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(E)-1-Methyl-4-[2-(1-naphth­yl)vin­yl]pyridinium 4-bromo­benzene­sulfonate

In the title compound, C(18)H(16)N(+)·C(6)H(4)BrO(3)S(−), the cation exists in the E configuration and the whole mol­ecule of the cation is disordered with a refined site-occupancy ratio of 0.733 (1):0.267 (1). The naphthalene system is not planar, the inter­planar angle between the two aromatic rin...

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Detalles Bibliográficos
Autores principales: Chantrapromma, Suchada, Chanawanno, Kullapa, Fun, Hoong-Kun
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977813/
https://www.ncbi.nlm.nih.gov/pubmed/21583950
http://dx.doi.org/10.1107/S1600536809014974
Descripción
Sumario:In the title compound, C(18)H(16)N(+)·C(6)H(4)BrO(3)S(−), the cation exists in the E configuration and the whole mol­ecule of the cation is disordered with a refined site-occupancy ratio of 0.733 (1):0.267 (1). The naphthalene system is not planar, the inter­planar angle between the two aromatic rings being 5.0 (5)° for the major component and 5.7 (10)° for the minor component. The cation is twisted with dihedral angles between the pyridinium ring and the two aromatic rings of the naphthalene system of 56.3 (5) and 51.4 (5)° (for the major component) and 52.2 (11) and 53.4 (11)° (for the minor component). The pyridinium ring and the benzene ring of the anion are inclined to each other at inter­planar angles of 85.0 (4) and 71.5 (9)° for the major and minor components, respectively. In the crystal packing, the cations and anions are alternately arranged with the cations stacked in an anti­parallel manner along the c axis and the anions linked together into chains along the same direction. The cations are linked to the anions into chains along [102] by weak C—H⋯O inter­actions. The crystal structure is further stabilized by C—H⋯π inter­actions and π–π contacts, with Cg⋯Cg distances of 3.502 (9) and 3.698 (6) Å. A short Br⋯O contact [3.029 (4) Å] is also present.