10 págs; 14 figs.; 2 tabs.State-to-state cross-sections for the S + H(v,j) → SH(v′,j′) + H endothermic reaction are obtained using quantum wave packet (WP) and quasi-classical (QCT) methods for different initial ro-vibrational H(v,j) over a wide range of translation energies. The final state distribution as a function of the initial quantum number is obtained and discussed. Additionally, the effect of the internal excitation of H on the reactivity is carefully studied. It appears that energy transfer among modes is very inefficient that vibrational energy is the most favorable for the reaction, and rotational excitation significantly enhances the reactivity when vibrational energy is sufficient to reach the product. Special attention is also paid to an unusual discrepancy between classical and quantum dynamics for low rotational levels while agreement improves with rotational excitation of H. An interesting resonant behaviour found in WP calculations is also discussed and associated with the existence of roaming classical trajectories that enhance the reactivity of the title reaction. Finally, a comparison with the experimental results of Stowe et al. for S + HD and S + D reactions exhibits a reasonably good agreement with those results.O. R. and N. B. acknowledge CSIC for the travelling grant
I-LINK0775. Financial support from the Scientific and Technological
Research Council of TURKEY (TUBITAK) (Project No. TBAG-
112T827) and the Ministerio de Economía e Innovación (Spain),
for grants CSD2009-00038 and FIS2014-52172-C2, is gratefully
acknowledged. The computations have been performed on the
High Performance and Grid Computing Center (TR-Grid) at
ULAKBIM/TURKEY and CESGA computer center. We also thank
the support from the European Research Council under the
European Union’s Seventh Framework Programme (FP/2007-
2013)/ERC Grant Agreement no. 610256 (NANOCOSMOS). We
also acknowledge the COST action CM1401 ‘Our Astrochemical
History’.Peer Reviewe
