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trans-[(4-dimethylaminopyridine)Ru(pyridine)4Cl](PF6) | 1320358-23-3

中文名称
——
中文别名
——
英文名称
trans-[(4-dimethylaminopyridine)Ru(pyridine)4Cl](PF6)
英文别名
——
trans-[(4-dimethylaminopyridine)Ru(pyridine)4Cl](PF6)化学式
CAS
1320358-23-3
化学式
C27H30ClN6Ru*F6P
mdl
——
分子量
720.063
InChiKey
BIBNDPPGLAKDSS-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

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:
    potassium hexacyanoferrate trihydrate 、 trans-[(4-dimethylaminopyridine)Ru(pyridine)4Cl](PF6)四苯基氯化膦甲醇 为溶剂, 以30%的产率得到
    参考文献:
    名称:
    Exploring the properties of mixed valence cyanide bridged dinuclear complexes: Solvent stabilization of electronic isomers
    摘要:
    We report here the synthesis and properties of a family of mixed-valence cyanide-bridged dinuclear complex ions trans-[(L'L(4)Ru(II)(mu-NC)Fe(III)(CN)(5)] (with L = pyridine or 4-dimethylaminopyridine (dmap) and L' = pyridine, 4-methoxypyridine (meopy) or 4-dimethylaminopyridine)) whose properties could be adjusted smoothly by changing the acceptor properties of the solvent and the sigma donor properties of the L' pyridine ligand. In solution these complexes exhibit an intense solvent-dependent MM'CT (Ru(II) -> FeIII) absorption in the near infrared region. Analysis of this band in different complexes and solvents suggests an enhanced interaction as the energies of the metal centers come closer. From this trend the anion trans-[(dmap)(5)Ru(mu-NC)Fe(CN)(5)] (dmap = 4-dimethylaminopyridine) in water is expected to belong to the class II-III, but its spectral properties indicates a ground state with Ru(III)-Fe(II) character. The stabilization of this electronic isomer is probably related to the better donor properties of the hexacyanoferrate( II) moiety and its stronger interaction with water. (C) 2011 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.ica.2011.03.032
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