Ab initio electronic structure methods are used to estimate the cross sections for electron transfer from donor anions having electron binding energies ranging from 0.001 to 0.6 eV to each of three sites in a model disulfide-linked molecular cation. The three sites are (1) the S-S sigma* orbital to which electron attachment is rendered exothermic by Coulomb stabilization from the nearby positive site, (2) the ground Rydberg orbital of the -NH3+ site, and (3) excited Rydberg orbitals of the same -NH3+ site. It is found that attachment to the ground Rydberg orbital has a somewhat higher cross section than attachment to either the sigma* orbital or the excited Rydberg orbital. However, it is through attachment either to the sigma* orbital or to certain excited Rydberg orbitals that cleavage of the S-S bond is most likely to occur. Attachment to the sigma* orbital causes prompt cleavage because the sigma* energy surface is repulsive (except at very long range). Attachment to the ground or excited Rydberg state causes the S-S bond to rupture only once a through-bond electron transfer from the Rydberg orbital to the S-S sigma* orbital takes place. For the ground Rydberg state, this transfer requires surmounting an similar to 0.4 eV barrier that renders the S-S bond cleavage rate slow. However, for the excited Rydberg state, the intramolecular electron transfer has a much smaller barrier and is prompt.