不同芳香族化合物在聚对苯二甲酸丁二酯固定相上的液相色谱保留行为

Koki Nakagami, Misato Amiya, K. Shimizu, Ohjiro Sumiya, Ryota Koike, I. Ueta, Yoshihiro Saito
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引用次数: 1

摘要

将聚对苯二甲酸丁二酯包被二氧化硅(PBT)作为液相色谱(LC)的固定相,并在反相色谱(LC)中评价了多环芳香族化合物(PACs)的保留行为。并与两种市售的十八烷基二氧化硅(ODS)相和苯基丁基二氧化硅(PBS)相的保留趋势进行了比较。在PBT固定相上证实了平面PACs的分子大小与相应的对数保留因子之间存在良好的线性关系,其趋势与传统聚合物ODS固定相上的趋势非常相似。此外,PBT固定相对由平面和非平面PACs组成的具有相似二维分子大小的溶质对具有良好的分子形状识别能力。PBT固定相对某些平面/非平面溶质对的选择性明显优于传统的ODS相,甚至与典型的聚合物ODS固定相在相似的实验条件下进行比较也是如此。对于二氯苯和二溴苯的结构异构体,PBT固定相的洗脱顺序为0 -、p-,而典型ODS相和PBS相的洗脱顺序不同,为0 -、p-和m-。由于PBT固定相与二氧化硅载体上的这些对异构体具有相似的部分化学结构,因此可以根据固定相配体与分析物分子之间的分子-分子相互作用来解释这一结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Retention Behavior of Various Aromatic Compounds on Poly(butylene terephthalate) Stationary Phase in Liquid Chromatography
Poly(butylene terephthalate)-coated silica (PBT) have been introduced as a stationary phase in liquid chromatography (LC) and the retention behavior of polycyclic aromatic compounds (PACs) was evaluated in reversed-phase LC. The trend for the retention was compared with that obtained on two types of commercially-available octadecylsilica (ODS) phases and phenylbutylsilica (PBS) phase. A good liner relationship between molecular size of planar PACs and the corresponding logarithmic retention factor was confirmed on the PBT stationary phase, and the trend is quite similar to that obtained on a conventional polymeric ODS stationary phase. In addition, a good molecular shape recognition capability of the PBT stationary phase was confirmed for several solute pairs consisted of planar and non-planar PACs with a similar two-dimensional molecular size. The selectivities to some planar/non-planar solute pairs on the PBT stationary phase were significantly better than conventional ODS phases, even when compared with that of typical polymeric ODS stationary phases operated in a similar experimental condition. In the case of structural isomers of dichlorobenzene and dibromobenzene, the elution order on the PBT stationary phase was o-, mand p-, however the corresponding elution order in typical ODS phases, and PBS phase was different, o-, pand m-. The results can be explained on the basis of the molecular-molecular interaction between the stationary phase ligand and the analyte molecule, because the PBT stationary phase has a similar partial chemical structure to these p-isomers on the silica support.
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