6533b829fe1ef96bd128a576
RESEARCH PRODUCT
Photografted methacrylate-based monolithic columns coated with cellulose tris(3,5-dimethylphenylcarbamate) for chiral separation in CEC
Enrique Javier Carrasco-correaMario RetaRomina Noel EchevarriaSonia KeunchkarianJosé Manuel Herrero-martínezsubject
inorganic chemicalsCHIRAL MONOLITHIC ORGANIC COLUMNSMonolithic HPLC columnFiltration and Separation02 engineering and technology01 natural sciencesEnantioseparationAnalytical Chemistry//purl.org/becyt/ford/1 [https]chemistry.chemical_compoundCapillary electrochromatographyMonolithic hplc columnPhotografting//purl.org/becyt/ford/1.4 [https]AcetonitrileCelluloseMonolithCelluloseAcetonitrileCELLULOSE TRIS(35-DIMETHYLPHENYLCARBAMATE)ChromatographyCapillary electrochromatographygeographyCellulose tris(35-dimethylphenylcarbamate)Chromatographygeography.geographical_feature_categoryCAPILLARY ELECTROCHROMATOGRAPHYEnantiomer010401 analytical chemistryCiencias QuímicasENANTIOSEPARATIONQuímica021001 nanoscience & nanotechnologyChiral monolithic organic columns0104 chemical sciencesMonomerChemistryMonomerchemistryPhotograftingPHOTOGRAFTINGQuímica AnalíticaEnantiomer0210 nano-technologyMonolithCIENCIAS NATURALES Y EXACTASdescription
A chiral capillary monolithic column for enantiomer separation in capillary electrochromatography was prepared by coating cellulose tris(3,5-dimethylphenylcarbamate) on porous glycidyl methacrylate-co-ethylene dimethacrylate monolith in capillary format grafted with chains of [2(methacryloyloxy)ethyl] trimethylammonium chloride. The surface modification of the monolith by the photografting of [2(methacryloyloxy)ethyl] trimethylammonium chloride monomer as well as the coating conditions of cellulose tris(3,5-dimethylphenylcarbamate) onto the grafted monolithic scaffold were optimized to obtain a stable and reproducible chiral stationary phase for capillary electrochromatography. The effect of organic modifier (acetonitrile) in aqueous mobile phase for the enantiomer separation by capillary electrochromatography was also investigated. Several pairs of enantiomers including acidic, neutral, and basic analytes were tested and most of them were partially or completely resolved under aqueous mobile phases. The prepared monolithic chiral stationary phases exhibited a good stability, repeatability, and column-to-column reproducibility, with relative standard deviations below 11% in the studied electrochromatographic parameters.
year | journal | country | edition | language |
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2018-03-01 |