1,8-Bis(tos­yloxy)-9,10-anthraquinone

In the crystal structure of the title compound, C(28)H(20)O(8)S(2), adjacent anthracene skeletons are parallel or inclined at an angle of 20.6 (1)°. In the mol­ecular structure, the mean plane of the anthracene skeleton makes dihedral angles of 49.6 (1) and 76.8 (1)° with the tosyl rings, and the tw...

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Autores principales: Niedziałkowski, Paweł, Trzybiński, Damian, Sikorski, Artur, Ossowski, Tadeusz
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980119/
https://www.ncbi.nlm.nih.gov/pubmed/21580139
http://dx.doi.org/10.1107/S1600536809051009
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author Niedziałkowski, Paweł
Trzybiński, Damian
Sikorski, Artur
Ossowski, Tadeusz
author_facet Niedziałkowski, Paweł
Trzybiński, Damian
Sikorski, Artur
Ossowski, Tadeusz
author_sort Niedziałkowski, Paweł
collection PubMed
description In the crystal structure of the title compound, C(28)H(20)O(8)S(2), adjacent anthracene skeletons are parallel or inclined at an angle of 20.6 (1)°. In the mol­ecular structure, the mean plane of the anthracene skeleton makes dihedral angles of 49.6 (1) and 76.8 (1)° with the tosyl rings, and the two terminal benzene rings are oriented at an angle of 74.5 (1)° with respect to each other. The crystal structure is stabilized by inter­molecular C—H⋯O and C—O⋯π inter­actions.
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spelling pubmed-29801192010-12-30 1,8-Bis(tos­yloxy)-9,10-anthraquinone Niedziałkowski, Paweł Trzybiński, Damian Sikorski, Artur Ossowski, Tadeusz Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal structure of the title compound, C(28)H(20)O(8)S(2), adjacent anthracene skeletons are parallel or inclined at an angle of 20.6 (1)°. In the mol­ecular structure, the mean plane of the anthracene skeleton makes dihedral angles of 49.6 (1) and 76.8 (1)° with the tosyl rings, and the two terminal benzene rings are oriented at an angle of 74.5 (1)° with respect to each other. The crystal structure is stabilized by inter­molecular C—H⋯O and C—O⋯π inter­actions. International Union of Crystallography 2009-12-04 /pmc/articles/PMC2980119/ /pubmed/21580139 http://dx.doi.org/10.1107/S1600536809051009 Text en © Niedziałkowski 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
Niedziałkowski, Paweł
Trzybiński, Damian
Sikorski, Artur
Ossowski, Tadeusz
1,8-Bis(tos­yloxy)-9,10-anthraquinone
title 1,8-Bis(tos­yloxy)-9,10-anthraquinone
title_full 1,8-Bis(tos­yloxy)-9,10-anthraquinone
title_fullStr 1,8-Bis(tos­yloxy)-9,10-anthraquinone
title_full_unstemmed 1,8-Bis(tos­yloxy)-9,10-anthraquinone
title_short 1,8-Bis(tos­yloxy)-9,10-anthraquinone
title_sort 1,8-bis(tos­yloxy)-9,10-anthraquinone
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980119/
https://www.ncbi.nlm.nih.gov/pubmed/21580139
http://dx.doi.org/10.1107/S1600536809051009
work_keys_str_mv AT niedziałkowskipaweł 18bistosyloxy910anthraquinone
AT trzybinskidamian 18bistosyloxy910anthraquinone
AT sikorskiartur 18bistosyloxy910anthraquinone
AT ossowskitadeusz 18bistosyloxy910anthraquinone

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