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N,N′-Bis[(E)-quinoxalin-2-ylmethyl­idene]­ethane-1,2-diamine

In the mol­ecule of the title compound, C(20)H(16)N(6), the central C—C bond lies on a crystallographic inversion centre. The quinoxalidine ring is nearly planar, with a maximum deviation of 0.021 (2) Å from the mean plane. The crystal structure is stabilized by inter­molecular C—H⋯N inter­actions,...

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Detalles Bibliográficos
Autores principales: Varghese, Digna, Arun, V., Sebastian, Manju, Leeju, P., Varsha, G., Yusuff, K. K. M.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968406/
https://www.ncbi.nlm.nih.gov/pubmed/21582020
http://dx.doi.org/10.1107/S1600536809003006
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author Varghese, Digna
Arun, V.
Sebastian, Manju
Leeju, P.
Varsha, G.
Yusuff, K. K. M.
author_facet Varghese, Digna
Arun, V.
Sebastian, Manju
Leeju, P.
Varsha, G.
Yusuff, K. K. M.
author_sort Varghese, Digna
collection PubMed
description In the mol­ecule of the title compound, C(20)H(16)N(6), the central C—C bond lies on a crystallographic inversion centre. The quinoxalidine ring is nearly planar, with a maximum deviation of 0.021 (2) Å from the mean plane. The crystal structure is stabilized by inter­molecular C—H⋯N inter­actions, leading to the formation of a layer-like structure, which extends along the a axis.
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spelling pubmed-29684062010-12-30 N,N′-Bis[(E)-quinoxalin-2-ylmethyl­idene]­ethane-1,2-diamine Varghese, Digna Arun, V. Sebastian, Manju Leeju, P. Varsha, G. Yusuff, K. K. M. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the mol­ecule of the title compound, C(20)H(16)N(6), the central C—C bond lies on a crystallographic inversion centre. The quinoxalidine ring is nearly planar, with a maximum deviation of 0.021 (2) Å from the mean plane. The crystal structure is stabilized by inter­molecular C—H⋯N inter­actions, leading to the formation of a layer-like structure, which extends along the a axis. International Union of Crystallography 2009-01-31 /pmc/articles/PMC2968406/ /pubmed/21582020 http://dx.doi.org/10.1107/S1600536809003006 Text en © Varghese 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
Varghese, Digna
Arun, V.
Sebastian, Manju
Leeju, P.
Varsha, G.
Yusuff, K. K. M.
N,N′-Bis[(E)-quinoxalin-2-ylmethyl­idene]­ethane-1,2-diamine
title N,N′-Bis[(E)-quinoxalin-2-ylmethyl­idene]­ethane-1,2-diamine
title_full N,N′-Bis[(E)-quinoxalin-2-ylmethyl­idene]­ethane-1,2-diamine
title_fullStr N,N′-Bis[(E)-quinoxalin-2-ylmethyl­idene]­ethane-1,2-diamine
title_full_unstemmed N,N′-Bis[(E)-quinoxalin-2-ylmethyl­idene]­ethane-1,2-diamine
title_short N,N′-Bis[(E)-quinoxalin-2-ylmethyl­idene]­ethane-1,2-diamine
title_sort n,n′-bis[(e)-quinoxalin-2-ylmethyl­idene]­ethane-1,2-diamine
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968406/
https://www.ncbi.nlm.nih.gov/pubmed/21582020
http://dx.doi.org/10.1107/S1600536809003006
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