离子液体
金属有机骨架
差示扫描量热法
酰胺
红外光谱学
吸附
材料科学
相(物质)
光谱学
化学工程
化学
物理化学
有机化学
热力学
量子力学
物理
工程类
催化作用
作者
Kazuyuki Fujie,Teppei Yamada,Ryuichi Ikeda,Hiroshi Kitagawa
标识
DOI:10.1002/anie.201406011
摘要
Abstract Controlling the dynamics of ionic liquids (ILs) is a significant issue for widespread use. Metal–organic frameworks (MOFs) are ideal host materials for ILs because of their small micropores and tunable host–guest interactions. Herein, we demonstrate the first example of an IL incorporated within the micropores of a MOF. The system studied consisted of EMI‐TFSA (1‐ethyl‐3‐methylimidazolium bis(trifluoromethylsulfonyl)amide) and ZIF‐8 (composed of Zn(MeIM) 2 ; H(MeIM)=2‐methylimidazole) as the IL and MOF, respectively. Construction of the EMI‐TFSA in ZIF‐8 was confirmed by X‐ray powder diffraction, nitrogen gas adsorption, and infrared absorption spectroscopy. Differential scanning calorimetry and solid‐state NMR measurements showed that the EMI‐TFSA inside the micropores demonstrated no freezing transition down to 123 K, whereas bulk EMI‐TFSA froze at 231 K. Such anomalous phase behavior originates from the nanosize effect of the MOF on the IL. This result provides a novel strategy for stabilizing the liquid phase of the ILs down to a lower temperature region.
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