Infinite Twisted Polycatenanes

Author:

Liu Jiali12ORCID,Wu Mengqi2ORCID,Wu Lin2ORCID,Liang Yimin2ORCID,Tang Zheng‐Bin2ORCID,Jiang Liang2ORCID,Bian Lifang2ORCID,Liang Kejiang2ORCID,Zheng Xiaorui2ORCID,Liu Zhichang2ORCID

Affiliation:

1. Department of Chemistry Zhejiang University Zhejiang University Hangzhou Zhejiang 310027 China

2. Key Laboratory of Precise Synthesis of Functional Molecules of Zhejiang Province Department of Chemistry School of Science, School of Engineering, and Research Center for Industries of the Future Westlake University Westlake Institute for Advanced Study 600 Dunyu Road Hangzhou Zhejiang 310030 China

Abstract

AbstractPoly[n]catenanes have exceptional mechanical bonding properties that give them tremendous potential for use in the development of molecular machines and soft materials. Synthesizing these compounds has, however, proven to be a formidable challenge. Herein, we describe a concise method for the construction of twisted polycatenanes. Our approach involves using preorganized double helicates as templates, linked crosswise in a linear fashion by either silver ions or triple bonds. By using this approach, we successfully synthesized twisted polycatenanes with both coordination and covalent bonding employing Ag(I) ions and ethynylene units, respectively, as the linkages and leveraging the same Ag(I)‐templated double helicate in both cases. Synthesis with Ag(I) ions formed a single‐crystalline one‐dimensional (1D) coordination poly[n]catenane, and synthesis using ethynylene units generated 1D fibers which self‐assembled with solvents to form a gel. Our results confirm the potential of multi‐stranded metallohelicates for creating sophisticated mechanically interlocked molecules and polymers, which could pave the way for exploration in the realms of molecular nanotopology and materials design.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Zhejiang Province

Publisher

Wiley

Subject

General Medicine

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