Complexation kinetics cyclodextrins

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 inclusion complexes of cyclodextrins have been studied since about 30 years using chemical, spectroscopic, kinetic, potentiometric methods. The obtained data have led to the conclusion that the adduct formation of the cyclodextrin molecules in solution is due to their annular structure and that they provide space for the substrate molecules in their annular cavity. The only obvious requirement for inclusion is that the dimensions of the guest molecules must be small enough to fit into the cyclodextrin cavity. 

Owing to the inclusion complex formation cyclodextrins offer an excellent model system to study intermolecular interactions as different substrate molecules can be accommodated into their cavity. In the following some of these complexes are described structurally and the structural data and data from kinetic measurements are combined to derive a picture of the inclusion mechanism and to show which intermolecular interactions are involved in the inclusion process. 

Insoluble drug compounds complexed with cyclodextrins in the presence of water-soluble polymers tend to achieve kinetic solubility in aqueous media several times... 

Key words. Cyclodextrin-catalyzed, hydrolysis, hydrophobic cavity, inclusion complex, kinetic parameter RMP. 

Water plays a crucial role in the inclusion process. Although cyclodextrin does form inclusion complexes in such nonaqueous solvents as dimethyl sulfoxide, the binding is very weak compared with that in water 13 Recently, it has been shown that the thermodynamic stabilities of some inclusion complexes in aqueous solutions decrease markedly with the addition of dimethyl sulfoxide to the solutions 14,15>. Kinetic parameters determined for inclusion reactions also revealed that the rate-determining step of the reactions is the breakdown of the water structure around a substrate molecule and/or within the cyclodextrin cavity 16,17). 

Nishioka and Fujita78) have also determined the Kd values fora- and (S-cyclodextrin complexes with p- and/or m-substituted phenyl acetates through kinetic investigations on the alkaline hydrolysis of the complexes. The Kd values obtained were analyzed in the same manner as those for cyclodextrin-phenol complexes to give the Kd(X) values (Table 5). The quantitative structure-activity relationships were formulated as Eqs. 30 to 32 ... 

Mikolajczyk and coworkers have summarized other methods which lead to the desired sulfmate esters These are asymmetric oxidation of sulfenamides, kinetic resolution of racemic sulfmates in transesterification with chiral alcohols, kinetic resolution of racemic sulfinates upon treatment with chiral Grignard reagents, optical resolution via cyclodextrin complexes, and esterification of sulfinyl chlorides with chiral alcohols in the presence of optically active amines. None of these methods is very satisfactory since the esters produced are of low enantiomeric purity. However, the reaction of dialkyl sulfites (33) with t-butylmagnesium chloride in the presence of quinine gave the corresponding methyl, ethyl, n-propyl, isopropyl and n-butyl 2,2-dimethylpropane-l-yl sulfinates (34) of 43 to 73% enantiomeric purity in 50 to 84% yield. This made available sulfinate esters for the synthesis of t-butyl sulfoxides (35). 

By virtue of their complexing ability, CDs may influence the course of chemical reactions in respect of rates and/or product selectivity. In consequence, there is a large body of data in the literature on the effect of CDs on many types of reactions (Fendler and Fendler, 1975 Bender and Komiyama, 1978 Szejtli, 1982 Tabushi, 1982 Sirlin, 1984 Ramamurthy, 1986 Ramamurthy and Eaton, 1988). The present review concentrates on reactions for which sufficient kinetic data are available to allow quantification of the effects of CDs on transition state stability, in an attempt to understand how cyclodextrins influence reactivity in either a positive or negative sense. 

In order to determine the mechanism of complex-formation, however, kinetic methods must be used. Consider one host-two guests complex-ation. The two possible mechanisms are dimerization of the guest outside the cyclodextrin cavity followed by inclusion, and dimerization within the cyclodextrin cavity. Equilibrium measurements alone cannot distinguish between these two possibilities. The same is the case for 2 2 complex-formation, where a larger number of possible mechanisms exist. 

Until 1984, all of the stopped-flow and temperature-jump kinetic studies of alpha cyclodextrin inclusion-complex formation were explainable in terms of a single-step, binding mechanism. According to this mechanism, the observed rate constant, kobs, (for stopped-flow) and the reciprocal relaxation time, 1/t, (for temperature-jump) should show a linear dependence on the edpha cyclodextrin concentration. Sano and coworkers, however, in the case of the iodide-alpha cyclodextrin interaction, and Hersey and Robinson,in the case of various azo dye-alpha cyclodextrin interactions (see Fig. 7), found that certain guest species exhibit a limiting value of kobs and 1/t at high concentrations of alpha cyclodextrin. This behavior can most simply be explained in terms of a mechanism of the type,... 

A study similar to that of Hersey and Robinson has been reported by Seiyama and coworkers.From a stopped-flow, kinetic study of the interaction of various azo dyes and some azo dye-metal complexes with alpha cyclodextrin, they observed two kinetic processes. The dependence of the observed rate-constants for these two processes on the alpha cyclodextrin concentration was found to be explainable in terms of a mechanism identical to that proposed earlier by Hersey and Robinson. In the case of the guests used by Seiyama and coworkers, however, values for the rate constants of the binding step could be determined from the concentration dependence of kobs for the faster process thus,... 

Reddy L. R. Bhanumathi, N. Rao, K. R. (2000) Dynamis kinetic asymmetric synthesis of y -aminoalcohols from racemic epoxides in cyclodextrin complexes under solid state conditions., Chem. Commun. 2321-2322. 

Prbpy, 5-(2-MePr)bpy and 5-(2,2-Mc2Pr)bpy have been prepared and characterized. The mer-and /uc-isomers of each complex have been isolated by use of cation-exchange column chromatography as the steric requirements of the R group increase, the percentage of the /uc-isomer decreases. Enantiomers of [Ru(5-Prbpy)3] + were separated on SP Sephadex C-25. Electro-kinetic chromatography has been used to separate the enantiomers of [Ru(104)3] " anionic carboxymethyl-/ -cyclodextrin was employed as the chiral mobile phase additive. ... 

Zhang, X., Gramlich, G., Wang, X. and Nau, W.M. (2002) A joint structural, kinetic, and thermodynamic investigation of substituent effects on host-guest complexation of bicyclic azoalkanes by -cyclodextrin./. Am. Chem. Soc., 124 (2), 254-263. 

A review with ca 500 references has appeared on the stability of cyclodextrin complexes in solution. The principal headings in it are nature of cyclodextrins (CDs) binding equilibria and kinetics strengths of CD complexes structures of CD complexes sources of CD complex stability and prediction of CD stability.168... 

In other media like micelles, cyclodextrin, binary solvent mixtures, and proteins (47-55), lifetime distributions are routinely used to model the decay kinetics. In all of these cases the distribution is a result of the (intrinsic or extrinsic) fluorescent probe distributing simultaneously in an ensemble of different local environments. For example, in the case of the cyclodextrin work from our laboratory (53-55), the observed lifetime distribution is a result of an ensemble of 1 1 inclusion complexes forming and coexisting. These complexes are such that the fluorescent probe is located simultaneously in an array of environments (polarities, etc.) in, near, and within the cyclodextrin cavity, which manifest themselves in a distribution of excited-state lifetimes (53-55). In the present study our experimental results argue for a unimodal lifetime distribution for PRODAN in pure CF3H. The question then becomes, how can a lifetime distribution be manifest in a pure solvent ... 

Complexes of unsymmetrically substituted conjugated dienes are chiral. Racemic planar chiral complexes are separated into their enantiomers 84 and 85 by chiral HPLC on commercially available /f-cyclodextrin columns and used for enantioseletive synthesis [25]. Kinetic resolution was observed during the reaction of the meso-type complex 86 with the optically pure allylboronate 87 [26], The (2R) isomer reacted much faster with 87 to give the diastereomer 88 with 98% ee. The complex 88 was converted to 89 by the reaction of meldrum acid. Stereoselective Michael addition of vinylmagnesium bromide to 89 from the opposite side of the coordinated Fe afforded 90, which was converted to 91 by acetylation of the 8-OH group and displacement with EtjAl. Finally, asymmetric synthesis of the partial structure 92 of ikarugamycin was achieved [27],... 

Cyclodextrins have a large range of industrial applications. The market for them is growing as a consequence of their unique inclusion properties and decomplexation kinetics in conjunction with their stability, non-toxicity and relative cheapness. Cyclodextrins are the main active ingredient in Procter and Gamble s deodorising product Febreze, for example, where their complexation ability binds molecules responsible for household odours. The principal areas of interest are summarised in Figure 6.26. Some 1,649 research papers were published with the word cyclodextrin in the title in 2006 alone. 

Abou-Hamdan, A. Bugnon, P. Saudan, Ch. Lye, P.G. and Merbach, A.E. (2000) High-Pressure Studies as a Novel Approach in Determining Inclusion Mechanisms Thermodynamics and Kinetics of the Host-Guest Interactions for a-Cyclodextrin Complexes, J. Am. Chem. Soc. 122, 592-602. 

Different cyclodextrin monolayers have been synthesized and their surface properties have been characterized. Kaifer et al. prepared per-6-thiol-cyclodextrins, and described the interfacial monovalent ferrocene complexation at the monolayer.55 Mittler-Neher et al. studied the kinetics of the adsorption of mono- and multithiolate-functionalized CD SAMs.56,57 Beulen et al.,58 Huskens et al.,59 Auletta et al.,60 and Nijhuis et al.61 reported on the concept of molecular printboards, that is, (3-cyclodextrin ((3-CD) SAMs on gold or silicon oxide substrates, onto which complementary multivalent guest-functionalized dendrimer molecules were adsorbed, resulting in the formation of kinetically stable supramolecular assemblies. With the... 

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