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| 151709-47-6

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
151709-47-6
化学式
C31H23ClN5Ru*F6P
mdl
——
分子量
747.044
InChiKey
CSXQKNSMGRCJDN-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:
    为溶剂, 以0%的产率得到(6-phenyl-2,2'-bipyridine(1-))(2,2':6',2''-terpyridine)ruthenium(II) hexafluorophosphate
    参考文献:
    名称:
    Solvent effects in the reactions of 6-phenyl-2,2′-bipyridine with ruthenium(II)
    摘要:
    The reaction of [Ru(tpy)Cl3] with the potentially cyclometallating ligand 6-phenyl-2,2'-bipyridine (HL) has been examined in a variety of solvents. In glacial acetic acid the ligand acts as a substituted 2,2'-bipyridine and reacts to give the complex cation [Ru(tpy)(HL)Cl]+, containing a bidentate N,N'-bonded HL ligand. The structure of this complex has been unambiguously established from its H-1 NMR spectrum. In contrast, the use of water as a solvent gives the cyclometallated complex cation [Ru(tpy)(L)]+. In methanol and butan-1-ol, mixtures of these two products are formed. The work has been extended to 2,2':6',2''-terpyridines with aromatic substituents in the 4' position and the complexes have been characterised by H-1 NMR, electronic and FAB mass spectroscopic techniques and also by cyclic voltammetry.
    DOI:
    10.1016/s0020-1693(00)82850-9
  • 作为产物:
    描述:
    (6-phenyl-2,2'-bipyridine(1-))(2,2':6',2''-terpyridine)ruthenium(II) hexafluorophosphate 以 溶剂黄146 为溶剂, 以0%的产率得到
    参考文献:
    名称:
    Solvent effects in the reactions of 6-phenyl-2,2′-bipyridine with ruthenium(II)
    摘要:
    The reaction of [Ru(tpy)Cl3] with the potentially cyclometallating ligand 6-phenyl-2,2'-bipyridine (HL) has been examined in a variety of solvents. In glacial acetic acid the ligand acts as a substituted 2,2'-bipyridine and reacts to give the complex cation [Ru(tpy)(HL)Cl]+, containing a bidentate N,N'-bonded HL ligand. The structure of this complex has been unambiguously established from its H-1 NMR spectrum. In contrast, the use of water as a solvent gives the cyclometallated complex cation [Ru(tpy)(L)]+. In methanol and butan-1-ol, mixtures of these two products are formed. The work has been extended to 2,2':6',2''-terpyridines with aromatic substituents in the 4' position and the complexes have been characterised by H-1 NMR, electronic and FAB mass spectroscopic techniques and also by cyclic voltammetry.
    DOI:
    10.1016/s0020-1693(00)82850-9
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文献信息

  • Reversible cyclometallation at a ruthenium(II) centre
    作者:Edwin C. Constable、Simon J. Dunne、David G. F. Rees、Chantal X. Schmitt
    DOI:10.1039/cc9960001169
    日期:——
    The metallated complex [Ru(tbp)(tpy)][PF6][Htbp = 6-(2-thienyl)-2,2′-bipyridine, tpy = 2,2′:6′,2″-terpyridine] is converted to the non-metallated species [Ru(Htbp)(tpy)][PF6] containing an N,N,S-bonded Htbp ligand upon treatment with acid; this process is reversed upon reaction of [Ru(Htbp)(tpy)][PF6] with aqueous sodium hydroxide solution.
    属络合物[Ru(tbp)(tpy)][PF6][Htbp = 6-(2-噻吩基)-2,2′-联吡啶,tpy = 2,2′:6′,2″-三联吡啶]在酸处理后转化为非属络合物[Ru(Htbp)(tpy)][PF6],其中含有N,N,S键合的Htbp配体;当[Ru(Htbp)(tpy)][PF6]与氢氧化钠溶液反应时,该过程可逆。
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