Affiliation:
1. Department of Basic Science Graduate School of Arts and Sciences, The University of Tokyo 3-8-1 Komaba, Meguro-ku 153-8902 Tokyo Japan
2. PRESTO Japan Science and Technology Agency 4-1-8 Honcho 332-0012 Kawaguchi Saitama Japan
Abstract
AbstractCatenanes with multistate switchable properties are promising components for next‐generation molecular machines and supramolecular materials. Herein, we report a ligand‐controlled switching method, a novel method for the multistate switching of catenanes controlled by complexation with added amine ligands. To verify this method, a [3]catenane comprising cyclic porphyrin dimers with a rigid π‐system has been synthesized. Owing to the rigidity, the relative positions among the cyclic components of the [3]catenane can be precisely controlled by complexation with various amine ligands. Moreover, ligand‐controlled multistate switching affects the optical properties of the [3]catenanes: the emission intensity can be tuned by modulating the sizes and coordination numbers of integrated amine ligands. This work shows the utility of using organic ligands for the structural switching of catenanes, and will contribute to the further development of multistate switchable mechanically interlocked molecules.
Funder
Japan Society for the Promotion of Science London
Japan Science and Technology Corporation
Subject
General Chemistry,Catalysis
Cited by
5 articles.
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