HPLC enantioseparation on a homochiral MOF-silica composite as a novel chiral stationary phase
The last frontier in the development of chiral stationary phases for chromatographic enantioseparation involves homochiral metal-organic frameworks (MOFs). Using enantiopure ( R )-2,2′-dihydroxy-1,1′-binaphthalene-6,6′-dicarboxylic acid as a starting material, we prepared three homochiral MOFs that...
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Veröffentlicht in: | RSC advances 2016-01, Vol.6 (26), p.21293-2131 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The last frontier in the development of chiral stationary phases for chromatographic enantioseparation involves homochiral metal-organic frameworks (MOFs). Using enantiopure (
R
)-2,2′-dihydroxy-1,1′-binaphthalene-6,6′-dicarboxylic acid as a starting material, we prepared three homochiral MOFs that were further used as chiral stationary phases for high-performance liquid chromatography to separate the enantiomers of various kinds of racemic sulfoxides,
sec
-alcohols, β-lactams, benzoins, flavanones and epoxides. The experimental results showed excellent performances for enantioseparation, and highlighted that enantioseparation on homochiral MOF columns is practical.
Using enantiopure (
R
)-2,2′-dihydroxy-1,1′-binaphthalene-6,6′-dicarboxylic acid as a starting material, we prepared three homochiral MOFs that were further used as chiral stationary phases for HPLC to separate the enantiomers. |
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ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/c5ra26520g |