Intramolecular hydrogen-bond-directed coordination: trans-bis(N-benzoyl-N′-propyl­thio­urea-κS)di­iodo­platinum(II) and trans-bis(N-benzoyl-N′-propyl­thio­urea-κS)di­bromo­platinum(II)

In the title compounds, trans-[PtI₂(C₁₁H₁₄N₂OS)₂], (I), and trans-[PtBr₂(C₁₁H₁₄N₂OS)₂], (II), respectively, intramolecular N—H⋯O (propyl­amine side) hydrogen bonds in the potentially bidentate thio­urea ligands lock the carbonyl O atoms into six-membered rings, determining the S-mono­dentate mode of coordination of these ligands. Intramolecular N—H⋯X (X is I or Br) interactions (benzoyl­amine side) lead to slight distortions of the Pt^II coordination spheres from ideal square-planar geometry. The Pt^II ion is located on an inversion centre in both structures.