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Isolation of the Elusive Heptavanadate Anion with Trisalkoxide Ligands
[Image: see text] The unprecedented heptavanadate cluster has been isolated from reactions between trisalkoxide ligands and vanadate in water at pH = 2 as a series of alkylammonium [H(x)V(7)O(18)(H(2)O)((OCH(2))(3)CR)]((4–x)-) salts (1–3, R = CH(2)OH; 4, R = CH(3)). Their structures have been determ...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9157487/ https://www.ncbi.nlm.nih.gov/pubmed/33818060 http://dx.doi.org/10.1021/acs.inorgchem.1c00448 |
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author | Fernández-Navarro, Leticia Nunes-Collado, Aitor Artetxe, Beñat Ruiz-Bilbao, Estibaliz San Felices, Leire Reinoso, Santiago San José Wéry, Ana Gutiérrez-Zorrilla, Juan M. |
author_facet | Fernández-Navarro, Leticia Nunes-Collado, Aitor Artetxe, Beñat Ruiz-Bilbao, Estibaliz San Felices, Leire Reinoso, Santiago San José Wéry, Ana Gutiérrez-Zorrilla, Juan M. |
author_sort | Fernández-Navarro, Leticia |
collection | PubMed |
description | [Image: see text] The unprecedented heptavanadate cluster has been isolated from reactions between trisalkoxide ligands and vanadate in water at pH = 2 as a series of alkylammonium [H(x)V(7)O(18)(H(2)O)((OCH(2))(3)CR)]((4–x)-) salts (1–3, R = CH(2)OH; 4, R = CH(3)). Their structures have been determined and the partial stability of 4 in water assessed by a combination of multinuclear NMR spectroscopy and ESI-MS. The heptavanadate unit reported herein could represent an intermediate species in the formation of decavanadate that is blocked by attachment of tripodal ligands. |
format | Online Article Text |
id | pubmed-9157487 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-91574872022-06-02 Isolation of the Elusive Heptavanadate Anion with Trisalkoxide Ligands Fernández-Navarro, Leticia Nunes-Collado, Aitor Artetxe, Beñat Ruiz-Bilbao, Estibaliz San Felices, Leire Reinoso, Santiago San José Wéry, Ana Gutiérrez-Zorrilla, Juan M. Inorg Chem [Image: see text] The unprecedented heptavanadate cluster has been isolated from reactions between trisalkoxide ligands and vanadate in water at pH = 2 as a series of alkylammonium [H(x)V(7)O(18)(H(2)O)((OCH(2))(3)CR)]((4–x)-) salts (1–3, R = CH(2)OH; 4, R = CH(3)). Their structures have been determined and the partial stability of 4 in water assessed by a combination of multinuclear NMR spectroscopy and ESI-MS. The heptavanadate unit reported herein could represent an intermediate species in the formation of decavanadate that is blocked by attachment of tripodal ligands. American Chemical Society 2021-04-05 2021-04-19 /pmc/articles/PMC9157487/ /pubmed/33818060 http://dx.doi.org/10.1021/acs.inorgchem.1c00448 Text en © 2021 American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Fernández-Navarro, Leticia Nunes-Collado, Aitor Artetxe, Beñat Ruiz-Bilbao, Estibaliz San Felices, Leire Reinoso, Santiago San José Wéry, Ana Gutiérrez-Zorrilla, Juan M. Isolation of the Elusive Heptavanadate Anion with Trisalkoxide Ligands |
title | Isolation of the Elusive Heptavanadate Anion with
Trisalkoxide Ligands |
title_full | Isolation of the Elusive Heptavanadate Anion with
Trisalkoxide Ligands |
title_fullStr | Isolation of the Elusive Heptavanadate Anion with
Trisalkoxide Ligands |
title_full_unstemmed | Isolation of the Elusive Heptavanadate Anion with
Trisalkoxide Ligands |
title_short | Isolation of the Elusive Heptavanadate Anion with
Trisalkoxide Ligands |
title_sort | isolation of the elusive heptavanadate anion with
trisalkoxide ligands |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9157487/ https://www.ncbi.nlm.nih.gov/pubmed/33818060 http://dx.doi.org/10.1021/acs.inorgchem.1c00448 |
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