Kawano Masahiro, Sadakane Koichiro, Iwase Hiroki, Matsugami Masaru, Marekha Bogdan A, Idrissi Abdenacer, Takamuku Toshiyuki
Department of Chemistry and Applied Chemistry, Graduate School of Science and Engineering, Saga University, Honjo-machi, Saga 840-8502, Japan.
Phys Chem Chem Phys. 2020 Mar 7;22(9):5332-5346. doi: 10.1039/c9cp05258e. Epub 2020 Feb 25.
The mixing states of an imidazolium-based ionic liquid (IL), 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide ([Cmim][TFSI]), with cycloethers, tetrahydrofuran (THF), 1,4-dioxane (1,4-DIO), and 1,3-dioxane (1,3-DIO), have been clarified on the meso- and microscopic scales using small-angle neutron scattering (SANS), IR, and NMR experiments and molecular dynamics (MD) simulations. SANS profiles of [Cmim][TFSI]-THF-d and -1,4-DIO-d solutions at various mole fractions x of molecular liquid (ML) have shown that [Cmim][TFSI] is heterogeneously mixed with THF and 1,4-DIO on the mesoscopic scale, to a high extent in the case of the latter solution. In fact, [Cmim][TFSI] and 1,4-DIO are not miscible with each other above the 1,4-DIO mole fraction x of 0.903, whereas the IL can be mixed with THF over the entire range of THF mole fraction x. The results of IR and H and C NMR measurements and MD simulations showed that cycloether molecules are more strongly hydrogen-bonded with the imidazolium ring H atoms in the order of THF > 1,3-DIO > 1,4-DIO. Although 1,4-DIO and 1,3-DIO molecules are structural isomers, our results point out that 1,4-DIO cannot be strongly hydrogen-bonded with the ring H atoms. The solvation of [TFSI] by cycloethers through the dipole-dipole interaction promotes hydrogen bonding between the ring H atoms and cycloethers. Thus, 1,4-DIO with the lowest dipole moment cannot easily eliminate [TFSI] from the imidazolium ring. This results in the weakest hydrogen bonds of 1,4-DIO with the ring H atoms. 2D-NMR of H{H} rotating-frame nuclear Overhauser effect spectroscopy (ROESY) showed the interaction of the three cycloethers with the butyl group of [Cmim]. 1,4-DIO mainly interacts with the butyl group by the dispersion force, whereas THF interacts with the IL by both hydrogen bonding and dispersion force. This leads to the higher heterogeneity of the 1,4-DIO solutions compared to the THF solutions.
利用小角中子散射(SANS)、红外光谱(IR)、核磁共振(NMR)实验以及分子动力学(MD)模拟,在介观和微观尺度上阐明了基于咪唑鎓的离子液体(IL)1-丁基-3-甲基咪唑双(三氟甲磺酰)亚胺([Cmim][TFSI])与环醚、四氢呋喃(THF)、1,4-二氧六环(1,4-DIO)和1,3-二氧六环(1,3-DIO)的混合状态。[Cmim][TFSI]-THF-d和-1,4-DIO-d溶液在不同分子液体(ML)摩尔分数x下的SANS曲线表明,在介观尺度上,[Cmim][TFSI]与THF和1,4-DIO呈非均相混合,对于后一种溶液而言程度较高。实际上,当1,4-DIO的摩尔分数x高于0.903时,[Cmim][TFSI]和1,4-DIO彼此不互溶,而IL在THF摩尔分数x的整个范围内都能与THF混合。红外光谱、氢核磁共振和碳核磁共振测量结果以及分子动力学模拟表明,环醚分子与咪唑环H原子之间的氢键作用强度顺序为THF > 1,3-DIO > 1,4-DIO。尽管1,4-DIO和1,3-DIO分子是结构异构体,但我们的结果指出,1,4-DIO无法与环H原子形成强氢键。环醚通过偶极-偶极相互作用对[TFSI]的溶剂化作用促进了环H原子与环醚之间的氢键形成。因此,偶极矩最低的1,4-DIO不易将[TFSI]从咪唑环上消除。这导致1,4-DIO与环H原子之间的氢键最弱。氢{H}旋转框架核Overhauser效应光谱(ROESY)的二维核磁共振显示了三种环醚与[Cmim]丁基之间的相互作用。1,4-DIO主要通过色散力与丁基相互作用,而THF与离子液体通过氢键和色散力相互作用。这导致1,4-DIO溶液相比THF溶液具有更高的非均质性。