Capillary electrophoretic separation of weak base enantiomers using the single-isomer heptakis-(2,3-dimethyl-6-sulfato)-β-cyclodextrin as resolving agent and methanol as background electrolyte solvent
被引:38
作者:
Cai, H
论文数: 0引用数: 0
h-index: 0
机构:
Texas A&M Univ, Dept Chem, College Stn, TX 77842 USATexas A&M Univ, Dept Chem, College Stn, TX 77842 USA
Cai, H
[1
]
Vigh, G
论文数: 0引用数: 0
h-index: 0
机构:
Texas A&M Univ, Dept Chem, College Stn, TX 77842 USATexas A&M Univ, Dept Chem, College Stn, TX 77842 USA
Vigh, G
[1
]
机构:
[1] Texas A&M Univ, Dept Chem, College Stn, TX 77842 USA
The sodium salt of the single-isomer, heptakis-(2,3-dimethyl-6-sulfato)-beta-cyclodextrin (HDMS-beta CD) was used as resolving agent in the capillary electrophoretic (CE) separation of weak base enantiomers in pure methanol background electrolytes (BEs). According to the requirements of the charged resolving agent migration model of CE enantiomer separations (CHARM model), a high buffer-capacity, low pH methanolic BE was created from 25 mM phosphoric acid and 12.5 mM NaOH. In this BE, the solubility of HDMS-beta CD was as high as 50 mM, permitting the realization of very high separation selectivities and short separation times for the fully protonated weak base enantiomers. (C) 1998 Elsevier Science B.V. All rights reserved.