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The thermal decomposition of trifluoroacetic acid and carbonyl fluoride (CF 2 O) has been extensively studied because of their importance in the oxidation of hydrochlorofluorocarbons in the atmosphere. We hitherto present the study of the thermal reaction between these two molecules. The reaction mechanism was studied using Fourier transform infrared spectroscopy in the temperature range of 513-573 K. The reaction proceeds homogeneously in the gas phase through the formation of a reaction intermediate, here characterized as CF 3 C(O)OC(O)F (detected for the first time in this work), the major final products being CF 3 C(O)F, HF, and CO 2 . We demonstrate that the reaction is first-order with respect to each reagent, second-order global and the mechanism consists of two steps, the first being the rate-determining one. The E a = 110.1 ± 6.1 kJ mol -1 and A = (1.2 ± 0.2) × 10 -12 cm 3 molec -1 s -1 values were obtained from the experimental data. The low activation energy is explained by the hydrogen-bond interactions between the -OH group of the acid and the F atom of the CF 2 O. First-principles calculations at the G4MP2 level of theory were carried out to understand the dynamics of the decomposition. Thermodynamic activation values found for this reaction are as follows: Δ H ⧧ = 105.6 ± 6.4 kJ mol -1 , Δ S ⧧ = -88.6 ± 9.7 J mol -1 K -1 , and Δ G ⧧ = 153.7 ± 13.5 kJ mol -1 . The comparison between theory and experimental results showed excellent similarities, thus strengthening the proposed mechanism.

Gas-Phase Reaction between CF2O and CF3C(O)OH: Characterization of CF3C(O)OC(O)F

Gas-Phase Reaction between CF₂O and CF₃C(O)OH: Characterization of CF₃C(O)OC(O)F