metal-organic compounds
Open access
In the title coordination polymer, [Ag2Cl2(C10H8N2)(C18H15P)2]n, the AgI cation is coordinated by a 4,4′-bipyridine N atom, a triphenylphosphane P atom and two Cl− anions in a distorted tetrahedral geometry. The 4,4-bipyridine and Cl− anions bridge the AgI cations, forming polymeric chains running along [21-1]. In the crystal, weak C—HCl interactions link the polymeric chains into a three-dimensiona supramolecular architecture.
organic compounds
Open access
The asymmetric unit of the title compound, C38H34Cl2O2Te2·H2O, contains two independent TeIV cations, each coordinated by three phenyl ligands, two Cl− anions and one acetic acid molecule in a distorted octahedral C3Cl2O geometry; the longer TeCl distances ranging from 3.2007 (11) to 3.4407 (11) Å and the longer TeO distances of 3.067 (3) and 3.113 (3) Å indicate the weak bridge coordination. The Cl− anion and acetic acid molecule bridge the two independent TeIV cations, forming the dimeric complex molecule, in which the TeTe separation is 3.7314 (4) Å. In the crystal, the water molecules of crystallization link the TeIV complex molecules into chains running along the b-axis direction via O—HO and O—HCl hydrogen bonds.