Conductive and photosensitive polymers

Abstract

The present invention relates to newly functionalized polythiophenes and the syntheses thereof. The present invention also demonstrates that the new polythiophenes and their derivatives are suitable for fabricating organic light emitting diodes (OLEDs), light emitting diodes (PLEDs), organic photovoltaic devices (OPVs) and conducting polymers for printed electronic devices.

Claims

1. A compound of formula Ic, comprising: ##STR00042## wherein X is selected from the group consisting of hydrogen, bromine, chlorine, and methyl group; m is equal or greater than one; k is equal to or greater than one; n is equal to or greater than one; R* is selected from the group consisting of ethanol, substituted ethanol, ethyl formate, substituted ethyl formate, ethoxy silane, and substituted ethoxy silane; and R is hydrogen or alkyl chain comprising C.sub.6H.sub.13, C.sub.8H.sub.17, and C.sub.12H.sub.25.

2. A compound of formula Id, comprising: ##STR00043## wherein X is selected from the group consisting of hydrogen, bromine, chlorine, and methyl group; k is equal to or greater than one; n is equal to or greater than one; R is NR.sup.1R.sup.2 or an alkoxy group, said alkoxy group is further selected from the group consisting of ethanol, substituted ethanol, ethyl formate, substituted ethyl formate, ethoxy silane, and substituted ethoxy silane, and wherein R.sup.1 and R.sup.2 are independently selected from the group consisting of hydrogen, aldehyde, acid chloride, acid bromide, and isocyanate.

3. A composition comprising at least a compound according to claim 1 or 2 admixed with a solvent.

4. The composition according to claim 3, wherein said solvent comprises an organic solvent selected from the group consisting of acetone, acetonitrile, tetrahydrofuran, ethyl acetate, toluene, benzene, methanol, ethanol, 1-propanol, iso-propanol, DMSO, DMF, and halogenated hydrocarbon solvent.

5. The composition according to claim 4, wherein said solvent further comprises water.

6. A conductive polymer comprising at least a compound according to claim 1 or 2.

7. A solution comprising at least a compound according to claim 1 or 2, wherein said solution is adapted for using or making a thin film on a substrate.

8. The solution according to claim 7, wherein said solution is adapted for fabrication of a layer by using spin coating process or roll-to-roll process; wherein said layer is selected from the group consisting of a thin layer on a LED device as an active layer, a conductive layer for thermal management, and an active light absorption layer on an organic photovoltaic solar device.

9. An ink formulation comprising at least a compound according to claim 1 or 2, wherein said ink formulation is adapted for using or making a thin film on printed electronic devices.

10. The ink formulation according to claim 9, wherein said ink formulation is adapted for fabrication of a layer by using spin coating process or roll-to-roll process; wherein said layer is selected from the group consisting of a thin layer on a LED device as an active layer, a conductive layer for thermal management, and an active light absorption layer on an organic photovoltaic solar device.

Description

BRIEF DESCRIPTION OF FIGURES

(1) FIG. 1 shows the fabrication process for the NH.sub.2-functionalized polythiophene according to one embodiment of the present invention. The resulting NH.sub.2-functionalized polythiophene is soluble in organic solvents and is processable for reforming and thin film formation for devices.

(2) FIG. 2 shows the UV-vis absorption spectrum of the functionalized polythiophene according to the same embodiment of the present invention.

(3) FIG. 3 shows the UV-vis absorption spectrum of polythiophene 1 (where R is ethyl).

(4) FIG. 4 shows the UV-vis absorption spectrum of polythiophene 2.

(5) FIG. 5 shows the UV-vis absorption spectrum of polythiophene 4.

(6) FIG. 6 shows the UV-vis absorption spectrum of polythiophene 11.

(7) FIG. 7 shows the solubility of the NH.sub.2-functionalized polythiophene obtained according to Example 1 of the present invention in (A) ethanol, (B) acetone, (C) ethyl acetate, and (D) toluene.

(8) FIG. 8 shows the solubility of polythiophene 1 in (A) methanol, (B) acetonitrile, (C) acetone, (D) chloroform, and (E) 1,2-dichlorobenzene according to one embodiment of the present invention

(9) FIG. 9 shows the solubility of polythiophene 2 in (A) methanol, (B) acetonitrile, (C) acetone, (D) chloroform, and (E) 1,2-dichlorobenzene according to one embodiment 190 of the present invention.

(10) FIG. 10 shows the solubility of polythiophene 4 in (A) methanol, (B) acetonitrile, (C) acetone, (D) chloroform, and (E) 1,2-dichlorobenzene according to one embodiment of the present invention.

(11) FIG. 11 shows the photoluminescence spectrum of polythiophene 12 in DMF.

(12) FIG. 12 shows the photoluminescence spectrum of polythiophene 13 in DMF.

(13) FIG. 13 shows the photoluminescence spectrum of polythiophene 14 in DMF.

(14) FIG. 14 shows the photoluminescence spectrum of polythiophene 15 in CHCl.sub.3.

(15) FIG. 15 shows the photoluminescence spectrum of polythiophene 16 in CHCl.sub.3.

(16) FIG. 16 shows the photoluminescence spectrum of polythiophene 17 in DCB.

(17) FIG. 17 shows the photoluminescence spectrum of polythiophene 18 in CHCl.sub.3.

(18) FIG. 18 shows the photoluminescence spectrum of polythiophene 19 in CHCl.sub.3.

(19) FIG. 19 shows the J-V characteristics of polythiophenes 15-19 doped with PCBM under illumination.

(20) FIG. 20 shows the J-V characteristics of polythiophenes 16, 17, and 19 under dark condition. The hollowed symbols are the experimental data, while the solid is the fitted curve of J.sub.SCL.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

(21) As used herein and in the claims, comprising means including the following elements but not excluding others.

(22) The present invention relates to new functionalized polythiophene compound. In particular, amine group directly bonds to the thiophene repeating unit of the polythiophene compound. The amine group allows ease of further functionalization to prepare new polymer derivatives with different chemical and physical properties. These new functionalized polythiophenes and their derivatives can be used for the fabrications of organic light emitting diodes (OLEDs), polymer light emitting diodes (PLEDs), organic photovoltaic devices (OPVs) and conducting polymers for printed electronic devices. The amine-functionalized polythiophene is soluble in commonly used organic solvents including acetone, ethyl acetate, ethanol, and toluene, etc. The resulting solution amine-functionalized polythiophene is processable and suitable for printing thin-films in the field of printed electronics and roll-to-roll processing.

(23) Another aspect of the present invention discloses a new low-cost methodology to functionalize the native polythiophene through simple and mild chemical processes to produce new polythiophene compounds. The process is able to be scaled up for large production. The new compounds are soluble in common organic solvents including acetone, acetonitrile, tetrahydrofuran, ethyl acetate, chloroform, toluene, methanol, ethanol, 1-propanol, isopropanol, DMSO, DMF, other halogenated hydrocarbon solvents and etc.

(24) The exemplary embodiments of the present invention are thus fully described. Although the description referred to particular embodiments, it will be clear to one skilled in the art that the present invention may be practiced with variation of these specific details. Hence this invention should not be construed as limited to the embodiments set forth herein.

(25) Fabrication processes are described in Examples 1-9 below. Referring now to FIGS. 1-5, the present invention discloses the fabrication processes and UV-vis absorption spectrum of solution processable polythiophene.

Example 1

Fabrication of NH2-Functionalized Polythiophene

(26) Polymerization of Thiophene

(27) 50 ml acetonitrile was cooled in a flask in an ice bath. 38.44 g of anhydrous FeCl.sub.3 were added to the flask. 5 g of thiophene and 20 ml acetonitrile were added to another flask in a 40 C. water bath. FeCl.sub.3 solution was added to the thiophene solution drop by drop. The mixture was kept in a water bath at 40 C. for overnight. The resulting mixture was filtered and the dark reddish solid was collected. The solid was washed with methanol and then water. Reddish brown solid obtained. The compound was characterized by UV-vis. The process is summarized in Equation (1) below.

(28) ##STR00010##

(29) Observation: Solid is not soluble ethanol, ethyl acetate, acetone, etc. It is slightly soluble in hot dichlorobenzene.

Step 1: Nitration of Polythiophene to NO2-polythiophene (NO2-PT)

(30) HNO.sub.3 (8 ml) and H.sub.2SO.sub.4 (20 ml) were put in an ice bath for 30 min. The two acids and 3 ml H.sub.2O were added to a flask with stirring in an ice bath and was kept for 30 min. Polythiophene (1 g) was added to the flask slowly. The mixture was then heated to 50 C. for 4 h after all solids were dissolved. The reaction mixture was then cooled to room temperature and then was poured to a beaker with ice-water slowly. Reddish brown precipitates were formed and the solid was filtered out. The compound was characterized by UV-vis. The process is summarized in Equation (2) below.

(31) ##STR00011##

(32) Observation: Reddish brown solid collected which was highly soluble in EtOH and acetone.

Step 2: Reduction of NO2-Polythiophene to NH2-Polythiophene

(33) NO.sub.2-PT (0.2 g), Fe powder (0.3 g), CaCl.sub.2 (0.2 g), EtOH (10 ml), and H.sub.2O (0.5 ml) were added to a flask. The mixture was stirred and heated to 78 C. for 2.5 h. The mixture was then cooled to room temperature and the reaction mixture was filtered. The filtrate was collected, extracted with ethyl acetate and then was washed with water. The organic phase was collected and recrystallized. Black solid was obtained. The compound was characterized by UV-vis, which is shown in FIG. 2, whereas the solubility test results are shown in FIG. 7.

(34) Observation: Black solid collected which was soluble in ethanol, ethyl acetate, and acetone.

Example 2

Fabrication of Polythiophene 1

(35) Step 1: Modification of Thiophene-3-Ethanol with Various Acyl Chlorides (where R can be any Alkyl Chains Comprising Methyl, Ethyl, Propyl, i-Propyl, Butyl, Etc.)

(36) ##STR00012##

(37) Procedures:

(38) 1. 1.0 ml of thiophene-3-ethanol was placed with 30 ml of CHCl.sub.3, 4.96 ml of triethylamine and was cooled in ice-bath.

(39) 2. 3.1 ml of propionyl chloride was added to thiophene solution dropwise for 15 min.

(40) 3. The mixture was stirred at 0-2 C. for 2 h and then stirred at room temperature for 10 h and subsequently washed with DI water to obtain the product.

(41) The process is summarized in Equation (3) above.

(42) Step 2: Synthesis of Polythiophene 1 (where R can be any Alkyl Chains Comprising Methyl, Ethyl, Propyl, i-Propyl, Butyl, Etc.)

(43) ##STR00013##

(44) Procedures:

(45) 1. 50 ml acetonitrile was cooled in an ice-bath. FeCl.sub.3 (6.8 g, 41.8 mmol) was added to the flask with stirring.

(46) 2. 2-(3-Thienyl)ethyl propanoate (1.9 g, 10.4 mmol) was dissolved in 20 mL acetonitrile and the solution was added to a dropping funnel.

(47) 3. The 2-(3-Thienyl)ethyl propanoate solution (monomer) was added to the cooled FeCl.sub.3 solution dropwise for a period of 0.5 h.

(48) 4. The mixture was stirred at 0-2 C. for 2 h and then stirred at room temperature for 10 h.

(49) 5. The precipitate was filtrated and washed with DI water and MeOH.

(50) 6. The precipitate was poured into 12.5% of ammonium solution and stirred overnight at room temperature.

(51) 7. The precipitate was filtrated and washed with DI water and MeOH. The collected precipitate was poured into an aqueous solution of EDTA (pH=8) and stirred overnight at room temperature.

(52) 8. The precipitate was then filtrated and washed with DI water and MeOH.

(53) The process is summarized in Equation (4) above.

(54) The UV-vis spectrum of polythiophene 1 obtained is shown in FIG. 3, whereas the solubility test results are shown in FIG. 8 and summarized in Table 1 below, in which the R group is ethyl group in this specific embodiment of polythiophene 1.

(55) As observed from Table 1, polythiophene 1 is soluble in acetone, chloroform, and 1,2-dichlorobenzene.

(56) TABLE-US-00001 TABLE 1 Sample Solvent Solubility, g/ml at 23 C. A Methanol Insoluble B Acetonitrile Insoluble C Acetone 0.43 mg/mL D Chloroform 0.93 mg/mL E 1,2-Dichlorobenzene 1.03 mg/mL

Example 3

Fabrication of Silyl-Polythiophene

(57) Step 1: Modification of Thiophene-3-Ethanol with Various Silyl Chlorides ((R).sub.3SiCl, where R.sup.1, R.sup.2, and R.sup.3 can be any Alkyl Chains Comprising Methyl, Ethyl, Propyl, i-Propyl, Butyl, Etc.)

(58) ##STR00014##

(59) Procedures:

(60) 1. Imidazole (4.9 g, 73.0 mmol) was added to a solution of 6.0 g (21.0 mmol) of 2-hydroxyethylthiophene in 60 mL of DMF, and the resulting mixture was stirred at room temperature for 15 min.

(61) 2. The reaction was followed by addition of 5.2 g (34.4 mmol) of silyl chlorides in 10 mL of DMF.

(62) 3. The reaction mixture was stirred for 16 h at room temperature, and then was poured into a water-ice solution. The solution was extracted with hexane (360 mL). The organic fraction is washed with water and dry over Na.sub.2SO.sub.4.

(63) 4. Concentration in vacuum affords crude product which was purified by column chromatography on silica gel as colorless oil.

(64) The process is summarized in Equation (5) above.

(65) Step 2: Synthesis of Silyl-Polythiophene (where R can be any Alkyl Chains Comprising Methyl, Ethyl, Propyl, i-Propyl, Butyl, Etc.)

(66) ##STR00015##

(67) The polymerization procedure was the same as described in step 2 in Example 2. The process is summarized in Equation (6) above.

Example 4

Fabrication of New Polythiophene with Mixed-Blocks

(68) 4.1 Synthesis of Polythiophene 2 Using Thiophene Monomer (A) and 3-Alkyl-Substituted Thiophene Monomer (B) (where R can be any Alkyl Chains Comprising Methyl, Ethyl, Propyl, i-Propyl, Butyl, Etc.)

(69) ##STR00016##

(70) Procedures:

(71) 1. 50 ml acetonitrile was cooled in an ice-bath. FeCl.sub.3 (5.3 g 32.8 mmol) was added to the flask with stirring.

(72) 2. Thiophene A (444 uL, 5.54 mmol) and 3-methylthiophene (268 uL, 2.77 mmol) B were dissolved in 20 mL of acetonitrile and added to a dropping funnel.

(73) 3. The solution of the mixed thiophene monomers was added to FeCl.sub.3 solution dropwise for a period of 0.5 h.

(74) 4. The mixture was stirred at 0-2 C. for 2 h and then stirred at room temperature for 10 h.

(75) 5. The precipitate was filtrated and washed with DI water and MeOH.

(76) 6. The precipitate was poured into 12.5% of ammonium solution and stirred overnight at room temperature.

(77) 7. The precipitate was filtrated and washed with DI water and MeOH. The collected precipitate was then poured into an aqueous solution of EDTA (pH=8) and stirred overnight at room temperature.

(78) 8. The precipitate was filtrated and washed with DI water and MeOH.

(79) The process is summarized in Equation (7) above. The UV-vis spectrum of polythiophene 2 obtained was shown in FIG. 4.

(80) The UV-vis spectrum of polythiophene 2 obtained is shown in FIG. 4, whereas the solubility test results are shown in FIG. 9 and summarized in Table 2 below, in which the R group is methyl group, n is greater than 1 and m is greater than 1.

(81) As observed from Table 2, polythiophene 2 is soluble in acetone, chloroform, and 1,2-dichlorobenzene.

(82) TABLE-US-00002 TABLE 2 Test number Solvent Solubility, mg/ml at 23 C. A Methanol Insoluble B Acetonitrile Insoluble C Acetone 0.07 mg/mL D Chloroform 0.57 mg/mL E 1,2-Dichlorobenzene 0.83 mg/mL

(83) 4.2 Polymerization Using Thiophene Monomer (A) and Thiophene-3-Ethanol Monomer (B)

(84) ##STR00017##

(85) The polymerization procedure was the same as described in section 4.1 in Example 4. The process is summarized in Equation (8) above.

(86) 4.3 Synthesis Using Thiophene Monomer (A) and Thiophene-3-Ethyl-Ester Monomer (B) (Referring to Step 1 in Example 2, where R can be any Alkyl Chains Comprising Methyl, Ethyl, Propyl, i-Propyl, Butyl, Etc.)

(87) ##STR00018##

(88) The synthesis procedure was the same as described in section 4.1 in Example 4. The process is summarized in Equation (9) above.

(89) 4.4 Synthesis Using Thiophene Monomer (A) and Thiophene-3-Ethyl-Silyl Monomer (B) (Referring to Step 1 in Example 3, where R.sup.1, R.sup.2, and R.sup.3 can be any Alkyl Chains Comprising Methyl, Ethyl, Propyl, i-Propyl, Butyl, Etc.)

(90) ##STR00019##

(91) The synthesis procedure was the same as described in section 4.1 in Example 4. The process is summarized in Equation (10) above.

Example 5

Synthesis Using Polythiophene and 2,7-dibromo-9,9-dioctylfluorene

(92) Step 1: Synthesis of Polythiophene 3

(93) ##STR00020##

(94) Procedures:

(95) 1. 50 m acetonitrile was cooled in an ice-bath. FeCl.sub.3 (5.3 g, 32.8 mmol) was added to the flask with stirring.

(96) 2. Thiophene monomer (660 uL, 8.31 mmol) was dissolved in 20 mL acetonitrile and then was added to a dropping funnel.

(97) 3. The solution of the thiophene monomer was added to FeCl.sub.3 solution dropwise in a period of 0.5 h.

(98) 4. The mixture was stirred at 0-2 C. for 2 h and then stirred at room temperature for 10 h.

(99) 5. The precipitate was filtrated and washed with DI water and followed by MeOH.

(100) 6. The precipitate was poured into 12.5% of ammonium solution and was stirred overnight at room temperature.

(101) 7. The precipitate was filtrated and washed with DI water and then MeOH. The collected precipitate was poured into an aqueous solution of EDTA (pH=8) and stirred overnight at room temperature.

(102) 8. The precipitate was filtrated and washed with DI water and MeOH.

(103) The process is summarized in Equation (11) above.

(104) Step 2: Coupling Reaction of Polythiophene 3 (where the Repeating Unit, n, is Greater than 6) with 2,7-Dibromo-9,9-Dialkylfluorene (where R can be n-Alkyl Chain Comprising: RC.sub.6H.sub.13, or C.sub.8H.sub.17, or C.sub.12H.sub.25) or 2,7-Dibromofluorene (where RH)

(105) ##STR00021##

(106) Procedures:

(107) 1. A mixture of Pd(OAc).sub.2 (2 mg), pivalic acid (10 uL), K.sub.2CO.sub.3 (87 mg), 2,7-dibromo-9,9-dioctylfluorene (137 mg), polythiophene 3 (124 mg) were stirred in dimethylacetamide for 1 d at 120 C. under nitrogen.

(108) 2. After cooling to room temperature, the mixture was poured into an aqueous solution of EDTA (pH=8).

(109) 3. The suspension was stirred overnight at room temperature.

(110) 4. The precipitate was filtrated and washed with 0.1 M HCl, then followed by DI water, MeOH and hexane successively.

(111) 5. The precipitate was dissolved in CHCl.sub.3 and the solution was filtrated to remove the insoluble matters.

(112) 6. The Re-precipitation in CHCl.sub.3/MeOH solution to obtain the product.

(113) The process is summarized in Equation (12) above. The UV-vis spectrum of polythiophene 4 obtained was shown in FIG. 5. The UV-vis spectrum of polythiophene 4 obtained is shown in FIG. 5, whereas the solubility test results are shown in FIG. 10 and summarized in Table 3 below in which n is greater than 6 in this specific embodiment of polythiophene 4.

(114) As observed from Table 3, polythiophene 4 is soluble in acetone, chloroform, and 1,2-dichlorobenzene.

(115) TABLE-US-00003 TABLE 3 Test number Solvent Solubility, g/ml at 23 C. A Methanol Insoluble B Acetonitrile Insoluble C Acetone 0.07 mg/mL D Chloroform 0.20 mg/mL E 1,2-Dichlorobenzene 0.37 mg/mL

Example 6

Synthesis Using 3-Substituted Polythiophene and 2,7-dibromo-9,9-Dialkylfluorene (where R can be n-Alkyl Chain Comprising: RC6H13, or C8H17, or C12H25) or 2,7-Dibromofluorene (where RH)

(116) ##STR00022##

(117) Step 1: Synthesis of 3-Substituted Polythiophene 5 (where the Repeating Unit, n, is Greater than 1.

(118) ##STR00023##

(119) Procedures:

(120) 1. 50 ml acetonitrile was cooled in an iced-bath. FeCl.sub.3 (5.8 g, 35.7 mmol) was added to the flask with stirring.

(121) 2. Thiophene-3-ethanol monomer (1.0 mL, 8.9 mmol) was dissolved in 20 mL acetonitrile and added to a dropping funnel.

(122) 3. The thiophene solution was added to FeCl.sub.3 solution dropwise over a period of 0.5 h.

(123) 4. The mixture was stirred at 0-2 C. for 2 h and then stirred at room temperature for 10 h.

(124) 5. The precipitate was filtrated and washed with DI water and MeOH.

(125) 6. The precipitate was poured into 12.5% of ammonium solution and stirred overnight at room temperature.

(126) 7. The precipitate was filtrated and washed with DI water and MeOH. The precipitate was poured into an aqueous solution of EDTA (pH=8) and stirred overnight at room temperature.

(127) 8. The precipitate was filtrated and washed with DI water and MeOH.

(128) The process is summarized in Equation (14) above.

(129) Step 2: Coupling reaction of polythiophene 5 (where the repeating unit, n, is greater than 1) with 2,7-dibromo-9,9-dialkylfluorene (Where R can be n-alkyl chain comprising: RC.sub.6H.sub.13, or C.sub.8H.sub.17, or C.sub.12H.sub.25) or 2,7-Dibromofluorene (where RH)

(130) ##STR00024##

(131) Procedures:

(132) 1. A mixture of Pd(OAc).sub.2 (2 mg), pivalic acid (10 uL), K.sub.2CO.sub.3 (87 mg), 2,7-dibromo-9,9-dioctylfluorene (137 mg), polythiophene 5 (124 mg) were stirred in dimethylacetamide for 1 d at 120 C. under N.sub.2.

(133) 2. After cooling to room temperature, the mixture was poured into an aqueous solution of EDTA (pH=8).

(134) 3. The suspension was stirred overnight at room temperature.

(135) 4. The precipitate was filtrated and washed with 0.1 M HCl, DI water, MeOH and hexane.

(136) 5. The precipitate was dissolved in CHCl.sub.3 and the solution was filtrated to remove the insoluble material.

(137) 6. Re-precipitation in a CHCl.sub.3/MeOH solution to result in the product of polythiophene 6.

(138) The process is summarized in Equation (15) above.

Example 7

Synthesis Using 3-Substituted Polythiophene (where R can be any Alkyl Chains Comprising Methyl, Ethyl, Propyl, i-Propyl, Butyl, Etc.) with 2,7-dibromo-9,9-dialkylfluorene (where R can be n-Alkyl Chain Comprising: RC6H13, or C8H17, or C12H25) or 2,7-Dibromofluorene (where RH)

(139) ##STR00025##

(140) Procedures:

(141) 1. A mixture of Pd(OAc).sub.2 (2 mg), pivalic acid (10 uL), K.sub.2CO.sub.3 (87 mg), 2,7-dibromo-9,9-dioctylfluorene (137 mg), polythiophene 7 (124 mg) were stirred in dimethylacetamide for 1 d at 120 C. under N.sub.2.

(142) 2. After cooling to room temperature, the mixture was poured into an aqueous solution of EDTA (pH=8).

(143) 3. The suspension was stirred overnight at room temperature.

(144) 4. The precipitate was filtrated and washed with 0.1 M HCl, DI water, MeOH and hexane.

(145) 5. The precipitate was dissolved in CHCl.sub.3 and the solution was filtrated to remove the insoluble material.

(146) 6. Re-precipitation in a CHCl.sub.3/MeOH solution to result in the product of polythiophene 8.

(147) The process is summarized in Equation (16) above.

Example 8

Synthesis Using New Mix-Block Polythiophene with 2,7-Dibromo-9,9-Dialkylfluorene (where R can be n-Alkyl Chain Comprising: RC6H13, or C8H17, or C12H25) or 2,7-Dibromofluorene (where RH)

(148) 8.1 Reaction of the New Mix-Block Polythiophene (Referring to Product of Example 4, where R can be any Alkyl Chains Comprising Methyl, Ethyl, Propyl, i-Propyl, Butyl, Etc.) and 2,7-Dibromo-9,9-Dialkylfluorene (where R can be n-Alkyl Chain Comprising: RC.sub.6H.sub.13, or C.sub.8H.sub.17, or C.sub.12H.sub.25) or 2,7-Dibromofluorene (where RH).

(149) ##STR00026##

(150) The process is summarized in Equation (17) above in which polythiophene 11 is obtained.

(151) The UV-vis spectrum of a specific embodiment of polythiophene 11, in which R group is methyl, n is greater than 1, and m is greater than 1, is shown in FIG. 6.

(152) 8.2 Reaction of the New Mix-Block Polythiophene (Refer to the Product of Example 4) and 2,7-Dibromo-9,9-Dialkylfluorene (where R can be n-Alkyl Chain Comprising: RC.sub.6H.sub.13, or C.sub.8H.sub.17, or C.sub.12H.sub.25) or 2,7-Dibromofluorene (where RH).

(153) The process is summarized in Equation (18) above.

(154) ##STR00027##

(155) 8.3 Reaction of the New Mix-Block Polythiophene (Referring to the Product of Example 4, where R can be any Alkyl Chains Comprising Methyl, Ethyl, Propyl, i-Propyl, Butyl, Etc.) with 2,7-Dibromo-9,9-Dialkylfluorene (where R can be n-Alkyl Chain Comprising: RC.sub.6H.sub.13, or C.sub.8H.sub.17, or C.sub.12H.sub.25) or 2,7-Dibromofluorene (where RH).

(156) ##STR00028##

(157) The process is summarized in Equation (19) above.

(158) 8.4 Reaction of the New Mix-Block Polythiophene (Referring to the Product of Example 4, where R.sup.1, R.sup.2, and R.sup.3 can be any Alkyl Chains Comprising Methyl, Ethyl, Propyl, i-Propyl, Butyl, Etc.) with 2,7-Dibromo-9,9-Dialkylfluorene (where R can be n-Alkyl Chain Comprising: RC.sub.6H.sub.13, or C.sub.8H.sub.17, or C.sub.12H.sub.25) or 2,7-Dibromofluorene (where RH).

(159) ##STR00029##

(160) The process is summarized in Equation (20) above.

Example 9

Synthesis Using New Polythiophene (where R can be any Alkyl Chains Comprising Methyl, Ethyl, Propyl, i-Propyl, Butyl, Etc.) with Benzothiadiazole (BT)

(161) ##STR00030##

(162) 9.1 Coupling Reaction of New Polythiophene 5 with Benzothiadiazole (BT) to Synthesize Polythiophene 9

(163) ##STR00031##

(164) Procedures:

(165) 1. A mixture of Pd(OAc).sub.2 (2 mg), pivalic acid (10 uL), K.sub.2CO.sub.3 (87 mg), benzothiadiazole (137 mg), polythiophene 5 (124 mg) were stirred in dimethylacetamide for 1 d at 120 C. under N.sub.2.

(166) 2. After cooling to room temperature, the mixture was poured into an aqueous solution of EDTA (pH=8).

(167) 3. The suspension was stirred overnight at room temperature.

(168) 4. The precipitate was filtrated and washed with 0.1 M HCl, DI water, MeOH and hexane.

(169) 5. The precipitate was dissolved in CHCl.sub.3 and the solution was filtrated to remove the insoluble material.

(170) 6. Re-precipitation in a CHCl.sub.3/MeOH solution to result in the product of polythiophene 9.

(171) The process is summarized in Equation (22) above.

(172) 9.2 Coupling Reaction of New Polythiophene 7 (where R can be any Alkyl Chains Comprising Methyl, Ethyl, Propyl, i-Propyl, Butyl, Etc.) with Benzothiadiazole (BT) to Synthesize to Synthesize Polythiophene 10

(173) ##STR00032##

(174) Procedures:

(175) 1. A mixture of Pd(OAc).sub.2 (2 mg), pivalic acid (10 uL), K.sub.2CO.sub.3 (87 mg), benzothiadiazole (137 mg), polythiophene 7 (124 mg) were stirred in dimethylacetamide for 1 d at 120 C. under N.sub.2.

(176) 2. After cooling to room temperature, the mixture was poured into an aqueous solution of EDTA (pH=8).

(177) 3. The suspension was stirred overnight at room temperature.

(178) 4. The precipitate was filtrated and washed with 0.1 M HCl, DI water, MeOH and hexane.

(179) 5. The precipitate was dissolved in CHCl.sub.3 and the solution was filtrated to remove the insoluble material.

(180) 6. Re-precipitation in a CHCl.sub.3/MeOH solution to result in the product of polythiophene 10.

(181) The process is summarized in Equation (23) above.

(182) 9.3 Coupling Reaction of New Polythiophene (where R.sup.1, R.sup.2, and R.sup.3 can be any Alkyl Chains Comprising Methyl, Ethyl, Propyl, i-Propyl, Butyl, Etc.) with Benzothiadiazole (BT)

(183) ##STR00033##

(184) The process is summarized in Equation (24) above.

(185) Referring now to FIGS. 7(A), 7(B), 7(C), and 7(D), the solubility tests of the polythiophene compounds of the present invention demonstrate that the new compounds are soluble in ethanol, acetone, ethyl acetate, and toluene.

Example 10

Study on the Solubility of NH2-Functionalized Polythiophene in Ethanol

(186) A reddish brown solid sample of NH.sub.2-functionalized polythiophene (15 mg) was put into a glass bottle and 2 ml of ethanol was added to dissolve the compound at room temperature. A deep reddish-brown homogeneous solution was obtained as shown in FIG. 7 (A). The test demonstrated that NH.sub.2-functionalized polythiophene is soluble in ethanol.

Example 11

Study on the Solubility of NH2-Functionalized Polythiophene in Acetone

(187) A reddish brown solid sample of NH.sub.2-functionalized polythiophene (15 mg) was put into a glass bottle and 2 ml of acetone was added to dissolve the compound at room temperature. A deep reddish-brown homogeneous solution was obtained as shown in FIG. 7 (B). The test demonstrated that NH.sub.2-functionalized polythiophene is soluble in acetone.

Example 12

Study on the Solubility of NH2-Functionalized Polythiophene in Ethyl Acetate

(188) A reddish brown solid sample of NH.sub.2-functionalized polythiophene (10 mg) was put into a glass bottle and 2 ml of ethyl acetate was added to dissolve the compound at room temperature. A reddish-brown homogeneous solution was obtained as shown in FIG. 7 (C). The test demonstrated that NH.sub.2-functionalized polythiophene is soluble in ethyl acetate.

Example 13

Study on the Solubility of NH2-Functionalized Polythiophene in Toluene

(189) A reddish brown solid sample of NH.sub.2-functionalized polythiophene (5 mg) was put into a glass bottle and 2 ml of toluene was added to dissolve the compound at room temperature. A reddish-brown homogeneous solution was obtained as shown in FIG. 7 (D). The test demonstrated that NH.sub.2-functionalized polythiophene is soluble in toluene.

Example 14

Study on the Potential Application of Polythiophenes for Electroluminescent Devices, Such as Organic Light Emitting Diode and Polymer Light-Emitting Diode

(190) All of the polythiophenes in Table 4 were readily dissolved in DMF, chloroform or dichlorobenzene, and were filtered by 0.45 m PTFE filter. They display photoluminescence at room temperature under ambient condition when they are excited at their respective absorption bands and the maximum fluorescence peaks are found in the range of 505 to 630 nm.

(191) TABLE-US-00004 TABLE 4 Excitation Emission wavelength wavelength Polythiophene Chemical structure Solvent (nm), .sub.ex (nm), .sub.em 12 DMF 500 588 13 DMF 480 512, 630 14 DMF 480 559 15 CHCl.sub.3 470 505 16 CHCl.sub.3 470 570 17 DCB 420 562 18 0 CHCl.sub.3 470 550 19 CHCl.sub.3 470 580, 613

(192) Polythiophene 14-19 emit green light in the range of 505 nm to 570 nm. Polythiophene 12 shows yellow emission color at 588 nm while polythiophene 13 exhibits green and red light emission with two peaks at 512 nm and 630 nm respectively. Polythiophene 19 shows emission color in the range from yellow to orange at 580 nm to 613 nm.

(193) Similar polythiophene materials were previously shown to fabricate high efficient electroluminescent devices (I. F. Perepichka, et al., 2005; G. G. Malliaras, et al., 1993; J.-L. Bredas, et al., 1983; F. Chen, et al., 1996; M. Pomerantz, et al., 1999). Thus polythiophenes 12-19 as shown in Table 4, or other polythiophenes of the present invention, could be used in fabricating high efficient electroluminescent devices.

(194) The photoluminescence spectra of polythiophenes 12-19 obtained are shown in FIGS. 11-18.

Example 15

Study on the Potential Application of Polythiophenes 16, 17, and 19 for Fabricating Organic Photovoltaic Solar Cells, Transistor or Other Conducting Devices

(195) For photovoltaic (PV) measurements, the structure of fabricated device is ITO/PEDOT:PSS (30 nm)/Polymer:PCBM (1:1 wt %)/LiF (1 nm)/Al (120 nm) and the active area is 0.16 cm.sup.2. The J-V characteristic under illumination is plotted in FIG. 19 and the PV parameters are summarized in Table 5. All of the polythiophenes have shown the PV characteristics, and so it is proven that the selected polythiophenes are the potential materials for PV cells fabrication.

(196) TABLE-US-00005 TABLE 5 Thickness Voc Jsc FF PCE Polythiophene (nm) (V) (mA/cm.sup.2) (%) (%) 15 162 0.97 0.69 41.0 0.3 16 55 0.91 1.91 30.6 0.5 17 118 0.63 0.33 28.0 0.1 18 127 0.68 0.37 28.4 0.1 19 65 0.98 0.45 22.9 0.1

(197) To investigate the conductivity (a) of synthesized polythiophene, mobility (p) determination should be the most directly method according to the following equation:
=nq,
where n is the carrier concentration and q is the elementary charge.

(198) In the study, J-V measurement in dark condition is employed for 16, 17 and 19 with the unipolar device structure, ITO/PEDOT:PSS (30 nm)/Polymer/Al (100 nm). The J-V characteristics are shown in FIG. 10. The hollowed symbols are the experimental data, while the solid lines are the fitted curve of space-charge-limited current (J.sub.SCL). The mobility () can then be obtained from the fitting parameters in the following equation:

(199) $J=\frac{9}{8}\mathrm{.Math.}\frac{E^2}{d},$

(200) where is permittivity, E is electric field and d is the device thickness.

(201) The results are summarized in Table 6. It shows clearly that polythiophenes 16, 17 and 19 are conducting polythiophenes with the magnitude between 110.sup.7 to 110.sup.6 cm.sup.2/Vs. Therefore, all these investigated polythiophenes can be used for the fabrication of transistor or other conducting devices.

(202) TABLE-US-00006 TABLE 6 Polythiophene Thickness (nm) Mobility (cm.sup.2/Vs) 16 255 8.49 10.sup.7 17 152 1.34 10.sup.6 19 173 1.64 10.sup.7