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bis(di(1H-indazol-1-yl)methane)cadmium(II) dinitrate | 1255147-95-5

中文名称
——
中文别名
——
英文名称
bis(di(1H-indazol-1-yl)methane)cadmium(II) dinitrate
英文别名
——
bis(di(1H-indazol-1-yl)methane)cadmium(II) dinitrate化学式
CAS
1255147-95-5
化学式
C30H24CdN10O6
mdl
——
分子量
732.994
InChiKey
FNNVTHQKFIJDIF-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

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:
    cadmium(II) nitrate tetrhydrate二(1H-吲唑-1-基)甲烷乙腈 为溶剂, 以65%的产率得到bis(di(1H-indazol-1-yl)methane)cadmium(II) dinitrate
    参考文献:
    名称:
    Synthesis and Coordination Chemistry of Two N2-Donor Chelating Di(indazolyl)methane Ligands: Structural Characterization and Comparison of Their Metal Chelation Aptitudes
    摘要:
    The N-2-donor bidentate ligands di(1H-indazol-1-yl)methane (L-1) and di(2H-indazol-2-yl)methane (L-2) (L in general) have been synthesized, and their coordination behavior toward Zn-II, Cd-II, and Hg-II salts has been studied. Reaction of L-1 and L-2 with ZnX2 (X = Cl, Br, or I) yields [ZnX2L] species (1-6), that, in the Gold state, show a tetrahedral structure with dihapto ligand coordination via the pyrazolyl arms. The reaction of L-1 and L-2 with Zn(NO3)(2)center dot 6H(2)O is strongly dependent on the reaction conditions and on the ligand employed. Reaction of L-1 with equimolar quantities of Zn(NO3)(2)center dot 6H(2)O yields the neutral six-coordinate species [Zn(NO3)(2)(L-1)], 7. On the other hand the use of L-1 excess gives the 2:1 adduct [Zn(NO3)(2)(L-1)(2)], 8 where both nitrates act as a unidentate coordinating ligand. Analogous stoichiometry is found in the compound obtained from the reaction of L-2 with Zn(NO3)(2)center dot 6H(2)O which gives the ionic [Zn(NO3)(L-2)(2)](NO3), 10. Complete displacement of both nitrates from the zinc coordination sphere is observed when the reaction between L-1 excess and the zinc salt was carried out in hydrothermal conditions. The metal ion type is also determining structure and stoichiometry: the reaction of L-2 with CdCl2 gave the 2:1 adduct [CdCl2(L-2)(2)] 11 where both chlorides complete the coordination sphere of the six-coordinate cadmium center; on the other hand from the reaction of L-1 with CdBr2 the polynuclear [CdBr2(L-1)](n) 12 is obtained, the Br- anion acting as bridging ligands in a six-coordinate cadmium coordination environment. The reaction of L-1 and L-2 with HgX2 (X = Cl, I, SCN) is also dependent on the reaction condition's and the nature of X, two different types of adducts being formed [HgX(L)](14: L = L-1, 16, 17: L = L-1 or L-2, X=I, 19: L=L-2, X = SCN) and [HgX(L)(2)] (15:L = L-2, X = Cl, 18: L = L-1, X = SCN). The X-ray diffraction analyses of compounds 1, 2, 4, 5, 7, 8, 10-12, 14, 15,; and 19 are also reported. The variations of the coordination geometry parameters in the complexes are compared and discussed.
    DOI:
    10.1021/ic101577k
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