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Facile modification of phosphole-based aggregation-induced emission luminogens with sulfonyl isocyanates

Phosphole oxides undergo a highly chemoselective reaction with sulfonyl isocyanates forming sulfonylimino phospholes in high yields. This facile modification proved to be a powerful tool for obtaining new phosphole-based aggregation-induced emission (AIE) luminogens with high fluorescence quantum yi...

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Autores principales: König, Nils, Godínez-Loyola, Yokari, Yang, Fangshun, Laube, Christian, Laue, Michael, Lönnecke, Peter, Strassert, Cristian A., Hey-Hawkins, Evamarie
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/PMC9977459/
https://www.ncbi.nlm.nih.gov/pubmed/36873851
http://dx.doi.org/10.1039/d3sc00308f
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author König, Nils
Godínez-Loyola, Yokari
Yang, Fangshun
Laube, Christian
Laue, Michael
Lönnecke, Peter
Strassert, Cristian A.
Hey-Hawkins, Evamarie
author_facet König, Nils
Godínez-Loyola, Yokari
Yang, Fangshun
Laube, Christian
Laue, Michael
Lönnecke, Peter
Strassert, Cristian A.
Hey-Hawkins, Evamarie
author_sort König, Nils
collection PubMed
description Phosphole oxides undergo a highly chemoselective reaction with sulfonyl isocyanates forming sulfonylimino phospholes in high yields. This facile modification proved to be a powerful tool for obtaining new phosphole-based aggregation-induced emission (AIE) luminogens with high fluorescence quantum yields in the solid state. Changing the chemical environment of the phosphorus atom of the phosphole framework results in a significant shift of the fluorescence maximum to longer wavelengths.
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spelling pubmed-99774592023-03-02 Facile modification of phosphole-based aggregation-induced emission luminogens with sulfonyl isocyanates König, Nils Godínez-Loyola, Yokari Yang, Fangshun Laube, Christian Laue, Michael Lönnecke, Peter Strassert, Cristian A. Hey-Hawkins, Evamarie Chem Sci Chemistry Phosphole oxides undergo a highly chemoselective reaction with sulfonyl isocyanates forming sulfonylimino phospholes in high yields. This facile modification proved to be a powerful tool for obtaining new phosphole-based aggregation-induced emission (AIE) luminogens with high fluorescence quantum yields in the solid state. Changing the chemical environment of the phosphorus atom of the phosphole framework results in a significant shift of the fluorescence maximum to longer wavelengths. The Royal Society of Chemistry 2023-02-03 /pmc/articles/PMC9977459/ /pubmed/36873851 http://dx.doi.org/10.1039/d3sc00308f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
König, Nils
Godínez-Loyola, Yokari
Yang, Fangshun
Laube, Christian
Laue, Michael
Lönnecke, Peter
Strassert, Cristian A.
Hey-Hawkins, Evamarie
Facile modification of phosphole-based aggregation-induced emission luminogens with sulfonyl isocyanates
title Facile modification of phosphole-based aggregation-induced emission luminogens with sulfonyl isocyanates
title_full Facile modification of phosphole-based aggregation-induced emission luminogens with sulfonyl isocyanates
title_fullStr Facile modification of phosphole-based aggregation-induced emission luminogens with sulfonyl isocyanates
title_full_unstemmed Facile modification of phosphole-based aggregation-induced emission luminogens with sulfonyl isocyanates
title_short Facile modification of phosphole-based aggregation-induced emission luminogens with sulfonyl isocyanates
title_sort facile modification of phosphole-based aggregation-induced emission luminogens with sulfonyl isocyanates
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9977459/
https://www.ncbi.nlm.nih.gov/pubmed/36873851
http://dx.doi.org/10.1039/d3sc00308f
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