11077 results about "Phenyl group" patented technology

The invention relates to a phenyl-containing heterocyclic derivative regulator as well as a preparation method and application thereof. In particular, the present invention relates to a compound represented by general formula (XVI), a preparation method thereof, a pharmaceutical composition containing the compound, and an application of the compound as a regulator in the preparation of drugs for treating metabolic diseases and related diseases, each substituent in the general formula (XVI) being as defined in the specification # imgabs0 #

A compound of formula (I) or a pharmaceutically acceptable salt or hydrate thereof wherein X-Y is -NHSO2- or -SO2NH-; R1 is H, CN or alkyl; R2 is selected from COOH and a tetrazolyl group; R3 is selected from H, Cl and alkyl; R4 is selected from H and halo; R5 is selected from H, alkyl, haloalkyl, SO2-alkyl, Cl, alkoxy, OH, CN, hydroxyalkyl, alkylthio, heteroaryl, cycloalkyl, heterocycloalkyl and haloalkoxy; R6 is H; R7 is selected from H, CN, haloalkyl, halo, SO2-alkyl, optionally substituted heteroaryl, SO2NR14R15, CONR10R11 and alkyl; R8 is selected from H, alkyl, haloalkyl and halo; R9 is H or halo; and R10, R11, R12, R14, and R15 are H or alkyl; R13 is selected from alkyl, halo, alkoxy, CN, haloalkyl and OH; and m is 0-3. The compounds of formula (I) modulate ERAP1 (endoplasmic reticulum aminopeptidase 1) and are for use in treating proliferative, immune or inflammatory disorders, particularly cancer or leukemia. The compounds of formula (I) stimulate a neo-antigen directed immune response in the subject. A method for producing an antigen-presenting cell which presents a neo-antigen using compounds of formula (I) is disclosed. An immunogenic composition comprising an antigen-presenting cell is also disclosed. Exemplified compounds include 4-cyclopropyl-3-(N-(2-(morpholin-3-yl)-5-(trifluoromethyl)phenyl)sulfamoyl)benzoic acid.

The invention discloses a thiapyran molecule modified solar cell and a preparation method thereof. The cell sequentially comprises an ITO (Indium Tin Oxide) conductive glass layer, a 4-aminotetrahydro-2H-thiapyran-1, 1-dioxide hydrochloride modified [4-(3, 6-dimethoxy-9H-carbazole-9-yl) butyl] phosphonic acid hole transport layer, a Cs0.05 (FA < 0.77 > MA < 0.23 >) < 0.95 > Pb < (I < 0.77 > Br < 0.23 >) 3 wide-band gap perovskite thin film, a phenethyl ammonium iodide passivation layer, an electron transport layer of [6, 6]-phenyl-C61-butyric acid isomethyl ester, a 2, 9-dimethyl-4, 6, 7-tetrahydro-2H-thiapyran-1, 1-dioxide hydrochloride modified [4-(3, 6-dimethoxy-9H-carbazole-9-yl) butyl] the hole barrier layer is made of 1, 7-biphenyl-1, 10-phenanthroline; the electrode layer is made of metal Ag; according to the scheme, the hole transport layer is modified through thiapyran molecules, agglomeration of the hole transport layer is relieved, and a more compact and more uniform self-assembled single layer is generated by inducing favorable crystal orientation. A good bottom interface is obtained based on thiapyran molecule modification, and ordered growth of high-quality perovskite crystal grains is promoted. In addition, the energy level of the hole transport layer is effectively adjusted through thiapyran molecule treatment, and the extraction and transmission of carriers by the hole transport layer are enhanced.

The invention discloses a novel synthetic method for 5-phenyl tetrazole, which includes the following steps: firstly performing acid neutralization to hydrazine hydrate; then adding mixing solution formed by cyanobenzene, water and ethyl alcohol to generate phenyl aminoguanidine salt; adopting sodium nitrite for diazotization to obtain nitrine amidine under the acidic condition; obtaining 5-phenyl tetrazole crude product through closed loop under the alkaline condition; obtaining 5-phenyl tetrazole acceptable product through adopting ethyl alcohol for refining. The method has the advantages of simple technology, simplicity in operation and high product yield.

The invention discloses a blue light-emitting main body composition, and an organic electroluminescent device, a display panel and a display device comprising the same. The blue light-emitting main body composition comprises a first component and a second component, the structural general formula of the first component is shown as a formula I, and the structural general formula of the second component is shown as a formula II; ar1 is selected from deuterated or unsubstituted phenyl or naphthyl; l is selected from deuterated or non-deuterated phenyl; and Ar22 is a deuterated structure of Ar21. In the invention, the compound in the formula I containing the deuterated anthracene nucleus and the non-deuterated Ar21 group is combined with the compound in the formula II containing the non-deuterated anthracene nucleus and the deuterated Ar22 group in a differentiated manner, so that the carrier balance of the organic electroluminescent device can be further adjusted, the efficiency of the organic electroluminescent device is improved, and the service life of the organic electroluminescent device is prolonged. # imgabs0 #

The invention discloses a wear-resistant and high-temperature-resistant synchronous belt and a preparation method thereof. The wear-resistant and high-temperature-resistant synchronous belt comprises a synchronous belt framework and a synchronous belt rubber sheet, the synchronous belt rubber sheet is prepared from the following raw materials: a fluorosilicone thermoplastic polyurethane elastomer containing a benzene ring structure, an amino-containing hyperbranched liquid crystal polymer, methyl vinyl phenyl silicone rubber, epoxidized natural rubber, molybdenum sulfide nanosheets, reinforced fibers, bis (1-vinyl imidazole-2-) ketone, 2-acrylamido-2-methylpropanesulfonic acid, 4, 4 '-difluoro-1, 3, 4-trimethyl-1, 3, 4-trimethyl-1, 3, 4-trimethyl-1, 3, 4-trimethyl-1, 3, 4-trimethyl-1, 3, 4-trimethyl-1, 3, 4-trimethyl-1, 3, 4-trimethyl-1 The high-temperature-resistant rubber is prepared from 2, 6-hydroxy-2-cyanobenzothiazole, bis (3-aminophenyl) 3, 5-bis (trifluoromethyl) phenylphosphine oxide, a catalyst, a coupling agent, a vulcanizing agent, an anti-aging agent, a scorch retarder and a lubricating agent. The synchronous belt is good in mechanical property, sufficient in high-temperature resistance and cold resistance, good in wear resistance and excellent in aging resistance and flame retardance.

The invention relates to a flame-retardant inorganic quick-setting material and a preparation method thereof, and the flame-retardant inorganic quick-setting material is prepared from the following raw materials: sulphoaluminate cement, aluminum-magnesium hydrotalcite, phosphorus slag powder, waste PBO fiber, an accelerator, a water reducer, a functional auxiliary agent, and 3, 3 '-diamino-4, 4'-difluorodiphenyl sulfone. The functional auxiliary agent comprises structural units introduced by the following monomers: 3-[N, N-dimethyl-[2-(2-methylpropyl-2-enoyloxy) ethyl] ammonium] propane-1-sulfonic acid inner salt, diphenyl (4-vinyl phenyl) phosphine oxide, 1, 3-bis (oxirane methyl)-5-(2-allyl)-1, 3, 5-triazine-2, 4, 6 (1H, 3H, 5H)-triketone, 10-(4-vinyl phenyl)-10H-phenoxazine and itaconic acid. The material is high in strength, remarkable in rapid hardening and flame-retardant effect, and safe and environment-friendly to use.

The invention relates to a synthesis method of 1, 2-bis (4-vinyl phenyl) ethane, which comprises the following steps: 1) under the action of magnesium or zinc, carrying out self-coupling reaction on benzyl halide at a benzyl position to obtain 1, 2-bis (4-halogen phenyl) ethane, and 2) preparing the 1, 2-bis (4-vinyl phenyl) ethane from the 1, 2-bis (4-halogen phenyl) ethane, which is selected from any one of the following schemes: 2i: carrying out self-coupling reaction on the 1, 2-bis (4-vinyl phenyl) ethane obtained in the step 1) to obtain the 1, 2-bis (4-vinyl phenyl) ethane. The preparation method comprises the following steps: preparing a Grignard reagent from 1, 2-bis (4-halogen phenyl) ethane, and coupling the Grignard reagent with vinyl chloride to prepare 1, 2-bis (4-vinyl phenyl) ethane; and (2iii) coupling the 1, 2-bis (4-halogen phenyl) ethane obtained in the step (1) with vinyl magnesium chloride to prepare the 1, 2-bis (4-vinyl phenyl) ethane. According to the invention, the 1, 2-bis (4-vinyl phenyl) ethane is prepared from p-benzyl halide through two-step reaction at a relatively high yield, and the yield of the two-step reaction can reach 86.9%.

The invention belongs to the technical field of polyurethane pouring sealants, and particularly relates to a two-component hydrophobic heat-resistant polyurethane pouring sealant and a preparation method thereof. The pouring sealant is prepared by reacting a component A and a component B, the component A is prepared from the following raw materials in parts by weight: 17 to 33 parts of modified polyether polyol I; 15 to 27 parts of modified polyether polyol II; 18 to 30 parts of diisocyanate; 20 to 34 parts of a plasticizer; the component B is prepared from the following raw materials in parts by weight: 47 to 64 parts of polyether polyol III; 36 to 53 parts of filler; and 0.15 to 0.35 part of a catalyst. Introducing a silicon-oxygen-silicon chain segment into a polyether polyol structure through acrylic acid bridging to prepare siloxane modified polyether polyol; more side ethyl, phenyl and neopentyl structures are introduced into the polyether polyol, so that the intrinsic hydrophobicity and temperature resistance of the raw materials are further improved, and the polyurethane pouring sealant shows relatively high hydrophobicity and heat resistance.

The invention provides a redox imidazole covalent organic framework material as well as a preparation method and application thereof, belongs to the technical field of material preparation and photocatalytic preparation of hydrogen peroxide, and aims to solve the technical problem of low activity of a current covalent organic framework in preparation of hydrogen peroxide. The preparation method of the imidazole-connected redox type imidazole covalent organic framework material comprises the following steps: respectively reacting a reactant 2, 7-di-tert-butylpyrene-4, 5, 9, 10-tetraketone monomer with 4, 4 ', 4', 4 ', 4', 4 ', 4', 4 ', 4', 4 ', 4', 4 ', 4', 4 ', 4', 4 ', 4', 4 ' The preparation method comprises the following steps: mixing 4, 4 '-(pyridine-2, 4, 6-triyl) tribenzaldehyde and a tri (4-formylphenyl) amine monomer, adding a solvent and a catalyst, uniformly stirring, and reacting to obtain the redox type imidazole covalent organic framework material after the reaction is finished. The application comprises the following steps: adding the covalent organic framework, oxygen and the sacrificial agent into water, and reacting under the irradiation of visible light. The preparation method is green, environment-friendly, simple and easy to implement, the prepared material has good thermal stability, and efficient visible light photocatalysis preparation of hydrogen peroxide can be achieved; meanwhile, the catalyst can be recycled and has good photocatalytic stability.

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 belongs to the field of pesticides, and relates to a 2-cyano-3-disubstituted phenyl acrylate compound as well as a preparation method and application thereof in pesticides. Carrying out alcoholysis reaction on the benzonitrile compound a and a hydrogen chloride absolute ethyl alcohol solution to obtain an intermediate b; carrying out condensation reaction on the intermediate b and ethyl cyanoacetate under the action of alkali to obtain an intermediate c; the intermediate c and a substituted compound are subjected to a substitution reaction under the action of alkali and a catalyst, and the 2-cyano-3-disubstituted phenyl acrylate compound I is obtained. The 2-cyano-3-disubstituted phenylacrylate compound provided by the invention has good bactericidal activity, and has relatively high bactericidal activity on pathogenic bacteria of chlorosclerotium, fusarium, acrocyst, colletotrichum, cercospora, verticillium and black beancurd skin; the compound can be used for preparing bactericides in the fields of agriculture, horticulture, industry and the like, and has the advantages of broad spectrum, high efficiency, low toxicity and environmental friendliness.

The invention discloses a film-forming composition and a lip makeup product containing the same. The film-forming composition comprises the following components: phenyl silicone oil, wherein the phenyl silicone oil comprises two or more than two of diphenyl polydimethylsiloxane, trimethyl pentaphenyl trisiloxane, phenyl polytrimethyl siloxane and trimethyl siloxy phenyl polydimethylsiloxane; the viscosity of the phenyl silicone oil at the temperature of 25 DEG C is 50 mPa.s to 500 mPa.s; the film-forming agent comprises at least one of hydrogenated polyisobutene and polyisobutene; and the viscosity of the film forming agent at 75 DEG C is 1500 mPa.s to 2500 mPa.s. The mass ratio of the phenyl silicone oil to the film-forming agent is (2-5): 1. The film-forming composition provided by the invention is applied to a formula system of a lip makeup product, and the phenomena of cup staining, fading and the like of the lip makeup product can be reduced.

Herein is provided a novel process for the preparation of methyl 6-(2,4-dichlorophenyl)-5-[4-[(3S)-1-(3-fluoropropyl)pyrrolidin-3-yl]oxyphenyl]-8,9-dihydro-7H-benzo[7]annulene-2-carboxylate by a Suzuki coupling of compound (3), wherein LG represents a leaving group, with an organoboron reagent:Compound (3) is obtained by activation of compound (4) with a leaving group LG, and compound (4) is obtained by alpha-arylation of methyl 5-oxo-6,7,8,9-tetrahydro-5H-benzo[7]annulene-2-carboxylate with 1-LG′-2,4-dichlorobenzene, wherein LG′ represents a leaving group:

The invention discloses a waterproof heat-resistant adhesive and a preparation method thereof, and relates to the technical field of adhesives. Tetramethyltri-3-trifluoropropyl cyclotetrasiloxane is used as a raw material to prepare hydroxyl-terminated organic fluorosilicone oil and modified epoxy resin, fluorine atoms are closely arranged around a main chain of the hydroxyl-terminated organic fluorosilicone oil and modified epoxy resin in an umbrella shape, and the hydroxyl-terminated organic fluorosilicone oil and modified epoxy resin cooperate with organic silicon to improve the waterproof and heat-resistant effects; hydroxyl groups on the oxidized carbon nanofibers are reacted and combined with thiocyanate in vulcanized rubber powder, and hybrid filler is formed; residual active groups on the surface of the oxidized carbon fiber are combined and crosslinked with epoxy resin, so that the heat resistance of the epoxy resin is greatly improved; secondly, phenyl maleic anhydride is used as a cross-linking agent to form a three-dimensional cross-linked structure, and meanwhile, phenyl is introduced into the structure, so that the heat-resistant effect and the waterproof effect of the epoxy resin are further improved, and the adhesive prepared by taking the epoxy resin as the raw material has excellent waterproof and heat-resistant performance. The adhesive prepared by the invention has waterproof and heat-resistant effects.

The invention relates to a crown ether covalent organic framework material as well as a preparation method and application thereof. The preparation method comprises the following steps: dissolving a crown ether monomer and an amino monomer in an o-dichlorobenzene solvent, adding a catalyst acetic acid aqueous solution, and uniformly dispersing to form a reaction solution; the method comprises the following steps: freezing a reaction solution through a liquid nitrogen bath, vacuumizing, filling nitrogen, carrying out a heating reaction, and carrying out post-treatment operations such as washing and drying on a reaction product, so as to obtain the crown ether covalent organic framework material BADT-DB18C6-COF. The crown ether covalent organic framework material is formed by condensation of a crown ether aldehyde monomer and an amino monomer, the crown ether monomer is 4, 4 ', 4' ', 4 '''-(6, 7, 9, 10, 17, 18, 20, 21-octahydrodibenzo [B, K] [1, 4, 7, 10, 13, 16] hexaoxacyclo octadecene-2, 3, 13, 14-tetrayl) tetrabenzaldehyde, and the crown ether monomer is 4, 4 ', 4' ', 4'''-(6, 7, 9, 10, 17, 18, 20, 21-octahydrodibenzo [B, K] [1, 4, 7, 10, 13, 16] hexaoxacyclo octadecene-2, 3, 13, 14-tetrayl) tetrabenzaldehyde. The amino monomer is 4 ', 5'-bis (4-aminophenyl)-[1, 1 ': 2', 1 ''-terphenyl]-4, 4''-diamine. The crown ether covalent organic framework material BADT-DB18C6-COF prepared by the invention is mainly used as an adsorbent, is used for adsorbing and recovering uranium, thorium and americium ions from a solution, shows good adsorption capacity on radionuclides U-238, Th-232 and Am-243, and is particularly suitable for the field of spent fuel post-treatment in the nuclear industry.

Disclosed herein are novel methods for preparing 2-[(3R)-2-[4-amino-3-(2-fluoro-4-phenoxy-phenyl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carbonyl]-4-methyl-4[4-(oxetan-3-yl)piperazin-1-yl]-pent-2-enenitrile, including various solvate forms and intermediates thereof. Also disclosed herein are novel solvate forms and intermediates of 2-[(3R)-2-[4-amino-3-(2-fluoro-4-phenoxy-phenyl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carbonyl]-4-methyl-4[4-(oxetan-3-yl)piperazin-1-yl]-pent-2-enenitrile.

The invention discloses an organic electroluminescent compound and a luminescent device. The organic electroluminescent compound has a structure as shown in a formula (1). In the structure of the N-type compound provided by the invention, an electron-rich group formed by carbazole and phenyl connected with the carbazole is substituted by deuterium, and the deuterated P-type compound in the core region is matched, so that the chemical stability, photoelectric stability and thermal stability of the structure of the luminescent material can be effectively improved, the stability of a luminescent device using the material is further improved, and the service life of the luminescent device is prolonged; meanwhile, the N-type compound and the deuterated P-type compound in the core area can form a good Premix material, good P / N stability and mass production stability are achieved in the evaporation process, the formed Premix material has more balanced carrier mobility, the efficiency of a device is greatly improved, and the service life of the device is greatly prolonged. And # imgabs0 #.

The preparation method comprises the following steps: by taking 2, 2 '-[4-(4-aminophenylazo) phenylimine] diethanol and phenol as raw materials, preparing a bisazobenzene compound according to a molar ratio of 1: 1, carrying out nucleophilic substitution on the compound and alkyl bromide according to a molar ratio of 1: 1 to prepare a bisazobenzene monomer, and carrying out side-chain type photoresponse bisazobenzene polyurethane on the bisazobenzene monomer to prepare the side-chain type photoresponse bisazobenzene polyurethane. And carrying out a reaction on the bisazobenzene monomer and diisocyanate urethane to obtain the side chain type photoresponse bisazobenzene polyurethane. The bis-azobenzene polyurethane has obvious trans-cis configuration change along with the increase of ultraviolet irradiation time in a tetrahydrofuran solution, and gradually recovers the trans configuration under the irradiation of visible light. Besides, the bisazobenzene polyurethane and polyurethane are subjected to melt blending to prepare a composite material film, and the composite material film has an obvious light-induced bending phenomenon under ultraviolet irradiation.

The present invention relates to crystal modifications of 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methylthio-8-(N-{(R)-α-[N-((S)-1-carboxypropyl)carbamoyl]-4-hydroxybenzyl}carbamoylmethoxy)-2,3,4,5-tetrahydro-1,2,5-benzothiadiazepine (odevixibat), more specifically crystal modifications 1 and 2 of odevixibat. The invention also relates to a process for the preparation of crystal modification 1 of odevixibat, to a pharmaceutical composition comprising crystal modification 1, and to the use of this crystal modification in the treatment of various conditions as described herein.

The invention belongs to the field of medical chemistry, and particularly relates to a crystal form of a heterocyclic compound and a pharmaceutical composition thereof. Specifically, the invention relates to a crystal form of 4-((2R, 3S, 5R)-3-(3, 4-difluoro-2-methoxyphenyl)-5-methyl-5-(trifluoromethyl) thiacyclopentane-2-formamido) pyridine-2-formamide and a pharmaceutical composition of the crystal form of 4-((2R, 3S, 5R)-3-(3, 4-difluoro-2-methoxyphenyl)-5-methyl-5-(trifluoromethyl) thiacyclopentane-2-formamido) pyridine-2-formamide. The crystal form is good in crystallinity, excellent in chemical stability and crystal form stability, high in process safety and capable of playing a good drug effect in various animal models.

The invention discloses a UV photocureable coating as well as a preparation method and application thereof in automobiles, and relates to the technical field of coatings. When the UV photocureable coating is prepared, 4-aminophenylboronic acid is dehydrated to prepare aminated boron oxygen six-ring; carrying out a reaction on the aminated boroxane and diallyl chlorophosphate to prepare functionalized boroxane; the preparation method comprises the following steps: sequentially reacting graphene oxide with 3-chloropropyltriethoxysilane and 1, 3-diallyl-1, 3, 5-triazine-2, 4, 6-triketone, so as to obtain modified graphene; the preparation method comprises the following steps: reacting epoxy resin with 2-butenal thiosemicarbazone to prepare modified epoxy resin; and uniformly mixing the modified epoxy resin, the epoxy acrylate resin, the modified graphene, the functionalized boroxane, the 1, 6-hexanediol diacrylate and the 1-hydroxycyclohexyl phenyl ketone, so as to obtain the UV photocureable coating. The UV photocureable coating prepared by the invention has excellent flame retardant, self-repairing and mechanical properties.

The invention discloses a high-temperature-resistant power tube and a production process thereof, and belongs to the technical field of power tube preparation. The high-temperature-resistant electric power tube is prepared from, by weight, 60-80 parts of a high-temperature-resistant base material, 10-30 parts of carbon fibers and 1-5 parts of a modified anti-aging agent, the high-temperature-resistant base material is prepared from 2, 3, 4-trifluorobenzaldehyde, malonic acid, oxynaphthalene propionic acid, trifluoroacetic anhydride and 2, 2-bis [4-(4-aminophenoxy) phenyl] propane, and the modified anti-aging agent is prepared from 2, 3, 4-trifluorobenzaldehyde, malonic acid, oxynaphthalene propionic acid, trifluoroacetic anhydride and 2, 2-bis [4-(4-aminophenoxy) phenyl] propane. The modified anti-aging agent is prepared from absolute ethyl alcohol, paeonol, sodium hydroxide and 2-methoxybenzaldehyde. The power tube prepared by the method has excellent high temperature resistance, mechanical property and aging resistance.

The present invention relates to novel (3,3-dimethyl-2-oxo-butoxy)phenyl derivatives and (2- aryl-2-oxo-ethoxy]phenyl derivatives and to their application in a process for the preparation of (3,3,3-trifluoro-2-oxo-propoxy)phenyl derivatives and their further transformation into [(2- trifluoromethyl-1,3-dioxolan-2-yl)methoxy]phenyl derivatives and (2-ethoxy-3,3,3-trifluoro- prop-1-enoxy)phenyl derivatives suitable for use, e.g., as active ingredients, which have microbiocidal activity, in particular, fungicidal activity.

The invention discloses a battery and a preparation method thereof. The battery comprises a positive electrode lithium supplementing material and an electrolyte, the positive electrode lithium supplementing material comprises at least one of lithium nickelate, lithium ferrite and lithium oxide; the electrolyte comprises a silicon-based fluorophosphate compound as shown in a formula I: # imgabs0 #, wherein R1, R2 and R3 are independently H, F, alkyl of C1-C4, fluoroalkyl of C1-C4, alkenyl of C2-C4, fluoroalkenyl of C2-C4, alkynyl of C2-C4, fluoroalkynyl of C2-C4, cycloalkane of C5-C7, phenyl substituted by R4 or benzyl substituted by R5; r1, R2, R3, R4 and R5 are independently alkyl groups of C1-C4, alkylene groups of C2-C4, alkyne groups of C2-C4, fluoro alkyl groups of C1-C4, fluoro alkylene groups of C2-C4 or fluoro alkyne groups of C2-C4. The compound shown in the formula I is added into the electrolyte, so that the problems of gas expansion and lithium precipitation caused by a positive electrode lithium supplementing material can be solved, and the battery performance is improved.

The invention discloses a high-efficiency near-infrared two-region aggregation-induced emission material, a preparation method thereof and application of the high-efficiency near-infrared two-region aggregation-induced emission material in bimodal surgical navigation. According to the molecular structure, the organic near-infrared two-region material with an intramolecular charge transfer characteristic is constructed by taking thionaphthalene tetracarboxylic acid diimide as an electron acceptor group and tetraphenylethylene as a molecular rotor and an electron donor unit. By expanding the length of a pi conjugate fragment and introducing an isotope effect, the oscillator strength can be improved, and high-frequency vibration can be inhibited, so that the radiative transition rate of molecules is promoted, and the non-radiative transition rate is inhibited. The nanoparticles prepared from the aggregation-induced emission material have the advantages of high brightness, large Stokes shift and good light stability, and have an excellent effect in bimodal imaging guided mouse in-situ breast cancer and sentinel lymph node operation excision.

The invention belongs to the technical field of OLEDs, and provides a polycyclic compound containing triphenyl silicon and a polyalkyl substituent group and an organic electroluminescent device containing the polycyclic compound. The structural general formula of the polycyclic compound is as shown in formula I in the specification. Benzofuran with higher electronegativity is introduced to a ring structure composed of nitrogen atoms and boron atoms, triphenyl silicon is introduced to the para-position of boron, and the synergistic effect of benzofuran and triphenyl silicon can significantly enhance the multiple resonance of a light-emitting core and reduce vibration relaxation. Due to simultaneous use of the benzofuran and the triphenyl silicon, the problems of vibration relaxation increase, spectrum widening and the like caused by introduction of the polyalkyl substituent are remarkably improved, the luminous efficiency of the material is remarkably improved, and the color purity is improved, so that the requirement of BT.2020 wide color gamut display standard on a luminescent spectrum is met. I

Compounds having herbicidal activity effective against economically important harmful plants are disclosed. The disclosed compounds exhibit herbicidal activity even at relatively low application rates, while at the same time may exhibit compatibility with crop plants. The disclosed compounds may further be effective and efficient against a large number of weeds and against a broad spectrum of weed grasses. As disclosed herein, 3-phenylisoxazoline-5-carboxamides of S-containing cyclopentenylcarboxylic esters of formula (I) and their salts exhibit herbicidal activity against a broad spectrum of economically important mono- and dicotyledonous annual harmful plants.

The phosphazene covalent organic framework (COF) is a material with high efficiency to improve the removal of iodine from nuclear waste. The COF can be obtained by a solvothermal reaction of hexa(4-formyl-phenoxy)cyclotriphosphazene and 1,3,6,8-tetra(aminophenyl)pyrene. The resulting three-dimensional phosphazene COF has iodine uptakes as high as 9.4 g g−1 due to its 3D framework with higher specific surface areas and interconnected channels.

The invention belongs to the technical field of electrochemistry, and particularly relates to a negative electrode binder which is composed of a core layer and a shell layer, and the core layer is coated with the shell layer. In one negative electrode binder, a core layer monomer used for synthesizing a core layer comprises ethylene glycol phenyl ether unsaturated acid ester. In the other negative electrode binder, the diameter of the core layer is 50-500 nm, and the thickness of the shell layer is 1-10 nm; or the glass transition temperature of the shell layer is greater than the glass transition temperature of the core layer; or the swelling degree of the core layer in the electrolyte is 20%-200%, and the swelling degree of the shell layer in the electrolyte is 1%-10%. The negative electrode binders have good flexibility, dispersibility, mechanical modulus and bonding strength, are beneficial to inhibition of volume expansion generated by a negative electrode active material in the charging and discharging process, and are beneficial to maintenance of structural stability in the long cycle process, so that the cycle performance of the battery is improved.