693results about "Group 2/12 organic compounds without C-metal linkages" patented technology

An isoreticular metal-organic framework (IRMOF) and method for systematically forming the same. The method comprises the steps of dissolving at least one source of metal cations and at least one organic linking compound in a solvent to form a solution; and crystallizing the solution under predetermined conditions to form a predetermined IRMOF. At least one of functionality, dimension, pore size and free volume of the IRMOF is substantially determined by the organic linking compound.

A zinc amino acid chelate formulation is disclosed comprising zinc ions being chelated by an amino acid ligand mixture comprising glycine and a sulfur-containing amino acid wherein the ligand to zinc molar ratio is from about 1:1 to 2:1 and wherein the glycine to sulfur-containing amino acid molar ratio is between about 1:6 to 6:1.

The present invention provides a metal-organic framework (“MOF”) comprising a plurality of metal clusters and a plurality of multidentate linking ligands. Each metal of the plurality of metal clusters comprises one or more metal ions. Each ligand of the plurality of multidentate linking ligands connects adjacent metal clusters. The present invention also provides a method of forming the metal-organic framework. The method of the invention comprises combining a solution comprising one or metal ions with a multidentate linking ligand having a sufficient number of accessible sites for atomic or molecular adsorption that the surface area of the resulting metal-organic framework is greater than 2,900 m²/g.

An overbased magnesium composition deposit control additive for residual fuel oils and turbine fuels is an overbased magnesium sulfonate, carboxylate or phenate or mixtures thereof containing at least 14% and upwards to about 18% by weight of magnesium and containing a succinic anhydride and lower carboxylic acid co-promoter reaction product. The additive when added to fuel oils, such as residual fuel oils containing high asphaltenes, reduces, if not eliminates, magnesium/asphaltene deposits or sediment and the consequential plugging of filters. The additive also reduces, if not eliminates, vanadium caused corrosion in the turbine. The invention is also the process for preparing the overbased composition or deposit control additive, wherein the overbasing reaction incorporates the combination of a lower carboxylic acid, preferably acetic acid and a succinic anhydride, preferably dodecenyl succinic anhydride (DDSA), as the co-promoter.

The present invention discloses a method for preparing a metal organic framework film. The method comprises a step of contacting a metal source with an organic ligand to form the metal organic framework film on a substrate by a hot-pressing method. By means of the method provided by the present invention, a large number of metal organic framework films with quite high purity can be obtained conveniently and rapidly, so that industrialized production and application are implemented, and the method has the advantages of low costs, simplicity in operation, rapid production, mass production of products, high purity and the like.

Embodiments of the invention relate to a method for preparing crystalline metal-organic frameworks (MOFs). The method includes the steps of providing an electrolyte solution in contact with a conductive surface, and applying a current or potential to the conductive surface in contact with the electrolyte solution. The electrolyte solution includes a protonated organic ligand, a metal ion, and a probase. Application of the reductive current or potential to the conductive surface produces the crystalline metal-organic framework (MOF) deposited on the conductive surface. The MOFs produced by the method may be incorporated into a gas separation membrane, a purification filter, and/or a sensor.

The invention discloses synthesis methods of a tri-(4-triazolyl phenyl) amine and a tri-(4-triazolyl phenyl) amine cadmium complex, and relates to the field of luminescent materials. The synthesis method of the tri-(4-triazolyl phenyl) amine takes copper oxide as a catalyst and dimethylsulfoxide as a solvent, tri-(4-iodobenzene) amine and triazole react at the temperature of 120-170 DEG C, then the mixture is diluted by the solvent, filtered, decolored, separated and purified sequentially to obtain the tri-(4-triazolyl phenyl) amine; the synthesis method of the cadmium complex is carried out by mixing 5-aminoisophthalic acid, 3-(4-triazolyl phenyl) amine and cadmium acetate into a mixed solution of water and alcohol, then the mixture is uniformly stirred under the acid or neutral condition to obtain a reaction liquid, and the reaction liquid is put into a reaction kettle to crystalize and react to obtain the tri-(4-triazolyl phenyl) amine cadmium complex. The synthesis methods obtain the tri-(4-triazolyl phenyl) amine and the tri-(4-triazolyl phenyl) amine cadmium complex, whose crystal purities are more than 95% and whose yields are more than 85%, through the simple synthesis route.

A method is disclosed for the formation of metal chelates which are able to remain stable in high alkaline environments when compared to metal chelates produced from a reaction with amino acids. The method involves the reaction of sugars, amino groups, and metal components for a sufficient period of time and temperature in a water solution. Additionally, the stability of metal chelates can be enhanced by oxidation of the sugars with an oxidizing agent such as hydrogen peroxide which form an MRP which will react with the metal component to form a more stable metal chelate than if oxidation were not utilized.

The present invention relates to sorbants such as metal-organic frameworks (MOFs), covalent organic frameworks (COFs), porous aromatic frameworks (PAFs) or porous polymer networks (PPNs) for separations of gases or liquids, gas storage, cooling, and heating applications, including, but not limited to, adsorption chillers.

A hybrid porous material including at least a first and a second porous material portion which are chemically bonded to each other and are each a different type of material.

Group II metal MOCVD precursor compositions are described having utility for MOCVD of the corresponding Group II metal-containing films. The complexes are Group II metal beta-diketonate adducts of the formula M(beta-diketonate)2(L)4 wherein M is the Group II metal and L is tetrahydrofuran. Such source reagent complexes of barium and strontium are usefully employed in the formation of barium strontium titanate and other Group II thin films on substrates for microelectronic device applications, such as integrated circuits, ferroelectric memories, switches, radiation detectors, thin-film capacitors, microelectromechanical structures (MEMS) and holographic storage media.

There is provided a metal-containing azo compound suitably used for an recording layer of an optical medium, which is represented by at least one of the following general formulae:wherein M(II) is a bivalent metal, X1 and X2 are each a residue that forms a monocyclic or polycyclic aromatic ring, Y1 and Y2 are each a residue that forms a nitrogen-containing aromatic heterocycle, and one residue is different from the other in at least one of a combination of X1 and X2, and a combination of Y1 and Y2; and there is also provided an optical recording medium of which recording layer comprises said metal-containing azo compound.

A MOF production system and method of making are detailed for continuous and controlled synthesis of MOFs and MOF composites. The system can provide optimized yields of MOFs and MOF composites greater than or equal to 95%.

The purpose of the invention is providing a micro-channel chemical preparation method of porous metal-organic framework material. The method comprises the following steps: respectively injecting a liquid medium containing one or more organic compounds with at least one unidentate ligand, a liquid medium containing one or more metal ions, a liquid medium containing a deprotonation assistant and an inert gas into a micro-channel reactor through different inlets, carrying out a coordination reaction on the above obtained mixed material liquid in the micro-channel at a certain temperature under a certain pressure to form a coordination compound, crystallizing, filtering, washing, and drying to prepare the porous metal-organic framework material, wherein the micro-channel reactor has at least two inlets and one outlet; the addition amount of the deprotonation assistant is 0-50% of the mole number of all metal ions; a ratio of the volume velocity of inert gas added into the micro-channel reactor to the bulk volume velocity of the liquid phase is 0-100:1; and the crystallization process can be omitted. The method has the characteristics of simple and safe operation, high efficiency, large throughput and easy amplification.

The invention discloses a baicalin metal complex of which the molecular formula is (C21H17O11) xM (H2O) y, wherein M in the formula is Cu (II), x is 1 and y is 2; or M is Fe (III), x is 2 and y is 0; or M is La (III) or Y (III), x is 3 and y is 0. The preparation method comprises the following steps: adding aqueous alkali into baicalin until the baicalin and alkali (sodium bicarbonate, potassium bicarbonate, sodium formate, potassium formate, sodium acetate, potassium acetate, disodium hydrogen phosphate, dipotassium hydrogen phosphate, sodium phosphate or potassium phosphate) are just completely reacted, then adding metal salt (copper salt, ferric salt, lanthanum salt or yttrium salt) for reaction to obtain the baicalin metal complex. The baicalin metal complex has obviously stronger antibacterial and antitumor activities than the baicalin, can be used for preparing antibacterial drugs and antitumor drugs, and has good development and application prospects. In the preparation method, an organic solvent is not used, a strong basic condition is not adopted, and the method is simple and feasible, is green and environment-friendly and has the advantages of low cost, high product purity and high yield.

Metal-organic framework-based molecular sieves comprising pores with a temperature-adjustable pore opening. The temperature-adjustable pore size molecular sieves comprise a plurality of metal clusters bound with a plurality of amphiphilic ligands, each ligand comprising a functionalized hydrophobic moiety and a functionalized hydrophilic moiety, and wherein the metal clusters and amphiphilic ligand hydrophilic moieties form a metal cluster layer, the metal cluster layer forming at least one hydrophilic pore. On each side of the metal cluster layer, a plurality of associated amphiphilic ligand hydrophobic moieties cooperate with the metal cluster layer to form a tri-layer and a plurality of tri-layers are held in proximity with each other to form at least one hydrophobic chamber. The hydrophobic moieties form temperature-adjustable pore size hydrophobic pores. When adjusted to a pre-selected temperature the temperature-adjustable pore openings allow for the passage of molecules having a size less than the size of the pre-selected temperature-adjustable pore opening.

Methods of forming metal alkoxides and methods of forming precursor solutions of metal alkoxides suitable for the coating of glass in the manufacture of electrochromic devices are disclosed. The method of forming metal alkoxides involves dissolving the metal halide in an anhydrous solvent and reacting it with an alcohol and (together with the addition of the alcohol or subsequently) adding an epoxide, and then evaporating-off the volatile components of the reaction product to leave a solid metal alkoxide that is substantially free of halide. The alkoxide may then be dissolved in a solvent including an alcohol (preferably ethanol) containing a small proportion of water to produce a precursor solution suitable for coating glass, the coating then being hydrolyzed to form a sol-gel and then baked to remove volatile components and to yield a thin layer of metal oxide.

A process for the preparation of a dry crystalline metal organic framework which comprises: a) spray drying at least one metal ion and at least one organic ligand which is at least bidentate into a spray dryer in the presence of a solvent, wherein the reaction of the at least one metal ion with the at least one organic ligand to yield the metal organic framework and the drying of the obtained metal organic framework take place simultaneously inside the spray dryer, and b) collecting the formed dry crystalline metal organic framework.

A method for forming a protective layer for a dielectric material in an alternating current type plasma display is provided. In this connection, a coating sol solution is provided which can form a protective layer on a large area substrate without the need to introduce any expensive equipment, the protective layer thus formed being excellent in properties such as strength, adhesion, transparency, and protective properties and capable of being formed by a sol-gel process without use of the conventional vacuum process. The sol solution comprises a dispersion of a precursor to magnesium oxide in a specific form. A method for film formation, using this solution is also provided.

Metal-organic frameworks (MOFs) are provided. An exemplary MOF includes a plurality of metal clusters, at least one linking ligand, and at least one dopant. Doped MOFs according to embodiments of the present invention have significantly increased H2 uptake capacity, and some embodiments meet the 2010 DOE H2 storage target of 6 wt % at a temperature ranging from −30 to 80° C. and a pressure less than or equal to 100 bar.

A zinc-based metal organic framework and method of making is described. The zinc-based metal organic framework is in the form of an interpenetrating diamondoid framework where each Zn²⁺ ion center is linked with four other Zn²⁺ ion centers in a distorted tetrahedral geometry. The linking occurs through diamine and dicarboxylic acid linkers. The zinc-based metal organic framework may be deposited on a transparent conducting film and used as a photoelectrode for photoelectrochemical water splitting.