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In the pharmaceutical industry, the analysis of atropisomers is of considerable interest from both scientific and regulatory perspectives. The compound of interest contains two stereogenic axes due to the hindered rotation around the single bonds connecting the aryl groups, which results in four potential configurational isomers(atropisomers). The separation of the four atropisomers was achieved on a derivatized β-cyclodextrin bonded stationary phase. Further investigation showed that low temperature conditions, including sample preparation(-70 °C), sample storage(-70 °C), and chromatographic separation(6 °C), were critical to preventing interconversion. LC-UV-laser polarimetric analysis identified peaks 1 and 2 as a pair of enantiomers and peaks3 and 4 as another. Thermodynamic analysis of the retention data indicated that the separation of the pairs of enantiomers is primarily enthalpy controlled as indicated by the positive slope of the van’t Huff plot. The difference in absolute Δ(Δ H), ranged from 2.20 k J/mol to 2.42 k J/mol.
In the pharmaceutical industry, the analysis of atropisomers is of may interest from both scientific and regulatory perspectives. The compound of interest contains two stereogenic axes due to the hindered rotation around the single bonds connecting the aryl groups, which results in four potential configurational isomers ( The separation of the four atropisomers was achieved on a derivatized β-cyclodextrin bonded stationary phase. Further investigation showed that low temperature conditions, including sample preparation (-70 ° C), sample storage (-70 ° C), and chromatographic LC-UV-laser polarimetric analysis identified peaks 1 and 2 as a pair of enantiomers and peaks 3 and 4 as another. Thermodynamic analysis of the retention data indicated that the separation of the pairs of enantiomers is to enthalpy controlled as indicated by the positive slope of the van’t Huff plot. The difference in absolut e Δ (ΔH), ranged from 2.20 kJ / mol to 2.42 kJ / mol.