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(S)-2,8-diethyl-5-fluoro-1,3,7,9-tetramethyl-5-(perfluorophenyl)-5H-5l4-dipyrrolo[1,2-c:2',1'-f][1,3,2]diazaborinin-4-ium | 1183675-97-9

中文名称
——
中文别名
——
英文名称
(S)-2,8-diethyl-5-fluoro-1,3,7,9-tetramethyl-5-(perfluorophenyl)-5H-5l4-dipyrrolo[1,2-c:2',1'-f][1,3,2]diazaborinin-4-ium
英文别名
——
(S)-2,8-diethyl-5-fluoro-1,3,7,9-tetramethyl-5-(perfluorophenyl)-5H-5l4-dipyrrolo[1,2-c:2',1'-f][1,3,2]diazaborinin-4-ium化学式
CAS
1183675-97-9
化学式
C23H23BF6N2
mdl
——
分子量
452.25
InChiKey
CAVPGHVRQJLENP-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):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Perfluoroaryl-Substituted Boron Dipyrrinato Complexes
    摘要:
    A methodology for the incorporation of fluoroaryl groups into boron dipyrrinato complexes (modified BODIPY dyes) is reported. Two hexaalkylated dipyrrinato ligands with either H or CH3 occupying the meso position were employed; when they were treated with fluoroaryl haloboranes in the presence of a weak base, the title compounds were prepared in good to excellent yields. The structures of seven derivatives were determined using X-ray crystallography, and their spectroscopic, photophysical, and redox properties are compared.
    DOI:
    10.1021/om900402e
  • 作为产物:
    描述:
    difluoro (pentafluorophenyl)borane1,3,7,9-tetramethyl-2,8-diethyl-4,6-dipyrrin hydrobromide 在 Et3N 作用下, 以 二氯甲烷 为溶剂, 以48%的产率得到(S)-2,8-diethyl-5-fluoro-1,3,7,9-tetramethyl-5-(perfluorophenyl)-5H-5l4-dipyrrolo[1,2-c:2',1'-f][1,3,2]diazaborinin-4-ium
    参考文献:
    名称:
    Perfluoroaryl-Substituted Boron Dipyrrinato Complexes
    摘要:
    A methodology for the incorporation of fluoroaryl groups into boron dipyrrinato complexes (modified BODIPY dyes) is reported. Two hexaalkylated dipyrrinato ligands with either H or CH3 occupying the meso position were employed; when they were treated with fluoroaryl haloboranes in the presence of a weak base, the title compounds were prepared in good to excellent yields. The structures of seven derivatives were determined using X-ray crystallography, and their spectroscopic, photophysical, and redox properties are compared.
    DOI:
    10.1021/om900402e
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相关结构分类