Enantiomeric separation by capillary electrochromatography - II. Chiral separation of dansyl amino acids and phenoxy acid herbicides on sulfonated silica having surface-bound hydroxypropyl-beta-cyclodextrin
Mq. Zhang et Z. El Rassi, Enantiomeric separation by capillary electrochromatography - II. Chiral separation of dansyl amino acids and phenoxy acid herbicides on sulfonated silica having surface-bound hydroxypropyl-beta-cyclodextrin, ELECTROPHOR, 21(15), 2000, pp. 3135-3140
A chiral silica-based stationary phase having surface-bound hydroxypropyl-b
eta-cyclodextrin (HP-beta-CD) with a relatively strong electroosmotic flow
(EOF) was introduced for enantioseparation by capillary electrochromatograp
hy (CEC). The stationary phase contained a hydrophilic sulfonated sublayer
to which a chiral top layer of HP-beta-CD was immobilized. While the sulfon
ated sublayer was to provide a relatively strong EOF, the top HP-beta-CD wa
s to confer the desired chiral recognition towards enantiomeric solutes. Th
is HP-beta-CD sulfonated silica (CDSS) stationary phase proved useful for t
he rapid separation of anionic enantiomers such as dansyl amino acids and p
henoxy acid herbicides. The effects of the organic modifier content, pH, an
d ionic strength of the mobile phase on enantioseparation were investigated
. Under the optimized separation conditions, ten dansyl amino acids and six
phenoxy acid herbicides were enantioseparated with a resolution greater th
an unity.