Schiff bases derived from aminoguanidine are extensively investigated for their structural versatility. The tridentate 2-formylpyridine guanylhydrazones act as analogues of 2-formyl or 2-acetylpyridine thiosemicarbazones, where the thioamide unit is replaced by the guanidyl group. Six derivatives of 2-formylpyridine guanylhydrazone were synthesized and their proton dissociation and complex formation processes with Cu(II), Fe(II) and Fe(III) ions were studied using pH-potentiometry, UV-visible, NMR and electron paramagnetic resonance spectroscopic methods.
View Article and Find Full Text PDFStructure-activity studies aiming to understand the role of each coligand in the formulation of new metallodrugs is an important subject. In that frame, six new compounds with general formula [Fe(η-CH)(dppe)(L)][CFSO] with L = benzonitriles (1-4) or carbon monoxide (5) and compound [Fe(η-CH)(CO)(PPh)][CFSO] (6) were synthesized and compared with three other previously reported compounds [Fe(η-CH)(CO)(L)(PPh)][CFSO]. We were particularly interested in assessing the effect of dppe vs.
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