1335 results about "Thiophene" patented technology

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 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 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 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 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 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 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.

4, 4 '-bipyridine (Bpy), 2, 5-thiophenedicarboxylic acid (Tdc), FeCl3. 6H2O, NiCl2. 6H2O, urea and tetrabutylammonium bromide are used as raw materials, a simple hydrothermal-calcination method is adopted to prepare the Fe2O3-coated Ni-MOF composite nanomaterial catalyst, X-ray diffraction (XRD), a scanning electron microscope (SEM) and a N2 adsorption and desorption technology are adopted to characterize a prepared sample, and the electro-catalytic oxygen evolution reaction (OER) activity of the Fe2O3-coated Ni-MOF composite nanomaterial catalyst is tested. Results show that compared with a single component, the activity of the composite nano-material catalyst is greatly improved, especially the composition-optimized Fe2O3-coated Ni-MOF-1 composite nano-material catalyst shows the highest catalytic activity, the composite nano-material catalyst catalyzes OER in 1M KOH, and the overpotential (eta 10) is only 330mV when the current density is 10mA / cm < 2 > and is close to the overpotential 291mV of a noble metal catalyst RuO2.

The invention relates to a compound containing a thiophene group, a device and equipment. In the structural formula of the compound, R1, R2, R3, R4, R5, R6, R7, R8, R9 and R10 are independently selected from hydrogen, halogen, cyano, trifluoromethyl, triphenylamine and derivatives thereof, methoxyl, aryl and derivatives thereof, cyanobiphenyl and naphthyl; the compound can be used for preparing a photovoltaic device and photovoltaic equipment and is used for improving the efficiency and stability of the photovoltaic device.

The invention discloses a carbazole phosphonate-thiophene copolymer as well as a preparation method and application thereof. The structural formula of the carbazole phosphonate-thiophene copolymer is shown as a formula (I), according to the invention, the carbazole phosphonate compound and the thiophene compound are copolymerized, and the obtained copolymer is used for preparing the hole transport layer of the perovskite solar cell, so that the perovskite solar cell has relatively high photoelectric conversion efficiency, and the relatively high photoelectric conversion efficiency can be kept in a humid and hot environment.

The invention belongs to the technical field of organic dye synthesis and application, and discloses a conjugated compound containing a benzothiophenazine structure as well as a preparation method and application thereof, and the conjugated compound containing the benzothiophenazine structure has excellent photophysical properties, singlet oxygen yield and superoxide anion generation capacity. The novel conjugated compounds ENBO-NI and ENBS-NI containing benzothiophenazine structures are successfully prepared by replacing a benzene ring of Nile blue with a cycloalkane structure and adjusting the electron donating ability of an R1 group. The two compounds have near infrared fluorescence emission, good solubility and relatively high ROS yield. Compared with a classical photosensitizer NB, the singlet oxygen yield of ENBO-NI is increased by about 117.65%, and the singlet oxygen yield of ENBS-NI is as high as 70%. The absorption wavelength of the conjugated compound is in a red light wave band. The preparation process is simple and efficient, large-scale production is easy, and the preparation method has a wide clinical application prospect.

The invention provides an optical monomer as well as a preparation method and application thereof, the structural general formula of the optical monomer is shown in the specification, in the formula, R1 and R2 are groups with the structural formula shown in the specification; or, one of R1 and R2 is hydrogen, and the other one of R1 and R2 is a group shown in the structural formula; r0 in the group represents hydrogen or methyl. The optical monomer provided by the invention has a (methyl) acrylate group and has the properties of high refractive index and low volume shrinkage; the monomer contains a plurality of aromatic rings with high molar refractive index and low molar volume, sulfur atoms with higher molar refractive index and dibenzothiophene groups with both aromatic rings and sulfur, so that the whole molecule of the monomer has extremely high refractive index, and the whole optical monomer is small in molecular weight and convenient to migrate.

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 crystalline allyl covalent organic framework material and application research of the crystalline allyl covalent organic framework material in benzamide cyclization green photocatalytic conversion. The SF-COF material is prepared by adopting a step-by-step synthesis method. The preparation method comprises the following steps: synthesizing a COF precursor by taking 1, 3-benzenetricarboxaldehyde and p-aminophenylacetonitrile as raw materials, and preparing the allylation covalent organic framework material with the electronic push-pull effect from the COF precursor and 5, 5 ', 5'-(benzene-1, 3, 5-triyl) tri (thiophene-2-formaldehyde) through a solvothermal method. The material is applied to the field of photocatalytic organic conversion, and benzamide cyclization and conversion of derivatives of benzamide are achieved under irradiation of a blue light LED. The prepared SF-COF has the advantages of efficient charge separation and electron conduction performance, good structural stability and chemical stability and the like. And a catalyzed organic reaction substrate has the advantages of wide universality range, good cycle stability and the like, and shows excellent photocatalytic conversion capability.

The invention discloses a precise construction strategy of a dibenzothiophene sulfuryl covalent organic framework material and systematically explains efficient application of the dibenzothiophene sulfuryl covalent organic framework material in photocatalytic synthesis of thiadiazole and derivatives thereof. The achievement relates to a plurality of leading subjects such as catalytic chemistry, organic synthesis, material science, environmental engineering and green chemistry. According to the method, 2, 4, 6-triformyl phloroglucinol and 3, 7-diaminodibenzo [b, d] thiophene-5, 5-dioxide are taken as construction units, and the crystalline S-COF rich in sulfuryl active sites can be quantitatively obtained through topology-oriented Schiff base condensation under the conditions of protonic acid catalysis, no water and no oxygen. Under the radiation condition of visible blue light, S-COF is used as a heterogeneous photocatalyst to drive green synthesis of 3, 5-di-p-tolyl-1, 2, 4-thiadiazole and series of derivatives thereof; the invention provides a new catalyst design normal form for light-induced organic conversion, and lays a solid foundation for sustainable development-oriented efficient synthesis chemistry.

The invention discloses a method for preparing a single-walled carbon nanotube, and belongs to the technical field of single-walled carbon nanotubes. When the single-walled carbon nanotube is prepared, the single-walled carbon nanotube is grown by using a chemical vapor deposition method; then, the grown single-walled carbon nanotubes are subjected to acid pickling, then, the carbon tubes are sorted and purified by adopting a polymer dispersant, and finally, the polymer dispersant is removed to obtain the single-walled carbon nanotubes; the polymer dispersant disclosed by the invention is obtained by reacting an aldehyde-terminated fluorenyl surfactant with diamino dipyridyl; wherein the aldehyde-terminated fluorenyl surfactant is obtained by polymerizing 9, 9-di-n-octylfluorene-2, 7-diboric acid di-pinacol ester and quaternary ammonium salt containing 2, 7-dibromofluorene, and then reacting with 5-formyl-2-thiopheneboronic acid pinacol ester for end capping; the prepared single-walled carbon nanotube is relatively high in purity and relatively high in finished product conversion rate.

The invention belongs to the technical field of self-repairing materials, and particularly relates to a double-microcapsule self-repairing waterborne polyurethane material and a preparation method thereof. Comprising the following steps: ultrasonically dispersing cellulose nanocrystals in deionized water to form a water phase, adding drying oil and lauryl sodium sulfate, and stirring to obtain the drying oil microcapsule taking Pickering emulsion as a template. Preparing a polyvinylpyrrolidone aqueous solution, a non-polar solvent solution of thiophene monomers and an ammonium persulfate aqueous solution; and mixing and ultrasonically dispersing the two, mixing with an ammonium persulfate aqueous solution, stirring and polymerizing to obtain a polythiophene microcapsule suspension after the reaction is completed, centrifuging until the supernatant is colorless, and washing and drying the solid to obtain the polythiophene microcapsule. And finally, adding the two microcapsules into waterborne polyurethane, uniformly mixing, and drying at room temperature to form the double-microcapsule self-repairing waterborne polyurethane material. According to the invention, the self-repairing and mechanical property improvement of the double-microcapsule self-repairing waterborne polyurethane material under room-temperature natural light are realized.

The invention provides an electrolyte and application thereof, and relates to the technical field of secondary batteries. Specifically, the electrolyte comprises an alternating copolymer, a first solvent, a second solvent, a third solvent, a lithium salt and an additive, the alternating copolymer is obtained by polymerizing a first monomer and a second monomer; the first monomer comprises terminal alkenyl, terminal halogen atoms and ether bonds, and the second monomer comprises at least one of maleic anhydride, citraconic anhydride, itaconic anhydride, maleimide and 2, 5-thiophenedione. The electrolyte disclosed by the invention has relatively high low-temperature ionic conductivity while having high-temperature safety; the electrolyte is in a liquid state at a low temperature, has relatively high ionic conductivity, is in a solid state after reversible phase change along with temperature rise, has safety and stability in a high-temperature state, and has a good application prospect.

The invention relates to a high-toughness anti-crack magnetic decorative film and a preparation method thereof. The decorative film is prepared from the following raw materials in parts by weight: 40 to 60 parts of poly (dihydrothiophene-vinyl ether) copolymer, 10 to 25 parts of shell layer self-assembly modified Fe3O4 nanosheets, 5 to 15 parts of polyether ester block elastomer, 0.5 to 2 parts of sodium dodecyl benzene sulfonate, 0.5 to 1.5 parts of fluorosilane coupling agent, 0.1 to 1.0 part of 2-hydroxybenzotriazole ultraviolet absorbent, 3 to 6 parts of bisphenol A type epoxy curing agent and 0.05 to 0.5 part of imidazole catalyst. The flexible copolymer is synthesized through copolymerization of dihydrothiophene and vinyl ether, the modified Fe3O4 nanosheets form a Fe3O4 structure through coprecipitation of ferric chloride and ferrous chloride and regulation and control of ammonia water, and shell self-assembly coating is carried out through tetraethoxysilane and a block micromolecule interface agent. The material has excellent tensile strength, elongation at break, magnetic adsorption force and cycling stability, and is suitable for the application fields of flexible magnetic films and high-adhesion decorations.

The invention discloses a carboxymethyl beta-cyclodextrin modified D-A COF material and a preparation method and application thereof.Benzotrithiophene is used as an electron donor, triazine is used as an electron withdrawing unit, imine-connected D-A COFs are successfully synthesized through a solvothermal method, the imino COFs and carboxymethyl beta-cyclodextrin are treated through a Ugi multi-component reaction, and the COF material is prepared. And the COFBTT-TAPT photoactive material containing the beta-cyclodextrin group is obtained through preparation. COFBTT-TAPT-beta-CD and Mxene form a heterojunction to further enhance the photoelectric conversion efficiency of the photoactive material, and the photoactive material is used for preparing a photoelectrochemical sensor, so that high-sensitivity field screening of PFOS (perfluorooctane sulfonate) can be carried out in a low concentration range.

This invention belongs to the field of chemical synthesis and relates to a method for achieving deuterated methylation of a nucleophile. The invention provides a deuterated methylating reagent, which is obtained by reacting formic acid with deuterated methanol under acidic conditions, followed by a second reaction with thiaanthracite and trifluoromethanesulfonic acid. The nucleophile is then reacted with the deuterated methylating reagent described in claim 1, a base, and a solvent to obtain the deuterated methylated product. This invention also provides a method for achieving deuterated methylation of a nucleophile, which involves dissolving the nucleophile and 5-deuterated methyl-5H-thiophene-5-onium trifluoromethanesulfonate in a suitable solvent, adding a base, and then performing the deuterated methylation reaction at room temperature. In the method provided by this invention, the yield of the product after nucleophile methylation can reach 52% to 95%.

The invention belongs to the technical field of photocatalyst synthesis, and particularly relates to a benzothiophene-naphthalimide covalent organic framework as well as a preparation method and application thereof. A benzothiophene-naphthalimide covalent organic framework (named as SF-COF, formula I) which is novel in structure and relatively high in photocatalytic activity is obtained by assembling a compound with a naphthalimide and benzotrithiophene core framework into a molecule, and the SF-COF is applied to photocatalytic synthesis of polysubstituted olefins.

This application provides a method for preparing compound I-b or a pharmaceutically acceptable salt thereof, wherein (S)-N-methylamino-1-(2-thiophene)-1-propanol reacts with 4-fluorobenzo[1,3]dioxolane in a system containing sodium hydride and potassium benzoate to obtain compound I-b. This method has short steps, mild reaction conditions, and is simple to operate, making it suitable for industrial scale-up; moreover, the obtained product has high purity and low isomer content.

Liquid-crystalline compounds with a terminal 5,6-difluoro-benzo[b]thiophene ring as provided by formula I, liquid crystal mixtures using the compounds, the use of the compounds in an electro-optical display, particularly in an active-matrix display based on the IPS or FFS effect, and liquid crystal displays that contain a liquid crystal material of this type.

A cosmetic composition comprising: (a) 2-mercaptonicotinoyl glycine; (b) acyl glycinate surfactant; (c) a salt providing divalent cations having a charge density of about 40 to about 200 C / mm3 and a water solubility of at least 400 g / L; (d) anionic polymer; (e) glycerin; (f) water; and (g) reducing agent. The cosmetic composition is particularly useful in a method for brightening skin, depigmenting skin, treating hyperpigmentation of skin, treating melasmic skin, or evening skin tone.

The invention relates to the technical field of hydrodesulfurization catalysts, and discloses a molecular sieve hydrodesulfurization catalyst and a preparation method thereof.Active Si-Cl bonds of maleate methyl dichlorosilane react with hydroxyl in an MCM-41 molecular sieve, then hydrolysis is conducted through sodium hydroxide, and therefore a large number of carboxyl groups are grafted in the molecular sieve; carboxyl can form a strong coordination effect with metal ions such as nickel and the like, so that nickel and molybdenum are uniformly adsorbed into a matrix of the molecular sieve, a nickel-molybdenum oxide catalytic active center is uniformly generated in the molecular sieve through high-temperature roasting, catalytic sites are not easy to agglomerate, the dispersity is good, and the catalytic activity is stable. The catalyst can effectively perform hydrogenation reaction on sulfur-containing substances such as thiophenes in straight-run diesel oil, and has higher desulfurization rate. The catalyst has good practical application in the aspects of oil hydrodesulfurization catalysis and the like.

A novel salt form of Compound (I) represented by the following structural formula, and its corresponding pharmaceutical compositions, are disclosed.Particular single crystalline forms of 1:1 Compound (I) tartrate salt are characterized by a variety of properties and physical measurements. Methods of preparing specific crystalline forms are also disclosed. The present disclosure also provides methods of treating cancer in a subject.

The invention relates to the field of antitumor drugs, in particular to a thiophene acetyl tetrahydro-beta-carboline compound and application thereof. The thiophene acetyl tetrahydro-beta-carboline compound or the pharmaceutically acceptable salt thereof, and the pharmaceutical composition containing the compound can be used for preparing medicines for preventing and / or treating various cancers. The cancer is at least one of breast cancer, lung cancer, osteosarcoma, melanoma, gastric cancer, pancreatic cancer, kidney cancer, glioma and ovarian cancer. Activity screening is carried out on various compounds, it is found for the first time that the 12 compounds provided by the invention have remarkable broad-spectrum inhibitory activity on various human cancer cell lines, and key candidate compounds are provided for developing novel anti-cancer drugs.