10-Methoxy­benzo[g]imidazo[1,2-a][1,8]naphthyridine-4-carbonitrile

In the title compound, C(16)H(10)N(4)O, both the meth­oxy and nitrile substituents lie in the plane defined by the benzo[g]imidazo[1,2-a]-1,8-naphthyridine ring system, resulting in a nearly planar geometry for the entire mol­ecule (r.m.s. deviation of the non-H atoms from the mean plane is 0.044 Å)...

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Autores principales: Tarasov, Andrii V., Volovnenko, Tatyana A., Lugan, Noël, Volovenko, Yulian M.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970372/
https://www.ncbi.nlm.nih.gov/pubmed/21577970
http://dx.doi.org/10.1107/S1600536809037544
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author Tarasov, Andrii V.
Volovnenko, Tatyana A.
Lugan, Noël
Volovenko, Yulian M.
author_facet Tarasov, Andrii V.
Volovnenko, Tatyana A.
Lugan, Noël
Volovenko, Yulian M.
author_sort Tarasov, Andrii V.
collection PubMed
description In the title compound, C(16)H(10)N(4)O, both the meth­oxy and nitrile substituents lie in the plane defined by the benzo[g]imidazo[1,2-a]-1,8-naphthyridine ring system, resulting in a nearly planar geometry for the entire mol­ecule (r.m.s. deviation of the non-H atoms from the mean plane is 0.044 Å). In the solid-state, the mol­ecules form a three-dimensional polymer through inter­molecular C—H⋯N and C—H⋯O hydrogen bonds. In addition, the packing mode results in stabilizing π–π stacking inter­actions between the asymmetric units.
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spelling pubmed-29703722010-12-30 10-Methoxy­benzo[g]imidazo[1,2-a][1,8]naphthyridine-4-carbonitrile Tarasov, Andrii V. Volovnenko, Tatyana A. Lugan, Noël Volovenko, Yulian M. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(16)H(10)N(4)O, both the meth­oxy and nitrile substituents lie in the plane defined by the benzo[g]imidazo[1,2-a]-1,8-naphthyridine ring system, resulting in a nearly planar geometry for the entire mol­ecule (r.m.s. deviation of the non-H atoms from the mean plane is 0.044 Å). In the solid-state, the mol­ecules form a three-dimensional polymer through inter­molecular C—H⋯N and C—H⋯O hydrogen bonds. In addition, the packing mode results in stabilizing π–π stacking inter­actions between the asymmetric units. International Union of Crystallography 2009-09-26 /pmc/articles/PMC2970372/ /pubmed/21577970 http://dx.doi.org/10.1107/S1600536809037544 Text en © Tarasov 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
Tarasov, Andrii V.
Volovnenko, Tatyana A.
Lugan, Noël
Volovenko, Yulian M.
10-Methoxy­benzo[g]imidazo[1,2-a][1,8]naphthyridine-4-carbonitrile
title 10-Methoxy­benzo[g]imidazo[1,2-a][1,8]naphthyridine-4-carbonitrile
title_full 10-Methoxy­benzo[g]imidazo[1,2-a][1,8]naphthyridine-4-carbonitrile
title_fullStr 10-Methoxy­benzo[g]imidazo[1,2-a][1,8]naphthyridine-4-carbonitrile
title_full_unstemmed 10-Methoxy­benzo[g]imidazo[1,2-a][1,8]naphthyridine-4-carbonitrile
title_short 10-Methoxy­benzo[g]imidazo[1,2-a][1,8]naphthyridine-4-carbonitrile
title_sort 10-methoxy­benzo[g]imidazo[1,2-a][1,8]naphthyridine-4-carbonitrile
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970372/
https://www.ncbi.nlm.nih.gov/pubmed/21577970
http://dx.doi.org/10.1107/S1600536809037544
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