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The mol­ecular structure of the title salt, C6H16N+·C20H11N6O12S, shows a planar geometry of the benzamido–phen­yl–sulfonyl moiety, with a dihedral angle of 1.59 (9)° between the aromatic ring planes. The central ring and the aromatic ring of the other dinitro­benzamide group are nearly perpendicular, making a dihedral angle of 89.55 (9)°. All nitro groups lie almost in plane with the associated aromatic rings, the O—N—C—C torsion angles ranging from 9.2 (2) to 24.3 (2)°. In the crystal, strong anion–anion N—H...O and anion–cation hydrogen bonds form inversion dimers stacked along the a axis. Less prominent anion–anion C—H...O inter­actions lead to the formation of a three-dimensional network including anion–anion dimers as well as anion–anion chains along [100?].

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The mol­ecule of the title compound, C19H13Br2N3O2, lies about a twofold rotation axis. The benzene ring makes dihedral angles of 8.9 (2) and 16.4 (2)° with the central pyridine ring and the second benzene ring, respectively. An intra­molecular N—H...N contact occurs. In the crystal, mol­ecules are connected by pairs of N—H...O hydrogen bonds into chains along the c axis.

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The mol­ecular structure of the pyridine derivative, C19H15N3O4·C3H7NO, shows almost planar geometry with dihedral angles of 6.9 (1) and 13.4 (1)° between the pyridine ring and the two benzene rings. This conformation is stabilized by two intra­molecular N—H...N(pyridine) bonds. In the crystal, strong O—H...O(carboxamide) and N—H...O(hy­droxy­phen­yl) hydrogen bonds link the mol­ecules, forming a three-dimensional structure. The di­methyl­formamide solvent mol­ecules are not involved in the hydrogen bonding. The structure shows pseudosymmetry, but refinement in the space group Pbcn leads to significantly worse results and a disordered di­methyl­formamide mol­ecule.
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