Beyond the First Coordination Sphere─Manipulating the Excited-State Landscape in Iron(II) Chromophores with Protons.

Abstract

Molecular transition metal chromophores play a central role in light harvesting and energy conversion. Recently, earth-abundant transition-metal-based chromophores have begun to challenge the dominance of platinum group metal complexes in this area. However, the development of new chromophores with optimized photophysical properties is still limited by a lack of synthetic methods, especially with respect to heteroleptic complexes with functional ligands. Here, we demonstrate a facile and efficient method for the combination of strong-field carbenes with the functional 2,2'-bibenzimidazole ligand in a heteroleptic iron(II) chromophore complex. Our approach yields two isomers that differ predominantly in their excited-state lifetimes based on the symmetry of the ligand field. Deprotonation of both isomers leads to a significant red-shift of the metal-to-ligand charge transfer (MLCT) absorption and a shortening of excited-state lifetimes. Femtosecond transient absorption spectroscopy in combination with quantum chemical simulations and resonance Raman spectroscopy reveals the complex relationship between protonation and photophysical properties. Protonation is found to tip the balance between MLCT and metal-centered (MC) excited states in favor of the former. This study showcases the first example of fine-tuning of the excited-state landscape in an iron(II) chromophore through second-sphere manipulations and provides a new perspective to the challenge of excited-state optimizations in 3d transition metal chromophores.