Share Email Print

Proceedings Paper

Molecular rotation based on the minimization of the ro-vibrational Hamilton function
Author(s): Sergei V. Petrov
Format Member Price Non-Member Price
PDF $14.40 $18.00
cover GOOD NEWS! Your organization subscribes to the SPIE Digital Library. You may be able to download this paper for free. Check Access

Paper Abstract

Our method of attack of the molecular rotation in the case when the ro-vib interaction can not be considered as a small one involves three steps. Firstly, so called effective classical energy of the molecular rotation is defined as the minimum of the exact classical ro-vib Hamilton function (it is suggested that the dependence of Hamilton function on the angular momentum components is the parametric one). The second step consists in the qualitative analysis of the classical rotational energy function using well known conception of the rotational energy surface (RES). The non- local bifurcation in rotational dynamics of isotopically substituted P4 molecule is considered as an example. The third step consists in the construction of an effective quantum rotational Hamiltonian from the classical rotational energy function. As an example, the rotational levels of KCN molecule in the ground vibrational state are calculated.

Paper Details

Date Published: 3 March 1997
PDF: 6 pages
Proc. SPIE 3090, 12th Symposium and School on High-Resolution Molecular Spectroscopy, (3 March 1997); doi: 10.1117/12.267810
Show Author Affiliations
Sergei V. Petrov, Moscow State Univ. (Russia)

Published in SPIE Proceedings Vol. 3090:
12th Symposium and School on High-Resolution Molecular Spectroscopy
Leonid N. Sinitsa; Yurii N. Ponomarev; Valery I. Perevalov, Editor(s)

© SPIE. Terms of Use
Back to Top