Please use this identifier to cite or link to this item: https://doi.org/10.1002/chir.20983
Title: Preparation and application of methylcalix[4]resorcinarene-bonded silica particles as chiral stationary phase in high-performance liquid chromatography
Authors: Tan, H.M.
Soh, S.F.
Zhao, J.
Yong, E.L.
Gong, Y. 
Keywords: C-methylcalix[4]resorcinarene
chiral separation
chiral stationary phase
high-performance liquid chromatography
Issue Date: 2011
Citation: Tan, H.M., Soh, S.F., Zhao, J., Yong, E.L., Gong, Y. (2011). Preparation and application of methylcalix[4]resorcinarene-bonded silica particles as chiral stationary phase in high-performance liquid chromatography. Chirality 23 (1 E) : E91-E97. ScholarBank@NUS Repository. https://doi.org/10.1002/chir.20983
Abstract: Two new types of methylcalix[4]resorcinarene-bonded stationary phases, (3-(C-methylcalix[4]resorcinarene)-2-hydroxypropoxy)-propylsilyl-appended silica particles (MCR-HPS) and bromoacetate-substituted MCR-HPS particles (BAMCR-HPS), have been synthesized and used as chiral stationary phases for high-performance liquid chromatography (HPLC) for the first time. The synthetic stationary phases are characterized by means of elemental analysis and Fourier-transform infrared spectroscopy. The chromatographic behavior of MCR-HPS and BAMCR-HPS was studied with several disubstituted benzenes and some chiral drug compounds under both normal phase and reversed-phase conditions. The results show that MCR-HPS has excellent selectivity for the separation of aromatic positional isomers and BAMCR-HPS exhibits excellent performance for separation of enantiomers of chiral compounds. © 2011 Wiley Periodicals, Inc.
Source Title: Chirality
URI: http://scholarbank.nus.edu.sg/handle/10635/109529
ISSN: 08990042
DOI: 10.1002/chir.20983
Appears in Collections:Staff Publications

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