Loading…

Separation of racemic 2,4-dinitrophenyl amino acids on zirconia-immobilized quinine carbamate in reversed-phase liquid chromatography

Zirconia is known to be one of the best chromatographic support materials due to its excellent chemical, thermal, and mechanical stability. A quinine carbamate‐coated zirconia was prepared as a chiral stationary phase for separation of enantiomers of DNP‐amino acids in reversed‐phase liquid chromato...

Full description

Saved in:
Bibliographic Details
Published in:Journal of separation science 2004-08, Vol.27 (12), p.977-982
Main Authors: Park, Jung Hag, Lee, Joon Woo, Song, Young Tae, Ra, Chun Sup, Cha, Jin Soon, Ryoo, Jae Jeong, Lee, Wonjae, Kim, In Whan, Jang, Myung Duk
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Zirconia is known to be one of the best chromatographic support materials due to its excellent chemical, thermal, and mechanical stability. A quinine carbamate‐coated zirconia was prepared as a chiral stationary phase for separation of enantiomers of DNP‐amino acids in reversed‐phase liquid chromatography. Retention and enantioselectivity of this phase were compared to those for quinine carbamate bonded onto silica. Most amino acids studied were separated on the quinine carbamate‐zirconia CSP although retention was longer and chiral selectivity was somewhat lower than on the corresponding silica CSP. Increased retention and decreased selectivity are probably due to strong non‐enantioselective Lewis acid‐base interactions between the amino acid molecule and the residual Lewis acid sites on the zirconia surface.
ISSN:1615-9306
1615-9314
DOI:10.1002/jssc.200301713