Molecular structure, conformational mobility, vibrational spectra, and thermochemistry of peroxyacetic acid: an ab initio and density functional study

Abstract

The structure of the peroxyacetic acid (PAA) molecule and its conformational mobility under rotation about the peroxide bond was studied by ab initio and density functional methods. The free rotation is hindered by the trans-barrier of height 22.3 kJ mol–1. The equilibrium molecular structure of AcOOH (Cs symmetry) is a result of intramolecular hydrogen bond. The high energy of hydrogen bonding (∼46 kJ mol–1 according to natural bonding orbital analysis) hampers formation of intermolecular associates of AcOOH in the gas and liquid phases. The standard enthalpies of formation for AcOOH (–353.2 kJ mol–1) and products of radical decomposition of the peroxide — AcO· (–190.2 kJ mol–1) and AcOO· (–153.4 kJ mol–1) — were determined by the G2 and G2(MP2) composite methods. The O—H and O—O bonds in the PAA molecule (bond energies are 417.8 and 202.3 kJ mol–1, respectively) are much stronger than in alkyl hydroperoxide molecules. This provides an explanation for substantial contribution of non-radical channels of the decomposition of peroxyacetic acid. The electron density distribution and gas-phase acidity of PAA were determined. The transition states of the ethylene and cyclohexene epoxidation reactions were located (Ea = 71.7 and 50.9 kJ mol–1 respectively).