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Improved Access to Organo‐Soluble Di‐ and Tetrafluoridochlorate(I)/(III) Salts

18

Citations

37

References

2020

Year

Abstract

A facile one-pot gram-scale synthesis of tetraalkylammonium tetrafluoridochlorate(III) [cat][ClF<sub>4</sub> ] ([cat]=[NEt<sub>3</sub> Me]<sup>+</sup> , [NEt<sub>4</sub> ]<sup>+</sup> ) is described. An acetonitrile solution of the corresponding alkylammonium chloride salt is fluorinated with diluted fluorine at low temperatures. The reaction proceeds via the [ClF<sub>2</sub> ]<sup>-</sup> anion which is structurally characterized for the first time. The potential application of [ClF<sub>4</sub> ]<sup>-</sup> salts as fluorinating agents is evaluated by the reaction with diphenyl disulfide, Ph<sub>2</sub> S<sub>2</sub> , to pentafluorosulfanyl benzene, PhSF<sub>5</sub> . The CN moieties in acetonitrile and [B(CN)<sub>4</sub> ]<sup>-</sup> are transferred in CF<sub>3</sub> groups. Exposure of carbon monoxide, CO, leads to the formation of carbonyl fluoride, COF<sub>2</sub> , and elemental gold is dissolved under the formation of tetrafluoridoaurate [AuF<sub>4</sub> ]<sup>-</sup> .

References

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