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Abstract

4-(pentafluorosulfanyl)benzenediazonium tetrafluoroborate salt was synthesized and isolated. The pentafluorosulfanyl salt was examined in a wide assortment of reactions to form novel SF₅-bearing alkenes, alkynes, and biaryl derivatives using Heck-Matsuda, Sonogashira, and Suzuki coupling protocols. Dediazoniation of the salt furnished the corresponding p-SF₅—C₆H₄X,C₆H₄OS(O)(CF₃)═NSO₂CF₃, and p-SF₅—C₆H₄—NTf₂ derivatives. The azide derivative p-SF₅—C₆H₄N₃ entered into click chemistry with phenylacetylenes to furnish the corresponding triazoles. Various SF₅-bearing alkenes were synthesized by coupling reactions using a metal catalyst. Fluorodediazoniation selectively furnished the fluoro derivative p-SF₅—C₆H₄F. Homolytic dediazoniation gave the unsymmetrical biaryls, thus demonstrating the broad utility of pentafluorosulfanyl diazonium salts as building blocks of SF5-aromatics that are in high demand in many branches of chemistry including biomedicine and materials chemistry.

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First Claim