Abstract

By means of EPR spectroscopy the behaviour of the vanadocene dichloride (I), Cp2VCl2(Cp=η5-C5H5), in various deoxygenated and non-deoxygenated physiological media and therapeutic solution as well as in blood plasma and stabilized human blood was studied. On the basis of measured values of isotropic spectroscopic splitting factor giso and isotropic hyperfine coupling constant Aiso, the vanadocene species, [Cp2V(H2O)Cl]+ (II; giso= 1.985, |Aiso| = 7.68 mT), [Cp2V(H2O)2]2+ (III; giso= 1.983, |Aiso| = 7.92 mT), Cp2V(OH)2 (IV; giso= 1.991, |Aiso| = 6.285 mT), [Cp2VCl(DMSO)]+ (V; giso= 1.985, |Aiso| = 7.69 mT), the vanadyl species [VO(DMSO)5]2+ (VI; giso= 1.964, |Aiso| = 10.78mT) and [VO(H2O)5]2+ (VII; giso= 1.955, |Aiso| = 11.56 mT) have been identified. From the measurements it follows that I does not react in its first coordination sphere with any component of a system used other than water and DMSO, resp. As to water-containing media, its behaviour is fully consistent with that of I in pure aqueous media. It was found the only vanadocene species present after application of the therapeutic solution of I into human blood to be IV not interacting in its first coordination sphere with any blood component.