voltages have been determined for 10 %, 50 % and 90 % relative contrast, respectively.

The liquid-crystalline media are investigated with respect to their properties in the microwave frequency range as described in A.

Penirschke et al.“Cavity Perturbation Method for Characterization of Liquid Crystals up to 35 GHz“, 34 ^th European Microwave Conference - Amsterdam, pp. 545-548. Compare in this respect also A. Gaebler et al. “Direct Simulation of Material Permittivities ...“, 12MTC 2009 - International Instrumentation and Measurement Technology Conference, Singapore, 2009 (IEEE), pp. 463-467, and DE 10 2004 029 429 A, in which a measurement method is likewise described in detail.

The liquid crystal is introduced into a polytetrafluoroethylene (PTFE) or quartz capillary. The capillary has an inner diameter of 0.5mm and an outer diameter of 0.78mm. The effective length is 2.0 cm. The filled capil lary is introduced into the centre of the cylindrical cavity with a resonance frequency of 19 GHz. This cavity has a length of 1 1 .5 mm and a radius of 6 mm. The input signal (source) is then applied, and the frequency depending response of the cavity is recorded using a commercial vector network analyser (N5227A PNA Microwave Network Analyzer, Keysight Technologies Inc. USA. For other frequencies, the dimensions of the cavity are adapted correspondingly.

The change in the resonance frequency and the Q factor between the measurement with the capillary filled with the liquid crystal and the meas urement without the capillary filled with the liquid crystal is used to deter mine the dielectric constant and the loss angle at the corresponding target frequency by means of equations 10 and 11 in the above-mentioned publi cation A. Penirschke et al., 34 ^th European Microwave Conference - Amsterdam, pp. 545-548, as described therein.

The values for the components of the properties perpendicular and parallel to the director of the liquid crystal are obtained by alignment of the liquid crystal in a magnetic field. To this end, the magnetic field of a permanent magnet is used. The strength of the magnetic field is 0.35 tesla.

Preferred components are phase shifters, varactors, wireless and radio wave antenna arrays, matching circuit adaptive filters and others.

Herein, the term“compounds” is taken to mean both one compound and a plurality of compounds, unless expressly stated otherwise. The liquid-crystal media according to the invention preferably have nema tic phases in preferred ranges given above. The expression have a nematic phase here means on the one hand that no smectic phase and no crystallisation are observed at low temperatures at the corresponding temperature and on the other hand that no clearing occurs on heating from the nematic phase. At high temperatures, the clearing point is measured in capillaries by conventional methods. The investigation at low temperatures is carried out in a flow viscometer at the corresponding temperature and checked by storage of bulk samples: The storage stability in the bulk (LTS) of the media according to the invention at a given temperature T is determined by visual inspection. 2 g of the media of interest are filled into a closed glass vessel (bottle) of appropriate size placed in a refrigerator at a predetermined temperature. The bottles are checked at defined time intervals for the occurrence of smectic phases or crystallisation. For every material and at each temperature two bottles are stored. If crystallisation or the appearance of a smectic phase is observed in at least one of the two correspondent bottles the test is terminated and the time of the last inspection before the one at which the occurrence of a higher ordered phase is observed is recorded as the respective storage stability. The test is finally terminated after 1000 h, i.e an LTS value of 1000 h means that the mixture is stable at the given temperature for at least 1000 h.

The liquid crystals employed preferably have a positive dielectric anisot ropy. This is preferably 2 or more, preferably 4 or more, particularly pref- erably 6 or more and very particularly preferably 10 or more.

Furthermore, the liquid-crystal media according to the invention are char acterised by high anisotropy values in the microwave range. The birefrin gence at about 19 GFIz is, for example, preferably 0.14 or more, particu- larly preferably 0.15 or more, particularly preferably 0.20 or more, particu- larly preferably 0.25 or more and very particularly preferably 0.30 or more. In addition, the birefringence is preferably 0.80 or less.

The dielectric anisotropy in the microwave range is defined as

De _{G º} (e r, | I - 8r,±) .

The tunability (t) is defined as t º (De _G / e r, 1 1 ) .

The material quality (h) is defined as

h º (t / tan d _e , _ma ), where the maximum dielectric loss is tan de º max. { tan d _e tan d _{e r,} } .

The material quality (h) of the preferred liquid-crystal materials is 6 or more, preferably 8 or more, preferably 10 or more, preferably 15 or more, preferably 17 or more, preferably 20 or more, particularly preferably 25 or more and very particularly preferably 30 or more.

In the corresponding components, the preferred liquid-crystal materials have phase shifter qualities of 157dB or more, pre ferably 207dB or more, preferably 307dB or more, preferably 407dB or mor e, preferably 507dB or more, particularly preferably 807dB or more and ve ry particularly preferably 1007dB or more. in some embodiments, however, liquid crystals having a negative value of the dielectric anisotropy can also advantageously be used. The liquid crystals employed are either individual substances or mixtures. They preferably have a nematic phase.

In the present application, high-frequency technology means applications of electromagnetic radiation having frequencies in the range of from

1 MHz to 1 THz, preferably from 1 GHz to 500 GHz, more preferably

2 GHz to 300 GHz, particularly preferably from about 5 GHz to 150 GHz.

Preferably, the devices according to the invention are operable in the microwave range.

The liquid-crystal media in accordance with the present invention may comprise further additives and chiral dopants in the usual concentrations. The total concentration of these further constituents is in the range from 0 % to 10 %, preferably 0.1 % to 6 %, based on the mixture as a whole. The concentrations of the individual compounds used are each preferably in the range from 0.1 % to 3 %. The concentration of these and similar additives is not taken into consideration when quoting the values and concentration ranges of the liquid-crystal components and liquid-crystal compounds of the liquid-crystal media in this application.

Preferably the media according to the present invention comprise one or more chiral compounds as chiral dopants in order to adjust their cholesteric pitch. Their total concentration in the media according to the instant invention is preferably in the range 0.05 % to 15 %, more preferably from 1 % to 10 % and most preferably from 2 % to 6 %.

Optionally the media according to the present invention may comprise further liquid crystal compounds in order to adjust the physical properties. Such compounds are known to the expert. Their concentration in the media according to the instant invention is preferably 0 % to 30 %, more preferably 0.1 % to 20 % and most preferably 1 % to 15 %.

The response times are given as rise time (t _oh ) for the time for the change of the relative tuning, respectively of the relative contrast for the electro- optical response, from 0 % to 90 % (tsio - to), i.e. including the delay time (tio - to), as decay time (x _0ff ) for the time for the change of the relative tuning, respectively of the relative contrast for the electro-optical response, from 100 % back to 10 % (tioo - tio) and as the total response time

(xtotai = Xon + Xoff), respectively.

The liquid-crystal media according to the invention consist of a plurality of compounds, preferably 3 to 30, more preferably 4 to 20 and very prefera bly 4 to 16 compounds. These compounds are mixed in a conventional manner. In general, the desired amount of the compound used in the smaller amount is dissolved in the compound used in the larger amount. If the temperature is above the clearing point of the compound used in the higher concentration, it is particularly easy to observe completion of the dissolution process. It is, however, also possible to prepare the media in other conventional ways, for example using so-called pre-mixes, which can be, for example, homologous or eutectic mixtures of compounds, or using so-called“multibottle” systems, the constituents of which are themselves ready-to-use mixtures.

All temperatures, such as, for example, the melting point T(C,N) or T(C,S), the transition from the smectic (S) to the nematic (N) phase T(S,N) and the clearing point T(N,I) of the liquid crystals, are quoted in degrees Celsius.

All temperature differences are quoted in differential degrees.

In the present invention and especially in the following examples, the structures of the mesogenic compounds are indicated by means of abbre- viations, also referred to as acronyms. In these acronyms, the chemical formulae are abbreviated as follows using Tables A to D below. All groups

C _n H _2n+1 , C _m H _2m+i and C1H21+1 or C _n H _2n , C _m H _2m and C1H21 denote straight- chain alkyl or alkylene, , where n, m and I are 1 , 2, 3, 4, 5, 6 or 7. Table A lists the codes used for the ring elements of the core structures of the compounds, while Table B shows the linking groups. Table C gives the meanings of the codes for the left-hand or right-hand end groups. Table D shows illustrative structures of compounds with their respective

abbreviations.

Table A: Ring elements

 Table B: Linking groups

E -CH2CH2- Z -CO-O-

V -CH=CH- Zl -o-co-

X -CF=CH- O -CH2-0- XI -CH=CF- 01 -0-CH2- B -CF=CF- Q -CF2-O-

T -CºC- Ql -O-CF2- w -CF2CF2-

Table B: End groups

Left-hand side Right-hand side

Used alone

-n- CnH2n ₊ 1- -n -CnH2n ₊ 1

-nO- CnH2n ₊₁ -0- -On -0-CnH2n+1

-V- CH =CH- -V -CH=CH

-nV- CnH n ₊ i-CH=CH- -nV -CnH2n-CH=CH

-Vn- CH =CH- CnH ₂ n _+i - -Vn -CH=CH-CnH2n ₊₁

-nVm- CnH2n+i-CH=CH-CmH2m- -nVm -CnH2n-CH=CH-C, H2m+1

-N- NºC- -N -CºN

-S- S=C=N- -S -N=C=S

-F- F- -F -F

-CL- Cl- -CL -Cl

-M- CFH2- -M -CFH2

-D- CF2H- -D -CF2H

-T- CF ₃ - -T -CF ₃

-MO- CFH2O- -OM -OCFH2

-DO- CF2HO- -OD -OCF2H

-TO- CF3O- -OT -OCF ₃

-FXO- CF =CH-0- -OXF -0-CH=CF

-A- H-CºC- -A -CºC-H

-nA- CnH2n ₊₁ -CºC- -An -CºC-CnH2n+1

-NA- NºC-CºC- -AN -CºC-CºN

Used in combination with others

-...A...- -Cº- -...A... -Cº-

-...V...- -CH=CH- -...V... -CH=CH- F- in which n and m each denote integers, and the three dots are place holders for other abbreviations from this table. The following table shows illustrative structures together with their respec tive abbreviations. These are shown in order to illustrate the meaning of the rules for the abbreviations. They furthermore represent compounds which are preferably used.

Table C: Illustrative structures

The following illustrative structures are compounds, which are preferably additionally used in the media:

MGTU-nMm-S

PPG-n-S

CGG-n-S

PTU-n-S PTG(c3)TU-n-F GGP-n-F PGU-n-CL PGGP-n-m CPGU-n-OT APGP-n-m

The following table, Table E, shows illustrative compounds which can be used as stabiliser in the mesogenic media in accordance with the present invention. The total concentration of these and similar compounds in the media is preferably 5 % or less. Table E



In a preferred embodiment of the present invention, the mesogenic media comprise one or more compounds selected from the group of the com pounds from Table E.

The following table, Table F, shows illustrative compounds which can pref erably be used as chiral dopants in the mesogenic media in accordance with the present invention.

Table F

CM 44

 In a preferred embodiment of the present invention, the mesogenic media comprise one or more compounds selected from the group of the com pounds of Table F. The mesogenic media in accordance with the present application prefera bly comprise two or more, preferably four or more, compounds selected from the group consisting of the compounds from the above tables.

The liquid-crystal media in accordance with the present invention prefera bly comprise seven or more, preferably eight or more, compounds, preferably compounds having three or more, preferably four or more, different formulae, selected from the group of the compounds from Table D.

Examples

The following examples illustrate the present invention without limiting it in any way.

However, it is clear to the person skilled in the art from the physical prop erties what properties can be achieved and in what ranges they can be modified. In particular, the combination of the various properties which can preferably be achieved is thus well defined for the person skilled in the art. Mixture Examples

Liquid-crystal host mixture H1 having the compositions and properties as indicated in the following tables are prepared and characterized with respect to their general physical properties and their applicability in microwave components at 19 GHz and 20*0.

Mixture H1

BCH-3F.F 12.0 % T(N,I) = 92Ό BCH-5F.F 10.0 % Dh (20Ό, 589.3 nm) = 0.0969 ECCP-30CF3 5.0 % De (20Ό, 1 kHz) = 5.2

ECCP-50CF3 5.0 %

CBC-33F 2.0 %

CBC-53F 2.0 %

CBC-55F 2.0 %

PCH-6F 8.0 %

PCH-7F 6.0 %

CCP-20CF3 8.0 %

CCP-30CF3 12.0 %

CCP-40CF3 7.0 %

CCP-50CF3 1 1.0 %

PCH-5F 10.0 %

å 100.0%

A nematic liquid-crystal medium N1 consisting of 90% of the medium H 1 and 10% of the compound of Synthesis Example 1 (compound (1 )) has the following properties: N1 90.0 % T(N,I) 93 Ό

(1) 10.0 % Dh (20Ό, 589.3 nm) 0.1341 å 100.0 % De (20Ό, 1 kHz) 6.7

The compound (1 ) is well soluble in the medium H1. The addition of the compound (1 ) to the medium H1 has no negative influence in the properties of the host H1. The addition of the compound (1 ) to the medium H1 has the effect that the material quality h is significantly improved due to a higher tunability (t) and lower dielectric loss (tan de _,± ) of the medium, as shown in the following table.

Further mixtures are prepared and charactersied as follows:

Mixture N2

PTU-3-S 10.0 % T(N,i). [ ^* C]: 140.0 PTU-5-S 8.0 % Dh (589.3 nm, 20Ό): 0.3777

PGU-3-S 18.0 % De (1 kHz, 20Ό): 21 .8

PPTU-4-S 7.0 %

PPTU-5-S 9.0 %

PGTU-4-S 6.0 %

CPU-2-S 22.0 %

CPU-4-S 10.0 %

ThTU-5-S 10.0 %

å 100.0 %

Mixture N3

PTU-3-S 8.0 % T(N,I). [ ^* C]: 148.5 PGU-3-S 18.0 % Dh (589.3 nm, 20Ό): 0.3801 PPTU-4-S 7.0 % De (1 kHz, 20Ό): 21 .1

PPTU-5-S 9.0 %

PGTU-4-S 6.0 %

CPU-2-S 22.0 %

CPU-4-S 10.0 %

ThTU-5-S 10.0 % Thll-5-S 10.0%

å 100.0%

Mixture N4

PGU-3-S 18.0% T(N,i). [*C]: 151.0 PPTU-4-S 7.0 % Dh (589.3 nm, 20Ό): 0.3900 PPTU-5-S 9.0 % De (1 kHz, 20Ό): 21.1 PGTU-4-S 6.0 %

CPU-2-S 22.0 %

CPU-4-S 6.0 %

ThTU-5-S 16.0%

ThU-5-S 16.0%

å 100.0%