Synthesis and spectroscopic studies (moessbauer, IR and NMR) of biologically active organotin(IV) complexes of Schiff bases derived from 2-amino-5-phenyl-1,3,4-oxadiazole

Article abstract of DOI:10.1080/00945719608005147

A few new organotin(IV) complexes of tridentate ONN donor Schiff bases of salicylaldehyde, 4-hydroxybenzaldehyde, 2-hydroxyacetophenone, 4-hydroxyacetophenone with 2-amino-5-phenyl-1,3,4-oxadiazole have been synthesised and characterised by elemental analyses. ¹H NMR, UV, IR and Moessbauer spectroscopic studies show hexa-coordination about the tin atom which is arranged in a distorted octahedral geometry. Representative complexes have been screened for their fungicidal as well as bactericidal activity and found to be quite active.

Full text of DOI:10.1080/00945719608005147

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Synthesis and Reactivity in
Inorganic and Metal-Organic
Chemistry
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Synthesis and Spectroscopic
Studies (Mössbauer, IR and
NMR) of Biologically Active
Organotin(IV) Complexes of
Schiff Bases Derived from
2-Amino-5-phenyl-1,3,4-
oxadiazole
M. S. Raizada a
a Department of Chemistry , University of
Allahabad , Allahabad, 211004, India
Published online: 15 Aug 2006.
To cite this article: M. S. Raizada (1996) Synthesis and Spectroscopic Studies
(Mössbauer, 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, 1563-1576, DOI: 10.1080/00945719608005147
To link to this article: http://dx.doi.org/10.1080/00945719608005147
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