Title of article :
Crystal structure of bis[μ-2-(diisopropylphosphoryl)propan-2-olato-κ3O1,O2:O1]bis[chloridooxidovanadium(IV)]
Author/Authors :
Glatz, Mathias Institute of Applied Synthetic Chemistry - Vienna University of Technology, Austria , Stöger, Berthold Institute of Chemical Technologies and Analytics - Vienna University of Technology, Austria , Weil, Matthias Institute of Chemical Technologies and Analytics - Vienna University of Technology, Austria , Kirchnera, Karl Institute of Applied Synthetic Chemistry - Vienna University of Technology, Austria
Abstract :
The dinuclear molecule of the title complex, [VOCl{μ-OC(Me)2P(iPr)2-κ2O}]2 or [V2(C9H20O2P)2Cl2O2], which was obtained due to an unexpected oxidation reaction, is centrosymmetric, with the inversion centre located in the middle of the central V2O2 core. These core O atoms arise from the symmetry-related 2-(diisopropylphosphoryl)propan-2-olate dianions. The VIV atom is additionally bonded to one terminal Cl ligand, the second O atom of the dianion and double bonded to a vanadyl O atom, leading to an overall distorted square-pyramidal VO4Cl coordination polyhedron with the vanadyl O atom as the apex. An intramolecular C—H⋯Cl contact helps to establish the molecular configuration. In the crystal, molecules are stacked in rows parallel to [001] and are linked by C—H⋯Cl contacts to form chains running in the same direction.
Keywords :
crystal structure , square-pyramidal coordination geometry , vanadium , binuclear centrosymmetric complex
Journal title :
Acta Crystallographica Section E: Crystallographic Communications
