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Tytuł artykułu

Cyclic Voltammetry and Electronic Absorption Spectroscopy in Investigations of the Nature of the Electrochemical reduction of Phenyldiazonium and Phenyl-bis-diazonium Cations

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
The electrochemical reduction of phenyldiazonium and phenyl-bis-diazonium cations on mercury drop and platinum cathodes exhibits a multistep nature, as demonstrate the results of polarographic and cyclic voltammetry measurements. The primarily formed radicals participate in various secondary processes, as a result of which occur species absorbing UV-VIS radiation. Electronic absorption in the visible region can be ascribed to entities forming from the recombination of two azophenyl or azophenyl and phenyl radicals, originating from the one- or two-electron reduction of primarily or secondary formed cations.
Rocznik
Strony
139--147
Opis fizyczny
Bibliogr. 23 poz., rys.
Twórcy
  • Ivan Franko L’viv National University, Department of Chemistry, Kyrylo and Mefodiy 8, 79005 L’viv, Ukraine
  • Ivan Franko L’viv National University, Department of Chemistry, Kyrylo and Mefodiy 8, 79005 L’viv, Ukraine
autor
  • University of Warsaw, Faculty of Chemistry, L. Pasteura 1, 02-093 Warszawa, Poland
autor
  • V.N. Karazin Kharkiv National University, Institute of Chemistry, Svobody Sq. 4, 61077 Kharkiv, Ukraine
  • Ivan Franko L’viv National University, Department of Chemistry, Kyrylo and Mefodiy 8, 79005 L’viv, Ukraine
  • University of Gdańsk, Faculty of Chemistry, J. Sobieskiego 18, 80-952 Gdańsk, Poland
  • Ivan Franko L'viv National University, Department of Chemistry, Kyrylo and Mefodiy 8, 79005 L'viv, Ukraine
Bibliografia
  • 1. Bahr J.L., Yang J., Kosynkin D.V., Bronikowski M.J., Smalley R.E. and Tour J.M., J. Am. Chem. Soc., 123, 6536(2001).
  • 2. Kariuki J.K. and McDermott M.T., Langmuir, 17, 5947 (2001).
  • 3. Hamisch J.A., Gazda D.B., Anderegg J.W. and Porter M.D., Anal. Chem., 73, 3954 (2001).
  • 4. Elofson R.M., Edsberg R.L. and Mercherly P.A., J. Electrochem. Soc., 97, 166 (1950).
  • 5. Alkinson E.R., Warren H.H., Abell P.I. and Wing R.E., J. Am. Chem. Soc., 72, 915 (1950).
  • 6. KovarchukE.P.,GanuschakN.I.,PrysyazhnyiV.M. and ObushakN.D., Ukr.Khim. Zh.. 48,491 (1982).
  • 7. Koval’chuk E.P., Ganuschak N.I., Obushak N.D. and Krupak I.N., Ukr. Khim. Zh., 49, 161 (1983).
  • 8. Koval’chuk E.P., Kozlowska Z.E., Jozwiak L. and Blalejowski J., Polish J. Chem., 74, 67 (2000).
  • 9. Reshetnyak O.V., Kozlovs’ka Z.E., Koval’chuk E.P., Obushak M.D., Rak J. and Biazejowski J., Electrochem. Commun., 3, 1 (2001).
  • 10. Galli C„ Chem. Rev., 88, 765 (1988).
  • 11. Efros L.S. and Gorclic M.V., Chemistry and Technology of Intermediate Products (in Russian), Khimia, Leningrad, 1980, p. 554.
  • 12. Oliver O., Elfakir-Hamet C. and Connlet C., J. Electrochem. Soc., 128, 1889 (1981).
  • 13. Dombrovskiy A. V. and Najdan V.M., Organic Chemistry (in Russian), Vysha shkola, Kyiv, 1992, p. 426.
  • 14. Dewar M.J.S., Zoebisch E.G., Healy E.F. and Stewart J.J.P., J. Am. Chem. Soc., 107, 3902 (1985).
  • 15. Baker ].,J. Comput. Chem., 9, 465 (1988).
  • 16. Stewart J.J.P., MOPAC 93, Copyright Fujitsu, Tokyo, Japan, 1993.
  • 17. Stewart J.J.P., J. Comput.-Aided Mol. Des., 4, 1 (1990).
  • 18. HyperChem 5.0, HyperCube Inc., Waterloo, ON, Canada, 1995.
  • 19. Armstrong D.R., Perkins P.G. and Stewart J.J.P., J. Chem. Soc., Farad. Trans. 2, 68, 1839 (1972).
  • 20. The Methods in Elementorganic Chemistry. Mercury (in Russian), A.N. Nesmeyanov and K.A. Kocheshkov (Eds.), Nauka, Moscow, 1965, p. 182.
  • 21. Elofson R.M., Gadallah F.F., Schulz K.F. and Laidler J.K., Can. J. Chem., 62, 1772 (1984).
  • 22. Feoktistov L.G. and Lund H., Organic Electrochemistry (in Russian), vol. 1, Khimia, Moscow, 1988, p. 319.
  • 23. Argonomov A.E., Selected Chapters ofOrganic Chemistry (in Russian), Khimia, Moscow, 1990, p. 433.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUJ1-0023-0152
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