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A Systematic Survey of the Reactivity of Chlorinated N(2)P(2), NP(3) and P(4) Ring Systems
The reactivity of the four‐membered NP(3) ring system [RN(μ‐PCl)(2)PR] (R=Mes*=2,4,6‐tri‐tert‐butylphenyl) towards Lewis acids, Lewis bases, and reducing agents was investigated. Comparisons with the literature‐known, analogous cyclic compounds [ClP(μ‐NR)](2) (R=Ter=2,6‐dimesitylphenyl) and [ClP(μ‐P...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6973262/ https://www.ncbi.nlm.nih.gov/pubmed/31589354 http://dx.doi.org/10.1002/chem.201903410 |
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author | Bresien, Jonas Eickhoff, Liesa Schulz, Axel Suhrbier, Tim Villinger, Alexander |
author_facet | Bresien, Jonas Eickhoff, Liesa Schulz, Axel Suhrbier, Tim Villinger, Alexander |
author_sort | Bresien, Jonas |
collection | PubMed |
description | The reactivity of the four‐membered NP(3) ring system [RN(μ‐PCl)(2)PR] (R=Mes*=2,4,6‐tri‐tert‐butylphenyl) towards Lewis acids, Lewis bases, and reducing agents was investigated. Comparisons with the literature‐known, analogous cyclic compounds [ClP(μ‐NR)](2) (R=Ter=2,6‐dimesitylphenyl) and [ClP(μ‐PR)](2) (R=Mes*) are drawn, to obtain a better systematic understanding of the reactivity of cyclic NP species. Apart from experimental results, DFT computations are discussed to further the insight into bonding and electronic structure of these compounds. |
format | Online Article Text |
id | pubmed-6973262 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69732622020-01-27 A Systematic Survey of the Reactivity of Chlorinated N(2)P(2), NP(3) and P(4) Ring Systems Bresien, Jonas Eickhoff, Liesa Schulz, Axel Suhrbier, Tim Villinger, Alexander Chemistry Full Papers The reactivity of the four‐membered NP(3) ring system [RN(μ‐PCl)(2)PR] (R=Mes*=2,4,6‐tri‐tert‐butylphenyl) towards Lewis acids, Lewis bases, and reducing agents was investigated. Comparisons with the literature‐known, analogous cyclic compounds [ClP(μ‐NR)](2) (R=Ter=2,6‐dimesitylphenyl) and [ClP(μ‐PR)](2) (R=Mes*) are drawn, to obtain a better systematic understanding of the reactivity of cyclic NP species. Apart from experimental results, DFT computations are discussed to further the insight into bonding and electronic structure of these compounds. John Wiley and Sons Inc. 2019-11-22 2019-12-18 /pmc/articles/PMC6973262/ /pubmed/31589354 http://dx.doi.org/10.1002/chem.201903410 Text en © 2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the 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 | Full Papers Bresien, Jonas Eickhoff, Liesa Schulz, Axel Suhrbier, Tim Villinger, Alexander A Systematic Survey of the Reactivity of Chlorinated N(2)P(2), NP(3) and P(4) Ring Systems |
title | A Systematic Survey of the Reactivity of Chlorinated N(2)P(2), NP(3) and P(4) Ring Systems |
title_full | A Systematic Survey of the Reactivity of Chlorinated N(2)P(2), NP(3) and P(4) Ring Systems |
title_fullStr | A Systematic Survey of the Reactivity of Chlorinated N(2)P(2), NP(3) and P(4) Ring Systems |
title_full_unstemmed | A Systematic Survey of the Reactivity of Chlorinated N(2)P(2), NP(3) and P(4) Ring Systems |
title_short | A Systematic Survey of the Reactivity of Chlorinated N(2)P(2), NP(3) and P(4) Ring Systems |
title_sort | systematic survey of the reactivity of chlorinated n(2)p(2), np(3) and p(4) ring systems |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6973262/ https://www.ncbi.nlm.nih.gov/pubmed/31589354 http://dx.doi.org/10.1002/chem.201903410 |
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