The separation of three pairs of enantiomeric herbicides has been successfully achieved by capillary electrophoresis at two different pH values in the presence of cyclodextrin derivatives previously synthesized in our laboratory. Two of these derivatives constitute a new class of receptor, the hemispherodextrins, in which a trehalose capping moiety is bonded to β-cyclodextrin. Because of their peculiar structure hemispherodextrins have very promising characteristics and the low receptor concentra- tion required to achieve separation deserves particular in- terest.

New cyclodextrins derivatives as chiral selectors in capillar electrophoresis,

GRASSO G;MAZZAGLIA A;
2001

Abstract

The separation of three pairs of enantiomeric herbicides has been successfully achieved by capillary electrophoresis at two different pH values in the presence of cyclodextrin derivatives previously synthesized in our laboratory. Two of these derivatives constitute a new class of receptor, the hemispherodextrins, in which a trehalose capping moiety is bonded to β-cyclodextrin. Because of their peculiar structure hemispherodextrins have very promising characteristics and the low receptor concentra- tion required to achieve separation deserves particular in- terest.
2001
Istituto per lo Studio dei Materiali Nanostrutturati - ISMN
Istituto di Cristallografia - IC - Sede Secondaria Catania
Algorithms, Carbohydrate Sequence, Cyclodextrins, Electrophoresis, Capillary, Molecular Sequence Data, Stereoisomerism
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/487614
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