Probing Gas Adsorption in Metal–Organic Framework ZIF-8 by EPR of Embedded Nitroxides

电子顺磁共振 一氧化氮介导的自由基聚合 吸附 金属有机骨架 吸附 化学 分子 金属 化学工程 纳米技术 聚合物 化学物理 材料科学 有机化学 核磁共振 聚合 工程类 物理 自由基聚合
作者
Alena M. Sheveleva,А. В. Аникеенко,Artem S. Poryvaev,Diana Kuzmina,Inna K. Shundrina,Daniil I. Kolokolov,Alexander G. Stepanov,Matvey V. Fedin
出处
期刊:Journal of Physical Chemistry C [American Chemical Society]
卷期号:121 (36): 19880-19886 被引量:26
标识
DOI:10.1021/acs.jpcc.7b06884
摘要

Metal–organic frameworks (MOFs) are being increasingly considered as promising materials for gas separation and storage, yet specific interactions between gas molecules and the inner surface of pores are still not well understood. In this work, we propose a new approach for investigation of such interactions by Electron Paramagnetic Resonance (EPR). We use stable nitroxide radicals as multifunctional agents embedded into the pores of a MOF prior to the gas sorption. They act as EPR-active reporters, and simultaneously as competitor molecules during the gas adsorption process. We exemplify this approach using a ZIF-8 framework, nitroxide TEMPO ((2,2,6,6-tetramethylpiperidin-1-yl)oxyl), and CO2, N2, and O2 gases. The mobility of nitroxide monitored by continuous wave EPR behaves differently upon adsorption of each of these gases. In particular, a noticeable increase of mobility in the presence of CO2 reveals the weakening of guest–host interactions TEMPO–MOF induced by CO2, which was qualitatively supported by molecular dynamic calculations. The nitroxides can be embedded in MOFs postsynthetically, and their negligible amounts (≤1 per 1000 cells) are required due to a high sensitivity of EPR. Therefore, the proposed approach is sufficiently versatile and might find broad applications for various MOFs.

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