Abstract: Provided are a novel fullerene derivative which can adsorb quickly and efficiently an allergen which may cause a pollen allergy without releasing the allergen again, does not contain a metal or the like which may cause a harmful effect to a human body, and is easily applicable, impregnable, or chemically bondable onto surface of various materials: and a process for producing the same. The fullerene derivative is characterized in that a halogen group and many hydroxyl groups are bonded directly to a fullerene nucleus. In the case that the halogen group is chlorine, the fullerene derivative can be synthesized by a partial hydroxylation of a chlorinated fullerene or a partial chlorination of a hydroxylated fullerene.

Abstract: Provided are a novel fullerene derivative which can adsorb quickly and efficiently an allergen which may cause a pollen allergy without releasing the allergen again, does not contain a metal or the like which may cause a harmful effect to a human body, and is easily applicable, impregnable, or chemically bondable onto surface of various materials; and a process for producing the same. The fullerene derivative is characterized in that a halogen group and many hydroxyl groups are bonded directly to a fullerene nucleus. In the case that the halogen group is chlorine, the fullerene derivative can be synthesized by a partial hydroxylation of a chlorinated fullerene or a partial chlorination of a hydroxylated fullerene.

Abstract: The present application discloses novel endohedral fullerenes having enclosed therein one or more ozone molecules, e.g. fullerenes selected from C60-fullerene (Buckminsterfullerene), C70-fullerene, C76-fullerene, C78-fullerene, C82-fullerene, C84-fullerene, and C120-fullerene. The application further discloses a composition comprising the endohedral fullerene and a carrier material, e.g. where the carrier material is a skin lotion, such as a skin lotion comprising L-ascorbic acid or Vitamin E. Moreover, various uses of the novel fullerenes are disclosed, e.g. for skin UV-protection; in or on the surface of sun glasses; in or on the surface of window glass; in or on the surface of textiles, fabrics, clothes, wood, paint, paper, cushions, leather, hair-care products, and plants.

Abstract: Core shell particles and bulk-heterojunction organic photovoltaic devices using the core shell particles are described. In particular, core shell particles having a core particle and a shell of a second material and bulk-heterojunction organic photovoltaic devices using the core-shell particles are described. The core-shell particles can have a core particle with an electron donating material or a core particle with an electron donating material. Formation of a hulk-heterojunction organic photovoltaic device using such an core-shell particles forming an interpenetrating network with the an electron donating or electron accepting phase is also described.

Abstract: In order to isolate and purify an endohedral fullerene, a solvent washing was performed using toluene to concentrate the endohedral fullerene in a residual, but endohedral fullerene could not be efficiently purified because impurities other than the endohedral fullerene could not be sufficiently removed. Thus, the endohedral fullerene is isolated and purified by using a solvent such as chloronaphthalene or tetralin having a high solubility for the endohedral fullerene and concentrating the endohedral fullerene in the solvent. The endohedral fullerene isolated and purified by solvent extraction has a cluster structure where the endohedral fullerene is surrounded with empty fullerenes. Thus, this endohedral fullerene is highly stable and is a useful material applicable to various fields such as medical care and electronics.

Abstract: This invention provides a composition of polyhydroxylated metallofullerene compound and its application in the preparation of antitumor pharmaceutical. In one embodiment, metallofullerol comprising the formula, M@C2m(OH)x, wherein M is selected from rare earth elements such as La or Gd; m is carbon atoms of 41 or 30; x is a number of hydroxyl group of from 10 to about 50. Actually, due to the reset of the neighboring hydroxyl, the numbers of O and H in Carbon cage are different, formula are thus written as M@C2mOxHy. Comparing to the clinical anticancer drugs such as Paclitaxel, Cyclophosphamide, and Cisplatin, metallofullerol of M@C2m(OH)x or M@C2mOxHy has superior advantages of higher antitumor efficiency, low dosage, low toxicity, and better biocompatibility.

Abstract: A pegylated and hydroxlated trimetallic nitride endohedral metallofullerene is provided comprising a plurality of hydroxyl groups and one or more polyethylene glycol (PEG) moieties covalently bonded to a fullerene encapsulating a trimetallic nitride. Methods of pegylation and hydroxylation of trimetallic nitride endohedral metallofullerene and methods of using pegylated and hydroxlated trimetallic nitride endohedral metallofullerene are described.

Abstract: The present invention provides: a carbon nanohorn composite including a carbon nanohorn, a substance encapsulated in the carbon nanohorn, and a polyamine adsorbed by chemical reaction firmly to a surface functional group present on the opening part on the surface of the carbon nanohorn, wherein the release amount and release rate of the encapsulated substance can be controlled using the difference in size, substituent or three-dimensional structure of the polyamine, which is used as a plug; a method of controlling the release of the encapsulated substance; and a process for producing the carbon nanohorn composite. The release amount and release rate of the substance encapsulated in the carbon nanohorn composite is controlled by selecting a polyamine molecule, which plugs the opening part formed in the carbon nanohorn by oxidation, by its size, substituent or three-dimensional structure.

Abstract: A method is disclosed whereby a functional nanomaterial such as a monolayer carbon nanotube, a monolayer boron nitride nanotube, a monolayer silicon carbide nanotube, a multilayer carbon nanotube with the number of layers controlled, a multilayer boron nitride nanotube with the number of layers controlled, a multilayer silicon carbide nanotube with the number of layers controlled, a metal containing fullerene, and a metal containing fullerene with the number of layers controlled is produced at a high yield. According to the method, when a multilayer carbon nanotube (3) is formed by a chemical vapor deposition or a liquid phase growth process, an endothermic reaction aid (H2S) is introduced in addition to a primary reactant (CH4, H2) in the process to form a monolayer carbon nanotube (4).

Abstract: Self-assembled, closed and hollow chemical multimer structures having a dodecahedral morphology, composed of chemical monomers having a structurally symmetric core which possess a 5-fold rotational symmetry, are provided. Also provided are methods of creating such chemical monomers, methods of creating such chemical multimer structures and compositions comprising these chemical multimer structures. Also provided are uses of these chemical multimer structures in applications such as drug delivery, imaging, immunization, formation of plastic crystals and nanoparticle matrices and other medical and material science applications.

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: Trimetallic nitride endohedral metallofullerene derivatives and their preparation are described. The trimetallic nitride endohedral metallofullerene derivatives have the general formula A3-nXn@Cm(R) 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, m is between about 60 and about 200, and R is preferably an organic group. Derivatives where the R group forms cyclized derivatives with the fullerene cage are also described.

Abstract: A fusion fuel composition has two or more light nuclei combined with a cage-like molecule. The light nuclei may be, for example, deuterium and tritium, and the cage-like molecule may be, for example, a fullerene molecule. A fusion reaction to consume the fusion fuel may be ignited, for example, via compression methods including chemical or laser.

Abstract: Methods for separating and purifying carbon nanomaterials such as trimetallic nitride endohedral metallofullerenes are described. In certain embodiments, carbon nanomaterials are contacted with a carbon nanomaterial reactive agent. The reactive agent binds empty cage fullerenes, nanotubes, and endohedral metallofullerenes without appreciably binding trimetallic nitride endohedral metallofullerenes. According to some embodiments, purified forms of trimetallic nitride endohedral metallofullerenes may be prepared.

Abstract: This invention is directed to the fluorination (or derivatization with alternative chemical species) of fullerene carbon nanocages as an efficient way to (a) facilitate synthesis of endohedral complexes by a significant reduction or elimination of the barriers for the entry of guest-ions, -atoms or molecules, and (b) to preserve the chemical stability of final product.