Theoretical investigation of the gas-phase reactions of CFClC(O)OCH with the hydroxyl radical and the chlorine atom at 298 K.

A Theoretical study on the mechanism of the reactions of CFClC(O)OCH with the OH radical and Cl atom is presented. Geometry optimization and frequency calculations have been performed at the MPWB1K/6-31+G(d,p) level of theory and energetic information is further refined by calculating the energy of the species using G2(MP2) theory. Transition states are searched on the potential energy surface involved during the reaction channels and each of the transition states are characterized by presence of only one imaginary frequency. The existence of transition states on the corresponding potential energy surface is ascertained by performing intrinsic reaction coordinate (IRC) calculation. Theoretically calculated rate constants at 298 K and atmospheric pressure using the canonical transition state theory (CTST) are found to be in good agreement with the experimentally measured ones. Using group-balanced isodesmic reactions as working chemical reactions, the standard enthalpies of formation for CFClC(O)OCH CFClC(O)OCH and CFC(O)OCH are also reported for the first time. [ABSTRACT FROM AUTHOR]