Abstract
Detailed photophysical investigation of a Mn(IV)-carbene complex has revealed that excitation into its lowest-energy absorption band (∼500 nm) results in the formation of an energetic ligand-to-metal charge-transfer (LMCT) state with a lifetime of 15 ns. To the best of our knowledge, this is the longest lifetime reported for charge-transfer states of first-row-based transition metal complexes in solution, barring those based on Cu, with a d10 configuration. A so-called superoxidant, Mn(IV)-carbene exhibits an excited state potential typically only harnessed via excited states of reactive organic radical species. Furthermore, the long-lived excited state in this case is found to be a dark doublet, with its transition to the quartet ground state being spin-forbidden, a contrast to most first-row literature examples, and a possible cause of the long lifetime. Showcasing excited state properties which in some cases exceed those of complexes based on precious metals, these findings not only advance the library of earth-abundant photosensitizers but also shed general insight into the photophysics of d3 and related Mn complexes.