(3E,5E)-3,5-Bis(naphthalen-1-yl­methyl­idene)piperidin-4-one

In the title compound, C(27)H(21)NO, the piperidine ring adopts a chair conformation. The mean plane through the piperidine ring makes dihedral angles of 49.27 (5) and 63.07 (5)° with the naphthalene ring systems. In the crystal, mol­ecules are linked into dimers via pairs of inter­molecular C—H⋯O i...

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Detalles Bibliográficos
Autores principales: Kia, Yalda, Osman, Hasnah, Murugaiyah, Vikneswaran, Arshad, Suhana, Razak, Ibrahim Abdul
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/PMC3297868/
https://www.ncbi.nlm.nih.gov/pubmed/22412671
http://dx.doi.org/10.1107/S1600536812006307
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author Kia, Yalda
Osman, Hasnah
Murugaiyah, Vikneswaran
Arshad, Suhana
Razak, Ibrahim Abdul
author_facet Kia, Yalda
Osman, Hasnah
Murugaiyah, Vikneswaran
Arshad, Suhana
Razak, Ibrahim Abdul
author_sort Kia, Yalda
collection PubMed
description In the title compound, C(27)H(21)NO, the piperidine ring adopts a chair conformation. The mean plane through the piperidine ring makes dihedral angles of 49.27 (5) and 63.07 (5)° with the naphthalene ring systems. In the crystal, mol­ecules are linked into dimers via pairs of inter­molecular C—H⋯O inter­actions, generating ten-membered R (2) (2)(10) ring motifs. C—H⋯π inter­actions further stabilize the crystal structure.
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spelling pubmed-32978682012-03-12 (3E,5E)-3,5-Bis(naphthalen-1-yl­methyl­idene)piperidin-4-one Kia, Yalda Osman, Hasnah Murugaiyah, Vikneswaran Arshad, Suhana Razak, Ibrahim Abdul Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(27)H(21)NO, the piperidine ring adopts a chair conformation. The mean plane through the piperidine ring makes dihedral angles of 49.27 (5) and 63.07 (5)° with the naphthalene ring systems. In the crystal, mol­ecules are linked into dimers via pairs of inter­molecular C—H⋯O inter­actions, generating ten-membered R (2) (2)(10) ring motifs. C—H⋯π inter­actions further stabilize the crystal structure. International Union of Crystallography 2012-02-24 /pmc/articles/PMC3297868/ /pubmed/22412671 http://dx.doi.org/10.1107/S1600536812006307 Text en © Kia et al. 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
Kia, Yalda
Osman, Hasnah
Murugaiyah, Vikneswaran
Arshad, Suhana
Razak, Ibrahim Abdul
(3E,5E)-3,5-Bis(naphthalen-1-yl­methyl­idene)piperidin-4-one
title (3E,5E)-3,5-Bis(naphthalen-1-yl­methyl­idene)piperidin-4-one
title_full (3E,5E)-3,5-Bis(naphthalen-1-yl­methyl­idene)piperidin-4-one
title_fullStr (3E,5E)-3,5-Bis(naphthalen-1-yl­methyl­idene)piperidin-4-one
title_full_unstemmed (3E,5E)-3,5-Bis(naphthalen-1-yl­methyl­idene)piperidin-4-one
title_short (3E,5E)-3,5-Bis(naphthalen-1-yl­methyl­idene)piperidin-4-one
title_sort (3e,5e)-3,5-bis(naphthalen-1-yl­methyl­idene)piperidin-4-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3297868/
https://www.ncbi.nlm.nih.gov/pubmed/22412671
http://dx.doi.org/10.1107/S1600536812006307
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