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(2,2'-bipyridine)(O2NO)Cu(μ-N3)2Cu(ONO2)(2,2'-bipyridine) | 212001-04-2

中文名称
——
中文别名
——
英文名称
(2,2'-bipyridine)(O2NO)Cu(μ-N3)2Cu(ONO2)(2,2'-bipyridine)
英文别名
——
(2,2'-bipyridine)(O2NO)Cu(μ-N3)2Cu(ONO2)(2,2'-bipyridine)化学式
CAS
212001-04-2
化学式
C20H16Cu2N12O6
mdl
——
分子量
647.516
InChiKey
XBDMPCRZOPBEAF-UHFFFAOYSA-N
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

反应信息

  • 作为产物:
    描述:
    Cu(2,2′-bipyridine)(NO3)2 、 sodium azide 以 甲醇 为溶剂, 以74%的产率得到(2,2'-bipyridine)(O2NO)Cu(μ-N3)2Cu(ONO2)(2,2'-bipyridine)
    参考文献:
    名称:
    The chemistry of dinitrato-2, 2′-bipyridinecopper(II): preparation and characterization of binuclear complexes having a Cu(μ-OH)2Cu and Cu(μ-N3)2Cu core
    摘要:
    The mononuclear Cu(II) complex (bipy)Cu(O2NO)(ONO2) (1) has been obtained by the reaction of bipyridine (bipy) with Cu(NO2)(2).3H2O in methanol solution. 1 reacts with anionic ligands OH- and N-3(-) in methanolic solution to form the stable binuclear complexes (bipy)(O3N)Cu(mu-OH)(2)Cu(NO3) (bipy) (2) and (bipy)(O3N)Cu(mu-N-3)(2)Cu(NO3)(bipy) (3). Complexes 1-3 were characterized including X-ray crystallographic analyses. 1: triclinic P-l with a = 7.9659(4), b = 7.9963(4), c = 10.7860(6) Angstrom, alpha = 81.5070(10), beta = 86.6530( 10), gamma = 63.2120( 10)degrees, V = 606.56(5) Angstrom(3), Z = 2, R = 0.040; 2: triclinic P-1 with a = 7.6167(3), b = 8.4889(3), c=9.8989(3) Angstrom, alpha = 110.583(12), beta = 108.866(15), gamma = 97.802(11)degrees, V = 544.05(3) Angstrom(3), Z = 1, R = 0.042;3: monoclinic with a = 6.8101 (3), b = 17.5101(8), c = 10.5084(5) Angstrom, beta = 98.2940( 10)degrees, V = 1239.97( 10) Angstrom(3), Z = 4, R = 0.029. 1 has a monodentate and a semi-bidentate nitrate ligand and is structurally related to (bipy)Cu(NO2)(2) rather than to its silver analog, (bipy)Ag(NO3)(2), which forms a polymeric chain. Complexes 2 and 3 are dimeric in nature and possess bridging OH- and N-3(-) ligands, respectively. (C) 1998 Elsevier Science S.A. All rights reserved.
    DOI:
    10.1016/s0020-1693(98)00007-3
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