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Antimony(III) complexes of bifunctional tridentateSchiff bases

  • Anorganische, Struktur- und Physikalische Chemie
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Abstract

Several newSchiff base derivatives of antimony(III) have been synthesized by the reaction of antimony(III) isopropoxide with theSchiff bases having the donor system, O−N−O. The reactions in 1:1 and 2:3 molar ratios [Sb(O-i-C3H7)3: :Schiff base] have yielded Sb(O-i-C3H7) (SB) and Sb2 (SB)3 type of derivatives (whereSB represents the anion of theSchiff base andSBH2=o-hydroxyacetophenone-2-hydroxy-1-propylimine, o-hydroxycetophenone-3-hydroxy-1-propylimine, salicylidene-2-hydroxyethylamine, salicylidene-2-hydroxy-1-propylamine and 2-hydroxy-1-naphthylidene-2-hydroxyethylamine) resp. In the resultingSchiff base derivatives, the central antimony atom appears to be tetracoordinated as indicated by their monomeric state determined ebullioscopically. The infrared spectra of the resulting complexes have been recorded and tentative structures indicated. The thermogravimetric analysis of antimony-monoisopropoxysalicylidene-2-hydroxy-1-propylamine has also been carried out.

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Singh, O.P., Tandon, J.P. Antimony(III) complexes of bifunctional tridentateSchiff bases. Monatshefte für Chemie 108, 1353–1357 (1977). https://doi.org/10.1007/BF01046448

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