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Electron transfer reactions associated with ethyl viologen-β-cyclodextrin complexation: equilibrium and kinetic aspects

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Abstract

Formation of the complex of ethyl viologen in its cationic (Ev+•) and neutral (Ev) forms with β-cyclodextrin (β-CD) was investigated by means of voltammetric technique in buffer solution of pH 7.00. The number of βCD (n or m) per viologen species (Ev+•) or (Ev), bonding equilibrium constants as well as bonding rate constants was calculated. The calculated values of \(K_{\text{eq}}^{(1)}\) and \(K_{\text{eq}}^{ ( 2)}\) (pertaining to the bonding of Ev+• and Ev with βCD) are 13.6 Mn and 2.1 × 103 Mm, respectively, whereas the calculated values of n and m are 0.54 and 1.25, respectively. The bimolecular rate constant for the Ev−βCD inclusion complex formation is 3.03 × 103 M−1s−1. These results are supported by the simulation of the experimental cyclic voltammograms. This study also highlights the significance of the proposed electrochemical method as compared to earlier studies on viologen-Cyclodextrin systems.

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Acknowledgments

Shaz Akber is thankful to Dr. M Tariq and Dr. Lubna Naz, ICCBS Karachi University for their useful suggestions and help in connection with the digital simulation.

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Correspondence to Shazia Akbar.

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Akbar, S., Naqvi, I.I. & Mohammad, M. Electron transfer reactions associated with ethyl viologen-β-cyclodextrin complexation: equilibrium and kinetic aspects. J IRAN CHEM SOC 11, 615–621 (2014). https://doi.org/10.1007/s13738-013-0331-4

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  • DOI: https://doi.org/10.1007/s13738-013-0331-4

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