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Electrochemical Behaviors of 4-(2-thiazolylazo)-resorcinol in Acetonitrile

  • Bae, Zun-Ung (Department of Chemistry, Kyungpook National University) ;
  • Lee, Heung-Lark (Department of Chemistry, Kyungpook National University) ;
  • Seo, Moo-Lyung (Department of Chemistry, Gyeongsang National University)
  • Published : 1989.06.20

Abstract

The electrochemical behaviors of 4-(2)-thiazolylazo)-resorcinol (TAR) in acetonitrile solution was studied by DC polarography, cyclic voltammetry, controlled-potential coulometry and UV-Vis spectroscopy. The electrochemical reduction of TAR occurs in four-one electron reduction steps in acetonitrile solution. The products of the first and the third electron transfer are speculated to be a relatively stable anion radical. The second electron transfer to the dianion is followed by a chemical reaction producing a protonated species. The product of the fourth electron transfer also produces the corresponding amine compounds with a following reaction. Also every reduction wave was diffusion controlled. The first reduction wave is considerably reversible and the other waves are less reversible.

Keywords

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Cited by

  1. On the Electrochemical Reduction of 4‐(Thiazol‐2‐ylazo)‐Substituted 1‐Chloronaphthalenes: Formation and Characterization of Stable Radical Anions vol.7, pp.7, 1989, https://doi.org/10.1002/celc.202000121