4-Acetamido-N-(λ(5)-triphenyl­phospho­ranyl­idene)benzene­sulfonamide

There are two independent mol­ecules per asymmetric unit of the title compound, C(26)H(23)N(2)O(3)PS. Their superposition shows that they differ in the conformation of the CH(3)CO– group and the benzene rings from the triphenyl­phospho­rane group. In the crystal structure, independent mol­ecules are...

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Detalles Bibliográficos
Autores principales: Prugovečki, Biserka, Marinković, Marina, Vinković, Mladen, Dumić, Miljenko
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979042/
https://www.ncbi.nlm.nih.gov/pubmed/21579151
http://dx.doi.org/10.1107/S1600536810013620
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author Prugovečki, Biserka
Marinković, Marina
Vinković, Mladen
Dumić, Miljenko
author_facet Prugovečki, Biserka
Marinković, Marina
Vinković, Mladen
Dumić, Miljenko
author_sort Prugovečki, Biserka
collection PubMed
description There are two independent mol­ecules per asymmetric unit of the title compound, C(26)H(23)N(2)O(3)PS. Their superposition shows that they differ in the conformation of the CH(3)CO– group and the benzene rings from the triphenyl­phospho­rane group. In the crystal structure, independent mol­ecules are inter­conected by strong N—H⋯O hydrogen bonds, forming infinite chains along the a axis.
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spelling pubmed-29790422010-12-30 4-Acetamido-N-(λ(5)-triphenyl­phospho­ranyl­idene)benzene­sulfonamide Prugovečki, Biserka Marinković, Marina Vinković, Mladen Dumić, Miljenko Acta Crystallogr Sect E Struct Rep Online Organic Papers There are two independent mol­ecules per asymmetric unit of the title compound, C(26)H(23)N(2)O(3)PS. Their superposition shows that they differ in the conformation of the CH(3)CO– group and the benzene rings from the triphenyl­phospho­rane group. In the crystal structure, independent mol­ecules are inter­conected by strong N—H⋯O hydrogen bonds, forming infinite chains along the a axis. International Union of Crystallography 2010-04-17 /pmc/articles/PMC2979042/ /pubmed/21579151 http://dx.doi.org/10.1107/S1600536810013620 Text en © Prugovečki et al. 2010 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
Prugovečki, Biserka
Marinković, Marina
Vinković, Mladen
Dumić, Miljenko
4-Acetamido-N-(λ(5)-triphenyl­phospho­ranyl­idene)benzene­sulfonamide
title 4-Acetamido-N-(λ(5)-triphenyl­phospho­ranyl­idene)benzene­sulfonamide
title_full 4-Acetamido-N-(λ(5)-triphenyl­phospho­ranyl­idene)benzene­sulfonamide
title_fullStr 4-Acetamido-N-(λ(5)-triphenyl­phospho­ranyl­idene)benzene­sulfonamide
title_full_unstemmed 4-Acetamido-N-(λ(5)-triphenyl­phospho­ranyl­idene)benzene­sulfonamide
title_short 4-Acetamido-N-(λ(5)-triphenyl­phospho­ranyl­idene)benzene­sulfonamide
title_sort 4-acetamido-n-(λ(5)-triphenyl­phospho­ranyl­idene)benzene­sulfonamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979042/
https://www.ncbi.nlm.nih.gov/pubmed/21579151
http://dx.doi.org/10.1107/S1600536810013620
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AT marinkovicmarina 4acetamidonl5triphenylphosphoranylidenebenzenesulfonamide
AT vinkovicmladen 4acetamidonl5triphenylphosphoranylidenebenzenesulfonamide
AT dumicmiljenko 4acetamidonl5triphenylphosphoranylidenebenzenesulfonamide

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