Kinetics for the Reactions of HO(HO) with Isoprene (2-Methyl-1,3-butadiene) as a Function of Temperature (300-500 K).

We report kinetics studies of HO(HO) with isoprene (2-methyl-1,3-butadiene, CH) as a function of temperature (300-500 K) measured using a flowing afterglow-selected ion flow tube. Results are supported by density functional (DFT) calculations at the B3LYP/def2-TZVP level. HO ( = 0) reacts with isoprene near the collision limit exclusively via proton transfer to form CH. The first hydrate ( = 1) also reacts at the collision limit and only the proton transfer product is observed, although hydrated protonated isoprene may have been produced and dissociated thermally. Addition of a second water ( = 2) lowers the rate constant by about a factor of 10. The proton transfer of HO(HO) to isoprene is endothermic, but transfer of the water ligands lowers the thermicity and the likely process occurring is HO(HO) + CH → CH(HO) + HO, followed by thermal dissociation of CH(HO). Statistical modeling indicates the amount of reactivity is consistent with the process being slightly endothermic, as is indicated by the DFT calculations. This reactivity was obscured in past experiments due to the presence of water in the reaction zone. The third hydrate is observed not to react and helps explain the past results for = 2, as = 2 and 3 were in equilibrium in that flow tube experiment. Very little dependence on temperature was found for the three species that did react. Finally, the CH proton transfer product further reacted with isoprene to produce mainly CH along with a small amount of clustering.