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Phosphide Delivery to a Cyclotrisilene**
The reactivity of the 2-phosphaethynolate anion (PCO(−)) towards a cyclic trisilene (cSi(3)(Tip)(4)) is reported. The result is the net activation of the P=C and Si=Si multiple bonds of the precursors affording a heteroatomic bicyclo[1.1.1]pentan-2-one analogue ([P(CO)Si(3)(Tip)(4)](−); 1). This rea...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
WILEY-VCH Verlag
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4506556/ https://www.ncbi.nlm.nih.gov/pubmed/25418506 http://dx.doi.org/10.1002/anie.201409908 |
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author | Robinson, Thomas P Cowley, Michael J Scheschkewitz, David Goicoechea, Jose M |
author_facet | Robinson, Thomas P Cowley, Michael J Scheschkewitz, David Goicoechea, Jose M |
author_sort | Robinson, Thomas P |
collection | PubMed |
description | The reactivity of the 2-phosphaethynolate anion (PCO(−)) towards a cyclic trisilene (cSi(3)(Tip)(4)) is reported. The result is the net activation of the P=C and Si=Si multiple bonds of the precursors affording a heteroatomic bicyclo[1.1.1]pentan-2-one analogue ([P(CO)Si(3)(Tip)(4)](−); 1). This reaction can be interpreted as the formal addition of a phosphide and a carbonyl across the Si=Si double bond. Photolytic decarbonylation of 1 results in the incorporation of the phosphide vertex into the cyclotrisilene scaffold, yielding a congener of the cyclobutene anion with considerable allylic character. |
format | Online Article Text |
id | pubmed-4506556 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | WILEY-VCH Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-45065562015-07-22 Phosphide Delivery to a Cyclotrisilene** Robinson, Thomas P Cowley, Michael J Scheschkewitz, David Goicoechea, Jose M Angew Chem Int Ed Engl Communications The reactivity of the 2-phosphaethynolate anion (PCO(−)) towards a cyclic trisilene (cSi(3)(Tip)(4)) is reported. The result is the net activation of the P=C and Si=Si multiple bonds of the precursors affording a heteroatomic bicyclo[1.1.1]pentan-2-one analogue ([P(CO)Si(3)(Tip)(4)](−); 1). This reaction can be interpreted as the formal addition of a phosphide and a carbonyl across the Si=Si double bond. Photolytic decarbonylation of 1 results in the incorporation of the phosphide vertex into the cyclotrisilene scaffold, yielding a congener of the cyclobutene anion with considerable allylic character. WILEY-VCH Verlag 2015-01-07 2014-11-21 /pmc/articles/PMC4506556/ /pubmed/25418506 http://dx.doi.org/10.1002/anie.201409908 Text en © 2014 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Communications Robinson, Thomas P Cowley, Michael J Scheschkewitz, David Goicoechea, Jose M Phosphide Delivery to a Cyclotrisilene** |
title | Phosphide Delivery to a Cyclotrisilene** |
title_full | Phosphide Delivery to a Cyclotrisilene** |
title_fullStr | Phosphide Delivery to a Cyclotrisilene** |
title_full_unstemmed | Phosphide Delivery to a Cyclotrisilene** |
title_short | Phosphide Delivery to a Cyclotrisilene** |
title_sort | phosphide delivery to a cyclotrisilene** |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4506556/ https://www.ncbi.nlm.nih.gov/pubmed/25418506 http://dx.doi.org/10.1002/anie.201409908 |
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