The di-CO2+ complex, [Co2+(mu-OH)(oxapyme)Co2+(H2O)](+), contains an unsymmetrical binucleating ligand (oxapyme) which provides five- and six-coordinate metal sites when a hydroxide bridge is introduced. This complex absorbs 1 equiv of O-2 irreversibly in solution, producing an unstable di-Co3+ oxygenated product. The oxygenated product has been studied at low temperatures, where its electronic absorption and H-1 NMR spectra were recorded. It is probable that the oxygenation reaction involves a one-site addition two-metal oxidation reaction to produce an end-on-bonded peroxide ligand at the available coordination site, giving the complex [Co3+(mu-OH)(oxapyme)Co3+(eta(1)-O-2)](+). Addition of 1 equiv of HClO4 to this oxygenation product gives a stable peroxide complex, [Co3+(mu,eta(1):eta(2)-O-2)(oxapyme)Co3+](2+), where one of the oxygen atoms bridges the two metals and is sideways bonded to one of the metals. The formation of this stable complex involves expulsion of the OH- bridge. Addition of NO2- to the sideways-bonded peroxide complex leads to the formation of another stable complex, [Co3+(mu,eta(1):eta(1)-O-2)(oxapyme)Co3+(NO2)](+), where the peroxide forms a classic di-end-on bridge to the two metals. Both of these complexes have been fully characterized. Addition of acid to this second stable dioxygen complex leads to the release of HNO2 and the formation of the mu,eta(1):eta(2) sideways-bonded peroxide complex.