We compare different vibrational analysis methods and examine the effect of hindered internal rotation treatments on predicting thermodynamic properties.

We study the chemical kinetics of hydrogen addition reactions of unsaturated methyl esters, methyl 2-butenoate and methyl 3-butenoate, and compare the rate constants with those of hydrogen abstraction reactions by H atom.

In this study, to determine an efficient and accurate method for predicting standard enthalpy of formation (Δf H o) of oxygenated species, we calculated Δf H o for several typical C2–C4 oxygenated species using atomization and isodesmic reactions in combination with various quantum chemical methods, including six density functional theory methods, three compound methods, and CCSD­(T)/CBS. Compared with experimental values, at the same quantum chemical level, Δf H o values predicted by using isodesmic reactions are more accurate than those using atomization reactions. Comparing various quantum chemical methods when isodesmic reactions are used, the performance of G4 is the best with a mean unsigned deviation (MUE) of 0.3 kcal/mol and a standard deviation (SD) of 0.3 kcal/mol, while M06-2X can predict Δf H o efficiently and accurately with an MUE of 0.6 kcal/mol and SD of 0.5 kcal/mol. Using the best methods we have found, we calculated the enthalpies of formation and other thermodynamic properties for dimethyl carbonate (DMC) and its associated species and then applied them in a DMC combustion model for predicting ignition delay times. Better agreement with the experiments is achieved when the newly computed thermodynamic properties are adopted.

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