Abstract:In this communication, we present studies of the oxidative homocoupling of arylboronic acids catalyzed by immobilised palladium nanoparticles in aqueous solution. This reaction is of significant interest because it shares a key transmetallation step with the well-known Suzuki-Miyaura cross-coupling reaction. Additives can have significant effects on catalysis, both in terms of reaction mechanism and recovery of catalytic species, and our aim was to study the effect of added halides on catalytic efficiency and catalyst recovery. Using kinetic studies, we have shown that added halides (added as NaCl and NaBr) can increase the catalytic activity of the palladium nanoparticles more than 10-fold, allowing reactions to be completed in less than half a day at 30 • C. However, this increased activity comes at the expense of catalyst recovery. The results are in agreement with a reaction mechanism in which, under conditions involving high concentrations of chloride or bromide, palladium leaching plays an important role. Considering the evidence for analogous reactions occurring on the surface of palladium nanoparticles under different reaction conditions, we conclude that additives can exert a significant effect on the mechanism of reactions catalyzed by nanoparticles, including switching from a surface reaction to a solution reaction. The possibility of this switch in mechanism may also be the cause for the disagreement on this topic in the literature.

The stability of synthesized Schiff base [Bis-(2-chlorobenzalidene) benzidine] have been studied under different types of light (UV , Visible and sunlight) kinetic study of photolysis was done in DMF solvent by monitoring the concentration of Schiff base, using UV-Vis spectroscopy . The High Performance Liquid Chromatography analytical technique coupled with UV-visible spectrophotometer used to detect the intermediate compounds formed in the photolysis it was found that the photolysis process exhibited pseudo-first-order kinetics. The results show the photolysis rate constants in the process using UV light is higher than that using visible or sunlight radiation.

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Zeolites are compounds which have many applications in chemistry and industry; therefore, studies of synthesis of zeolites are of great importance. In this work, kinetic and thermodynamic study of hydrothermal crystallization for zeolite synthesis process performed at different time intervals (17, 20, 23 and 26 h) and various temperatures (70, 90, 110 and 125 0 C). By time intervals we got out the rate of the zeolite synthesis reaction in this research was first order. The synthesized zeolites were similar in their crystallinity according to the Zeolites synthesis at different of the time intervals. The thermodynamic parameters indicated that the change in Gibbs free energy was negative value. The degrees of crystallinity of the synthesized zeolites decreased with increasing the hydrothermal crystallization temperature. Moreover, the change of hydrothermal crystallization time and temperature caused synthesis of different types of zeolites. The synthesized zeolite samples characterized by Infra-Red (IR), X-ray diffraction (XRD), X-ray Fluorescence (XRF) and scanning electron microscopy (SEM). The variation of chemical compositions led to differences in morphologies and crystallinity of the synthesized zeolites.