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[PtCl2(4-ClC6H4CH2NH2)(SOMe2)] | 1063991-19-4

中文名称
——
中文别名
——
英文名称
[PtCl2(4-ClC6H4CH2NH2)(SOMe2)]
英文别名
——
[PtCl2(4-ClC6H4CH2NH2)(SOMe2)]化学式
CAS
1063991-19-4
化学式
C9H14Cl3NOPtS
mdl
——
分子量
485.721
InChiKey
BTHOOCVEAGTTRJ-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:
    参考文献:
    名称:
    Novel platinum(II) compounds with N-benzylidenebenzylamines: Synthesis, crystal structures and the effect of cis or trans geometry on cycloplatination
    摘要:
    Coordination compounds with a trans-stereochemistry were prepared for ligands (4-ClC6H4)CH=NCH2(4'-ClC6H4) (L-a), (2,4,6-Me3C6H2)CH=NCH2(4'-ClC6H4) (L-b) and (2,6-Cl2C6H3)CH=NCH2(4'-ClC6H4) (L-c) and were shown to be precursors of the corresponding cyclometallated compounds. The reactions between cis-[PtCl2(dmso)(2)] and ligands ArCH=NCH2(4'-ClC6H4) (Ar = 2-BrC6H4 (L-d); 2-ClC6H4 (L-e); C6F5 (L-f); 2,6-F2C6H3 (L-g)) under previously described conditions for cycloplatination of N-benzylidenebenzylamines gave a cyclometallated compound only for imine L-f; the other imines produced coordination compounds with a cis arrangement from which cyclometallation could not be achieved. Formation of either cis or trans coordination compounds [PtCl2(L)dmso] (L = N-benzylidenebenzylamine) can be related to steric effects and to the E/Z configuration of the C=N bond. All compounds were fully characterized including structure determinations for trans-[PtCl2{(4-ClC6H4)CH=NCH2(4'-ClC6H4)}SOMe2] (2a), trans-[PtCl2[{2,6-Cl2C6H3)CH=NCH2(4'-ClC6H4)}SOMe2] (2c) and the amine derivative trans-[PtCl2(4-ClC6H4CH2NH2)SOMe2] (2) obtained as a by-product. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2008.05.001
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