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. 2008 Jul 12;64(Pt 8):m1020-1.
doi: 10.1107/S1600536808021004.

Bis(μ-N-benzyl-N-methyl-dithio-carbamato)-1:2κS,S':S';1:2κS:S,S'-bis-[bis-(N-benzyl-N-methyl-dithio-carbamato-κS,S')thallium(III)]

Bis(μ-N-benzyl-N-methyl-dithio-carbamato)-1:2κS,S':S';1:2κS:S,S'-bis-[bis-(N-benzyl-N-methyl-dithio-carbamato-κS,S')thallium(III)]

Corrado Rizzoli et al. Acta Crystallogr Sect E Struct Rep Online. .

Abstract

The molecule of the dinuclear title compound, [Tl(2)(C(9)H(10)NS(2))(6)], possesses a crystallographically imposed centre of symmetry. Each Tl(III) atom is seven-coordinated by S atoms of four different dithio-carbamate anions in a distorted penta-gonal-bipyramidal coordination geometry. The crystal structure is stabilized by a C-H⋯S hydrogen-bond inter-action linking complex mol-ecules into chains running parallel to the b axis. Intramolecular C-H⋯S hydrogen bonds are also present.

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Figures

Fig. 1.
Fig. 1.
View of the title dinuclear complex molecule with displacement ellipsoids drawn at the 30% probability level. Hydrogen atoms are omitted for clarity [Symmetry code: (i) = 1 - x, -y, -z].
Fig. 2.
Fig. 2.
View of the crystal packing of the title compound. Intermolecular hydrogen bonds are shown as dashed lines. H atoms not involved in hydrogen bonds are omitted for clarity. Colour codes: Tl red, S yellow, N blue, C grey and H white.

References

    1. Abrahamson, H., Heiman, J. R. & Pignolet, L. H. (1975). Inorg. Chem.14, 2070–2075.
    1. Altomare, A., Burla, M. C., Camalli, M., Cascarano, G. L., Giacovazzo, C., Guagliardi, A., Moliterni, A. G. G., Polidori, G. & Spagna, R. (1999). J. Appl. Cryst.32, 115–119.
    1. Bruker (1997). SMART, SAINT and SADABS Bruker AXS Inc., Madison, Wisconsin, USA.
    1. Burschka, C. H. (1982). Z. Anorg. Allg. Chem.485, 217–224.
    1. Casas, J. S., Castaño, M. V., Freire, C., Sanchez, A., Sordo, J., Castellano, E. E. & Zukerman-Schpector, J. (1994). Inorg. Chim. Acta, 216, 15–20.