Chen Xiong, Addicoat Matthew, Jin Enquan, Xu Hong, Hayashi Taku, Xu Fei, Huang Ning, Irle Stephan, Jiang Donglin
Department of Materials Molecular Science, Institute for Molecular Science, National Institutes of Natural Sciences, 5-1 Higashiyama, Myodaiji, Okazaki 444-8787, Japan.
WPI-Research Initiative-Institute of Transformative Bio-Molecules and Department of Chemistry, Graduate School of Science, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8602, Japan.
Sci Rep. 2015 Oct 12;5:14650. doi: 10.1038/srep14650.
Covalent organic frameworks (COFs) are an emerging class of crystalline porous polymers in which organic building blocks are covalently and topologically linked to form extended crystalline polygon structures, constituting a new platform for designing π-electronic porous materials. However, COFs are currently synthesised by a few chemical reactions, limiting the access to and exploration of new structures and properties. The development of new reaction systems that avoid such limitations to expand structural diversity is highly desired. Here we report that COFs can be synthesised via a double-stage connection that polymerises various different building blocks into crystalline polygon architectures, leading to the development of a new type of COFs with enhanced structural complexity and diversity. We show that the double-stage approach not only controls the sequence of building blocks but also allows fine engineering of pore size and shape. This strategy is widely applicable to different polymerisation systems to yield hexagonal, tetragonal and rhombus COFs with predesigned pores and π-arrays.
共价有机框架(COFs)是一类新兴的结晶多孔聚合物,其中有机结构单元通过共价键和拓扑连接形成扩展的结晶多边形结构,构成了设计π电子多孔材料的新平台。然而,目前COFs是通过少数化学反应合成的,这限制了对新结构和性质的获取与探索。迫切需要开发新的反应体系以避免此类限制,从而扩大结构多样性。在此,我们报告COFs可通过双阶段连接合成,即将各种不同的结构单元聚合成结晶多边形结构,从而开发出一种具有更高结构复杂性和多样性的新型COFs。我们表明,双阶段方法不仅能控制结构单元的序列,还能对孔径和形状进行精细设计。该策略广泛适用于不同的聚合体系,可生成具有预先设计的孔和π阵列的六边形、四边形和菱形COFs。