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

Authors
Citation
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
Citations number
24
Categorie Soggetti
Chemistry Inorganic & Nuclear
ISSN journal
00945714
Volume
26
Issue
9
Year of publication
1996
Pages
1563 - 1576
Database
ISI
SICI code
0094-5714(1996)26:9<1563:SASS(I>2.0.ZU;2-J
Abstract
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.