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In the polymeric title compound, {[Ag(C8H10N4S4)]ClO4·1.5H2O}n, the AgI atom has a slightly distorted trigonal-planar coordination geometry provided by three N-atom donors from the thia­diazole rings of three symmetry-related 2,2′-[butane-1,4-diylbis(sulfanedi­yl)]bis­(1,3,4-thia­diazole) ligands. Centrosymmetrically related AgI atoms are bridged by the N–N fragments of rings, forming six-membered dinuclear metallacycles, which are further linked by the alkyl spacers of the thia­diazole ligands into a layer network extending parallel to (0-21). The crystal structure is stabilized by inter­molecular O—H...O hydrogen bonds. The O atoms of the perchlorate anion and one water mol­ecule are disordered over two sets of sites with refined occupancy ratios of 0.640 (6):0.360 (6) and 0.663 (11):0.337 (11), respectively. The second water molecule shows half-occupancy.

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The three-dimensional coordination polymer, [Eu2(C6H2O4S)3(H2O)4]n, has been synthesized under hydro­thermal conditions. The asymmetric unit comprises one Eu3+ cation, two aqua ligands and one and a half thiophene-2,5-dicarboxylate anions (the half-anion being completed by a twofold rotation axis). The Eu3+ cation is eight-coordinated in a distorted dodeca­hedral geometry. The crystal structure features O—H...O hydrogen bonds.

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The title compound, C9H8N2O4, adopts an E conformation about the C=C bond. The CHphen­yl—Cphen­yl—CH—C(—NO2) torsion angle is −57.7 (3)°. The crystal structure features weak inter­molecular C—H...O inter­actions.
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