1,3-Diethyl-1,3-diphenyl­urea

The mol­ecule of the title compound, C(17)H(20)N(2)O, a symmetrical derivative of urea, shows non-crystallographic C (2) symmetry. Inter­action with the aromatic system of the phenyl substituents as well as amide-type resonance is responsible for the marked planarization of the coordination environm...

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Detalles Bibliográficos
Autores principales: Betz, Richard, Gerber, Thomas, Schalekamp, Henk
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3100078/
https://www.ncbi.nlm.nih.gov/pubmed/21754111
http://dx.doi.org/10.1107/S1600536811008294
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author Betz, Richard
Gerber, Thomas
Schalekamp, Henk
author_facet Betz, Richard
Gerber, Thomas
Schalekamp, Henk
author_sort Betz, Richard
collection PubMed
description The mol­ecule of the title compound, C(17)H(20)N(2)O, a symmetrical derivative of urea, shows non-crystallographic C (2) symmetry. Inter­action with the aromatic system of the phenyl substituents as well as amide-type resonance is responsible for the marked planarization of the coordination environments of the N atoms. C—H⋯O contacts give rise to the formation of centrosymmetric dimers in the crystal structure. The closest distance between the centroids of two adjacent rings is 3.8938 (11) Å.
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spelling pubmed-31000782011-07-13 1,3-Diethyl-1,3-diphenyl­urea Betz, Richard Gerber, Thomas Schalekamp, Henk Acta Crystallogr Sect E Struct Rep Online Organic Papers The mol­ecule of the title compound, C(17)H(20)N(2)O, a symmetrical derivative of urea, shows non-crystallographic C (2) symmetry. Inter­action with the aromatic system of the phenyl substituents as well as amide-type resonance is responsible for the marked planarization of the coordination environments of the N atoms. C—H⋯O contacts give rise to the formation of centrosymmetric dimers in the crystal structure. The closest distance between the centroids of two adjacent rings is 3.8938 (11) Å. International Union of Crystallography 2011-03-09 /pmc/articles/PMC3100078/ /pubmed/21754111 http://dx.doi.org/10.1107/S1600536811008294 Text en © Betz et al. 2011 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
Betz, Richard
Gerber, Thomas
Schalekamp, Henk
1,3-Diethyl-1,3-diphenyl­urea
title 1,3-Diethyl-1,3-diphenyl­urea
title_full 1,3-Diethyl-1,3-diphenyl­urea
title_fullStr 1,3-Diethyl-1,3-diphenyl­urea
title_full_unstemmed 1,3-Diethyl-1,3-diphenyl­urea
title_short 1,3-Diethyl-1,3-diphenyl­urea
title_sort 1,3-diethyl-1,3-diphenyl­urea
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3100078/
https://www.ncbi.nlm.nih.gov/pubmed/21754111
http://dx.doi.org/10.1107/S1600536811008294
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AT gerberthomas 13diethyl13diphenylurea
AT schalekamphenk 13diethyl13diphenylurea

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