2D conjugated microporous polyacetylenes synthesized via halogen-bond-assisted radical solid-phase polymerization for high-performance metal-ion absorbents

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作者
Hong Tho Le
Chen-Gang Wang
Atsushi Goto
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[1] Nanyang Technological University,School of Chemistry, Chemical Engineering and Biotechnology
[2] Institute of Sustainability for Chemicals,undefined
[3] Energy and Environment (ISCE2),undefined
[4] Agency for Science Technology and Research (A*STAR),undefined
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Nature Communications | / 14卷
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摘要
The paper reports the first free-radical solid-phase polymerization (SPP) of acetylenes. Acetylene monomers were co-crystalized using halogen bonding, and the obtained cocrystals were polymerized. Notably, because of the alignment of acetylene monomers in the cocrystals, the adjacent C≡C groups were close enough to undergo radical polymerization effectively, enabling the radically low-reactive acetylene monomers to generate high-molecular-weight polyacetylenes that are unattainable in solution-phase radical polymerizations. Furthermore, the SPP of a crosslinkable diacetylene monomer yielded networked two-dimensional conjugated microporous polymers (2D CMPs), where 2D porous polyacetylene nanosheets were cumulated in layer-by-layer manners. Because of the porous structures, the obtained 2D CMPs worked as highly efficient and selective adsorbents of lithium (Li+) and boronium (B3+) ions, adsorbing up to 312 mg of Li+ (31.2 wt%) and 196 mg of B3+ (19.6 wt%) per 1 g of CMP. This Li+ adsorption capacity is the highest ever record in the area of Li+ adsorption.
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