Silicon dioxide surface modified with cholesterol derivatives

被引:30
作者
Buszewski, B
Jezierska, M
Ostrowska-Gumkowska, B
机构
[1] Nicholas Copernicus Univ, Fac Chem, Dept Environm Chem & Ecoanalyt, PL-87100 Torun, Poland
[2] Nicholas Copernicus Univ, Fac Chem, Dept Phys Chem, PL-87100 Torun, Poland
关键词
silica; surface modification; physicochemical characterization; chromatography;
D O I
10.1016/S0254-0584(01)00320-0
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The major aim of the presented work was focused on the preparation and characterization of surface architecture of home-made packing materials for liquid chromatography and related techniques. Four stationary phases were synthesized on the basis of the same batch of silica gel. Two of them were obtained using compounds possessing liquid crystalline properties, one consisted of alkylamide ligands and one was conventionally prepared hydrocarbonaceous material. Properties of the silica matrix as well as the preparation of phases were discussed. Various physicochemical techniques were applied for the characterization of the surface of obtained packings. The progress of the modification reactions was confirmed by elemental analysis, which allowed calculation of the surface coverage density with bonded ligands. Created undersurface structure was examined by means of the solid-state NMR and FT-IR spectroscopy. Thermal analysis revealed the presence of phase transitions. The chromatographic experiments were designed and performed to prove the evidence of the non-homogenous nature of the surface of the packing materials and to create a relative hydrophobicity scale. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:30 / 41
页数:12
相关论文
共 54 条
[1]   Test analytes for studies of the molecular mechanism of chromatographic separations by quantitative structure-retention relationships [J].
Al-Haj, MA ;
Kaliszan, R ;
Nasal, A .
ANALYTICAL CHEMISTRY, 1999, 71 (15) :2976-2985
[2]   Mechanism of separation on cholesterol-silica stationary phase for high-performance liquid chromatography as revealed by analysis of quantitative structure-retention relationships [J].
Al-Haj, MA ;
Haber, P ;
Kaliszan, R ;
Buszewski, B ;
Jezierska, M ;
Chilmonzyk, Z .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1998, 18 (4-5) :721-728
[3]   Correlation between chromatographic and physicochemical properties of stationary phases in HPLC:: C30 bonded reversed-phase silica [J].
Albert, K .
TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 1998, 17 (10) :648-658
[4]   CHARACTERIZATION OF BONDED PHASES BY SOLID-STATE NMR-SPECTROSCOPY [J].
ALBERT, K ;
BAYER, E .
JOURNAL OF CHROMATOGRAPHY, 1991, 544 (1-2) :345-370
[5]  
BERENDSEN GE, 1980, J LIQ CHROMATOGR, V296, P3
[6]   Cholesteryl-silica stationary phase for liquid chromatography - Comparative study of retention behavior and selectivity [J].
Buszewski, B ;
Jezierska, M ;
Welniak, M ;
Kaliszan, R .
JOURNAL OF CHROMATOGRAPHY A, 1999, 845 (1-2) :433-445
[7]   CHEMICALLY BONDED PHASES FOR THE REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC SEPARATION OF BASIC SUBSTANCES [J].
BUSZEWSKI, B ;
SCHMID, J ;
ALBERT, K ;
BAYER, E .
JOURNAL OF CHROMATOGRAPHY, 1991, 552 (1-2) :415-427
[8]   ISOLATION AND DETERMINATION OF SUGARS IN NICOTIANA-TABACUM ON AMINOPROPYL CHEMICALLY BONDED PHASE USING SPE AND HPLC [J].
BUSZEWSKI, B ;
LODKOWSKI, R .
JOURNAL OF LIQUID CHROMATOGRAPHY, 1991, 14 (06) :1185-1201
[9]  
BUSZEWSKI B, 1987, CHEM LISTY, V81, P552
[10]   THE EFFECT OF THE REACTION MEDIUM ON THE COVERAGE DENSITY OF C-18 CHEMICALLY BONDED PHASE [J].
BUSZEWSKI, B ;
JURASEK, A ;
GARAJ, J ;
NONDEK, L ;
NOVAK, I ;
BEREK, D .
JOURNAL OF LIQUID CHROMATOGRAPHY, 1987, 10 (11) :2325-2336