In this study, five ruthenium arene complexes with fluorene-bearing N,N-(1) and N,O-(2) donor Schiff base ligands were synthesized and fully characterized. Cationic ruthenium complexes 3[X], ([Ru(η-CH)(Cl)(fluorene-N[double bond, length as m-dash]CH-pyridine)][X] (where X = BF, PF, BPh), were obtained by reacting ligand 1 with [Ru(η-CH)Cl] in the presence of NHX salts, whereas neutral complex 4, Ru(η-CH)(Cl)(fluorene-N[double bond, length as m-dash]CH-naphtholate), was isolated by reacting ligand 2 with the same precursor. It was possible to obtain a cationic version of the latter, 5[BF], by reacting 4 with AgBF in the presence of pyridine.
View Article and Find Full Text PDFThe special ability of organometallic complexes to catalyze various transformations might offer new effective mechanisms for the treatment of cancer. Studies that report both the biological properties and the ability of metallic complexes to promote therapeutically relevant catalytic reactions are limited. Herein, we report the anticancer activity and catalytic potential of some ruthenium(II)-arene complexes bearing bidentate Schiff base ligands (2a and 2b) and their reduced analogues (5a and 5b, respectively).
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