3628 results about "Methyl group" patented technology

A production method for an aqueous dispersion according to the present invention comprises polymerizing a first monomer that includes tetrafluoroethylene in the presence of a compound represented by formula (X) and a polymerization initiator under conditions in which an aqueous medium is present but an emulsifier that includes fluorine atoms is substantially absent to produce an aqueous dispersion that includes particles of a first fluorine-containing polymer that has an average particle diameter of no more than 500 nm and does not have a melting point.　Formula (X): C(X1)(X2)=C(X3)-L-Z. In formula (X), X1, X2, and X3 are each independently a hydrogen atom, a fluorine atom, a perfluoromethyl group, or an alkyl group, L is a single bond or a divalent linking group, and Z is an anionic group or a salt of an anionic group.

The invention provides a photosensitive resin composition containing a photobleaching aminomethyl anthracene photosensitizer and application thereof.The structural main body anthracene ring of the photosensitizer introduces an aminomethyl functional group to the 9th and / or 10th site: through introduction of the aminomethyl functional group, while the electron cloud density of polycyclic aromatic hydrocarbon is maintained, the maximum absorption wavelength is subjected to red shift, and the photosensitive resin composition is especially suitable for a 405nm illumination system; the initiation efficiency is obviously improved; the exposure energy is reduced; compared with an existing DBA type photoinitiator, the problem of alkoxy carbon-oxygen bond breakage caused by p-pi conjugation of DBA is avoided, generation of small molecule fragments is effectively inhibited, defects are reduced, and the yield is increased. In addition, compared with DPHA and DAcOA, the photosensitizer also shows better solubility and formula compatibility. The preparation method has the characteristics of simple preparation process and low cost, and can be widely applied to the photocuring fields of dry films, paints, coatings, printing inks, forming materials and the like.

The invention belongs to the field of organic photoelectric materials, and discloses an electroluminescent material and a preparation method and application thereof. The structure of the electroluminescent material is as shown in a formula I: # imgabs0 #. According to the electroluminescent material compound provided by the invention, on the basis of a 9-methyl-9-phenylfluorene group, triarylamine and an aromatic ring are connected through 2 and 4 sites, when the triarylamine group is substituted by aryl, the energy level is relatively low, carrier migration localization is avoided, and a hole transport energy barrier can be reduced, so that the migration rate and the luminous efficiency are improved; triarylamine has excellent hole transport performance, a triarylamine material is used as a light-emitting auxiliary layer, a group with a high triplet state energy level is introduced, the energy range between energy levels can be reduced, and the service life of the device is greatly prolonged.

The invention relates to the technical field of petrochemical engineering, and discloses a temperature-resistant anti-swelling agent for fracturing and a preparation process thereof.The preparation method comprises the steps that glycerol triglycidyl ether and diethanol amine are subjected to a ring-opening reaction, a polyhydroxy tertiary amine monomer is obtained, then the polyhydroxy tertiary amine monomer and chloromethylated polystyrene are subjected to a quaternization reaction, and the temperature-resistant anti-swelling agent for fracturing is obtained. Quaternary ammonium salt groups of the anti-swelling agent and negative charges on the surface of clay form electrostatic interaction, and hydroxyl groups and the surface of the clay form hydrogen-bond interaction, so that the anti-swelling agent can be firmly adsorbed on the surface of the clay to form a layer of polymer film, the clay is prevented from being in contact with water, the phenomenon that the clay swells when encountering water is effectively inhibited, and the anti-swelling rate is very high. And the anti-swelling agent contains a heat-resistant polystyrene molecular chain, has excellent high temperature resistance, can maintain good structural stability at high temperature, still maintains high anti-swelling rate, and is suitable for a fracturing fluid system for high-temperature oil reservoir exploitation.

The invention provides a light conversion film composition. The light conversion film composition comprises the following components in percentage by weight: matrix resin, a light conversion agent and an auxiliary agent, the light conversion agent is a benzotriazole compound, and the auxiliary agent is an organic solvent. The structural general formula of the benzotriazole compound is as follows: # imgabs0 # R1 and R2 are respectively and independently selected from any one or more of H, C1-C20 alkyl and C1-C20 alkyl with at least one methylene substituted by a polyether chain segment, and R3 is independently a chain segment containing a carbon-carbon unsaturated double bond.

The invention discloses an organic silicon cooling liquid and a preparation method thereof, the product has low viscosity and high flash point, and relates to the field of application of single-phase cooling liquid for heat dissipation of heating equipment, and the specific method comprises the following steps: uniformly mixing olefin and a catalyst at 20-30 DEG C, heating to 35-45 DEG C, dropwise adding hydrogen-containing siloxane, and controlling the temperature of the reaction liquid to be in a range of 60-130 DEG C; after adding, continuously stirring; cooling after the reaction is finished, and removing residual olefin to obtain a final product with a general formula of (CH3) 3SiO-[R1R2SiO] nSi (CH3) 3, wherein R1 is an alkyl group ranging from 8 to 16; r2 is a methyl group or a trimethylsiloxy group; n is equal to 1-2. The prepared single-phase organic silicon cooling liquid has the performance of high flash point and low viscosity, is low in surface tension, good in fluidity, more comprehensive in coverage, better in heat dissipation effect, good in compatibility with materials of a data center, free of swelling and other damage with related materials, and safe and long-acting.

Disclosed is a printing ink for heat-sensitive recording media, which is (A) or (B) below: (A) a heat-sensitive color-developing printing ink containing a leuco dye, a color developer, a vinylpyrrolidone-vinyl acetate copolymer, and a solvent, wherein the color developer is at least one selected from the group consisting of an N,N'-diaryl urea-based compound represented by general formula (1) (in the formula, R0 represents a C1-12 alkyl group, a C7-12 aralkyl group, or a C6-12 aryl group. The aralkyl group and the aryl group may be substituted with a C1-12 alkyl group, a C1-12 alkoxy group, a C6-12 aryl group, or a halogen atom. A plurality of R0s may be the same or different. A1 represents a hydrogen atom or a C1-4 alkyl group. A plurality of A1s may be the same or different.), a compound represented by general formula (2) (in the formula, R1 to R5 are the same or different, and represent a hydrogen atom, a halogen atom, a nitro group, an amino group, an alkyl group, an alkoxy group, an aryloxy group, an alkylcarbonyloxy group, an arylcarbonyloxy group, an alkylcarbonylamino group, an arylcarbonylamino group, an alkylsulfonylamino group, an arylsulfonylamino group, a monoalkylamino group, a dialkylamino group, or an arylamino group.), and 5-(N-3-methylphenyl-sulfonamide)-N',N''-bis-(3-methylphenyl)-isophthalic acid diamide; and (B) a protective layer printing ink for heat-sensitive recording media, the protective layer printing ink containing an adhesive, a slipperiness imparting agent, and a solvent, wherein the adhesive is a polyvinyl acetal resin, and the slipperiness imparting agent is an alkyl phosphate ester and / or a salt thereof.

The invention relates to the field of biomedical materials, in particular to a composite hydrogel microsphere with excellent cell adhesion performance and a preparation method and application thereof, and the preparation method comprises the following steps: (1) modifying silk fibroin with glutathione to obtain sulfydryl modified silk fibroin SF-GSH; (2) adopting methacrylic anhydride as a double-bond introduction reagent, introducing a methacrylate group on hyaluronic acid and forming a carbon-carbon double bond to obtain double-bond modified hyaluronic acid HA-MA; (3) mixing the sulfydryl modified silk fibroin SF-GSH with double bond modified hyaluronic acid HA-MA, and adding lactobionic acid to prepare a composite hydrogel microsphere precursor solution; and (4) preparing the composite hydrogel microsphere precursor solution into the composite hydrogel microsphere containing lactobionic acid. Compared with single hyaluronic acid hydrogel, the composite hydrogel microspheres prepared by the preparation method provided by the invention have good biocompatibility.

The invention relates to the technical field of dielectric materials, and discloses polyimide, a polyimide film and a preparation method and application thereof, the polyimide is obtained by a polymerization reaction of a dianhydride monomer and a diamine monomer, the diamine monomer comprises a methylene bridging group and a phenyl group with a substituent group, and the methylene bridging group is a phenyl group with a substituent group. The substituent group at least comprises one methyl group. The molecular twisted conformation lock structure provided by the invention not only can improve the tolerance of polyimide, but also can doubly inhibit intrachain and inter-chain charge migration of the dielectric film, so that the dielectric film still has extremely high energy storage density and energy storage efficiency at a service temperature close to a glass-transition temperature.

The present invention relates to a preparation method of an intelligent self-repairing, flame-retardant and light-resistant water-based polyurethane coating. The method comprises the following steps: preparing a self-made hyperbranched flame retardant and using it in the synthesis of a polyurethane prepolymer; cooling the mixture to 58° C., adding 2,2-dimethylolpropionic acid, reacting the mixture for 1 to 2 hours, adding 1 to 2 parts of a disulfide compound, reacting the mixture for 1 to 2 hours at 60 to 80° C., adding 1 to 2 parts of a hydrogen bonding agent, reacting the mixture for 1 hour at 60 to 80° C., adding 0.5 to 1.5 parts of a coumarin derivative, and reacting the mixture for 60 to 90° C. The mixture was stirred for 1-2 hours, and then spiropyran, diethanol monoisopropanolamine, and 0.01 parts of p-toluenesulfonamide were added, and the mixture was reacted at 50°C for 30 minutes. The temperature was lowered to 40-45°C, and 1-2 parts of triethylamine were added, and the mixture was reacted for 1-2 hours. The mixture was cooled to room temperature, and 60-65 parts of water were added. The mixture was stirred at a speed of 1800-2000 r / min for 0.5-1 hour to obtain an intelligent self-healing, flame-retardant, and light-resistant water-based polyurethane coating. The flame retardancy and self-healing properties of the obtained water-based polyurethane were significantly improved.

The invention discloses a modified amine curing agent and a preparation method thereof, and an epoxy resin composite material and a preparation method thereof, and belongs to the field of resin and composite materials. According to the curing agent, a C2-C8 alkyl chain is grafted to a methylene site of 4, 4 '-diaminodiphenylmethane (MDA) through free radical substitution and alkylation reaction, and a molecular structure with a flexible alkyl chain and a rigid benzene ring is formed. The preparation method comprises the following two steps: generating a halogenated intermediate from MDA and a halogen simple substance under certain reaction conditions, alkylating the halogenated intermediate with a Grignard reagent (RMgX), and purifying. The curing agent and epoxy resin are compounded, heated and cured, so that the epoxy resin composite material has relatively high impact strength and fracture toughness, has good tensile strength and hardness, has double functions of reinforcing and toughening, and solves the problem that reinforcing and toughening of traditional epoxy resin are difficult to be compatible; the method is suitable for the fields of aerospace, composite material adhesives and the like with harsh requirements on mechanical properties.

The present invention relates to compounds of formula (I) possessing an indole moiety linked to an indazole moiety, to compounds having similar core structures, and to associated salts, solvates, prodrugs and pharmaceutical compositions. The present invention further relates to methods of synthesising such compounds, and to the use of such compounds in the treatment and prevention of medical disorders and diseases, most especially by Factor B inhibition.

The invention belongs to the field of cation exchange membranes, and discloses a monovalent selective cation exchange membrane with crown ether encapsulated in the membrane and a preparation method of the monovalent selective cation exchange membrane. Firstly, a sulfonated chloromethylated polymer is synthesized, a solvent is evaporated to form a membrane, and a chemical reaction of chloromethyl and amido contained in the membrane endows a growth site of a covalent organic framework. And then constructing a covalent organic framework in a membrane channel by an in-situ growth method, and packaging the crown ether nano material in the membrane. A regular porous channel of the covalent organic framework and a sulfonic acid group in the base membrane have a synergistic effect, so that good ion flux of monovalent ions is ensured. Meanwhile, the crown ether structure has a special recognition complexing effect on alkali metal ions and has different affinity to different metal ions, so that the monovalent cation selective separation is achieved, and the prepared monovalent selective cation exchange membrane is suitable for an electrodialysis process.

The invention discloses a construction method and application of a zwitter-ion antifouling and dual-signal-ratio electrochemical biosensor, and belongs to the technical field of biochemical sensing analysis and life science. According to the invention, 3-aminopropyl dimethylamine oxide (APDMAO) zwitterions are prepared to be used as an antifouling interface. Specific positive and negative charges (N < + >-O-) of APDMAO promote hydrogen bond combination with water molecules, and a firm hydration barrier is formed. Meanwhile, the development of APDMAO overcomes the defect that zwitterions are difficult to synthesize and modify, and the application of APDMAO in biosensing analysis is expanded. A methylene blue (MB) internal standard modified alpha fetoprotein (AFP) aptamer is coupled with APDMAO under a controllable potential, so that the detection precision of the sensor is improved. The constructed ratio type electrochemical antifouling biosensor realizes sensitive and accurate detection of AFP, and the detection limit is as low as 3.41 fg / mL.

The invention discloses a pure silicon Beta molecular sieve packaging metal catalyst and a preparation method and application thereof, and the preparation method comprises the following steps: dissolving a silicon source, a template agent, a ligand, a metal salt and a mineralizer in water, carrying out a crystallization reaction at 120-200 DEG C, and carrying out calcination treatment and reduction treatment on the crystallized solid to obtain the pure silicon Beta molecular sieve packaging metal catalyst. The pure silicon Beta molecular sieve packaged metal catalyst is obtained. The pure silicon twelve-membered ring macroporous Beta molecular sieve encapsulated metal catalyst is prepared through a ligand protection in-situ hydrothermal synthesis strategy, so that the size of a metal nanocluster can be reduced, the high-temperature thermal stability of the metal nanocluster is improved, the adsorption and diffusion processes of guest molecules can be regulated and controlled, and the stability of the metal nanocluster is improved. Furthermore, the catalyst shows excellent catalytic performance when being used for catalyzing a propane dehydrogenation reaction and a methyl cyclohexane dehydrogenation reaction, and efficient and stable propane and methyl cyclohexane dehydrogenation performance is achieved.

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 discloses an organic electroluminescent material and an organic electroluminescent device and application thereof.The organic electroluminescent material can serve as a functional layer of the organic electroluminescent device, 9-alkyl-9-phenyl-9H-fluorene serves as a parent nucleus and is directly connected with arylamine on the parent nucleus, one side chain of the arylamine is aryl or heteroaryl, the other side chain of the arylamine is 1, 1, 4, 5, 6-tetramethyl-1, 3, 5-tetramethyl-1, 3, 5-tetramethyl-1, 3, 5-tetramethyl-1, 3, 5-tetramethyl-1, 3, 5-tetramethyl-1, 3-tetramethyl-1, 3-tetramethyl-1, 3-tetramethyl-1, 3-tetramethyl-1, 3-tetramethyl-1, 3-tetramethyl-1, 3-tetramethyl-1 Compared with other compounds, the organic electroluminescent material compound disclosed by the invention has the advantages that the transverse electric leakage is small, and the phenomena that adjacent pixels are lightened, transverse crosstalk is generated between adjacent sub-pixels and color display is influenced due to transverse leakage current of the adjacent pixels in a device can be reduced. The organic electroluminescent material is used as a functional layer of the organic electroluminescent device, and the problems that color display is affected and picture display is abnormal due to transverse electric leakage of an OLED display device can be solved.

The invention provides a perovskite passivation layer and a preparation method thereof. According to the invention, a perovskite passivation layer is arranged on the surface of a perovskite absorption layer, and the material of the perovskite passivation layer contains an alkyl diamine compound and a phenylethyl ammonium compound; the phenethyl ammonium compound is selected from p-trifluoromethyl phenylethylamine hydrochloride and / or p-fluorophenethyl hydriodate. According to the perovskite solar cell and the preparation method thereof, the alkyl diamine compound and the phenylethyl ammonium compound are cooperated to form the passivation layer, the simultaneous effect of surface passivation and interface passivation can be exerted, the carrier recombination of the surface and the interface is reduced, the electron extraction capability is improved, and the energy conversion efficiency of the perovskite solar cell is further improved.

The invention belongs to the technical field of flame-retardant materials, and particularly relates to a halogen-free flame retardant containing a Schiff base structure, a preparation method of the halogen-free flame retardant and application of the halogen-free flame retardant in epoxy resin. An intermediate is prepared through nucleophilic substitution reaction between an aldehyde group-containing phenolic compound and an acyl chloride compound, and a halogen-free flame retardant containing phosphorus and nitrogen elements and a Schiff base structure is obtained through Schiff base reaction between the intermediate and 1, 3-bis (3-aminopropyl)-1, 1, 3, 3-tetramethyldisiloxane. The flame retardant combines a Schiff base structure, phosphorus and silicon elements, and has the advantages of good thermal stability, significantly improved char yield, excellent flame retardant effect and significantly improved mechanical properties. The modified epoxy resin is further used for modifying the epoxy resin to prepare the flame-retardant epoxy resin; under the condition that the influence on the thermal performance of an epoxy resin cured product is small, the charring performance and the mechanical performance of the epoxy resin cured product can be remarkably improved, and the flame-retardant efficiency is excellent.

A cosmetic containing (A) an alkali metal salt of an alkanoyl N-methyltaurine having an alkanoyl group having 8-20 carbon atoms, (B) a plant extract, (C) one or more compounds selected from the group consisting of compounds represented by general formula (1) and pharmacologically acceptable salts thereof, and (D) water (in general formula (1), R1, R3, R4 and R6 are each independently an alkyl group having 1-3 carbon atoms, R2 is an alkyl group having 1-3 carbon atoms, and R3 is an alkyl group having 1-3 carbon atoms; and R2 and R5 each independently represent a hydrogen atom or an alkyl group having 1-3 carbon atoms. ). # imgabs0 #

The invention belongs to the technical field of organic radiation luminescence and radiation imaging, and discloses an aggregation-induced delayed fluorescence (AIDF) type organic scintillator material and a preparation method thereof, and a preparation method and application of a flexible organic scintillation film. The molecular structure of the material comprises carbonyl, methylene, sulfuryl and other connecting units, phthalonitrile is used as an acceptor unit, carbazole is used as a donor unit, an aggregation-induced excitation state is formed through space charge transfer among molecules, efficient AIDF luminescence and large Stokes shift characteristics are realized, the self-absorption phenomenon is effectively avoided, and the luminescent efficiency is improved. The X-ray fluorescence probe is suitable for a luminescence process under an X-ray excitation condition, the sensitivity of X-ray detection is remarkably improved, and the lowest detection limit can reach 276nGy.s <-1 > and is far superior to the 5.5 mu Gy.s <-1 > standard required by medical diagnosis. Besides, the flexible scintillator film prepared based on the material system radiates and emits light within the waveband range of 450-750 nm and is perfectly matched with the response area of a silicon-based detector, X-ray imaging with the high signal-to-noise ratio is achieved, and the imaging resolution is as high as 20.01 lp.mm <-1 >.

The disclosure aims to provide a method for producing a refined polytetrafluoroethylene powder, in which a short-chain fluorine compound is reduced from low-molecular-weight polytetrafluoroethylene. The disclosure relates to a method for producing a refined polytetrafluoroethylene powder, including a step of reducing a short-chain fluorine compound from a low-molecular weight polytetrafluoroethylene powder obtained by radical polymerization. The step includes at least reducing a compound represented by the following formula (1) to 179 ppb or less and a compound represented by the following formula (2) to 6900 ppb or less:         Formula (1):     (H-(CF2)m-COO)pM1 wherein m is 3 to 20; M1 is H, a metal atom, NR54 (where R5s are optionally the same as or different from each other and each represent H or a C1-C10 organic group), imidazolium optionally containing a substituent, pyridinium optionally containing a substituent, or phosphonium optionally containing a substituent; and p is 1 or 2, and         Formula (2) :     (H-(CF2)n-SO3)qM2 wherein n is 4 to 21; M2 is H, a metal atom, NR54 (where R5 is as defined above), imidazolium optionally containing a substituent, pyridinium optionally containing a substituent, or phosphonium optionally containing a substituent; and q is 1 or 2.

The invention relates to the field of organic synthesis, in particular to a synthetic method of 1-(2, 6, 6-trimethyl-1, 3-cyclohexadiene-1-yl) ethanone, and particularly relates to a synthetic method of 1-(2, 6, 6-trimethyl-1, 3-cyclohexadiene-1-yl) ethanone by taking 4-acetyl-3, 5, 5-trimethylcyclohexene as a raw material and carrying out bromination and elimination steps to synthesize the 1-(2, 6, 6-trimethyl-1, 3-cyclohexadiene-1-yl) ethanone. The method has the advantages of easily available raw materials and high reaction yield, and can be industrially implemented on a large scale.

The invention discloses a synthesis method of an aryl bidentate phosphine compound, which comprises the following steps of: (1) reacting benzene or alkylbenzene with benzyl chloride or 4-alkyl benzyl chloride at 0-100 DEG C for 0.5-5 hours in the absence of oxygen and under the condition of a lewis acid catalyst to prepare a first intermediate; (2) dropwise adding an alkyl lithium reagent into tetramethylethylenediamine at the temperature of-30 to 40 DEG C under the conditions of no water, no oxygen and a solvent, stirring for 1 to 3 hours, dropwise adding the first intermediate into the mixed solution at normal temperature, and reacting for 4 to 20 hours at the temperature of-20 to 40 DEG C to prepare a second intermediate; and (3) under anhydrous and anaerobic conditions, adding diphenyl phosphine chloride into the second intermediate obtained in the step (2), and reacting at-20 to 80 DEG C for 5-60 hours to obtain the aryl bidentate phosphine compound. The synthesis method disclosed by the invention is simple in process, mild in condition and high in product yield, and has a relatively good industrial prospect.

The present invention discloses a Pt-based catalyst and its preparation method and application, belonging to the technical field of dehydrogenation catalysts. The preparation method of the Pt-based catalyst comprises the following steps: mixing an aqueous solution I containing magnesium ions, aluminum ions and platinum ions with an aqueous solution II containing a hydroxide-containing alkaline compound and a carbonate, and reacting to obtain a Pt-based catalyst. The preparation method of the present invention utilizes PtCl6 2‑ The strong electrostatic interaction with the magnesium-aluminum hydrotalcite layer (positively charged) and the change of Pt loading amount realize the microstructural regulation of Pt in the Pt-based catalyst. The Pt-based catalyst prepared by this method has a small Pt particle size, a highly dispersed state, and a high atomic utilization rate. When it is used for the dehydrogenation reaction of methylcyclohexane, compared with the catalyst prepared by the traditional impregnation method, under the same reaction conditions, the methylcyclohexane conversion rate is increased by 3.3 times, and it also has good stability.

The invention relates to the field of electrochemical energy storage electrode materials, in particular to a method for preparing a coal-based carbon material through chemical crosslinking coupling high-temperature carbonization and application of the coal-based carbon material. The method comprises the following steps: crushing and deliming raw material coal to obtain ultra-pure coal powder; then dissolving the ultra-pure coal powder and a cross-linking agent in an organic solvent, under the action of a catalyst, inducing methyl, ethyoxyl, aldehyde and other groups to uniformly introduce polycyclic aromatic hydrocarbon molecules, and finally forming a super-cross-linked structure; and performing high-temperature carbonization to recombine the coal into closed pores, thereby forming the disordered coal-based carbon material with small microcrystal size. The method has the advantages that the raw material source is stable, the cost is low, the carbon yield is high, the treatment process is simple, large-scale preparation of the high-performance coal-based carbon material is easy to realize, and the like; and the prepared coal-based carbon material shows excellent electrochemical performance as a sodium ion / lithium ion battery negative electrode.

The invention relates to application of a heterocyclic compound as a fluorescent probe. The structural formula of the heterocyclic compound is shown as a general formula I, and R1, R2, R3, R4, R5, R6, R7 and R8 are independently one of hydrogen, alkyl, hydroxyl, phenyl, hydroxyphenyl, indole and oxymethyl. According to the present invention, the heterocyclic compounds represented by the general formula I can be specifically positioned in mitochondria, and have long fluorescence lifetime, such that the heterocyclic compounds are suitable for being used as mitochondria fluorescence probes.

The invention relates to an aqueous adhesive composition, comprising a thermosetting resin based on: - at least one aromatic compound A1 comprising at least one aromatic ring bearing at least two functions, one of these functions being an aldehyde function or a hydroxymethyl function, the other being an aldehyde function or a hydroxymethyl function; - at least one aromatic polyphenol A2 comprising at least one aromatic ring bearing at least two hydroxyl functions in the meta position relative to one another, the two positions ortho to at least one of the hydroxyl functions being unsubstituted; and a compound (III): R3NH-C=X-N(R1R2) in which each group R1, R2, R3 represents, independently of one another, an alkyl, alkenyl, aryl, arylalkyl, alkylaryl or cycloalkyl group or hydrogen, X represents S, O or N-R4 with R4 representing an alkyl, aryl, arylalkyl, alkylaryl or cycloalkyl group or compound (III) is melamine or uracil; with compound (I) being at a weight content of solids of the aqueous adhesive composition ranging from 0.003 to 0.160.

The embodiment of the invention discloses a preparation method of trifluoromethyl sulfinate. The preparation method comprises the following steps: reacting a trifluoromethyl sulfinyl reagent with an amino compound containing hydroxyl to obtain a trifluoromethyl sulfinate intermediate; and reacting the trifluoromethyl sulfinate intermediate with alkali metal salt in an organic solvent to obtain the trifluoromethyl sulfinate. According to the embodiment of the invention, firstly, the trifluoromethyl sulfinyl reagent reacts with the amino compound containing the hydroxyl group to obtain the trifluoromethyl sulfinate intermediate, and then the trifluoromethyl sulfinate and the alkali metal salt react in the organic solvent, so that the high-purity trifluoromethyl sulfinate can be prepared with high yield under mild conditions. The yield and the purity of the target product are effectively improved, and meanwhile, the production condition requirement and the environmental pollution degree are reduced, so that large-scale production and application are facilitated.

The invention discloses a near-infrared two-region aggregation-induced emission material as well as a preparation method and application thereof, and belongs to the technical field of aggregation-induced emission materials. The invention provides a fluorescent material with aggregation-induced emission (AIE) property, which can have high luminous efficiency in an NIR-II (1000 nm to 1500 nm) region. The invention aims to carry out rational structure design through the multilevel space confinement effect of molecule and aggregate levels. Through modification of a methyl group and a side chain substituent group, free rotation of an aromatic ring is effectively inhibited, and a rigid mortise and tenon interlocking structure is formed in the crystal. The water-soluble nanoparticles prepared from the synthesized aggregation-induced emission material can achieve a fluorescence quantum yield of 28.2%. By utilizing the nanoparticles with high fluorescence efficiency, the application of real-time dynamic monitoring and the like on intestinal vessels of a living body can be realized, and a new method is provided for early diagnosis and surgical intervention of acute intestinal ischemia.