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dc.date.accessioned 2021-09-17T14:16:22Z
dc.date.available 2021-09-17T14:16:22Z
dc.date.issued 2018
dc.identifier.uri http://sedici.unlp.edu.ar/handle/10915/125064
dc.description.abstract 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. en
dc.format.extent 1424-1432 es
dc.language en es
dc.subject Monolithic hplc column es
dc.subject Monolith es
dc.subject Monomer es
dc.subject Chemistry es
dc.subject Acetonitrile es
dc.subject Photografting es
dc.subject Cellulose es
dc.subject Capillary electrochromatography es
dc.subject Chromatography es
dc.subject Enantiomer es
dc.subject Cellulose tris(3,5-dimethylphenylcarbamate) es
dc.subject Chiral monolithic organic columns es
dc.subject Enantioseparation es
dc.title Photografted methacrylate-based monolithic columns coated with cellulose tris(3,5-dimethylphenylcarbamate) for chiral separation in CEC en
dc.type Articulo es
sedici.identifier.other pmid:29385319 es
sedici.identifier.other doi:10.1002/jssc.201701234 es
sedici.identifier.issn 1615-9314 es
sedici.identifier.issn 1615-9306 es
sedici.creator.person Echevarría, Romina Noel es
sedici.creator.person Carrasco Correa, Enrique Javier es
sedici.creator.person Keunchkarian, Sonia es
sedici.creator.person Reta, Mario Roberto es
sedici.creator.person Herrero Martínez, José Manuel es
sedici.subject.materias Química es
sedici.description.fulltext true es
mods.originInfo.place Laboratorio de Investigación y Desarrollo de Métodos Analíticos (LIDMA) es
sedici.subtype Preprint es
sedici.rights.license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
sedici.rights.uri http://creativecommons.org/licenses/by-nc-sa/4.0/
sedici.description.peerReview peer-review es
sedici.relation.journalTitle Journal of Separation Science es
sedici.relation.journalVolumeAndIssue vol. 41, no. 6 es


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Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) Excepto donde se diga explícitamente, este item se publica bajo la siguiente licencia Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)