Spectroelectrochemical Investigation of TPPMn(III/II)-Driven Liquid Liquid | Electrode Triple Phase Boundary Anion Transfer into 4-(3-Phenylpropyl)-Pyridine: ClO4-, CO3H-, Cl-, and F

Reference:

Collins, A. M., Blanchard, G. J. and Marken, F., 2012. Spectroelectrochemical Investigation of TPPMn(III/II)-Driven Liquid Liquid | Electrode Triple Phase Boundary Anion Transfer into 4-(3-Phenylpropyl)-Pyridine: ClO4-, CO3H-, Cl-, and F. Electroanalysis, 24 (2), pp. 246-253.

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Official URL:

http://dx.doi.org/10.1002/elan.201100623

Abstract

The triple phase boundary transfer of anions from the aqueous into an organic phase can be driven electrochemically here with the tetraphenylporphyrinato-Mn(III/II) (or TPPMn) redox system in 4-(3-phenylpropyl)-pyridine) (or PPP). Anions investigated are perchlorate, chloride, fluoride, and bicarbonate. The bicarbonate and fluoride transfer processes are shown to be chemically more complex compared to the perchlorate and chloride cases with UV-vis-spectroelectrochemical measurements indicating a combination of HCO3-/CO32- transfer processes and association of fluoride with TPPMn(III)+, respectively. In situ spectroelectrochemistry is developed for ion-transfer voltammetry into sub-microliter organic phase regions on mesoporous ITO conducting film electrodes.

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