147results about "Bismuth organic compounds" patented technology

By providing a novel polycyclic aromatic compound in which a plurality of aromatic rings are linked via a boron atom, a nitrogen atom, or the like, options of a material for an organic EL element are increased. In addition, by using the novel polycyclic aromatic compound as a material for an organic electroluminescent element, an excellent organic EL element is provided.

A process for producing bismuth-containing oxide thin films by Atomic Layer Deposition, including using an organic bismuth compound having at least one silylamido ligand as a source material for the bismuth oxide. Bismuth-containing oxide thin films produced by the preferred embodiments can be used, for example, as ferroelectric or dielectric material in integrated circuits and / or as superconductor materials.

In a method for functionalizing a carbon nanotube surface, the nanotube surface is exposed to at least one vapor including at least one functionalization species that non-covalently bonds to the nanotube surface, providing chemically functional groups at the nanotube surface, producing a functionalized nanotube surface. A functionalized nanotube surface can be exposed to at least one vapor stabilization species that reacts with the functionalization layer to form a stabilization layer that stabilizes the functionalization layer against desorption from the nanotube surface while providing chemically functional groups at the nanotube surface, producing a stabilized nanotube surface. The stabilized nanotube surface can be exposed to at least one material layer precursor species that deposits a material layer on the stabilized nanotube surface.

The invention discloses a dark blue organic light-emitting material and a preparation method and application thereof. The dark blue organic light-emitting material contains a structural unit disclosedin the invention, wherein, M is B or Bi; X is O, S or NR4; R1-R4 are independently selected from connecting bonds or groups obtained from H-H, H-F, H-O-H, H-S-H, H-CN, saturated hydrocarbons, unsaturated hydrocarbons, fluorinated hydrocarbons, heterocyclic compounds, organoboron, organosilicone, alcohols, mercaptans, ethers, thioethers, phenols, thiophenol, aldehydes, ketones, amines, amides, nitriles or sulfones losing one or more H; R1-R3 are located at any substitution position on rings of the structural unit where R1-R3 are located, and the bond energy between the ring where R3 is locatedand M is greater than or equal to the bond energy between the ring where R2 is located and M. The dark blue organic light-emitting material containing the B / Bi-N main body structure has very narrow light-emitting spectrum and TADF properties; the color purity is high, and the stability is good.

The invention provides a coordination polymer material with a multistage pore passage structure and a preparation method thereof. The coordination polymer material with a multistage pore passage structure is internally provided with the multistage pore passage structure, the multistage pore passage structure is a microporous and / or mesoporous and / or macroporous multistage pore passage structure which is formed by the self assembly between the metal ion and the organic ligand, the apertures of the micropores are less than or equal to 2nm, the apertures of the mesopores are from 2nm to 50nm, and the apertures of the macropores are more than 50nm. The coordination polymer material with a multistage pore passage structure is large in specific surface, the large-size organic ligand does not need to be synthesized, and the coordination polymer material with larger porous sizes can be obtained without the template agent and the pore assisting agent, so that the invention is simple in preparation method, and low in cost.

The present invention is directed to novel non-invasive diagnostic tools to image cancers, especially, leukemia and non-Hodgkin's lymphomas (NHL) with minimal toxicity in vivo. The present invention represents a clear advance in the art which presently relies on tissue biopsy for diagnoses of these cancers. The novel imaging probe is capable of detecting precancerous cells, as well as their metastatic spread in tissues. This represents a quantum step forward in the diagnosis and staging of NHL using non-invasively molecular imaging techniques. This novel probe will also be useful to monitor patients response to chemotherapy treatments and other interventions or therapies used in the treatment of NHL. Compounds according to the present invention may be used as diagnostic tools for a number of conditions and diseases states as well as therapeutic agents for treating such conditions and disease states.

The present invention relates to bismuth dithiocarbamate compounds of general formula I: wherein R and R1 are the same or different, and each is an alkyl, substituted alkyl, aryl or a substituted aryl; X is a halide or a pseudo-halide; and n is either 2 or 3, for use as an active pharmaceutical substance. In particular, they can be used as anti-tumour agents and for the treatment of various forms of tumours. Also provided are some novel bismuth dithiocarbamate compounds and the process for preparing these compounds.

The invention discloses a bismuth metal organic framework material, a preparation method of the bismuth metal organic framework material and an application of the bismuth metal organic framework material in lead storage battery anode additives. The bismuth metal organic framework material disclosed by the invention is a porous material, so that the material has high porosity, a large pore volume, a large superficial area and good water solubility and acid stability, and the material can be dispersed in deionized water in advance. The bismuth metal organic framework material can be used as a lead storage battery anode doping material and can improve the utilization rate of active substance and enhance the charge acceptance.

Enclosed are high refractive index and low birefringence organic / inorganic hybrid materials useful for optical applications. They are prepared from solventless metal aliphatic acryl alkoxides. The metal acryl alkoxides are synthesized from exchanging acryl alcohol with metal alkoxides, and are hydrolyzed into metal oxide nanoparticles and are well dispersed in the acrylate matrix. Then they are polymerized into organic / inorganic hybrid materials containing metal oxide in polyacrylate.

Semiconductor nano-sized particles possess unique properties, which make them ideal candidates for applications in solar electrochemical cells to produce chemical energy from solar energy. Coupled nanocrystal photoelectrochemical cells and several applications improve the efficiency of solar to chemical energy conversion.

The invention discloses a novel organic bismuth ion compound containing bridged nitrogen atom ligand. The structural formula of the ligand is (R<1>)(R<2>)(R<3>)(R<4>)PhCH2N[R']CH2Ph(R<5>)(R<6>)(R<7>)(R<8>), wherein, R<1>, R<2>, R<3>, R<4>, R<5>, R<6>, R<7> and R<8> are any same or different radicals on a benzene ring; R' is substituents on nitrogen atoms; radicals X directly connected with bismuth are anions with stronger electrolysis capacity; and in the bismuth compound, Bi<3+> forms bonds with two carbon atoms in the ligand, a coordination bond with N atoms in the ligand and an ionic bond with the corresponding anions. The invention also provides a preparation method of the organic bismuth ion compound and application thereof to organic synthesis as a catalyst.

A novel bismuth compound having excellent vaporization characteristic and / or thermal stability, a process of producing the same and a process of producing a film in the film formation by the CVD process are disclosed. Bismuth compounds each represented by the following formula 1, 5 and 9, processes of producing the same, and processes of producing a film. In the formulae, R1 and R7 each represents a lower alkyl group; R2, R8, R12, and R13 each represents a lower alkyl group, a lower alkoxy group, or the like; m represents the number of the substituent R12 in the range of 0-5; n1, n2, and n3 respectively represent the number of the substituent R2, the number of the substituent R8, and the number of the substituent R13 each in the range of 0-4; and R3 to R6, R9 to R11, R14, and R15 each represents hydrogen, a lower alkyl group, or the like, provided that specific combinations of the substituents are excluded.

The invention discloses a novel organic bismuth ion compound containing bridged sulfur atom ligand. The structural formula of the ligand is (R)(R)(R)(R)PhCH2SCH2Ph(R)(R)(R)(R), wherein, R, R, R, R, R, R, R and R are any same or different radicals on a benzene ring; other radicals X directly connected with bismuth are anions with stronger electrolysis capacity; and in the bismuth compound, Bi forms bonds with two carbon atoms in the ligand, a coordination bond with the sulfur atoms in the ligand and an ionic bond with the corresponding anions. The invention also provides a preparation method of the organic bismuth ion compound and application thereof to organic synthesis as a catalyst.

The invention discloses a novel metal bismuth compound, preparation method and application thereof. The novel compound has the formula as above, i.e., contains bridge type N atom bisphenolate as the ligand, and Bi<3+> and the bridge type N atom form intramolecular coordination. The preparation method includes allowing bisphenolate [(R1)(R2)(ONa)Ph(CH2)]N[R'][(R1)(R2)(ONa)Ph(CH2)] and bismuth trihalogen to directly react if X is halogen atom to obtain objective product (I); and allowing sodium alkoxide (RCH2ONa) and bismuth trihalogen to react to produce Bi(OCH2R)3, and reacting with precursor [(R1)(R2) (OH)Ph(CH2)]N[R'][(R1)(R2)(OH)Ph(CH2)] to obtain objective product (II) if X in the formula is alkoxyl; or allowing the objective product (I) and RCH2ONa to react to produce objective product (II). The metal bismuth compound has novel structure, simple process, and high catalytic activity and selectivity for cyclic carbonate made by coupling of CO2 and epoxy compound, and has wide prospect in the fields of catalysis, organic synthesis and medicine.

The invention relates to preparation of a mononuclear (polynuclear) complex of Schiff's base and bismuth. The method comprises the main steps of: adding Schiff's base, an organic solvent, a bismuth salt and a chelating agent in a suitable container; heating with stirring; and after thorough reaction, treating the products to obtain a pure product. The invention uses the rich and fine bismuth resources in Chenzhou, Hunan Province to synthesize the bismuth complex with biological activity, and plays important role in promoting the improvement on comprehensive utilization of nonferrous metals in Hunan, formation of an industrial chain, and comprehensive increase of local economic efficiency.

To provide a novel material exhibiting excellent light-emitting characteristics using a heavy metal element having relatively abundant reserve.A thin film containing a compound of Formula (1):wherein Ar1 and Ar2 are each independently a C3-30 aromatic ring; R1 and R2 are a substituent; a and b are each independently an integer of 0 to 12, wherein when a is 2 or more, each R1 is optionally different from each other and two R1 are optionally bonded with each other to form a ring structure, and when b is 2 or more, each R2 is optionally different from each other and two R2 are optionally bonded with each other to form a ring structure; A1 is any of direct bond, —O—, —S—, —S(═O)—, —S(═O)2—, —PR3—, —NR4—, and —C(—R5)2—; R3 is a hydrogen atom or a substituent; R4 is a hydrogen atom or a substituent; R5 is a hydrogen atom or a substituent and two R5 are optionally different from each other; E1 is a monovalent group having 50 or less carbon atoms; L1 is a ligand having 50 or less carbon atoms; c is an integer of 0 to 3, wherein when c is 2 or more, each L1 is optionally different from each other; and each combination of a combination of E1 and Ar1 and a combination of E1 and Ar2 optionally forms a bond; and when c is 1 to 3, each combination of a combination of L1 and E1, a combination of L1 and Ar1, a combination of L1 and Ar2, and a combination of L1 and L1 optionally forms a bond.

A method of preparing Group VA organometal compounds in high yield and high purity by the reaction of a Grignard reagent with a Group VA metal halide in certain ethereal solvents is provided. A method of preparing Group VA organometal hydrides is also provided.

The invention provides a carbon-metal composite material which has improved conductivity, specific surface area and regularity and a shape which is easily controlled, and a process of preparing the same. The carbon-metal composite material includes carbon and metal, has a sheet resistance of 8m CR / sq. or less under a pressure of 100 kg f / cm2 and a specific surface area of 30 m2 / g or greater, shows an X-ray pattern having at least one peak at d-spacing of 6 nm or greater.

The invention relates to a metal-organic framework MOF material with the high methane adsorption and storage density. According to the metal-organic framework MOF material, naphthalene binary or ternary carboxylic acid organic ligands and derivatives of naphthalene binary or ternary carboxylic acid organic ligands are used in match with metal cations of ferric iron, lanthanum, bismuth, nickel, aluminum and cerium to form a three-dimensional neat network porous channel structure in the presence of coordinate bonds or ionic bonds; nitrogenous, oxygenic and sulfuric functional groups with the extremely strong polarity are introduced into the organic ligands, so that the methane adsorption and storage amount of the MOF material can be effectively increased; the metal-organic framework material has a suitable porous channel size being 1.0-2.0nm, a specific surface area being greater than 2000m<2> / g, a pore volume performance and the good heat stability, so that the material can be reused; meanwhile, the material is relatively low in synthetic cost and has the methane absorption and storage amount of 190-210V / V under 3.5MPa. By adopting the metal-organic framework MOF material with the high methane adsorption and storage density, the problems of low methane absorption capacity, high operation pressure and dissatisfactory absorption / desorption rate in the prior art are solved. The metal-organic framework material can be used as an efficient methane adsorbent and is wide in application prospects.

The present invention discloses industrial preparation process of serial triphenyl bismuth compounds. Serial benzene bromide compounds as material are made to produce Grignard reaction with metal magnesium in anhydrous solvent to produce organic magnesium compounds, which are then reacted with anhydrous bismuth trichloride at 20-120 deg.c to produce serial triphenyl bismuth compounds. The serial benzene bromide compounds include bromobenzene, parabromotoluene, m-bromotoluene, o-bromotoluene, etc; and the anhydrous solvent may be tetrahydrofuran, benzene, toluene, ethyl benzene, etc or their mixture. The reaction time is 2-24 hr. The present invention adopts organic solvent with high boiling point for high safety and easy activation of magnesium, and has mild reaction condition and yield over 90 %.

The invention relates to metal complex compounds of the formula Mk(L)x(Y)kz-nx, where the ligand L has the formula (I), and to metal complex compounds which include the reaction product of at least one salt or a complex of a transition metal or a main group metal element of the groups 13 to 15 and at least one 1,3-ketoamide. Such complex compounds are suitable in particular as catalysts for polyurethane compositions. The invention also relates to two-component polyurethane compositions including at least one polyisocyanate as the first component, at least one polyol as the second component, and at least one such metal complex compound as the catalyst. The invention additionally relates to different uses of the two-component polyurethane compositions.

The invention discloses a bismuth compound with 2-acetyl-3-ethylpyrazine thiosemicarbazone as a ligand and a synthesis method of the bismuth compound. The method comprises the steps of dissolving 2-acetyl-3-ethylpyrazine in methyl alcohol to prepare a solution; taking thiosemicarbazone into methyl alcohol, then dropping the prepared solution into a methyl alcohol solution containing the thiosemicarbazone, conducting a backflow mixing reaction, cooling to the room temperature, afterwards, pouring the solution into a beaker for volatilization, filtering an obtained precipitate, afterwards, utilizing absolute ethyl alcohol for washing of 2-3 times, and obtaining the ligand after drying; taking BiCl3 to be dissolved into the methyl alcohol solution, then dropwise adding the methyl alcohol solution into an ethanol solution containing the ligand, conducting a backflow mixing reaction, filtering the solution after the reaction into the beaker, replenishing methyl alcohol, utilizing preservative film for sealing, utilizing a needle for punching out several holes, and conducting volatilization for several days at 4 DEG C to obtain a bismuth compound crystal. The synthesized bismuth compoundis subjected to in-vitro proliferation inhibition activity experiments, it is proved that for cancer cells, the activity of the pure 2-acetyl-3-ethylpyrazine thiosemicarbazone ligand is not high, andafter the ligand is coordinated with bismuth ions, the activity is greatly improved.

The invention provides a bismuth-based metal organic framework material and a preparation method and application thereof, and belongs to the technical field of metal organic framework material preparation and photocatalysis. The preparation method of the bismuth-based metal organic framework material (namely Bi-MBA) provided by the invention is simple, and has the advantages of mild reaction conditions, low cost, high yield and the like; meanwhile, the prepared Bi-MBA single crystal belongs to an orthogonal space group Cmcm and is structurally characterized by being a Bi2S4 long chain; the photo-induced electron-holes of the Bi-MBA can be effectively separated; the electronic structure has the characteristics that an organic ligand mainly occupies a conduction band, so that the conductionband potential reaches -1.38 eV; and thus, the Bi-MBA exhibits good photocatalytic reduction properties, including reduction of O2, Cr(VI) and CO2, and the reaction conditions are all at room temperature. Therefore, good practical application value is achieved.

The invention provides a preparation method of a metal-organic frame material Bi-BTC for adsorbing CO2. The preparation method comprises steps as follows: dissolving Bi(NO3)3*5H2O in an absolute ethyl alcohol and ethylene glycol mixed solution or an ethylene glycol and glycerin mixed solution to form a solution A; dissolving 1,3,5-benzenetricarboxylic acid in absolute ethyl alcohol or N-N-dimethylformamide to form a solution B; slowly adding the solution B into the solution A at the room temperature to obtain a first mixed solution, crystalizing the first mixed solution at the temperature of 120-130 DEG C for 2-3 days to obtain a first solid product, washing the first product with an alcoholic solution, and placing the washed first solid product in a drying oven at the temperature of 110-130 DEG C for 10-16 h to obtain the metal-organic frame material Bi-BTC. The material has the better CO2 adsorbing capacity in a lower-temperature lower-CO2-pressure environment.

Radiopaque bismuth particles and methods of making and using the radiopaque bismuth particles are disclosed. The radiopaque bismuth particles include an elemental bismuth core and an outer coating comprising one or more coating agents. Disclosed radiopaque bismuth particles are suitable for use in surgical sponges and plastic objects.

The present invention relates complexes comprising a PSMA targeting compound linked to a radionuclide, such as 212Pb or 227Th. These compounds, and pharmaceutical compositions comprising them, can be used for medical applications. These applications include the treatment of prostate cancer, and the complexes allow for dual targeting of cancers.

(Pentafluorophenyl) Group 11 and 12 metal compounds and processes for preparing (pentafluorophenyl) Group 11 and 12 metal compounds are disclosed. Also, disclosed are processes for preparing (pentafluorophenyl) Group 13 or 15 metal compounds useful as Lewis acids. Compositions with low levels of base impurities and products produced by the novel processes are also disclosed.

Diazaphosphacycles comprising compounds having the formula XI and salts of the compound are provided, wherein the variables W, T, R1, R14, and R15 are as described herein. Transition metal catalysts incorporating such diazaphosphacycles and methods of use thereof are also disclosed. There are further provided compositions comprising diazaphosphacycles covalently attached to a solid support and methods of use thereof.