462results about "Zinc organic compounds" patented technology

The present invention relates to: an electrochemical biosensor capable of effectively and sensitively detecting alfuzosin; an electrode applied thereto; a metal-organic framework (MOF) which includes a zinc / cobalt oxide and is applied in manufacturing the electrode; and methods for manufacturing same.

The present invention provides an amidinate compound represented by the following general formula (1) or a dimer compound thereof, and a method of producing a thin-film including using the compound as a raw material:where R1 and R2 each independently represent an alkyl group having 1 to 5 carbon atoms, R3 represents a hydrogen atom or an alkyl group having 1 to 5 carbon atoms, M represents a metal atom or a silicon atom, and “n” represents the valence of the atom represented by M, provided that at least one hydrogen atom of R1 to R3 is substituted with a fluorine atom.

The invention discloses a preparation method and application of a bio-based zinc adenine salt environment-friendly PVC heat stabilizer, and belongs to the field of fine chemical synthesis and plastic additive application. The nitrogen-containing organic metal heat stabilizer adenine zinc complex is prepared by taking adenine and zinc acetate as main raw materials through a one-step method. The method is simple and environment-friendly in preparation process, easily available in raw materials and suitable for industrial production. The prepared heat stabilizer zinc adenine is used as a heat stabilizer, can effectively absorb hydrogen chloride generated by PVC thermal decomposition, and can replace allyl chlorine atoms, so that the heat stability of a PVC product is improved, PVC has more excellent heat stability, and the heat stabilizer is expected to replace a traditional commercially available heat stabilizer.

Mixed metal metal-organic frameworks (MM-MOFs) of copper-1,3,5-benzenetricarboxylate (BTC), M-Cu-BTC, wherein M is Zn(II), Ni(II), Co(II), and / or Fe(II) may be made using post-synthetic exchange (PSE) with metal ions. Such MM-MOFs may be used in H2 storage, especially Ni(II) and Co(II) MM-MOFs. Selected metal exchanged materials can provide gravimetric H2 uptake around 1.63 wt. % for Zn—Cu-BTC, around 1.61 wt. % for Ni—Cu-BTC, around 1.63 wt. % for Fe—Cu-BTC, and around 1.12 wt. % for Co—Cu-BTC.

The invention provides a novel D-A-D type fluorescent probe material as well as a preparation method and application thereof. The fluorescent probe material has good stability, the preparation process is simple, and the synthesis condition is mild. Moreover, the D-A-D type fluorescent probe material has good solubility and stability, and a complex of the D-A-D type fluorescent probe material and zinc ions can identify pyrophosphate ions with high selectivity and high sensitivity. The interference of phosphate ions, hydrogen phosphate ions, dihydrogen phosphate ions, fluorine ions, chloride ions, nitrate ions, acetate ions, sulfate ions and carbonate ions is avoided; after the zinc ion complex of the D-A-D type fluorescent probe material is combined with PPi, the fluorescence intensity is remarkably enhanced, the D-A-D type fluorescent probe material has a higher signal-to-noise ratio, in-situ imaging detection of a target object in living cells or tissues is realized, the defects of a traditional molecule and ion detection method are overcome, and the D-A-D type fluorescent probe material is suitable for being widely applied to the field of biological imaging. # imgabs0 #

Proposed is a conductive hydrogel including a micelle and a metal-organic framework / surfactant composite.

The heat resistance of an organic semiconductor device including a step of forming an aluminum oxide film over and in contact with an organic semiconductor layer is improved. A heating step is performed after a layer containing an organometallic compound for a mask for an organic semiconductor layer, which is represented by General Formula (G1) below, is provided over the organic semiconductor layer.In General Formula (G1), Ar represents a substituted or unsubstituted aryl group having 6 to 30 carbon atoms or a substituted or unsubstituted heteroaryl group having 1 to 30 carbon atoms, X represents oxygen or sulfur, M represents a metal, n represents an integer greater than or equal to 1 and less than or equal to 5, and n is the same as the valence of the metal M. Note that when n is greater than or equal to 2, a plurality of Ars may be the same or different and Xs may be the same or different. When Ar represents the substituted or unsubstituted heteroaryl group having 1 to 30 carbon atoms, a heteroatom of the heteroaryl group may be coordinated to the metal M.

Disclosed herein are transition and / or heavy metal cation-capturing membranes constructed from zinc imidazole salicylaldoxime (ZIOS) nanosheets deposited on membrane supports, and methods of making and using such metal cation-capturing membranes. In a non-limiting embodiment, the membrane support comprises polyvinylidene fluoride (PVDF) membranes which have been modified with polydopamine (PDA) and polyethyleneimine (PEI). Three exemplary methods for fabricating the metal cation-capturing membranes include (1) in-solution hydrothermal growth, (2) vacuum-assisted coordination growth, and (3) interfacial coordination growth methods. The membranes may be tuned regarding textural properties and the adhesion of the ZIOS to the membrane support.

The invention discloses a Schiff base catalyst for copolymerization of epoxide and carbon disulfide, and relates to the technical field of Schiff base catalysts. The invention provides a structural general formula of the Schiff base catalyst and a specific structural formula in 6, and also provides a preparation method of the Schiff base catalyst. Different numbers of methyl, fluorine and other functional groups are introduced to improve the selectivity of the catalyst to the reaction.

The invention provides a complex comprising Zn2+ and a compound of formula (I): or a deuterated analog thereof, or an ion or poly-ion thereof, or a salt thereof that is useful for treating cancer, as well as compositions and kits comprising such complexes.

The present application discloses a dialkylphosphinic acid hybrid salt and its preparation method and use, and the dialkylphosphinic acid hybrid salt is at least one selected from compounds having the chemical formula shown in formula (I). The dialkylphosphinic acid hybrid salt having the composition of formula (I) according to the present application has a small amount of addition, a high flame retardant efficiency for various polymeric materials, and is economically excellent, which not only overcomes the disadvantages of diethylphosphinic acid salt, which is low in flame retardant efficiency for polymeric materials, but also overcomes the disadvantages of diisobutylphosphinic acid salt, which is too volatile and low in flame retardant efficiency for polyester, but can also be widely used in the flame retardancy of various polymeric materials that require high-temperature processing. JPEG2024536906000030.jpg50153

A method of promoting growth in a photosynthetic organism comprising treating the photosynthetic organism with a metal complex or a precursor thereof, wherein the metal complex comprises a metal selected from the group consisting of zinc (Zn), cobalt (Co), copper (Cu), nickel (Ni) and iron (Fe), and a ligand, which is a bidentate or tridentate ligand. Metal complexes and their ligands are also describe.

To provide a polystyrene-polyolefin-polystyrene triblock copolymer and a method for producing the same.SOLUTION: There is provided a polystyrene-polyolefin-polystyrene triblock copolymer represented by the following chemical formula 7. (Ar is an aryl group having 6 to 20 carbon atoms; the average value of m is 20 to 10000; Y and Y' independently are any one of H, methyl, ethyl, butyl, hexyl and octyl and Y and Y' are not identical to each other; p and 1-p are a molar fraction of each repeating unit constituting a repeating unit body n and the value of p is 0 to 1; the average value of n is 40 to 10000; R2 to R3 independently are H or hydrocarbyl having 1 to 20 carbon atoms; and z is an integer of 0 to 10.)SELECTED DRAWING: None

The application discloses an energetic material, a preparation method thereof and application of the energetic material as explosives and self-ignition propellants. I C 12 H 12 N 10 or M Ⅱ C8H6N8; wherein, M I is selected from Co, Ni and Cu; M Ⅱ is selected from Zn. The energetic material is convenient to synthesize, has good thermal stability, excellent mechanical sensitivity, excellent propelling performance and specific impulse, has a significant energy density advantage, can effectively solve the problem of continuous evaporation of hydrazine propellants during storage, avoid the risk of internal pressure increase of a fuel tank, and overcome the problems of liquid fuel in the storage and transportation process. Therefore, the innovative high-performance energetic material has excellent performance and wide application potential, and has great commercial value in the fields of aviation, aerospace and military.

The present invention discloses a method and system for producing hexafluorobutadiene, which includes the following steps: In step (1), an organic solution of bromotrifluoroethylene and zinc powder are respectively introduced into a first reactor containing an initiator, zinc powder, and an organic solvent, followed by a second reactor, and reacted to obtain a trifluorovinylzinc bromide solution. The reaction solution is then introduced into a precipitator to separate excess zinc powder, resulting in a zinc-free trifluorovinylzinc bromide solution. The excess zinc powder is then filtered and reused. In step (2), the trifluorovinylzinc bromide solution obtained above and a pre-prepared composite catalyst solution are introduced into a third reactor and subjected to a coupling reaction to obtain crude hexafluorobutadiene. In step (3), the crude hexafluorobutadiene obtained above is purified to obtain a product with a purity of ≥ 99.9%.

The application discloses an 8-hydroxyquinoline anticancer zinc (II) complex and a synthesis method and application thereof. The 8-hydroxyquinoline anticancer zinc (II) complex is synthesized by taking 5,7-diiodo-8-hydroxyquinoline, 5,7-dichloro-8-hydroxyquinoline, 5-chloro-7-iodo-8-hydroxyquinoline, 5,7-dibromo-8-hydroxyquinoline and 5-chloro-8-hydroxyquinoline as a first ligand and taking 4,4'-dimethoxy-2,2'-bipyridine, 4,4-di-tert-butyl-2,2-bipyridine, 5,5'-dimethyl-2,2-bipyridine, 2,2-bipyridine and 4,4'-dimethyl-2,2'-bipyridine as auxiliary ligands. The 8-hydroxyquinoline anticancer zinc (II) complex has good inhibiting effect on SK-OV-3CR cells of an ovarian cancer drug-resistant strain, is higher than that of cisplatin drugs, overcomes drug resistance of clinical drugs, has potential medicinal value and can be used for preparation of various antitumor drugs.

The invention relates to a hydrogen sensor material comprising at least one rod-shaped single crystal having wurtzite structure composed of a semiconductor and a conversion layer formed by an MOF on the surface of the single crystal, where the single crystal has a length of 100 nm to 100 pm and a lateral extent of 500 nm to 10 pm and where the aspect ratio of the single crystal of length to lateral extent is greater than 3. The invention further relates to a production process for a hydrogen sensor material.

The present invention relates to a display device comprisinga plurality of OLED pixels comprising at least two OLED pixels, the OLED pixels comprising an anode, a cathode, and a stack of organic layers, wherein the stack of organic layersis arranged between and in contact with the cathode and the anode, andcomprises a first electron transport layer, a first hole transport layer, and a first light emitting layer provided between the first hole transport layer and the first electron transport layer, anda driving circuit configured to separately driving the pixels of the plurality of OLED pixels,wherein, for the plurality of OLED pixels, the first hole transport layer is provided in the stack of organic layers as a common hole transport layer shared by the plurality of OLED pixels, and the first hole transport layer comprises(i) at least one first hole transport matrix compound consisting of covalently bound atoms and(ii) at least one electrical p-dopant selected from metal salts and from electrically neutral metal complexes comprising a metal cation and at least one anion and / or at least one anionic ligand consisting of at least 4 covalently bound atoms,wherein the metal cation of the electrical p-dopant is selected from alkali metals; alkaline earth metals, Pb, Mn, Fe, Co, Ni, Zn, Cd; rare earth metals in oxidation state (II) or (III); Al, Ga, In; and from Sn, Ti, Zr, Hf, V, Nb, Ta, Cr, Mo and W in oxidation state (IV) or less, a method for preparing the display device and a chemical compound for use therein.

A coloring composition includes at least one compound S selected from a compound S-1 represented by Formula (1) or a compound S-2 in which the compound S-1 is coordinated to a metal atom, a pigment, a resin P, and a solvent, in which the resin P includes at least one selected from a graft resin P-1 having a specific graft chain, a block copolymer P-2 including a specific structure, or a resin P-3 in which at least one terminal of a polymer chain including a specific structure is capped with an acid group.

Provided are bacteriochlorin derivatives with narrow band emission. In some embodiments, the bacteriochlorin derivatives are PEGylated. In some embodiments, the bacteriochlorin derivatives have high water solubility (e.g., 10 mg / mL or more). In some embodiments the bacteriochlorin derivatives are PEGylated and have high water solubility. The bacteriochlorin derivatives can include bioconjugatable groups for forming conjugates, for example, with antibodies and nanoparticles. The bacteriochlorin derivatives and their conjugates can be used in imaging and therapeutic applications. Methods of synthesizing the bacteriochlorin derivatives are also provided.

The invention relates to the technical field of metal organic complexes, in particular to a fluorene-containing alkyl zinc complex and a preparation method and application thereof, and the preparation method comprises the following steps: adding fluorene, potassium tert-butoxide and sodium methoxide into a solvent, and reacting to obtain 9-fluorene formaldehyde; the preparation method comprises the following steps: dissolving 9-fluorene formaldehyde in a solvent, adding an amino compound and a catalyst, and reacting to obtain a formyl fluorene imine ligand; and reacting the formyl fluorene imine ligand with zinc alkyl to obtain the zinc alkyl complex. The invention provides a fluorenyl-containing zinc complex as well as a preparation method and application thereof. The fluorenyl-containing zinc complex is short in reaction route, simple and convenient to operate and capable of efficiently catalyzing an imine hydroboration reaction. Meanwhile, the fluorenyl-containing zinc complex disclosed by the invention is used as a catalyst, is small in usage amount, mild in reaction condition and high in yield, and can catalyze hydroboration reaction of various compounds.

A metal-organic framework according to the present invention provides a metal-organic framework satisfying chemical formula 1. (Chemical formula 1) M+COO--(CH2)n- COO-M+ (M is a metal having a standard reduction potential of -0.8 V to 1.8 V, and n is an integer between 2 and 15.)

Disclosed is a compound of formula (I), its hydrate, anhydrous or salt form thereof, wherein M, X and n are as disclosed herein. The compounds can be used modulating activity of aryl hydrocarbon receptor (AhR), and for treatment of diseases associated with modulating AhR activity. Also disclosed are pharmaceutical compositions containing the compound of formula (I), its hydrate, anhydrous or salt form thereof. (Formula I)

To provide a novel electrofluorochromic sheet containing a metallosupramolecular polymer.SOLUTION: An electrofluorochromic sheet includes a metallosupramolecular polymer formed by alternately connecting a cation of an element A selected from metal elements or lanthanoid elements and an organic ligand by a binding form containing at least one selected from the group consisting of a coordination bond and an organometallic bond, in which the organic ligand has, between cations, depending on the binding form, two or more coordination sites forming at least one luminous complex selected from the group consisting of the metal complex and an organometallic complex in one molecule, and has one or more redox response sites causing a redox reaction by application of a potential, the redox response site has at least one or more nitrogen atoms, and in the organic ligand, the coordination site and the redox response site are directly bonded or are bonded via a spacer site.SELECTED DRAWING: Figure 9

A zinc carboxylate salt used in production of a semiconductor nanoparticle, in which a ratio of carboxylic acids having 8 to 10 carbon atoms in whole of carboxylic acids that form the zinc carboxylate salt is 80.0% by mass or more, and an average branching degree of the whole of the carboxylic acids that form the zinc carboxylate salt is in the range of 1.1 to 2.9. The present invention can provide a zinc salt used for easily producing a semiconductor nanoparticle having a core / shell type structure that has excellent optical properties in the case where two or more types of shell precursors are used to produce the semiconductor nanoparticle having a core / shell type structure.

The invention relates to a multi-metal zinc complex, a preparation method and application in polymer depolymerization. The multi-metal zinc complex forms a stable coordinate bond with an organic ligand molecular skeleton, shows excellent chemical stability and substrate adaptability, and can efficiently catalyze the depolymerization reaction of various polymers in a temperature range of 100-250 DEG C. In addition, the ligand framework has adjustability, polymer substrates with different compositions and structures can be optimized, and high-yield recovery of various types of monomers is realized. The catalytic system has wide applicability, can catalyze the bulk depolymerization of the polymer, and also can catalyze the depolymerization in the presence of a nucleophilic reagent. Through a multi-metal concerted catalysis mechanism, the dosage of the catalyst is remarkably reduced, various polymers with the number-average molecular weight in the range of 3.8-807.5 kg / mol can be depolymerized, the depolymerization reaction time is 0.5-24.0 h, side reactions are remarkably inhibited, and excellent industrial application prospects are shown.

To provide a production method for a phthalocyanine compound that enables high-purity production of a phthalocyanine compound having an ester side chain.SOLUTION: A method for producing a phthalocyanine compound comprises a step of mixing a phthalonitrile compound represented by general formula (1), a metal compound, and a compound represented by general formula (5), wherein in general formula (1), Z1 to Z4 each independently represent a hydrogen atom, a halogen atom, an alkoxy group, or the like, and at least one of Z1 to Z4 is a substituent represented by general formula (2); in general formula (2), L represents an alkylene or arylene group, and R represents an alkyl group or an aryl group; and in general formula (5), R is the same as R in general formula (2).SELECTED DRAWING: None