Polymers that repair themselves after mechanical damage can significantly improve their durability and safety. A major goal in the field of self-healing materials is to combine robust mechanical and efficient healing properties. Here, we show that incorporation of sacrificial bonds into a self-repairable network dramatically improves the overall mechanical properties. Specifically, we use simple secondary amide side chains to create dynamic energy dissipative hydrogen bonds in a covalently cross-linked polymer network, which can self-heal via olefin cross-metathesis. We envision that this straightforward sacrificial bonding strategy can be employed to improve mechanical properties in a variety of self-healing systems.

Vitrimers are a new class of polymeric materials that simultaneously offer the desired physical properties of thermosets and malleability/reprocessability of thermoplastics. Despite significant progress being made in the field of vitrimers, there exists a critical need for the development of robust dynamic covalent chemistries for the production of strong and thermally stable vitrimers. In this work, we discovered a new silyl ether metathesis reaction and used it for the preparation of vitrimers with exceptional thermal stability. In small-molecule model studies, we observed that silyl ether motifs directly exchange under anhydrous conditions catalyzed by a Brønsted or Lewis acid catalyst. For initial vitrimer demonstration, a commodity polymer, poly­(ethylene-co-vinyl alcohol) (PEOH), was silylated with trimethylsilyl (TMS) groups followed by cross-linking with a bis-silyl ether cross-linker. The resulting thermoset showed exceptional thermal stability while maintaining malleability/reprocessability at elevated temperatures. The vitrimer properties such as recyclability and stress relaxation at various temperatures were carefully investigated. The material was reprocessable at 150 °C while also exhibiting good creep resistance at temperatures below its melting transition (T m). This work demonstrates the silyl ether metathesis reaction as a new, robust dynamic covalent chemistry to introduce plasticity, reprocessability, and recyclability to thermosets.

Tunable mechanical response under dynamic and static loading is desirable for many technological applications. Traditionally, mechanical performance of polymeric materials is controlled by modulating structural (i.e., molecular weight, chain packing, or cross-link density) or temporal parameters (such as kinetics of the exchange of dynamic cross-linkers). Metal–ligand interactions are uniquely suited to control both structural and temporal parameters as the thermodynamics and kinetics of mechanically active cross-linkers can be varied by careful selection of metal without significant synthetic modification of the polymer backbone. Here, we have demonstrated that it is possible to engineer desired mechanical properties in a metallopolymer with a high degree of tunability by simply changing the type and amount of added metal. Specifically, we cross-linked an imidazole-containing brush copolymer system with the divalent cations of zinc, copper, and cobalt. Using rheology and tensile experiments, we have correlated the emergent mechanical properties to the stoichiometric ratio of ligand to metal as well as the coordination number and ligand exchange mechanism of the imidazole–metal cross-links. In contrary to the general view that unbound free ligands are normally regarded as mechanically inactive dangling chains in metallopolymer networks, this study clearly shows that they can play a critical role in stress distribution and chain relaxation. Importantly, this work shows for the first time that it is possible to simultaneously control both the structure of networks and the temporal response of bulk materials using dynamic association of weak and monodentate ligands with transition metals.

Mechanical gradients are often employed in nature to prevent biological materials from damage by creating a smooth transition from strong to weak that dissipates large forces. Synthetic mimics of these natural structures are highly desired to improve distribution of stresses at interfaces and reduce contact deformation in manmade materials. Current synthetic gradient materials commonly suffer from non-continuous transitions, relatively small gradients in mechanical properties, and difficult syntheses. Inspired by the polychaete worm jaw, we report a novel approach to generate stiffness gradients in polymeric materials via incorporation of dynamic monodentate metal-ligand crosslinks. Through spatial control of metal ion content, we created a continuous mechanical gradient that spans over a 200-fold difference in stiffness, approaching the mechanical contrast observed in biological gradient materials.

Mechanical gradients are often employed in nature to prevent biological materials from damage by creating as mooth transition from strong to weak that dissipates large forces.S ynthetic mimics of these natural structures are highly desired to improve distribution of stresses at interfaces and reduce contact deformation in manmade materials.C urrent synthetic gradient materials commonly suffer from non-continuous transitions,r elatively small gradients in mechanical properties,a nd difficult syntheses.I nspired by the polychaete worm jaw,w er eport an ovel approach to generate stiffness gradients in polymeric materials via incorporation of dynamic monodentate metal-ligand crosslinks.Through spatial control of metal ion content, we created ac ontinuous mechanical gradient that spans over a2 00-fold difference in stiffness, approaching the mechanical contrast observed in biological gradient materials.