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Borazatruxenes

We report the synthesis and characterization of a series of arene-borazine hybrids called borazatruxenes. These molecules are BN-isosteres of truxene whereby the central benzene core has been replaced by a borazine ring. The straightforward three step synthesis, stability and their chiroptical and e...

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Detalles Bibliográficos
Autores principales: Limberti, Simone, Emmett, Liam, Trandafir, Anamaria, Kociok-Köhn, Gabriele, Pantoş, G. Dan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6979502/
https://www.ncbi.nlm.nih.gov/pubmed/32055329
http://dx.doi.org/10.1039/c9sc02489a
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author Limberti, Simone
Emmett, Liam
Trandafir, Anamaria
Kociok-Köhn, Gabriele
Pantoş, G. Dan
author_facet Limberti, Simone
Emmett, Liam
Trandafir, Anamaria
Kociok-Köhn, Gabriele
Pantoş, G. Dan
author_sort Limberti, Simone
collection PubMed
description We report the synthesis and characterization of a series of arene-borazine hybrids called borazatruxenes. These molecules are BN-isosteres of truxene whereby the central benzene core has been replaced by a borazine ring. The straightforward three step synthesis, stability and their chiroptical and electronic properties recommend them as new scaffolds for BN–carbon hybrid materials. Computational studies at DFT level, closely matching the experimental data, provided insights in the electronic structure of these molecules.
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spelling pubmed-69795022020-02-13 Borazatruxenes Limberti, Simone Emmett, Liam Trandafir, Anamaria Kociok-Köhn, Gabriele Pantoş, G. Dan Chem Sci Chemistry We report the synthesis and characterization of a series of arene-borazine hybrids called borazatruxenes. These molecules are BN-isosteres of truxene whereby the central benzene core has been replaced by a borazine ring. The straightforward three step synthesis, stability and their chiroptical and electronic properties recommend them as new scaffolds for BN–carbon hybrid materials. Computational studies at DFT level, closely matching the experimental data, provided insights in the electronic structure of these molecules. Royal Society of Chemistry 2019-08-28 /pmc/articles/PMC6979502/ /pubmed/32055329 http://dx.doi.org/10.1039/c9sc02489a Text en This journal is © The Royal Society of Chemistry 2019 https://creativecommons.org/licenses/by/3.0/This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0)
spellingShingle Chemistry
Limberti, Simone
Emmett, Liam
Trandafir, Anamaria
Kociok-Köhn, Gabriele
Pantoş, G. Dan
Borazatruxenes
title Borazatruxenes
title_full Borazatruxenes
title_fullStr Borazatruxenes
title_full_unstemmed Borazatruxenes
title_short Borazatruxenes
title_sort borazatruxenes
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6979502/
https://www.ncbi.nlm.nih.gov/pubmed/32055329
http://dx.doi.org/10.1039/c9sc02489a
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AT pantosgdan borazatruxenes