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Synthesis and spectroscopic properties of benzo- and naphthofuryl-3-hydroxychromones

Klymchenko, AS; Ozturk, T; Pivovarenko, VG; Demchenko, AP


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{
  "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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