## Abstract Crown etherβbased chiral stationary phases (CSPs) have been known to be quite useful for the liquid chromatographic resolution of racemic compounds containing a primary amino group. Chiral separations on crown etherβbased CSPs are characterized by several factors. In this paper, the str
Chromatographic retention and thermodynamics of adsorption of dipeptides on a chiral crown ether stationary phase
β Scribed by Leonid Asnin; Kavita Sharma; Se Won Park
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 223 KB
- Volume
- 34
- Category
- Article
- ISSN
- 1615-9306
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
The enantioselective adsorption of several dipeptides on the crown etherβbased stationary phase ChiroSil RCA(+) was studied by means of the linear chromatography method. The retention of analytes was measured with acidified waterβmethanol mobile phases with varied concentration of methanol (from 60 to 90%, v/v) at different temperatures. Thermodynamic characteristics of adsorption were determined and analyzed applying extrathermodynamic relationships. A considerable difference in adsorption mechanisms of dipeptides with a chiral and achiral Nβterminal fragment was proved. An explanation to this fact was proposed assuming that the enantiorecognition of the dipeptides of the first type occurred through the interaction of side groups of the Nβterminus with the chiral cavity formed by the crown ether ring. The enantiorecognition of the dipeptides of the second type occurs through the interaction of the Cβterminal residue with the side groups of the crown ether moiety. The study also demonstrates how extrathermodynamic concepts can be used for obtaining additional information about retention mechanisms from a limited amount of chromatographic data.
π SIMILAR VOLUMES
## Liquid chromatographic direct resolution of b-amino acids on a chiral crown ether stationary phase A chiral stationary phase (CSP) prepared by bonding (+)-(18-crown-6)-2,3,11,12tetracarboxylic acid to silica gel was used for the direct resolution of b-amino acids. To determine the optimum mobil
A direct, isocratic high-performance liquid chromatographic method is described for the enantiomeric resolution of a number of phenylalkylamines, namely, racemic cathinone, amphetamine, norephedrine, and norphenylephrhe, without sample derivatization. The separations were achieved on an S-18-crownd-