Crystal structure of 3,6-bis­­(pyridin-2-yl)-1,4-di­hydro-1,2,4,5-tetra­zine

Wzgarda-Raj, Kinga; Rybarczyk-Pirek, Agnieszka; Palusiak, Marcin; Wojtulewski, Sławomir

dc.contributor.author	Wzgarda-Raj, Kinga
dc.contributor.author	Rybarczyk-Pirek, Agnieszka
dc.contributor.author	Palusiak, Marcin
dc.contributor.author	Wojtulewski, Sławomir
dc.date.accessioned	2022-01-26T18:32:57Z
dc.date.available	2022-01-26T18:32:57Z
dc.date.issued	2019
dc.identifier.issn	2056-9890
dc.identifier.uri	http://hdl.handle.net/11089/40503
dc.description	The structure of the title compound, C12H10N6, at 100 K has monoclinic (P21/n) symmetry. Crystals were obtained as a yellow solid by reduction of 3,6-bis(pyridin-2-yl)-1,2,4,5-tetrazine. The structure displays intermolecular hydrogen bonding of the N—H⋯N type, ordering molecules into infinite ribbons extending along the [100] direction.	pl_PL
dc.description.sponsorship	Funding for this research was provided by: Narodowe Centrum Nauki (grant No. 2015/19/B/ST4/01773); EFRD in Operational Programme Development of Eastern Poland 2007–2013, the Oxford Diffraction SuperNova DualSource diffractometer (award No. POPW.01.03.00-20-004/11).	pl_PL
dc.language.iso	en	pl_PL
dc.publisher	International Union of Crystallography	pl_PL
dc.relation.ispartofseries	Acta Crystallographica Section E: Crystallographic Communications;75
dc.rights	Uznanie autorstwa 4.0 Międzynarodowe	*
dc.rights.uri	http://creativecommons.org/licenses/by/4.0/	*
dc.subject	crystal structure	pl_PL
dc.subject	1,2,4,5-tetrazine	pl_PL
dc.subject	hydrogen bond	pl_PL
dc.title	Crystal structure of 3,6-bis(pyridin-2-yl)-1,4-dihydro-1,2,4,5-tetrazine	pl_PL
dc.type	Article	pl_PL
dc.page.number	86-88	pl_PL
dc.contributor.authorAffiliation	Group of Theoretical and Structural Chemistry, Department of Physical Chemistry, Faculty of Chemistry, University of Łódź, Pomorska 163/165, 90-236, Łódź, Poland	pl_PL
dc.contributor.authorAffiliation	Group of Theoretical and Structural Chemistry, Department of Physical Chemistry, Faculty of Chemistry, University of Łódź, Pomorska 163/165, 90-236, Łódź, Poland	pl_PL
dc.contributor.authorAffiliation	Group of Theoretical and Structural Chemistry, Department of Physical Chemistry, Faculty of Chemistry, University of Łódź, Pomorska 163/165, 90-236, Łódź, Poland	pl_PL
dc.contributor.authorAffiliation	Department of Theoretical Chemistry, University of Białystok, Ciołkowskiego, 1K, 15-245 Białystok, Poland	pl_PL
dc.references	Allen, F. H., Kennard, O., Watson, D. G., Brammer, L., Orpen, A. G. & Taylor, R. (1987). J. Chem. Soc. Perkin Trans. 2, pp. S1–S19.	pl_PL
dc.references	Brooker, P. J., Parsons, J. H., Reid, J. & West, P. (1987). Pestic. Sci. 18, 179–190.	pl_PL
dc.references	Churakov, A. M. & Tartakovsky, V. A. (2004). Chem. Rev. 104, 2601–2616.	pl_PL
dc.references	Clavier, G. & Audebert, P. (2010). Chem. Rev. 110, 3299–3314.	pl_PL
dc.references	Etter, M. C., MacDonald, J. C. & Bernstein, J. (1990). Acta Cryst. B46, 256–262.	pl_PL
dc.references	Farrugia, L. J. (2012). J. Appl. Cryst. 45, 849–854.	pl_PL
dc.references	Groom, C. R., Bruno, I. J., Lightfoot, M. P. & Ward, S. C. (2016). Acta Cryst. B72, 171–179.	pl_PL
dc.references	Kaim, W. (2002). Coord. Chem. Rev. 230, 127–139.	pl_PL
dc.references	Kamal, M. D., Hassan, A. G., Money, E., Hanan, A. M. & Bahira, H. (2006). Arch. Pharm. Chem. Life Sci. 339, 133.	pl_PL
dc.references	Klein, A., McInnes, E. J. L., Scheiring, T. & Zališ, S. (1998). Faraday Trans. 94, 2979–2984.	pl_PL
dc.references	Neunhoeffer, H. (1984). Comprehensive Heterocyclic Chemistry, Vol. 3, 1st ed , edited by A. R. Katritzky and C. W. Rees, p. 531. Oxford: Pergamon Press.	pl_PL
dc.references	Rao, G. W. & Hu, W. X. (2006). Bioorg. Med. Chem. Lett. 16, 3702–3705.	pl_PL
dc.references	Rigaku OD (2015). CrysAlisPRO. Rigaku Oxford Diffraction, Yarnton, England.	pl_PL
dc.references	Saghatforoush, L., Khoshtarkib, Z., Amani, V., Bakhtiari, A., Hakimi, M. & Keypour, H. (2016). J. Solid State Chem. 233, 311–319.	pl_PL
dc.references	Saracoglu, N. (2007). Tetrahedron, 63, 4199–4236.	pl_PL
dc.references	Sauer, J. (1996). Comprehensive Heterocyclic Chemistry, Vol. 6, 2nd ed., edited by A. J. Boulton, C. W. Rees and E. F. V. Scriven, pp. 901–955. Oxford: Pergamon.	pl_PL
dc.references	Šečkutė, J. & Devaraj, N. K. (2013). Curr. Opin. Chem. Biol. 17, 761–767.	pl_PL
dc.references	Sheldrick, G. M. (2015a). Acta Cryst. A71, 3–8.	pl_PL
dc.references	Sheldrick, G. M. (2015b). Acta Cryst. C71, 3–8.	pl_PL
dc.references	Spek, A. L. (2009). Acta Cryst. D65, 148–155.	pl_PL
dc.references	Westrip, S. P. (2010). J. Appl. Cryst. 43, 920–925.	pl_PL
dc.contributor.authorEmail	kinga.raj@chemia.uni.lodz.pl	pl_PL
dc.identifier.doi	10.1107/S205698901801753X
dc.relation.volume	1	pl_PL
dc.discipline	nauki chemiczne	pl_PL