Monoclinic form of 1,2,4,5-tetra­cyclo­hexyl­benzene

The mol­ecule of the title compound, C(30)H(46), has a crystallographically imposed inversion center and the cyclo­hexyl groups are oriented with their methine H atoms pointing towards one another (H⋯H = 1.99 Å). The cyclohexyl groups adopt chair conformations. A significant C—H⋯π inter­action assem...

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Detalles Bibliográficos
Autores principales: Mague, Joel T., Linhardt, Lisa, Medina, Iliana, Sattler, Daniel J., Fink, Mark J.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960273/
https://www.ncbi.nlm.nih.gov/pubmed/21201406
http://dx.doi.org/10.1107/S160053680706758X
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author Mague, Joel T.
Linhardt, Lisa
Medina, Iliana
Sattler, Daniel J.
Fink, Mark J.
author_facet Mague, Joel T.
Linhardt, Lisa
Medina, Iliana
Sattler, Daniel J.
Fink, Mark J.
author_sort Mague, Joel T.
collection PubMed
description The mol­ecule of the title compound, C(30)H(46), has a crystallographically imposed inversion center and the cyclo­hexyl groups are oriented with their methine H atoms pointing towards one another (H⋯H = 1.99 Å). The cyclohexyl groups adopt chair conformations. A significant C—H⋯π inter­action assembles mol­ecules into layers parallel to (100).
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spelling pubmed-29602732010-12-30 Monoclinic form of 1,2,4,5-tetra­cyclo­hexyl­benzene Mague, Joel T. Linhardt, Lisa Medina, Iliana Sattler, Daniel J. Fink, Mark J. Acta Crystallogr Sect E Struct Rep Online Organic Papers The mol­ecule of the title compound, C(30)H(46), has a crystallographically imposed inversion center and the cyclo­hexyl groups are oriented with their methine H atoms pointing towards one another (H⋯H = 1.99 Å). The cyclohexyl groups adopt chair conformations. A significant C—H⋯π inter­action assembles mol­ecules into layers parallel to (100). International Union of Crystallography 2008-01-04 /pmc/articles/PMC2960273/ /pubmed/21201406 http://dx.doi.org/10.1107/S160053680706758X Text en © Mague et al. 2008 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
Mague, Joel T.
Linhardt, Lisa
Medina, Iliana
Sattler, Daniel J.
Fink, Mark J.
Monoclinic form of 1,2,4,5-tetra­cyclo­hexyl­benzene
title Monoclinic form of 1,2,4,5-tetra­cyclo­hexyl­benzene
title_full Monoclinic form of 1,2,4,5-tetra­cyclo­hexyl­benzene
title_fullStr Monoclinic form of 1,2,4,5-tetra­cyclo­hexyl­benzene
title_full_unstemmed Monoclinic form of 1,2,4,5-tetra­cyclo­hexyl­benzene
title_short Monoclinic form of 1,2,4,5-tetra­cyclo­hexyl­benzene
title_sort monoclinic form of 1,2,4,5-tetra­cyclo­hexyl­benzene
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960273/
https://www.ncbi.nlm.nih.gov/pubmed/21201406
http://dx.doi.org/10.1107/S160053680706758X
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AT sattlerdanielj monoclinicformof1245tetracyclohexylbenzene
AT finkmarkj monoclinicformof1245tetracyclohexylbenzene

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