Abstract
ABSTRACTTwo nickel complexes with metallodithiolate ligands, which can be regarded as the active site models of the acetyl coenzyme A synthase, were prepared and structurally characterized by X-ray crystallography. Reactions of Ni(PPh3)2Cl2 with Ni(bme-dach) [bme-dach = N,N'-bis(mercaptoethyl)-1,4-diazacycloheptane] or Ni(bme-dach*) [bme-dach* = N,N'-bis(mercaptoethyl)-1,4-diazacyclohexane] in MeCN in the presence of NH4PF6 resulted in the formation of a trinuclear nickel complex {Ni[Ni(bme-dach)]2}[PF6-]2 (1) and a hexanuclear nickel complex {Ni2[Ni(bme-dach*)]4}[PF6−]4 (2). The crystal structure of 1·2MeCN shows a square planar geometry of nickel atom that is coordinated by four sulfur atoms of the metallodithiolate ligands Ni(bme-dach). The crystal structure of 2·4MeCN reveals that each of the two nickel atoms is ligated by four sulfur atoms of the metallodithiolate ligands Ni(bme-dach*) to form a square planar coordination sphere.
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