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[RuCl(bsp)2(PPh3)] | 1589490-12-9

中文名称
——
中文别名
——
英文名称
[RuCl(bsp)2(PPh3)]
英文别名
——
[RuCl(bsp)<sub>2</sub>(PPh<sub>3</sub>)]化学式
CAS
1589490-12-9
化学式
C46H33ClN4O2PRuS2
mdl
——
分子量
905.422
InChiKey
YMXWZNHVWGLCKP-UZAQZMKHSA-K
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:
    tris(triphenylphosphine)ruthenium(II) chloride2-((benzo[d]thiazol-2-ylimino)methyl)phenol甲苯 为溶剂, 反应 6.0h, 以66%的产率得到[RuCl(bsp)2(PPh3)]
    参考文献:
    名称:
    Ruthenium complexes with Schiff base ligands containing benz(othiazole/imidazole) moieties: Structural, electron spin resonance and electrochemistry studies
    摘要:
    Novel ruthenium(II/III) complexes of Schiff bases containing benzimidazole (bz) or benzothiazole (bs) moieties were isolated: the diamagnetic ruthenium complex, cis-[(RuCl2)-Cl-11(bzpy)(PPh3)(2)] (1) was formed from the 1:1 M reaction between N-((pyridine-2-yl)methylene)-1H-benzimidazole (bzpy) and metal precursor, trans-[RuCl2(PPh3)(3)]. The same metal precursor, when reacted with the benzimidazole-derived Schiff bases N-(2-hydroxybenzylidene)-benzothiazole (Hbsp) and N-(2-hydroxybenzylidene)-benzimidazole (Hbzp)], afforded the paramagnetic ruthenium(III) complexes [RuCl(bsp)(2)(PPh3)] (2) and trans-[RuCl(bzp)(PPh3)(2)] (3), respectively. These metal complexes were characterized via IR, mass and UV-Vis spectroscopy, elemental analysis, single crystal XRD analysis as well as conductivity measurements. Their redox properties were probed by voltammetry and accompanying UV-Vis spectroelectro-chemistry experiments. Structural features of complex I were further investigated by multinuclear and P-31) NMR spectroscopy. The presence of the paramagnetic metal centres of 2 and 3 were confirmed by X-band ESR spectroscopy. (C) 2014 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2014.02.009
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