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| 1042334-04-2

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1042334-04-2
化学式
C23H17MoO5PS2
mdl
——
分子量
564.431
InChiKey
HTGRWSHSKHREJC-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:
    氘代氯仿 为溶剂, 生成
    参考文献:
    名称:
    Dithiafulvenylphosphine as P- and P,S-ligand towards metal carbonyl fragments
    摘要:
    The ability of the dithiafulvenylphosphine ( P-DTF) to react as a monodentate ( P) or a bidentate ( P, S) ligand with metal carbonyl complexes such as Mo(CO)(6) and MnBr(CO)(5) is presented. A series of metal carbonyl complexes are synthesised and characterised by IR, H-1 NMR and P-31 NMR spectroscopy. X-ray crystallographic analyses on the Mo( CO)(5)(P-DTF) and Mo(CO)(4)( P, S-DTF) complexes are reported together with the structural investigations on the dithiafulvenes precursors. The electrochemical properties of the various complexes investigated by cyclic voltammetry are discussed. (C) 2008 Elsevier B. V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2008.04.011
  • 作为产物:
    参考文献:
    名称:
    Dithiafulvenylphosphine as P- and P,S-ligand towards metal carbonyl fragments
    摘要:
    The ability of the dithiafulvenylphosphine ( P-DTF) to react as a monodentate ( P) or a bidentate ( P, S) ligand with metal carbonyl complexes such as Mo(CO)(6) and MnBr(CO)(5) is presented. A series of metal carbonyl complexes are synthesised and characterised by IR, H-1 NMR and P-31 NMR spectroscopy. X-ray crystallographic analyses on the Mo( CO)(5)(P-DTF) and Mo(CO)(4)( P, S-DTF) complexes are reported together with the structural investigations on the dithiafulvenes precursors. The electrochemical properties of the various complexes investigated by cyclic voltammetry are discussed. (C) 2008 Elsevier B. V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2008.04.011
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