Preparation and Application of Aza-15-crown-5-capped Methylcalix[4]resorcinarene-Bonded Silica Particles for Use as Chiral Stationary Phase in HPLC

Aza-15-crown-5-capped (3-( C -methylcalix[4]resorcinarene)-2-hydroxypropoxy)-propylsilyl (MCR-HP)-appended silica particles (15C5-MCR-HPS), a new type of substituted C -methylcalix[4]resorcinarene (MCR)-bonded chiral stationary phase (CSP) for high-performance liquid chromatography (HPLC), have been...

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Veröffentlicht in:Chromatographia 2017-07, Vol.80 (7), p.1007-1014
Hauptverfasser: Ma, Mingxuan, Wei, Qunli, Meng, Min, Yin, Jiale, Shan, Yu, Du, Lei, Zhu, Xia, Soh, Shu Fang, Min, Mengjun, Zhou, Xueyan, Yin, Xiaoxing, Gong, Yinhan
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Sprache:eng
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Zusammenfassung:Aza-15-crown-5-capped (3-( C -methylcalix[4]resorcinarene)-2-hydroxypropoxy)-propylsilyl (MCR-HP)-appended silica particles (15C5-MCR-HPS), a new type of substituted C -methylcalix[4]resorcinarene (MCR)-bonded chiral stationary phase (CSP) for high-performance liquid chromatography (HPLC), have been synthesized by reaction of bromoacetate-substituted MCR-HPS with excessive aza-15-crown-5 in anhydrous acetonitrile in the presence of potassium carbonate. The bonded phase 15C5-MCR-HPS is characterized by elemental analysis and further evaluated by separating several disubstituted benzenes and some chiral drug compounds in HPLC. The new CSP has a chiral selector with two recognition sites: 15-crown-5 and MCR-HP, which can provide cooperative multiple interactions with solutes to enhance chiral recognition and to improve chromatographic separation. The chromatographic evaluation results show that 15C5-MCR-HPS has excellent selectivity for the separation of aromatic positional isomers and enantiomers of some chiral compounds under multiple-mode mobile phase conditions including normal phase, reversed phase, and polar organic mobile phase conditions. Graphical abstract
ISSN:0009-5893
1612-1112
DOI:10.1007/s10337-017-3312-4