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  • 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)
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)
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)
skos:notation
  • RIV/61388955:_____/06:00085403!RIV08-MSM-61388955
http://linked.open.../vavai/riv/strany
  • 5845;5852
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(1P05ME785), Z(AV0Z40400503)
http://linked.open...iv/cisloPeriodika
  • 26
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
  • 504638
http://linked.open...ai/riv/idVysledku
  • RIV/61388955:_____/06:00085403
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • oximes; electroreduction; polarography (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • GB - Spojené království Velké Británie a Severního Irska
http://linked.open...ontrolniKodProRIV
  • [CF13E3FA9FB2]
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
  • 51
http://linked.open...iv/tvurceVysledku
  • Ludvík, Jiří
  • Celik, H.
  • Zuman, P.
http://linked.open...n/vavai/riv/zamer
issn
  • 0013-4686
number of pages
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