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An Isolable Bis(Silanone–Borane) Adduct
The reaction of bis(silylenyl)‐substituted ferrocene 1 with two molar equivalents of BPh(3) yields the corresponding bis(silylene–borane) Lewis adduct 2. The latter is capable to activate CO(2) to furnish the borane‐stabilized bis(silanone) 3 through mono‐oxygenation of the dative Si(II)→B silicon c...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7187440/ https://www.ncbi.nlm.nih.gov/pubmed/32017257 http://dx.doi.org/10.1002/chem.202000235 |
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author | Luecke, Marcel‐Philip Pens, Elron Yao, Shenglai Driess, Matthias |
author_facet | Luecke, Marcel‐Philip Pens, Elron Yao, Shenglai Driess, Matthias |
author_sort | Luecke, Marcel‐Philip |
collection | PubMed |
description | The reaction of bis(silylenyl)‐substituted ferrocene 1 with two molar equivalents of BPh(3) yields the corresponding bis(silylene–borane) Lewis adduct 2. The latter is capable to activate CO(2) to furnish the borane‐stabilized bis(silanone) 3 through mono‐oxygenation of the dative Si(II)→B silicon centers under release of CO. Removal of BPh(3) from 3 with PMe(3) affords the corresponding 1,3,2,4‐cyclodisiloxane and the Me(3)P−BPh(3) adduct. All isolated new compounds were characterized and their molecular structures were determined by single‐crystal X‐ray diffraction analyses. |
format | Online Article Text |
id | pubmed-7187440 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71874402020-04-29 An Isolable Bis(Silanone–Borane) Adduct Luecke, Marcel‐Philip Pens, Elron Yao, Shenglai Driess, Matthias Chemistry Communications The reaction of bis(silylenyl)‐substituted ferrocene 1 with two molar equivalents of BPh(3) yields the corresponding bis(silylene–borane) Lewis adduct 2. The latter is capable to activate CO(2) to furnish the borane‐stabilized bis(silanone) 3 through mono‐oxygenation of the dative Si(II)→B silicon centers under release of CO. Removal of BPh(3) from 3 with PMe(3) affords the corresponding 1,3,2,4‐cyclodisiloxane and the Me(3)P−BPh(3) adduct. All isolated new compounds were characterized and their molecular structures were determined by single‐crystal X‐ray diffraction analyses. John Wiley and Sons Inc. 2020-03-11 2020-04-06 /pmc/articles/PMC7187440/ /pubmed/32017257 http://dx.doi.org/10.1002/chem.202000235 Text en © 2020 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-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Communications Luecke, Marcel‐Philip Pens, Elron Yao, Shenglai Driess, Matthias An Isolable Bis(Silanone–Borane) Adduct |
title | An Isolable Bis(Silanone–Borane) Adduct |
title_full | An Isolable Bis(Silanone–Borane) Adduct |
title_fullStr | An Isolable Bis(Silanone–Borane) Adduct |
title_full_unstemmed | An Isolable Bis(Silanone–Borane) Adduct |
title_short | An Isolable Bis(Silanone–Borane) Adduct |
title_sort | isolable bis(silanone–borane) adduct |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7187440/ https://www.ncbi.nlm.nih.gov/pubmed/32017257 http://dx.doi.org/10.1002/chem.202000235 |
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