Bis(2-hy­droxy­phen­yl)methanone

In the title compound, C(13)H(10)O(3), a benzophenone derivative, the least-squares planes defined by the C atoms of the 2-hy­droxy­phenyl rings inter­sect at an angle of 45.49 (3)°. The substituents on the aromatic systems are both orientated towards the central O atom. Intra- as well as inter­mole...

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Detalles Bibliográficos
Autores principales: Betz, Richard, Gerber, Thomas, Schalekamp, Henk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3212291/
https://www.ncbi.nlm.nih.gov/pubmed/22090948
http://dx.doi.org/10.1107/S1600536811025438
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author Betz, Richard
Gerber, Thomas
Schalekamp, Henk
author_facet Betz, Richard
Gerber, Thomas
Schalekamp, Henk
author_sort Betz, Richard
collection PubMed
description In the title compound, C(13)H(10)O(3), a benzophenone derivative, the least-squares planes defined by the C atoms of the 2-hy­droxy­phenyl rings inter­sect at an angle of 45.49 (3)°. The substituents on the aromatic systems are both orientated towards the central O atom. Intra- as well as inter­molecular O—H⋯O hydrogen bonds are observed, the latter giving rise to the formation of centrosymmetric dimers. The closest centroid–centroid distance between two π-systems is 3.7934 (7) Å.
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spelling pubmed-32122912011-11-16 Bis(2-hy­droxy­phen­yl)methanone Betz, Richard Gerber, Thomas Schalekamp, Henk Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(13)H(10)O(3), a benzophenone derivative, the least-squares planes defined by the C atoms of the 2-hy­droxy­phenyl rings inter­sect at an angle of 45.49 (3)°. The substituents on the aromatic systems are both orientated towards the central O atom. Intra- as well as inter­molecular O—H⋯O hydrogen bonds are observed, the latter giving rise to the formation of centrosymmetric dimers. The closest centroid–centroid distance between two π-systems is 3.7934 (7) Å. International Union of Crystallography 2011-07-02 /pmc/articles/PMC3212291/ /pubmed/22090948 http://dx.doi.org/10.1107/S1600536811025438 Text en © Betz et al. 2011 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
Betz, Richard
Gerber, Thomas
Schalekamp, Henk
Bis(2-hy­droxy­phen­yl)methanone
title Bis(2-hy­droxy­phen­yl)methanone
title_full Bis(2-hy­droxy­phen­yl)methanone
title_fullStr Bis(2-hy­droxy­phen­yl)methanone
title_full_unstemmed Bis(2-hy­droxy­phen­yl)methanone
title_short Bis(2-hy­droxy­phen­yl)methanone
title_sort bis(2-hy­droxy­phen­yl)methanone
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3212291/
https://www.ncbi.nlm.nih.gov/pubmed/22090948
http://dx.doi.org/10.1107/S1600536811025438
work_keys_str_mv AT betzrichard bis2hydroxyphenylmethanone
AT gerberthomas bis2hydroxyphenylmethanone
AT schalekamphenk bis2hydroxyphenylmethanone

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