Cargando…
Dimethylnonacethrene – en route to a magnetic switch
Dimethylnonacethrene is the first derivative of the cethrene family that is energetically more stable than the product of its electrocyclic ring closure. Compared to the shorter homologue dimethylcethrene, the new system is EPR-active, because of a significantly lowered singlet–triplet gap, and disp...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10281489/ https://www.ncbi.nlm.nih.gov/pubmed/37221917 http://dx.doi.org/10.1039/d3cc01301d |
_version_ | 1785061013182218240 |
---|---|
author | Čavlović, Daniel Blacque, Olivier Krummenacher, Ivo Braunschweig, Holger Ravat, Prince Juríček, Michal |
author_facet | Čavlović, Daniel Blacque, Olivier Krummenacher, Ivo Braunschweig, Holger Ravat, Prince Juríček, Michal |
author_sort | Čavlović, Daniel |
collection | PubMed |
description | Dimethylnonacethrene is the first derivative of the cethrene family that is energetically more stable than the product of its electrocyclic ring closure. Compared to the shorter homologue dimethylcethrene, the new system is EPR-active, because of a significantly lowered singlet–triplet gap, and displays remarkable stability. Our results suggest that adjustment of the steric bulk in the fjord region can enable realisation of diradicaloid-based magnetic photoswitches. |
format | Online Article Text |
id | pubmed-10281489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-102814892023-06-21 Dimethylnonacethrene – en route to a magnetic switch Čavlović, Daniel Blacque, Olivier Krummenacher, Ivo Braunschweig, Holger Ravat, Prince Juríček, Michal Chem Commun (Camb) Chemistry Dimethylnonacethrene is the first derivative of the cethrene family that is energetically more stable than the product of its electrocyclic ring closure. Compared to the shorter homologue dimethylcethrene, the new system is EPR-active, because of a significantly lowered singlet–triplet gap, and displays remarkable stability. Our results suggest that adjustment of the steric bulk in the fjord region can enable realisation of diradicaloid-based magnetic photoswitches. The Royal Society of Chemistry 2023-05-17 /pmc/articles/PMC10281489/ /pubmed/37221917 http://dx.doi.org/10.1039/d3cc01301d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Čavlović, Daniel Blacque, Olivier Krummenacher, Ivo Braunschweig, Holger Ravat, Prince Juríček, Michal Dimethylnonacethrene – en route to a magnetic switch |
title | Dimethylnonacethrene – en route to a magnetic switch |
title_full | Dimethylnonacethrene – en route to a magnetic switch |
title_fullStr | Dimethylnonacethrene – en route to a magnetic switch |
title_full_unstemmed | Dimethylnonacethrene – en route to a magnetic switch |
title_short | Dimethylnonacethrene – en route to a magnetic switch |
title_sort | dimethylnonacethrene – en route to a magnetic switch |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10281489/ https://www.ncbi.nlm.nih.gov/pubmed/37221917 http://dx.doi.org/10.1039/d3cc01301d |
work_keys_str_mv | AT cavlovicdaniel dimethylnonacethreneenroutetoamagneticswitch AT blacqueolivier dimethylnonacethreneenroutetoamagneticswitch AT krummenacherivo dimethylnonacethreneenroutetoamagneticswitch AT braunschweigholger dimethylnonacethreneenroutetoamagneticswitch AT ravatprince dimethylnonacethreneenroutetoamagneticswitch AT juricekmichal dimethylnonacethreneenroutetoamagneticswitch |