Abstract
Theoretical investigations are made for elastic scattering and vibrational excitation via a vibrationally excited transient ionic state, following the reaction e+AB→AB−**(υ′)→AB(υ)+e. Restrictions on the electronic wave number k and on the resonant partial wave angular momentum l are such that k<<1 and l≥1. A threshold law is proposed: a resonance width between the vibrational υ and υ′ states, Γυυ′, is proportional to k2l+1 multiplied by a square of the Franck-Condon factor Fυυ′. This is an extention of the usual Wigner rule, Γυυ′∝k2l+1.
The results of semi-empirical calculations are presented for O2 and NO. By using only one calibration parameter, satisfactory results are obtained. Resonance widths of the transient υ′ states and energy integrated vibrational excitation cross sections are calculated. For the life time of O2−**(υ′=4), 7.2×10−11sec is obtained. This value is consistent with all available experimental data.