We have examined whether the Co ions crystallographically substitute on the
Ti sites in rutile and anatase Ti_{1-x}Co_{x}O_{2-delta}thinfilmsthatexhibitroom−temperatureferromagnetism.Intensitiesofthex−rayBraggreflectionfromthefilmsweremeasuredaroundtheK−absorption−edgeofCo.IftheCoionsrandomlysubstituteontheTisites,theintensityshouldexhibitananomalyduetotheanomalousdispersionoftheatomicscatteringfactorofCo.However,noneoftheanataseandrutilesamplesdidexhibitananomaly,unambiguouslyshowingthattheCoionsinTi_{1-x}Co_{x}O_{2-delta}arenotexactlylocatedattheTisitesofTiO_2.TheabsenceoftheanomalyisprobablycausedbyasignificantdeformationofthelocalstructurearoundCoduetotheoxygenvacancy.WehaveappliedthesamemethodtoparamagneticZn_{1-x}Co_{x}$O thin films and
obtained direct evidence that the Co ions are indeed substituted on the Zn
sites.Comment: 5 pages, 4 figures, accepted in PR
To understand the possible physiological roles of the neuromelanins, we examined effects of synthetic dopamine-melanins on oxygen radical formation by metal ions with dopamine. Oxygen radical formation was detected by DNA cleavage analysis. Addition of metal-free synthetic dopamine-melanins inhibited DNA cleavage induced by Fe or Cu ions with dopamine. On the other hand, in the presence of dopamine, dopamine-melanins loaded with Cu and Fe induced DNA cleavage without addition of free metal ions. It was clarfied that dopamine-melanins loaded with Cu and Fe generated hydroxyl radicals in the presence of dopamine, on the basis of the findings thet catalase and mannitol inhibited the DNA cleavage. Our results suggest that metal-free neromalanins inhibit hydroxyl radical formation induced by ions with dopamine by sequestering metal ions