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In the colourless title compound, [Pr(CF3O3S)3(CH3CN)3]n, the three trifluoro­methane­sulfonate anions form three bridges via O:O′-coordination between two PrIII atoms. The structure contains [Pr(NCMe)32(OTf)3—Pr(NCMe)32(OTf)3]n (NCMe is acetonitrile; OTf is trifluoromethanesulfonate) chains parallel to the a axis. The PrIII atom is nine-coordinate in a distorted tricapped trigonal-prismatic environment.

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The colourless title complex, [Zn2(C10H11O5)4(C2H6OS)2], crystallizes with one half-mol­ecule in the asymmetric unit, the other half of the mol­ecule being generated by a crystallographic inversion center. The structure shows a μ2-O:O′-bridging mode of the four 3,4,5-tri­meth­oxy­benzoate ligands finally stabilizing the two ZnII atoms in the dinuclear complex in a distorted square-pyramidal environment. The fifth coord­in­ation site in the apical position of the pyramid is occupied by a coordinating dimethyl sulfoxide solvent mol­ecule equally disordered over two positions.

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The title compound, C12H20N2O4, represents one example of a zwitterionic imidazolium salt with a carboxyl­ate group at the 2-position of the imidazolium ring. The dihedral angle between the heterocyclic ring and the carboxyl­ate group is 31.3 (1)°. The side chain linking the N atom of the ring and the methine C atom has a gaucheantianti conformation [torsion angles = −60.3 (2), −175.7 (2) and 178.7 (2)°, respectively]. In the crystal, mol­ecules are linked by short C—H...O hydrogen bonds involving the C—H groups in the aromatic ring to generate (001) sheets.
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