(2-Hy­droxy-4-meth­oxy­phen­yl)(2-hy­droxy­phen­yl)methanone

The title compound, C(14)H(12)O(4), is an asymmetric substitution product of benzophenone. Both hy­droxy groups are orientated towards the O atom of the keto group. Intra­molecular as well as inter­molecular O—H⋯O hydrogen bonds can be observed in the crystal structure, with the latter connecting th...

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Detalles Bibliográficos
Autores principales: Betz, Richard, Gerber, Thomas, Hosten, Eric, 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/PMC3213614/
https://www.ncbi.nlm.nih.gov/pubmed/22091191
http://dx.doi.org/10.1107/S1600536811030042
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author Betz, Richard
Gerber, Thomas
Hosten, Eric
Schalekamp, Henk
author_facet Betz, Richard
Gerber, Thomas
Hosten, Eric
Schalekamp, Henk
author_sort Betz, Richard
collection PubMed
description The title compound, C(14)H(12)O(4), is an asymmetric substitution product of benzophenone. Both hy­droxy groups are orientated towards the O atom of the keto group. Intra­molecular as well as inter­molecular O—H⋯O hydrogen bonds can be observed in the crystal structure, with the latter connecting the mol­ecules into chains along the crystallographic b axis. C—H⋯O contacts [C⋯O = 3.3297 (18) Å] are also apparent. The closest centroid–centroid distance between two aromatic systems is 4.9186 (9) Å.
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spelling pubmed-32136142011-11-16 (2-Hy­droxy-4-meth­oxy­phen­yl)(2-hy­droxy­phen­yl)methanone Betz, Richard Gerber, Thomas Hosten, Eric Schalekamp, Henk Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(14)H(12)O(4), is an asymmetric substitution product of benzophenone. Both hy­droxy groups are orientated towards the O atom of the keto group. Intra­molecular as well as inter­molecular O—H⋯O hydrogen bonds can be observed in the crystal structure, with the latter connecting the mol­ecules into chains along the crystallographic b axis. C—H⋯O contacts [C⋯O = 3.3297 (18) Å] are also apparent. The closest centroid–centroid distance between two aromatic systems is 4.9186 (9) Å. International Union of Crystallography 2011-07-30 /pmc/articles/PMC3213614/ /pubmed/22091191 http://dx.doi.org/10.1107/S1600536811030042 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
Hosten, Eric
Schalekamp, Henk
(2-Hy­droxy-4-meth­oxy­phen­yl)(2-hy­droxy­phen­yl)methanone
title (2-Hy­droxy-4-meth­oxy­phen­yl)(2-hy­droxy­phen­yl)methanone
title_full (2-Hy­droxy-4-meth­oxy­phen­yl)(2-hy­droxy­phen­yl)methanone
title_fullStr (2-Hy­droxy-4-meth­oxy­phen­yl)(2-hy­droxy­phen­yl)methanone
title_full_unstemmed (2-Hy­droxy-4-meth­oxy­phen­yl)(2-hy­droxy­phen­yl)methanone
title_short (2-Hy­droxy-4-meth­oxy­phen­yl)(2-hy­droxy­phen­yl)methanone
title_sort (2-hy­droxy-4-meth­oxy­phen­yl)(2-hy­droxy­phen­yl)methanone
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3213614/
https://www.ncbi.nlm.nih.gov/pubmed/22091191
http://dx.doi.org/10.1107/S1600536811030042
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AT gerberthomas 2hydroxy4methoxyphenyl2hydroxyphenylmethanone
AT hosteneric 2hydroxy4methoxyphenyl2hydroxyphenylmethanone
AT schalekamphenk 2hydroxy4methoxyphenyl2hydroxyphenylmethanone

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