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Benzoic acid–3,4-bis[(pyridin-3-ylmethyl)amino]cyclobut-3-ene-1,2-dione (1/2)
In the title co-crystal, C(16)H(14)N(4)O(2)·2C(7)H(6)O(2), the 3,4-bis[(pyridin-3-ylmethyl)amino]cyclobut-3-ene-1,2-dione squareamide molecules assemble into chains along the b axis via N—H⋯O hydrogen bonds. The benzoic acid molecules then hydrogen bond to the pyridine rings via O—H⋯N hydrogen...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275061/ https://www.ncbi.nlm.nih.gov/pubmed/22347006 http://dx.doi.org/10.1107/S1600536812000220 |
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author | Lemmerer, Andreas Bourne, Susan A. |
author_facet | Lemmerer, Andreas Bourne, Susan A. |
author_sort | Lemmerer, Andreas |
collection | PubMed |
description | In the title co-crystal, C(16)H(14)N(4)O(2)·2C(7)H(6)O(2), the 3,4-bis[(pyridin-3-ylmethyl)amino]cyclobut-3-ene-1,2-dione squareamide molecules assemble into chains along the b axis via N—H⋯O hydrogen bonds. The benzoic acid molecules then hydrogen bond to the pyridine rings via O—H⋯N hydrogen bonds, supported by weaker C—H⋯O hydrogen bonds, forming extended ribbons. The asymmetric unit consists of a half squareamide molecule, sitting on a special position around a twofold axis, and one benzoic acid molecule on a general position. |
format | Online Article Text |
id | pubmed-3275061 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32750612012-02-15 Benzoic acid–3,4-bis[(pyridin-3-ylmethyl)amino]cyclobut-3-ene-1,2-dione (1/2) Lemmerer, Andreas Bourne, Susan A. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title co-crystal, C(16)H(14)N(4)O(2)·2C(7)H(6)O(2), the 3,4-bis[(pyridin-3-ylmethyl)amino]cyclobut-3-ene-1,2-dione squareamide molecules assemble into chains along the b axis via N—H⋯O hydrogen bonds. The benzoic acid molecules then hydrogen bond to the pyridine rings via O—H⋯N hydrogen bonds, supported by weaker C—H⋯O hydrogen bonds, forming extended ribbons. The asymmetric unit consists of a half squareamide molecule, sitting on a special position around a twofold axis, and one benzoic acid molecule on a general position. International Union of Crystallography 2012-01-14 /pmc/articles/PMC3275061/ /pubmed/22347006 http://dx.doi.org/10.1107/S1600536812000220 Text en © Lemmerer and Bourne 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 Lemmerer, Andreas Bourne, Susan A. Benzoic acid–3,4-bis[(pyridin-3-ylmethyl)amino]cyclobut-3-ene-1,2-dione (1/2) |
title | Benzoic acid–3,4-bis[(pyridin-3-ylmethyl)amino]cyclobut-3-ene-1,2-dione (1/2) |
title_full | Benzoic acid–3,4-bis[(pyridin-3-ylmethyl)amino]cyclobut-3-ene-1,2-dione (1/2) |
title_fullStr | Benzoic acid–3,4-bis[(pyridin-3-ylmethyl)amino]cyclobut-3-ene-1,2-dione (1/2) |
title_full_unstemmed | Benzoic acid–3,4-bis[(pyridin-3-ylmethyl)amino]cyclobut-3-ene-1,2-dione (1/2) |
title_short | Benzoic acid–3,4-bis[(pyridin-3-ylmethyl)amino]cyclobut-3-ene-1,2-dione (1/2) |
title_sort | benzoic acid–3,4-bis[(pyridin-3-ylmethyl)amino]cyclobut-3-ene-1,2-dione (1/2) |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275061/ https://www.ncbi.nlm.nih.gov/pubmed/22347006 http://dx.doi.org/10.1107/S1600536812000220 |
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