Depending on the dynamics of the crosslinks, polymer networks can have distinct bulk mechanical behaviors, from viscous liquids to tough solids. Here, by means of designing a crosslink with variable molecular dynamics, we show the control of viscoelasticity of polymer networks in a broad range quantitatively. The hexanoate-isoquinoline@cucurbit[7]uril (HIQ@CB[7]) crosslink exhibits in a combination of protonated and deprotonated states of similar association affinity but distinct molecular dynamics. The molecular property of this crosslink is contributed by linear combination of the parameters at the two states, which is precisely tuned by pH. Using this crosslink, we achieve the quantitative control of viscoelasticity of quasi-ideal networks in 5 orders of magnitude, and we show the reversible control of mechanical response, such as stiffness, strength and extensibility, of tough random polymer networks. This strategy offers a way to tailor the mechanical properties of polymer networks at the molecular level and paves the way for engineering "smart" responsive materials.
Keywords: cucurbituril; self-assembly; supramolecular chemistry; supramolecular networks; viscoelasticity.
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