{"title":"Rotational‐level‐dependent radiative lifetimes and branching ratios in NO(B 2Π) (v=7, Ω=1/2,3/2)","authors":"G. E. Gadd, D. Huestis, T. Slanger","doi":"10.1063/1.460801","DOIUrl":null,"url":null,"abstract":"The previous study [G. E. Gadd and T. G. Slanger, J. Chem. Phys. 92, 2194 (1990)] of the v=0–6 levels of the NO(B 2Π) valence state has been extended to the v=7 level, which is of particular interest because it lies at the first dissociation limit of the molecule, and also in a region where strong homogeneous mixing with the C 2Π Rydberg state manifests itself. Thus, the v=7 radiative lifetime can be affected by both these interactions, which are dependent on rotational level. It has often been argued that the B 2Π3/2 spin–orbit component interacts strongly with C 2Π1/2,3/2, whereas the B 2Π1/2 component is unperturbed. We show here that ‘‘unperturbed’’ is a relative term and that a sensitive way to demonstrate that even the B 2Π1/2 levels are mixed with the C 2Π state is to measure the intensity branching in the B–X 7–v‘ vibrational progression from fluorescent spectra, for different rotational levels. In the present study, excitation of these levels is carried out on the B–X 7–0 band at 191–192 nm. We h...","PeriodicalId":15313,"journal":{"name":"Journal of Chemical Physics","volume":"95 1","pages":"3944-3954"},"PeriodicalIF":3.1000,"publicationDate":"1991-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1063/1.460801","citationCount":"11","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Physics","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1063/1.460801","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 11
Abstract
The previous study [G. E. Gadd and T. G. Slanger, J. Chem. Phys. 92, 2194 (1990)] of the v=0–6 levels of the NO(B 2Π) valence state has been extended to the v=7 level, which is of particular interest because it lies at the first dissociation limit of the molecule, and also in a region where strong homogeneous mixing with the C 2Π Rydberg state manifests itself. Thus, the v=7 radiative lifetime can be affected by both these interactions, which are dependent on rotational level. It has often been argued that the B 2Π3/2 spin–orbit component interacts strongly with C 2Π1/2,3/2, whereas the B 2Π1/2 component is unperturbed. We show here that ‘‘unperturbed’’ is a relative term and that a sensitive way to demonstrate that even the B 2Π1/2 levels are mixed with the C 2Π state is to measure the intensity branching in the B–X 7–v‘ vibrational progression from fluorescent spectra, for different rotational levels. In the present study, excitation of these levels is carried out on the B–X 7–0 band at 191–192 nm. We h...
期刊介绍:
The Journal of Chemical Physics publishes quantitative and rigorous science of long-lasting value in methods and applications of chemical physics. The Journal also publishes brief Communications of significant new findings, Perspectives on the latest advances in the field, and Special Topic issues. The Journal focuses on innovative research in experimental and theoretical areas of chemical physics, including spectroscopy, dynamics, kinetics, statistical mechanics, and quantum mechanics. In addition, topical areas such as polymers, soft matter, materials, surfaces/interfaces, and systems of biological relevance are of increasing importance.
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