Title of article :
Crystal structure of (μ-1,4-dicarboxybutane-1,4-dicarboxylato)bis[bis(triphenylphosphane)silver(I)] dichloromethane trisolvate
Author/Authors :
Frenzel, Peter Technische Universita¨t Chemnitz - Fakulta¨t fu¨r Naturwissenschaften - Institut fu¨r Chemie, Anorganische Chemie - D-09107 Chemnitz , Korb, Marcus Technische Universita¨t Chemnitz - Fakulta¨t fu¨r Naturwissenschaften - Institut fu¨r Chemie, Anorganische Chemie - D-09107 Chemnitz , Lang, Heinrich Technische Universita¨t Chemnitz - Fakulta¨t fu¨r Naturwissenschaften - Institut fu¨r Chemie, Anorganische Chemie - D-09107 Chemnitz
Abstract :
The molecular structure of the tetrakis(triphenylphosphanyl)disilver salt of butane-1,1,4,4-tetracarboxylic acid, [Ag2(C8H8O8)(C18H15P)4]·3CH2Cl2, crystallizes with one and a half molecules of dichloromethane in the asymmetric unit. The coordination complex exhibits an inversion centre through the central CH2—CH2 bond. The AgI atom has a distorted trigonal–planar P2O coordination environment. The packing is characterized by intermolecular T-shaped π–π interactions between the phenyl rings of the PPh3 substituents in neighbouring molecules, forming a ladder-type superstructure parallel to [010]. These ladders are arranged in layers parallel to (101). Intramolecular hydrogen bonds between the OH group and one O atom of the Ag-bonded carboxylate group results in an asymmetric bidendate coordination of the carboxylate moiety to the AgI ion.
Keywords :
crystal structure , bridges , silver , hydrogen bond , tetracarboxylic acid , triphenylphosphane
Journal title :
Acta Crystallographica Section E: Crystallographic Communications