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A Monoanionic Arsenide Source: Decarbonylation of the 2‐Arsaethynolate Anion upon Reaction with Bulky Stannylenes
We report fundamental studies on the reactivity of the 2‐arsaethynolate anion (AsCO(−)), a species that has only recently become synthetically accessible. The reaction of AsCO(−) with the bulky stannylene Ter(2)Sn (Ter=2,6‐bis[2,4,6‐trimethylphenyl]phenyl) is described, which leads to the unexpected...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5299489/ https://www.ncbi.nlm.nih.gov/pubmed/27862768 http://dx.doi.org/10.1002/anie.201609309 |
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author | Hinz, Alexander Goicoechea, Jose M. |
author_facet | Hinz, Alexander Goicoechea, Jose M. |
author_sort | Hinz, Alexander |
collection | PubMed |
description | We report fundamental studies on the reactivity of the 2‐arsaethynolate anion (AsCO(−)), a species that has only recently become synthetically accessible. The reaction of AsCO(−) with the bulky stannylene Ter(2)Sn (Ter=2,6‐bis[2,4,6‐trimethylphenyl]phenyl) is described, which leads to the unexpected formation of a [Ter(3)Sn(2)As(2)](−) cluster compound. On the reaction pathway to this cluster, several intermediates were identified and characterized. After the initial association of AsCO(−) to Ter(2)Sn, decarbonylation occurs to give an anion featuring monocoordinate arsenic, [Ter(2)SnAs](−). Both species are not stable under ambient conditions, and [Ter(2)SnAs](−) rearranges to form [TerSnAsTer](−), an unprecedented anionic mixed Group 14/15 alkene analogue. |
format | Online Article Text |
id | pubmed-5299489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-52994892017-02-22 A Monoanionic Arsenide Source: Decarbonylation of the 2‐Arsaethynolate Anion upon Reaction with Bulky Stannylenes Hinz, Alexander Goicoechea, Jose M. Angew Chem Int Ed Engl Communications We report fundamental studies on the reactivity of the 2‐arsaethynolate anion (AsCO(−)), a species that has only recently become synthetically accessible. The reaction of AsCO(−) with the bulky stannylene Ter(2)Sn (Ter=2,6‐bis[2,4,6‐trimethylphenyl]phenyl) is described, which leads to the unexpected formation of a [Ter(3)Sn(2)As(2)](−) cluster compound. On the reaction pathway to this cluster, several intermediates were identified and characterized. After the initial association of AsCO(−) to Ter(2)Sn, decarbonylation occurs to give an anion featuring monocoordinate arsenic, [Ter(2)SnAs](−). Both species are not stable under ambient conditions, and [Ter(2)SnAs](−) rearranges to form [TerSnAsTer](−), an unprecedented anionic mixed Group 14/15 alkene analogue. John Wiley and Sons Inc. 2016-11-15 2016-12-12 /pmc/articles/PMC5299489/ /pubmed/27862768 http://dx.doi.org/10.1002/anie.201609309 Text en © 2016 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution (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 Hinz, Alexander Goicoechea, Jose M. A Monoanionic Arsenide Source: Decarbonylation of the 2‐Arsaethynolate Anion upon Reaction with Bulky Stannylenes |
title | A Monoanionic Arsenide Source: Decarbonylation of the 2‐Arsaethynolate Anion upon Reaction with Bulky Stannylenes |
title_full | A Monoanionic Arsenide Source: Decarbonylation of the 2‐Arsaethynolate Anion upon Reaction with Bulky Stannylenes |
title_fullStr | A Monoanionic Arsenide Source: Decarbonylation of the 2‐Arsaethynolate Anion upon Reaction with Bulky Stannylenes |
title_full_unstemmed | A Monoanionic Arsenide Source: Decarbonylation of the 2‐Arsaethynolate Anion upon Reaction with Bulky Stannylenes |
title_short | A Monoanionic Arsenide Source: Decarbonylation of the 2‐Arsaethynolate Anion upon Reaction with Bulky Stannylenes |
title_sort | monoanionic arsenide source: decarbonylation of the 2‐arsaethynolate anion upon reaction with bulky stannylenes |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5299489/ https://www.ncbi.nlm.nih.gov/pubmed/27862768 http://dx.doi.org/10.1002/anie.201609309 |
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