Abstract

Auricyanide [Au(CN) 4] − interaction with biologically important thiols, thioether and selenoether were carried out and monitored using 1H, 13C NMR and UV spectroscopy. These ligands include l-cysteine, glutathione, captopril, l-methionine and dl-seleno-methionine. Thiols show very strong affinity to be oxidized into the disulfide by auricyanide, which gets reduced to aurocyanide [Au(CN) 2] −. l-cysteine reaction mechanism with [Au(CN) 4] − was found to be dependent on reactants mole ratio. While l-methionine was completely inert toward auricyanide, dl-Se-methionine showed some reactivity with [Au(CN) 4] − after raising solution pH to 12 that facilitated cyanide exchange.

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