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6-[6-(Pyridin-2-yl)-1,2,4,5-tetrazin-3-yl]pyridin-3-amine monohydrate
The packing of the title compound, C(12)H(9)N(7)·H(2)O, is dominated by hydrogen bonding and π-stacking. Layers parallel to [010] are established by hydrogen bonds involving all amine donor functions and one of the water donor functions, while the remaining water donor function enables the stacking...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4770950/ https://www.ncbi.nlm.nih.gov/pubmed/26958397 http://dx.doi.org/10.1107/S2056989016000608 |
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author | Broichhagen, Johannes Klingl, Yvonne E. Trauner, Dirk Mayer, Peter |
author_facet | Broichhagen, Johannes Klingl, Yvonne E. Trauner, Dirk Mayer, Peter |
author_sort | Broichhagen, Johannes |
collection | PubMed |
description | The packing of the title compound, C(12)H(9)N(7)·H(2)O, is dominated by hydrogen bonding and π-stacking. Layers parallel to [010] are established by hydrogen bonds involving all amine donor functions and one of the water donor functions, while the remaining water donor function enables the stacking of the layers along [10-1], which is accompanied by π-stacking. In the molecule, the plane of the central tetrazine ring forms angles of 5.33 (7) and 19.84 (8)° with the adjacent 3-amine-pyridine and pyridine rings, respectively. |
format | Online Article Text |
id | pubmed-4770950 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-47709502016-03-08 6-[6-(Pyridin-2-yl)-1,2,4,5-tetrazin-3-yl]pyridin-3-amine monohydrate Broichhagen, Johannes Klingl, Yvonne E. Trauner, Dirk Mayer, Peter Acta Crystallogr E Crystallogr Commun Research Communications The packing of the title compound, C(12)H(9)N(7)·H(2)O, is dominated by hydrogen bonding and π-stacking. Layers parallel to [010] are established by hydrogen bonds involving all amine donor functions and one of the water donor functions, while the remaining water donor function enables the stacking of the layers along [10-1], which is accompanied by π-stacking. In the molecule, the plane of the central tetrazine ring forms angles of 5.33 (7) and 19.84 (8)° with the adjacent 3-amine-pyridine and pyridine rings, respectively. International Union of Crystallography 2016-01-27 /pmc/articles/PMC4770950/ /pubmed/26958397 http://dx.doi.org/10.1107/S2056989016000608 Text en © Broichhagen et al. 2016 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 | Research Communications Broichhagen, Johannes Klingl, Yvonne E. Trauner, Dirk Mayer, Peter 6-[6-(Pyridin-2-yl)-1,2,4,5-tetrazin-3-yl]pyridin-3-amine monohydrate |
title | 6-[6-(Pyridin-2-yl)-1,2,4,5-tetrazin-3-yl]pyridin-3-amine monohydrate |
title_full | 6-[6-(Pyridin-2-yl)-1,2,4,5-tetrazin-3-yl]pyridin-3-amine monohydrate |
title_fullStr | 6-[6-(Pyridin-2-yl)-1,2,4,5-tetrazin-3-yl]pyridin-3-amine monohydrate |
title_full_unstemmed | 6-[6-(Pyridin-2-yl)-1,2,4,5-tetrazin-3-yl]pyridin-3-amine monohydrate |
title_short | 6-[6-(Pyridin-2-yl)-1,2,4,5-tetrazin-3-yl]pyridin-3-amine monohydrate |
title_sort | 6-[6-(pyridin-2-yl)-1,2,4,5-tetrazin-3-yl]pyridin-3-amine monohydrate |
topic | Research Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4770950/ https://www.ncbi.nlm.nih.gov/pubmed/26958397 http://dx.doi.org/10.1107/S2056989016000608 |
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