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1-Benzyl-3-(1-benzyl-2-methylindol-3-yl)-4-phenanthren-9-ylpyrrole-2,5-dione | 1263758-09-3

中文名称
——
中文别名
——
英文名称
1-Benzyl-3-(1-benzyl-2-methylindol-3-yl)-4-phenanthren-9-ylpyrrole-2,5-dione
英文别名
1-benzyl-3-(1-benzyl-2-methylindol-3-yl)-4-phenanthren-9-ylpyrrole-2,5-dione
1-Benzyl-3-(1-benzyl-2-methylindol-3-yl)-4-phenanthren-9-ylpyrrole-2,5-dione化学式
CAS
1263758-09-3
化学式
C41H30N2O2
mdl
——
分子量
582.701
InChiKey
YZGOLWDJRSQFTQ-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

计算性质

  • 辛醇/水分配系数(LogP):
    8.8
  • 重原子数:
    45
  • 可旋转键数:
    6
  • 环数:
    8.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    42.3
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    3-(2'-methyl-3'-indolyl)-4-(9-phenanthryl)-N-benzylmaleimide 、 溴甲苯 在 sodium hydroxide 作用下, 以 丙酮 为溶剂, 以82%的产率得到1-Benzyl-3-(1-benzyl-2-methylindol-3-yl)-4-phenanthren-9-ylpyrrole-2,5-dione
    参考文献:
    名称:
    Asymmetric indolylmaleimides as non-dopant type red color emitting dyes
    摘要:
    The photophysical properties of asymmetric indolylmaleimide derivatives (4a-4f) with a variety of aryl substituents at C(4) were analyzed. Their absorption spectra vary in the region of aryl substituents, whereas their emission spectra are nearly identical. The red emission is derived from a charge transfer transition along the indole-maleimide chromophore, which is not significantly disturbed by the introduction of a nearby aryl substituent at C(4). All compounds displayed intensive emissions both in solutions as well as in the form of solid films. Light emitting diodes (LED) were fabricated successfully by using the neat film of these materials as emitters. The performance of devices among the series varied slightly as a result of different film morphology. The best performance was found on the compound with a pyrene substituent, which exhibited optimal external quantum efficiency of 1.1%. This device could be turned on at 4 V and reached to optimal brightness of 9750 cd/m(2). The red color, according to the Commission Internationale de l'Eclairage (CIE) coordinates at (0.65, 0.34), was very close to pure red (0.67, 0.33). (C) 2009 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.orgel.2009.12.025
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文献信息

  • Asymmetric indolylmaleimides as non-dopant type red color emitting dyes
    作者:Ying-Shin Lee、Zhenghuan Lin、Yu-Yuan Chen、Ching-Yang Liu、Tahsin J. Chow
    DOI:10.1016/j.orgel.2009.12.025
    日期:2010.4
    The photophysical properties of asymmetric indolylmaleimide derivatives (4a-4f) with a variety of aryl substituents at C(4) were analyzed. Their absorption spectra vary in the region of aryl substituents, whereas their emission spectra are nearly identical. The red emission is derived from a charge transfer transition along the indole-maleimide chromophore, which is not significantly disturbed by the introduction of a nearby aryl substituent at C(4). All compounds displayed intensive emissions both in solutions as well as in the form of solid films. Light emitting diodes (LED) were fabricated successfully by using the neat film of these materials as emitters. The performance of devices among the series varied slightly as a result of different film morphology. The best performance was found on the compound with a pyrene substituent, which exhibited optimal external quantum efficiency of 1.1%. This device could be turned on at 4 V and reached to optimal brightness of 9750 cd/m(2). The red color, according to the Commission Internationale de l'Eclairage (CIE) coordinates at (0.65, 0.34), was very close to pure red (0.67, 0.33). (C) 2009 Elsevier B.V. All rights reserved.
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