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Synthesis and Reactivity of the First Isolated Hydrogen‐Bridged Silanol–Silanolate Anions

We report on the first examples of isolated silanol–silanolate anions, obtained by utilizing weakly coordinating phosphazenium counterions. The silanolate anions were synthesized from the recently published phosphazenium hydroxide hydrate salt with siloxanes. The silanol–silanolate anions are postul...

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Autores principales: Weitkamp, Robin F., Neumann, Beate, Stammler, Hans‐Georg, Hoge, Berthold
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7154667/
https://www.ncbi.nlm.nih.gov/pubmed/31833629
http://dx.doi.org/10.1002/anie.201914339
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author Weitkamp, Robin F.
Neumann, Beate
Stammler, Hans‐Georg
Hoge, Berthold
author_facet Weitkamp, Robin F.
Neumann, Beate
Stammler, Hans‐Georg
Hoge, Berthold
author_sort Weitkamp, Robin F.
collection PubMed
description We report on the first examples of isolated silanol–silanolate anions, obtained by utilizing weakly coordinating phosphazenium counterions. The silanolate anions were synthesized from the recently published phosphazenium hydroxide hydrate salt with siloxanes. The silanol–silanolate anions are postulated intermediates in the hydroxide‐mediated polymerization of aryl and alkyl siloxanes. The silanolate anions are strong nucleophiles because of the weakly coordinating character of the phosphazenium cation, which is perceptible in their activity in polysiloxane depolymerization.
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spelling pubmed-71546672020-04-14 Synthesis and Reactivity of the First Isolated Hydrogen‐Bridged Silanol–Silanolate Anions Weitkamp, Robin F. Neumann, Beate Stammler, Hans‐Georg Hoge, Berthold Angew Chem Int Ed Engl Communications We report on the first examples of isolated silanol–silanolate anions, obtained by utilizing weakly coordinating phosphazenium counterions. The silanolate anions were synthesized from the recently published phosphazenium hydroxide hydrate salt with siloxanes. The silanol–silanolate anions are postulated intermediates in the hydroxide‐mediated polymerization of aryl and alkyl siloxanes. The silanolate anions are strong nucleophiles because of the weakly coordinating character of the phosphazenium cation, which is perceptible in their activity in polysiloxane depolymerization. John Wiley and Sons Inc. 2020-02-11 2020-03-27 /pmc/articles/PMC7154667/ /pubmed/31833629 http://dx.doi.org/10.1002/anie.201914339 Text en © 2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Communications
Weitkamp, Robin F.
Neumann, Beate
Stammler, Hans‐Georg
Hoge, Berthold
Synthesis and Reactivity of the First Isolated Hydrogen‐Bridged Silanol–Silanolate Anions
title Synthesis and Reactivity of the First Isolated Hydrogen‐Bridged Silanol–Silanolate Anions
title_full Synthesis and Reactivity of the First Isolated Hydrogen‐Bridged Silanol–Silanolate Anions
title_fullStr Synthesis and Reactivity of the First Isolated Hydrogen‐Bridged Silanol–Silanolate Anions
title_full_unstemmed Synthesis and Reactivity of the First Isolated Hydrogen‐Bridged Silanol–Silanolate Anions
title_short Synthesis and Reactivity of the First Isolated Hydrogen‐Bridged Silanol–Silanolate Anions
title_sort synthesis and reactivity of the first isolated hydrogen‐bridged silanol–silanolate anions
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7154667/
https://www.ncbi.nlm.nih.gov/pubmed/31833629
http://dx.doi.org/10.1002/anie.201914339
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