A ruthenium catalyst linked to a redox-active ruthenium polypyridine for water oxidation

Chromophore-catalyst assemblies are interesting benchmark molecules for photocatalysis. We have prepared two examples of these assemblies and characterized their behaviour as catalysts for the water oxidation reaction. In the bimetallic complexes [Ru(tpy)(4,4 '-X2-bpy)(mu-CN)Ru(bda)(DMSO)](PF6) (X = -H (1), -OCH3 (2), tpy = 2,2 ':6 ',2 ''-terpyridine, bpy = 2,2 '-bipyridine, H2bda = 2,2 '-bipyridine-6,6 '-dicarboxylic acid and DMSO = (CH3)2SO), a Ru(ii)-polypiridine chromophore {Ru(tpy)(4,4 '-X2-bpy)} is linked by a cyanide bridge to a {Ru(bda)} water oxidation catalyst. Both complexes catalyze water oxidation both chemically, using Ce(iv) as the terminal oxidant, and electrochemically. Electrochemical and spectroelectrochemical studies, aided with (TD)DFT calculations, allowed us to study the different species involved in the catalytic cycle. For the RuIIRuIII, an intense MMCT (metal-to-metal charge transfer) band suggests a geometrical reorganization during the oxidation process. The wave associated with oxidation to the RuIIIRuIV species shows an increased current that suggests that it may be a catalyst for the water oxidation reaction. Further oxidation results in the RuIIIRuV redox state which is an active catalyst for the water oxidation reaction as demonstrated by the evolution of oxygen. Two Ru polypyridine-catalyst-assemblies show activity in the water oxidation reaction both in their RuIII-RuIV and RuIII-RuV redox states.