Collisions between I 2+ and CO have been investigated using time-of flight mass spectrometry at a range of centre-of-mass collision energies between 0.5 eV and 3.0 eV. Following I 2+ + CO collisions we detect I + + CO + from a single-electron transfer reaction and IO + + C + from bond-forming reactivity. Reaction-window calculations, based on Landau-Zener theory, have been used to rationalise the electron transfer reactivity and computational chemistry has been used to explore the [I-CO] 2+ potential energy surface to account for the observation of IO +. In addition, collisions between I 2+ and CS2 have been investigated over a range of centre-of-mass collision energies between 0.8 eV and 6.0 eV. Both single and double electron transfer reactions are observed in the I 2+ /CS2 collision system, an observation again rationalized by reaction-window theory. The monocations IS + and IC + are also detected following collisions of I 2+ with CS2, and these ions are clearly products from a bond-forming reaction. We present a simple model based on the structure of the [I-CS2] 2+ collision complex to rationalize the significantly larger yield of IS + than IC + in this bond-forming process.