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First-principle calculation of reduced masses in vibrational analysis using generalized internal coordinates: Some crucial aspects and examples

Journal of Chemical Information and Modeling, ISSN: 1549-960X, Vol: 47, Issue: 3, Page: 840-850
2007
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Article Description

In this paper we present and analyze the most essential aspects of reduced masses along generalized internal coordinates. The definition of reduced masses in the internal coordinate formalism is established through the Wilson G-matrix concept and includes sophisticated relations between internal and Cartesian coordinates. Moreover, reduced masses in internal coordinates are, in general, no longer constant but coordinate-dependent. Based on the approach presented earlier [Stare, J.; Balint-Kurti, G. G. J. Phys. Chem. A 2003, 107, 7204-7214] and on our experience with reduced masses discussed in this paper, we have developed a robust program for the calculation of Wilson G-matrix elements and their functional coordinate dependence. The approach is based on the first principles and can be used in virtually any (internal) coordinate set. Since the program allows for projection of any kind of nuclear motion on the selected internal coordinates, the method is particularly suitable for ab initio or DFT potential energy functions calculated by partial geometry optimization. Moreover, reduced masses obtained by this program can be used as a decision tool for selecting the most appropriate internal coordinates for the considered vibrational problem and for the inclusion or omission of the kinetic coupling terms in the vibrational Hamiltonian. © 2007 American Chemical Society.

Bibliographic Details

Stare, Jernej

American Chemical Society (ACS)

Chemistry; Chemical Engineering; Computer Science; Social Sciences

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