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A novel aggregation-induced enhanced emission aromatic molecule: 2-aminophenylboronic acid dimer
Aggregation-induced enhanced emission (AIEE) molecules have significant applications in optoelectronics, biomedical probes and chemical sensors, and large amounts of AIEE molecules have been reported since the concept of AIEE was proposed. Most aromatic AIEE molecules have complex structures consist...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8480421/ https://www.ncbi.nlm.nih.gov/pubmed/34603674 http://dx.doi.org/10.1039/d1sc03765j |
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author | Li, Xiaopei Wang, Dongdong Zhang, Yongjie Lu, Wenqi Yang, Songqiu Hou, Guangjin Zhao, Zhenchao Qin, Haijuan Zhang, Yahui Li, Minmin Qing, Guangyan |
author_facet | Li, Xiaopei Wang, Dongdong Zhang, Yongjie Lu, Wenqi Yang, Songqiu Hou, Guangjin Zhao, Zhenchao Qin, Haijuan Zhang, Yahui Li, Minmin Qing, Guangyan |
author_sort | Li, Xiaopei |
collection | PubMed |
description | Aggregation-induced enhanced emission (AIEE) molecules have significant applications in optoelectronics, biomedical probes and chemical sensors, and large amounts of AIEE molecules have been reported since the concept of AIEE was proposed. Most aromatic AIEE molecules have complex structures consisting of multiple aromatic rings and/or polycyclic skeletons. In this study, we find that 2-aminophenylboronic acid (2-APBA) with a simple structure is highly emissive in the solid state. Further studies reveal that 2-APBA exists in a dimeric form, and the 2-APBA dimer is a novel AIEE molecule. The underlying AIEE mechanism is that the 2-APBA dimeric units aggregate through intermolecular interactions to produce highly ordered molecular packing without the presence of π–π stacking interactions that would lead to aggregation-caused quenching. Furthermore, the 2-APBA dimer aggregates could reversibly transform into its non-fluorescent monomer form driven by new kinds of dynamic covalent B–N and B–O bonds, illustrating its good potential in molecular recognition, nanogating, chemo/bio-sensing and controlled drug release. |
format | Online Article Text |
id | pubmed-8480421 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-84804212021-10-01 A novel aggregation-induced enhanced emission aromatic molecule: 2-aminophenylboronic acid dimer Li, Xiaopei Wang, Dongdong Zhang, Yongjie Lu, Wenqi Yang, Songqiu Hou, Guangjin Zhao, Zhenchao Qin, Haijuan Zhang, Yahui Li, Minmin Qing, Guangyan Chem Sci Chemistry Aggregation-induced enhanced emission (AIEE) molecules have significant applications in optoelectronics, biomedical probes and chemical sensors, and large amounts of AIEE molecules have been reported since the concept of AIEE was proposed. Most aromatic AIEE molecules have complex structures consisting of multiple aromatic rings and/or polycyclic skeletons. In this study, we find that 2-aminophenylboronic acid (2-APBA) with a simple structure is highly emissive in the solid state. Further studies reveal that 2-APBA exists in a dimeric form, and the 2-APBA dimer is a novel AIEE molecule. The underlying AIEE mechanism is that the 2-APBA dimeric units aggregate through intermolecular interactions to produce highly ordered molecular packing without the presence of π–π stacking interactions that would lead to aggregation-caused quenching. Furthermore, the 2-APBA dimer aggregates could reversibly transform into its non-fluorescent monomer form driven by new kinds of dynamic covalent B–N and B–O bonds, illustrating its good potential in molecular recognition, nanogating, chemo/bio-sensing and controlled drug release. The Royal Society of Chemistry 2021-08-18 /pmc/articles/PMC8480421/ /pubmed/34603674 http://dx.doi.org/10.1039/d1sc03765j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Li, Xiaopei Wang, Dongdong Zhang, Yongjie Lu, Wenqi Yang, Songqiu Hou, Guangjin Zhao, Zhenchao Qin, Haijuan Zhang, Yahui Li, Minmin Qing, Guangyan A novel aggregation-induced enhanced emission aromatic molecule: 2-aminophenylboronic acid dimer |
title | A novel aggregation-induced enhanced emission aromatic molecule: 2-aminophenylboronic acid dimer |
title_full | A novel aggregation-induced enhanced emission aromatic molecule: 2-aminophenylboronic acid dimer |
title_fullStr | A novel aggregation-induced enhanced emission aromatic molecule: 2-aminophenylboronic acid dimer |
title_full_unstemmed | A novel aggregation-induced enhanced emission aromatic molecule: 2-aminophenylboronic acid dimer |
title_short | A novel aggregation-induced enhanced emission aromatic molecule: 2-aminophenylboronic acid dimer |
title_sort | novel aggregation-induced enhanced emission aromatic molecule: 2-aminophenylboronic acid dimer |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8480421/ https://www.ncbi.nlm.nih.gov/pubmed/34603674 http://dx.doi.org/10.1039/d1sc03765j |
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