61/985,872 titled "SYNTHESIS OF NEW SMALL MOLECULES/OLIGOMERS WITH HIGH CONDUCTIVITY AND ABSORPTION FOR OPTOELECTRONIC APPLICATION" filed April 29, 2014. The entire contents of the referenced patent application are incorporated into the present application by reference.

[0002] The invention generally concerns small molecules and oligomers based on an anthradithiophene core combined with conjugated oligomer side groups comprising Group 16 elements sulfur, selenium, or tellurium, or combinations thereof. These compounds have electron rich and electron deficient regions and can be used in organic electronic applications.

Bo Description of Related Art

[0003] The search for more efficient and economically viable electronic devices is an ongoing process. This is especially the case for organic electronic applications (e.g., both photovoltaic and non-photovoltaic applications).

[0004] While conjugated organic polymers have found widespread use in organic electronic devices including organic light emitting diodes (OLEDs), organic photovoltaics (OPVs) and organic field effect transistors (OFETs), their small molecule/oligomer counterparts have not. One of the reasons for this is that polymers have continuous π- electron systems, and consequent electron-transport properties make them ideal candidates for a variety of electronic devices. Strategic chemical modification of different polymer moieties with varying electron-rich and electron-poor functionalities allows these electron- transporting molecules to be "tuned" for specific applications. [0005] Some of the potential issues with polymeric-based electronic devices, however, are that they are more complicated to make, more difficult to characterize, and more likely to fail (i.e., lack longevity of use) when compared with small-molecule or oligomer-based devices. Despite these issues with polymer-based electronics, the electronics industry continues to implement and develop the use of polymers in electronics to the detriment of small-molecule/oiigomer based electronics.

[0006] For instance, there are only a handful of small molecules and oligomers that have been demonstrated to lead to moderate-to-high efficiency OPV devices (efficiencies greater than 4%). One of the reasons for this is due to the challenges encountered in designing small molecules and oligomers with both the correct electronic and absorption characteristics and the ability to form nanoscale, phase-segregated, donor-acceptor pairings in the solid state. In terms of the required electronic properties, a suitable band gap is needed for absorption of a broad swath of the solar spectrum, proper alignment of energy levels for charge transfer to the donor or acceptor partner, and suitable (matching) charge carrier mobilities for the balanced transport and extraction of charge from the OPV device.

SUM ARY OF THE I VENTION

[0007] The present invention offers a solution to the aforementioned problems associated with both current polymer-based as well as small-molecule and oligomer-based electronics. The solution is premised on a donor-acceptor (D-A) when creating small molecules or oligomers of the present invention, which can be semiconducting or conducting molecules or oligomers. In particular, the small molecules and oligomers of the present invention have been shown to have low band gap semiconducting properties due to the presence of a deloeal zed π-electron system comprising electron-rich (donor) and electron- deficient (acceptor) units. The donor unit comprises an anthradithiophene core. The acceptor unit utilizes group 16 elements (S, Se, or Te, or any combination or all thereof— e.g., S and S, S and Se, S and Te, Se and Se and Se, Se and Te, or Te and Te, etc. ) to allow for improved light absorption properties and enhanced electronic properties, including increased charge carrier mobility. Further, the light absorption properties of the small molecules and oligomers of the present invention can be extended into the ultraviolet and near infrared regions of solar radiation, which allows for increased efficiency as well as fabrication of visibly transparent solar cells. Additional advantages of the small molecules and oligomers of the present invention include: straight forward synthesis, scalable reaction and purification

7 conditions; high degree of solubility in common organic solvents, thereby allowing for efficient solution-based processing during device fabrication; tunable electronic and optical properties via the presence of sulfur, selemum, or tellurium (or any combination or all thereof), which allows for the formation of hypervalent coordination complexes; and photo! minescence properties. Still further, the compounds and oligomers of the present invention can have an overall flat planar stmcture, which allows for acceptable conjugation lengths.

[0008] In one embodiment of the present invention, there is disclosed a compound havina the following staicture:

where one of X ¹ and Y is ( ^" 1 1 or ί 1 1- and the other is S, O, (Ί I■ or NR. ¹ ; one of and Y ² is -CH= or =CH- and the other is S, O, CH ₂ or R ¹ ; R ¹ is H or a linear or branched aliphatic group of up to 20 carbon atoms. R ² and R' can each independently be

or

R ⁴ can be

R ⁹ , R ^I0 , R ^U , R ¹² , R°, R ^{F 5} , R ⁵⁶ , R ¹ ', R ^IS and R ^I9 are each independently H, or a linear, branched or cyclic aliphatic, aryl or heteroaiyl group of up to 20 carbon atoms, with the proviso that both of R ⁶ and R are not H, both of R and R ^IU are not H, both of ^U and R ^IJ are not H, and both of R ¹⁵ and R ¹⁶ are not H; M ¹ , M ² , and M ^J are each individually S, Se, or Te; Li, L?, and L ₃ are each individually a coordination ligand bound to M ¹ , M ² , and M\ respectively, through a coordination bond, with q being an integer from 0 to 4; Zi, Z ₂ , Z ₃ , Z _4> Z ₅ and Z ₆ are each independently H, CI, Br, F, N0 ₂ , CN, N(¾2o)2, OR21, CF ₃ , or C ₆ H _Z E6. _Z , or Zi and Z ₂ or Z ₃ and Z ₄ or Z ₅ and Z ₆ are each N and are connected by a metal bridge atom to form, together with the carbon atoms to which they are attached, a 5 member ring system; R ₂ o and R ₂ i are each independently a linear, branched or cyclic aliphatic, aiyl or heteroaiyl group of up to 20 carbon atoms: z can be an integer from 0 to 5; and n can be an integer from 0 to 5. By way of explanation, the curved lines spanning the X ^f , C, and Y ^f atoms and the X ² , C, and Y ² atoms represent double bonds that can either be present between X' and C or C and Y ³ and between X and C or C and Y ² . In some particular instances, M ¹ is S and M ² is S, M ¹ is S and M ² is Se, or M' is S and M" is Te. In other instances, M ¹ is Se and M ² is Se or M' is Se and M ² is Te. In still other instances, M ¹ is Te and IVP is Te. Still further, the number and combination of group 16 elements (e.g., where at least 3 or more such elements are present in a given compound or polyme— M ^J , M ⁴ , M ⁵ , etc.) can be selected to achieve a desired result. Such a selection process allows for wider flexibility and tunability in obtaining desired band gaps. In one particular instance, the compound can have the following structure:

In still another aspect, the compound can have the following structure:

wherein M ^' is S, Se, or Te, and M ⁵ is S, Se, or Te, In another aspect, the compound can have the following structure:

In siili another embodiment, the compound can have the following stmcture:

yet another aspect, the compound can have one of the following structures

[0009] Any of the compounds of the present invention can be purified or isolated by techniques known to those of skill in the art (e.g., filtration, precipitation, steam distillation, distillation evaporation, sublimation, centiifugation, decantation, or the like). The purified or isolated compound can be in a dry or powdered form or can be stored within a liquid. The produced compound can be further modified with a dopant so as to enhance its p-type or n- type properties. The produced compounds can be conductive or semi-conductive compounds and can be used in such electronic applications and devices.

[0010] In another embodiment of the present invention, the compounds (e.g., small molecules and oligomers) of the present invention can be used in electronic applications. These compounds can be used in an active layer of an electronic device. The active layer can be an organic or hybrid semiconducting or conducting layer. The device can include a substrate, the photoactive layer, and at least two electrodes, one of which is transparent, wherein at least a portion or all of the photoactive layer is disposed between said electrodes. The transparent electrode can be a cathode and the other electrode can be an anode. Alternatively, the transparent electrode can be an anode and the other electrode can be a cathode. In some instances both of the aforementioned electrodes can be transparent. In other instances, one of the electrodes can be transparent while the other is non-transparent (e.g., opaque) or reflective, such that it can reflect electromagnetic radiation such as ultraviolet light or visible light or sun light. Still further, the substrate can be opaque, reflective, or transparent. In particular instances, the electronic device can be a photovoltaic cell or can include a photovoltaic cell. Said cell may not include an electrolyte. The photovoltaic cell can be designed such that it is a single active layer or bi-layer photovoltaic ceil . A bulk-heteroj unction layer can be produced by using the compounds of the present invention alone or in combination with known small molecule, oligomers, or polymers, or combinations thereof. The photovoltaic cell can be included in an organic electronic device. Examples of such devices include organic light-emitting diodes (OLEDs) (e.g., polymeric organic light-emitting diodes (PLEDs), small-molecule organic light-emitting diodes (SM- OLEDs), organic integrated circuits (O-ICs), organic field effect transistors (OFETs), organic thin film transistors (OTFTs), organic solar cell (O-SCs), and organic laser diodes (Q-iasers).

[0011] Also disclosed is a process for applying an organic or hybrid semiconducting or conducting layer on a substrate or an electrode, wherein the semiconducting or conducting layer comprises any one of the compounds of the present invention. The process can include disposing said semiconducting or conducting layer on said substrate or said electrode. The semiconducting layer can be photoactive. The conducting layer can be photoactive. The substrate can be rigid or flexible. The substrate can include an electrode and the photoactive layer can be disposed on said electrode. The substrate may not include an electrode, and the photoactive layer can be disposed on the substrate. The substrate can include an electrode and the photoactive layer can be disposed on the subsirate or the electrode or onto both. Deposition of said layer can be by spray coating, ultra sonic spray coating, roll-to-roil coating, drop casting, dip coating, Mayer rod coating, gravure coating, slot die coating, doctor blade coating, spin coating, meniscus coating, transfer printing, ink-jet printing, offset printing or screen printing process. Alternatively, deposition of said layer can be by vacuum deposition or organic vapor phase deposition (OVPD), solution precipitation, organic molecular beam deposition, or vacuum thermal evaporation (VTE). In preferred aspects, vacuum deposition is vacuum thermal deposition.

[0012] A linear aliphatic group is a substituted or un substituted, saturated hydrocarbon with no tertiary or quaternary carbons. Aliphatic group substituents include, but are not limited to halogen, hydroxy!, alkyoxy, haloalkyl, haloaikoxy, carboxyiic acid, ester, amine, amide, nitrile, acvi, thiol and thioether.

[0013] A branched aliphatic group is a substituted or nsubstituted, saturated hydrocarbon that includes at least one tertiary and/or quaternary carbon. Branched aliphatic group substituents include, but are not limited to alkyl, halogen, hydroxy!, alkyoxy, haloalkyl, haloaikoxy, carboxyiic acid, ester, amine, amide, nitrile, acyl, thiol and thioether. [0014] A cyclic aliphatic group is a substituted or unsubstituted, saturated, hydrocarbon that includes at least one ring in its structure. Polycyciic aliphatic groups may include fused, e.g., decalin, and/or spiro, e.g., spiro[5.5]undecane, polycyciic groups. Cyclic aliphatic group substituents include, but are not limited to aikyi, halogen, hydroxvl, alkvoxy, haloalkvl, haloalkoxy, carboxylic acid, ester, amine, amide, nitrile, acyl, thiol and thioether.

[0015] An aryl group is a substituted or unsubstituted, mono- or polycyciic hydrocarbon with alternating single and double bonds within each ring structure. Aryl group substituents include, but are not limited to alkvl, halogen, hydroxy!, alkyoxv, haloalkvl, haloalkoxy, carboxylic acid, ester, amine, amide, nitrile, acyl, thiol and thioether.

[0016] A heteroaryl group is a mono-or polycyciic hydrocarbon with alternating single and double bonds within each ring structure, and at least one atom within at least one ring is not carbon. Heteroaryl group substituents include, but are not limited to alky I, halogen, hydroxyl, alkvoxy, haioalkyl, haloalkoxy, carboxylic acid, ester, amine, amide, nitrile, acyl, thiol and thioether.

[0017] An aromatic group is a substituted or unsubstituted, mono- or polycyciic hydrocarbon with alternating single and double bonds within each ring structure. Aromatic group substituents include, but are not limited to alkyl, halogen, hydroxy!, alkyoxv, haioalkyl, haloalkoxy, carboxylic acid, ester, amine, amide, nitrile, acyl, thiol and thioether.

[0018] A hetero-aromatic group is a mono-or polycyciic hydrocarbon with alternating single and double bonds within each ring structure, and at least one atom within at least one ring is not carbon. Hetero-aromatic group substituents include, but are not limited to alkyl, halogen, hydroxyl, alkyoxv, haioalkyl, haloalkoxy, carboxylic acid, ester, amine, amide, nitrile, acyl, thiol and thioether.

[0019] An alkyl group is linear or branched, substituted or unsubstituted, saturated hydrocarbon. Alkyl group substituents may include, but are not limited to alkyl, halogen, hydroxyl, alk oxy, haioalkyl, haloalkoxy, carboxylic acid, ester, amine, amide, nitrile, acyl, thiol and thioether.

[0020] The term "about" or "approximately" are defined as being close to as understood by one of ordinary skill in the art, and in one non-limiting embodiment the terms are defined to be within 10%, preferably within 5%, more preferably within 1%, and most preferably within 0.5%.

[0021] The use of the word "a" or "an" when used in conjunction with the term

"comprising" in the claims or the specification may mean "one," but it is al so consistent with the meaning of "one or more," "at least one," and "one or more than one."

[0022] The words "comprising" (and any form of comprising, such as "comprise" and

"compri ses"), "having" (and any form of having, such as "have" and "has"), "including" (and any form of including, such as "includes" and "include") or "containing" (and any form of containing, such as "contains" and "contain") are inclusive or open-ended and do not exclude additional, unrecited elements or method steps.

[0023] The compounds and related processes of making and using said compounds, the photoactive layers, the photovoltaic cells, and the organic electronic devices of the present invention can "comprise," "consist essentially of," or "consi st of" particular ingredients, components, compounds, compositions, etc. disclosed throughout the specification. With respect to the transitional phase "consisting essentially of," in one non- limiting aspect, a basic and novel characteristic of the aforesaid compounds are their light absorption and charge carrier mobility properties.

[0024] Other objects, features and advantages of the present invention will become apparent from the following figures, detailed description, and examples. It should be understood, however, that the figures, detailed description, and examples, while indicating specific embodiments of the invention, are given by way of illustration only and are not meant to be limiting. Additionally, it is contemplated that changes and modifications within the spirit and scope of the invention will become apparent to those skilled in the art from this detail ed descripti on.

BRIEF DESCRIPTION OF THE DRAWINGS

[0025] FIG. It Illustration of an organic photovoltaic cell incorporating the small molecules or oligomers or polymers or all types of the present invention.

[0026] FIGS. 2A-B: Thermal ellipsoid plots of compound 6. FIGS. 3A-C: Scanning electron microscopy (SEM) images of QuIS-S crystals suspended on standard transmission electron microscopy (TEM) grids.

[0028] FIG. 4: XRD of QuIS-S prepared under different conditions.

[0029] FIGS. 5A-D: Atomic Force Microscopy (AFM) images showing the determination of thickness of films of QuIS-S and QuIS-Se on glass.

FIG. 6: UV-Vis spectra of both QuIS-S and QuIS-Se films.

FIGS. 7: Tauc plots for QuIS-S and QuiS-Se films.

[0032] FIG. 8: Ultraviolet photoelectron spectroscopy (UPS) for QuIS-S and QuIS-Se films.

FIG. 9i Proposed band diagram for both QuIS-S and QuIS-Se. FIG. 10: Illustration of a bilayer OPV using a QulS-S film and a PC71 BM film .

I-V curve using QuIS-S in a bilayer configuration with PC71 Illustration of PC71 BM and QuIS-S films intermingling to form

As explained above, the present invention offers a solution to the problems associated with current small molecules and oligomers that are used in organic electronic devices. The solution resides in the creation of small molecules or oligomers that have low band gap semiconducting properties due to the presence of a delocalized π-electron system that has an electron rich (donor) anthradithiophene core and an electron-deficien (acceptor) unit having group 16 elements such as sulfur, selenium, or tellurium. The compounds and oligomers have good light absorption and electronic properties, including increased charge carrier mobility.

[0038] These and other non-limiting aspects of the present invention are discussed in detail in the following sections. A. Semi-Conductive or Conductive Compounds

[0039] The compounds of the present invention can be prepared as small molecules or oligomers that contain a central electron rich monomelic unit (or electron donor unit) or units in instances where oligomers or polymers are concerned that have an electron rich monomelic unit that is connected to at least one or two comparatively electron deficient monomelic unit or units (or electron acceptor units) that feature group 16 heteroatoms of sulfur, selenium, or tellurium or combinations thereof. The compounds and oligomers can be semi-conductive or conductive. Larger units are also contemplated and can be prepared to achieve a desired compound or oligomer. Further each small molecule or oligomer can be terminated with a thiophene capping unit. In addition to the compounds prepared in the Examples, the following provides non-limiting schemes that can be used to prepare small molecules and oligomers of the present invention. Notably, the small molecules and oligomers can be modified with additional non-functional or functional groups as desired. Further the small molecules and oligomers can be soluble in common organic solvents, examples of which are provided below, and are stable for extended periods of time under ambient conditions.

L Electron Acceptor Units

[0040] The following reaction scheme 1 illustrates a non-limiting process to make monomeric electron acceptor units that can be used with the small molecules and oligomers of the present invention:

Referring to Scheme 1, excess (5-10) of equivalent Na[BH ₄ ] can be used to synthesize compound A. In preferred embodiments, compounds B L B2, B3 are attached directly to an electron donor unit by using the processes described throughout this specification or processes known to those of ordinary skill in the art. However, each of compounds B l, B2, and B3 can be linked together to create small oligomers (e.g., the oligomers contain up to 5 monomelic units (i.e., n can be an integer of L 2, 3, 4, or 5 or more). This oligomerization step can be performed by using well established coupling reactions such as Suzuki coupling where compounds B l, B2, and/or B3 are coupled with a boronic acid or boronic ester containing moiety. The desired coupling reaction can also be carried out using Stilie coupling when compounds B l, B2, and/or B3 are reacted with a tin containing organic moiety to produce compounds B4, B5, and B6

, and

[0041 ] The produced Bl, B2, B3, B4, B5, and B6 compounds can then be used in reaction scheme 2 to obtain thiophene end units or caps:

Reaction Scheme 2

Referring to scheme 2, the reaction can be performed under Suzuki coupling reaction conditions and the catalyst Pd(P! ³ h ;) ;. solvent (toluene) and activator (Na ₂ C0 ₃ ) can vary depending on the reaction. In some cases, different sets of catalysts, solvents and activators can be used. Also the percentage of product formation can change by modifying these parameters. Alternatively, the small molecule or oligomer can be terminated with an aromatic, hetero-aromatic, or alkyl functional group rather than with a thiophene capping unit. The R ⁹ , R ¹ , R ^l \ R ¹² , R ^lj , and Z ¹ and Z ² groups are defined above in the summary of the invention section and in the claims, the definitions of which are incorporated into this section by reference. The CI , C2, C3,€4, C5, and C6 compounds can then be covalently linked to an electron donor unit.

2, Electron Donor Units

[0042] Reaction scheme 3 provides a non-limiting process to make an electron donor unit that can be used with the molecules and oligomers of the present invention.

Reaction Scheme 3

The X ¹ and Y ¹ groups can be switched with the aforementioned X ² and Y to obtain compounds D3 and D4, respectively, with D3 having a single Br group and D4 having two Br groups. Additionally, the Br? and acetic acid can be used in excess of the stoichiometric amount to synthesize compounds Dl, D2, D3, and D4. Any one of, or any combination of, Dl, D2, D3, and D4, can then be reacted with 1,4-cyclohexanedione and an ethanol solution of KOH under room temperature conditions (20 to 25 °C) and mixed until the reaction is complete (e.g., about 2 to 4 hours). In preferred embodiments, Dl and D3 can be used. The amounts of Dl , D2, D3, D4, 1,4-cyclohexanedione, and the ethanol solution of KOH can be varied as needed to produce a desired amount of the following compound D5. This is illustrated in reaction scheme 4:

Alternatively, compound D6 can be prepared according to the following reaction scheme 5:

Either one of D5 or D6 can be used in the following reaction scheraes 6 and 7, respectively, to produce compounds D7 and D8:

and

[0043] Referring to reaction schemes 6 and 7, the n~BuLi can be added to the R ^; R ^* substituted acetylene compound and heated (e.g., about 60 °C) for a sufficient period of time (e.g., about 1 hour) to form a reaction mixture. Subsequently, the mixture can be cooled to room temperature and compound D5 or D6 can be added under a nitrogen stream and heated (e.g., about 60 °C) for a sufficient period of time (e.g., about 12 hours). Subsequently, the reaction mixture can be cooled to room temperature and a solution of stannyl chloride hydrate in a 10% HCl solution can be added. The reaction mixture can then be heated (e.g., about 60 °C) for a sufficient period of time (e.g., about 2 hours) to produce compounds D7 and D8, respectively. The compounds can be purified via filtration through a silica gel flask column using hexane as an eluent.

[0044] Additionally, either of compounds D7 and D8 can be further used to produce compounds D9 and D10, respectively under the following reaction scheme 8 (notably, D7 and D8 are identical to D9 and D10, respectively, when rs is 1):

Reaction Scheme 8

The above reaction can be performed by deprotecting and removing R ² and R ^' using tetrabutyl ammonium fluoride or CsF or KF to form alkyne functionality, followed by Cu catalyzed coupling reaction. The general non-limiting reaction conditions can include: 5mol% Cul or Cu(OAc)2, tri ethyl amine solvent,€b. Both steps can be peiformed separately or i one pot. [0045] Compounds D7, D8, D9, or D10 can then be placed in THF and reacted in the presence of lithium di-isopropyl amide (LDA) at a sufficiently cold temperature (e.g., about - 78 °C) for a sufficient period of time (e.g., about 1 hour) to produce a reaction mixture. Subsequently, trimethyitin chloride can be added to the reaction mixture at approximately the same temperature and then gradually warmed to room temperature under continuous stirring for a sufficient period of time (e.g., about 12 hours) to obtain compound Dl l, where n is from 1 to 5. Reaction scheme 9 illustrates this:

3, Attachment of the Electron Acceptor and Donor Units

[0046] Each of the produced electron acceptor and donor units can then be covalently linked together to form a variety of compounds (i.e., small molecules and oligomers) of the present invention. The covalent linkage can be made by reacting the bromine group on the electron donor unit with the trimethyitin group(s) present on the electron donor unit by using the following reaction conditions. A microwave glass tube can be charged with compound C (e.g., C I , C2, C3, C4, C5, or C6 or combinations thereof), compound D (e.g., Dl l ), iVii'P h ;) : and dry THF. The glass tube can be sealed with a Teflon® cap and stirred at room temperature following by heating the reaction mixture in a microwave to form covalent links between the electron acceptor (C) and electron donor (D) units. This is illustrated in reaction scheme 10:

As noted in a non-limiting aspect, the stirring step can be for a sufficient period of time (e.g., about 15 minutes) at room temperature conditions (20 to 25 °C), and the heating step can be performed in stages (e.g., about 100 °C for 2 minutes, followed by 125 °C for 2 minutes, followed by 140 °C for 10 minutes, followed by 150 °C for 10 minutes, followed by 160 °C for 20 minutes, followed by 170 °C for 30 minutes. ).

[0047] Additionally, coordination complexes can be formed between the sulfur, selenium and tellurium atoms (i.e., M groups) on the compounds of the present invention with a coordination ligand, such as CI, Br, I, a linear, branched or cyclic aliphatic, aryl or heteroaryl group of up to 20 carbon atoms. The formation of these coordination complexes can be used to increase the charge carrier mobility of the compounds of the present invention and further enhance their tunability for use in electronic devices.

[0048] The following includes non-limiting compounds of the present invention that can be made by utilizing the aforesaid reaction schemes, in which the various M, R, X, Y, and n groups and integers are those that have been previously defined in the summary of the invention section and claims of the specification:

Organic Photovoltaic Cells

The small molecules and oligomers of the present invention can be used in photovoltaic applications, such as organic photovoltaic cells. FIG. 1 is a cross-sectional view of a non-limiting organic photovoltaic cell of the present invention, in which the photoactive layer is formed with the small molecules or oligomers of the present invention, or combinations thereof. Notably, polymers do not have to be used to form said photoactive layer. However, and if desired, polymers can be used in combination with the disclosed small molecules or oligomers. The organic photovoltaic cell ( 1 ) can include a transparent substrate (10), a front electrode (1 1), a photoactive layer (12), and a back electrode (13). Additional materials, layers, and coatings (not shown) known to those of ordinary skill in the art can be used with photovoltaic cell (1), some of which are described below.

)] Generally speaking, the organic photovoltaic cell (1) can convert light into usable energy by: (a) photon absorption to produce excitons; (b) exciton diffusion; (c) charge transfer; and (d) charge separation and transportation to the electrodes. With respect to (a), the excitons are produced by photon absorption by the photoactive layer (12), which can be a single layer such that the compounds of the present invention are the active light absorbing component in the layer. In preferred aspects, and given that the compounds of the present invention have both electron donor and acceptor regions, the preferred layer ( 12) is a bulk heteroj unction single layer. However, multiple layers are also contemplated in the context of the present invention (e.g., a bi-iayer, tri-layer, or multiple-layer staking or bulk heteroj unction layers). For (b), the generated excitons diffuse to the p-n junction. Then in (c), the charge is transferred to the other constituent of the BHJ. For (d), electrons and holes are separated and transported to the electrodes (11) and (13) and are used in a circuit. 1. Substrate (10)

[0051 ] The substrate (10) can be used as support. For organic photovoltaic cells, it is typically transparent or translucent, which allows light to efficiently enter the cell. It is typically made from material that is not easily altered or degraded by heat or organic solvents, and as already noted, has excellent optical transparency. Non-limiting examples of such materials include inorganic materials such as alkali-free glass and quartz glass, polymers such as polyethylene, PET, PEN, polyimide, polyamide, polyamidoimide, polycarbonate (e.g., Lexan™, which is a polycarbonate resin offered by SABIC Innovative Plastics), liquid crystal polymer, and cycloolefin polymer, silicon, and metal.

2. Front Electrode and Back Electrodes (11) and (13)

[0052] The front electrode (1 1 ) can be used as a cathode or anode depending on the set-up of the circuit. It is stacked on the substrate (10). The front electrode (1 1 ) can be made of a transparent or translucent conductive material. Alternatively, the front electrode (1 1) can be made of opaque or reflective material. Typical ly, the front electrode (1 1 ) is obtained by forming a film using such a material (e.g. , vacuum deposition, sputtering, ion-plating, plating, coating, etc.). Non-limiting examples of transparent or translucent conductive material include metal oxide films, metal films, and conductive polymers. Non-limiting examples of metal oxides that can be used to form a film include indium oxide, zinc oxide, tin oxide, and their complexes such as indium stamiate (ITO), fluorine-doped tin oxide (FTO), and indium zinc oxide films. Non-limiting examples of metals that can be used to form a film include gold, platinum, silver, and copper. Non-limiting examples of conductive polymers include polyaniline and poiythiophene. The thickness of the film for the front electrode (1 1) is typically between from 30 to 300 nm. If the film thickness is less than 30 nm, then the conductivity can be reduced and the resi stance increased, which results in a decrease in photoelectric conversion efficiency. If the film thickness is greater than 300 nm, then light transmittance may be lowered. Also, the sheet resistance of the front electrode (11) is typical ly Ι ΟΩ/D or less. Further, the front electrode (1 1 ) may be a single layer or laminated layers formed of materials each having a different work function.

[0053] The back electrode (13) can be used as a cathode or anode depending on the set-up of the circuit. Thi s electrode (13) can be made of a transparent or translucent conductive material. Alternatively, it (13) can be made of opaque or reflective material . This electrode (13) can be stacked on the photoactive layer (12). The material used for the back electrode (13) can be conductive. Non-limiting examples of such materials include metals, metal oxides, and conductive polymers (e.g., polyaniiine, polythiophene, etc.) such as those discussed above in the context of the front electrode (1 1 ). When the front electrode (1 1) is formed using a material having high work function, then the back electrode (13) can be made of material having a low work function. Non-limiting examples of materials having a low work function include Li, In, Al, Ca, Mg, Sm, Tb, Yb, Zr, Na, K, Rb, Cs, Ba, and the alloys thereof The back electrode (13) can be a single layer or laminated layers formed of materials each having a different work function. Further, it may be an alloy of one or more of the materials having a low work function and at least one selected from the group consisting of gold, silver, platinum, copper, manganese, titanium, cobalt, nickel, tungsten, and tin. Examples of the alloy include a lithium-aluminum alloy, a lithium-magnesium alloy, a lithium-indium alloy, a magnesium-silver alloy, a magnesium-indium alloy, a magnesium- aluminum alloy, an indium-silver alloy, and a calcium-aluminum alloy. The film thickness of the back electrode (13) can be from 1 to 1000 nm or from 10 to 500 ran. If the film thickness is too small, then the resistance can be excessively large and the generated charge may not be sufficiently transmitted to the external circuit.

[0054] In some embodiments, the front (11 ) and back (13) electrodes can be further coated with hole transport or electron transport layers (not shown in FIG. 1) to increase the efficiency and prevent short circuits of the organic photovoltaic cell (1). The hole transport layer and the electron transport layer can be interposed between the electrode and the photoactive layer (12). Non-limiting examples of the materials that can be used for the hole transport layer include polythiophene-based polymers such as PEDOT/PSS (poly (3,4- ethylenedioxythiophene)-poly(styrene sulfonate)) and organic conductive polymers such as polyaniiine and polypy rrole. The film thickness of the hole transport layer can be from 20 to 100 nm. If the film thickness is too low, short circuit of the electrode can occur more readily. If the film thickness is too high, the film resistance is large and the generated electric current could be limited and optical conversion efficiency can be reduced. As for the electron transport layer, it can function by blocking holes and transporting electrons more efficiently. Non-limiting examples of the type of material that the electron transport layer can be made of include metal oxides {e.g., amorphous titanium oxide). When titanium oxide is used, the film thickness can range from 5 to 20 nm. If the film thickness is too low, the hole blocking effect can be reduced and thus the generated excitons are deactivated before the excitons dissociate into electrons and holes. By comparison, when the film thickness is too high, the film resistance is large, the generated electric current is limited, resulting in reduction of optical conversion efficiency.

3, Photoactive Layer (12)

[0055] The photoactive layer (12) can be an organic or hybrid semiconducting or conducting layer. The layer (12) can he interposed between the front electrode (10) and the back electrode (13). In one preferred instance, the photoactive layer (12) can be a bulk hetero-j unction single layer such that the compounds of the present invention are the active light absorbing component in the layer. The layer (12) can absorb light and allow for the flow of electrons to and from the electrodes (1 1 and 13 ). Further, there can be multiple photoactive layers used for a given photovoltaic cell (e.g., 2, 3, 4, or more).

[0056] Given the unique properties of the compounds (i.e., small molecules and oligomers) of the present invention, many options are available for forming the photoactive photoactive layer (12) on at least a portion of a surface of the electrodes (11 and 13) or on the substrate (10) or both. By way of example, vacuum thermal evaporation, which involves the heating of an organic material in vacuum and depositing said material, or organic vapor phase deposition, which involves evaporation of the organic material over a substrate in the presence of an inert carrier gas, can be used. However, the increased solubility of the compounds of the present invention also allows for the formation of a solution that can then be deposited onto said surfaces. In particular, the compounds of the present invention can be fully or partially solubilized within a solution and then deposited onto a given surface via solution-based deposition techniques (e.g., spray coating, role-to-role coating, drop casting, dip coating, Mayer rod coating, doctor blade coating, spin coating, meniscus coating, transfer printing, ink jet printing, offset printing, screen printing, gravure printing, flexo printing, dispenser coating, nozzle coating, capillar} _' coating, etc.). Non-limiting examples of solvents that can be used in the context of the present invention include unsaturated hydrocarbon- based solvents (such as toluene, xylene, tetralin, decalin, mesitylene, n-butylhenzene, sec- butylbutylbenzene, and tert-butylbenzene), halogenated aromatic hydrocarbon-based solvents (such as chlorobenzene, dichiorobenzene, and trichlorobenzene), halogenated saturated hydrocarbon-based solvents (such as carbon tetrachloride, chloroform, dichloromethane, dichloroethane, chlorobutane, bromobutane, chlo opentane, chlorohexane, bromohexane, and chlorocyclohexane), ethers (such as tetrahydrofuran and tetrahydropyran), and polar aprotic solvents (such as dichloromethane (DCM), tetrahydrofuran (THF), ethyl acetate, propyl acetate, butyl acetate, isobutyl acetate (and the like), acetone, dimethylformamide (DMF), acetonitrile (MeCN), benzonitrile, nitromethane, dimethyl sulfoxide (DMSO), propylene carbonate, or -met.hyl-2-pyrrolidone (NMP), sulfolane (tetramethylene su!fone, 2,3,4,5- tetrahydrothiophene- 1, 1 -dioxide), hexamethylphosphoramide (HMPA), methyl ethyl ketone, methyl isobutyl ketone, acetophenone, benzophenone, or the like), or any combination of said solvents.

[0057] The present invention will be described in greater detail by way of specific examples. The following examples are offered for illustrative purposes only, and are not intended to limit the invention in any manner. Those of skill in the art will readily recognize a variety of noncritical parameters which can be changed or modified to yield essentially the same results.

1

(Synthesis of 2,8~Bis(5~fluoro~7-(5'~hexyi~[2,2'~^^

l,2,5]thiadiazole)-5 1-Bis(triisopro and 2,8-Bi$(5-fli5oro-7-(5'-hexy!-[2,2 >ithM

(tnisopropylsHyiethynyl)anthra[2,3-b:7,6~b']dithiophene)

[0058] Synthesis of 5-Bromo-2,3-thiophenedkarboxaIdehyde (1 ): Bromine (6.0 mL, 1 16.3 mrnol) was added drop wise at room temperature to a solution of 2,3- thiophenedicarboxaldehyde (5.1g, 36.38 mmol) in 100 mL of CHCI ₃ . The reaction mixture was stirred overnight and then excess bromine was quenched with a saturated solution of a ₂ S ₂ 0 ₃ . The organic layer was extracted with CHCL, dried over Na ₂ SO, _¾ and volatiles were removed in vacuo to obtain 1 as a brown solid. Spectroscopicaily pure compound was isolated by column chromatography using silica gel as stationaiy phase and a 4: 1 mixture of

CH7CI7 :hexanes. 1H NMR (500 MHz, CDC1 ₃ ): 61 0.37 (s, 1H), 10.26 (s, 1H), 7.59 (s, 1H).

[0059] Alternate procedure for the synthesis of 5~Bro o-2,3-thiophenedi~ carboxaldehyde (1 assd 2): Bromine (1.2 mL, 7.5 mmol) was added drop wise to a solution of 2,3-thiophenedicarboxaldehyde (1.0 g, 7.1 mmol) in 20 ml, of glacial acetic acid. The reaction mixture was stirred overnight at 70 °C and then excess bromine was quenched with a saturated solution of a ₂ S ₂ 0 ₃ . The organic layer was extracted with CH ₂ C1 ₂ , dried over Xa -SO i and volatiles were removed in vacuo to obtain a mixture of 1 and 4,5~dibromo-2,3- thiophenedicarboxaldehyde 2 as a brown solid (30:65 by ^l H NMR spectroscopy). Spectroscopically pure compound was isolated by column chromatography using silica gel as stationary phase and a 4: 1 mixture of C¾C! ₂ :hexanes. ^' Ί NMR (500 MHz, CDC1 ₃ ): δ 10.37 is, 1H), 10.26 (s, 1H), 7.59 (s, 1H). 1H NMR data for 4,5-dibromo-2,3- thiophenedicarboxaldehyde (500 MHz, CDC1 ₃ ): δ 9.81 (s, i l l ). 7,36 is. 1H).

[0060] Synthesis of 2,8-dibromoaiithradithiophenequinones (3): To a mixture of 1

(2.0 g, 9.18 mmol) and 1 ,4-cy clohexanedione (50 mg, 0.46 mmol) 10 mL of ethanol was added and afterwards an ethanol solution of OH ( 15%, 0.5 ml,) was added to the reaction mixture. The resulting brown slurry was stirred at room temperature for 3 hours and then filtered and washed with ethanol to obtain 3 as a pale brown powder.

[0061] Synthesis of Anihra 2,3-b:6,7-b']dithiophene-5,ll-dione and Anthra] ^" 2,3- b:7,6~b']dithiophene-5,n-dione (4); To a solution of thiophene-2,3-dicarboxaldehyde (2.0 g, 1 7.2 mmol ) in 200 mL of EtOH was stirred at room temperature followed by addition of 1 ,4-cy clohexane dione (0.96 g, 8.6 mmol). Afterwards, a solution of 15% KOH was added to the reaction mixture to form brown precipitate. The resulting reaction mixture was stirred for an additional 3h and then filtered to obtain a pale yellow powder in quantitative yield. Compounds 4 and 6 could not be characterized due to their poor solubility in common organic solvents, HR-mass spectroscopy confirmed formation of the products.

[0062] Synthesis of 5,1 i-Bis(irHsopropy!si!yiethyny!)aiiihrax 2,3~b:6,7~ b ^' jdithiophene asid 5,ll-Bis(triisopropylsiiyleihynyI)anthraxj ^" 2,3-b:7,6-b' ^' Sdiihiophene (5): nBuLi (7.8 mL, 1.6 M solution in hexanes) was added drop wise to triisopropysilylacetylene (2.95 mL, 13.2 niniol) and then heated at 60 °C for 1 hour. After cooling the reaction mixture to room temperature, compound 4 was added under nitrogen stream and heated overnight at 60 °C to obtain a dark brown solution. Afterwards, a solution of stannyl chloride dehydrate (3.0 g, 13.8 mmol) in 10% HQ solution was added and heated again to 60 °C for 2 hours to yield a dark pink solution. The crude product was obtained after filtering through a silica gel flash column using hexanes as eluent. Spectroscopically pure 5 was isolated as dark red crystals after reerystallization from hexanes at 35 ^C C in 38% yield.

[0063] Synthesis of 2,8~Bis(trimethylstannyl)~5,l l~Bis(triisopropyisi!ylethynyi)- aiiihra 2,3~b:6,J~b']dit ophe55e and 2,8-Bis(inmethyistannyI)-5,l.l-Bis(inisopropylsiIy!~ ethyny!)antfara[2^~b:7,6 )']diihiophene (6): To a cold (-78 °C) solution of compound 5, (1.0 g, 1.54 mmol) in 15 mL of dry THF was added LDA (1.6 mL, 2 M solution in THF) and stirred at that temperature for 1 hour. Afterwards, trimethyltin chloride (3.4 mL, 1 M solution in THF) was added to the reaction mixture drop wise at -78 °C, then warmed gradually to room temperature and stirred overnight. After quenching the reaction with water organic layer was extracted with hexanes, dried over Na ₂ S0 ₄ and volatiles were removed to obtain 95% pure 6 as red powder. Crystals suitable for X-ray crystallography were obtained by reerystallization from hexanes at -35 °C. ^l ll NMR (500 MHz, CDC1 ₃ ): δ 9.19 (m, 2H), 9.10 (m, 21 ! }. 7.50 (s, 21 1. 3JSnH === ^: 29.5 Hz), 1.32 (m, 42! I s. 0.49 (s, 18H). 13C (1 H) (500 MHz, CDCI ₃ ): δ - 8,4 (Sn(CH ₃ ) ₃ ), 1 1.7 (CH(CH ) ₃ ), 19.1 (Π !i Ci S : ) .5, 104.5 (CC-Si), 105.5 (-CC), 1 16.4 (ArC), 117.7 (ArC), 118.9 (ArC), 120.1 (ArC), 129.6 (ArC), 129.8 (ArC), 129.9 (ArC), 130.2, (ArC), 131.7 (ArC), 141.2 (ArC), 141.3 (ArC), 143.1 (ArC), 143.2 (ArC), 145.9 (ArC), 146.1 (ArC). 119Sn NMR (185 MHZ, CDCI ₃ ): δ -23.7. LR MALDI, Calculated for C ₄₆ H ₆₆ S ₂ Si ₂ Sn ₂ : 976[M+]. Anal , calculated for C ₄₆ H ₆₆ S ₂ Si ₂ Sn ₂ : C, 56.57; H, 6.81 ; S, 6.57. Found: C, 56.89; H, 6.93; S, 6.18.

FIGS. 2 A. and B provide two different view of thermal ellipsoid plots of compound 6.

[0064] Synthesis of 2,8-Bis(5~fluoro-7-(5 ^, ~hexyI~ 2,2 ^, ~bithiopheiie]~5~yI)besizo[c]~ l,2,5jifoiadiazok)~5 i }is(ir¾ and 2,8~Bis(5-fluoro~7-(5'-faexyH2,2'~bit

(inisopropylsilyieihyny^anihraP^-bjT^-fo'Jdithiophene (8): A 20 mL microwave glass tube was charged with 7 (196 nig, 0.41 miiiol), 6 (200 nig, 0.2 nimol), Pd(PPh ₃ ) ₄ (15 mg, 0.01 3 mmol) and 15 mL dry Π IF. The glass tube was sealed with a Teflon© cap and stirred at room temperature for 15 minutes. Afterwards, the reaction mixture was heated to 100 °C for 2 minutes, 125 °C for 2 minutes, 140 °C for 10 minutes, 150 °C for 12 minutes and 160 °C for 15 minutes in a Biotage microwave reactor. After cooling the reaction mixture to room temperature, the crude product mixture was then added to a aqueous solution of sodium diethyldithiocarbamate (1 g/lQO mL) and stirred for 12 hours at room temperature. Afterwards, the organic layer was separated and volatiles were removed to obtain crude product as a dark brown powder. Compound 8 was purified by washing with toluene, dichloromethane and methanol (278 mg, 70%). NMR studies are incomplete due to insolubility of 7 in common organic solvents (only dissolves in dichlorobenzene at 170 °C ). LR MALDL calculated for CeoHwFii SeSa: 1,450 [M+], Anal, calculated for C ₈ oHg4F ₂ N ₄ S ₈ S _i2 : C, 66.16; I I 5.83; N, 3.86; S, 17.66. Found: C, 63.29, H, 5.56; N, 3.61 ; S, 18.01. Compound 8 is highly crystalline and forms wire like structure during the reaction probably due to the presence of strong intermolecular π-π stacking.

Example 2

(Synthesis of 2,8~Bis(5~fliioro~7-(5'~hexyl~[2,2'~bithiophesie]~5~yl)beiiz o c.]- l,2,5]seIeiio- diazo!e)-5,l l-bis(iriisopropyIsiIy!eihynyI)anthra[2,3-b:6,7-b'jdithiophe ne and 2,8-Bis(5- fluoro-7-(5'~hexyi- 2,2'-bithiophene]^

(triisopropylsilyiethynyl)anihra[2,3~b:7,6-b'jdithiophene (10))

[0065] Synthesis of 10: A 20 mL microwave vial was charged with 9 (216 mg, 0.41 mmoi), 6 (200 mg, 0.2 mmol ), Pd(PPh ₃ ) ₄ ( 15 mg, 0.013 mmol) and 15 mL of dry TFTF. The glass tube was sealed with a Teflon® cap and stirred at room temperature for 15 minutes. Afterwards, the reaction mixture was heated to 100 °C for 2 minutes, 125 °C for 2 minutes, 140 °C for 10 minutes, 150 °C for 10 minutes, 160 °C for 20 minutes and 170 °C for 30 minutes in a Biotage microwave reactor. After cooling the reaction mixture to room temperature, the crude product mixture was then added to a aqueous solution of sodium diethyldithiocarbarnate (1 g/100 mL) and stirred for 12 hours at room temperature. Afterwards, the organic layer was separated and voiatiles were removed to obtain crude product as a dark brown powder. The crude material was washed with a mixture of CH?Cl?/hexanes (5: 1, 4 - 30 mL) to obtain pure 10 as a dark brown powder (210 mg, 54%). NMR studies are incomplete due to insolubility of 9 in common organic solvents. LR MALDI, calculated for C _S0 i½F ₂ N ₄ S ₆ Se ₂ Si ₂ : 1546.1 [M+l]. Anal, calculated for ( iK ii ;\ _; S,' _; e :S -: C, 62.15; H, 5.48; N, 3.62; S, 12.44. Found: C, 62.04; H, 5.44; N, 3.62; S, 12.41. HRMS (MALDI-TOF), Calculated for C» l lk J- _. -N i Si.Se .Sl· . 1546.2870 [M+], found 1546.2850.

(Data Concerning Compounds 8 and 10)

[0066] Crystal Structure: Compound 8 has a crystalline structure as suggested by the uniform and linear staictures viewed by scanning electron microscope (SEM) and X-ray diffraction (XRD) patterns, illustrated in FIGS. 3 and 4, respectively.

[0067] Solsibility: Compounds 8 and 10 were screened with a variety of polar and non-polar solvents to try to dissolve the compounds. No dissolution occurred. It was discovered that heating the compounds in dichlorobenzene to 160 to 165 °C, without stirring, iiiduced the formation of a dark transparent solution that could be used to produce coherent films with the compounds. The FIG. 4 XRD spectra refer to three situations: (i) "Solution" refers to getting the compounds to solubilize prior to casting a film (165 °C, no stirring); (ii) "Stirred" refers to stirring the solution without heating and prior to casting of a film; and (iii) "Suspension" refers to the addition of a solvent without any noticeable dissolution of the compound. A difference in the higher 2 theta values in FIG. 4, near 25°, is suggestive of a hypothesized switch between a molecule with a Cy-symmetric rotation axis, and one without a rotational axis. The compounds 8 and 10 have the C ₂ - rotation axis.

[0068] Film Formation on Glass Substrate: FIG, 5 illustrates atomic force microscopy (ATM) images of films formed from compounds 8 (QuIS-S) and 10 (QuIS-Se) on a glass substrate. The films were cast from a solution of 5 mg/ml of compounds 8 and 10, respectively, in dichiorobenzene at 165 °C. FIG. 6 provides UV-Vis spectra of the compound QuIS-S and QuIS-Se films. The glass background has been subtracted and the absorbance normalized in FIG. 6. Once smooth and relatively defect-free films were prepared via the higher temperature odichlorobenzene processing to yield a solution, the thickness can be controlled, and thus electronic properties can be measured with accuracy. Tauc plots in FIG. 7 of the QuIS-S and QuIS-Se films illustrate the presence of direct arid indirect band gaps. For QuIS-S, the gaps are 1.32 eV for the indirect, and 1 .56 eV for the direct gap, whereas with QuIS-Se, the gaps are 1.26 eV for the indirect, and 1.50 eV for the direct gap. FIG. 8 provides ultraviolet photoelectron spectroscopy (UPS) for both films. The top two plots show the measurements from a work function scan, while the bottom two plots show the values of the valence band scan. FIG. 9 provides a proposed band diagram for both films, based upon the data from the Tauc plots and known values for ΠΌ, PEDOT:PSS, PC71BM, and LiF/Al .

[0069] Bi- Layer Electronic Device: FIG, 10 illustrates a produced bilayer OPV with a QuIS-S film and a PC71BM film. Table 1 provides data concerning the produced OPV:

Table 1

FIG. 1 1 provides I-V curve illustrating the best results obtained using the QuIS-S film in a bilayer configuration with a PC71 BM film . [0070] Proposed Bulkheterojunction (BHJ) Electronic Device: FIG. 12 provides an illustration of a PC7IBM and QuIS-S bulkheterojunction (BHJ) electronic device that could be prepared in the context of the present invention.