Cyclodextrins between

To be selective, heterocapping of cyclodextrins has to control both the distance and the direction between the grafting hydroxyls. This was achieved in a two-step manner on the primary rim of P-cyclodextrin between the positions 6A and 6G. The thiol group of t- or D-cysteine reacted with the 6A-tosyl group of cyclodextrin 13b to give monofunctionalized P-cyclodextrins 35a-b (Scheme 9.15). The amino group was functionalized with a dansyl moiety, and the free carboxyUc acid was subjected to esterification conditions. The esterification only happened on the position 6G, leading to cyclodextrins 36a-b in about 80% yield [49]. It has to be noted that this... 

Fig. 8. A hydrophobic inclusion complex between a chiral analyte and a cyclodextrin.

Table 4-3. Binding Constants and Rate Constants for Complex Formation between a-Cyclodextrin and Azo Dyes ...

Figure 10.2 MDGC-MS differentiation between the enantiomers of theaspiranes in an aglycone fraction from puiple passion fruit DB5 pre-column (25 m X 0.25 mm i.d., 0.25 p.m film thickness canier gas He, 0.66 ml/min oven temperature, 60-300 °C at 10 °C/min with a final hold of 25 min) permethylated /3-cyclodextrin column (25 m X 0.25 mm i.d., 0.25 p.m film thickness canier gas He, 1.96 ml/min 80 °C isothermal for 20 min and then programmed to 220 °C at 2 °C/min). Reprinted from Journal of High Resolution Chromatography, 16, G. Full et al., MDGC- MS a powerful tool for enantioselective flavor analysis , pp. 642-644, 1993, with permission from Wiley-VCH.

Righetti and co-workers [11] were one of the first to demonstrate the utility of classical isoelectric focusing for the chiral separation of small molecules in a slab gel configuration. In their system, dansylated amino acids were resolved enan-tiomerically through complexation with (i-cyclodextrin. Preferential complexation between the cyclodextrin and the derivatized amino acid induced as much as a 0.1 pH unit difference in the pK s of the dansyl group. 

Matsui441 has computed energies (Evdw) due to the van der Waals interaction between a-cyclodextrin and some guest molecules by the use of Hill s potential equation 451 ... 

The results were simple and clear-cut Only the two terms ofa° and Emin were involved for the a-cyclodextrin systems, and the two terms of k and Emin, for (S-cyclodextrin systems. This means that the stabilities of the inclusion complexes are mainly governed by the electronic and steric interactions in a-cyclodextrin systems and by the hydro-phobic and steric interactions in (i-cyclodextrin systems, regardless of the position of the substituents in the phenols. These observations agree well with those by Harata23), who showed that there is no appreciable difference in thermodynamic parameters between cyclodextrin complexes of m- and p-di substituted benzenes and that the contribution of the enthalpy term to the complexation is more significant in a-cyclodextrin systems than in P-cyclodextrin systems, where the inhibitory effect... 

Only the hydrophobic and steric terms were involved in these equations. There are a few differences between these equations and the corresponding equations for cyclo-dextrin-substituted phenol systems. However, it is not necessarily required that the mechanism for complexation between cyclodextrin and phenyl acetates be the same as that for cyclodextrin-phenol systems. The kinetically determined Kj values are concerned only with productive forms of inclusion complexes. The productive forms may be similar in structure to the tetrahedral intermediates of the reactions. To attain such geometry, the penetration of substituents of phenyl acetates into the cyclodextrin cavity must be shallow, compared with the cases of the corresponding phenol systems, so that the hydrogen bonding between the substituents of phenyl acetates and the C-6 hydroxyl groups of cyclodextrin may be impossible. 

The importance of the proximity effect in cyclodextrin catalysis has been discussed on the basis of the structural data. Harata et al. 31,35> have determined the crystal structures of a-cyclodextrin complexes with m- and p-nitrophenols by the X-ray method. Upon the assumption that m- and p-nitrophenyl acetates form inclusion complexes in the same manner as the corresponding nitrophenols, they estimated the distances between the carbonyl carbon atoms of the acetates and the adjacent second-... 

Fig. 8. Parabolic relationship between reactivity with cyclodextrin and substituent diameter of m-substituted phenyl acetates...

The more useful types of chirally active bonded phases are those based on the cyclodextrins. There are a number of different types available, some of which have both dispersive or polar groups bonded close to the chirally active sites to permit mixed interactions to occur. This emphasizes the basic entropic differences between the two isomers being separated. A range of such products is available from ASTEC Inc. and a separation of the d and / isomers of scopolamine and phenylephrine are shown in figure 4. The separations were carried out on a cyclodextrin bonded phase (CYCLOBOND 1 Ac) that had been acetylated to provide semi-polar interacting groups in close proximity to the chiral centers of the cyclodextrin. The column was 25 cm long, 4.6 mm in diameter and packed with silica based spherical bonded phase particles 5pm in diameter. Most of the columns supplied by ASTEC Inc. have these dimensions and, consequently, provide a... 

It is seen that, providing the isomers are eluted at a (kf) value greater than about 2.0, the column will separate those solute pairs having separation ratios as low as about 1.03. This, however, assumes that the column is very well packed and is operated at about the optimum mobile phase velocity. In practice, a more realistic minimum separation ratio would be between 1.035 and 1.04. However, as it will be seen, the cyclodextrin bonded phases can easily provide separation ratios significantly greater than these values. This is achieved by... 

Micellar medium has received great attention because it solubilizes, concentrates and orientates the reactants within the micelle core and in this way accelerates the reaction and favors the regio- and stereoselectivity of the process [68], In addition the micellar medium is cheap, can be reused, is more versatile than cyclodextrins and more robust than enzymes. With regard to Diels Alder reactions, we may distinguish between (i) those in which one or both reagents are surfactants which make up the micellar medium, and (ii) those that are carried out in a micellar medium prepared by a suitable surfactant. 

The fact that f.a.b.-m.s. can be used to observe cluster ions has been exploited in a study of metal binding to cyclodextrins, and in an investigation of the complexes formed between a 3-O-methylmannose dodecasac-charide and alkyltrimethylammonium ions having decyl and hexadecyl as alkyl chains. In the latter study, the larger organic cation was shown to form the stronger complex. 

The well-known reaction between phenol and chloroform in the presence of concentrated sodium hydroxide is amenable to dramatic changes with cyclodextrins. -cyclodextrin, immobilized with epichlorohydrin, seems to give 100 % selectivity for para... 

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