Synthesis of furanochromones: a new step in improvement of fluorescence properties


Klymchenko A., Ozturk T., DEMCHENKO A.

TETRAHEDRON LETTERS, cilt.43, sa.39, ss.7079-7082, 2002 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 43 Sayı: 39
  • Basım Tarihi: 2002
  • Doi Numarası: 10.1016/s0040-4039(02)01547-2
  • Dergi Adı: TETRAHEDRON LETTERS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.7079-7082
  • İstanbul Teknik Üniversitesi Adresli: Hayır

Özet

New 3-hydroxychromone derivatives with a fused furan heterocycle (2-aryl-3-hydroxyfurano[3,2-g]chromones) have been synthesized. This was achieved by an important improvement in the synthetic procedure. Like their parent analogs, these new compounds exhibit two intensive fluorescence emission bands belonging to normal (N*) and tautomer (T*) excited-state forms. While the spectral position of the N* band remains unchanged, the T* band is shifted to longer wavelengths, providing larger separation between the two bands. The new compounds exhibit increased molecular extinction and, more importantly, have about twice as high fluorescence quantum yields. These properties make them very promising for designing new two-band fluorescence sensors. (C) 2002 Elsevier Science Ltd. All rights reserved.