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133 results about "Diazo" patented technology

The diazo group is an organic moiety consisting of two linked nitrogen atoms (azo) at the terminal position. Overall charge neutral organic compounds containing the diazo group bound to a carbon atom are called diazo compounds or diazoalkanes and are described by the general structural formula R₂C=N⁺=N⁻, and the simplest example of a diazo compound is diazomethane. Compounds with the diazo moiety should be distinguished from diazonium compounds, which have the same terminal azo group but bear an overall positive charge, and azo compounds in which the azo group bridges two organic substituents. The electronic structure of diazo compounds is characterized by π electron density delocalized over the α-carbon and two nitrogen atoms, along with an orthogonal π system with electron density delocalized over only the terminal nitrogen atoms. Because all octet rule-satisfying resonance forms of diazo compounds have formal charges, they are members of a class of compounds known as 1,3-dipoles. Some of the most stable diazo compounds are α-diazo-β-diketones and α-diazo-β-diesters with the electron density further delocalized into an electron-withdrawing carbonyl group. In contrast, most diazoalkanes without electron-withdrawing substituents, including diazomethane itself, are explosive. A commercially relevant diazo compound is ethyl diazoacetate (N₂CHCOOEt). A group of isomeric compounds with only few similar properties are the diazirines, where the carbon and two nitrogens are linked as a ring.

Synthetic method of glutaric acid ester compound

The invention discloses a synthesis method of a glutaric acid ester compound, which comprises the following steps: reacting a propionate compound as shown in a formula 1 with a diazo compound as shown in a formula 2 in a solvent in a nitrogen atmosphere in the presence of a reducing agent under the illumination condition of visible light, and after the reaction is completed, separating out the glutaric acid ester compound, thereby obtaining the glutaric acid ester compound. And separating and purifying the reaction mixture to obtain the glutaric acid ester compound as shown in the formula 3. The propionate compound and the diazo compound are used as reaction substrates, the compound can be generated through reaction under mild conditions, the yield of the target product is improved, operation is easy and convenient, the reaction conditions are mild, the price of raw materials and solvents used in the whole process is low, and cost control is facilitated.
Owner:ZHEJIANG UNIV OF TECH

Method for catalytically synthesizing secondary amine acetate derivatives by using lignite residues

The invention discloses a method for catalytically synthesizing a secondary amine acetate derivative by using lignite residues, which comprises the following steps: taking an amine (primary amine) compound and an aryl diazo ester compound as raw materials to react for preparation, and taking the lignite residues as a catalyst. The catalyst lignite residue adopted by the method is wide in source, low in cost and easy to obtain, the reaction condition is mild, the yield is good, gram-scale reaction can be achieved, and the method has industrialization prospects. The lignite residues are high in catalytic activity and can be recycled, recycling of waste resources is achieved, the problem that the lignite residues are difficult to treat is solved, and the method conforms to the sustainable development concepts of environmental protection and green chemistry.
Owner:THE SECOND AFFILIATED HOSPITAL ARMY MEDICAL UNIV

Polyhydroxy phenolic compounds and methods for their preparation, diazonium naphthoquinone sulfonic acid esters and methods for their preparation, and photoresist compositions

The application provides a polyhydroxy phenolic compound, a preparation method thereof, a diazonium naphthoquinone sulfonate, a preparation method thereof and a photoresist composition. The polyhydroxy phenolic compound has the following structure shown in formula (I). The diazonium naphthoquinone sulfonate prepared by using the polyhydroxy phenolic compound provided by the application as an intermediate is applied to the photoresist composition as a photosensitive agent, and the obtained photoresist not only has clear resolution and high photosensitivity, but also has excellent thermal stability and etching resistance, and has a wide application prospect in the field of semiconductors.
Owner:CHANGZHOU TRONLY NEW ELECTRONICS MATERIALS CO LTD +2

Diazo compounds with Anti-trypanosomal activities

PCT designated stageWO2026110111A1Organic chemistryAntiparasitic agentsAntiparasiticSide effect
The present invention provides diazo compounds having anti-trypanosomal activity, with less or no side-effects. The diazo compounds are structural analogue of quinapyramine and possess characteristics necessary for the targeted pharmacologic action of anti trypanosomosis, with reduced cytotoxicity. The compounds were found to have less cytotoxicity, and identical or better anti- parasitemia effect as compared to conventional quinapyramine sulfate.
Owner:INDIAN COUNCIL OF AGRI RES

Process for the preparation of an organic pigment yellow free of residual aromatic amine

PendingCN122080664ASolve the industry problem of "controlling disability will inevitably lead to loss of performance"Improve applicabilityMonoazo dyesDisazo dyesAcetic acidActive agent
This invention discloses a method for preparing an aromatic amine-free organic pigment yellow, comprising the following steps: S1, preparing a diazo solution by sequentially adding water, inorganic acid, and diazo components to a diazo tank, stirring and slurrying, then cooling the mixture in the diazo tank to below 0°C and adding nitrite; S2, preparing a coupling solution by sequentially adding water, inorganic alkali, and coupling components to a dissolving tank, stirring and dissolving until clear; S3, coupling reaction by adding water, acetic acid, and surfactant to a coupling tank, stirring and mixing evenly, then slowly adding the diazo solution and coupling solution simultaneously to the coupling tank for a coupling reaction; S4, pigmentation by heating to above 60°C and maintaining the temperature, adjusting the pH of the solution to alkaline; S5, filtering, washing, and drying to obtain an aromatic amine-free organic pigment yellow. This invention is applicable to the synthesis of most mono- and diazo organic pigment yellows, reducing aromatic amine residues during the synthesis process and ensuring that the organic pigment yellow product is free of aromatic amine residues.
Owner:SHANDONG YUHONG NEW PIGMENT CO LTD

A gas-liquid separator for separating diazomethane from a diazomethane mixed solution

ActiveCN117654113BLiquid degasification arrangementsVapor–liquid separatorMechanical engineering
This invention provides a gas-liquid separator for separating diazonium methane from a diazonium methane mixture. The separator comprises an upper cylinder, a middle cylinder, and a lower cylinder connected sequentially from top to bottom. The upper cylinder has a gas outlet at its top center, surrounded by gas moisture detection ports, diazonium methane content detection ports, gas temperature detection ports, and an explosion vent. A pressure detection port is located on the side. The middle cylinder has a refrigerant inlet and a refrigerant outlet at its upper part, and a refrigerant coil is installed inside the middle cylinder. The refrigerant coil inlet is connected to the refrigerant outlet, and the refrigerant coil outlet is connected to the refrigerant outlet. The lower cylinder has a liquid level-above gas inlet and a liquid level-below gas inlet at its upper part. The liquid level-above gas inlet is connected to a gas distributor above the liquid level via a pipe, and the liquid level-below gas inlet is connected to a gas distributor below the liquid level via a pipe. A feed inlet is located on the middle side wall of the lower cylinder. This gas-liquid separator offers high gas-liquid separation efficiency, is explosion-proof, and can be used for continuous automated production.
Owner:ABA CHEM SHANGHAI +1

Pyrazolo [5, 1-a] isoindole derivative as well as synthesis method and application thereof

The invention discloses a pyrazolo [5, 1-a] isoindole derivative as well as a synthesis method and application thereof, and belongs to the technical field of organic chemical synthesis. The invention solves the problems of harsh reaction conditions, limited substrate range and the like of continuous multi-step synthesis of a precursor in the existing pyrazolo [5, 1-a] isoindole compound synthesis process. According to the invention, a polarity reversal strategy is adopted, a cyano group is introduced into 1, 5-enyne to change the electronic characteristics of 1, 5-enyne, diazo, olefin and ethynyl benzene are reacted under mild conditions, two rings and three new chemical bonds are constructed through a series of intermolecular [3 + 2] cycloaddition, intramolecular cycloaddition and elimination reactions, and pyrazolo [5, 5-a]-1, 5-a-phenanthrene is efficiently synthesized. According to the present invention, the 1, 1-a] isoindole derivative has characteristics of good synthesis yield, simple operation of the synthesis method, easily available raw materials, good substrate universality and step economy, and provides the effective strategy for the drug design synthesis.
Owner:LIAONING UNIVERSITY OF PETROLEUM AND CHEMICAL TECHNOLOGY

A neutral reverse electron state carbene and a preparation method and application thereof

This invention provides a neutral-electron-reversed carbene, its preparation method, and its applications, belonging to the fields of organic chemistry and organic catalysis. The neutral-electron-reversed carbene described in this invention has the structure shown in formula (I). This invention synthesizes the neutral-electron-reversed carbene in one step by reacting a diazo compound as a precursor with a rhodium complex, followed by nitrogen removal and COD (1,5-cyclooctadiene) removal processes. The reaction conditions of this invention are simple, and the yield is good. Stable separation of neutral-electron-reversed carbene is achieved for the first time.
Owner:SOUTHERN UNIVERSITY OF SCIENCE AND TECHNOLOGY

Heterogeneous photocatalyst and method of making and using same

ActiveCN118146412BPolyolefinPtru catalyst
The present disclosure provides a heterogeneous photocatalyst, a preparation method and application thereof. The heterogeneous photocatalyst comprises a nano semiconductor with photocatalytic performance, polyolefin acid particles and an alpha-diazo nickel metal catalyst. The polyolefin acid particles are formed with the nano semiconductor as a condensation nucleus to form a catalytically active layer on the surface thereof, and the alpha-diazo nickel metal catalyst is loaded by using the carboxyl-metal ion dynamic crosslinking point contained in the polyolefin acid particles. The present disclosure also provides a preparation method of the heterogeneous photocatalyst, comprising: dissolving and uniformly mixing the nano semiconductor and alkyl aluminum protected olefin acid monomers at a first reaction temperature, and then adding a cocatalyst and an alpha-diazo nickel metal catalyst; allowing the polymerization reaction of the olefin acid monomers to occur at a second reaction temperature, and forming a polyolefin acid catalytically active layer on the surface of the nano semiconductor after heterogeneous nucleation, and then cooling to a third reaction temperature after standing or stirring for a period of time to obtain the heterogeneous photocatalyst.
Owner:UNIV OF SCI & TECH OF CHINA

S-alkyl isothiourea compounds and methods for their preparation

The application discloses a method for preparing S-alkyl isothiourea under visible light irradiation, and a structural formula of the S-alkyl isothiourea is shown in formula 1. The preparation method comprises the following steps: adding secondary amine, aryl isothiocyanate, aryl alpha-diazo ester and cyclic ether as reaction raw materials into a reactor, adding an organic solvent, and stirring and reacting at room temperature under visible light irradiation for 3 hours. After the reaction is completed, the reactants are concentrated under reduced pressure, and the target product S-alkyl isothiourea is obtained through column chromatography separation. According to the application, secondary amine, aryl isothiocyanate, aryl alpha-diazo ester and cyclic ether are reacted under the promotion of visible light, and a series of S-alkyl isothiourea is efficiently synthesized in one-step operation. The process of the application is completed at room temperature under the condition that no heating and any metal catalyst, base, ligand and other additives are needed, and clean visible light energy is used as a reaction energy source. The process of the application has the advantages of simple operation, mild reaction condition, high efficiency, low energy consumption, high safety and small pollution.
Owner:QUFU NORMAL UNIV

A photocatalytic synthesis method of 1,2-naphthalene dicarboxylic acid diethyl ester compounds

The application discloses a kind of 1,2-naphthalene dicarboxylic acid diethyl compound photocatalytic synthesis method, it includes the following steps: styrene compound, alpha-diazo iodonium salt and catalyst are dispersed in organic solvent, then coupling cyclization reaction is carried out under light, obtains 1,2-naphthalene dicarboxylic acid diethyl compound.The 1,2-naphthalene dicarboxylic acid diethyl compound photocatalytic synthesis method of the application has the advantages that raw material is cheap and easy to obtain, simple and efficient, reaction condition is mild, atom economy is high, product is easy to purify, production cost is low, green and safe, suitable for large-scale industrial production.
Owner:SOUTH CHINA UNIV OF TECH +1

Functionalised crosslinker

PCT designated stageWO2026139298A1ArylPolymer science
The invention relates to a polymer for treating a surface, which polymer comprises: n reactive intermediate precursor groups, wherein n is an integer equal to or greater than 3; and m groups which comprise an atom-transfer radical polymerization (ATRP) initiator, wherein m is an integer equal to or greater than 3, wherein the reactive intermediate precursor groups are selected from carbene precursor groups and nitrene precursor groups, wherein the carbene precursor groups are selected from hydrazone groups of formula (A), diazo groups of formula (B) and diazirine groups of formula (C), and the nitrene precursor groups are azide groups of formula (D), wherein R1 is H or -S(O)2R2, and R2 is an unsubstituted or substituted C1-6 alkyl group or an unsubstituted or substituted aryl group. The invention also relates to a process for producing a treated substrate, which treated substrate has a surface suitable for surface -initiated atom-transfer radical polymerization (SIATRP). The invention also relates to a treated substrate having a surface suitable for SIATRP, and to treated substrates obtainable by the aforementioned process of the invention. The invention also relates to a treated substrate which comprises: a substrate, a reacted polymer disposed on a surface of the substrate, and a further polymer, grown by SIATRP, bonded to the reacted polymer.
Owner:OXFORD ADVANCED SURFACES

Diazo compounds, chemical mechanical polishing slurry compositions and polishing methods

ActiveCN116462637BImprove polishing flatnessImprove polishing rateOrganic chemistryOther chemical processesSlurryMaterials science
A diazo compound of Formula 1 or a salt thereof, a chemical mechanical polishing slurry composition comprising the compound, and a polishing method using the chemical mechanical polishing slurry composition are disclosed.
Owner:SAMSUNG SDI CO LTD

Environment-friendly disperse dye and preparation method thereof

The invention provides an environment-friendly disperse dye and a preparation method thereof. The preparation method comprises the following steps: a pretreatment step: refining 3, 4-dichlorophenyl thiourea by using an organic solvent to obtain refined 3, 4-dichlorophenyl thiourea; a closed loop step: under an acidic condition, the refined 3, 4-dichlorophenyl thiourea is subjected to closed loop to obtain a thiazole mixed slurry, and the thiazole mixed slurry comprises 2-amino-5, 6-dichlorobenzothiazole and 2-amino-6, 7-dichlorobenzothiazole; a diazotization step: under an acidic condition, carrying out a diazotization reaction on the thiazole mixed slurry and a diazotization reagent to obtain a diazotization liquid; and a coupling step: carrying out a coupling reaction on the diazonium liquid and an esterification reagent, and carrying out crystal transformation to obtain the environment-friendly disperse dye. The environment-friendly disperse dye disclosed by the invention is qualified in environment-friendly index, high in yield and purity and suitable for mass production.
Owner:ZHEJIANG RUNTU

A method for preparing minocycline hydrochloride and its intermediates

This invention discloses a compound of formula I and a method for preparing minocycline hydrochloride. The method for preparing compound I involves dissolving 6-demethyltetracycline in acidic water, adding a chlorination reagent for chlorination, then adding p-aminobenzenesulfonic acid diazonium hydrochloride and alkaline solution for coupling reaction, followed by post-treatment. The method for preparing minocycline hydrochloride uses 6-demethyltetracycline as a starting material, proceeding through the intermediate of compound I, and removing the C7 chlorine, p-aminobenzenesulfonic acid group, and C6 hydroxyl group via catalytic hydrogenation, followed by reductive amination and post-treatment. This invention achieves low-pressure palladium-carbon catalytic removal of the C6 hydroxyl group by introducing an electron-donating amino group at the C7 position, eliminating the need for expensive rhodium-carbon catalysts. The reaction conditions are mild, column chromatography purification is unnecessary, the overall yield is ≥85%, and the product purity is ≥96%, making it suitable for industrial production.
Owner:CHONGQING SHENGHUAXI PHARMA CO LTD +1

Electroactive compounds, compositions comprising the compounds, and methods of pattern forming

The present application relates to an electroactive compound, a composition comprising the same, and a pattern forming method, and more particularly, to a composition comprising an acid-sensitive polymer comprising a first repeating unit derived from a monomer containing an acid-decomposable group; a photoacid generator compound; a non-polymeric electron acceptor compound, the non-polymeric electron acceptor compound having an electron affinity greater than that of the photoacid generator compound, where the non-polymeric electron acceptor compound does not generate a photoacid, and where the non-polymeric electron acceptor compound does not include a plurality of diazonaphthoquinone (DNQ) groups; and a solvent, where the solvent is present in the composition in an amount greater than 50% by weight, based on the total weight of the composition, where the composition is a positive EUV photoresist or an electron beam photoresist.
Owner:杜邦电子材料国际有限责任公司

[3+2] cycloaddition method of amino acid active ester and diazo compound and its application in synthetic chemistry

ActiveCN119462537Befficient connectionFast and efficient orthogonal connectionGroup 5/15 element organic compoundsOrganic synthesisCycloaddition
This invention belongs to the field of organic synthesis and relates to a [3+2] orthogonal cycloaddition method for the reaction of an active amino acid ester with a diazo compound and its application in synthetic chemistry. The method comprises: under inert gas protection and in the presence of a base and solvent, contacting the active amino acid ester with a diazo compound to undergo a [3+2] orthogonal cycloaddition reaction to obtain the 1,2,4-triazole compound represented by Formula I. The method of this invention uses readily available active amino acids and diazo compounds as starting materials, enabling the efficient and selective synthesis of highly functionalized, fully substituted 1,2,4-triazoles, and achieving a rapid and efficient orthogonal connection between two molecules linked to the diazo compound and the active ester.
Owner:WUHAN ORGANIC PHOTOCHEMICAL TECHNOLOGY CO LTD

Preparation method of tetrahydroxy tetraphenyl ethylene photoinitiator and ultraviolet light absorber

PendingCN121850908AHigh molar extinction coefficientStrong UV Absorbing PropertiesSulfonic acid esters preparationPhotosensitive materials for photomechanical apparatusSulfonyl chloridePtru catalyst
The invention relates to a preparation method of a tetrahydroxy tetraphenyl ethylene photoinitiator. According to the method, tetrahydroxy tetraphenyl ethylene and a diazo naphthoquinone sulfonyl chloride compound are subjected to a condensation reaction to prepare the diazo naphthoquinone photoinitiator, and the photolysis rate of the diazo naphthoquinone photoinitiator is tested. The preparation method specifically comprises the following steps: in an organic solvent, taking tetrahydroxy tetraphenyl ethylene and diazonaphthoquinone sulfonyl chloride as raw materials, and carrying out esterification condensation reaction under the action of a catalyst to obtain the tetrahydroxy tetraphenyl ethylene photoinitiator. The tetrahydroxy tetraphenyl ethylene photoinitiator synthesized by the invention has the following advantages: compared with the traditional photoinitiator, the light sensitivity is obviously improved; the ultraviolet absorption capability is stronger, and the photosensitive performance is more excellent.
Owner:HUBEI SINOPHORUS ELECTRONIC MATERIALS CO LTD

Preparation method and application of suzertraline intermediate

The invention relates to a preparation method and application of a suzertraline intermediate, 3, 4-difluoro-2-methoxyaniline is taken as a raw material, diazotization is carried out to obtain a stable intermediate compound 3, 4-difluoro-2-methoxybenzene diazonium tetrafluoroborate, then coupling is carried out through a copper catalyst to obtain (R)-3-(3, 4-difluoro-2-methoxyphenyl)-4, 4-difluoro-2-methoxyphenyl)-4, 4-difluoro-2-methoxybenzene diazonium tetrafluoroborate, and then the (R)-3-(3, 4-difluoro-2-methoxyphenyl)-4, 4-difluoro-2-methoxybenzene diazonium tetrafluoroborate is taken as a raw material to obtain the suzertraline intermediate. The catalyst is 2, 5-dimethyl-5-(trifluoromethyl) furan-2 (5H) ketone. A diazotization reaction site is an amino group of 3, 4-difluoro-2-methoxyaniline, a copper catalyst coupling reaction site is a diazonium tetrafluoroboric acid group of 3, 4-difluoro-2-methoxybenzene diazonium tetrafluoroborate and one end of a hydrogen atom on a carbon-carbon double bond in (R)-4, 5-dimethyl-5-(trifluoromethyl) furan-2 (5H) ketone, and by-products are not easy to generate.
Owner:ZHEJIANG MENOVO PHARMA

A method for preparing an electrocatalytic scf-substituted dihydrofuran compound

The application provides a preparation method of an electrocatalytic SCF-substituted dihydrofuran compound, and belongs to the technical field of compound preparation. The application uses diazonium and ethylene compounds as substrates, uses an SCF source as a sulfur-containing and fluorine-containing fragment donor, realizes a one-pot cascade reaction of ring formation through electrolysis, and thus constructs the SCF-substituted dihydrofuran compound. The raw material of the application has a wide source, uses electric current as a reaction driving force, avoids or reduces the use of additional photosensitizers and chemical oxidation-reduction reagents, and has the one-pot cascade characteristics of ring C-N bond breaking, C-O bond construction, trifluoromethylation and ring formation and the like, so that the step economy can be improved.
Owner:JINING UNIV

Flexible display device and dual-curing photosensitive material

The invention discloses a flexible display device and a photosensitive material or a compound suitable for forming patterns of an insulating film or a protective film in flexible display manufacturing, and the compound is shown as a structural formula (I). The photosensitive material has the advantages of low curing temperature, high elastic recovery rate and high light transmittance; the technical contradiction of a traditional insulating film material is overcome, and the problem of color development of diazonaphthoquinone is solved.
Owner:LIANYUNGANG SUIZHU TECH CO LTD

Antimony nanopowder, preparation method and application thereof

ActiveCN122076979AAddressing pulmonary toxicity issuesReduce Occupational Health RisksTransportation and packagingMetal-working apparatusPulmonary effectsChemical reaction
This invention relates to antimony nanopowder, its preparation method, and its applications, belonging to the field of metal powder processing technology. The method includes dispersing antimony nanopowder in a solvent to obtain a dispersion, mixing the dispersion with 5-10 times the mass of nitrobenzene diazonium salt (p-NBD) of the antimony nanopowder, and reacting under light irradiation at 0-4°C for 30-60 hours to obtain passivated antimony nanopowder. The diazo chemical reaction forms stable covalent bonds on the surface of Sb NPs, blocking their interaction with respiratory cells. Compared with the original Sb NPs group, the nitrobenzene diazonium salt modification reverses the GPX4 activity inhibition effect, upregulates GPX4 protein expression and restores it to near the control group level, and eliminates the ability to induce ferroptosis, thus addressing the pulmonary toxicity problem of Sb NPs from the perspective of ferroptosis mechanism.
Owner:SHANDONG UNIV +1

Protamine-mediated fluorescence resonance energy transfer sensing system and application

The invention discloses a protamine mediated fluorescence resonance energy transfer (FRET) sensing system and application thereof. According to the protamine, a tetraphenylethylene-derived anionic molecule (4, 4 '-(((1, 2-stilbene-1, 2-disubunit) bis (4, 1-phenyl)) bis (aza-disubunit)) bis (4-sodium oxobutyrate)) is electrostatically enriched on the surface of the protamine, and a tetraphenylethylene group emits fluorescence after being aggregated and acts as an energy donor; furthermore, cationic dye (4-(4-dimethylaminostyryl)-1-methyl iodide pyridine) is added as an energy receptor, and a fluorescence resonance energy transfer (FRET) system is constructed. Through construction of the FRET system, long-wavelength fluorescence emission can be obtained, high-sensitivity detection of trypsin and screening of enzyme preparations are achieved, and the FRET system is expected to be applied to complex media.
Owner:BEIJING TECH & BUSINESS UNIV

Cholic acid derivative resin and preparation method thereof, photoresist and application thereof, and photoetching method

The invention provides cholic acid derivative resin and a preparation method thereof, photoresist and application thereof, and a photoetching method, and can be applied to the technical field of photoresist. According to the cholic acid derivative resin, bio-based cholic acid tert-butyl ester is used as a skeleton, and two functional groups including a diazonaphthoquinone sulfonate group and a tert-butyl ester group are introduced into molecules of the bio-based cholic acid tert-butyl ester to form a resin structure with a dual-sensitization characteristic. The photoresist composition comprises 10%-20% of the resin, 1%-5% of a photoacid generator, 1%-2% of an additive and an organic solvent. The composition shows high light transmittance in i-line photoetching, the sensitivity of the composition is lower than 130 mJ / cm, and patterning with the resolution of 64 nm can be achieved. The invention also provides a corresponding resin preparation method and a photoetching process, which are suitable for i-line projection photoetching, interference photoetching, near-field photoetching and super-resolution photoetching, and have the advantages of high resolution, environmental friendliness and good process compatibility.
Owner:INST OF OPTICS & ELECTRONICS CHINESE ACAD OF SCI

Direct coupling type double-chromosome disperse dye as well as synthesis method and application thereof

PendingCN121471727ADisazo dyesDyeing processDisperse dyeChromophore
The invention provides a direct coupling type double-chromophore disperse dye as well as a synthesis method and application thereof, and belongs to the technical field of disperse dyes. Introducing a reaction active group into the coupling component I to obtain a coupling component I containing the reaction active group; directly coupling a coupling component II with a reaction site with a coupling component I containing a reaction active group to obtain a coupling component with double coupling sites; the coupling component of the double coupling sites and the diazo component are subjected to bilateral coupling, and the direct coupling type double-chromophoric disperse dye is obtained.
Owner:SHAOXING UNIVERSITY

Method for preparing red pigment by coating nano calcium carbonate with pigment red 2

The invention discloses a method for preparing a red pigment by coating nano calcium carbonate with pigment red 2, and belongs to the technical field of pigments. The preparation method comprises the following steps: dispersing nano calcium carbonate into absolute ethyl alcohol to obtain a nano calcium carbonate suspension, and preparing a diazo component A solution and a coupling component B solution; and simultaneously dropwise adding the solution A and the solution B into the nano calcium carbonate suspension, controlling the molar ratio of the raw materials, the reaction temperature and the reaction time, and carrying out post-treatment to obtain the red pigment with the nano calcium carbonate coated with the pigment red 2. The binding force of the pigment red 2 and calcium carbonate in the obtained red pigment is remarkably enhanced, compared with commercially available pigment red 2, the hue, colored light, brightness and tinting strength of the red pigment are not reduced, and the prepared product is expected to replace the commercially available pigment red 2 product to be applied.
Owner:ZHEJIANG HAOCHUAN TECH CO LTD

Diazirine-based molecules and uses thereof

A family of novel diazirine-based molecules as well as methods of manufacture and uses thereof are disclosed. These compounds allow non-functionalized polymers, such as polyolefins, to crosslink via C—H insertion. Such a C—H insertion process is useful, for example, for forming protective topical coatings on low surface energy films, for the covalent adhesive bonding of such films, or for creating rigid 3-dimensional polymeric structures by in-situ doping and activation of the crosslinker. The crosslinkers can be activated thermally, by UV radiation or by an electric potential.
Owner:XLYNX MATERIALS INC

Preparation method of azo reactive dye

The invention discloses a preparation method of an azo reactive dye, which comprises the following steps: reacting cyanuric chloride with sodium 2, 5-diaminobenzene sulfonate to obtain a first condensate, diazotizing the first condensate, performing acidic coupling on the first condensate and acetyl J acid, performing alkaline coupling on the first condensate and a diazo solution of 6-beta-ethyl sulfuryl sulfate-2-naphthylamine-1-sulfonic acid, and finally performing secondary condensation on the second condensate and nicotinic acid to obtain the azo reactive dye. Reacting to obtain azo reactive dye primary pulp, wherein the structure of the dye is shown in the specification; the prepared dye is bright in color, excellent in solubility, high in storage stability, good in lifting power and good in fixation rate and color fastness.
Owner:ZHEJIANG JINGGUANG IND

Sulfonate synthesis method based on flowing photochemical technology

PendingCN121974832ASulfonic acid esters preparationPhenylacetatesOrganic solvent
The invention discloses a method for synthesizing a sulfonate compound based on a flowing photochemical technology, which comprises the following steps: (1) carrying out azidation reaction on a phenylacetate compound and p-toluenesulfonyl azide under the action of alkali to obtain an alpha-diazophenylacetate compound; and (2) respectively dissolving a sulfonic acid compound and the alpha-diazophenylacetate compound obtained in the step (1) in an organic solvent to form solutions, then continuously inputting the solutions into a microchannel reactor, carrying out an illumination reaction under an illumination condition, and after the reaction is finished, carrying out post-treatment to obtain the sulfonate compound. The preparation method can realize continuous reaction and is high in yield.
Owner:SHAOXING UNIVERSITY