O. Zerbinati et al., Optimization of the cyclodextrin-assisted capillary electrophoresis separation of the enantiomers of phenoxyacid herbicides, J CHROMAT A, 875(1-2), 2000, pp. 423-430
An ethylcarbonate derivative of beta-cyclodextrin (beta-CD) with three subs
tituents per molecule, hydroxypropyl-beta-CD and native alpha-CD have been
tested as resolving agents in the capillary zone electrophoresis (CZE) sepa
ration of the four enantiomers of the herbicides mecoprop and dichlorprop.
The performances of the three compounds have been quantified by means of tw
o-levels full factorial design and the inclusion constants were calculated
from CZE migration time data. Possible structure of inclusion complexes hav
e been proposed, on the basis of molecular mechanics simulations. (C) 2000
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