Molecular organization of reactants in the kinetics and catalysis of liquid phase reactions: XII. Mechanism of the boron trifluoride-catalyzed Curtius thermal rearrangement of benzoyl azide into phenyl isocyanate

Abstract

The kinetics of the thermal decomposition and rearrangement of benzoyl azide into phenyl isocyanate was studied in n-heptane in the presence of boron trifluoride etherate as the catalyst. The apparent activation energy of the noncatalytic reaction is 28.0 kcal/mol, and that of the catalytic reaction is 11.0 kcal/mol. The electronic structure and geometry of various complexes between benzoyl azide and BF3 were studied using the PBE/TZ2P density functional method, and fragments of the potential energy surface were calculated for the catalytic rearrangement. Comparatively stable 1: 1 and 1: 2 complexes between the syn conformer of benzoyl azide and the catalyst can form in the system by coordination to the oxygen and nitrogen atoms of the acyl azide group. The heats of formation of these complexes are between −1.7 and −6.4 kcal/mol. The main consequence of the formation of these complexes is that the acyl azide group comes out of the benzene ring plane and thus becomes more reactive. The effective activation energies calculated for the catalytic rearrangement involving complexes of different compositions are 12–15 kcal/mol lower the effective activation energy of the noncatalytic reaction. Information has been obtained about the structure of the transition state of the catalytic reaction, in which a nitrogen molecule is abstracted from benzoyl azide with a synchronous rearrangement of other atoms, resulting in the formation of the ultimate product.