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Description
| - The separation of the two two-electron waves in acidic media in solutions of some aromatic aldoximes and ketoximes is attributed to differences between the pK(a)-values of oximes (which are smaller than about 1.0) and those of protonated forms of corresponding in-tines. Dependences of halfwave potentials on pH show that the lower limit pK(a) of imine varies from -0.25 for p-formylbenzaldehyde oxime to 2.2 for p-fluorobenzaldehyde oxime. For the benzaldehyde and acetophenone oximes bearing substituents, which have pKa higher than -1.50, a good agreement was observed for pK(a)-values obtained spectrophotometrically and pK(ox) values obtained from the change in the slope of E-1/2(1) = f(H-0) plots. Past misrepresentations of the electroreduction mechanism of protonated forms of imines is attributed to insufficiently controlled compositions of supporting electrolytes.
- The separation of the two two-electron waves in acidic media in solutions of some aromatic aldoximes and ketoximes is attributed to differences between the pK(a)-values of oximes (which are smaller than about 1.0) and those of protonated forms of corresponding in-tines. Dependences of halfwave potentials on pH show that the lower limit pK(a) of imine varies from -0.25 for p-formylbenzaldehyde oxime to 2.2 for p-fluorobenzaldehyde oxime. For the benzaldehyde and acetophenone oximes bearing substituents, which have pKa higher than -1.50, a good agreement was observed for pK(a)-values obtained spectrophotometrically and pK(ox) values obtained from the change in the slope of E-1/2(1) = f(H-0) plots. Past misrepresentations of the electroreduction mechanism of protonated forms of imines is attributed to insufficiently controlled compositions of supporting electrolytes. (en)
- Separace dvou 2-elektronových redukčních vln aromatických aldoximů a ketoximů v kyselém prostředí je způsobena rozdílem mezi pKa výchozích oximů a pKa protonované formy příslušného iminového meziproduktu. Na základě elektrochemických dat bylo zjištěno, že hodnoty pKa studovaných iminů jsou mezi -1,5 až 2,2 a tyto výsledky byly potvrzeny spektrofotometricky. Byl diskutován vliv koncentrace halogenidů v základním elektrolytu. (cs)
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Title
| - Two reduction waves of oximes and imine formation in acidic media
- Dvě redukční vlny oximů a tvorba iminů v kyselém prostředí (cs)
- Two reduction waves of oximes and imine formation in acidic media (en)
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skos:prefLabel
| - Two reduction waves of oximes and imine formation in acidic media
- Dvě redukční vlny oximů a tvorba iminů v kyselém prostředí (cs)
- Two reduction waves of oximes and imine formation in acidic media (en)
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skos:notation
| - RIV/61388955:_____/06:00085403!RIV08-MSM-61388955
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http://linked.open.../vavai/riv/strany
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http://linked.open...avai/riv/aktivita
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http://linked.open...avai/riv/aktivity
| - P(1P05ME785), Z(AV0Z40400503)
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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:_____/06:00085403
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http://linked.open...riv/jazykVysledku
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http://linked.open.../riv/klicovaSlova
| - oximes; electroreduction; polarography (en)
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http://linked.open.../riv/klicoveSlovo
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http://linked.open...odStatuVydavatele
| - GB - Spojené království Velké Británie a Severního Irska
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http://linked.open...ontrolniKodProRIV
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http://linked.open...i/riv/nazevZdroje
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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
| - Ludvík, Jiří
- Celik, H.
- Zuman, P.
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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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