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Rotational effects on intramolecular radiationless transitions in a large molecule
Affiliation:1. Department of Applied Chemistry, School of Science, Xi''an Jiaotong University, Xi''an 710049, China;2. Key Laboratory for Physical Electronics and Devices of the Ministry of Education, School of Electronic and Information Engineering, Xi''an Jiaotong University, Xi''an 710049, China;1. Department of Chemistry, M. V. Lomonosov Moscow State University, 1 Leninskie Gory, 119992 Moscow, Russian Federation;2. A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 119991 Moscow, Russian Federation;1. Vip mobile d.o.o., Belgrade, Serbia;2. School of Electrical Engineering, University of Belgrade, Serbia;3. Centre Suisse d''Electronique et de Microtechnique (CSEM), Neuchâtel, Switzerland;1. Tyndall National Institute, Dyke Parade, Cork, Ireland;2. Intel Corporation, 2200 Mission College Blvd., Santa Clara, CA 95054-1549, USA
Abstract:We report the observation of a pronounced rotational-state dependence for the fluorescence quantum yield and fluorescence decay from the S1(0,0+1160 cm−1) state of jet-cooled 9-cyanoanthracene. We attribute these results to the effects of Coriolis rotational-vibrational interaction on intramolecular vibrational energy redistribution, which influence electronic relaxation.
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