Abstract
Voltammetry of [5,10,15-tris(pentafluorophenylcorrole)]Mn(III) was investigated in four different ionic liquids (ILs): 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (BMIm-TFSI); 1-ethyl-3-methylimidazolium ethylsulfate (EMIm-EtOSO3); 1-ethyl-3-methylimidazolium triflate (EMIm-OTf); and 1-ethyl-3-methylimidazolium tetracyanoborate (EMIm-TCB). We found that MnIV/III E 1/2 values depend on IL counter anion: OTf–< EtOSO3 − < TFSI− < TCB−. In EMIm-TCB and BMIm- TFSI, reversible, diffusion-controlled MnIV/III reactions occurred, as evidenced in each case by the ratio of anodic to cathodic diffusion coefficients over a range of scan rates. Axial coordination was evidenced by a cathodic to anodic diffusion coefficient ratio greater than one, an increasing cathodic to anodic peak current ratio with increasing scan rate, and a split Soret band in the UV-vis spectrum of the complex.
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Published in Russian in Elektrokhimiya, 2017, Vol. 53, No. 10, pp. 1342–1347.
This paper is the authors’ contribution to the special issue of Russian Journal of Electrochemistry dedicated to the 100th anniversary of the birth of the outstanding Soviet electrochemist Veniamin G. Levich.
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McNicholas, B.J., Blumenfeld, C., Kramer, W.W. et al. Electrochemistry in ionic liquids: Case study of a manganese corrole. Russ J Electrochem 53, 1189–1193 (2017). https://doi.org/10.1134/S1023193517100068
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DOI: https://doi.org/10.1134/S1023193517100068