
Mono-(6-azido-6-deoxy)-β-cyclodextrin (CD) was covalently attached to an alkyne-modified 5-methyl-2-(pyridin-2-yl)thiazol-4-ol yielding a fluorophore containing CD in a click-type reaction. Intermolecular complexes were formed by poly(host–guest)-interactions. The supramolecular structures were characterized by 1H NMR-ROESY spectroscopy, dynamic light scattering, UV–vis spectroscopy, fluorescence spectroscopy, and asymmetric flow field-flow fractionation. By adding potassium adamantane-1-carboxylate, the thiazol dye is displaced from the CD-cavity and the elongated noncovalent polymeric structures collapse.
cyclodextrins, QD241-441, Science, Q, host–guest interaction, Organic chemistry, fluorescent dye, supramolecular polymer, Full Research Paper
cyclodextrins, QD241-441, Science, Q, host–guest interaction, Organic chemistry, fluorescent dye, supramolecular polymer, Full Research Paper
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