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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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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. |
format | Online Article Text |
id | pubmed-9093196 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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