Homolytic X‐H Bond Cleavage at a Gold(III) Hydroxide: Insights into One‐Electron Events at Gold

C(sp3)‐H and O−H bond breaking steps in the oxidation of 1,4‐cyclohexadiene and phenol by a Au(III)‐OH complex were studied computationally. The analysis reveals that for both types of bonds the initial X−H cleavage step proceeds via concerted proton coupled electron transfer (cPCET), reflecting electron transfer from the substrate directly to the Au(III) centre and proton transfer to the Au‐bound oxygen. This mechanistic picture is distinct from the analogous formal Cu(III)‐OH complexes studied by the Tolman group (J. Am. Chem. Soc. 2019, 141, 17236–17244), which proceed via hydrogen atom transfer (HAT) for C−H bonds and cPCET for O−H bonds. Hence, care should be taken when transferring concepts between Cu−OH and Au−OH species. Furthermore, the ability of Au−OH complexes to perform cPCET suggests further possibilities for one‐electron chemistry at the Au centre, for which only limited examples exist. The mechanism of homolytic X‐H bond cleavage by a Au(III)‐OH complex was investigated computationally. Both C−H and O−H bonds are cleaved via a concerted proton coupled electron transfer mechanism (cPCET) rather than a hydrogen atom transfer mechanism (HAT). The results suggest that one‐electron events at gold may be more accessible than anticipated.