Shape-shifting molecule behaviour during comprehensive two-dimensional gas chromatography analysis—A review

Philip J. Marriott , Yong Foo Wong , Michelle S.S. Amaral , Yuesong Wu
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Abstract

This research considers a number of molecular structural changes that have been reported in gas chromatography (GC), which take place during the chromatographic separation process of a molecule, and leads to an observation of an elevated baseline between the molecule and its product in a single column (1D) GC analysis. This phenomenon has been termed dynamic gas chromatography (DGC) in the case of interconverting compounds or reaction chromatography for a reaction process (RGC), and has also been referred to as forming a ‘bridge’. This is distinct from the conventional (dynamic) equilibrium process that defines chromatography. In order to observe this effect, the precursor (PRE) and product (PRO) must have resolvable peaks i.e., they must have a sufficient magnitude difference in their retention factors. Comprehensive two-dimensional gas chromatography (GC×GC) offers particular advantages to examine the nature of this elevated baseline phenomenon in the 2D space of GC×GC, provided the relative retentions of the respective PRE and PRO of the transformation are now resolved in the second dimension. This leads to the observation of what may appear as ‘streaking’ effects in the 2D plot, with theoretical terminal positions due to both the PRE and PRO components. These streaking effects should not be confused with adsorption (e.g., tailing) effects. The elevated baseline may comprise a single species, such as for a decomposition process, PRE → PRO, or may comprise more components such as when a reversible or interconversion process occurs, PRE ⇌ PRO. If degradation occurs in the heated injector, PRO may generate an elevated peak at its characteristic first and second column retention times (1tR and 2tR) as more PRO is produced. Considerations of different shapes arising from the different processes and their kinetics will also be discussed. This review introduces general aspects of dynamic GC, with a range of applications reported for this phenomenon. The manner in which this on-column process may be illustrated in GC×GC analysis to produce certain patterns in the 2D space are highlighted. Two recent examples of rearrangements in essential oil samples and irreversible changes in pyrethrins are considered in more depth, and experimental details are provided for these two cases.

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二维气相色谱综合分析过程中的变形分子行为--综述
本研究考虑了气相色谱(GC)中已报道的一些分子结构变化,这些变化发生在分子的色谱分离过程中,并导致在单柱(1D)气相色谱分析中观察到分子与其产物之间的基线升高。这种现象在化合物相互转化的情况下被称为动态气相色谱(DGC),在反应过程中被称为反应色谱(RGC),也被称为形成 "桥"。这与定义色谱的传统(动态)平衡过程不同。为了观察到这种效果,前体(PRE)和产物(PRO)必须具有可分辨的峰值,即它们的保留因子必须有足够大的差异。综合二维气相色谱法(GC×GC)在 GC×GC 的二维空间中研究这种基线升高现象的性质方面具有特殊的优势,前提是转化过程中各自的前体(PRE)和产物(PRO)的相对保留因子现在可以在二维空间中解析。这就导致在二维图中观察到可能出现的 "条纹 "效应,即 PRE 和 PRO 两部分的理论终点位置。这些条纹效应不应与吸附效应(如拖尾)相混淆。升高的基线可能由单一物质组成,如分解过程中的 PRE → PRO,也可能由更多的组分组成,如发生可逆或相互转化过程时的 PRE ⇌ PRO。如果在加热的进样器中发生降解,PRO 可能会在其特征的第一和第二色谱柱保留时间(1tR 和 2tR)处产生一个较高的峰值,因为会产生更多的 PRO。此外,还将讨论不同过程及其动力学所产生的不同形状。本综述介绍了动态气相色谱的一般方面,并报告了这一现象的一系列应用。重点介绍了柱上过程在 GC×GC 分析中产生特定二维空间模式的方式。更深入地探讨了精油样品中的重排和除虫菊素中的不可逆变化这两个最新实例,并提供了这两个实例的实验细节。
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来源期刊
Journal of chromatography open
Journal of chromatography open Analytical Chemistry
CiteScore
2.50
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0.00%
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0
审稿时长
50 days
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