Journal of the American Chemical Society, Vol.118, No.21, 5039-5046, 1996
Controlled Orientation of Cyclodextrin Derivatives Immobilized on Gold Surfaces
Several different cyclodextrinthiol derivatives have been immobilized on gold surfaces through a chemisorption process to form films which exhibit significantly different features. Three monothiolated cyclodextrin derivatives with different spacers between the cyclodextrin cavity and the thiol group and a mixture of multithiolated cyclodextrins were synthesized and characterized. Chemisorption of these compounds onto gold surfaces gave films which were investigated by Fourier transform infrared (FTIR) spectroscopy, time-of-flight mass spectrometry, contact angle measurements, plasmon surface polariton (PSP) spectroscopy, and cyclic voltammetry. It was found that the chemical structure of each cyclodextrin derivative had a strong influence on the molecular architecture in the resulting films, and in particular on the orientation of the cyclodextrin torus. Models were developed to describe the molecular arrangement in the films.
Keywords:ORGANIZED MOLECULAR ASSEMBLIES;BETA-CYCLODEXTRIN;ALPHA-CYCLODEXTRIN;MONOLAYERS;ELECTRODES;INTERFACE;FILMS