Directional Ring Translocation in a pH‐ and Redox‐Driven Tristable [2]Rotaxane
We describe the synthesis and characterization of a [2]rotaxane comprising a dibenzo-24-crown-8 (DB24C8) macrocyclic component and a thread containing three recognition sites: ammonium (AmH<sup>+</sup>), bipyridinium (Bpy<sup>2+</sup>) and triazolium (Trz<sup>+</sup>). AmH<sup>+</sup> and Bpy<sup>2+</sup> are responsive to fully orthogonal stimuli, pH and electrochemical, which allows to precisely control the directional translation of the macrocycle along the axle. A better understanding of the processes driving the operation of the system was obtained thanks to an in-depth thermodynamic characterization. Orthogonal stimuli responsive tristable rotaxanes represent the starting point for the creation of linear motors and the development of molecular logic gates.
Authors
- Özlem Seven (ORCID: https://orcid.org/0000-0002-6993-0711)
- Serena Silvi (ORCID: https://orcid.org/0000-0001-9273-4148)
- Leonardo Andreoni (ORCID: https://orcid.org/0000-0001-6027-0326)
- Jessica Groppi (ORCID: https://orcid.org/0000-0003-0307-9781)
- Massimo Baroncini (ORCID: https://orcid.org/0000-0002-8112-8916)
- Alberto Credi
Institutions
- Institute of Nanostructured Materials (IT)
- Institute of Organic Synthesis and Photoreactivity (IT)
- University of Bologna (IT)
Publication Details
- Journal
- Angewandte Chemie International Edition
- Published
- 2024-09-20
- DOI
- https://doi.org/10.1002/anie.202414609
- Citations
- 7
- Primary Topic
- Supramolecular Chemistry and Complexes
- Type
- article
- Field-Weighted Citation Impact
- 1.75
Funders
- European Commission