Ab initio kinetics for decomposition/isomerization reactions of C ₂H₅O radicals

The ground-state potential energy surface of the C₂H ₅O system, including the decomposition and isomerization of the ethoxy (CH₃CH₂O), 1-hydroxyethyl (CH₃CHOH), and 2-hydroxyethyl (CH₂CH₂OH) radicals, is computed by the modified Gaussian-2 (G2M) and CCSD(T)/6-311 +G(3df,2p) methods by using the geometries optimized at the B3LYP/6-311 + G(3df,2p) level of theory. These detailed reaction pathways are used to calculate the rate constants for the unimolecular isomerization and decomposition reactions of the three radicals by the microcanonical transition-state theory and Rice-Ramsperger-Kassel-Marcus (RRKM) theory in the temperature range of 200-3000 K at varying pressures of He and other diluents. The predicted rate constants are in reasonable agreement with the available experimental data, in addition, the predicted heats of formation of the three isomeric radicals are compared with available experimental and theoretical values.