Room-Temperature Synthesis of Thiostannates from {[Ni(tren)]2[Sn2S6]}n.

The compound {[Ni(tren)]2[Sn2S6]}n (1) (tren = tris(2-aminoethyl)amine, C6H18N4) was successfully applied as source for the room-temperature synthesis of the new thiostannates [Ni(tren)(ma)(H2O)]2[Sn2S6]·4H2O (2) (ma = methylamine, CH5N) and [Ni(tren)(1,2-dap)]2[Sn2S6]·2H2O (3) (1,2-dap = 1,2-diaminopropane, C3H10N2). The Ni-S bonds in the Ni2S2N8 bioctahedron in the structure of 1 are analyzed with density functional theory calculations demonstrating significantly differing Ni-S bond strengths. Because of this asymmetry they are easily broken in the presence of an excess of ma or 1,2-dap immediately followed by Ni-N bond formation to N donor atoms of the amine ligands thus generating [Ni(tren)(amine)](2+) complexes.

Crystal structure of tris-(N-methyl-salicyl-aldiminato-κ(2) N,O)chromium(III).

The crystal structure of the title compound, [Cr(C8H8NO)3], is isotypic with the vanadium(III) analogue. The asymmetric unit consists of one Cr(3+) cation and three N-methyl-salicylaldiminate anions. The metal cation is octa-hedrally coordinated by three N,O-chelating N-methyl-salicylaldiminate ligands, leading to discrete and neutral complexes.

Crystal structure of tris-(N-methyl-salicylaldiminato-κ(2) N,O)vanadium(III).

The structure of the title complex, [V(C8H8NO)3], comprises neutral and discrete complexes, in which the V(III) cation is coordinated by three anionic N-methyl-alicylaldiminate ligands within a slightly distorted mer-N3O3 octa-hedral geometry. In the crystal structure, the mol-ecules are linked via C-H⋯O hydrogen bonds into supra-molecular chains that extend along the c axis.

Influence of the synthesis parameters onto nucleation and crystallization of five new tin-sulfur containing compounds.

The distinct control of the synthesis parameters achieved crystallization of five new inorganic-organic hybrid tin sulfides with 1,10-phenanthroline (phen) as the organic component: {[Mn(phen)2]2(μ2-Sn2S6)} (1, 3), {[Mn(phen)2]2(μ2-Sn2S6)}·phen (2), {[Mn(phen)2]2(μ2-Sn2S6)}·phen·H2O (4), and {[Mn(phen)2]2[μ-η(2)-η(2)-SnS4]2[Mn(phen)]2}·H2O (5). Compounds 1, 3, and 4 occur successively under static conditions by increasing the reaction time up to 8 weeks. Stirring the reaction mixtures and keeping the educt ratio constant allow preparation of distinct phase pure samples within very short reaction times.