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[PtMe2Cl{C6H4CH=NCH2(4-ClC6H4)}SMe2] | 1448617-19-3

中文名称
——
中文别名
——
英文名称
[PtMe2Cl{C6H4CH=NCH2(4-ClC6H4)}SMe2]
英文别名
——
[PtMe<sub>2</sub>Cl{C<sub>6</sub>H<sub>4</sub>CH=NCH<sub>2</sub>(4-ClC<sub>6</sub>H<sub>4</sub>)}SMe<sub>2</sub>]化学式
CAS
1448617-19-3
化学式
C18H23Cl2NPtS
mdl
——
分子量
551.439
InChiKey
OGLNUFBFXGBHRT-BADOYKKRSA-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:
    [PtMe2Cl{C6H4CH=NCH2(4-ClC6H4)}SMe2]丙酮甲苯 为溶剂, 反应 4.5h, 生成 [PtCl{2-MeC6H3CH=NCH2(4-ClC6H4)}PPh3]
    参考文献:
    名称:
    Regioselective C–H Activation Preceded by Csp2–Csp3 Reductive Elimination from Cyclometalated Platinum(IV) Complexes
    摘要:
    Reductive elimination reactions of the cyclometalated platinum-(IV) compounds [PtMe2Cl{C6H4CH=NCH2(4-ClC6H4)}L] and [PtMe2Br{C6H4CH=NCH2(C6H5)}L] (L = SMe2, PPh3) to form C-sp3-C-sp2 bonds, followed by either exclusive C H bond activation (L = SMe2) or competition between C-sp2-H and C-sp3-H bond activation (L = PPh3), are reported. Isomerization to give endo products instead of the expected exo complex was observed for the ligand C6H4CH=NCH2(2-BrC6H5), and formation of an endo six-membered platinacycle occurs for the ligand 2,4,6-Me3C6H2CH=NCH2(2-BrC6H4).
    DOI:
    10.1021/om400398g
  • 作为产物:
    描述:
    bis[dimethyl(μ-dimethylsulfide)platinum(II)] 、 1-(2-chlorophenyl)-N-[(4-chlorophenyl)methyl]methanimine丙酮 为溶剂, 反应 16.0h, 以87%的产率得到[PtMe2Cl{C6H4CH=NCH2(4-ClC6H4)}SMe2]
    参考文献:
    名称:
    Regioselective C–H Activation Preceded by Csp2–Csp3 Reductive Elimination from Cyclometalated Platinum(IV) Complexes
    摘要:
    Reductive elimination reactions of the cyclometalated platinum-(IV) compounds [PtMe2Cl{C6H4CH=NCH2(4-ClC6H4)}L] and [PtMe2Br{C6H4CH=NCH2(C6H5)}L] (L = SMe2, PPh3) to form C-sp3-C-sp2 bonds, followed by either exclusive C H bond activation (L = SMe2) or competition between C-sp2-H and C-sp3-H bond activation (L = PPh3), are reported. Isomerization to give endo products instead of the expected exo complex was observed for the ligand C6H4CH=NCH2(2-BrC6H5), and formation of an endo six-membered platinacycle occurs for the ligand 2,4,6-Me3C6H2CH=NCH2(2-BrC6H4).
    DOI:
    10.1021/om400398g
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