Abstract
Rotational distributions of the product H2 formed in resonant scattering of H + H2 are presented based on an extension of the reduced dimensionality theory of reactive scattering. The reduced dimensionality theory is based on an adiabatic treatment of the three-atom bending motion in the strong interaction region. The final rotational distributions are obtained by making a simple Franck–Condon projection of the bending states onto the final rotational states of the product H2. We focus in particular on the rotational distributions which may result from bend-excited resonances which have been recently identified in this system.
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