Synthesis, structural peculiarities, and photosensitivity of fluorinated dibenzo-1,2,5,6-tetrathiocines
Alexander A. Buravlev,
Alexander Yu. Makarov,
Georgy E. Salnikov
et al.
Abstract:Synthesized fluorinated dibenzo-1,2,5,6-tetrathiocines are structurally flexible in the solid state (XRD), solution (NMR, NOESY), and gas phase (DFT). In solution under sunlight, they isomerize in rare dibenzo-1,2,3,6-tetrathiocines (XRD).
By heating polyfluoroarenethiols with potassium iodate at 150–235°C in ampoules, a number of iodopolyfluoroarenes were obtained as the main products along with dipolyfluoroarylsulfanes.
By heating polyfluoroarenethiols with potassium iodate at 150–235°C in ampoules, a number of iodopolyfluoroarenes were obtained as the main products along with dipolyfluoroarylsulfanes.
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