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Asymmetrically bridged aroyl-S,N-ketene acetal-based multichromophores with aggregation-induced tunable emission

Asymmetrically bridged aroyl-S,N-ketene acetals and aroyl-S,N-ketene acetal multichromophores can be readily synthesized in consecutive three-, four-, or five-component syntheses in good to excellent yields by several successive Suzuki-couplings of aroyl-S,N-ketene acetals and bis(boronic)acid ester...

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Detalles Bibliográficos
Autores principales: Biesen, Lukas, Krenzer, Julius, Nirmalananthan-Budau, Nithiya, Resch-Genger, Ute, Müller, Thomas J. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9093196/
https://www.ncbi.nlm.nih.gov/pubmed/35655556
http://dx.doi.org/10.1039/d2sc00415a
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author Biesen, Lukas
Krenzer, Julius
Nirmalananthan-Budau, Nithiya
Resch-Genger, Ute
Müller, Thomas J. J.
author_facet Biesen, Lukas
Krenzer, Julius
Nirmalananthan-Budau, Nithiya
Resch-Genger, Ute
Müller, Thomas J. J.
author_sort Biesen, Lukas
collection PubMed
description Asymmetrically bridged aroyl-S,N-ketene acetals and aroyl-S,N-ketene acetal multichromophores can be readily synthesized in consecutive three-, four-, or five-component syntheses in good to excellent yields by several successive Suzuki-couplings of aroyl-S,N-ketene acetals and bis(boronic)acid esters. Different aroyl-S,N-ketene acetals as well as linker molecules yield a library of 23 multichromophores with substitution and linker pattern-tunable emission properties. This allows control of different communication pathways between the chromophores and of aggregation-induced emission (AIE) and energy transfer (ET) properties, providing elaborate aggregation-based fluorescence switches.
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spelling pubmed-90931962022-06-01 Asymmetrically bridged aroyl-S,N-ketene acetal-based multichromophores with aggregation-induced tunable emission Biesen, Lukas Krenzer, Julius Nirmalananthan-Budau, Nithiya Resch-Genger, Ute Müller, Thomas J. J. Chem Sci Chemistry Asymmetrically bridged aroyl-S,N-ketene acetals and aroyl-S,N-ketene acetal multichromophores can be readily synthesized in consecutive three-, four-, or five-component syntheses in good to excellent yields by several successive Suzuki-couplings of aroyl-S,N-ketene acetals and bis(boronic)acid esters. Different aroyl-S,N-ketene acetals as well as linker molecules yield a library of 23 multichromophores with substitution and linker pattern-tunable emission properties. This allows control of different communication pathways between the chromophores and of aggregation-induced emission (AIE) and energy transfer (ET) properties, providing elaborate aggregation-based fluorescence switches. The Royal Society of Chemistry 2022-04-12 /pmc/articles/PMC9093196/ /pubmed/35655556 http://dx.doi.org/10.1039/d2sc00415a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Biesen, Lukas
Krenzer, Julius
Nirmalananthan-Budau, Nithiya
Resch-Genger, Ute
Müller, Thomas J. J.
Asymmetrically bridged aroyl-S,N-ketene acetal-based multichromophores with aggregation-induced tunable emission
title Asymmetrically bridged aroyl-S,N-ketene acetal-based multichromophores with aggregation-induced tunable emission
title_full Asymmetrically bridged aroyl-S,N-ketene acetal-based multichromophores with aggregation-induced tunable emission
title_fullStr Asymmetrically bridged aroyl-S,N-ketene acetal-based multichromophores with aggregation-induced tunable emission
title_full_unstemmed Asymmetrically bridged aroyl-S,N-ketene acetal-based multichromophores with aggregation-induced tunable emission
title_short Asymmetrically bridged aroyl-S,N-ketene acetal-based multichromophores with aggregation-induced tunable emission
title_sort asymmetrically bridged aroyl-s,n-ketene acetal-based multichromophores with aggregation-induced tunable emission
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9093196/
https://www.ncbi.nlm.nih.gov/pubmed/35655556
http://dx.doi.org/10.1039/d2sc00415a
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