Chiral recognition by enantioselective liquid chromatography: Mechanisms and modern chiral stationary phases |
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Authors: | Michael Lä mmerhofer |
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Affiliation: | Christian Doppler Laboratory for Molecular Recognition Materials, Department of Analytical Chemistry and Food Chemistry, University of Vienna, Waehringer Strasse 38, A-1090 Vienna, Austria |
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Abstract: | An overview of the state-of-the-art in LC enantiomer separation is presented. This tutorial review is mainly focused on mechanisms of chiral recognition and enantiomer distinction of popular chiral selectors and corresponding chiral stationary phases including discussions of thermodynamics, additivity principle of binding increments, site-selective thermodynamics, extrathermodynamic approaches, methods employed for the investigation of dominating intermolecular interactions and complex structures such as spectroscopic methods (IR, NMR), X-ray diffraction and computational methods. Modern chiral stationary phases are discussed with particular focus on those that are commercially available and broadly used. It is attempted to provide the reader with vivid images of molecular recognition mechanisms of selected chiral selector–selectand pairs on basis of solid-state X-ray crystal structures and simulated computer models, respectively. Such snapshot images illustrated in this communication unfortunately cannot account for the molecular dynamics of the real world, but are supposed to be helpful for the understanding. The exploding number of papers about applications of various chiral stationary phases in numerous fields of enantiomer separations is not covered systematically. |
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Keywords: | Ac-Phe, N-acetyl-phenylalanine AGP, α1-acid glycoprotein ADMPC, amylose tris(3,5-dimethylphenylcarbamate) ANN, artificial neural networks ANOVA, analysis of variance ATR, attenuated total reflectance AX, anion-exchanger CBH, cellobiohydrolase CE, crown-ether (in context of chiral selector) CD, circular dichroism (in context of spectroscopy) CD, cyclodextrin (in context of chiral selector) CDMPC, cellulose tris(3,5-dimethylphenylcarbamate) CIS, complexation-induced chemical shift (Δδ) CLEC, chiral ligand exchange chromatography CMPA, chiral mobile phase additive CoMFA, comparative molecular field analysis CoMSIA, comparative molecular similarity index analysis CS, chiral selector CSP, chiral stationary phase DEA, diethylamine DNB, 3,5-dinitrobenzoyl DNP, 2,4-dinitrophenyl EEC, enthalpy&ndash entropy compensation ELSD, evaporative light scattering detection FMOC, fluorenylmethoxycarbonyl Glob-MolInE, global molecular interaction evaluation HOMO, highest occupied molecular orbital HILIC, hydrophilic interaction chromatography HR/MAS, high-resolution magic angle spinning HSA, human serum albumin IRE, internal reflection element Leu, leucine LFER, linear free energy relationship LSER, linear solvation energy relationship LUMO, lowest unoccupied molecular orbital MCTA, microcrystalline cellulose triacetate MD, molecular dynamic MLR, multiple linear regression MM, molecular mechanics N-Me-Leu, N-methyl leucine NOE, nuclear Overhauser effect NOESY, nuclear Overhauser effect spectroscopy NP, normal-phase OVM, ovomucoid PLS, partial least squares in latent variables PO, polar organic (mode) QD, quinidine QM, quantum mechanical QN, quinine QSERR, quantitative structure&ndash enantioselective retention relationship QSPR, quantitative structure&ndash property relationship QSRR, quantitative structure&ndash retention relationship ROE, rotating frame nuclear Overhauser effect ROESY, rotating frame nuclear Overhauser effect spectroscopy SA, selectand SCX, strong cation exchanger SFC, super-/subcritical fluid chromatography SMB, simulated moving bed TAG, teicoplanin aglycone TFA, trifluoroacetic acid trNOE, transferred nuclear Overhauser effect VCD, vibrational circular dichroism WAX, weak anion-exchanger (WAX) Wf, warfarin XRD, X-ray diffraction ZWIX, zwitterionic ion-exchanger |
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