Crystal structure of azido-(η(5)-cyclo-penta-dien-yl)bis-(tri-phenyl-phosphane-κP)ruthenium(II) di-chloro-methane hemisolvate.

The title solvated complex, [Ru(η(5)-C5H5)(N3){P(C6H5)3}2]·0.5CH2Cl2, displays a typical piano-stool geometry about the Ru(II) atom. The bond lengths and angles of the cyclo-penta-dienyl and phosphane ligands are very similar to that of the unsolvated complex [Taqui Khan et al. (1994 ▶). Acta Cryst. C50, 502-504]. The azide anion displays similar N-N distances of 1.173 (3) and 1.156 (3) Šand has an N-N-Ru angle of 119.20 (15)°, indicating a greater contribution of the canonical form Ru-N=N((+))=N((-)) for the bonding situation. An intra-molecular C-H⋯N hydrogen-bonding inter-action between one ortho H atom of a phosphane ligand and the N atom coordinating to the metal is observed. A similar inter-molecular inter-action is observed between a meta H atom of a phosphane ligand and the terminal azide N atom of a neighbouring complex. Finally, two C-H⋯N inter-actions exists between the H atoms of the di-chloro-methane solvent mol-ecule and the terminal N atom of two azide anions. The solvent mol-ecule is located about a twofold rotation axis and shows disorder of the Cl atoms with an occupancy ratio of 0.62 (3):0.38 (3).

(E)-1,1-Diphenyl-2-(thio-phen-2-yl-methyl-idene)hydrazine.

The asymmetric unit of the title compound, C17H14N2S, consists of two crystallographically independent mol-ecules with similar conformations. The dihedral angles between the phenyl rings are 89.32 (5) and 82.80 (5)° in the two mol-ecules. In the crystal, mol-ecules are linked by C-H⋯π inter-actions, forming a three-dimensional network.