CN109791980A - 共轭聚合物及其在有机电子器件的应用 - Google Patents
共轭聚合物及其在有机电子器件的应用 Download PDFInfo
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- CN109791980A CN109791980A CN201780059466.0A CN201780059466A CN109791980A CN 109791980 A CN109791980 A CN 109791980A CN 201780059466 A CN201780059466 A CN 201780059466A CN 109791980 A CN109791980 A CN 109791980A
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- organic
- aromatic
- alkyl chain
- conjugated polymer
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- 229920000547 conjugated polymer Polymers 0.000 title claims abstract description 64
- 230000003252 repetitive effect Effects 0.000 claims abstract description 20
- 239000000463 material Substances 0.000 claims description 81
- -1 siloxanes Chemical class 0.000 claims description 62
- 125000003118 aryl group Chemical group 0.000 claims description 55
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 46
- 239000000178 monomer Substances 0.000 claims description 40
- 125000003709 fluoroalkyl group Chemical group 0.000 claims description 34
- 239000000758 substrate Substances 0.000 claims description 31
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 30
- 239000000203 mixture Substances 0.000 claims description 29
- 238000007639 printing Methods 0.000 claims description 28
- 125000000217 alkyl group Chemical group 0.000 claims description 25
- 125000004432 carbon atom Chemical group C* 0.000 claims description 23
- 125000003545 alkoxy group Chemical group 0.000 claims description 22
- 125000004429 atom Chemical group 0.000 claims description 22
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 22
- 125000004104 aryloxy group Chemical group 0.000 claims description 19
- 125000004122 cyclic group Chemical group 0.000 claims description 18
- 229910052732 germanium Inorganic materials 0.000 claims description 18
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 claims description 18
- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 claims description 18
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 17
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- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 claims description 16
- 238000002347 injection Methods 0.000 claims description 16
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- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 13
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims description 12
- 125000001072 heteroaryl group Chemical group 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 12
- 229910052757 nitrogen Inorganic materials 0.000 claims description 12
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 claims description 10
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- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 claims description 10
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- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 claims description 10
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- 125000000623 heterocyclic group Chemical group 0.000 claims description 9
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- DZBUGLKDJFMEHC-UHFFFAOYSA-N acridine Chemical compound C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 claims description 8
- 239000011248 coating agent Substances 0.000 claims description 8
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- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 8
- BNRDGHFESOHOBF-UHFFFAOYSA-N 1-benzoselenophene Chemical compound C1=CC=C2[se]C=CC2=C1 BNRDGHFESOHOBF-UHFFFAOYSA-N 0.000 claims description 7
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 claims description 7
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- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 claims description 6
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- IYYZUPMFVPLQIF-UHFFFAOYSA-N dibenzothiophene Chemical class C1=CC=C2C3=CC=CC=C3SC2=C1 IYYZUPMFVPLQIF-UHFFFAOYSA-N 0.000 claims description 6
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- KTZQTRPPVKQPFO-UHFFFAOYSA-N 1,2-benzoxazole Chemical compound C1=CC=C2C=NOC2=C1 KTZQTRPPVKQPFO-UHFFFAOYSA-N 0.000 claims description 5
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 claims description 5
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 claims description 5
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- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims description 5
- 125000005605 benzo group Chemical group 0.000 claims description 5
- WCZVZNOTHYJIEI-UHFFFAOYSA-N cinnoline Chemical compound N1=NC=CC2=CC=CC=C21 WCZVZNOTHYJIEI-UHFFFAOYSA-N 0.000 claims description 5
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- QDLAGTHXVHQKRE-UHFFFAOYSA-N lichenxanthone Natural products COC1=CC(O)=C2C(=O)C3=C(C)C=C(OC)C=C3OC2=C1 QDLAGTHXVHQKRE-UHFFFAOYSA-N 0.000 claims description 5
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- 150000004866 oxadiazoles Chemical class 0.000 claims description 5
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- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 claims description 5
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 claims description 5
- 229910052710 silicon Inorganic materials 0.000 claims description 5
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 claims description 5
- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 claims description 4
- TZMSYXZUNZXBOL-UHFFFAOYSA-N 10H-phenoxazine Chemical compound C1=CC=C2NC3=CC=CC=C3OC2=C1 TZMSYXZUNZXBOL-UHFFFAOYSA-N 0.000 claims description 4
- BAXOFTOLAUCFNW-UHFFFAOYSA-N 1H-indazole Chemical compound C1=CC=C2C=NNC2=C1 BAXOFTOLAUCFNW-UHFFFAOYSA-N 0.000 claims description 4
- IEBQZJXMAOMNBO-UHFFFAOYSA-N 1h-indole;pyridine Chemical class C1=CC=NC=C1.C1=CC=C2NC=CC2=C1 IEBQZJXMAOMNBO-UHFFFAOYSA-N 0.000 claims description 4
- AGIJRRREJXSQJR-UHFFFAOYSA-N 2h-thiazine Chemical compound N1SC=CC=C1 AGIJRRREJXSQJR-UHFFFAOYSA-N 0.000 claims description 4
- BWCDLEQTELFBAW-UHFFFAOYSA-N 3h-dioxazole Chemical compound N1OOC=C1 BWCDLEQTELFBAW-UHFFFAOYSA-N 0.000 claims description 4
- QJTQKPNNQVLHHO-UHFFFAOYSA-N 9h-carbazole;1h-indole Chemical compound C1=CC=C2NC=CC2=C1.C1=CC=C2C3=CC=CC=C3NC2=C1 QJTQKPNNQVLHHO-UHFFFAOYSA-N 0.000 claims description 4
- 125000003302 alkenyloxy group Chemical group 0.000 claims description 4
- RFRXIWQYSOIBDI-UHFFFAOYSA-N benzarone Chemical compound CCC=1OC2=CC=CC=C2C=1C(=O)C1=CC=C(O)C=C1 RFRXIWQYSOIBDI-UHFFFAOYSA-N 0.000 claims description 4
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- 230000005284 excitation Effects 0.000 claims description 4
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- 125000004437 phosphorous atom Chemical group 0.000 claims description 4
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- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 3
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- YRTCKZIKGWZNCU-UHFFFAOYSA-N furo[3,2-b]pyridine Chemical class C1=CC=C2OC=CC2=N1 YRTCKZIKGWZNCU-UHFFFAOYSA-N 0.000 claims description 3
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- ODHXBMXNKOYIBV-UHFFFAOYSA-N triphenylamine Chemical compound C1=CC=CC=C1N(C=1C=CC=CC=1)C1=CC=CC=C1 ODHXBMXNKOYIBV-UHFFFAOYSA-N 0.000 claims description 3
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- ONCNIMLKGZSAJT-UHFFFAOYSA-N thieno[3,2-b]furan Chemical compound S1C=CC2=C1C=CO2 ONCNIMLKGZSAJT-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
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Abstract
本发明涉及一种共轭聚合物,包含通式(I)所示的重复单元:其中,p为重复单元数,所述p是大于或等于1的整数;D1具有通式(II)所示的结构:B1具有通式(III)所示的结构:上述共轭聚合物,具有较高的三线态能级及高的电荷传输性能。
Description
PCT国内申请,说明书已公开。
Claims (18)
- PCT国内申请,权利要求书已公开。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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CN201611147726 | 2016-12-13 | ||
CN2016111477263 | 2016-12-13 | ||
PCT/CN2017/115981 WO2018108107A1 (zh) | 2016-12-13 | 2017-12-13 | 共轭聚合物及其在有机电子器件的应用 |
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CN109791980A true CN109791980A (zh) | 2019-05-21 |
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CN (1) | CN109791980A (zh) |
WO (1) | WO2018108107A1 (zh) |
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CN110698475A (zh) * | 2018-12-10 | 2020-01-17 | 广州华睿光电材料有限公司 | 稠环有机化合物及其应用 |
Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20080061685A1 (en) * | 2006-08-24 | 2008-03-13 | Chesterfield Reid J | Organic electronic devices |
CN102449796A (zh) * | 2009-05-29 | 2012-05-09 | 默克专利有限公司 | 包含至少一种发光体化合物和至少一种具有共轭间断单元的聚合物的组合物 |
US20130006119A1 (en) * | 2010-03-11 | 2013-01-03 | Merck Patent Gmbh | Fibers in therapy and cosmetics |
US20140117289A1 (en) * | 2011-06-17 | 2014-05-01 | Merck Patent Gmbh | Materials for organic electroluminescent devices |
US20140155600A1 (en) * | 2012-11-30 | 2014-06-05 | Samsung Display Co., Ltd. | Hole transport material for organic electroluminescence device and organic electroluminescence device comprising the same |
CN103880849A (zh) * | 2014-03-05 | 2014-06-25 | 南京邮电大学 | 一种窄带隙共轭分子及其制备方法与应用 |
CN104629006A (zh) * | 2013-11-13 | 2015-05-20 | 北京师范大学 | 一类基于含氟咔唑共轭聚合物、其制备方法及其在有机光电子器件中的应用 |
CN105102582A (zh) * | 2013-04-08 | 2015-11-25 | 默克专利有限公司 | 有机电致发光器件 |
CN105860034A (zh) * | 2016-05-03 | 2016-08-17 | 桂林理工大学 | 一种聚合物太阳能电池共混活性层中的共轭聚合物电子给体材料及其制备方法 |
-
2017
- 2017-12-13 CN CN201780059466.0A patent/CN109791980A/zh active Pending
- 2017-12-13 US US16/469,471 patent/US20200109235A1/en not_active Abandoned
- 2017-12-13 WO PCT/CN2017/115981 patent/WO2018108107A1/zh active Application Filing
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20080061685A1 (en) * | 2006-08-24 | 2008-03-13 | Chesterfield Reid J | Organic electronic devices |
CN102449796A (zh) * | 2009-05-29 | 2012-05-09 | 默克专利有限公司 | 包含至少一种发光体化合物和至少一种具有共轭间断单元的聚合物的组合物 |
US20130006119A1 (en) * | 2010-03-11 | 2013-01-03 | Merck Patent Gmbh | Fibers in therapy and cosmetics |
US20140117289A1 (en) * | 2011-06-17 | 2014-05-01 | Merck Patent Gmbh | Materials for organic electroluminescent devices |
US20140155600A1 (en) * | 2012-11-30 | 2014-06-05 | Samsung Display Co., Ltd. | Hole transport material for organic electroluminescence device and organic electroluminescence device comprising the same |
CN105102582A (zh) * | 2013-04-08 | 2015-11-25 | 默克专利有限公司 | 有机电致发光器件 |
CN104629006A (zh) * | 2013-11-13 | 2015-05-20 | 北京师范大学 | 一类基于含氟咔唑共轭聚合物、其制备方法及其在有机光电子器件中的应用 |
CN103880849A (zh) * | 2014-03-05 | 2014-06-25 | 南京邮电大学 | 一种窄带隙共轭分子及其制备方法与应用 |
CN105860034A (zh) * | 2016-05-03 | 2016-08-17 | 桂林理工大学 | 一种聚合物太阳能电池共混活性层中的共轭聚合物电子给体材料及其制备方法 |
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