Study of polyaniline-coated silica gel as a stationary phase in different modes of capillary liquid chromatography
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F17%3A10362649" target="_blank" >RIV/00216208:11310/17:10362649 - isvavai.cz</a>
Výsledek na webu
<a href="http://dx.doi.org/10.1007/s00706-017-1965-1" target="_blank" >http://dx.doi.org/10.1007/s00706-017-1965-1</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1007/s00706-017-1965-1" target="_blank" >10.1007/s00706-017-1965-1</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Study of polyaniline-coated silica gel as a stationary phase in different modes of capillary liquid chromatography
Popis výsledku v původním jazyce
Separation potential of a stationary phase based on polyaniline-coated silica gel porous spherical particles was investigated in different chromatographic modes of capillary liquid chromatography. L-Tryptophan and three of its structural derivatives with modified amino or carboxylic functionality were used to investigate the retention factor curves under different mobile phase composition including pH variation. Some retention curves pass minimum which indicates that more than one chromatographic mode can be employed to retain the relevant solute. The positional isomers of aminoacetophenone and caffeine and its demethylated analogs-theobromine and theophylline-were used as separation probes in normal phase, hydrophilic interaction liquid chromatography, and reversed phase modes. The stationary phase exhibits the mixed-mode retention mechanism; therefore, it is not easy to predict the elution order of the solutes only according to their polarity. Even slightly hydrophilic compounds can be sufficiently retained in reversed phase mode using polyaniline-coated silica gel stationary phase. All positional isomers of aminoacetophenone were separated for the first time in normal phase and reversed phase modes.
Název v anglickém jazyce
Study of polyaniline-coated silica gel as a stationary phase in different modes of capillary liquid chromatography
Popis výsledku anglicky
Separation potential of a stationary phase based on polyaniline-coated silica gel porous spherical particles was investigated in different chromatographic modes of capillary liquid chromatography. L-Tryptophan and three of its structural derivatives with modified amino or carboxylic functionality were used to investigate the retention factor curves under different mobile phase composition including pH variation. Some retention curves pass minimum which indicates that more than one chromatographic mode can be employed to retain the relevant solute. The positional isomers of aminoacetophenone and caffeine and its demethylated analogs-theobromine and theophylline-were used as separation probes in normal phase, hydrophilic interaction liquid chromatography, and reversed phase modes. The stationary phase exhibits the mixed-mode retention mechanism; therefore, it is not easy to predict the elution order of the solutes only according to their polarity. Even slightly hydrophilic compounds can be sufficiently retained in reversed phase mode using polyaniline-coated silica gel stationary phase. All positional isomers of aminoacetophenone were separated for the first time in normal phase and reversed phase modes.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10406 - Analytical chemistry
Návaznosti výsledku
Projekt
—
Návaznosti
S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2017
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Monatshefte für Chemie - Chemical Monthly
ISSN
0026-9247
e-ISSN
—
Svazek periodika
148
Číslo periodika v rámci svazku
9
Stát vydavatele periodika
AT - Rakouská republika
Počet stran výsledku
7
Strana od-do
1605-1611
Kód UT WoS článku
000407126500007
EID výsledku v databázi Scopus
2-s2.0-85021811931