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By means of the Stopped—Flow Spectrophotometry,the kinetics of the reactions betweennickel(Ⅱ)and the ligand 5—bromopyridylazo diethylaminophenol(5-BrPADAP)and 3,5—dibromopyridylazo diethylaminophenol(3,5—2BrPADAP)have been investigated in themicellar solution of sodium dodecyl sulfate(SDS).The reaction rate(compared with thatmeasured in aqueous solution for the same Ni~(2+)concentration)was enhanced up to a factorof 400.Kinetic analysis indicates that the rate enhancement can be explained in terms of theconcentration effect of the micelles on the rcactants(i.e.partitioning coefficient effects).Aquantitative expression for the rate enhancement is derived,using the psudo—phase modeland Berezin’s original micellar-catalysis coneepts.The influenccs of hydrophobic character-istics of ligands on the micellar-catalysis effect have been studied also.
The means of the Stopped-Flow Spectrophotometry, the kinetics of the reactions between nick (II) and the ligand 5-bromopyridylazo diethylaminophenol (5-BrPADAP) and 3,5-dibromopyridylazo diethylaminophenol (3,5-2 BrpADAP) have been investigated in themicellar solution of sodium dodecyl sulfate (SDS). The reaction rate (compared with that measured in aqueous solution for the same Ni 2+ concentration) was enhanced up to a factor of 400. Kinetic analysis indicates that the rate enhancement can be explained in terms of theconcentration effect of the micelles on the rcactants (iepartitioning coefficient effects). Quantitative expression for the rate enhancement is derived, using the psudo-phase modeland Berezin’s original micellar-catalysis coneepts.The influenccs of hydrophobic character-istics of ligands on the micellar- catalysis effect have been studied also.