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Chiral Triptycenes: Concepts, Progress and Prospects
Triptycenes have been established as unique scaffolds because of their backbone π‐structure with a propeller‐like shape and saddle‐like cavities. They are some of the key organic molecules that have been extensively studied in polymer chemistry, in supramolecular chemistry and in material science. T...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8248085/ https://www.ncbi.nlm.nih.gov/pubmed/33433031 http://dx.doi.org/10.1002/chem.202005317 |
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author | Khan, Md. Nasim Wirth, Thomas |
author_facet | Khan, Md. Nasim Wirth, Thomas |
author_sort | Khan, Md. Nasim |
collection | PubMed |
description | Triptycenes have been established as unique scaffolds because of their backbone π‐structure with a propeller‐like shape and saddle‐like cavities. They are some of the key organic molecules that have been extensively studied in polymer chemistry, in supramolecular chemistry and in material science. Triptycenes become chiral molecules when substituents are unsymmetrically attached in at least two of their different aromatic rings. This Minireview highlights the chirality of triptycenes from basics to an advanced stage for the development of functional molecules. |
format | Online Article Text |
id | pubmed-8248085 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82480852021-07-02 Chiral Triptycenes: Concepts, Progress and Prospects Khan, Md. Nasim Wirth, Thomas Chemistry Minireviews Triptycenes have been established as unique scaffolds because of their backbone π‐structure with a propeller‐like shape and saddle‐like cavities. They are some of the key organic molecules that have been extensively studied in polymer chemistry, in supramolecular chemistry and in material science. Triptycenes become chiral molecules when substituents are unsymmetrically attached in at least two of their different aromatic rings. This Minireview highlights the chirality of triptycenes from basics to an advanced stage for the development of functional molecules. John Wiley and Sons Inc. 2021-02-26 2021-04-26 /pmc/articles/PMC8248085/ /pubmed/33433031 http://dx.doi.org/10.1002/chem.202005317 Text en © 2021 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Minireviews Khan, Md. Nasim Wirth, Thomas Chiral Triptycenes: Concepts, Progress and Prospects |
title | Chiral Triptycenes: Concepts, Progress and Prospects |
title_full | Chiral Triptycenes: Concepts, Progress and Prospects |
title_fullStr | Chiral Triptycenes: Concepts, Progress and Prospects |
title_full_unstemmed | Chiral Triptycenes: Concepts, Progress and Prospects |
title_short | Chiral Triptycenes: Concepts, Progress and Prospects |
title_sort | chiral triptycenes: concepts, progress and prospects |
topic | Minireviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8248085/ https://www.ncbi.nlm.nih.gov/pubmed/33433031 http://dx.doi.org/10.1002/chem.202005317 |
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