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cis-tetracarbonylpyrazinetrimethylphosphitetungsten(0) | 897939-16-1

中文名称
——
中文别名
——
英文名称
cis-tetracarbonylpyrazinetrimethylphosphitetungsten(0)
英文别名
——
cis-tetracarbonylpyrazinetrimethylphosphitetungsten(0)化学式
CAS
897939-16-1
化学式
C11H13N2O7PW
mdl
——
分子量
500.057
InChiKey
AYDZDNXGVRGJSW-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

  • 作为产物:
    描述:
    四氢呋喃吡嗪pentacarbonyl(trimethyl phosphite)tungsten(0)四氢呋喃 为溶剂, 以10%的产率得到cis-tetracarbonylpyrazinetrimethylphosphitetungsten(0)
    参考文献:
    名称:
    A stable carbonyl–pyrazine–metal(0) complex: Synthesis and characterization of cis-tetracarbonylpyrazinetrimethylphosphitetungsten(0)
    摘要:
    Pentacarbonylpyrazinetungsten(0), (CO)(5)W(pyz), is not stable in solution in polar solvents such as acetone or dichloromethane and undergoes conversion to a bimetallic complex, (CO)(5)W(pyz)W(CO)(5) plus free pyrazine. These three species exist at equilibrium. Using the quantitative H-1 NMR spectroscopy, the equilibrium constant could be determined to be K-eq = (5.9 +/- 0.8) x 10(-2) at 25 degrees C. Introducing a second pyrazine ligand into the molecule does not stabilize the complex, as CiS-W(CO)(4)(pyz)(2) was found to be less stable than W(CO)(5)(pyz) and, therefore, could not be isolated. However, introducing trimethylphosphite as a donor ligand into the complex leads to the stabilization of the carbonyl-pyrazine-metal(0) complexes, as shown by the synthesis Of CiS-W(CO)(4)[P(OCH3)(3)](pyz). This complex could be isolated from the reaction of the photogenerated W(CO)(4)[P(OCH3)(3)](tetrahydrofuran) with trimethylphosphite upon mixing for 2 h at 10 degrees C in tetrahydrofuran and characterized by elemental analysis, IR, MS, H-1, C-13 and P-31 NMR spectroscopy. (c) 2006 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2006.02.005
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