Abstract
Paula Fanlo, Guillem Seychal, Haritz Sardón, Alaitz Rekondo, Hans Jürgen Grande, Alaitz Ruiz de Luzuriaga, Marta Ximenis
Abstract
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Production, Use, and Fate of All Plastics Ever Made
10.1126/sciadv.1700782 · 2017
Advances in Sustainable Thermosetting Resins: From Renewable Feedstock to High Performance and Recyclability
10.1016/j.progpolymsci.2020.101353 · 2021
Covalent Adaptable Networks: Smart, Reconfigurable and Responsive Network Systems
10.1039/c3cs60046g · 2013
Dynamic Covalent Polymer Networks: From Old Chemistry to Modern Day Innovations
10.1002/adma.201606100 · 2017
Covalent Adaptable Networks (CANs): A Unique Paradigm in Cross-Linked Polymers
10.1021/ma902596s · 2010
A Thermally Re-Mendable Cross-Linked Polymeric Material
10.1126/science.1065879 · 2002
Dynamers: Polyacylhydrazone Reversible Covalent Polymers, Component Exchange, and Constitutional Diversity
10.1073/pnas.0401885101 · 2004
Silica-Like Malleable Materials from Permanent Organic Networks
10.1126/science.1212648 · 2011
Covalent Adaptable Networks: Reprocessable Cross-Linked Polymers
10.1021/acs.chemrev.4c00994 · 2026
Biobased Transesterification Vitrimers
Provenance
crossref
Confidence 100%
ror
Confidence 99%
openalex
Confidence 95%
datacite
Confidence 0%
10.1002/marc.202200892 · 2023
Designed from Biobased Materials for Recycling: Imine-Based Covalent Adaptable Networks
10.1002/marc.202100816 · 2022
Boronic Ester Based Vitrimers with Enhanced Stability via Internal Boron–Nitrogen Coordination
10.1021/jacs.0c10244 · 2020
Facile Control of Reversible Diels–Alder Polyester Networks from Biobased Furan Cross-Linkers and Aliphatic Bismaleimides
10.1021/acssuschemeng.5c06445 · 2025
Vinylogous Urethane Vitrimers
10.1002/adfm.201404553 · 2015
A Highly Dynamic Covalent Polymer Network without Creep: Mission Impossible?
10.1002/anie.202210405 · 2022
Taking Dynamic Covalent Chemistry out of the Lab and into Reprocessable Industrial Thermosets
10.1038/s41570-025-00686-7 · 2025
Sulfur in Dynamic Covalent Chemistry
10.1002/anie.202201168 · 2022
Recyclable Polythioesters and Polydisulfides with Near-Equilibrium Thermodynamics and Dynamic Covalent Bonds
10.1007/s11426-022-1418-9 · 2023
Acetal-thiol Click-like Reaction: Facile and Efficient Synthesis of Dynamic Dithioacetals and Recyclable Polydithioacetals
10.1002/anie.202405653 · 2024
Stress Relaxation Studies of the Viscoelastic Properties of Polymers
10.1063/1.1722465 · 1956
Self-Healing Materials Based on Disulfide Links
10.1021/ma2001492 · 2011
Disulfide-Mediated Reversible Polymerization toward Intrinsically Dynamic Smart Materials
10.1021/jacs.1c10359 · 2022
Density Functional Theory Calculations on S–S Bond Dissociation Energies of Disulfides
10.1002/poc.3480 · 2016
Combined DFT and MD Simulation Protocol to Characterize Self-Healing Properties in Disulfide-Containing Materials: Polyurethanes and Polymethacrylates as Case Studies
10.3389/fmats.2022.859482 · 2022
Design of New Disulfide-Based Organic Compounds for the Improvement of Self-Healing Materials
10.1039/c5cp06660c · 2016
The Underlying Mechanisms for Self-Healing of Poly(Disulfide)s
10.1039/c6cp04028d · 2016
Disulfide-Initiated Addition–Fragmentation Chain Transfer in Allyl Sulfide-Based Vitrimers
10.1002/anie.202519880 · 2025
Thermally Adjustable Dynamic Disulfide Linkages Mediated by Highly Air-Stable 2,2,6,6-Tetramethylpiperidine-1-sulfanyl (TEMPS) Radicals
10.1002/anie.201611049 · 2017
Sulfenamides as Building Blocks for Efficient Disulfide-Based Self-Healing Materials A Quantum Chemical Study
10.1002/open.201800003 · 2018
Amines, Aromatic
10.1002/14356007.a02_037 · 2000
Tetrahedron Report Number 163
10.1016/s0040-4020(01)91791-0 · 1984
10.1002/14356007
10.1002/14356007 · 2000
10.1007/978-3-642-73432-8
10.1007/978-3-642-73432-8 · 1988
The Processability of a Poly(Urea-Urethane) Elastomer Reversibly Crosslinked with Aromatic Disulfide Bridges
10.1039/c3ta14927g · 2014
Vanillin-Based Dual Dynamic Epoxy Building Block: A Promising Accelerator for Disulfide Vitrimers
10.1039/d4py00038b · 2024
Aero Grade Epoxy Vitrimer towards Commercialization
10.3390/polym14153180 · 2022
Rapid Stress Relaxation and Degradable Aromatic Disulfide Vitrimer for Recyclable Carbon Fiber Reinforced Composite
10.1007/s10965-024-03939-z · 2024
Chemical Control of the Aromatic Disulfide Exchange Kinetics for Tailor-Made Epoxy Vitrimers
10.1016/j.polymer.2021.124457 · 2022
Synthesis and Characterization of Redox-Responsive Disulfide Cross-Linked Polymer Particles for Energy Storage Applications
10.1021/acsmacrolett.1c00682 · 2021
Dynamic by Design: Unlocking Full Relaxation in Disulfide Epoxy Networks
10.1039/d5py00124b · 2025
A Safe Operating Space for Humanity
10.1038/461472a · doi-reference
Rapid Repair and Degradation: A Study of High-Performance Recyclable Vitrimer Epoxy Resin Based on Disulfide Bonds
10.1016/j.polymertesting.2024.108528 · doi-reference
Thermal and Flame Retardant Properties of Recyclable Disulfide Based Epoxy Vitrimers
10.1016/j.polymdegradstab.2024.111145 · doi-reference
Recyclable Flame-Retardant Epoxy Composites Based on Disulfide Bonds: Flammability and Recyclability
10.1016/j.coco.2021.100754 · doi-reference
Design and Preparation of a High Mechanical Strength Recyclable Polyurethane Adhesive Based on Dynamic Disulfide Bonds
10.1002/pol.20241146 · doi-reference
Self-Healing Organic Coatings – Fundamental Chemistry to Commercial Application
10.1016/j.porgcoat.2023.107759 · doi-reference
Reconciling Ultrahigh-Temperature Capability and Chemical Degradation in Bismaleimide Diphenyldisulfide-Based Polymers and Composites
10.1021/acsami.5c24646 · doi-reference
Mode-I and Mode-II Interlaminar Fracture Properties of High Strength Polyacrylonitrile-Based Carbon Fiber Reinforced Disulfide-Based Epoxy-Covalent Adaptable Network Polymer Composite
10.1016/j.mtcomm.2026.114737 · doi-reference
Design, Production and Characterization of High Performance 3R Composites Based on Dynamic Chemistry for the Aerospace Industry
10.23967/r.matcomp.2022.11.03 · doi-reference
Characterization and Modeling of an Epoxy Vitrimer Based on Disulfide Exchange for Wet Filament Winding Applications
10.1002/pen.26805 · doi-reference
Vitrimer Composites: Current Status and Future Challenges
10.1039/d2ma00654e · doi-reference
A Comprehensive Review on Fiber-Reinforced Polymer Composites: Raw Materials to Applications, Recycling, and Waste Management
10.1016/j.pmatsci.2024.101326 · doi-reference
Synergistic Enhancement of the Robustness of Multifunctional Polyurethane via an Ionic Noncovalent Cross-Linking Network and Aromatic Disulfides
10.1016/j.cej.2023.148229 · doi-reference
A Wear-Resistant, Self-Healing and Recyclable Multifunctional Waterborne Polyurethane Coating with Mechanical Tunability Based on Hydrogen Bonding and an Aromatic Disulfide Structure
10.1039/d2py00958g · doi-reference
Recyclable Polymer-Bonded Explosives Enabled by Thiol-Cured Disulfide-Based Epoxy Vitrimers
10.1016/j.polymer.2023.125949 · doi-reference
Reprocessable and Recyclable Crosslinked Poly(Urea-Urethane)s Based on Dynamic Amine/Urea Exchange
10.1016/j.polymer.2018.04.076 · doi-reference
Development and Characterisation of Dynamic Bi-Phase (Epoxy/PU) Composites for Enhanced Impact Resistance
10.1016/j.compositesb.2018.08.039 · doi-reference
Unraveling the Thermal Stability of Aromatic Disulfide Epoxy Vitrimers: A Comprehensive Study Using Principal Component Analysis (PCA)
10.1039/d4lp00156g · doi-reference
Thermoformable and Recyclable CFRP Pultruded Profile Manufactured from an Epoxy Vitrimer
10.1016/j.polymertesting.2020.106931 · doi-reference
Epoxy Vitrimer Formulation for Resin Transfer Molding: Reactivity, Process, and Material Characterization
10.1021/acsapm.4c00796 · doi-reference
Epoxy Resin with Exchangeable Disulfide Crosslinks to Obtain Reprocessable, Repairable and Recyclable Fiber-Reinforced Thermoset Composites
10.1039/c6mh00029k · doi-reference
Aromatic Disulfide Crosslinks in Polymer Systems: Self-Healing, Reprocessability, Recyclability and More
10.1016/j.eurpolymj.2016.09.023 · doi-reference
Exploring the Limits of High- Tg Epoxy Vitrimers Produced through Resin-Transfer Molding
10.1021/acsami.3c10007 · doi-reference
Analysis of the Effect of Network Structure and Disulfide Concentration on Vitrimer Properties
10.3390/polym15204123 · doi-reference
Polymer Engineering Based on Reversible Covalent Chemistry: A Promising Innovative Pathway towards New Materials and New Functionalities
10.1016/j.progpolymsci.2018.03.002 · doi-reference
Self-Healing, Reprocessable, and Degradable Bio-Based Epoxy Elastomer Bearing Aromatic Disulfide Bonds and Its Application in Strain Sensors
10.1021/acsapm.1c00865 · doi-reference
Stretchable, Robust and Reprocessable Poly(Siloxane-Urethanes) Elastomers Based on Exchangeable Aromatic Disulfides
10.1016/j.polymer.2021.123588 · doi-reference
Network Topology and Percolation in Model Covalent Adaptable Networks
10.1021/acsmacrolett.4c00523 · doi-reference
Disulfides as Mercapto-Precursors in Nucleophilic Ring Opening Reaction of Polymeric Epoxides: Establishing Equimolar Stoichiometric Conditions in a Thiol–Epoxy ‘Click’ Reaction
10.1039/d0cc02601h · doi-reference
Thermally Reversible Organocatalyst for the Accelerated Reprocessing of Dynamic Networks with Creep Resistance
10.1021/acsmacrolett.3c00544 · doi-reference
Ultrafast Poly(Disulfide) Synthesis in the Presence of Organocatalysts
10.1021/acs.macromol.2c01228 · doi-reference
Solid-State Dynamic Combinatorial Chemistry: Reversibility and Thermodynamic Product Selection in Covalent Mechanosynthesis
10.1039/c0sc00533a · doi-reference
The Role of Tertiary Amines as Internal Catalysts for Disulfide Exchange in Covalent Adaptable Networks
10.1039/d2py01406h · doi-reference
Internal Catalysis for Dynamic Covalent Chemistry Applications and Polymer Science
10.1039/d0cs00452a · doi-reference
Epoxy-Based Catalyst-Free Self-Healing Elastomers at Room Temperature Employing Aromatic Disulfide and Hydrogen Bonds
10.1021/acsomega.2c04559 · doi-reference
High Strength, Recyclable, Durable Polydimethylsiloxanes Based on Carboxylic Acid Aromatic Disulfides with Highly Efficient Room-Temperature Self-Healing
10.1016/j.polymer.2025.128125 · doi-reference
The Role of Non-Covalent Interactions in the Self-Healing Mechanism of Disulfide-Based Polymers
10.1039/c7cp03570e · doi-reference
Hardener Isomerism and Content of Dynamic Disulfide Bond Effect on Chemical Recycling of Epoxy Networks
10.1021/acsapm.2c00598 · doi-reference
Self-healing Polyurethane Based on Disulfide Bond and Hydrogen Bond
10.1002/pat.4135 · doi-reference
Reprocessable Covalent Adaptable Networks via Free-Radical Polymerization with an Aromatic Disulfide Cross-Linker
10.1021/acsapm.4c01580 · doi-reference