Journal of the American Chemical Society · 2019 · 219 citations · 38 references
Natural SciencesChemistryMaterials ScienceMaterials ChemistryPolymer ChemistryPolymer MaterialsPolymer CharacterizationPolymer Phase BehaviorPolymer PhysicsPolymer ProcessingPolymerization ChemistrySelf-healing MaterialsCopolymerizationGlass TransitionSelf-healing Polymer MaterialsSelf-healing PolymersShape Memory EffectsShape-memory Polymers
Self-healing materials are of fundamental interest and practical importance. Herein we report the synthesis of a new class of self-healing materials, formed by the copolymerization of ethylene and anisyl-substituted propylenes using a sterically demanding half-sandwich scandium catalyst. The copolymerization proceeded in a controlled fashion, affording unique multi-block copolymers composed of relatively long alternating ethylene-alt-anisylpropylene sequences and short ethylene–ethylene units. By controlling the molecular weight and varying the anisyl substituents, a series of copolymers that show a wide range of glass-transition temperatures (Tg) and mechanical properties have been obtained. The copolymers with Tg below room temperature showed high elastic modulus, high toughness, and remarkable self-healability, being able to autonomously self-heal upon mechanical damage not only in a dry environment but also in water and aqueous acid and alkaline solutions, while those with Tg around or above room temperature exhibited excellent shape-memory property. The unique mechanical properties may be ascribed to the phase separation of the crystalline ethylene–ethylene nanodomains from the ethylene-alt-anisylpropylene matrix.
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