Simulation of the effect of vibrational pre-excitation on the dynamics of pyrrole photo-dissociation

Photo-dissociation dynamics is simulated for vibrationally pre-excited pyrrole molecules using an ab initio multiple cloning approach. Total kinetic energy release (TKER) spectra and dissociation times are calculated. It is found that pre-excitation of N-H bond vibrations facilitates fast direct dissociation, which results in a significant increase in the high-energy wing of TKER spectra. The results are in very good agreement with the recent vibrationally mediated photo-dissociation experiment, where the TKER spectrum was measured for pyrrole molecules excited by a combination of IR and UV laser pulses. Calculations for other vibrational modes show that this effect is specific for N-H bond vibrations: Pre-excitation of other modes does not result in any significant changes in TKER spectra.

Automated summary

The research shows that pre-excitation of N-H bond vibrations facilitates fast direct dissociation, resulting in a significant increase in the high-energy wing of TKER spectra. The simulations are in good agreement with recent experimental results, indicating the specificity of this effect for N-H bond vibrations.