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基于三蝶烯的氢键有机框架中的互穿异构现象。

Interpenetration Isomerism in Triptycene-Based Hydrogen-Bonded Organic Frameworks.

作者信息

Li Penghao, Li Peng, Ryder Matthew R, Liu Zhichang, Stern Charlotte L, Farha Omar K, Stoddart J Fraser

机构信息

Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, IL, 60208, USA.

Neutron Scattering Division, Oak Ridge National Laboratory, Oak Ridge, TN, 37831, USA.

出版信息

Angew Chem Int Ed Engl. 2019 Feb 4;58(6):1664-1669. doi: 10.1002/anie.201811263. Epub 2019 Jan 9.

Abstract

We describe an example of "interpenetration isomerism" in three-dimensional hydrogen-bonded organic frameworks. By exploiting the crystallization conditions for a peripherally extended triptycene H PET, we can modulate the interpenetration of the assembled frameworks, yielding a two-fold interpenetrated structure PETHOF-1 and a five-fold interpenetrated structure PETHOF-2 as interpenetration isomers. In PETHOF-1, two individual nets are related by inversion symmetry and form an interwoven topology with a large guest-accessible volume of about 80 %. In PETHOF-2, five individual nets are related by translational symmetry and are stacked in an alternating fashion. The activated materials show permanent porosity with Brunauer-Emmett-Teller surface areas exceeding 1100 m  g . Synthetic control over the framework interpenetration could serve as a new strategy to construct complex supramolecular architectures from simple organic building blocks.

摘要

我们描述了三维氢键有机框架中“互穿异构现象”的一个例子。通过利用外围扩展的三蝶烯H PET的结晶条件,我们可以调节组装框架的互穿情况,得到作为互穿异构体的二重互穿结构PETHOF-1和五重互穿结构PETHOF-2。在PETHOF-1中,两个独立的网络通过反演对称性相关联,并形成一种具有约80%的大客体可及体积的交织拓扑结构。在PETHOF-2中,五个独立的网络通过平移对称性相关联,并以交替方式堆叠。活化后的材料表现出永久孔隙率,其布鲁诺尔-埃米特-泰勒表面积超过1100 m² g⁻¹。对框架互穿的合成控制可作为一种从简单有机构建块构建复杂超分子结构的新策略。

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