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N,N′-Bis(1-ethynylcyclo­hexyl)­pyro­mellitic diimide

The title compound, C(26)H(24)N(2)O(4), consists of a symmetrical mol­ecule that lies across a crystallographic inversion centre. The C—C distance in the triple bond is 1.188 (2) Å and there is also an inter­molecular C—H⋯O contact from a terminal acetyl­ene C—H to one of the dimiide O atoms [3.4349...

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Detalles Bibliográficos
Autores principales: Gondo, Chenaimwoyo A., Lynch, Daniel E., Hamilton, Darren G.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970110/
https://www.ncbi.nlm.nih.gov/pubmed/21577536
http://dx.doi.org/10.1107/S1600536809030979
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author Gondo, Chenaimwoyo A.
Lynch, Daniel E.
Hamilton, Darren G.
author_facet Gondo, Chenaimwoyo A.
Lynch, Daniel E.
Hamilton, Darren G.
author_sort Gondo, Chenaimwoyo A.
collection PubMed
description The title compound, C(26)H(24)N(2)O(4), consists of a symmetrical mol­ecule that lies across a crystallographic inversion centre. The C—C distance in the triple bond is 1.188 (2) Å and there is also an inter­molecular C—H⋯O contact from a terminal acetyl­ene C—H to one of the dimiide O atoms [3.4349 (19) Å].
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spelling pubmed-29701102010-12-30 N,N′-Bis(1-ethynylcyclo­hexyl)­pyro­mellitic diimide Gondo, Chenaimwoyo A. Lynch, Daniel E. Hamilton, Darren G. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(26)H(24)N(2)O(4), consists of a symmetrical mol­ecule that lies across a crystallographic inversion centre. The C—C distance in the triple bond is 1.188 (2) Å and there is also an inter­molecular C—H⋯O contact from a terminal acetyl­ene C—H to one of the dimiide O atoms [3.4349 (19) Å]. International Union of Crystallography 2009-08-08 /pmc/articles/PMC2970110/ /pubmed/21577536 http://dx.doi.org/10.1107/S1600536809030979 Text en © Gondo 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
Gondo, Chenaimwoyo A.
Lynch, Daniel E.
Hamilton, Darren G.
N,N′-Bis(1-ethynylcyclo­hexyl)­pyro­mellitic diimide
title N,N′-Bis(1-ethynylcyclo­hexyl)­pyro­mellitic diimide
title_full N,N′-Bis(1-ethynylcyclo­hexyl)­pyro­mellitic diimide
title_fullStr N,N′-Bis(1-ethynylcyclo­hexyl)­pyro­mellitic diimide
title_full_unstemmed N,N′-Bis(1-ethynylcyclo­hexyl)­pyro­mellitic diimide
title_short N,N′-Bis(1-ethynylcyclo­hexyl)­pyro­mellitic diimide
title_sort n,n′-bis(1-ethynylcyclo­hexyl)­pyro­mellitic diimide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970110/
https://www.ncbi.nlm.nih.gov/pubmed/21577536
http://dx.doi.org/10.1107/S1600536809030979
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