Bimodal internal energy distribution as a consequence of Cul‐de‐sac isomerization reactions

Abstract

AbstractA simple model is developed to examine the internal energy distribution for metastable ions and the probability of reaction in the field‐free regions of sector mass spectrometers in systems where the reactant ions in the ion source react by dissociation in competition with reversible isomerization to non‐dissociating species. The internal energy distribution for the reacting ions is strongly dependent on whether dissociation is preceded by isomerization and back‐isomerization, and it is shown that a range of reasonable combinations of rate constants for the forward and reverse isomerization result in a bimodal distribution of the internal energy for the ions that dissociate in the field‐free regions. The isomerization effectively provides a kinetic reservoir of higher energy reactant ions. The reaction probability of the metastable ions varies strongly with internal energy, and the back‐isomerized ions may in some instances be responsible for most of the reactions observed. A bimodal energy distribution will give rise to composite metastable peaks even though neither non‐statistical behavior nor multiple reaction channels are involved.