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Reinterpreting the Fate of Iridium(III) Photocatalysts-Screening a Combinatorial Library to Explore Light-Driven Side-Reactions

journal contribution
posted on 2022-09-29, 10:17 authored by Joseph BawdenJoseph Bawden, Paul FrancisPaul Francis, S DiLuzio, David HayneDavid Hayne, Egan DoevenEgan Doeven, J Truong, Richard AlexanderRichard Alexander, Luke HendersonLuke Henderson, D E Gómez, Massimiliano Massi, B I Armstrong, F A Draper, S Bernhard, Tim ConnellTim Connell
Photoredox catalysts are primarily selected based on ground and excited state properties, but their activity is also intrinsically tied to the nature of their reduced (or oxidized) intermediates. Catalyst reactivity often necessitates an inherent instability, thus these intermediates represent a mechanistic turning point that affords either product formation or side-reactions. In this work, we explore the scope of a previously demonstrated sidereaction that partially saturates one pyridine ring of the ancillary ligand in heteroleptic iridium(III) complexes. Using highthroughput synthesis and screening under photochemical conditions, we identified different chemical pathways, ultimately governed by ligand composition. The ancillary ligand was the key factor that determined photochemical stability. Following photoinitiated electron transfer from a sacrificial tertiary amine, the reduced intermediate of complexes containing 1,10-phenanthroline derivatives exhibited long-term stability. In contrast, complexes containing 2,2′-bipyridines were highly susceptible to hydrogen atom transfer and ancillary ligand modification. Detailed characterization of selected complexes before and after transformation showed differing effects on the ground and excited state reduction potentials dependent on the nature of the cyclometalating ligands and excited states. The implications of catalyst stability and reactivity in chemical synthesis was demonstrated in a model photoredox reaction.



Journal of the American Chemical Society






11189 - 11202