The nature of frontier orbitals under systematic ligand exchange in pseudo octahedral Fe II complexes

Understanding and controlling properties of transition metal complexes is a crucial step towards tailoring materials for sustainable energy applications. In a systematic approach, we use resonant inelastic X ray scattering to study the influence of ligand substitution on the valence electronic structure around an aqueous iron II center. Exchanging cyanide with 2 20 bipyridine ligands reshapes frontier orbitals in a way that reduces metal 3d charge delocalization onto the ligands. This net decrease of metal ligand covalency results in lower metal centered excited state energies in agreement with previously reported excited state dynamics. Furthermore, traces of solvent effects were found indicating a varying interaction strength of the solvent with ligands of different character. Our results demonstrate how ligand exchange can be exploited to shape frontier orbitals of transition metal complexes in solution phase chemistry; insights upon which future efforts can built when tailoring the functionality of photoactive systems for light harvesting application