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2,3-bis(4-bromophenyl)-1,4-bis(4-methoxyphenyl)butane-1,4-dione | 944344-62-1

中文名称
——
中文别名
——
英文名称
2,3-bis(4-bromophenyl)-1,4-bis(4-methoxyphenyl)butane-1,4-dione
英文别名
2,3-Bis(4-bromophenyl)-1,4-bis(4-methoxyphenyl)butane-1,4-dione
2,3-bis(4-bromophenyl)-1,4-bis(4-methoxyphenyl)butane-1,4-dione化学式
CAS
944344-62-1
化学式
C30H24Br2O4
mdl
——
分子量
608.326
InChiKey
GLGFQOYDWNGSQZ-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):
    7.6
  • 重原子数:
    36
  • 可旋转键数:
    9
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    52.6
  • 氢给体数:
    0
  • 氢受体数:
    4

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

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Peripheral aryl-substituted pyrrole fluorophores for glassy blue-light-emitting diodes
    摘要:
    In this work, a series of aryl-substituted pyrrole analogues were synthesized. These pyrrole analogues emit violet to blue light. Fluorescence and amorphous glassy properties of these pyrrole analogues were induced by manipulating the peripheral aryl groups. These crowded peripheral aryl groups would effectively prevent the fluorophores from aggregation, resulting in higher quantum efficiency and a stable emission spectrum in the solid state. One of the aryl-substituted pyrrole analogues, namely NPANPy can be used as hole-transporting material or hole-transporting/emitting material. The devices would emit blue light when the fluorophore NPANPy acts as the hole-transporting/ emitting material. Their CIE coordinate is around (0.16, 0.14), whereas the maximum brightness can reach 4300-5000 cd m(-2). Apart from that, when the fluorophore was used only as the hole-transporting material, better device performances, especially in low current density, were found, as compared with the standard device. (C) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2007.05.032
  • 作为产物:
    参考文献:
    名称:
    Peripheral aryl-substituted pyrrole fluorophores for glassy blue-light-emitting diodes
    摘要:
    In this work, a series of aryl-substituted pyrrole analogues were synthesized. These pyrrole analogues emit violet to blue light. Fluorescence and amorphous glassy properties of these pyrrole analogues were induced by manipulating the peripheral aryl groups. These crowded peripheral aryl groups would effectively prevent the fluorophores from aggregation, resulting in higher quantum efficiency and a stable emission spectrum in the solid state. One of the aryl-substituted pyrrole analogues, namely NPANPy can be used as hole-transporting material or hole-transporting/emitting material. The devices would emit blue light when the fluorophore NPANPy acts as the hole-transporting/ emitting material. Their CIE coordinate is around (0.16, 0.14), whereas the maximum brightness can reach 4300-5000 cd m(-2). Apart from that, when the fluorophore was used only as the hole-transporting material, better device performances, especially in low current density, were found, as compared with the standard device. (C) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2007.05.032
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文献信息

  • Peripheral aryl-substituted pyrrole fluorophores for glassy blue-light-emitting diodes
    作者:Wen-Jang Kuo、Ying-Hsiao Chen、Ru-Jong Jeng、Li-Hsin Chan、Wen-Peng Lin、Zhe-Ming Yang
    DOI:10.1016/j.tet.2007.05.032
    日期:2007.7
    In this work, a series of aryl-substituted pyrrole analogues were synthesized. These pyrrole analogues emit violet to blue light. Fluorescence and amorphous glassy properties of these pyrrole analogues were induced by manipulating the peripheral aryl groups. These crowded peripheral aryl groups would effectively prevent the fluorophores from aggregation, resulting in higher quantum efficiency and a stable emission spectrum in the solid state. One of the aryl-substituted pyrrole analogues, namely NPANPy can be used as hole-transporting material or hole-transporting/emitting material. The devices would emit blue light when the fluorophore NPANPy acts as the hole-transporting/ emitting material. Their CIE coordinate is around (0.16, 0.14), whereas the maximum brightness can reach 4300-5000 cd m(-2). Apart from that, when the fluorophore was used only as the hole-transporting material, better device performances, especially in low current density, were found, as compared with the standard device. (C) 2007 Elsevier Ltd. All rights reserved.
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同类化合物

苯基(2,4,5-三苯基-2-环戊烯-1-基)甲酮 肠二醇 珠子草素 开环异落叶松树脂酚 安五脂素 外消旋肠二醇-13C3 去甲二氢愈创木酸 半去甲二氢愈创木酸 二甲基2,5-二苯基-3,4-二氢-2H-吡咯-3,4-二羧酸酯 二氢荜澄茄脂素 9,9'-二-O-(E)-阿魏酰开环异落叶松脂素 4-[4-(4-羟基-3-甲氧基苯基)-2,3-二甲基丁基]-2-甲氧基苯酚 2,6-二甲氧基-4-羟基苯甲醛 2,6-二甲氧基-4-[(2R,3R)-4-甲氧基-3-[(7-甲氧基-1,3-苯并二噁唑-5-基)甲基]-2-(甲氧基甲基)丁基]苯酚 2,3-双[(4-羟基-3-甲氧基苯基)甲基]丁烷-1,4-二醇 2,3-双[(3,4-二甲氧基苯基)甲基]丁烷-1,4-二醇 2,3-双[(3,4-二甲氧基苯基)甲基]丁二酸 2,3-双(4-羟基-3-甲氧基苄基)琥珀酸二甲酯 2,3-双(3,4-二甲氧基苄基)-4-甲氧基-4-氧代丁酸 2,3-二苄基丁烷-1,4-二醇 2,3-二甲基-1,4-二苯基丁烷-2,3-二醇 2,3-二甲基-1,4-二苯基丁烷-1,4-二酮 2,3-二异丙基-1,2-二苯基-1,4-丁二酮 2,3-二[(3-羟基苯基)甲基]丁烷-1,4-二醇 2,2,3,3-四甲基-1,4-二苯基丁烷-1,4-二酮 1,4-丁烷二酮 1,2,3,4-四苯基环戊烷 1,2,3,4-四苯基丁烷 1,2,3,4-四苯基-1,4-丁烷二酮 1,2,3,4-四-(4-甲氧基-苯基)-丁烷-1,4-二酮 1,1'-[(2S,3S)-2,3-双(甲氧基甲基)-1,4-丁二基]双[3,4-二甲氧基苯] 1,1'-(2,3-二甲基-1,4-丁烷二基)二(3,4-二甲氧基苯) 1,1',2,2',3,3'-六苯基-1,1'-联(2-环丙烯) (3,3,4,4-四甲基-2-苯基环丁烯-1-基)苯 (2R,3S)-1,4-二(4-羟基-3-甲氧基苯基)-2,3-二甲基丁烷-1-酮 (-)-二氢愈创木脂酸 (+)-开环异落叶松树脂酚 1,4-difluoro-1,2,34,-tetrahydrophenylbutane (1R*,2R*,3R*,4S*)-2,3-bis(hydroxymethyl)-1-(3,4-dimethoxyphenyl)-4-<3,4-(methylenedioxy)phenyl>butane-1,4-diol 2,5-diphenyl-3,4-dimethylhexa-1,5-diene meso-1,4-bis-(3,4-dihydroxyphenyl)-2,3-dimethylbutane bis-cyclic carbonate (2R,3R)-2-(4'-hydroxy-3'-methoxybenzyl)-3-(3'',4''-dimethoxybenzyl)-4-hydroxy-N-benzylbutyramide (2R,3R)-2-(3',4'-dihydroxybenzyl)-3-(3'',4''-dimethoxybenzyl)-4-hydroxy-N-benzylbutyramide 2,5-di(3-nitrophenyl)-3,3,4,4-tetracyanopyrrolidine 4,5-dihydroxy-2,4,5-triphenyl-3-(2-pyridyl)-1-pyrroline (+/-)-(1R,2S,3R,4R)-2,3-bis(hydroxymethyl)-1,4-bisphenyl-2-hydroxybutane-1,4-diol α,β-dimethyl-γ-phenylbutyrophenone meso-2,3-bis(3,4-dihydroxybenzyl)succinic acid (±)-1-(4-hydroxy-3-methoxyphenyl)-(2R,3S)-dimethyl-4-[3-methoxy-4-(picolinoyloxy)phenyl]butane meso-1,4-bis[3-methoxy-4-(picolinoyloxy)phenyl]-(2R,3S)-dimethylbutane