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Self-assembly directed one-step synthesis of [4]radialene on Cu(100) surfaces
The synthetic challenges of radialenes have precluded their practical applications. Here, we report a one-step synthetic protocol of [4]radialene on a copper surface. High-resolution scanning tunneling microscopy measurements reveal that such catalytic reaction proceeds readily with high selectivity...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6078953/ https://www.ncbi.nlm.nih.gov/pubmed/30082699 http://dx.doi.org/10.1038/s41467-018-05472-2 |
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author | Li, Qing Gao, Jianzhi Li, Youyong Fuentes-Cabrera, Miguel Liu, Mengxi Qiu, Xiaohui Lin, Haiping Chi, Lifeng Pan, Minghu |
author_facet | Li, Qing Gao, Jianzhi Li, Youyong Fuentes-Cabrera, Miguel Liu, Mengxi Qiu, Xiaohui Lin, Haiping Chi, Lifeng Pan, Minghu |
author_sort | Li, Qing |
collection | PubMed |
description | The synthetic challenges of radialenes have precluded their practical applications. Here, we report a one-step synthetic protocol of [4]radialene on a copper surface. High-resolution scanning tunneling microscopy measurements reveal that such catalytic reaction proceeds readily with high selectivity at the temperature below 120 K. First-principles calculations show that the reaction pathway is characterized by firstly the cooperative inter-molecular hydrogen tautomerization and then the C–C bond formation. The feasibility of such cyclotetramerization reaction can be interpreted by the surface effect of Cu(100), which firstly plays an important role in directing the molecular assembly and then serves as an active catalyst in the hydrogen tautomerization and C–C coupling processes. This work presents not only a novel strategy to the scant number of synthetic methods to produce [4]radialenes via a novel [1 + 1 + 1 + 1] reaction pathway, but also a successful example of C–C bond coupling reactions guided by the surface-induced C–H/π assembly. |
format | Online Article Text |
id | pubmed-6078953 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60789532018-08-08 Self-assembly directed one-step synthesis of [4]radialene on Cu(100) surfaces Li, Qing Gao, Jianzhi Li, Youyong Fuentes-Cabrera, Miguel Liu, Mengxi Qiu, Xiaohui Lin, Haiping Chi, Lifeng Pan, Minghu Nat Commun Article The synthetic challenges of radialenes have precluded their practical applications. Here, we report a one-step synthetic protocol of [4]radialene on a copper surface. High-resolution scanning tunneling microscopy measurements reveal that such catalytic reaction proceeds readily with high selectivity at the temperature below 120 K. First-principles calculations show that the reaction pathway is characterized by firstly the cooperative inter-molecular hydrogen tautomerization and then the C–C bond formation. The feasibility of such cyclotetramerization reaction can be interpreted by the surface effect of Cu(100), which firstly plays an important role in directing the molecular assembly and then serves as an active catalyst in the hydrogen tautomerization and C–C coupling processes. This work presents not only a novel strategy to the scant number of synthetic methods to produce [4]radialenes via a novel [1 + 1 + 1 + 1] reaction pathway, but also a successful example of C–C bond coupling reactions guided by the surface-induced C–H/π assembly. Nature Publishing Group UK 2018-08-06 /pmc/articles/PMC6078953/ /pubmed/30082699 http://dx.doi.org/10.1038/s41467-018-05472-2 Text en © The Author(s) 2018 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/. |
spellingShingle | Article Li, Qing Gao, Jianzhi Li, Youyong Fuentes-Cabrera, Miguel Liu, Mengxi Qiu, Xiaohui Lin, Haiping Chi, Lifeng Pan, Minghu Self-assembly directed one-step synthesis of [4]radialene on Cu(100) surfaces |
title | Self-assembly directed one-step synthesis of [4]radialene on Cu(100) surfaces |
title_full | Self-assembly directed one-step synthesis of [4]radialene on Cu(100) surfaces |
title_fullStr | Self-assembly directed one-step synthesis of [4]radialene on Cu(100) surfaces |
title_full_unstemmed | Self-assembly directed one-step synthesis of [4]radialene on Cu(100) surfaces |
title_short | Self-assembly directed one-step synthesis of [4]radialene on Cu(100) surfaces |
title_sort | self-assembly directed one-step synthesis of [4]radialene on cu(100) surfaces |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6078953/ https://www.ncbi.nlm.nih.gov/pubmed/30082699 http://dx.doi.org/10.1038/s41467-018-05472-2 |
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