2-Meth­oxy-3,4-diphenyl­phenol

The title compound, C(19)H(16)O(2), was isolated as the major product after the solid-state photochemical reaction of 2-meth­oxy-4,4-diphenyl­cyclo­hexa-2,5-dienone. The dihedral angles between the central ring and pendant benzene rings are 60.76 (6) and 51.64 (6)°. The O—C vector of the meth­oxy gr...

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Detalles Bibliográficos
Autores principales: Guzei, Ilia A., Annamalai, Senthilvelan, Zimmerman, Howard E.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980045/
https://www.ncbi.nlm.nih.gov/pubmed/21580173
http://dx.doi.org/10.1107/S1600536809050855
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author Guzei, Ilia A.
Annamalai, Senthilvelan
Zimmerman, Howard E.
author_facet Guzei, Ilia A.
Annamalai, Senthilvelan
Zimmerman, Howard E.
author_sort Guzei, Ilia A.
collection PubMed
description The title compound, C(19)H(16)O(2), was isolated as the major product after the solid-state photochemical reaction of 2-meth­oxy-4,4-diphenyl­cyclo­hexa-2,5-dienone. The dihedral angles between the central ring and pendant benzene rings are 60.76 (6) and 51.64 (6)°. The O—C vector of the meth­oxy group is almost perpendicular to the plane of the central ring as indicated by the C—C—O—C torsion angle of 94.89 (18)°. Hydrogen-bonded dimers are formed in the crystal structure via O—H⋯O inter­actions. The data were collected at room temperature on a Bruker SMART X2S diffractometer in the automated mode and processed manually thereafter.
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spelling pubmed-29800452010-12-30 2-Meth­oxy-3,4-diphenyl­phenol Guzei, Ilia A. Annamalai, Senthilvelan Zimmerman, Howard E. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(19)H(16)O(2), was isolated as the major product after the solid-state photochemical reaction of 2-meth­oxy-4,4-diphenyl­cyclo­hexa-2,5-dienone. The dihedral angles between the central ring and pendant benzene rings are 60.76 (6) and 51.64 (6)°. The O—C vector of the meth­oxy group is almost perpendicular to the plane of the central ring as indicated by the C—C—O—C torsion angle of 94.89 (18)°. Hydrogen-bonded dimers are formed in the crystal structure via O—H⋯O inter­actions. The data were collected at room temperature on a Bruker SMART X2S diffractometer in the automated mode and processed manually thereafter. International Union of Crystallography 2009-12-09 /pmc/articles/PMC2980045/ /pubmed/21580173 http://dx.doi.org/10.1107/S1600536809050855 Text en © Guzei 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
Guzei, Ilia A.
Annamalai, Senthilvelan
Zimmerman, Howard E.
2-Meth­oxy-3,4-diphenyl­phenol
title 2-Meth­oxy-3,4-diphenyl­phenol
title_full 2-Meth­oxy-3,4-diphenyl­phenol
title_fullStr 2-Meth­oxy-3,4-diphenyl­phenol
title_full_unstemmed 2-Meth­oxy-3,4-diphenyl­phenol
title_short 2-Meth­oxy-3,4-diphenyl­phenol
title_sort 2-meth­oxy-3,4-diphenyl­phenol
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980045/
https://www.ncbi.nlm.nih.gov/pubmed/21580173
http://dx.doi.org/10.1107/S1600536809050855
work_keys_str_mv AT guzeiiliaa 2methoxy34diphenylphenol
AT annamalaisenthilvelan 2methoxy34diphenylphenol
AT zimmermanhowarde 2methoxy34diphenylphenol

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