In the title complex, [U(C17H14BrN3O2S)O2(C2H5OH)], the UVI cation has a distorted pentagonal–bipyramidal environment with the pentagonal plane defined by two N and two O atoms of the tetradentate Schiff base ligand and the O atom of the ethanol molecule. Two oxide O atoms occupy the axial positions. The azomethine C N group and the Br atom are disordered over two positions in a 0.8356 (18):0.1644 (18) ratio. The ethylthiolyl group is disordered over three conformations in a 0.8356 (18):0.085 (6):0.079 (6) ratio, and the ethanol ligand is also disordered over three orientations in a 0.470 (16):0.277 (19):0.253 (18) ratio. In the crystal, molecules form centrosymmetric dimers through hydrogen bonding between ethanol O—H donors and phenolate Oatom acceptors. Weak C—H O interactions consolidate the crystal packing.

{4-Bromo-2-[(2-{(ethylsulfanyl)[(2-oxidobenzylidene- κO)amino-κN]methylidene}hydrazinylidene-κN1)methyl] phenolato-κO}(ethanol-κO)dioxidouranium(VI)

PELUSO, Andrea
2013-01-01

Abstract

In the title complex, [U(C17H14BrN3O2S)O2(C2H5OH)], the UVI cation has a distorted pentagonal–bipyramidal environment with the pentagonal plane defined by two N and two O atoms of the tetradentate Schiff base ligand and the O atom of the ethanol molecule. Two oxide O atoms occupy the axial positions. The azomethine C N group and the Br atom are disordered over two positions in a 0.8356 (18):0.1644 (18) ratio. The ethylthiolyl group is disordered over three conformations in a 0.8356 (18):0.085 (6):0.079 (6) ratio, and the ethanol ligand is also disordered over three orientations in a 0.470 (16):0.277 (19):0.253 (18) ratio. In the crystal, molecules form centrosymmetric dimers through hydrogen bonding between ethanol O—H donors and phenolate Oatom acceptors. Weak C—H O interactions consolidate the crystal packing.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11386/4101455
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