JP6675124B2 - アントラビスチアジアゾール誘導体及びこれを用いて得られるπ共役系重合体 - Google Patents
アントラビスチアジアゾール誘導体及びこれを用いて得られるπ共役系重合体 Download PDFInfo
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- JP6675124B2 JP6675124B2 JP2016044905A JP2016044905A JP6675124B2 JP 6675124 B2 JP6675124 B2 JP 6675124B2 JP 2016044905 A JP2016044905 A JP 2016044905A JP 2016044905 A JP2016044905 A JP 2016044905A JP 6675124 B2 JP6675124 B2 JP 6675124B2
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- 229920000547 conjugated polymer Polymers 0.000 title claims description 30
- 125000000217 alkyl group Chemical group 0.000 claims description 119
- -1 sulfonyloxy, amino, amide Chemical class 0.000 claims description 97
- 125000005843 halogen group Chemical group 0.000 claims description 71
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 68
- 125000003545 alkoxy group Chemical group 0.000 claims description 57
- 125000003118 aryl group Chemical group 0.000 claims description 56
- 125000001072 heteroaryl group Chemical group 0.000 claims description 55
- 125000002252 acyl group Chemical group 0.000 claims description 48
- 125000004185 ester group Chemical group 0.000 claims description 37
- 229910052717 sulfur Inorganic materials 0.000 claims description 36
- 125000004434 sulfur atom Chemical group 0.000 claims description 36
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims description 35
- 150000001875 compounds Chemical class 0.000 claims description 34
- 239000000463 material Substances 0.000 claims description 34
- 125000004414 alkyl thio group Chemical group 0.000 claims description 29
- 239000004065 semiconductor Substances 0.000 claims description 28
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical group [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 claims description 27
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 27
- 229910052711 selenium Inorganic materials 0.000 claims description 27
- 125000000304 alkynyl group Chemical group 0.000 claims description 25
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 25
- 125000003342 alkenyl group Chemical group 0.000 claims description 24
- 125000005110 aryl thio group Chemical group 0.000 claims description 21
- 125000003441 thioacyl group Chemical group 0.000 claims description 21
- 125000005103 alkyl silyl group Chemical group 0.000 claims description 20
- 125000005104 aryl silyl group Chemical group 0.000 claims description 20
- 125000004432 carbon atom Chemical group C* 0.000 claims description 19
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 19
- 150000007970 thio esters Chemical class 0.000 claims description 19
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 18
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 17
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 17
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 16
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M thiocyanate group Chemical group [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 claims description 16
- 125000003368 amide group Chemical group 0.000 claims description 11
- 239000000758 substrate Substances 0.000 claims description 11
- 125000003277 amino group Chemical group 0.000 claims description 10
- 239000010409 thin film Substances 0.000 claims description 10
- 150000002148 esters Chemical class 0.000 claims description 9
- 125000001391 thioamide group Chemical group 0.000 claims description 9
- AEOCXXJPGCBFJA-UHFFFAOYSA-N ethionamide Chemical compound CCC1=CC(C(N)=S)=CC=N1 AEOCXXJPGCBFJA-UHFFFAOYSA-N 0.000 claims description 7
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 6
- KYPOHTVBFVELTG-UHFFFAOYSA-N but-2-enedinitrile Chemical group N#CC=CC#N KYPOHTVBFVELTG-UHFFFAOYSA-N 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 6
- 238000006880 cross-coupling reaction Methods 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- BMIBJCFFZPYJHF-UHFFFAOYSA-N 2-methoxy-5-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine Chemical compound COC1=NC=C(C)C=C1B1OC(C)(C)C(C)(C)O1 BMIBJCFFZPYJHF-UHFFFAOYSA-N 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
- 125000001424 substituent group Chemical group 0.000 description 69
- 238000000034 method Methods 0.000 description 20
- 238000006243 chemical reaction Methods 0.000 description 19
- 229920000642 polymer Polymers 0.000 description 18
- 230000015572 biosynthetic process Effects 0.000 description 16
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 15
- 239000002904 solvent Substances 0.000 description 15
- 238000003786 synthesis reaction Methods 0.000 description 15
- 239000007787 solid Substances 0.000 description 11
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 238000010898 silica gel chromatography Methods 0.000 description 9
- 230000000704 physical effect Effects 0.000 description 8
- 239000000049 pigment Substances 0.000 description 8
- XMWRBQBLMFGWIX-UHFFFAOYSA-N C60 fullerene Chemical compound C12=C3C(C4=C56)=C7C8=C5C5=C9C%10=C6C6=C4C1=C1C4=C6C6=C%10C%10=C9C9=C%11C5=C8C5=C8C7=C3C3=C7C2=C1C1=C2C4=C6C4=C%10C6=C9C9=C%11C5=C5C8=C3C3=C7C1=C1C2=C4C6=C2C9=C5C3=C12 XMWRBQBLMFGWIX-UHFFFAOYSA-N 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 6
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 6
- 239000000460 chlorine Substances 0.000 description 6
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 6
- UDGKZGLPXCRRAM-UHFFFAOYSA-N 1,2,5-thiadiazole Chemical compound C=1C=NSN=1 UDGKZGLPXCRRAM-UHFFFAOYSA-N 0.000 description 5
- 125000000732 arylene group Chemical group 0.000 description 5
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 0 *C(*1)=C(*)C(*)=C1c1cc2c(*)c(c3n[s]nc3c(C3=C(*)C(*)=C(*)*3)c3)c3c(*)c2c2n[s]nc12 Chemical compound *C(*1)=C(*)C(*)=C1c1cc2c(*)c(c3n[s]nc3c(C3=C(*)C(*)=C(*)*3)c3)c3c(*)c2c2n[s]nc12 0.000 description 4
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 4
- 125000005278 alkyl sulfonyloxy group Chemical group 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 125000005279 aryl sulfonyloxy group Chemical group 0.000 description 4
- 229910052731 fluorine Inorganic materials 0.000 description 4
- 125000001153 fluoro group Chemical group F* 0.000 description 4
- 238000005227 gel permeation chromatography Methods 0.000 description 4
- 125000003707 hexyloxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 4
- 239000010410 layer Substances 0.000 description 4
- 239000011259 mixed solution Substances 0.000 description 4
- 238000004528 spin coating Methods 0.000 description 4
- 125000001302 tertiary amino group Chemical group 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 3
- 239000012300 argon atmosphere Substances 0.000 description 3
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 3
- 125000004744 butyloxycarbonyl group Chemical group 0.000 description 3
- 150000001721 carbon Chemical group 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 229910003472 fullerene Inorganic materials 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 239000012044 organic layer Substances 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 150000003254 radicals Chemical class 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
- 239000011787 zinc oxide Substances 0.000 description 3
- FNQJDLTXOVEEFB-UHFFFAOYSA-N 1,2,3-benzothiadiazole Chemical group C1=CC=C2SN=NC2=C1 FNQJDLTXOVEEFB-UHFFFAOYSA-N 0.000 description 2
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
- QLIMAARBRDAYGQ-UHFFFAOYSA-N 1,6-diiodohexane Chemical compound ICCCCCCI QLIMAARBRDAYGQ-UHFFFAOYSA-N 0.000 description 2
- PBLNBZIONSLZBU-UHFFFAOYSA-N 1-bromododecane Chemical compound CCCCCCCCCCCCBr PBLNBZIONSLZBU-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- IYBLVRRCNVHZQJ-UHFFFAOYSA-N 5-Hydroxyflavone Chemical compound C=1C(=O)C=2C(O)=CC=CC=2OC=1C1=CC=CC=C1 IYBLVRRCNVHZQJ-UHFFFAOYSA-N 0.000 description 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- KDCGOANMDULRCW-UHFFFAOYSA-N 7H-purine Chemical compound N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- ISZWRZGKEWQACU-UHFFFAOYSA-N Primuletin Natural products OC1=CC=CC(C=2OC3=CC=CC=C3C(=O)C=2)=C1 ISZWRZGKEWQACU-UHFFFAOYSA-N 0.000 description 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 2
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 125000001309 chloro group Chemical group Cl* 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- 125000005678 ethenylene group Chemical group [H]C([*:1])=C([H])[*:2] 0.000 description 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 2
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 2
- 125000004705 ethylthio group Chemical group C(C)S* 0.000 description 2
- 230000005669 field effect Effects 0.000 description 2
- 239000010408 film Substances 0.000 description 2
- 125000002541 furyl group Chemical group 0.000 description 2
- 125000005935 hexyloxycarbonyl group Chemical group 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 125000002883 imidazolyl group Chemical group 0.000 description 2
- 230000009878 intermolecular interaction Effects 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- 125000002510 isobutoxy group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])O* 0.000 description 2
- 125000005929 isobutyloxycarbonyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])OC(*)=O 0.000 description 2
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 2
- 125000005928 isopropyloxycarbonyl group Chemical group [H]C([H])([H])C([H])(OC(*)=O)C([H])([H])[H] 0.000 description 2
- 239000002932 luster Substances 0.000 description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 2
- JKQOBWVOAYFWKG-UHFFFAOYSA-N molybdenum trioxide Chemical compound O=[Mo](=O)=O JKQOBWVOAYFWKG-UHFFFAOYSA-N 0.000 description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000001624 naphthyl group Chemical group 0.000 description 2
- 125000005029 naphthylthio group Chemical group C1(=CC=CC2=CC=CC=C12)S* 0.000 description 2
- 125000005484 neopentoxy group Chemical group 0.000 description 2
- 125000002971 oxazolyl group Chemical group 0.000 description 2
- 125000004115 pentoxy group Chemical group [*]OC([H])([H])C([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 2
- 125000001148 pentyloxycarbonyl group Chemical group 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 2
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 description 2
- 229920000301 poly(3-hexylthiophene-2,5-diyl) polymer Polymers 0.000 description 2
- NROKBHXJSPEDAR-UHFFFAOYSA-M potassium fluoride Chemical compound [F-].[K+] NROKBHXJSPEDAR-UHFFFAOYSA-M 0.000 description 2
- 238000007639 printing Methods 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000004742 propyloxycarbonyl group Chemical group 0.000 description 2
- 125000003373 pyrazinyl group Chemical group 0.000 description 2
- 125000003226 pyrazolyl group Chemical group 0.000 description 2
- 125000004076 pyridyl group Chemical group 0.000 description 2
- 125000000168 pyrrolyl group Chemical group 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 125000005920 sec-butoxy group Chemical group 0.000 description 2
- 125000005930 sec-butyloxycarbonyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(OC(*)=O)C([H])([H])[H] 0.000 description 2
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 description 2
- 125000000335 thiazolyl group Chemical group 0.000 description 2
- 125000001544 thienyl group Chemical group 0.000 description 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
- 150000003613 toluenes Chemical class 0.000 description 2
- SLLFVLKNXABYGI-UHFFFAOYSA-N 1,2,3-benzoxadiazole Chemical compound C1=CC=C2ON=NC2=C1 SLLFVLKNXABYGI-UHFFFAOYSA-N 0.000 description 1
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- MNDIARAMWBIKFW-UHFFFAOYSA-N 1-bromohexane Chemical compound CCCCCCBr MNDIARAMWBIKFW-UHFFFAOYSA-N 0.000 description 1
- MVWPVABZQQJTPL-UHFFFAOYSA-N 2,3-diphenylcyclohexa-2,5-diene-1,4-dione Chemical class O=C1C=CC(=O)C(C=2C=CC=CC=2)=C1C1=CC=CC=C1 MVWPVABZQQJTPL-UHFFFAOYSA-N 0.000 description 1
- WQOWBWVMZPPPGX-UHFFFAOYSA-N 2,6-diaminoanthracene-9,10-dione Chemical compound NC1=CC=C2C(=O)C3=CC(N)=CC=C3C(=O)C2=C1 WQOWBWVMZPPPGX-UHFFFAOYSA-N 0.000 description 1
- STTGYIUESPWXOW-UHFFFAOYSA-N 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline Chemical compound C=12C=CC3=C(C=4C=CC=CC=4)C=C(C)N=C3C2=NC(C)=CC=1C1=CC=CC=C1 STTGYIUESPWXOW-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- NSMJMUQZRGZMQC-UHFFFAOYSA-N 2-naphthalen-1-yl-1H-imidazo[4,5-f][1,10]phenanthroline Chemical compound C12=CC=CN=C2C2=NC=CC=C2C2=C1NC(C=1C3=CC=CC=C3C=CC=1)=N2 NSMJMUQZRGZMQC-UHFFFAOYSA-N 0.000 description 1
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 1
- MGADZUXDNSDTHW-UHFFFAOYSA-N 2H-pyran Chemical compound C1OC=CC=C1 MGADZUXDNSDTHW-UHFFFAOYSA-N 0.000 description 1
- RFKWIEFTBMACPZ-UHFFFAOYSA-N 3-dodecylthiophene Chemical compound CCCCCCCCCCCCC=1C=CSC=1 RFKWIEFTBMACPZ-UHFFFAOYSA-N 0.000 description 1
- 125000004217 4-methoxybenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1OC([H])([H])[H])C([H])([H])* 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical group C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- KESRRRLHHXXBRW-UHFFFAOYSA-N C1=CC=NC2=C3C(O)=CC=CC3=CC=C21 Chemical compound C1=CC=NC2=C3C(O)=CC=CC3=CC=C21 KESRRRLHHXXBRW-UHFFFAOYSA-N 0.000 description 1
- 125000003184 C60 fullerene group Chemical group 0.000 description 1
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 1
- MWCLLHOVUTZFKS-UHFFFAOYSA-N Methyl cyanoacrylate Chemical group COC(=O)C(=C)C#N MWCLLHOVUTZFKS-UHFFFAOYSA-N 0.000 description 1
- 238000006411 Negishi coupling reaction Methods 0.000 description 1
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 description 1
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 description 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
- 238000000944 Soxhlet extraction Methods 0.000 description 1
- 238000006161 Suzuki-Miyaura coupling reaction Methods 0.000 description 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
- CPDJESQRPVLWKV-UHFFFAOYSA-N [4-(2-hexyldecyl)thiophen-2-yl]-trimethylstannane Chemical compound CCCCCCCCC(CCCCCC)CC1=CSC([Sn](C)(C)C)=C1 CPDJESQRPVLWKV-UHFFFAOYSA-N 0.000 description 1
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- 125000001931 aliphatic group Chemical group 0.000 description 1
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- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
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- 125000005135 aryl sulfinyl group Chemical group 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 description 1
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- 125000001231 benzoyloxy group Chemical group C(C1=CC=CC=C1)(=O)O* 0.000 description 1
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- 229910052790 beryllium Inorganic materials 0.000 description 1
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- 239000004305 biphenyl Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
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- 238000007766 curtain coating Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
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- DGBWPZSGHAXYGK-UHFFFAOYSA-N perinone Chemical compound C12=NC3=CC=CC=C3N2C(=O)C2=CC=C3C4=C2C1=CC=C4C(=O)N1C2=CC=CC=C2N=C13 DGBWPZSGHAXYGK-UHFFFAOYSA-N 0.000 description 1
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- 239000011698 potassium fluoride Substances 0.000 description 1
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- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 description 1
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- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical class C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
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- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
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- 125000000037 tert-butyldiphenylsilyl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1[Si]([H])([*]C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- YJSKZIATOGOJEB-UHFFFAOYSA-N thieno[2,3-b]pyrazine Chemical compound C1=CN=C2SC=CC2=N1 YJSKZIATOGOJEB-UHFFFAOYSA-N 0.000 description 1
- ONCNIMLKGZSAJT-UHFFFAOYSA-N thieno[3,2-b]furan Chemical compound S1C=CC2=C1C=CO2 ONCNIMLKGZSAJT-UHFFFAOYSA-N 0.000 description 1
- VJYJJHQEVLEOFL-UHFFFAOYSA-N thieno[3,2-b]thiophene Chemical compound S1C=CC2=C1C=CS2 VJYJJHQEVLEOFL-UHFFFAOYSA-N 0.000 description 1
- CRUIOQJBPNKOJG-UHFFFAOYSA-N thieno[3,2-e][1]benzothiole Chemical group C1=C2SC=CC2=C2C=CSC2=C1 CRUIOQJBPNKOJG-UHFFFAOYSA-N 0.000 description 1
- JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical compound S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-N 0.000 description 1
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- TVIVIEFSHFOWTE-UHFFFAOYSA-K tri(quinolin-8-yloxy)alumane Chemical compound [Al+3].C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1 TVIVIEFSHFOWTE-UHFFFAOYSA-K 0.000 description 1
- 125000005259 triarylamine group Chemical class 0.000 description 1
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- 150000003852 triazoles Chemical class 0.000 description 1
- 125000005951 trifluoromethanesulfonyloxy group Chemical group 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 125000000025 triisopropylsilyl group Chemical group C(C)(C)[Si](C(C)C)(C(C)C)* 0.000 description 1
- RLKUQAZUYUQVOW-UHFFFAOYSA-N trimethyl-[4-(2-octyldodecyl)thiophen-2-yl]stannane Chemical compound CCCCCCCCCCC(CCCCCCCC)CC1=CSC([Sn](C)(C)C)=C1 RLKUQAZUYUQVOW-UHFFFAOYSA-N 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
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- YZYKBQUWMPUVEN-UHFFFAOYSA-N zafuleptine Chemical compound OC(=O)CCCCCC(C(C)C)NCC1=CC=C(F)C=C1 YZYKBQUWMPUVEN-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/549—Organic PV cells
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
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- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
- Photovoltaic Devices (AREA)
Description
[式(1)−(a1)で示される6,12-Dihydroxyanthra[1,2-c:5,6-c’]bis[1,2,5]thiadiazoleの合成]
1H NMR (600 MHz, CDCl3, rt) : δ 7.87 (t, J = 9.6 Hz, 2H), δ 8.66 (d, J = 9.6 Hz, 2H), δ 10.87 (s, 2H).
[式(1)−(a2)で示される6,12-bis(dodecyloxy)anthra[1,2-c:5,6-c’]bis[1,2,5]thiadiazoleの合成]
シリカゲルカラムクロマトグラフィー(Rf = 0.84,CH2Cl2)
1H NMR (600 MHz, CDCl3, rt) : δ 0.88 (t, J = 6.6 Hz, 6H), δ 1.28-1.55 (m, 32H), δ 1.67 (m, 4H), δ 2.21 (m, 4H), δ 4.22 (t, J = 6.6 Hz, 4H), δ 7.97 (d, J = 9.6 Hz, 2H), δ 8.55 (d, J = 9.6 Hz, 2H).
[式(2)−(a1)で示される4,10-bis(4-(2-hexyldecyl)thiophene-2-yl)-6,12-bis(dodecyloxy)anthra[1,2-c:5,6-c’]bis[1,2,5]thiadiazoleの合成]
次に、アルゴン雰囲気下、50 mLシュレンク管に、式(1)−(a3)で示される化合物 (710 mg, 0.86 mmol)、3-(2-へキシルデシル)-5-トリメチルスタニルチオフェン (1.0 g, 2.2 mmol)、脱水トルエン (45 mL)を加え、30 分間脱気した。その後、Pd(PPh3)4 (40 mg, 4 mol %)を加え、24 時間加熱還流した。反応終了後、1 M フッ化カリウム水溶液 (20 mL)を加えることで反応を停止し、ジクロロメタンで抽出した。飽和塩化ナトリウム水溶液で有機層を洗浄した後、無水硫酸マグネシウムで乾燥し、この混合溶液をろ過後、ロータリーエバポレーターを用いて溶媒を留去した。その後、シリカゲルカラムクロマトグラフィーにより精製することで、式(2)−(a1)で示される化合物を橙色固体として収率 45% (2 step,546 mg, 0.53 mmol)で得た。
シリカゲルカラムクロマトグラフィー (Rf = 0.62,Hexane/CH2Cl2 = 5/2)
1H NMR (600 MHz, CDCl3, rt) : δ 0.88 (m, 18H), δ 1.20-1.55 (m, 84H), δ 1.81 (m, 2H), δ 2.23 (m, 4H), δ 2.68 (d, J = 6.6 Hz, 4H), δ 4.28 (t, J = 6.6 Hz, 4H), δ 7.05 (s, 2H), δ 8.15 (s, 2H), δ 8.81 (s, 2H).
[式(2)−(a2)で示される4,10-bis(5-bromo-4-(2-hexyldecyl)thiophene-2-yl)-6,12-bis(dodecyloxy)anthra[1,2-c:5,6-c’]bis[1,2,5]thiadiazoleの合成]
シリカゲルカラムクロマトグラフィー (Rf = 0.95,Hexane/CH2Cl2 = 2/1)
1H NMR (600 MHz, CDCl3, rt) : δ 0.87 (m, 18H), δ 1.20-1.56 (m, 84H), δ 1.81 (m, 2H), δ 2.22 (m, 4H), δ 2.62 (d, J = 6.6 Hz, 4H), δ 4.27 (t, J = 6.6 Hz, 4H), δ 7.98 (s, 2H), δ 8.72 (s, 2H).
[式(3)−(a1)で示される重合体(P1:PATz4T-o12HD)の合成]
GPC (o-DCB,140 ℃): Mn = 63.3 kDa,Mw = 124.6 kDa,PDI = 1.97.
[式(1)−(b2)で示される6,12-bis(hexyloxy)anthra[1,2-c:5,6-c’]bis[1,2,5]thiadiazoleの合成]
シリカゲルカラムクロマトグラフィー (Rf = 0.82,CH2Cl2)
1H NMR (300 MHz, CDCl3, rt) : δ 0.97 (t, J = 6.9 Hz, 6H), δ 1.46 (m, 8H), δ 1.68 (m, 4H), δ 2.21 (m, 4H), δ 4.22 (t, J = 6.6 Hz, 4H), δ 7.97 (d, J = 9.6 Hz, 2H), δ 8.56 (d, J = 9.6 Hz, 2H).
[式(2)−(b1)で示される4,10-bis(4-(2-octyldodecyl)thiophene-2-yl)-6,12-bis(hexyloxy)anthra[1,2-c:5,6-c’]bis[1,2,5]thiadiazoleの合成]
シリカゲルカラムクロマトグラフィー (Rf = 0.45,Hexane/CH2Cl2 = 5/2)
1H NMR (400 MHz, CDCl3, rt) : δ 1.86 (t, 12H), δ 0.98 (t, 6H), δ 1.25-1.35 (m, 64H), δ 1.44-1.54 (m, 8H), δ 1.74 (m, 2H), δ 1.79-1.862 (m, 4H), δ 2.20-2.27 (m, 4H), δ 2.67 (d, J = 6.8 Hz, 4H), δ 4.28 (t, J = 6.4 Hz, 4H), δ 7.06 (s, 2H), δ 8.14 (s, 2H), δ 8.80 (s, 2H). Anal. Calcd for C74H114N4O2S4: C, 72.85; H, 9.42; N, 4.59%. Found: C, 73.02; H, 9.62; N, 4.56%.
[式(2)−(b2)で示される4,10-bis(5-bromo-4-(2-octyldodecyl)thiophene-2-yl)-6,12-bis(hexyloxy)anthra[1,2-c:5,6-c’]bis[1,2,5]thiadiazoleの合成]
シリカゲルカラムクロマトグラフィー (Rf = 0.96,Hexane/CH2Cl2 = 2/1)
1H NMR (400 MHz, CDCl3, rt) : δ 0.85 (t, J = 7.2 Hz, 12H), δ 1.01 (t, J = 7.2 Hz,6H), δ 1.23-1.55 (m, 72H), δ 1.82 (m, 6H), δ 2.19 (m, 4H), δ 2.61 (d, J = 7.2 Hz, 4H), δ 4.22 (t, J = 6.4 Hz, 4H), δ 7.94 (s, 2H), δ 8.62 (s, 2H). Anal. Calcd for C74H112N4O2S4Br2: C, 64.51; H, 8.19; N, 4.07%. Found: C, 64.60; H, 8.24; N, 4.00%.
[式(3)−(b1)で示される重合体(P2:PATz4T-o6OD)の合成]
GPC (o-DCB,140 ℃): Mn = 41.5 kDa,Mw = 68.3 kDa,PDI = 1.64.
[逆型バルクヘテロ接合型太陽電池素子の作製]
ITO基板 (ジオマテック社,膜厚: 150 nm,抵抗率: < 12 Ω/□,透過率: (λ = 550 nm) ≧ 85%)を中性洗剤、イオン交換水、アセトンおよびイソプロパノールを用いてそれぞれ10分間超音波洗浄した。その後、基板の入ったイソプロパノールを10分間煮沸し、乾燥後、UV−オゾン洗浄を20分間行った。洗浄した基板上に、酢酸亜鉛二水和物 0.87 g、エタノールアミン 0.24 gを10 mLの2-メトキシエタノールに溶解した溶液を滴下し、4000 rpmで30秒間スピンコートした。200 ℃で30分間ホットプレート上で加熱し、徐冷することで酸化亜鉛薄膜を形成した。その後、先ほどの基板をアセトン、イソプロパノールを用いて10分間超音波洗浄し、煮沸後、基板を乾燥させ直ちにグローブボックス内に搬入した。濃度13.3 g/Lの式(3)−(a1)で示される重合体 (P1:PATz4T-o12HD)の無水o-ジクロロベンゼン溶液に、1 vol%の1,6-ジヨードヘキサン (DIH)と重量比 1:1となるように可溶性フラーレン誘導体 (PC61BM)を加え、100 ℃に保ったまま、400 rpmで30秒、続いて600 rpmで180秒間スピンコートすることで酸化亜鉛をコートした基板上にP1活性層を作製した。また、濃度8.3 g/Lの式(3)−(b1)で示される重合体 (P2:PATz4T-o6OD)の無水クロロベンゼン溶液に、重量比 1:2となるように可溶性フラーレン誘導体 (PC61BM)を加え、100 ℃に保ったまま、400 rpmで30秒、続いて1000 rpmで5秒間スピンコートすることで酸化亜鉛をコートした基板上にP2活性層を作製した。室温で乾燥後、シャドーマスクを装着した基板を真空蒸着装置に移し、3×10-5 Pa程度の減圧下でホール注入層として6 nmの三酸化モリブデン、続いて陽極として50 nmの銀を真空蒸着することで、活性エリア0.16 cm2のバルクヘテロ接合型太陽電池素子を作製した。作製した太陽電池素子の室温、不活性雰囲気下、ソーラーシミュレータ (AM 1.5 G, 100 mW cm-2)照射下での光電変換特性を図1および表1に示す。作製した太陽電池素子は、いずれも高い開放電圧およびFFを示し、P2においては高い短絡電流密度を示したため、最大で5.66%の光電変換効率を示した。このことから、太陽電池材料として高い可能性を持つことが明らかとなった。
Claims (9)
- 下記式(1)で示されるアントラビスチアジアゾール誘導体。
- Yが水素原子である請求項1記載のアントラビスチアジアゾール誘導体。
- 下記式(2)で示されるアントラビスチアジアゾール誘導体。
- 下記式(3)で示される構成単位を有するπ共役系重合体。
- Wが下記式(4)及び(5)で示される2価の共役系基からなる群から選択される少なくとも1種である請求項4記載のπ共役系重合体。
- 請求項4又は5記載のπ共役系重合体を含む有機半導体材料。
- 請求項4又は5記載のπ共役系重合体が基材に塗布されてなる有機半導体材料。
- 請求項6又は7記載の有機半導体材料を含む有機薄膜太陽電池。
- 下記式(2)で示されるアントラビスチアジアゾール誘導体と、下記式(6)で示される化合物とをクロスカップリング反応させる請求項4又は5記載のπ共役系重合体の製造方法。
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