The visible-light-mediated synthesis of trifluoromethylthiolated arenes in the presence
of ruthenium-based photocatayst under mild reaction conditions is reported. The trifluoromethylthiolated
arenes are obtained using the shelf-stable reagent trifluoromethyl toluenethiosulfonate
at room temperature. The reaction proceeds selectively and does not require the presence
of any additive. A mechanism is proposed based on the obtained results of EPR as well
as luminescence
Key words
visible light - trifluoromethylthiolation - arenediazonium - radical - reaction mechanism