9,10-Dioxoanthracene-1,4-diyl bis­(4-methyl­benzene­sulfonate)

The title mol­ecule, C(28)H(20)O(8)S(2), has a T-shaped conformation. The central 9,10-anthraquinone moiety is bow-shaped with the two outer aromatic rings being inclined to one another by 13.99 (11)°. The benzenesulfonate rings are inclined to one another by 47.35 (12)°, and by 34.51 (11) and 17.88...

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Detalles Bibliográficos
Autores principales: Teerawatananond, Thapong, Kerdsamut, Chiaranan, Kokpol, Sirirat, Muangsin, Nongnuj
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344545/
https://www.ncbi.nlm.nih.gov/pubmed/22590307
http://dx.doi.org/10.1107/S1600536812015814
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author Teerawatananond, Thapong
Kerdsamut, Chiaranan
Kokpol, Sirirat
Muangsin, Nongnuj
author_facet Teerawatananond, Thapong
Kerdsamut, Chiaranan
Kokpol, Sirirat
Muangsin, Nongnuj
author_sort Teerawatananond, Thapong
collection PubMed
description The title mol­ecule, C(28)H(20)O(8)S(2), has a T-shaped conformation. The central 9,10-anthraquinone moiety is bow-shaped with the two outer aromatic rings being inclined to one another by 13.99 (11)°. The benzenesulfonate rings are inclined to one another by 47.35 (12)°, and by 34.51 (11) and 17.88 (11)° to the bridging aromatic ring of the 9,10-anthraquinone moiety. In the crystal, C—H⋯O interactions link the mol­ecules into ribbons in [100].
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spelling pubmed-33445452012-05-15 9,10-Dioxoanthracene-1,4-diyl bis­(4-methyl­benzene­sulfonate) Teerawatananond, Thapong Kerdsamut, Chiaranan Kokpol, Sirirat Muangsin, Nongnuj Acta Crystallogr Sect E Struct Rep Online Organic Papers The title mol­ecule, C(28)H(20)O(8)S(2), has a T-shaped conformation. The central 9,10-anthraquinone moiety is bow-shaped with the two outer aromatic rings being inclined to one another by 13.99 (11)°. The benzenesulfonate rings are inclined to one another by 47.35 (12)°, and by 34.51 (11) and 17.88 (11)° to the bridging aromatic ring of the 9,10-anthraquinone moiety. In the crystal, C—H⋯O interactions link the mol­ecules into ribbons in [100]. International Union of Crystallography 2012-04-18 /pmc/articles/PMC3344545/ /pubmed/22590307 http://dx.doi.org/10.1107/S1600536812015814 Text en © Teerawatananond et al. 2012 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
Teerawatananond, Thapong
Kerdsamut, Chiaranan
Kokpol, Sirirat
Muangsin, Nongnuj
9,10-Dioxoanthracene-1,4-diyl bis­(4-methyl­benzene­sulfonate)
title 9,10-Dioxoanthracene-1,4-diyl bis­(4-methyl­benzene­sulfonate)
title_full 9,10-Dioxoanthracene-1,4-diyl bis­(4-methyl­benzene­sulfonate)
title_fullStr 9,10-Dioxoanthracene-1,4-diyl bis­(4-methyl­benzene­sulfonate)
title_full_unstemmed 9,10-Dioxoanthracene-1,4-diyl bis­(4-methyl­benzene­sulfonate)
title_short 9,10-Dioxoanthracene-1,4-diyl bis­(4-methyl­benzene­sulfonate)
title_sort 9,10-dioxoanthracene-1,4-diyl bis­(4-methyl­benzene­sulfonate)
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344545/
https://www.ncbi.nlm.nih.gov/pubmed/22590307
http://dx.doi.org/10.1107/S1600536812015814
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