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1D Heterometallic Oxalate Compounds as Precursors for Mixed Ca–Cr Oxides – Synthesis, Structures, and Magnetic Studies
24
Citations
37
References
2014
Year
Materials ScienceInorganic ChemistryCrystal StructureEngineeringHeterometallic Oxalate CompoundsCrystallographyChemistryMagnetic StudiesO 4Inorganic MaterialFunctional MaterialsIr SpectroscopyInorganic SynthesisInorganic Compound
Abstract The heterodimetallic compounds {[CaCr 2 (L) 2 (C 2 O 4 ) 4 ] · x H 2 O} n [L = 2,2′‐bipyridine (bpy), x = 0.83 ( 1 ); L = 1,10‐phenanthroline (phen), x = 0.33 ( 2 )] were synthesized and characterized by IR spectroscopy, X‐ray diffraction and magnetic measurements. The crystal structure of 2 is reported: the chelation of a [Cr(phen)(C 2 O 4 ) 2 ] – units towards Ca cations results in 1D double zigzag chains. The ability of 1 and 2 to act as single‐source precursors for the formation of Ca–Cr oxides is explored by thermal analysis, powder X‐ray diffraction and IR spectroscopy. The thermal processing of 1 and 2 at 1100 °C in air led to the appearance of the β‐CaCr 2 O 4 phase as the major crystalline oxide. By heating the samples up to 1100 °C in nitrogen, only the β‐CaCr 2 O 4 phase formed, whereas heating at 1400 °C caused the crystallization of two polymorphs, α‐ and β‐CaCr 2 O 4 . The magnetic behaviour of β‐CaCr 2 O 4 pointed to the freezing of magnetic moments in coexistence with a weak ferromagnetic order.
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