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Cp(CO)(triphenylphosphite)Mo*CBu | 213621-42-2

中文名称
——
中文别名
——
英文名称
Cp(CO)(triphenylphosphite)Mo*CBu
英文别名
——
Cp(CO)(triphenylphosphite)Mo*CBu化学式
CAS
213621-42-2
化学式
C29H29MoO4P
mdl
——
分子量
568.461
InChiKey
AIURKBCCOSXKFN-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

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Effect of Ligand Variation on the Site of Protonation in the Metal Carbynes CpL2Mo⋮CBu and TpL2Mo⋮CBu [L = CO, P(OR)3]
    摘要:
    The site of thermodynamic protonation of the Fischer carbynes CpL2Mo=CBu and TpL(2)Mo=CBu [L = CO, P(OR)(3)] with HBF4 depends on the number of pi-acid CO ligands. As the number of carbonyls increases from zero to two and the electron density at the metal center is decreased by back-bonding, the protonation site shifts from the metal to the carbyne carbon. Parallel behavior in the Tp and Cp series of complexes allows the change in protonation site to be attributed to electronic effects in the ancillary ligands.
    DOI:
    10.1021/om990047x
  • 作为产物:
    参考文献:
    名称:
    Effect of Ligand Variation on the Site of Protonation in the Metal Carbynes CpL2Mo⋮CBu and TpL2Mo⋮CBu [L = CO, P(OR)3]
    摘要:
    The site of thermodynamic protonation of the Fischer carbynes CpL2Mo=CBu and TpL(2)Mo=CBu [L = CO, P(OR)(3)] with HBF4 depends on the number of pi-acid CO ligands. As the number of carbonyls increases from zero to two and the electron density at the metal center is decreased by back-bonding, the protonation site shifts from the metal to the carbyne carbon. Parallel behavior in the Tp and Cp series of complexes allows the change in protonation site to be attributed to electronic effects in the ancillary ligands.
    DOI:
    10.1021/om990047x
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文献信息

  • Oxidation of Metal Carbynes in the Presence of Alkynes. Alkyne Addition vs H-Shift in the Carbene Intermediate
    作者:Karen E. Torraca、Khalil A. Abboud、Lisa McElwee-White
    DOI:10.1021/om980534x
    日期:1998.9.1
    One-electron oxidation of the carbyne complex (eta(5)-C5H5)(CO)P(OPh)(3)}Mo=CCH2CH2CH2CH3 (1a) in the presence of phenylacetylene results in H-abstraction and addition of the alkyne to the resulting metal carbene. The final product of the addition is the eta(1)eta(2)-allyl complex (eta(5)-C5H5)(CO)P(OPh)(3)}Mo[eta(1):eta(2)-CHP(OPh)(3)}C(Ph)=CH(Ch(2)CH(2)CH(2)CH(3))] (2a), the structure of which was confirmed by X-ray crystallography.
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