A rotational spectroscopy study of microsolvation effects on intramolecular proton transfer in trifluoroacetylacetone-(H 2 O) 1-3

Trifluoroacetylacetone (TFAA) has two enol forms, which can switch to each other proton transfer. While much attention has been paid to their conformational preferences, the influence of microsolvation on regulating the proton position remains unexplored. Herein, we report the rotational spectra of trifluoroacetylacetone-(water) ( = 1-3) investigated by chirped pulse Fourier transform microwave spectroscopy in the 2-8 GHz frequency range. Two conformers were identified for both TFAA-H O and TFAA-(H O) , while only one conformer was characterized for TFAA-(H O) . The results indicate that water binding on the CH side stabilizes the enol form, whereas water binding on the CF side stabilizes the enol form. The enol form predominates over the enol form in these hydrated complexes, which contrasts with the fact that only enol exists in isolated TFAA. Enol becomes preferred only when water inserts itself into the intramolecular hydrogen bond. Instanton theory calculations reveal that the proton transfer reaction is dominated by quantum tunneling at low temperatures, leading to the stable existence of only one enol form in each configuration of the hydrated clusters.