Synthesis, electrochemical, kinetic and thermodynamic properties of new ferrocene-containing betadiketonato rhodium(I) complexes with biomedical applications
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Klaas, Palesa
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University of the Free State
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English: Synthetic routes to prepare new ferrocene-containing β-diketones, FcCOCH2COR, with Fc =
ferrocenyl, R = H, CH3, CH2CH3, CH(CH3)2 and C(CH3)3, have been developed. Rhodium
complexes of the type [Rh(FcCOCHCOR)(cod)] were obtained in yields approaching 80% by
treating these β-diketones with [Rh2Cl2-(cod)2]. Group electronegativities XR of R substituents were
determined from a linear relationship between ethyl ester IR carbonyl stretching frequencies of the
type RCOOCH2CH3 and group electronegativities of known R groups. pKa values of new β -diketones were determined. 1H NMR studies on FcCOCH2COR indicated that enolisation in the
direction furthest from the ferrocenyl group always dominate. This finding is considered to be the
result of resonance driving force rather than inductive electronic effects of substituents on the
pseudo-aromatic β-diketone core.
Formal reduction potentials (Eol values vs. Ag/Ag+) of the iron core in the free β-diketones,
FcCOCH2COR, and in [Rh(FcCOCHCOR)(cod)] complexes as well as the peak anodic oxidation
potentials, Epa, of the rhodium(I) nucleus were determined. The roles of pKa and group electronegativities on redox potentials are also discussed.
Second-order rate constants, k2, for the substitution of the β-diketonato ligand, (FcCOCHCOR),
from the complexes [Rh(FcCOCHCOR)(cod)] with 1,10-phenanthroline at 25°C in methanol were
determined. Large negative values obtained for entropy of activation suggested an associative
substitution mechanism. All substitution reactions were independent of a solvent step.
Cytotoxic properties in terms of potential anticancer applications of these newly synthesised β- diketones and their rhodium complexes on cancer cells are described. Cytotoxicity was tested on
HeLa, A2780 and A2780 platinum resistant cancer cells lines. Rhodium complexes were observed to
be more effective in killing cancer cells than the free β-diketones.