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Ni(3-([4',5'-bis(butylthio)-5-(methylthio)-2,2'-bi-1,3-dithol-4-yl]thio)pentane-2,4-dione(1-))2(pyridine)2 | 870813-96-0

中文名称
——
中文别名
——
英文名称
Ni(3-([4',5'-bis(butylthio)-5-(methylthio)-2,2'-bi-1,3-dithol-4-yl]thio)pentane-2,4-dione(1-))2(pyridine)2
英文别名
——
Ni(3-([4',5'-bis(butylthio)-5-(methylthio)-2,2'-bi-1,3-dithol-4-yl]thio)pentane-2,4-dione(1-))2(pyridine)2化学式
CAS
870813-96-0
化学式
C50H64N2NiO4S16
mdl
——
分子量
1328.82
InChiKey
DFBLRBCFZBJEFD-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:
    吡啶nickel(II) acetate tetrahydrate3-([4',5'-bis(butylthio)-5-(methylthio)-2,2'-bi-1,3-ditol-4-yl]thio)pentane-2,4-dione四氢呋喃甲醇 为溶剂, 以71%的产率得到Ni(3-([4',5'-bis(butylthio)-5-(methylthio)-2,2'-bi-1,3-dithol-4-yl]thio)pentane-2,4-dione(1-))2(pyridine)2
    参考文献:
    名称:
    Electroactive Ligands:  The First Metal Complexes of Tetrathiafulvenyl−Acetylacetonate
    摘要:
    The reaction of tris(alkylthio)tetrathiafulvalene thiolates with 3-chloro-2,4-pentanedione affords tetrathiafulvalene (TTF) moieties substituted by the acetylacetone function (TTFSacacH), precursors of novel redox-active ligands: the acetylacetonate ions (TTFSacac). These TTFSacacHs have been characterized by X-ray diffraction analyses, and similar trends have been observed, such as a TTF core almost planar and the acetylacetone substituent located in a plane almost perpendicular to the plane formed by the TTF core. Their chelating ability has been demonstrated by the formation of the corresponding M(TTFSacac)(2)(pyridine)(2) complexes in the presence of M-II(OAc)(2)center dot H2O (M = Ni2+, Zn2+). These complexes with TTFSacac moieties, Ni(TTFSacac)(2)(pyridine)(2), 6b, and Zn(TTFSacac)(2)(pyridine)(2), 7b, have been characterized by X-ray diffraction analyses, showing in all structures the metal(II) center chelated by two TTFacac units in the equatorial plane and the octahedral coordination geometry around the metal completed by two axial pyridine ligands. Cyclic voltammetry and UV-visible-near infrared spectroscopic measurements have evidenced a sizable interaction between the two electroactive ligands and the stabilization of a mixed-valence state in the one-electron oxidized complexes.
    DOI:
    10.1021/ic051017r
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