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Selective Intramolecular Dehydrocyclization of Co-Porphyrin on Au(111)
The on-surface C–H bond activation and coupling reaction is a powerful approach to constructing fine-tuned surface nanostructures. It is quite challenging to control its regioselectivity due to the inertness of the C–H bond involved. With scanning tunneling microscopy/spectroscopy and theoretical ca...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7503656/ https://www.ncbi.nlm.nih.gov/pubmed/32824933 http://dx.doi.org/10.3390/molecules25173766 |
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author | Yin, Cen Peng, Zhantao Liu, Dan Song, Huanjun Zhu, Hao Chen, Qiwei Wu, Kai |
author_facet | Yin, Cen Peng, Zhantao Liu, Dan Song, Huanjun Zhu, Hao Chen, Qiwei Wu, Kai |
author_sort | Yin, Cen |
collection | PubMed |
description | The on-surface C–H bond activation and coupling reaction is a powerful approach to constructing fine-tuned surface nanostructures. It is quite challenging to control its regioselectivity due to the inertness of the C–H bond involved. With scanning tunneling microscopy/spectroscopy and theoretical calculations, the C–H activation and sequential intramolecular dehydrocyclization of meso-tetra(p-methoxyphenyl)porphyrinatocobalt(II) was explored on Au(111), showing that the methoxy groups in the molecule could kinetically mediate the selectivity of the intramolecular reaction over its intermolecular coupling counterpart. The experimental results demonstrate that the introduced protecting group could help augment the selectivity of such on-surface reaction, which can be applied to the precise fabrication of functional surface nanostructures. |
format | Online Article Text |
id | pubmed-7503656 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-75036562020-09-27 Selective Intramolecular Dehydrocyclization of Co-Porphyrin on Au(111) Yin, Cen Peng, Zhantao Liu, Dan Song, Huanjun Zhu, Hao Chen, Qiwei Wu, Kai Molecules Communication The on-surface C–H bond activation and coupling reaction is a powerful approach to constructing fine-tuned surface nanostructures. It is quite challenging to control its regioselectivity due to the inertness of the C–H bond involved. With scanning tunneling microscopy/spectroscopy and theoretical calculations, the C–H activation and sequential intramolecular dehydrocyclization of meso-tetra(p-methoxyphenyl)porphyrinatocobalt(II) was explored on Au(111), showing that the methoxy groups in the molecule could kinetically mediate the selectivity of the intramolecular reaction over its intermolecular coupling counterpart. The experimental results demonstrate that the introduced protecting group could help augment the selectivity of such on-surface reaction, which can be applied to the precise fabrication of functional surface nanostructures. MDPI 2020-08-19 /pmc/articles/PMC7503656/ /pubmed/32824933 http://dx.doi.org/10.3390/molecules25173766 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Yin, Cen Peng, Zhantao Liu, Dan Song, Huanjun Zhu, Hao Chen, Qiwei Wu, Kai Selective Intramolecular Dehydrocyclization of Co-Porphyrin on Au(111) |
title | Selective Intramolecular Dehydrocyclization of Co-Porphyrin on Au(111) |
title_full | Selective Intramolecular Dehydrocyclization of Co-Porphyrin on Au(111) |
title_fullStr | Selective Intramolecular Dehydrocyclization of Co-Porphyrin on Au(111) |
title_full_unstemmed | Selective Intramolecular Dehydrocyclization of Co-Porphyrin on Au(111) |
title_short | Selective Intramolecular Dehydrocyclization of Co-Porphyrin on Au(111) |
title_sort | selective intramolecular dehydrocyclization of co-porphyrin on au(111) |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7503656/ https://www.ncbi.nlm.nih.gov/pubmed/32824933 http://dx.doi.org/10.3390/molecules25173766 |
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