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(η6-toluene)dicarbonyl-η1-bis(diphenylphosphino)ethanemanganese hexafluorophosphate | 138033-24-6

中文名称
——
中文别名
——
英文名称
(η6-toluene)dicarbonyl-η1-bis(diphenylphosphino)ethanemanganese hexafluorophosphate
英文别名
——
(η6-toluene)dicarbonyl-η1-bis(diphenylphosphino)ethanemanganese hexafluorophosphate化学式
CAS
138033-24-6
化学式
C35H32MnO2P2*F6P
mdl
——
分子量
746.488
InChiKey
YSWQAGSGOGKINC-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:
    参考文献:
    名称:
    Reactions of ditertiary phosphines with η6-arenetricarbonylmanganese cations
    摘要:
    Ditertiaryphosphines PPh2(CH2)nPPh2 (n = 1-3) react at room temperature with the eta-6-arenetricarbonylmanganese cations [(eta-6-XYC6H4)Mn(CO)3]+ (Ia, X = Y = H; Ib, X = Me, Y = H) by monocarbonyl substitution and formation of [(eta-6-XYC6H4)Mn(CO)2(eta-1-PPh2(CH2)nPPh2)]+. Prolonged refluxing results in metal-ring bond breaking and formation of cis- and trans-[Mn(CO)2(eta-2-PPh2CH2PPh2)2]+ and trans-[Mn(CO)2(eta-2-PPh2(CH2)2PPh2)2]+.Activation of a carbonyl group in [(eta-6-XYC6H4Mn(CO),(eta-1-PPh2(CH2)nPPh2)]+ by TMNO gives the series of chelate complexes [(eta-6-XYC6H4Mn(CO)(eta-2-PPh2(CH2)nPPh2)]+ (n = 1-3). The X-ray structure of the chelate with n = 3 is reported. In the case of [(eta-6-XYC6H4)Mn(CO)3]+ (Ic, X = Cl, Y = H); Id, X = Cl, Y = Me), formation of fac-Mn(CO)3(eta-2-PPh2(CH2)nPPh2)Cl (n = 1, 2) occurs, in a reaction analogous to that with monophosphines, see D.A. Brown, W.K. Glass and K.M. Kreddan, J. Organomet. Chem., 413 (1991) 233, but there was no evidence for ring adducts as intermediates.
    DOI:
    10.1016/0022-328x(91)86349-u
  • 作为产物:
    参考文献:
    名称:
    Reactions of ditertiary phosphines with η6-arenetricarbonylmanganese cations
    摘要:
    Ditertiaryphosphines PPh2(CH2)nPPh2 (n = 1-3) react at room temperature with the eta-6-arenetricarbonylmanganese cations [(eta-6-XYC6H4)Mn(CO)3]+ (Ia, X = Y = H; Ib, X = Me, Y = H) by monocarbonyl substitution and formation of [(eta-6-XYC6H4)Mn(CO)2(eta-1-PPh2(CH2)nPPh2)]+. Prolonged refluxing results in metal-ring bond breaking and formation of cis- and trans-[Mn(CO)2(eta-2-PPh2CH2PPh2)2]+ and trans-[Mn(CO)2(eta-2-PPh2(CH2)2PPh2)2]+.Activation of a carbonyl group in [(eta-6-XYC6H4Mn(CO),(eta-1-PPh2(CH2)nPPh2)]+ by TMNO gives the series of chelate complexes [(eta-6-XYC6H4Mn(CO)(eta-2-PPh2(CH2)nPPh2)]+ (n = 1-3). The X-ray structure of the chelate with n = 3 is reported. In the case of [(eta-6-XYC6H4)Mn(CO)3]+ (Ic, X = Cl, Y = H); Id, X = Cl, Y = Me), formation of fac-Mn(CO)3(eta-2-PPh2(CH2)nPPh2)Cl (n = 1, 2) occurs, in a reaction analogous to that with monophosphines, see D.A. Brown, W.K. Glass and K.M. Kreddan, J. Organomet. Chem., 413 (1991) 233, but there was no evidence for ring adducts as intermediates.
    DOI:
    10.1016/0022-328x(91)86349-u
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