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P,P-Bis[4-(dimethylamino)phenyl]-N,N-bis(propan-2-yl)phosphinic amide
The molecular structure of the title compound, C(22)H(34)N(3)OP, adopts a distorted tetrahedral geometry at the P atom, with the most noticeable distortion being for the O—P—N angle [117.53 (10)°]. An effective cone angle of 187° was calculated for the compound. In the crystal, weak C—H⋯O interac...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569256/ https://www.ncbi.nlm.nih.gov/pubmed/23424479 http://dx.doi.org/10.1107/S1600536812050398 |
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author | Evans, Stephen J. Renison, C. Alicia Williams, D. Bradley G. Muller, Alfred |
author_facet | Evans, Stephen J. Renison, C. Alicia Williams, D. Bradley G. Muller, Alfred |
author_sort | Evans, Stephen J. |
collection | PubMed |
description | The molecular structure of the title compound, C(22)H(34)N(3)OP, adopts a distorted tetrahedral geometry at the P atom, with the most noticeable distortion being for the O—P—N angle [117.53 (10)°]. An effective cone angle of 187° was calculated for the compound. In the crystal, weak C—H⋯O interactions create infinite chains along [100], whereas C—H⋯π interactions propagating in [001] generate a herringbone motif. |
format | Online Article Text |
id | pubmed-3569256 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-35692562013-02-19 P,P-Bis[4-(dimethylamino)phenyl]-N,N-bis(propan-2-yl)phosphinic amide Evans, Stephen J. Renison, C. Alicia Williams, D. Bradley G. Muller, Alfred Acta Crystallogr Sect E Struct Rep Online Organic Papers The molecular structure of the title compound, C(22)H(34)N(3)OP, adopts a distorted tetrahedral geometry at the P atom, with the most noticeable distortion being for the O—P—N angle [117.53 (10)°]. An effective cone angle of 187° was calculated for the compound. In the crystal, weak C—H⋯O interactions create infinite chains along [100], whereas C—H⋯π interactions propagating in [001] generate a herringbone motif. International Union of Crystallography 2013-01-09 /pmc/articles/PMC3569256/ /pubmed/23424479 http://dx.doi.org/10.1107/S1600536812050398 Text en © Evans et al. 2013 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited. |
spellingShingle | Organic Papers Evans, Stephen J. Renison, C. Alicia Williams, D. Bradley G. Muller, Alfred P,P-Bis[4-(dimethylamino)phenyl]-N,N-bis(propan-2-yl)phosphinic amide |
title |
P,P-Bis[4-(dimethylamino)phenyl]-N,N-bis(propan-2-yl)phosphinic amide |
title_full |
P,P-Bis[4-(dimethylamino)phenyl]-N,N-bis(propan-2-yl)phosphinic amide |
title_fullStr |
P,P-Bis[4-(dimethylamino)phenyl]-N,N-bis(propan-2-yl)phosphinic amide |
title_full_unstemmed |
P,P-Bis[4-(dimethylamino)phenyl]-N,N-bis(propan-2-yl)phosphinic amide |
title_short |
P,P-Bis[4-(dimethylamino)phenyl]-N,N-bis(propan-2-yl)phosphinic amide |
title_sort | p,p-bis[4-(dimethylamino)phenyl]-n,n-bis(propan-2-yl)phosphinic amide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569256/ https://www.ncbi.nlm.nih.gov/pubmed/23424479 http://dx.doi.org/10.1107/S1600536812050398 |
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