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On-surface synthesis and spontaneous segregation of conjugated tetraphenylethylene macrocycles
Creating conjugated macrocycles has attracted extensive research interest because their unique chemical and physical properties, such as conformational flexibility, intrinsic inner cavities and aromaticity/antiaromaticity, make these systems appealing building blocks for functional supramolecular ma...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9814618/ https://www.ncbi.nlm.nih.gov/pubmed/36697742 http://dx.doi.org/10.1038/s42004-022-00794-1 |
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author | Li, En Lyu, Cheng-Kun Chen, Chengyi Xie, Huilin Zhang, Jianyu Lam, Jacky Wing Yip Tang, Ben Zhong Lin, Nian |
author_facet | Li, En Lyu, Cheng-Kun Chen, Chengyi Xie, Huilin Zhang, Jianyu Lam, Jacky Wing Yip Tang, Ben Zhong Lin, Nian |
author_sort | Li, En |
collection | PubMed |
description | Creating conjugated macrocycles has attracted extensive research interest because their unique chemical and physical properties, such as conformational flexibility, intrinsic inner cavities and aromaticity/antiaromaticity, make these systems appealing building blocks for functional supramolecular materials. Here, we report the synthesis of four-, six- and eight-membered tetraphenylethylene (TPE)-based macrocycles on Ag(111) via on-surface Ullmann coupling reactions. The as-synthesized macrocycles are spontaneously segregated on the surface and self-assemble as large-area two-dimensional mono-component supramolecular crystals, as characterized by scanning tunneling microscopy (STM). We propose that the synthesis benefits from the conformational flexibility of the TPE backbone in distinctive multi-step reaction pathways. This study opens up opportunities for exploring the photophysical properties of TPE-based macrocycles. |
format | Online Article Text |
id | pubmed-9814618 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98146182023-01-10 On-surface synthesis and spontaneous segregation of conjugated tetraphenylethylene macrocycles Li, En Lyu, Cheng-Kun Chen, Chengyi Xie, Huilin Zhang, Jianyu Lam, Jacky Wing Yip Tang, Ben Zhong Lin, Nian Commun Chem Article Creating conjugated macrocycles has attracted extensive research interest because their unique chemical and physical properties, such as conformational flexibility, intrinsic inner cavities and aromaticity/antiaromaticity, make these systems appealing building blocks for functional supramolecular materials. Here, we report the synthesis of four-, six- and eight-membered tetraphenylethylene (TPE)-based macrocycles on Ag(111) via on-surface Ullmann coupling reactions. The as-synthesized macrocycles are spontaneously segregated on the surface and self-assemble as large-area two-dimensional mono-component supramolecular crystals, as characterized by scanning tunneling microscopy (STM). We propose that the synthesis benefits from the conformational flexibility of the TPE backbone in distinctive multi-step reaction pathways. This study opens up opportunities for exploring the photophysical properties of TPE-based macrocycles. Nature Publishing Group UK 2022-12-22 /pmc/articles/PMC9814618/ /pubmed/36697742 http://dx.doi.org/10.1038/s42004-022-00794-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Li, En Lyu, Cheng-Kun Chen, Chengyi Xie, Huilin Zhang, Jianyu Lam, Jacky Wing Yip Tang, Ben Zhong Lin, Nian On-surface synthesis and spontaneous segregation of conjugated tetraphenylethylene macrocycles |
title | On-surface synthesis and spontaneous segregation of conjugated tetraphenylethylene macrocycles |
title_full | On-surface synthesis and spontaneous segregation of conjugated tetraphenylethylene macrocycles |
title_fullStr | On-surface synthesis and spontaneous segregation of conjugated tetraphenylethylene macrocycles |
title_full_unstemmed | On-surface synthesis and spontaneous segregation of conjugated tetraphenylethylene macrocycles |
title_short | On-surface synthesis and spontaneous segregation of conjugated tetraphenylethylene macrocycles |
title_sort | on-surface synthesis and spontaneous segregation of conjugated tetraphenylethylene macrocycles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9814618/ https://www.ncbi.nlm.nih.gov/pubmed/36697742 http://dx.doi.org/10.1038/s42004-022-00794-1 |
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