Abstract
Potential energy curves for twelve valence states of O2 are calculated with fully linked renormalized Feynman diagrams which dissociate properly. Compared with experiment, average errors of spectroscopic constants are: 18 kJ mol-1 for D e, 2•1 pm for R e, 81 cm-1 for ωe 15 kJ mol-1 for T e, and 16 kJ mol-1 for the sum of asymptotic atomic excitation energies.