Chiral recognition of binaphthyl derivatives: A chiral recognition model on the basis of chromatography, spectroscopy, and molecular mechanistic calculations for the enantioseparation of 1,1′-binaphthyl derivatives on cholic acid-bonded stationary phases

✍ Scribed by L. Vaton-Chanvrier; H. Oulyadi; Y. Combret; G. Coquerel; J.C. Combret

• Publisher: John Wiley and Sons
• Year: 2001
• Tongue: English
• Weight: 199 KB
• Volume: 13
• Category: Article
• ISSN: 0899-0042
• DOI: 10.1002/chir.10053

✦ Synopsis

Abstract

In an effort to elucidate the mechanism of chiral discrimination of cholic acid‐based stationary phases, the enantiomeric recognition ability of six chiral stationary phases (CSPs), prepared from differently substituted cholic acid derivatives, was evaluated in normal phase high‐performance liquid chromatography (HPLC) with a series of 1,1′‐binaphthyl compounds. The influence of structural variations of analytes on retention and enantioselectivity was investigated. Particularly high values of enantioselectivity were observed for the binaphthol enantiomers on a CSP prepared from the allyl 7α,12α‐dihydroxy‐3α‐phenylcarbamoyloxy‐5β‐cholan‐24‐oate. The complexes of this chiral selector with both enantiomers of binaphthol were studied as models for the interactions responsible for the enantioseparation with the cholic acid‐based stationary phases. The 1:1 stoichiometry of the complex in solution was determined by UV titration. The chiral selector dissolved in chloroform exhibited a chiral discrimination for the binaphthol in ^1^H and ^13^C nuclear magnetic resonance (NMR) spectroscopies. Some aromatic proton and carbon resonances of binaphthol were clearly separated into a pair of peaks due to enantiomers in the presence of the chiral selector. Moreover, on the basis of molecular mechanics calculation, a chiral discrimination model was proposed which nicely explains the relevant chromatographic behavior of the 1,1′‐binaphthyl derivatives. Chirality 13:668–674, 2001. © 2001 Wiley‐Liss, Inc.