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Self-Assembly of Stimuli-Responsive [2]Rotaxanes by Amidinium Exchange

Oleg BorodinInstitute of Organic Chemistry, Ulm University, Albert-Einstein-Allee 11, 89081 Ulm, GermanyYevhenii ShchukinInstitute of Organic Chemistry, Ulm University, Albert-Einstein-Allee 11, 89081 Ulm, GermanyCraig C. RobertsonDepartment of Chemistry, University of Sheffield, Brook Hill, Sheffield S3 7HF, U.KStefan RichterInstitute of Organic Chemistry, Ulm University, Albert-Einstein-Allee 11, 89081 Ulm, GermanyMax von DeliusInstitute of Organic Chemistry, Ulm University, Albert-Einstein-Allee 11, 89081 Ulm, Germany
2021en
ABI

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Advances in supramolecular chemistry are often underpinned by the development of fundamental building blocks and methods enabling their interconversion. In this work, we report the use of an underexplored dynamic covalent reaction for the synthesis of stimuli-responsive [2]rotaxanes. The formamidinium moiety lies at the heart of these mechanically interlocked architectures, because it enables both dynamic covalent exchange and the binding of simple crown ethers. We demonstrated that the rotaxane self-assembly follows a unique reaction pathway and that the complex interplay between crown ether and thread can be controlled in a transient fashion by addition of base and fuel acid. Dynamic combinatorial libraries, when exposed to diverse nucleophiles, revealed a profound stabilizing effect of the mechanical bond as well as intriguing reactivity differences between seemingly similar [2]rotaxanes.

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