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Trimesityltriangulene: a persistent derivative of Clar's hydrocarbon
Triangulene, known as Clar's hydrocarbon, is a prototypical non-Kekulé diradical comprised of six benzenoid rings fused in a triangular shape. We synthesized and characterized its trimesityl derivative, illustrating that three bulky substituents installed in the centers of the zigzag edges suff...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8886921/ https://www.ncbi.nlm.nih.gov/pubmed/35156113 http://dx.doi.org/10.1039/d2cc00352j |
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author | Valenta, Leoš Mayländer, Maximilian Kappeler, Pia Blacque, Olivier Šolomek, Tomáš Richert, Sabine Juríček, Michal |
author_facet | Valenta, Leoš Mayländer, Maximilian Kappeler, Pia Blacque, Olivier Šolomek, Tomáš Richert, Sabine Juríček, Michal |
author_sort | Valenta, Leoš |
collection | PubMed |
description | Triangulene, known as Clar's hydrocarbon, is a prototypical non-Kekulé diradical comprised of six benzenoid rings fused in a triangular shape. We synthesized and characterized its trimesityl derivative, illustrating that three bulky substituents installed in the centers of the zigzag edges suffice to protect all reactive positions. This work brings prospects to use triangulene and its open-shell analogs in spintronic materials via solution-phase synthesis. |
format | Online Article Text |
id | pubmed-8886921 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-88869212022-03-24 Trimesityltriangulene: a persistent derivative of Clar's hydrocarbon Valenta, Leoš Mayländer, Maximilian Kappeler, Pia Blacque, Olivier Šolomek, Tomáš Richert, Sabine Juríček, Michal Chem Commun (Camb) Chemistry Triangulene, known as Clar's hydrocarbon, is a prototypical non-Kekulé diradical comprised of six benzenoid rings fused in a triangular shape. We synthesized and characterized its trimesityl derivative, illustrating that three bulky substituents installed in the centers of the zigzag edges suffice to protect all reactive positions. This work brings prospects to use triangulene and its open-shell analogs in spintronic materials via solution-phase synthesis. The Royal Society of Chemistry 2022-02-04 /pmc/articles/PMC8886921/ /pubmed/35156113 http://dx.doi.org/10.1039/d2cc00352j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Valenta, Leoš Mayländer, Maximilian Kappeler, Pia Blacque, Olivier Šolomek, Tomáš Richert, Sabine Juríček, Michal Trimesityltriangulene: a persistent derivative of Clar's hydrocarbon |
title | Trimesityltriangulene: a persistent derivative of Clar's hydrocarbon |
title_full | Trimesityltriangulene: a persistent derivative of Clar's hydrocarbon |
title_fullStr | Trimesityltriangulene: a persistent derivative of Clar's hydrocarbon |
title_full_unstemmed | Trimesityltriangulene: a persistent derivative of Clar's hydrocarbon |
title_short | Trimesityltriangulene: a persistent derivative of Clar's hydrocarbon |
title_sort | trimesityltriangulene: a persistent derivative of clar's hydrocarbon |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8886921/ https://www.ncbi.nlm.nih.gov/pubmed/35156113 http://dx.doi.org/10.1039/d2cc00352j |
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