2243 results about "Thiophene" patented technology

The invention relates to a pharmaceutically acceptable salt of a benzothiophene substituted fused ring compound, and a crystal form and application thereof. Specifically, the present disclosure provides a pharmaceutically acceptable salt of 2-amino-7-fluoro-4-((5S, 5aS, 6S, 9R)-1-fluoro-12-((1-((4-(fluoromethylsubunit) piperidine-1-yl) methyl) cyclopropyl) methoxyl)-5-methyl-5a, 6, 7, 8, 9, 10-hexahydro-5H-4-oxa-3, 10a, 11, 13, 14-pentaaza-6, 9-methylbridged naphtho [1, 8-ab] heptano-2-yl) benzo [b] thiophene-3-formonitrile, a crystal form and a preparation method thereof, and a preparation method of the pharmaceutically acceptable salt, the crystal form and the preparation method thereof. Corresponding salts have good stability and can be better used for clinical treatment. # imgabs0 #

The invention relates to a crystal form of a benzothiophene substituted fused ring compound and a preparation method thereof. Specifically, the invention provides a crystal form A and a crystal form D of 2-amino-7-fluoro-4-((5S, 5aS, 6S, 9R)-1-fluoro-12-((1-((4-(fluoromethylsubunit) piperidine-1-yl) methyl) cyclopropyl) methoxyl)-5-methyl-5a, 6, 7, 8, 9, 10-hexahydro-5H-4-oxa-3, 10a, 11, 13, 14-pentaaza-6, 9-methylbridged naphtho [1, 8-ab] heptano-2-yl) benzo [b] thiophene-3-formonitrile, and the crystal form A and the crystal form D have the advantages that the crystal form A and the crystal form D are good in stability; and the medicine can be better used for clinical treatment. # imgabs0 #

The invention relates to a crystal form of a benzothiophene substituted fused ring compound and a preparation method thereof. Specifically, the invention provides a crystal form E, a crystal form G and a crystal form H of 2-amino-7-fluoro-4-((5S, 5aS, 6S, 9R)-1-fluoro-12-((1-((4-(fluoromethylsubunit) piperidine-1-yl) methyl) cyclopropyl) methoxyl)-5-methyl-5a, 6, 7, 8, 9, 10-hexahydro-5H-4-oxa-3, 10a, 11, 13, 14-pentaaza-6, 9-methylbridged naphtho [1, 8-ab] heptano-2-yl) benzo [b] thiophene-3-formonitrile, and the crystal form E, the crystal form G and the crystal form H have the advantages that the stability is good; and the medicine can be better used for clinical treatment. # imgabs0 #

The present disclosure relates to a pharmaceutically acceptable salt of a G12D inhibitor compound and a crystal form thereof. Specifically, provided in the present disclosure are a salt of 2-amino-4-((5S,5aS,6S,9R)-12-((1-((4-(difluoromethylene)piperidin-1-yl)methyl)cyclopropyl)methoxy)-1-fluoro-5-methyl-5a,6,7,8,9,10-hexahydro-5H-4-oxa-3,10a,11,13,14-pentaaza-6,9-methanonaphtho[1,8-ab]cyclohepten-2-yl)-7-fluorobenzo[b]thiophene-3-carbonitrile and a crystal form thereof.

The invention relates to an antistatic MLCC release film base film and a preparation method thereof. The antistatic MLCC release film base film is prepared by melt blending and biaxial stretching of PET master batch, an antistatic composition and a nano filler, wherein the antistatic composition is prepared by compounding modified PET-PEG and thiophene modified aromatic polyamide; the nano filler is prepared by carrying out melt extrusion on KH550 modified talcum powder and MAH-g-PET (maleic anhydride-grafted polyethylene terephthalate). The antistatic composition disclosed by the invention has the beneficial effects that the antistatic composition is formed by interweaving two polymers, and a stable three-dimensional conductive network is constructed in the PET film, so that the antistatic performance is more efficient, lasting and stable. In addition, through chemically bonded modified talcum powder, the smoothness and low roughness are provided, and meanwhile reinforcing and toughening are achieved; and the single-layer extrusion process can realize ultrathin thin film, the production process is simplified, and the production cost is greatly reduced.

The present invention provides a production method of a thienopyrimidine derivative or a salt thereof which has a gonadotropin releasing hormone (GnRH) antagonistic action with high quality in high yield. The present invention provides a method of producing a thienopyrimidine derivative, which comprises reacting 6-(4-aminophenyl)-1-(2,6-difluorobenzyl)-5-dimethylaminomethyl-3-(6-methoxypyridazin-3-yl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione or salt thereof, 1,1′-carbonyldiimidazole or a salt thereof and methoxyamine or a salt thereof, and the like.

The invention relates to preparation of a covalent organic framework material (COF) containing methyl and thiophene and application of the covalent organic framework material in production of hydrogen peroxide. Two thienyl covalent organic framework materials are prepared respectively, and the problem that the yield of hydrogen peroxide produced through photocatalysis of an existing covalent organic framework material is not high is solved. A solvothermal method is adopted for preparation, the preparation process is simple and efficient, the solvent consumption is low, the method is green and environmentally friendly, the yield is high, the problem that the energy utilization efficiency is too low due to mutual compounding of photon-generated carriers and electrons in the photocatalysis process is solved, and the efficiency of photocatalytic production of hydrogen peroxide is effectively improved. The BTTPa-2COF is applied to photocatalytic production of hydrogen peroxide, experimental results show that the BTTPa-2COF has excellent performance of photocatalytic production of hydrogen peroxide, and the performance of hydrogen peroxide production can reach 3680 [mu] molg <-1 > h <-1 > under visible light irradiation.

The invention relates to the technical field of photovoltaic cells, in particular to a hole transport material and a preparation method thereof, a solar cell and an optoelectronic device. The hole transport material comprises a hole transport polymer, and the hole transport polymer has at least one of repetitive units shown in formulas (I)-(III). According to the hole transport material provided by the invention, thienopyrrole, carbazole and phenothiazine are adopted as conjugated units of the hole transport polymer, a cyano phosphate group is adopted as an anchoring unit of the hole transport polymer, and through the synergistic effect of the conjugated units and the anchoring unit, the efficiency and stability of a perovskite solar cell are improved, and the service life of the perovskite solar cell is prolonged.

The invention relates to a low-temperature graphite negative electrode material and a preparation method thereof, and belongs to the technical field of high polymer materials. According to the prepared low-temperature graphite negative electrode material, firstly, the surface of graphite is pre-oxidized through potassium persulfate, phosphorus pentoxide and concentrated sulfuric acid, and then under the action of sodium nitrate, potassium permanganate and hydrogen peroxide, graphite oxide is prepared; then, ammonium molybdate hydrate and thioacetamide are used as a molybdenum source and a sulfur source, graphite oxide is used as a supporting material, a molybdenum disulfide-graphite compound is synthesized, and the conductivity and the cycling stability are improved; secondly, the surface of the negative electrode is coated with amorphous resin carbon / nickel oxide, so that the ion diffusion efficiency of the low-temperature graphite negative electrode material is enhanced, and the electrochemical lithium storage performance is improved in a low-temperature environment; and finally, the surface of the amorphous resin carbon / nickel oxide is coated with a layer of polythiophene film, so that the rate capability of the negative electrode material is improved due to large surface area and high pores.

The invention provides a hole transport material, a preparation method thereof and a perovskite solar cell. The chemical structural formula of the hole transport material is # imgabs0 #, wherein each A is independently a heteroatom. A thiophene-methoxy triphenylamine group and a thiophene-methylthio triphenylamine group are introduced into an acridine phosphate side chain, and a series of novel hole transport materials are provided. The hole transport material has higher decomposition temperature, better thermal stability and higher hole mobility, thereby being beneficial to hole extraction and transport. The hole transport material has a deep HOMO energy level matched with perovskite, and can be used in a perovskite solar cell without doping any additive, so that the perovskite solar cell has higher photoelectric conversion efficiency, photovoltaic performance and stability, and the material has repeatability.

The invention discloses a preparation method and an application of an S and N co-doped small-nano-size high-entropy intermetallic compound. 2, 2 '-bithiophene is simultaneously used as a metal ligand and a sulfur source to be applied to synthesis of the high-entropy intermetallic compound, and sulfur atoms in the substance can form a complex with metal ions, so that a metal precursor can be uniformly and firmly distributed on the surface of a commercial carbon carrier, and formation of the high-entropy intermetallic compound in the subsequent annealing process is facilitated; the S and N co-doped high-entropy alloy intermetallic compound catalyst synthesized by the invention has excellent electrochemical performance in a fuel cell, and particularly has remarkable performance in the aspect of stability; wherein the mass activity of the S and N co-doped high-entropy alloy intermetallic compound PtCuNiCoFe / C-SN (PCNCF-SN) catalyst under the condition of 0.9 V (vs.RHE) reaches 2.7 A * mg <-1 > Pt, which is more than 12.3 times of that of commercial Pt / C; and in the aspect of stability, the mass activity can still be kept at 65% or above after 100000 circles of accelerated durability.

The invention discloses a wear-resistant vehicle body film and a preparation method thereof, and relates to the technical field of films. The wear-resistant automobile body film prepared by the invention is prepared from polytetrahydrofuran ether glycol, isophorone diisocyanate, a catalyst, dihydric alcohol quaternary ammonium salt, a functional aid, modified silicon dioxide and a chain extender. The dihydric alcohol quaternary ammonium salt is obtained by reacting N, N '-dihexyl-N, N'-dimethyl propane-1, 3-diamine with monochloroacetone and then condensing with glycerol; the functional additive is obtained by reacting 2-boric acid thiophene-4-methyl acetate with 2, 7-dibromofluorene and then carrying out bromination hydrolysis; the modified silicon dioxide is obtained by reacting pretreated silicon dioxide with melamine and then reacting with sodium hypophosphite. The wear-resistant vehicle body film prepared by the invention has good anti-aging, wear-resistant, antibacterial and flame-retardant properties.

The invention discloses a compound as well as a preparation method and application thereof, and belongs to the field of organic materials. The compound includes a first chain hydrocarbon group, a first phenyl group, a second phenyl group, a thieno [3, 2-b] thienyl group, and a second chain hydrocarbon group. The first chain alkyl is connected to one carbon atom of the first phenyl group, the other carbon atom of the first phenyl group is connected with one carbon atom of the second phenyl group through a first connecting bond, the other carbon atom of the second phenyl group is connected with one carbon atom of the thieno [3, 2-b] thienyl through a second connecting group, and the other carbon atom of the thieno [3, 2-b] thienyl is connected with the second chain alkyl. The first phenyl group has one or two first substituents which are F,-CF3 or-OCF3; the first and second chain hydrocarbon groups are linear alkyl groups, alkoxy groups, fluoroalkyl groups, alkenyl groups, alkenyloxy groups or difluorovinyl groups. The compound can be used as a liquid crystal monomer to improve birefringence, low-temperature stability, high-temperature stability and nematic phase temperature range of a liquid crystal material.

The invention provides a compound shown in the following structure, or a tautomer, a stereoisomer, a hydrate, a solvate, a pharmaceutically acceptable salt or a prodrug thereof. These compounds useful as agonists of AT2R, # imgabs0

The invention relates to the technical field of adhesives, and particularly discloses an electrogenerated viscosity-reducing adhesive as well as a preparation method and application thereof. The electrogenerated viscosity-reducing glue is prepared from the following raw materials in parts by weight: 100 to 150 parts of polyacrylate, 30 to 50 parts of polyvinyl alcohol, 20 to 40 parts of functional monomer, 1 to 5 parts of conductive agent, 2 to 6 parts of alkenyl-containing ionic liquid, 1 to 5 parts of lithium salt, 1 to 5 parts of tackifier, 1 to 2 parts of dispersant, 0.1 to 2 parts of initiator and 60 to 100 parts of organic solvent, and the conductive agent is obtained by synergistically modifying hydroxylated carbon nanotubes with 2-thiophenecarboxylic acid and 2-picolinic acid. The electrogenerated viscosity-reducing adhesive is applied to the electrogenerated viscosity-reducing adhesive tape, and the obtained adhesive tape is excellent in peel strength and shear strength, high in power-on viscosity-reducing efficiency, free of adhesive residue during peeling, reusable and wide in application prospect.

The invention discloses an organic compound, a composition, an electronic device and a display panel. The organic compound has a structure as shown in formula (1): (1); the organic compound provided by the invention is an arylamine compound taking dibenzofuran or dibenzothiophene substituted by a heterocyclic group containing a nitrogen atom, an oxygen atom or a sulfur atom as a core structure, and can have a relatively high refractive index; when the organic compound provided by the invention is used in a covering layer of an electronic device, the refractive index of the covering layer can be effectively improved, so that the luminous efficiency of the electronic device is improved, and the electronic device with excellent performance can be realized.

The invention discloses a method for green and efficient removal of thiophene sulfides in fuel oil by using Q [8]. According to the method provided by the invention, a Q [8] solid powder material is adopted to carry out removal treatment on simulated fuel oil containing the thiophene sulfides in a subject-object interaction mode, and the Q [8] solid powder material can be subjected to a regeneration process for reuse through ethanol desorption. The Q [8] solid powder material used in the method is low in cost, the urea is a main raw material for synthesis of the Q [8] solid powder material, and the Q [8] solid powder material is high in selectivity, can be recycled and is more environmentally friendly. The method is simple to operate, convenient to use and low in cost, the combustion simulation oil can be efficiently desulfurized, and environmental pollution is effectively reduced.

The invention relates to the technical field of marine chemical engineering, in particular to thiolated chitosan quaternary ammonium salt containing thiophene groups as well as a preparation method and application of the thiolated chitosan quaternary ammonium salt. The thiolated chitosan quaternary ammonium salt containing the thiophene group has a structure as shown in a formula I in the specification. The preparation method comprises the following steps: further reacting sulfhydrylated chitosan to obtain sulfhydrylated chitosan quaternary ammonium salt, and further introducing thiophene groups into the chitosan quaternary ammonium salt by taking the sulfhydrylated chitosan quaternary ammonium salt as a reaction raw material. Antioxidant activity experiments prove that the obtained thiolated chitosan quaternary ammonium salt derivative has good antioxidant activity, and can be widely researched and applied as an antioxidant in the fields of biological medicine, agriculture and the like. And the # imgabs0 # is shown in the formula 1.

The invention relates to a compound, a preparation method, a hole transport layer material, a photovoltaic device and a photovoltaic module. R1 and R4 are respectively and independently selected from amino and derivatives thereof, hydroxyl and derivatives thereof, methoxyl and derivatives thereof, sulfydryl and derivatives thereof, methylthio and derivatives thereof, thiophene groups and derivatives thereof, phosphate groups and derivatives thereof, carboxylic acid groups and derivatives thereof, and sulfonic acid groups and derivatives thereof; r2 and R3 are independently selected from alkyl, a phosphate group and derivatives thereof, a carboxylic acid group and derivatives thereof, a sulfonic acid group and derivatives thereof, and trimethoxysilyl propyl and derivatives thereof. The material is beneficial to improving the photoelectric conversion efficiency of photovoltaic devices and photovoltaic modules.

The invention relates to the technical field of luminescent materials, and discloses an aggregation-induced emission material, nanoparticles as well as a preparation method and application thereof, the structural general formula of the aggregation-induced emission material is as follows: # imgabs0 #, R is selected from one of the following structures: # imgabs1 # aggregation-induced emission material takes a pyridine group as an acceptor unit, and the acceptor unit is selected from one of the following structures: 1 # imgabs2 # aggregation-induced emission material; a carbon-carbon double bond and a thiophene unit are used as pi bridges, and diphenylamine, bis (4-ethylphenyl) amine and bis (4-(tert-butyl) phenyl) amine are used as strong electron donors. The donors not only provide strong electron supply ability, but also become efficient rotors due to highly twisted molecular conformation, and endow the aggregation-induced emission material with long emission wavelength and aggregation-induced emission activity.

The invention provides an aza-BODIPY dye molecule with near-infrared two-region absorption, 4-cyanophenyl is used as an electron acceptor for modification at 1, 7 sites, thiophene-triphenylamine is used as a strong electron donor for modification at 3, 5 sites, an aza-BODIPY dye with extremely strong intramolecular charge transfer is constructed, the absorption spectrum of the aza-BODIPY dye is extended to 1100 nm, and after the aza-BODIPY dye molecule forms an aggregation state, the absorption spectrum of the aza-BODIPY dye molecule has strong absorption spectrum. The aza-BODIPY dye molecule has the advantages that the absorption spectrum of the aza-BODIPY dye molecule is extended to 1250nm, the aza-BODIPY dye molecule has good absorption in an NIR-II region, and the nano-particles prepared by self-assembling the aza-BODIPY dye molecule and the amphiphilic polymer F127 show 46.2% of high photothermal conversion efficiency under the excitation of 1060nm laser, can be used for photoacoustic imaging and photothermal therapy, and can be used for preparing the nano-particles. The problems that tissue penetrability is insufficient and deep tumors cannot be diagnosed and treated in traditional tumor light diagnosis and treatment are solved.

The invention discloses a preparation method of a grafted and substituted thiophene polymer material, which comprises the following steps: mixing poly (3-hexylthiophene), a grafting monomer, a catalyst and an auxiliary agent, and heating for reaction to obtain the grafted and substituted thiophene polymer material, the structural formula of the grafting monomer is as shown in formula (I); wherein B is fluorine, chlorine, bromine or iodine, A is a carbon atom or a nitrogen atom, and R is cyano, formyl, methoxycarbonyl or; according to the method, pre-synthesis of complex functional monomers is avoided, the main chain of the poly (3-hexylthiophene) can be directly modified without using an expensive catalyst or ligand, the polymerization reaction of the poly (3-hexylthiophene) is not interfered, and meanwhile, the method has the advantages of simplified steps and low cost.

The invention belongs to the technical field of medicines, and particularly relates to a benzothiophene compound as well as a pharmaceutical composition, a pharmaceutical preparation and application thereof. The benzothiophene compound has a structure as shown in a formula (I), has a very strong excitation effect on an STING-mediated interferon signal channel, can be used as a small-molecule STING agonist, and is used for clinical treatment (especially immunotherapy) of tumors or infectious diseases. # imgabs0 #

The invention discloses a phosphorus-sulfur synergistic flame retardant with high gas phase activity, a durable flame-retardant nylon fabric and a preparation method of the flame-retardant nylon fabric, and relates to the technical field of flame-retardant nylon fabric preparation.The preparation method of the phosphorus-sulfur synergistic flame retardant comprises the steps that 9, 10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide and polyepoxide are mixed and heated to be molten for a reaction, and the phosphorus-sulfur synergistic flame retardant is obtained; obtaining an intermediate after the reaction is finished; the intermediate and a thiophenethiol derivative are subjected to a click chemical reaction, and a 9, 10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide derivative containing phosphorus and sulfur is obtained; the preparation method comprises the following steps: dissolving a 9, 10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide derivative containing phosphorus and sulfur into a mixed solvent of ethanol and water, so as to obtain the phosphorus-sulfur synergistic flame retardant with high gas phase activity. The raw materials are safe and environmentally friendly, the preparation method is simple, and the prepared flame-retardant nylon fabric is excellent in flame retardance and washing resistance and free of pollution in the using process.

The invention discloses a high-impact material prepared from recycled polypropylene and a preparation method of the high-impact material, and relates to the field of materials. When recycled polypropylene is used for preparing the high-impact material, firstly, polypropylene is grafted with vinyl diphenylphosphine, then the grafted polypropylene is reacted with 1-(3-chlorphenyl)-2-propyn-1-ol, and then the reacted polypropylene is reacted with 6-(methyl formate) pyridine-3-boric acid to obtain modified polypropylene; secondly, the calcium carbonate pretreated by 3-aminopropyltrimethoxysilane reacts with 3-thiophenecarboxaldehyde, thiophene, 6-(thiophene-2-yl) pyridine-2-carboxylic acid and 6-(3-thienyl) pyridine-2-formaldehyde are polymerized on the surface of the calcium carbonate, and modified calcium carbonate is obtained; and finally, carrying out melt blending on recycled polypropylene, modified polypropylene, modified calcium carbonate, sodium cyanide and bismaleimide, and carrying out extrusion granulation to obtain the high-impact material. The high-impact material prepared by the invention has good impact resistance, aging resistance and antibacterial property.

The invention relates to the technical field of polyether-ether-ketone composite materials, in particular to a conjugated polythiophene-polyether-ether-ketone-based high-antibacterial coating and a preparation method thereof.The preparation method comprises the steps that hydroxyl modified boron nitride with photocatalytic capacity and aminated PEEK are subjected to melt blending to generate chemical bonding, and a BN-OH / PEEK-NH2 composite fine powder material is formed; then carrying out oxidative polymerization on the BN-OH / PEEK-NH2 composite fine powder and a thiophene monomer under the action of an oxidizing agent, carrying out in-situ synthesis to obtain a polythiophene / BN-OH / PEEK-NH2 conjugated composite material, and subsequently spraying the polythiophene / BN-OH / PEEK-NH2 conjugated composite material to the surface of a base material to prepare a composite coating with excellent antibacterial property, high thermal stability and low friction coefficient; the antibacterial rate of the coating on escherichia coli and staphylococcus aureus under illumination reaches 90% or above, and the coating is suitable for the medical antibacterial field.

The invention belongs to the technical field of electrolyte additives, and discloses a thiophenesulfonyl electrolyte additive, an electrolyte and a lithium ion battery, the thiophenesulfonyl electrolyte additive has the following structural formula: # imgabs0 #, in which R1 is selected from F, H or sulfonyl fluoride; r2 is selected from F, H or sulfonyl fluoride; r3 is selected from F, H or sulfonyl fluoride; and R1, R2 and R3 at least comprise one fluorine atom. Through the synergistic effect of the thiophenesulfonyl electrolyte additive and the FEC, the positive and negative electrode film-forming impedance can be effectively improved, the side reaction is inhibited, and the high-temperature and high-voltage cycle performance of the battery is improved.

The invention discloses a fuel cell cathode catalyst and a preparation method thereof, and belongs to the technical field of fuel cells. The preparation method of the fuel cell cathode catalyst comprises the following steps: adding a modified multi-walled carbon nanotube into a chloroplatinic acid aqueous solution with the mass concentration of 5g / L, carrying out ultrasonic treatment at 30-50 DEG C for 1-2 hours, and then carrying out freeze drying; and putting the dry powder into a horizontal tube furnace, introducing inert gas as protective gas, heating to 450-500 DEG C, preserving heat for 1 hour, cooling to room temperature along with the furnace, and taking out to obtain the fuel cell cathode catalyst. The modified multi-walled carbon nanotube is MWCNT / PEI / 5-formyl-2-thiopheneboronic acid, and the 5-formyl-2-thiopheneboronic acid is grafted after the PEI is grafted on the surface of the MWCNT, so that the dispersity of the MWCNT can be obviously improved, the agglomeration phenomenon of the MWCNT is reduced, the dispersion is more uniform, the loading capacity of platinum is high, the electrocatalytic activity of the catalyst is obviously enhanced, and the dosage of platinum is reduced.

The invention discloses a thiophene monomer, a holographic recording medium, a preparation method and a related device, the structural general formula of the thiophene monomer is shown in the specification, the refractive index of the monomer is larger than 1.8 and smaller than 1.9, the diffraction efficiency can be remarkably improved, the thiophene monomer is applied to preparation of a photopolymer type holographic recording medium, and the photopolymer type holographic recording medium with the sensitivity larger than 100 cm / mJ can be obtained. According to the holographic recording medium, the diffraction efficiency of the recording grating is larger than 95%, the refractive index modulation degree is larger than 0.1, and the shrinkage rate is lower than 1%, and further, the holographic recording medium can be used for preparing a volume holographic grating, a holographic optical element and an optical device.

The invention provides a packaging adhesive film for a perovskite assembly and a photovoltaic assembly and application thereof. The adhesive film comprises organic ammonium salt and a packaging adhesive film base material, wherein the organic ammonium salt is selected from one or more of diammonium halogen ammonium salt, phenyl halogen ammonium salt and thiophene halogen ammonium salt. According to the invention, the organic ammonium salt is used as the passivation material and is combined with the adhesive film matrix material to prepare the packaging adhesive film, so that the process step of post-passivation of the perovskite assembly and corresponding expensive vacuum equipment can be omitted, and the packaging cost is greatly reduced while the service life of the perovskite assembly is prolonged.