The thermally unstable, primary perfluoroalcohols, CF3 OH, C2 F5 OH, and nC3 F7 OH, were conveniently prepared from the corresponding carbonyl compounds in anhydrous HF solution. Experimental values for the reaction enthalpies and entropies were derived from the temperature dependence of the Rf COF+HF⇄Rf CF2 OH (Rf =F, CF3 , CF3 CF2 ) equilibria by NMR spectroscopy. Electronic structure calculations of the gas-phase and solution reaction energies, gas-phase acidities and heats of formation were carried out at the G3MP2 level, showing that these compounds are strong acids. Protonation of these alcohols in HF/SbF5 produced the perfluoroalkyl oxonium salts Rf CF2 OH2 + SbF6 - .
Keywords: NMR spectroscopy; acidity; electronic structure calculations; fluorine; α-perfluoroalcohols.
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