| Abstrakt: |
A glycol ether modified precursor, [Nb{O(CHCHO)}(OPr)] ( A) was prepared by the reaction of Nb(OPr) with O(CHCHOH) in 1:1 molar ratio in anhydrous benzene. Further reactions of A with a variety of internally functionalized oximes in different molar ratios, yielded heteroleptic complexes of the type, [Nb{O(CHCHO)}(OPr){ON = C(CH)(Ar)}] ( 1-9) {where Ar = CHO-2, n = 1 [ 1], n = 2 [ 2], n = 3 [ 3]; CHS-2, n = 1 [ 4], n = 2 [ 5], n = 3 [ 6]; CHN-2, n = 1 [ 7], n = 2 [ 8], n = 3 [ 9]}. All the above derivatives have been characterized by elemental analyses, FT-IR, NMR (H, C {H}) and FAB mass studies. Spectral studies of 1-9 suggest the presence of mono- and bi-dentate mode of oxime moieties, in the solution and in the solid states, respectively. FAB mass studies indicate monomeric nature for 3 and dimeric nature for A. TG curves of A and 6 show their low thermal stability. Soft transformation of A and 3 to pure niobia, a and b, respectively have been carried out by sol-gel technique. The XRD patterns of niobia a and b suggest the formation of nano-size crystallites of average size of 10.8 and 19.5 nm, respectively. The XRD patterns also indicate the formation of monoclinic phase of the niobia in both the cases. Absorption spectra of a and b suggest energy band gaps of 4.95 and 4.39 eV, respectively. [ABSTRACT FROM AUTHOR] |
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