3.8 Article

Crystal structure of (μ-trans-1,2-bis{2-[(2-oxidophenyl)methylidene]hydrazin-1-ylidene}ethane1,2-diolato-κ3O,O′,N)bis[di-tert-butyltin(IV)]

Publisher

INT UNION CRYSTALLOGRAPHY
DOI: 10.1107/S2056989018007077

Keywords

crystal structure; tin; Schiff base

Funding

  1. Sonatel Foundation

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The binuclear complex, [Sn-2(C4H9)(4)(C16H10N4O4)], contains two Sn4+ ions, connected by doubly N-deprotonated oxalylbis[(2-oxidobenzylidene)hydrazide] ligands, and each Sn4+ ion is linked to two tert-butyl groups. The coordination sphere of each Sn atom is best described as a distorted trigonal bipyramid. Each stannic ion in the complex is in a C2O2N environment. The two homologous parts of the doubly deprotonated ligand are located in trans positions with respect to the C-C bond of the oxalamide group. The oxalamide group exhibits an asymmetric coordination geometry, as seen by the slight difference between the C-O and C-N bond lengths. The three-dimensional network is a multilayer of complex molecules with no strong supramolecular interactions.

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