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[(Ph3PNC(C6H4)C(Ph)=N(4-MeC6H4)PdCl2] | 1160221-90-8

中文名称
——
中文别名
——
英文名称
[(Ph3PNC(C6H4)C(Ph)=N(4-MeC6H4)PdCl2]
英文别名
——
[(Ph3PNC(C6H4)C(Ph)=N(4-MeC6H4)PdCl2]化学式
CAS
1160221-90-8
化学式
C38H31Cl2N2PPd
mdl
——
分子量
723.977
InChiKey
BVFANTDMXALWSE-MDMSKSMXSA-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:
    参考文献:
    名称:
    Reversible Orthopalladation of Phosphinimine−Imine Dichloropalladium(II) Complexes
    摘要:
    The synthesis and characterization of triphenylphosphinimine-arylimine bidentate ligands (aryl = 2,4,6-trimethylphenyl or 4-methylphenyl) along with their dichloropalladium(II) complexes are reported. These complexes form tridentate orthopalladated species upon heating in the presence or sodium acetate. The reverse reaction occurs upon addition of HCl center dot Et2O. The rate of orthopalladation and reprotonation is highly dependent on the steric bulk of the ligand. Related cationic species were also synthesized and characterized and found to be inert in the presence of 1-hexene and styrene.
    DOI:
    10.1021/om900194s
  • 作为产物:
    描述:
    [(C6H4P(Ph)2NC(C6H4)C(Ph)=N(4-MeC6H4))PdCl]*CH2Cl2 、 hydrochloric acid diethyl ether 以 氯仿 为溶剂, 以85%的产率得到[(Ph3PNC(C6H4)C(Ph)=N(4-MeC6H4)PdCl2]
    参考文献:
    名称:
    Reversible Orthopalladation of Phosphinimine−Imine Dichloropalladium(II) Complexes
    摘要:
    The synthesis and characterization of triphenylphosphinimine-arylimine bidentate ligands (aryl = 2,4,6-trimethylphenyl or 4-methylphenyl) along with their dichloropalladium(II) complexes are reported. These complexes form tridentate orthopalladated species upon heating in the presence or sodium acetate. The reverse reaction occurs upon addition of HCl center dot Et2O. The rate of orthopalladation and reprotonation is highly dependent on the steric bulk of the ligand. Related cationic species were also synthesized and characterized and found to be inert in the presence of 1-hexene and styrene.
    DOI:
    10.1021/om900194s
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