Research graph
References from Biobased N,O-acetal covalent adaptable networks with enhanced thermomechanical properties and flame-retardancy. Local targets link to admitted publications; unresolved targets remain external evidence.
Plastic or plastic-free life: from formation to removal
10.1016/j.scitotenv.2023.164359 · 2023 · External reference
Designing a circular carbon and plastics economy for a sustainable future
10.1038/s41586-023-06939-z · 2024 · External reference
Evaluating scenarios toward zero plastic pollution
10.1126/science.aba9475 · 2020 · External reference
State of the art in recycling waste thermoplastics and thermosets and their applications in construction
10.1016/j.resconrec.2021.105776 · 2021 · External reference
Advances in sustainable thermosetting resins: from renewable feedstock to high performance and recyclability
10.1016/j.progpolymsci.2020.101353 · 2021 · External reference
Covalent adaptable networks: reprocessable cross-linked polymers
10.1021/acs.chemrev.4c00994 · 2026 · External reference
A thermally re-mendable cross-linked polymeric material
10.1126/science.1065879 · 2002 · External reference
Rheological and chemical analysis of reverse gelation in a covalently cross-linked diels−alder polymer network
10.1021/ma801863d · 2008 · External reference
Covalent adaptable network enables sustainable polyethylene for next‐generation cable insulation
2025 · External reference
Silica-like malleable materials from permanent organic networks
10.1126/science.1212648 · 2011 · External reference
Scalable upcycling of thermoplastic polyolefins into vitrimers through transesterification
10.1039/d0ta07339c · 2020 · External reference
Introduction of photolatent bases for locally controlling dynamic exchange reactions in thermo‐activated vitrimers
10.1002/anie.202102946 · 2021 · External reference
Biobased transesterification vitrimers
10.1002/marc.202200892 · 2023 · External reference
Self-healing materials based on disulfide links
10.1021/ma2001492 · 2011 · External reference
Orthogonal imine and disulfide exchange in a biobased covalent adaptable network: toward healable and recyclable thermosets
10.1016/j.eurpolymj.2025.114473 · 2026 · External reference
Photoinduced plasticity in cross-linked polymers
10.1126/science.1110505 · 2005 · External reference
Disulfide‐initiated addition–fragmentation chain transfer in allyl sulfide‐based vitrimers
2025 · External reference
Malleable and self-healing covalent polymer networks through tunable dynamic boronic ester bonds
10.1021/jacs.5b03551 · 2015 · External reference
Room-temperature self-healing polymers based on dynamic-covalent boronic esters
10.1021/acs.macromol.5b00210 · 2015 · External reference
A combined computational and experimental study of metathesis and nucleophile-mediated exchange mechanisms in boronic ester-containing vitrimers
10.1039/d3py01047c · 2024 · External reference
Adaptive and robust vitrimers fabricated by synergy of traditional and supramolecular polymers
10.1002/anie.202405761 · 2024 · External reference
Boronic ester-enabled covalent adaptable networks in hydrogenated nitrile butadiene rubber for reprocessable high-performance elastomers
2026 · External reference
Heat- or water-driven malleability in a highly recyclable covalent network polymer
10.1002/adma.201400317 · 2014 · External reference
Repairable woven carbon fiber composites with full recyclability enabled by malleable polyimine networks
10.1002/adma.201505245 · 2016 · External reference
Solvent-free preparation of imine vitrimers: leveraging benzoxazine crosslinking for melt processability and tunable mechanical performance
10.1039/d3ta04351g · 2023 · External reference
Chemical Control of the viscoelastic properties of vinylogous urethane vitrimers
10.1038/ncomms14857 · 2017 · External reference
Block copolymer vitrimers
10.1021/jacs.9b10360 · 2020 · External reference
Suppressing creep and promoting fast reprocessing of vitrimers with reversibly trapped amines
10.1002/anie.202113872 · 2022 · External reference
Vinylogous urea—urethane vitrimers: accelerating and inhibiting network dynamics through hydrogen bonding
10.1002/anie.202318412 · 2024 · External reference
Understanding the reshaping of fluorinated polyester vitrimers by kinetic and DFT studies of the transesterification reaction
10.1002/chem.202201135 · 2022 · External reference
Catalyst-free epoxy vitrimers based on transesterification internally activated by an α–CF 3 group
10.1021/acs.macromol.1c02538 · 2022 · External reference
From vineyards to reshapable materials: α-CF 2 activation in 100% resveratrol-based catalyst-free vitrimers
10.1039/d3py00017f · 2023 · External reference
Transamidation vitrimers enabled by neighbouring fluorine atom activation
10.1039/d3py00577a · 2023 · External reference
Combination of fluorine and tertiary amine activation in catalyst-free thia-michael covalent adaptable networks
10.1021/acs.macromol.3c01129 · 2023 · External reference
Biobased catalyst-free covalent adaptable networks based on CF 3 -activated synergistic aza-michael exchange and transesterification
10.1039/d2ta05067f · 2022 · External reference
Trifluoromethylated N,S-acetal as a chemical platform for covalent adaptable networks: fast thiol exchange and strong hydrostability for a highly transparent material
10.1021/acs.macromol.4c01359 · 2024 · External reference
Ethoxycarbonyl-stabilized N,S -acetals as a fast exchange platform for catalyst-free covalent adaptable networks
10.1021/acs.macromol.5c01637 · 2025 · External reference
From Formica® to FormiCAN: one-pot synthesis of melamine-based covalent adaptable network endowed with high transition temperature and fast stress relaxation
10.1002/marc.202500280 · 2025 · External reference
Degradable Thermosets Based On Labile Bonds Or Linkages: A Review
10.1016/j.progpolymsci.2017.07.008 · 2018 · External reference
Facile catalyst-free synthesis, exchanging, and hydrolysis of an acetal motif for dynamic covalent networks
10.1039/c9ta04073k · 2019 · External reference
Fast reprocessing of acetal covalent adaptable networks with high performance enabled by neighboring group participation
10.1021/acs.macromol.1c01046 · 2021 · External reference
One‐pot synthesis of depolymerizable δ ‐lactone based vitrimers
10.1002/adma.202300954 · 2023 · External reference
Recyclable, strong thermosets and organogels via paraformaldehyde condensation with diamines
10.1126/science.1251484 · 2014 · External reference
Tunable and processable shape-memory materials based on solvent-free, catalyst-free polycondensation between formaldehyde and diamine at room temperature
10.1021/acsmacrolett.9b00199 · 2019 · External reference
Novel green reversible humidity-responsive hemiaminal dynamic covalent network for smart window
10.1021/acsami.2c21717 · 2023 · External reference
Hemiaminal dynamic covalent networks with rapid stress relaxation, reprocessability and degradability endowed by the synergy of disulfide and hemiaminal bonds
10.1039/d3ra05413f · 2023 · External reference
Covalent adaptable networks through dynamic N , S -Acetal chemistry: toward recyclable CO2 -based thermosets
10.1021/jacs.3c10080 · 2023 · External reference
Unprecedented associative exchange in CO2 -sourced cyclic S , O -acetal-based covalent adaptable networks
10.1039/d4py00359d · 2024 · External reference
10.1039/d5ta07881d
10.1039/d5ta07881d · External reference
Tailoring biobased epoxy systems: unraveling the structure-property relationship of polyfurfurylamines
10.1007/s10924-025-03671-9 · 2025 · External reference
Review on intrinsically recyclable flame retardant thermosets enabled through covalent bonds
10.1002/app.52493 · 2022 · External reference
Effect of addition of aluminum phosphinate as fire retardant in a PBT vitrimer
10.1016/j.polymer.2023.126559 · 2024 · External reference
Recent developments in the fire retardancy of polymeric materials
10.1016/j.progpolymsci.2013.06.006 · 2013 · External reference
Phosphorus acid: an asset for flame-retardant sustainable vitrimers
10.1039/d3py01328f · 2024 · External reference
Bio-based anhydride crosslinked furan-derived vitrimeric epoxy networks with intrinsic flame retardancy, self-healing capacity and recyclability
10.1016/j.jclepro.2025.147301 · 2026 · External reference
A phosphorus/silicon-containing flame retardant based on eugenol for improving flame retardancy and smoke suppression of epoxy resin
10.1002/app.54474 · 2023 · External reference
Recent advances in fire-retardant silicone rubber composites
10.3390/polym16172442 · 2024 · External reference
Catalyst-free β-hydroxy phosphate ester exchange for robust fire-proof vitrimers
10.1016/j.cej.2021.129132 · 2021 · External reference
A phosphonate-derived epoxy vitrimer with intrinsic flame retardancy and catalyst-free reprocessability
10.1002/pol.20230211 · 2024 · External reference
A curing agent for facile fabrication of intrinsically flame-retardant epoxy vitrimers with catalyst-free mixed carboxylate/phosphonate transesterification
10.1021/acsapm.4c01048 · 2024 · External reference
Furan-derived Schiff base covalent adaptable thermosets with recyclability and anti-flammability
10.1016/j.gce.2023.08.005 · 2024 · External reference
Biobased heat resistant epoxy resin with extremely high biomass content from 2,5-furandicarboxylic acid and eugenol
10.1021/acssuschemeng.7b01222 · 2017 · External reference
A furan-derived epoxy thermoset with inherent anti-flammability, degradability, and raw material recycling
2023 · External reference
How to make furfural and HMF production greener? lessons from life cycle assessments
10.1039/d5gc03729h · 2025 · External reference
A Bio-based intrinsically flame-retardant epoxy vitrimer from furan derivatives and its application in recyclable carbon fiber composites
10.1016/j.polymdegradstab.2022.110206 · 2023 · External reference
Estimation of rate of heat release by means of oxygen consumption measurements
10.1002/fam.810040202 · 1980 · External reference
A microscale combustion calorimeter study of gas phase combustion of polymers
10.1016/j.combustflame.2014.08.008 · 2015 · External reference
A molecular basis for polymer flammability
10.1016/j.polymer.2009.03.047 · 2009 · External reference
Predicting the flammability of polymers from their chemical structure: an improved model based on group contributions
10.1016/j.polymer.2016.01.046 · 2016 · External reference
Prediction of thermosets flammability using a model based on group contributions
10.1016/j.polymer.2017.09.012 · 2017 · External reference
Exploring the contribution of two phosphorus-based groups to polymer flammability via pyrolysis–combustion flow calorimetry
10.3390/ma12182961 · 2019 · External reference
FTIR–PCFC coupling: a new method for studying the combustion of polymers
10.1016/j.combustflame.2013.11.011 · 2014 · External reference
CF3CH(ONO)CF3: synthesis, IR spectrum, and use as OH radical source for kinetic and mechanistic studies
10.1002/kin.10116 · 2003 · External reference
Heat- or water-driven malleability in a highly recyclable covalent network polymer
10.1002/adma.201400317 · ExternalCitation · doi-reference
Repairable woven carbon fiber composites with full recyclability enabled by malleable polyimine networks
10.1002/adma.201505245 · ExternalCitation · doi-reference
One‐pot synthesis of depolymerizable δ ‐lactone based vitrimers
10.1002/adma.202300954 · ExternalCitation · doi-reference
Introduction of photolatent bases for locally controlling dynamic exchange reactions in thermo‐activated vitrimers
10.1002/anie.202102946 · ExternalCitation · doi-reference
Suppressing creep and promoting fast reprocessing of vitrimers with reversibly trapped amines
10.1002/anie.202113872 · ExternalCitation · doi-reference
Vinylogous urea—urethane vitrimers: accelerating and inhibiting network dynamics through hydrogen bonding
10.1002/anie.202318412 · ExternalCitation · doi-reference
Adaptive and robust vitrimers fabricated by synergy of traditional and supramolecular polymers
10.1002/anie.202405761 · ExternalCitation · doi-reference
Review on intrinsically recyclable flame retardant thermosets enabled through covalent bonds
10.1002/app.52493 · ExternalCitation · doi-reference
A phosphorus/silicon-containing flame retardant based on eugenol for improving flame retardancy and smoke suppression of epoxy resin
10.1002/app.54474 · ExternalCitation · doi-reference
Understanding the reshaping of fluorinated polyester vitrimers by kinetic and DFT studies of the transesterification reaction
10.1002/chem.202201135 · ExternalCitation · doi-reference
Estimation of rate of heat release by means of oxygen consumption measurements
10.1002/fam.810040202 · ExternalCitation · doi-reference
CF3CH(ONO)CF3: synthesis, IR spectrum, and use as OH radical source for kinetic and mechanistic studies
10.1002/kin.10116 · ExternalCitation · doi-reference
Biobased transesterification vitrimers
10.1002/marc.202200892 · ExternalCitation · doi-reference
From Formica® to FormiCAN: one-pot synthesis of melamine-based covalent adaptable network endowed with high transition temperature and fast stress relaxation
10.1002/marc.202500280 · ExternalCitation · doi-reference
A phosphonate-derived epoxy vitrimer with intrinsic flame retardancy and catalyst-free reprocessability
10.1002/pol.20230211 · ExternalCitation · doi-reference
Tailoring biobased epoxy systems: unraveling the structure-property relationship of polyfurfurylamines
10.1007/s10924-025-03671-9 · ExternalCitation · doi-reference
Catalyst-free β-hydroxy phosphate ester exchange for robust fire-proof vitrimers
10.1016/j.cej.2021.129132 · ExternalCitation · doi-reference
FTIR–PCFC coupling: a new method for studying the combustion of polymers
10.1016/j.combustflame.2013.11.011 · ExternalCitation · doi-reference
A microscale combustion calorimeter study of gas phase combustion of polymers
10.1016/j.combustflame.2014.08.008 · ExternalCitation · doi-reference
Orthogonal imine and disulfide exchange in a biobased covalent adaptable network: toward healable and recyclable thermosets
10.1016/j.eurpolymj.2025.114473 · ExternalCitation · doi-reference
Furan-derived Schiff base covalent adaptable thermosets with recyclability and anti-flammability
10.1016/j.gce.2023.08.005 · ExternalCitation · doi-reference
Bio-based anhydride crosslinked furan-derived vitrimeric epoxy networks with intrinsic flame retardancy, self-healing capacity and recyclability
10.1016/j.jclepro.2025.147301 · ExternalCitation · doi-reference
A Bio-based intrinsically flame-retardant epoxy vitrimer from furan derivatives and its application in recyclable carbon fiber composites
10.1016/j.polymdegradstab.2022.110206 · ExternalCitation · doi-reference
A molecular basis for polymer flammability
10.1016/j.polymer.2009.03.047 · ExternalCitation · doi-reference
Predicting the flammability of polymers from their chemical structure: an improved model based on group contributions
10.1016/j.polymer.2016.01.046 · ExternalCitation · doi-reference
Prediction of thermosets flammability using a model based on group contributions
10.1016/j.polymer.2017.09.012 · ExternalCitation · doi-reference
Effect of addition of aluminum phosphinate as fire retardant in a PBT vitrimer
10.1016/j.polymer.2023.126559 · ExternalCitation · doi-reference
Recent developments in the fire retardancy of polymeric materials
10.1016/j.progpolymsci.2013.06.006 · ExternalCitation · doi-reference
Degradable Thermosets Based On Labile Bonds Or Linkages: A Review
10.1016/j.progpolymsci.2017.07.008 · ExternalCitation · doi-reference
Advances in sustainable thermosetting resins: from renewable feedstock to high performance and recyclability
10.1016/j.progpolymsci.2020.101353 · ExternalCitation · doi-reference
State of the art in recycling waste thermoplastics and thermosets and their applications in construction
10.1016/j.resconrec.2021.105776 · ExternalCitation · doi-reference
Plastic or plastic-free life: from formation to removal
10.1016/j.scitotenv.2023.164359 · ExternalCitation · doi-reference
Covalent adaptable networks: reprocessable cross-linked polymers
10.1021/acs.chemrev.4c00994 · ExternalCitation · doi-reference
Fast reprocessing of acetal covalent adaptable networks with high performance enabled by neighboring group participation
10.1021/acs.macromol.1c01046 · ExternalCitation · doi-reference
Catalyst-free epoxy vitrimers based on transesterification internally activated by an α–CF 3 group
10.1021/acs.macromol.1c02538 · ExternalCitation · doi-reference
Combination of fluorine and tertiary amine activation in catalyst-free thia-michael covalent adaptable networks
10.1021/acs.macromol.3c01129 · ExternalCitation · doi-reference
Trifluoromethylated N,S-acetal as a chemical platform for covalent adaptable networks: fast thiol exchange and strong hydrostability for a highly transparent material
10.1021/acs.macromol.4c01359 · ExternalCitation · doi-reference
Room-temperature self-healing polymers based on dynamic-covalent boronic esters
10.1021/acs.macromol.5b00210 · ExternalCitation · doi-reference
Ethoxycarbonyl-stabilized N,S -acetals as a fast exchange platform for catalyst-free covalent adaptable networks
10.1021/acs.macromol.5c01637 · ExternalCitation · doi-reference
Novel green reversible humidity-responsive hemiaminal dynamic covalent network for smart window
10.1021/acsami.2c21717 · ExternalCitation · doi-reference
A curing agent for facile fabrication of intrinsically flame-retardant epoxy vitrimers with catalyst-free mixed carboxylate/phosphonate transesterification
10.1021/acsapm.4c01048 · ExternalCitation · doi-reference
Tunable and processable shape-memory materials based on solvent-free, catalyst-free polycondensation between formaldehyde and diamine at room temperature
10.1021/acsmacrolett.9b00199 · ExternalCitation · doi-reference
Biobased heat resistant epoxy resin with extremely high biomass content from 2,5-furandicarboxylic acid and eugenol
10.1021/acssuschemeng.7b01222 · ExternalCitation · doi-reference
Covalent adaptable networks through dynamic N , S -Acetal chemistry: toward recyclable CO2 -based thermosets
10.1021/jacs.3c10080 · ExternalCitation · doi-reference
Malleable and self-healing covalent polymer networks through tunable dynamic boronic ester bonds
10.1021/jacs.5b03551 · ExternalCitation · doi-reference
Block copolymer vitrimers
10.1021/jacs.9b10360 · ExternalCitation · doi-reference
Self-healing materials based on disulfide links
10.1021/ma2001492 · ExternalCitation · doi-reference
Rheological and chemical analysis of reverse gelation in a covalently cross-linked diels−alder polymer network
10.1021/ma801863d · ExternalCitation · doi-reference
Chemical Control of the viscoelastic properties of vinylogous urethane vitrimers
10.1038/ncomms14857 · ExternalCitation · doi-reference
Designing a circular carbon and plastics economy for a sustainable future
10.1038/s41586-023-06939-z · ExternalCitation · doi-reference
Facile catalyst-free synthesis, exchanging, and hydrolysis of an acetal motif for dynamic covalent networks
10.1039/c9ta04073k · ExternalCitation · doi-reference
Scalable upcycling of thermoplastic polyolefins into vitrimers through transesterification
10.1039/d0ta07339c · ExternalCitation · doi-reference
Biobased catalyst-free covalent adaptable networks based on CF 3 -activated synergistic aza-michael exchange and transesterification
10.1039/d2ta05067f · ExternalCitation · doi-reference
From vineyards to reshapable materials: α-CF 2 activation in 100% resveratrol-based catalyst-free vitrimers
10.1039/d3py00017f · ExternalCitation · doi-reference
Transamidation vitrimers enabled by neighbouring fluorine atom activation
10.1039/d3py00577a · ExternalCitation · doi-reference
A combined computational and experimental study of metathesis and nucleophile-mediated exchange mechanisms in boronic ester-containing vitrimers
10.1039/d3py01047c · ExternalCitation · doi-reference
Phosphorus acid: an asset for flame-retardant sustainable vitrimers
10.1039/d3py01328f · ExternalCitation · doi-reference
Hemiaminal dynamic covalent networks with rapid stress relaxation, reprocessability and degradability endowed by the synergy of disulfide and hemiaminal bonds
10.1039/d3ra05413f · ExternalCitation · doi-reference
Solvent-free preparation of imine vitrimers: leveraging benzoxazine crosslinking for melt processability and tunable mechanical performance
10.1039/d3ta04351g · ExternalCitation · doi-reference
Unprecedented associative exchange in CO2 -sourced cyclic S , O -acetal-based covalent adaptable networks
10.1039/d4py00359d · ExternalCitation · doi-reference
How to make furfural and HMF production greener? lessons from life cycle assessments
10.1039/d5gc03729h · ExternalCitation · doi-reference
10.1039/d5ta07881d
10.1039/d5ta07881d · ExternalCitation · doi-reference
A thermally re-mendable cross-linked polymeric material
10.1126/science.1065879 · ExternalCitation · doi-reference
Photoinduced plasticity in cross-linked polymers
10.1126/science.1110505 · ExternalCitation · doi-reference
Silica-like malleable materials from permanent organic networks
10.1126/science.1212648 · ExternalCitation · doi-reference
Recyclable, strong thermosets and organogels via paraformaldehyde condensation with diamines
10.1126/science.1251484 · ExternalCitation · doi-reference
Evaluating scenarios toward zero plastic pollution
10.1126/science.aba9475 · ExternalCitation · doi-reference
Exploring the contribution of two phosphorus-based groups to polymer flammability via pyrolysis–combustion flow calorimetry
10.3390/ma12182961 · ExternalCitation · doi-reference
Recent advances in fire-retardant silicone rubber composites
10.3390/polym16172442 · ExternalCitation · doi-reference
