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Cp*IrCl[κ2(N,C)-(NH2CH2-2-C6H4)] | 1033052-17-3

中文名称
——
中文别名
——
英文名称
Cp*IrCl[κ2(N,C)-(NH2CH2-2-C6H4)]
英文别名
——
Cp*IrCl[κ2(N,C)-(NH2CH2-2-C6H4)]化学式
CAS
1033052-17-3
化学式
C17H23ClIrN
mdl
——
分子量
469.049
InChiKey
QQEZVCWXXGNXCT-UHFFFAOYSA-M
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

反应信息

  • 作为产物:
    描述:
    苄胺 、 bis[dichloro(pentamethylcyclopentadienyl)iridium(III)] 在 sodium acetate 作用下, 以 乙腈 为溶剂, 以50%的产率得到Cp*IrCl[κ2(N,C)-(NH2CH2-2-C6H4)]
    参考文献:
    名称:
    Synthesis and Reactivities of Cp*Ir Amide and Hydride Complexes Bearing C−N Chelate Ligands
    摘要:
    A series of 16-electron Cp*Ir amide complexes with C-N chelating ligands, Cp*Ir[kappa(2)(NC)-(NHCR2-2-C6H4)] (2a: R = C6H5, 2b: R = CH3) and the chiral version, Cp*Ir[kappa(2)(N,C)-(R)-{NHCH(CH3)-2-C10H6}] (2e), were obtained in good to excellent yields from reactions of 18-electron iridium amine complexes, Cp*IrCl[kappa(2)(N,C)-(NH2CR2-2-C6H4)] (1a: R = C6H5, 1b: R = CH3) and Cp*IrCl[kappa(2)(N,C)-(R)-{NH2CH(CH3)-2-C10H6}] (le), with a base. The amido complexes 2 readily reacted with 2-propanol to convert into hydrido(amine) complexes 3 in almost quantitative yields. The chiral amido complex has proven to serve as an efficient catalyst for asymmetric transfer hydrogenation of acetophenone with 2-propanol, giving 1-phenylethanol with a moderate ee. The Bronsted basicity on the metal-NH moiety in the amido complexes was evaluated by deprotonation of acetic acid, dimethyl malonate, and acetone, leading to the corresponding acetato(amine) complex 4 and alkyl(amine) complexes 5 and 6, respectively, indicating that the amido-Ir complexes bearing the C-N chelate have more basic properties than those with N-sulfonylated diamine ligands.
    DOI:
    10.1021/om800124f
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