Cytenamide–1,4-dioxane (2/1)

In the crystal structure of the title compound [systematic name: 5H-dibenzo[a,d]cyclo­hepta­triene-5-carboxamide–1,4-dioxane (2/1)], 2C(16)H(13)NO·C(4)H(8)O(2), the cytenamide mol­ecules form a hydrogen-bonded R (2) (2)(8) dimer. The solvent mol­ecule is located between two adjacent cytenamide dimer...

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Detalles Bibliográficos
Autores principales: Johnston, Andrea, Florence, Alastair J., Fabbiani, Francesca J. A., Shankland, Kenneth, Bedford, Colin T.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961860/
https://www.ncbi.nlm.nih.gov/pubmed/21202967
http://dx.doi.org/10.1107/S1600536808018709
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author Johnston, Andrea
Florence, Alastair J.
Fabbiani, Francesca J. A.
Shankland, Kenneth
Bedford, Colin T.
author_facet Johnston, Andrea
Florence, Alastair J.
Fabbiani, Francesca J. A.
Shankland, Kenneth
Bedford, Colin T.
author_sort Johnston, Andrea
collection PubMed
description In the crystal structure of the title compound [systematic name: 5H-dibenzo[a,d]cyclo­hepta­triene-5-carboxamide–1,4-dioxane (2/1)], 2C(16)H(13)NO·C(4)H(8)O(2), the cytenamide mol­ecules form a hydrogen-bonded R (2) (2)(8) dimer. The solvent mol­ecule is located between two adjacent cytenamide dimers and forms N—H⋯O hydrogen bonds with one cytenamide mol­ecule from each dimer.
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spelling pubmed-29618602010-12-30 Cytenamide–1,4-dioxane (2/1) Johnston, Andrea Florence, Alastair J. Fabbiani, Francesca J. A. Shankland, Kenneth Bedford, Colin T. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal structure of the title compound [systematic name: 5H-dibenzo[a,d]cyclo­hepta­triene-5-carboxamide–1,4-dioxane (2/1)], 2C(16)H(13)NO·C(4)H(8)O(2), the cytenamide mol­ecules form a hydrogen-bonded R (2) (2)(8) dimer. The solvent mol­ecule is located between two adjacent cytenamide dimers and forms N—H⋯O hydrogen bonds with one cytenamide mol­ecule from each dimer. International Union of Crystallography 2008-06-28 /pmc/articles/PMC2961860/ /pubmed/21202967 http://dx.doi.org/10.1107/S1600536808018709 Text en © Johnston 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
Johnston, Andrea
Florence, Alastair J.
Fabbiani, Francesca J. A.
Shankland, Kenneth
Bedford, Colin T.
Cytenamide–1,4-dioxane (2/1)
title Cytenamide–1,4-dioxane (2/1)
title_full Cytenamide–1,4-dioxane (2/1)
title_fullStr Cytenamide–1,4-dioxane (2/1)
title_full_unstemmed Cytenamide–1,4-dioxane (2/1)
title_short Cytenamide–1,4-dioxane (2/1)
title_sort cytenamide–1,4-dioxane (2/1)
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961860/
https://www.ncbi.nlm.nih.gov/pubmed/21202967
http://dx.doi.org/10.1107/S1600536808018709
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AT shanklandkenneth cytenamide14dioxane21
AT bedfordcolint cytenamide14dioxane21

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