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  • 1
    ISSN: 1040-7685
    Keywords: capillary column gas chromatography ; nitrophenyl polysiloxanes ; stationary phases ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Nitrophenyl-, nitrophenylethyl-, dinitrophenylethyl-, and methoxynitrophen- ylethyl-substituted polysiloxanes (25-50% substitution) have been synthesized and evaluated as stationary phases in capillary column gas chromatography. Phases with 25% substitution and with ethylene spacers between the phenyl substituents and the polysiloxane backbone were found to provide high efficiencies, moderate thermal stabilities, and useful selectivities. Without flexible hydrocarbon spacers, the station- ary phases exhibited poor efficiencies. The 50% substituted phases generally provided narrower operational temperature ranges and lower efficiencies, and they were more difficult to immobilize by free radical crosslinking. Several methods of immobilization were evaluated, and a dynamic procedure with dicumylperoxide (DCP) was found to produce the best results for these nitrophenyl-containing phases. The enhancements in polarity resulting from the resonances of the nitrophenyl substituent groups pro- vided unique selectivities for specific applications involving aromatic compounds. The dinitrophenyl-containing phases showed, in addition, selectivity based on charge transfer complex formation.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1040-7685
    Keywords: capillary column gas chromatography ; cyanophenyl polysiloxane ; stationary phases ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New p-cyanophenylethylpolysiloxane and p-cyanophenylpolysiloxane stationary phases exhibiting high efficiency, cross-Iinkability, and thermal stability up to 300°C are reported in this paper. These stationary phases possess a unique blend of polar and polarizable character that has resulted in excellent selectivities for compounds having delocalized nelectrons. Another advantage of the p-cyanophenyl phases is their demonstrated relatively low elution temperatures for polar materials compared with the typical cyanopropyl polysiloxane phases.
    Additional Material: 7 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electrophoresis 18 (1997), S. 1002-1006 
    ISSN: 0173-0835
    Keywords: Chiral separations ; Disopyramide ; Capillary electrophoresis ; Cyclodextrin additives ; Role of pH ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Enantiomers of disopyramide display different biological actions, and therefore chiral selective analysis is necessary. Fifteen different cyclodextrins (CDs) and CD derivatives were tested as capillary electrophoresis (CE) additives for the chiral separation of disopyramide. Eleven types of CDs showed chiral recognition features and four types had a baseline or close to baseline separation. The best resolution (Rs = 3.0) was with 15 mM carboxymethylated β-CD (pH 4.9). A sharp decrease in the selectivity of γ-phosphate (γ-PhoCD) was observed in the pH range of 2-3, indicating a structural change of γ-PhoCD. The enantiomers of disopyramide were separated in its ionized as well as neutral forms using acidic substituted CDs. The results show that the size of the CD cavity can not be used as a guide to estimate chiral separations, suggesting a more complex separation mechanism of these CDs towars disopyramide.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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