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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...

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Detalles Bibliográficos
Autores principales: Kirschbaum, Tobias, Rominger, Frank, Mastalerz, Michael
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/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.
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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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