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    Synthesis, crystal structure and magnetic properties of an octanuclear cerium(III) complex of pyridine-2,6-dicarboxylate
    (Walter De Gruyter Gmbh, 2019) Sharif, Shahzad; Khan, Islam Ullah; Sahin, Onur; Jabeen, Nadia; Ahmad, Saeed; Khan, Bushra
    An octanuclear compound of cerium(III), [Ce-8(Pydc)(10)(HPydc)(4)center dot 22H(2)O]center dot 11H(2)O (1) (Pydc = pyridine-2,6-dicarboxylate anion) was prepared under mild solvothermal conditions and its crystal structure was determined by single-crystal X-ray diffraction. Three kinds of coordination environments are observed, which include: [Ce(Pydc)(3)], [Ce(Pydc)(H2O)(4)(O,O)], and [Ce(H2O)(7) (O,O)]. Each cerium atom in 1 is nine-coordinated but two different geometries are found. The Ce1 and Ce2 atoms exhibit a nearly tricapped trigonal prismatic CeN3O8 geometry, while Ce3 and Ce4 possess CeNO8 and CeO9 coordination polyhedra, which approximate to slightly distorted mono-capped square antiprisms having 12 triangular faces. The Pydc ligands adopt tri-, tetra-, and penta-coordination modes through tridentate chelating and, mu(2) and mu(3)-bridging modes, respectively. The clusters are joined by O-II center dot center dot center dot O hydrogen bonds to generate 3D supramolecular network. Magnetic susceptibility measurements for 1 indicate that the chi(m) values obey the Curie-Weiss law. The overall magnetic behavior is typical for the presence of antiferromagnetic exchange coupling interactions between the cerium(III) ions.