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[PdCl(benzylidenepropylamine(-1H))]2 | 1338077-47-6

中文名称
——
中文别名
——
英文名称
[PdCl(benzylidenepropylamine(-1H))]2
英文别名
——
[PdCl(benzylidenepropylamine(-1H))]2化学式
CAS
1338077-47-6
化学式
C20H24Cl2N2Pd2
mdl
——
分子量
576.17
InChiKey
AJLAXURRUIFODL-LGTVYGGGSA-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

  • 作为反应物:
    描述:
    [PdCl(benzylidenepropylamine(-1H))]2三苯基膦二氯甲烷 为溶剂, 以89%的产率得到[PdCl(triphenylphosphine)(benzylidenepropylamine(-1H))]
    参考文献:
    名称:
    Cationic palladacycles as catalyst precursors for phenyl acetylene polymerization
    摘要:
    Novel cationic palladacycles based on benzylidene-2,6-diisopropylphenylimines were prepared via C-H activation using Pd(CH(3)CN)(2)Cl(2) as metal precursor. The complexes were fully characterized by IR and NMR spectroscopy, mass spectrometry and elemental analysis. The cationic palladacycles were found to be active catalysts for the polymerization of phenylacetylene producing largely trans-cisoidal PPA. (C) 2011 Elsevier B. V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2011.07.044
  • 作为产物:
    描述:
    双(乙腈)氯化钯(II)N-丙基苄亚基胺 在 sodium acetate 作用下, 以 二氯甲烷 为溶剂, 以70%的产率得到[PdCl(benzylidenepropylamine(-1H))]2
    参考文献:
    名称:
    Cationic palladacycles as catalyst precursors for phenyl acetylene polymerization
    摘要:
    Novel cationic palladacycles based on benzylidene-2,6-diisopropylphenylimines were prepared via C-H activation using Pd(CH(3)CN)(2)Cl(2) as metal precursor. The complexes were fully characterized by IR and NMR spectroscopy, mass spectrometry and elemental analysis. The cationic palladacycles were found to be active catalysts for the polymerization of phenylacetylene producing largely trans-cisoidal PPA. (C) 2011 Elsevier B. V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2011.07.044
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