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[Cu4(μ4-O)(μ-H2bpmp)2(μ1,3-O2CCH2Ph)4] | 1428987-74-9

中文名称
——
中文别名
——
英文名称
[Cu4(μ4-O)(μ-H2bpmp)2(μ1,3-O2CCH2Ph)4]
英文别名
[Cu44-O)(μ-2,6-bis[(3-hydroxypropylimino)methyl]-4-methylphenol)21,3-phenylacetate)4];[Cu44-O)(μ-H2bpmp)21,3-O2CCH2Ph)4]
[Cu4(μ4-O)(μ-H2bpmp)2(μ1,3-O2CCH2Ph)4]化学式
CAS
1428987-74-9
化学式
C62H70Cu4N4O15
mdl
——
分子量
1365.44
InChiKey
INDFIYDHUQNQTP-UVGXFSDVSA-H
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) phenylacetate monohydrate 、 2,6-bis-[(3-hydroxy-propylimino)-methyl]-4-methyl-phenol三乙胺 作用下, 以 甲醇 为溶剂, 反应 2.0h, 以78%的产率得到[Cu4(μ4-O)(μ-H2bpmp)2(μ1,3-O2CCH2Ph)4]
    参考文献:
    名称:
    New μ-hydroxido-bridged copper nitrate dimer and μ4-oxido-bridged copper phenylacetate quasi-tetrahedron: Direct synthesis and uphill conversion
    摘要:
    Dinuclear [Cu-2(mu-OH)] fragment and its self-assembled tetranuclear part [Cu-2(mu(4)-O)Cu-2] are found in two copper(II) complexes of ligand H3bpmp: [Cu-2(mu(2)-OH)(mu-H(2)bpmp)(mu(1.3)-NO3)][Cu-2(mu(2)-OH)(mu-H(2)bpmp)(NO3)(H2O)](NO3)2 center dot 2H(2)O (1 center dot 2H(2)O) and [Cu-4(mu(2)-OH)(mu-H(2)bpmp)(2)(mu(1.3)-O2CCH2Ph)(4)] (2) [H(3)bpmp = 2,6-bis-[(3-hydroxy-propylimino)-methyl]-4-methylphenoll. These complexes have been synthesized and characterized by single crystal X-ray crystallography. Complex 1 showed unique reactivity with phenylacetate anions to provide 2 in which two [Cu-2(mu(2)-OH)] units available within same crystal lattice collapsed to give [Cu-4(mu(4)-O)] hub. Formation of the [Cu-4] compound is also achieved from individual components and phenylacetate ligands, which allows an effective tuning of the self-assembly of two ligand bound [Cu-2] fragments and removal of H+ from hydroxido bridges to provide oxido nucleus. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2012.08.064
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