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A Phosphanyl‐Phosphagallene that Functions as a Frustrated Lewis Pair

Phosphagallenes (1 a/1 b) featuring double bonds between phosphorus and gallium were synthesized by reaction of (phosphanyl)phosphaketenes with the gallium carbenoid Ga(Nacnac) (Nacnac=HC[C(Me)N(2,6‐i‐Pr(2)C(6)H(3))](2)). The stability of these species is dependent on the saturation of the phosphany...

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Detalles Bibliográficos
Autores principales: Wilson, Daniel W. N., Feld, Joey, Goicoechea, Jose M.
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/PMC7693089/
https://www.ncbi.nlm.nih.gov/pubmed/32615007
http://dx.doi.org/10.1002/anie.202008207
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author Wilson, Daniel W. N.
Feld, Joey
Goicoechea, Jose M.
author_facet Wilson, Daniel W. N.
Feld, Joey
Goicoechea, Jose M.
author_sort Wilson, Daniel W. N.
collection PubMed
description Phosphagallenes (1 a/1 b) featuring double bonds between phosphorus and gallium were synthesized by reaction of (phosphanyl)phosphaketenes with the gallium carbenoid Ga(Nacnac) (Nacnac=HC[C(Me)N(2,6‐i‐Pr(2)C(6)H(3))](2)). The stability of these species is dependent on the saturation of the phosphanyl moiety. 1 a, which bears an unsaturated phosphanyl ring, rearranges in solution to yield a spirocyclic compound (2) which contains a P=P bond. The saturated variant 1 b is stable even at elevated temperatures. 1 b behaves as a frustrated Lewis pair capable of activation of H(2) and forms a 1:1 adduct with CO(2).
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spelling pubmed-76930892020-12-08 A Phosphanyl‐Phosphagallene that Functions as a Frustrated Lewis Pair Wilson, Daniel W. N. Feld, Joey Goicoechea, Jose M. Angew Chem Int Ed Engl Communications Phosphagallenes (1 a/1 b) featuring double bonds between phosphorus and gallium were synthesized by reaction of (phosphanyl)phosphaketenes with the gallium carbenoid Ga(Nacnac) (Nacnac=HC[C(Me)N(2,6‐i‐Pr(2)C(6)H(3))](2)). The stability of these species is dependent on the saturation of the phosphanyl moiety. 1 a, which bears an unsaturated phosphanyl ring, rearranges in solution to yield a spirocyclic compound (2) which contains a P=P bond. The saturated variant 1 b is stable even at elevated temperatures. 1 b behaves as a frustrated Lewis pair capable of activation of H(2) and forms a 1:1 adduct with CO(2). John Wiley and Sons Inc. 2020-09-09 2020-11-16 /pmc/articles/PMC7693089/ /pubmed/32615007 http://dx.doi.org/10.1002/anie.202008207 Text en © 2020 The Authors. Published by Wiley-VCH GmbH 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
Wilson, Daniel W. N.
Feld, Joey
Goicoechea, Jose M.
A Phosphanyl‐Phosphagallene that Functions as a Frustrated Lewis Pair
title A Phosphanyl‐Phosphagallene that Functions as a Frustrated Lewis Pair
title_full A Phosphanyl‐Phosphagallene that Functions as a Frustrated Lewis Pair
title_fullStr A Phosphanyl‐Phosphagallene that Functions as a Frustrated Lewis Pair
title_full_unstemmed A Phosphanyl‐Phosphagallene that Functions as a Frustrated Lewis Pair
title_short A Phosphanyl‐Phosphagallene that Functions as a Frustrated Lewis Pair
title_sort phosphanyl‐phosphagallene that functions as a frustrated lewis pair
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7693089/
https://www.ncbi.nlm.nih.gov/pubmed/32615007
http://dx.doi.org/10.1002/anie.202008207
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