2,3-Dihydro-1H-cyclo­penta­[b]naph­tha­len-1-ol

In the title compound, C(13)H(12)O, the cyclo­pentene ring fused with the naphthalene group adopts an envelope conformation. The cyclo­pentene torsion angle, with the fusion bond at the centre, has a magnitude of 1.16 (16)°. In the crystal, neigh­bouring mol­ecules are connected through O—H⋯O hydrog...

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Autores principales: Çelik, Ísmail, Akkurt, Mehmet, Tutar, Ahmet, Erenler, Ramazan, García-Granda, Santiago
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3295469/
https://www.ncbi.nlm.nih.gov/pubmed/22412580
http://dx.doi.org/10.1107/S1600536812005181
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author Çelik, Ísmail
Akkurt, Mehmet
Tutar, Ahmet
Erenler, Ramazan
García-Granda, Santiago
author_facet Çelik, Ísmail
Akkurt, Mehmet
Tutar, Ahmet
Erenler, Ramazan
García-Granda, Santiago
author_sort Çelik, Ísmail
collection PubMed
description In the title compound, C(13)H(12)O, the cyclo­pentene ring fused with the naphthalene group adopts an envelope conformation. The cyclo­pentene torsion angle, with the fusion bond at the centre, has a magnitude of 1.16 (16)°. In the crystal, neigh­bouring mol­ecules are connected through O—H⋯O hydrogen bonds into an R (4) (4)(8) ring motif. The crystal packing also features weak π–π stacking inter­actions [centroid–centroid distance = 3.8981 (8) Å] and C—H⋯π inter­actions.
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spelling pubmed-32954692012-03-12 2,3-Dihydro-1H-cyclo­penta­[b]naph­tha­len-1-ol Çelik, Ísmail Akkurt, Mehmet Tutar, Ahmet Erenler, Ramazan García-Granda, Santiago Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(13)H(12)O, the cyclo­pentene ring fused with the naphthalene group adopts an envelope conformation. The cyclo­pentene torsion angle, with the fusion bond at the centre, has a magnitude of 1.16 (16)°. In the crystal, neigh­bouring mol­ecules are connected through O—H⋯O hydrogen bonds into an R (4) (4)(8) ring motif. The crystal packing also features weak π–π stacking inter­actions [centroid–centroid distance = 3.8981 (8) Å] and C—H⋯π inter­actions. International Union of Crystallography 2012-02-10 /pmc/articles/PMC3295469/ /pubmed/22412580 http://dx.doi.org/10.1107/S1600536812005181 Text en © Çelik 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
Çelik, Ísmail
Akkurt, Mehmet
Tutar, Ahmet
Erenler, Ramazan
García-Granda, Santiago
2,3-Dihydro-1H-cyclo­penta­[b]naph­tha­len-1-ol
title 2,3-Dihydro-1H-cyclo­penta­[b]naph­tha­len-1-ol
title_full 2,3-Dihydro-1H-cyclo­penta­[b]naph­tha­len-1-ol
title_fullStr 2,3-Dihydro-1H-cyclo­penta­[b]naph­tha­len-1-ol
title_full_unstemmed 2,3-Dihydro-1H-cyclo­penta­[b]naph­tha­len-1-ol
title_short 2,3-Dihydro-1H-cyclo­penta­[b]naph­tha­len-1-ol
title_sort 2,3-dihydro-1h-cyclo­penta­[b]naph­tha­len-1-ol
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3295469/
https://www.ncbi.nlm.nih.gov/pubmed/22412580
http://dx.doi.org/10.1107/S1600536812005181
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