Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1506927 | Solid State Sciences | 2006 | 5 Pages |
We report the synthesis, crystal structures, magnetic properties, and thermal behavior of a family of isostructural transition metal gallate dihydrates containing infinite chains of trans -corner-sharing MO6MO6 octahedra. The gallates crystallize in the enantiomorphic space groups P3121P3121 and P3221P3221, chirality being imparted by helical motifs in the structure. Ni(C7O5H4)⋅2H2O: a=8.824(2) Åa=8.824(2) Å, c=10.644(2) Åc=10.644(2) Å; Mn(C7O5H4)⋅2H2O: a=9.063(2) Åa=9.063(2) Å, c=10.947(2) Åc=10.947(2) Å; Co(C7O5H4)⋅2H2O: a=8.910(2) Åa=8.910(2) Å, c=10.887(2) Åc=10.887(2) Å. The Co(II) and Ni(II) gallates exhibit antiferromagnetic behavior, with TN=43TN=43 and 19 K, respectively, while Mn(II) gallate is paramagnetic down to 5 K. High-temperature X-ray powder diffraction indicates that crystallinity is lost near 200 °C in all of the compounds. Decarboxylation of the gallate moieties is believed to facilitate this thermal decomposition.
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