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Photophysical properties of β-(1-pyrenyl)ethyl p-cyanobenzoate in binary solvents of isooctane-ethyl acetate and ethyl acetate-acetonitrile
Authors:Jun Kawakami  Junko Nakamura  Michiko Iwamura  
Institution:

a Department of Biomolecular Science, Faculty of Science, Toho University, 2-2-1 Miyama, Funabashi, Chiba 274-8510, Japan

b Institute of Physical and Chemical Research, Wako, Saitama 351-0198, Japan

Abstract:The effects of solvent polarity on the fluorescence spectra and fluorescence decays of β-(1-pyrenyl)ethyl p-cyanobenzoate (P2CN) were investigated in detail using binary solvents consisting of various mixing ratios of isooctane-ethyl acetate or ethyl acetate-acetonitrile (dielectric constants (var epsilon)=1.94–36.2). Whereas both the intensity and wavelength maxima of an intramolecular exciplex emission (EX) are dependent on the solvent polarity, only the intensity of an emission from the locally excited pyrene (LE) is dependent on the solvents used. When monitored at 377 nm, the picosecond SPC (single photon counting) measurements reveal a slow decay (>150 ns) in addition to a fast decay (<1 ns) of the locally excited P2CN. There are also two decays for the EX which vary the intensity ratios by the monitored wavelength. The decay rate constants, kEX1 and kEX2, have a good linear correlation with the dielectric constants of the solvents, indicating that there exist two kinds of exciplexes. It is suggested that the decays of the locally excited-state of P2CN are so fast due to result of the efficient electron transfer that the two kinds of intramolecular exciplexes are formed from the two discrete conformers in the ground state.
Keywords:Intramolecular exciplex  Solvent effect  Pyrene derivatives  Fluorescence lifetimes
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