Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9589573 | Journal of Molecular Spectroscopy | 2005 | 10 Pages |
Abstract
The rotational spectra of 3-fluoropropyne in the ground and first excited acetylenic C-H stretch vibrational state have been measured. The pure rotational spectrum of the normal species and the 13C isotopomers were measured using FTMW-cwMW double-resonance spectroscopy based on the Autler-Townes (AC Stark) effect. The lineshape properties of this measurement make it possible to determine the transition strength, ÎJ-selection rules, and the relative energy ordering of the quantum states. The frequency accuracy of this technique is tested against a previous pure rotational study of 3-fluoropropyne. The rotational spectrum of vibrationally excited state was obtained through IR-FTMW-cwMW methods. In this technique a single-longitudinal-mode pulsed infrared laser source vibrationally excites the acetylenic C-H stretch with J-selectivity. The rotational spectrum of the excited state is then obtained by FTMW and FTMW-cwMW double-resonance methods. The excited-state measurements have a signal-to-noise ratio comparable to the pure rotational spectrum. The residuals in the excited-state fit are larger than those obtained in the ground-state fit. This greater deviation from a standard asymmetric top spectrum is most likely due to weak perturbations to the acetylenic C-H spectrum.
Related Topics
Physical Sciences and Engineering
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Physical and Theoretical Chemistry
Authors
Kevin O. Douglass, Frances S. Rees, Richard D. Suenram, Brooks H. Pate, Igor Leonov,