We report the preparation and characterization of two meso-alkyl substituted porphyrin pi-cation radical derivatives, [Fe(TalkylP(center dot))(Cl)]SbCl6 (alkyl = ethyl or propyl). Both complexes have been characterized by UV/vis/near-IR, IR, and Mossbauer spectroscopy, temperature-dependent solid-state magnetic susceptibility measurements, and X-ray structure determinations. All data for both oxidized species are consistent with the formulation of the complexes as ring-oxidized iron(III) porphyrin species. The molecular structures of the two five-coordinate species have the typical square-pyramidal coordination group of high-spin iron(III) derivatives. The crystal structures also reveal that the species form cofacial pi-pi dimers with lateral shifts of 1.44 angstrom and 3.22 angstrom, respectively, for the propyl and ethyl radical derivatives. Both radicals exhibit porphyrin cores with alternating bond distance patterns in the inner 16-membered ring. In addition, [Fe(TEtP center dot)(Cl)]SbCl6 and [Fe(TPrP center dot)(Cl)]SbCl6 have been characterized by temperature-dependent (6-300 K) magnetic susceptibility studies, the best fitting of the temperature-dependent moments reveal strong coupling between iron spins and porphyrin radical, and a smaller magnitude of antiferromagnetic coupling between ring radicals, which are opposite to those found in the five-coordinate iron(III) OEP radicals. The differences in structure and properties of the cation radical meso-alkyl and beta-alkyl derivatives possibly reflect differences in properties of a(1u)- and a(2u)-forming radicals.