亚胺
聚合
共价键
共轭体系
拓扑(电路)
材料科学
模板
聚合物
共价有机骨架
纳米技术
碳纤维
四方晶系
动态共价化学
分子
化学
有机化学
催化作用
晶体结构
超分子化学
复合材料
复合数
数学
组合数学
作者
Enquan Jin,Keyu Geng,Ka Hung Lee,Weiming Jiang,Juan Li,Qiuhong Jiang,Stephan Irle,Donglin Jiang
标识
DOI:10.1002/ange.202004728
摘要
Abstract A strategy is presented for the synthesis of crystalline porous covalent organic frameworks via topology‐templated polymerization. The template is based on imine‐linked frameworks and their (001) facets seed the C=C bond formation reaction to constitute 2D sp 2 carbon‐conjugated frameworks. This strategy is applicable to templates with different topologies, enables designed synthesis of frameworks that cannot be prepared via direct polymerization, and creates a series of sp 2 carbon frameworks with tetragonal, hexagonal, and kagome topologies. The sp 2 carbon frameworks are highly luminescent even in the solid state and exhibit topology‐dependent π transmission and exciton migration; these key fundamental π functions are unique to sp 2 carbon‐conjugated frameworks and cannot be accessible by imine‐linked frameworks, amorphous analogues, and 1D conjugated polymers. These results demonstrate an unprecedented strategy for structural and functional designs of covalent organic frameworks.
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