Photocatalyzed CO(2) reduction to CO by supramolecular photocatalysts made of Ru(II) photosensitizers and Re(I) catalytic subunits containing preformed CO(2)TEOA adducts

Two new supramolecular photocatalysts containing Ru(II) polypyridine units as light-harvesting photosensitizers and Re(I) polypyridine subunits as catalytic centers have been prepared. The new species, RuRe2A and Ru2ReA, contain catalytic Re(I) subunits coordinated by the preformed CO(2)TEOA adduct (known to be the effective catalytic subunits; TEOA is triethanolamine) and exhibit quite efficient and selective photoreduction of CO(2) to CO, with outstanding TONs of 2368 and 2695 and a selectivity of 99.9% and 98.9%, respectively. Such photocatalytic properties are significantly improved with respect to those of previously studied RuRe2 and Ru2Re parent compounds, containing chloride ligands instead of the CO(2)TEOA adduct. Comparison between photocatalytic performance of the new species and their parent compounds allows to investigate the effect of the CO(2)TEOA insertion process as well as the eventual effect of the presence of chloride ions in solution on the photocatalytic processes. The improved photocatalytic properties of RuRe2A and Ru2ReA compared with their parent species are attributed to a combined effect of different distribution of the one-electron reduced form of the supramolecular photocatalysts on the Ru-subunit(s) (leading to decreased CO formation due to a poisoning ligand loss process) and on the Re-subunit(s) and to the presence of chloride ions in solution for RuRe2 and Ru2Re, which could interfere with the CO(2)TEOA adduct formation, a needed requisite for CO forming catalysis. These results strongly indicate the utility of preparing supramolecular photocatalysts containing preformed adducts.