Abstract: The present invention is directed to a family of trimetallic nitride endohedral metalloheterofullerenes having the formula Ax X3-x N@Cn N, (x=0, 1, 2 or 3) (n=number of carbon atoms in the cage, typically between 59 and 199), wherein A and X are metal atoms encased within the cage, C is carbon and N is nitrogen. A and X are preferably selected from rare earth elements or group IIIB elements. A or X metal atoms are scandium, yttrium, lanthanum, gadolinium, lutetium, holmium, erbium, thulium, dysprosium, neodymium, cerium, praseodymium and ytterbium. Representative embodiments include Sc3N@C79N, Y3N@C79N, La3N@C79N, Tb3N@C79N, Ho3N@C79N, LaSc2N@C79N, PrSc2N@C79N, GdSc2N@C79N, La2ScN@C79N, and Gd2ScN@C79N. The present invention is also directed to a method of making the inventive endohedral metalloheterofullerenes having the formula AxX3-xN@CnN. These methods involve use of oxidizing gases (e.g.

Abstract: An exemplary optical limiter device (100) has an optically transmissive substrate (102) and a layer (104) on a first surface (106) of the substrate, the layer having a trimetallic nitride endohedral metallofullerene. The layer can be a thin film of the trimetallic nitride endohedral metallofullerene, a layer material with a cavity containing a solution with the trimetallic nitride endohedral metallofullerene, a sol-gel with a trimetallic nitride endohedral metallofullerene, and a self assembled monolayer with a trimetallic nitride endohedral metallofullerene. The layers of trimetallic nitride endohedral metallofullerenes can be vapor deposited, solution deposited and/or self assembled onto optical components. The third-order nonlinear properties of these films provide desired transmission characteristics.

Abstract: A method of making multiple carbonaceous nanomaterials is provided. Embodiments of the method can produce a reaction product that includes trimetaspheres, nanotubes, and at least one of fullerenes and metallofullerenes. A preferred embodiment of the method includes reacting at least one carbon source, nitrogen source, copper source, yttrium source, transition metal, and trimetasphere-forming metal in a reaction chamber. The reaction product can be produced by arc discharge in the presence of nitrogen gas.

Abstract: The present invention is directed toward a tunable dielectric device comprising: a substrate and an endohedral fullerene encapsulating trimetallic nitride template compound disposed on the substrate. The endohedral fullerene encapsulating trimetallic nitride template compound has a dipole moment that is oriented when a voltage of less than about 5 volts is applied thereto causing a change in the orientation of the dipole moment of the compound. The physical dimension of the compound is essentially unchanged.

Abstract: A method for imagining and treating a body employing at least one trimetallic nitride template endohedral metallofullerene compound is disclosed. The compound has at least one diagnostic and at least one treatment atom encapsulated within a fullerene cage. The two atoms are different from each other. The compound is administered into a body, traced, and allowed to react at a targeted area of the body.

Abstract: A family of trimetallic nitride endohedral metallofullerenes and their preparation are described. The trimetallic nitride endohedral metallofullerenes have the general formula A3-nXn@Cm where n ranges from 0 to 3, A and X may be trivalent metals and may be either rare earth metal or group IIIB metals, and m is between about 60 and about 200. Further, the A3-nXn@C68, A3-nXn@C78, A3-nXn@C80 families of endohedral fullerenes are described. The trimetallic nitride endohedral metallofullerenes are produced by charging a reactor with a cored graphite rod that has been filled with a metal oxide graphite mixture. The metal oxides correspond to the metals for A and X. The graphite rod is arc discharged in a helium and nitrogen atmosphere to produce the desired trimetallic nitride endohedral metallofullerenes.