Effects of solvent density on retention in gas-liquid chromatography II.: Polar solutes in poly(ethylene glycol) stationary phases

被引:10
作者
González, FR
Pérez-Parajón, J
机构
[1] CSIC, Inst Quim Fis Rocasolano, E-28006 Madrid, Spain
[2] Natl Univ La Plata, Fac Ciencias Exactas, Div Quim Analit, RA-1900 La Plata, Argentina
关键词
density; partition coefficients; stationary phases; GC; thermodynamic parameters; molecular dynamics; computer simulations; poly(ethylene oxide);
D O I
10.1016/S0021-9673(03)00085-2
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Effects of solvent density on the solubility of polar probes which undergo specific interactions with poly(oxyethylene) are studied. The analysis of retention data on capillary columns coated with oligomeric poly(oxyethylene) stationary phases shows that, within the experimental error, the enthalpic contribution to the solubility is practically independent of variations in the solvent density. Average values of enthalpies of solute transfer are reported for different probes and temperatures. The observed systematic decrease of solubility with the increasing density is due to a change of entropy. Some thermodynamic consequences inferred from these general results are discussed. One relevant observation is that the influence of solvent's final groups must be negligible. This is even the case for oligomers with number-average degrees of polymerization as low as 13, hosting solutes capable of strong interactions with the end hydroxyl groups of linear poly(ethylene glycols). Possible explanations for this behavior are explored through molecular dynamics simulations of the liquid solvent. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:265 / 276
页数:12
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