Quinine bonded to superficially porous particles for high-efficiency and ultrafast liquid and supercritical fluid chromatography

被引:57
作者
Patel, Darshan C. [1 ]
Breitbach, Zachary S. [1 ]
Yu, JeongJae [1 ,2 ]
Nguyen, Kate A. [1 ]
Armstrong, Daniel W. [1 ]
机构
[1] Univ Texas Arlington, Dept Chem & Biochem, 700 Planetarium Pl, Arlington, TX 76019 USA
[2] Kyungpook Natl Univ, Dept Chem, Daegu 702701, South Korea
关键词
Chiral separations; Superficially porous particles; High-efficiency chiral stationary phase; Ultra-high performance liquid; chromatography (UHPLC); Sub/ supercritical fluid chromatography (SFC); Kinetic plots; CHIRAL STATIONARY PHASES; CORE-SHELL; REPRESENTATION METHODS; MESOPOROUS SILICA; ANION-EXCHANGERS; AMINO-ACIDS; PERFORMANCE; SEPARATION; RESOLUTION; SELECTORS;
D O I
10.1016/j.aca.2017.02.005
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Two new anion-exchange columns were prepared by bonding tert-butyl carbamoylated quinine to 2.7 mu m superficially porous particle (SPP) silica to create chiral stationary phases for high-efficiency and ultrafast chromatography. Performance and retention parameters of these new columns are compared with an analogous 5 mu m fully porous particle (FPP) based Chiralpak QNAX column and a 3-4 fold increase in efficiency was observed. Ultrafast separations ranging from 12 s down to sub-second are shown using 2.7 mu m SPPs bonded via hydrosilation to the selector. Potential benefits of 2.7 mu m SPP based columns for increased LC-MS compatibility were investigated. A van Deemter plot comparison showed 2.7 mu m SPP based columns provided a lower reduced plate height and a higher optimal linear velocity compared to the 5 mm FPP based column. With geometry-independent kinetic plots, 2.7 mu m SPP and 5 mu m FPP based columns were assessed for their kinetic performance and the maximal number of plates each column can generate in a given analysis time. The 2.7 mu m SPP based column showed remarkable performance improvements in speed and efficiency as indicated by the kinetic plots. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:164 / 174
页数:11
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