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Tough, High-Strength and Recyclability Polyurethane Elastomers Via Woven Crosslinking Strategy

https://doi.org/10.2139/ssrn.5145766
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Energy Dissipation and Toughening of Covalent Networks via a Sacrificial Conformation Approach
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Synergistic enhancement of the robustness of multifunctional polyurethane via an ionic noncovalent cross-linking network and aromatic disulfides
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Hydrogen and DA bond-based self-healing epoxy-modified polyurea composite coating with anti-cavitation, anticorrosion, antifouling, and strong adhesion properties
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Adaptable Strategy to Fabricate Self-Healable and Reprocessable Poly(thiourethane-urethane) Elastomers via Reversible Thiol–Isocyanate Click Chemistry
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Woven Polymer Networks via the Topological Transformation of a [2]Catenane
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Boronic Ester Based Vitrimers with Enhanced Stability via Internal Boron–Nitrogen Coordination
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Mechanically Interlocked Vitrimers
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Oligo[2]catenane That Is Robust at Both the Microscopic and Macroscopic Scales
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Doubly Threaded Slide-Ring Polycatenane Networks
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Oxime-Based and Catalyst-Free Dynamic Covalent Polyurethanes
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A Synthetic Route for Crystals of Woven Structures, Uniform Nanocrystals, and Thin Films of Imine Covalent Organic Frameworks
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Recyclable, Strong, and Highly Malleable Thermosets Based on Boroxine Networks
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Phase-locked constructing dynamic supramolecular ionic conductive elastomers with superior toughness, autonomous self-healing and recyclability
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Closed-loop chemical recycling of cross-linked polymeric materials based on reversible amidation chemistry
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