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Klymchenko, AS; Pivovarenko, VG; Demchenko, AP
{ "URL": "https://aperta.ulakbim.gov.tr/record/93679", "abstract": "In order to understand the unexpectedly low quantum yields of 3-hydroxyflavones (3-HFs) in certain solvents, such as acetonitrile or ethyl acetate, the comparative study of solvent-dependent properties of parent 3-HF, 2-furyl-3-hydroxychromone and 2-benzofuryl-3-hydroxychromone derivatives have been pin-formed. The results suggest that the formation of intermolecular hydrogen bond of 3-hydroxy group with the solvent favors non-planar conformations of phenyl group with respect to chromone system. This steric hindrance is not observed in the case of furan- and benzofuran-substituted 3-hydroxychromones (3-HCs). These results suggesting, new strategy for dramatic improvement of fluorescence properties of 3-HCs as two-wavelength ratiometric fluorescence probes. (C) 2002 Elsevier Science B.V. All rights reserved.", "author": [ { "family": "Klymchenko", "given": " AS" }, { "family": "Pivovarenko", "given": " VG" }, { "family": "Demchenko", "given": " AP" } ], "container_title": "SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY", "id": "93679", "issue": "4", "issued": { "date-parts": [ [ 2003, 1, 1 ] ] }, "page": "787-792", "title": "Perturbation of planarity as the possible mechanism of solvent-dependent variations of fluorescence quantum yield in 2-aryl-3-hydroxychromones", "type": "article-journal", "volume": "59" }
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