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The structural, optical and magnetic properties of the Zn 1-x Mn x O (0 < x < 0.05) thin films synthesized by sol-gel technique have been analyzed in the light of modification of the electronic structure and disorder developed in the samples due to Mn doping. The films are of single phase in nature and no formation of any secondary phase has been detected from structural analysis.Absence of magnetic impurity phase in these films confirmed from morphological study also.Increasing tendency of lattice parameters and unit cell volume has been observed with increasing Mn doping concentration. The incorporation of Mn 2+ ions introduces disorder in the system. That also leads to slight degradation in crystalline quality of the films with increasing doping. The grain size reduces with increase in Mn doping proportion. The band gaps shows red shift with doping and the width of localized states shows an increasing tendency with doping concentration. It is due to the formation of impurity band and trapping of Mn atoms, which leads to the generation of the defect states within the forbidden band. Photoluminescence (PL) spectra shows gradual decrease of intensity of exitonic and defect related peaks with increasing Mn doping. Defect mediated intrinsic ferromagnetism has been observed even at room temperature for 5at% Mn doped ZnO film. The strong presence of antiferromagnetic (AFM) interaction reduces the observed ferromagnetic moments.

Thiamethoxam at normal and double the recommended use rate effectively controlled aphids, whiteflies and Helicoverpa, as the insect population decreased to a minimum within 10 days of spraying in comparison with the control. There was no significant difference between the two rates of application, and both thiamethoxam treatments significantly increased tomato fruit yield compared with the untreated control. A maximum residue limit (MRL) of 0.05 mg kg(-1) for tomato has been proposed, with a corresponding preharvest interval (PHI) of 8 days. These parallel advances in toxicology and analytical chemistry have strengthened the observations that thiamethoxam can be used safely and efficiently in crop protection programmes.

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The degradation of thiamethoxam [(EZ)-3-(2-chloro-1,3-thiazol-5-yl-methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene (nitro) amine] insecticide in buffers at different pH and temperature levels was investigated in laboratory studies. Acidic hydrolysis under conventional heating conditions and alkaline hydrolysis under both conventional heating and microwave conditions were carried out. Different hydrolysis products were found to form under alkaline and acidic conditions. Hydrolysis of thiamethoxam in acidic, neutral and alkaline buffers followed first-order reaction rate kinetics at pH 4, 7 and 9.2, respectively. Thiamethoxam readily hydrolyzed in alkaline buffer but was comparatively stable in neutral buffer solution. The main products formed under different conditions were characterized on the basis of infrared (IR), (1)H-NMR and Mass spectroscopy. The possible mechanisms for the formation of these hydrolysis products have also been proposed.