JP4922301B2 - 有機電子素子における正孔注入の改善のための新規材料並びに前記材料の使用 - Google Patents
有機電子素子における正孔注入の改善のための新規材料並びに前記材料の使用 Download PDFInfo
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- JP4922301B2 JP4922301B2 JP2008529595A JP2008529595A JP4922301B2 JP 4922301 B2 JP4922301 B2 JP 4922301B2 JP 2008529595 A JP2008529595 A JP 2008529595A JP 2008529595 A JP2008529595 A JP 2008529595A JP 4922301 B2 JP4922301 B2 JP 4922301B2
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- Prior art keywords
- organic
- organic electronic
- materials
- hole transport
- substituents
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- 239000000463 material Substances 0.000 title claims description 27
- 238000002347 injection Methods 0.000 title description 5
- 239000007924 injection Substances 0.000 title description 5
- 230000006872 improvement Effects 0.000 title description 2
- 230000005525 hole transport Effects 0.000 claims description 13
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 239000000460 chlorine Substances 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 125000001424 substituent group Chemical group 0.000 claims description 4
- 238000009834 vaporization Methods 0.000 claims description 4
- 230000008016 vaporization Effects 0.000 claims description 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 3
- 230000005669 field effect Effects 0.000 claims description 3
- 229910052731 fluorine Inorganic materials 0.000 claims description 3
- 239000011737 fluorine Substances 0.000 claims description 3
- 238000007496 glass forming Methods 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- -1 heterocyclic quinodimethane derivative Chemical class 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 238000013086 organic photovoltaic Methods 0.000 claims description 2
- 239000004065 semiconductor Substances 0.000 claims description 2
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- 150000003549 thiazolines Chemical class 0.000 description 3
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 2
- 125000005002 aryl methyl group Chemical group 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 230000005684 electric field Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 235000003913 Coccoloba uvifera Nutrition 0.000 description 1
- 229910021591 Copper(I) chloride Inorganic materials 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-L Malonate Chemical compound [O-]C(=O)CC([O-])=O OFOBLEOULBTSOW-UHFFFAOYSA-L 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 240000008976 Pterocarpus marsupium Species 0.000 description 1
- 239000000370 acceptor Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000005251 aryl acyl group Chemical group 0.000 description 1
- 230000031709 bromination Effects 0.000 description 1
- 238000005893 bromination reaction Methods 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000005137 deposition process Methods 0.000 description 1
- 239000002019 doping agent Substances 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000005691 oxidative coupling reaction Methods 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- ZNNZYHKDIALBAK-UHFFFAOYSA-M potassium thiocyanate Chemical compound [K+].[S-]C#N ZNNZYHKDIALBAK-UHFFFAOYSA-M 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000027756 respiratory electron transport chain Effects 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- PCCVSPMFGIFTHU-UHFFFAOYSA-N tetracyanoquinodimethane Chemical class N#CC(C#N)=C1C=CC(=C(C#N)C#N)C=C1 PCCVSPMFGIFTHU-UHFFFAOYSA-N 0.000 description 1
- 238000005019 vapor deposition process Methods 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/611—Charge transfer complexes
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/14—Carrier transporting layers
- H10K50/15—Hole transporting layers
- H10K50/155—Hole transporting layers comprising dopants
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/656—Aromatic compounds comprising a hetero atom comprising two or more different heteroatoms per ring
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/17—Carrier injection layers
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K71/00—Manufacture or treatment specially adapted for the organic devices covered by this subclass
- H10K71/30—Doping active layers, e.g. electron transporting layers
-
- 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
Landscapes
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Optics & Photonics (AREA)
- Electroluminescent Light Sources (AREA)
- Thiazole And Isothizaole Compounds (AREA)
Description
1. アリールメチルケトンの臭素化
相応のアリールメチルケトンを、酢酸中で臭素によって臭素化する。
前記の1.)によるブロモメチル−アリールケトンを、カリウムローダニドを用いて沸騰エタノール中で転化させる。
前記の2.)によるアリールアシルローダニドを、マロン酸ジニトリルとトリエチルアミンによって沸騰エタノール中で転化させて、相応のチアゾリン誘導体が得られる。
前記の3.)による相応のチアゾリン誘導体を、−70℃でブチルリチウムによって脱プロトン化し、引き続き酸化剤(例えばCuCl2)を用いて酸化させて、所望の4,4′−ジアリール−キノ−5,5′−ビスチアゾリル−2,2′−ジシアノジメタンが得られる。
Claims (4)
- 請求項1に記載の材料を、有機電子素子において用いる使用。
- 前記有機電子素子は、有機発光ダイオード(OLED)、有機電界効果トランジスタ(OFET)及び/又は有機光電池素子から選択される、請求項2に記載の使用。
- 少なくとも2つの電極と、その間に1つの活性層を有する有機電子素子であって、少なくとも1つの電極と活性層との間に、1つの正孔輸送層が配置されている有機電子素子であって、正孔輸送層に、請求項1記載の材料が混ぜられていることを特徴とする有機電子素子。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102005042105 | 2005-09-05 | ||
DE102005042105.9 | 2005-09-05 | ||
PCT/EP2006/065726 WO2007028733A1 (de) | 2005-09-05 | 2006-08-28 | Neue materialien zur verbesserung der lochinjektion in organischen elektronischen bauelementen und verwendung des materials |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2009507386A JP2009507386A (ja) | 2009-02-19 |
JP4922301B2 true JP4922301B2 (ja) | 2012-04-25 |
Family
ID=37137540
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2008529595A Active JP4922301B2 (ja) | 2005-09-05 | 2006-08-28 | 有機電子素子における正孔注入の改善のための新規材料並びに前記材料の使用 |
Country Status (7)
Country | Link |
---|---|
US (1) | US7947975B2 (ja) |
EP (1) | EP1938398B1 (ja) |
JP (1) | JP4922301B2 (ja) |
KR (1) | KR101339712B1 (ja) |
CN (1) | CN101273480B (ja) |
DE (1) | DE502006007053D1 (ja) |
WO (1) | WO2007028733A1 (ja) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5306341B2 (ja) * | 2007-07-04 | 2013-10-02 | コーニンクレッカ フィリップス エヌ ヴェ | パターン化された層を基板上に形成する方法 |
JP5488473B2 (ja) * | 2008-11-19 | 2014-05-14 | 日産化学工業株式会社 | 電荷輸送性ワニス |
KR102442614B1 (ko) | 2015-08-07 | 2022-09-14 | 삼성디스플레이 주식회사 | 디벤조보롤계 화합물 및 이를 포함한 유기 발광 소자 |
CN110483529B (zh) * | 2019-08-09 | 2021-04-13 | 宁波卢米蓝新材料有限公司 | 一种稠杂环化合物及其应用 |
CN113809246B (zh) * | 2020-06-15 | 2024-06-11 | Tcl科技集团股份有限公司 | 复合材料及其制备方法和量子点发光二极管 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000196140A (ja) * | 1998-12-28 | 2000-07-14 | Sharp Corp | 有機エレクトロルミネッセンス素子とその製造法 |
JP2005167175A (ja) * | 2003-12-04 | 2005-06-23 | Novaled Gmbh | 有機半導体をキノンジイミン誘導体によってドーピングする方法 |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3515373A1 (de) * | 1985-04-27 | 1986-11-06 | Merck Patent Gmbh, 6100 Darmstadt | Stickstoffhaltige heterocyclen |
JPH09512572A (ja) | 1994-04-28 | 1997-12-16 | ビーエーエスエフ アクチェンゲゼルシャフト | チアゾールメチン染料 |
EP0941990A3 (de) | 1998-03-09 | 2002-07-24 | Siemens Aktiengesellschaft | Verfahren zur Herstellung von Azamethinen sowie Azamethine selbst |
WO2002012212A1 (de) | 2000-08-07 | 2002-02-14 | Siemens Aktiengesellschaft | Di(het)arylaminothiazol-derivate und ihre verwendung in organischen lichtemittierenden dioden (oleds) und organischen photovoltaischen bauelemente |
WO2006102620A2 (en) * | 2005-03-24 | 2006-09-28 | Northwestern University | TWISTED π-ELECTRON SYSTEM CHROMOPHORE COMPOUNDS WITH VERY LARGE MOLECULAR HYPERPOLARIZABILITIES AND RELATED COMPOSITIONS AND DEVICES |
-
2006
- 2006-08-28 US US12/065,814 patent/US7947975B2/en active Active
- 2006-08-28 KR KR1020087007903A patent/KR101339712B1/ko active IP Right Grant
- 2006-08-28 CN CN2006800323603A patent/CN101273480B/zh active Active
- 2006-08-28 DE DE502006007053T patent/DE502006007053D1/de active Active
- 2006-08-28 EP EP06778379A patent/EP1938398B1/de active Active
- 2006-08-28 WO PCT/EP2006/065726 patent/WO2007028733A1/de active Application Filing
- 2006-08-28 JP JP2008529595A patent/JP4922301B2/ja active Active
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000196140A (ja) * | 1998-12-28 | 2000-07-14 | Sharp Corp | 有機エレクトロルミネッセンス素子とその製造法 |
JP2005167175A (ja) * | 2003-12-04 | 2005-06-23 | Novaled Gmbh | 有機半導体をキノンジイミン誘導体によってドーピングする方法 |
Also Published As
Publication number | Publication date |
---|---|
JP2009507386A (ja) | 2009-02-19 |
CN101273480B (zh) | 2010-09-15 |
EP1938398A1 (de) | 2008-07-02 |
WO2007028733A1 (de) | 2007-03-15 |
US7947975B2 (en) | 2011-05-24 |
EP1938398B1 (de) | 2010-05-26 |
US20090152535A1 (en) | 2009-06-18 |
KR20080052634A (ko) | 2008-06-11 |
DE502006007053D1 (de) | 2010-07-08 |
CN101273480A (zh) | 2008-09-24 |
KR101339712B1 (ko) | 2013-12-11 |
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