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The document discusses the anodic oxidation of triphenylphosphine using cyclic voltammetry and controlled potential electrolysis in acetonitrile, resulting in the formation of monoalkylaminotriphenylphosphonium salts with yields of 50-70%. It outlines the reaction mechanism involving one-electron oxidation and nucleophilic attack by primary amines, leading to stable products. The study provides insights into the electrochemical behavior of organophosphorus compounds and compares the electrochemical method w

Author

bondatom

Language

EN