Abstract

Abstract Syntheses were performed at room temperature using Ni(NO3)2·6H2O, cyclam (cyclam = 1,4,8,11-tetraazacyclotetradecane) and the precursors Li8[Nb6O19]· ≈22H2O or Na7[HNb6O19]·15H2O in a DMSO-H2O mixture. Yellow crystals of the new compound {[Ni(cyclam)]2H4Nb6O19}·12H2O could be obtained after one week applying the Li+ or Na+ salt as starting materials. The crystal structure is unique in polyoxoniobate (PONb) chemistry and displays two interpenetrating three-dimensional (3D) networks. The [Nb6O19]8– anion is expanded by four Ni2+ centered complexes via Ni–O bonds to terminal O2− anions of the hexaniobate anion. The 3D networks are generated by further Ni–O bond formation between neighboring [Nb6O19]8− anions. The remaining void space is occupied by H2O molecules which form a water cluster.

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