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Vinylpyrroles: solid-state structures and aggregation-induced emission properties

An aggregation-induced emission chromophore, vinylpyrrole, was prepared from a formylpyrrole derivative, Meldrum's acid, and 1,3-dimethylbarbituric acid. The optical properties of the chromophore both in the solution and solid states were investigated by UV-vis and fluorescence spectroscopy. Si...

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Detalles Bibliográficos
Autores principales: Okawara, Toru, Matsufuji, Yurina, Mizuno, Kouhei, Takehara, Kenji, Nagamura, Toshihiko, Iwasa, Seiji
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/PMC9067133/
https://www.ncbi.nlm.nih.gov/pubmed/35514514
http://dx.doi.org/10.1039/c9ra04088a
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author Okawara, Toru
Matsufuji, Yurina
Mizuno, Kouhei
Takehara, Kenji
Nagamura, Toshihiko
Iwasa, Seiji
author_facet Okawara, Toru
Matsufuji, Yurina
Mizuno, Kouhei
Takehara, Kenji
Nagamura, Toshihiko
Iwasa, Seiji
author_sort Okawara, Toru
collection PubMed
description An aggregation-induced emission chromophore, vinylpyrrole, was prepared from a formylpyrrole derivative, Meldrum's acid, and 1,3-dimethylbarbituric acid. The optical properties of the chromophore both in the solution and solid states were investigated by UV-vis and fluorescence spectroscopy. Single crystal X-ray diffraction measurements revealed that the dimethylbarbituric acid adduct formed a J-aggregate in the solid and resulted in higher fluorescence quantum yield compared to the Meldrum's acid adduct. Emission enhancement was found to occur by the restriction of molecular rotation in the solid state.
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spelling pubmed-90671332022-05-04 Vinylpyrroles: solid-state structures and aggregation-induced emission properties Okawara, Toru Matsufuji, Yurina Mizuno, Kouhei Takehara, Kenji Nagamura, Toshihiko Iwasa, Seiji RSC Adv Chemistry An aggregation-induced emission chromophore, vinylpyrrole, was prepared from a formylpyrrole derivative, Meldrum's acid, and 1,3-dimethylbarbituric acid. The optical properties of the chromophore both in the solution and solid states were investigated by UV-vis and fluorescence spectroscopy. Single crystal X-ray diffraction measurements revealed that the dimethylbarbituric acid adduct formed a J-aggregate in the solid and resulted in higher fluorescence quantum yield compared to the Meldrum's acid adduct. Emission enhancement was found to occur by the restriction of molecular rotation in the solid state. The Royal Society of Chemistry 2019-07-23 /pmc/articles/PMC9067133/ /pubmed/35514514 http://dx.doi.org/10.1039/c9ra04088a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Okawara, Toru
Matsufuji, Yurina
Mizuno, Kouhei
Takehara, Kenji
Nagamura, Toshihiko
Iwasa, Seiji
Vinylpyrroles: solid-state structures and aggregation-induced emission properties
title Vinylpyrroles: solid-state structures and aggregation-induced emission properties
title_full Vinylpyrroles: solid-state structures and aggregation-induced emission properties
title_fullStr Vinylpyrroles: solid-state structures and aggregation-induced emission properties
title_full_unstemmed Vinylpyrroles: solid-state structures and aggregation-induced emission properties
title_short Vinylpyrroles: solid-state structures and aggregation-induced emission properties
title_sort vinylpyrroles: solid-state structures and aggregation-induced emission properties
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9067133/
https://www.ncbi.nlm.nih.gov/pubmed/35514514
http://dx.doi.org/10.1039/c9ra04088a
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