Co-function Mechanisms of Chlorine and Alkoxy Radicals in Cerium-Catalyzed C–H Functionalization of Alkane Mediated by Visible Light

Identification of radical intermediates for the catalytic functionalization of alkanes offers a number of unique challenges and has recently raised a controversial issue concerning the subtle role of chlorine versus alkoxy radicals in cerium photocatalysis. This study is an attempt to settle the controversy within the theoretical frameworks of Marcus electron transfer and transition state theory. Co-function mechanisms were proposed together with a scheme of kinetic evaluations to account for ternary dynamic competition among photolysis, back electron transfer, and hydrogen atom transfer (HAT). Cl•-based HAT has been proven to initially control the early dynamics of the photocatalytic transformation on the picosecond to nanosecond time scale, which is subsequently taken over by a postnanosecond event of alkoxy radical-mediated HAT. The theoretical models developed herein provide a uniform understanding of the continuous time dynamics of photogenerated radicals to address some paradoxical arguments in lanthanide photocatalysis.