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2-[(2-Hydroxynaphthalen-1-yl)methylideneamino]-5,6,7,8-tetrahydro-4H-cyclohepta[b]thiophene-3-carbonitrile
Two independent molecules, A and B, comprise the asymmetric unit of the title compound, C(21)H(18)N(2)OS, with the difference in the angle of orientation between the naphthalene ring system and the mean plane of the cycloheptyl ring [16.13 (1) in A and 11.48 (5)° in B], being evident. The cyclohe...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569254/ https://www.ncbi.nlm.nih.gov/pubmed/23424477 http://dx.doi.org/10.1107/S160053681300007X |
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author | Asiri, Abdullah M. Arshad, Muhammad Nadeem Sobahi, Tariq R. Mustafa, Ghulam |
author_facet | Asiri, Abdullah M. Arshad, Muhammad Nadeem Sobahi, Tariq R. Mustafa, Ghulam |
author_sort | Asiri, Abdullah M. |
collection | PubMed |
description | Two independent molecules, A and B, comprise the asymmetric unit of the title compound, C(21)H(18)N(2)OS, with the difference in the angle of orientation between the naphthalene ring system and the mean plane of the cycloheptyl ring [16.13 (1) in A and 11.48 (5)° in B], being evident. The cycloheptyl ring adopts a distorted chair conformation in each molecule with r.m.s. deviations of 0.2345 (4) (A) and 0.2302 (4) Å (B). Intramolecular O—H⋯N hydrogen bonding generates planar six-membered S(6) loops with r.m.s. deviations of 0.0099 (1) (A) and 0.0286 (1) Å (B). |
format | Online Article Text |
id | pubmed-3569254 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-35692542013-02-19 2-[(2-Hydroxynaphthalen-1-yl)methylideneamino]-5,6,7,8-tetrahydro-4H-cyclohepta[b]thiophene-3-carbonitrile Asiri, Abdullah M. Arshad, Muhammad Nadeem Sobahi, Tariq R. Mustafa, Ghulam Acta Crystallogr Sect E Struct Rep Online Organic Papers Two independent molecules, A and B, comprise the asymmetric unit of the title compound, C(21)H(18)N(2)OS, with the difference in the angle of orientation between the naphthalene ring system and the mean plane of the cycloheptyl ring [16.13 (1) in A and 11.48 (5)° in B], being evident. The cycloheptyl ring adopts a distorted chair conformation in each molecule with r.m.s. deviations of 0.2345 (4) (A) and 0.2302 (4) Å (B). Intramolecular O—H⋯N hydrogen bonding generates planar six-membered S(6) loops with r.m.s. deviations of 0.0099 (1) (A) and 0.0286 (1) Å (B). International Union of Crystallography 2013-01-09 /pmc/articles/PMC3569254/ /pubmed/23424477 http://dx.doi.org/10.1107/S160053681300007X Text en © Asiri et al. 2013 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 Asiri, Abdullah M. Arshad, Muhammad Nadeem Sobahi, Tariq R. Mustafa, Ghulam 2-[(2-Hydroxynaphthalen-1-yl)methylideneamino]-5,6,7,8-tetrahydro-4H-cyclohepta[b]thiophene-3-carbonitrile |
title | 2-[(2-Hydroxynaphthalen-1-yl)methylideneamino]-5,6,7,8-tetrahydro-4H-cyclohepta[b]thiophene-3-carbonitrile |
title_full | 2-[(2-Hydroxynaphthalen-1-yl)methylideneamino]-5,6,7,8-tetrahydro-4H-cyclohepta[b]thiophene-3-carbonitrile |
title_fullStr | 2-[(2-Hydroxynaphthalen-1-yl)methylideneamino]-5,6,7,8-tetrahydro-4H-cyclohepta[b]thiophene-3-carbonitrile |
title_full_unstemmed | 2-[(2-Hydroxynaphthalen-1-yl)methylideneamino]-5,6,7,8-tetrahydro-4H-cyclohepta[b]thiophene-3-carbonitrile |
title_short | 2-[(2-Hydroxynaphthalen-1-yl)methylideneamino]-5,6,7,8-tetrahydro-4H-cyclohepta[b]thiophene-3-carbonitrile |
title_sort | 2-[(2-hydroxynaphthalen-1-yl)methylideneamino]-5,6,7,8-tetrahydro-4h-cyclohepta[b]thiophene-3-carbonitrile |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569254/ https://www.ncbi.nlm.nih.gov/pubmed/23424477 http://dx.doi.org/10.1107/S160053681300007X |
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