Abstract
Two novel oxorhenium complexes containing the 2,6-dimercaptomethylpyridine ligand were synthesized and characterized by classical methods of analysis. The [2,6-dimercaptomethylpyridinato][ p-methoxybenzenethiolato]oxorhenium complex 1, was produced by simultaneous action of equimolar quantities of 2,6-dimercaptomethylpyridine and p-methoxybenzenethiol on the precursor [(n-C 4H 9) 4N][ReOCl 4] in EtOH. As revealed by spectroscopic data as well as X-ray structure analysis, complex 1 adopts a distorted square pyramidal geometry around the metal with the SNS/S donors forming the basal plane and the oxygen occupying the apex of the pyramid. When the same tridentate ligand reacts with [(n-C 4H 9) 4N][ReOCl 3(PO)] (PO= o-diphenylphosphinophenolato) as a precursor, complex 2a, [2,6-dimercaptomethylpyridinato][ o-diphenylphosphinophenolato]-oxorhenium, is obtained. The latter is a six-coordinate rhenium species to which the distorted octahedral geometry is assigned, according to the analytical findings. In this case, the SNS/P donors occupy the equatorial plane and the two oxygen atoms the apices of the distorted octahedron positioned trans to each other.
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