Abstract
An original design of a fluorescent dithienylethene (DTE)-based bipyridine, where donor (D) and acceptor (A) groups are located on the same thiophene ring of the DTE unit, is reported; in non-polar solvents, UV or visible excitation triggers a photochromic reaction, disrupting the conjugation and quenching the fluorescence. © The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 2009.
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CITATION STYLE
Aubert, V., Ishow, E., Ibersiene, F., Boucekkine, A., Williams, J. A. G., Toupet, L., … Le Bozec, H. (2009). A “reverse interrupter”: The novel molecular design of a fluorescent photochromic DTE-based bipyridine. New Journal of Chemistry, 33(6), 1320–1323. https://doi.org/10.1039/b823113c
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