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[Co(1,4-bis(4-oxy-1,2-benzenedicarboxylic acid)benzene(-2H))(1,10-phenanthroline)2(H2O)] | 1477517-85-3

中文名称
——
中文别名
——
英文名称
[Co(1,4-bis(4-oxy-1,2-benzenedicarboxylic acid)benzene(-2H))(1,10-phenanthroline)2(H2O)]
英文别名
[Co(1,4-bis(4-oxy-1,2-benzenedicarboxylic acid)benzene(-2H))(phen)2(H2O)]
[Co(1,4-bis(4-oxy-1,2-benzenedicarboxylic acid)benzene(-2H))(1,10-phenanthroline)<sub>2</sub>(H<sub>2</sub>O)]化学式
CAS
1477517-85-3
化学式
C46H30CoN4O11
mdl
——
分子量
873.758
InChiKey
UPYVIINWGSSOTP-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:
    1,10-菲罗啉cobalt(II) nitrate hexahydrate1,4-bis(4-oxy-1,2-benzenedicarboxylic acid)benzene 为溶剂, 反应 92.0h, 以57%的产率得到[Co(1,4-bis(4-oxy-1,2-benzenedicarboxylic acid)benzene(-2H))(1,10-phenanthroline)2(H2O)]
    参考文献:
    名称:
    Syntheses, crystal structures and properties of five divalent transition metal coordination compounds based on a semirigid tetracarboxylic acid ligand
    摘要:
    Five divalent transition metal coordination compounds based on a semirigid tetracarboxylic acid have been synthesized by the hydrothermal method, namely, [MnL(0.5)phen](n) (1), [CdL(0.5)phen](n) (2), [Co(H2L)(phen).2H(2)O] n (3), {[Ni2L(phen) 2(H2O) 6].2H(2)O} n (4) {[Zn2L(phen) 4(H2O) 2].2H(2)O}(n) (5) (H4L = 1,4-bis(4-oxy-1,2-benzene dicarboxylic acid) benzene, phen = 1,10-phenanthroline). These compounds were structurally characterized by infrared spectra, thermogravimetric analyses and single crystal X-ray diffractions. The isostructural 1 and 2 exhibit the two-dimensional layered structures. Compound 3 and 4-5 reveal a mononuclear and two dinuclear structures, respectively. In addition, the magnetic property of 1 and the photoluminescence of 2 and 5 were also investigated, respectively. (C) 2013 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.ica.2013.08.022
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