948 results about "Diimine" patented technology

The invention discloses an alpha-nickel diimine compound olefin polymerization catalyst and a preparation method thereof, and a method for preparing branched polyethylene. Structural formulas of the alpha-nickel diimine compound olefin polymerization catalyst are shown as a formula (I) and a formula (II), and the preparation method of the alpha-nickel diimine compound olefin polymerization catalyst is simple and low in cost, and can catalyze ethylene polymerization with high activity at a temperature of more than or equal to 80 DEG C to obtain high molecular weight polyethylene. The polyethylene prepared by catalyzing of the alpha-nickel diimine compound olefin polymerization catalyst has high molecular weight, and can prepare molecular weight which reaches more than 10<2>*kg / mol in the temperature range of between 0 and 80 DEG C.

The invention discloses an alpha-nickel diimine compound olefin polymerization catalyst, a preparation method and a method for preparing branched polyethylene. The structural formula of the alpha-nickel diimine compound olefin polymerization catalyst is shown as the formula (I) and the formula (II). The alpha-nickel diimine compound olefin polymerization catalyst has simple preparation method and low cost, and ethylene can be catalyzed to polymerize with high activity at a temperature not lower than 80 DEG C to obtain high molecular weight polyethylene. The polyethylene prepared from the alpha-nickel diimine compound olefin polymerization catalyst by catalyzing has high molecular weight, and the molecular weight can reach higher than 102x kg / mol within the range of 0-80 DEG C.

The invention relates to the use of an organic mesomeric compound as organic dopant for doping an organic semiconducting matrix material for varying the electrical properties thereof. In order to be able to handle organic semiconductors more easily in the production process and to be able to produce electronic components with doped organic semiconductors more reproducibly, a quinone or quinone derivative or a 1,3,2-dioxaborine or a 1,3,2-dioxaborine derivative may be used as a mesomeric compound, which under like evaporation conditions has a lower volatility than tetrafluorotetracyanoquinonedimethane (F4TCNQ).

Disclosed herein are manganese, iron, cobalt, or nickel complexes containing terdentate pyridine diimine ligands and their use as efficient and selective hydrosilylation catalysts.

The invention relates to the field of catalytic polymerization of olefins, aiming at providing an ethylene acenaphthylene (alpha-diimine) nickel complex / alkyl aluminum chloride combined catalyst. The combined catalyst consists of an ethylene acenaphthylene (alpha-diimine) nickel complex and alkyl aluminum chloride, wherein the molar ratio of aluminum in alkyl aluminum chloride to nickel in the ethylene acenaphthylene (alpha-diimine) nickel complex is 20-800:1. Compared with the prior art, the combined catalyst provided by the invention has higher activity and better stability in catalyzing polymerization of ethylene and propene. According to the invention, alkyl aluminum chloride is used as a cocatalyst. Compared with that of using methylaluminoxane or modified methyl aluminoxane, cost is significantly reduced, and in addition, localization of alkyl aluminum chloride is realized, saving the need of importing.

A metalorganic complex composition comprising a metalorganic complex selected from the group consisting of: metalorganic complexes comprising one or more metal central atoms coordinated to one or more monodentate or multidentate organic ligands, and complexed with one or more complexing monodentate or multidentate ligands containing one or more atoms independently selected from the group consisting of atoms of the elements C, N, H, S, O and F; wherein when the number of metal atoms is one and concurrently the number of complexing monodentate or multidentate ligands is one, then the complexing monodentate or multidentate ligand of the metalorganic complex is selected from the group consisting of beta-ketoiminates, beta-diiminates, C2-C10 alkenyl, C2-C15 cycloalkenyl and C6-C10 aryl.

The invention provides an ionic liquid consisting of the anions of diimine (vikane) and (perfluoroalkglsulfonyl fluorosulfonyl group) imine and the cation of sulfonium salt, ammonium salt or phosphor salt, as well as method for preparing the ionic liquid through diimine (vikane) and (perfluoroalkglsulfonyl fluorosulfonyl group) imine alkali salt. The ionic liquid can be used as an electrolyte material and applied on the fields like secondary lithium ion batteries, super capacitors, etc.

The invention relates to neutral mononuclear copper (I) complexes for emitting light and with a structure according to formula (A) in which: M represents: Cu(I); L∩L represents: a single, negatively charged, bidentate ligand; N∩N represents: a diimine ligand (substituted with R and FG), in particular a substituted 2,2′-bipyridine derivative (bpy) or a substituted 1,10-phenanthroline derivative (phen); R represents: at least one sterically demanding substituent for preventing the planarisation of the complex in the excited state; FG=functional group, and represents: at least one second substituent for increasing solubility in organic solvents. The substituent can also be used for electron transport or alternatively for hole transport, said functional group being bound to the diimine ligands either directly or by means of suitable bridges; and the copper (I) complex: having a ΔE(S1−T1) value of less than 2500 cm−1 between the lowest excited singlet state (S1) and the triplet state (T1) which lies below; having an emission lifespan of at most 20 μs; having an emission quantum yield of greater than 40%, and a solubility of at least 1 g / L in organic solvents, in particular polar organic hydrocarbons such as acetone, methyl ethyl ketone, benzene, toluene, chlorobenzene, dichlorobenzene, dichloromethane, chloroform, dichloroethane, tetrachloroethylene, alcohols, acetonitrile or water.

A UV-protective composition comprising a water-soluble polyaminoamide containing 1,3-diimine groups, wherein the polyaminoamide containing 1,3-diimine groups absorbs ultraviolet light radiation having a wavelength of about 200 nm to about 420 nm, and methods of treating substrates with the UV-protective polyaminoamide containing 1,3-diimine groups.

The invention provides a diimine ligand compound as shown in a formula (I) which is defined in the specification and a preparation method thereof. In the formula I, R1 to R10 are same or different and are independently selected from a group consisting of hydrogen, saturated or unsaturated alkyl groups, oxyl groups and halogen. The invention also relates to the preparation method for the diimine ligand compound, a complex containinging the diimine ligand compound, and a preparation method and application of the complex. As a catalyst composition obtained in the invention is applied to ethylene homopolymerization, polymerization activity is high under a high-temperature polymerization condition (50 to 100 DEG C); and an obtained polymer has high molecular weight and narrow molecular weight distribution.

The invention provides a diimine ligand compound as shown in a formula (I) which is defined in the specification and a preparation method thereof. In the formula I, R1 to R10 are same or different and are independently selected from a group consisting of hydrogen, saturated or unsaturated alkyl groups, oxyl groups and halogen. The invention also relates to the preparation method for the diimine ligand compound, a complex containinging the diimine ligand compound, and a preparation method and application of the complex. As a catalyst composition obtained in the invention is applied to ethylene homopolymerization, polymerization activity is as high as 3.84 * 10<6> g / mol(Ni) / h under a high-temperature polymerization condition (50 to 100 DEG C); and an obtained polymer has high molecular weight and narrow molecular weight distribution.

The invention discloses a preparation method for binuclear acenaphthene (alpha-diimine) nickel / palladium catalysts for olefins and application of the catalysts in catalysis of polymerization of olefins. The binuclear acenaphthene (alpha-diimine) nickel / palladium catalysts for olefins in the invention have structural formulas as represented by formula (I) and formula (II) in the specification. The binuclear acenaphthene (alpha-diimine) palladium catalyst for polymerization of olefins has high activity and good stability and can be used for preparing high-molecular-weight hyperbranched polyethylene with bimodal distribution; the binuclear acenaphthene (alpha-diimine) nickel catalyst for polymerization of olefins has high activity and good stability and can be used for preparing polypropylene with a weight-average molecular weight of more than 100,000 and thermoplastic elastomers with elasticity and a high molecular weight. The preparation method for the synthesized catalysts used for polymerization of olefins has the advantages of a simple process, a short synthetic route, low cost, high yield and easy industrialization.

An adhesive composition that is capable of achieving a superior combination of process characteristics such as adherend fill properties (embedability) and low-temperature lamination properties, and semiconductor device reliability such as reflow resistance, as well as a film-like adhesive, an adhesive sheet that exhibits excellent process characteristics including ready releasability from dicing sheets, and a semiconductor device that exhibits excellent productivity, superior adhesive strength when heated and superior moisture resistance, all of which use the adhesive composition. The adhesive composition comprises (A) a thermoplastic resin, (B) a bisallylnadimide represented by a general formula (I) shown below, and (C) a bifunctional or higher (meth)acrylate compound.(wherein, R1 represents a bivalent organic group containing an aromatic ring and / or a straight-chain, branched or cyclic aliphatic hydrocarbon).

The invention discloses a tridentate nitrogen ligand 2,6-diimine pyridine contained iron or cobalt complex and a preparation method thereof. The structural formula of the complex is shown in a formula I, wherein M is iron or cobalt, and R1 and R2 are selected from any one of hydrogen and alkyl. The preparation method is as follows: under anaerobic conditions, a ligand shown in a formula IV is reacted with FeCl2 4H2O or CoCl2 to obtain the complex shown in the formula I. The N ^ N ^ N ligand containing asymmetric 2,6-diimine pyridine ligand and iron metal complex is synthesized, and the metal complex is used for catalyzing an ethylene polymerization reaction, and shows high catalytic activity. The obtained polymer has a high molecular weight, the catalyst has strong tolerance to high temperature, for example, at a higher temperature (80 DEG C), the iron (II) complex shows high polymerization activity on ethylene, and the polymerization activity can reach 2.2*107g mol<-1> (Fe) h<-1>; and the metal complex has wide industrial application prospects. (Formula I) (Formula IV).

The present invention relates to the use of perylene diimide derivatives as air-stable n-type organic semiconductors.

A polyolefin polymer comprising one or more terminal polymerizable methacryloyl groups (i.e. tethered to the main body of the polymer) and a novel process for preparing same are herein disclosed. A hyperbranched polyethylene polymer and a process for preparing same are also disclosed. The polymer is prepared by a novel one-pot copolymerization reaction of an olefin, such as ethylene, and a heterobifunctional comonomer comprising a methacryloyl group, catalyzed by a late transition metal α-diimine catalyst which is selectively non-reactive towards methacryloyl groups. The process allows for preparation of polymers with various chain topologies, including linear, branched, and hyperbranched topologies. The terminal methacryloyl groups within the polymer are reactive in further polymerization reactions. Thus, the polymer may be used in materials and applications which require cross-linking or further polymerization, for example, UV / thermal / radical curable crosslinkers for use in thermoset applications.

The invention discloses a preparation method of a polyamide composite nanofiltration membrane, which comprises the following steps of partially hydrolyzing a polyacrylonitrile-based membrane under alkaline and heat treatment conditions, and activating the membrane in 1-ethyl-(3-dimethyl amino propyl) carbonyl diimine hydrochloride ethylene dichloride-hydrogen chloride (EDC-HCl) and N-hydroxyl succinimide (NHS); and then sequentially immersing the membrane in water phase monomer piperazine with low concentration and organic phase monomer benzenetricarbonyl trichloride, and the polyamide composite nanofiltration membrane is prepared by interfacial polymerization. The preparation method of the polyamide composite nanofiltration membrane has the advantages that compared with a traditional method, the method utilizes monomer solution with low concentration to perform the interfacial polymerization, high permeation flux can be obtained under ultra-low pressure (0.1MPa), and filter dye solution and saline solution have high separation selectivity.

The present invention relates to novel 1,3-diimine copper complexes and the use of 1,3-diimine copper complexes for the deposition of copper on substrates or in or on porous solids in an Atomic Layer Deposition process.

The invention discloses a bis (imino) pyridine iron olefin polymerization catalyst and a preparation method and application thereof. The catalyst is a novel bis(imino)pyridine iron complex with the asymmetric substitution of position 2 and 6 of an aromatic ring; and the structural formula of the catalyst is shown in formula (I), wherein X is halogen, R1 is alkyl, and R2 is the alkyl or oxyl. The catalyst can be obtained through a Friedel-Crafts reaction, a ketoamine condensation reaction and a coordination reaction. The preparation method is simple, and raw materials are cheap. The catalyst can catalyze the polymerization of ethylene under the activation of MAO to prepare polyethylene with high molecular weight and wide distribution.

The invention discloses a novel late transition metal alpha-diimine nickel (II) olefin polymerization catalyst with a symmetrical structure. The catalyst is a didentate coordination compound formed by an alpha-diimine ligand with a symmetrical Schiff base structure and a halogenide of later transition metal nickel (II). In the presence of diethyl aluminium chloride (DEAC) used as a cocatalyst, the coordination compound catalyst of nickel has higher activity for catalyzing ethylene to polymerize, which can reach 107gPE / (mol Ni h Bar), and obtained polyethylene has higher degree of branching, which can reach 114 branched chains per 1,000C.

The invention discloses a preparation method of an injectable hyaluronic acid hydrogel. The method comprises the following steps: initiating a condensation reaction of an amino group of adipic dihydrazide and a carboxyl group of the main chain of HA (hyaluronic acid) by 1-ethyl-3-(3-dimethylamino)carbodiimide hydrochloride to obtain a hyaluronic acid-adipic dihydrazide (HA-ADH) derivative with the main chain possessing the amino group, and reacting N-acryloxysuccinimide with the amino group of the HA-ADH to obtain an acrylate functionalized hyaluronic acid derivative; and cross-linking the acrylate functionalized hyaluronic acid derivative with a bismercapto cross-linking agent to form the injectable hyaluronic acid hydrogel. The above acrylate functionalized HA-AC synthesis method is simple and easy, and is suitable for industrial amplified production; the environmental protection, biological inertness and reaction speed controllability of a Michael addition reaction lay a good foundation for the application of the Michael addition reaction in the injectable hyaluronic acid hydrogel; and the HA-AC chemically cross-linked hydrogel has better stability and mechanical performances than physically associated injectable gels.

Metal ketoiminate or diiminate complexes, containing copper, silver, gold, cobalt, ruthenium, rhodium, platinum, palladium, nickel, osmium, or indium, and methods for making and using same are described herein. In certain embodiments, the metal complexes described herein may be used as precursors to deposit metal and metal-containing films on a substrate through, for example, atomic layer deposition or chemical vapor deposition conditions.

α-Olefins are made in a modified plug flow reactor system by the oligomerization of ethylene using an iron complex of a selected diimine of a 2,6-pyridinecarboxaldehyde(bisimine) or 2,6-diacylpyridine(bisimine) as the oligomerization catalyst. The reactor is modified to add the iron complex at two or more points along the length of the plug flow reactor, the distance between addition points being dependent on the half-life of the active ethylene oligomerization catalyst.

The invention discloses a beta-diketiminate divalent rare earth boron hydrogen complex and a preparation method and application thereof. In the method, a beta-diimine rare earth dichloride and NaBH4 have a reaction in a tetrahydrofuran solvent and are reduced through in-situ Na / K to obtain the beta-diketiminate divalent rare earth boron hydrogen complex with the molecular structural formula being [2,6-ipr2-(C6H3)-NC(Me) CHC (Me) N-(C6H3)-2,6-ipr2] Ln-BH4.2THF. The beta-diketiminate divalent rare earth boron hydrogen complex can highly actively catalyze the reaction between aldehyde and phosphite ester under the mild condition and has the advantages that the reaction time is short, the reaction condition is mild, and a follow-up treatment method is easy and convenient to implement.

An organic semiconducting composition consists essentially of an N,N-dicycloalkyl-substituted naphthalene diimide and a polymer additive comprising an insulating or semiconducting polymer having a permittivity at 1000 Hz of at least 1.5 and up to and including 5. This composition can be used to provide a semiconducting layer in a thin-film transistor that can be incorporated into a variety of electronic devices.

The invention relates to a synthesis method of a cooper (I) phosphorescent complexes using a 8-phosphinoquinoline derivative as a ligand and application thereof in an organic electroluminescence device. The cooper (I) complexes has an asymmetric bidentate N^P type ligand, and compared with the traditional cooper (I) phosphorescent complexes using a diimine / triphenylphosphine mixed ligand, the invention has better photochemical and electrochemical stability, which ensures that the invention becomes an ideal material for preparing the organic electroluminescence device.

The invention discloses a preparation method of an amido-imine nickel catalyst and application of the amido-imine nickel catalyst to catalyzing vinyl polymerization. The complex has the structures of a formula (I) and a formula (II) shown in the specification, wherein R1 is hydrogen or alkyl, R2 is hydrogen or alkyl, R3 is hydrogen or alkyl, R4 is hydrogen or alkyl, and X is halogen. The preparation method of the complex comprises the following steps of: carrying out condensation reaction on a diketone compound and phenylamine through ketoamine to obtain an diimine compound; then reacting with trimethyl aluminum, and hydrolyzing to obtain an amido-imine ligand; finally carrying out coordination reaction on the amido-imine ligand and (DME)NiX2 under the condition without water and oxygen to obtain a nickel complex. The complex disclosed by the invention has a specific ligand replacement structure and can be used for catalyzing the vinyl polymerization under the activation of modified methyl aluminium oxane or alkyl aluminum, showing the characteristics of living polymerization under specific conditions and obtaining the high-molecular-weight narrowly-distributed branched polyethylene.

The invention provides a chemical approach which can adopt point-and-click chemistry to realize functional grouping on the bodies or the surfaces of high molecular hydrogel particles. The high molecular hydrogel particles are generally formed by the cross linking of a hydrophilic monomer and a functional group monomer. The invention mainly puts forward a point-and-click functional group which can be introduced by adopting a copolymerization mode and can carry out a 1,3-dipolar cycloaddition reaction of triazo-end alkynyl catalyzed by Cu (I). Simultaneously, a point-and-click reaction catalyzed by the Cu (I) and a coupling reaction of carboxyl-primary amine radicals initiated by 1-(3-dimethylin propyl)-3-ethyl carbon diimine hydrochloride are carried out in a water phase, are not disturbed mutually and are mutually orthogonal. The characteristic can be beneficial to the multi-function grouping of the microgel simultaneously. The temperature / pH-sensibility microgel containing the point-and-click functional group has potential application value in the aspects of targeting medicine release, molecular treatment, chemical / biologic sensors, water treatment and the like.

The invention discloses a catalyst system for ethylene polymerization, comprising three components a, b and c. The component a is a pyridine diimine ligand with a structural formula (I) or a structural formula (II); the component b is an acetylacetone salt compound; the component c is an aid catalyst; a mol ratio of the component b to the component a is (0.01-100):1; and a mol ratio of the component c to the component b is (10-10,000):1. The invention also discloses the applications of the catalyst system in the preparation of single-peak distributed polyethylene, double-peak distributed polyethylene, polyethylene with super high molecular weight and an ethylene oligomer by the ethylene polymerization.