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Anomalous Intensities in the 2+1 REMPI Spectrum of the E 1Π-X 1Σ+ Transition of CO.
Gunthardt, C E; Wallace, C J; Hall, G E; Field, R W; North, S W.
Afiliação
  • Gunthardt CE; Department of Chemistry , Texas A&M University , College Station , Texas 77843 , United States.
  • Wallace CJ; Department of Chemistry , Texas A&M University , College Station , Texas 77843 , United States.
  • Hall GE; Chemistry Division , Brookhaven National Laboratory , Upton , New York 11973 , United States.
  • Field RW; Department of Chemistry , Massachusetts Institute of Technology , Cambridge , Massachusetts 02139 , United States.
  • North SW; Department of Chemistry , Texas A&M University , College Station , Texas 77843 , United States.
J Phys Chem A ; 123(13): 2780-2788, 2019 Apr 04.
Article em En | MEDLINE | ID: mdl-30811199
We report on one-color experiments near 214 nm involving the photodissociation of jet-cooled OCS to produce high rotational states (40 < J < 80) of CO (X 1Σ+, v = 0, 1) which were then ionized by 2+1 resonance-enhanced multiphoton ionization via the E 1Π state. The nominally forbidden Q-branch of the two-photon E 1Π-X 1Σ+ transition is observed with intensity comparable to the allowed R-branch. The bright character of the high- J Q-branch lines can be described quantitatively as intensity borrowing due to mixing of the E 1Π and C 1Σ+ states, using J-dependent mixing coefficients extrapolated from the observed Λ-doubling in the lower rotational levels of the E state. In addition to the significant enhancement of Q-branch intensities above the values predicted by conventional two-photon line strengths for a 1Π-1Σ+ transition, the high- J lines of the R- and P-branches appear to be suppressed in intensity by approximately a factor of 3 compared to the unperturbed low- J line strengths, most likely due to perturbations associated with a 1Σ- state. The E-state rotational term values for J < 80, v = 0 derived from the present spectra agree within our measurement and calibration uncertainties with the extrapolations based on the molecular constants previously derived from rotational levels with J < 50. The E-X transition is attractive for future application to photodissociation dynamics and rotational polarization measurements of CO photofragments, with convenient access to state-selective probing on multiple rotational branches, which exhibit different sensitivity to fragment alignment.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: J Phys Chem A Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: J Phys Chem A Ano de publicação: 2019 Tipo de documento: Article