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N,N′-Bis(di­phenyl­meth­yl)benzene-1,4-di­amine

The complete mol­ecule of the title compound, C(32)H(28)N(2), is generated by crystallographic inversion symmetry. The dihedral angles between the central aromatic ring and the pendant adjacent rings are 61.37 (16) and 74.20 (14)°. The N—H group does not participate in hydrogen bonds and there are n...

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Autores principales: Al-Fahdawi, Aeed S., Al-Kafajy, Hussain A., Al-Jeboori, Mohamad J., Coles, Simon J., Wilson, Claire, Potgieter, Herman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3914097/
https://www.ncbi.nlm.nih.gov/pubmed/24527002
http://dx.doi.org/10.1107/S1600536813033497
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author Al-Fahdawi, Aeed S.
Al-Kafajy, Hussain A.
Al-Jeboori, Mohamad J.
Coles, Simon J.
Wilson, Claire
Potgieter, Herman
author_facet Al-Fahdawi, Aeed S.
Al-Kafajy, Hussain A.
Al-Jeboori, Mohamad J.
Coles, Simon J.
Wilson, Claire
Potgieter, Herman
author_sort Al-Fahdawi, Aeed S.
collection PubMed
description The complete mol­ecule of the title compound, C(32)H(28)N(2), is generated by crystallographic inversion symmetry. The dihedral angles between the central aromatic ring and the pendant adjacent rings are 61.37 (16) and 74.20 (14)°. The N—H group does not participate in hydrogen bonds and there are no aromatic π–π stacking inter­actions in the crystal.
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spelling pubmed-39140972014-02-13 N,N′-Bis(di­phenyl­meth­yl)benzene-1,4-di­amine Al-Fahdawi, Aeed S. Al-Kafajy, Hussain A. Al-Jeboori, Mohamad J. Coles, Simon J. Wilson, Claire Potgieter, Herman Acta Crystallogr Sect E Struct Rep Online Organic Papers The complete mol­ecule of the title compound, C(32)H(28)N(2), is generated by crystallographic inversion symmetry. The dihedral angles between the central aromatic ring and the pendant adjacent rings are 61.37 (16) and 74.20 (14)°. The N—H group does not participate in hydrogen bonds and there are no aromatic π–π stacking inter­actions in the crystal. International Union of Crystallography 2013-12-14 /pmc/articles/PMC3914097/ /pubmed/24527002 http://dx.doi.org/10.1107/S1600536813033497 Text en © Al-Fahdawi et al. 2014 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
Al-Fahdawi, Aeed S.
Al-Kafajy, Hussain A.
Al-Jeboori, Mohamad J.
Coles, Simon J.
Wilson, Claire
Potgieter, Herman
N,N′-Bis(di­phenyl­meth­yl)benzene-1,4-di­amine
title N,N′-Bis(di­phenyl­meth­yl)benzene-1,4-di­amine
title_full N,N′-Bis(di­phenyl­meth­yl)benzene-1,4-di­amine
title_fullStr N,N′-Bis(di­phenyl­meth­yl)benzene-1,4-di­amine
title_full_unstemmed N,N′-Bis(di­phenyl­meth­yl)benzene-1,4-di­amine
title_short N,N′-Bis(di­phenyl­meth­yl)benzene-1,4-di­amine
title_sort n,n′-bis(di­phenyl­meth­yl)benzene-1,4-di­amine
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3914097/
https://www.ncbi.nlm.nih.gov/pubmed/24527002
http://dx.doi.org/10.1107/S1600536813033497
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