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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...
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/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. |
format | Online Article Text |
id | pubmed-5074235 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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