封装(网络)
金属有机骨架
离子键合
分子
化学
金属
纳米技术
组合化学
材料科学
离子
有机化学
吸附
计算机科学
计算机网络
作者
José de Jesús Velazquez-Garcia,L. De Los Santos Valladares,C. H. W. Barnes,Sandra König,Michael Fröba,Volodymyr Baran,Bassima Knjo,Faegheh Khademhir,Aliyenur Ekineken,Fabienne Hain,Evke Carstensen,Tom Spillner,Luis A. Alfonso‐Herrera,Weronika Łukaszczyk,Simone Techert
摘要
Two Co(II) mixed-ligand metal-organic frameworks (MOFs) based on 2-methylimidazole and trimesate were synthesised at room temperature. The structure and properties of the two MOFs, named material Deutsches Elektronen Synchrotron-1 and -2 (mDESY-1 and mDESY-2), were verified by single crystal X-ray diffraction (SCXRD), powder X-ray diffraction (PXRD), SQUID magnetic susceptibility and N2 adsorption. The structural analysis indicates that mDESY-1 is a 3D ionic framework with 2-methyl-1H-imidazol-3-ium counterions residing in its pores, while mDESY-2 is a 2D neutral framework isostructural to ITH-1, with water as a co-crystallising solvent. PXRD data demonstrates that mDESY-1 exhibits better crystallinity than mDESY-2. Magnetic measurements indicate that both MOFs are paramagnetic with a weak ferromagnetic transition above room temperature. Although both structures suggest the presence of voids, N2 adsorption data confirms that these voids are not accessible in either MOF. Nevertheless, mDESY-1 was capable of encapsulating azobenzene during synthesis, which was observed via SCXRD. The encapsulated molecules were then slowly released in ethanol, with a release of up to 30 mg of azobenzene per g of MOF in a period of 60 days.
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