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Über grünes Bis-(2-Iminoisopropyl-thiophenolato)-nickel(II) und weitere, ähnliche NiII-Komplexe
Authors:A. Mü  ller,K. U. Johannes,W. Plass,H. B  gge,E. Krahn,K. Schneider
Affiliation:A. Müller,K. U. Johannes,W. Plass,H. Bögge,E. Krahn,K. Schneider
Abstract:Green Bis-(2-iminoisopropyl-thiophenolato)nickel(II) and other Similar NiII Complexes The compounds [NiII(iitp)2] 1 (iitp = 2-iminoisopropyl-thiophenolate), [Niurn:x-wiley:00442313:media:ZAAC19966221022:tex2gif-stack-3(imptp)2] · 2 CH3OH 2 , a dinuclear compound with an Ni? Ni distance of 276 pm, and [PPh4] · [NiII(imptp)(SCN)] 3 (imptp = 2-(2-iminopentane-4-on)-thiophenolate) have been prepared by the reaction of nickel(II)-acetate-tetrahydrate with 2-iminoisopropyl-thiophenole and 2-(2-iminopentane-4-on)-thiophenole in methanol, respectively. They have been characterized by single-crystal X-ray structure analysis and other physical methods. The redox behaviour of 1–3 has been studied in detail (chemically as well as by cyclovoltammetry and ESR spectroscopy). Particularly interesting are the electronic properties of 1 and its reduction with NaBH4 and the following reaction of the product with O2. The complexes are model compounds for some Ni-containing enzymes. For details of the crystal structure determination see “Inhaltsübersicht”.
Keywords:Nickel  Schiff base complexes  synthesis  crystal structure  hydrogenase
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