133results about "Nickel organic compounds" patented technology

This invention relates to nickel catalysts with alkali ions for homopolymerization and copolymerization.

The invention discloses a neutral phosphine phenol nickel catalyst based on a tert-butyl structure. The catalyst has a structure shown as a formula (I), wherein R1 and R2 are respectively and independently selected from hydrogen, C1-C20 alkyl, fluorine, chlorine, bromine, iodine, nitryl, hydroxyl, substituted silicon group and C1-C20 substituted alkyl; r3 is independently selected from C1-C20 alkyl, C1-C20 substituted alkyl, phenyl or substituted phenyl, R4 and R5 are independently selected from hydrogen, fluorine, chlorine, bromine, iodine, C1-C20 alkyl, aryl, an oxygen-containing group, a nitrogen-containing group, a sulfur-containing group, a boron-containing group, an aluminum-containing group, a phosphorus-containing group, a silicon-containing group or a tin-containing group; tert-butyl is introduced into para-position and meta-position of a ligand phenol oxygen ring, and a protection barrier is formed by utilizing the steric hindrance effect of the t-butyl, so that decomposition and deactivation of the catalyst under a high-temperature condition are inhibited, the catalyst can stably play a catalytic role in an industrial common medium-high-temperature polymerization environment, and the process adaptation range of the catalyst is widened.

The invention provides an alpha-diimine ligand compound, an alpha-diimine nickel catalyst and a preparation method and application of the alpha-diimine ligand compound and the alpha-diimine nickel catalyst, and belongs to the technical field of organic synthesis. Wherein R1 is selected from hydrogen, methoxyl or tertiary butyl; r2 is selected from methyl, ethyl or isopropyl; and R3 is selected from hydrogen or methyl. The alpha-diimine nickel catalyst prepared by adopting the alpha-diimine ligand compound can catalyze olefin to carry out homopolymerization reaction or copolymerization reaction, so that not only is excellent catalytic performance shown, but also a polyolefin material obtained by catalyzing olefin monomer homopolymerization reaction has excellent elastic recovery performance; and the catalyst has certain application potential in olefin polymerization industry.

The invention provides a transition metal nickel complex as well as a preparation method and application thereof. The transition metal nickel complex has a structure as shown in a formula (I), wherein R1, R2, R3, R4 and R5 are independently selected from the following groups substituted by one or more Ra: H, C1-6 alkyl, C1-6 alkoxy, C6-20 aryl or C6-20 heteroatom aryl. The complex provided by the invention has higher catalytic activity and stability in catalysis of olefin polymerization, especially for polymerization of ethylene, has very strong regulation and control performance on the molecular weight of polyethylene, and can be used for preparing highly branched polyethylene.

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.)

A method for producing a metal-organic framework, a metal-organic framework produced therefrom, and a solid-state battery anode comprising the metal-organic framework are provided. The method comprises preparing a precursor solution by introducing a basic additive into a mixed solution containing a co-precursor and an organic ligand (S1), introducing a nickel precursor into the precursor solution and obtaining a precipitate (S2), and obtaining the metal-organic framework by purifying and drying the precipitate (S3).

The present invention relates to a method for the deuteration of organic compounds, particularly the deuteration of silanes (primary, secondary, and tertiary), as well as of the particular borane "pinacolborane", by reacting deuterium gas (D2) and said silanes and / or borane at certain deuteration reaction conditions in the presence of a deuteration reaction catalyst which is an organometallic complex comprising Ni (II) and an organic ligand comprising phosphorous and boron.

The invention provides a bidentate aza-matched nickel complex, a preparation method and a nickel metal catalyst for catalyzing olefin polymerization, the bidentate aza-matched nickel complex has a structure as shown in a formula (I), in the formula (I), R1 and R2 are the same or different, and are independently selected from substituted or unsubstituted C1-C10 alkyl, C1-C10 alkoxy, C2-C10 alkenyl or C6-C10 aryl, and R2 and R3 are the same or different and are independently selected from substituted or unsubstituted C1-C10 alkyl, C1-C10 alkoxy, C2-C10 alkenyl or C6-C10 aryl; r3 is selected from hydrogen, methyl, methoxyl and trifluoromethyl; x is selected from chlorine or bromine. According to the bidentate aza-nickel complex provided by the invention, the binding force between amido and nickel metal is stronger, and meanwhile, the imine is substituted by aryl, so that the nickel metal catalyst has a higher heat stabilizer, and is obviously superior to the traditional alpha-diimine nickel catalyst.

The invention relates to the technical field of catalysts, in particular to a neutral nickel catalyst as well as a ligand, a preparation method and application thereof, and the ligand has a structure as shown in a formula I. According to the invention, a series of novel neutral nickel complexes with sandwich-like structures are developed based on an amide-aryl ketone skeleton structure for the first time; the series of catalysts are simple and efficient to synthesize, the ligand synthesis yield is greater than or equal to 80%, and the catalyst synthesis yield is greater than or equal to 80%; nuclear magnetic resonance monitoring shows that the nickel catalyst provided by the invention has high stability in air and does not deteriorate within 72 hours; during polymerization, no extra cocatalyst needs to be added, and the catalyst shows extremely excellent thermal stability and capability of inhibiting chain transfer side reaction in a solution copolymerization process and can resist poisoning of acrylate monomers at the same time.

The application provides an alpha-diamino nickel complex for catalytically preparing polyethylene, realizes control of polymer molecular weight and branching degree by regulating N-aryl ortho groups in the alpha-diamino nickel complex molecules and polymerization conditions, and has the advantages of high catalytic activity, low cost, stable performance and the like. The prepared polyethylene has high molecular weight, narrow molecular weight distribution, high branching degree and excellent mechanical mechanical performance.

The present application relates to a kind of diimine ligand with the general structure shown in formula L, the post-transition metal catalyst prepared by its coordination and its preparation method and application, wherein R1-R6 are independently selected from H, C1-C6 alkyl, C1-C6 alkoxy, C6-C 12 Aryl or halogen. The present application constructs diimine post-transition metal catalyst with different chemical environment of bimetallic active site and rigid parent ring skeleton structure, not only improves catalytic activity and thermal stability, but also can be used for preparing bimodal UHMWPE by ethylene polymerization.

This invention provides a highly thermally stable, photoresponsive α-diimine nickel complex, its synthesis method, and its applications, aiming to develop novel olefin polymerization catalysts with both excellent thermal stability and photoresponsive properties. The core photoresponsive switch of this type of nickel complex is a rigid diphenylethylene derivative, which can achieve reversible photoisomerization of the E / Z configuration under 365 nm and 405 nm ultraviolet light irradiation: the E configuration has a relatively open coordination environment; after light irradiation, the Z configuration has a more compact spatial structure, which can form a dual regulatory mechanism: steric hindrance and potential metal-aryl π interactions. Due to this dual regulatory mechanism, the complex exhibits excellent thermal stability at 150 °C. o Even at high temperatures, it still maintains a high value of 0.8 × 10⁻⁶. 6 g·mol ‑1 ·h ‑1 The nickel complex of this invention exhibits enhanced catalytic activity and effectively inhibits chain transfer and chain walking reactions during high-temperature polymerization. By synergistically enhancing thermal stability through configurational tautomerism, and possessing both photoresponsive properties and high catalytic activity, it holds significant research value and broad application prospects in the precise synthesis of functionalized polyolefin materials.

The application discloses a kind of vinylidene acenaphthene double asymmetric alpha-diimine chemical intermediates and catalyst prepared from it, intermediate and the preparation method and application of catalyst. 2,4,6-tri-tert-butyl aniline is used as raw material, in the presence of catalyst, under the condition of 120 DEG C, the vinylidene acenaphthene double asymmetric alpha-diimine chemical intermediate with structure as shown in formula (I) is obtained.Compared with prior art, the application uses commercially available, low-cost and storage condition loose 2,4,6-tri-tert-butyl aniline instead of high-cost, storage harsh 2,4-di-tert-butyl aniline as reaction raw material, which effectively reduces the raw material procurement threshold and comprehensive production cost, and simplifies the storage condition.The raw material of the method is easy to obtain, low in cost, easy to operate, high in yield, and suitable for industrial scale-up production.

The invention relates to ylide-functionalized phosphane ligands, the production of same and use in transition metal compounds, as well as the use of same as catalysts in organic reactions.

The invention discloses an energetic material, a preparation method thereof and application of the energetic material as an initiating explosive, an explosive and a pyrotechnic compound. The chemical formula of the energetic material is MC10H18B2N6; wherein M is selected from at least one of Mn, Fe, Co, Ni, Cu, Zn and Cd; the crystal structure of the energetic material belongs to a monoclinic system, and the space group is P21 / n. The obtained energetic material has excellent stability and safety, and is green and environment-friendly. Through experimental determination, the thermal stability is greater than or equal to 120 DEG C, the impact sensitivity is greater than or equal to 40J, and the friction sensitivity is greater than or equal to 240N. Compared with an existing commercial propellant (unsymmetrical dimethylhydrazine), the ignition delay time of the energetic material is equivalent, the defects that fuel and an oxidizing agent are seriously mixed and the combustion efficiency is low are overcome, and the energetic material has important commercial application value in the field of green high-performance energetic materials.

The application provides an alpha-carboxyl-beta-diimine nickel complex and a preparation method and application thereof and a preparation method of ethylene-methyl acrylate copolymer. The alpha-carboxyl-beta-diimine nickel complex has a structure shown in general formula (I): in the general formula (I), Ar is selected from 2,6-dialkylphenyl; X is chlorine or bromine; and L is acetonitrile or benzonitrile. The preparation method of the alpha-carboxyl-beta-diimine nickel complex is that acetylacetone is reacted with 2,6-dialkylaniline, then reacted with ammonium formate under the action of alkyl lithium, and then reacted with a halogenated nickel salt in an acetonitrile or benzonitrile solvent to obtain the alpha-carboxyl-beta-diimine nickel complex. The application further provides a preparation method of ethylene-methyl acrylate copolymer, which uses the alpha-carboxyl-beta-diimine nickel complex as a main catalyst. The application improves the copolymer molecular weight and the methyl acrylate insertion rate, and makes the prepared EMA similar to the branched structure of a commercial product prepared by a free radical process.

The present invention relates to air stable, binary Ni(0)-olefin complexes and their use in organic synthesis.

The invention discloses a metal complex with anti-tumor activity, and relates to the technical field of medicines. The invention relates to a metal complex with anti-tumor activity, the metal complex provided by the invention has a remarkable inhibition effect on proliferation of human lung cancer PC-9 cells and nasopharyngeal carcinoma cells Hone1 cells, the unique chemical structure of the metal complex endows higher selectivity for tumor treatment, and the problem of drug resistance of traditional drugs is effectively solved; important technical support is provided for developing novel efficient anti-tumor drugs.

An olefin polymerization catalyst composition comprising a compound represented by the following general formula (A) and a transition metal compound represented by the following general formula (E) or (F): (the definitions of the general formulae are as described in the DESCRIPTION.)

The present invention relates to novel ligands of formula 1, their metal complexes and their use for catalytic purposes. In Formula 1, R1 is alkyl, perfluoroalkyl, aryl, or cycloalkyl, each of which is unsubstituted or substituted with cyano, sulfonyl: -SO2-R10 (R10 = C1-C5 alkyl, C5-C6 cycloalkyl, C5-C10 aryl, each of which is unsubstituted or substituted with C1-C4 alkyl or C1-C4 perfluoroalkyl), or silyl: Si(R20R30R40) (R20, R30, and R40 are, independently of one another, C1-C6 alkyl or C5-C10 aryl, each of which is unsubstituted or substituted with C1-C4 alkyl); R2 is alkyl, cycloalkyl, adamantyl, or aryl, each of which is substituted or unsubstituted; and R3, R4, and R5 are alkyl, cycloalkyl, or aryl. R3 and R6, and / or R4 and R7, and / or R5 and R8 together form an alkyl bridge or alkyl ether bridge which, together with the nitrogen atom to which they are attached, forms a heterocyclyl ring; R6, R7, and R8 are alkyl or aryl which are unsubstituted or substituted, or which, individually or collectively, form a heterocyclyl ring with R3, R4, or R5 and the nitrogen atom to which they are attached; and m, n, and o are 0 or 1, provided that at least one of m, n, and o is 1.

The invention provides preparation and application of an acyl chloride imine nickel catalyst. The invention designs and synthesizes a series of acyl chloride imine nickel catalysts aiming at different steric hindrances, and application of the catalysts in ethylene homogeneous polymerization and ethylene / polar monomer copolymerization. The high activity of the nickel acyl chloride imine catalyst not only can catalyze the synthesis of high-molecular-weight linear polyethylene, but also can efficiently realize the copolymerization of ethylene and polar monomers such as various norbornene. For example, in copolymerization of ethylene / norbornene carboxylic acid methyl ester or norbornene-2-yl acetate, under the condition of maintaining a relatively high insertion ratio of polar monomers such as norbornene, the nickel acyl chloride imine catalyst can still maintain relatively high activity. Introduction of polar functional groups into polyolefin is always an important subject for limiting expansion of the application field of polyolefin, and the acyl chloride imine nickel-based catalyst has important industrial application value in the technical field of olefin polymerization.

The invention relates to the technical field of olefin polymerization catalysts, and discloses a pyridylamino group VIII binuclear metal organic complex as well as a preparation method and application thereof. The structural formula is shown as a formula (I). The pyridylamine group VIII binuclear metal organic complex disclosed by the invention is applied to olefin polymerization and has higher polymerization activity under similar polymerization conditions, the number-average molecular weight of the obtained polymer is obviously higher than that of a polymer obtained in a contrast, and the molecular weight distribution of the obtained polymer is narrow.

The invention discloses a dithiocarbamate nickel (II) complex as well as a preparation method and application thereof, the chemical formula of the nickel (II) complex is [NiIILCl], and L is (E)-2-(phenyl (pyridine-2-yl) methylene) hydrazino methyl dithioformate. The nickel (II) complex is mild in synthesis condition and high in target yield. In-vitro MTT activity evaluation proves that the introduction of copper ions has a synergistic effect on the anticancer activity of the nickel (II) complex, so that the activity of the nickel (II) complex is improved from a micromole level to a nanomole level, and the amplification is as high as 200 times or more. Cell scratch experiments prove that the nickel (II) complex and copper (II) ions are combined for use, so that the migration resistance is achieved. A nickel (II) complex and copper ion combination strategy provided by the invention not only has a direct killing effect on cancer cells, but also can effectively inhibit the migration ability of the cancer cells, and shows huge application potential in the field of cancer treatment.

The present specification relates to a compound represented by Chemical Formula 1, a composition for forming an optical film and an optical film including the same, and a display device including the optical film.

A method for producing a two-dimensional coordination polymer, a two-dimensional coordination polymer, and a solution for forming the two-dimensional coordination polymer. This method for producing a two-dimensional coordination polymer comprises: a preparation step for preparing a solution of a Ni compound, a Pd compound, or a Pt compound, or a solution of a Ni compound, a Pd compound, or a Pt compound, and preparing a solution of at least one of benzenehexanethiol, a derivative of benzenehexanethiol, or benzenehexanethiol and a derivative of benzenehexanethiol; and a polymer formation step in which a single-phase solution containing the Ni compound, the Pd compound or the Pt compound, and the benzene hexaphosphol is prepared, and a two-dimensional coordination polymer is prepared in the single-phase solution. The two-dimensional coordination polymer has a structural unit represented by formula (2) and a structural unit represented by formula (3). M1 is Ni or Pt, and M2 is Mn, Fe, Co, Ni, Cu, Zn, Pd or Ag.

The invention relates to the technical field of olefin polymerization catalysts, and discloses a group VIII metal organic complex as well as a preparation method and application thereof. The structural formula of the group VIII metal organic complex is shown as a formula (I). The group VIII metal organic complex disclosed by the invention is applied to olefin polymerization and has higher polymerization activity under similar polymerization conditions, the number-average molecular weight of the obtained polymer is obviously higher than that of a polymer obtained in a contrast, the molecular weight distribution of the obtained polymer is narrow, and the molecular weight of a catalyzed polymerization product is in double-peak or broad-peak distribution, so that the molecular weight of the polymer is greatly reduced. The molecular weight of the obtained polymer can be regulated.

The invention discloses synthesis and application of a pyridine-containing asymmetric alpha-diimine nickel catalyst and application of Lewis acid regulation in olefin polymerization, and belongs to the technical field of olefin polymerization. In the olefin polymerization reaction catalyzed by the diimine nickel catalyst, the Lewis acid plays a very ingenious role of a regulator, and the electronic property and space environment of the active center of the catalyst are changed by introducing the Lewis acid salt, so that the dual regulation of the steric hindrance and the electronic effect of the catalyst is realized; the performance of the catalyst is improved; and the structure of the final polymer is changed. Compared with known alpha-diimine nickel catalysts, the alpha-diimine nickel catalyst has the advantages of high polymerization activity, strong thermal stability and improvement of monomer insertion rate.

The invention provides a complex, a catalyst composition, a preparation method and application and an ethylene oligomerization reaction method, and relates to the technical field of ethylene oligomerization. The structural formula of the complex is shown as a formula (I), in the formula (I), R1-R13 are the same or different and are independently selected from any one of hydrogen, C1-C6 alkyl, halogen, C1-C6 alkoxy, nitryl and C6-C10 aryl; and R14-R16 are the same or different and are respectively and independently hydrogen or C1-C20 alkyl groups. The complex can be completely dissolved in an organic solvent, the concentration of the complex can be accurately metered in industrial operation, and stable operation of the reaction is ensured. The catalyst composition comprises the complex, so that under the action of the catalyst composition, the ethylene oligomerization reaction is rapid in initiation, stable in operation and good in repeatability.

The present application relates to the technical field of nickel-based catalyst, and discloses a diimine ligand, a preparation method and application thereof, wherein the raw materials for preparing the diimine ligand contain acenaphthenequinone, a protective agent, substituted aniline and a catalyst, the protective agent is selected from one or more than two of ortho ester, amine, hydrazine and substituted hydrazine; and the molar ratio of the acenaphthenequinone, the protective agent, the substituted aniline and the catalyst is 1:(0.5-3):(1.6-2.4):(0.1-10). In the present application, a certain amount of protective agent is added to the reaction system, the acenaphthenequinone is reacted with the ortho ester or low-molecular-weight amine to generate ketal or imine, the ketal or imine is separated or not separated, and then reacted with the substituted aniline to generate the target product diimine ligand, no water is generated in the synthesis reaction of the diimine ligand, the balance can be effectively promoted to the forward reaction, and the reaction yield is improved.

The invention discloses a biquinoline nickel complex as well as a preparation method and application thereof. The preparation method comprises the following steps: taking 8-hydroxyquinoline-N-oxide, 2, 2 '-biquinoline and NiCl2. 6H2O with the same amount of substance, and carrying out sealed reaction at 65-80 DEG C for 3 days; and after the reaction is finished, cooling to room temperature to obtain the novel biquinoline nickel complex. The research also finds that the biquinoline nickel complex has low toxicity to normal HL-7702 cells; it is indicated that the biquinoline nickel complex can inhibit growth of SK-OV-3 / DDP cancer cells in a targeted mode, shows excellent anti-tumor activity, has potential medicinal value and is expected to be used for preparing various anti-tumor drugs.