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9-Allyl-9H-fluoren-9-ol
The asymmetric unit of the title compound, C(16)H(14)O, contains two independent molecules differing in the orientations of the allyl groups; the corresponding O—C—C(H(2))—C(H) torsion angles are −61.01 (13) and −177.43 (10)°. In the crystal, O—H⋯O hydrogen bonds link four molecules into a centros...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4051071/ https://www.ncbi.nlm.nih.gov/pubmed/24940257 http://dx.doi.org/10.1107/S1600536814010290 |
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author | Knight, Kyle S. Wood, Harvey B. |
author_facet | Knight, Kyle S. Wood, Harvey B. |
author_sort | Knight, Kyle S. |
collection | PubMed |
description | The asymmetric unit of the title compound, C(16)H(14)O, contains two independent molecules differing in the orientations of the allyl groups; the corresponding O—C—C(H(2))—C(H) torsion angles are −61.01 (13) and −177.43 (10)°. In the crystal, O—H⋯O hydrogen bonds link four molecules into a centrosymmetric tetramer, in which each hydroxy group acts as a donor and an acceptor of hydrogen bonds. |
format | Online Article Text |
id | pubmed-4051071 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-40510712014-06-17 9-Allyl-9H-fluoren-9-ol Knight, Kyle S. Wood, Harvey B. Acta Crystallogr Sect E Struct Rep Online Organic Papers The asymmetric unit of the title compound, C(16)H(14)O, contains two independent molecules differing in the orientations of the allyl groups; the corresponding O—C—C(H(2))—C(H) torsion angles are −61.01 (13) and −177.43 (10)°. In the crystal, O—H⋯O hydrogen bonds link four molecules into a centrosymmetric tetramer, in which each hydroxy group acts as a donor and an acceptor of hydrogen bonds. International Union of Crystallography 2014-05-17 /pmc/articles/PMC4051071/ /pubmed/24940257 http://dx.doi.org/10.1107/S1600536814010290 Text en © Knight and Wood 2014 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 Knight, Kyle S. Wood, Harvey B. 9-Allyl-9H-fluoren-9-ol |
title | 9-Allyl-9H-fluoren-9-ol |
title_full | 9-Allyl-9H-fluoren-9-ol |
title_fullStr | 9-Allyl-9H-fluoren-9-ol |
title_full_unstemmed | 9-Allyl-9H-fluoren-9-ol |
title_short | 9-Allyl-9H-fluoren-9-ol |
title_sort | 9-allyl-9h-fluoren-9-ol |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4051071/ https://www.ncbi.nlm.nih.gov/pubmed/24940257 http://dx.doi.org/10.1107/S1600536814010290 |
work_keys_str_mv | AT knightkyles 9allyl9hfluoren9ol AT woodharveyb 9allyl9hfluoren9ol |