摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

Cp*Ta(CH2SiMe3)2(Cp*IrH2) | 1383607-91-7

中文名称
——
中文别名
——
英文名称
Cp*Ta(CH2SiMe3)2(Cp*IrH2)
英文别名
——
Cp*Ta(CH2SiMe3)2(Cp*IrH2)化学式
CAS
1383607-91-7
化学式
C28H54IrSi2Ta
mdl
——
分子量
820.076
InChiKey
RSIOSNKSIRLZSQ-UHFFFAOYSA-N
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:
    Cp*Ta(CH2SiMe3)2(Cp*IrH2) 生成 Cp*TaO(CH2SiMe3)(Cp*Ir)(μ-H)3
    参考文献:
    名称:
    Early–Late Heterobimetallic Complexes with a Ta–Ir Multiple Bond: Bimetallic Oxidative Additions of C–H, N–H, and O–H Bonds
    摘要:
    A heterobinuclear transition metal complex with a Ta-Ir multiple bond, Cp*(Me3SiCH2)(2)Ta-IrCp*(H)(2) (1), was synthesized using a salt elimination reaction. The isolable complex was characterized by NMR, IR, UV-vis spectroscopy, and X-ray crystallography. Compound I features an exceptionally short intermetallic distance (Ta-Ir 2.4457(3) angstrom). DFT calculation for 1 revealed the presence of a highly covalent bonding nature in spite of the involvement of such disparate d elements. Oxidative additions of C-H, N-H, and O-H bonds to 1 were also investigated.
    DOI:
    10.1021/om300429u
  • 作为产物:
    描述:
    Li[(eta.5-C5Me5)IrH3] 、 chloro(pentamethylcyclopentadienyl)(trimethylsilylmethyl)(trimethylsilylmethylidene)tantalum(V) 以 甲苯 为溶剂, 生成 Cp*Ta(CH2SiMe3)2(Cp*IrH2)
    参考文献:
    名称:
    Early–Late Heterobimetallic Complexes with a Ta–Ir Multiple Bond: Bimetallic Oxidative Additions of C–H, N–H, and O–H Bonds
    摘要:
    A heterobinuclear transition metal complex with a Ta-Ir multiple bond, Cp*(Me3SiCH2)(2)Ta-IrCp*(H)(2) (1), was synthesized using a salt elimination reaction. The isolable complex was characterized by NMR, IR, UV-vis spectroscopy, and X-ray crystallography. Compound I features an exceptionally short intermetallic distance (Ta-Ir 2.4457(3) angstrom). DFT calculation for 1 revealed the presence of a highly covalent bonding nature in spite of the involvement of such disparate d elements. Oxidative additions of C-H, N-H, and O-H bonds to 1 were also investigated.
    DOI:
    10.1021/om300429u
点击查看最新优质反应信息