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meta-Oligoazobiphenyls – synthesis via site-selective Mills reaction and photochemical properties

The investigation of multi-photochromic compounds constitutes a great challenge, not only from a synthetic point of view, but also with respect to the analysis of the photochemical properties. In this context we designed a novel strategy to access meta-oligoazobiphenyls via site-selective Mills reac...

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Detalles Bibliográficos
Autores principales: Reuter, Raphael, Wegner, Hermann A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3388877/
https://www.ncbi.nlm.nih.gov/pubmed/23015837
http://dx.doi.org/10.3762/bjoc.8.99
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author Reuter, Raphael
Wegner, Hermann A
author_facet Reuter, Raphael
Wegner, Hermann A
author_sort Reuter, Raphael
collection PubMed
description The investigation of multi-photochromic compounds constitutes a great challenge, not only from a synthetic point of view, but also with respect to the analysis of the photochemical properties. In this context we designed a novel strategy to access meta-oligoazobiphenyls via site-selective Mills reaction and Suzuki cross-coupling in a highly efficient iterative way. Photochemical examination of the resulting monomeric and oligomeric azo compounds revealed that the overall degree of switching was independent of the connected azo-units. However, one of the azobonds in the bis-azobiphenyl is isomerized preferentially despite the high structural similarity.
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spelling pubmed-33888772012-09-26 meta-Oligoazobiphenyls – synthesis via site-selective Mills reaction and photochemical properties Reuter, Raphael Wegner, Hermann A Beilstein J Org Chem Full Research Paper The investigation of multi-photochromic compounds constitutes a great challenge, not only from a synthetic point of view, but also with respect to the analysis of the photochemical properties. In this context we designed a novel strategy to access meta-oligoazobiphenyls via site-selective Mills reaction and Suzuki cross-coupling in a highly efficient iterative way. Photochemical examination of the resulting monomeric and oligomeric azo compounds revealed that the overall degree of switching was independent of the connected azo-units. However, one of the azobonds in the bis-azobiphenyl is isomerized preferentially despite the high structural similarity. Beilstein-Institut 2012-06-13 /pmc/articles/PMC3388877/ /pubmed/23015837 http://dx.doi.org/10.3762/bjoc.8.99 Text en Copyright © 2012, Reuter and Wegner https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Reuter, Raphael
Wegner, Hermann A
meta-Oligoazobiphenyls – synthesis via site-selective Mills reaction and photochemical properties
title meta-Oligoazobiphenyls – synthesis via site-selective Mills reaction and photochemical properties
title_full meta-Oligoazobiphenyls – synthesis via site-selective Mills reaction and photochemical properties
title_fullStr meta-Oligoazobiphenyls – synthesis via site-selective Mills reaction and photochemical properties
title_full_unstemmed meta-Oligoazobiphenyls – synthesis via site-selective Mills reaction and photochemical properties
title_short meta-Oligoazobiphenyls – synthesis via site-selective Mills reaction and photochemical properties
title_sort meta-oligoazobiphenyls – synthesis via site-selective mills reaction and photochemical properties
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3388877/
https://www.ncbi.nlm.nih.gov/pubmed/23015837
http://dx.doi.org/10.3762/bjoc.8.99
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