The applicability of the pyrene@2β-cyclodextrin complex as a fluorescent chemosensor for aromatic amino acids has been studied by fluorescence spectroscopy. For the first time, it has been that the sensitivity of the complex to the implementation of D-enantiomers into its cavity is higher in comparison with the L-enantiomers of aromatic amino acids. Quantum-chemical calculations confirmed that the binding of the D-enantiomers of aromatic amino acids with P@2βCD is characterized by a greater energy of complexation in comparison with the L-enantiomers.
High Energy Chemistry – Springer Journals
Published: Jun 1, 2018
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