Cu-catalyzed 1,3-dipolar cycloaddition of methyl 2-azidoacetate to iodobuta-1,3-diynes and subsequent Suzuki-Miyaura cross-coupling were used to synthesize new triazoles derivatives: 5aryl-4-arylethynyl-1H-1,2,3-triazoles. Investigation of their optical properties by using UV absorption and fluorescence emission spectroscopies revealed that all molecules possess fluorescence properties with the values of the Stokes shift more than 100 nm. The photophysical behavior of the two most promising triazoles in polar and non-polar solvents was also studied.

Original languageEnglish
Article number2801
Number of pages14
JournalMolecules
Volume26
Issue number9
DOIs
StatePublished - 10 May 2021

    Research areas

  • 1,2,3-triazoles, 1,3-diynes, Antimicrobial activity, Azide–alkyne cycloaddition, Cytotoxity, Fluorescence, Solvatochromism, Suzuki-Miyaura cross-coupling, Solvents, Humans, Molecular Conformation, Spectrometry, Fluorescence, Triazoles/chemical synthesis, Light, HEK293 Cells, HeLa Cells, Physical Phenomena, cytotoxity, ORGANIC-DYES, COMPLEXES, azide&#8211, BRIDGE, alkyne cycloaddition, fluorescence, CYCLOADDITIONS, 3-diynes, CHARGE-TRANSFER, CLICK CHEMISTRY, antimicrobial activity, 1, 2, 3-triazoles, TRIAZOLE, 1,2,3-TRIAZOLES, solvatochromism

    Scopus subject areas

  • Drug Discovery
  • Analytical Chemistry
  • Chemistry (miscellaneous)
  • Molecular Medicine
  • Physical and Theoretical Chemistry
  • Pharmaceutical Science
  • Organic Chemistry

ID: 76918505