PHOTOPHYSICAL PROPERTIES AND CONFORMATIONAL EQUILIBRIA OF TRANS-1-(N-PYRIDYL)-2-(2-QUINOXALINYL)ETHENES

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The photophysical properties of trans-2-styrylnaphthalene (2-StN) and trans-1-(n-pyridyl)-2-(2-quinoxalinyl)ethenes (n,2-PQxE, n = 2 and 3) were studied. Conformational equilibrium was verified by the solvent dependence of the photophysical properties, the wavelength dependence of the fluorescence spectra (emission and excitation) and comparison with conformationally restricted trans-1-(n-pyridyl)-2-(3-methyl-2-quinoxalinyl)ethenes. The positional effect of the nitrogen atom in the pyridine ring was not observed in these compounds.
Publisher
ELSEVIER SCIENCE SA LAUSANNE
Issue Date
1994-04
Language
English
Article Type
Article
Keywords

EMISSION-SPECTRA; AZA AROMATICS; PHOTOISOMERIZATION; FLUORESCENCE; TRANS-1,2-DIARYLETHYLENES; STYRYLPYRIDINES; DERIVATIVES; CONFORMERS; BEHAVIOR

Citation

JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, v.79, no.1-2, pp.39 - 47

ISSN
1010-6030
URI
http://hdl.handle.net/10203/59290
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