Response to “Comment on ‘Ab initio dynamic dipole polarizabilities for O2, its photoabsorption spectrum in the Schumann–Runge region, and long-range interaction coefficients for its dimer’ ” [J. Chem. Phys. 111, 11236 (1999)]

Abstract

The oscillator strengths of the discrete part of the Schumann–Runge band system is recalculated from single-state calculations using the adiabatic potential curve. Potential curves for three Πu3 states are computed. The integrated oscillator strength for the Πu3←Σu3 transition is recalculated from four-state coupled diabatic calculations.