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通过自牺牲客体策略合成高质量二维共价有机框架

Synthesis of high quality two dimensional covalent organic frameworks through a self-sacrificing guest strategy.

作者信息

Xue Tianwei, Peng Li, Liu Chengbin, Li Ruiqing, Qiu Rongxing, Qian Yunyang, Guan Xinyu, Shi Shanshan, Xu Guangkuo, Zhu Lilin, Yang Shuliang, Li Jun, Jiang Hai-Long

机构信息

College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, Fujian, 361005, China.

Hefei National Research Center for Physical Sciences at the Microscale, Department of Chemistry, University of Science and Technology of China, Hefei, Anhui, 230026, China.

出版信息

Nat Commun. 2025 Feb 27;16(1):2023. doi: 10.1038/s41467-025-57311-w.

Abstract

The quality of covalent organic frameworks (COFs) crucially influences their mechanistic research and subsequent practical implementations. However, it has been widely observed that the structure damage induced by the activation procedure could compromise the quality of COFs. Here we develop a self-sacrificing guest method for synthesizing high-quality two-dimensional COFs (SG-COFs) by incorporating salt guests into the pores of the COF structure. These introduced salts play an indispensable role in supporting COF pores and mitigating quality loss during the activation process. Interestingly, due to the unique characteristic of salts decomposing into gases upon heating, this method can ultimately enable the synthesis of highly pure, high-quality COFs without the presence of residual guest molecules. The resulting sixteen COFs display superior crystallinity and porosity compared to those synthesized using conventional routes. Moreover, these high-quality SG-COFs have demonstrated to be highly efficient adsorbents for removal of per- and polyfluoroalkyl substances.

摘要

共价有机框架材料(COFs)的质量对其机理研究及后续实际应用有着至关重要的影响。然而,人们普遍观察到,活化过程引起的结构损伤可能会损害COFs的质量。在此,我们开发了一种自牺牲客体法,通过将盐客体引入COF结构的孔中,来合成高质量的二维COFs(SG-COFs)。这些引入的盐在支撑COF孔以及减轻活化过程中的质量损失方面发挥着不可或缺的作用。有趣的是,由于盐在加热时会分解成气体这一独特特性,该方法最终能够在不存在残留客体分子的情况下合成高纯度、高质量的COFs。与采用传统路线合成的COFs相比,所得的16种COFs表现出优异的结晶度和孔隙率。此外,这些高质量的SG-COFs已被证明是去除全氟和多氟烷基物质的高效吸附剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cf0/11868610/9123e74366a8/41467_2025_57311_Fig1_HTML.jpg

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