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Multistimuli‐Responsive [3]Dioxaphosphaferrocenophanes with Orthogonal Switches
Novel multistimuli‐responsive phosphine ligands comprising a redox‐active [3]dioxaphosphaferrocenophane backbone and a P‐bound imidazolin‐2‐ylidenamino entity that allows switching by protonation are reported. Investigation of the corresponding metal complexes and their redox behaviour are reported...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8596786/ https://www.ncbi.nlm.nih.gov/pubmed/34459528 http://dx.doi.org/10.1002/chem.202101969 |
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author | Birenheide, Bernhard S. Krämer, Felix Bayer, Lea Mehlmann, Paul Dielmann, Fabian Breher, Frank |
author_facet | Birenheide, Bernhard S. Krämer, Felix Bayer, Lea Mehlmann, Paul Dielmann, Fabian Breher, Frank |
author_sort | Birenheide, Bernhard S. |
collection | PubMed |
description | Novel multistimuli‐responsive phosphine ligands comprising a redox‐active [3]dioxaphosphaferrocenophane backbone and a P‐bound imidazolin‐2‐ylidenamino entity that allows switching by protonation are reported. Investigation of the corresponding metal complexes and their redox behaviour are reported and show the sensitivity of the system towards protonation and metal coordination. The experimental findings are supported by DFT calculations. Protonation and oxidation events are applied in Rh‐catalysed hydrosilylations and demonstrate a remarkable influence on reactivity and/or selectivity. |
format | Online Article Text |
id | pubmed-8596786 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85967862021-11-22 Multistimuli‐Responsive [3]Dioxaphosphaferrocenophanes with Orthogonal Switches Birenheide, Bernhard S. Krämer, Felix Bayer, Lea Mehlmann, Paul Dielmann, Fabian Breher, Frank Chemistry Communications Novel multistimuli‐responsive phosphine ligands comprising a redox‐active [3]dioxaphosphaferrocenophane backbone and a P‐bound imidazolin‐2‐ylidenamino entity that allows switching by protonation are reported. Investigation of the corresponding metal complexes and their redox behaviour are reported and show the sensitivity of the system towards protonation and metal coordination. The experimental findings are supported by DFT calculations. Protonation and oxidation events are applied in Rh‐catalysed hydrosilylations and demonstrate a remarkable influence on reactivity and/or selectivity. John Wiley and Sons Inc. 2021-09-06 2021-11-02 /pmc/articles/PMC8596786/ /pubmed/34459528 http://dx.doi.org/10.1002/chem.202101969 Text en © 2021 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Communications Birenheide, Bernhard S. Krämer, Felix Bayer, Lea Mehlmann, Paul Dielmann, Fabian Breher, Frank Multistimuli‐Responsive [3]Dioxaphosphaferrocenophanes with Orthogonal Switches |
title | Multistimuli‐Responsive [3]Dioxaphosphaferrocenophanes with Orthogonal Switches |
title_full | Multistimuli‐Responsive [3]Dioxaphosphaferrocenophanes with Orthogonal Switches |
title_fullStr | Multistimuli‐Responsive [3]Dioxaphosphaferrocenophanes with Orthogonal Switches |
title_full_unstemmed | Multistimuli‐Responsive [3]Dioxaphosphaferrocenophanes with Orthogonal Switches |
title_short | Multistimuli‐Responsive [3]Dioxaphosphaferrocenophanes with Orthogonal Switches |
title_sort | multistimuli‐responsive [3]dioxaphosphaferrocenophanes with orthogonal switches |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8596786/ https://www.ncbi.nlm.nih.gov/pubmed/34459528 http://dx.doi.org/10.1002/chem.202101969 |
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