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Ionic partition diagram of tetraphenylporphyrin at the water|1,2-dichloroethane interface

Hubert Girault, Manuel Alejandro Méndez Agudelo, Bin Su, Raheleh Partovi Nia, Zdenek Samec

diagram of 5,10,15,20-tetraphenyl-21H,23H-porphine (H2TPP) at the water|1,2-dichloroethane interface using a simple Born solvation model. This zone diagram shows under which form this porphyrin is present, i.e. neutral, monoprotonated or diprotonated, and in which phase i.e. either in the aqueous or the organic phase as a function of the aqueous pH and the interface polarisation that can be controlled externally or by the distribution of supporting electrolytes. This diagram explains why the monoprotonated form has been difficult to observe when doing biphasic pH titrations

Elsevier2011

Oxygen and proton reduction by decamethylferrocene in non-aqueous acidic media

Hubert Girault, Manuel Alejandro Méndez Agudelo, Bin Su, Peiyu Ge, Imren Hatay, Zdenek Samec

Experimental studies and density functional theory (DFT) computations suggest that oxygen and proton reduction by decamethylferrocene (DMFc) in 1,2-dichloroethane involves protonated DMFc, DMFcH+, as an active intermediate species, producing hydrogen peroxide and hydrogen in aerobic and anaerobic conditions, respectively.

Royal Society of Chemistry2010

Oxygen reduction by decamethylferrocene at liquid/liquid interfaces catalyzed by dodecylaniline

Hubert Girault, Manuel Alejandro Méndez Agudelo, Bin Su, Raheleh Partovi Nia, Imren Hatay, Zdenek Samec

Molecular oxygen (O2) reduction by decamethylferrocene (DMFc) was investigated at a polarized water/ 1,2-dichloroethane (DCE) interface. Electrochemical results point to a mechanism similar to the EC type reaction at the conventional electrode/solution interface, in which an assisted proton transfer (APT) by DMFc across the water/DCE interface via the formation of DMFcH+ corresponds to the electrochemical step and O2 reduction to hydrogen peroxide (H2O2) represents the chemical step. The proton transfer step can also be driven using lipophilic bases such as 4-dodecylaniline. Finally, voltammetric data shows that lipophilic DMFc can also be extracted to the aqueous acidic phase to react homogeneously with oxygen.

Elsevier2010