Iodine-Catalysed Dissolution of Elemental Gold in Ethanol

Abstract

Gold is a scarce element in the Earth's crust but indispensable in modern electronic devices. New, sustainable methods of gold recycling are essential to meet the growing eco-social demand of gold. Here, we describe a simple, inexpensive, and environmentally benign dissolution of gold under mild conditions. Gold dissolves quantitatively in ethanol using 2-mercaptobenzimidazole as a ligand in the presence of a catalytic amount of iodine. Mechanistically, the dissolution of gold begins when I₂ oxidizes Au⁰ and forms a [Au^I I₂ ]^- species, which undergoes subsequent ligand-exchange reactions and forms a stable bis-ligand Au^I complex. H₂ O₂ oxidizes free iodide and regenerated I₂ returns back to the catalytic cycle. Addition of a reductant to the reaction mixture precipitates gold quantitatively and partially regenerates the ligand. We anticipate our work will open a new pathway to more sustainable metal recycling with the utilization of just catalytic amounts of reagents and green solvents.

Keywords: Catalysis; Gold; Iodine; Recycling; Sustainable Chemistry.