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Ultrasonic Exfoliation of Hydrophobic and Hydrophilic Metal–Organic Frameworks To Form Nanosheets

机译:疏水性和亲水性金属-有机骨架的超声剥离形成纳米片

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摘要

The modular structure of metal–organic framework nanosheets (MONs) provides a convenient route to creating two‐dimensional materials with readily tuneable surface properties. Here, the liquid exfoliation of two closely related layered metal–organic frameworks functionalised with either methoxy‐propyl (>1) or pentyl (>2) pendent groups intended to bestow either hydrophilic or hydrophobic character to the resulting nanosheets is reported. Exfoliation of the two materials in a range of different solvents highlighted significant differences in their dispersion properties, as well as their molecular and nanoscopic structures. Exchange or loss of solvent was found to occur at the labile axial position of the paddle‐wheel based MONs and DFT calculations indicated that intramolecular coordination by the oxygen of the methoxy‐propyl pendant groups may take place. The nanoscopic dimensions of the MONs were further tuned by varying the exfoliation conditions and through “liquid cascade centrifugation”. Aqueous suspensions of the nanosheets were used as sensors to detect aromatic heterocycles with clear differences in binding behaviour observed and quantified.
机译:金属-有机框架纳米片(MONs)的模块化结构为创建具有易于调整的表面特性的二维材料提供了便利的途径。在这里,两个紧密相关的层状金属-有机骨架的液体剥落被甲氧基丙基(> 1 )或戊基(> 2 )侧基官能化,旨在赋予亲水性或亲水性。报告了所得纳米片的疏水性。两种材料在一系列不同溶剂中的剥离突出了它们的分散性能以及分子和纳米结构的显着差异。发现基于桨轮的MONs的不稳定轴向位置发生溶剂的交换或损失,DFT计算表明,甲氧基-丙基侧基的氧可能发生分子内配位。通过改变剥落条件并通过“液体级联离心”进一步调整了MONs的纳米尺寸。纳米片的水悬浮液用作传感器来检测芳香杂环,并观察到并量化结合行为的明显差异。

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