Symmetry, vibrational energy redistribution and vibronic coupling: The internal conversion processes of cycloketones

Publication: Research - peer-reviewJournal article – Annual report year: 2012

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In this paper, we discern two basic mechanisms of internal conversion processes; one direct, where immediate activation of coupling modes leads to fast population transfer and one indirect, where internal vibrational energy redistribution leads to equidistribution of energy, i.e., ergodicity, and slower population transfer follows. Using model vibronic coupling Hamiltonians parameterized on the basis of coupled-cluster calculations, we investigate the nature of the Rydberg to valence excited-state internal conversion in two cycloketones, cyclobutanone and cyclopentanone. The two basic mechanisms can amply explain the significantly different time scales for this process in the two molecules, a difference which has also been reported in recent experimental findings [T. S. Kuhlman, T. I. Sølling, and K. B. Møller, ChemPhysChem. 13, 820 (2012)]
Original languageEnglish
JournalJournal of Chemical Physics
Publication date2012
Volume137
PagesPaper 22A522
Number of pages31
ISSN0021-9606
DOIs
StatePublished

Bibliographical note

Copyright (2012) American Institute of Physics.
This article may be downloaded for personal use only. Any other use requires prior permission of the author and the American Institute of Physics. The following article appeared in J. Chem. Phys. 137, 22A522 (2012) and may be found at http://jcp.aip.org/resource/1/jcpsa6/v137/i22/p22A522_s1

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