Rational Synthesis of Functionalized Covalent Organic Frameworks via Four-Component Reaction

• Published in: Journal of the American Chemical Society Vol. 146; no. 7; pp. 4822 - 4829
• Main Authors: Zhang, Zhi-Cong, Wang, Peng-Lai, Sun, Yi-Fan, Yang, Tong, Ding, San-Yuan, Wang, Wei
• Format: Journal Article
• Language: English
• Published: WASHINGTON American Chemical Society 21.02.2024; Amer Chemical Soc
• Subjects: adsorption; Chemistry; Chemistry, Multidisciplinary; imidazole; Physical Sciences; Science & Technology; society
• ISSN: 0002-7863; 1520-5126; 1520-5126
• DOI: 10.1021/jacs.3c13172

The construction of function-oriented covalent organic frameworks (COFs) remains a challenge as it requires simultaneous consideration of diversified structures, robust linkage, and tailorable functionalities. Herein, we report the rational synthesis of functionalized COFs via a four-component reaction strategy. Through the four-component Debus–Radziszewski reaction, 11 N-substituted imidazole-based COFs with diversified structures were facilely constructed from readily available building blocks. By forming the N-substituted imidazole linkage, these synthesized COFs displayed ultrastability toward strong acids and base. Moreover, the four components reaction allows the rational synthesis of COFs with tailorable functionalities. As an example, the phosphonate-functionalized COF (LZU-530) was rationally constructed for the efficient adsorption of uranium­(VI). The uranium­(VI) uptake of LZU-530 reaches up to 95 mg·g–1 in 2 M HNO3, which is the highest uptake of the existing organic porous materials under such harsh conditions. Our results highlight the use of multicomponent reaction for the rational synthesis of robust and functionalized COFs toward targeted applications.