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WO2009066666A1 - 高分子化合物及びそれを用いた有機エレクトロルミネッセンス素子 - Google Patents

高分子化合物及びそれを用いた有機エレクトロルミネッセンス素子 Download PDF

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WO2009066666A1
WO2009066666A1 PCT/JP2008/070949 JP2008070949W WO2009066666A1 WO 2009066666 A1 WO2009066666 A1 WO 2009066666A1 JP 2008070949 W JP2008070949 W JP 2008070949W WO 2009066666 A1 WO2009066666 A1 WO 2009066666A1
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substituted
ring
unsubstituted
polymeric compound
carbon atoms
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PCT/JP2008/070949
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French (fr)
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Mitsunori Ito
Yumiko Mizuki
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Idemitsu Kosan Co., Ltd.
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Priority to US12/743,509 priority Critical patent/US8558221B2/en
Priority to JP2009542558A priority patent/JPWO2009066666A1/ja
Priority to EP08852465A priority patent/EP2213693A4/en
Publication of WO2009066666A1 publication Critical patent/WO2009066666A1/ja

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    • C08G61/00Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
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  • Optics & Photonics (AREA)
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  • Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)

Abstract

 下記式(1)で表される化合物から誘導される繰り返し単位と特定構造の芳香族化合物から誘導される繰り返し単位とを含む高分子化合物。 (式中、Ar1~Ar4は、それぞれ独立に、置換もしくは無置換の環形成炭素数6~40のアリール基、置換もしくは無置換の環形成原子数3~40の複素環基、または、置換もしくは無置換の炭素数1~50のアルキル基であり;Xは、置換もしくは無置換の環形成炭素数6~40アリール基、置換もしくは無置換の環形成原子数3~40の複素環基、または、置換もしくは無置換の2~4価のスチレン誘導基であり、sは0~3の整数である)。上記高分子化合物は発光材料として有用で、寿命、発光効率等の素子特性に優れた高分子エレクトロルミネッセンス素子を実現することができる。
PCT/JP2008/070949 2007-11-20 2008-11-18 高分子化合物及びそれを用いた有機エレクトロルミネッセンス素子 WO2009066666A1 (ja)

Priority Applications (3)

Application Number Priority Date Filing Date Title
US12/743,509 US8558221B2 (en) 2007-11-20 2008-11-18 Polymeric compound containing dopant and host repeating units and organic electroluminescence element
JP2009542558A JPWO2009066666A1 (ja) 2007-11-20 2008-11-18 高分子化合物及びそれを用いた有機エレクトロルミネッセンス素子
EP08852465A EP2213693A4 (en) 2007-11-20 2008-11-18 POLYMER COMPOUND AND ORGANIC ELECTROLUMINESCENT ELEMENT THEREWITH

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JP2007-300088 2007-11-20
JP2007300088 2007-11-20

Publications (1)

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WO2009066666A1 true WO2009066666A1 (ja) 2009-05-28

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US (1) US8558221B2 (ja)
EP (1) EP2213693A4 (ja)
JP (1) JPWO2009066666A1 (ja)
KR (1) KR20100077200A (ja)
WO (1) WO2009066666A1 (ja)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010189454A (ja) * 2009-02-13 2010-09-02 Mitsubishi Chemicals Corp 共役ポリマー、ポリマー組成物、電荷輸送材料、有機電界発光素子、有機elディスプレイ及び有機el照明
WO2011019058A1 (ja) * 2009-08-13 2011-02-17 住友化学株式会社 高分子化合物及びその製造方法
WO2011105622A1 (ja) * 2010-02-25 2011-09-01 住友化学株式会社 フルオランテン系高分子化合物
WO2012086670A1 (ja) * 2010-12-21 2012-06-28 住友化学株式会社 組成物及びブロック型共重合体
WO2012086671A1 (ja) * 2010-12-21 2012-06-28 住友化学株式会社 高分子化合物及びそれを用いた有機el素子
JP2012524139A (ja) * 2009-04-16 2012-10-11 ケンブリッジ ディスプレイ テクノロジー リミテッド 有機発光材料および素子
JP2012241170A (ja) * 2011-05-24 2012-12-10 Sumitomo Chemical Co Ltd ピレン系高分子化合物及びそれを用いた発光素子
JP2013227401A (ja) * 2012-04-25 2013-11-07 Sumitomo Chemical Co Ltd 高分子化合物及びそれを用いた発光素子
JP2018184603A (ja) * 2012-12-24 2018-11-22 ケンブリッジ ディスプレイ テクノロジー リミテッド ポリマーおよびデバイス
JP2022506658A (ja) * 2018-11-07 2022-01-17 メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング アミン基含有繰り返し単位を有するポリマー

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WO2009075203A1 (ja) * 2007-12-11 2009-06-18 Idemitsu Kosan Co., Ltd. 高分子化合物及びそれを用いた有機エレクトロルミネッセンス素子
CN103107284A (zh) 2007-12-28 2013-05-15 出光兴产株式会社 芳胺衍生物及使用该芳胺衍生物的有机电致发光元件
CN104795495B (zh) 2009-04-24 2017-09-29 出光兴产株式会社 芳香族胺衍生物和使用其的有机电致发光元件
JP5587302B2 (ja) 2009-12-16 2014-09-10 出光興産株式会社 芳香族アミン誘導体及びそれを用いた有機エレクトロルミネッセンス素子
JP5866990B2 (ja) * 2010-11-15 2016-02-24 住友化学株式会社 高分子化合物及びその製造方法
KR101848118B1 (ko) 2011-03-25 2018-04-11 스미또모 가가꾸 가부시키가이샤 고분자 화합물 및 그것을 사용하여 이루어지는 발광 소자
KR101980759B1 (ko) * 2012-12-18 2019-05-21 엘지디스플레이 주식회사 유기 발광 표시 장치
WO2016042781A1 (ja) 2014-09-19 2016-03-24 出光興産株式会社 新規な化合物
KR102343572B1 (ko) * 2015-03-06 2021-12-28 삼성디스플레이 주식회사 유기 발광 소자
KR102385225B1 (ko) * 2017-07-12 2022-04-11 삼성디스플레이 주식회사 유기막 형성용 조성물, 이를 이용한 표시 장치 및 표시 장치의 제조 방법
CN111233676B (zh) * 2020-01-17 2022-03-29 华南理工大学 一种高性能空穴传输材料及其制备与应用
DE102023122545A1 (de) 2023-08-23 2025-02-27 Technische Universität Chemnitz, Körperschaft des öffentlichen Rechts Neues aromatisches Copolymer, welches Sulfonat-substituierte Naphthalin-Wiederholeinheiten sowie aromatische Phenyl-, Biphenyl- oder Terphenyl-Wiederholeinheiten umfasst, dessen Herstellung und Verwendung

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