SYNTHESIS AND SPECTROSCOPIC STUDIES (MOSSBAUER, IR AND NMR) OF BIOLOGICALLY-ACTIVE ORGANOTIN(IV) COMPLEXES OF SCHIFF-BASES DERIVED FROM 2-AMINO-5-PHENYL-1,3,4-OXADIAZOLE
Ms. Raizada, SYNTHESIS AND SPECTROSCOPIC STUDIES (MOSSBAUER, IR AND NMR) OF BIOLOGICALLY-ACTIVE ORGANOTIN(IV) COMPLEXES OF SCHIFF-BASES DERIVED FROM 2-AMINO-5-PHENYL-1,3,4-OXADIAZOLE, Synthesis and reactivity in inorganic and metal-organic chemistry, 26(9), 1996, pp. 1563-1576
A few new organotin(IV) complexes of tridentate (ONN) over bar donor S
chiff bases of salicylaldehyde, 4-hydroxybenzaldehyde, 2-hydroxyacetop
henone, 4-hydroxyacetophenone with 2-amino-5-phenyl-1,3,4-oxadiazole h
ave been synthesised and characterised by elemental analyses, H-1 NMR,
UV, IR and Mossbauer spectroscopic studies show hexa-coordination abo
ut the tin atom which is arranged in a distorted octahedral geometry.
Representative complexes have been screened for their fungicidal as we
ll as bactericidal activity and found to be quite active.