Phases chirality

Most chiral chromatographic separations are accompHshed using chromatographic stationary phases that incorporate a chiral selector. The chiral separation mechanisms are generally thought to involve the formation of transient diastereomeric complexes between the enantiomers and the stationary phase chiral ligand. Differences in the stabiHties of these complexes account for the differences in the retention observed for the two enantiomers. Often, the use of a... 

An interesting and practical example of the use of thermodynamic analysis is to explain and predict certain features that arise in the application of chromatography to chiral separations. The separation of enantiomers is achieved by making one or both phases chirally active so that different enantiomers will interact slightly differently with the one or both phases. In practice, it is usual to make the stationary phase comprise one specific isomer so that it offers specific selectivity to one enantiomer of the chiral solute pair. The basis of the selectivity is thought to be spatial, in that one enantiomer can approach the stationary phase closer than the other. If there is no chiral selectivity in the stationary phase, both enantiomers (being chemically identical) will coelute and will provide identical log(Vr ) against 1/T curve. If, however, one... 

T. Foi nstedt, A.-M. Hesselgren and M. Johansson, Chiral assay of atenolol present in microdialysis and plasma samples of rats using chiral CBH as stationaiy phase . Chirality 9 329-334 (1997). 

C. J. Harding, Photoelectron Circular Dichroism in Gas Phase Chiral Molecules, Ph.D. thesis. University of Nottingham, UK, 2005. 

Diaz-Perez, M.J., Chen, J.C., Aubry, A.F., Wainer, I.W. (1994). The direct determination of the enantiomers of Ketorlac and parahydroxyketorlac in plasma and urine using enantiose-lective liquid chromatography on a human semm albumin-based chiral stationary phase. Chirality 6, 283-289. 

Enantiomers of the 8,9-dichloro-2,3,4,4 ,5,6-hexahydro-177-pyrazino[l,2-tf]quinoxalin-5-one (structure 249 Rz = R3 = Cl R1 = R4 = H) could be separated by normal-phase, chiral high-performance liquid chromatography (HPLC) with increased retention and separation factors if ethoxynonafluorobutane was used as solvent, instead of -hexane <2001JCH(918)293>. 

Aboul-Enein and Ali [78] compared the chiral resolution of miconazole and two other azole compounds by high performance liquid chromatography using normal-phase amylose chiral stationary phases. The resolution of the enantiomers of ( )-econazole, ( )-miconazole, and (i)-sulconazole was achieved on different normal-phase chiral amylose columns, Chiralpak AD, AS, and AR. The mobile phase used was hexane-isopropanol-diethylamine (400 99 1). The flow rates of the mobile phase used were 0.50 and 1 mL/min. The separation factor (a) values for the resolved enantiomers of econazole, miconazole, and sulconazole in the chiral phases were in the range 1.63-1.04 the resolution factors Rs values varied from 5.68 to 0.32. 

The study of the cholesteric mesophases obtained by doping thermotropic nematics with chiral, nonracemic compounds, has lead to relevant information about the stereochemistry of the dopants. Chiral interactions change the structure of the phase and therefore molecular chirality can be mapped onto an achiral (nematic) phase to yield a superstructural phase chirality. In 1984 Sol-ladie and Zimmermann published the first review summarizing the state of the art at that time.52 Later on, several review articles updated this subject.53-55... 

This banana phase nomenclature was established at the first international conference specifically focused on banana phases Chirality by Achiral Molecules, held in Berlin, Germany, in December, 1997. 

Figure 9.9 Simulated normalized line shapes of -polarized (a-c) and p-polarized (if-/) second-harmonic signals for quarter waveplate measurements (a) and (if) hypothetical achiral surface (hs = 0.5 fp = 0.75, gp = —0.5), (b) and (if) hypothetical chiral surface with in-phase chiral coefficient (fs = 0.75, hs = 0.5 fp = 0.75, gp = —0.5, hp = 0.25), (c) and (/) hypothetical chiral surface with out-of-phase chiral coefficient ( fs = 0.75 0.25i, hs = 0.5 fp = 0.75, gp = —0.5, hp = 0.25z). Upper (solid line) and lower (dashed line) sign in expansion coefficients correspond to two enantiomers. Rotation angles of 45° and 225° (135° and 315°) correspond to right-hand (left-hand) circularly polarized light and are indicated for one of enantiomers with open and filled circles, respectively.

The rate of reaction 29 is found to be sensitive to the configuration of the guest A, making p-CD a gas-phase chiral selector. Its enantioselectivity, defined by the measured ko/kL ratio, is as large as far kolkL is from unit. Table 12 indicates that the /3-CD increases from alanine kolk = 0.62) to valine kolkL = 0.32), leucine... 

Ekborg-Ott, K.H., Liu, Y, and Armstrong, D.W., Highly enantioselective HPLC separations using the covalently bonded macrocyclic antibiotic, ristocetin A, chiral stationary phase. Chirality, 10, 434, 1998. 

Sun, Q. and Olesik, S.V., Chiral separation by simultaneous use of vancomycin as stationary phase chiral selector and chiral mobile phase additive, J. Chromatogr. B, 745, 159, 2000. 

Torok, G. et al.. Direct chiral separation of unnatural amino acids by high performance liquid chromatography on a ristocetin A-bonded stationary phase. Chirality, 13, 648, 2001. 

Fried, K.M., Koch, P, and Wainer, I.W., Determination of the enantiomers of albuterol in human and canine plasma by enantioselective high-performance liquid chromatography on a teicoplanin-based chiral stationary phase. Chirality, 10, 484, 1998. 

Aqueous surfactants are another class of catalysts. Substantial rate enhancement is seen in the reaction occurring at the micellar hydrocarbon-water interface, which is ascribed to a concentration of the reactant in the micellar pseudo-phase. Chiral p-nitrophenyl esters derived from phenylalanine are hydrolyzed by a histidine-containing dipeptide at a micellar interphase, at which a very high enantiomer discrimination, kR/ks up to 30.4 at 0°C, is observed (49). As shown in Scheme 20, the enantioselectivity is expressed at the stage at which a transient, zwitter-ionic tetrahedral intermediate leading to the acylimidazole is formed,... 

Another method for creating a chiral environment is lo add an optically pure chiral selector to a bulk liquid phase. Chiral additives have several advanlages over chiral stationary phases and continue lo be the predominant mode for chiral separations by tic and capillary electrophoresis (cc). First of all, the chiral selector added to a bulk liquid phase can be readily changed. The use of chiral additives allows chiral separations lo be done using less expensive, conventional stationary phases. A wider variety of chiral selectors are available [ be used as chiral additives than are available as chiral stationary phases, thus, providing the analyst with considerable flexibility. Finally, the use of chiral additives may provide valuable insight into (he chromatographic conditions and/or likelihood ol success with a potential chiral stationary-phase chiral selector. This is particularly important for the development of new chiral stationary phases because of the difficulty and cosl involved. 

Among the most successful of the liquid chromatographic reversed-phase chiral stationary phases have been the cyclodextrin-based phases, introduced by Armstrong and commercially available through Advanced... 

Frustrated Phases. Chiral molecules normally form chiral phases, hui in some cases this is dune in an interesting way. For example, it is not... 

Scheme 22 Synthesis of solid-phase chiral catalyst 83...

Cr Cub, Cubv d E G HT Iso Isore l LamN LaniSm/col Lamsm/dis LC LT M N/N Rp Rh Rsi SmA Crystalline solid Spheroidic (micellar) cubic phase Bicontinuous cubic phase Layer periodicity Crystalline E phase Glassy state High temperature phase Isotropic liquid Re-entrant isotropic phase Molecular length Laminated nematic phase Correlated laminated smectic phase Non-correlated laminated smectic phase Liquid crystal/Liquid crystalline Low temperature phase Unknown mesophase Nematic phase/Chiral nematic Phase Perfluoroalkyl chain Alkyl chain Carbosilane chain Smectic A phase (nontilted smectic phase)... 

SmB SmC SmC SmCA SmCPA SmCPp SmCo, SmIA SmX UCST XRD Smectic B phase Smectic C phase (synclinic tilted smectic C phase) Chiral (synclinic tilted) smectic C phase Chiral anticlinic tilted (antiferroelectric switching) SmC phase Antiferroelectric switching polar smectic C phase Ferroelectric switching polar smectic C phase Chiral smectic C alpha phase Chiral antiferroelectric switching smectic I phase Smectic phase with unknown structure Upper critical solution temperature X-ray diffraction... 

Martens-Lobenhoffer et al. [119] used chiral HPLC-atmospheric pressure photoionization tandem mass-spectrometric method for the enantio-selective quantification of omeprazole and its main metabolites in human serum. The method features solid-phase separation, normal phase chiral HPLC separation, and atmospheric pressure photoionization tandem mass spectrometry. The internal standards serve stable isotope labeled omeprazole and 5-hydroxy omeprazole. The HPLC part consists of Agilent 1100 system comprising a binary pump, an autosampler, a thermo-stated column component, and a diode array UV-VIS detector. The enantioselective chromatographic separation took place on a ReproSil Chiral-CA 5 ym 25 cm x 2 mm column, protected by a security guard system, equipped with a 4 mm x 2-mm silica filter insert. The analytes were detected by a Thermo Scientific TSQ Discovery Max triple quadrupole mass spectrometer, equipped with an APPI ion source with a... 

Franco et al. [45] described an HPLC method for simultaneous determination of the R-( ) and (S)-(+)-enantiomers of vigabatrin in human serum after precolumn derivatization with 2,4,6-trinitrobenzene sulfonic acid (TNBSA) and detection at 340 nm. Separation was achieved on a reversed phase chiral column (Chiralcel-ODR, 25 cm x 4.6 mm) using 0.05 M potassium hexafluorophosphate (pH4.5) acetonitrile ethanol (50 40 10) as a mobile phase at a flow rate of 0.9 ml/min. The calibration graphs for each enantiomer were linear over the concentration range of 0.5-40 fig/ml with a limit of quantification of 0.5 fig/ml. No interferences were found from commonly coadministered antiepileptic drugs. 

Okamoto, Y., Aburatani, R., Kaida, Y., Hatada, K., Inotsume, N., and Nakano, M. (1989) Direct chromatographic separation of 2-arylpropionic acid enantiomers using tris(3,5-dimethylphenylcarbamate)s of cellulose and amylose as chiral stationary phases, Chirality 1, 239-242. 

Pu G.-Q., Yamamoto M., Takeuchi Y., Yamazawa H. and Ando T. (1999) Resolution of epoxydienes by reversed-phase chiral HPLC and its application to stereochemistry assignment of mulberry looper sex pheromone. J. Chem. Ecol. 25, 1151-1162. 

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