6,7-Dimeth­oxy-1,4-anthraquinone

The mol­ecule of the title compound, C(16)H(12)O(4), is almost planar; the two meth­oxy groups are slightly out of the plane of the anthraquinone ring system, with C—C—O—C torsion angles of −6.25 (19) and −10.22 (19)°. In the crystal structure, the mol­ecules adopt a herringbone arrangement and form...

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Detalles Bibliográficos
Autores principales: Kitamura, Chitoshi, Akamatsu, Naoki, Yoneda, Akio, Kawase, Takeshi
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960635/
https://www.ncbi.nlm.nih.gov/pubmed/21201781
http://dx.doi.org/10.1107/S1600536808026500
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author Kitamura, Chitoshi
Akamatsu, Naoki
Yoneda, Akio
Kawase, Takeshi
author_facet Kitamura, Chitoshi
Akamatsu, Naoki
Yoneda, Akio
Kawase, Takeshi
author_sort Kitamura, Chitoshi
collection PubMed
description The mol­ecule of the title compound, C(16)H(12)O(4), is almost planar; the two meth­oxy groups are slightly out of the plane of the anthraquinone ring system, with C—C—O—C torsion angles of −6.25 (19) and −10.22 (19)°. In the crystal structure, the mol­ecules adopt a herringbone arrangement and form face-to-face slipped anti­parallel π–π stacking inter­actions along the b axis, with an inter­planar distance of 3.278 (2) Å.
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spelling pubmed-29606352010-12-30 6,7-Dimeth­oxy-1,4-anthraquinone Kitamura, Chitoshi Akamatsu, Naoki Yoneda, Akio Kawase, Takeshi Acta Crystallogr Sect E Struct Rep Online Organic Papers The mol­ecule of the title compound, C(16)H(12)O(4), is almost planar; the two meth­oxy groups are slightly out of the plane of the anthraquinone ring system, with C—C—O—C torsion angles of −6.25 (19) and −10.22 (19)°. In the crystal structure, the mol­ecules adopt a herringbone arrangement and form face-to-face slipped anti­parallel π–π stacking inter­actions along the b axis, with an inter­planar distance of 3.278 (2) Å. International Union of Crystallography 2008-08-23 /pmc/articles/PMC2960635/ /pubmed/21201781 http://dx.doi.org/10.1107/S1600536808026500 Text en © Kitamura et al. 2008 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
Kitamura, Chitoshi
Akamatsu, Naoki
Yoneda, Akio
Kawase, Takeshi
6,7-Dimeth­oxy-1,4-anthraquinone
title 6,7-Dimeth­oxy-1,4-anthraquinone
title_full 6,7-Dimeth­oxy-1,4-anthraquinone
title_fullStr 6,7-Dimeth­oxy-1,4-anthraquinone
title_full_unstemmed 6,7-Dimeth­oxy-1,4-anthraquinone
title_short 6,7-Dimeth­oxy-1,4-anthraquinone
title_sort 6,7-dimeth­oxy-1,4-anthraquinone
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960635/
https://www.ncbi.nlm.nih.gov/pubmed/21201781
http://dx.doi.org/10.1107/S1600536808026500
work_keys_str_mv AT kitamurachitoshi 67dimethoxy14anthraquinone
AT akamatsunaoki 67dimethoxy14anthraquinone
AT yonedaakio 67dimethoxy14anthraquinone
AT kawasetakeshi 67dimethoxy14anthraquinone

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