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Phosphine and carbene azido-cations: [(L)N(3)](+) and [(L)(2)N(3)](+)
The cationic N(3)-species [(p-HC(6)F(4))(3)PN(3)](+) (1) featuring a perfluoro-arene phosphonium group serves as a N(3)(+)-source in stoichiometric reactions with several Lewis bases (L) allowing for the stepwise formation of [(L)N(3)](+) and [(L)(2)N(3)](+) cations (L = phosphine, carbene) with lib...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Royal Society of Chemistry
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6054069/ https://www.ncbi.nlm.nih.gov/pubmed/30090255 http://dx.doi.org/10.1039/c5sc02336j |
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author | Winkelhaus, Daniel Holthausen, Michael H. Dobrovetsky, Roman Stephan, Douglas W. |
author_facet | Winkelhaus, Daniel Holthausen, Michael H. Dobrovetsky, Roman Stephan, Douglas W. |
author_sort | Winkelhaus, Daniel |
collection | PubMed |
description | The cationic N(3)-species [(p-HC(6)F(4))(3)PN(3)](+) (1) featuring a perfluoro-arene phosphonium group serves as a N(3)(+)-source in stoichiometric reactions with several Lewis bases (L) allowing for the stepwise formation of [(L)N(3)](+) and [(L)(2)N(3)](+) cations (L = phosphine, carbene) with liberation of (p-HC(6)F(4))(3)P. X-Ray diffraction analysis and computational studies provide insight into the bonding in these remarkably stable azido-cations. |
format | Online Article Text |
id | pubmed-6054069 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-60540692018-08-08 Phosphine and carbene azido-cations: [(L)N(3)](+) and [(L)(2)N(3)](+) Winkelhaus, Daniel Holthausen, Michael H. Dobrovetsky, Roman Stephan, Douglas W. Chem Sci Chemistry The cationic N(3)-species [(p-HC(6)F(4))(3)PN(3)](+) (1) featuring a perfluoro-arene phosphonium group serves as a N(3)(+)-source in stoichiometric reactions with several Lewis bases (L) allowing for the stepwise formation of [(L)N(3)](+) and [(L)(2)N(3)](+) cations (L = phosphine, carbene) with liberation of (p-HC(6)F(4))(3)P. X-Ray diffraction analysis and computational studies provide insight into the bonding in these remarkably stable azido-cations. Royal Society of Chemistry 2015-11-01 2015-07-21 /pmc/articles/PMC6054069/ /pubmed/30090255 http://dx.doi.org/10.1039/c5sc02336j Text en This journal is © The Royal Society of Chemistry 2015 https://creativecommons.org/licenses/by/3.0/This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0) |
spellingShingle | Chemistry Winkelhaus, Daniel Holthausen, Michael H. Dobrovetsky, Roman Stephan, Douglas W. Phosphine and carbene azido-cations: [(L)N(3)](+) and [(L)(2)N(3)](+) |
title | Phosphine and carbene azido-cations: [(L)N(3)](+) and [(L)(2)N(3)](+)
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title_full | Phosphine and carbene azido-cations: [(L)N(3)](+) and [(L)(2)N(3)](+)
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title_fullStr | Phosphine and carbene azido-cations: [(L)N(3)](+) and [(L)(2)N(3)](+)
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title_full_unstemmed | Phosphine and carbene azido-cations: [(L)N(3)](+) and [(L)(2)N(3)](+)
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title_short | Phosphine and carbene azido-cations: [(L)N(3)](+) and [(L)(2)N(3)](+)
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title_sort | phosphine and carbene azido-cations: [(l)n(3)](+) and [(l)(2)n(3)](+) |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6054069/ https://www.ncbi.nlm.nih.gov/pubmed/30090255 http://dx.doi.org/10.1039/c5sc02336j |
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