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Complexes of Dichlorogermylene with Phosphine/Sulfoxide-Supported Carbone as Ligand †

Due to their remarkable electronic features, recent years have witnessed the emergence of carbones L(2)C, which consist in two donating L ligands coordinating a central carbon atom bearing two lone pairs. In this context, the phosphine/sulfoxide-supported carbone 4 exhibits a strong nucleophilic cha...

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Autores principales: Authesserre, Ugo, Hameury, Sophie, Dajnak, Aymeric, Saffon-Merceron, Nathalie, Baceiredo, Antoine, Madec, David, Maerten, Eddy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8037485/
https://www.ncbi.nlm.nih.gov/pubmed/33916075
http://dx.doi.org/10.3390/molecules26072005
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author Authesserre, Ugo
Hameury, Sophie
Dajnak, Aymeric
Saffon-Merceron, Nathalie
Baceiredo, Antoine
Madec, David
Maerten, Eddy
author_facet Authesserre, Ugo
Hameury, Sophie
Dajnak, Aymeric
Saffon-Merceron, Nathalie
Baceiredo, Antoine
Madec, David
Maerten, Eddy
author_sort Authesserre, Ugo
collection PubMed
description Due to their remarkable electronic features, recent years have witnessed the emergence of carbones L(2)C, which consist in two donating L ligands coordinating a central carbon atom bearing two lone pairs. In this context, the phosphine/sulfoxide-supported carbone 4 exhibits a strong nucleophilic character, and here, we describe its ability to coordinate dichlorogermylene. Two original stable coordination complexes were obtained and fully characterized in solution and in the solid state by NMR spectroscopy and X-ray diffraction analysis, respectively. At 60 °C, in the presence of 4, the Ge(II)-complex 5 undergoes a slow isomerization that transforms the bis-ylide ligand into an yldiide.
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spelling pubmed-80374852021-04-12 Complexes of Dichlorogermylene with Phosphine/Sulfoxide-Supported Carbone as Ligand † Authesserre, Ugo Hameury, Sophie Dajnak, Aymeric Saffon-Merceron, Nathalie Baceiredo, Antoine Madec, David Maerten, Eddy Molecules Article Due to their remarkable electronic features, recent years have witnessed the emergence of carbones L(2)C, which consist in two donating L ligands coordinating a central carbon atom bearing two lone pairs. In this context, the phosphine/sulfoxide-supported carbone 4 exhibits a strong nucleophilic character, and here, we describe its ability to coordinate dichlorogermylene. Two original stable coordination complexes were obtained and fully characterized in solution and in the solid state by NMR spectroscopy and X-ray diffraction analysis, respectively. At 60 °C, in the presence of 4, the Ge(II)-complex 5 undergoes a slow isomerization that transforms the bis-ylide ligand into an yldiide. MDPI 2021-04-01 /pmc/articles/PMC8037485/ /pubmed/33916075 http://dx.doi.org/10.3390/molecules26072005 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Authesserre, Ugo
Hameury, Sophie
Dajnak, Aymeric
Saffon-Merceron, Nathalie
Baceiredo, Antoine
Madec, David
Maerten, Eddy
Complexes of Dichlorogermylene with Phosphine/Sulfoxide-Supported Carbone as Ligand †
title Complexes of Dichlorogermylene with Phosphine/Sulfoxide-Supported Carbone as Ligand †
title_full Complexes of Dichlorogermylene with Phosphine/Sulfoxide-Supported Carbone as Ligand †
title_fullStr Complexes of Dichlorogermylene with Phosphine/Sulfoxide-Supported Carbone as Ligand †
title_full_unstemmed Complexes of Dichlorogermylene with Phosphine/Sulfoxide-Supported Carbone as Ligand †
title_short Complexes of Dichlorogermylene with Phosphine/Sulfoxide-Supported Carbone as Ligand †
title_sort complexes of dichlorogermylene with phosphine/sulfoxide-supported carbone as ligand †
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8037485/
https://www.ncbi.nlm.nih.gov/pubmed/33916075
http://dx.doi.org/10.3390/molecules26072005
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