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Journal ArticleDOI

Dynamic Covalent Polymer Networks: from Old Chemistry to Modern Day Innovations.

Weike Zou, +4 more
- 01 Apr 2017 - 
- Vol. 29, Iss: 14, pp 1606100
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TLDR
This work designs dynamic covalent polymer networks with unique adaptive properties for vitrimeric rheological behavior and solid-state plasticity for this type of material, and suggests a promising future for this class of materials.
Abstract
Dynamic covalent polymer networks have long been recognized. With the initial focus on the unintended impact of dynamic covalent linkages on the viscoelasticity of commercial rubbers, efforts in modern times have transitioned into designing dynamic covalent polymer networks with unique adaptive properties. Whereas self-healing and thermoset reprocessing have been the primary motivations for studying dynamic covalent polymer networks, the recent discovery of the vitrimeric rheological behavior and solid-state plasticity for this type of material have opened up new opportunities in material innovations. This, coupled with the revelation of the dynamic characteristics of commercially relevant polymer building blocks such as esters and urethanes, suggests a promising future for this class of materials.

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Citations
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Strong, Self-Healing Gelatin Hydrogels Cross-Linked by Double Dynamic Covalent Chemistry.

TL;DR: Biocompatible gelatin hydrogels, double cross-linked via imine and Diels-Alder (DA) dynamic covalent frameworks, showed integrated advantages of adjustable and durable mechanical strength, good thermal stability, biocompatibility for promoting cell growth and reasonable degradable rate as mentioned in this paper.
Journal ArticleDOI

A facile one-pot route to elastomeric vitrimers with tunable mechanical performance and superior creep resistance

TL;DR: In this article, the authors demonstrate a one-pot approach to prepare covalently cross-linked diene-rubbers by engineering dynamic silyl ether linkages into the networks.
Journal ArticleDOI

Photoresponsive dynamic covalent bond based on addition–fragmentation chain transfer of allyl selenides

TL;DR: In this paper, a new dynamic C-Se bond-based addition-fragmentation chain transfer (AFCT) reaction of allyl selenides was performed under irradiation without any catalyst.
Journal ArticleDOI

Disulfide Metathesis-Assisted Lithium-Ion Conduction for PEO-Based Polymer Electrolytes.

TL;DR: The disulfide metathesis is a promising candidate in the dynamically exchanged strategy for improving the self-healing ability of polymer electrolytes (PEs), however, the enhancement effects on the ionic conductivities of PEs are generally ignored while introducing a dynamic covalent bond to PEs as discussed by the authors .
References
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Journal ArticleDOI

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TL;DR: In this article, a review of recent mechanistic developments in the field of controlled/living radical polymerization (CRP) is presented, with particular emphasis on structure-reactivity correlations and "rules" for catalyst selection in ATRP, for chain transfer agent selection in reversible addition-fragmentation chain transfer (RAFT) polymerization, and for the selection of an appropriate mediating agent in stable free radical polymerisation (SFRP), including organic and transition metal persistent radicals.
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Self-healing and thermoreversible rubber from supramolecular assembly

TL;DR: The design and synthesis of molecules that associate together to form both chains and cross-links via hydrogen bonds and the system shows recoverable extensibility up to several hundred per cent and little creep under load are designed and synthesized.
Journal ArticleDOI

A Thermally Re-mendable Cross-Linked Polymeric Material

TL;DR: A transparent organic polymeric material that can repeatedly mend or “re-mend” itself under mild conditions and is a tough solid at room temperature and below with mechanical properties equaling those of commercial epoxy resins.
Journal ArticleDOI

Silica-Like Malleable Materials from Permanent Organic Networks

TL;DR: In this paper, the authors designed epoxy networks that can rearrange their topology by exchange reactions without depolymerization, and showed that they are insoluble and processable.
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