Monitoring dediazoniation product formation by high-performance liquid chromatography after derivatization

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A derivatization protocol that exploits the rapid reaction between arenediazonium ions and a suitable coupling agent followed by high-performance liquid chromatography analyses of the reaction mixture was employed to determine the product distribution, the rate constants for product formation and the association constant of 4-nitrobenzenediazonium, PNBD, ion with β-cyclodextrin, β-CD. The derivatization of PNBD with the coupling agent leads to the formation of a stable azo dye that prevents by-side reactions of PNBD with the solvents of the mobile phase, including water, or the metallic parts of the chromatographic system that would eventually lead to erroneous identification and quantification of dediazoniation products. The results show that in the presence of β-CD, nitrobenzene is formed at the expense of 4-nitrophenol, which is the major product in its absence. The observed rate constants for the interaction between PNBD and β-CD increase upon increasing [β-CD] showing a saturation profile indicative of the formation of an inclusion complex between PNBD and β-CD. By fitting the experimental data to a simplified Lineaweaver-Burk equation, the corresponding association constant and the maximum acceleration rate of β-CD towards PNBD were estimated. The protocol is applicable under a variety of experimental conditions provided that the rate of the coupling reaction is much faster than that of dediazoniation. © 2003 Elsevier Science B.V. All rights reserved.




Bravo-Díaz, C., & González-Romero, E. (2003). Monitoring dediazoniation product formation by high-performance liquid chromatography after derivatization. Journal of Chromatography A, 989(2), 221–229.

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