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Extremely Bent Cyanide Coordination at a Preorganized Dinickel Site and Assembly of a Starlike Nonanuclear Complex from the Constrained Dinickel Building Blocks
Author(s) -
Franc Meyer,
Rainer F. Winter,
Elisabeth Kaifer
Publication year - 2001
Publication title -
inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.348
H-Index - 233
eISSN - 1520-510X
pISSN - 0020-1669
DOI - 10.1021/ic010249x
Subject(s) - chemistry , cyanide , ligand (biochemistry) , bimetallic strip , coordination sphere , nickel , crystallography , bent molecular geometry , metal , moiety , metal ions in aqueous solution , ion , stereochemistry , photochemistry , crystal structure , inorganic chemistry , organic chemistry , biochemistry , receptor
An extremely bent cyanide coordination at a dinickel scaffold is reported. Preorganization of two nickel ions is achieved by means of a compartmental dinucleating pyrazolate ligand L(-), setting up a bimetallic coordination pocket with constrained metal-metal separation. The mixed-spin dinickel(II) complex [LNi2(CN)(MeCN)](ClO4)2 (1) has been characterized by X-ray diffraction. The MeCN bound to the high-spin nickel(II) ion can be removed or replaced by other ligands, e.g., by the cyanide ligand of a tetracyanonickelate(II) moiety to give the starlike nonanuclear complex ([LNi2(CN)]4[Ni(CN)4])(ClO4)6 (2) that contains four of the constrained pyrazolate-based dinickel(II) fragments grouped around a central tetracyanonickelate(II) unit, as revealed by X-ray crystallography. Spectral and electrochemical properties of 1 and 2 are reported, and the formation of reduced mixed-valent Ni(I)Ni(II) species is investigated by IR and UV/vis spectroelectrochemistry.

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