Hydrophobic N‐Diazeniumdiolates and the Aqueous Interface of Sodium Dodecyl Sulfate (SDS) Micelles

Abstract

Zwitterionic diazeniumdiolates of the form RN[N(O)NO(-)](CH(2))(2)NH(2) (+)R, where R=CH(3) (1), (CH(2))(3)CH(3) (2), (CH(2))(5)CH(3) (3), and (CH(2))(7)CH(3) (4) were synthesized by reaction of the corresponding diamines with nitric oxide. Spectrophotometrically determined pK(a)(O) values, attributed to protonation at the terminal oxygen of the diazeniumdiolate group, show shifts to higher values in dependence of the chain lengths of R. The pH dependence of the decomposition of NO donors 1-3 was studied in buffered solution between pH 5 and 8 at 22 degrees C, from which pK(a)(N) values for protonation at the amino nitrogen, leading to release of NO, were estimated. It is shown that the decomposition of these diazeniumdiolates is markedly catalyzed by anionic SDS micelles. First-order rate constants for the decay of 1-4 were determined in phosphate buffer pH 7.4 at 22 degrees C as a function of SDS concentration. Micellar binding constants, K(SM), for the association of diazeniumdiolates 1-3 with the SDS micelles were also determined, again showing a significant increase with increasing length of the alkyl side chains. The decomposition of 1-3 in micellar solution is quantitatively described by using the pseudo-phase ion-exchange (PIE) model, in which the degree of micellar catalysis is taken into account through the ratio of the second-order rate constants (k(2m)/k(2w)) for decay in the micelles and in the bulk aqueous phase. The decay kinetics of 1-3 were further studied in the presence of cosolvents and nonionic surfactants, but no effect on the rate of NO release was observed. The kinetic data are discussed in terms of association to the micelle-aqueous phase interface of the negatively charged micelles. The apparent interfacial pH value of SDS micelles was evaluated from comparison of the pH dependence of the first-order decay rate constants of 2 and 3 in neat buffer and the rate data obtained for the surfactant-mediated decay. For a bulk phase of pH 7.4, an interfacial pH of 5.7-5.8 was determined, consistent with the distribution of H(+) in the vicinity of the negatively charged micelles. The data demonstrate the utility of 2 and 3 as probes for the determination of the apparent pH value in the Stern region of anionic micelles.