两个基于Calix冠的固定相。合成、色谱性能及X射线光电子能谱研究

Giuseppe Arena, Annalinda Contino, Elisa Longo, Domenico Sciotto, Giuseppe Spoto, Alberto Torrisi
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引用次数: 13

摘要

本文描述了通过将两个适当衍生的杯[4]冠-6和杯[4]冠-5受体共价连接到硅胶上而获得的两个色谱固定相。报道了它们的色谱行为及其表面组成的研究。填料对碱金属离子表现出高选择性。当使用水/甲醇混合物(80∶20)作为流动相时,获得了Cs+与K+和Na+的完全分离。在这些条件下,用硅胶结合的杯[4]冠-6实现了选择性因子Cs+/Na+=4.10。通过X射线光电子能谱(XPS)估计了大环共价连接后活性硅胶表面的覆盖度。该技术允许对材料的前几层单层进行分析,因此对于类似的研究而言,该技术优于传统的元素分析。针对有机污染物的存在,提出了三种适当校正XP信号的方法,并进行了严格的比较。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Two Calix-Crown Based Stationary Phases. Synthesis, Chromatographic Performance and X-ray Photoelectron Spectroscopy Investigation

Two chromatographic stationary phases, obtained by covalently linking two suitably derivatized calix[4]crown-6 and calix[4]crown-5 receptors onto silica gel, are described here. A study of their chromatographic behaviour as well as their surface composition is reported. The packing materials exhibit high selectivity toward alkali metal ions. Complete separations of Cs+ from K+ and Na+ were obtained when using a water/methanol mixture (80:20) as the mobile phase. In these conditions, a selectivity factor Cs+/Na+=4.10 was achieved with the silica gel-bound calix[4]crown-6. The degree of coverage of the activated silica-gel surface following the covalent attachment of the macrocycle was estimated by mean of X-ray photoelectron spectroscopy (XPS). This technique allows the first few monolayers of the material to be analysed and thus is to be preferred to conventional Elemental Analysis for similar studies. Three methods for an adequate correction of the XP signals for the presence of organic contaminants are suggested and critically compared.

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