Dinuclear PhotoCORMs: Dioxygen-Assisted Carbon Monoxide Uncaging from Long-Wavelength-Absorbing Metal–Metal-Bonded Carbonyl Complexes

High Resolution Image Download MS PowerPoint Slide We describe a new strategy for triggering the photochemical release of caged carbon monoxide (CO) in aerobic media using long-wavelength visible and near-infrared (NIR) light. The dinuclear rhenium–manganese carbonyl complexes (CO) 5 ReMn(CO) 3 (L), where L = phenanthroline ( 1 ), bipyridine ( 2 ), biquinoline ( 3 ), or phenanthrolinecarboxaldehyde ( 4 ), each show a strong metal–metal-bond-to-ligand (σ MM → π L *) charge-transfer absorption band at longer wavelengths. Photolysis with deep-red ( 1 and 2 ) or NIR ( 3 and 4 ) light leads to homolytic cleavage of the Re–Mn bonds to give mononuclear metal radicals. In the absence of trapping agents, these radicals primarily recombine to reform dinuclear complexes. In oxygenated media, however, the radicals react with dioxygen to form species much more labile toward CO release via secondary thermal and/or photochemical reactions. Conjugation of 4, with an amine-terminated poly(ethylene glycol) oligomer, gives a water-soluble derivative with similar photochemistry. In this context, we discuss the potential applications of these dinuclear complexes as visible/NIR-light-photoactivated CO-releasing moieties (photoCORMs).