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Synthesis, electrochemical and spectroelectrochemical studies of octaphenylthio-substituted phthalocyanines

    https://doi.org/10.1142/S1088424605000605Cited by:30 (Source: Crossref)

    Cobalt (4) and iron (5) phenylthio-substituted phthalocyanines (MPc(SR)8) have been synthesized and characterized. Cyclic square wave voltammetry in dimethylformamide containing tetrabutylammonium perchlorate revealed five and six redox processes, respectively, for complexes 4 and 5. The complexes are easier to reduce compared to the corresponding unsubstituted MPc and to butylthio substituted derivatives. The first oxidation and reduction occurs on the metal for both complexes. Spectroelectrochemistry (in dimethylformamide containing tetrabutylammonium perchlorate) was employed to assign the cyclic voltammetry peaks, and gave spectra characteristic of FeIPc for reduction of 5 and CoIPc for the reduction of 4. The spectrum of the former is particularly of importance since such species have not received much attention in the literature.

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