Dissociative electron transfer to haloacetonitriles. An example of the dependency of in-cage ion-radical interactions upon the leaving group.

Abstract

The reductive cleavage of the haloacetonitriles (Cl, Br, I) in DMF provides additional examples of the formation of a fragment cluster upon dissociative electron transfer, which is able to survive in this polar solvent thanks to the electron-withdrawing character of the cyano group. The remarkable sensitivity of the activation energy to small changes of the interaction energies allows, with help of the "sticky" dissociative electron-transfer model, the precise determination of interaction energies down to a few millielectronvolts from the cyclic voltammetric data. The interaction energy rapidly decreases from Cl to Br and to I, correlated with the increase of the halide radius. These observations add to the previously gathered evidence to confirm the existence of such interactions and to highlight their electrostatic character. This is further corroborated by the quantum chemical computation of the potential energy profiles, which exhibit a long-distance energy minimum. This revisiting of the notion of sigma-ion radicals and of their status in a polar medium makes them appear as an electrostatic radical-ion pair rather than covalently bound molecules. Their stability is a function of the Lewis acid-base properties of both the radical and the leaving ion and is strongly influenced by the nature of the solvent.