Rotaxane synthesis exploiting the M( i )/M( iii ) redox couple - Dalton Transactions (RSC Publishing) DOI:10.1039/C7DT02648J
Dynamic Covalently Bonded Rotaxanes Cross‐Linked by Imine Bonds between the Axle and Ring: Inverse Temperature Dependence of Subunit Mobility - Kawai - 2006 - Angewandte Chemie - Wiley Online Library
The application of CuAAC 'click' chemistry to catenane and rotaxane synthesis - Chemical Society Reviews (RSC Publishing) DOI:10.1039/B901974J
Exchange of rings shows off molecular machine's clever trick | Research | Chemistry World
![Controlling co-conformation in a [2]rotaxane molecular shuttle using... | Download Scientific Diagram](https://www.researchgate.net/publication/259770322/figure/fig21/AS:668358999552000@1536360611027/Controlling-co-conformation-in-a-2rotaxane-molecular-shuttle-using-a-changes-in-the.png "Controlling co-conformation in a [2]rotaxane molecular shuttle using... | Download Scientific Diagram")
Controlling co-conformation in a [2]rotaxane molecular shuttle using... | Download Scientific Diagram
Development of Pseudorotaxanes and Rotaxanes: From Synthesis to Stimuli-Responsive Motions to Applications. | Semantic Scholar
![Molecules | Free Full-Text | Calix[6]arene-Based [3]Rotaxanes as Prototypes for the Template Synthesis of Molecular Capsules](https://www.mdpi.com/molecules/molecules-28-00595/article_deploy/html/images/molecules-28-00595-g001.png "Molecules | Free Full-Text | Calix[6]arene-Based [3]Rotaxanes as Prototypes for the Template Synthesis of Molecular Capsules")
Molecules | Free Full-Text | Calix[6]arene-Based [3]Rotaxanes as Prototypes for the Template Synthesis of Molecular Capsules
![Symmetry | Free Full-Text | Template-Free Synthesis of a Phenanthroline-Containing [2]Rotaxane: A Reversible pH-Controllable Molecular Switch](https://www.mdpi.com/symmetry/symmetry-11-01137/article_deploy/html/images/symmetry-11-01137-sch001.png "Symmetry | Free Full-Text | Template-Free Synthesis of a Phenanthroline-Containing [2]Rotaxane: A Reversible pH-Controllable Molecular Switch")
Symmetry | Free Full-Text | Template-Free Synthesis of a Phenanthroline-Containing [2]Rotaxane: A Reversible pH-Controllable Molecular Switch
Rotaxane - an overview | ScienceDirect Topics
![2]Rotaxane End‐Capping Synthesis by Click Michael‐Type Addition to the Vinyl Sulfonyl Group - David - 2019 - Chemistry – A European Journal - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/989863d4-a105-4b25-9425-9d42180fc720/chem201900156-toc-0001-m.png "2]Rotaxane End‐Capping Synthesis by Click Michael‐Type Addition to the Vinyl Sulfonyl Group - David - 2019 - Chemistry – A European Journal - Wiley Online Library")
2]Rotaxane End‐Capping Synthesis by Click Michael‐Type Addition to the Vinyl Sulfonyl Group - David - 2019 - Chemistry – A European Journal - Wiley Online Library
![Mechanically linked supramolecular polymer architectures derived from macromolecular [2]rotaxanes: Synthesis and topology transformation - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0032386117307851-gr5.jpg "Mechanically linked supramolecular polymer architectures derived from macromolecular [2]rotaxanes: Synthesis and topology transformation - ScienceDirect")
Mechanically linked supramolecular polymer architectures derived from macromolecular [2]rotaxanes: Synthesis and topology transformation - ScienceDirect
![Synthesis of triazolium-based mono- and tris-branched [1]rotaxanes using a molecular transporter of dibenzo-24-crown-8 - Chemical Science (RSC Publishing) DOI:10.1039/C5SC01722J](https://pubs.rsc.org/image/article/2015/SC/c5sc01722j/c5sc01722j-f3_hi-res.gif "Synthesis of triazolium-based mono- and tris-branched [1]rotaxanes using a molecular transporter of dibenzo-24-crown-8 - Chemical Science (RSC Publishing) DOI:10.1039/C5SC01722J")
Synthesis of triazolium-based mono- and tris-branched [1]rotaxanes using a molecular transporter of dibenzo-24-crown-8 - Chemical Science (RSC Publishing) DOI:10.1039/C5SC01722J
Switchable Polymer Materials Controlled by Rotaxane Macromolecular Switches. - Abstract - Europe PMC
![A [2]Rotaxane Capped by a Cyclodextrin and a Guest: Formation of Supramolecular [2]Rotaxane Polymer | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/ja042840+/asset/images/medium/ja0428401h00001.gif "A [2]Rotaxane Capped by a Cyclodextrin and a Guest: Formation of Supramolecular [2]Rotaxane Polymer | Journal of the American Chemical Society")
A [2]Rotaxane Capped by a Cyclodextrin and a Guest: Formation of Supramolecular [2]Rotaxane Polymer | Journal of the American Chemical Society
![Chemical templated routes to [1]rotaxanes. | Download Scientific Diagram](https://www.researchgate.net/publication/277603931/figure/fig1/AS:400694726152194@1472544475329/Chemical-templated-routes-to-1rotaxanes_Q640.jpg "Chemical templated routes to [1]rotaxanes. | Download Scientific Diagram")
Chemical templated routes to [1]rotaxanes. | Download Scientific Diagram
![Schematic plan of the synthesis of a [2]catenane (2) and a [2]rotaxane... | Download Scientific Diagram](https://www.researchgate.net/publication/356711517/figure/fig1/AS:1098726189875200@1638968145229/Schematic-plan-of-the-synthesis-of-a-2catenane-2-and-a-2rotaxane-3-from-a-common.png "Schematic plan of the synthesis of a [2]catenane (2) and a [2]rotaxane... | Download Scientific Diagram")
Schematic plan of the synthesis of a [2]catenane (2) and a [2]rotaxane... | Download Scientific Diagram
Rotaxane - Wikipedia
Figure 3 from Discovery and early development of squaraine rotaxanes. | Semantic Scholar
Synthesis of water soluble polyrotaxanes by end-capping polypseudo-rotaxanes of γ-CDs with PHEMA-PPO-PEO-PPO-PHEMA using ATRP of MPC - Polymer Chemistry (RSC Publishing) DOI:10.1039/C5PY00674K
Dr. Frédéric Coutrot - Glycorotaxane - Rotaxane - Publications
![Synthesis of spiro quasi[1]catenanes and quasi[1]rotaxanes via a templated backfolding strategy | Nature Communications](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fncomms15392/MediaObjects/41467_2017_Article_BFncomms15392_Fig1_HTML.jpg "Synthesis of spiro quasi[1]catenanes and quasi[1]rotaxanes via a templated backfolding strategy | Nature Communications")
Synthesis of spiro quasi[1]catenanes and quasi[1]rotaxanes via a templated backfolding strategy | Nature Communications
![Synthesis and characterization of original [2]rotaxanes including cyclodextrin | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs42452-019-0350-6/MediaObjects/42452_2019_350_Sch4_HTML.png "Synthesis and characterization of original [2]rotaxanes including cyclodextrin | SpringerLink")