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Synthesis of Polypyrrole Induced by [Fe(CN)(6)](3−) and Redox Cycling of [Fe(CN)(6)](4−)/[Fe(CN)(6)](3−)

Chemical synthesis of the conducting polymer polypyrrole induced by [Fe(CN)(6)](3−) is reported. Reaction kinetics were characterized spectrophotometrically. Reaction rate was evaluated at several different pH levels in the presence of [Fe(CN)(6)](3−) and [Fe(CN)(6)](4−) ions. The formation of polyp...

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Detalles Bibliográficos
Autores principales: Andriukonis, Eivydas, Ramanaviciene, Almira, Ramanavicius, Arunas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6403579/
https://www.ncbi.nlm.nih.gov/pubmed/30960674
http://dx.doi.org/10.3390/polym10070749
Descripción
Sumario:Chemical synthesis of the conducting polymer polypyrrole induced by [Fe(CN)(6)](3−) is reported. Reaction kinetics were characterized spectrophotometrically. Reaction rate was evaluated at several different pH levels in the presence of [Fe(CN)(6)](3−) and [Fe(CN)(6)](4−) ions. The formation of polypyrrole at aerobic and anaerobic conditions was evaluated. We report that at anaerobic conditions [Fe(CN)(6)](4−) cannot initiate oxidative polymerization, while its oxidized form [Fe(CN)(6)](3−) successfully initiates and maintains the pyrrole polymerization reaction. The formation of polypyrrole was also observed in the solution containing a pyrrole monomer, [Fe(CN)(6)](4−) and dissolved oxygen due to re-oxidation (redox cycling) of [Fe(CN)(6)](4−) into [Fe(CN)(6)](3−) by dissolved oxygen. Experiments to determine the polymerization reaction rate were performed and showed the highest rate in the presence of 0.5 mM of [Fe(CN)(6)](3−) at pH 9.0, while the polymerization reaction performed at pH 7.0 was determined as the slowest. This investigation opens new horizons for the application of [Fe(CN)(6)](4−)/[Fe(CN)(6)](3−)-based redox cycling reactions in the synthesis of the conducting polymer polypyrrole and potentially in the formation of other conducting polymers which can be formed by oxidative polymerization.