Li Hui, Chen Fengqian, Guan Xinyu, Li Jiali, Li Cuiyan, Tang Bin, Valtchev Valentin, Yan Yushan, Qiu Shilun, Fang Qianrong
State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, Jilin University, Changchun 130012, P. R. China.
Deakin University, Institute for Frontier Materials, Geelong, Victoria 3216, Australia.
J Am Chem Soc. 2021 Feb 24;143(7):2654-2659. doi: 10.1021/jacs.0c12499. Epub 2021 Feb 10.
The growth of three-dimensional covalent organic frameworks (3D COFs) with new topologies is still considered as a great challenge due to limited availability of high-connectivity building units. Here we report the design and synthesis of 3D triptycene-based COFs, termed JUC-568 and JUC-569, following the deliberate symmetry-guided design principle. By combining a triangular prism (6-connected) node with a planar triangle (3-connected) or another triangular prism node, the targeted COFs adopt non-interpenetrated or topology, respectively. Both materials show permanent porosity and impressive performance in the adsorption of CO (∼98 cm/g at 273 K and 1 bar), CH (∼48 cm/g at 273 K and 1 bar), and especially H (up to 274 cm/g or 2.45 wt % at 77 K and 1 bar), which is highest among porous organic materials reported to date. This research thus provides a promising strategy for diversifying 3D COFs based on complex building blocks and promotes their potential applications in energy storage and environment-related fields.
由于高连接性构建单元的可用性有限,具有新拓扑结构的三维共价有机框架(3D COFs)的生长仍然被认为是一项巨大的挑战。在此,我们报告了基于对称引导设计原则设计和合成的3D三蝶烯基COFs,命名为JUC - 568和JUC - 569。通过将三角棱柱(6连接)节点与平面三角形(3连接)或另一个三角棱柱节点相结合,目标COFs分别采用非互穿或拓扑结构。两种材料均表现出永久孔隙率,并且在CO(273 K和1 bar下约为98 cm³/g)、CH₄(273 K和1 bar下约为48 cm³/g)尤其是H₂(77 K和1 bar下高达274 cm³/g或2.45 wt%)的吸附方面表现出令人印象深刻的性能,这在迄今为止报道的多孔有机材料中是最高的。因此,这项研究为基于复杂构建块的3D COFs多样化提供了一种有前景的策略,并促进了它们在储能和环境相关领域的潜在应用。