Structural and Nanotribological Properties of a BODIPY Self-Assembly
Boron-dipyrromethenes (BODIPY) are promising functional dyes, whose exceptional optical properties are closely related to their supramolecular assembly. Herein, the self-assembly of a BODIPY derivative functionalized with uracil groups is explicitly and thoroughly investigated by using scanning tunn...
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2021-08-01
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Online Access: | https://www.frontiersin.org/articles/10.3389/fchem.2021.704915/full |
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doaj-6a5e603227bc47928cf5165307fb43a92021-08-06T05:14:20ZengFrontiers Media S.A.Frontiers in Chemistry2296-26462021-08-01910.3389/fchem.2021.704915704915Structural and Nanotribological Properties of a BODIPY Self-AssemblyShanchao Tan0Shanchao Tan1Wendi Luo2Yongjie Zhang3Xiang-Kui Ren4Yuhong Liu5Zhijian Chen6Qingdao Zeng7Qingdao Zeng8State Key Laboratory of Tribology, Tsinghua University, Beijing, ChinaCAS Key Laboratory of Standardization and Measurement for Nanotechnology, CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology (NCNST), Beijing, ChinaLaboratory of Theoretical and Computational Nanoscience, CAS Key Laboratory of Nanophotonic Materials and Devices, CAS Center for Excellence in Nanoscience, Beijing Key Laboratory of Ambient Particles Health Effects and Prevention Techniques, National Center for Nanoscience and Technology, Chinese Academy of Sciences, Beijing, ChinaSchool of Chemical Engineering and Technology, Tianjin University, Tianjin, ChinaSchool of Chemical Engineering and Technology, Tianjin University, Tianjin, ChinaState Key Laboratory of Tribology, Tsinghua University, Beijing, ChinaSchool of Chemical Engineering and Technology, Tianjin University, Tianjin, ChinaCAS Key Laboratory of Standardization and Measurement for Nanotechnology, CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology (NCNST), Beijing, ChinaCenter of Materials Science and Optoelectonics Engineering, University of Chinese Academy of Sciences, Beijing, ChinaBoron-dipyrromethenes (BODIPY) are promising functional dyes, whose exceptional optical properties are closely related to their supramolecular assembly. Herein, the self-assembly of a BODIPY derivative functionalized with uracil groups is explicitly and thoroughly investigated by using scanning tunneling microscopy (STM). Based on the simulation and calculation by density functional theory (DFT) method, it can be concluded that the construction of ordered self-assembly structure is attributed to the formation of hydrogen bonds between uracil groups. Moreover, the nanotribological property of the self-assembly on HOPG surface is measured by using atomic force microscopy (AFM). The effort on self-assembly of the BODIPY derivative could enhance the understanding of surface assembly mechanism.https://www.frontiersin.org/articles/10.3389/fchem.2021.704915/fullself-assemblybodipy dyescanning tunneling microscopynanotribologyhydrogen bond |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Shanchao Tan Shanchao Tan Wendi Luo Yongjie Zhang Xiang-Kui Ren Yuhong Liu Zhijian Chen Qingdao Zeng Qingdao Zeng |
spellingShingle |
Shanchao Tan Shanchao Tan Wendi Luo Yongjie Zhang Xiang-Kui Ren Yuhong Liu Zhijian Chen Qingdao Zeng Qingdao Zeng Structural and Nanotribological Properties of a BODIPY Self-Assembly Frontiers in Chemistry self-assembly bodipy dye scanning tunneling microscopy nanotribology hydrogen bond |
author_facet |
Shanchao Tan Shanchao Tan Wendi Luo Yongjie Zhang Xiang-Kui Ren Yuhong Liu Zhijian Chen Qingdao Zeng Qingdao Zeng |
author_sort |
Shanchao Tan |
title |
Structural and Nanotribological Properties of a BODIPY Self-Assembly |
title_short |
Structural and Nanotribological Properties of a BODIPY Self-Assembly |
title_full |
Structural and Nanotribological Properties of a BODIPY Self-Assembly |
title_fullStr |
Structural and Nanotribological Properties of a BODIPY Self-Assembly |
title_full_unstemmed |
Structural and Nanotribological Properties of a BODIPY Self-Assembly |
title_sort |
structural and nanotribological properties of a bodipy self-assembly |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Chemistry |
issn |
2296-2646 |
publishDate |
2021-08-01 |
description |
Boron-dipyrromethenes (BODIPY) are promising functional dyes, whose exceptional optical properties are closely related to their supramolecular assembly. Herein, the self-assembly of a BODIPY derivative functionalized with uracil groups is explicitly and thoroughly investigated by using scanning tunneling microscopy (STM). Based on the simulation and calculation by density functional theory (DFT) method, it can be concluded that the construction of ordered self-assembly structure is attributed to the formation of hydrogen bonds between uracil groups. Moreover, the nanotribological property of the self-assembly on HOPG surface is measured by using atomic force microscopy (AFM). The effort on self-assembly of the BODIPY derivative could enhance the understanding of surface assembly mechanism. |
topic |
self-assembly bodipy dye scanning tunneling microscopy nanotribology hydrogen bond |
url |
https://www.frontiersin.org/articles/10.3389/fchem.2021.704915/full |
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