3409 results about "Aryl" patented technology

An aqueous ultraviolet-absorbing resin emulsion, and an aqueous resin emulsion composition containing the emulsion is provided, wherein the emulsion is excellent in compatibility with a synthetic resin and light resistance. Also, the emulsion improves stability in blending with an aqueous emulsion of the synthetic resin, and prevents bleed out of the ultraviolet-absorbing resin on the surface of a coating film. Further, the aqueous ultraviolet-absorbing resin emulsion imparts excellent alkali or solvent resistance to a synthetic resin poor in alkali or solvent resistance. More specifically, an aqueous resin emulsion composition comprising (I) an aqueous ultraviolet-absorbing resin emulsion and (II) an other aqueous resin emulsion is provided, wherein the emulsion (I) is obtained by urethanizing (A) a polyol component having an ultraviolet-absorbing group {e.g., 1,1-bis[3-(2H-benzotriazol-2-yl)-4-hydroxy-benzeneethanol]methane}, (B) a polyol if necessary, (C) an alkyl or aryl dialkanolamine compound, and (D) an organic polyisocyanate in (E) an organic solvent, diluting the reaction mixture with (F) an organic solvent having a boiling point lower than 100° C. to give a resin solution, neutralizing the resin solution with (G) a neutralizing agent, and dispersing the resultant in water.

The invention provides a novel polynorbornene anion exchange ionomer containing a polar functional group as well as a preparation method and application of the novel polynorbornene anion exchange ionomer. The polynorbornene has excellent thermal stability and chemical stability. Meanwhile, the AEI main chain of the polynorbornene has no aryl group, so that the adsorption influence caused by the aryl group is avoided. The synthesized addition polynorbornene AEI in the form of quaternary ammonium salt can be dissolved in a low-boiling-point solvent, and it is ensured that a membrane electrode can be prepared through a solvent casting method. Besides the solubility of the AEI, the addition polynorbornene-based AEI in the form of quaternary ammonium salt is modified by utilizing a thiol-ene click reaction, an anion exchange ionomer containing a polar functional group can be prepared, the interaction between the AEI and an electrolytic catalyst is improved, the reaction is simple and easy to operate, the universality is high, and the method is suitable for industrial production. And the current density in the AEMWE system containing the AEI can be effectively improved.

Provided is an arylalkyl-modified indene composition comprising a plurality of compounds, each of the compounds having one or more arylalkyl groups on an indene ring and differing from the others in the number of arylalkyl groups in one molecule. The content of the compound or compounds having a single arylalkyl group in one molecule is 1% or less in the composition at the percentage calculated on the basis of the area ratio in a GPC chart. At least one of the arylalkyl groups present in the composition is an arylalkyl group having a polymerizable unsaturated bond-containing group, while at least one of the arylalkyl groups present in the composition is an arylalkyl group having no polymerizable unsaturated bond-containing group.

A corrosion inhibitor composition includes a fatty acid ethoxylate, a thiourea, an arylthiourea, a thiazole, and two or more solvents. A metal article in contact with the composition has a corrosion rate of about 25 to about 45 mils penetration per year (mpy), as determined by an ASTM G111 standard test method. A method for inhibiting corrosion of a metal in contact with a corrosive fluid.

Provided is an arylalkyl-modified indene composition that contains a plurality of types of compounds having an arylalkyl group on an indene ring, the compounds having different numbers of arylalkyl groups in one molecule, wherein: the content of a compound in which the number of arylalkyl groups in one molecule is 1 is 1% or less as calculated from the area ratio of the GPC chart; at least one of the arylalkyl groups present in the composition has a polymerizable unsaturated bond-containing group; and at least one of the arylalkyl groups present in the composition does not have a polymerizable unsaturated bond-containing group.

This method for producing an aryl-alkylated indene composition involves: adding an arylalkyl group having a polymerizable unsaturated bond-containing group to an indene compound; and adding an arylalkyl group having no polymerizable unsaturated bond-containing group to the indene compound to which the arylalkyl group having a polymerizable unsaturated bond-containing group is added.

The invention relates to the technical field of quantum computing and molecular electronic devices, in particular to a probabilistic bit device based on polyfluoroaryl methyl free radicals and a preparation method of the probabilistic bit device. According to the probabilistic bit device, the coupling efficiency of molecules and electrodes is improved by virtue of the characteristic that the paramagnetic unpaired electron spin state of tri (polyfluoroaryl) methyl free radical molecules can be used as a random expansion physical entropy source and high electronegativity and stability formed by modification of a plurality of strong electron-withdrawing fluorine atoms in the molecules. During the operation period of the device, the spin fluctuation can efficiently regulate and control tunneling current passing through molecules, promote random conversion between output high and low current states, show excellent random binary fluctuation characteristics, and simultaneously have high sensitivity and long coherence time. Compared with the prior art, the device has remarkable advantages in the aspects of device stability, energy efficiency ratio and external field controllability. The preparation method is simple and convenient to operate, mild in reaction condition and beneficial to large-scale production.

The invention provides a substituted amino bipyridine derivative as well as a preparation method and application thereof, the structure of the substituted amino bipyridine derivative is as shown in formula I. In the formula, R1, R2, R3 and R4 are independently selected from any one of H, C1-C6 alkyl, C2-C6 alkenyl, C2-C20 alkynyl, C3-C6 cycloalkyl, C5-C20 aryl or C5-C20 heterocyclic radical; when R1, R2, R3 and R4 are not methyl, no more than one of R1, R2, R3 and R4 is H; and when any one of R1, R2, R3 and R4 is methyl, the rest groups are independently selected from H or methyl. When the substituted amino dipyridyl derivative provided by the invention is used as a blue dye, the dyed blue dye is bright in color, deep in dyeing and comprehensive in dyeing fastness; the preparation process is simple, convenient to purify, safe, simple, convenient and energy-saving, the product quality is stable, the reproducibility is good, the yield is high, and the method is suitable for industrial production.

The invention provides a self-assembled monomolecular layer hole transport material based on a polycarbazole derivative and a preparation method and application thereof, and the self-assembled monomolecular layer hole transport material has a structure as shown in a formula I. The self-assembled monomolecular layer hole transport material is simple in structure, high in hole transport property, strong in interface passivation ability, high in thermal stability, and suitable for large-scale application; a polycarbazole derivative is taken as a mother nucleus, an alkyl / aryl chain is taken as a linking group, phosphoric acid is taken as an anchoring group, and rigid conjugated large-plane polycarbazole with a specific structure is taken as the mother nucleus, so that molecular accumulation can be improved, and the hole transport performance of the material can be improved. By taking a phosphate group as a tail end, single-molecule self-assembly can be realized, a perovskite interface can be passivated, the energy loss at the interface is reduced, and the battery performance is improved.

The invention relates to a compound, a composition, an organic optoelectronic device, and a display device. The compound is represented by Chemical Formula 1, where X1 and X2 are each independently NRa, O, S, Se, or Te, any one of R1 to R10 is a group represented by Chemical Formula A, the remaining ones of R1 to R10 and Ra are each independently hydrogen, deuterium, a substituted or unsubstituted C1 to C20 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C2 to C30 heterocyclic group, a substituted or unsubstituted amine group, a substituted or unsubstituted silyl group, a cyano group, or a halogen, and R1 to R10 and Ra are each independently present, or adjacent two of R1 to R10 and Ra are linked to form a ring.

A polysubstituted aryl compound as shown in formula (I) or a stereoisomer thereof or a pharmaceutically acceptable salt thereof, a pharmaceutical composition containing same, and a use of the polysubstituted aryl compound or the stereoisomer thereof or the pharmaceutically acceptable salt thereof as an NMT (N-myristoyltransferase) inhibitor in the prevention or treatment of NMT-related diseases.

The invention discloses a method for preparing a carbon monoxide normal-temperature oxidation catalyst based on electrolytic manganese residues and landfill leachate. The method comprises the following steps: soaking and purifying the electrolytic manganese residues with deionized water to obtain preliminarily purified electrolytic manganese residues; mixing aryl alcohol dehydrogenase, the preliminarily purified electrolytic manganese residues and the landfill leachate, and standing to obtain enzymolysis electrolytic manganese residue slurry; mixing fly ash, red mud and the enzymolysis electrolytic manganese slag slurry, uniformly stirring, drying and grinding to obtain a multi-component composite raw material; placing the multi-component composite raw material in low-temperature plasma equipment for irradiation to obtain a plasma activated composite material; and carrying out hydrothermal reaction on the plasma activated composite material to obtain a hydrothermal structure composite material, dipping the hydrothermal structure composite material in a solution containing cerium nitrate, drying, and roasting to obtain the carbon monoxide normal-temperature oxidation catalyst. The carbon monoxide normal-temperature oxidation catalyst with high activity and high moisture resistance is prepared by utilizing industrial wastes and landfill leachate enzymolysis derivative liquid.

The invention relates to the technical field of adsorption materials, and discloses a post-modified imine-COF adsorbent and a preparation method and application thereof, the adsorbent comprises the following structural units: a COF skeleton, which is a two-dimensional or three-dimensional porous skeleton formed by an aromatic aldehyde monomer and an amino monomer through a Schiff base reaction; the imine group is formed in a COF skeleton through a post-modification reaction, and the imine group is-C = NR, r is selected from one or more of a substituted or unsubstituted alkyl group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted alkenyl group, a substituted or unsubstituted cycloalkenyl group, a substituted or unsubstituted aryl group, a substituted or unsubstituted aralkyl group, a substituted or unsubstituted heterocyclic group and a hydrogen atom. The adsorbent retains excellent structural characteristics of the COF material, realizes high density and uniform distribution of functional groups, and avoids interference of functional monomers on crystal nucleation and growth, so that the adsorption performance of the adsorbent is improved, and the adsorbent can efficiently capture rare earth when being applied to a rare earth-containing solution.

The invention provides a halohydrin dehalogenase mutant and an application of the halohydrin dehalogenase mutant in synthesis of a chiral gamma-amino alcohol compound. Halogenated alcohol dehalogenase mutants enabling 2-substituted oxetane to be subjected to ring opening are obtained through the technologies of gene mining, directed evolution and the like, and the enzymes can directly perform ring opening on a substrate 2-aryl oxetane under the action of a nucleophilic reagent to generate a series of chiral gamma-amino alcohol compounds which are important precursors for synthesizing drugs. Therefore, the halohydrin dehalogenase mutants have important application value in the industry.

The invention provides a benzotriazole light conversion agent, a light conversion adhesive film composition, a light conversion adhesive film and a packaging device. The benzotriazole light conversion agent has a structure as shown in a formula (I). Compared with a traditional benzotriazole light conversion agent, the benzotriazole light conversion agent has higher light conversion efficiency; carbon-carbon triple bonds are respectively introduced between a benzotriazole group and substituent groups R2 and R2'on two sides of the benzotriazole group, and R2 and R2 'are limited as specific types of aryl groups, so that a D (aryl)-A (benzotriazole group)-D (aryl)-like structure can be converted into a D (aryl)-pi (alkynyl)-A (benzotriazole group)-pi (alkynyl)-D (aryl) structure, and the structural formula of the benzotriazole compound is as shown in the specification. Therefore, the conjugation range and conjugation degree of molecules are effectively expanded, and the purposes of enhancing the absorption strength and widening the absorption wave band range are achieved. (I)

The present invention belongs to the technical field of pesticides and specifically relates to a substituted pyrazole compound containing pyrimidine and a use thereof. The compound is represented by general formula I: where Q represents an aryl group or a heterocyclic group; Y1 and Y2 each independently represent hydrogen, alkyl, or the like; R1 and R2 each independently represent hydrogen, halogen, nitro, or the like; R3 represents hydrogen, alkyl, or the like; R4, R5, R6, and R7 each independently represent hydrogen, alkyl, or halogenated alkyl; and R8 and R9 each independently represent hydrogen, halogen, cyano, alkyl, or the like. The described compound exhibits good control activity against fungi, etc.

The invention belongs to the technical field of lithium / sodium batteries, and particularly relates to a method for pre-embedding lithium / sodium into a battery. The preparation method comprises the following steps: firstly, preparing a lithium / sodium pre-embedded material of the lithium / sodium battery, namely putting a sodium salt of the material into an organic solvent, dropwise adding acid, stirring for reaction, extracting and drying, and evaporating the solvent to dryness; placing the product in deionized water, adding lithium salt, stirring for reaction, and evaporating the solvent to dryness; recrystallizing the solid by using ethyl acetate and dichloromethane; and drying the obtained solid powder to obtain a final material. Dissolving the prepared lithium / sodium pre-intercalation material in a battery electrolyte to realize lithium / sodium pre-intercalation of the battery; the sodium salt of the material takes organic sodium sulfinate as a skeleton, and side groups are substituted with different alkyl groups or aryl groups; the prepared lithium / sodium pre-embedded material is high in specific capacity, good in compatibility with a battery system and good in material stability; lithium / sodium pre-embedding is carried out on the battery through an electrolyte adding method, the lithium / sodium pre-embedding process is safe and convenient, the process is simple, the cost is low, and large-scale production can be realized.

The invention provides high-grinding-efficiency color paste, a preparation method thereof and dispersed ink, and belongs to the technical field of dispersed ink, and the high-grinding-efficiency color paste comprises the following components in percentage by weight: 15%-30% of disperse dye toner, 15%-25% of a dispersing agent, 5%-15% of resin ammonium salt, 10%-20% of a dissolution promoting mixture, 0.5%-2% of a wetting agent and the balance of water; the dispersing agent comprises a hyperbranched polymer and a sodium naphthalene sulfonate improved polymer; the hyperbranched polymer takes a benzene ring as a center, hydrophobic groups and hydrophilic groups on a branched chain are randomly distributed, the hydrophilic groups of the branched chain comprise carboxylate and sulfonate, and the hydrophobic groups of the branched chain comprise alkane, ester and aryl. According to the invention, the hyperbranched polymer and the sodium naphthalene sulfonate improved polymer are mixed with the dispersing agent, so that the problem of abrupt change of ink viscosity can be avoided when the content of ink toner is relatively high, thereby obtaining the color paste with strong dispersion and high stability, and further obtaining the dispersed ink with good stability.

The invention discloses hydrolysis-resistant liquid phosphite ester and a preparation method and application thereof.The hydrolysis-resistant liquid phosphite ester is prepared by the steps that 2, 2, 4-trimethyl-1, 3-pentanediol and phosphorus trichloride or phosphite triester serve as raw materials, a cyclization reaction is conducted firstly, and then the hydrolysis-resistant liquid phosphite ester is obtained; and then carrying out nucleophilic substitution on Cl or aryl and alkyl on the cyclized intermediate by using higher saturated monohydric alcohol with more than C8, wherein the molecular structure is as shown in formula I in the specification. The liquid phosphite ester is novel liquid phosphite ester, the main body of the liquid phosphite ester is of a six-membered ring structure, the basic structure of the phosphite ester is reserved to the maximum extent, and the anti-oxidation effect of the phosphite ester is guaranteed; hydrophobic aliphatic chain structures on phosphorus atoms and branched chains of the phosphorus atoms prevent water molecules from approaching P-O bonds, so that the phosphorus atoms and the branched chains are prevented from being attacked by the water molecules, and the hydrolysis resistance is improved under the conditions that any additional amine hydrolysis-resistant agent is not used and any steric hindrance group is not introduced; good practical value, economic value and market prospect are realized.

The invention relates to the technical field of organic synthesis and the technical field of fluorescent materials, in particular to a boron coordination salicylhydrazone double-state emission fluorophore as well as a preparation method and application of the boron coordination salicylhydrazone double-state emission fluorophore. The structure of the boron coordination salicylazone double-state emission fluorophore is shown as I, II or III; wherein R1 is selected from one of H, halogen atoms, diethylamino and thienyl, R2 is selected from one of H, halogen atoms, diethylamino and thienyl, and R3 is selected from one of aryl, 9, 9 '-spirobifluorenyl, alkoxy and halogen atoms. The boron coordination salicylazone double-state emission fluorophore is diversified in structure and good in solubility, has excellent photophysical properties and extremely high quantum yield, and also shows excellent biocompatibility and remarkable liposome targeting property at the same time. Moreover, the preparation method of the boron-coordinated salicylazone double-state emission fluorophore adopts a one-pot two-step method, is simple and convenient, is high in yield, is green and environment-friendly, and has a wide application prospect.

The present disclosure provides, in part, five-membered heteroarylcarboxamide compounds useful for disrupting HBV core protein assembly, and pharmaceutical compositions thereof, and methods for treating hepatitis B (HBV) infection. In another aspect, the present disclosure provides a method of treating HBV infection in a subject in need thereof, the method comprising administering to the subject a pharmaceutical composition comprising a therapeutically effective amount of a compound of Formula I, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable excipient.

The present invention relates to a solid laundry composition. More particularly it relates to a solid laundry composition which provides improved fragrance perception. It is desired to provide solid laundry composition which provides improved fragrance intensity on wet fabrics, also preferably on both wet fabrics and post drying the fabrics. The present inventors have found that when a solid laundry composition has a surfactant system comprising alkyl aryl sulphonate surfactant and an amino acid-based surfactant in combination with specific chelating agents it provides for surprisingly higher fragrance intensity, preferably on wet fabrics, more preferably both on the wet fabrics and after drying the fabrics. It was also found that the composition according to the first aspect of the present invention provides for reducing / removing the malodour producing soil from the fabrics.

This invention belongs to the field of veterinary drug technology, specifically relating to a 2,3-disubstituted naphthoquinone compound, its uses, and a preparation method. The 2,3-disubstituted naphthoquinone compound has the general formula: where X is selected from C, NH, O, and S; where X is selected from C, the X-R1 substituent represents an aryl substituent; when X is selected from NH, R1 is selected from hydrogen atom, C1-6 alkyl, C3-6 cycloalkyl, substituted aryl, substituted benzyl, or substituted acyl; when X is selected from O, R1 is selected from hydrogen atom, C1-6 alkyl, C3-6 cycloalkyl, C4-6 cycloalkyl, C5-6 cycloalkyl, C6-6 cyclo ... 3-6 cycloalkyl, substituted benzyl, substituted acyl; when X is selected from S, R1 is selected from C1-6 alkyl, substituted aryl, substituted benzyl; R2 is selected from C1-16 alkyl, substituted aryl, Ra-(CH2)n-, Ra-CO-(CH2)n-; This series of compounds has novel structures, excellent antiparasitic activity, and has been successfully applied in the field of veterinary drugs, solving long-standing safety and toxicity problems; its synthesis process is simple, the conditions are mild, and it can efficiently prepare a variety of 2,3-disubstituted naphthoquinone compounds.

Disclosed herein is an organic light emitting diode device. The organic light emitting diode device includes an anode, a cathode and a light emitting layer. The light emitting layer has a structure where a blue light emitter and a red / green simultaneous light emitter are stacked. The red / green simultaneous light emitter has a structure where a red light emitter and a green light emitter are stacked. The red light emitter includes a red host compound, and in some embodiments, the red host compound includes a spirobisfluorene-based compound where an aryl amino group is substituted. The green light emitter includes a green host compound, and the green host compound includes a mixture of a first green host compound and a second green host compound. In some embodiments, the first green host compound includes a biscarbazole-based compound and the second green host compound includes an indolocarbazole-based compound.

The present disclosure relates to pyrazoloheteroaryl derivatives, their preparation methods, and their pharmaceutical applications. Specifically, the present disclosure relates to pyrazoloheteroaryl derivatives represented by general formula (I), their preparation methods, pharmaceutical compositions containing the derivatives, and their use as therapeutic agents, particularly their use as ATR kinase inhibitors and in the preparation of medicaments for treating and / or preventing hyperproliferative diseases. The definitions of each group in general formula (I) are as described in the specification. TIFF2023502458000095.tif4136

The invention discloses a dual-band acridine formic acid anthracene methyl ester photocatalyst as well as a preparation method and application thereof, and belongs to the field of heterocyclic compounds. The invention designs and synthesizes a novel acridine formic acid anthracene methyl ester photocatalyst, which has good compatibility in two wavebands of 365 nm and 405 nm, can realize photocatalysis of disulfide compounds and aryl formyl peroxide compounds, and provides a new thought for preparation of sulfoxide compounds with asymmetric structures; the reaction conditions are mild, the reaction time is short, the photocatalyst can be recycled, the circulation loss is low, the circulation efficiency is high, the production efficiency is greatly improved, and the production period and cost are reduced; the product is free of transition metal residues and high in yield.

The invention relates to the technical field of polymer dye synthesis, and discloses a monomer for a blue polyester fiber and a preparation method thereof.According to the monomer for the blue polyester fiber, 1, 4-arylamino substituted anthraquinone serves as a color development mother nucleus, a benzoate group is introduced to aryl of the 1, 4-arylamino substituted anthraquinone mother nucleus, and the monomer for the blue polyester fiber is obtained; the benzoate group is connected with the chromophoric parent nucleus through a carbon-carbon bond; the molecular terminal of the monomer for the blue polyester fiber is connected with an exposed ester group through an aryl group, and the exposed ester group is used for transesterification with dihydric alcohol under the melt polycondensation condition of polyester. The novel monomer for the blue polyester fiber, provided by the invention, has excellent color development performance and thermal stability, can be directly used for in-situ synthesis of blue polyester and can be directly used for melt spinning, and the color fastness and coloring uniformity of a product are improved; meanwhile, the monomer for the blue polyester fiber, provided by the invention, is simple in preparation method, low in cost and easy for large-scale production.

The invention discloses a battery, a positive pole piece, slurry, a dispersing agent, a preparation method and electric equipment. The battery comprises a positive electrode plate, the positive electrode plate comprises a current collector and a positive electrode material layer arranged on at least one side of the current collector, the positive electrode material layer comprises a positive electrode active material and a dispersant, the dispersant comprises a polyester compound, the polyester compound comprises a structural unit A and / or a structural unit B, the chemical formula of the structural unit A is shown in the specification, and the chemical formula of the structural unit B is shown in the specification. R1 and R2 are respectively selected from at least one of C0, a C1-C18 alkyl group and a C6-C18 aryl group; and R3 and R4 are respectively selected from at least one of H, C1-C18 alkyl groups, C6-C18 aryl groups and ester groups. The dispersing agent can improve the dispersibility of the positive electrode slurry and improve the uniformity and flexibility of the positive electrode plate, so that the battery has relatively high capacity and stability.

The present invention provides an electronic or electrical device or component thereof comprising a cross-linked polymeric coating on a surface of the electronic or electrical device or component thereof; wherein the cross-linked polymeric coating is obtainable by exposing the electronic or electrical device or component thereof to a plasma comprising a monomer compound and a crosslinking reagent for a period of time sufficient to allow formation of the cross-linked polymeric coating on a surface thereof,wherein the monomer compound has the following formula:where R1, R2 and R4 are each independently selected from hydrogen, optionally substituted branched or straight chain C1-C6 alkyl or halo alkyl or aryl optionally substituted by halo, and R3 is selected from:where each X is independently selected from hydrogen, a halogen, optionally substituted branched or straight chain C1-C6 alkyl, halo alkyl or aryl optionally substituted by halo; and n1 is an integer from 1 to 27; and wherein the crosslinking reagent comprises two or more unsaturated bonds attached by means of one or more linker moieties and has a boiling point at standard pressure of less than 500° C.