Vibrational study of the S0and S1states of 2-naphthyl-1-ethanol/(water)2and 2-naphthyl-1-ethanol/(methanol)2complexes by IR/UV double resonance spectroscopy
Seurre, N.; Sepioł, J.; Lahmani, F.; Zehnacker-Rentien, A.; Le Barbu-Debus, K.; Seurre N.; Laboratoire de Photophysique Moléculaire du CNRS; SepioÅ J.; Institute of Physical Chemistry, Polish Academy of Sciences; Lahmani F.; Laboratoire de Photophysique Moléculaire du CNRS; Zehnacker-Rentien A.; Laboratoire de Photophysique Moléculaire du CNRS; Le Barbu-Debus K.; Laboratoire de Photophysique Moléculaire du CNRS
Журнал:
Physical Chemistry Chemical Physics
Дата:
2004
Аннотация:
2-naphthyl-1-ethanol/(water)2 and 2-naphthyl-1-ethanol/(methanol)2 complexes have been formed in a supersonic expansion and studied by laser induced fluorescence (LIF) and IR/UV double resonance spectroscopy in the region of the Oâ H stretch. Comparison of the measured frequencies with DFT calculations has led to the attribution of the observed 2-naphthyl-1-ethanol/(water)2 and 2-naphthyl-1-ethanol/(methanol)2 complexes to bridged structures. In these structures the solvent dimer is inserted in between the OH group of the chromophore which acts as a hydrogen bond donor, and the electron Ï system of the aromatic ring. Electronic excitation results in a red shift of all the νOH stretch frequencies.
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