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Rigidity and Flexibility in Rotaxanes and Their Relatives; On Being Stubborn and Easy-Going
Rotaxanes are an emerging class of molecules composed of two building blocks: macrocycles and threads. Rotaxanes, and their pseudorotaxane and polyrotaxane relatives, serve as prototypes for molecular-level switches and machines and as components in materials like elastic polymers and 3D printing in...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9022846/ https://www.ncbi.nlm.nih.gov/pubmed/35464214 http://dx.doi.org/10.3389/fchem.2022.856173 |
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author | Fadler, Rachel E. Flood, Amar H. |
author_facet | Fadler, Rachel E. Flood, Amar H. |
author_sort | Fadler, Rachel E. |
collection | PubMed |
description | Rotaxanes are an emerging class of molecules composed of two building blocks: macrocycles and threads. Rotaxanes, and their pseudorotaxane and polyrotaxane relatives, serve as prototypes for molecular-level switches and machines and as components in materials like elastic polymers and 3D printing inks. The rigidity and flexibility of these molecules is a characteristic feature of their design. However, the mechanical properties of the assembled rotaxane and its components are rarely examined directly, and the translation of these properties from molecules to bulk materials is understudied. In this Review, we consider the mechanical properties of rotaxanes by making use of concepts borrowed from physical organic chemistry. Rigid molecules have fewer accessible conformations with higher energy barriers while flexible molecules have more accessible conformations and lower energy barriers. The macrocycles and threads become rigidified when threaded together as rotaxanes in which the formation of intermolecular interactions and increased steric contacts collectively reduce the conformational space and raise barriers. Conversely, rotational and translational isomerism in rotaxanes adds novel modes of flexibility. We find that rigidification in rotaxanes is almost universal, but novel degrees of flexibility can be introduced. Both have roles to play in the function of rotaxanes. |
format | Online Article Text |
id | pubmed-9022846 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90228462022-04-22 Rigidity and Flexibility in Rotaxanes and Their Relatives; On Being Stubborn and Easy-Going Fadler, Rachel E. Flood, Amar H. Front Chem Chemistry Rotaxanes are an emerging class of molecules composed of two building blocks: macrocycles and threads. Rotaxanes, and their pseudorotaxane and polyrotaxane relatives, serve as prototypes for molecular-level switches and machines and as components in materials like elastic polymers and 3D printing inks. The rigidity and flexibility of these molecules is a characteristic feature of their design. However, the mechanical properties of the assembled rotaxane and its components are rarely examined directly, and the translation of these properties from molecules to bulk materials is understudied. In this Review, we consider the mechanical properties of rotaxanes by making use of concepts borrowed from physical organic chemistry. Rigid molecules have fewer accessible conformations with higher energy barriers while flexible molecules have more accessible conformations and lower energy barriers. The macrocycles and threads become rigidified when threaded together as rotaxanes in which the formation of intermolecular interactions and increased steric contacts collectively reduce the conformational space and raise barriers. Conversely, rotational and translational isomerism in rotaxanes adds novel modes of flexibility. We find that rigidification in rotaxanes is almost universal, but novel degrees of flexibility can be introduced. Both have roles to play in the function of rotaxanes. Frontiers Media S.A. 2022-04-07 /pmc/articles/PMC9022846/ /pubmed/35464214 http://dx.doi.org/10.3389/fchem.2022.856173 Text en Copyright © 2022 Fadler and Flood. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Chemistry Fadler, Rachel E. Flood, Amar H. Rigidity and Flexibility in Rotaxanes and Their Relatives; On Being Stubborn and Easy-Going |
title | Rigidity and Flexibility in Rotaxanes and Their Relatives; On Being Stubborn and Easy-Going |
title_full | Rigidity and Flexibility in Rotaxanes and Their Relatives; On Being Stubborn and Easy-Going |
title_fullStr | Rigidity and Flexibility in Rotaxanes and Their Relatives; On Being Stubborn and Easy-Going |
title_full_unstemmed | Rigidity and Flexibility in Rotaxanes and Their Relatives; On Being Stubborn and Easy-Going |
title_short | Rigidity and Flexibility in Rotaxanes and Their Relatives; On Being Stubborn and Easy-Going |
title_sort | rigidity and flexibility in rotaxanes and their relatives; on being stubborn and easy-going |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9022846/ https://www.ncbi.nlm.nih.gov/pubmed/35464214 http://dx.doi.org/10.3389/fchem.2022.856173 |
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