in Wiley Online Library (wileyonlinelibrary.com).The enantioselective extraction of hydrophobic oxybutynin (OBN) enantiomers by hydrophilic b-cyclodextrin (b-CD) derivatives was studied. The efficiency of extraction depends strongly on a number of process variables such as types of organic solvents and b-CD derivatives, concentration of selector, pH, and temperature. The experimental data were described by a reactive extraction model with a homogeneous aqueous phase reaction of R,S-OBN with b-CD. Important parameters of this model were determined experimentally. The physical distribution coefficients for molecular and ionic OBN were 4.96 Â 10 À3 and 9.52, respectively. The equilibrium constants of the complexation reactions were 1770 and 1340 L/mol for S-and R-OBN, respectively. By modeling and experiment, an optimal extraction condition with pH of 5 and HP-b-CD concentration of 0.1 mol/L was obtained with enantioselectivity (a) of 1.26, which was close to the theoretical maximum of 1.32 and performance factor (pf i ) of 0.036. The model was verified experimentally with excellent results.
This article reports a new chiral separation method-biphasic recognition chiral extraction for the separation of mandelic acid enantiomers. Distribution behavior of mandelic acid enantiomers was studied in the extraction system with
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.