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N‐Heterocyclic Carbenes: Molecular Porters of Surface Mounted Ru‐Porphyrins
Ru‐porphyrins act as convenient pedestals for the assembly of N‐heterocyclic carbenes (NHCs) on solid surfaces. Upon deposition of a simple NHC ligand on a close packed Ru‐porphyrin monolayer, an extraordinary phenomenon can be observed: Ru‐porphyrin molecules are transferred from the silver surface...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092334/ https://www.ncbi.nlm.nih.gov/pubmed/36200438 http://dx.doi.org/10.1002/anie.202211877 |
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author | Knecht, Peter Meier, Dennis Reichert, Joachim Duncan, David A. Schwarz, Martin Küchle, Johannes T. Lee, Tien‐Lin Deimel, Peter S. Feulner, Peter Allegretti, Francesco Auwärter, Willi Médard, Guillaume Seitsonen, Ari Paavo Barth, Johannes V. Papageorgiou, Anthoula C. |
author_facet | Knecht, Peter Meier, Dennis Reichert, Joachim Duncan, David A. Schwarz, Martin Küchle, Johannes T. Lee, Tien‐Lin Deimel, Peter S. Feulner, Peter Allegretti, Francesco Auwärter, Willi Médard, Guillaume Seitsonen, Ari Paavo Barth, Johannes V. Papageorgiou, Anthoula C. |
author_sort | Knecht, Peter |
collection | PubMed |
description | Ru‐porphyrins act as convenient pedestals for the assembly of N‐heterocyclic carbenes (NHCs) on solid surfaces. Upon deposition of a simple NHC ligand on a close packed Ru‐porphyrin monolayer, an extraordinary phenomenon can be observed: Ru‐porphyrin molecules are transferred from the silver surface to the next molecular layer. We have investigated the structural features and dynamics of this portering process and analysed the associated binding strengths and work function changes. A rearrangement of the molecular layer is induced by the NHC uptake: the NHC selective binding to the Ru causes the ejection of whole porphyrin molecules from the molecular layer on silver to the layer on top. This reorganisation can be reversed by thermally induced desorption of the NHC ligand. We anticipate that the understanding of such mass transport processes will have crucial implications for the functionalisation of surfaces with carbenes. |
format | Online Article Text |
id | pubmed-10092334 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100923342023-04-13 N‐Heterocyclic Carbenes: Molecular Porters of Surface Mounted Ru‐Porphyrins Knecht, Peter Meier, Dennis Reichert, Joachim Duncan, David A. Schwarz, Martin Küchle, Johannes T. Lee, Tien‐Lin Deimel, Peter S. Feulner, Peter Allegretti, Francesco Auwärter, Willi Médard, Guillaume Seitsonen, Ari Paavo Barth, Johannes V. Papageorgiou, Anthoula C. Angew Chem Int Ed Engl Research Articles Ru‐porphyrins act as convenient pedestals for the assembly of N‐heterocyclic carbenes (NHCs) on solid surfaces. Upon deposition of a simple NHC ligand on a close packed Ru‐porphyrin monolayer, an extraordinary phenomenon can be observed: Ru‐porphyrin molecules are transferred from the silver surface to the next molecular layer. We have investigated the structural features and dynamics of this portering process and analysed the associated binding strengths and work function changes. A rearrangement of the molecular layer is induced by the NHC uptake: the NHC selective binding to the Ru causes the ejection of whole porphyrin molecules from the molecular layer on silver to the layer on top. This reorganisation can be reversed by thermally induced desorption of the NHC ligand. We anticipate that the understanding of such mass transport processes will have crucial implications for the functionalisation of surfaces with carbenes. John Wiley and Sons Inc. 2022-11-02 2022-12-05 /pmc/articles/PMC10092334/ /pubmed/36200438 http://dx.doi.org/10.1002/anie.202211877 Text en © 2022 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Knecht, Peter Meier, Dennis Reichert, Joachim Duncan, David A. Schwarz, Martin Küchle, Johannes T. Lee, Tien‐Lin Deimel, Peter S. Feulner, Peter Allegretti, Francesco Auwärter, Willi Médard, Guillaume Seitsonen, Ari Paavo Barth, Johannes V. Papageorgiou, Anthoula C. N‐Heterocyclic Carbenes: Molecular Porters of Surface Mounted Ru‐Porphyrins |
title | N‐Heterocyclic Carbenes: Molecular Porters of Surface Mounted Ru‐Porphyrins |
title_full | N‐Heterocyclic Carbenes: Molecular Porters of Surface Mounted Ru‐Porphyrins |
title_fullStr | N‐Heterocyclic Carbenes: Molecular Porters of Surface Mounted Ru‐Porphyrins |
title_full_unstemmed | N‐Heterocyclic Carbenes: Molecular Porters of Surface Mounted Ru‐Porphyrins |
title_short | N‐Heterocyclic Carbenes: Molecular Porters of Surface Mounted Ru‐Porphyrins |
title_sort | n‐heterocyclic carbenes: molecular porters of surface mounted ru‐porphyrins |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092334/ https://www.ncbi.nlm.nih.gov/pubmed/36200438 http://dx.doi.org/10.1002/anie.202211877 |
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