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230 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.

Preparation method of 4-fluoro-3, 5-dimethylphenylhydrazine hydrochloride

PendingCN120757464AHydrazine preparationDimethylaniline N-oxidePhenylhydrazine hydrochloride
The invention provides a preparation method of 4-fluoro-3, 5-dimethylphenylhydrazine hydrochloride, which comprises the following steps: salifying 4-fluoro-3, 5-dimethylaniline serving as a substrate with concentrated hydrochloric acid, reacting with sodium nitrite to prepare a diazo solution, reducing the diazo solution into corresponding phenylhydrazine by using alkaline sodium sulfite as a reducing agent system, and reacting the 4-fluoro-3, 5-dimethylphenylhydrazine hydrochloride with the diazo solution to prepare the 4-fluoro-3, 5-dimethylphenylhydrazine hydrochloride. And acidizing the 2, 5-dimethyl phenylhydrazine to obtain corresponding phenylhydrazine hydrochloride. According to the preparation method, sodium sulfite which is low in cost and easy to obtain is used as a reducing agent, the defects that metal residues are high, the environment is prone to being polluted and the raw material cost is high due to the fact that a metal reducing agent is adopted when phenylhydrazine hydrochloride is prepared in the prior art are overcome, the reaction is completed in a water phase, no organic solvent is adopted, and the concept of green chemistry is met; and the problems of complicated post-treatment and easy pollution caused by the adoption of an organic solvent can be effectively avoided.
Owner:INNER MONGOLIA XINGYUAN NEW MATERIAL TECH CO LTD

Method for detecting content of trace metal ions in diazo naphthoquinone photosensitizer

The invention discloses a method for detecting the content of trace metal ions in a diazo naphthoquinone photosensitizer. The method comprises the following steps: sample pretreatment: weighing diazonaphthoquinone photosensitizer powder in a clean room, putting the diazonaphthoquinone photosensitizer powder into a cleaned and dried wide-mouth PFA bottle, adding an organic reagent, and carrying out ultrasonic treatment until a solid is completely dissolved; the method comprises the following steps: testing: adding a metal standard substance into an organic solvent to prepare three standard solutions with different concentrations; debugging an instrument, determining target metal in the standard solution in a Cool mode, a No Gas mode and a He mode by using an inductively coupled plasma mass spectrometer to obtain a signal intensity value (CPS value) corresponding to each metal ion concentration in the standard solution, and establishing a standard curve; and measuring the sample in which the photosensitizer is dissolved by using the same steps to obtain the content of metal ions in the sample. According to the method, appropriate detection conditions are optimized for different elements to be detected in the diazo naphthoquinone photosensitizer, polyatomic ion interference and matrix effect in a sample are mainly reduced, the content of 16 metal ions can be accurately detected at the same time, and the test efficiency is high.
Owner:HUBEI THREE GORGES LAB

Preparation method and application of beta-functionalized cobalt phthalocyanine axial connection carbon nanotube electrocatalyst

The invention discloses a preparation method and application of a beta-functionalized cobalt phthalocyanine axial connection carbon nanotube electrocatalyst, and relates to a preparation method and application of an electrocatalyst. The invention aims to solve the problem of low selectivity of glycolaldehyde synthesis in the prior art, the CoPcX-CNT electrocatalyst is prepared by adopting a method of combining organic synthesis and diazo treatment, and CoPcCN-CNT containing cyano-functionalized cobalt phthalocyanine has optimal H2O2 selectivity. The Faraday efficiency of 95.7% and the H2O2 yield of 20320 mmol.g <-1 >. H <-1 > can be achieved in a flowing electrolytic tank under the industrial current density of 300 mA. Cm <-2 >. And finally, adjusting the permeability of H2O2 by using an ion exchange membrane, and finding that the AEM system with proper permeability of H2O2 has the highest glycolaldehyde selectivity (63.5%). The method is applied to the field of H2O2 in-situ production and efficient utilization.
Owner:JILIN AGRICULTURAL UNIV

A polyhydroxyazo-grafted graphene oxide-based material and its application in electromagnetic wave absorption.

This invention provides a benzene-azo group-grafted polyhydroxy graphene oxide-based material and its application in electromagnetic wave absorption. The material is synthesized using aniline compounds and polyhydroxy graphene oxide as raw materials via diazo coupling. The feasibility of the preparation method was verified by spectral characterization, demonstrating the feasibility of impedance matching through covalent grafting of functionalized functional groups. This preparation method is simple, low-cost, and yields high output.
Owner:NANJING UNIV OF INFORMATION SCI & TECH

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

A method for synthesizing a carbazole N-H functionalized product at room temperature and normal pressure based on Fe catalysis

This invention relates to a method for synthesizing N-H functionalized carbazole products based on Fe catalysis at room temperature and pressure. The method involves mixing α-aryl-α-diazo ester with carbazole or a carbazole derivative in an organic solvent, adding an Fe catalyst and additives, and reacting at room temperature and pressure to obtain the N-H functionalized carbazole product. This invention uses metallic Fe as a catalyst to react α-aryl-α-diazo ester to generate α-(N-carbazole)-α-aryl ester compounds under nitrogen atmosphere at room temperature and pressure. It also offers a wider range of selectable substrates and, compared to traditional synthesis methods, has many advantages such as high yield, simple conditions, low waste emissions, simple reaction equipment, and ease of industrial production.
Owner:SHANDONG 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

Photoresist and preparation method thereof

The invention relates to the technical field of photoresists, and particularly provides a photoresist and a preparation method thereof.The photoresist is prepared from phenolic resin, a diazonaphthoquinone photosensitizer, phenyl triphenyl phosphate and a solvent, and the stability and definition of an exposed pattern are optimized through the combination of a special polymer, a sensitizer and the solvent. In the embodiment, the sensitivity range of the formula is 55 mJ / cm < 2 > to 120 mJ / cm < 2 >, the resolution ratio reaches 0.05 mu m, and burrs are controlled to be 0.05 mu m or below. The technology can be widely applied to the fields of semiconductor chip manufacturing, microelectronic packaging, display devices and nanotechnology, meets the production requirements of high precision and high efficiency, and has good market prospects and commercial application value.
Owner:WUHAN BRIGHT DIODE LASER TECH CO LTD

Medical polyaryletherketone implant and surface modification method thereof

The invention discloses a medical polyaryletherketone implant and a surface modification method thereof, and the method comprises the following steps: immersing a polyaryletherketone material matrix into a saturated sodium carbonate solution used as a foaming agent, taking out the polyaryletherketone material matrix, and carrying out concentrated sulfuric acid ultrasonic treatment at room temperature; alternately treating with a saturated sodium carbonate solution and concentrated sulfuric acid until a microporous network is formed on the surface of the polyaryletherketone material matrix; carrying out surface phosphorylation on the polyaryletherketone material matrix with the microporous network formed on the surface by using a diazo reaction to obtain a surface phosphorylated matrix; treating the surface phosphorylated matrix by adopting a hydrothermal method and a chemical coprecipitation method, and forming a biomineralization layer doped with antibacterial metal ions on the surface of the matrix; and freeze-drying a hydrogel coating doped with antibacterial fatty acid on the surface of the matrix to obtain the medical polyaryletherketone implant.
Owner:ZHEJIANG UNIV

Universal polymer force-sensitive cross-linking agent based on combination of cross-linking functions of force-sensitive group and diaziridine, and preparation method and application of universal polymer force-sensitive cross-linking agent

The invention discloses a universal polymer force-sensitive cross-linking agent based on combination of a force-sensitive group and a bis-aziridine cross-linking function, and a preparation method and application thereof. The cross-linking agent is prepared by esterification of the force-sensitive group and a bis-aziridine group. The method comprises the following steps: in a nitrogen environment, carrying out a reaction on a force sensitive group, 4-[3-(trifluoromethyl) diazo-3-yl] benzoic acid, 4-dimethylaminopyridine (DMAP) and 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride (EDC-HCl) in anhydrous dichloromethane; and extracting the obtained mixture for three times, performing column chromatography purification on the obtained mixture on a silica gel column by using an eluent, and spin-drying to obtain a final product. The mechanical response sensitivity and structural stability of the material are remarkably improved, a mechanical force sensitive group introduction strategy suitable for various polymer systems is established, and a new technical path and theoretical support are provided for multifunctional design and wide application of the stress sensitive material.
Owner:TIANJIN UNIV

Method for preparing 9-(phenylsulfonyl)-xanthene derivatives by electrocatalysis

The present invention belongs to the technical field of electrocatalytic preparation of xanthene derivatives. The present invention provides a method for electrocatalytically preparing 9-(phenylsulfonyl)-xanthene derivatives, including: adding aryl diazonium tetrafluoroborate derivatives, xanthene, DABSO, tetrabutylammonium hexafluorophosphate, acetonitrile and acetic acid in an electrolytic cell, passing a direct current, and reacting for 2 hours at a certain temperature and under nitrogen protection conditions. The present invention adopts electrocatalytic synthesis of 9-(phenylsulfonyl)-xanthene, which uses electric current as an oxidant, does not require an external oxidant and other metal catalysts, and also provides higher catalytic activity and lower reaction energy barrier for the reaction; and there is no need to pre-functionalize the substrate, with high atom economy and good functional group tolerance, so various substituted 9-(phenylsulfonyl)-xanthene can be obtained with good yield. In the reaction, low-toxicity and economical acetonitrile is used as a solvent, which avoids the use of highly toxic solvents and is green and environmentally friendly.
Owner:NINGXIA MEDICAL UNIV

Ruthenium complex for inducing mitochondrial DNA polycondensation to overcome tumor drug resistance, anti-tumor drug and preparation method and application thereof

The invention discloses a ruthenium complex for inducing mitochondrial DNA polycondensation to overcome tumor drug resistance, an anti-tumor drug and a preparation method and application of the ruthenium complex and the anti-tumor drug. The ruthenium complex is connected with a triphenylphosphine structure-modified bipyridine diazo-anthracene ligand through an alkyl chain, so that the fat solubility of the complex is improved, and the complex can enter cells more easily; the complex has a mitochondrial enrichment function and can be enriched in mitochondria; the complex induces mitochondrial DNA polycondensation so as to cause cancer cell death; the targeting property on tumor cells is effectively improved; the IC50 of the compound on human non-small cell lung cancer cell strains and cis-platinum drug-resistant strains thereof is far lower than that of cis-platinum, and the compound can be used as an excellent anti-tumor drug. The complex takes a ruthenium-coordinated ruthenium precursor compound as a raw material, and the raw material is economical and easy to obtain; the selectivity of the ruthenium complex can be improved, and the cost is saved.
Owner:GUANGDONG UNIV OF TECH

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

Sulfur ylide diazo compounds and uses thereof

The present invention relates to sulfur ylide diazo compounds, their synthesis and their use for the transfer of a carbon atom or a CN2 group into an organic substrate comprising a pi electron system, in particular for C(sp3)-atom transfer to create carbon spiro centers. The invention further relates to related processes and the compounds thus obtained.
Owner:TECHN UNIV DORTMUND

Chiral fluorocyclopropane carboxylates and methods for their preparation

PendingCN122627914AArylCarboxylic acid
The application discloses a chiral fluorocyclopropane carboxylate and a preparation method thereof. Under the catalysis of divalent rhodium, ethyl aryl diazoacetate and fluorostyrene are reacted through an asymmetric cyclopropanation reaction to generate a chiral fluorocyclopropane compound. Different substitution types of substrates in the system are expanded, and good universality is shown. Various types of substituted substrates can smoothly participate in the reaction to synthesize 12 fluorocyclopropane ester substrates with a yield of 56-89%, 82-99% ee and a highest >20.0:1.0 dr. The application efficiently realizes the introduction of a fluorine atom to a cyclopropane skeleton, and efficiently constructs the fluorocyclopropane compound under mild conditions, thereby providing a new strategy which is simple, efficient and has strong universality for the synthesis of the important compound.
Owner:NINGXIA UNIVERSITY

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

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

Application of Nogo-B protein in preparation of medicine serving as anti-osteosarcoma target

The invention relates to application of Nogo-B protein in preparation of a medicine serving as an anti-osteosarcoma target spot. The invention discloses an alpha-hydroxyl / alkoxy / amino-beta-amino derivative, a synthesis method thereof and application of Nogo-B protein serving as a new osteosarcoma target, an osteosarcoma diagnostic reagent and a small-molecule inhibitor 4v serving as an osteosarcoma targeting drug. A diazo compound, water / alcohol / amide and imine are used as raw materials, rhodium acetate is used as a catalyst, a product is obtained in an organic solvent through a one-step reaction with high selectivity and high yield, then the small-molecule inhibitor 4v is obtained through osteosarcoma cell surface screening, a new osteosarcoma target Nogo-B is proposed based on a proteomics analysis technology, and the new target Nogo-B is used for inhibiting osteosarcoma. The effects of inhibiting cell proliferation and migration and tumor growth can be achieved through experiments such as knockout of Nogo-B protein. The invention discloses a novel application of Nogo-B protein. The Nogo-B protein is used for preventing, relieving and treating osteosarcoma and osteosarcoma-related complications of individuals in need. Also disclosed are methods of diagnosing, treating, and monitoring osteosarcoma or methods of inhibiting osteosarcoma, and methods of screening for osteosarcoma inhibitors.
Owner:EAST CHINA NORMAL UNIV

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

Carborane cage boron free radical as well as preparation method and application thereof

The invention relates to the technical field of organic electrochemical synthesis, and discloses a carborane cage boron free radical and a preparation method and application thereof.The structural formula of the carborane cage boron free radical is shown in the formula I. The preparation method has the advantages that in-situ generation of boron free radicals under the electrochemical condition is achieved for the first time; a B-N bond of diazo-carborane tetrafluoroborate is electrochemically reduced to generate a boron center free radical with reaction activity, the free radical can efficiently initiate a series cyclization reaction of 2-isocyano aryl sulfide, and a carborane benzothiazole skeleton is constructed in one step.
Owner:SOUTHERN UNIVERSITY OF SCIENCE AND 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

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 separation is carried out to obtain a stable solid intermediate compound 3, 4-difluoro-2-methoxybenzene diazonium tetrafluoroborate, and the suzertraline intermediate is prepared by a one-step method. Under the catalytic action of a titanium catalyst, coupling and configuration inversion are carried out to obtain a key intermediate (3S, 4S, 5R)-3-(3, 4-difluoro-2-methoxyphenyl) dihydro-4, 5-dimethyl-5-(trifluoromethyl)-2 (3H)-furanone, and the key intermediate is (3S, 4S, 5R)-3-(3, 4-difluoro-2-methoxyphenyl) dihydro-4, 5-dimethyl-5-(trifluoromethyl)-2 (3H)-furanone. The raw materials of the route are cheap and easy to obtain, the use of expensive palladium metal catalyst in the reaction route is reduced, the reaction site is single, byproducts are not easy to generate, and meanwhile, the quality control of the intermediate compound is facilitated.
Owner:ZHEJIANG MENOVO PHARMA

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

Indazole n-oxides, methods of synthesis and anticancer activity applications thereof

The application discloses indazole nitrogen oxide and a synthesis method and anticancer activity application thereof, and belongs to the technical field of organic synthesis and drug discovery. N-nitrosoaniline compound 1, diazindione compound 2, a catalyst, an additive and hexafluoroisopropanol are mixed, and the mixture is reacted by temperature rising to obtain indazole nitrogen oxide. The chemical structure of the indazole nitrogen oxide is as follows: researches show that the indazole nitrogen oxide has the activity of inhibiting the proliferation of Hela, A549 and HCT-116 cancer cells, and has potential medicinal value. Meanwhile, the synthesis method provided by the application is completed by one-pot multi-step tandem reaction, and the process is simple and efficient. The synthesis method has the following remarkable characteristics: raw materials are cheap and easy to obtain, the product is valuable, the steps are economical and atomic economy is high.
Owner:HENAN NORMAL UNIV

Method for detecting multiple chelating agents in daily chemical products

The application relates to the field of analysis and detection, and discloses a detection method for multiple chelating agents in daily chemical products, which comprises the following steps: methylating a to-be-detected sample by using a diazomethane methylating reagent to obtain a to-be-detected solution; detecting the to-be-detected solution by using a specific elution program to obtain a chromatogram; and qualitatively and / or quantitatively analyzing the chelating agents in the to-be-detected sample according to the chromatogram. By using the detection method, multiple chelating agents (including DTPA, DTPMP, EDTMPA, HDTEPA, EGTA, HEDP, EDTA, NTA, GLDA, PBTC, MGDA, IDS, HEDTA, HPAA, DTPA-OH, CA and ATMP) can be efficiently detected, meanwhile, the detection can be prevented from being disturbed by other components in the daily chemical products, and high detection sensitivity and accuracy can be realized for the chelating agents.
Owner:NICE ZHEJIANG TECH CO LTD +1

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