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Description
| - The reduction mechanism of ioxynil (3,5-diiodo-4-hydroxy-benzonitrile), bromoxynil (3,5-dibromo-4-hydroxybenzonitrile) and chloroxynil (3,5-dichloro-4-hydroxybenzonitrile) was studied in dimethylsulfoxide by the electrochemical methods combined with FTIR spectroelectrochemical and GC/MS identification of the products. Cyclic voltammetry at different scan rates and at various concentrations of pesticides is consistent with the radical anion formation followed by the subsequent chemical reactions. The main decomposition pathway includes the cleavage of the halogen atom and the dimerization of the dehalogenated intermediate. The differences in the mechanism of ioxynil, bromoxynil and chloroxynil are caused by the mutual differences in the rates of the bond cleavage and the dimerization process.
- The reduction mechanism of ioxynil (3,5-diiodo-4-hydroxy-benzonitrile), bromoxynil (3,5-dibromo-4-hydroxybenzonitrile) and chloroxynil (3,5-dichloro-4-hydroxybenzonitrile) was studied in dimethylsulfoxide by the electrochemical methods combined with FTIR spectroelectrochemical and GC/MS identification of the products. Cyclic voltammetry at different scan rates and at various concentrations of pesticides is consistent with the radical anion formation followed by the subsequent chemical reactions. The main decomposition pathway includes the cleavage of the halogen atom and the dimerization of the dehalogenated intermediate. The differences in the mechanism of ioxynil, bromoxynil and chloroxynil are caused by the mutual differences in the rates of the bond cleavage and the dimerization process. (en)
- Byl studován redukční mechanismus ioxynilu (3,5-diiodo-4-hydroxybenzonitril), bromoxynilu (3,5-dibromo-4-hydroxybenzonitril) a chloroxynilu (3,5-dichloro-4-hydroxybenzonitril) v prostředí dimethylsulfoxidu. Elektrochemické metody byly doplněny identifikací produktů pomocí FTIR spektroelektrochemie a GC/MS. Charakter cyklické voltametrie při různých rychlostech polarizace a různých koncentracích pesticidů odpovídá mechanismu tvorby radikálanionu s následnými chemickými reakcemi. Při rozkladu dochází k odštěpení atomu halogenu a k dimerizaci dehalogenovaného meziproduktu. Rozdíl v redukčním mechanismu ioxynilu, bromoxynilu a chloroxynilu je dán rozdílnou rychlostí odštěpení halogenu a rychlostí procesu dimerizace. (cs)
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Title
| - Reduction of substituted benzonitrile pesticides
- Redukce substituovaných benzonitrilových pesticidů (cs)
- Reduction of substituted benzonitrile pesticides (en)
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skos:prefLabel
| - Reduction of substituted benzonitrile pesticides
- Redukce substituovaných benzonitrilových pesticidů (cs)
- Reduction of substituted benzonitrile pesticides (en)
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skos:notation
| - RIV/61388955:_____/08:00312176!RIV09-AV0-61388955
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http://linked.open...avai/riv/aktivita
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http://linked.open...avai/riv/aktivity
| - P(IAA400400505), P(LC510), P(OC 140), Z(AV0Z40400503), Z(AV0Z40550506)
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http://linked.open...iv/cisloPeriodika
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http://linked.open...vai/riv/dodaniDat
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http://linked.open...aciTvurceVysledku
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http://linked.open.../riv/druhVysledku
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http://linked.open...iv/duvernostUdaju
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http://linked.open...titaPredkladatele
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http://linked.open...dnocenehoVysledku
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http://linked.open...ai/riv/idVysledku
| - RIV/61388955:_____/08:00312176
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http://linked.open...riv/jazykVysledku
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http://linked.open.../riv/klicovaSlova
| - benzonitrile pesticides; polarography; voltammetry (en)
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http://linked.open.../riv/klicoveSlovo
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http://linked.open...odStatuVydavatele
| - CH - Švýcarská konfederace
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http://linked.open...ontrolniKodProRIV
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http://linked.open...i/riv/nazevZdroje
| - Journal of the Electroanalytical Chemistry and Journal of Electroanalytical Chemistry and Interfacial Electrochemistry
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http://linked.open...in/vavai/riv/obor
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http://linked.open...ichTvurcuVysledku
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http://linked.open...cetTvurcuVysledku
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http://linked.open...vavai/riv/projekt
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http://linked.open...UplatneniVysledku
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http://linked.open...v/svazekPeriodika
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http://linked.open...iv/tvurceVysledku
| - Fiedler, Jan
- Hromadová, Magdaléna
- Pospíšil, Lubomír
- Sokolová, Romana
- Valášek, Michal
- Giannarelli, S.
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http://linked.open...ain/vavai/riv/wos
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http://linked.open...n/vavai/riv/zamer
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issn
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number of pages
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is http://linked.open...avai/riv/vysledek
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