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Klymchenko, AS; Ozturk, T; Pivovarenko, VG; Demchenko, AP
{ "URL": "https://aperta.ulakbim.gov.tr/record/95587", "abstract": "With the focus of designing new fluorescent probes, four new 3-hydroxy-chromone derivatives bearing benzofuran and naphthofuran groups were synthesized. They show bathochromic absorption shifts relative to 3-hydroxyflavone with the ability of retention to display the excited-state proton transfer. Disruption of the planarity by the methyl group in the furan ring leads to a decrease of both the extinction coefficient and the contribution of long wavelength absorption band, while molecules without a methyl group showed two distinct absorption bands. Shifts to longer wavelengths are also observed in fluorescent spectra, and the absence of the methyl group results in a dramatic increase of fluorescence quantum yield and lifetime. Of the extended 3-hydroxychromone derivatives, 3-hydroxy-2-naphtho[2,1-b]furan-2-yl-chromone has shown comparable, and in some cases better, absorption and fluorescence properties than the 3-hydroxychromones synthesized so far, which make it a highly promising candidate as molecular probe for analytical chemistry, biophysics, and cellular biology.", "author": [ { "family": "Klymchenko", "given": " AS" }, { "family": "Ozturk", "given": " T" }, { "family": "Pivovarenko", "given": " VG" }, { "family": "Demchenko", "given": " AP" } ], "container_title": "CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE", "id": "95587", "issue": "4", "issued": { "date-parts": [ [ 2001, 1, 1 ] ] }, "page": "358-363", "title": "Synthesis and spectroscopic properties of benzo- and naphthofuryl-3-hydroxychromones", "type": "article-journal", "volume": "79" }
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