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Vol. 11 No. 4 (1999): Vol 11 Issue 4

Synthesis and Biological Activity of 2-Methylpiperazine-Dithiocarbamato and Di-(2-Methyl-5-Chloro phenyl) Dithiophosphinato Derivatives of Triorganation(IV) Chloride

P.K. Gogoi
Department of Chemistry, Dibrugarh University, Dibrugarh-786 004, India
D.P. Phukan
Department of Chemistry, Dibrugarh University, Dibrugarh-786 004, India
D.K. Das
Department of Chemistry, Dibrugarh University, Dibrugarh-786 004, India

Corresponding Author(s) : P.K. Gogoi

Asian Journal of Chemistry, Vol. 11 No. 4 (1999): Vol 11 Issue 4

Abstract

Complexes of triphenyltin(IV) chloride with 2-methyl-piperazinedithiocarbamate (Na salt, 2-Mepipzdtc) and di-(2-methyl-5-chlorophenyl) diphosphinate (Na salt; MeCldtpi) have been synthesised and characterised by elemental analysis, IR and 1H-NMR studies. Unlike the symmetrical bidentate nature of the dithiocarbamato group an unsymmetrical
bidentate ligation is suggested for the dithiophosphinato group
towards organotin(IV) moiety. The thermal stability of the compounds,
biological activity against E. coli and potential antifungal role of the compounds
in wood preservation have been evaluated.

Keywords

Synthesis Biological Activity 2-Methylpiperazine-Dithiocarbamato Di-(2-Methyl-5-Chloro phenyl) Dithiophosphinato Derivatives Triorganation(IV) Chloride
Gogoi, P., Phukan, D., & Das, D. (2010). Synthesis and Biological Activity of 2-Methylpiperazine-Dithiocarbamato and Di-(2-Methyl-5-Chloro phenyl) Dithiophosphinato Derivatives of Triorganation(IV) Chloride. Asian Journal of Chemistry, 11(4), 1291–1295. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/23483
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