2D conjugated microporous polyacetylenes synthesized via halogen-bond-assisted radical solid-phase polymerization for high-performance metal-ion absorbents.
basic_science · Level V
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- Record sourced from PubMed, PMID 36635286.
- Also identified by DOI 10.1038/s41467-023-35809-5 and PMC identifier 9837052.
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Abstract
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<sup>+</sup>) and boronium (B<sup>3+</sup>) ions, adsorbing up to 312 mg of Li<sup>+</sup> (31.2 wt%) and 196 mg of B<sup>3+</sup> (19.6 wt%) per 1 g of CMP. This Li<sup>+</sup> adsorption capacity is the highest ever record in the area of Li<sup>+</sup> adsorption.