Exceptional Excited-State Lifetime of an Iron(II)-N-Heterocyclic Carbene Complex Explained.
2014
Earth-abundant transition-metal complexes are desirable for sensitizers in dye-sensitized solar cells or photocatalysts. Iron is an obvious choice, but the energy level structure of its typical polypyridyl complexes, featuring low-lying metal-centered states, has made such complexes useless as energy converters. Recently, we synthesized a novel iron–N-heterocyclic carbene complex exhibiting a remarkable 100-fold increase of the lifetime compared to previously known iron(II) complexes. Here, we rationalize the measured excited-state dynamics with DFT and TD-DFT calculations. The calculations show that the exceptionally long excited-state lifetime (∼9 ps) is achieved for this Fe complex through a significant destabilization of both triplet and quintet metal-centered scavenger states compared to other FeII complexes. In addition, a shallow 3MLCT potential energy surface with a low-energy transition path from the 3MLCT to 3MC and facile crossing from the 3MC state to the ground state are identified as key fea...
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