Answers are grounded in this paper and cite their sources.
Synthesis of ferrocenyl Schiff bases (1–6) was carried out by the condensation reaction of 4‐ferrocenyl aniline with different substituted aromatic aldehydes and acetyl acetone. Compounds were characterized by physical measurements, elemental analysis, FT‐IR, 1H‐NMR and 13C‐NMR spectroscopy. Single crystal X‐ray analysis of compound 2 showed the co‐planarity of both aromatic rings connected by a C–N double bond. Compounds demonstrated reversible one‐electron redox behavior and their peak currents were found to increase linearly with the square root of the sweep rate ν1/2. The overall electrode processes were found to be diffusion controlled. Compounds 1 and 4 showed low cytotoxicity and appreciable antifungal, antioxidant and DNA protection activities.
No takes yet. Share an insight, caveat, or question.
Zaheer et al. (2010) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: