Early View e202511493
Research Article

Mechanically Tunable Slide-Ring Polymers via Photo-Regulated Topological Control

Xiaoqing Wang

Xiaoqing Wang

Stoddart Institute of Molecular Science, Department of Chemistry, Zhejiang University, Hangzhou, 310058 China

Zhejiang-Israel Joint Laboratory of Self-Assembling Functional Materials, ZJU-Hangzhou Global Scientific and Technological Innovation Center, Zhejiang University, Hangzhou, 310058 China

Both authors contributed equally to this work.

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Chenjuan Yu

Chenjuan Yu

Stoddart Institute of Molecular Science, Department of Chemistry, Zhejiang University, Hangzhou, 310058 China

Both authors contributed equally to this work.

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Maolin Wang

Maolin Wang

Stoddart Institute of Molecular Science, Department of Chemistry, Zhejiang University, Hangzhou, 310058 China

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Shiyu Zhao

Shiyu Zhao

Stoddart Institute of Molecular Science, Department of Chemistry, Zhejiang University, Hangzhou, 310058 China

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Qimo Mao

Qimo Mao

Stoddart Institute of Molecular Science, Department of Chemistry, Zhejiang University, Hangzhou, 310058 China

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Prof. Yuping Wang

Corresponding Author

Prof. Yuping Wang

Stoddart Institute of Molecular Science, Department of Chemistry, Zhejiang University, Hangzhou, 310058 China

Zhejiang-Israel Joint Laboratory of Self-Assembling Functional Materials, ZJU-Hangzhou Global Scientific and Technological Innovation Center, Zhejiang University, Hangzhou, 310058 China

State Key Laboratory of Polymer Materials Engineering, Sichuan University, Chengdu, 610065 China

E-mail: [email protected]

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First published: 02 July 2025

Graphical Abstract

We developed light-responsive slide-ring polymer networks whose mechanical properties can be tuned through photoisomerization of the incorporated azobenzene units. The trans-state permits unhindered macrocycle sliding, yielding ductile materials, while UV-induced cis-configuration restricts macrocycle mobility to double Young's modulus. Furthermore, the azobenzene linkage confers controlled degradability under mild conditions.

Abstract

Post-synthetic dynamic control of polymer topology to modulate material properties on demand remains a grand challenge in polymer science. Here, we demonstrate a light-responsive slide-ring polymer network whose mechanical properties can be tuned through photoisomerization of incorporated azobenzene units. In the trans-state, azobenzene enables unhindered sliding of macrocycles along the polymer backbone, yielding a softer, more ductile material. UV-induced switching to the sterically demanding cis-configuration restricts ring mobility, thereby increasing the Young's modulus by two-fold while reducing toughness. Control experiments with noninterlocked analogs revealed the opposite mechanical response—light-induced softening—highlighting the pivotal role of topology in property regulation. Furthermore, the azobenzene linkage confers controlled degradability under mild conditions. This work establishes a versatile strategy for post-synthetic topological control via molecular photoswitches, enabling the design of adaptive polymers with stimuli-responsive mechanical properties for applications in smart materials.

Conflict of Interests

The authors declare no conflict of interest.

Data Availability Statement

The data that support the findings of this study are available in the Supporting Information of this article.

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