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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...

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Detalles Bibliográficos
Autores principales: Robinson, Thomas P, Cowley, Michael J, Scheschkewitz, David, Goicoechea, Jose M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: WILEY-VCH Verlag 2015
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.
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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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AT goicoecheajosem phosphidedeliverytoacyclotrisilene