Abstract
All the excited adiabatic electronic states of Na2 dissociating into 3d+4s, 4p+3s, and 5s+3s atoms are calculated using a nonempirical pseudopotential, a flexible basis set, and the exact valence configuration-interaction treatment. Together with a highly precise work [G. H. Jeung, J. Phys. B 16, 4289 (1983)], where all the electronic states dissociating into 3s+3s, 3p+3s, and 4s+3s atoms have been calculated, this work reveals the lowest 38 electronic states of Na2. Wherever possible, the comparison of the present data with the recent spectroscopic observations shows excellent agreement. The majority of the theoretically predicted states remains to be found experimentally.