ui Weng

Multi-responsive self-healing metallo-supramolecular gels based on 'click' ligand

Metallo-supramolecular gels were prepared using a ligand macromolecule containing the tridentate 2,6-bis(1,2,3-trizol-4-yl)pyridine (BTP) ligand unit synthesized via CuAAC “click” chemistry in the main chain, together with transition metal ions and/or lanthanide ions. The gelation and gel properties, e.g. swelling, emission, rheological properties, thermo- and chemo-responsive properties, can be tuned by the careful selection of metal ions and their combinations, solvents, concentration, etc. Most interestingly, the gels exhibited repeatable autonomic healing ability. Moreover, the repeatable self-healing ability of the gels found practical application in the repairing of metal coatings.

Mechanochromism and Mechanical‐Force‐Triggered Cross‐Linking from a Single Reactive Moiety Incorporated into Polymer Chains

Incorporation of small reactive moieties, the reactivity of which depends on externally imposed load (so-called mechanophores) into polymer chains offers access to a broad range of stress-responsive materials. Here, we report that polymers incorporating spirothiopyran (STP) manifest both green mechanochromism and load-induced addition reactions in solution and solid. Stretching a macromolecule containing colorless STP converts it into green thiomerocyanine (TMC), the mechanically activated thiolate moiety of which undergoes rapid thiol-ene click reactions with certain reactive C=C bonds to form a graft or a cross-link. The unique dual mechanochemical response of STP makes it of potentially great utility both for the design of new stress-responsive materials and for fundamental studies in polymer physics, for example, the dynamics of physical and mechanochemical remodeling of loaded materials.

Self-healing metallo-supramolecular polymers from a ligand macromolecule synthesized via copper-catalyzed azide–alkyne cycloaddition and thiol–ene double “click” reactions

In this study, we develop a series of new materials that can simultaneously and reversibly self-heal without external stimuli based on metallo-supramolecular interactions. Multiple tridentate 2,6-bis(1,2,3-trizaol-4-yl)pyridine (BTP) ligand units synthesized via a copper-catalyzed azide–alkyne cycloaddition (CuAAC) “click” reaction are incorporated into the polymer backbone of a ligand macromolecule through a thiol–ene “click” reaction. 3D transient supramolecular networks are formed from the ligand macromolecule upon coordination with transition and/or lanthanide metal ions. As compared to the ligand macromolecule, the resultant supramolecular films exhibit improved mechanical properties, such as Youngs modulus, strength and toughness, which can be readily tuned by the stoichiometric ratio of Zn2+ to Eu3+ to Tb3+. The supramolecular films exhibit characteristics of weakly crosslinked networks where the storage modulus G′ and loss modulus G′′ scaled with normalized frequency ωaT by the same slope of 0.5. Both the supramolecular bulk films and gels are found to exhibit fast and effective self-healing properties by virtue of the kinetically labile nature of the metal–ligand interactions.

Using metal-ligand interactions to access biomimetic supramolecular polymers with adaptive and superb mechanical properties

The development of polymer materials that exhibit excellent mechanical properties and can respond to environmental stimuli is of great scientific and commercial interest. In this work, we report a series of biomimetic supramolecular polymers using a ligand macromolecule carrying multiple tridentate ligand 2,6-bis(1,2,3-triazol-4-yl)pyridine (BTP) units synthesized via CuAAC in the polymer backbone together with transition and/or lanthanide metal salts. The metal-ligand complexes phase separate from soft linker segments, acting as physical crosslinking points in the materials. The metallo-supramolecular films exhibit superb mechanical properties, i.e., high tensile strength (up to 18 MPa), large strain at break (>1000%) and exceptionally high toughness (up to 70 MPa), which are much higher than those of the ligand macromolecule and are tunable by adjusting the stoichiometric ratio of Zn2+ to Eu3+ and the stoichiometry of metal ion to ligand. The metal-ligand hard phase domains are demonstrated to be thermally stable but mechanically labile, similar to the behaviors of covalent mechanophores. The thermal stability and mechanical responsiveness are also dependent on the compositions of metal ions. The disruption of the hard phase domains and the dissociation of metal-ligand complexes under stretching are similar to the unfolding of modular domains in modular biomacromolecules and are responsible for the superb mechanical properties. In addition, the biomimetic metallo-supramolecular materials display promising responsive properties to UV irradiation and chemicals. These well designed, created and characterized robust structures will inspire further accurate tailoring of biomimetic responsive materials at the molecular level and/or nanoscale.

Multi-modal mechanophores based on cinnamate dimers

Mechanochemistry offers exciting opportunities for molecular-level engineering of stress-responsive properties of polymers. Reactive sites, sometimes called mechanophores, have been reported to increase the material toughness, to make the material mechanochromic or optically healable. Here we show that macrocyclic cinnamate dimers combine these productive stress-responsive modes. The highly thermally stable dimers dissociate on the sub-second timescale when subject to a stretching force of 1–2 nN (depending on isomer). Stretching a polymer of the dimers above this force more than doubles its contour length and increases the strain energy that the chain absorbs before fragmenting by at least 600 kcal per mole of monomer. The dissociation produces a chromophore and dimers are reformed upon irradiation, thus allowing optical healing of mechanically degraded parts of the material. The mechanochemical kinetics, single-chain extensibility, toughness and potentially optical properties of the dissociation products are tunable by synthetic modifications.Mechanochemistry offers exciting opportunities for molecular engineering of stress-responsive properties of polymers. Here the authors show that macrocyclic cinnamate dimers in a polymer chain can undergo dissociation on the sub-second timescale under 1–2 nN stretching to yield a chromophore that then can be optically healed.