Molecular Inorganic Chemistry, Stratingh Institute for Chemistry, Faculty of Science and Engineering, University of Groningen, Nijenborgh 4, 9747 AG, Groningen (The, Netherlands.
Zernike Institute for Advanced Materials, Faculty of Science and Engineering, University of Groningen, Nijenborgh 4, 9747 AG, Groningen (The, Netherlands.
Chemistry. 2022 Jul 15;28(40):e202200599. doi: 10.1002/chem.202200599. Epub 2022 May 31.
C(sp )-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.
通过 Au(III)-OH 配合物对 1,4-环己二烯和苯酚的氧化作用,研究了 C(sp3)-H 和 O-H 键的断裂步骤。分析表明,对于这两种类型的键,初始 X-H 断裂步骤都通过协同质子耦合电子转移(cPCET)进行,这反映了电子从底物直接转移到 Au(III)中心和质子转移到 Au 结合的氧。这种机理图与 Tolman 小组研究的类似的形式 Cu(III)-OH 配合物不同(J. Am. Chem. Soc. 2019, 141, 17236-17244),后者对于 C-H 键通过氢原子转移(HAT)进行,对于 O-H 键通过 cPCET 进行。因此,在将 Cu-OH 和 Au-OH 物种之间的概念转移时应谨慎。此外,Au-OH 配合物进行 cPCET 的能力表明,Au 中心的单电子化学具有进一步的可能性,而这种可能性是有限的。