HIGH RESOLUTION, ROTATIONALLY RESOLVED ELECTRONIC SPECTRA OF $ZnCH_{3}$ AND $CdCH_{3}$

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1993

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Ohio State University

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We present the rotationally resolved, laser-induced fluorescence spectra of jet-cooled ZnCH3 and CdCH3. The preliminary analysis of the origin band for both spin-orbit components of the A¯2EX¯2A1 electronic transition for ZnCH3 was reported at the 47th Symposium.1 Since that report, a final fit has been performed. Additionally, a spectrum for the CdCH3A¯2E1/22E3/2X¯2A1 transition has been recorded and globally fit with the previously reported A¯2E1/2X¯2A1 transition. The A¯2E3/2 state of CdCH3 exhibits a reduced lifetime, correspondingly broader linewidths and reduced intensity pointing to the existence of a nearby non-radiative perturbing state postulated in earlier work.2 This non-radiative state is thought to be responsible for significant Jahn-Teller-like interactions that alter the spectrum of the A¯2E3/2X¯2A1CdCH3 transition compared to the other bands reported here. Results of the fit will be discussed for both species.

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1 T.M. Cerny, E.S.J. Robles, A.M. Ellis, J.M. Williamson, D.W. Cullin, X.Q. Tan and T.A. Miller, 47th Ohio State University Symposium on Molecular Spectroscopy, June 1992, Paper RC6. 2 A.M. Ellis, E.S.J. Robles and T.A. Miller, Chem. Phys. Lett. 190, 599 (1992).


Author Institution: Laser Spectroscopy Facility, Department of Chemistry, The Ohio State University; Chemistry Department, Harvard University; Department of Chemistry, University of Leicester

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