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Preparation of chiral metal-organic framework L-his-MIL-53-NH2@SiO2 composite by in situ growth and chiral post-modification strategies for HPLC enantiomeric separation.

Authors :
An-Xu Ma
Cai-Fang Liu
Yu-Lan Zhu
Zong-Hong Luo
Hong-Mei Zhou
Yue Zhang
Bang-Jin Wang
Jun-Hui Zhang
Sheng-Ming Xie
Li-Ming Yuan
Source :
New Journal of Chemistry. 6/7/2024, Vol. 48 Issue 21, p9702-9708. 7p.
Publication Year :
2024

Abstract

In this work, a chiral core-shell microspheres composite, L-his-MIL-53-NH2@SiO2, was prepared through in situ growth and chiral post-modification strategies. The core-shell microspheres were applied as a novel chiral stationary phase for HPLC enantiomeric separation. Various racemates were separated on the L-his-MIL-53-NH2@SiO2 packed column using n-hexane/isopropanol as the mobile phase. The chiral column showed excellent separation efficiency for fourteen chiral compounds, including alcohols, alkanes, esters, phenols, ketones, and organic acids. The influence of injection mass and temperature on the separation performance of the chiral column were investigated. The relative standard deviations (n = 5) of the retention time and peak area by repeated separation of benzoin are 0.28% and 0.63%, respectively. The results show that the L-his-MIL-53-NH2@SiO2 packed column exhibited good reproducibility and stability. In addition, the chiral resolution ability of the L-his-MIL-53-NH2@SiO2 packed column was compared with that of a commercial chiral column (Chiralpak AD-H). The L-his-MIL-53-NH2@SiO2 packed column exhibits unique advantages in chiral separations that can be complementary to the commercial chiral column. It was demonstrated that the chiral core-shell microspheres composite L-his-MIL-53-NH2@SiO2 prepared based on in situ growth and chiral postmodification strategies has great potential for enantiomeric separation by HPLC. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
11440546
Volume :
48
Issue :
21
Database :
Academic Search Index
Journal :
New Journal of Chemistry
Publication Type :
Academic Journal
Accession number :
177548928
Full Text :
https://doi.org/10.1039/d4nj00557k