Periodic Trends in Intra-ionic Excited State Quenching by Halide

• Published in: Inorganic chemistry 2024-08, Vol.63 (34), p.15772-15783
• Main Authors: Goodwin, Matthew J., Deetz, Alexander M., Griffin, Paul J., Meyer, Gerald J.
• Format: Article
• Language: English
• ISSN: 0020-1669; 1520-510X; 1520-510X
• DOI: 10.1021/acs.inorgchem.4c01726

The preassociation of reactants in a photoinitiated redox reaction through the use of noncovalent interactions can have a significant impact on excited state reactivity. As these noncovalent interactions render some stabilization to the associated species, they impact the kinetics and thermodynamics of photoinitiated electron transfer. Reported herein is a novel iridium­(III) photocatalyst, equipped with an anion-sensitive, amide-substituted bipyridine ligand, and its reactivity with the halides (X = I–, Br–, Cl–) in acetonitrile and dichloromethane. A noteworthy periodic trend was observed, where the size and electron affinity dramatically altered the observed photoredox behavior. The binding affinity for the halides increased with decreasing ionic radius (K eq ∼103 to >106) in a polar medium but association was stoichiometric for each halide in a nonpolar medium. Evidence for the static quenching of iodide and bromide is presented while dynamic quenching was observed with all halides. These results highlight how the photophysics of halide adducts and the thermodynamics of intra-ionic photo-oxidation are impacted as a consequence of preassociation of a quencher through hydrogen bonding.