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Complexes of Uracil (2,4-Dihydroxypyrimidine) Derivatives. Part II. Potentiometric and Luminescence Studies with Eu(III)

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Luminescence spectroscopy studies were carried out on europium(III) complexation with HL = uracil, thymine (5-methyluracil), 6-chloromethyluracil, 5-hydroxymethyluracil and 6-methyluracil in acidic perchlorate solutions. In acidic medium the decrease of the hydration number with increasing the ligand excess indicates a consecutive complexation via metal - O4 coordination. The potentiometric method confirmed the possibility of coordination by N3 at higher pH for thymine, 6-chloromethyluracil and 6-methyluracil. The formation of hydroxo species has been ascertained for all the ligands.
Rocznik
Strony
1019--1025
Opis fizyczny
Bibliogr. 15 poz., rys.
Twórcy
  • Laboratory of Physical and Biocoordination Chemistry, Medical University of Łódź 1 Muszyński Str., 90-151 Łódź, Poland
autor
  • Laboratory of Physical and Biocoordination Chemistry, Medical University of Łódź 1 Muszyński Str., 90-151 Łódź, Poland
autor
  • Department of Rare Earths, Faculty of Chemistry, Adam Mickiewicz University, Grunwaldzka 6, 60-780 Poznań, Poland
autor
  • Department of Rare Earths, Faculty of Chemistry, Adam Mickiewicz University, Grunwaldzka 6, 60-780 Poznań, Poland
Bibliografia
  • 1. Lönnberg H., Proton and Metal Interaction with Nucleic Acid Bases, Nucleosides and Nucleoside Monophosphates, in „Biocoordination Chemistry: Coordination Equilibria in Biologically Active Systems”, Ed. K. Burger, Ellis Horwood Limited, Chichester 1990, pp. 308-312.
  • 2. Kufelnicki A., Kupinska I., Jezierska J. and Ochocki J., Polish J. Chem., 76, 1559 (2002).
  • 3. Emsley J., The Elements, Polish Edition, Warsaw 1997, pp. 66, 218.
  • 4. Horrocks W. DeW, jr. and Sudnick D.R., J. Am. Chem. Soc., 101, 334 (1979).
  • 5. Lis S. and Choppin G.R., Mater. Chem. Phys., 31, 159 (1992).
  • 6. Lis S., J. Alloys Comp., 341, 45 (2002).
  • 7. Smith R., Martell A. and Chen Y., Pure & Appl. Chem., 63, 1015 (1991).
  • 8. Gran G., Acta Chem. Scand., 4, 559 (1950).
  • 9. Stryla Z., Lis S. and Elbanowski M., Opt. Appl., 23, 163 (1993).
  • 10. Lis S., Hnatejko Z. and Stryla Z., Opt. Appl., 31, 643 (2001).
  • 11. Pettit L.D. and Powell K.J., Stability Constants Database, IUPAC and Academic Software, Royal Society of Chemistry, London 1993-2000.
  • 12. Sabatini A., Vacca A. and Gans P., Coord. Chem. Rev., 120, 389 (1992).
  • 13. Barthelemy P.P. and Choppin G.R., Inorg. Chem., 28, 3354 (1989).
  • 14. Frolova U., Kumok V. and Serebrennikov V., Izv. VUZ. Khim., 6, 176 (1966).
  • 15. Casassas E., Izquierdo-Ridorsa A. and Tauler R., J. Inorg. Biochem., 39, 327 (1990).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUJ1-0021-0066
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