A combined experimental-theoretical study of the vibrational predissociation and product rotational distributions for high vibrational levels of He79Br2

• Published in: The Journal of chemical physics 1999-01, Vol.110 (1), p.256-266
• Main Authors: Rohrbacher, Andreas, Ruchti, Thomas, Janda, Kenneth C., Buchachenko, Alexei A., Hernández, Marta I., González-Lezana, Tomás, Villarreal, Pablo, Delgado-Barrio, G.
• Format: Article
• Language: English
• ISSN: 0021-9606; 1089-7690
• DOI: 10.1063/1.478101

Pump-probe spectra of HeBr2 in vibrational states v′=10 and 39 through 48 of the B electronic state are reported and the fragment rotational distributions from vibrational predissociation of the cluster are extracted from the measured E(0g+)←B(3Π0u+) spectra of Br2. The experimental results are compared to theoretical calculations on the B←X spectra using atom-atom model potentials and performing a thermal average over transitions that contribute to the net excitation. Very good agreement between experiment and theory is obtained, except in the region of v′=44, where the Δv=−1 channel closes, and in the region of v′=48 where the Δv=−2 channel closes. For v′=43, and v′=44, the agreement is less satisfactory because the dynamics are extremely sensitive to details of the potential energy surface due to threshold effects associated with the Δv=−1 channel closing. Similar sensitivity to the potential due to the Δv=−2 channel closing impairs the agreement between experiment and theory for v′=48. Below v′=43, the rotational distributions for Δv=−1 and Δv=−2 are quite similar. Above v′=43 the peaks of the rotational distributions for Δv=−2 move to higher values of j. These results are compatible with the theoretical conclusion that dissociation shifts from a direct mechanism to one involving intramolecular vibrational distribution in the region of the closing of the Δv=−1 channel. Although the simple additive potential model used in this work succeeds in reproducing most of the experimental data for this system, further improvements in the potential energy surface will be required to achieve precise agreement between experiment and theory for large Br-Br separations.