Multisite Proton‐Coupled Electron Transfer Facilitates Oxidative Photocatalysis in a Molecular Zr‐Based Coordination Compound

The development of mediators that harness visible light to drive proton-coupled electron transfer (PCET) offers a promising pathway to achieving challenging redox transformations in a more sustainable manner and with enhanced thermochemical efficiency. However, designing photocatalytic systems based on earth-abundant metals while gaining precise control over their excited-state reactivity remains a significant challenge. Here, deprotonation of the hydroxy ligands in the Zr₃(O)(OH)₃ nodes of a photoactive coordination cage is shown to unlock the photocatalytic oxidation of strong O─H and C─H bonds (70-100 kcal mol⁻1). Mechanistic investigations reveal that this oxidative process proceeds via a multisite PCET pathway involving ground-state, pre-association followed by a static quenching mechanism. This contrasts with the dynamic quenching mechanism governing the reductive PCET previously reported for the same system. Collectively, these findings establish an unprecedented ambipolar PCET mechanism with a new class of photocatalytic mediators based on an earth abundant metal.