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[Rh(κ2P,P':η5-C5Me3-1,3-(CH2CPh=CHPPh2)2)Cl](CF3SO3) | 1095268-31-7

中文名称
——
中文别名
——
英文名称
[Rh(κ2P,P':η5-C5Me3-1,3-(CH2CPh=CHPPh2)2)Cl](CF3SO3)
英文别名
——
[Rh(κ2P,P':η5-C5Me3-1,3-(CH2CPh=CHPPh2)2)Cl](CF3SO3)化学式
CAS
1095268-31-7
化学式
CF3O3S*C50H45ClP2Rh
mdl
——
分子量
995.284
InChiKey
RFLYRGDYHKLRQK-FSSOOTDASA-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

  • 作为产物:
    参考文献:
    名称:
    Facile Single or Double C−H Bond Activation on a Cp* Ligand Promoted by the Presence of Alkynylphosphine Ligands
    摘要:
    The behavior of the cationic alkynylphosphine complex [Rh(eta(5)-Cp*)Cl(PPh2C CPh)(2)](CF3SO3) (1) under thermal or basic conditions is described. Complex 1 rearranges thermally (toluene, reflux) to generate a solution from which a mixture formed by 1, the motrohydroalkylated derivative [Rh{kP:eta Me-5(4)(CH2CPh=CHPPh2)}Cl(PPh2C equivalent to CPh)](CF3SO3) (2), and the symmetrical 1,2 -dihydroalkylated derivative [Rh{k(2)PP':eta(5)-C5Me3-1,2-(CH2CPh=CHPPh2)(2)}]Cl](CF3SO3) (3') (similar to 30:60:10, respectively) can be isolated. From this mixture, compounds 1 and 2 cocrystallize together, giving rise to a solid solution, as has been confirmed by X-ray crystallography. In contrast, treatment of [Rh(eta(5)-Cp*)Cl(PPh2C CPh)(2)](CF3SO3) (1) with Na2CO3 evolves with the formation of the new asymmetrical 1,2- and 1,3-dihydroactivated isomers [Rh{k(2)PP':eta(5)-1,2-(PPh2CH2CPh=CH)C5Me3(CH2CPh=CHPPh2)}]Cl](CF3SO3) (3, X-ray) and [Rh{k(2)PP':eta(5)-1,3-(PPh2CH2CPh=CH)C5Me3(CH2CPh=CHPPh2)}]Cl](CF3SO3) (4), generated by the occurrence of a simultaneous 1,2- or 1,3-double C-H bond addition to the triple bonds, together with an additional isomerization process. A detailed study of this reaction (reflux or room temperature) provides evidence that these asymmetrical deactivated complexes (3, 4) are generated by initial formation of the corresponding symmetrical 1,2- and 1,3-dihydroalkylated species 3' and 4', respectively.
    DOI:
    10.1021/om800867h
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