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通过将易于获得的亚胺键进行顺序氧化/环化反应来制备苯并恶唑连接的共价有机框架材料。

Sequential Oxidation/Cyclization of Readily Available Imine Linkages to Access Benzoxazole-Linked Covalent Organic Frameworks.

作者信息

Zhu Yanqiu, Huang Dekang, Wang Wanqin, Liu Gang, Ding Chizhu, Xiang Yonggang

机构信息

College of Chemistry, Huazhong Agricultural University, Wuhan, 430070, PR China.

College of Resources and Environment, Huazhong Agricultural University, Wuhan, 430070, PR China.

出版信息

Angew Chem Int Ed Engl. 2024 Mar 11;63(11):e202319909. doi: 10.1002/anie.202319909. Epub 2024 Feb 2.

Abstract

Benzoxazole-linked covalent organic frameworks (BO-COFs), despite their exceptional chemical stability, are still in their infancy. This is primarily because the current prevalent methods require the use of special ortho-hydroxyl-substituted aromatic amines as monomers. Herein, we report an innovative strategy to access BO-COFs directly from imine-linked COFs (Im-COFs) without pre-embedded OH groups, using a two-step sequential oxidation/cyclization process. The two-step process included the oxidation of Im-COFs into amide-linked COFs, followed by a copper-catalyzed oxidative cyclization. Five representative BO-COFs were synthesized with retained crystallinity and high oxidization efficiency, offering the potential to convert a significant portion of Im-COFs into BO-COFs. The structural advantages of the newly designed BO-COFs were demonstrated through their application to photocatalytic organic transformations.

摘要

苯并恶唑连接的共价有机框架(BO-COFs),尽管具有出色的化学稳定性,但仍处于起步阶段。这主要是因为当前普遍使用的方法需要使用特殊的邻羟基取代的芳香胺作为单体。在此,我们报告了一种创新策略,通过两步连续氧化/环化过程,直接从没有预嵌入羟基的亚胺连接的COFs(Im-COFs)制备BO-COFs。两步过程包括将Im-COFs氧化为酰胺连接的COFs,然后进行铜催化的氧化环化。合成了五种具有保留结晶度和高氧化效率的代表性BO-COFs,为将大部分Im-COFs转化为BO-COFs提供了潜力。通过将新设计的BO-COFs应用于光催化有机转化,展示了其结构优势。

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