Study of Reactive and Non-Reactive Chemical Processes in Condensed Phase

Chemical dynamics in condensed phase environments is dictated by an intricate interplay between reactive and competing non-reactive processes. This dissertation is aimed at the molecular level understanding of both types of processes in liquid solution environments within the framework of nonequilibrium statistical mechanics and using advanced molecular dynamics simulation techniques.;The first part of this thesis is focused on understanding quantum effects on the rates of non-reactive vibrational energy relaxation processes in several experimentally relevant systems. The systems studied include neat liquid HCl and DCl and CN--isotopomers dissolved in H2O and D2O. The vibrational energy relaxation rates constants for those systems were calculated within the framework of the Landau-Teller formula. Accounting for quantum effects was achieved by calculating the vibrational energy relaxation rate constants via the linearized semiclassical method. The rate constants calculated via the linearized semiclassical method for both systems are in excellent agreement with the experimentally measured rate constants. Furthermore, comparison to the corresponding classical results suggest that quantum effects are strongly pathway dependent and that failure to account for them can lead to misinterpretation of the molecular mechanism underlying vibrational energy relaxation in liquid solution.;The second part of this thesis is focused on understanding solvent effects on single-bond cZt-tZt isomerization rate constant of 1,3,5- cis -hexatriene dissolved in a series of explicit alkane (cyclohexane, n -heptane and cycloheptane) and alcohol (methanol, ethanol and n -propanol) solvents. The isomerization rate constants are calculated within the framework of reactive flux theory and transition state theory, at different temperatures (275-325K), via classical molecular dynamics simulations. Our results reproduce the experimentally observed trend of slower isomerization rate constants in alcohol solvents in comparison to alkane solvents. Further analysis also reveals that the experimentally observed solvent dependence may be traced back to the fundamentally different structure of the solvation shell in alcohol and alkane solvents. More specifically, whereas in alcohol solvents, hexatriene fits inside a rigid cavity formed by the hydrogen-bonded network, which is relatively insensitive to conformational dynamics, alkane solvents form a cavity around hexatriene that adjusts to the conformational state of hexatriene, thereby increasing the entropy of transition state configurations relative to reactant configurations and giving rise to faster isomerization.