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Fluorescence spectroscopy of C60 in toluene solutions at 5 K
Institution:1. Laboratoire Aimé Cotton, CNRS-UPR 3321, Bât. 505, Centre Universitaire d''Orsay, 91405-Orsay Cedex, France;2. DAMAP, CNRS-UMR 8588, Observatoire de Paris-Meudon, 92195-Meudon, France;1. Center for Photochemical Sciences, Bowling Green State University, Bowling Green, OH 43402, USA;2. Department of Physics, Bowling Green State University, Bowling Green, OH 43402, USA;3. Department of Chemistry, Bowling Green State University, Bowling Green, OH 43402, USA;1. School of Chemical Sciences, Mahatma Gandhi University, Priyadarsini Hills, Kottayam 686560, Kerala, India;2. Research Institute for Electronic Science, Hokkaido University, Sapporo 001-0200, Japan;3. Graduate School of Environmental Science, Hokkaido University, Sapporo 001-0020, Japan;1. National Reference Centre for Bacterial Meningitis (NRCBM), National Medicines Institute, Warsaw, Poland;2. Institute Pasteur, Invasive Bacterial Infections Unit, Paris, France;3. Novartis Vaccines and Diagnostics, Siena, Italy;2. Department of Medical Physics, University of Wisconsin–Madison, Madison, Wisconsin, U.S.A.
Abstract:We have recorded the dispersed fluorescence and the fluorescence excitation spectra of C60 in toluene matrices at 5 K. Upon excitation with the green Ar+ laser line (λ=514 nm) we obtained for the first time in this matrix well resolved visible fluorescence spectra which we have compared with those observed in other low temperature matrices. Our spectra were interpreted and assigned using theoretical assessments of vibronic activities of transitions between the three lowest excited electronic states 1T1g, 1T2g, 1Gg and the totally symmetric ground state, and on the basis of a single 00 level which has pseudo-Jahn–Teller (JT) components of the three near-degenerate excited states. The fluorescence spectra exhibit prominent JT induced hg(1) progressions, Herzberg–Teller-induced hu and other ungerade mode vibrations, including a very active t1u(4) mode. Excitation wavelength independent bands are assigned to the fluorescence of C60 molecules in toluene microcrystals embedded in the toluene glass whereas excitation wavelength dependent features are interpreted as originating from C60 molecules isolated in the toluene glass itself. These interpretations are supported by the results of spectrally selective detected fluorescence excitation spectra.
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