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Role of water in complexation of 147101316-hexaoxacyclooctadecane (18-crown-6) with Li+ and K+ in hydrophobic 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)amide ionic liquid

机译:水在疏水性1-乙基-3-甲基咪唑双(三氟甲磺酰基)酰胺离子液体中的147101316-六氧杂环十八烷(18-crown-6)与Li +和K +络合中的作用

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摘要

Complexation characteristics of 1,4,7,10,13,16-hexaoxacyclooctadecane (18-crown-6, 18C6) with Li+ and K+ in a hydrophobic ionic liquid of 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)amide under dry and humid conditions at 298.2 K were studied by 1H and 13C NMR chemical shifts. The comparison of the 1H and 13C chemical shifts of 18C6 molecule between the dry and humid IL solutions without the alkali metal ions showed that uncomplexed 18C6 molecules are solvated by water molecules in the humid ionic liquid solution. The changes in the 1H and 13C chemical shifts of 18C6 ligand molecule with the increases in the Li+ and K+ concentrations revealed that in both dry and humid ionic liquid solutions 18C6 molecule forms 1:1 complexes with Li+ and K+. The 1H NMR data of water molecules in the humid ionic liquid solutions demonstrated that water molecules interact with Li+-18C6 complexes and free Li+, but do not with K+-18C6 complexes and free K+. The mechanisms of the formation of the Li+ and K+ complexes in the humid ionic liquid solution are different from each other due to the differences in the complex-water interactions.
机译:1,4,7,10,13,16-六氧杂环十八烷(18-crown-6,18C6)与Li + 和K + 在疏水性离子液体中的络合特性通过 1 H和 13 C NMR化学位移研究在298.2K下干燥和潮湿条件下的1-乙基-3-甲基咪唑鎓双(三氟甲磺酰基)酰胺。在没有碱金属离子的干燥和潮湿IL溶液中18C6分子的 1 H和 13 C化学位移的比较表明,未络合的18C6分子被水分子溶剂化在潮湿的离子液体溶液中。 18C6配体分子 1 H和 13 C化学位移随Li + 和K + < / sup>浓度表明,在干燥和潮湿的离子液体溶液中,18C6分子均与Li + 和K + 形成1:1配合物。湿离子液体溶液中水分子的 1 H NMR数据表明,水分子与Li + -18C6络合物和游离的Li + 相互作用,但不适用于K + -18C6配合物和游离K + 。湿离子液体溶液中Li + 和K + 络合物的形成机理由于络合物与水之间的相互作用而不同。

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