Construction of Slide-Ring Polymers Based on Pillar[5]Arene/Alkyl Chain Host−Guest Interactions

Abstract

Slide-ring polymers exhibit distinctive mechanical properties, making them highly promising for applications in emerging fields such as energy storage devices and smart sensing. However, existing slide-ring polymer systems primarily rely on hydrophilic-hydrophobic interactions to achieve ring-axle interlocking in aqueous phases. This reliance limits the construction of slide-ring networks mainly to water-soluble polymers, excluding a diverse range of lipophilic polymers. Therefore, it is crucial to introduce efficient construction strategies that facilitate interpenetration in organic solvents, enabling the development of diverse slide-ring polymers and expanding their range and applications. Herein, by utilizing the pillar[5]arene/alkyl chain host−guest interactions, we successfully facilitated the interpenetration of a pillar[5]arene and poly(caprolactone), enabling the efficient construction of two slide-ring polymer networks in organic solvents. One of these two slide-ring polymers demonstrates a unique network deformation mechanism along with outstanding mechanical properties compared with the control covalently cross-linked polymer network, including maximum stress (4.43 vs 1.98 MPa), maximum strain (1285 vs 330 %), and toughness (35.4 vs 3.92 MJ/m³). More importantly, this strategy of making slide-ring polymers is highly versatile, given the wide range of macrocyclic arenes and alkyl chain-containing polymers it can accommodate.