Reactivity of 3-Methylbenzenediazonium ions with Gallic Acid. Kinetics and Mechanism of the Reaction

19 October 2009

Helvetica Chimica Acta. 92, pp. 1 - 15.

Sonia Losada-Barreiroa, Carlos Bravo-Díaz*a

Autor affilations:

*Corresponding authors
aDpt. Química Física, Facultad de Química, Universidad de Vigo, Vigo-Pontevedra, Spain
E-mail: cbravo@uvigo.es

Abstract

We investigated the kinetics and mechanism of the reaction between the 3-methylbenzenediazonium ions (3MBD), and gallic acids (=3,4,5-trihydroxybenzoic acid; GA) in aqueous buffer solution under acidic conditions by employing spectrometric, electrochemical, and chromatographic techniques and computational methods. To discern which of the three OH groups of GA is the first one undergoing deprotonation, the geometries of the resulting dianions were optimized by using B3LYP hybrid density-functional theory (DFT) and a 6-31G(++d,p) basis set, and the results suggest that the OH group at the 4-position is the first one which is deprotonated. The variation of the observed rate constant, kobs, with the acidity at a given [GA] follows an upward curve suggesting that the reaction takes place with the dianionic form of gallic acid, GA2−, and rate enhancements of ca. 23000 fold are obtained on going from pH 3.5 up to pH 7.5. At relatively high acidities, the variation of kobs with [GA] is linear with an intercept very close to the value for the thermal decomposition of 3MBD; however, a decrease in the acidity leads to saturation-kinetics profiles with nonzero, pH-dependent intercepts. The saturation-kinetics patterns found suggest the formation of an intermediate in a rapid pre-equilibrium step, but the nonzero, pH-dependent intercepts cause the double reciprocal plots of 1/kobsvs. 1/[GA] to curve. This prompts us to propose an alternative reaction mechanism comprising consecutive equilibrium processes involving the bimolecular, reversible formation of a highly unstable (Z)-diazo ether which undergoes isomerization to the (E)-isomer through a unimolecular step. The results obtained indicate the complexity of reactions of arenediazonium ions with nucleophilic arenes containing three or more OH groups.