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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...

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Detalles Bibliográficos
Autores principales: Khan, Md. Nasim, Wirth, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
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
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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.
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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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