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- W2001261138 abstract "Abstract The three novel amino acid β-cyclodextrin derivatives, l -methionine ( l -Met-β-CD, 2 ), l -proline ( l -Pro-β-CD, 3 ), and l -isoleucine ( l -Ile-β-CD, 4 ) modified β-cyclodextrins have been synthesized, and their inclusion complexation behavior was investigated through fluorescence spectrometry. Selecting both 8-anilino-1-napthalenesulfonic acid ammonium salt (ANS) and Rhodamine B (RhB) as spectral probes, spectrofluorometric titrations have been performed in aqueous phosphate buffer solution (pH 7.20) to calculate the complex stability constants ( K s ) for 1:1 inclusion complexation of amino acid modified β-cyclodextrins ( 2–4 ) with the two guest molecules. The results obtained indicate that the binding ability of modified β-cyclodextrins ( 2–4 ) with ANS increased as compared with the parent β-CD ( 1 ), where decreased with RhB. The molecular binding ability of ANS and RhB guests by natural ( 1 ) and modified β-cyclodextrins ( 2–4 ) was discussed from the size/shape fit concept." @default.
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- W2001261138 date "2000-01-01" @default.
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- W2001261138 title "Molecular recognition studies on supramolecular systems. 26. Inclusion complexation of natural and amino acid modified β-cyclodextrins with model substances: ANS and RhB molecules" @default.
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- W2001261138 doi "https://doi.org/10.1016/s0026-265x(99)00006-5" @default.
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