Vitrimer-like elastomers with rapid stress-relaxation by high-speed carboxy exchange through conjugate substitution reaction

We report vitrimer-like elastomers that exhibit significantly fast stress relaxation using carboxy exchange via the conjugate substitution reaction of α-(acyloxymethyl) acrylate skeletons. This network design is inspired by a small-molecule model that shows the carboxy exchange reaction even at ambient temperature in the presence of 1,4-diazabicyclo[2.2.2]octane (DABCO). The acrylate and acrylic acid copolymers are cross-linked using bis[α-(bromomethyl)acrylates] and doped with 10 wt% DABCO, exhibiting processability to obtain a transparent film by hot pressing. The high-speed bond exchange in the network, validated by stress-relaxation tests, allows quick molding with household iron. In addition, the material is applied as an adhesion sheet for plastic and metal substrates. Because dynamic cross-linking with the proposed bond exchange mechanism can be implemented for any polymer bearing carboxyl pendants, our approach can be applied to versatile backbones, which must thus be meaningful in the practical sense.

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Publication Details

Journal
Nature Communications
Published
2024-10-05
DOI
https://doi.org/10.1038/s41467-024-53043-5
Citations
25
Primary Topic
Polymer composites and self-healing
Type
article
Field-Weighted Citation Impact
4.22

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article

Vitrimer-like elastomers with rapid stress-relaxation by high-speed carboxy exchange through conjugate substitution reaction

Mikihiro Hayashi, Ryo Kawatani, Yasuhiro Kohsaka, Natsumi Nishiie et al.
25 citations
Nature Communications
Polymer composites and self-healing
4.22
article

Vitrimer-like elastomers with rapid stress-relaxation by high-speed carboxy exchange through conjugate substitution reaction

Mikihiro Hayashi, Ryo Kawatani, Yasuhiro Kohsaka, Natsumi Nishiie, Sae Tezuka, Miu Mizuma
article en
25 citations

Abstract

We report vitrimer-like elastomers that exhibit significantly fast stress relaxation using carboxy exchange via the conjugate substitution reaction of α-(acyloxymethyl) acrylate skeletons. This network design is inspired by a small-molecule model that shows the carboxy exchange reaction even at ambient temperature in the presence of 1,4-diazabicyclo[2.2.2]octane (DABCO). The acrylate and acrylic acid copolymers are cross-linked using bis[α-(bromomethyl)acrylates] and doped with 10 wt% DABCO, exhibiting processability to obtain a transparent film by hot pressing. The high-speed bond exchange in the network, validated by stress-relaxation tests, allows quick molding with household iron. In addition, the material is applied as an adhesion sheet for plastic and metal substrates. Because dynamic cross-linking with the proposed bond exchange mechanism can be implemented for any polymer bearing carboxyl pendants, our approach can be applied to versatile backbones, which must thus be meaningful in the practical sense.

Nature CommunicationsVol. 15(1)
Shinshu University (JP), Nagoya Institute of Technology (JP)
Japan Science and Technology Agency, Precursory Research for Embryonic Science and Technology
Openalex Percentile: Top 4%
Polymer composites and self-healing
4.22
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Vitrimer-like elastomers with rapid stress-relaxation by high-speed carboxy exchange through conjugate substitution reaction — Mikihiro Hayashi, Ryo Kawatani, et al. · Nature Communications (2024) | TGRS Research Map | TGRS