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拟五重对称配体在多孔金属-有机和氢键框架中诱导几何阻挫。

Pseudo-5-Fold-Symmetrical Ligand Drives Geometric Frustration in Porous Metal-Organic and Hydrogen-Bonded Frameworks.

机构信息

Institute for Integrated Cell-Material Sciences (WPI-iCeMS), Kyoto University, iCeMS Research Building, Yoshida, Sakyo-ku, Kyoto 606-8501, Japan.

Japan Synchrotron Radiation Research Institute/SPring-8, Kouto, Sayo, Hyogo 679-5198, Japan.

出版信息

J Am Chem Soc. 2020 Aug 12;142(32):13839-13845. doi: 10.1021/jacs.0c04450. Epub 2020 Jul 29.

Abstract

Reticular framework materials thrive on designability, but unexpected reaction outcomes are crucial in exploring new structures and functionalities. By combining "incompatible" building blocks, we employed geometric frustration in reticular materials leading to emergent structural features. The combination of a pseudo-C-symmetrical organic building unit based on a pyrrole core with a C-symmetrical copper paddlewheel synthon led to three distinct frameworks by tuning the synthetic conditions. The frameworks show structural features typical for geometric frustration: self-limiting assembly, internally stressed equilibrium structures, and topological defects in the equilibrium structure, which manifested in formation of a hydrogen-bonded framework, distorted and broken secondary building units, and dangling functional groups, respectively. The influence of geometric frustration on the CO sorption behavior and the discovery of a new secondary building unit shows geometric frustration can serve as a strategy to obtain highly complex porous frameworks.

摘要

网状框架材料在设计上具有优势,但探索新结构和功能时,意外的反应结果至关重要。通过组合“不兼容”的构建块,我们在网状材料中引入了几何阻碍,从而产生了新的结构特征。结合基于吡咯核心的伪 C 对称有机构建单元和 C 对称铜桨轮合成子,通过调整合成条件,得到了三种不同的框架。这些框架表现出典型的几何阻碍结构特征:自限制组装、内部应力平衡结构和平衡结构中的拓扑缺陷,分别表现为氢键框架的形成、扭曲和断裂的次级构建单元以及悬垂官能团。几何阻碍对 CO 吸附行为的影响和新次级构建单元的发现表明,几何阻碍可以作为获得高度复杂多孔框架的策略。

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