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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...

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Detalles Bibliográficos
Autores principales: Yin, Cen, Peng, Zhantao, Liu, Dan, Song, Huanjun, Zhu, Hao, Chen, Qiwei, Wu, Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
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.
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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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