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N,N′-Bis[2,6-bis­(1-methyl­eth­yl)phen­yl]pyridine-4-carboximidamide toluene hemisolvate

The title compound, C(30)H(39)N(3)·0.5C(7)H(8), is a symmetrically N,N′-disubstituted aryl­amidine containing a 4-pyridyl substituent on the carbon atom of the N–C–N linkage and bulky 2,6-diiso­propyl­phenyl groups on the nitro­gen atoms. It crystallizes in the Z-anti configuration and its amidine C...

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Detalles Bibliográficos
Autores principales: Cottin, Lola, Girard, Sarah, Hanan, Garry S., Cibian, Mihaela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7869534/
https://www.ncbi.nlm.nih.gov/pubmed/33614137
http://dx.doi.org/10.1107/S2056989021000141
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author Cottin, Lola
Girard, Sarah
Hanan, Garry S.
Cibian, Mihaela
author_facet Cottin, Lola
Girard, Sarah
Hanan, Garry S.
Cibian, Mihaela
author_sort Cottin, Lola
collection PubMed
description The title compound, C(30)H(39)N(3)·0.5C(7)H(8), is a symmetrically N,N′-disubstituted aryl­amidine containing a 4-pyridyl substituent on the carbon atom of the N–C–N linkage and bulky 2,6-diiso­propyl­phenyl groups on the nitro­gen atoms. It crystallizes in the Z-anti configuration and its amidine C—N bonds present amine [1.368 (1) Å] and imine [1.286 (1) Å] features. Intra­molecular hydrogen bonds are present in the structure together with inter­molecular N—H⋯N and C—H⋯N inter­actions linking the mol­ecules in chains along the a- and c-axis directions.
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spelling pubmed-78695342021-02-19 N,N′-Bis[2,6-bis­(1-methyl­eth­yl)phen­yl]pyridine-4-carboximidamide toluene hemisolvate Cottin, Lola Girard, Sarah Hanan, Garry S. Cibian, Mihaela Acta Crystallogr E Crystallogr Commun Research Communications The title compound, C(30)H(39)N(3)·0.5C(7)H(8), is a symmetrically N,N′-disubstituted aryl­amidine containing a 4-pyridyl substituent on the carbon atom of the N–C–N linkage and bulky 2,6-diiso­propyl­phenyl groups on the nitro­gen atoms. It crystallizes in the Z-anti configuration and its amidine C—N bonds present amine [1.368 (1) Å] and imine [1.286 (1) Å] features. Intra­molecular hydrogen bonds are present in the structure together with inter­molecular N—H⋯N and C—H⋯N inter­actions linking the mol­ecules in chains along the a- and c-axis directions. International Union of Crystallography 2021-01-12 /pmc/articles/PMC7869534/ /pubmed/33614137 http://dx.doi.org/10.1107/S2056989021000141 Text en © Cottin et al. 2021 http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.http://creativecommons.org/licenses/by/4.0/
spellingShingle Research Communications
Cottin, Lola
Girard, Sarah
Hanan, Garry S.
Cibian, Mihaela
N,N′-Bis[2,6-bis­(1-methyl­eth­yl)phen­yl]pyridine-4-carboximidamide toluene hemisolvate
title N,N′-Bis[2,6-bis­(1-methyl­eth­yl)phen­yl]pyridine-4-carboximidamide toluene hemisolvate
title_full N,N′-Bis[2,6-bis­(1-methyl­eth­yl)phen­yl]pyridine-4-carboximidamide toluene hemisolvate
title_fullStr N,N′-Bis[2,6-bis­(1-methyl­eth­yl)phen­yl]pyridine-4-carboximidamide toluene hemisolvate
title_full_unstemmed N,N′-Bis[2,6-bis­(1-methyl­eth­yl)phen­yl]pyridine-4-carboximidamide toluene hemisolvate
title_short N,N′-Bis[2,6-bis­(1-methyl­eth­yl)phen­yl]pyridine-4-carboximidamide toluene hemisolvate
title_sort n,n′-bis[2,6-bis­(1-methyl­eth­yl)phen­yl]pyridine-4-carboximidamide toluene hemisolvate
topic Research Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7869534/
https://www.ncbi.nlm.nih.gov/pubmed/33614137
http://dx.doi.org/10.1107/S2056989021000141
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