Thirteen enantiomeric pairs of alpha-amino acids derivatised with fluorescein isothiocyanate (FITC-AAs) were separated in capillary electrophoresis (CE) using as chiral selectors the single isomer derivatives (SIDs) 3-monodeoxy-3-monoamino-beta- and gamma-cyclodextrins. The chiral separation data obtained by these strictly homologous compounds, show different behaviours, allowing to hypothesise a possible structure of the obtained selector-analyte complexes, as well as highlighting the crucial role of the cavity size and the significant effects on the resolution obtained by small differences in the structural characteristics of these analytes. (c) 2012 Elsevier B.V. All rights reserved.

Chiral separation of amino acids derivatised with fluorescein isothiocyanate by single isomer derivatives 3-monodeoxy-3-monoamino-beta- and gamma-cyclodextrins: the effect of the cavity size

GIUFFRIDA, ALESSANDRO;MACCARRONE, Giuseppe;Contino A;CUCINOTTA, Vincenzo
2012

Abstract

Thirteen enantiomeric pairs of alpha-amino acids derivatised with fluorescein isothiocyanate (FITC-AAs) were separated in capillary electrophoresis (CE) using as chiral selectors the single isomer derivatives (SIDs) 3-monodeoxy-3-monoamino-beta- and gamma-cyclodextrins. The chiral separation data obtained by these strictly homologous compounds, show different behaviours, allowing to hypothesise a possible structure of the obtained selector-analyte complexes, as well as highlighting the crucial role of the cavity size and the significant effects on the resolution obtained by small differences in the structural characteristics of these analytes. (c) 2012 Elsevier B.V. All rights reserved.
Capillary Electrophoresis; Cyclodetrin derivatives; Molecular Recognition; Chiral Separation; Amino acids
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/20.500.11769/16080
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