Evaluation of silica from different vendors as the solid support of anion-exchange chiral stationary phases by means of preferential sorption and liquid chromatography.

0511718 - ÚCHP 2020 RIV DE eng J - Journal Article
Kohout, P. - Hovorka, Š. - Herciková, J. - Wilk, M. - Sysel, P. - Izák, Pavel - Bartůněk, V. - von Baeckmann, C. - Pícha, Jan - Frühauf, P.
Evaluation of silica from different vendors as the solid support of anion-exchange chiral stationary phases by means of preferential sorption and liquid chromatography.
Journal of Separation Science. Roč. 42, č. 24 (2019), s. 3653-3661. ISSN 1615-9306. E-ISSN 1615-9314
R&D Projects: GA ČR(CZ) GA17-00089S
Institutional support: RVO:67985858 ; RVO:61388963
Keywords : chiral anion exchanger * preferential sorption * liquid chromatography
OECD category: Chemical process engineering; Analytical chemistry (UOCHB-X)
Impact factor: 2.878, year: 2019
Method of publishing: Limited access

Chromatographic performance of a chiral stationary phase is significantly influenced by the employed solid support. Properties of the most commonly used support, silica particles, such as size and size distribution, and pore size are of utmost importance for both superficially porous particles and fully porous particles. In this work, we have focused on evaluation of fully porous particles from three different vendors as solid supports for a brush-type chiral stationary phase based on 9-O-tert-butylcarbamoyl quinidine. We have prepared corresponding stationary phases under identical experimental conditions and determined the parameters of the modified silica by physisorption measurements and scanning electron microscopy. Enantiorecognition properties of the chiral stationary phases have been studied using preferential sorption experiments. The same material was slurry-packed into chromatographic columns and the chromatographic properties have been evaluated in liquid chromatography. We show that preferential sorption can provide valuable information about the influence of the pore size and total pore volume on the interaction of analytes of different size with the chirally-modified silica surface. The data can be used to understand differences observed in chromatographic evaluation of the chiral stationary phases. The combination of preferential sorption and liquid chromatography separation can provide detailed information on new chiral stationary phases.
Permanent Link: http://hdl.handle.net/11104/0303439