Facile Preparation of a Poly[2]Catenane Network Using Self‐Assembled [2]Catenane Unit

J Jinsa Li (Key Laboratory of Material Chemistry for Energy Conversion and Storage, Ministry of Education Hubei Key Laboratory of Material Chemistry and Service Failure State Key Laboratory of Materials Processing and Die & Mould Technology School of Chemistry and Chemical Engineering Huazhong University of Science and Technology Wuhan People's Republic of China) R Rui Hu Y Yuxin Fu X Xiaohe Zhou (Key Laboratory of Material Chemistry for Energy Conversion and Storage, Ministry of Education Hubei Key Laboratory of Material Chemistry and Service Failure State Key Laboratory of Materials Processing and Die & Mould Technology School of Chemistry and Chemical Engineering Huazhong University of Science and Technology Wuhan People's Republic of China) J Jonathan L. Sessler X Xiaofan Ji (Key Laboratory of Material Chemistry for Energy Conversion and Storage, Ministry of Education Hubei Key Laboratory of Material Chemistry and Service Failure State Key Laboratory of Materials Processing and Die & Mould Technology School of Chemistry and Chemical Engineering Huazhong University of Science and Technology Wuhan People's Republic of China)

Abstract

ABSTRACT Polycatenanes are an emerging class of polymeric materials linked through interlocked rings, possessing a higher degree of conformational freedom and mobility. However, the number of its studies is far lower than that of other dynamic polymers. This may reflect the fact that the preparation of polycatenanes involves the complicated synthesis of a covalent catenation (ring closing) step. Here we report a self‐assembly approach that allows the facile preparation of a poly[2]catenane network with good material properties. First, a clip‐type self‐associated dimer is generated through a spontaneous self‐assembly process driven by hydrogen bonding interactions between two individual isophthaloyl bis(diamine) subunits modified with olefin groups. Next, polymerization via a thiol‐alkene click reaction is used to produce an H‐bond‐based polymer network. Finally, ring closure involving the formation of dynamic imine bonds was used to create a series of poly[2]catenane‐containing networks. The resulting polymer networks not only demonstrated excellent mechanical features and stimuli‐responsiveness but also proved ready degradability. We believe that this work will significantly accelerate the development of polycatenane materials.

Article Details

Volume / Issue Vol. 65, Issue 29
Published July 13, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (6)

J

Jinsa Li

Key Laboratory of Material Chemistry for Energy Conversion and Storage, Ministry of Education Hubei Key Laboratory of Material Chemistry and Service Failure State Key Laboratory of Materials Processing and Die & Mould Technology School of Chemistry and Chemical Engineering Huazhong University of Science and Technology Wuhan People's Republic of China

R

Rui Hu

Y

Yuxin Fu

X

Xiaohe Zhou

Key Laboratory of Material Chemistry for Energy Conversion and Storage, Ministry of Education Hubei Key Laboratory of Material Chemistry and Service Failure State Key Laboratory of Materials Processing and Die & Mould Technology School of Chemistry and Chemical Engineering Huazhong University of Science and Technology Wuhan People's Republic of China

J

Jonathan L. Sessler

X

Xiaofan Ji

Key Laboratory of Material Chemistry for Energy Conversion and Storage, Ministry of Education Hubei Key Laboratory of Material Chemistry and Service Failure State Key Laboratory of Materials Processing and Die & Mould Technology School of Chemistry and Chemical Engineering Huazhong University of Science and Technology Wuhan People's Republic of China