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Ab Initio Variational Calculations of Molecular Vibrational-Rotational Spectra

  • Debra J. Searles
  • Ellak I. von Nagy-Felsobuki

Part of the Lecture Notes in Chemistry book series (LNC, volume 61)

Table of contents

  1. Front Matter
    Pages I-IX
  2. Debra J. Searles, Ellak I. von Nagy-Felsobuki
    Pages 1-23
  3. Debra J. Searles, Ellak I. von Nagy-Felsobuki
    Pages 24-39
  4. Debra J. Searles, Ellak I. von Nagy-Felsobuki
    Pages 40-56
  5. Debra J. Searles, Ellak I. von Nagy-Felsobuki
    Pages 57-81
  6. Debra J. Searles, Ellak I. von Nagy-Felsobuki
    Pages 82-106
  7. Debra J. Searles, Ellak I. von Nagy-Felsobuki
    Pages 107-125
  8. Debra J. Searles, Ellak I. von Nagy-Felsobuki
    Pages 126-145
  9. Debra J. Searles, Ellak I. von Nagy-Felsobuki
    Pages 146-156
  10. Debra J. Searles, Ellak I. von Nagy-Felsobuki
    Pages 157-190
  11. Back Matter
    Pages 187-190

About this book

Introduction

This work had its beginnings in the early 1980s at the University ofWollongong, with significant contributions from Dr. Margret Hamilton, Professors Peter G. Burton and Greg Doherty. The emphasis was to develop computer code to solve the nuclear Schrodinger problem. For bent triatomic molecules the project was fmally realized at the University of Newcastle a decade or so later, with the contribution from Ms. Feng Wan g. Aspects of this work are now taught in the quantum mechanics and electron spectroscopy courses at The University of Newcastle. Even now "complete" ab initio solutions of the time-independent SchrOdinger equation is not commonplace for molecules containing four atoms or more. In fact, when using the Eckart-Watson nuclear Hamiltonian a further restriction needs to be imposed; that is, the molecule is restricted to undergoing small amplitudes of vibration. This Hamiltonian is useful for molecules containing massive nuclei and moreover, has been extremely useful in interpreting the rovibrational spectra of small molecules. Nevertheless, a number of nuclear Hamiltonians that do not embed an equilibrium geometry have become well established and are extremely successful in interpreting rovibrational spectra of floppy molecules. Furthermore, solution algorithms vary greatly from research group to research group and it is still unclear which aspects will survive the next decade. For example, even for a triatomic molecule a general form of a potential function has not yet been uncovered that will generally interpolate with accuracy and precision ab initio discrete surfaces.

Keywords

Atom Molecular spectroscopy Molekülspektroskopie Schrödinger equation Theoretische Chemie Vibration algorithms energy molecule spectra system theoretical chemistry

Authors and affiliations

  • Debra J. Searles
    • 1
  • Ellak I. von Nagy-Felsobuki
    • 2
  1. 1.Research School of ChemistryAustralian National UniversityCanberraAustralia
  2. 2.Department of ChemistryThe University of NewcastleCallaghanAustralia

Bibliographic information

  • DOI https://doi.org/10.1007/978-3-662-05561-8
  • Copyright Information Springer-Verlag Berlin Heidelberg 1993
  • Publisher Name Springer, Berlin, Heidelberg
  • eBook Packages Springer Book Archive
  • Print ISBN 978-3-540-57465-1
  • Online ISBN 978-3-662-05561-8
  • Series Print ISSN 0342-4901
  • Series Online ISSN 2192-6603
  • Buy this book on publisher's site
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