化学
共聚物
介孔材料
化学工程
整体
共价键
单体
催化作用
粒子(生态学)
纳米技术
高分子化学
聚合物
有机化学
材料科学
海洋学
工程类
地质学
作者
Wei Li,Zhengwei Bie,Chi Zhang,Xintong Xu,Song Wang,Yuhao Yang,Ziyang Zhang,Xuan Yang,Khak Ho Lim,Qingyue Wang,Wenjun Wang,Bo‐Geng Li,Pingwei Liu
摘要
Precise tailoring of the aggregation state of covalent organic frameworks (COFs) to form a hierarchical porous structure is critical to their performance and applications. Here, we report a one-pot and one-step strategy of using dynamic combinatorial chemistry to construct imine-based hollow COFs containing meso- and macropores. It relies on a direct copolymerization of three or more monomers in the presence of two monofunctional competitors. The resulting particle products possess high crystallinity and hierarchical pores, including micropores around 0.93 nm, mesopores widely distributed in the range of 3.1-32 nm, and macropores at about 500 nm, while the specific surface area could be up to 748 m2·g-1, with non-micropores accounting for 60% of the specific surface area. The particles demonstrate unique advantages in the application as nanocarriers for in situ loading of Pd catalysts at 93.8% loading efficiency in the copolymerization of ethylene and carbon monoxide. The growth and assembly of the copolymer could thus be regulated to form flower-shaped particles, efficiently suppressing the fouling of the reactor. The copolymer's weight-average molecular weight and the melting temperature are also highly improved. Our method provides a facile way of fabricating COFs with hierarchical pores for advanced applications in catalysis.
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