Supramolecular Hydrogen Bonding Assembly from Non-Coplanar Aromatic Tetra-(1)H-Pyrazoles with Crystallization-Induced Emission (CIE)

Here, we report a design strategy for constructing supramolecular organic frameworks by introducing (1)H-pyrazole groups to aromatic cores as non-coplanar molecules to form diverse supramolecular assemblies through multiple (1)H-pyrazole [N−H···N] hydrogen bonds as well as other weak interactions. T...

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Detalles Bibliográficos
Autores principales: Wang, Ji, Zhao, Li-Rong, Tong, Jin, Yu, Yan-Min, Wang, Xia-Yan, Yu, Shu-Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9026852/
https://www.ncbi.nlm.nih.gov/pubmed/35457024
http://dx.doi.org/10.3390/ijms23084206
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author Wang, Ji
Zhao, Li-Rong
Tong, Jin
Yu, Yan-Min
Wang, Xia-Yan
Yu, Shu-Yan
author_facet Wang, Ji
Zhao, Li-Rong
Tong, Jin
Yu, Yan-Min
Wang, Xia-Yan
Yu, Shu-Yan
author_sort Wang, Ji
collection PubMed
description Here, we report a design strategy for constructing supramolecular organic frameworks by introducing (1)H-pyrazole groups to aromatic cores as non-coplanar molecules to form diverse supramolecular assemblies through multiple (1)H-pyrazole [N−H···N] hydrogen bonds as well as other weak interactions. The new supramolecular organic frameworks displayed interesting crystallization-induced emission (CIE) behavior.
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spelling pubmed-90268522022-04-23 Supramolecular Hydrogen Bonding Assembly from Non-Coplanar Aromatic Tetra-(1)H-Pyrazoles with Crystallization-Induced Emission (CIE) Wang, Ji Zhao, Li-Rong Tong, Jin Yu, Yan-Min Wang, Xia-Yan Yu, Shu-Yan Int J Mol Sci Communication Here, we report a design strategy for constructing supramolecular organic frameworks by introducing (1)H-pyrazole groups to aromatic cores as non-coplanar molecules to form diverse supramolecular assemblies through multiple (1)H-pyrazole [N−H···N] hydrogen bonds as well as other weak interactions. The new supramolecular organic frameworks displayed interesting crystallization-induced emission (CIE) behavior. MDPI 2022-04-11 /pmc/articles/PMC9026852/ /pubmed/35457024 http://dx.doi.org/10.3390/ijms23084206 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Wang, Ji
Zhao, Li-Rong
Tong, Jin
Yu, Yan-Min
Wang, Xia-Yan
Yu, Shu-Yan
Supramolecular Hydrogen Bonding Assembly from Non-Coplanar Aromatic Tetra-(1)H-Pyrazoles with Crystallization-Induced Emission (CIE)
title Supramolecular Hydrogen Bonding Assembly from Non-Coplanar Aromatic Tetra-(1)H-Pyrazoles with Crystallization-Induced Emission (CIE)
title_full Supramolecular Hydrogen Bonding Assembly from Non-Coplanar Aromatic Tetra-(1)H-Pyrazoles with Crystallization-Induced Emission (CIE)
title_fullStr Supramolecular Hydrogen Bonding Assembly from Non-Coplanar Aromatic Tetra-(1)H-Pyrazoles with Crystallization-Induced Emission (CIE)
title_full_unstemmed Supramolecular Hydrogen Bonding Assembly from Non-Coplanar Aromatic Tetra-(1)H-Pyrazoles with Crystallization-Induced Emission (CIE)
title_short Supramolecular Hydrogen Bonding Assembly from Non-Coplanar Aromatic Tetra-(1)H-Pyrazoles with Crystallization-Induced Emission (CIE)
title_sort supramolecular hydrogen bonding assembly from non-coplanar aromatic tetra-(1)h-pyrazoles with crystallization-induced emission (cie)
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9026852/
https://www.ncbi.nlm.nih.gov/pubmed/35457024
http://dx.doi.org/10.3390/ijms23084206
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