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[bis(triphenylphosphoranylidene)ammonium][(catBOBcat)*(OAc)] | 858865-56-2

中文名称
——
中文别名
——
英文名称
[bis(triphenylphosphoranylidene)ammonium][(catBOBcat)*(OAc)]
英文别名
[PPN][(catBOBcat)*(OAc)]
[bis(triphenylphosphoranylidene)ammonium][(catBOBcat)*(OAc)]化学式
CAS
858865-56-2
化学式
C14H11B2O7*C36H30NP2
mdl
——
分子量
851.448
InChiKey
NZMIFUXGORJSCX-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

  • 作为产物:
    参考文献:
    名称:
    Complementary anion binding by bidentate boron-containing Lewis acids
    摘要:
    Anion binding by the pyroborates (catB)(2)O (1, cat = O2C6H4-1,2) and (S,S-Ph2C2H2O2B)(2)O (2) has been investigated by spectroscopic, structural and titration methods. 1 has been shown to act as a bifunctional Lewis acid, exemplified by the complementary (1:1) binding of bidentate bases such as acetate and dihydrogen phosphate. The former complex has been characterized in the solid state by X-ray diffraction and a binding constant of 1500 +/- 550 M-1 determined in chloroform solution. The reaction of 2 with acetate, by contrast, leads to breakdown of the Lewis acid chelate and to the formation of the homochiral borate anion [(S,S-Ph2C2H2O2)(2)B](-) in good yield (84% based on the chiral component). (c) 2005 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2005.01.015
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