Spectroscopic properties and bending potential energy surfaces of 2B1, 2A1, 2A2, 2A2(2Πg), 4A2(4Πg),
and 2B2 electronic states of SbCl2 and SbBr2, and three low-lying electronic states of SbCl2
+ and
SbBr2
+, (1A1, 3B1, 1B1), have been studied with complete active space self-consistent field (CASSCF) followed
by multireference singles and doubles configuration interaction (MRSDCI) methods that included nearly 2
million configurations. The bond dissociation and adiabatic ionization energies of SbCl2, SbBr2, SbCl, and
SbBr have been computed. The computed properties of these species are extensively compared with other
group V dihalides.