Payagala Tharanga, Zhang Ying, Wanigasekara Eranda, Huang Ke, Breitbach Zachary S, Sharma Pritesh S, Sidisky Leonard M, Armstrong Daniel W
Department of Chemistry and Biochemistry, University of Texas at Arlington, Arlington, Texas 76019, USA.
Anal Chem. 2009 Jan 1;81(1):160-73. doi: 10.1021/ac8016949.
Trigonal tricationic ionic liquids (ILs) are a new class of ILs that appear to be unique when used as gas chromatographic stationary phases. They consist of four core structures; (1) A = mesitylene core, (2) B = benzene core, (3) C = triethylamine core, and (4) D = tri(2-hexanamido)ethylamine core; to which three identical imidazolium or phosphonium cationic moieties were attached. These were coated on fused silica capillaries, and their gas chromatographic properties were evaluated. They were characterized using a linear solvation parameter model and a number of test mixtures. On the basis of the literature, it is known that both monocationic and dicationic ILs possess almost identical polarities, solvation characteristics, and chromatographic selectivities. However, some of the trigonal tricationic ILs were quite different. The different solvation parameters and higher apparent polarities appear to generate from the more rigid trigonal geometry of these ILs, as well as their ability to retain the positive charges in relatively close proximity to one another in some cases. Their unique selectivities, retention behaviors, and separation efficiencies were demonstrated using the Grob mixture, a flavor and fragrance test mixture, alcohols/alkanes test, and FAME isomer separations. Two ILs C1 (methylimidazolium substitution) and C4 (2-hydroxyethylimidazolium substitution) had higher apparent polarities than any know IL (mono, di, and tricationic ILs) or commercial stationary phases. The tri(2-hexanamido)ethylamine core IL series proved to be very interesting in that it not only showed the highest separation efficiency for all test mixtures, but it also is the first IL stationary phase (containing NTf(2)(-) anions) that eliminates peak tailing for alcohols and other H-bonding analytes. The thermal stabilities were investigated using three methods: thermogravimetric analysis (TGA) method, temperature programmed gas chromatographic method (TPGC), and isothermal gas chromatographic method. The D core series had a high working temperature range, exceptional selectivities, and higher separation efficiencies than comparable polarity commercial columns. It appears that this specific type of multifunctional ILs may have the most promising future as a new generation of gas chromatographic stationary phases.
三角三阳离子离子液体(ILs)是一类新型离子液体,用作气相色谱固定相时显得很独特。它们由四种核心结构组成:(1)A = 均三甲苯核心,(2)B = 苯核心,(3)C = 三乙胺核心,以及(4)D = 三(2 - 己酰胺基)乙胺核心;其上连接有三个相同的咪唑鎓或鏻阳离子部分。将这些涂覆在熔融石英毛细管上,并对其气相色谱性质进行评估。使用线性溶剂化参数模型和多种测试混合物对它们进行表征。根据文献可知,单阳离子和双阳离子离子液体具有几乎相同的极性、溶剂化特性和色谱选择性。然而,一些三角三阳离子离子液体却有很大不同。不同的溶剂化参数和更高的表观极性似乎源于这些离子液体更刚性的三角几何形状,以及它们在某些情况下使正电荷相对彼此保持较近距离的能力。使用格罗布混合物、一种香精香料测试混合物、醇类/烷烃测试以及脂肪酸甲酯(FAME)异构体分离展示了它们独特的选择性、保留行为和分离效率。两种离子液体C1(甲基咪唑鎓取代)和C4(2 - 羟乙基咪唑鎓取代)具有比任何已知离子液体(单、双和三阳离子离子液体)或商业固定相更高的表观极性。三(2 - 己酰胺基)乙胺核心离子液体系列被证明非常有趣,因为它不仅对所有测试混合物显示出最高的分离效率,而且它也是第一个消除醇类和其他氢键分析物峰拖尾现象的离子液体固定相(含有NTf(2)(-)阴离子)。使用三种方法研究了热稳定性:热重分析(TGA)法、程序升温气相色谱法(TPGC)和等温气相色谱法。D核心系列具有较宽的工作温度范围、出色的选择性以及比具有可比极性商业柱更高的分离效率。看来这种特定类型的多功能离子液体作为新一代气相色谱固定相可能具有最广阔的前景。