Multivalency in healable supramolecular polymers: the effect of supramolecular cross-link density on the mechanical properties and healing of non-covalent polymer networksElectronic supplementary information (ESI) available. See DOI: 10.1039/c4py00292j

Polymers with the ability to heal themselves could provide access to materials with extended lifetimes in a wide range of applications such as surface coatings, automotive components and aerospace composites. Here we describe the synthesis and characterisation of two novel, stimuli-responsive, supra...

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Hauptverfasser: Hart, Lewis R, Hunter, James H, Nguyen, Ngoc A, Harries, Josephine L, Greenland, Barnaby W, Mackay, Michael E, Colquhoun, Howard M, Hayes, Wayne
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Sprache:eng
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Zusammenfassung:Polymers with the ability to heal themselves could provide access to materials with extended lifetimes in a wide range of applications such as surface coatings, automotive components and aerospace composites. Here we describe the synthesis and characterisation of two novel, stimuli-responsive, supramolecular polymer blends based on π-electron-rich pyrenyl residues and π-electron-deficient, chain-folding aromatic diimides that interact through complementary π-π stacking interactions. Different degrees of supramolecular "cross-linking" were achieved by use of divalent or trivalent poly(ethylene glycol)-based polymers featuring pyrenyl end-groups, blended with a known diimide-ether copolymer. The mechanical properties of the resulting polymer blends revealed that higher degrees of supramolecular "cross-link density" yield materials with enhanced mechanical properties, such as increased tensile modulus, modulus of toughness, elasticity and yield point. After a number of break/heal cycles, these materials were found to retain the characteristics of the pristine polymer blend, and this new approach thus offers a simple route to mechanically robust yet healable materials. Mechanical properties of healable supramolecular polymer blends correlate to non-covalent "crosslink density".
ISSN:1759-9954
1759-9962
DOI:10.1039/c4py00292j