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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
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.
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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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