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Control over molecular motion using the cis–trans photoisomerization of the azo group

Control over molecular motion represents an important objective in modern chemistry. Aromatic azobenzenes are excellent candidates as molecular switches since they can exist in two forms, namely the cis (Z) and trans (E) isomers, which can interconvert both photochemically and thermally. This transf...

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Detalles Bibliográficos
Autores principales: Merino, Estíbaliz, Ribagorda, María
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3458724/
https://www.ncbi.nlm.nih.gov/pubmed/23019434
http://dx.doi.org/10.3762/bjoc.8.119
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author Merino, Estíbaliz
Ribagorda, María
author_facet Merino, Estíbaliz
Ribagorda, María
author_sort Merino, Estíbaliz
collection PubMed
description Control over molecular motion represents an important objective in modern chemistry. Aromatic azobenzenes are excellent candidates as molecular switches since they can exist in two forms, namely the cis (Z) and trans (E) isomers, which can interconvert both photochemically and thermally. This transformation induces a molecular movement and a significant geometric change, therefore the azobenzene unit is an excellent candidate to build dynamic molecular devices. We describe selected examples of systems containing an azobenzene moiety and their motions and geometrical changes caused by external stimuli.
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spelling pubmed-34587242012-09-27 Control over molecular motion using the cis–trans photoisomerization of the azo group Merino, Estíbaliz Ribagorda, María Beilstein J Org Chem Review Control over molecular motion represents an important objective in modern chemistry. Aromatic azobenzenes are excellent candidates as molecular switches since they can exist in two forms, namely the cis (Z) and trans (E) isomers, which can interconvert both photochemically and thermally. This transformation induces a molecular movement and a significant geometric change, therefore the azobenzene unit is an excellent candidate to build dynamic molecular devices. We describe selected examples of systems containing an azobenzene moiety and their motions and geometrical changes caused by external stimuli. Beilstein-Institut 2012-07-12 /pmc/articles/PMC3458724/ /pubmed/23019434 http://dx.doi.org/10.3762/bjoc.8.119 Text en Copyright © 2012, Merino and Ribagorda 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 Review
Merino, Estíbaliz
Ribagorda, María
Control over molecular motion using the cis–trans photoisomerization of the azo group
title Control over molecular motion using the cis–trans photoisomerization of the azo group
title_full Control over molecular motion using the cis–trans photoisomerization of the azo group
title_fullStr Control over molecular motion using the cis–trans photoisomerization of the azo group
title_full_unstemmed Control over molecular motion using the cis–trans photoisomerization of the azo group
title_short Control over molecular motion using the cis–trans photoisomerization of the azo group
title_sort control over molecular motion using the cis–trans photoisomerization of the azo group
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3458724/
https://www.ncbi.nlm.nih.gov/pubmed/23019434
http://dx.doi.org/10.3762/bjoc.8.119
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