6533b831fe1ef96bd129874e

RESEARCH PRODUCT

Electrochemical determination of the stability of complexes formed by proton-ionizable ligands of 3,5-disubstituted 1H-pyrazole with phenethylamine

Enrique García-españaAntonio DoménechFelipe ReviriegoPilar Navarro

subject

chemistry.chemical_compoundchemistryStability constants of complexesLigandComputational chemistryInorganic chemistryRotating disk electrodePyrazoleElectrochemistryEquilibrium constantAnalytical ChemistryCyclophaneInclusion compound

description

The application of two extreme models for diffusion in two-component systems to electrochemically determine equilibrium constants is discussed. The application of cyclic voltammetric, diferential pulse and rotating-disc electrode voltammetric data to elucidate the stoichiometry and formation constant of complex species by applying a generalization of the molar-ratio method is described. Molar-ratio experiments permit the distinction between the limiting diffusive regimes. The values of the equilibrium stability constants for complexation of phenethylamine and phenethylammonium ions by a 26-membered dioxotetraester crown of 3,5-disubstituted 1H-pyrazole as free ligand 1[L] and as dipyrazolate anion 1%[L 2 ]2Na, respectively, were determined. © 2000 Elsevier Science B.V. All rights

https://doi.org/10.1016/s0039-9140(99)00325-2