Literature DB >> 21826428

Purine scaffold effect on fluorescence properties of purine-hydroxyquinolinone bisheterocycles.

Kamil Motyka1, Barbora Vaňková, Jan Hlaváč, Miroslav Soural, Petr Funk.   

Abstract

The fluorescence properties of bisheterocyclic compounds that contain purine and the 3-hydroxyquinolin-4(1H)-one skeleton connected with an aliphatic spacer of a different length/structure (3HQP) were examined. It was found that the introducing of the spacer-purine scaffold led in the comparison to 3HQs themselves to (1) the possibility of the effectual excitation in the wider range of excitation wavelengths, moreover, some derivatives can be excited at relatively high wavelengths around 400 nm, (2) the lowering of the quantum yield and (3) the slight longer wavelength shift of the dual emission spectra. Tested organic solvents did not affect significantly the 3HQP fluorescence properties. The characters of emission spectra as well as the quantum yields of 3HQPs were notably influenced by the ratio of water and DMSO in their composed mixture applied as a solvent. With increasing water content in the mixture both I(1)/I(2) and the quantum yield decreased.

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Year:  2011        PMID: 21826428     DOI: 10.1007/s10895-011-0925-0

Source DB:  PubMed          Journal:  J Fluoresc        ISSN: 1053-0509            Impact factor:   2.217


  3 in total

1.  Solid-phase synthesis of highly diverse purine-hydroxyquinolinone bisheterocycles.

Authors:  Barbora Vanková; Jan Hlavác; Miroslav Soural
Journal:  J Comb Chem       Date:  2010-09-17

2.  Steric control of the excited-state intramolecular proton transfer in 3-hydroxyquinolones: steady-state and time-resolved fluorescence study.

Authors:  Dmytro A Yushchenko; Volodymyr V Shvadchak; Andrey S Klymchenko; Guy Duportail; Vasyl G Pivovarenko; Yves Mély
Journal:  J Phys Chem A       Date:  2007-08-24       Impact factor: 2.781

3.  Dual-fluorescence probe of environment basicity (hydrogen bond accepting ability) displaying no sensitivity to polarity.

Authors:  Mykhailo D Bilokin'; Volodymyr V Shvadchak; Dmytro A Yushchenko; Guy Duportail; Yves Mély; Vasyl G Pivovarenko
Journal:  J Fluoresc       Date:  2008-11-20       Impact factor: 2.217

  3 in total

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