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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...

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Detalles Bibliográficos
Autores principales: Steiner, Ann‐Kristin, Sharapa, Dmitry I., Troyanov, Sergey I., Nuss, Jürgen, Amsharov, Konstantin
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/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.
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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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