Gas Phase Elimination Kinetics of Methyl Mandelate: Experimental and DFT Studies

• Published in: The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory Molecules, spectroscopy, kinetics, environment, & general theory, 2009-11, Vol.113 (44), p.12157-12162
• Main Authors: Rotinov, Alexandra, Escalante, Luz, Ramirez, Beatriz, Pereira, Desiree, Córdova, Tania, Chuchani, Gabriel
• Format: Article
• Language: English
• Subjects: A: Kinetics, Spectroscopy
• ISSN: 1089-5639; 1520-5215
• DOI: 10.1021/jp9046424

The gas phase elimination kinetics of racemic methyl mandelate was determined in a static system, and yielded on decomposition benzaldehyde, methanol, and carbon monoxide. The reaction was homogeneous, unimolecular, and follows a first-order law in the temperature range 379.5−440 °C and pressure range of 21.5−71.1 Torr. The variation of the rate coefficient with temperature is expressed by the following Arrhenius equation: log k 1 = (12.70 ± 0.14) − (206.5 ± 1.9) kJ/mol (2.303RT)−1. The theoretical estimations of the kinetics and thermodynamics parameters were carried out using DFT methods B3LYP, B3PW91, MPW1PW91, and PBEPBE. Calculation results are in reasonably good agreement with the experimental energy and enthalpy values when using the PBEPBE DFT functional. However, regarding the entropy of activation, the MPW1PW91 functional is more adequate to describe the reaction. These calculations imply a molecular concerted nonsynchronous mechanism involving a two-step process, where the formation of the unstable α-lactone intermediate is the rate-determining factor. The lactone intermediate rapidly decarbonylates to produce benzaldehyde and carbon monoxide. The transition state is late in the reaction coordinate, resembling the lactone configuration.