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使用反相气相色谱法阐明温度和水对含铜(I)离子液体π络合强度的作用。

Elucidating the role of temperature and water on the π-complexation strength of copper(I) ion-containing ionic liquids using inverse gas chromatography.

作者信息

Eor Philip, Tryon-Tasson Nicholas, Anderson Jared L

机构信息

Ames National Laboratory-USDOE and Department of Chemistry, Iowa State University, Ames, IA, 50011, USA.

Ames National Laboratory-USDOE and Department of Chemistry, Iowa State University, Ames, IA, 50011, USA.

出版信息

Anal Chim Acta. 2024 Jan 25;1287:342021. doi: 10.1016/j.aca.2023.342021. Epub 2023 Nov 11.

Abstract

BACKGROUND

The π-complexation capability of copper(I) ion has been exploited in olefin/paraffin separations, but its propensity of undergoing disproportionation to copper(II) ion and copper metal has limited its use. Imidazolium-based ionic liquids (ILs) can serve as solvents for copper(I) ions as they facilitate copper(I) ion-olefin complexation and can enhance its stability. To precisely monitor how copper(I) ions complex with olefins in ILs and evaluate the effects of environmental factors, it is necessary to construct an experimental platform capable of quantitatively measuring their molecular-level interactions.

RESULTS

This study employs an innovative inverse chromatography platform to measure changes in molecular-level interactions between copper(I) ions and olefins when the temperature and water content in the system are carefully controlled. Gas chromatographic stationary phases comprised of the 1-decyl-3-methylimidazolium bis[(trifluoromethyl)sulfonyl]imide ([CMIM][NTf]) IL containing 0.5 M [Cu][NTf] were pre-heated to 140 °C maximizing copper(I) ion's π-complexation capability. The chromatographic retention of alkenes, dienes, and alkynes on the copper(I) ion/IL stationary phase was observed to be predominantly influenced by their partitioning between the carrier gas and copper(I) ion as well as between the IL and copper(I) ion. Upon introducing water to the system, the Gibbs free energy of solvation for olefins showed less favorable solvation into the stationary phase. In contrast, their solvation was significantly enhanced when the [Cu][NTf]/[CMIM][NTf] stationary phase was heated to an elevated temperature, indicating that the π-complexation capability of copper(I) ion can be regenerated as needed.

SIGNIFICANCE

This study demonstrates that the stability of copper(I) ions can be improved by dissolving them into appropriate IL solvents. Moreover, the olefin separation performance of the copper(I) ion/IL stationary phase was found to be adjustable by the application of different column treatment conditions (i.e., heating and water introduction), opening the possibility of devising more stable, reliable, and efficient olefin separation systems based on copper(I) ion and IL solvents.

摘要

背景

铜(I)离子的π络合能力已被用于烯烃/石蜡分离,但它歧化为铜(II)离子和铜金属的倾向限制了其应用。基于咪唑鎓的离子液体(ILs)可作为铜(I)离子的溶剂,因为它们促进铜(I)离子与烯烃的络合,并能增强其稳定性。为了精确监测铜(I)离子在离子液体中如何与烯烃络合,并评估环境因素的影响,有必要构建一个能够定量测量其分子水平相互作用的实验平台。

结果

本研究采用了一种创新的反相色谱平台,在系统温度和含水量得到仔细控制的情况下,测量铜(I)离子与烯烃之间分子水平相互作用的变化。由含有0.5 M [Cu][NTf]的1-癸基-3-甲基咪唑鎓双[(三氟甲基)磺酰基]亚胺([CMIM][NTf])离子液体组成的气相色谱固定相被预热到140°C,以最大化铜(I)离子的π络合能力。观察到烯烃、二烯烃和炔烃在铜(I)离子/离子液体固定相上色谱保留主要受它们在载气和铜(I)离子之间以及离子液体和铜(I)离子之间的分配影响。当向系统中引入水时,烯烃的溶剂化吉布斯自由能显示出在固定相中溶剂化不太有利。相比之下,当[Cu][NTf]/[CMIM][NTf]固定相加热到较高温度时,它们的溶剂化显著增强,表明铜(I)离子的π络合能力可以根据需要再生。

意义

本研究表明,将铜(I)离子溶解在合适的离子液体溶剂中可以提高其稳定性。此外,发现铜(I)离子/离子液体固定相的烯烃分离性能可通过应用不同的柱处理条件(即加热和引入水)来调节,这为设计基于铜(I)离子和离子液体溶剂的更稳定、可靠和高效的烯烃分离系统开辟了可能性。

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