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The data presented in this paper is related to the research article entitled “Synthesis, Spectroscopy, Electrochemistry and DFT of Electron-Rich Ferrocenylsubphthalocyanines” [1] where electrochemical redox data and cyclic voltammograms at only a scan rate of 0.10 V s−1 of four ferrocenylsubphthalocyanine dyads Fc(CH2)nCO2BSubPc(H)12 (n = 0, 1 or 3) and FcCO(CH2)2CO2BSubPc(H)12, are presented. This data article provides extensive electrochemical redox data and cyclic voltammograms at various scan rates from 0.05 up to 5.00 V s−1 to illustrate the effect of the different scan rates on the electrochemical behaviour of the four ferrocenylsubphthalocyanine dyads.

Redox data obtained from cyclic voltammetry experiments of the FeII/III and ring-based oxidation and reductions of subphthalocyanines containing a ferrocenylcarboxylic acid as axial ligand, is presented in this data in brief article. The FeII/III oxidation of ferrocenylsubphthalocyanines which containing the electron-withdrawing fluorine atoms at the peripheral and non-peripheral positions, are ca. 0.100 V more positive than FeII/III oxidation of ferrocenylsubphthalocyanines containing hydrogens at the peripheral and non-peripheral positions. For more insight into the reported data, see the related research article “Redox and photophysical properties of four subphthalocyanines containing ferrocenylcarboxylic acid as axial ligands” [1].

The data presented in this paper is related to the research article entitled " Synthesis, Spectroscopy, Electrochemistry and DFT of Electron-Rich Ferrocenylsubphthalocyanines " [1] where electrochemical redox data and cyclic voltammograms at only a scan rate of 0.10 V s -1 of four ferrocenylsubphthalocyanine dyads Fc(CH 2 ) n CO 2 BSubPc(H) 12 (n = 0, 1 or 3) and FcCO(CH 2 ) 2 CO 2 BSubPc(H) 12 , are presented. This data article provides extensive electrochemical redox data and cyclic voltammograms at various scan rates from 0.05 up to 5.00 V s -1 to illustrate the effect of the different scan rates on the electrochemical behaviour of the four ferrocenylsubphthalocyanine dyads., Competing Interests: The authors declare that they have no known competing financial interests or personal relationships which have, or could be perceived to have, influenced the work reported in this article., (© 2020 The Author(s).)

Redox data obtained from cyclic voltammetry experiments of the Fe II/III and ring-based oxidation and reductions of subphthalocyanines containing a ferrocenylcarboxylic acid as axial ligand, is presented in this data in brief article. The Fe II/III oxidation of ferrocenylsubphthalocyanines which containing the electron-withdrawing fluorine atoms at the peripheral and non-peripheral positions, are ca. 0.100 V more positive than Fe II/III oxidation of ferrocenylsubphthalocyanines containing hydrogens at the peripheral and non-peripheral positions. For more insight into the reported data, see the related research article " Redox and photophysical properties of four subphthalocyanines containing ferrocenylcarboxylic acid as axial ligands " [1]., Competing Interests: The authors declare that they have no known competing financial interests or personal relationships which have, or could be perceived to have, influenced the work reported in this article., (© 2020 The Author(s).)