Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Hinz, Alexander, Goicoechea, Jose M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
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
_version_ 1782506035909492736
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
work_keys_str_mv AT hinzalexander amonoanionicarsenidesourcedecarbonylationofthe2arsaethynolateanionuponreactionwithbulkystannylenes
AT goicoecheajosem amonoanionicarsenidesourcedecarbonylationofthe2arsaethynolateanionuponreactionwithbulkystannylenes
AT hinzalexander monoanionicarsenidesourcedecarbonylationofthe2arsaethynolateanionuponreactionwithbulkystannylenes
AT goicoecheajosem monoanionicarsenidesourcedecarbonylationofthe2arsaethynolateanionuponreactionwithbulkystannylenes