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- W1967868049 abstract "The synthesis of the novel tripodal ligand [N(CH2CH2CH2OH)(CH2CH2SH)2] H3-4 is reported. The aliphatic tetradentate ligand is equipped with an unsymmetrical NOS2 donor set. It reacts with Ni(OAc)2·4H2O or Zn(BF4)2·xH2O to give the complexes [Ni(H-4)]2 5 and [Zn(H-4)]4 6, respectively. The molecular structures of 5 and 6 have been determined by X-ray diffraction. In both cases multinuclear, μ-thiolato-bridged complexes, wherein the ligand coordinates with only three (NS2) of the four donor groups, had formed. The dinuclear complex 5 adopts a butterfly geometry and contains nickel(II) ions in a square-planar NS3 coordination environment. Cyclic voltammetry experiments indicate that the nickel centers in 5 are electron-rich but not overly sensitive toward oxidation. Complex 6 is tetranuclear and the four thiolato-bridged metal centers form a ring. It shows a distorted tetrahedral coordination geometry for the zinc(II) ions in an NS3 coordination sphere. In both complexes the hydroxyl functionalized ligand arm of the tripodal ligand remains uncoordinated." @default.
- W1967868049 created "2016-06-24" @default.
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- W1967868049 date "2004-08-25" @default.
- W1967868049 modified "2023-10-17" @default.
- W1967868049 title "An Unsymmetrical Tripodal Ligand with NOS<sub>2</sub>-Donor Set: Coordination Chemistry with Nickel(II) and Zinc(II)" @default.
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- W1967868049 doi "https://doi.org/10.1021/ic0491940" @default.
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