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[(Z,Z-1,5-cyclooctadiene)Rh(N,N-di-[(1-methyl-1H-2-imidazolyl)methyl]amine)]PF6 | 496789-14-1

中文名称
——
中文别名
——
英文名称
[(Z,Z-1,5-cyclooctadiene)Rh(N,N-di-[(1-methyl-1H-2-imidazolyl)methyl]amine)]PF6
英文别名
——
[(Z,Z-1,5-cyclooctadiene)Rh(N,N-di-[(1-methyl-1H-2-imidazolyl)methyl]amine)]PF6化学式
CAS
496789-14-1
化学式
C18H27N5Rh*F6P
mdl
——
分子量
561.316
InChiKey
ACJZIYZRZUBYKD-ONEVTFJLSA-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

  • 作为产物:
    描述:
    ammonium hexafluorophosphate 、 bis<(1-methylimidazol-2-yl)methyl>amine 、 chloro(1,5-cyclooctadiene)rhodium(I) dimer 以 甲醇 为溶剂, 以59.3%的产率得到[(Z,Z-1,5-cyclooctadiene)Rh(N,N-di-[(1-methyl-1H-2-imidazolyl)methyl]amine)]PF6
    参考文献:
    名称:
    Amido-bridged dinuclear rhodium(I) complexes by deprotonation of mononuclear rhodium(I) amine complexes
    摘要:
    The preparation of a series of new amido bridged binuclear complexes [(N-N-N)Rh-2(1) (cod)(2)] (cod = Z,Z- 1,5-cyclooctadiene), [(N-N-N)Rh-2(1) (hed)(2)] (hed = 1,5-hexadiene) and [(N-N-N)Rh-2(1) (CO)(4)] is reported. These complexes contain chelating imidazoleamido-imidazole, pyridine-amido-pyridine and pyridine-amido-pyrrolate ligands (N-N-N). The cod complexes have been prepared through deprotonation of their mononuclear amine precursors [(N-HN-N)Rh-1(cod)] in the presence of [Rh-1(cod)](+). Reaction of the binuclear complexes [(N-N-N)Rh-2(1) (cod)(2)] with CO results in the complexes [(N-N-N)Rh-2(1) (CO)(4)]. For N-N-N= chelating imidazole-amido-imidazole ligand, the X-ray structures of [(N-N-N)Rh-2(1)(cod)(2)], [(N-N-N)Rh-2(1)(CO)(4)], and their mononuclear amine precursor [(N-HN-N)Rh-1(cod)] are reported. Electrochemical oxidation of the complexes is related to the relative donor strength of the N-ligands. (C) 2002 Elsevier Science B.V. All rights reserved.
    DOI:
    10.1016/s0020-1693(02)01030-7
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