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Axially chiral 1,4-dihydropyridine derivatives: aggregation-induced emission in exciplexes and application as viscosity probes
By combining the fluorophores of axially chiral 1,1′-binaphthol (BINOL) and 1,4-dihydropyridine derivatives, axially chiral 1,4-dihydropyridine derivatives ((R)-/(S)-2) with aggregation-induced emission (AIE) in exciplexes were designed and synthesized. (R)-/(S)-2 emitted low fluorescence in THF sol...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072944/ https://www.ncbi.nlm.nih.gov/pubmed/35530811 http://dx.doi.org/10.1039/c9ra06553a |
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author | Yang, Zeren Huo, Yanmin Liu, Yanke Du, Guifen Zhang, Wenhao Zhou, Lijie Zhan, Lihui Ren, Xuerui Duan, Wenzeng Gong, Shuwen |
author_facet | Yang, Zeren Huo, Yanmin Liu, Yanke Du, Guifen Zhang, Wenhao Zhou, Lijie Zhan, Lihui Ren, Xuerui Duan, Wenzeng Gong, Shuwen |
author_sort | Yang, Zeren |
collection | PubMed |
description | By combining the fluorophores of axially chiral 1,1′-binaphthol (BINOL) and 1,4-dihydropyridine derivatives, axially chiral 1,4-dihydropyridine derivatives ((R)-/(S)-2) with aggregation-induced emission (AIE) in exciplexes were designed and synthesized. (R)-/(S)-2 emitted low fluorescence in THF solutions of their locally excited states; however, they emitted red-shifted fluorescence in the aggregate state upon exciplex formation. Moreover, (R)-/(S)-2 showed linear and multi-exponential relationships between their local excited and exciplex fluorescence intensities and the viscosity of the medium, which allowed us to determine the viscosities of different mixed solvents. In addition, as an axially chiral viscosity probe, (R)-/(S)-2 show excellent CD signals and have potential applications in the fields of chiral recognition and fluorescence imaging, which will broaden the new family of AIE fluorophores. To the best of our knowledge, there are few reports of axially chiral intramolecular exciplex-mediated AIE molecules. |
format | Online Article Text |
id | pubmed-9072944 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90729442022-05-06 Axially chiral 1,4-dihydropyridine derivatives: aggregation-induced emission in exciplexes and application as viscosity probes Yang, Zeren Huo, Yanmin Liu, Yanke Du, Guifen Zhang, Wenhao Zhou, Lijie Zhan, Lihui Ren, Xuerui Duan, Wenzeng Gong, Shuwen RSC Adv Chemistry By combining the fluorophores of axially chiral 1,1′-binaphthol (BINOL) and 1,4-dihydropyridine derivatives, axially chiral 1,4-dihydropyridine derivatives ((R)-/(S)-2) with aggregation-induced emission (AIE) in exciplexes were designed and synthesized. (R)-/(S)-2 emitted low fluorescence in THF solutions of their locally excited states; however, they emitted red-shifted fluorescence in the aggregate state upon exciplex formation. Moreover, (R)-/(S)-2 showed linear and multi-exponential relationships between their local excited and exciplex fluorescence intensities and the viscosity of the medium, which allowed us to determine the viscosities of different mixed solvents. In addition, as an axially chiral viscosity probe, (R)-/(S)-2 show excellent CD signals and have potential applications in the fields of chiral recognition and fluorescence imaging, which will broaden the new family of AIE fluorophores. To the best of our knowledge, there are few reports of axially chiral intramolecular exciplex-mediated AIE molecules. The Royal Society of Chemistry 2019-10-10 /pmc/articles/PMC9072944/ /pubmed/35530811 http://dx.doi.org/10.1039/c9ra06553a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Yang, Zeren Huo, Yanmin Liu, Yanke Du, Guifen Zhang, Wenhao Zhou, Lijie Zhan, Lihui Ren, Xuerui Duan, Wenzeng Gong, Shuwen Axially chiral 1,4-dihydropyridine derivatives: aggregation-induced emission in exciplexes and application as viscosity probes |
title | Axially chiral 1,4-dihydropyridine derivatives: aggregation-induced emission in exciplexes and application as viscosity probes |
title_full | Axially chiral 1,4-dihydropyridine derivatives: aggregation-induced emission in exciplexes and application as viscosity probes |
title_fullStr | Axially chiral 1,4-dihydropyridine derivatives: aggregation-induced emission in exciplexes and application as viscosity probes |
title_full_unstemmed | Axially chiral 1,4-dihydropyridine derivatives: aggregation-induced emission in exciplexes and application as viscosity probes |
title_short | Axially chiral 1,4-dihydropyridine derivatives: aggregation-induced emission in exciplexes and application as viscosity probes |
title_sort | axially chiral 1,4-dihydropyridine derivatives: aggregation-induced emission in exciplexes and application as viscosity probes |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072944/ https://www.ncbi.nlm.nih.gov/pubmed/35530811 http://dx.doi.org/10.1039/c9ra06553a |
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