Cargando…

1-(Hydroxy­meth­yl)pyrene

The asymmetric unit of the title compound, C(17)H(12)O, contains two molecules, in which the fused aromatic ring systems are almost planar [maximum deviations = 0.0529 (9) and 0.0256 (9) Å]. In the crystal, aromatic π–π stacking inter­actions (perpendicular distance of centroids of about 3.4 Å) and...

Descripción completa

Detalles Bibliográficos
Autores principales: Gruber, Tobias, Seichter, Wilhelm, Weber, Edwin
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979693/
https://www.ncbi.nlm.nih.gov/pubmed/21579858
http://dx.doi.org/10.1107/S1600536810002424
_version_ 1782191475394609152
author Gruber, Tobias
Seichter, Wilhelm
Weber, Edwin
author_facet Gruber, Tobias
Seichter, Wilhelm
Weber, Edwin
author_sort Gruber, Tobias
collection PubMed
description The asymmetric unit of the title compound, C(17)H(12)O, contains two molecules, in which the fused aromatic ring systems are almost planar [maximum deviations = 0.0529 (9) and 0.0256 (9) Å]. In the crystal, aromatic π–π stacking inter­actions (perpendicular distance of centroids of about 3.4 Å) and strong O—H⋯O hydrogen bonds result in a helical arrangement of pyrenyl dimers.
format Text
id pubmed-2979693
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-29796932010-12-30 1-(Hydroxy­meth­yl)pyrene Gruber, Tobias Seichter, Wilhelm Weber, Edwin Acta Crystallogr Sect E Struct Rep Online Organic Papers The asymmetric unit of the title compound, C(17)H(12)O, contains two molecules, in which the fused aromatic ring systems are almost planar [maximum deviations = 0.0529 (9) and 0.0256 (9) Å]. In the crystal, aromatic π–π stacking inter­actions (perpendicular distance of centroids of about 3.4 Å) and strong O—H⋯O hydrogen bonds result in a helical arrangement of pyrenyl dimers. International Union of Crystallography 2010-01-23 /pmc/articles/PMC2979693/ /pubmed/21579858 http://dx.doi.org/10.1107/S1600536810002424 Text en © Gruber 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
Gruber, Tobias
Seichter, Wilhelm
Weber, Edwin
1-(Hydroxy­meth­yl)pyrene
title 1-(Hydroxy­meth­yl)pyrene
title_full 1-(Hydroxy­meth­yl)pyrene
title_fullStr 1-(Hydroxy­meth­yl)pyrene
title_full_unstemmed 1-(Hydroxy­meth­yl)pyrene
title_short 1-(Hydroxy­meth­yl)pyrene
title_sort 1-(hydroxy­meth­yl)pyrene
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979693/
https://www.ncbi.nlm.nih.gov/pubmed/21579858
http://dx.doi.org/10.1107/S1600536810002424
work_keys_str_mv AT grubertobias 1hydroxymethylpyrene
AT seichterwilhelm 1hydroxymethylpyrene
AT weberedwin 1hydroxymethylpyrene