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Dibismuthanes in catalysis: from synthesis and characterization to redox behavior towards oxidative cleavage of 1,2-diols

A family of aryl dinuclear bismuthane complexes has been successfully synthesized and characterized. The two bismuth centers are bonded to various xanthene-type backbones, which differ in ring-size and flexibility, resulting in complexes with different intramolecular Bi⋯Bi distances. Moreover, their...

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Detalles Bibliográficos
Autores principales: Magre, Marc, Kuziola, Jennifer, Nöthling, Nils, Cornella, Josep
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8188851/
https://www.ncbi.nlm.nih.gov/pubmed/33955447
http://dx.doi.org/10.1039/d1ob00367d
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author Magre, Marc
Kuziola, Jennifer
Nöthling, Nils
Cornella, Josep
author_facet Magre, Marc
Kuziola, Jennifer
Nöthling, Nils
Cornella, Josep
author_sort Magre, Marc
collection PubMed
description A family of aryl dinuclear bismuthane complexes has been successfully synthesized and characterized. The two bismuth centers are bonded to various xanthene-type backbones, which differ in ring-size and flexibility, resulting in complexes with different intramolecular Bi⋯Bi distances. Moreover, their pentavalent Bi(v) analogues have also been prepared and structurally characterized. Finally, the synergy between bismuth centers in catalysis has been studied by applying dinuclear bismuthanes 5–8 to the catalytic oxidative cleavage of 1,2-diols. Unfortunately, no synergistic effects were observed and the catalytic activities of dinuclear bismuthanes and triphenylbismuth are comparable.
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spelling pubmed-81888512021-06-23 Dibismuthanes in catalysis: from synthesis and characterization to redox behavior towards oxidative cleavage of 1,2-diols Magre, Marc Kuziola, Jennifer Nöthling, Nils Cornella, Josep Org Biomol Chem Chemistry A family of aryl dinuclear bismuthane complexes has been successfully synthesized and characterized. The two bismuth centers are bonded to various xanthene-type backbones, which differ in ring-size and flexibility, resulting in complexes with different intramolecular Bi⋯Bi distances. Moreover, their pentavalent Bi(v) analogues have also been prepared and structurally characterized. Finally, the synergy between bismuth centers in catalysis has been studied by applying dinuclear bismuthanes 5–8 to the catalytic oxidative cleavage of 1,2-diols. Unfortunately, no synergistic effects were observed and the catalytic activities of dinuclear bismuthanes and triphenylbismuth are comparable. The Royal Society of Chemistry 2021-05-06 /pmc/articles/PMC8188851/ /pubmed/33955447 http://dx.doi.org/10.1039/d1ob00367d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Magre, Marc
Kuziola, Jennifer
Nöthling, Nils
Cornella, Josep
Dibismuthanes in catalysis: from synthesis and characterization to redox behavior towards oxidative cleavage of 1,2-diols
title Dibismuthanes in catalysis: from synthesis and characterization to redox behavior towards oxidative cleavage of 1,2-diols
title_full Dibismuthanes in catalysis: from synthesis and characterization to redox behavior towards oxidative cleavage of 1,2-diols
title_fullStr Dibismuthanes in catalysis: from synthesis and characterization to redox behavior towards oxidative cleavage of 1,2-diols
title_full_unstemmed Dibismuthanes in catalysis: from synthesis and characterization to redox behavior towards oxidative cleavage of 1,2-diols
title_short Dibismuthanes in catalysis: from synthesis and characterization to redox behavior towards oxidative cleavage of 1,2-diols
title_sort dibismuthanes in catalysis: from synthesis and characterization to redox behavior towards oxidative cleavage of 1,2-diols
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8188851/
https://www.ncbi.nlm.nih.gov/pubmed/33955447
http://dx.doi.org/10.1039/d1ob00367d
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