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A Comparison of Basicities of Substituted Pyridines and Pyridine N-Oxides

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
The basicity of pyridine and its derivatives, as representatives of monocyclic heterocyclic N-bases, has been compared with that of pyridine N-oxide and its derivatives representing the class of heterocyclic monocyclic oxygen-containing bases. The basicities have been compared both in the gas phase and in solution. To do this, correlated were both calculated (at RHF, MP2 levels and using SCRF and PCM methods) energy parameters, _Eprot and _Gprot, with experimental pKa values for a particular class of the bases, as well as theoretical and experimental characteristics of the two classes of compounds studied. Results of the correlations paved the way to discussion of the effect of the medium on basicity of both classes of compounds, as well as enabled to compare the basicities of these very important classes of organic bases in a quantitative way.
Rocznik
Strony
581--588
Opis fizyczny
Bibliogr. 22 poz., rys.
Twórcy
autor
  • Department of General Chemistry, University of Gdańsk, Sobieskiego 18, 80-952, Gdańsk, Poland
autor
  • Department of General Chemistry, University of Gdańsk, Sobieskiego 18, 80-952, Gdańsk, Poland
  • Department of General Chemistry, University of Gdańsk, Sobieskiego 18, 80-952, Gdańsk, Poland
Bibliografia
  • 1. Augustin-Nowacka D. and Chmurzyński L., Anal. Chim. Acta, 381, 215 (1999).
  • 2. Augustin-Nowacka D and Chmurzyński L., J. Solution Chem., 29, 837 (2000).
  • 3. Augustin-Nowacka D., Makowski M. and Chmurzyński L., Anal. Chim. Acta, 418, 233 (2000).
  • 4. Augustin-Nowacka D., Makowski M. and Chmurzyński L., J. Chem. Thermodyn., (in press).
  • 5. Wawrzynów A. and Chmurzyński L., J. Chem. Thermodyn., 30, 713 (1998).
  • 6. Chmurzyński L., Solvent Effect on Acidic-Basic Interactions of Pyridine N-Oxide Derivatives, University of Gdańsk, Gdańsk, 1994 (in Polish).
  • 7. Chmurzyński L., Anal. Chim. Acta, 321, 237 (1996).
  • 8. Chmurzyński L., Anal. Chim. Acta, 326, 267 (1996).
  • 9. Makowski M., Liwo A., Wróbel R. and Chmurzyński L., J. Phys. Chem. A, 103, 11104 (1999).
  • 10. Sadowski R., Makowski M., Augustin-Nowacka D. and Chmurzyński L., J. Phys. Chem. A, 105, 6743 (2001).
  • 11. Schmidt M.W., Boldridge K.K., Boatz J.A., Elbert S.T., Gordon M.S., Jensen J.A., Koseki S., MatsunagaN., Nguyen K.A., Su S., Windus T.L., Dupuis M. and Montgomery J.A.,7. Comput. Chem., 14, 1347(1993).
  • 12. Schaftenaar G. and Noordik J.H., J. Comput.-AidedMol. Design, 14, 123 (2000).
  • 13. Onsager L., J. Am. Chem. Soc., 58, 1486 (1936).
  • 14. Karelson M., Tamm T. and Zemer M. C., J. Phys. Chem., 97, 11901 (1993).
  • 15. Cammi R. and Tomasi J., J. Comput. Chem., 16, 1449 (1995).
  • 16. Reichardt Ch., Solvents and Solvent Effects in Organic Chemistry, VCH Verlaggesellschaft GmbH, Weinheim, Germany, 1988; pp. 407-410.
  • 17. Gardner J.N. and Katritzky A.R., J. Chem. Soc., 4375 (1957).
  • 18. Klotufar C., Krasovec F. and KusarM., Croat. Chim. Acta, 40, 23 (1968).
  • 19. Perrin D.D., Dissociation Constants of Organic Bases in Aqueous Solutions, Butterworths, London, 1965.
  • 20. Christensen J.J., Hansen L.D. and Izatt R.M., Handbook of Proton Ionization Heats and Related Thermodynamic Quantities, Brigham Young University, Provo, UT, 1976.
  • 21. Jaffe H.H., J. Am. Chem. Soc., 77, 4445 (1955).
  • 22. Barthel J., Wächter R. and Gores H. H., Modem Aspects of Electrochemistry, 13, Plenum Publ. Corp., 1979, pp. 112-114.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUJ1-0020-0062
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