1-(Anthracen-1-yl)pyrrolidine-2,5-dione

In the mol­ecular structure of title compound, C(18)H(13)NO(2), the succinimide ring is orientated away from the plane of the anthracene moiety by 71.94 (4)°. The crystal structure features three different types of inter­molecular inter­actions, viz. C—H⋯O, C—H⋯π and π–π bonds. Mol­ecules along the...

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Detalles Bibliográficos
Autores principales: Khorasani, Sanaz, Fernandes, Manuel A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344612/
https://www.ncbi.nlm.nih.gov/pubmed/22590374
http://dx.doi.org/10.1107/S160053681201536X
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author Khorasani, Sanaz
Fernandes, Manuel A.
author_facet Khorasani, Sanaz
Fernandes, Manuel A.
author_sort Khorasani, Sanaz
collection PubMed
description In the mol­ecular structure of title compound, C(18)H(13)NO(2), the succinimide ring is orientated away from the plane of the anthracene moiety by 71.94 (4)°. The crystal structure features three different types of inter­molecular inter­actions, viz. C—H⋯O, C—H⋯π and π–π bonds. Mol­ecules along the b axis stack on each other as a result of π–π inter­actions which have a centroid–centroid distance of 3.6780 (15) Å, while C—H⋯π inter­actions are present between neigbouring stacks. Also, acting between the stacks are the C—H⋯O inter­actions between the aromatic H atoms of the anthracene and the O atoms of the succinimide.
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spelling pubmed-33446122012-05-15 1-(Anthracen-1-yl)pyrrolidine-2,5-dione Khorasani, Sanaz Fernandes, Manuel A. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the mol­ecular structure of title compound, C(18)H(13)NO(2), the succinimide ring is orientated away from the plane of the anthracene moiety by 71.94 (4)°. The crystal structure features three different types of inter­molecular inter­actions, viz. C—H⋯O, C—H⋯π and π–π bonds. Mol­ecules along the b axis stack on each other as a result of π–π inter­actions which have a centroid–centroid distance of 3.6780 (15) Å, while C—H⋯π inter­actions are present between neigbouring stacks. Also, acting between the stacks are the C—H⋯O inter­actions between the aromatic H atoms of the anthracene and the O atoms of the succinimide. International Union of Crystallography 2012-04-21 /pmc/articles/PMC3344612/ /pubmed/22590374 http://dx.doi.org/10.1107/S160053681201536X Text en © Khorasani and Fernandes 2012 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
Khorasani, Sanaz
Fernandes, Manuel A.
1-(Anthracen-1-yl)pyrrolidine-2,5-dione
title 1-(Anthracen-1-yl)pyrrolidine-2,5-dione
title_full 1-(Anthracen-1-yl)pyrrolidine-2,5-dione
title_fullStr 1-(Anthracen-1-yl)pyrrolidine-2,5-dione
title_full_unstemmed 1-(Anthracen-1-yl)pyrrolidine-2,5-dione
title_short 1-(Anthracen-1-yl)pyrrolidine-2,5-dione
title_sort 1-(anthracen-1-yl)pyrrolidine-2,5-dione
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344612/
https://www.ncbi.nlm.nih.gov/pubmed/22590374
http://dx.doi.org/10.1107/S160053681201536X
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