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Chiral Triptycenes in Supramolecular and Materials Chemistry

Triptycenes are an intriguing class of organic molecules with several unusual characteristics, such as a propeller‐like shape, saddle‐like cavities around a symmetrical scaffold, a rigid π‐framework. They have been extensively studied and proposed as key synthons for a variety of applications in sup...

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Detalles Bibliográficos
Autores principales: Preda, Giovanni, Nitti, Andrea, Pasini, Dario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7290281/
https://www.ncbi.nlm.nih.gov/pubmed/32547902
http://dx.doi.org/10.1002/open.202000077
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author Preda, Giovanni
Nitti, Andrea
Pasini, Dario
author_facet Preda, Giovanni
Nitti, Andrea
Pasini, Dario
author_sort Preda, Giovanni
collection PubMed
description Triptycenes are an intriguing class of organic molecules with several unusual characteristics, such as a propeller‐like shape, saddle‐like cavities around a symmetrical scaffold, a rigid π‐framework. They have been extensively studied and proposed as key synthons for a variety of applications in supramolecular chemistry and materials science. When decorated with an appropriate substitution pattern, triptycenes can be chiral, and, similarly to other popular chiral π‐extended synthons, can express chirality robustly, efficiently, and with relevance to chiroptical spectroscopies. This minireview highlights and encompasses recent advances in the synthesis of chiral triptycenes and in their introduction as molecular scaffolds for the assembly of functional supramolecular materials.
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spelling pubmed-72902812020-06-15 Chiral Triptycenes in Supramolecular and Materials Chemistry Preda, Giovanni Nitti, Andrea Pasini, Dario ChemistryOpen Minireviews Triptycenes are an intriguing class of organic molecules with several unusual characteristics, such as a propeller‐like shape, saddle‐like cavities around a symmetrical scaffold, a rigid π‐framework. They have been extensively studied and proposed as key synthons for a variety of applications in supramolecular chemistry and materials science. When decorated with an appropriate substitution pattern, triptycenes can be chiral, and, similarly to other popular chiral π‐extended synthons, can express chirality robustly, efficiently, and with relevance to chiroptical spectroscopies. This minireview highlights and encompasses recent advances in the synthesis of chiral triptycenes and in their introduction as molecular scaffolds for the assembly of functional supramolecular materials. John Wiley and Sons Inc. 2020-06-12 /pmc/articles/PMC7290281/ /pubmed/32547902 http://dx.doi.org/10.1002/open.202000077 Text en © 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Minireviews
Preda, Giovanni
Nitti, Andrea
Pasini, Dario
Chiral Triptycenes in Supramolecular and Materials Chemistry
title Chiral Triptycenes in Supramolecular and Materials Chemistry
title_full Chiral Triptycenes in Supramolecular and Materials Chemistry
title_fullStr Chiral Triptycenes in Supramolecular and Materials Chemistry
title_full_unstemmed Chiral Triptycenes in Supramolecular and Materials Chemistry
title_short Chiral Triptycenes in Supramolecular and Materials Chemistry
title_sort chiral triptycenes in supramolecular and materials chemistry
topic Minireviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7290281/
https://www.ncbi.nlm.nih.gov/pubmed/32547902
http://dx.doi.org/10.1002/open.202000077
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