1,3-Diallyl-1H-anthra[1,2-d]imidazole-2,6,11(3H)-trione

In the title compound, C(21)H(16)N(2)O(3), the fused-ring system (r.m.s. deviation = 0.067 Å) is slightly buckled at the carbonyl C atom of the anthracenyl ring system [deviation = 0.177 (1) Å] that is closer to an allyl substituent. The two allyl units lie on the same side of the fused-ring plane b...

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Autores principales: Afrakssou, Zahra, Rodi, Youssef Kandri, Zouihri, Hafid, Essassi, El Mokhtar, Ng, Seik Weng
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3007069/
https://www.ncbi.nlm.nih.gov/pubmed/21588049
http://dx.doi.org/10.1107/S1600536810024748
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author Afrakssou, Zahra
Rodi, Youssef Kandri
Zouihri, Hafid
Essassi, El Mokhtar
Ng, Seik Weng
author_facet Afrakssou, Zahra
Rodi, Youssef Kandri
Zouihri, Hafid
Essassi, El Mokhtar
Ng, Seik Weng
author_sort Afrakssou, Zahra
collection PubMed
description In the title compound, C(21)H(16)N(2)O(3), the fused-ring system (r.m.s. deviation = 0.067 Å) is slightly buckled at the carbonyl C atom of the anthracenyl ring system [deviation = 0.177 (1) Å] that is closer to an allyl substituent. The two allyl units lie on the same side of the fused-ring plane but are oriented in opposite directions, with N—C—C—C torsion angles of 126.9 (2) and 116.7 (2)°. In the crystal, the mol­ecules are linked into chains propagating along the b axis by C—H⋯O hydrogen bonds.
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spelling pubmed-30070692010-12-30 1,3-Diallyl-1H-anthra[1,2-d]imidazole-2,6,11(3H)-trione Afrakssou, Zahra Rodi, Youssef Kandri Zouihri, Hafid Essassi, El Mokhtar Ng, Seik Weng Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(21)H(16)N(2)O(3), the fused-ring system (r.m.s. deviation = 0.067 Å) is slightly buckled at the carbonyl C atom of the anthracenyl ring system [deviation = 0.177 (1) Å] that is closer to an allyl substituent. The two allyl units lie on the same side of the fused-ring plane but are oriented in opposite directions, with N—C—C—C torsion angles of 126.9 (2) and 116.7 (2)°. In the crystal, the mol­ecules are linked into chains propagating along the b axis by C—H⋯O hydrogen bonds. International Union of Crystallography 2010-06-26 /pmc/articles/PMC3007069/ /pubmed/21588049 http://dx.doi.org/10.1107/S1600536810024748 Text en © Afrakssou et al. 2010 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
Afrakssou, Zahra
Rodi, Youssef Kandri
Zouihri, Hafid
Essassi, El Mokhtar
Ng, Seik Weng
1,3-Diallyl-1H-anthra[1,2-d]imidazole-2,6,11(3H)-trione
title 1,3-Diallyl-1H-anthra[1,2-d]imidazole-2,6,11(3H)-trione
title_full 1,3-Diallyl-1H-anthra[1,2-d]imidazole-2,6,11(3H)-trione
title_fullStr 1,3-Diallyl-1H-anthra[1,2-d]imidazole-2,6,11(3H)-trione
title_full_unstemmed 1,3-Diallyl-1H-anthra[1,2-d]imidazole-2,6,11(3H)-trione
title_short 1,3-Diallyl-1H-anthra[1,2-d]imidazole-2,6,11(3H)-trione
title_sort 1,3-diallyl-1h-anthra[1,2-d]imidazole-2,6,11(3h)-trione
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3007069/
https://www.ncbi.nlm.nih.gov/pubmed/21588049
http://dx.doi.org/10.1107/S1600536810024748
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