Potential energy profiles for unimolecular reactions of organic ions: [C3H8N]+ and [C3H7O]+

Abstract

The unimolecular decompositions of two isomers of [C₃H₈N]⁺, \documentclass{article}\pagestyle{empty}$ {\rm CH}_{\rm 3} {\rm CH}_{\rm 2} {\rm CH} = \mathop {\rm N}\limits^ + {\rm H}_2 $ and \documentclass{article}\pagestyle{empty}$ {\rm CH}_{\rm 3} {\rm CH}_{\rm 2} \mathop {\rm N}\limits^ + {\rm H = CH}_{\rm 2} $ , are discussed in terms of the potential energy profile over which reaction may be considered to occur. The energy needed to promote slow (metastable) dissociations of either ion is found to be less than that required to cause isomerization to the other structure. This finding is supported by the observation of different decomposition pathways, different metastable peak shapes for C₂H₄ loss, the results of ²H labelling studies, and energy measurements on the two ions. The corresponding potential energy profile for decomposition of the oxygen analogues, \documentclass{article}\pagestyle{empty}${\rm CH}_{\rm 3} {\rm CH}_{\rm 2} {\rm CH =\!= }\mathop {\rm O}\limits^ + {\rm H} $ and \documentclass{article}\pagestyle{empty}$ {\rm CH}_{\rm 3} {\rm CH}_{\rm 2} \mathop {\rm O}\limits^ + {\rm = CH}_{\rm 2} $ , is compared and contrasted with that proposed for the [C₃H₈N]⁺ isomers. This analysis indicates that for the oxygen analogues, the energy needed to decompose either ion is very similar to that required to cause isomerization to the other structure. Consequently, dissociation of either ion is finely balanced with rearrangement to the other and similar reactions are observed. Detailed mechanisms are proposed for loss of H₂O and C₂H₄ from each ion and it is shown that these mechanisms are consistent with ²H and ¹³C labelling studies, the kinetic energy release associated with each decomposition channel, the relative competition between H₂O and C₂H₄ loss and energy measurements.