KR102252884B1 - 신규한 화합물 및 이를 이용한 유기발광 소자 - Google Patents
신규한 화합물 및 이를 이용한 유기발광 소자 Download PDFInfo
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- KR102252884B1 KR102252884B1 KR1020190103963A KR20190103963A KR102252884B1 KR 102252884 B1 KR102252884 B1 KR 102252884B1 KR 1020190103963 A KR1020190103963 A KR 1020190103963A KR 20190103963 A KR20190103963 A KR 20190103963A KR 102252884 B1 KR102252884 B1 KR 102252884B1
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- MIHGLWBVTFFWJB-UHFFFAOYSA-N CC(C)(C)c(cc1)ccc1-c(cc1)ccc1N(c(cc1)cc(C2(C)C)c1-c(cc1)c2c(C2(C3CC(C4)CC2CC4C3)c2c3)c1-c2ccc3N(c(cc1)ccc1-c1ccc(C(C)(C)C)cc1)c1ccc(c2ccccc2[o]2)c2c1)c1ccc(c(cccc2)c2[o]2)c2c1 Chemical compound CC(C)(C)c(cc1)ccc1-c(cc1)ccc1N(c(cc1)cc(C2(C)C)c1-c(cc1)c2c(C2(C3CC(C4)CC2CC4C3)c2c3)c1-c2ccc3N(c(cc1)ccc1-c1ccc(C(C)(C)C)cc1)c1ccc(c2ccccc2[o]2)c2c1)c1ccc(c(cccc2)c2[o]2)c2c1 MIHGLWBVTFFWJB-UHFFFAOYSA-N 0.000 description 2
- LBMANLRDCSBXSA-UHFFFAOYSA-N CC(C)(C)c(cc1)ccc1N(c(cc1C23C4CC(C5)CC2CC5C4)ccc1-c(c-1c2C(C)(C)c4ccccc-14)c3cc2N(c1ccc(C(C)(C)C)cc1)c(cc1)cc(c2c3cccc2)c1[n]3-c1ccccc1)c(cc1c2ccccc22)ccc1[n]2-c1ccccc1 Chemical compound CC(C)(C)c(cc1)ccc1N(c(cc1C23C4CC(C5)CC2CC5C4)ccc1-c(c-1c2C(C)(C)c4ccccc-14)c3cc2N(c1ccc(C(C)(C)C)cc1)c(cc1)cc(c2c3cccc2)c1[n]3-c1ccccc1)c(cc1c2ccccc22)ccc1[n]2-c1ccccc1 LBMANLRDCSBXSA-UHFFFAOYSA-N 0.000 description 2
- AZEKMNYGCGTYBL-UHFFFAOYSA-N Brc1ccc(c(cc(c(C23C4CC(C5)CC2CC5C4)c2)-c(c4c5[s]c6c4cccc6)c3cc5Br)c2[s]2)c2c1 Chemical compound Brc1ccc(c(cc(c(C23C4CC(C5)CC2CC5C4)c2)-c(c4c5[s]c6c4cccc6)c3cc5Br)c2[s]2)c2c1 AZEKMNYGCGTYBL-UHFFFAOYSA-N 0.000 description 1
- DSKHQAQLBMBLGB-UHFFFAOYSA-N Brc1ccc(cc2-c3ccc(ccc(Br)c4)c4c3C3(C4CC(C5)CC3CC5C4)c2c2)c2c1 Chemical compound Brc1ccc(cc2-c3ccc(ccc(Br)c4)c4c3C3(C4CC(C5)CC3CC5C4)c2c2)c2c1 DSKHQAQLBMBLGB-UHFFFAOYSA-N 0.000 description 1
- UXRLWBNNINJNFQ-UHFFFAOYSA-N C(C(CC1C2)C3)C2CC3C1(c1c2)c3cc(N(c4ccccc4)c4ccc(c(cc(cccc5)c5c5)c5[o]5)c5c4)c4[s]c(cccc5)c5c4c3-c1cc1c2[s]c2c1ccc(N(c1ccccc1)c1ccc(c3cc(cccc4)c4cc3[o]3)c3c1)c2 Chemical compound C(C(CC1C2)C3)C2CC3C1(c1c2)c3cc(N(c4ccccc4)c4ccc(c(cc(cccc5)c5c5)c5[o]5)c5c4)c4[s]c(cccc5)c5c4c3-c1cc1c2[s]c2c1ccc(N(c1ccccc1)c1ccc(c3cc(cccc4)c4cc3[o]3)c3c1)c2 UXRLWBNNINJNFQ-UHFFFAOYSA-N 0.000 description 1
- RQMBVURAUYSEBX-UHFFFAOYSA-N CC(C)(C)c(cc1)ccc1-c(cc1)ccc1N(c(cc1)cc2c1c(cccc1)c1[o]2)c1ccc(c(ccc-2c3C4(C5CC(C6)CC4CC6C5)c(cc4)c-2c([o]c2c5)c4c2ccc5N(c(cc2)ccc2-c2ccc(C(C)(C)C)cc2)c2ccc(c(cccc4)c4[o]4)c4c2)c3[o]2)c2c1 Chemical compound CC(C)(C)c(cc1)ccc1-c(cc1)ccc1N(c(cc1)cc2c1c(cccc1)c1[o]2)c1ccc(c(ccc-2c3C4(C5CC(C6)CC4CC6C5)c(cc4)c-2c([o]c2c5)c4c2ccc5N(c(cc2)ccc2-c2ccc(C(C)(C)C)cc2)c2ccc(c(cccc4)c4[o]4)c4c2)c3[o]2)c2c1 RQMBVURAUYSEBX-UHFFFAOYSA-N 0.000 description 1
- ZEIJKKNWPJCBFQ-UHFFFAOYSA-N CC(C)(C)c(cc1)ccc1N(C(C)(C)c1ccccc1)c(cc1)cc2c1c(cc(C1(C3CC(C4)CC1CC4C3)c1ccc(c(c([o]3)c4)ccc4N(C(C)(C)c4ccccc4)c4ccc(C(C)(C)C)cc4)c3c1-1)c-1c1)c1[o]2 Chemical compound CC(C)(C)c(cc1)ccc1N(C(C)(C)c1ccccc1)c(cc1)cc2c1c(cc(C1(C3CC(C4)CC1CC4C3)c1ccc(c(c([o]3)c4)ccc4N(C(C)(C)c4ccccc4)c4ccc(C(C)(C)C)cc4)c3c1-1)c-1c1)c1[o]2 ZEIJKKNWPJCBFQ-UHFFFAOYSA-N 0.000 description 1
- XFEOGSLVYOOBCX-UHFFFAOYSA-N CC(C)(C)c(cc1)ccc1N(c(cc1)cc(C2(C)C)c1-c1c2ccc2c1cccc2)c1ccc(c(cc2-c3c4[o]c5cc(N(c6ccc(C(C)(C)C)cc6)c(cc6)cc7c6-c6c(cccc8)c8ccc6C7(C)C)ccc5c4ccc3C3(C4CC(C5)CC3CC5C4)c2c2)c2[o]2)c2c1 Chemical compound CC(C)(C)c(cc1)ccc1N(c(cc1)cc(C2(C)C)c1-c1c2ccc2c1cccc2)c1ccc(c(cc2-c3c4[o]c5cc(N(c6ccc(C(C)(C)C)cc6)c(cc6)cc7c6-c6c(cccc8)c8ccc6C7(C)C)ccc5c4ccc3C3(C4CC(C5)CC3CC5C4)c2c2)c2[o]2)c2c1 XFEOGSLVYOOBCX-UHFFFAOYSA-N 0.000 description 1
- CXVJKWCCAJIUTE-UHFFFAOYSA-N CC(C)(C)c(cc1)ccc1N(c(cc1c2c3cccc2)ccc1[n]3-c1ccccc1)c(cc1C23C4CC(C5)CC2CC5C4)c(c2ccccc2[o]2)c2c1-c(c1c2[o]c4c1cccc4)c3cc2N(c1ccc(C(C)(C)C)cc1)c(cc1)cc(c2c3cccc2)c1[n]3-c1ccccc1 Chemical compound CC(C)(C)c(cc1)ccc1N(c(cc1c2c3cccc2)ccc1[n]3-c1ccccc1)c(cc1C23C4CC(C5)CC2CC5C4)c(c2ccccc2[o]2)c2c1-c(c1c2[o]c4c1cccc4)c3cc2N(c1ccc(C(C)(C)C)cc1)c(cc1)cc(c2c3cccc2)c1[n]3-c1ccccc1 CXVJKWCCAJIUTE-UHFFFAOYSA-N 0.000 description 1
- QXLJZIFAARPSNO-UHFFFAOYSA-N CC(C)(c1ccccc1)N(c1cc(-c2ccccc2)cc(-c2ccccc2)c1)c(cc1C2(C3CC(C4)CC2CC4C3)c2c3)c(c4ccccc4[o]4)c4c1-c2c1[o]c(cccc2)c2c1c3N(C(C)(C)c1ccccc1)c1cc(-c2ccccc2)cc(-c2ccccc2)c1 Chemical compound CC(C)(c1ccccc1)N(c1cc(-c2ccccc2)cc(-c2ccccc2)c1)c(cc1C2(C3CC(C4)CC2CC4C3)c2c3)c(c4ccccc4[o]4)c4c1-c2c1[o]c(cccc2)c2c1c3N(C(C)(C)c1ccccc1)c1cc(-c2ccccc2)cc(-c2ccccc2)c1 QXLJZIFAARPSNO-UHFFFAOYSA-N 0.000 description 1
- GHKIZKSZYYAOHS-UHFFFAOYSA-N CC(C)(c1ccccc1)c(cc1)ccc1N(c1ccccc1)c1ccc(c2ccc(C3(C4CC(C5)CC3CC5C4)c3c(c(ccc(N(c4ccccc4)c4ccc(C(C)(C)c5ccccc5)cc4)c4)c4[o]4)c4ccc3-3)c-3c2[o]2)c2c1 Chemical compound CC(C)(c1ccccc1)c(cc1)ccc1N(c1ccccc1)c1ccc(c2ccc(C3(C4CC(C5)CC3CC5C4)c3c(c(ccc(N(c4ccccc4)c4ccc(C(C)(C)c5ccccc5)cc4)c4)c4[o]4)c4ccc3-3)c-3c2[o]2)c2c1 GHKIZKSZYYAOHS-UHFFFAOYSA-N 0.000 description 1
- ZWDMHZYFGNKPHW-UHFFFAOYSA-N c(cc1)ccc1Nc(cc1)cc2c1c1cc(cccc3)c3cc1[o]2 Chemical compound c(cc1)ccc1Nc(cc1)cc2c1c1cc(cccc3)c3cc1[o]2 ZWDMHZYFGNKPHW-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/43—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
- C07C211/57—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings being part of condensed ring systems of the carbon skeleton
- C07C211/61—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings being part of condensed ring systems of the carbon skeleton with at least one of the condensed ring systems formed by three or more rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- H01L51/0058—
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- H01L51/006—
-
- H01L51/0073—
-
- H01L51/50—
-
- 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
-
- 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
- H10K85/626—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene containing more than one polycyclic condensed aromatic rings, e.g. bis-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
- H10K85/631—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine
- H10K85/633—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine comprising polycyclic condensed aromatic hydrocarbons as substituents on the nitrogen atom
-
- 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
- H10K85/6574—Polycyclic condensed heteroaromatic hydrocarbons comprising only oxygen in the heteroaromatic polycondensed ring system, e.g. cumarine dyes
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Optics & Photonics (AREA)
- Electroluminescent Light Sources (AREA)
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CN201980052918.1A CN112585115B (zh) | 2018-08-29 | 2019-08-26 | 新的化合物和包含其的有机发光器件 |
PCT/KR2019/010852 WO2020045924A1 (ko) | 2018-08-29 | 2019-08-26 | 신규한 화합물 및 이를 이용한 유기발광 소자 |
US17/267,560 US20220017544A1 (en) | 2018-08-29 | 2019-08-26 | Novel compound and organic light emitting device comprising the same |
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KR20180102199 | 2018-08-29 |
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KR20200026080A KR20200026080A (ko) | 2020-03-10 |
KR102252884B1 true KR102252884B1 (ko) | 2021-05-17 |
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Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
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CN112209944B (zh) * | 2020-03-04 | 2022-01-28 | 陕西莱特光电材料股份有限公司 | 含氮化合物、有机电致发光器件和电子装置 |
KR20210115259A (ko) * | 2020-03-12 | 2021-09-27 | 에스에프씨 주식회사 | 축합 고리를 갖는 아민 화합물 및 이를 포함하는 유기발광소자 |
CN112209840B (zh) * | 2020-03-13 | 2022-01-28 | 陕西莱特光电材料股份有限公司 | 含氮化合物、电子元件和电子装置 |
CN115700046A (zh) * | 2020-03-19 | 2023-02-03 | Sfc株式会社 | 使用多环芳族化合物的有机电致发光器件 |
CN113292566B (zh) * | 2020-04-28 | 2022-04-29 | 陕西莱特光电材料股份有限公司 | 一种有机化合物和应用以及使用其的有机电致发光器件和电子装置 |
CN111620855B (zh) * | 2020-06-12 | 2022-03-25 | 烟台九目化学股份有限公司 | 一种含苯并氧杂蒽类化合物材料及其应用 |
CN114456158A (zh) * | 2020-11-10 | 2022-05-10 | 广州华睿光电材料有限公司 | 有机化合物、混合物、组合物及有机电子器件 |
CN112661706B (zh) * | 2020-12-22 | 2023-01-20 | 陕西莱特光电材料股份有限公司 | 一种螺环化合物以及使用其的电子元件和电子装置 |
CN113105420B (zh) * | 2021-04-13 | 2023-06-16 | 浙江虹舞科技有限公司 | 一种稠环芳胺类化合物及其应用以及包含该化合物的有机电致发光器件 |
CN113402526B (zh) * | 2021-07-26 | 2023-07-18 | 武汉天马微电子有限公司 | 一种有机化合物、电致发光材料及其应用 |
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CN101421226B (zh) * | 2006-04-13 | 2013-05-22 | 东曹株式会社 | 苯并芴化合物及其用途 |
KR101497133B1 (ko) | 2011-12-23 | 2015-02-27 | 제일모직 주식회사 | 유기광전자소자용 화합물, 이를 포함하는 유기발광소자 및 상기 유기발광소자를 포함하는 표시장치 |
KR20160050827A (ko) * | 2014-10-31 | 2016-05-11 | 롬엔드하스전자재료코리아유한회사 | 감광성 수지 조성물 및 이를 이용한 절연막 |
KR102593531B1 (ko) * | 2015-05-27 | 2023-10-26 | 삼성디스플레이 주식회사 | 유기 발광 소자 |
KR102093535B1 (ko) * | 2016-04-25 | 2020-03-25 | 주식회사 엘지화학 | 화합물 및 이를 포함하는 유기 발광 소자 |
KR101917953B1 (ko) * | 2016-06-02 | 2018-11-13 | 주식회사 엘지화학 | 화합물 및 이를 포함하는 유기 전자 소자 |
CN106397398A (zh) * | 2016-08-31 | 2017-02-15 | 北京绿人科技有限责任公司 | 一种有机化合物及其在有机电致发光器件中的应用 |
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2019
- 2019-08-23 KR KR1020190103963A patent/KR102252884B1/ko active IP Right Grant
- 2019-08-26 CN CN201980052918.1A patent/CN112585115B/zh active Active
Non-Patent Citations (1)
Title |
---|
C.H. Chen et al, Synthesis and characterization of spiro(adamantane-2,9-fluorene)-based triaryldiamines: thermally stable hole-transporting materials, Synthetic Metals, 2004, 143(2), pp.215-220 1부.* |
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CN112585115A (zh) | 2021-03-30 |
KR20200026080A (ko) | 2020-03-10 |
CN112585115B (zh) | 2023-06-27 |
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