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  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    4.8
  • 重原子数:
    21
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    34.1
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • BENZANTHRACENE DERIVATIVES FOR ORGANIC ELECTROLUMINESCENT DEVICES
    申请人:Stoessel Philipp
    公开号:US20100187505A1
    公开(公告)日:2010-07-29
    The present invention relates to the compounds of the formula (1) and to organic electroluminescent devices, in particular blue-emitting devices, in which these compounds are used as host material or dopant in the emitting layer and/or as hole-transport material and/or as electron-transport material.
    本发明涉及公式(1)的化合物,以及有机电致发光器件,特别是蓝色发光器件,在这些器件中,这些化合物被用作发射层的主体材料或掺杂剂,和/或作为空穴传输材料和/或电子传输材料。
  • MATERIALS FOR ELECTRONIC DEVICES
    申请人:Buesing Arne
    公开号:US20120326602A1
    公开(公告)日:2012-12-27
    The invention relates to an organic electroluminescent device comprising an anode and a cathode and at least one electroluminescent layer arranged between the anode and cathode which comprises at least one compound of the formula (I) and at least one compound of the formula (II). The invention furthermore relates to the production of an organic electroluminescent device by means of a sublimation process and/or by application from solution and to a mixture comprising at least one compound of the formula (I) and at least one compound of the formula (II).
    本发明涉及一种有机电致发光器件,包括阳极和阴极以及至少一个电致发光层,该电致发光层位于阳极和阴极之间,其中包括公式(I)的至少一个化合物和公式(II)的至少一个化合物。本发明还涉及通过升华工艺和/或溶液涂覆的方式制备有机电致发光器件以及包括至少一个公式(I)的化合物和至少一个公式(II)的化合物的混合物。
  • BENZANTHRACEN-DERIVATE FÜR ORGANISCHE ELEKTROLUMINESZENZVORRICHTUNGEN
    申请人:Merck Patent GmbH
    公开号:EP2148909B1
    公开(公告)日:2012-05-30
  • US8986852B2
    申请人:——
    公开号:US8986852B2
    公开(公告)日:2015-03-24
  • [DE] NEUE MATERIALIEN FÜR ORGANISCHE ELEKTROLUMINESZENZVORRICHTUNGEN<br/>[EN] NOVEL MATERIALS FOR ORGANIC ELECTROLUMINESCENT DEVICES<br/>[FR] NOUVEAUX MATÉRIAUX DESTINÉS À DES DISPOSITIFS ÉLECTROLUMINESCENTS ORGANIQUES
    申请人:MERCK PATENT GMBH
    公开号:WO2008145239A2
    公开(公告)日:2008-12-04
    [EN] The invention relates to the compounds of formula (1) and to organic electroluminescent devices, in particular blue-emitting devices, in which said compounds are used as the host material or doping agent in the emitting layer and/or as the hole transport material and/or as the electron transport material.
    [FR] L'invention concerne des composés de formule (1) et des dispositifs électroluminescents organiques, notamment des dispositifs à émission bleue, dans lesquels ces composés sont utilisés comme matériau hôte ou dopant dans la couche émettrice et/ou comme matériau de transport de trous et/ou comme matériau de transport d'électrons.
    [DE] Die vorliegende Erfindung betrifft die Verbindungen der Formel (1) und organische Elektrolumineszenzvorrichtungen, insbesondere blau emittierende Vorrichtungen, in denen diese Verbindungen als Hostmaterial oder Dotand in der emittierenden Schicht und/oder als Lochtransportmaterial und/oder als Elektronentransportmaterial verwendet werden.
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同类化合物

酒色霉素 A1 萘并[1,2-b]菲-7,14-二酮 苯并蒽-7,12-二酮 腊伯罗霉素 浅内红霉素 水绫霉素 棣棠霉素 C 抑胃酶氨酰-21 富士霉素A 四角霉素 丙酸,2-甲基-,(3R,4S)-1,2,3,4,7,12-六氢-8-甲氧基-3-甲基-1,7,12-三羰基苯并[a]蒽-4-基酯 丁二酸,碘-,4-乙基1-甲基酯(9CI) N-{4-[(4-吡啶-2-基哌嗪-1-基)羰基]苯基}-7-(三氟甲基)喹啉-4-胺 8-羟基-3-甲基-3,4-二氢-1,7,12(2H)-苯并[a]蒽三酮 8-甲氧基-3-甲基-3,4-二氢-1,7,12(2H)-四苯e三酮 8,11-二[2-(2-羟基乙基氨基)乙基氨基]-6-甲氧基-1,2,3,4-四氢苯并[a]蒽-7,12-二酮 4a,8,12b-三羟基-4-甲基-1H-苯并[a]蒽-2,7,12-三酮 3-甲氧基苯并(a)蒽-7,12-二酮 1,3-二羟基-8-甲氧基-3-甲基-2,4-二氢-1H-苯并[a]蒽-7,12-二酮 (R)-8-羟基-3-甲基-1,2,3,4-四氢苯并[a]蒽-7,12-二酮 (3S)-6-羟基-8-甲氧基-3-甲基-3,4-二氢-2H-苯并[a]蒽-1,7,12-三酮 (3S)-3-甲基-8-[(2S,3R,4R,5R,6S)-3,4,5-三羟基-6-甲基四氢吡喃-2-基]氧基-3,4-二氢-2H-苯并[a]蒽-1,7,12-三酮 (3S)-11-羟基-8-甲氧基-3-甲基-3,4-二氢-2H-苯并[a]蒽-1,7,12-三酮 (3R)-9-[(2R,4R,5R,6R)-4-[(2S,5S,6S)-5-[(2S,4R,5S,6R)-4,5-二羟基-6-甲基四氢吡喃-2-基]氧基-6-甲基四氢吡喃-2-基]氧基-5-羟基-6-甲基四氢吡喃-2-基]-3,8-二羟基-3-甲基-2,4-二氢苯并[b]菲-1,7,12-三酮 (2S,4S,5S)-4-[(1E,3E,5E)-7-[(2R,6R)-6-[(2R,3S,4aR,12bS)-2,3,4A,8,12B-五羟基-3-甲基-1,7,12-三氧代-2,4-二氢苯并[h]菲-9-基]-2-甲基四氢吡喃-3-基]氧基-7-氧代庚-1,3,5-三烯基]-2,5-二甲基-1,3-二氧戊环-2-羧酸 (2R,3S,4aR,12bS)-2,3,4a,8,12b-五羟基-3-甲基-3,4,4a,12b-四氢-1,7,12(2H)-四苯e三酮 (1S,3S)-10-[[(1S,3S)-1,11-二羟基-8-甲氧基-3-甲基-7,12-二氧代-1,2,3,4-四氢苯并[h]菲-10-基]甲基]-1,11-二羟基-8-甲氧基-3-甲基-1,2,3,4-四氢苯并[B]菲-7,12-二酮 (1S,3S)-1-羟基-8-甲氧基-3-甲基-1,2,3,4-四氢苯并[a]蒽-7,12-二酮 (-)-8-O-甲基四角霉素 methyl 9-fluoro-6-hydroxy-8-methoxy-1,2,3,4-tetrahydrobenz[a]anthracene-7,12-dione-2-carboxylate urdamycinone B amycomycin B 6-hydroxy-5-hydroxymethylbenz[a]anthracene-7,12-dione 6-hydroxy-5-methylbenz[a]anthracene-7,12-dione 6-hydroxy-1,5,8-trimethoxy-3-methyltetraphene-7,12-dione 3,6-Dihydroxy-3-methyl-1,2,3,4-tetrahydrobenzanthracene-7,12-dione Moromycin B Moromycin A 1,2,3,11,12,13-Hexamethoxydibenzanthracen-7,14-chinon 4-methoxybenzanthracene-7,12-dione Fujianmycin B (3R,4aR,12bS)-4a,8,12b-trihydroxy-9-[5-(5-hydroxy-6-methyloxan-2-yl)oxy-6-methyloxan-2-yl]-3-methyl-3-[(6-methyl-5-oxo-2H-pyran-2-yl)oxy]-2,4-dihydrobenzo[a]anthracene-1,7,12-trione 4,11-dihydroxy-dibenz[a,h]anthracene-7,14-dione 5-fluoro-1,2,3,4-tetrahydrobenzanthracene-7,12-dione 10-fluoro-1,2,3,4-tetrahydrobenzanthracene-7,12-dione 3-methoxydibenzanthracene-7,14-dione 4-Hydroxy-benzanthracen-7,12-dion 8-Methoxy-1,2,3,4-tetrahydro-benzo[a]anthracene-7,12-dione 1-Hydroxybenzantracen-7,12-chinon 8-methoxy-3-methyl-7,12-dioxy-1,2,3,4-tetrahydro-benzoanthracene-2-dimethylene dithioacetal