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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2014
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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. |
format | Online Article Text |
id | pubmed-3998285 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
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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