Synthesis and anticancer activity of chalcogenide derivatives and platinum(II) and palladium(II) complexes derived from a polar ferrocene phosphanyl-carboxamide
The polar phosphinyl carboxamide, 1'-(diphenylphosphino)-1-[N-(2-hydroxyethyl)carbamoyl]ferrocene [I; Z = null; (1)] , reacts readily with H2O2 and elemental S to give the corresponding phosphine oxide I [Z = O (2)] and phosphine sulfide I [Z = S (3)], resp., and with Pt(II) and Pd(II) precursors to afford various bis(phosphine) complexes [MCl2(1-κP)2] (M = trans-Pd, trans-Pt and cis-Pt). The structures of 2 and 3 were detd. by x-ray crystallog. The anticancer activity of the compds. was evaluated in vitro with the complexes showing moderate cytotoxicities towards human ovarian cancer cells. Also, the biol. activity is strongly influenced by the stereochem., with trans-[PtCl2(1-κP)2] being an order of magnitude more active than the corresponding cis isomer. Copyright © 2010 John Wiley and Sons, Ltd.
Keywords: ferrocene ; phosphanyl-carboxamides ; complexes ; anticancer properties ; X-ray crystallography ; Asymmetric Allylic Alkylation ; Catalytic Use ; Drug-Resistance ; Ferrocenecarboxylic Ligands ; Enantioselective Synthesis ; Antitumor Complexes ; Molecular-Structure ; Crystal-Structure ; Planar Chirality ; Pendant Groups
Record created on 2010-12-15, modified on 2016-08-09