Controlling the Photophysical Properties of a Series of Isostructural d 6 Complexes Based on Cr 0 , Mn I , and Fe II .

Development of first-row transition metal complexes with similar luminescence and photoredox properties as widely used Ru II polypyridines is attractive because metals from the first transition series are comparatively abundant and inexpensive. The weaker ligand field experienced by the valence d-electrons of first-row transition metals challenges the installation of the same types of metal-to-ligand charge transfer (MLCT) excited states as in precious metal complexes, due to rapid population of energetically lower-lying metal-centered (MC) states. In a family of isostructural tris(diisocyanide) complexes of the 3d 6 metals Cr 0 , Mn I , and Fe II , the increasing effective nuclear charge and ligand field strength allow us to control the energetic order between the 3 MLCT and 3 MC states, whereas pyrene decoration of the isocyanide ligand framework provides control over intraligand (IL Pyr ) states. The chromium(0) complex shows red 3 MLCT phosphorescence because all other excited states are higher in energy. In the manganese(I) complex, a microsecond-lived dark 3 IL Pyr state, reminiscent of the types of electronic states encountered in many polyaromatic hydrocarbon compounds, is the lowest and becomes photoactive. In the iron(II) complex, the lowest MLCT state has shifted to so much higher energy that 1 IL Pyr fluorescence occurs, in parallel to other excited-state deactivation pathways. Our combined synthetic-spectroscopic-theoretical study provides unprecedented insights into how effective nuclear charge, ligand field strength, and ligand π-conjugation affect the energetic order between MLCT and ligand-based excited states, and under what circumstances these individual states become luminescent and exploitable in photochemistry. Such insights are the key to further developments of luminescent and photoredox-active first-row transition metal complexes.