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An Isosteric Triaza Analogue of a Polycyclic Aromatic Hydrocarbon Monkey Saddle
Since a few years, the interest in negatively‐curved fused polycyclic aromatic hydrocarbons (PAHs) has significantly increased. Recently, the first chiral negatively‐curved PAH with the topology of a monkey saddle was introduced. Herein the synthesis of its triaza congener is reported. The influence...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756504/ https://www.ncbi.nlm.nih.gov/pubmed/32539193 http://dx.doi.org/10.1002/chem.202002826 |
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author | Kirschbaum, Tobias Rominger, Frank Mastalerz, Michael |
author_facet | Kirschbaum, Tobias Rominger, Frank Mastalerz, Michael |
author_sort | Kirschbaum, Tobias |
collection | PubMed |
description | Since a few years, the interest in negatively‐curved fused polycyclic aromatic hydrocarbons (PAHs) has significantly increased. Recently, the first chiral negatively‐curved PAH with the topology of a monkey saddle was introduced. Herein the synthesis of its triaza congener is reported. The influence of this CH↔N exchange on photophysical and electrochemical properties is studied as well as the isomerization process of the enantiomers. The aza analogue has a significantly higher inversion barrier, which makes it easier to handle at room temperature. All experimental results are underpinned by theoretical DFT calculations. |
format | Online Article Text |
id | pubmed-7756504 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77565042020-12-28 An Isosteric Triaza Analogue of a Polycyclic Aromatic Hydrocarbon Monkey Saddle Kirschbaum, Tobias Rominger, Frank Mastalerz, Michael Chemistry Communications Since a few years, the interest in negatively‐curved fused polycyclic aromatic hydrocarbons (PAHs) has significantly increased. Recently, the first chiral negatively‐curved PAH with the topology of a monkey saddle was introduced. Herein the synthesis of its triaza congener is reported. The influence of this CH↔N exchange on photophysical and electrochemical properties is studied as well as the isomerization process of the enantiomers. The aza analogue has a significantly higher inversion barrier, which makes it easier to handle at room temperature. All experimental results are underpinned by theoretical DFT calculations. John Wiley and Sons Inc. 2020-10-12 2020-11-17 /pmc/articles/PMC7756504/ /pubmed/32539193 http://dx.doi.org/10.1002/chem.202002826 Text en © 2020 The Authors. Published by Wiley-VCH GmbH This is an open access article under the terms of the http://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 | Communications Kirschbaum, Tobias Rominger, Frank Mastalerz, Michael An Isosteric Triaza Analogue of a Polycyclic Aromatic Hydrocarbon Monkey Saddle |
title | An Isosteric Triaza Analogue of a Polycyclic Aromatic Hydrocarbon Monkey Saddle |
title_full | An Isosteric Triaza Analogue of a Polycyclic Aromatic Hydrocarbon Monkey Saddle |
title_fullStr | An Isosteric Triaza Analogue of a Polycyclic Aromatic Hydrocarbon Monkey Saddle |
title_full_unstemmed | An Isosteric Triaza Analogue of a Polycyclic Aromatic Hydrocarbon Monkey Saddle |
title_short | An Isosteric Triaza Analogue of a Polycyclic Aromatic Hydrocarbon Monkey Saddle |
title_sort | isosteric triaza analogue of a polycyclic aromatic hydrocarbon monkey saddle |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756504/ https://www.ncbi.nlm.nih.gov/pubmed/32539193 http://dx.doi.org/10.1002/chem.202002826 |
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