TY - JOUR
T1 - Resolution and determination of enantiomeric purity of new chiral derivatives of xanthones using polysaccharide-based stationary phases
AU - Fernandes, Carla
AU - Brandão, Pedro
AU - Santos, Alexandre
AU - Tiritan, Maria Elizabeth
AU - Afonso, Carlos
AU - Cass, Quezia B.
AU - Pinto, Madalena M.
N1 - Funding Information:
This work was funded by FCT – Fundação para a Ciência e a Tecnologia under the project CEQUIMED-PEst-OE/SAU/UI4040/2011; under the project FCT-GRICES/CAPES 00770 29/05/08, University of Porto/Santander Totta (Investigação Científica na Pré-Graduação) projects, and also funded by FEDER funds through the COMPETE program under the project FCOMP-01-0124-FEDER-011057.
PY - 2012/12/21
Y1 - 2012/12/21
N2 - The enantioresolution and determination of the enantiomeric purity of 24 new chiral derivatives of xanthones (CDXs) were investigated on polysaccharide-based chiral stationary phases (CSPs). The tris-3,5-dimethylphenylcarbamates of cellulose and amylose and tris-3,5-dimethoxyphenylcarbamate of amylose were selected as CSPs for this work. The separation of enantiomeric mixtures of CDXs was explored under multimodal elution conditions. All the enantiomeric mixtures of CDXs were enantioseparated with very high enantioselectivity and resolution with α and RS ranging from 1.43 to 12.41 and from 1.48 to 10.29, respectively. The best performances were achieved on amylose tris-3,5-dimethylphenylcarbamate stationary phase under polar organic elution conditions. Furthermore the enantiomeric purity for all the CDXs was measured, achieving values higher than 99%. Based on the obtained results, the influence of the mobile phases and structural features of the CSPs and CDXs on chiral discrimination are also discussed.
AB - The enantioresolution and determination of the enantiomeric purity of 24 new chiral derivatives of xanthones (CDXs) were investigated on polysaccharide-based chiral stationary phases (CSPs). The tris-3,5-dimethylphenylcarbamates of cellulose and amylose and tris-3,5-dimethoxyphenylcarbamate of amylose were selected as CSPs for this work. The separation of enantiomeric mixtures of CDXs was explored under multimodal elution conditions. All the enantiomeric mixtures of CDXs were enantioseparated with very high enantioselectivity and resolution with α and RS ranging from 1.43 to 12.41 and from 1.48 to 10.29, respectively. The best performances were achieved on amylose tris-3,5-dimethylphenylcarbamate stationary phase under polar organic elution conditions. Furthermore the enantiomeric purity for all the CDXs was measured, achieving values higher than 99%. Based on the obtained results, the influence of the mobile phases and structural features of the CSPs and CDXs on chiral discrimination are also discussed.
KW - Chiral derivatives of xanthones
KW - Enantiomeric purity
KW - Enantioselectivity
KW - Multimodal elution
KW - Polysaccharide-based stationary phases
UR - http://www.scopus.com/inward/record.url?scp=84870339987&partnerID=8YFLogxK
U2 - 10.1016/j.chroma.2012.07.058
DO - 10.1016/j.chroma.2012.07.058
M3 - Article
C2 - 22889602
AN - SCOPUS:84870339987
SN - 0021-9673
VL - 1269
SP - 143
EP - 153
JO - Journal of Chromatography A
JF - Journal of Chromatography A
ER -