Modifying the endohedral La-ion location in both neutral and positively charged polyhydroxylated metallofullerenes

q=0, 1, 2, 4, 6, and 8 metallofullerenes. Interestingly we obtain, for the neutral hydroxylated structures, that the location of the encapsulated La atom strongly depends on the precise distribution of the OH groups on the carbon surface. Actually, we found atomic configurations in which the La ion is attached to different regions of the inner surface as well as atomic arrays in which weakly bonded endohedral species are obtained, being located near the center of the structure. The previous strong variations in the endohedral position of the lanthanum atom leads to sizable modifications in its valence state as well as to notable changes in the electronic spectra and in the lowest-energy spin configuration of the molecules, which are all facts that could be used to better identify the atomic structure of these highly relevant metallofullerenes. The positive charging by means of simply electron detachment of our here-considered La@C60 OH 32 compounds reveals that the rupture of various C-C bonds of the carbon network can be achieved. However, even if the previous bond breakage leads to the formation of sizable holes in the C60 cavity made of nine-membered rings , we obtain that the encapsulated La atom was unable to escape from the cage. In contrast, in the polyhydroxylated La@C82 OH 20 fullerene, no C-C bond breakage is induced with increasing charge state of the cage, defining thus a more stable molecular compound. The previous results are expected to be of fundamental importance in medical and biological applications where the permanent encapsulation of these highly toxic atomic species is required.