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2-溴-13,13-二甲基-6H-茚并[1,2-b]蒽-6,11(13H)-二酮 | 1196107-73-9

中文名称
2-溴-13,13-二甲基-6H-茚并[1,2-b]蒽-6,11(13H)-二酮
中文别名
2-溴-13,13-二甲基-13H-茚并[1,2-b]蒽-6,11-二酮;119617-73-9
英文名称
2-bromo-13,13-dimethyl-13H-indeno[1,2-b]anthracene-6,11-dione
英文别名
2-bromo-13,13-dimethyl-6H-indeno[1,2-b]anthracene-6,11(13H)-dione;7-bromo-10,10-dimethylpentacyclo[11.8.0.03,11.04,9.015,20]henicosa-1(13),2,4(9),5,7,11,15,17,19-nonaene-14,21-dione
2-溴-13,13-二甲基-6H-茚并[1,2-b]蒽-6,11(13H)-二酮化学式
CAS
1196107-73-9
化学式
C23H15BrO2
mdl
——
分子量
403.275
InChiKey
NREMKCAHBDRWFB-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 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

物化性质

  • 沸点:
    570.7±49.0 °C(Predicted)
  • 密度:
    1.479±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    6.1
  • 重原子数:
    26
  • 可旋转键数:
    0
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    34.1
  • 氢给体数:
    0
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2914700090
  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H302,H315,H319
  • 储存条件:
    室温且干燥

SDS

SDS:f048f4e723424e111186740371fef42b
查看

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    2-溴-13,13-二甲基-6H-茚并[1,2-b]蒽-6,11(13H)-二酮 在 sodium tetrahydroborate 作用下, 以 异丙醇 为溶剂, 反应 6.0h, 以87.2%的产率得到2-溴-13,13-二甲基-13H-茚并[1,2-b]蒽
    参考文献:
    名称:
    一种茚并蒽衍生物化合物及其应用
    摘要:
    本发明公开了一种茚并蒽衍生物化合物及其应用,属于有机电致发光材料技术领域;该类化合物的结构通式如下式(I)所示:其中,L1、L2、L3为亚苯基或取代的亚苯基,n为0~3之间的任意整数,Ar1、Ar2相同或者不同,Ar1、Ar2各自独立为给电子基团,X可以是C原子、O原子、S原子、N原子、Si原子,A表示二苯基氧磷分子或二苯基硼分子衍生物;本发明提供的化合物作为OLED的掺杂材料和/或主体材料可以实现有机电致发光器件高亮度、低电压、高效率、使用寿命长;这些化合物制成的材料具有较高的热稳定性,可显著提高发光器件的发光稳定性,广泛应用于OLED发光器件及显示装置。
    公开号:
    CN110041366B
  • 作为产物:
    参考文献:
    名称:
    Synthesis and characterization of solution processable 6,11-dialkynyl substituted indeno[1,2-b]anthracenes
    摘要:
    Twelve indene-fused dialkynyl substituted anthracene derivatives (indenoanthracenes) were synthesized and their optical, electrochemical and thermal properties were described. These small molecules possess high quantum yields, thermal and photoxidative stabilities, and solubility in common organic solvents. Indenoanthracenes (57-92%) were prepared in two steps from four different indenoanthraquinones obtained via a highly selective and practical benzocyclobutendione based methodology. The photophysical properties of indenoanthracenes were investigated by UV-vis and fluorescence spectroscopies. From spectroscopic data of indenoanthracenes, quantum yields (Phi(f), 0.28-0.71) and optical HOMO-LUMO energy gaps were determined. Electrochemistry of indenoanthracenes was studied and electrochemical HOMO-LUMO energy gaps were also determined from the onset oxidation and reduction potentials. Density functional theory calculations were performed to obtain the geometry optimized structures and HOMO-LUMO energy levels. Fluorenylethynyl substituted indenoanthracene was employed as an emitting layer in a solution processed OLED device and the maximum current efficiency and luminance were found to be 1.02 cd/A and 1284 cd/m(2), respectively. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.dyepig.2013.08.024
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文献信息

  • 一种芴基蒽醌类有机电致发光材料及其制备 方法和应用
    申请人:中节能万润股份有限公司
    公开号:CN106800525B
    公开(公告)日:2019-04-02
    本发明公开了一种芴基蒽醌类化合物类有机电致发光材料及其制备方法和应用,上述有机电致发光材料的结构式为本发明提供的芴基蒽醌类有机电致发光材料应用于OLED发光器件中,使得器件的电流效率、功率效率和外量子效率均得到很大改善。本发明提供的芴基蒽醌类有机电致发光材料具有良好的应用效果,具有良好的产业化前景。
  • ANTHRACENE DERIVATIVES AND ORGANIC ELECTROLUMINESCENT DEVICE USING SAME
    申请人:LEE Eunjung
    公开号:US20110057182A1
    公开(公告)日:2011-03-10
    Provided are a novel anthracene derivative and an organic light-emitting device using the same, and more particularly, an anthracene derivative having a core (e.g., an indenoanthracene core) where an anthracene moiety with excellent device characteristics is fused with a fluorene moiety or the like with excellent fluorescent properties, wherein an aryl group is introduced at the core, and an organic light-emitting device using the anthracene derivative, which is enhanced in efficiency, operating voltage, lifetime, etc.
    提供了一种新的蒽衍生物和使用该蒽衍生物的有机发光器件,更具体地说,一种具有核心(例如,吲哚蒽核心)的蒽衍生物,其中具有出色器件特性的蒽基与具有出色荧光特性的萘基或类似基团融合在一起,并且在核心引入芳基团,以及使用该蒽衍生物的有机发光器件,其在效率、工作电压、寿命等方面得到增强。
  • AMINOANTHRACENE DERIVATIVE AND AN ORGANIC ELECTROLUMINESCENT ELEMENT EMPLOYING THE SAME
    申请人:Hong Jin-Seok
    公开号:US20120161615A1
    公开(公告)日:2012-06-28
    Disclosed are a novel amino anthracene derivative and an organic electro-luminescence device using the same. More specifically, the disclosed amino anthracene derivative has a core (e.g., indenoanthracene core) of an anthracene moiety (with a high device characteristic) linked to a fluorene moiety (with a high fluorescence characteristic), in which in the core is substituted with at least one amine group represented by Formula 2 and the disclosed organic electro-luminescence device uses the amino anthracene derivative as a light emitting layer material so as to be enhanced in efficiency, operating voltage, and life span.
    揭示了一种新型氨基蒽衍生物及其所使用的有机电致发光器件。具体来说,所揭示的氨基蒽衍生物具有一个核心(例如,吲哚蒽核心),该核心是蒽基(具有高设备特性)连接到萘基(具有高荧光特性),其中核心被至少一个由化学式2表示的胺基取代,所揭示的有机电致发光器件使用氨基蒽衍生物作为发光层材料,以提高效率、工作电压和寿命。
  • ANTHRACENE DERIVATIVE AND ORGANIC ELECTROLUMINESCENCE ELEMENT USING THE SAME
    申请人:Shin Chang-Ju
    公开号:US20110210320A1
    公开(公告)日:2011-09-01
    The present invention relates to an anthracene derivative and an organic electroluminescent device using the same. More specifically, the present invention relates to: a novel compound which has a core (for example, an indenoanthracene core) where both an anthracene moiety with excellent device characteristics and a fluorene moiety with excellent fluorescent properties are fused, wherein substituents (for example, a heterocyclic group such as a benzimidazole group, a benzothiazole group, a benzoxazole group, a pyridinyl group or a bipyridinyl group) with an electron transfer capacity are substituted to the core; and an organic electroluminescence element which has improved luminous efficiency, brightness, thermal stability, driving voltage, and lifetime, by comprising an organic layer which is positioned between a positive electrode and negative electrode and contains the novel compound.
    本发明涉及一种蒽衍生物及其应用于有机电致发光器件中。更具体地,本发明涉及一种新型化合物,其具有一个核心(例如,一个茚并蒽核心),其中蒽基具有优异的器件特性,荧光基团具有优异的荧光性能,并且向核心取代基(例如,带有电子转移能力的杂环基团,如苯并咪唑基团、苯并噻唑基团、苯并噁唑基团、吡啶基团或联吡啶基团)被取代;以及一种有机电致发光元件,通过包含新型化合物的有机层位于正电极和负电极之间,其具有改善的发光效率、亮度、热稳定性、驱动电压和寿命。
  • Anthracene derivative and organic electroluminescence element using the same
    申请人:Shin Chang-Ju
    公开号:US08525158B2
    公开(公告)日:2013-09-03
    The present invention relates to an anthracene derivative and an organic electroluminescent device using the same. More specifically, the present invention relates to: a novel compound which has a core (for example, an indenoanthracene core) where both an anthracene moiety with excellent device characteristics and a fluorene moiety with excellent fluorescent properties are fused, wherein substituents (for example, a heterocyclic group such as a benzimidazole group, a benzothiazole group, a benzoxazole group, a pyridinyl group or a bipyridinyl group) with an electron transfer capacity are substituted to the core; and an organic electroluminescence element which has improved luminous efficiency, brightness, thermal stability, driving voltage, and lifetime, by comprising an organic layer which is positioned between a positive electrode and negative electrode and contains the novel compound.
    本发明涉及一种蒽衍生物及其在有机电致发光器件中的应用。更具体地说,本发明涉及一种新型化合物,其具有一个核心(例如,一个茚并蒽核心),其中蒽基具有优异的器件特性,荧光基具有优异的荧光性能,并且核心上取代基(例如,具有电子转移能力的杂环基,如苯并咪唑基、苯并噻唑基、苯并噁唑基、吡啶基或联吡啶基)被取代;以及一种有机电致发光元件,其通过包含所述新型化合物的有机层,位于正极和负极之间,从而提高了发光效率、亮度、热稳定性、驱动电压和寿命。
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齐斯托醌 黄决明素 马普替林杂质E(N-甲基马普替林) 马普替林杂质D 马普替林 颜料黄199 颜料黄147 颜料黄123 颜料黄108 颜料红89 颜料红85 颜料红251 颜料红177 颜料紫27 顺式-1-(9-蒽基)-2-硝基乙烯 阿美蒽醌 阳离子蓝3RL 长蠕孢素 镁蒽四氢呋喃络合物 镁蒽 锈色洋地黄醌醇 锂钠2-[[4-[[3-[(4-氨基-9,10-二氧代-3-磺基-1-蒽基)氨基]-2,2-二甲基-丙基]氨基]-6-氯-1,3,5-三嗪-2-基]氨基]苯-1,4-二磺酸酯 锂胭脂红 链蠕孢素 铷离子载体I 铝洋红 铂(2+)二氯化1-({2-[(2-氨基乙基)氨基]乙基}氨基)蒽-9,10-二酮(1:1) 钾6,11-二氧代-6,11-二氢-1H-蒽并[1,2-d][1,2,3]三唑-4-磺酸酯 钠6,11-二氧代-6,11-二氢-1H-蒽并[1,2-d][1,2,3]三唑-4-磺酸酯 钠4-({4-[乙酰基(乙基)氨基]苯基}氨基)-1-氨基-9,10-二氧代-9,10-二氢-2-蒽磺酸酯 钠2-[(4-氨基-9,10-二氧代-3-磺基-9,10-二氢-1-蒽基)氨基]-4-{[2-(磺基氧基)乙基]磺酰基}苯甲酸酯 钠1-氨基-9,10-二氢-4-[[4-(1,1-二甲基乙基)-2-甲基苯基]氨基]-9,10-二氧代蒽-2-磺酸盐 钠1-氨基-4-[(3-{[(4-甲基苯基)磺酰基]氨基}苯基)氨基]-9,10-二氧代-9,10-二氢-2-蒽磺酸酯 钠1-氨基-4-[(3,4-二甲基苯基)氨基]-9,10-二氧代-9,10-二氢-2-蒽磺酸酯 钠1-氨基-4-(1,3-苯并噻唑-2-基硫基)-9,10-二氧代蒽-2-磺酸盐 醌茜隐色体 醌茜素 酸性蓝127:1 酸性紫48 酸性紫43 酸性兰62 酸性兰25 酸性兰182 酸性兰140 酸性兰138 酸性兰 129 透明蓝R 透明蓝AP 透明红FBL 透明紫BS