Time‐dependence of the isotope effects in the unimolecular dissociation of tertiary amine molecular ions

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Abstract
The intramolecular secondary isotope effects on the α‐cleavage of deuterium‐labelled N‐methyldipentylamine radical cations have been studied as a function of ion lifetime by field ionization kinetics. The isotope effects observed are all normal and increase in magnitude with increasing ion lifetime, with the exception of the δ‐labelled compound which shows an inverse effect (predominant loss of the labelled radical) at times shorter than 10−9 s, and a normal effect at longer times. The isotope effects reflect differences in zero‐point energies of the transition states as well as the influence of slight reductions of isotope‐dependent frequencies on the state sums–a statistical weight effect. The latter is particularly important at high ion energies and is the primary reason for the occurrence of the inverse isotope effect. The time dependence of the normal and inverse isotope effect is reproduced by QET/RRKM calculations.

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