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Cyclodextrin stationary phase elution order

Using a chiral column, coated with a definite modified cyclodextrin as the chiral stationary phase, the elution orders of furanoid and pyranoid linalool oxides are not comparable [11, 12]. Consistently, the chromatographic behaviour of diastereomers and/or enantiomers on modified cyclodextrins is not predictable (Fig. 17.1, Table 17.1). Even by changing the non-chiral polysiloxane part of the chiral stationary phase used, the order of elution may significantly be changed [13]. The reliable assignment of the elution order in enantio-cGC implies the coinjection of structurally well defined references [11-13]. [Pg.380]

Table 17.1 Elution order of the furanoid linalool oxides using different modified cyclodextrins (CD) as chiral stationary phases [11, 13]... Table 17.1 Elution order of the furanoid linalool oxides using different modified cyclodextrins (CD) as chiral stationary phases [11, 13]...
All three stationary phases are permethylated cyclodextrins and for the most part the separations obtained from each are very similar. However, it is clear that there is a reversal in the order of elution for the isomenthol isomers on the y-PM stationary phase. It is also seen, that this phase shows distinctly less selectivity for the other enantiomeric pairs. This reversal of elution is also demonstrated in figure 6.4. [Pg.147]

The low vapor pressure and high thermal stability of CILs render them suitable for enantioseparations in gas chromatography (GC). Recently, CILs have been used as chiral stationary phases (CSPs) in GC [40]. Armstrong and coworkers carried out enantiomeric separation of chiral alcohols and diols, chiral sulfoxides, some chiral epoxides and acetamides using a CIL based on ephedrinium salt. Using an ephedrinium CIL (4) as the CSP, enantiomeric separation of alcohols and diols was achieved (Fig. 1). The presence of both enantiomeric forms of ephedrine makes it possible to produce CSPs of opposite stereochemistry, which could reverse the enantiomeric elution order of the analytes. This offers an additional advantage that may not be easily achieved with common and widely used chiral selectors in GC such as the cyclodextrins. However, there was a decrease in enantiomeric recognition ability of the CSP after a week which the authors attributed to dehydration-induced... [Pg.294]


See other pages where Cyclodextrin stationary phase elution order is mentioned: [Pg.235]    [Pg.44]    [Pg.949]    [Pg.181]    [Pg.110]    [Pg.387]    [Pg.238]    [Pg.148]    [Pg.172]    [Pg.21]    [Pg.17]    [Pg.199]    [Pg.365]    [Pg.385]   
See also in sourсe #XX -- [ Pg.235 ]




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Cyclodextrin phase

Ordered phases

Phases ordering

Stationary phases cyclodextrins

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