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2,2′-(1,4-Phenyl­ene)bis­(propane-2,2-di­yl) bis­(benzodi­thio­ate)

The title compound, C(26)H(26)S(4), shows a dihedral angle of 76.64 (15)° between the central and peripheral benzene rings. An inversion center is located at the centroid of the thio­benzoyl ring. In the crystal, weak C—H⋯S inter­actions form C(5) chains along [001]. There are no classical hydrogen...

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Detalles Bibliográficos
Autores principales: Moreno-Fuquen, Rodolfo, Grande, Carlos, Advincula, Rigoberto C., Tenorio, Juan C., Ellena, Javier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3998285/
https://www.ncbi.nlm.nih.gov/pubmed/24764846
http://dx.doi.org/10.1107/S160053681303465X
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author Moreno-Fuquen, Rodolfo
Grande, Carlos
Advincula, Rigoberto C.
Tenorio, Juan C.
Ellena, Javier
author_facet Moreno-Fuquen, Rodolfo
Grande, Carlos
Advincula, Rigoberto C.
Tenorio, Juan C.
Ellena, Javier
author_sort Moreno-Fuquen, Rodolfo
collection PubMed
description The title compound, C(26)H(26)S(4), shows a dihedral angle of 76.64 (15)° between the central and peripheral benzene rings. An inversion center is located at the centroid of the thio­benzoyl ring. In the crystal, weak C—H⋯S inter­actions form C(5) chains along [001]. There are no classical hydrogen bonds.
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spelling pubmed-39982852014-04-24 2,2′-(1,4-Phenyl­ene)bis­(propane-2,2-di­yl) bis­(benzodi­thio­ate) Moreno-Fuquen, Rodolfo Grande, Carlos Advincula, Rigoberto C. Tenorio, Juan C. Ellena, Javier Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(26)H(26)S(4), shows a dihedral angle of 76.64 (15)° between the central and peripheral benzene rings. An inversion center is located at the centroid of the thio­benzoyl ring. In the crystal, weak C—H⋯S inter­actions form C(5) chains along [001]. There are no classical hydrogen bonds. International Union of Crystallography 2014-01-08 /pmc/articles/PMC3998285/ /pubmed/24764846 http://dx.doi.org/10.1107/S160053681303465X Text en © Moreno-Fuquen et al. 2014 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
Moreno-Fuquen, Rodolfo
Grande, Carlos
Advincula, Rigoberto C.
Tenorio, Juan C.
Ellena, Javier
2,2′-(1,4-Phenyl­ene)bis­(propane-2,2-di­yl) bis­(benzodi­thio­ate)
title 2,2′-(1,4-Phenyl­ene)bis­(propane-2,2-di­yl) bis­(benzodi­thio­ate)
title_full 2,2′-(1,4-Phenyl­ene)bis­(propane-2,2-di­yl) bis­(benzodi­thio­ate)
title_fullStr 2,2′-(1,4-Phenyl­ene)bis­(propane-2,2-di­yl) bis­(benzodi­thio­ate)
title_full_unstemmed 2,2′-(1,4-Phenyl­ene)bis­(propane-2,2-di­yl) bis­(benzodi­thio­ate)
title_short 2,2′-(1,4-Phenyl­ene)bis­(propane-2,2-di­yl) bis­(benzodi­thio­ate)
title_sort 2,2′-(1,4-phenyl­ene)bis­(propane-2,2-di­yl) bis­(benzodi­thio­ate)
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3998285/
https://www.ncbi.nlm.nih.gov/pubmed/24764846
http://dx.doi.org/10.1107/S160053681303465X
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