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The 2‐Arsaethynolate Anion: Synthesis and Reactivity Towards Heteroallenes

The synthesis and isolation of the 2‐arsaethynolate anion, AsCO(−), and its subsequent reactivity towards heteroallenes is reported. Reactions with ketenes and carbodiimides afford four‐membered anionic heterocycles in formal [2+2] cycloaddition reactions. By contrast, reaction with an isocyanate yi...

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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/PMC5074235/
https://www.ncbi.nlm.nih.gov/pubmed/27093942
http://dx.doi.org/10.1002/anie.201602310
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author Hinz, Alexander
Goicoechea, Jose M.
author_facet Hinz, Alexander
Goicoechea, Jose M.
author_sort Hinz, Alexander
collection PubMed
description The synthesis and isolation of the 2‐arsaethynolate anion, AsCO(−), and its subsequent reactivity towards heteroallenes is reported. Reactions with ketenes and carbodiimides afford four‐membered anionic heterocycles in formal [2+2] cycloaddition reactions. By contrast, reaction with an isocyanate yielded a 1,4,2‐diazaarsolidine‐3,5‐dionide anion and the unprecedented cluster anions As(10) (2−) and As(12) (4−). These preliminary reactivity studies hint at the enormous potential synthetic utility of this novel anion, which may be employed as an arsenide (As(−)) source.
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spelling pubmed-50742352016-11-04 The 2‐Arsaethynolate Anion: Synthesis and Reactivity Towards Heteroallenes Hinz, Alexander Goicoechea, Jose M. Angew Chem Int Ed Engl Communications The synthesis and isolation of the 2‐arsaethynolate anion, AsCO(−), and its subsequent reactivity towards heteroallenes is reported. Reactions with ketenes and carbodiimides afford four‐membered anionic heterocycles in formal [2+2] cycloaddition reactions. By contrast, reaction with an isocyanate yielded a 1,4,2‐diazaarsolidine‐3,5‐dionide anion and the unprecedented cluster anions As(10) (2−) and As(12) (4−). These preliminary reactivity studies hint at the enormous potential synthetic utility of this novel anion, which may be employed as an arsenide (As(−)) source. John Wiley and Sons Inc. 2016-04-20 2016-07-18 /pmc/articles/PMC5074235/ /pubmed/27093942 http://dx.doi.org/10.1002/anie.201602310 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.
The 2‐Arsaethynolate Anion: Synthesis and Reactivity Towards Heteroallenes
title The 2‐Arsaethynolate Anion: Synthesis and Reactivity Towards Heteroallenes
title_full The 2‐Arsaethynolate Anion: Synthesis and Reactivity Towards Heteroallenes
title_fullStr The 2‐Arsaethynolate Anion: Synthesis and Reactivity Towards Heteroallenes
title_full_unstemmed The 2‐Arsaethynolate Anion: Synthesis and Reactivity Towards Heteroallenes
title_short The 2‐Arsaethynolate Anion: Synthesis and Reactivity Towards Heteroallenes
title_sort 2‐arsaethynolate anion: synthesis and reactivity towards heteroallenes
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5074235/
https://www.ncbi.nlm.nih.gov/pubmed/27093942
http://dx.doi.org/10.1002/anie.201602310
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