ArticleMacromolecules2023
Benzene Tetraamide: A Covalent Supramolecular Dual Motif in Dynamic Covalent Polymer Networks.
Article in Macromolecules, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
What it found
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Who cites it
6 citing papers in PubMed.
- A Practical User Guide to Stress Relaxation Spectra of Dynamic Covalent Networks.ACS polymers Au · 2026Article
- Low-Viscosity, Dynamic Amidoamine Hardeners with Tunable Curing Kinetics for Epoxy Adhesives.Macromolecules · 2025Article
- Engineering Supramolecular Hydrogen Bonding Interactions into Dynamic Covalent Polymers To Obtain Double Dynamic Biomaterials.Journal of the American Chemical Society · 2025Article
- Structure-property relationships to direct the dynamic properties of acylsemicarbazide-based materials.Polymer chemistry · 2025Article
- Supramolecular Polymer Additives as Repairable Reinforcements for Dynamic Covalent Networks.Advanced materials (Deerfield Beach, Fla.) · 2024Article
- Internal catalysis significantly promotes the bond exchange of covalent adaptable polyurethane networks.Proceedings of the National Academy of Sciences of the United States of America · 2024Article
Corrections and comments
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Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
In dynamic polyamide networks, 1,2,4,5-benzene tetraamide (B4A) units act simultaneously as a dynamic covalent cross-linker and as supramolecular stacking motif. This results in materials with a rubbery plateau modulus that is about 20 times higher than that of a corresponding reference network in which the supramolecular interaction is suppressed. In branched polyamides with the same B4A dynamic motif, hydrogen bonding and stacking lead to strong and reversible supramolecular networks, whereas a branched polyamide with the nonstacking reference linker is a viscous liquid under the same conditions. Wide-angle X-ray scattering and variable-temperature infrared experiments confirm that covalent cross-linking and stacking cooperatively contribute to the dynamics of the network. Stress relaxation in the reference network is dominated by a single mode related to the dynamic covalent chemistry, whereas relaxation in the B4A network has additional modes assigned to the stacking dynamics.
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Registered trials
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