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cis-Cycloheptane-1,2-diol
The title compound, C(7)H(14)O(2), is a vicinal diol derived from cycloheptane with cis-orientated hydroxy groups. The molecules shows no non-crystallographic symmetry. The O—C—C—O torsion angles of both molecules present in the asymmetric unit [−66.4 (2) and −66.9 (2)°] are similar to those in...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971971/ https://www.ncbi.nlm.nih.gov/pubmed/21578965 http://dx.doi.org/10.1107/S160053680905051X |
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author | Betz, Richard Klüfers, Peter Mayer, Peter |
author_facet | Betz, Richard Klüfers, Peter Mayer, Peter |
author_sort | Betz, Richard |
collection | PubMed |
description | The title compound, C(7)H(14)O(2), is a vicinal diol derived from cycloheptane with cis-orientated hydroxy groups. The molecules shows no non-crystallographic symmetry. The O—C—C—O torsion angles of both molecules present in the asymmetric unit [−66.4 (2) and −66.9 (2)°] are similar to those in trans-configured cyclohexane derivatives (including pyranoses) as well as rac-trans-cycloheptane-1,2-diol, but smaller than those in trans-configured cyclopentane derivatives (including furanoses). In the crystal structure, O—H⋯O hydrogen bonds furnish the formation of sheets parallel to [110]. |
format | Text |
id | pubmed-2971971 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29719712010-12-30 cis-Cycloheptane-1,2-diol Betz, Richard Klüfers, Peter Mayer, Peter Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(7)H(14)O(2), is a vicinal diol derived from cycloheptane with cis-orientated hydroxy groups. The molecules shows no non-crystallographic symmetry. The O—C—C—O torsion angles of both molecules present in the asymmetric unit [−66.4 (2) and −66.9 (2)°] are similar to those in trans-configured cyclohexane derivatives (including pyranoses) as well as rac-trans-cycloheptane-1,2-diol, but smaller than those in trans-configured cyclopentane derivatives (including furanoses). In the crystal structure, O—H⋯O hydrogen bonds furnish the formation of sheets parallel to [110]. International Union of Crystallography 2009-11-28 /pmc/articles/PMC2971971/ /pubmed/21578965 http://dx.doi.org/10.1107/S160053680905051X Text en © Betz et al. 2009 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 Betz, Richard Klüfers, Peter Mayer, Peter cis-Cycloheptane-1,2-diol |
title |
cis-Cycloheptane-1,2-diol |
title_full |
cis-Cycloheptane-1,2-diol |
title_fullStr |
cis-Cycloheptane-1,2-diol |
title_full_unstemmed |
cis-Cycloheptane-1,2-diol |
title_short |
cis-Cycloheptane-1,2-diol |
title_sort | cis-cycloheptane-1,2-diol |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971971/ https://www.ncbi.nlm.nih.gov/pubmed/21578965 http://dx.doi.org/10.1107/S160053680905051X |
work_keys_str_mv | AT betzrichard ciscycloheptane12diol AT kluferspeter ciscycloheptane12diol AT mayerpeter ciscycloheptane12diol |