Electronic spectroscopy techniques with the aid of quantum chemical calculations, and notably the Time-Dependent Density Functional Theory, can be used to probe the structure of metal complexes in solution. Here, we report the characterization of Al(III)-protocatechuate in aqueous solution, at pH = 6.5. The exploitation of the UV-vis spectra of the system by chemometric methods highlights the formation of a single complex of stoichiometry 1:1. From different structural hypothesis, the comparison of theoretical and experimental spectra shows that Al(III) forms a monodentate complex with the carboxylate function. This hypothesis is confirmed by the calculation of the complexation reaction pathways. Previous studies report the formation of a chelate involving the ortho-dihydroxyl group, at pH = 3.5. These results illustrate the important dependence of the protonation state of the carboxylic function on the Al(III) fixation site on the studied ligand.
