The electronic structures of the radical cations of two dithienylperfluorocyclopentene molecules with appended tertiary amine units were investigated by electrochemical and optical spectroscopic methods. The through-bond N-N distances in the photocyclized (closed) forms of the two systems are 9.3 and 17.6 angstrom, respectively, depending on whether the nitrogen atoms are attached directly to the two thienyl units or whether xylyl spacers are in between. In the case of the radical cation with the longer N-N distance, photocyclization of the dithienylperfluorocyclopentene core induces a changeover from class I to class II mixed valence behavior. In the case of the shorter system, the experimental data is consistent with assignment of the photocyclized form to a class III mixed valence species.