FUNCTIONAL-GROUP SELECTIVITY USING FLUOROFORM AS A MOBILE-PHASE FOR SUPERCRITICAL-FLUID CHROMATOGRAPHY

Citation
Ja. Blackwell et Le. Schallinger, FUNCTIONAL-GROUP SELECTIVITY USING FLUOROFORM AS A MOBILE-PHASE FOR SUPERCRITICAL-FLUID CHROMATOGRAPHY, The Journal of microcolumn separations, 6(5), 1994, pp. 475-482
Citations number
12
Categorie Soggetti
Chemistry Analytical
ISSN journal
10407685
Volume
6
Issue
5
Year of publication
1994
Pages
475 - 482
Database
ISI
SICI code
1040-7685(1994)6:5<475:FSUFAA>2.0.ZU;2-2
Abstract
The eluotropic strength and chromatographic selectivity of fluoroform is compared to that of carbon dioxide and methanol-modified carbon dio xide. Naphthalene derivatives were used as probe solutes in capillary supercritical fluid chromatography to determine the effects of fluid t ype, pressure, and temperature on selectivity and retention. Fluorofor m is much stronger in eluotropic strength than carbon dioxide or metha nol-modified carbon dioxide at the same temperature and pressure. Unde r the same reduced conditions, fluoroform is lower in eluotropic stren gth than carbon dioxide. Specific interactions between hydrogen bond a ccepting functional groups and fluoroform are observed. Functional gro ups capable of accepting hydrogen bonds contribute less of an increase in retention when using fluoroform while those capable of dispersive interactions contribute less of an increase in retention when using ca rbon dioxide.