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4,4′-Bipyridine–3,3′-disulfanediylbis(1H-1,2,4-triazole-5-amine) (1/1)
In the title 1:1 adduct, C(10)H(8)N(2)·C(4)H(6)N(8)S(2)·, the components are connected through N—H⋯N hydrogen bonds, leading to a two-dimensional structure. The C—S—S—C torsion angle is −83.6 (1)°. The dihedral angle between pyridine rings is 1.86 (15)°.
| 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/PMC3515285/ https://www.ncbi.nlm.nih.gov/pubmed/23284505 http://dx.doi.org/10.1107/S1600536812042742 |
| _version_ | 1782252151726145536 |
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| author | Yang, Wei Qiu, Qi-Ming Jin, Qiong-Hua Zhang, Cun-Lin |
| author_facet | Yang, Wei Qiu, Qi-Ming Jin, Qiong-Hua Zhang, Cun-Lin |
| author_sort | Yang, Wei |
| collection | PubMed |
| description | In the title 1:1 adduct, C(10)H(8)N(2)·C(4)H(6)N(8)S(2)·, the components are connected through N—H⋯N hydrogen bonds, leading to a two-dimensional structure. The C—S—S—C torsion angle is −83.6 (1)°. The dihedral angle between pyridine rings is 1.86 (15)°. |
| format | Online Article Text |
| id | pubmed-3515285 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2012 |
| publisher | International Union of Crystallography |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-35152852013-01-02 4,4′-Bipyridine–3,3′-disulfanediylbis(1H-1,2,4-triazole-5-amine) (1/1) Yang, Wei Qiu, Qi-Ming Jin, Qiong-Hua Zhang, Cun-Lin Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title 1:1 adduct, C(10)H(8)N(2)·C(4)H(6)N(8)S(2)·, the components are connected through N—H⋯N hydrogen bonds, leading to a two-dimensional structure. The C—S—S—C torsion angle is −83.6 (1)°. The dihedral angle between pyridine rings is 1.86 (15)°. International Union of Crystallography 2012-10-20 /pmc/articles/PMC3515285/ /pubmed/23284505 http://dx.doi.org/10.1107/S1600536812042742 Text en © Yang et al. 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 Yang, Wei Qiu, Qi-Ming Jin, Qiong-Hua Zhang, Cun-Lin 4,4′-Bipyridine–3,3′-disulfanediylbis(1H-1,2,4-triazole-5-amine) (1/1) |
| title | 4,4′-Bipyridine–3,3′-disulfanediylbis(1H-1,2,4-triazole-5-amine) (1/1) |
| title_full | 4,4′-Bipyridine–3,3′-disulfanediylbis(1H-1,2,4-triazole-5-amine) (1/1) |
| title_fullStr | 4,4′-Bipyridine–3,3′-disulfanediylbis(1H-1,2,4-triazole-5-amine) (1/1) |
| title_full_unstemmed | 4,4′-Bipyridine–3,3′-disulfanediylbis(1H-1,2,4-triazole-5-amine) (1/1) |
| title_short | 4,4′-Bipyridine–3,3′-disulfanediylbis(1H-1,2,4-triazole-5-amine) (1/1) |
| title_sort | 4,4′-bipyridine–3,3′-disulfanediylbis(1h-1,2,4-triazole-5-amine) (1/1) |
| topic | Organic Papers |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3515285/ https://www.ncbi.nlm.nih.gov/pubmed/23284505 http://dx.doi.org/10.1107/S1600536812042742 |
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