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(2-diphenylphosphinocyclopentene-1-(tert-butyl)imine)(allyl)palladium(II) chloride | 1014625-63-8

中文名称
——
中文别名
——
英文名称
(2-diphenylphosphinocyclopentene-1-(tert-butyl)imine)(allyl)palladium(II) chloride
英文别名
——
(2-diphenylphosphinocyclopentene-1-(tert-butyl)imine)(allyl)palladium(II) chloride化学式
CAS
1014625-63-8
化学式
C25H31ClNPPd
mdl
——
分子量
518.375
InChiKey
KEBRWXBUKPCXLL-UHFFFAOYSA-M
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:
    描述:
    (2-diphenylphosphinocyclopentene-1-(tert-butyl)imine)(allyl)palladium(II) chloridesilver trifluoromethanesulfonate二氯甲烷 为溶剂, 以89.7%的产率得到(2-diphenylphosphinocyclopentene-1-(tert-butyl)imine)(allyl)palladium(II) triflate
    参考文献:
    名称:
    Palladium(II) 3-Iminophosphine Complexes as Intermolecular Hydroamination Catalysts for the Formation of Imines and Enamines
    摘要:
    Palladium(II) 3-iminophosphine derivatives were screened as intermolecular hydroamination catalysts, with (3-iminophosphine)(allyl)palladium triflate determined to be the most active for the hydroamination of 1,3-cyclohexadiene and phenyl acetylene. The iminophosphine ligands were synthesized by a three-step process and coordinated in an eta(2) and eta(1) manner to palladium(II) chloride and (allyl)palladium(II) chloride, respectively.
    DOI:
    10.1021/om701106q
  • 作为产物:
    描述:
    bis(η3-allyl-μ-chloropalladium(II)) 、 2-diphenylphosphinocyclopentene-1-(tert-butyl)imine二氯甲烷 为溶剂, 以73.7%的产率得到(2-diphenylphosphinocyclopentene-1-(tert-butyl)imine)(allyl)palladium(II) chloride
    参考文献:
    名称:
    Palladium(II) 3-Iminophosphine Complexes as Intermolecular Hydroamination Catalysts for the Formation of Imines and Enamines
    摘要:
    Palladium(II) 3-iminophosphine derivatives were screened as intermolecular hydroamination catalysts, with (3-iminophosphine)(allyl)palladium triflate determined to be the most active for the hydroamination of 1,3-cyclohexadiene and phenyl acetylene. The iminophosphine ligands were synthesized by a three-step process and coordinated in an eta(2) and eta(1) manner to palladium(II) chloride and (allyl)palladium(II) chloride, respectively.
    DOI:
    10.1021/om701106q
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文献信息

  • Reactivity of (3-Iminophosphine)palladium(II) Complexes: Evidence of Hemilability
    作者:Andrew R. Shaffer、Joseph A. R. Schmidt
    DOI:10.1021/om900066t
    日期:2009.4.27
    Several palladium(II) 3-iminophosphine complexes were synthesized in moderate to high yield. With relevance to many palladium-catalyzed coupling reactions, these complexes incorporate a wide variety of ligands, including amines, alkyls, allyls, and triflates. The presence of both eta'- and eta(2)-coordination modes demonstrates the hemilability of the 3-iminophosphine ligand class, as determined by X-ray crystallography and NMR spectroscopy.
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