Synthesis of a Station‐Less Molecular Daisy Chain
A daisy chain architecture without a preferred low energy arrangement of the mechanically linked components is presented. The molecular design combines a rigid-rod type oligophenylene ethynylene subunit with an oligoethylene glycol macrocycle that features a bipyridine coordination site. The daisy chain dimer was synthesized via kinetic trapping of the interlocked structure using a Cadiot-Chodkiewicz active metal template reaction. Comparison of the isolated interlocked dimer with its monomeric analogue indicates the presence of a variety of different geometries for the molecular daisy chain. The dynamic sliding motion in the daisy chain is studied by variable temperature UV-vis and nuclear magnetic resonance (NMR) spectroscopy experiments, which point to a highly mobile system even at low temperatures.
Authors
- Marcel Mayor (ORCID: https://orcid.org/0000-0002-8094-7813)
- David A. Leigh (ORCID: https://orcid.org/0000-0002-1202-4507)
- Daniel Häußinger (ORCID: https://orcid.org/0000-0002-4798-0072)
- Charlotte Kress (ORCID: https://orcid.org/0000-0002-6683-787X)
Institutions
- Karlsruhe Institute of Technology (DE)
- Sun Yat-sen University (CN)
- University of Basel (CH)
- University of Manchester (GB)
- Institute of Nanotechnology (GB)
- East China Normal University (CN)
Publication Details
- Journal
- Chemistry - A European Journal
- Published
- 2025-04-29
- DOI
- https://doi.org/10.1002/chem.202501369
- Primary Topic
- Supramolecular Chemistry and Complexes
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Science Foundation
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
- Higher Education Discipline Innovation Project