Sougata Datta
Self-assembled poly-catenanes from supramolecular toroidal building blocks
Datta, Sougata; Kato, Yasuki; Higashiharaguchi, Seiya; Aratsu, Keisuke; Isobe, Atsushi; Saito, Takuho; Prabhu, Deepak D.; Kitamoto, Yuichi; Hollamby, Martin J.; Smith, Andrew J.; Dalgliesh, Robert; Mahmoudi, Najet; Pesce, Luca; Perego, Claudio; Pavan, Giovanni M.; Yagai, Shiki
Authors
Yasuki Kato
Seiya Higashiharaguchi
Keisuke Aratsu
Atsushi Isobe
Takuho Saito
Deepak D. Prabhu
Yuichi Kitamoto
Martin Hollamby m.hollamby@keele.ac.uk
Andrew J. Smith
Robert Dalgliesh
Najet Mahmoudi
Luca Pesce
Claudio Perego
Giovanni M. Pavan
Shiki Yagai
Abstract
Mechanical interlocking of molecules (catenation) is a nontrivial challenge in modern synthetic chemistry and materials science1,2. One strategy to achieve catenation is the design of pre-annular molecules that are capable of both efficient cyclization and of pre-organizing another precursor to engage in subsequent interlocking3,4,5,6,7,8,9. This task is particularly difficult when the annular target is composed of a large ensemble of molecules, that is, when it is a supramolecular assembly. However, the construction of such unprecedented assemblies would enable the visualization of nontrivial nanotopologies through microscopy techniques, which would not only satisfy academic curiosity but also pave the way to the development of materials with nanotopology-derived properties. Here we report the synthesis of such a nanotopology using fibrous supramolecular assemblies with intrinsic curvature. Using a solvent-mixing strategy, we kinetically organized a molecule that can elongate into toroids with a radius of about 13 nanometres. Atomic force microscopy on the resulting nanoscale toroids revealed a high percentage of catenation, which is sufficient to yield ‘nanolympiadane’10, a nanoscale catenane composed of five interlocked toroids. Spectroscopic and theoretical studies suggested that this unusually high degree of catenation stems from the secondary nucleation of the precursor molecules around the toroids. By modifying the self-assembly protocol to promote ring closure and secondary nucleation, a maximum catenation number of 22 was confirmed by atomic force microscopy.
Citation
Datta, S., Kato, Y., Higashiharaguchi, S., Aratsu, K., Isobe, A., Saito, T., …Yagai, S. (2020). Self-assembled poly-catenanes from supramolecular toroidal building blocks. Nature, 583, 400 - 405. https://doi.org/10.1038/s41586-020-2445-z
Journal Article Type | Article |
---|---|
Acceptance Date | May 19, 2020 |
Publication Date | Jul 15, 2020 |
Journal | Nature |
Print ISSN | 0028-0836 |
Publisher | Nature Publishing Group |
Peer Reviewed | Peer Reviewed |
Volume | 583 |
Pages | 400 - 405 |
DOI | https://doi.org/10.1038/s41586-020-2445-z |
Keywords | Interlocked molecules; Supramolecular polymers |
Publisher URL | https://www.nature.com/articles/s41586-020-2445-z |
Files
370066_1_art_file_3417960_q989lr(1).pdf
(1.8 Mb)
PDF
Publisher Licence URL
https://creativecommons.org/licenses/by-nc/4.0/
You might also like
Diarylethene-Powered Light-Induced Folding of Supramolecular Polymers.
(2021)
Journal Article
Laboratory Safety for Undergraduate Chemistry Students
(2020)
Book Chapter
Developing the Scientific Reporting Skills of Chemistry Students
(2020)
Book Chapter
Downloadable Citations
About Keele Repository
Administrator e-mail: research.openaccess@keele.ac.uk
This application uses the following open-source libraries:
SheetJS Community Edition
Apache License Version 2.0 (http://www.apache.org/licenses/)
PDF.js
Apache License Version 2.0 (http://www.apache.org/licenses/)
Font Awesome
SIL OFL 1.1 (http://scripts.sil.org/OFL)
MIT License (http://opensource.org/licenses/mit-license.html)
CC BY 3.0 ( http://creativecommons.org/licenses/by/3.0/)
Powered by Worktribe © 2024
Advanced Search