CN111683948B8 - 菲咯啉化合物以及包含该菲咯啉化合物的有机发光器件 - Google Patents

菲咯啉化合物以及包含该菲咯啉化合物的有机发光器件 Download PDF

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CN111683948B8
CN111683948B8 CN201780098097.6A CN201780098097A CN111683948B8 CN 111683948 B8 CN111683948 B8 CN 111683948B8 CN 201780098097 A CN201780098097 A CN 201780098097A CN 111683948 B8 CN111683948 B8 CN 111683948B8
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same
phenanthroline compound
emitting device
organic light
phenanthroline
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CN111683948A (zh
CN111683948B (zh
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李宗仑
朴宽熙
柳智淑
李善桂
相 赵
赵相
柳承一
鞠昌勋
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
    • C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
    • 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]
    • H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
    • H10K50/125—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers specially adapted for multicolour light emission, e.g. for emitting white light
    • H10K50/13—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers specially adapted for multicolour light emission, e.g. for emitting white light comprising stacked EL layers within one EL unit
    • 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
    • H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
    • 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
    • H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
    • H10K85/622—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene containing four rings, e.g. pyrene
    • 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
    • H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
    • 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
    • H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
    • H10K85/6572—Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ring system, e.g. phenanthroline or carbazole
    • 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]
    • H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Optics & Photonics (AREA)
  • Electroluminescent Light Sources (AREA)

Abstract

本发明涉及一种菲咯啉化合物，以及通过在至少一个有机物层中包含该菲咯啉化合物而表现出优秀的效率特性的有机电致发光器件。
CN201780098097.6A 2017-11-07 2017-11-10 菲咯啉化合物以及包含该菲咯啉化合物的有机发光器件 Active CN111683948B8 (zh)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
KR10-2017-0147651 2017-11-07
KR1020170147651A KR101984676B1 (ko) 2017-11-07 2017-11-07 페난트롤린 화합물 및 이를 포함하는 유기발광소자
PCT/KR2017/012705 WO2019093544A1 (ko) 2017-11-07 2017-11-10 페난트롤린 화합물 및 이를 포함하는 유기발광소자

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CN111683948A CN111683948A (zh) 2020-09-18
CN111683948B CN111683948B (zh) 2023-06-27
CN111683948B8 true CN111683948B8 (zh) 2023-12-01

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WO (1) WO2019093544A1 (zh)

Families Citing this family (5)

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Publication number Priority date Publication date Assignee Title
CN109608452B (zh) * 2018-12-24 2020-12-04 武汉天马微电子有限公司 有机化合物、显示面板及显示装置
KR20210081637A (ko) * 2019-12-24 2021-07-02 솔루스첨단소재 주식회사 유기 화합물 및 이를 이용한 유기 전계 발광 소자
KR102423258B1 (ko) * 2020-07-02 2022-07-21 솔루스첨단소재 주식회사 유기 화합물 및 이를 이용한 유기 전계 발광 소자
KR20220081021A (ko) * 2020-12-08 2022-06-15 엘지디스플레이 주식회사 유기 화합물, 이를 포함하는 유기발광다이오드 및 유기발광장치
WO2023125541A1 (zh) * 2021-12-27 2023-07-06 浙江光昊光电科技有限公司 一种有机电子器件

Citations (2)

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CN104953037A (zh) * 2014-03-31 2015-09-30 乐金显示有限公司 有机发光二极管
JP2017191661A (ja) * 2016-04-11 2017-10-19 出光興産株式会社 有機エレクトロルミネッセンス素子

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KR20170104718A (ko) * 2016-03-07 2017-09-18 덕산네오룩스 주식회사 유기전기 소자용 화합물, 이를 이용한 유기전기소자 및 그 전자 장치

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* Cited by examiner, † Cited by third party
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CN104953037A (zh) * 2014-03-31 2015-09-30 乐金显示有限公司 有机发光二极管
JP2017191661A (ja) * 2016-04-11 2017-10-19 出光興産株式会社 有機エレクトロルミネッセンス素子

Non-Patent Citations (3)

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Title
; Rajendran Suresh 等.SnCl2-Catalyzed Selective Atom Economic Imino Diels−Alder Reaction: Synthesis of 2-(1H-Pyrrolo[2,3-b]pyridin-3-yl)quinolines.《JOURNAL OF ORGANIC CHEMISTRY》.2012,第77卷(第3期),第1468−1476页. *
Diphenanthroline Electron Transport Materials for the Efficient Charge Generation Unit in Tandem Organic Light-Emitting Diodes;Gyeong Woo Kim 等;《Chemistry of Materials》;20170911;第29卷(第19期);第8299-8312页 *
New Sterically Encumbered 2,9-Diarylphenanthrolines for the Selective Formation of Heteroleptic Bis(phenanthroline)copper(I) Complexes;Michael Schmittel等;《European Journal of Inorganic Chemistry》;20010321(第5期);第1155-1166页 *

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KR20190051714A (ko) 2019-05-15
KR101984676B1 (ko) 2019-05-31
WO2019093544A1 (ko) 2019-05-16
CN111683948A (zh) 2020-09-18
CN111683948B (zh) 2023-06-27

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CI03 Correction of invention patent

Correction item: Inventor

Correct: Li Zonglun|Park Kuan hee|Liu Zhishu|Li Shangui|Zhao Jianxiang|Liu Chengyi|Ju Changxun

False: Li Zonglun|Park Kuan hee|Liu Zhishu|Li Shangui|Zhao Congxiang|Liu Chengyi|Ju Changxun

Number: 26-01

Volume: 39

Correction item: Inventor

Correct: Li Zonglun|Park Kuan hee|Liu Zhishu|Li Shangui|Zhao Jianxiang|Liu Chengyi|Ju Changxun

False: Li Zonglun|Park Kuan hee|Liu Zhishu|Li Shangui|Zhao Congxiang|Liu Chengyi|Ju Changxun

Number: 26-01

Page: The title page

Volume: 39

CI03 Correction of invention patent
OR01 Other related matters
OR01 Other related matters