Genetic Algorithm Driven Force Field Parameterization for Molten Alkali-Metal Carbonate and Hydroxide Salts.

Molten alkali-metal carbonates and hydroxides play important roles in the molten carbonate fuel cell and in Earth's geochemistry. Molecular simulations allow us to study these systems at extreme conditions without the need for difficult experimentation. Using a genetic algorithm to fit molecular dynamics-computed densities and radial distribution functions, as well as experimental enthalpies of formation, we derive new classical force fields able to accurately predict liquid chemical potentials.

Partial oxidation of alkanes by dioxiranes formed at low temperature.

Partial oxidation catalysts capable of efficiently operating at low temperatures may limit the over-oxidation of alkane substrates and thereby improve selectivity. This work focuses on examining alkane oxidation using completely metal-free organocatalysts, dioxiranes. The dioxiranes employed here are synthesized by oxidation of a ketone using a terminal oxidant, such as hydrogen peroxide.

Thermal decomposition of ethylene oxide: potential energy surface, master equation analysis, and detailed kinetic modeling.

The unimolecular decomposition of ethylene oxide (oxirane) and the oxiranyl radial is examined by molecular orbital calculations, Rice-Ramsperger-Kassel-Marcus (RRKM)/Master Equation analysis, and detailed kinetic modeling of ethylene oxide pyrolysis in a single-pulse shock tube. It was found that the largest energy barrier to the decomposition of ethylene oxide lies in its initial isomerization to form acetaldehyde, and in agreement with previous studies, the isomerization was found to proceed through the *CH2CH2O* biradical. Because of the biradical nature of the transition states and intermediate, the energy barriers for the initial C-O rupture in ethylene oxide and the subsequent 1,2-H shift remain highly uncertain.

Explorations of conical intersections and their ramifications for chemistry through the Jahn-Teller effect.

Much recent progress has been made theoretically and computationally towards understanding the importance of conical intersections for chemical reactions. Nonetheless, experimental characterization of conical intersections has proven extremely difficult with one striking exception: the Jahn-Teller conical intersection. This article overviews the fundamental similarity of a variety of conical intersections and demonstrates how the spectroscopy of Jahn-Teller active molecules can be used to characterize them.