The activation of SF , a potent greenhouse gas, under metal-free and visible light conditions is reported. Herein, mechanistic investigations including EPR spectroscopy, NMR studies and cyclic voltammetry allowed the rational design of a new fluorinating reagent which was synthesized from the 2-electron activation of SF with commercially available TDAE. This new SF -based reagent was efficiently employed for the deoxyfluorination of CO and the fluorinative desulfurization of CS allowing the formation of useful fluorinated amines.
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