Topology-Templated Synthesis of Crystalline Porous Covalent Organic Frameworks

被引:98
作者
Jin, Enquan [1 ]
Geng, Keyu [1 ]
Lee, Ka Hung [2 ,3 ]
Jiang, Weiming [1 ]
Li, Juan [1 ]
Jiang, Qiuhong [1 ]
Irle, Stephan [2 ,3 ,4 ]
Jiang, Donglin [1 ,5 ]
机构
[1] Natl Univ Singapore, Dept Chem, Fac Sci, 3 Sci Dr 3, Singapore 117543, Singapore
[2] Oak Ridge Natl Lab, Computat Sci & Engn Div, Oak Ridge, TN USA
[3] Oak Ridge Natl Lab, Div Chem Sci, Oak Ridge, TN USA
[4] Univ Tennessee, Bredesen Ctr Interdisciplinary Res & Grad Educ, Knoxville, TN 37996 USA
[5] Tianjin Univ, Joint Sch Natl Univ Singapore & Tianjin Univ, Int Campus, Fuzhou 350207, Peoples R China
关键词
covalent organic frameworks; exciton migration; luminescence; topology template; pi transmission;
D O I
10.1002/anie.202004728
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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 pi transmission and exciton migration; these key fundamental pi 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.
引用
收藏
页码:12162 / 12169
页数:8
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