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混合金属对苯二甲酸金属有机框架的经济高效氧富集与核磁共振光谱分析

Cost-effective O enrichment and NMR spectroscopy of mixed-metal terephthalate metal-organic frameworks.

作者信息

Bignami Giulia P M, Davis Zachary H, Dawson Daniel M, Morris Samuel A, Russell Samantha E, McKay David, Parke Richard E, Iuga Dinu, Morris Russell E, Ashbrook Sharon E

机构信息

School of Chemistry , EaStCHEM and Centre of Magnetic Resonance , University of St Andrews , North Haugh, St Andrews , Fife , KY16 9ST , UK . Email:

UK 850 MHz Solid-State NMR Facility , Department of Physics , University of Warwick , Millburn House , Coventry , CV4 7AL , UK.

出版信息

Chem Sci. 2017 Nov 23;9(4):850-859. doi: 10.1039/c7sc04649a. eCollection 2018 Jan 28.

Abstract

O solid-state NMR spectroscopy is employed to investigate the cation disorder in metal-organic frameworks containing two different types of metal cations. Although NMR offers exquisite sensitivity to the local, atomic-scale structure, making it an ideal tool for the characterisation of disordered materials, the low natural abundance of O (0.037%) necessitates expensive isotopic enrichment to acquire spectra on a reasonable timescale. Using dry gel conversion and a novel steaming method we show that cost-effective and atom-efficient enrichment of MOFs is possible, and that high-resolution O NMR spectra are sensitive both to the structural forms of the MOF and the presence of guest molecules. For mixed-metal forms of MIL-53, NMR can also provide information on the final composition of the materials (notably different to that of the initial starting material) and the preference for cation clustering/ordering within the MOFs. For Al, Ga MIL-53, the distribution of cations results in a mixed-pore form upon exposure to water, unlike the different structures seen for the corresponding end members. This work shows that as good levels of enrichment can be achieved at reasonable cost, O NMR spectroscopy should be an invaluable tool for the study of these important functional materials.

摘要

采用固态核磁共振光谱法研究含有两种不同类型金属阳离子的金属有机框架中的阳离子无序情况。尽管核磁共振对局部原子尺度结构具有极高的灵敏度,使其成为表征无序材料的理想工具,但氧的天然丰度较低(0.037%),这就需要进行昂贵的同位素富集才能在合理的时间尺度上获取光谱。通过干凝胶转化和一种新型的蒸汽处理方法,我们表明对金属有机框架进行经济高效且原子利用率高的富集是可行的,并且高分辨率的氧核磁共振光谱对金属有机框架的结构形式和客体分子的存在都很敏感。对于MIL - 53的混合金属形式,核磁共振还可以提供有关材料最终组成(与初始原料明显不同)以及金属有机框架内阳离子聚集/有序化偏好的信息。对于铝、镓取代的MIL - 53,阳离子的分布在暴露于水时会导致形成混合孔形式,这与相应端基成员所呈现的不同结构不同。这项工作表明,由于可以以合理的成本实现良好的富集水平,氧核磁共振光谱法应该是研究这些重要功能材料的宝贵工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4007/5873045/52fd186d9720/c7sc04649a-f1.jpg

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