• Nuclear Engineering and Technology
• /
• v.8 no.2
• /
• pp.77-80
• /
• 1976

The halogen exchange reactions of 2-naphylmethyl chloride have been investigated in actone and acetonitrile. The results were in good accord with PMO theory and HSAB principle.

• Nuclear Engineering and Technology
• /
• v.7 no.4
• /
• pp.311-316
• /
• 1975

Kinetic studies on the halide exchange reactions of substituted benzoyl chlorides have been carried out. The experimental result has been explained reasonably in terms of HSAB principle and EH-Theory, and addition elimination mechanism has been proposed for this type of reaction.

• Nuclear Engineering and Technology
• /
• v.1 no.2
• /
• pp.87-90
• /
• 1969

Halogen exchange reactions of trans-cinnnamyl chloride and bromide with radioactive chloride, bromide and iodide ions in acetone have teen studied. Relative nucleophilicity of halide ions and relative leaving ability have been discussed invoking the principle of HSAB.

• Journal of Soil and Groundwater Environment
• /
• v.6 no.3
• /
• pp.21-29
• /
• 2001

Organobentonite modified with hexadecyltrimethylammonium (HDTMA) was used to quantify adsorption of heavy metals. Adsorption of cadmium and lead increased with increasing pH and soil/solution ratio. Based on these experiments, an optimal soil/solution ratio and an optimal pH was selected. Adsorption experiments with cadmium and lead were conducted to quantify adsorption selectivity on bentonite and organobentonite. Adsorption of heavy metals on organobentonite was slightly reduced relative to bentonite. Because of competition between cadmium and lead, adsorption of each metal was reduced due to the presence of the other. Adsorption selectivity of cadmium was higher than lead. This study used the principle of hard soft-acid-base (HSAB) to interpret adsorption.

• Nuclear Engineering and Technology
• /
• v.5 no.1
• /
• pp.20-25
• /
• 1973

Kinetics of halogen exchange reactions of phenacyl halides using radioisotope tracer halide ions in anhydrous acetone have been studied. The reactions wore believed to be SN2 processes and the orders of relative nucleophilicity of halide ions were Cl->I->Br- for the phenacyl chloride and I->Cl->Br- for the phenacyl bromide. These were interpreted in terms of solvation effect of halide ions and HSAB principle.

• Journal of the Korean Chemical Society
• /
• v.13 no.4
• /
• pp.281-287
• /
• 1969

Rate constans for the chloride exchange of some arylmethylchloride in dry acetone have been determined, and activation parameters have been evaluated. The reactivities of substates are explained with perturbational molecular orbital (PMO) method and HSAB principle. It was found that carbon-chlorine resonance integral at the transition state is a out 67% of ${\beta}$, the carbon-carbon resonance integral.

• Nuclear Engineering and Technology
• /
• v.7 no.1
• /
• pp.25-29
• /
• 1975

Kinetics of halogen exchange reaction of 1-phenthyl chloride and 2-phenethyl chloride using radioisotopic tracer halide ions in acetone have been studied. The reactions were belived to be S$_{N}$2 processes and the orders of relative nucleophilicity of halide ions were Cl->Br->I-. The reaction rate is slower than that of benzyl chloride. These were interpreted in terms of solvation effect of halide ions and HSAB principle.

• Journal of the Korean Chemical Society
• /
• v.13 no.2
• /
• pp.109-114
• /
• 1969

Halogen exchange reactions of benzyl halides have been studied in absolute acetone. Rate constants were calculated using an integrated rate expression derived for the reaction involving ion-pair association. The order of nucleophilicity of halide ions in acetone was found to be a reverse of the order in 90% aqueous enthanol solvent. This was interpreted by means of HSAB principle and solvation of halide ions. Net increase in rate of reaction in acetone compared with the rate in protic solvent resulted from large increase in ${\Delta}S^\neq$ rather than decrease in ${\Delta}H^\neq$. The solvation of the transition state also contribute to the net increase in rate.

• Journal of the Korean Chemical Society
• /
• v.17 no.6
• /
• pp.406-410
• /
• 1973

Kinetic study of halide exchange for dimethylsulfamoyl chloride in dry acetone by using radioisotopic halide ions has been carried out at two temperatures. The result of the order of nucleophilicity, as compared with benzenesulfonyl chloride, shows a similar tendency but reaction rate is slower, more than $10^{-2}$times, than benzenesulfonyl chloride. The activation parameter, ${\Delta}H^{\neq}\;and\;{\Delta}S^{\neq}$ decrease in sequence $Cl^-\;>\;Br^-\;>\;I^-$ in dimethylsulfamoyl chloride but it is the reverse order found for benzenesulfonyl chloride. The results are interpreted with bond-breaking, bond-formation, and electronic requirments, and in the light of HSAB Principle.

• Bulletin of the Korean Chemical Society
• /
• v.1 no.3
• /
• pp.83-87
• /
• 1980

The Murrell-Fueno type of the intermolecular perturbation approach was applied to the acid-catalyzed hydrolysis of diformamide. The results show that: (1) the attack of a water molecule on the protonated carbonyl carbon is favored over that on the unprotonated carbonyl carbon; (2) the ${\sigma}$-approach model of water is preferred to the ${\pi}$-approach model; (3) the major contributing term to the total energy is the Coulomb energy, $E_q$, especially in the ${\sigma}$-approach, while the contribution of $E_{ct}$ (and $E_k$) increases moderately in the ${\pi}$-approach; (4) the reaction is a charge-controlled one, a hard-hard type in the language of the HSAB principle.