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NO(3)(−) anions can act as Lewis acid in the solid state

Identifying electron donating and accepting moieties is crucial to understanding molecular aggregation, which is of pivotal significance to biology. Anions such as NO(3)(−) are typical electron donors. However, computations predict that the charge distribution of NO(3)(−) is anisotropic and minimal...

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Detalles Bibliográficos
Autores principales: Bauzá, Antonio, Frontera, Antonio, Mooibroek, Tiddo J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5321794/
https://www.ncbi.nlm.nih.gov/pubmed/28220788
http://dx.doi.org/10.1038/ncomms14522
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author Bauzá, Antonio
Frontera, Antonio
Mooibroek, Tiddo J.
author_facet Bauzá, Antonio
Frontera, Antonio
Mooibroek, Tiddo J.
author_sort Bauzá, Antonio
collection PubMed
description Identifying electron donating and accepting moieties is crucial to understanding molecular aggregation, which is of pivotal significance to biology. Anions such as NO(3)(−) are typical electron donors. However, computations predict that the charge distribution of NO(3)(−) is anisotropic and minimal on nitrogen. Here we show that when the nitrate's charge is sufficiently dampened by resonating over a larger area, a Lewis acidic site emerges on nitrogen that can interact favourably with electron rich partners. Surveys of the Cambridge Structural Database and Protein Data Bank reveal geometric preferences of some oxygen and sulfur containing entities around a nitrate anion that are consistent with this ‘π-hole bonding' geometry. Computations reveal donor–acceptor orbital interactions that confirm the counterintuitive Lewis π–acidity of nitrate.
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spelling pubmed-53217942017-03-01 NO(3)(−) anions can act as Lewis acid in the solid state Bauzá, Antonio Frontera, Antonio Mooibroek, Tiddo J. Nat Commun Article Identifying electron donating and accepting moieties is crucial to understanding molecular aggregation, which is of pivotal significance to biology. Anions such as NO(3)(−) are typical electron donors. However, computations predict that the charge distribution of NO(3)(−) is anisotropic and minimal on nitrogen. Here we show that when the nitrate's charge is sufficiently dampened by resonating over a larger area, a Lewis acidic site emerges on nitrogen that can interact favourably with electron rich partners. Surveys of the Cambridge Structural Database and Protein Data Bank reveal geometric preferences of some oxygen and sulfur containing entities around a nitrate anion that are consistent with this ‘π-hole bonding' geometry. Computations reveal donor–acceptor orbital interactions that confirm the counterintuitive Lewis π–acidity of nitrate. Nature Publishing Group 2017-02-21 /pmc/articles/PMC5321794/ /pubmed/28220788 http://dx.doi.org/10.1038/ncomms14522 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Bauzá, Antonio
Frontera, Antonio
Mooibroek, Tiddo J.
NO(3)(−) anions can act as Lewis acid in the solid state
title NO(3)(−) anions can act as Lewis acid in the solid state
title_full NO(3)(−) anions can act as Lewis acid in the solid state
title_fullStr NO(3)(−) anions can act as Lewis acid in the solid state
title_full_unstemmed NO(3)(−) anions can act as Lewis acid in the solid state
title_short NO(3)(−) anions can act as Lewis acid in the solid state
title_sort no(3)(−) anions can act as lewis acid in the solid state
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5321794/
https://www.ncbi.nlm.nih.gov/pubmed/28220788
http://dx.doi.org/10.1038/ncomms14522
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