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[dicopper(I)(1,10-phenanthroline)2(4,4'-bisphenyl diphosphonate)] | 1262957-62-9

中文名称
——
中文别名
——
英文名称
[dicopper(I)(1,10-phenanthroline)2(4,4'-bisphenyl diphosphonate)]
英文别名
[Cu2(phen)2(C12H6(PO3H)2)]
[dicopper(I)(1,10-phenanthroline)2(4,4'-bisphenyl diphosphonate)]化学式
CAS
1262957-62-9
化学式
C36H26Cu2N4O6P2
mdl
——
分子量
799.665
InChiKey
RCOKDVIEFPSSEG-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 、 Cu(acac)2 H2O 、 [4-(4-膦酰苯基)苯基]膦酸 在 hydrofluoric acid 、 MoO2 作用下, 以 为溶剂, 以10%的产率得到[dicopper(I)(1,10-phenanthroline)2(4,4'-bisphenyl diphosphonate)]
    参考文献:
    名称:
    Metal-organodiphosphonates: Structural consequences of introducing aromatic tethering groups. The structures of [Cu(phen){HO3P(C12H8)PO3H}], [{Cu(phen)}2{HO3P(C12H8)PO3H}] and [Cu(terpy){HO3P(C12H8)PO3H}] and of the bimetallic materials [{Cu(LL)}2MoO2{HO3P(C12H8)PO3H}3] (LL=2,2-bipyridine, o-phenanthroline)
    摘要:
    Hydrothermal reactions were used to prepare three copper-organodiphosphonate compounds and two copper-molybdate-organodiphosphonate chains. Compound 1, [Cu(phen){HO3P(C12H8)PO3H}] is a binuclear Cu(II) compound, while [{Cu(phen)}(2){HO3P(C12H8)PO3H}] (2) is a Cu(I) species with distorted "T" shaped copper coordination geometry. In contrast, [Cu(terpy){HO3P(C12H8)PO3H}]center dot 1.5H(2)O (3.1.5H(2)O) exhibits a zig-zag chain structure. The isomorphous bimetallic diphosphonates, [{Cu(LL)}(2)MoO2 {HO3P(C12H8)PO3H}(3)]center dot H2O (LL = bpy (4.H2O), phen (5.H2O)) also exhibit chain structures, constructed from {Cu2MoO2} clusters, bridging aromatic diphosphonate ligands, and diphosphonates coordinating to the clusters at one terminus and projecting a second pendant terminus. (C) 2010 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.ica.2010.07.030
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