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Cu(1,2-bis(pyridine-2-carboxamido)-4,5-dimethylbenzene-2H) | 1053232-07-7

中文名称
——
中文别名
——
英文名称
Cu(1,2-bis(pyridine-2-carboxamido)-4,5-dimethylbenzene-2H)
英文别名
Cu(Me2bpb)
Cu(1,2-bis(pyridine-2-carboxamido)-4,5-dimethylbenzene-2H)化学式
CAS
1053232-07-7
化学式
C20H16CuN4O2
mdl
——
分子量
407.919
InChiKey
ATQGFQIQWPMPEZ-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:
    copper(II) perchlorate hexahydrate 、 N,N'-(4,5-dimethyl-1,2-phenylene)dipicolinamide甲醇 为溶剂, 以65%的产率得到Cu(1,2-bis(pyridine-2-carboxamido)-4,5-dimethylbenzene-2H)
    参考文献:
    名称:
    Steric effect on construction of Cu(II) complexes with pyridine carboxamide ligands
    摘要:
    The structures of three new Cu(II) complexes with pyridine carboxamide ligands (Me(2)bpb, 6-Me-2-Mebpb, and 6-Me-2-Me(2)bpb) have been determined. 6-Methyl-substituted pyridyl bpb ligands produced dimeric compounds with Cu(II) ions, and weak interactions between dimers can make even polymeric compounds, while bpb ligands without 6-methyl substitution produced monomeric Cu(II) complexes. The large distortion effects of 6-methyl-substitution are shown in Cu(II) complexes with 6-methyl-substituted pyridyl bpb ligands. This result suggests that the steric effect of 6-methyl-substitution plays important role for distortion of the structure, and 6-methyl-substitution can also influence to make polymeric compounds with interactions between Cu(II) ions and neighbor carbonyl oxygen atoms. In addition, the voltammetric behaviors of the Cu complexes were examined and classified into two groups, with/without 6-methyl group. The complexes without 6-methyl group show reversible redox waves at similar to-1.6 V, and the complexes with 6-methyl group do irreversible redox ones at similar to-1.3 V, indicating that the presence of the methyl group of 6-position of the complex makes the reduction of the complexes easier. (C) 2007 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.molstruc.2007.10.006
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