Department of Chemistry, Iowa State University, 1605 Gilman Hall, Ames, IA, 50011, USA.
Department of Chemistry, Concordia College, Moorhead, MN, 56562, USA.
Anal Bioanal Chem. 2018 Jul;410(19):4597-4606. doi: 10.1007/s00216-017-0802-z. Epub 2017 Dec 23.
Ionic liquids (IL) have been utilized as gas chromatography stationary phases due to their high thermal stability, negligible vapor pressure, wide liquid range, and the ability to solvate a range of analytes. In this study, the solvation properties of eight room temperature ILs containing various transition and rare earth metal centers [e.g., Mn(II), Co(II), Ni(II), Nd(III), Gd(III), and Dy(III)] are characterized using the Abraham solvation parameter model. These metal-containing ILs (MCILs) consist of the trihexyl(tetradecyl)phosphonium cation and functionalized acetylacetonate ligands chelated to various metals. They are used in this study as gas chromatographic stationary phases to investigate the effect of the metal centers on the separation selectivities for various analytes. In addition, two MCILs comprised of tetrachloromanganate and tris(trifluoromethylphenylacetylaceto)manganate anions were used to study the effect of chelating ligands on the selectivity of the stationary phases. Depending on the metal center and chelating ligand, significant differences in solvation properties were observed. MCILs containing Ni(II) and Mn(II) metal centers exhibited higher retention factors and higher peak asymmetry factors for amines (e.g., aniline and pyridine). Alcohols (e.g., phenol, p-cresol, 1-octanol, and 1-decanol) were strongly retained on the MCIL stationary phase containing Mn(II) and Dy(III) metal centers. This study presents a comprehensive evaluation into how the solvation properties of ILs can be varied by incorporating transition and rare earth metal centers into their structural make-up. In addition, it provides insight into how these new classes of ILs can be used for solute-specific gas chromatographic separations. Graphical abstract The solvation properties of eight metal-containing ionic liquids (MCILs) comprised of transition and rare-earth metal centers are evaluated for the first time using gas chromatography. The results reveal that metals comprising the MCILs provide unique separation selectivities for various analytes and that these materials can be exploited as stationary phases in solute-specific gas chromatographic separations.
离子液体 (IL) 由于其高热稳定性、可忽略的蒸气压、宽液相范围以及溶解一系列分析物的能力,已被用作气相色谱固定相。在这项研究中,使用 Abraham 溶剂化参数模型来表征八种含有各种过渡金属和稀土金属中心的室温离子液体(例如 Mn(II)、Co(II)、Ni(II)、Nd(III)、Gd(III) 和 Dy(III))的溶剂化性质。这些含金属的离子液体(MCIL)由三己基(十四烷基)膦阳离子和与各种金属螯合的功能化乙酰丙酮配体组成。在这项研究中,它们被用作气相色谱固定相,以研究金属中心对各种分析物分离选择性的影响。此外,还使用了两种由四氯锰酸盐和三(三氟甲基苯乙酰丙酮)锰酸盐阴离子组成的 MCIL,以研究螯合配体对固定相选择性的影响。根据金属中心和螯合配体的不同,观察到溶剂化性质有显著差异。含有 Ni(II)和 Mn(II)金属中心的 MCIL 表现出更高的保留因子和更高的峰不对称因子对于胺(例如苯胺和吡啶)。醇(例如苯酚、对甲酚、1-辛醇和 1-癸醇)强烈保留在含有 Mn(II)和 Dy(III)金属中心的 MCIL 固定相上。这项研究全面评估了通过将过渡金属和稀土金属中心纳入其结构来改变离子液体溶剂化性质的方法。此外,它还提供了有关如何将这些新型 IL 用于特定溶质的气相色谱分离的深入了解。