dc.contributor.author | Aydoǧan, C. and Denizli, A. | |
dc.date.accessioned | 2021-04-08T12:09:29Z | |
dc.date.available | 2021-04-08T12:09:29Z | |
dc.date.issued | 2014 | |
dc.identifier | 10.1016/j.ab.2013.11.006 | |
dc.identifier.issn | 00032697 | |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-84891368607&doi=10.1016%2fj.ab.2013.11.006&partnerID=40&md5=68a0d016401098ed316bfa55cbf88da3 | |
dc.identifier.uri | http://acikerisim.bingol.edu.tr/handle/20.500.12898/4841 | |
dc.description.abstract | Chiral ligand-exchange enantioseparation of aliphatic and aromatic amino acids was successfully performed using a new open-tubular zwitterionic column with tentacle-type polymer stationary phase. The polymeric stationary phase was prepared using 3-chloro-2-hydroxypropyl methacrylate (HPMA-Cl), a new reactive monomer. The preparation procedure of the open-tubular column included silanization, in situ graft polymerization with HPMA-Cl, and l-histidine (l-His) modification. l-His was used as a chiral ligand-exchange selector and copper(II) as a central ion. Successful enantioseparation of six pairs of amino acid enantiomers was achieved with a buffer of 5 mM CuSO4, 20 mM (NH4)2SO4 at pH 3.0. © 2013 Elsevier Inc. All rights reserved. | |
dc.language.iso | English | |
dc.source | Analytical Biochemistry | |
dc.title | Chiral separation-based ligand exchange by open-tubular capillary electrochromatography | |