Abstract
A facile one-pot gram-scale synthesis of tetraalkylammonium tetrafluoridochlorate(III) [cat][ClF4] ([cat]=[NEt3Me]+, [NEt4]+) is described. An acetonitrile solution of the corresponding alkylammonium chloride salt is fluorinated with diluted fluorine at low temperatures. The reaction proceeds via the [ClF2]− anion which is structurally characterized for the first time. The potential application of [ClF4]− salts as fluorinating agents is evaluated by the reaction with diphenyl disulfide, Ph2S2, to pentafluorosulfanyl benzene, PhSF5. The CN moieties in acetonitrile and [B(CN)4]− are transferred in CF3 groups. Exposure of carbon monoxide, CO, leads to the formation of carbonyl fluoride, COF2, and elemental gold is dissolved under the formation of tetrafluoridoaurate [AuF4]−.
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Pröhm, P., Schmid, J. R., Sonnenberg, K., Voßnacker, P., Steinhauer, S., Schattenberg, C. J., … Riedel, S. (2020). Improved Access to Organo-Soluble Di- and Tetrafluoridochlorate(I)/(III) Salts. Angewandte Chemie - International Edition, 59(37), 16002–16006. https://doi.org/10.1002/anie.202006268
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