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The oxidation state in low-valent beryllium and magnesium compounds

Low-valent group 2 (E = Be and Mg) stabilized compounds have been long synthetically pursued. Here we discuss the electronic structure of a series of Lewis base-stabilized Be and Mg compounds. Despite the accepted zero(0) oxidation state nature of the group 2 elements of some recent experimentally a...

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Autores principales: Gimferrer, Martí, Danés, Sergi, Vos, Eva, Yildiz, Cem B., Corral, Inés, Jana, Anukul, Salvador, Pedro, Andrada, Diego M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9172369/
https://www.ncbi.nlm.nih.gov/pubmed/35756523
http://dx.doi.org/10.1039/d2sc01401g
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author Gimferrer, Martí
Danés, Sergi
Vos, Eva
Yildiz, Cem B.
Corral, Inés
Jana, Anukul
Salvador, Pedro
Andrada, Diego M.
author_facet Gimferrer, Martí
Danés, Sergi
Vos, Eva
Yildiz, Cem B.
Corral, Inés
Jana, Anukul
Salvador, Pedro
Andrada, Diego M.
author_sort Gimferrer, Martí
collection PubMed
description Low-valent group 2 (E = Be and Mg) stabilized compounds have been long synthetically pursued. Here we discuss the electronic structure of a series of Lewis base-stabilized Be and Mg compounds. Despite the accepted zero(0) oxidation state nature of the group 2 elements of some recent experimentally accomplished species, the analysis of multireference wavefunctions provides compelling evidence for a strong diradical character with an oxidation state of +2. Thus, we elaborate on the distinction between a description as a donor–acceptor interaction L(0) ⇆ E(0) ⇄ L(0) and the internally oxidized situation, better interpreted as a diradical L(−1) → E(+2) ← L(−1) species. The experimentally accomplished examples rely on the strengthened bonds by increasing the π-acidity of the ligand; avoiding this interaction could lead to an unprecedented low-oxidation state.
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spelling pubmed-91723692022-06-23 The oxidation state in low-valent beryllium and magnesium compounds Gimferrer, Martí Danés, Sergi Vos, Eva Yildiz, Cem B. Corral, Inés Jana, Anukul Salvador, Pedro Andrada, Diego M. Chem Sci Chemistry Low-valent group 2 (E = Be and Mg) stabilized compounds have been long synthetically pursued. Here we discuss the electronic structure of a series of Lewis base-stabilized Be and Mg compounds. Despite the accepted zero(0) oxidation state nature of the group 2 elements of some recent experimentally accomplished species, the analysis of multireference wavefunctions provides compelling evidence for a strong diradical character with an oxidation state of +2. Thus, we elaborate on the distinction between a description as a donor–acceptor interaction L(0) ⇆ E(0) ⇄ L(0) and the internally oxidized situation, better interpreted as a diradical L(−1) → E(+2) ← L(−1) species. The experimentally accomplished examples rely on the strengthened bonds by increasing the π-acidity of the ligand; avoiding this interaction could lead to an unprecedented low-oxidation state. The Royal Society of Chemistry 2022-05-09 /pmc/articles/PMC9172369/ /pubmed/35756523 http://dx.doi.org/10.1039/d2sc01401g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Gimferrer, Martí
Danés, Sergi
Vos, Eva
Yildiz, Cem B.
Corral, Inés
Jana, Anukul
Salvador, Pedro
Andrada, Diego M.
The oxidation state in low-valent beryllium and magnesium compounds
title The oxidation state in low-valent beryllium and magnesium compounds
title_full The oxidation state in low-valent beryllium and magnesium compounds
title_fullStr The oxidation state in low-valent beryllium and magnesium compounds
title_full_unstemmed The oxidation state in low-valent beryllium and magnesium compounds
title_short The oxidation state in low-valent beryllium and magnesium compounds
title_sort oxidation state in low-valent beryllium and magnesium compounds
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9172369/
https://www.ncbi.nlm.nih.gov/pubmed/35756523
http://dx.doi.org/10.1039/d2sc01401g
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