SOLID-STATE NMR-STUDIES OF IONIC SURFACTANTS ADSORBED ON CYANOPROPYL-BONDED PHASES - IMPLICATIONS FOR MICELLAR LIQUID-CHROMATOGRAPHY

Citation
Bk. Lavine et al., SOLID-STATE NMR-STUDIES OF IONIC SURFACTANTS ADSORBED ON CYANOPROPYL-BONDED PHASES - IMPLICATIONS FOR MICELLAR LIQUID-CHROMATOGRAPHY, Journal of colloid and interface science, 179(2), 1996, pp. 341-349
Citations number
20
Categorie Soggetti
Chemistry Physical
ISSN journal
00219797
Volume
179
Issue
2
Year of publication
1996
Pages
341 - 349
Database
ISI
SICI code
0021-9797(1996)179:2<341:SNOISA>2.0.ZU;2-6
Abstract
Solid-state C-13 NMR spectroscopy techniques, including cross polariza tion (CP), magic angle spinning (MAS), and high-power proton decouplin g, have been used to study the interactions of two ionic surfactants, sodium dodecyl sulfate(SDS) and cetyltrimethylammonium bromide (CTAB), with the cyanopropyl bonded phase. Variable contact time CP/MAS C-13 NMR data suggest that the unusual behavior of cyanopropyl bonded phase columns in SDS and CTAB micellar reversed-phase liquid chromatography can be attributed to the strong interactions between the polar head g roup of SDS or CTAB and the cyano functionality of the polar bonded ph ase, Models which depict the structure of the surfactant-modified cyan opropyl bonded phase are proposed from the NMR data, and these models are in good agreement with the selectivity exhibited by cyanopropyl bo nded phase columns toward polar and ionogenic compounds in MLC. (C) 19 96 Academic Press, Inc.