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cis-dichlorobis(furfuryl-2-(N-diphenylphosphino)methylamine)platinum(II) | 1347752-18-4

中文名称
——
中文别名
——
英文名称
cis-dichlorobis(furfuryl-2-(N-diphenylphosphino)methylamine)platinum(II)
英文别名
——
cis-dichlorobis(furfuryl-2-(N-diphenylphosphino)methylamine)platinum(II)化学式
CAS
1347752-18-4
化学式
C34H32Cl2N2O2P2Pt
mdl
——
分子量
828.574
InChiKey
KPDLNGHVBQAMEZ-UHFFFAOYSA-L
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:
    描述:
    dichloro( 1,5-cyclooctadiene)platinum(ll)furfuryl-2-(N-diphenylphosphino)methylamine四氢呋喃 为溶剂, 以92.7%的产率得到cis-dichlorobis(furfuryl-2-(N-diphenylphosphino)methylamine)platinum(II)
    参考文献:
    名称:
    Aminophosphine–palladium(II) complexes: Synthsesis, structure and applications in Suzuki and Heck cross-coupling reactions
    摘要:
    Reaction of furfurylamine with 1 or 2 equivalents of PPh2Cl in the presence of Et3N, proceeds under anaerobic conditions in thf to give furfuryl-2-(N-diphenylphosphino)amine, Ph2PNHCH2-C4H3O, 1 and furfuryl-2-(N,N-bis(diphenylphosphino)amine), (Ph2P)(2)NCH2-C4H3O, 2, respectively. The reactions of 1 and 2 with MCl2(cod) (M = Pd, Pt; cod = 1,5-cyclooctadiene) or Pt(CH3)(2)(cod) yield complexes [M(Ph2PNHCH2-C4H3O)(2)Cl-2] (M= Pd 1a, Pt 1b), [Pt(Ph2PNHCH2-C4H3O)(2)(CH3)(2)] (1c), and [M((Ph2P)(2) NCH2-C4H3O)Cl-2] (M= Pd 2a, Pt 2b), [Pt((Ph2P)(2)NCH2-C4H3O)(CH3)(2)] (2c), respectively. All the compounds were isolated as analytically pure substances and characterized by NMR, IR spectroscopy and elemental analysis. Representative solid-state structures of 2a and 2b were also determined by X-ray single crystal diffraction technique. Furthermore, the palladium complexes 1a and 2a were tested and found to be highly active catalysts in the Suzuki coupling and Heck reaction affording biphenyls and trans-stilbenes, respectively. (C) 2011 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.ica.2011.07.056
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