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Optical characterization of supramolecular complexes of selected organic fluorophores with cyclodextrins
Haiklová, Simona ; Dian, Juraj (advisor) ; Červený, Václav (referee)
The content of this thesis is the optical characterization and determination of the strength of supramolecular interaction of selected organic fluorophores and cyclodextrins (CD) using the stability constant with optical methods: UV-Vis absorption and fluorescence. Two series of fluorophores differed in the presence of groups with two positive charges, and two types of cyclodextrins (-CD a -CD) with different cavity sizes were chosen for the study. Fluorophores with charged end groups can be efficiently bound by electrostatic interaction on solid surfaces of suitable chemical composition or thin films with an excess of negative charge and thus immobilized by a very strong interaction on a given support. These prepared surfaces or layers can then be used for the optical detection of chemical substances. The aim of this work was to determine the influence of cyclodextrin cavity size, the presence of a charged anchor, and solution pH on the supramolecular interaction of the studied systems and evaluate the application possibilities of the studied systems for optical chemosensors. In the presented thesis, the change in optical absorption and fluorescence intensity of four pairs of fluorophores: PRODAN, RhB, RhB-Si, DANSA, and their derivatives with a charged anchor was studied during supramolecular...
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Spectrophotometric determination of stability constants of cyclodextrin derivatives by phenolphthalein method
Haiklová, Simona ; Dian, Juraj (advisor) ; Červený, Václav (referee)
This bachelor thesis deals with the determination of stability constants of cyclodextrins and their derivatives in the formation of supramolecular complexes with phenolphthalein. Cyclodextrins - macrocyclic oligosaccharides - are characterized by the shape of a truncated cone, whose internal hydrophobic cavity can form, with suitable substances, host-guest inclusion complexes. The formation of these inclusion complexes is accompanied by a change of a number of physicochemical parameters of the included compounds. In this bachelor thesis, the change of optical absorption of phenolphthalein, which has characteristic violet color in the alkaline area, was studied during its interaction with selected CD macrocycles. The formation of a supramolecular complex resulted in a decrease in optical absorption, which was quantified and used to determine stability constant. In the bachelor thesis, the supramolecular interaction of phenolphthalein with six derivatives of cyclodextrins were studied - basic cyclodextrins β-CD a γ-CD and their two derivatives. In the selected derivatives of these CDs the -OH groups in positions 2, 3, and 6 were replaced either by hydroxypropyl groups (hydroxypropyl-β-CD and hydroxypropyl-γ- CD) or (randomly) by methyl groups (RaMe-β-CD and RaMe-γ-CD). For these CD derivatives, the...
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