Synthesis, Characterization, and Biotoxicity of <mml:math alttext="${fchem{N}hspace{-6.5pt} aisebox{9pt}{huge$frown$}hspace{-6.5pt}fchem{N}}$"> <mml:mrow> <mml:mover accent="true"> <mml:mrow> <mml:mtext>NN</mml:mtext> </mml:mrow> <mml:mo stretchy="true">&#x2322;</mml:mo> </mml:mover> </mml:mrow> </mml:math> Donor Sulphonamide Imine Silicon(IV) Complexes

<p>The organosilicon derivatives of <mml:math alttext="$2$"> <mml:mn>2</mml:mn> </mml:math>-[<mml:math alttext="$1$"> <mml:mn>1</mml:mn> </mml:math>-(<mml:math alttext...

Full description

Saved in:
Bibliographic Details
Format: Article
Language:English
Published: Wiley 2006-01-01
Series:Bioinorganic Chemistry and Applications
Online Access:http://www.hindawi.com/GetArticle.aspx?doi=10.1155/BCA/2006/13743
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:<p>The organosilicon derivatives of <mml:math alttext="$2$"> <mml:mn>2</mml:mn> </mml:math>-[<mml:math alttext="$1$"> <mml:mn>1</mml:mn> </mml:math>-(<mml:math alttext="$2$"> <mml:mn>2</mml:mn> </mml:math>-furayl)ethyledene]sulphathiazole with organosilicon chlorides have been synthesised and characterized on the basis of analytical, conductance, and spectroscopic techniques. Probable trigonal bipyramidal and octahedral structures for the resulting derivatives have been proposed on the basis of electronic, IR, <mml:math alttext="$^1 {ext{H}}$"> <mml:mrow> <mml:msup> <mml:mi/> <mml:mn>1</mml:mn> </mml:msup> <mml:mtext>H</mml:mtext> </mml:mrow> </mml:math>, <mml:math alttext="$^13 {ext{C}}$"> <mml:mrow> <mml:msup> <mml:mi/> <mml:mn>13</mml:mn> </mml:msup> <mml:mtext>C</mml:mtext> </mml:mrow> </mml:math> NMR, and <mml:math alttext="$^29 {ext{Si}}$"> <mml:mrow> <mml:msup> <mml:mi/> <mml:mn>29</mml:mn> </mml:msup> <mml:mtext>Si</mml:mtext> </mml:mrow> </mml:math> NMR spectral studies. In the search for better fungicides, bactericides, nematicides, and insecticides studies were conducted to assess the growth-inhibiting potential of the synthesized complexes against various pathogenic fungal, bacterial strains, root-knot nematode <emph>Meloidogyne incognita</emph>, and insect <emph>Trogoderma granarium</emph> These studies demonstrate that the concentrations reached levels which are sufficient to inhibit and kill the pathogens, nematode, and insect.</p>
ISSN:1565-3633