Abstract

A comparison of traditional and electrochemical synthetic techniques for obtaining metal complexes of azomethine and phthalocyanine is reported. It is shown that the electrochemical method affords azomethinic coordination compounds free of anions of precursors and with higher yields at ambient temperature. Electrolysis in a solid phase of phthalonitrile using a high-surface platinum cathode leads to metal-free phthalocyanine and metal phthalocyaninates at 0–25°C. The typical problems of the electrosynthetic procedures in different conditions are discussed in detail.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call