Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/165708
Title: 2D conjugated microporous polyacetylenes synthesized via halogen-bond-assisted radical solid-phase polymerization for high-performance metal-ion absorbents
Authors: Le, Hong Tho
Wang, Chen-Gang
Goto, Atsushi
Keywords: Science::Chemistry
Science::Chemistry::Organic chemistry::Polymers
Issue Date: 2023
Source: Le, H. T., Wang, C. & Goto, A. (2023). 2D conjugated microporous polyacetylenes synthesized via halogen-bond-assisted radical solid-phase polymerization for high-performance metal-ion absorbents. Nature Communications, 14(1), 171-. https://dx.doi.org/10.1038/s41467-023-35809-5
Project: MOE-MOET2EP10121-0005 
Journal: Nature Communications 
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+) 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.
URI: https://hdl.handle.net/10356/165708
ISSN: 2041-1723
DOI: 10.1038/s41467-023-35809-5
Schools: School of Chemistry, Chemical Engineering and Biotechnology 
Rights: © 2023 The Author(s). All rights reserved. This paper was published in Nature Communications and is made available with permission of The Author(s).
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:CCEB Journal Articles

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