Department of Chemistry , Technische Universität Berlin , BA2, Hardenbergstraße 40 , 10623 Berlin , Germany.
European Synchrotron Radiation Facility , CS40220 , 38043 Grenoble Cedex 9 , France.
J Am Chem Soc. 2018 Apr 25;140(16):5330-5333. doi: 10.1021/jacs.8b01774. Epub 2018 Apr 10.
The synthesis of 3D covalent organic frameworks (COFs) adopting novel topologies is challenging, and so far 3D COFs have only been reported for nets based on building blocks with tetrahedral geometry. We demonstrate the targeted synthesis of an anionic 3D COF crystallizing in a three-coordinated srs net by exploiting a recently developed linkage for the formation of anionic silicate COFs based on hypercoordinate silicon nodes. The framework, named SiCOF-5, was synthesized by reticulating dianionic hexacoordinate [SiO] nodes with triangular triphenylene building blocks and adopts a two-fold interpenetrated srs-c net with an overall composition of Na[Si(CHO)] (where CHO is triphenylene-2,3,6,7,10,11-hexakis(olate)). A key requirement for the crystallization of SiCOF-5 was the careful control over the nucleation and growth rate by gradual generation of the silicon source during the course of the reaction.
采用新拓扑结构合成 3D 共价有机骨架 (COFs) 具有挑战性,迄今为止,仅报道了基于具有四面体几何形状的构建块的 3D COFs。我们通过利用最近开发的用于形成基于超配位硅节点的阴离子硅酸盐 COFs 的连接来证明目标合成在三配位 srs 网上结晶的阴离子 3D COF。该骨架命名为 SiCOF-5,是通过用三角形三苯并[g,h,i]苝二炔构筑块与二价六配位 [SiO] 节点交联合成的,采用具有总体组成 Na[Si(CHO)] 的两倍互穿 srs-c 网(其中 CHO 是三苯并[g,h,i]苝-2,3,6,7,10,11-六羧酸根)。SiCOF-5 结晶的一个关键要求是通过在反应过程中逐渐生成硅源来仔细控制成核和生长速率。