Soluble Fluoridobromates as Well-Behaved Strong Fluorination Reagents

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Abstract

We present a facile synthesis of the soluble fluoridobromates [NEt3Me][BrF4] and [NEt3Me][Br2F7] via fluorination of the corresponding bromide salts in acetonitrile, propionitrile or bromine. We structurally characterized the [BrF2]– anion, an intermediate during the synthesis, for the first time. Additionally, the dissolution of noble metals to form the corresponding halometallates as well as the application of [NEt3Me][BrF4] as a fluorination agent for disulfides to form pentafluorosulfanyls was studied.

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Schmid, J. R., Pröhm, P., Voßnacker, P., Thiele, G., Ellwanger, M., Steinhauer, S., & Riedel, S. (2020). Soluble Fluoridobromates as Well-Behaved Strong Fluorination Reagents. European Journal of Inorganic Chemistry, 2020(47), 4497–4500. https://doi.org/10.1002/ejic.202000847

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