Litcius/Paper detail

Thiosulfonylation of Unactivated Alkenes with Visible-Light Organic Photocatalysis

Karthik Gadde, Pieter Mampuys, Andrea Guidetti, H. Y. Vincent Ching, Wouter Herrebout, Sabine Van Doorslaer, Kourosch Abbaspour Tehrani, Bert U. W. Maes

2020ACS Catalysis114 citationsDOIOpen Access PDF

Abstract

A metal-free method for the vicinal thiosulfonylation of unactivated alkenes with thiosulfonates using 9-mesityl-10-methylacridinium perchlorate as the photo-organocatalyst with visible-light irradiation has been developed. The method can be performed in dimethyl carbonate under air at room temperature and features a broad functional group compatibility. Metrics indicate the green potential of the developed versus the state-of-the-art methodologies. Mechanistic studies revealed no single electron transfer but involvement of an energy transfer from the excited photo-organocatalyst to thiosulfonate reactant, subsequently providing a sulfenyl and a sulfonyl radical via homolytic cleavage.

Topics & Concepts

ChemistryPhotocatalysisPhotochemistrySulfonylVicinalVisible spectrumPhotoredox catalysisCatalysisHomolysisElectron transferExcited stateCombinatorial chemistryOrganic chemistryAlkylRadicalOptoelectronicsNuclear physicsPhysicsSulfur-Based Synthesis TechniquesRadical Photochemical ReactionsCatalytic C–H Functionalization Methods