About: Advanced statistical evaluation of the complex formation constants from electrophoretic data II - Diastereomeric ion-pairs of (R,S)-N-(3,5-dinitrobenzoyl)leucine and tert-butylcarbamoylquinine     Goto   Sponge   NotDistinct   Permalink

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Description
  • Byla prováděna pokročilá statistická vyhodnocení konstant stability komplexů z elektroforetických dat II - diastereometrické iontové páry (R,S)-N-(3,5-dinitrobenzoyl)leucinu a terc-butylcarbamoylquininu. (cs)
  • Intermolecular association and ion-pair formation, respectively, between a cationic chiral selector, viz. o-9-(tert-butylcarbamoyl) quinine (CQN), and the both enantiomers of anionic N-(3,5-dinitrobenzoyl)leucine, (R)-DNB-Leu and (S)-DNB-Leu, were investigated by affinity capillary electrophoresis (ACE). Thus, binding constants of the both diastereomeric ion-pairs, (R) and (S)-DNB-Leu/CQN associates, were determined by different experimental setups and correction of nonlinear effects. A reciprocal setup was employed for the high-affinity (S)-enantiomer, and the experimental mobility data obtained for CQN at variable (S)-DNB-Leu concentrations in the background electrolyte were linearized and evaluated by advanced statistical model. A binding constant of K-S = 125.11 mol(-1) was afforded. The constant for the (R)-enantiomer, which is outside the range suitable for direct affinity CE, was obtained from indirect affinity CE utilizing the separation of the DNB-Leu racemate at a single appropriate CQN conc
  • Intermolecular association and ion-pair formation, respectively, between a cationic chiral selector, viz. o-9-(tert-butylcarbamoyl) quinine (CQN), and the both enantiomers of anionic N-(3,5-dinitrobenzoyl)leucine, (R)-DNB-Leu and (S)-DNB-Leu, were investigated by affinity capillary electrophoresis (ACE). Thus, binding constants of the both diastereomeric ion-pairs, (R) and (S)-DNB-Leu/CQN associates, were determined by different experimental setups and correction of nonlinear effects. A reciprocal setup was employed for the high-affinity (S)-enantiomer, and the experimental mobility data obtained for CQN at variable (S)-DNB-Leu concentrations in the background electrolyte were linearized and evaluated by advanced statistical model. A binding constant of K-S = 125.11 mol(-1) was afforded. The constant for the (R)-enantiomer, which is outside the range suitable for direct affinity CE, was obtained from indirect affinity CE utilizing the separation of the DNB-Leu racemate at a single appropriate CQN conc (en)
Title
  • Advanced statistical evaluation of the complex formation constants from electrophoretic data II - Diastereomeric ion-pairs of (R,S)-N-(3,5-dinitrobenzoyl)leucine and tert-butylcarbamoylquinine
  • Advanced statistical evaluation of the complex formation constants from electrophoretic data II - Diastereomeric ion-pairs of (R,S)-N-(3,5-dinitrobenzoyl)leucine and tert-butylcarbamoylquinine (en)
  • Pokročilé statistické vyhodnocení konstant stability komplexů z elektroforetických dat II - diastereometrické iontové páry (R,S)-N-(3,5-dinitrobenzoyl)leucinu a terc-butylcarbamoylquininu (cs)
skos:prefLabel
  • Advanced statistical evaluation of the complex formation constants from electrophoretic data II - Diastereomeric ion-pairs of (R,S)-N-(3,5-dinitrobenzoyl)leucine and tert-butylcarbamoylquinine
  • Advanced statistical evaluation of the complex formation constants from electrophoretic data II - Diastereomeric ion-pairs of (R,S)-N-(3,5-dinitrobenzoyl)leucine and tert-butylcarbamoylquinine (en)
  • Pokročilé statistické vyhodnocení konstant stability komplexů z elektroforetických dat II - diastereometrické iontové páry (R,S)-N-(3,5-dinitrobenzoyl)leucinu a terc-butylcarbamoylquininu (cs)
skos:notation
  • RIV/61989592:15310/04:00002045!RIV/2005/MSM/153105/N
http://linked.open.../vavai/riv/strany
  • 105-113
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • Z(MSM 153100013)
http://linked.open...iv/cisloPeriodika
  • 1
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
  • 553611
http://linked.open...ai/riv/idVysledku
  • RIV/61989592:15310/04:00002045
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • statistical theory of experiment;advanced statistical evaluation;binding constants;ion-pair formation constants;affinity capillary electrophoresis;leucine;tert-butyl carbamoyl quinine (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • NL - Nizozemsko
http://linked.open...ontrolniKodProRIV
  • [2A4D592998A6]
http://linked.open...i/riv/nazevZdroje
  • Analytica Chimica Acta
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 506
http://linked.open...iv/tvurceVysledku
  • Barták, Petr
  • Bednář, Petr
  • Kubáček, Lubomír
  • Stránský, Zdeněk
  • Lindner, W.
  • Lammerhofer, M.
http://linked.open...n/vavai/riv/zamer
issn
  • 0003-2670
number of pages
http://localhost/t...ganizacniJednotka
  • 15310
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