Synthesis of Conjugated Microporous Polymers through Cationic Cyclization Polymerization

被引:39
作者
Zhou, Hao [1 ]
Zhao, Bing [1 ]
Fu, Cheng [2 ]
Wu, Ziqi [1 ]
Wang, Chonggang [1 ]
Ding, Yun [1 ]
Han, Bao-Hang [2 ]
Hu, Aiguo [1 ]
机构
[1] East China Univ Sci & Technol, Sch Mat Sci & Engn, Shanghai Key Lab Adv Polymer Mat, Shanghai 200237, Peoples R China
[2] Natl Ctr Nanosci & Technol, CAS Ctr Excellence Nanosci, CAS Key Lab Nanosyst & Hierarch Fabricat, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
SURFACE-AREA; BERGMAN CYCLIZATION; ORGANIC POLYMERS; HIGHLY EFFICIENT; HYDROGEN STORAGE; LINKED POLYMERS; CO2; ADSORPTION; GAS-STORAGE; IODINE; NANOPARTICLES;
D O I
10.1021/acs.macromol.9b00437
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Conjugated microporous polymers (CMPs) are a kind of polymeric materials combining both high porosities and photoelectric functions and are applied in numerous fields. Herein, three CMPs are facilely synthesized through cationic cyclization polymerization of monomers with multiple enediyne moieties. The chemical structures of the CMPs were characterized with solid-state C-13 cross-polarization/magic-angle spinning NMR spectroscopy and Fourier transform infrared spectroscopy. The obtained CMPs exhibit high Brunauer-Emmett-Teller specific surface areas (up to 780 m(2) g(-1)) and excellent adsorption functionality. The highest uptake capacities are up to 12.7 wt % for carbon dioxide (1.0 bar, 273 K) and 246 wt % for iodine (353 K), which are superior to those of most porous organic polymers (POPs). We believe that this metal-free strategy will provide a novel approach toward the synthesis of CMPs and would further expand the application scope of POPs.
引用
收藏
页码:3935 / 3941
页数:7
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