Density functional theory (DFT) calculations, using the Becke-Perdew gradient-corrected functional with a triple-plus-polarization basis set, have been used to characterize the [(H2O)(H3N)(3)Mn(mu-O)(2)Mn(NH3)(3)(OH2)(q+) (q = 2-5) complexes. This structure has been proposed as a possible model for the oxygen-releasing site of the photosystern II (PSII) reaction center. We have performed full optimizations to locate stationary points in various spin states for each of the +2 to +5 charge states. Our calculations indicate that 02 release from the vacuum-phase +5 charge state complex is barrier inhibited, in contrast to the results of a recent DFT study. We report several new di-mu-oxo-bridged stationary points with spin multiplicities of S = 1/2, 3/2, and 5/2 and effective metal oxidation states of (MnMnV)-Mn-IV for the +5 charge state. Finally, calculations employing the 'conductorlike screening model' (COSMO), to address the inclusion of solvent effects, indicate that dissociative O-2 release from the +5 charge state model complex is inhibited by a major barrier and is therefore apparently highly disfavored.