Mechanophotocatalysis: A Generalizable Approach to Solvent-minimized Photocatalytic Reactions for Organic Synthesis

This proof-of-concept study cements the viability and generality of mechanophotocatalysis, merging mechanochemistry and photocatalysis to enable solvent-minimized photocatalytic reactions. We demonstrate the transmutation of four archetypal solution-state photocatalysis reactions to a solvent-minimized environment driven by the combined actions of milling, light, and photocatalysts. The chlorosulfonylation of alkenes and the pinacol coupling of aldehydes and ketones were conducted under solvent-free conditions with competitive or superior efficiencies to their solution-state analogues. Furthermore, decarboxylative alkylations are shown to function efficiently under solvent-minimized conditions, while the photoinduced energy transfer promoted [2+2] cycloaddition of chalcone experiences a significant initial rate enhancement over its solution-state variant. This work serves as a platform for future discoveries in an underexplored field: validating that solvent-minimized photocatalysis is not only generalizable and competitive with solution-state photocatalysis, but can also offer valuable advantages. Via the synergistic union with mechanochemistry, four archetypal photocatalysis reactions have been realized under solvent-free or solvent-minimized conditions. The mechanophotocatalytic versions feature competitive or superior efficiencies to the solution-state reactions, while also showcasing an enhanced tolerance to aerobic conditions. image