ArticleProceedings of the National Academy of Sciences of the United States of America2015
Electrochemically addressable trisradical rotaxanes organized within a metal-organic framework.
Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.
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Who cites it
16 citing papers in PubMed.
- Supramolecular Chemistry in Metal-Organic Framework Materials.Advanced materials (Deerfield Beach, Fla.) · 2025Review
- Mesoporous zirconium based metal-organic frameworks, a topological review.RSC advances · 2025Review
- Node Modification of Metal-Organic Frameworks for Catalytic Applications.ChemistryOpen · 2025Review
- The Story of the Little Blue Box: A Tribute to Siegfried Hünig.Angewandte Chemie (International ed. in English) · 2023Review
- Light-responsive rotaxane-based materials: inducing motion in the solid state.Beilstein journal of organic chemistry · 2023Article
- Controlling dynamics in extended molecular frameworks.Nature reviews. Chemistry · 2022Review
- Docking rings in a solid: reversible assembling of pseudorotaxanes inside a zirconium metal-organic framework.Chemical science · 2022Article
- Translational dynamics of a non-degenerate molecular shuttle imbedded in a zirconium metal-organic framework.Chemical science · 2021Article
- Visible-Light-Driven Rotation of Molecular Motors in a Dual-Function Metal-Organic Framework Enabled by Energy Transfer.Journal of the American Chemical Society · 2020Article
- Electrochemically switchable rotaxanes: recent strides in new directions.Chemical science · 2019Review
- Tetrathiafulvalene - a redox-switchable building block to control motion in mechanically interlocked molecules.Beilstein journal of organic chemistry · 2018Review
- Introducing Stable Radicals into Molecular Machines.ACS central science · 2017Review
- Piezochromism and hydrochromism through electron transfer: new stories for viologen materials.Chemical science · 2017Article
- QnAs with Fraser Stoddart.Proceedings of the National Academy of Sciences of the United States of America · 2017Article
- Post-synthetic modification of a macrocyclic receptorChemical science · 2016Article
- Article
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Authors and funding
15 authors.
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Abstract
The organization of trisradical rotaxanes within the channels of a Zr6-based metal-organic framework (NU-1000) has been achieved postsynthetically by solvent-assisted ligand incorporation. Robust Zr(IV)-carboxylate bonds are forged between the Zr clusters of NU-1000 and carboxylic acid groups of rotaxane precursors (semirotaxanes) as part of this building block replacement strategy. Ultraviolet-visible-near-infrared (UV-Vis-NIR), electron paramagnetic resonance (EPR), and 1H nuclear magnetic resonance (NMR) spectroscopies all confirm the capture of redox-active rotaxanes within the mesoscale hexagonal channels of NU-1000. Cyclic voltammetry measurements performed on electroactive thin films of the resulting material indicate that redox-active viologen subunits located on the rotaxane components can be accessed electrochemically in the solid state. In contradistinction to previous methods, this strategy for the incorporation of mechanically interlocked molecules within porous materials circumvents the need for de novo synthesis of a metal-organic framework, making it a particularly convenient approach for the design and creation of solid-state molecular switches and machines. The results presented here provide proof-of-concept for the application of postsynthetic transformations in the integration of dynamic molecular machines with robust porous frameworks.
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