Four novel diarylanthracene derivatives (1, 5a, 5b, 6) have been synthesized by Suzuki and Sonogashira coupling reactions, characterized and their structure assigned by (1)H and (13)C NMR spectroscopy. The spectral and photophysical properties of a series of symmetrically and asymmetrically disubstituted anthracene-based compounds (1-6) and of benzothiadiazole derivative 7 have been studied. All these photostable systems show high fluorescence emission and a batochromic shift of the absorption spectrum that increase with pi-conjugation. Flash photolysis measurements were carried out on the poor fluorescent compound 4.

Synthesis and photophysical properties of conjugated anthracene-based compounds

Seri M;
2010

Abstract

Four novel diarylanthracene derivatives (1, 5a, 5b, 6) have been synthesized by Suzuki and Sonogashira coupling reactions, characterized and their structure assigned by (1)H and (13)C NMR spectroscopy. The spectral and photophysical properties of a series of symmetrically and asymmetrically disubstituted anthracene-based compounds (1-6) and of benzothiadiazole derivative 7 have been studied. All these photostable systems show high fluorescence emission and a batochromic shift of the absorption spectrum that increase with pi-conjugation. Flash photolysis measurements were carried out on the poor fluorescent compound 4.
2010
Anthracene derivatives
Arylacetylenes
Spectral/photophysical properties
Synthesis
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/302040
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