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
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
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.