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aqua-(2,2-bipyridine-N,N')trichloro-chromium(III) | 1053059-79-2

中文名称
——
中文别名
——
英文名称
aqua-(2,2-bipyridine-N,N')trichloro-chromium(III)
英文别名
[Cr(bipy)(H2O)Cl3]
aqua-(2,2-bipyridine-N,N')trichloro-chromium(III)化学式
CAS
1053059-79-2
化学式
C10H10Cl3CrN2O
mdl
——
分子量
332.557
InChiKey
SMEMSDXGTHIOQR-UHFFFAOYSA-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:
    、 CrCl3*bpy*THF 以 四氢呋喃 为溶剂, 以95%的产率得到aqua-(2,2-bipyridine-N,N')trichloro-chromium(III)
    参考文献:
    名称:
    Substitution reactions of tetrahydrofuran in [Cr(thf)3Cl3] with mono and bidentate N-donor ligands: X-ray crystal structures of [Cr(bipy)(OH2)Cl3] and [HpyNH2][Cr(bipy)Cl4]
    摘要:
    Substitution of thf ligands in [Cr(thf)(3)Cl-3] and [Cr(thf)(2)(OH2)Cl-3] was investigated. 2,2'-Bipyridine (bipy) was reacted with [Cr(thf)(3)Cl-3] to form [Cr( bipy)(thf)Cl-3] (1), which was subsequently reacted with water to give [Cr(bipy)(OH2)Cl-3] (2). Reaction of 1 with acetonitrile (CH3CN), pyridine (py) and pyridine derivatives to form [Cr(bipy)(L)Cl-3] (L= CH3CN3, py 4 and 4-pyR with R = NH(2)5, Bu-t 6 and Ph7). In addition, the substitution of bipy in [Cr(thf)Cl-3(3)] was followed by H-1 NMR spectroscopy at room temperature, which showed completion of the reaction in ca. 100 min. Complex 2 was characterised by single crystal X-ray diffraction. The theoretical powder diffraction pattern of 2 was compared to the experimentally obtained powder X-ray diffraction pattern, and shows excellent agreement. The dimer [Cr-2(bipy)(2)Cl-4(mu-Cl)(2)] was cleaved asymmetrically to give the anionic complex [Cr(bipy)Cl-4](-) (8) and [Cr(bipy)(2)Cl-2](+) (9). Complexes 8 and 9 were characterised by single crystal X-ray diffraction. (c) 2008 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.ica.2008.01.033
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