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tris(3-ethynyl-2,4-pentanedionato)ruthenium(III) | 190510-74-8

中文名称
——
中文别名
——
英文名称
tris(3-ethynyl-2,4-pentanedionato)ruthenium(III)
英文别名
——
tris(3-ethynyl-2,4-pentanedionato)ruthenium(III)化学式
CAS
190510-74-8
化学式
C21H21O6Ru
mdl
——
分子量
470.464
InChiKey
JRCBMQUOXQJDNF-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

反应信息

  • 作为反应物:
    描述:
    tris(3-ethynyl-2,4-pentanedionato)ruthenium(III)四甲基乙二胺氧气copper(l) chloride 作用下, 以 二氯甲烷 为溶剂, 以18%的产率得到poly-tris(3-ethynyl-2,4-pentanedionato)ruthenium(III)
    参考文献:
    名称:
    Synthesis and characterization of a metal coordination polymer consisting of ruthenium(III) β-diketone units linked by butadiyne bridges
    摘要:
    A new metal coordination polymer consisting of ruthenium(III) beta-diketone units linked by butadiyne bridges was synthesized, and two mononuclear complexes, [Ru(mESima)(3)] and [Ru(mEma)(3)] (mESima(-) = 3-(trimethylsilyl)ethynyl-2,4-pentanedionate ion and mEma(-) = 3-ethynyl-2,4-pentanedionate ion), were also prepared as starting materials for the polymerization. The polymer was soluble in dichloromethane, chloroform, and benzene. The number-average molecular weight, 5400, corresponding to about 11 monomer units, was obtained from the FT-NMR integrated intensities for the protons on the ethynyl group of the mEma ligand end-group relative to the methyl protons of the entire chains. The NMR spectra also showed that the polymer structure was not a star-burst type but a chain-like type. The polymer exhibited one oxidation peak and one reduction peak on differential pulse voltammograms at 25 degrees C; however, the one anodic peak separated into two peaks at -36 degrees C. The difference in peak potentials between the first and the second oxidation waves was 0.23 V, which was very similar to the difference (0.22 V) in peak potentials for the corresponding binuclear complex. This indicated that metal-metal interactions in the polymer operate between only the closest neighboring units. Results of the controlled potential coulometry of the polymer in dichloromethane medium indicated that each monomer unit underwent a one-electron reduction. (C) 1999 Elsevier Science S.A. All rights reserved.
    DOI:
    10.1016/s0020-1693(99)00172-3
  • 作为产物:
    描述:
    tris(3-(trimethylsilyl)ethynyl-2,4-pentanedionato)ruthenium(III)四丁基氟化铵 作用下, 以 四氢呋喃 为溶剂, 以66%的产率得到tris(3-ethynyl-2,4-pentanedionato)ruthenium(III)
    参考文献:
    名称:
    Synthesis and characterization of a metal coordination polymer consisting of ruthenium(III) β-diketone units linked by butadiyne bridges
    摘要:
    A new metal coordination polymer consisting of ruthenium(III) beta-diketone units linked by butadiyne bridges was synthesized, and two mononuclear complexes, [Ru(mESima)(3)] and [Ru(mEma)(3)] (mESima(-) = 3-(trimethylsilyl)ethynyl-2,4-pentanedionate ion and mEma(-) = 3-ethynyl-2,4-pentanedionate ion), were also prepared as starting materials for the polymerization. The polymer was soluble in dichloromethane, chloroform, and benzene. The number-average molecular weight, 5400, corresponding to about 11 monomer units, was obtained from the FT-NMR integrated intensities for the protons on the ethynyl group of the mEma ligand end-group relative to the methyl protons of the entire chains. The NMR spectra also showed that the polymer structure was not a star-burst type but a chain-like type. The polymer exhibited one oxidation peak and one reduction peak on differential pulse voltammograms at 25 degrees C; however, the one anodic peak separated into two peaks at -36 degrees C. The difference in peak potentials between the first and the second oxidation waves was 0.23 V, which was very similar to the difference (0.22 V) in peak potentials for the corresponding binuclear complex. This indicated that metal-metal interactions in the polymer operate between only the closest neighboring units. Results of the controlled potential coulometry of the polymer in dichloromethane medium indicated that each monomer unit underwent a one-electron reduction. (C) 1999 Elsevier Science S.A. All rights reserved.
    DOI:
    10.1016/s0020-1693(99)00172-3
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