Theoretical characterization of gas-phase thermolysis products of ethane-1,2-diol, 2-chloroethanol and 2-fluoroethanol

• Published in: Molecular physics Vol. 111; no. 5; pp. 643 - 659
• Main Authors: Osman, Osman I., Elroby, Shabaan A. K., Hilal, Rifaat H., Aziz, Saadullah G.
• Format: Journal Article
• Language: English
• Published: Abingdon Taylor & Francis Group 01.03.2013; Taylor & Francis Ltd
• Subjects: activation energy; B3LYP; hyperconjugation; MP2; NBO analysis; thermal decomposition; vinyl alcohol
• ISSN: 0026-8976; 1362-3028
• DOI: 10.1080/00268976.2012.739716

The transition structures and the activation energies for the possible thermal elimination of H 2 O, HF and HCl from ethane-1,2-diol, 2-fluoroethanol and 2-chloroethanol respectively, were investigated. The relative stabilities and associated barrier heights of syn and anti vinyl alcohol isomers and their acetaldehyde tautomer were estimated. HF, DFT/B3LYP and MP2 methods at 3-21G, 6-31+G(d), 6-311++G(d,p) and aug-cc-pvdz basis sets were applied to identify the stationary points of the studied systems. The optimized geometries and electronic energies of reactants, transition states and products were analyzed. The dependence of these properties upon the theoretical level was discussed. A concerted proton release and a hydroxide or halide ion expulsion mechanism was proposed to account for the thermal rearrangement of reactants to products. A thorough understanding of syn vinyl alcohol preference is provided by performing natural bond orbital (NBO) analysis. The oxygen atom lone pair (LP) and periplanar hyperconjugative effects are responsible for this preference. It was suggested that the LP hyperconjugative interactions with the C=C σ and π antibonds were the most important origin of the structural differences between the two vinyl alcohol isomers.