1,5-Bis(piperidin-1-yl)-9,10-anthraquin­one

In the centrosymmetric title compound, C(24)H(26)N(2)O(2), the piperidine ring adopts a chair conformation and is inclined at a dihedral angle of 37.5 (1)°to the anthracene ring system. In the crystal, adjacent mol­ecules are linked through C—H⋯π and π–π [centroid–centroid distances = 3.806 (1) Å] i...

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Detalles Bibliográficos
Autores principales: Niedziałkowski, Paweł, Wnuk, Elżbieta, Wcisło, Anna, Trzybiński, Damian
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/PMC3588357/
https://www.ncbi.nlm.nih.gov/pubmed/23476373
http://dx.doi.org/10.1107/S1600536812050313
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author Niedziałkowski, Paweł
Wnuk, Elżbieta
Wcisło, Anna
Trzybiński, Damian
author_facet Niedziałkowski, Paweł
Wnuk, Elżbieta
Wcisło, Anna
Trzybiński, Damian
author_sort Niedziałkowski, Paweł
collection PubMed
description In the centrosymmetric title compound, C(24)H(26)N(2)O(2), the piperidine ring adopts a chair conformation and is inclined at a dihedral angle of 37.5 (1)°to the anthracene ring system. In the crystal, adjacent mol­ecules are linked through C—H⋯π and π–π [centroid–centroid distances = 3.806 (1) Å] inter­actions, forming a layer parallel to the bc plane.
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spelling pubmed-35883572013-03-08 1,5-Bis(piperidin-1-yl)-9,10-anthraquin­one Niedziałkowski, Paweł Wnuk, Elżbieta Wcisło, Anna Trzybiński, Damian Acta Crystallogr Sect E Struct Rep Online Organic Papers In the centrosymmetric title compound, C(24)H(26)N(2)O(2), the piperidine ring adopts a chair conformation and is inclined at a dihedral angle of 37.5 (1)°to the anthracene ring system. In the crystal, adjacent mol­ecules are linked through C—H⋯π and π–π [centroid–centroid distances = 3.806 (1) Å] inter­actions, forming a layer parallel to the bc plane. International Union of Crystallography 2012-12-19 /pmc/articles/PMC3588357/ /pubmed/23476373 http://dx.doi.org/10.1107/S1600536812050313 Text en © Niedziałkowski et al. 2013 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
Niedziałkowski, Paweł
Wnuk, Elżbieta
Wcisło, Anna
Trzybiński, Damian
1,5-Bis(piperidin-1-yl)-9,10-anthraquin­one
title 1,5-Bis(piperidin-1-yl)-9,10-anthraquin­one
title_full 1,5-Bis(piperidin-1-yl)-9,10-anthraquin­one
title_fullStr 1,5-Bis(piperidin-1-yl)-9,10-anthraquin­one
title_full_unstemmed 1,5-Bis(piperidin-1-yl)-9,10-anthraquin­one
title_short 1,5-Bis(piperidin-1-yl)-9,10-anthraquin­one
title_sort 1,5-bis(piperidin-1-yl)-9,10-anthraquin­one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588357/
https://www.ncbi.nlm.nih.gov/pubmed/23476373
http://dx.doi.org/10.1107/S1600536812050313
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AT trzybinskidamian 15bispiperidin1yl910anthraquinone

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