Photodissociation dynamics of the NO dimer. I. Theoretical overview of the ultraviolet singlet excited states

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DOIResolve DOI: http://doi.org/10.1063/1.2222355
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TypeArticle
Journal titleThe Journal Of Chemical Physics
Volume125
Issue8
Pages08430112; # of pages: 84290
Subjectconfiguration interactions; coupled cluster calculations; excited states; molecule-photon collisions; nitrogen compounds; orbital calculations; photodissociation; SCF calculations
AbstractMolecular orbital theory and calculations are used to describe the ultraviolet singlet excited states of NO dimer. Qualitatively, we derive and catalog the dimer states by correlating them with monomer states, and provide illustrative complete active space self-consistent field calculations. Quantitatively, we provide computational estimates of vertical transition energies and absorption intensities with multireference configuration interaction and equations-of-motion coupled-cluster methods, and examine an important avoided crossing between a Rydberg and a valence state along the intermonomer and intramonomer stretching coordinates. The calculations are challenging, due to the high density of electronic states of various types (valence and Rydberg, excimer and charge transfer) in the 6-8 eV region, and the multiconfigurational nature of the ground state. We have identified a bright charge-transfer (charge-resonance) state as responsible for the broadband seen in UV absorption experiments. We also use our results to facilitate the interpretation of UV photodissociation experiments, including the time-resolved 6 eV photodissociation experiments to be presented in the next two papers of this series.
Publication date
AffiliationNational Research Council Canada; NRC Steacie Institute for Molecular Sciences
Peer reviewedYes
NPARC number12339179
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Record identifier62f789f3-3bef-42a5-bc1d-eec72e103ffc
Record created2009-09-11
Record modified2016-05-09
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