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Stereoelectronic source of the anomalous stability of bis-peroxides

The unusual stability of bis- and tris-peroxides contradicts the conventional wisdom – some of them can melt without decomposition at temperatures exceeding 100 °C. In this work, we disclose a stabilizing stereoelectronic effect that two peroxide groups can exert on each other. This stabilization or...

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Detalles Bibliográficos
Autores principales: Gomes, Gabriel dos Passos, Vil', Vera, Terent'ev, Alexander, Alabugin, Igor V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5508698/
https://www.ncbi.nlm.nih.gov/pubmed/28757970
http://dx.doi.org/10.1039/c5sc02402a
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author Gomes, Gabriel dos Passos
Vil', Vera
Terent'ev, Alexander
Alabugin, Igor V.
author_facet Gomes, Gabriel dos Passos
Vil', Vera
Terent'ev, Alexander
Alabugin, Igor V.
author_sort Gomes, Gabriel dos Passos
collection PubMed
description The unusual stability of bis- and tris-peroxides contradicts the conventional wisdom – some of them can melt without decomposition at temperatures exceeding 100 °C. In this work, we disclose a stabilizing stereoelectronic effect that two peroxide groups can exert on each other. This stabilization originates from strong anomeric n(O) → σ*(CO) interactions that are absent in mono-peroxides but reintroduced in molecules where two peroxide moieties are separated by a CH(2) group. Furthermore, such effects can be induced by other σ-acceptors and amplified by structural constraints imposed by cyclic and bicyclic frameworks.
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spelling pubmed-55086982017-07-28 Stereoelectronic source of the anomalous stability of bis-peroxides Gomes, Gabriel dos Passos Vil', Vera Terent'ev, Alexander Alabugin, Igor V. Chem Sci Chemistry The unusual stability of bis- and tris-peroxides contradicts the conventional wisdom – some of them can melt without decomposition at temperatures exceeding 100 °C. In this work, we disclose a stabilizing stereoelectronic effect that two peroxide groups can exert on each other. This stabilization originates from strong anomeric n(O) → σ*(CO) interactions that are absent in mono-peroxides but reintroduced in molecules where two peroxide moieties are separated by a CH(2) group. Furthermore, such effects can be induced by other σ-acceptors and amplified by structural constraints imposed by cyclic and bicyclic frameworks. Royal Society of Chemistry 2015-12-01 2015-09-07 /pmc/articles/PMC5508698/ /pubmed/28757970 http://dx.doi.org/10.1039/c5sc02402a Text en This journal is © The Royal Society of Chemistry 2015 https://creativecommons.org/licenses/by-nc/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Chemistry
Gomes, Gabriel dos Passos
Vil', Vera
Terent'ev, Alexander
Alabugin, Igor V.
Stereoelectronic source of the anomalous stability of bis-peroxides
title Stereoelectronic source of the anomalous stability of bis-peroxides
title_full Stereoelectronic source of the anomalous stability of bis-peroxides
title_fullStr Stereoelectronic source of the anomalous stability of bis-peroxides
title_full_unstemmed Stereoelectronic source of the anomalous stability of bis-peroxides
title_short Stereoelectronic source of the anomalous stability of bis-peroxides
title_sort stereoelectronic source of the anomalous stability of bis-peroxides
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5508698/
https://www.ncbi.nlm.nih.gov/pubmed/28757970
http://dx.doi.org/10.1039/c5sc02402a
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