Generic placeholder image

Letters in Organic Chemistry

Editor-in-Chief

ISSN (Print): 1570-1786
ISSN (Online): 1875-6255

Fluorescence Changes of Glycyl-Tryptophan Peptide in the Presence of Some Newly Synthesized Azobenzene Compounds

Author(s): Catalina-Ionica Ciobanu, Laura Habasescu, Dan Scutaru and Gabi Drochioiu

Volume 12, Issue 2, 2015

Page: [91 - 99] Pages: 9

DOI: 10.2174/1570178612666150107235907

Price: $65

Abstract

Five newly synthesized bent-shaped compounds containing azobenzene chromophores have been prepared by resorcinol esterification with 4-(4-alkyloxyphenylazo) benzoic acid using DCC and DMAP. The structure of newly synthesized compounds was confirmed by MS and FT-IR spectroscopy. In addition, NMR spectroscopy also established the purity of these compounds. According to their azo-type chemical structure, the newly synthesized compounds are expected to be highly fluorescent. Consequently, their absorption and fluorescence properties were investigated using UVVis and fluorescence spectroscopy. The present paper also investigates the fluorescence evolution of glycyl-L-tryptophan dipeptide at different concentrations of the newly synthesized bent-shaped compounds. The intensity of their fluorescence band over 400 nm depends much on individual structures. Since the investigated compounds could have optical properties characteristic to liquid crystals, the interaction with fluorescent peptides, such as glycyl-tryptophan or proteins might enhance their utility.

Keywords: Azobenzene compounds, glycyl-tryptophan peptide, fluorescence, quenching, UV-Vis spectra.

« Previous
Graphical Abstract

Rights & Permissions Print Cite
© 2024 Bentham Science Publishers | Privacy Policy