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Carbon Origami via an Alumina‐Assisted Cyclodehydrofluorination Strategy
The synthesis of pristine non‐planar nanographenes (NGs) via a cyclodehydrofluorination strategy is reported and the creation of highly strained systems via alumina‐assisted C−F bond activation is shown. Steric hindrance could execute an alternative coupling program leading to rare octagon formation...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8048823/ https://www.ncbi.nlm.nih.gov/pubmed/32871018 http://dx.doi.org/10.1002/chem.202003448 |
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author | Steiner, Ann‐Kristin Sharapa, Dmitry I. Troyanov, Sergey I. Nuss, Jürgen Amsharov, Konstantin |
author_facet | Steiner, Ann‐Kristin Sharapa, Dmitry I. Troyanov, Sergey I. Nuss, Jürgen Amsharov, Konstantin |
author_sort | Steiner, Ann‐Kristin |
collection | PubMed |
description | The synthesis of pristine non‐planar nanographenes (NGs) via a cyclodehydrofluorination strategy is reported and the creation of highly strained systems via alumina‐assisted C−F bond activation is shown. Steric hindrance could execute an alternative coupling program leading to rare octagon formation offering access to elusive non‐classical NGs. The combination of two alternative ways of folding could lead to the formation of various 3D NG objects, resembling the Japanese art of origami. The power of the presented “origami” approach is proved by the assembly of 12 challenging nanographenes that are π‐isoelectronic to planar hexabenzocoronene but forced out of planarity. |
format | Online Article Text |
id | pubmed-8048823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80488232021-04-20 Carbon Origami via an Alumina‐Assisted Cyclodehydrofluorination Strategy Steiner, Ann‐Kristin Sharapa, Dmitry I. Troyanov, Sergey I. Nuss, Jürgen Amsharov, Konstantin Chemistry Full Papers The synthesis of pristine non‐planar nanographenes (NGs) via a cyclodehydrofluorination strategy is reported and the creation of highly strained systems via alumina‐assisted C−F bond activation is shown. Steric hindrance could execute an alternative coupling program leading to rare octagon formation offering access to elusive non‐classical NGs. The combination of two alternative ways of folding could lead to the formation of various 3D NG objects, resembling the Japanese art of origami. The power of the presented “origami” approach is proved by the assembly of 12 challenging nanographenes that are π‐isoelectronic to planar hexabenzocoronene but forced out of planarity. John Wiley and Sons Inc. 2021-03-23 2021-04-07 /pmc/articles/PMC8048823/ /pubmed/32871018 http://dx.doi.org/10.1002/chem.202003448 Text en © 2020 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Full Papers Steiner, Ann‐Kristin Sharapa, Dmitry I. Troyanov, Sergey I. Nuss, Jürgen Amsharov, Konstantin Carbon Origami via an Alumina‐Assisted Cyclodehydrofluorination Strategy |
title | Carbon Origami via an Alumina‐Assisted Cyclodehydrofluorination Strategy |
title_full | Carbon Origami via an Alumina‐Assisted Cyclodehydrofluorination Strategy |
title_fullStr | Carbon Origami via an Alumina‐Assisted Cyclodehydrofluorination Strategy |
title_full_unstemmed | Carbon Origami via an Alumina‐Assisted Cyclodehydrofluorination Strategy |
title_short | Carbon Origami via an Alumina‐Assisted Cyclodehydrofluorination Strategy |
title_sort | carbon origami via an alumina‐assisted cyclodehydrofluorination strategy |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8048823/ https://www.ncbi.nlm.nih.gov/pubmed/32871018 http://dx.doi.org/10.1002/chem.202003448 |
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