The equilibrium: 2 Bu(2)(CH2=CHCH2)SnCl reversible arrow Bu(2)Sn(CH2=CHCH2)(2)+Bu(2)SnCl(2) takes place when the allyltin chloride is stirred in water. This has been chosen as a model to understand the extent as well as the mechanistic pathways of the disproportionation reactions 2 R(3)SnX reversible arrow R(4)Sn+R(2)SnX(2) which are thought to occur in the aquatic environment. The behaviour of Bu(2)(CH2=CHCH2)SnCl has been studied in various media: water, water-acetone, water-ethanol and water-hexane. It has also been ascertained that Bu(2)(CH2=CHCH2)SnCl is a product arising at room temperature from the scrambling of Bu(2)Sn(CH2=CHCH2)(2) and Bu(2)SnCl(2) either neat, in organic solvents or also in the presence of water. Equilibrium [1] has been interpreted as arising from a bimolecular interaction between the electrophilic aquo-cation [Bu(2)(CH2=CHCH2)Sn(H2O)(n)](+) and the nucleophilic molecule Bu(2)(CH2=CHCH2)SnCl. Kinetic studies on R(3)SnMe/Me(2)SnX(2) (X=Cl, NO3) systems in alcoholic solvents (R=Me, Et, n-Pr, i-Pr, n-Bu) support the assumption that, in dissociating media, redistribution processes can be promoted by ionic electrophilic species

A STUDY OF THE DISPROPORTIONATION EQUILIBRIUM FOR ALLYLDIBUTYLTIN(IV) CHLORIDE AS AN APPROACH TO UNDERSTANDING THE ROLE OF ORGANOTINS IN THE AQUATIC ENVIRONMENT

MARTON, DANIELE;TAGLIAVINI, GIUSEPPE
1995

Abstract

The equilibrium: 2 Bu(2)(CH2=CHCH2)SnCl reversible arrow Bu(2)Sn(CH2=CHCH2)(2)+Bu(2)SnCl(2) takes place when the allyltin chloride is stirred in water. This has been chosen as a model to understand the extent as well as the mechanistic pathways of the disproportionation reactions 2 R(3)SnX reversible arrow R(4)Sn+R(2)SnX(2) which are thought to occur in the aquatic environment. The behaviour of Bu(2)(CH2=CHCH2)SnCl has been studied in various media: water, water-acetone, water-ethanol and water-hexane. It has also been ascertained that Bu(2)(CH2=CHCH2)SnCl is a product arising at room temperature from the scrambling of Bu(2)Sn(CH2=CHCH2)(2) and Bu(2)SnCl(2) either neat, in organic solvents or also in the presence of water. Equilibrium [1] has been interpreted as arising from a bimolecular interaction between the electrophilic aquo-cation [Bu(2)(CH2=CHCH2)Sn(H2O)(n)](+) and the nucleophilic molecule Bu(2)(CH2=CHCH2)SnCl. Kinetic studies on R(3)SnMe/Me(2)SnX(2) (X=Cl, NO3) systems in alcoholic solvents (R=Me, Et, n-Pr, i-Pr, n-Bu) support the assumption that, in dissociating media, redistribution processes can be promoted by ionic electrophilic species
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11577/2488473
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