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  • The reduction mechanism of ioxynil (3,5-diiodo-4-hydroxy-benzonitrile) was studied in dimethylsulfoxide using the electrochemical methods (tast polarography, cyclic voltammetry and controlled potential electrolysis) combined with GC/MS identification of products. The reduction is accompanied by the cleavage of iodide yielding 3-iodo-4-hydroxybenzonitrile. Surprisingly, this process requires only one electron for the exhaustive electrolysis of the starting compound. We showed that the apparent one electron reduction observed in the aprotic solvent is due to the autoprotonation by another molecule of ioxynil. The overall one electron reduction (uptake of two electrons per two molecules of ioxynil) is changed in the presence of a strong proton donor to a two electron process per one molecule.
  • The reduction mechanism of ioxynil (3,5-diiodo-4-hydroxy-benzonitrile) was studied in dimethylsulfoxide using the electrochemical methods (tast polarography, cyclic voltammetry and controlled potential electrolysis) combined with GC/MS identification of products. The reduction is accompanied by the cleavage of iodide yielding 3-iodo-4-hydroxybenzonitrile. Surprisingly, this process requires only one electron for the exhaustive electrolysis of the starting compound. We showed that the apparent one electron reduction observed in the aprotic solvent is due to the autoprotonation by another molecule of ioxynil. The overall one electron reduction (uptake of two electrons per two molecules of ioxynil) is changed in the presence of a strong proton donor to a two electron process per one molecule. (en)
Title
  • The autoprotonation in reduction mechanism of pesticide ioxynil
  • The autoprotonation in reduction mechanism of pesticide ioxynil (en)
skos:prefLabel
  • The autoprotonation in reduction mechanism of pesticide ioxynil
  • The autoprotonation in reduction mechanism of pesticide ioxynil (en)
skos:notation
  • RIV/61388955:_____/10:00348590!RIV11-GA0-61388955
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(GA203/08/1157), P(GA203/09/1607), P(LC510), P(OC 140), Z(AV0Z40400503)
http://linked.open...iv/cisloPeriodika
  • 27
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 248260
http://linked.open...ai/riv/idVysledku
  • RIV/61388955:_____/10:00348590
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • autoprotonation; organic halides; polarography (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • GB - Spojené království Velké Británie a Severního Irska
http://linked.open...ontrolniKodProRIV
  • [7BEEA4173BFA]
http://linked.open...i/riv/nazevZdroje
  • Electrochimica acta
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 55
http://linked.open...iv/tvurceVysledku
  • Hromadová, Magdaléna
  • Pospíšil, Lubomír
  • Sokolová, Romana
  • Ludvík, Jiří
  • Giannarelli, S.
http://linked.open...ain/vavai/riv/wos
  • 000284434700080
http://linked.open...n/vavai/riv/zamer
issn
  • 0013-4686
number of pages
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