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Updated: Jun 12, 2026

Spatial Separation of Molecular Conformers and Clusters
Published on: January 9, 2014
Mutual capture of dipolar molecules at low and very low energies. I. Approximate analytical treatment
1Schulich Faculty of Chemistry, Technion - Israel Institute of Technology, Haifa 32000, Israel.
Abstract:
Approximate analytical expressions are derived for the low-energy rate coefficients of capture of two identical dipolar polarizable rigid rotors in their lowest nonresonant (j(1) = 0 and j(2) = 0) and resonant (j(1) = 0,1 and j(2) = 1,0) states. The considered range extends from the quantum, ultralow energy regime, characterized by s-wave capture, to the classical regime described within fly wheel and adiabatic channel approaches, respectively. This is illustrated by the table of contents graphic (available on the Web) that shows the scaled rate coefficients for the mutual capture of rotors in the resonant state versus the reduced wave vector between the Bethe zero-energy (left arrows) and classical high-energy (right arrow) limits for different ratios δ of the dipole-dipole to dispersion interaction.
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