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Tautomeric photoswitches: anion-assisted azo/azine-to-hydrazone photochromism

The photoswitching properties of two easily synthesized isatin 4-nitrophenylhydrazones were investigated. Although the parent isatin 4-nitrophenylhydrazones exhibit low addressability which hampers their photochromic applications, the addition of strongly basic anions to phenylhydrazone solutions cr...

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Autores principales: Filo, Juraj, Tisovský, Pavol, Csicsai, Klaudia, Donovalová, Jana, Gáplovský, Martin, Gáplovský, Anton, Cigáň, Marek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9064339/
https://www.ncbi.nlm.nih.gov/pubmed/35521389
http://dx.doi.org/10.1039/c9ra02906k
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author Filo, Juraj
Tisovský, Pavol
Csicsai, Klaudia
Donovalová, Jana
Gáplovský, Martin
Gáplovský, Anton
Cigáň, Marek
author_facet Filo, Juraj
Tisovský, Pavol
Csicsai, Klaudia
Donovalová, Jana
Gáplovský, Martin
Gáplovský, Anton
Cigáň, Marek
author_sort Filo, Juraj
collection PubMed
description The photoswitching properties of two easily synthesized isatin 4-nitrophenylhydrazones were investigated. Although the parent isatin 4-nitrophenylhydrazones exhibit low addressability which hampers their photochromic applications, the addition of strongly basic anions to phenylhydrazone solutions creates a new Vis–Vis photochromic system with the unusual azo/azine-to-hydrazone photo-tautomerization process as the photoswitching mechanism. To the best of our knowledge, this is the first report related to the anion-assisted azo/azine-to-hydrazone photo-tautomerism.
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spelling pubmed-90643392022-05-04 Tautomeric photoswitches: anion-assisted azo/azine-to-hydrazone photochromism Filo, Juraj Tisovský, Pavol Csicsai, Klaudia Donovalová, Jana Gáplovský, Martin Gáplovský, Anton Cigáň, Marek RSC Adv Chemistry The photoswitching properties of two easily synthesized isatin 4-nitrophenylhydrazones were investigated. Although the parent isatin 4-nitrophenylhydrazones exhibit low addressability which hampers their photochromic applications, the addition of strongly basic anions to phenylhydrazone solutions creates a new Vis–Vis photochromic system with the unusual azo/azine-to-hydrazone photo-tautomerization process as the photoswitching mechanism. To the best of our knowledge, this is the first report related to the anion-assisted azo/azine-to-hydrazone photo-tautomerism. The Royal Society of Chemistry 2019-05-21 /pmc/articles/PMC9064339/ /pubmed/35521389 http://dx.doi.org/10.1039/c9ra02906k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Filo, Juraj
Tisovský, Pavol
Csicsai, Klaudia
Donovalová, Jana
Gáplovský, Martin
Gáplovský, Anton
Cigáň, Marek
Tautomeric photoswitches: anion-assisted azo/azine-to-hydrazone photochromism
title Tautomeric photoswitches: anion-assisted azo/azine-to-hydrazone photochromism
title_full Tautomeric photoswitches: anion-assisted azo/azine-to-hydrazone photochromism
title_fullStr Tautomeric photoswitches: anion-assisted azo/azine-to-hydrazone photochromism
title_full_unstemmed Tautomeric photoswitches: anion-assisted azo/azine-to-hydrazone photochromism
title_short Tautomeric photoswitches: anion-assisted azo/azine-to-hydrazone photochromism
title_sort tautomeric photoswitches: anion-assisted azo/azine-to-hydrazone photochromism
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9064339/
https://www.ncbi.nlm.nih.gov/pubmed/35521389
http://dx.doi.org/10.1039/c9ra02906k
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