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1.
A photometric method for the determination of malathion is described. Malathion dissolved in carbon tetrachloride is hydrolysed at room temperature with sodium ethoxide to dimethyl dithiophosphate (DMDTP) and fumarate. The DMDTP is converted into a molybdenum-DMDTP complex and determined spectrometrically. 相似文献
2.
T. Gangaiah P. Ramadevi G. R. K. Naidu K. Venugopal Chetty 《Journal of Radioanalytical and Nuclear Chemistry》1991,150(1):177-182
Isotopic exchange behaviour of bis(diethyldithio carbamate) nickel(II) complex with nickel(II) in chloroform and methanol medium was studied. The studies were carried out at different temperatures varying the concentration of both metal ion and the complex. The results show that the complex is labile in the kinetic sense. Increase in temperature increases the isotopic exchange rate. The increase in concentration also results in enhancement of the rate of reaction. 相似文献
3.
A. N. Chetty P. Ramadevi G. R. K. Naidu 《Journal of Radioanalytical and Nuclear Chemistry》1987,117(6):347-352
Isotope exchange behaviour of bis/diethyl dithiocarbamate/ copper/II/ complex has been studied at 30 °C and 40 °C varying the concentration of the complex and metal ion. Results indicate that the complex is labile in chloroform dimethyl sulphoxide medium. Increase in concentration has significant effect on the rate of the reaction. Similarly the increase in temperature increased the rate of the reaction. 相似文献
4.
Chandrashekar Ramarao Ramadevi Nandipati Rajasekhar Navakoti Ramanjaneyulu Kottamasu 《Tetrahedron letters》2012,53(6):637-640
1,2-Dihydroxy benzenes have been protected as cyclic diacetals using 2,3-butane dione. These diacetals are extremely robust and can be further chemically diversified and resolved with chirality embedded in the 1,4-dioxane ring attached to the aromatic back bone as a result of the anomeric effect. These systems can serve as ligands, auxiliaries or organocatalysts for asymmetric synthesis. 相似文献
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6.
Elayaraja Muthuswamy S. Sree Ramadevi H.N. Vasan Cécile Garcia Laure Noé Marc Verelst 《Journal of nanoparticle research》2007,9(4):561-567
A novel synthesis of inorganic–organic hybrid films containing well dispersed and almost uniform size Ag nanoparticles in
agar-agar matrix has been reported. The films are found to be highly stable for more than a year. The colloidal particles
of Ag can be obtained in large quantities in the form of a film or in the gel form when dispersed in agar-agar or by dissolving
in a suitable solvent as solution. Characterization has been done by UV–visible spectroscopy and TEM. The hybrid may be of
interest to study third-order non-linear susceptibility. 相似文献
7.
The kinetics of dissociation of tris-2,2′-bipyridyl-iron(II) complex ion have been examined in aqueous acetic acid solutions. The reaction is first order in the complex ion; the dependence of rate on H+ is somewhat like that observed in aqueous solutions approaching a limiting value at higher H+ concentrations. The influence of solvent composition on the reaction rate under acid-dependent and acid-independent conditions shows an initial retardation by acetic acid. The argument of ion-pair formation based on decrease of dielectric constant proposed to explain the kinetics in other aqueous solvent media was found useless to explain the behavior in acetic acid solutions. Other solvent parameters also did not provide satisfactory correlation with the kinetic results, thus, indicating the operation of more complex microscopic solute-solvent and solvent-solvent interactions. While solvent effects play some part in the rate process, the rate of reaction would tend to zero in the absence of H2O and H+. This interesting observation proved useful in proposing a reaction mechanism that is consistent with the rate behavior over the entire range of solvent composition. The activity of water in the reaction medium is controlled by the content of acetic acid which can effect the structure of water through operation of hydrophobic forces and formation of hydrates. While acetic acid cannot possibly fulfill the role of water in occupying the vacated coordination position, the anomalous rise in rate even under some water deficient conditions seems to be related to the coordinating ability of HSO4? derived from H2SO4 present in the solution. 相似文献
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Kambhampati Sriramam Janapati Sreelakshmi Lavu Ramadevi 《Transition Metal Chemistry》1990,15(2):126-131
Summary The kinetics of the iodine-catalysed reaction of vanadium(V) with arsenious acid in dilute H2SO4, leading to the formation of vanadium(IV) and arsenic acid, have been investigated spectrophotometrically. Plausible pathways consistent with the experimental rate law are discussed. An iodine bridged activated complex between reactant and substrate species is proposed to explain the electron mobility from arsenic to vanadium by resonance transfer. Applying other criteria, the heterolytic dissociation of the vanadium-iodine bond of the activated complex is considered rate-controlling. 相似文献
10.
P. Ramadevi U. V. Naidu G. R. K. Naidu 《Journal of Radioanalytical and Nuclear Chemistry》1988,128(4):257-261
Silver from aqueous solution was preconcentrated by adsorption on activated carbon as silver xanthate. Factors influencing the adsorption of silver have been studied. Optimum conditions for the preconcentration of silver have been established. 相似文献