Molecular Shape Selectivity for Polycyclic Aromatic Compoundson a Poly(4-vinylpyridine) Stationary Phase in Liquid Chromatography

Koki Nakagami, K. Shimizu, Ohjiro Sumiya, I. Ueta, Yoshihiro Saito
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Abstract

Poly(4-vinylpyridine) (P4VP) was introduced as a stationary phase in liquid chromatography (LC) and the retention behavior of polycyclic aromatic compounds (PACs) on the P4VP phase has been investigated by comparing with that observed on commercially-available octadecylsilica (ODS) and phenylbutylsilica (PBS) phases. On the P4VP phase, a good linear relationship between the logarithmic retention factor and the molecular size of planar PACs was obtained, however, a unique selectivity for some planar PACs was also observed. The P4VP phase demonstrated a specific retention trend, where planar PACs having "square-like" molecular shape were strongly retained. The above trend clearly suggested a unique selectivity of the P4VP phase for PACs. In addition, compared to the typical ODS and PBS phases, the P4VP phase showed a good molecular shape recognition capability for planar/non-planar PACs with a similar two-dimensional molecular size. The P4VP phase showed a very small retention for various alkylbenzenes, suggesting somewhat limited contribution of the hydrophobicity of the analytes to the retention. In the investigation for the selectivity to structural isomers, the P4VP phase exhibited a unique selectivity for isomers of dichlorobenzene and dibromobenzene when compared to the typical ODS and PBS phases. The trend can be interpreted as a dipole-dipole interaction between pyridyl groups in the P4VP ligands and the analyte.
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多环芳香族化合物在聚(4-乙烯基吡啶)固定相中的分子形状选择性
在液相色谱(LC)中引入了聚(4-乙烯基吡啶)(P4VP)作为固定相,并通过与市售十八烷基二氧化硅(ODS)和苯基丁基二氧化硅(PBS)相的保留行为进行比较,研究了多环芳烃(PAC)在P4VP相上的保留行为。在P4VP相上,对数保留因子与平面PAC的分子尺寸之间获得了良好的线性关系,然而,也观察到一些平面PAC具有独特的选择性。P4VP相表现出特定的保留趋势,其中具有“方形”分子形状的平面PAC被强烈保留。上述趋势清楚地表明P4VP相对PAC具有独特的选择性。此外,与典型的ODS和PBS相相比,P4VP相对具有相似二维分子尺寸的平面/非平面PAC表现出良好的分子形状识别能力。P4VP相对各种烷基苯显示出非常小的保留,这表明分析物的疏水性对保留的贡献有些有限。在对结构异构体的选择性研究中,与典型的ODS和PBS相相比,P4VP相对二氯苯和二溴苯的异构体表现出独特的选择性。该趋势可以解释为P4VP配体中的吡啶基与分析物之间的偶极-偶极相互作用。
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