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
Hauptverfasser: Tanaka, Koichi, Muraoka, Toshihide, Otubo, Yasuhiro, Takahashi, Hiroki, Ohnishi, Atsushi
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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.
ISSN:2046-2069
2046-2069
DOI:10.1039/c5ra26520g