Chemically bonded silica stationary phases: Synthesis, physicochemical characterization, and molecular mechanism of reversed phase HPLC retention

被引:111
作者
Buszewski, B [1 ]
GadzalaKopciuch, RM [1 ]
Markuszewski, M [1 ]
Kaliszan, R [1 ]
机构
[1] MED UNIV GDANSK,DEPT BIOPHARMACEUT & PHARMACODYNAM,PL-80416 GDANSK,POLAND
关键词
D O I
10.1021/ac9612032
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Two types of chemically bonded phases for high-performance liquid chromatography (HPLC) have been prepared: a conventional C18 and AP (N-acylaminopropylsilica), a novel one that contains specific interaction sites localized in the hydrophobic chain, Surface properties of stationary phases, before and after chemical modification, have been characterized by several physicochemical techniques, such as porosimetry, ICP atomic emission spectroscopy, elemental analysis, solid state CP/MAS NMR, and chromatography, For the studies of the reversed-phase HPLC retention mechanism under hydroorganic conditions, a test series of structurally diverse solutes has been selected, Sets of retention parameters and structural descriptors of the test solutes were subjected to multiparameter regression analysis, The quantitative structure-retention relationships derived demonstrated the typical reversed-phase partition mechanism to predominate in the separation on the C18 phases but not on the AP phases, The AP phases were demonstrated to provide significant input to retention due to the structurally specific dipole-dipole and charge transfer interactions with the solutes. The proposed AP phases for HPLC possess distinctive and interesting retentive properties, and chemometric analysis of retention data of appropriately designed series of test solutes appears to be a convenient, objective, and quantitative method to prove a new phase specificity.
引用
收藏
页码:3277 / 3284
页数:8
相关论文
共 61 条
[2]   THE USE OF CHARACTERISTIC VOLUMES TO MEASURE CAVITY TERMS IN REVERSED PHASE LIQUID-CHROMATOGRAPHY [J].
ABRAHAM, MH ;
MCGOWAN, JC .
CHROMATOGRAPHIA, 1987, 23 (04) :243-246
[3]   HYDROGEN-BONDING .38. EFFECT OF SOLUTE STRUCTURE AND MOBILE-PHASE COMPOSITION ON REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC CAPACITY FACTORS [J].
ABRAHAM, MH ;
ROSES, M .
JOURNAL OF PHYSICAL ORGANIC CHEMISTRY, 1994, 7 (12) :672-684
[4]  
ABRAHAM MH, 1996, U COLLEGE LONDON DAT
[5]   CP/MAS NMR INVESTIGATIONS OF SILICA-GEL SURFACES MODIFIED WITH AMINOPROPYLSILANE [J].
ALBERT, K ;
BRINDLE, R ;
SCHMID, J ;
BUSZEWSKI, B ;
BAYER, E .
CHROMATOGRAPHIA, 1994, 38 (5-6) :283-290
[6]  
[Anonymous], WIAD CHEM
[7]   Comparison and quantification of chromatographic retention mechanisms on three stationary phases using structure-retention relationships [J].
Azzaoui, K ;
MorinAllory, L .
CHROMATOGRAPHIA, 1996, 42 (7-8) :389-395
[8]   CHARACTERIZATION OF CHEMICALLY MODIFIED SILICA-GELS BY SI-29 AND C-13 CROSS-POLARIZATION AND MAGIC ANGLE SPINNING NUCLEAR MAGNETIC-RESONANCE [J].
BAYER, E ;
ALBERT, K ;
REINERS, J ;
NIEDER, M ;
MULLER, D .
JOURNAL OF CHROMATOGRAPHY, 1983, 264 (02) :197-213
[9]   PREPARATION AND CHROMATOGRAPHIC PROPERTIES OF SOME CHEMICALLY BONDED PHASES FOR REVERSED-PHASE LIQUID-CHROMATOGRAPHY [J].
BERENDSEN, GE ;
GALAN, LD .
JOURNAL OF LIQUID CHROMATOGRAPHY, 1978, 1 (05) :561-586
[10]   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