4-[(E)-1-Naphthyl­diazen­yl]phenol

The title compound (C. I. Solvent Yellow 8), C(16)H(12)N(2)O, crystallizes with two crystallographically independent mol­ecules in the asymmetric unit. The planarity of both mol­ecules is slightly distorted, the dihedral angles between the benzene ring and the naphthalene system being 9.04 (8) and 5...

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Detalles Bibliográficos
Autores principales: Aslanov, Leonid A., Paseshnichenko, Ksenia A., Yatsenko, Alexandr V.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968944/
https://www.ncbi.nlm.nih.gov/pubmed/21582541
http://dx.doi.org/10.1107/S1600536809009866
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author Aslanov, Leonid A.
Paseshnichenko, Ksenia A.
Yatsenko, Alexandr V.
author_facet Aslanov, Leonid A.
Paseshnichenko, Ksenia A.
Yatsenko, Alexandr V.
author_sort Aslanov, Leonid A.
collection PubMed
description The title compound (C. I. Solvent Yellow 8), C(16)H(12)N(2)O, crystallizes with two crystallographically independent mol­ecules in the asymmetric unit. The planarity of both mol­ecules is slightly distorted, the dihedral angles between the benzene ring and the naphthalene system being 9.04 (8) and 5.69 (3)°. In the crystal, O—H⋯N hydrogen bonds between the hydr­oxy groups and azo N atoms link the two symmetry-independent mol­ecules into a polymeric chain propagating in [001].
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spelling pubmed-29689442010-12-30 4-[(E)-1-Naphthyl­diazen­yl]phenol Aslanov, Leonid A. Paseshnichenko, Ksenia A. Yatsenko, Alexandr V. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound (C. I. Solvent Yellow 8), C(16)H(12)N(2)O, crystallizes with two crystallographically independent mol­ecules in the asymmetric unit. The planarity of both mol­ecules is slightly distorted, the dihedral angles between the benzene ring and the naphthalene system being 9.04 (8) and 5.69 (3)°. In the crystal, O—H⋯N hydrogen bonds between the hydr­oxy groups and azo N atoms link the two symmetry-independent mol­ecules into a polymeric chain propagating in [001]. International Union of Crystallography 2009-03-25 /pmc/articles/PMC2968944/ /pubmed/21582541 http://dx.doi.org/10.1107/S1600536809009866 Text en © Aslanov et al. 2009 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
Aslanov, Leonid A.
Paseshnichenko, Ksenia A.
Yatsenko, Alexandr V.
4-[(E)-1-Naphthyl­diazen­yl]phenol
title 4-[(E)-1-Naphthyl­diazen­yl]phenol
title_full 4-[(E)-1-Naphthyl­diazen­yl]phenol
title_fullStr 4-[(E)-1-Naphthyl­diazen­yl]phenol
title_full_unstemmed 4-[(E)-1-Naphthyl­diazen­yl]phenol
title_short 4-[(E)-1-Naphthyl­diazen­yl]phenol
title_sort 4-[(e)-1-naphthyl­diazen­yl]phenol
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968944/
https://www.ncbi.nlm.nih.gov/pubmed/21582541
http://dx.doi.org/10.1107/S1600536809009866
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AT paseshnichenkokseniaa 4e1naphthyldiazenylphenol
AT yatsenkoalexandrv 4e1naphthyldiazenylphenol

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