Synthesis and characterization of ruthenium(ii) complexes of 5‐hydroxyflavones

Abstract

AbstractBis(dimethyl sulfoxide)bis(flavonato)ruthenium(II) complexes, RuL2(DMSO)2, were synthesized by the reaction of dichlorotetrakis(dimethyl sulfoxide)ruthenium(II) with the sodium salts of 5‐hydroxyflavone, 5‐hydroxy‐4′‐methoxyflavone and 5‐hydroxy‐3′,4′,5′,7‐tetramethoxyflavone, (L). The complexation was followed by 1H nmr spectroscopy. The 1:1 kinetically favoured tris(dimethyl sulfoxide)chloroflavonatoruthenium(II) complexes, RuLCl(DMSO)3, were initially formed and then transformed into the thermodynamically more stable ones. Each one of these complexes, by reacting with another equivalent of lig‐and L, also gave rise to a mixture of 1:2 kinetic species, from which the 1:2 thermodynamically more stable bis(dimethyl sulfoxide)bis(flavonato)ruthenium(II) complexes, RuL2(DMSO)2, were formed. The complexes were characterized by extensive studies involving 1H, 13C nuclear magnetic resonance, infrared and ultraviolet‐visible spectroscopy, mass spectrometry, cyclic voltammetry and elemental analysis. Such 1:2 complexes exhibited properties of two nonequivalent flavonate ligands and also of two non‐equivalent dimethyl sulfoxide ligands; one of these dimethyl sulfoxide ligands is considered to be S‐bonded and the other O‐bonded. Also two quasireversible one‐electron redox steps were observed at 0.53 to 0.57 and 0.44 to 0.41 V (vs Saturated Calomel Electrode). The spectroscopic results obtained allow for the discussion of stereochemistry of each bis(dimethyl sulfoxide)bis(flavonato)ruthenium(II) complex and to postulate its possible structure as one corresponding to the more anisochronous species.