Synthesis and Characterization of Ruthenium bis-Bipyridine Mono- and Disulfinato Complexes
journal contributionposted on 02.03.2009, 00:00 by Rowshan Ara Begum, Abdiaziz A. Farah, Howard N. Hunter, A. B. P. Lever
Reaction of cis-Ru(bpy)2Cl2 with 1,2-benzenedithiol afforded a monosulfhydryl-monosulfinate complex, [Ru(bpy)2(S·SO2)] (1). Complex 1 readily undergoes oxidation when treated with 30% H2O2 and also upon exposure to atmospheric O2 (rapidly in bright light) to afford the disulfinate complex, [Ru(bpy)2(SO2.SO2)] (2). Complexes 1 and 2 were studied using various analytical techniques including elemental analysis, UV−vis, mass spectroscopy, NMR, IR spectroscopy, cyclic voltammetry, X-ray crystallography (for 2). Density functional theory computation was employed with extended charge decomposition and natural population analyses. The agreement between the observed electronic spectrum and that predicted by time dependent DFT, and between the observed infrared spectrum and that predicted by DFT, is truly exceptional. These molecules are relevant to the very unusual active site in the metalloenzyme nitrile hydratase.
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Rupopulation analysesDensitycrystallographycyclic voltammetryRutheniumtechniquedisulfinateSynthesiDisulfinato ComplexesReactionoxidationMonomoleculespectrumO 2benzenedithiol2OexposureDFTNMRCharacterizationUVanalysistheory computationmetalloenzyme nitrile hydrataseIR spectroscopycharge decompositionsite