Retention Mechanism for Ion-Pair Chromatography with Chaotropic Reagents. From Ion-Pair Chromatography toward a Unified Salt Chromatography.

4区 化学 Q4 Chemistry Advances in Chromatography Pub Date : 2011-01-01 DOI:10.1201/b10721-2
Teresa Cecchi
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引用次数: 9

Abstract

The breakthrough of chaotropic mobile phase modifiers in reversed-phase high-performance liquid chromatography (RP-HPLC) is due to their strong potential to provide adequate retention of ionic analytes without the blamed semipermanent modification of the chromatographic packing often connected to the use of classical ion-pair reagents. The lack of a physicochemical framework that is able to unify eclectic experimental evidence concerning the use of a wide gamut of ionic additives in RP-HPLC is the primary motive force for recent theoretical efforts to model their behavior. The time-honored solvophobic theory cannot properly explain salt effects. Its theoretical basis was recently questioned by breaking experimental evidence at variance with the textbook knowledge of ionic solutions interfaces; meanwhile, a recently proved extended thermodynamic approach to ion-pair chromatography (IPC) is challenged by the breakthrough of neoteric ionic additives whose behavior questions the rigidity of previous retention schemes and bridges salting chromatographic phenomena to IPC. Building on these research needs, the aims of this review are (1) to illustrate a comprehensive theory of analyte retention in the presence of any kind of electrolytes (hydrophobic ions, chaotropes, kosmotropes, ionic liquids [ILs]) to capture and rationalize the main salting effects and to support their strong practical impact for the separation of organic and inorganic ions, ionogenic, neutral, and zwitterionic analytes; (2) to explain why ion-specific salting chromatographic effects that represent a diachronic scientific consideration were not satisfactorily explained in the rubric of the solvophobic theory; and (3) to highlight the eligibility of chromatography as a basic technique that is able to clarify the currently hotly debated behavior of ions at water interfaces. The practical impact of chaotropic chromatography will also be detailed, and urgent research needs and suggestions will be illustrated.

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朝向试剂离子对色谱的保留机理。从离子对色谱到统一盐色谱。
朝向流动相改性剂在反相高效液相色谱(RP-HPLC)中的突破是由于它们具有强大的潜力,可以提供足够的离子分析物的保留,而不需要通常与使用经典离子对试剂相关的色谱填料的半永久性改性。缺乏能够统一RP-HPLC中广泛使用离子添加剂的折衷实验证据的物理化学框架是最近理论努力模拟其行为的主要动力。历史悠久的疏溶剂理论不能很好地解释盐的作用。它的理论基础最近受到质疑,因为它打破了与离子溶液界面课本知识不一致的实验证据;与此同时,新近离子添加剂的突破对离子对色谱(IPC)的扩展热力学方法提出了挑战,其行为质疑了先前保留方案的刚性,并将盐化色谱现象与IPC联系起来。基于这些研究需求,本综述的目的是:(1)阐述分析物在任何电解质(疏水离子、混沌性、宇宙性、离子液体[ILs])存在下的保留的综合理论,以捕获和合理的主要盐化效应,并支持它们对有机和无机离子、离子性、中性和两性离子分析物分离的强大实际影响;(2)解释为什么代表历时性科学考虑的离子特异性盐化色谱效应在疏溶剂理论的框架下不能令人满意地解释;(3)强调色谱作为一种基本技术的资格,它能够澄清目前热议的离子在水界面的行为。本文还将详细介绍朝向色谱的实际影响,并阐述迫切的研究需求和建议。
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来源期刊
Advances in Chromatography
Advances in Chromatography CHEMISTRY, ANALYTICAL-
CiteScore
1.40
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