The dynamics of the prototypical insertion reaction N( 2D) + D 2 have been investigated in a combined experimental and theoretical study. Angular and velocity distributions of the ND product have been obtained in crossed molecular beam experiments with mass spectrometric detection at two collision energies (E c = 3.8 and 5.1 kcal mol -1). The center-of-mass product angular and translational energy distributions have been derived; at both E c's, the former is found to be nearly backward-forward symmetric, reflecting an insertion dynamics, and the latter corresponds to a fraction of total available energy released in translation of 32%, indicating that the ND product is highly internally excited. Quasiclassical trajectory (QCT) calculations were performed on an accurate potential-energy surface obtained from large-scale ab initio electronic structure computations, and the results were compared to experiment. Generally good agreement was found between the experimental results and the theoretical predictions; however, small, yet significant, discrepancies point to some inaccuracy of the QCT treatment, calling for a quantum scattering study of the title reaction. © 2001 American Chemical Society.

Dynamics of the N( 2D) + D 2 reaction from crossed-beam and quasiclassical trajectory studies

Alagia;La;
2001

Abstract

The dynamics of the prototypical insertion reaction N( 2D) + D 2 have been investigated in a combined experimental and theoretical study. Angular and velocity distributions of the ND product have been obtained in crossed molecular beam experiments with mass spectrometric detection at two collision energies (E c = 3.8 and 5.1 kcal mol -1). The center-of-mass product angular and translational energy distributions have been derived; at both E c's, the former is found to be nearly backward-forward symmetric, reflecting an insertion dynamics, and the latter corresponds to a fraction of total available energy released in translation of 32%, indicating that the ND product is highly internally excited. Quasiclassical trajectory (QCT) calculations were performed on an accurate potential-energy surface obtained from large-scale ab initio electronic structure computations, and the results were compared to experiment. Generally good agreement was found between the experimental results and the theoretical predictions; however, small, yet significant, discrepancies point to some inaccuracy of the QCT treatment, calling for a quantum scattering study of the title reaction. © 2001 American Chemical Society.
2001
Quasiclassical trajectories (QCT)
Computational methods
Electronic structure
Ground state
Molecular beams
Nitrogen
Potential energy
Quantum theory
Scattering
Molecular dynamics
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/209672
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