Structure of phosphonium rhenates(VII)

Four phosphonium rhenates(VII) were prepared and crystallized: (A) 1,2-bis (triphenylphosphonium)ethane rhenate(VII) (Pī, a=8.298(2), b=10.638(3), c= 11.242(3) ?, α=64.96(2), β=80.49(2), γ=88.17(2)°), (B) methyltriphenylphosphonium rhenate(VII) (Pca2₁, a=15.096(3), b=12.627(3), c=19.353(3) ?), (C) benzyltriphenylphosphonium rhenate(VII) (Pī, a=9.648(2), b=11.689(2), c=20.806(3) ?, α=88.44(2), β=84.63(2), γ=77.33(3)°), and (D) orthorhombic form of (iodomethyl)triphenylphosphonium rhenate(VII) (Pca2₁, a=14.952(3), b=13.120(3), c=20.603(4) ?). Each crystal structure consists of separate phosphonium cations and rhenate(VII) anions. In A centrosymmetric 1,2-bis(triphenylphosphonium)ethane cations form layers perpendicular to 011]. In B the cations are set in chains along 100] forming layers perpendicular to 001]. In C two symmetrically-independent cations form double columns along 100] and these columns are arranged in puckered layers perpendicular to 001]. D is almost isomorphous to B. The crystal structures are stabilised by weak C–H⋯O hydrogen bonds as well as phenyl rings interactions. In all crystal structures supramolecular motifs of phenyl rings embraces could be distinguished.