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[1,3-dimethyl-2-(phenylazo)imidazolium][N,N-dimethylammonium][zinc(chloride)4] | 1239449-12-7

中文名称
——
中文别名
——
英文名称
[1,3-dimethyl-2-(phenylazo)imidazolium][N,N-dimethylammonium][zinc(chloride)4]
英文别名
[HaaiMe2][Me2NH2][ZnCl4]
[1,3-dimethyl-2-(phenylazo)imidazolium][N,N-dimethylammonium][zinc(chloride)4]化学式
CAS
1239449-12-7
化学式
C2H8N*C11H13N4*Cl4Zn
mdl
——
分子量
454.545
InChiKey
VUVKNEUKGPGRNN-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:
    [1,3-dimethyl-2-(phenylazo)imidazolium]2[zinc(chloride)4] 、 N,N-二甲基甲酰胺甲醇 为溶剂, 生成 [1,3-dimethyl-2-(phenylazo)imidazolium][N,N-dimethylammonium][zinc(chloride)4]
    参考文献:
    名称:
    Arylazoimidazoliumchloride and chlorometallates: Spectroscopic and structural characterization
    摘要:
    Protonation or dialkylation of 2-(arylazo)imidazoles (RaaiH) has generated azoimidazolium motif (RaaiH(2)(+), RaaiR'H+, RaaiR(2)'(+) where R = H, CH3 and R' = Me, Et, -CH2Ph). Electrostatic attraction between imdazolium cation and counter ions like Cl, ZnCl42-, PtCl62- has generated hydrogen bonded azoimidazolium-chloride/chlorometallated networks. The single crystal X-ray structure of 1-benzyl-2-(phenylazo) imidazolium chloride shows tape like 1-D network of [Cl(H2O)(4)]. Aquated Cl forms 10 membered supracycle through hydrogen bonding with imidazolium ion. The X-ray structures of [HaaiMe(2) (1,3)](+)[Me2NH2](+) [ZnCl4](2) and [MeaaiH(2)(+)center dot H2O](2)[PtCl6](2) show hydrogen bonded chlorometallate chain penetrated into the channel developed by organic motif. Azoimidazolium units are associated through pi center dot center dot center dot pi and C-H center dot center dot center dot pi interactions to strengthen the supramolecular geometry. (C) 2010 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.ica.2010.02.006
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