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cis-[Cl2Pt(II)(Cu(II)[N,N'-bis(2-aminoethyl)-2-(2-(4-pyridyl)ethyl)malondiamido(2-)])2] | 166403-90-3

中文名称
——
中文别名
——
英文名称
cis-[Cl2Pt(II)(Cu(II)[N,N'-bis(2-aminoethyl)-2-(2-(4-pyridyl)ethyl)malondiamido(2-)])2]
英文别名
——
cis-[Cl2Pt(II)(Cu(II)[N,N'-bis(2-aminoethyl)-2-(2-(4-pyridyl)ethyl)malondiamido(2-)])2]化学式
CAS
166403-90-3
化学式
C28H42Cl2Cu2N10O4Pt
mdl
——
分子量
975.784
InChiKey
DGLALGVRIFYYGO-UHFFFAOYSA-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

反应信息

  • 作为产物:
    参考文献:
    名称:
    {CuII[N,N'-bis(2-aminoethyl)-2-(2-(4-pyridyl)ethyl)malondiamido(2-)]}: A Convenient Building Block for the Construction of Supramolecular Coordination Compounds Containing Exchangeable Peripheral CuII Cations
    摘要:
    The ethylpyridino functionalized N,N'-bis(2-aminoethyl)-2-(2-(4-pyridil)ethyl)malondiamide ligand 1b has been prepared, its protonation and complexation properties (toward Cu-II) have been studied in aqueous solution, and the pertinent constants have been determined. The ligand is able to coordinate one Cu-II ion with the diamino-diamido binding unit, after the release of the two amido protons, thus forming complex 2, which still presents a free, outward-pointing pyridine unit, capable of coordinating a second metal center. Two 2 units have been appended, through their pyridine nitrogen atom, to the kinetically inert cis-Cl2PtII < fragment. The obtained supramolecular species 3 is able to release the peripheral Cu-II ions when the pH of the solution becomes acidic and to re-form the original complex when basicity is restored (the pertinent complexation constants have been determined). This system thus represents the first example of a supramolecular coordination compound which contains exchangeable peripheral transition metal cations. The crystal and molecular structure of 2 has been determined, disclosing the formation of ''head to tail'' dimers in the solid state, with an unusual coordination geometry of the Cu-II ions. Single-crystal X-ray diffraction data were collected with the use of Mo K alpha radiation: trigonal, space group P (3) over bar with a = b = 20.558(6) Angstrom, c = 7.562(3) Angstrom, V = 2768(2) Angstrom(3), and Z = 6 (R = 0.054, R(w) = 0.058). Finally, electrochemical studies revealed that both in the separate component and in the assembled system the Cu-II centers are reversibly oxidizable to Cu-III. In the supramolecular coordination compound, the two Cu-II centers weakly influence each other by means of electrostatic interactions.
    DOI:
    10.1021/ic00122a007
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