沸石咪唑盐骨架
物理吸附
金属有机骨架
微型多孔材料
材料科学
无定形固体
化学工程
多孔性
咪唑酯
纳米孔
亚稳态
结晶学
化学
纳米技术
无机化学
物理化学
有机化学
吸附
复合材料
工程类
作者
Min Tu,Dmitry E. Kravchenko,Benzheng Xia,Víctor Rubio‐Giménez,Nathalie Wauteraerts,Rhea Verbeke,Ivo F.J. Vankelecom,Timothée Stassin,Werner Egger,Marcel Dickmann,Heinz Wilfried Amenitsch,Rob Ameloot
标识
DOI:10.1002/anie.202014791
摘要
Abstract The landscape of possible polymorphs for some metal–organic frameworks (MOFs) can pose a challenge for controlling the outcome of their syntheses. Demonstrated here is the use of a template to control in the vapor‐assisted formation of zeolitic imidazolate framework (ZIF) powders and thin films. Introducing a small amount of either ethanol or dimethylformamide vapor during the reaction between ZnO and 4,5‐dichloroimidazole vapor results in the formation of the porous ZIF‐71 phase, whereas other conditions lead to the formation of the dense ZIF‐72 phase or amorphous materials. Time‐resolved in situ small‐angle X‐ray scattering reveals that the porous phase is metastable and can be transformed into its dense polymorph. This transformation is avoided through the introduction of template vapor. The porosity of the resulting ZIF powders and films was studied by N 2 and Kr physisorption, as well as positron annihilation lifetime spectroscopy. The templating principle was demonstrated for other members of the ZIF family as well, including the ZIF‐7 series, ZIF‐8_Cl, and ZIF‐8_Br.
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