The charge-transfer complex 1-aminoanthraquinone–7,70,8,80-tetracyanoquinodimethane (1/1)

Oliveira, Adriano Bof de; Beck, Johannes; Daniels, Jörg; Santos, Jaciara Nascimento; Feitosa, Bárbara Regina Santos

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Campo DC	Valor	Idioma
dc.contributor.author	Oliveira, Adriano Bof de	-
dc.contributor.author	Beck, Johannes	-
dc.contributor.author	Daniels, Jörg	-
dc.contributor.author	Santos, Jaciara Nascimento	-
dc.contributor.author	Feitosa, Bárbara Regina Santos	-
dc.date.accessioned	2025-11-12T20:34:59Z	-
dc.date.available	2025-11-12T20:34:59Z	-
dc.date.issued	2013	-
dc.identifier.citation	OLIVEIRA, A. B. et al. The charge-transfer complex 1-aminoanthraquinone–7,70,8,80-tetracyanoquinodimethane (1/1). Acta crystallographica Section E, Chester, v. 69, n. 2, p. o301, 2013. Disponível em: https://journals.iucr.org/e/issues/2013/02/00/bt6884/index.html. Acesso em: 12 nov. 2025.	pt_BR
dc.identifier.issn	1600-5368	-
dc.identifier.uri	https://ri.ufs.br/jspui/handle/riufs/23847	-
dc.language	eng	pt_BR
dc.publisher	International Union of Crystallography	pt_BR
dc.relation.ispartof	Acta Crystallographica Section E	pt_BR
dc.subject	Single-crystal X-ray study	eng
dc.subject	T = 293 K	eng
dc.subject	Mean (C–C) = 0.003 A˚	eng
dc.subject	R factor = 0.052	eng
dc.subject	WR factor = 0.135	eng
dc.subject	Data-to-parameter ratio = 11.3	eng
dc.title	The charge-transfer complex 1-aminoanthraquinone–7,70,8,80-tetracyanoquinodimethane (1/1)	pt_BR
dc.type	Artigo	pt_BR
dc.identifier.license	Creative Commons Atribuição 2.0 Reino unido: Inglaterra e País de Gales (CC BY 2.0 UK)	pt_BR
dc.description.resumo	The reaction of 1-aminoanthraquinone with 7,70 ,8,80 -tetracyanoquinodimethane yielded the title charge-transfer complex, C14H9NO2C12H4N4. The molecules have maximum deviations from the mean planes through the non-H atoms of 0.0769 (14) A˚ for an oxo O atom and 0.1175 (17) A˚ for a cyano N atom, respectively. The dihedral angle between the two planes is 3.55 (3). In the crystal, molecules are stacked into columns along the a-axis direction. Pairs of N—HN and N—HO interactions connect the molecules perpendicular to the stacking direction. Additionally, an intramolecular N— HO hydrogen-bond interaction is observed for 1-aminoanthraquinone.	pt_BR
dc.description.local	Chester	pt_BR
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