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[(pentamethylcyclopentadienyl)IrCl(η2-bis(diphenylphosphino)methane)]OTf | 240817-50-9

中文名称
——
中文别名
——
英文名称
[(pentamethylcyclopentadienyl)IrCl(η2-bis(diphenylphosphino)methane)]OTf
英文别名
chloroiridium(2+);diphenylphosphanylmethyl(diphenyl)phosphane;1,2,3,4,5-pentamethylcyclopenta-1,3-diene;trifluoromethanesulfonate
[(pentamethylcyclopentadienyl)IrCl(η2-bis(diphenylphosphino)methane)]OTf化学式
CAS
240817-50-9
化学式
CF3O3S*C35H37ClIrP2
mdl
——
分子量
896.37
InChiKey
KVRUBCRVSMYCMJ-UHFFFAOYSA-L
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:
    [(pentamethylcyclopentadienyl)IrCl(η2-bis(diphenylphosphino)methane)]OTfsodium ethanolate乙醇 为溶剂, 以78%的产率得到[(C5Me4CH2OEt)Ir(η2-bis(diphenylphosphino)methane)]
    参考文献:
    名称:
    Alkoxylation and Amination of Ring-Methyl Group in Pentamethylcyclopentadienyliridium Complexes
    摘要:
    Reactions of a unidentate bis(diphenylphosphino)methane (dppm) complex Cp*IrCl2(eta (1)-dppm) (1) with 2 equiv of NaOR (R = Et, Me, or Pr-i) give ring-methyl-alkoxylated complexes (C5Me4CH2OR)Ir(eta (2)-dppm) [R = Et (5a); R = Me (5b); R = Pr-i (5c)], respectively. Cationic complexes [Cp*IrCl(eta (2)-dppm)]OTf (2), [Cp*IrCl{P(OPh)(3)}(2)]OTf(3), and [Cp*IrCl(PPh3)(2)]OTf (4) react with 2 equiv of NaOEt to give (C5Me4CH2OEt)IrL2 [L-2 = dppm (5a); L = P(OPh)(3) (6a); L = PPh3 (7a)], respectively. The complex 3 reacts with 2 equiv of (NaOBu)-Bu-t in ethanol, methanol, 2-propanol, allyl alcohol, or propargyl alcohol to give (C5Me4CH2OR)Ir(P(OPh)3)2 [R = Et (6a); R = Me (6b); R = Pr-i (6c) R = allyl (6d); R = propargyl (6e)], respectively. Furthermore, treatment of 3 with 2 equiv of (BuLi)-Bu-n and excess diethylamine, propylamine, N-methylaniline, or aniline in triethylamine as solvent gives ring-methyl aminated complexes ((C5Me4CH2NRR2)-R-1)Ir(P(OPh)(3))(2) [R-1 = R-2 = Et (8a); R-1 = Pr-n, R-2 = H (sb); R-1 = Ph, R-2 = Me (8c); R-1 = Ph, R-2, H (8d)], respectively. The structure of 8a has been confirmed by X-ray analysis.
    DOI:
    10.1021/om000718n
  • 作为产物:
    描述:
    (η(5)-pentamethylcyclopentadienyl)IrCl2(η(1)-bis(diphenylphosphino)methane)silver trifluoromethanesulfonate四氢呋喃 为溶剂, 以44%的产率得到[(pentamethylcyclopentadienyl)IrCl(η2-bis(diphenylphosphino)methane)]OTf
    参考文献:
    名称:
    Alkoxylation and Amination of Ring-Methyl Group in Pentamethylcyclopentadienyliridium Complexes
    摘要:
    Reactions of a unidentate bis(diphenylphosphino)methane (dppm) complex Cp*IrCl2(eta (1)-dppm) (1) with 2 equiv of NaOR (R = Et, Me, or Pr-i) give ring-methyl-alkoxylated complexes (C5Me4CH2OR)Ir(eta (2)-dppm) [R = Et (5a); R = Me (5b); R = Pr-i (5c)], respectively. Cationic complexes [Cp*IrCl(eta (2)-dppm)]OTf (2), [Cp*IrCl{P(OPh)(3)}(2)]OTf(3), and [Cp*IrCl(PPh3)(2)]OTf (4) react with 2 equiv of NaOEt to give (C5Me4CH2OEt)IrL2 [L-2 = dppm (5a); L = P(OPh)(3) (6a); L = PPh3 (7a)], respectively. The complex 3 reacts with 2 equiv of (NaOBu)-Bu-t in ethanol, methanol, 2-propanol, allyl alcohol, or propargyl alcohol to give (C5Me4CH2OR)Ir(P(OPh)3)2 [R = Et (6a); R = Me (6b); R = Pr-i (6c) R = allyl (6d); R = propargyl (6e)], respectively. Furthermore, treatment of 3 with 2 equiv of (BuLi)-Bu-n and excess diethylamine, propylamine, N-methylaniline, or aniline in triethylamine as solvent gives ring-methyl aminated complexes ((C5Me4CH2NRR2)-R-1)Ir(P(OPh)(3))(2) [R-1 = R-2 = Et (8a); R-1 = Pr-n, R-2 = H (sb); R-1 = Ph, R-2 = Me (8c); R-1 = Ph, R-2, H (8d)], respectively. The structure of 8a has been confirmed by X-ray analysis.
    DOI:
    10.1021/om000718n
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