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(E)-2-tert-Butyl-6-[(naphthalen-1-yl)imino­meth­yl]phenol

The asymmetric unit of the title Schiff base compound, C(21)H(21)NO, contains two crystallographicaly independent mol­ecules. The dihedral angles between the naphthalene mean plane and the benzene ring are 29.28 (8) and 26.92.(8)° in the two mol­ecules. An intra­molecular O—H⋯N hydrogen bond and wea...

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Autores principales: Jamjah, Roghayieh, Nekoomanesh, Mehdi, Zahedi, Roya, Zohuri, Gholamhossein, Afshar Taromi, Faramarz, Notash, Behrouz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275263/
https://www.ncbi.nlm.nih.gov/pubmed/22347119
http://dx.doi.org/10.1107/S1600536812002395
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author Jamjah, Roghayieh
Nekoomanesh, Mehdi
Zahedi, Roya
Zohuri, Gholamhossein
Afshar Taromi, Faramarz
Notash, Behrouz
author_facet Jamjah, Roghayieh
Nekoomanesh, Mehdi
Zahedi, Roya
Zohuri, Gholamhossein
Afshar Taromi, Faramarz
Notash, Behrouz
author_sort Jamjah, Roghayieh
collection PubMed
description The asymmetric unit of the title Schiff base compound, C(21)H(21)NO, contains two crystallographicaly independent mol­ecules. The dihedral angles between the naphthalene mean plane and the benzene ring are 29.28 (8) and 26.92.(8)° in the two mol­ecules. An intra­molecular O—H⋯N hydrogen bond and weak intra­molecular C—H⋯O hydrogen bonds stabilize the structure of each independent mol­ecule.
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spelling pubmed-32752632012-02-15 (E)-2-tert-Butyl-6-[(naphthalen-1-yl)imino­meth­yl]phenol Jamjah, Roghayieh Nekoomanesh, Mehdi Zahedi, Roya Zohuri, Gholamhossein Afshar Taromi, Faramarz Notash, Behrouz Acta Crystallogr Sect E Struct Rep Online Organic Papers The asymmetric unit of the title Schiff base compound, C(21)H(21)NO, contains two crystallographicaly independent mol­ecules. The dihedral angles between the naphthalene mean plane and the benzene ring are 29.28 (8) and 26.92.(8)° in the two mol­ecules. An intra­molecular O—H⋯N hydrogen bond and weak intra­molecular C—H⋯O hydrogen bonds stabilize the structure of each independent mol­ecule. International Union of Crystallography 2012-01-25 /pmc/articles/PMC3275263/ /pubmed/22347119 http://dx.doi.org/10.1107/S1600536812002395 Text en © Jamjah et al. 2012 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
Jamjah, Roghayieh
Nekoomanesh, Mehdi
Zahedi, Roya
Zohuri, Gholamhossein
Afshar Taromi, Faramarz
Notash, Behrouz
(E)-2-tert-Butyl-6-[(naphthalen-1-yl)imino­meth­yl]phenol
title (E)-2-tert-Butyl-6-[(naphthalen-1-yl)imino­meth­yl]phenol
title_full (E)-2-tert-Butyl-6-[(naphthalen-1-yl)imino­meth­yl]phenol
title_fullStr (E)-2-tert-Butyl-6-[(naphthalen-1-yl)imino­meth­yl]phenol
title_full_unstemmed (E)-2-tert-Butyl-6-[(naphthalen-1-yl)imino­meth­yl]phenol
title_short (E)-2-tert-Butyl-6-[(naphthalen-1-yl)imino­meth­yl]phenol
title_sort (e)-2-tert-butyl-6-[(naphthalen-1-yl)imino­meth­yl]phenol
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275263/
https://www.ncbi.nlm.nih.gov/pubmed/22347119
http://dx.doi.org/10.1107/S1600536812002395
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