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2,6-Bis[1-(2-isopropylphenylimino)ethyl]pyridine
The title compound, C(27)H(31)N(3), has E substitution at each imine double bond where the two N atoms adopt a trans–trans relationship. The benzene rings are twisted out of the mean plane of the pyridine ring; the mean planes of the aromatic groups are rotated by 63.0 (1) and 72.58 (8)°. The crysta...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2914989/ https://www.ncbi.nlm.nih.gov/pubmed/21200845 http://dx.doi.org/10.1107/S1600536807060254 |
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author | Agrifoglio, Giuseppe Reyes, Julian Atencio, Reinaldo Briceño, Alexander |
author_facet | Agrifoglio, Giuseppe Reyes, Julian Atencio, Reinaldo Briceño, Alexander |
author_sort | Agrifoglio, Giuseppe |
collection | PubMed |
description | The title compound, C(27)H(31)N(3), has E substitution at each imine double bond where the two N atoms adopt a trans–trans relationship. The benzene rings are twisted out of the mean plane of the pyridine ring; the mean planes of the aromatic groups are rotated by 63.0 (1) and 72.58 (8)°. The crystal structure is sustained mainly by C—H⋯π and hydrophobic methyl–methyl interactions. |
format | Text |
id | pubmed-2914989 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29149892010-12-30 2,6-Bis[1-(2-isopropylphenylimino)ethyl]pyridine Agrifoglio, Giuseppe Reyes, Julian Atencio, Reinaldo Briceño, Alexander Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(27)H(31)N(3), has E substitution at each imine double bond where the two N atoms adopt a trans–trans relationship. The benzene rings are twisted out of the mean plane of the pyridine ring; the mean planes of the aromatic groups are rotated by 63.0 (1) and 72.58 (8)°. The crystal structure is sustained mainly by C—H⋯π and hydrophobic methyl–methyl interactions. International Union of Crystallography 2007-12-06 /pmc/articles/PMC2914989/ /pubmed/21200845 http://dx.doi.org/10.1107/S1600536807060254 Text en © International Union of Crystallography 2008 http://journals.iucr.org/services/termsofuse.html This is an open-access article distributed under the terms described at http://journals.iucr.org/services/termsofuse.html. |
spellingShingle | Organic Papers Agrifoglio, Giuseppe Reyes, Julian Atencio, Reinaldo Briceño, Alexander 2,6-Bis[1-(2-isopropylphenylimino)ethyl]pyridine |
title | 2,6-Bis[1-(2-isopropylphenylimino)ethyl]pyridine |
title_full | 2,6-Bis[1-(2-isopropylphenylimino)ethyl]pyridine |
title_fullStr | 2,6-Bis[1-(2-isopropylphenylimino)ethyl]pyridine |
title_full_unstemmed | 2,6-Bis[1-(2-isopropylphenylimino)ethyl]pyridine |
title_short | 2,6-Bis[1-(2-isopropylphenylimino)ethyl]pyridine |
title_sort | 2,6-bis[1-(2-isopropylphenylimino)ethyl]pyridine |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2914989/ https://www.ncbi.nlm.nih.gov/pubmed/21200845 http://dx.doi.org/10.1107/S1600536807060254 |
work_keys_str_mv | AT agrifogliogiuseppe 26bis12isopropylphenyliminoethylpyridine AT reyesjulian 26bis12isopropylphenyliminoethylpyridine AT atencioreinaldo 26bis12isopropylphenyliminoethylpyridine AT bricenoalexander 26bis12isopropylphenyliminoethylpyridine |