Molecular shape recognition of polycyclic aromatic hydrocarbons with a liquid-crystal bonded phase in supercritical fluid chromatography
β Scribed by Kiyokatsu Jinno; Hideo Mae; Yoshihiro Saito; Joseph J. Pesek; John C. Fetzer; Wilt R. Biggs
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 440 KB
- Volume
- 3
- Category
- Article
- ISSN
- 1040-7685
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β¦ Synopsis
Abstract
The chromatographic characteristics of a liquid crystal bonded phase have been evaluated for the separation of polycyclic aromatic hydrocarbons (PAHs), especially focusing on its shape recognition capability in supercritical fluid chromatography (SFC). The results clearly indicate that the phase has a stronger molecular planarity and shape recognition capability than typical polymeric and monomeric octadecylsilica (ODS) phases because of the very ordered bonded phase structure. The recognition capability was slightly dependent on SFC conditions such as column pressure, column temperature, and mobile phase density. Modifier addition did not make a large difference on the recognition capability. The phase seems to be a very promising stationary phase in SFC because the recognition capability is slightly influenced by the SFC conditions. Selectivity enhancement for molecular shape and planarity recognition has been found in SFC compared to reversedβphase LC separations with the same stationary phase.
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## Abstract A chemically bonded C~60~ silica phase was synthesized as a stationary phase for liquid chromatography (LC) and its retention behavior evaluated for various polycyclic aromatic hydrocarbons (PAHs) using microcolumn LC. The results indicate that the C~60~ bonded phase offers selectivity
A novel chemically bonded phase was evaluated for its applicability in Ε½ . discriminating among polycyclic aromatic hydrocarbons PAHs in terms of molecular size, planarity, and shape selectivity. It was observed that planar molecules were more retained than nonplanar analogues and that the retention