KR20120069675A - 유기 반도체 - Google Patents
유기 반도체 Download PDFInfo
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- KR20120069675A KR20120069675A KR1020127005640A KR20127005640A KR20120069675A KR 20120069675 A KR20120069675 A KR 20120069675A KR 1020127005640 A KR1020127005640 A KR 1020127005640A KR 20127005640 A KR20127005640 A KR 20127005640A KR 20120069675 A KR20120069675 A KR 20120069675A
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- 150000001875 compounds Chemical class 0.000 claims abstract description 31
- 125000003118 aryl group Chemical group 0.000 claims abstract description 24
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 13
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 13
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 13
- 125000006165 cyclic alkyl group Chemical group 0.000 claims abstract description 11
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 10
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 9
- 125000003368 amide group Chemical group 0.000 claims abstract description 9
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract description 9
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 claims abstract description 9
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract description 9
- -1 al Kenyl Chemical group 0.000 claims abstract description 6
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 5
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- 125000005842 heteroatom Chemical group 0.000 claims description 8
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- 239000001257 hydrogen Substances 0.000 claims description 2
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 1
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- 229910052737 gold Inorganic materials 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 238000004770 highest occupied molecular orbital Methods 0.000 description 1
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 1
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- 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 compound C1=C2SC=CC2=C2C=CSC2=C1 CRUIOQJBPNKOJG-UHFFFAOYSA-N 0.000 description 1
- PYJJCSYBSYXGQQ-UHFFFAOYSA-N trichloro(octadecyl)silane Chemical compound CCCCCCCCCCCCCCCCCC[Si](Cl)(Cl)Cl PYJJCSYBSYXGQQ-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D495/14—Ortho-condensed systems
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/22—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains four or more hetero rings
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- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
- C07F7/0812—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
- C07F7/0816—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring said ring comprising Si as a ring atom
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- H10K10/46—Field-effect transistors, e.g. organic thin-film transistors [OTFT]
- H10K10/462—Insulated gate field-effect transistors [IGFETs]
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Abstract
Description
도 2는 종래 기술에 따른 하부-게이트 유기 박막 필름 트랜지스터의 일반적 구조의 개략도이다.
도 3은 본 발명의 양태에 따라서 공통 기판상에 제작된 유기 박막 트랜지스터 및 인접 유기 발광 장치를 포함하는 픽셀의 개략도이다.
도 4는 본 발명의 양태에 따른 유기 발광 장치에 적층 관계로 제작된 유기 박막 트랜지스터의 개략도이다.
Claims (14)
- 하기 화학식 I의 반도체성 화합물:
화학식 I
상기 식에서,
R1 내지 R4는 독립적으로, 비제한적으로, 탄소수 2 내지 20의 선택적으로 치환된 선형, 분지형 또는 환형 알킬 쇄, 알콕시, 아미노, 아미도, 실릴, 알킬, 알켄일, 아릴 또는 헤테로아릴이고;
X1 및 X2는 독립적으로 S, O, NR5 또는 SiR6R7이고;
R5 내지 R7은 독립적으로 선형, 분지형 또는 환형 C1-C5 알킬 쇄이고;
Ar1은 바람직하게는 S, O, NR5 및 SiR6R7로 이루어진 군으로부터 선택된 하나 이상의 이종원자를 포함하는 이종환형 방향족 고리이고;
n은 1 내지 4의 정수이다. - 제 2 항에 있어서,
Ar2가 바람직하게는 S, O, NR5 및 SiR6R7로 이루어진 군으로부터 선택된 하나 이상의 이종원자를 포함하는 이종환형 방향족 고리인 반도체성 화합물. - 제 1 항 내지 제 3 항중 어느 한 항에 있어서,
Ar1 및/또는, 존재하는 경우, Ar2에 직렬로 융합된 하나 이상의 추가의 방향족 기를 포함하는 반도체성 화합물. - 제 4 항에 있어서,
추가의 방향족 기의 하나, 일부 또는 모두가 바람직하게는 S, O, NR5 및 SiR6R7로 이루어진 군으로부터 선택된 하나 이상의 이종원자를 포함하는 이종환형 기인 반도체성 화합물. - 제 1 항 내지 제 5 항중 어느 한 항에 있어서,
화합물의 말단 아릴 기중 하나 또는 둘다가 하나 이상의 치환기 T로 치환되되, 치환기 T중 하나 이상이 탄소수 1 내지 20, 예컨대 1 내지 12의 선택적으로 치환된 선형, 분지형 또는 환형 알킬 쇄, 알콕시, 아미노, 아미도, 실릴, 알킬, 알켄일, 아릴 또는 헤테로아릴이고, 나머지가 독립적으로 수소, 또는 탄소수 1 내지 20, 예컨대 1 내지 12의 선택적으로 치환된 선형, 분지형 또는 환형 알킬 쇄, 알콕시, 아미노, 아미도, 실릴, 알킬 또는 알켄일인 반도체성 화합물. - 하기 화학식 6의 반도체성 화합물:
화학식 6
상기 식에서,
R1 내지 R4는 독립적으로, 비제한적으로, 탄소수 1 내지 20, 예컨대 1 내지 12의 선택적으로 치환된 선형, 분지형 또는 환형 알킬 쇄, 알콕시, 아미노, 아미도, 실릴, 알킬, 알켄일, 아릴 또는 헤테로아릴이고;
X1 및 X2는 독립적으로 S, O, NR5 또는 SiR6R7이고;
R5 내지 R7은 독립적으로 선형, 분지형 또는 환형 C1-C5 알킬 쇄이고;
T1 및 T2는 독립적으로 탄소수 1 내지 20, 예컨대 1 내지 12의 선택적으로 치환된 선형, 분지형 또는 환형 알킬 쇄, 알콕시, 아미노, 아미도, 실릴, 알킬, 알켄일, 아릴 또는 헤테로아릴이고;
선택적인 아릴 기 Ar1 내지 Ar6중 하나 이상은 독립적으로 S, O, NR5 및 SiR6R7로 이루어진 군으로부터 선택된 하나 이상의 이종원자를 포함하는 이종환이다. - 제 8 항에 있어서,
말단 아릴 기중 하나 또는 둘다가 동종환형 고리인 반도체성 화합물. - 제 1 항 내지 제 9 항중 어느 한 항에 있어서,
R1 내지 R4가 동일하거나 상이하고, 독립적으로 탄소수 2 내지 12의 선택적으로 치환된 선형, 분지형 또는 환형 알킬 쇄인 반도체성 화합물. - 제 10 항에 있어서,
R1 내지 R4가 동일하거나 상이하고, 독립적으로 탄소수 2 내지 6의 선택적으로 치환된 선형, 분지형 또는 환형 알킬 쇄인 반도체성 화합물. - 제 1 항 내지 제 11 항중 어느 한 항에 따른 반도체성 화합물을 포함하는 반도체성 부분을 포함하는 전자 장치.
- 제 1 항 내지 제 11 항중 어느 한 항에 따른 반도체성 화합물을 포함하는, 기판의 표면에 적용하여 기판상에 반도체성 부분을 형성하기 위한 용액.
- 제 13 항에 따른 용액을 기판에 적용함을 포함하는, 전자 장치의 제조 방법.
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| PCT/GB2010/001485 WO2012017184A1 (en) | 2009-08-05 | 2010-08-05 | Organic semiconductors |
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| WO2020085579A1 (ko) * | 2018-10-22 | 2020-04-30 | 경상대학교산학협력단 | 신규한 스피로 화합물 및 이를 이용하는 유기 전자 소자 |
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| JP6392205B2 (ja) | 2012-04-25 | 2018-09-19 | メルク パテント ゲーエムベーハー | 共役ポリマー |
| EP2928939A1 (en) | 2012-12-07 | 2015-10-14 | Merck Patent GmbH | Polymer comprising a naphthalene group and its use in organic electronic devices |
| EP2935235B1 (en) * | 2012-12-18 | 2018-02-21 | Merck Patent GmbH | Indenophenanthrene based compounds |
| KR102173046B1 (ko) * | 2013-12-06 | 2020-11-03 | 삼성디스플레이 주식회사 | 축합환 화합물 및 이를 포함한 유기 발광 소자 |
| JP6252264B2 (ja) * | 2014-03-12 | 2017-12-27 | 住友化学株式会社 | 高分子化合物およびそれを用いた有機半導体素子 |
| CN105315298B (zh) * | 2014-08-04 | 2017-10-10 | 中国科学院化学研究所 | 基于七并稠环单元的a‑d‑a共轭分子及其制备方法和应用 |
| CN104557972B (zh) * | 2015-01-20 | 2017-02-22 | 武汉理工大学 | 双(噻吩并[3,2‑b]噻吩)并芴单体、共轭聚合物及其应用 |
| CN108699076B (zh) * | 2015-12-10 | 2021-07-16 | Clap有限公司 | 萘并引达省并二噻吩和聚合物 |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| KR20150067277A (ko) * | 2012-10-05 | 2015-06-17 | 메르크 파텐트 게엠베하 | 유기 반도체 |
| WO2020085579A1 (ko) * | 2018-10-22 | 2020-04-30 | 경상대학교산학협력단 | 신규한 스피로 화합물 및 이를 이용하는 유기 전자 소자 |
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| EP3447057A1 (en) | 2019-02-27 |
| CN102482291A (zh) | 2012-05-30 |
| GB2472413B (en) | 2014-04-23 |
| JP5812355B2 (ja) | 2015-11-11 |
| EP3524610A1 (en) | 2019-08-14 |
| EP3141551A1 (en) | 2017-03-15 |
| WO2012017184A1 (en) | 2012-02-09 |
| EP2462146A1 (en) | 2012-06-13 |
| EP3447057B1 (en) | 2021-10-06 |
| GB0913628D0 (en) | 2009-09-16 |
| EP3524610B1 (en) | 2022-10-05 |
| US20120184089A1 (en) | 2012-07-19 |
| JP6053880B2 (ja) | 2016-12-27 |
| US8853679B2 (en) | 2014-10-07 |
| KR101787121B1 (ko) | 2017-10-18 |
| JP2013501076A (ja) | 2013-01-10 |
| JP2015227461A (ja) | 2015-12-17 |
| GB2472413A (en) | 2011-02-09 |
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