Hydrophilic hosts

Solvation/desolvation effects in the cryptand also complicate the expected simple dependence of stability constant on host basicity. For example the aliphatic cryptand O-bistren shows lower formation constants than the less basic aromatic analogues such as R3F, which we attribute to the greater desolvation cost of complexation with the former, more hydrophilic host. 

Keywords Cyclodextrin, Cyclodextrin complex, Hydrophilic hosts, Inclusion, Polymerization... 

Pulse radiolytic reductions were conducted without employing a hydrophilic host molecule. Radical-induced reduction of e-C6o[C(COO )2]2 in N2-purged aqueous solution showed that the expected formation of the diagnostic NIR transition band occurs synchronously with the decay of the electron absorption. The fullerene 7t-radical anion, absorbs at 1055 nm, which is 5 nm blue-shifted relative to the analogous reduced ester derivative. 

Palladium-catalyzed reduction of carbon-halogen bonds can also be achieved by the formate anion in a biphasic system in the presence of cyclodextrins, which form a hydrophilic host-guest complex with hydrophobic substrates fitting into their cavities, and thus transfer them into the aqueous phase [86] ... 

The shape-persistent, structurally well-defined nature of PAMs and PDMs make them attractive models for binding guest molecules within their cavities. In 1995, Hoger and Enkelmann reported the construction of the first meta/para-PAM/PDM hybrid designed to possess hydrophobic and hydrophilic substituents for subsequent use in host guest chemistry [71]. Macrocyclic amphiphile 116 was assembled via the straightforward manner depicted in Scheme 26. 

The main peculiarity of solutions of reversed micelles is their ability to solubilize a wide class of ionic, polar, apolar, and amphiphilic substances. This is because in these systems a multiplicity of domains coexist apolar bulk solvent, the oriented alkyl chains of the surfactant, and the hydrophilic head group region of the reversed micelles. Ionic and polar substances are hosted in the micellar core, apolar substances are solubilized in the bulk apolar solvent, whereas amphiphilic substances are partitioned between the bulk apolar solvent and the domain comprising the alkyl chains and the surfactant polar heads, i.e., the so-called palisade layer [24],... 

In addition to the degree of hydrophilicity of the solubilizates, their size and structure, the size of the host microregions, or the occurrence of specific processes must be taken into account in order to rationalize the driving forces of the solubilization process and of the solubilization site within water-containing reversed micelles [25,138,139],... 

The concept of micelles consists of aggregation of amphiphilic molecules that contain polar and non-polar moieties, which associate in a manner that minimizes hydrophobic and lipophilic interactions. However, a cascade molecule consisting of an internal lipophilic framework and a external hydrophilic surface would effectively be a unimolecular micelle [59] capable of hosting molecular guest(s). 

Clay minerals or phyllosilicates are lamellar natural and synthetic materials with high surface area, cation exchange and swelling properties, exfoliation ability, variable surface charge density and hydrophobic/hydrophilic character [85], They are good host structures for intercalation or adsorption of organic molecules and macromolecules, particularly proteins. On the basis of the natural adsorption of proteins by clay minerals and various clay complexes that occurs in soils, many authors have investigated the use of clay and clay-derived materials as matrices for the immobilization of enzymes, either for environmental chemistry purpose or in the chemical and material industries. 

However, these elegant glycosylated nanostructures displayed only weak biological activity relative to their native glucan elicitor counterparts. Nevertheless, such glycoclusters provided unique environments for host-guest chemistry of amphi-pathic molecules owing to their lipophilic core surrounded by a hydrophilic periphery. 

A further category of cavitands are the calixarenes (Gutsche, Dhawan, No Muthukrishnan, 1981 Gutsche Levine, 1982). Structure (255) illustrates an example of this type which is readily prepared by treatment of 4-f-butylphenol with formaldehyde and base. The compound may exist in other conformations besides the saucer-shaped one illustrated by (255). Similarly, f-butyl-calix[4]arene (256 R = CH2COOH) has an enforced hydrophilic cavity in the shape of a cone the alkali and ammonium salts of this host are soluble in water (Arduini, Pochini, Reverberi Ungaro, 1984). 

Meijer et al [6] reported on inverted unimolecular micelle type dendrimers (Figure 13.4) which have a hydrophilic interior and a hydrophobic shell, synthesized by modifying the end groups of hydrophilic polypropylene imine) dendrimer with alkyl chains. It was shown that these dendrimers could host... 

In principle, there are four basic strategies to compensate for the repulsive effects between the hydrophobic fullerene surface and water (a) encapsulation in the internal hydrophobic moiety of water-soluble hosts like cyclodextrins (Andersson et al., 1992 Murthy and Geckeler, 2001), calixarenes (Kunsagi-Mate et al., 2004) or cyclotriveratrylenes (Rio and Nierengarten, 2002) (b) supramolecular or covalent incorporation of fullerenes or derivatives into water-soluble polymers (Giacalone and Martin, 2006) or biomolecules like proteins (Pellarini et al., 2001 Yang et al., 2007) (c) suspension with the aid of appropriate surfactants and (d) direct exohe-dral functionalization in order to introduce hydrophilic moieties. 

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