Oxidation of diclofenac in the presence of iron(II) octacarboxyphthalocyanine

Abstract

This paper presents the results of the research on the influence of catalytic activity of iron(II) octacarboxyphthalocyanines (FePcOC) on the transformation of diclofenac (DCF) which is the most popular anti-inflammatory analgesic. Diclofenac poses a serious threat to the natural environment. The paper demonstrates that diclofenac, in the presence a monomeric form of iron octacarboxyphthalocyanine and hydroxyl radicals (HO^•) (from H₂O₂), undergoes a transformation into diclofenac-2,5-iminoquinone (DCF-2,5-IQ), causing distinct changes in the UV-Vis absorption spectrum. In the presence of iron octacarboxyphthalocyanine and H₂O₂, the previously colourless diclofenac solution becomes intense orange. As a result, a new band at approx. 450 nm appears in the absorption spectrum. HPLC analysis has shown that the concentration of diclofenac decreases with time. TD-DFT calculations using the CAM-B3LYP/6-31+G (d, p) method have been conducted to confirm experimental data concerning the formation of a new band at λ_max = 450 nm.

Keywords: DFT calculations; Diclofenac; HPLC; Iron octacarboxyphthalocyanine; MS analysis; TD-DFT spectra; UV–Vis spectra.