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Cd(3,5-dimethylpyrazole)4(1,3-benzodioxole-5-carboxylate)2 | 1446905-55-0

中文名称
——
中文别名
——
英文名称
Cd(3,5-dimethylpyrazole)4(1,3-benzodioxole-5-carboxylate)2
英文别名
Cd(3,5-dimethylpyrazole)4(1,3-benzodioxole-5-carboxylate)2;Cd(Hdmpz)4(1,3-benzodioxole-5-carboxylate)2
Cd(3,5-dimethylpyrazole)4(1,3-benzodioxole-5-carboxylate)2化学式
CAS
1446905-55-0
化学式
C36H42CdN8O8
mdl
——
分子量
827.188
InChiKey
GUBCVINRQXVZLT-UHFFFAOYSA-L
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:
    3,5-二甲基吡唑胡椒酸cadmium(II) acetate dihydrate甲醇乙醇 为溶剂, 反应 2.0h, 以79.79%的产率得到Cd(3,5-dimethylpyrazole)4(1,3-benzodioxole-5-carboxylate)2
    参考文献:
    名称:
    Non-covalently bonded 2D–3D metal–organic frameworks from the reactions of Cd(II) and Zn(II) with 3,5-dimethylpyrazole and carboxylate ligands
    摘要:
    Seven new complexes, namely Cd(Hdmpz)(2)(L1)(2) (1) (Hdmpz = 3,5-dimethylpyrazole, L1 = N-phenylmaleamate), Cd(Hdmpz)(4)(L2)(2) (2) (L2 = 1,3-benzodioxole-5-carboxylate), Zn-2(mu-dmpz)(2)(Hdmpz)(2)(L3)(2) (3) (L3 = 2-chloronicotinate), Zn(Hdmpz)(2)(L4)(2) (4) (L4 = 3,5-dinitrobenzoate), Zn(Hdmpz)(2)(HL5)(2) (5) (HL5 = 5-chlorosalicylate), Cd(Hdmpz)(2)(HL6) (6) (HL6 = 5-sulfosalicylate) and Cd-2(Hdmpz)(4)(L7)(2) (7) (L7 = maleate), have been synthesized from the self-assembly of the Zn/Cd ions, 3,5-dimethylpyrazole and carboxylate ligands at room temperature. All the complexes were structurally characterized by different techniques, including elemental analysis, IR spectra, TG and single crystal X-ray diffraction analysis. The X-ray studies suggest that these complexes display mononuclear to dinuclear structures with a tetrahedral geometry around each zinc center, and an octahedral geometry around each cadmium center. The pyrazole ligands in all the compounds except compound 3 are coordinated only in the monodentate fashion by its neutral N group. In 2, 3, 4, 5 and 6, the carboxylate groups behave as monodentate ligands. The COO- group in 1 and the SO3- group in 6 both coordinate to the metal in a chelating bidentate fashion. The carboxylates in 7 functioned as a tetradentate bridging ligand. The uncoordinated oxygen atom of the carboxylate group in all of the compounds forms intramolecular hydrogen bonds with the N-H group of the coordinated 3,5-dimethylpyrazole ligand. On the basis of the X-ray crystallographic study, the rich intra- and intermolecular non-covalent interactions, such as classical hydrogen bonds, CH-Cl, CH3-Cl, Cl center dot center dot center dot Cl, Cl center dot center dot center dot O, C-H center dot center dot center dot O, CH3 center dot center dot center dot O, C-H center dot center dot center dot pi, CH2 center dot center dot center dot pi, CH3-pi, O-pi and pi-pi interactions, are analyzed. The various non-bonding interactions in these compounds are responsible for different structures, such as sheet, 3D network and 3D layer structures. The thermal stabilities of 1-7 were examined and the results show that the complexes seem to be good candidates for novel hybrid inorganic-organic materials with good thermal stability. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2013.04.056
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