Hydrogen host-guest

Fig. 18. Crystal structures of recent clathrate design (a) coordinatoclathrate between host (39) (Fig. 17) and / -butanol (host—guest hydrogen bonding in the shaded area) (b) perspective view of the hehcal inclusion channel formed by diol host (43) (Fig. 17 all except one host molecule are represented...

Fig. 5. The 1 2 host-guest complex (l-naphthyl)3SiOH-2p-xylene with hydrogen atoms omitted. The p-xylene molecules are shown drawn with solid lines. Drawn using coordinates taken from the Cambridge Crystallographic Database.

The H-bonding in the anhydrous 1 Im (Table 24) has topologic properties (Fig. 46) similar to those in the alcohol coordinatoclathrates of 1 with 1 2 host guest stoichiometry (cf. Fig. 17 a). Assuming a perfectly ordered crystal lattice, the resulting central loop of H-bonds should appear to have homodromic directionality with the donor/acceptor functions separated in space. This contrasts to the behavior in the dihydrated l Im where no such characteristic loops are formed. Involvement of the C—H hydrogen atoms of the imidazole molecule, however, is similar in both cases. 

Molecular imprinting can be accomplished in two ways (a), the self assembly approach and (b), the preorganisation approach3. The first involves host guest complexes produced from weak intermolecular interactions (such as ionic or hydrophobic interaction, hydrogen bonding) between the analyte molecule and the functional monomers. The self assembled complexes are spontaneously formed in the liquid phase and are sterically fixed by polymerisation. After extraction of the analyte, vacant recognition sites specific for the imprint are established. Monomers used for self assembly are methacrylic acid, vinylpyridine and dimethylamino methacrylate. 

Host-guest hydrogen bonds, 14 169 Host lattices, 14 172 phenol, 14 174... 

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