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Collect. Czech. Chem. Commun. 1993, 58, 41-46
https://doi.org/10.1135/cccc19930041

Electroreduction of Aromatic Nitro Compounds: Case for Comparison of Information Obtained by Polarography and Voltammetry

Petr Zuman

Department of Chemistry, Clarkson University, Potsdam, New York 13699-5810, U.S.A.

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  • Vidláková Pavlína, Pivoňková Hana, Fojta Miroslav, Havran Luděk: Electrochemical behavior of anthraquinone- and nitrophenyl-labeled deoxynucleoside triphosphates: a contribution to development of multipotential redox labeling of DNA. Monatsh Chem 2015, 146, 839. <https://doi.org/10.1007/s00706-015-1435-6>
  • Balintová Jana, Pohl Radek, Horáková Petra, Vidláková Pavlína, Havran Luděk, Fojta Miroslav, Hocek Michal: Anthraquinone as a Redox Label for DNA: Synthesis, Enzymatic Incorporation, and Electrochemistry of Anthraquinone‐Modified Nucleosides, Nucleotides, and DNA. Chemistry A European J 2011, 17, 14063. <https://doi.org/10.1002/chem.201101883>
  • Ghoneim Mohamed M., El-Desoky Hanaa S., Abdel-Galeil Mohamed M.: Electrochemistry of the antibacterial and antifungal drug nitroxoline and its determination in bulk form, pharmaceutical formulation and human blood. Bioelectrochem 2011, 80, 162. <https://doi.org/10.1016/j.bioelechem.2010.08.003>
  • Vyskočil Vlastimil, Labuda Ján, Barek Jiří: Voltammetric detection of damage to DNA caused by nitro derivatives of fluorene using an electrochemical DNA biosensor. Anal Bioanal Chem 2010, 397, 233. <https://doi.org/10.1007/s00216-010-3517-y>
  • Vyskočil Vlastimil, Barek Jiří: Polarographic and voltammetric study of genotoxic 2,7-dinitrofluoren-9-one and its determination using mercury electrodes. Collect. Czech. Chem. Commun. 2009, 74, 1675. <https://doi.org/10.1135/cccc2009108>
  • Čížek Karel, Barek Jiří, Zima Jiří: Polarographic and Voltammetric Determination of Trace Amounts of 3-Nitrofluoranthene. Collect. Czech. Chem. Commun. 2006, 71, 1571. <https://doi.org/10.1135/cccc20061571>
  • Martre Anne-Marie, Mousset Guy, Cosoveanu Veronica, Danciu Virginia: Electroréduction de dérivés dinitrés aromatiques. V. influences du matériau d'électrode et de systèmes rédox sur les réductions du 4,4′-dinitrodibenzyle et de l'acide 4,4′-dinitrostilbène-2,2′-disulfonique. Can J Chem 1996, 74, 1409. <https://doi.org/10.1139/v96-159>