![]()
![]()
Published: Journal of Chromatographic Science, Volume 33, Number 6, June 1995, pp. 281-284.
HPLC on Calixarene Bonded Silica Gels. I. Characterization
and Applications of the p-tert -Butyl-Calix[4]arene Bonded Material
S. Friebe, S. Gebauer, G.J. Krauss, G. Goermar and J. Krueger
Molecules containing cavities of well-defined dimensions are able to include guest molecules stereoselectively. This work is concerned with the introduction and evaluation of a newly developed high-performance liquid chromatographic packing material based on calix[4]arene chemically bonded to silica gel. It is well documented that calixarenes representing cyclic condensates of para substituted phenols and formaldehyde have the ability to form intracavity inclusion complexes with ions and organic molecules in aqueous solutions. The silica bonded macrocyclic ligands form truncated cones similar to cyclodextrins. Data are presented illustrating the resolution characteristics for disubstituted aromatics, peptides, nucleosides, and nucleobases. The results indicate that the calix[4]arene silica gel behaves predominantly as a reversed-phase material. Some effects support the assumption that the cavity acting as an electron donator can influence the elution order.
Reproduction of editorial content of this journal is prohibited without publishers permission.
| This article is available in its entirety by fax for $4.00 per page. Visa or MasterCard accepted. To order electronically click
here Please indicate JCS volume and issue along with page numbers. |
Site Map: Home
| Current Issue | Subscribe
|
| Back Issues | About
Us | Meetings | Advertising
|
| Books for Sale | For
the Author | Links |
| Supplier Info |Search
|