Capillary electrophoretic separation of the enantiomers of organophosphates with a phosphorus stereogenic center using the sodium salt of octakis(2,3-diacetyl-6-sulfo)-gamma-cyclodextrin as resolving agent

Citation
Wh. Zhu et al., Capillary electrophoretic separation of the enantiomers of organophosphates with a phosphorus stereogenic center using the sodium salt of octakis(2,3-diacetyl-6-sulfo)-gamma-cyclodextrin as resolving agent, J CHROMAT A, 895(1-2), 2000, pp. 247-254
Citations number
21
Categorie Soggetti
Chemistry & Analysis","Spectroscopy /Instrumentation/Analytical Sciences
Journal title
Volume
895
Issue
1-2
Year of publication
2000
Pages
247 - 254
Database
ISI
SICI code
Abstract
The sodium salt of the single-isomer, chiral resolving agent, octakis(2,3-d iacetyl-6-sulfo)-gamma -cyclodextrin (ODAS-gamma CD) has been used for the capillary electrophoretic separation of the enantiomers of alkylarylphospha tes which carry a phosphorus-based stereogenic center. The effective mobili ties and separation selectivities were measured at different ODAS-gamma CD and methanol concentrations to find the conditions under which the minor en antiomers could be adequately quantitated in samples obtained by chemical r esolution of the racemic mixtures. This work extends the utility of ODAS-ga mma CD to a hitherto unexplored field, the capillary electrophoretic separa tion of the enantiomers of organophosphorus compounds. (C) 2000 Elsevier Sc ience B.V. All rights reserved.