A visual approach to stationary phase selectivity classification based on the Snyder-Dolan Hydrophobic-Subtraction Model

被引:45
作者
Zhang, Yu [1 ]
Carr, Peter W. [1 ]
机构
[1] Univ Minnesota, Dept Chem, Smith & Kolthoff Hall,207 Pleasant St SE, Minneapolis, MN 55455 USA
基金
美国国家卫生研究院;
关键词
HPLC; Stationary phase; Reversed phase; Selectivity; Classification scheme; PERFORMANCE LIQUID-CHROMATOGRAPHY; SOLVATION ENERGY RELATIONSHIPS; UNIFIED MOLECULAR THEORY; ALKYL-SILICA COLUMNS; BONDED PHASES; SHAPE SELECTIVITY; HOMOLOGOUS SERIES; ORGANIC MODIFIER; SOLVENT STRENGTH; PARAMETER MODEL;
D O I
10.1016/j.chroma.2009.06.048
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A novel type of stationary phase selectivity classification "triangle" has been developed based on the Snyder-Dolan (S-D) Hydrophobic-Subtraction Model, wherein the apices of a set of four triangles represent the relative contributions of steric hindrance (chi(S)), hydrogen-bonding acidity (chi(A)), hydrogen-bonding basicity (chi(B)), cation-exchange capacity (chi(C)) to selectivity. We found that "effective selectivity" of a stationary phase is mathematically given by the ratio of system dependent interaction coefficients but not their absolute Values. Thus by normalizing the S*, A, B and C terms of the S-D model by H, we were able to obtain four parameters which fully define the chromatographic selectivity of the stationary phases. By examining the parameters in groups of three, we can represent all the result ill a set of four "selectivity triangles". The distinctive feature of this approach compared to the S-D phase classification scheme is that it allows the visualization of Column selectivity by plotting three-dimensional data in a two-dimensional space. Moreover. it very clearly shows that the RPLC columns thus far characterized cover only a small fraction of separation selectivity space leaving a great deal of room for researchers to develop novel RPC materials. Various applications of these "selectivity triangles" will be discussed in this paper. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:6685 / 6694
页数:10
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