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[1,1'-biphenyl]-2,2'-diylbis((4-(diphenylamino)phenyl)methanone) | 1432623-59-0

中文名称
——
中文别名
——
英文名称
[1,1'-biphenyl]-2,2'-diylbis((4-(diphenylamino)phenyl)methanone)
英文别名
[2-[2-[4-(N-phenylanilino)benzoyl]phenyl]phenyl]-[4-(N-phenylanilino)phenyl]methanone
[1,1'-biphenyl]-2,2'-diylbis((4-(diphenylamino)phenyl)methanone)化学式
CAS
1432623-59-0
化学式
C50H36N2O2
mdl
——
分子量
696.848
InChiKey
WKBXPYYWEYHJDT-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):
    12.7
  • 重原子数:
    54
  • 可旋转键数:
    11
  • 环数:
    8.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    40.6
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    phenyl 4-(diphenylamino)benzoate 在 1,1'-双(二苯基膦)二茂铁三氟甲磺酸potassium carbonate三乙胺联硼酸频那醇酯 、 palladium dichloride 作用下, 以 二氯甲烷二甲基亚砜 为溶剂, 反应 43.0h, 生成 [1,1'-biphenyl]-2,2'-diylbis((4-(diphenylamino)phenyl)methanone)
    参考文献:
    名称:
    Paraphenylene dimers with diphenylamine donor groups: synthesis and photophysics
    摘要:
    A novel paraphenylene dimer (D696) with electron donating diphenylamine side chain groups has been prepared. Optical absorption measurements were theoretically and experimentally determined showing a red shift in the absortivity relative to dialkylamine functionalized benzophenone dimers. The fluorescence of D696 was quenched in a concentration dependent manner in the presence of reduced graphene oxide (RGO). (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2013.03.141
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文献信息

  • Paraphenylene dimers with diphenylamine donor groups: synthesis and photophysics
    作者:Khoa Le、Lokendra B. Chand、Colette Griffin、Alfred L. Williams、Darlene K. Taylor
    DOI:10.1016/j.tetlet.2013.03.141
    日期:2013.6
    A novel paraphenylene dimer (D696) with electron donating diphenylamine side chain groups has been prepared. Optical absorption measurements were theoretically and experimentally determined showing a red shift in the absortivity relative to dialkylamine functionalized benzophenone dimers. The fluorescence of D696 was quenched in a concentration dependent manner in the presence of reduced graphene oxide (RGO). (C) 2013 Elsevier Ltd. All rights reserved.
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