The poly (vinyl chloride) (PVC) thin films embedding amphiphilic cyclodextrins at the one sides of the films have been prepared by spreading the solutions of the mixtures of PVC and cyclodextrin derivatives in THF-toluene on water. The XPS analyses indicate that the hydrophilic cyclodextrin head groups are arranged at the surfaces of the polymer films. The chiral recognition of such cyclodextrin films has been studied by dipping the films in the aqueous solutions of (
R) - and (
S) -1, 1′-binaphthy1-2, 2′-diylphosphates (BNP) and analyzing the films by means of XPS spectroscopy. The (
S) -BNP is preferentially bound to the cyclodextrin-embedding PVC films, which is in agreement with the results obtained for the homogeneous aqueous system as well as those for the cyclodextrin monolayer and LB membranes. The enantiomer selectivity of the film is altered by the dipping time. The XPS and FT-IR measurements indicate that the 2-naphthoate anion in water is bound to the cyclodextrin film in its salt form. Deducing from this result, the BNP anion in water seems to be transferred to the cyclodextrin film in its salt form. It is assumed that the chiral recognition is achieved by the enantioselective inclusion of BNP into the cyclodextrin cavity at the surface of the PVC film.
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