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A novel 8-carboxyindeno[1,2-b]quinoxalin-11-one thiosemicarbazone zinc(II) Schiff base complex.

In the novel title binuclear zinc(II) Schiff base complex, bis(mu-11-thiosemicarbazonoindeno[1,2-b]quinoxaline-8-carboxylato)bis[(dimethyl sulfoxide)zinc(II)] dimethyl sulfoxide trisolvate, [Zn2(C17H9N5O2S)2(C2H6OS)2].3C2H6OS, each ZnII atom is five-coordinated and situated in a distorted square-pyramidal environment, coordinated by two L2- ligands and one dimethyl sulfoxide molecule. Each L2- ligand, which coordinates to two ZnII atoms, has two parts. One part, acting in a tridentate chelating mode, coordinates to one ZnII atom through two N atoms and one S atom, while another part coordinates to another ZnII atom through a monodentate carboxylate group. The whole complex has a dimeric structure. The coordination mode of the nearly planar L2- ligand is quite different from the most common mode for Schiff bases.

Cations, Divalent↗

Structure of salicylaldehyde thiosemicarbazone.

C8H9N3OS, monoclinic, C2/c, a = 14.206 (3), b = 14.244 (4), c = 10.457 (4) A, beta = 116.18(2) degrees, V = 1898.9 (8) A3, Z = 8, Dm = 1.387, D chi = 1.366 g cm-3, lambda(Mo K alpha) = 0.71069 A, mu = 2.90 cm-1, F(000) = 816.0, T = 298 K, final R = 0.0429 for 1322 observed reflections. The S and hydrazinic N atoms lie trans. The lowering of antibacterial activity compared to that of 4-phenylthiosemicarbazide may be correlated with the decrease in negative charge on the hydrazinic N atom. The crystal structure is stabilized by hydrogen bonding, stacking interactions and van der Waals forces.

Aldehydes↗