Highly Emissive Covalent Organic Frameworks

被引:574
作者
Dalapati, Sasanka [1 ]
Jin, Enquan [2 ]
Addicoat, Matthew [3 ]
Heine, Thomas [3 ]
Jiang, Donglin [1 ]
机构
[1] Japan Adv Inst Sci & Technol, Sch Mat Sci, Field Energy & Environm, 1-1 Asahidai, Nomi 9231292, Japan
[2] SOKENDAI, Sch Phys Sci, Dept Struct Mol Sci, Hayama, Kanagawa 2400193, Japan
[3] Univ Leipzig, Wilhelm Ostwald Inst Phys & Theoret Chem, Linnestr 2, D-04103 Leipzig, Germany
关键词
AGGREGATION-INDUCED EMISSION; TRIAZINE-BASED FRAMEWORKS; SINGLE-LAYER GRAPHENE; CRYSTALLINE; CONSTRUCTION; FLUORESCENCE; GENERATION; ELECTRON; PLATFORM; DESIGN;
D O I
10.1021/jacs.6b02700
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Highly luminescent covalent organic frameworks (COFs) are rarely achieved because of the aggregation-caused quenching (ACQ) of pi-pi stacked layers. Here, we report a general strategy to design highly emissive COFs by introducing an aggregation-induced emission (AIE) mechanism. The integration of AIE-active units into the polygon vertices yields crystalline porous COFs with periodic pi-stacked columnar AIE arrays. These columnar AIE pi-arrays dominate the luminescence of the COFs, achieve exceptional quantum yield via a synergistic structural locking effect of intralayer covalent bonding and interlayer noncovalent pi-pi interactions and serve as a highly sensitive sensor to report ammonia down to sub ppm level. Our strategy breaks through the ACQ-based mechanistic limitations of COFs and opens a way to explore highly emissive COF materials.
引用
收藏
页码:5797 / 5800
页数:4
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