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Optical Characteristics and Applications of AIE Racemic C6-Unsubstituted Tetrahydropyrimidines

Racemic C6-unsubstituted tetrahydropyrimidines (THPs) are the products of an efficient five-component reaction that we developed. THPs show strong AIE characteristics, that is, completely no fluorescence in different solvents but strong emission with fluorescence quantum yields (Φ (F)) up to 100% up...

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Autor principal: Zhu, Qiuhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8664540/
https://www.ncbi.nlm.nih.gov/pubmed/34900949
http://dx.doi.org/10.3389/fchem.2021.800177
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author Zhu, Qiuhua
author_facet Zhu, Qiuhua
author_sort Zhu, Qiuhua
collection PubMed
description Racemic C6-unsubstituted tetrahydropyrimidines (THPs) are the products of an efficient five-component reaction that we developed. THPs show strong AIE characteristics, that is, completely no fluorescence in different solvents but strong emission with fluorescence quantum yields (Φ (F)) up to 100% upon aggregation. However, the Φ (F) values of their pure enantiomers are lower than 46%. Unlike common AIE compounds with crowded aryl rotors on a π-bond or on an aryl ring, THPs have three completely non-crowded aryl rotors on a non-aromatic chiral central ring (tetrahydropyrimidine). In this mini review, we first discuss the AIE characteristics of THPs and the influences of molecular structures on their molecular packing modes and optical properties, and then present their applications and forecast the development of other racemic AIE compounds.
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spelling pubmed-86645402021-12-11 Optical Characteristics and Applications of AIE Racemic C6-Unsubstituted Tetrahydropyrimidines Zhu, Qiuhua Front Chem Chemistry Racemic C6-unsubstituted tetrahydropyrimidines (THPs) are the products of an efficient five-component reaction that we developed. THPs show strong AIE characteristics, that is, completely no fluorescence in different solvents but strong emission with fluorescence quantum yields (Φ (F)) up to 100% upon aggregation. However, the Φ (F) values of their pure enantiomers are lower than 46%. Unlike common AIE compounds with crowded aryl rotors on a π-bond or on an aryl ring, THPs have three completely non-crowded aryl rotors on a non-aromatic chiral central ring (tetrahydropyrimidine). In this mini review, we first discuss the AIE characteristics of THPs and the influences of molecular structures on their molecular packing modes and optical properties, and then present their applications and forecast the development of other racemic AIE compounds. Frontiers Media S.A. 2021-11-26 /pmc/articles/PMC8664540/ /pubmed/34900949 http://dx.doi.org/10.3389/fchem.2021.800177 Text en Copyright © 2021 Zhu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Zhu, Qiuhua
Optical Characteristics and Applications of AIE Racemic C6-Unsubstituted Tetrahydropyrimidines
title Optical Characteristics and Applications of AIE Racemic C6-Unsubstituted Tetrahydropyrimidines
title_full Optical Characteristics and Applications of AIE Racemic C6-Unsubstituted Tetrahydropyrimidines
title_fullStr Optical Characteristics and Applications of AIE Racemic C6-Unsubstituted Tetrahydropyrimidines
title_full_unstemmed Optical Characteristics and Applications of AIE Racemic C6-Unsubstituted Tetrahydropyrimidines
title_short Optical Characteristics and Applications of AIE Racemic C6-Unsubstituted Tetrahydropyrimidines
title_sort optical characteristics and applications of aie racemic c6-unsubstituted tetrahydropyrimidines
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8664540/
https://www.ncbi.nlm.nih.gov/pubmed/34900949
http://dx.doi.org/10.3389/fchem.2021.800177
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