Charged Porous Polymers using a Solid CO Cross-Coupling Reaction

被引:19
作者
Zhang, Pengfei [1 ]
Jiang, Xueguang [2 ]
Wan, Shun [1 ]
Dai, Sheng [1 ,2 ]
机构
[1] Oak Ridge Natl Lab, Div Chem Sci, Oak Ridge, TN 37830 USA
[2] Univ Tennessee, Dept Chem, Knoxville, TN 37996 USA
关键词
acid gas capture; mechanochemistry; microporous materials; porous polyelectrolytes; porous polymers; SOLVENT-FREE SYNTHESIS; CONJUGATED MICROPOROUS POLYMERS; ORGANIC MATERIALS; IONIC LIQUIDS; CARBON; ADSORPTION; NETWORKS; MECHANOCHEMISTRY; ACTIVATION; FRAMEWORKS;
D O I
10.1002/chem.201501814
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Herein, we report a green, fast, efficient mechanochemical strategy for charged porous polymers (CPPs). A cationic CPP with basic anions and an anionic CPP with Li+ cations were fabricated by solid grinding under solvent-free conditions. Compared with solution-based synthesis, mechanochemical grinding can shorten the reaction time from dozens of hours to several minutes (60-90min) to form polymers possessing a high molecular mass and low polydispersity. During the construction of CPPs, a Pd-catalyzed solid polycondensation based on unactivated organic linkers was introduced. In particular, CPPs with basic phenolic or proline anions showed good activity and stability in SO2 capture, and Li+-functionalized CPPs can be post-modified to CPPs with other metal ions by ion exchange, highlighting the tailorable feature of ionic-modified CPPs.
引用
收藏
页码:12866 / +
页数:5
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