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[2-(4-bromo-phenoxy)-ethyl]-diphenyl-phosphane | 798548-31-9

中文名称
——
中文别名
——
英文名称
[2-(4-bromo-phenoxy)-ethyl]-diphenyl-phosphane
英文别名
[2-(4-Bromophenoxy)ethyl](diphenyl)phosphane;2-(4-bromophenoxy)ethyl-diphenylphosphane
[2-(4-bromo-phenoxy)-ethyl]-diphenyl-phosphane化学式
CAS
798548-31-9
化学式
C20H18BrOP
mdl
——
分子量
385.24
InChiKey
GBFWZVFZTVUYBI-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):
    5.4
  • 重原子数:
    23
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为产物:
    描述:
    4-溴苯基 2-氯乙基醚potassium diphenylphosphine四氢呋喃 为溶剂, 反应 0.25h, 以32%的产率得到[2-(4-bromo-phenoxy)-ethyl]-diphenyl-phosphane
    参考文献:
    名称:
    Halide-Induced Supramolecular Ligand Rearrangement
    摘要:
    A novel reaction involving the halide-induced rearrangement of ligands within supramolecular Rh(I) complexes containing hemilabile ligands is presented. Three analogous bis- and trishemilabile ligands have been synthesized to construct bi- and trimetallic Rh(I) macrocyclic complexes. An intentionally added halide source results in the formal rotation of only one hemilabile ligand along the axis that is perpendicular to the plane defined by the aryl backbone of the hemilabile ligands. X-ray structures, as determined by X-ray crystallography, of key intermediates and products are presented.
    DOI:
    10.1021/ja045316b
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文献信息

  • Halide-Induced Supramolecular Ligand Rearrangement
    作者:Aaron M. Brown、Maxim V. Ovchinnikov、Charlotte L. Stern、Chad A. Mirkin
    DOI:10.1021/ja045316b
    日期:2004.11.1
    A novel reaction involving the halide-induced rearrangement of ligands within supramolecular Rh(I) complexes containing hemilabile ligands is presented. Three analogous bis- and trishemilabile ligands have been synthesized to construct bi- and trimetallic Rh(I) macrocyclic complexes. An intentionally added halide source results in the formal rotation of only one hemilabile ligand along the axis that is perpendicular to the plane defined by the aryl backbone of the hemilabile ligands. X-ray structures, as determined by X-ray crystallography, of key intermediates and products are presented.
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