Supramolecular Hydrogen Bonding Assembly from Non-Coplanar Aromatic Tetra-<sup>1</sup>H-Pyrazoles with Crystallization-Induced Emission (CIE)
Here, we report a design strategy for constructing supramolecular organic frameworks by introducing <sup>1</sup>H-pyrazole groups to aromatic cores as non-coplanar molecules to form diverse supramolecular assemblies through multiple <sup>1</sup>H-pyrazole [N−H···N] hydrogen b...
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MDPI AG
2022-04-01
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Series: | International Journal of Molecular Sciences |
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Online Access: | https://www.mdpi.com/1422-0067/23/8/4206 |
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author | Ji Wang Li-Rong Zhao Jin Tong Yan-Min Yu Xia-Yan Wang Shu-Yan Yu |
author_facet | Ji Wang Li-Rong Zhao Jin Tong Yan-Min Yu Xia-Yan Wang Shu-Yan Yu |
author_sort | Ji Wang |
collection | DOAJ |
description | Here, we report a design strategy for constructing supramolecular organic frameworks by introducing <sup>1</sup>H-pyrazole groups to aromatic cores as non-coplanar molecules to form diverse supramolecular assemblies through multiple <sup>1</sup>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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id | doaj.art-109611b871dc4c2f8b63bf87f9c0cf81 |
institution | Directory Open Access Journal |
issn | 1661-6596 1422-0067 |
language | English |
last_indexed | 2024-03-09T10:33:43Z |
publishDate | 2022-04-01 |
publisher | MDPI AG |
record_format | Article |
series | International Journal of Molecular Sciences |
spelling | doaj.art-109611b871dc4c2f8b63bf87f9c0cf812023-12-01T21:02:56ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672022-04-01238420610.3390/ijms23084206Supramolecular Hydrogen Bonding Assembly from Non-Coplanar Aromatic Tetra-<sup>1</sup>H-Pyrazoles with Crystallization-Induced Emission (CIE)Ji Wang0Li-Rong Zhao1Jin Tong2Yan-Min Yu3Xia-Yan Wang4Shu-Yan Yu5Center of Excellence for Environmental Safety and Biological Effects, Beijing Key Laboratory for Green Catalysis and Separation, Department of Chemistry and Biology, Beijing University of Technology, Beijing 100124, ChinaCenter of Excellence for Environmental Safety and Biological Effects, Beijing Key Laboratory for Green Catalysis and Separation, Department of Chemistry and Biology, Beijing University of Technology, Beijing 100124, ChinaCenter of Excellence for Environmental Safety and Biological Effects, Beijing Key Laboratory for Green Catalysis and Separation, Department of Chemistry and Biology, Beijing University of Technology, Beijing 100124, ChinaCenter of Excellence for Environmental Safety and Biological Effects, Beijing Key Laboratory for Green Catalysis and Separation, Department of Chemistry and Biology, Beijing University of Technology, Beijing 100124, ChinaCenter of Excellence for Environmental Safety and Biological Effects, Beijing Key Laboratory for Green Catalysis and Separation, Department of Chemistry and Biology, Beijing University of Technology, Beijing 100124, ChinaCenter of Excellence for Environmental Safety and Biological Effects, Beijing Key Laboratory for Green Catalysis and Separation, Department of Chemistry and Biology, Beijing University of Technology, Beijing 100124, ChinaHere, we report a design strategy for constructing supramolecular organic frameworks by introducing <sup>1</sup>H-pyrazole groups to aromatic cores as non-coplanar molecules to form diverse supramolecular assemblies through multiple <sup>1</sup>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.https://www.mdpi.com/1422-0067/23/8/4206supramolecular assemblyhydrogen bondingaromatic multi-<sup>1</sup>H-pyrazolescrystallization-induced emission (CIE) |
spellingShingle | Ji Wang Li-Rong Zhao Jin Tong Yan-Min Yu Xia-Yan Wang Shu-Yan Yu Supramolecular Hydrogen Bonding Assembly from Non-Coplanar Aromatic Tetra-<sup>1</sup>H-Pyrazoles with Crystallization-Induced Emission (CIE) International Journal of Molecular Sciences supramolecular assembly hydrogen bonding aromatic multi-<sup>1</sup>H-pyrazoles crystallization-induced emission (CIE) |
title | Supramolecular Hydrogen Bonding Assembly from Non-Coplanar Aromatic Tetra-<sup>1</sup>H-Pyrazoles with Crystallization-Induced Emission (CIE) |
title_full | Supramolecular Hydrogen Bonding Assembly from Non-Coplanar Aromatic Tetra-<sup>1</sup>H-Pyrazoles with Crystallization-Induced Emission (CIE) |
title_fullStr | Supramolecular Hydrogen Bonding Assembly from Non-Coplanar Aromatic Tetra-<sup>1</sup>H-Pyrazoles with Crystallization-Induced Emission (CIE) |
title_full_unstemmed | Supramolecular Hydrogen Bonding Assembly from Non-Coplanar Aromatic Tetra-<sup>1</sup>H-Pyrazoles with Crystallization-Induced Emission (CIE) |
title_short | Supramolecular Hydrogen Bonding Assembly from Non-Coplanar Aromatic Tetra-<sup>1</sup>H-Pyrazoles with Crystallization-Induced Emission (CIE) |
title_sort | supramolecular hydrogen bonding assembly from non coplanar aromatic tetra sup 1 sup h pyrazoles with crystallization induced emission cie |
topic | supramolecular assembly hydrogen bonding aromatic multi-<sup>1</sup>H-pyrazoles crystallization-induced emission (CIE) |
url | https://www.mdpi.com/1422-0067/23/8/4206 |
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