649 results about "Bipyridine" patented technology

The invention provides a substituted amino bipyridine derivative as well as a preparation method and application thereof, the structure of the substituted amino bipyridine derivative is as shown in formula I. In the formula, R1, R2, R3 and R4 are independently selected from any one of H, C1-C6 alkyl, C2-C6 alkenyl, C2-C20 alkynyl, C3-C6 cycloalkyl, C5-C20 aryl or C5-C20 heterocyclic radical; when R1, R2, R3 and R4 are not methyl, no more than one of R1, R2, R3 and R4 is H; and when any one of R1, R2, R3 and R4 is methyl, the rest groups are independently selected from H or methyl. When the substituted amino dipyridyl derivative provided by the invention is used as a blue dye, the dyed blue dye is bright in color, deep in dyeing and comprehensive in dyeing fastness; the preparation process is simple, convenient to purify, safe, simple, convenient and energy-saving, the product quality is stable, the reproducibility is good, the yield is high, and the method is suitable for industrial production.

The invention relates to a preparation method of a high-lithium-affinity vinylene covalent organic framework material serving as a lithium metal negative electrode interface protective layer. The method comprises the following steps: firstly, by utilizing a simple hydrothermal synthesis method, taking 1, 3, 5-trimethyl-2, 4, 6-triazine (TMT) and 2, 2-bipyridine-5, 5-diformaldehyde (BPY) as monomers, and carrying out Aldol condensation reaction to synthesize a covalent organic framework material connected by a vinylene bond, which is named as viCOF-bpy; the electrochemical performance of the material is verified by modifying the surface of a copper pole piece with the viCOF-bpy material and then assembling a battery. The lithium-loving group on the material skeleton can promote the migration of lithium ions, and the vinylidene has very strong chemical stability, so that the electrochemical performance of the lithium metal battery can be effectively improved.

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.

This application relates to the field of microbial fermentation technology, and specifically discloses an N-hydroxyamino-N'-acetylguanine blue, its fermentation method and application. The chemical name of the N-hydroxyamino-N'-acetylguanine blue is N-(5'-hydroxyamino-2,6,2',6'-tetraoxo-1,6,1',6'-tetrahydro-2H,2'H-[3,3'] bipyridylmethylene)-acetamide, and the molecular formula is C 12 H 10 O6N4; compared with N-acetylguanine blue, the absorption of N-hydroxyamino-N'-acetylguanine blue is deeper in color at UV611, and at the same time, the formation of hydrogen bonds with amino groups on the fiber can enhance the dyeing property of the dye on the fiber and improve the wash fastness.

The present invention discloses a cobalt-based armor nanozyme and its preparation method and application. The method comprises uniformly mixing a cobalt salt solution, a 2,2'-bipyridine solution, and a g-C3N4 dispersion, performing sufficient reaction followed by pretreatment to obtain a precursor, and grinding and calcining the precursor to obtain the cobalt-based armor nanozyme. The cobalt-based armor nanozyme prepared by the present invention has high catalytic activity and the stability of carbonaceous materials. While ensuring efficient catalysis, it greatly reduces secondary pollution caused by cobalt metal leaching. The cobalt-based armor nanozyme can be used to remove organic pollutants from solid pollutants such as soil and water, and can also be used for targeted enrichment of numerous organic pollutants in contaminated wastewater, thereby improving removal efficiency.

The invention relates to a composite resin material for 3D printing and a preparation method thereof. The material is prepared from the following raw materials in parts by weight: 60-90 parts of polylactic acid, 5-15 parts of a toughening agent, 5-15 parts of a flame retardant, 5-10 parts of modified carbon nanotubes, 0.3-1 part of an anti-hydrolysis agent and 0.3-0.5 part of a lubricant. The flame retardant is added, a phosphate structure, a benzene ring and a hindered phenol structure are introduced into 5, 5 '-dibromo-[2, 2'-bipyridyl]-3, 3 '-diamine, and efficient flame retardance is achieved and the anti-aging performance of the composite resin material is enhanced through multiple synergistic effects of hindered phenol-phosphorus heterocycle-bipyridyl. The modified carbon nanotube is added as a reinforcing agent, so that the mechanical property of the composite resin material is remarkably improved, and the composite resin material is endowed with antibacterial property.

The invention discloses an organic rare earth luminescent complex scintillator as well as preparation and application thereof. The molecular structural formula of the complex is L13ML2, M is Tb, Eu or Er metal ions, and the valence state is + 3; l1 is a tetraphenyl diphosphine imide anion ligand (tpip) or a substituted tpip ligand; l2 is unsubstituted or substituted 2, 2 '-bipyridyl, 1, 10-phenanthroline and a non-ionic chelating group containing a polyheterocycle / fused heterocycle. The organic rare earth luminescent complex scintillator can effectively convert high-energy X-rays into narrow-band visible light and near-infrared light, and is suitable for being applied to the fields of high-energy ray detection and high-resolution imaging.

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 discloses a multi-metal active site covalent organic framework material, a preparation method thereof and application of the multi-metal active site covalent organic framework material in activating PMS to degrade pollutants, the multi-metal active site covalent organic framework material comprises metalloporphyrin and bipyridine groups, when porphyrin loads metal, metal atoms are connected through coordination of two nitrogen sources of bipyridine, the metal atoms are connected through coordination of two nitrogen sources of bipyridine, and therefore the multi-metal active site covalent organic framework material is obtained. Multi-metal active sites are formed; the metal active sites are increased, and the distance between metals is adjusted, so that the framework material shows excellent catalytic activity. The covalent organic framework material is prepared through a solvothermal reaction, the covalent organic framework material continues to react with a metal precursor to load metal, the preparation method is simple, a complex reaction process and harsh reaction conditions are not needed, and large-scale preparation can be achieved.

The invention relates to the technical field of nuclear waste treatment, in particular to a cucurbituril-based supramolecular organic framework material as well as a preparation method and application thereof. A construction unit of the supramolecular organic framework material is constructed by taking cucurbit [8] uril (CB8) as a subject and terephthalyl viologen ligand 1, 1 ''-(1, 4-phenylene) bis ([4, 4 '-bipyridyl]-1-onium) salt (PBV. 2X) as an object through the bonding effect of the subject and the object; in the molecular structure of the supramolecular organic framework material, the construction units are staggered and stacked in parallel in the space, and NO3 <-> is located at the gap of the adjacent CB8. The supramolecular organic framework material disclosed by the invention has high structural stability and cationic framework characteristics, and a rigid framework and a pyridine conjugated system of CB8 endow the material with excellent chemical / irradiation stability, so that the material shows ultrahigh removal rate on ReO4 <-> / TcO4 <-> in extreme environments (strong acid, strong alkali and high irradiation).

The invention relates to the field of copper plating solutions, and provides a low-stress chemical copper plating solution for a glass substrate and a preparation method of the low-stress chemical copper plating solution. The invention discloses a copper ion carboxyl chelate, which is composed of copper ion carboxyl chelate, 2, 2 '-bipyridine, polyethylene glycol-8000, lauryl sodium sulfate, a sodium carbonate buffer agent, deionized water and a pretreatment solvent, and the copper ion carboxyl chelate is prepared by chelating a polyacrylate-itaconic acid copolymer with copper chloride and then carrying out stepwise cross-linking with epichlorohydrin and N, N'-methylene bisacrylamide. The copper-bis-salicylaldehyde ethylenediamine complex is obtained by reacting bis-salicylaldehyde ethylenediamine with copper acetate, crystallizing and purifying. The preparation method comprises the steps of solvent premixing, chelating activation, staged additive integration, pH dynamic regulation and control and plating solution purification, through nitrogen protection, high-shear stirring and accurate pH regulation, the problems that a traditional chemical copper plating layer is high in stress and poor in conductivity are solved, and the method is suitable for high-precision glass substrate surface metallization.

The invention discloses a high-entropy metal organic framework compound, a high-entropy alloy composite material and a preparation method and application of the high-entropy metal organic framework compound and the high-entropy alloy composite material. The high-entropy metal organic framework compound comprises a reaction product of an organic ligand, a monometal complex and a cerium source, the organic ligand comprises 2, 2 '-bipyridine-5, 5'-dicarboxylic acid, and the monometal complex comprises at least five of a Pt complex, a Pd complex, a Ni complex, a Cu complex, an Ag complex, an Rh complex and an Ir complex. The high-entropy alloy composite material prepared from the high-entropy metal organic framework compound as a precursor through carbonization and reduction has adjustable metal content and excellent catalytic activity.

The invention belongs to the technical field of preparation of transition metal organic photocatalysts, and particularly relates to design and a preparation method of a carbazole terpyridyl nickel catalyst. The invention aims to design and synthesize a carbazole terpyridyl nickel catalyst with light / nickel synergistic catalytic activity. The preparation method comprises the following specific synthesis steps: reacting different types of alpha-pyridone pyridinium and alpha, beta-unsaturated ketone in methanol, and carrying out suction filtration, washing, drying and other operations to obtain the corresponding carbazole terpyridyl ligand. The carbazole terpyridyl ligand and anhydrous nickel bromide are subjected to a heating reflux reaction in a tetrahydrofuran solution, and the corresponding carbazole terpyridyl nickel catalyst is obtained through methanol washing, suction filtration, drying and other operations. The terpyridyl nickel catalyst has high catalytic activity in a C-N, C-O and C-S coupling reaction promoted by visible light.

The invention provides polyurethane serving as a hot melt adhesive and alcosol water as well as a preparation method and application thereof, and relates to the technical field of polyurethane binders. The preparation method comprises the following steps: mixing polydihydric alcohol, diisocyanate, an organic solvent and a catalyst to carry out polymerization reaction, and then mixing with chain extenders (dihydric alcohol containing 2-ureido-4-pyrimidone groups and dihydric alcohol containing bipyridine groups) to carry out chain extension reaction to obtain polyurethane. According to the invention, 2-ureido-4-pyrimidone and dipyridyl groups are introduced into a macromolecular chain of polyurethane, and a formed hydrogen bond can provide strong intermolecular cohesion in the adhesive, so that the strength of the material is improved, and the adhesive force with the surface of a base material can be enhanced; the bipyridine group can form a chelating structure with metal ions on the surface of a metal substrate, so that the bonding strength with the metal substrate is enhanced. According to the invention, a single polyurethane material has dual functions of hot-melt bonding and normal-temperature green solvent bonding, and has excellent bonding performance and milder bonding conditions.

The invention discloses a reinforced flame-retardant PC composite material and a preparation method thereof, and relates to the technical field of composite materials. Comprising the following raw materials in parts by weight: 80 parts of PC resin, 10-20 parts of hydroxyl-terminated hyperbranched polycarbonate, 5-8 parts of a micro-crosslinking agent, 3-5 parts of a coupling agent, 25-35 parts of a filler, 5-8 parts of hyperbranched tripolyphosphazene terpyridyl CTP-TPY, 2-4 parts of a compatilizer, 0.3-0.6 part of an antioxidant, 0.3-0.6 part of a lubricant, 0.8-1.2 parts of an initiator and 1-3 parts of 9, 10-di-tert-butyl-4-methylphenol. The invention relates to a high-temperature-resistant anti-corrosion coating which is prepared from the following components in parts by weight: 2-6 parts of 2-acrylamido-2-methylpropanesulfonic acid, 2-4 parts of 1, 10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide, 1-3 parts of octaphenylcyclotetrasiloxane, 4-6 parts of 2-acrylamido-2-methylpropanesulfonic acid and 0.8-1.2 parts of a catalyst. The reinforced flame-retardant PC composite material is good in mechanical property and excellent in flame retardance, impact toughness and weather resistance.

The invention discloses a preparation method and application of a layered column three-dimensional MOF enhanced mixed matrix membrane, and belongs to the technical field of pervaporation membrane separation. The preparation method comprises the following steps: firstly, dissolving a copper metal source and 2, 3, 6, 7, 10, 11-hexahydroxytribenzene in a solvent to obtain Cu < 2 + > and a deprotonated organic ligand, adding a pillar ligand bipyridine in situ, and co-coordinating the double ligand and Cu < 2 + > to generate a layered column three-dimensional MOF (Metal Organic Framework); and doping the layered column three-dimensional MOF into a polymer matrix to prepare a membrane casting solution, and coating the surface of a support body with the membrane casting solution to prepare the layered column three-dimensional MOF enhanced mixed matrix membrane. According to the invention, the pillar ligand dipyridyl provides a supporting effect for the three-dimensional MOF and constructs a three-dimensional pore channel at the same time; the affinity site of the three-dimensional MOF has conjugated pi-pi, hydrophobic and hydrogen bond interaction on the perfume; the three-dimensional MOF and a high-molecular polymer have excellent compatibility, and the mixed matrix membrane simultaneously has affinity of the three-dimensional MOF to 2-PE and hydrophobicity of a polymer matrix; the pervaporation membrane can be used for pervaporation membrane perfume separation.

Electrically neutral complex compounds of formula I including any stereoisomer or E / Z isomer thereof wherein: M is Fe < 2 + >, Ru < 2 + >, Os < 2 + >, Co < 3 + >, Rh < 2 + >, Rh < 3 + >, Ir < 3 + >, Ni < 2 + >, Pd < 2 + >, Pt < 2 + > or Pt < 4 + >, in particular Ru < 2 + >; t and T'are H or (C1-C3)-alkyl; lig is a bidentate ligand, in particular 2, 2 '-dipyridyl (bpy) or 4, 7-diphenyl-1, 10-phenanthroline (BPhen); and A is an anion from a pharmaceutically acceptable acid, the electrically neutral complex compounds of formula I are useful in human therapy, in particular as photosensitizers (PS) in photodynamic therapy (PDT) of cancer, skin diseases, fungal infections or microbial infections. They are almost non-toxic under dark conditions at therapeutic doses and exhibit good to excellent photoactivity under hypoxic conditions. They can be used for PDT treatment of deep hypoxia tumors by using light within a far-infrared to near-infrared light treatment window.

The invention discloses a covalent organic framework material, a preparation method thereof and application of the covalent organic framework material in degrading new pollutants in a water body by activating PMS, the covalent organic framework material contains a pyrene group and a bipyridine linking group, has a flat molecular structure and a laminated nanosheet morphology, and has a regular pore structure; the catalyst has a good crystal structure, reliable mechanical strength and excellent thermal chemical stability and catalytic activity, and is an excellent catalyst; and the subsequent modification and metal atom loading sites exist, so that the possibility is provided for further improving the catalytic activity. The bottleneck problems of low crystallinity and poor stability in the traditional preparation process are solved through solvothermal reaction preparation, use of a mixed solvent system and introduction of a weakly acidic solvent, the preparation method is simple, and large-scale production can be realized. The activated PMS degrades new pollutants in the water body; under the condition that the reaction time is 45 minutes, the degradation rate of the BPA can reach 100%.

The invention is suitable for the field of electrochemical luminescence detection equipment, and provides a dispersion device suitable for electrochemical luminescence detection, which comprises a monochromator body, the monochromator body is composed of a monochromator housing, a reflector assembly, a grating assembly, a collimating mirror assembly, a focus lens assembly, a slit, a flange snap ring and a flange; an M-shaped light path is arranged in the monochromator body, and a slit, a reflector assembly, a collimating mirror M1 in the collimating mirror assembly, a customized blazed grating G1 in the grating assembly and a focusing mirror M2 in the focusing mirror assembly are sequentially arranged in the light propagation direction. The customized blazed grating G1 is designed by adopting specific parameters including the scribed line density, the blazed wavelength, the notch groove depth and the groove width ratio, and primary light energy enhancement and secondary light intensity suppression can be realized; according to the invention, an optical filter is not needed, the diffraction efficiency of a monochromator is improved to 60-86%, the intensity ratio of luminol secondary light to primary light is less than or equal to 1.6%, the detection limit of ruthenium bipyridine is reduced from 100pmol / L to 50pmol / L, and the electrochemical luminescence detection device is suitable for various electrochemical luminescence detection scenes.

The invention provides a cobalt-doped nickel-based coordination polymer catalyst and a preparation method and application thereof.The preparation method comprises the following steps that S1, Schiff base and 4, 4 '-dipyridyl are placed in a mixed solvent to be mixed, acid is added into the mixed solvent to obtain a precursor solution, the precursor solution and foamed nickel are mixed, a coordination reaction is conducted through a hydrothermal method, and a nickel-based coordination polymer is obtained; and S2, dissolving cobalt salt in an organic solvent, adding into the nickel-based coordination polymer, mixing, and carrying out a hydrothermal method to obtain the cobalt-doped nickel-based coordination polymer catalyst. The preparation method is simple in process, low in cost and good in repeatability.

The invention belongs to the field of functional nano materials and optical imaging, and particularly relates to a gold nanocluster and a preparation method and application thereof. The surface of the gold nanocluster contains a sulfydryl ligand A and a sulfydryl ligand B, the sulfydryl ligand A is ATT, and the sulfydryl ligand B is a sulfydryl ligand containing arginine; fluorescence quantum efficiency and electron transfer efficiency are synergistically enhanced on the basis of interaction of hydrogen bonds in the gold nanoclusters, the ultra-small luminous gold nanoclusters protected by double ligands are synthesized, the electrochemical luminescence quantum efficiency of the ultra-small luminous gold nanoclusters is up to 13.0% and is 4.2 times of that of a standard compound terpyridyl ruthenium in the field of electrochemical luminescence, and the ultra-small luminous gold nanoclusters are high in electrochemical luminescence quantum efficiency. An electrochemical luminescence transition area can be narrowed by 10 times compared with a terpyridyl ruthenium imaging system, and zero-thickness ECL luminescent layer cell high-resolution imaging can be realized; good application prospects are realized in the fields of fluorescence detection, electrochemical luminescence detection, fluorescence imaging, electrochemical luminescence imaging and the like.

The invention discloses a monatomic covalent organic framework material with adjustable iron loading capacity, a preparation method of the monatomic covalent organic framework material and a sulfamethoxazole degradation method. COFs containing bipyridine groups are used as a framework, an anchoring point is provided for iron loading, the iron loading capacity can be regulated and controlled by controlling the adding amount of an iron precursor, and a degradation path is successfully regulated and controlled to be close to 100% high-valence iron; and after calcination, the spinning state of iron is changed, and the PMS utilization rate and the electron transmission efficiency of iron sites are improved, so that the degradation efficiency of new pollutants is remarkably improved. The preparation process has the core advantages of simple equipment, simplicity and convenience in operation, low production cost and the like, and has outstanding environmental compatibility, social and economic values and industrial mass production feasibility while practicing a green synthesis concept.

The invention discloses a preparation method of a functionalized carbon nanotube immobilized cobalt molecule complex and research on electrocatalytic CO2 reduction of the functionalized carbon nanotube immobilized cobalt molecule complex. The invention provides a dual combination strategy, specifically, a composite catalyst is prepared through an in-situ mixing process by taking a functionalized multi-walled carbon nanotube (MWCNT) as a conductive carrier and taking a peripheral modified cobalt tetrabipyridine molecular complex (Coqpy) as a catalytic active component. A carbon nanotube functional group is used as a first coordination ball to realize axial coordination bonding with a Co center, so that more electrochemical active cobalt complexes are allowed to be loaded, and interface electron transfer is accelerated. The pi-pi coupling effect of the peripheral conjugated group of Coqpy and MWCNT further strengthens the interaction and stability of electrons in the complex, and the CO Faraday efficiency and conversion frequency are respectively as high as 97.5% and 79s <-1 >. According to the composite electrode designed by the invention, the catalytic activity and stability of the catalyst are greatly improved, the process is simple, the method is novel, and the method is expected to become a universal and convenient method for preparing the heterogeneous molecular electrocatalyst.

The application discloses a kind of metal organic framework materials and preparation method and application thereof, belong to chemical separation technical field.The preparation method of metal organic framework material provided in the application includes the following steps: with water and methanol as solvent, with 4,4 '-dipyridyl and malic acid as organic ligand, zinc source is added, and reaction is carried out, in the reaction process, oxygen atom on malic acid is connected with zinc ion on zinc source to form 2D layered network structure, 2D layered network structure is bridged by 4,4 '-dipyridyl to form 3D rigid network framework, after reaction, metal organic framework material is prepared.The metal organic framework prepared by the application has super strong capture effect and large storage space for acetylene molecules, and also has excellent separation effect on acetylene carbon dioxide mixed system, to achieve the purpose of high-purity, high-yield acetylene purification in acetylene carbon dioxide mixture.

The invention discloses a preparation method of a modified lithium titanate battery negative electrode material. The preparation method comprises the following steps: S1, weighing zirconium chloride and benzoic acid, dissolving the zirconium chloride and benzoic acid in N, N-dimethylformamide, and mixing to obtain a first solution; s2, weighing 2, 2 '-bipyridine-5, 5'-dicarboxylic acid formic acid, dissolving the 2, 2 '-bipyridine-5, 5'-dicarboxylic acid formic acid into N, N-dimethylformamide, and mixing to obtain a second solution; s3, adding the first solution into the second solution, uniformly mixing, and reacting to obtain a third solution; s4, the third solution is subjected to suction filtration, washing and drying, and powdery UiO-bpy is obtained; s5, weighing lithium titanate powder and UiO-bpy, dissolving the weighed lithium titanate powder and UiO-bpy in ethanol to obtain a fourth solution, and drying the fourth solution to obtain an intermediate sample; and S6, heating the intermediate sample in a tubular furnace under the protection of Ar atmosphere, and cooling to obtain the battery negative electrode material UiO-bpy (LTO), thereby solving the problems of low electronic conductivity, poor rate capability and insufficient energy density of the lithium titanate (LTO) negative electrode material.

To provide a method for producing a bipyridine derivative, which enables obtaining a high-purity target compound (including an intermediate) without performing purification by column chromatography, provides a high yield, and is industrially advantageous.SOLUTION: A method for producing a bipyridine derivative represented by formula (3) comprises a step of obtaining a metal complex as an intermediate. In the formula, each of R13 to R20 is a hydrogen atom or a substituent; a plurality of R13 to R20 may be the same or different; at least one of six R14 to R16 is a substituent; at least one of two R17 is a hydrogen atom; any two substituents of R13 to R20 may be linked to each other to form a ring; R17 to R20 may contain a pyrrolyl group which may contain a halogen atom or a substituent; and at least one of R14 to R16 may have a halogen atom or a substituent.SELECTED DRAWING: None