Liu Jiaqiang, Su Xin, Xu Yan, Tang Weiwei, Yang Taimin, Gong Junbo
State Key Laboratory of Chemical Engineering, School of Chemical Engineering and Technology, Tianjin University Weijin Road 92 Tian-jin 300072 China.
Collaborative Innovation Center of Chemical Science and Engineering Weijin Road 92 Tianjin 300072 China.
Chem Sci. 2025 Jul 14. doi: 10.1039/d5sc04741b.
Covalent organic frameworks (COFs), an emerging class of porous crystalline materials, have potential applications ranging from separation to catalysis. However, the harsh conditions required by the classical amorphous transformation route limit the scalability of COF synthesis, especially for three-dimensional covalent organic frameworks (3D COFs). Here, we propose a novel crystalline intermediate (CIM) transformation method that circumvents the stage of amorphous phase generation, enabling the facile and scalable synthesis of imine-linked 3D COFs. In contrast with the classical route of 3D COF synthesis, the CIM transformation process requires no deoxygenation or high-temperature treatment and offers gram-scalable production with efficient and controllable structure interpenetration. The transformation mechanism from a CIM to a 3D COF was investigated in detail, showing a direct crystal-to-crystal pathway. The structure of a CIM nanocrystal, determined by scanning three-dimensional electron diffraction (3DED), reveals a tightly packed diamond-like structure. Furthermore, this strategy was also successfully applied to the synthesis of other three imine-linked 3D COFs that leads to the discovery of two new COFs, demonstrating its broad applicability.
共价有机框架(COFs)是一类新兴的多孔晶体材料,具有从分离到催化等潜在应用。然而,经典非晶态转变路线所需的苛刻条件限制了COF合成的可扩展性,特别是对于三维共价有机框架(3D COFs)。在此,我们提出了一种新颖的晶体中间体(CIM)转变方法,该方法绕过了非晶相生成阶段,能够实现亚胺连接的3D COFs的简便且可扩展的合成。与3D COF合成的经典路线相比,CIM转变过程不需要脱氧或高温处理,并且能够以高效且可控的结构互穿实现克级规模的生产。详细研究了从CIM到3D COF的转变机制,显示出直接的晶体到晶体途径。通过扫描三维电子衍射(3DED)确定的CIM纳米晶体结构揭示了一种紧密堆积的类金刚石结构。此外,该策略还成功应用于其他三种亚胺连接的3D COFs的合成,从而发现了两种新的COFs,证明了其广泛的适用性。