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Crystallographic and spectroscopic characterization of 5-chloropyridine-2,3-diamine
The two ortho-amino groups of the title compound, C(5)H(6)ClN(3), twist out of the plane of the molecule to minimize intramolecular interaction between the amino hydrogen atoms. In the crystal, the amino groups and the pyridine N atom engage in intermolecular hydrogen bonding. The molecules pac...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5598851/ https://www.ncbi.nlm.nih.gov/pubmed/28932439 http://dx.doi.org/10.1107/S2056989017010489 |
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author | Sulovari, Aron Tanski, Joseph M. |
author_facet | Sulovari, Aron Tanski, Joseph M. |
author_sort | Sulovari, Aron |
collection | PubMed |
description | The two ortho-amino groups of the title compound, C(5)H(6)ClN(3), twist out of the plane of the molecule to minimize intramolecular interaction between the amino hydrogen atoms. In the crystal, the amino groups and the pyridine N atom engage in intermolecular hydrogen bonding. The molecules pack into spiral hydrogen-bonded columns with offset face-to-face π-stacking. |
format | Online Article Text |
id | pubmed-5598851 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-55988512017-09-20 Crystallographic and spectroscopic characterization of 5-chloropyridine-2,3-diamine Sulovari, Aron Tanski, Joseph M. Acta Crystallogr E Crystallogr Commun Research Communications The two ortho-amino groups of the title compound, C(5)H(6)ClN(3), twist out of the plane of the molecule to minimize intramolecular interaction between the amino hydrogen atoms. In the crystal, the amino groups and the pyridine N atom engage in intermolecular hydrogen bonding. The molecules pack into spiral hydrogen-bonded columns with offset face-to-face π-stacking. International Union of Crystallography 2017-07-21 /pmc/articles/PMC5598851/ /pubmed/28932439 http://dx.doi.org/10.1107/S2056989017010489 Text en © Sulovari and Tanski 2017 http://creativecommons.org/licenses/by/2.0/uk/ 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/2.0/uk/ |
spellingShingle | Research Communications Sulovari, Aron Tanski, Joseph M. Crystallographic and spectroscopic characterization of 5-chloropyridine-2,3-diamine |
title | Crystallographic and spectroscopic characterization of 5-chloropyridine-2,3-diamine |
title_full | Crystallographic and spectroscopic characterization of 5-chloropyridine-2,3-diamine |
title_fullStr | Crystallographic and spectroscopic characterization of 5-chloropyridine-2,3-diamine |
title_full_unstemmed | Crystallographic and spectroscopic characterization of 5-chloropyridine-2,3-diamine |
title_short | Crystallographic and spectroscopic characterization of 5-chloropyridine-2,3-diamine |
title_sort | crystallographic and spectroscopic characterization of 5-chloropyridine-2,3-diamine |
topic | Research Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5598851/ https://www.ncbi.nlm.nih.gov/pubmed/28932439 http://dx.doi.org/10.1107/S2056989017010489 |
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