| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1166882 | Analytica Chimica Acta | 2012 | 10 Pages |
Chiral separation of iodiconazole, a new antifungal drug, and 12 new structurally related triadimenol analogues had been developed by capillary electrophoresis (CE) using hydroxypropyl-γ-cyclodextrin (HP-γ-CD) as the chiral selector. The effect of structural features of analytes on Δt and Rs was studied under the optimum separation conditions. Using molecular docking technique and binding energy calculations, the inclusion process between HP-γ-CD and enantiomers was investigated and chiral recognition mechanisms were discussed. The results suggest that hydrogen bonding between fluorine at position 4 of the phenyl group beside the chiral carbon and the hydroxyl group on the HP-γ-CD rim and face to face π–π interactions between two phenyl rings highly contributed to the enantiorecognition process between HP-γ-CD and iodiconazole. The N-methyl group beside chiral carbon also played an important role in enantiomeric separation. Additionally, the big difference in binding energy (ΔΔE) highly contributed to good separation in the presence of HP-γ-CD chiral selector, which may be a helpful initial guide for chiral selector selection and predicting the result of enantioseparation. Furthermore, the new mathematical equation established based on the results of molecular mechanics calculations exhibited good capability in predicting chiral separation of these triadimenol analogues using HP-γ-CD mediated CE.
Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slideHighlights► Molecular modeling studies chiral recognition mechanism of iodiconazole with HP-γ-CD. ► The good separation obtained is due to the big binding energy difference. ► A new mathematical equation is established to predict chiral separation. ► Molecular modeling serves as a useful method for studying chiral separation.
