1924 results about "Boronic acid" patented technology

The invention relates to the technical field of high polymer materials, and particularly provides a self-repairing type UV curing alumite color layer coating and a preparation method thereof. The water-based ink is prepared from, by weight, 30-50 parts of polyurethane acrylic resin, 10-25 parts of modified acrylic oligomer containing dynamic covalent bonds, 2-5 parts of photoinitiator, 3-8 parts of hydrophobic modified nano filler and 1-3 parts of cross-linking agent, and the dynamic covalent bonds are selected from at least one of hydrazide bonds, boric acid ester bonds and Diels-Alder bonds. By introducing a gradient energy collaborative network of dynamic covalent bonds and quadruple hydrogen bonds, rapid self-repairing of the coating at normal temperature and thermal triggering recombination of deep damage are achieved, and meanwhile through the micro-phase separation design of the hydrophobic core-shell filler and the graft modified silicon carbide nanowires, the hydrolysis resistance is improved.

The invention discloses a modified organic silicon resin, a high-temperature-resistant coating and a preparation method thereof, the modified organic silicon resin is prepared by hydrolyzing at least two different siloxane monomers and then carrying out condensation reaction on the hydrolyzed siloxane monomers and at least one boric acid monomer, and the main chain of the organic silicon resin is of a heteroatom doped structure formed by a Si-O bond, a B-O bond and a B-O-Si bond; at 200-250 DEG C, the modified organic-inorganic high-temperature-resistant composite material is subjected to a self-crosslinking reaction. The high-temperature-resistant coating overcomes the defect that the high-temperature-resistant coating in the prior art cannot meet the high-temperature test, and avoids the defects that organic and inorganic high-temperature-resistant coatings crack, the impact resistance and hardness are not matched, the water resistance is poor, and the wear resistance is poor.

The invention relates to a protein-based phenylboronic acid ester dynamic crosslinking hydrogel material as well as a preparation method and application thereof. The preparation method comprises the following steps: dissolving a component A, namely a phenylboronic acid modified protein polymer derivative, in a biocompatible medium to obtain a solution A; dissolving a component B, namely a macromolecular derivative containing a vicinal diol group, into a biocompatible medium to obtain a solution B; and mixing the solution A and the solution B with a certain concentration for a certain time to obtain the protein-based phenylboronic acid ester dynamic crosslinking hydrogel material. The boric acid ester dynamic cross-linking bond belongs to reversible chemical cross-linking reaction, and the prepared protein-based hydrogel material has enough mechanical strength and cheap operability. The protein-based hydrogel material disclosed by the invention can provide the effects of cell adhesion, proliferation and differentiation promotion, tissue regeneration and the like, can load and slowly release beneficial components for promoting tissue repair, is an ideal tissue engineering scaffold material, and can be applied to defect regeneration and repair of soft tissues, cartilages, bones and the like.

A compound or molecular complex. The compound or molecular complex comprises: a metal chelator configured for chelation with a radioactive isotope or a non-radioactive isotope; and a trifluoroborate (BF3)-containing moiety configured for 19F / 18F exchange or a precursor thereof; and optionally a cell-targeting domain.

The invention discloses a light-moisture dual-curing underwater epoxy coating with a self-repairing function as well as a preparation method and a construction method of the light-moisture dual-curing underwater epoxy coating. The epoxy coating comprises a component A and a component B, wherein the mass ratio of the component A to the component B is (1.5-3.5): 1; the component A is prepared from the following raw materials: bisphenol F type epoxy resin, dynamic disulfide bond modified polysulfide rubber, boron nitride nanosheet and silicon carbide nanowire hybrid filler, a photoinitiator and a silane coupling agent; the component B is prepared from the following raw materials: moisture-cured polyether amine, a boric acid ester bond cross-linking agent and hydrophobic modified graphene oxide. According to the invention, a light-moisture dual-curing mechanism is adopted, ultraviolet irradiation initiates rapid surface curing, and then environmental moisture permeates to complete deep curing. The material provided by the invention has the advantages of rapid curing, excellent self-repairing function, significantly improved underwater adhesion and good thermal conductivity, and provides a new solution for rapid repairing and long-acting protection of underwater structures.

The invention relates to the technical field of compound fertilizers, and discloses a boron-zinc-molybdenum synergistic compound fertilizer, which is prepared from the following raw materials in parts by weight: calcium nitrate, ammonium polyphosphate, potassium sulfate, magnesium sulfate, disodium octoborate tetrahydrate, sugar alcohol chelated zinc, sodium molybdate and a synergistic auxiliary agent, the feed additive is prepared from a feed additive, an activator, 5-alginic acid oligosaccharide, aminolevulinic acid, sugar alcohol chelated magnesium, an antagonist, a stress-resistant enhancer and a coating material. According to the boron-zinc-molybdenum synergistic interaction compound fertilizer and the preparation process thereof, the disodium octoborate tetrahydrate, the sugar alcohol chelated zinc and the sodium molybdate are compounded according to a specific proportion, antagonism is avoided through proportion limitation, the synergistic effect of the three elements is remarkably enhanced, and the problem that a single element is insufficient or excessive is solved; chelated elements such as sugar alcohol chelated zinc and sugar alcohol chelated magnesium are combined with an activating agent (humic acid chelated calcium and silica sol) to form a gel-state chelate, so that the trace elements can be prevented from being fixed by soil, and the transfer efficiency of the trace elements in crops is improved.

The invention provides a preparation method of a recombinant collagen dressing, and belongs to the technical field of medical dressings. According to the technical scheme, stacked short sequences and continuous human collagen amino acid short sequences are repeatedly combined for multiple times to form recombinant collagen with specificity, and high similarity of the recombinant collagen with human collagen is ensured. On the basis, 4-FPBA is used as a cross-linking agent to respectively form a Schiff base bond responsive to pH and a boric acid ester bond responsive to glucose with CMCS and two kinds of HA with different molecular weights, and then the double-dynamic covalent cross-linked network adhesive hydrogel is synthesized. The triple-helix structure of the recombinant collagen is combined with a specific receptor on a cell membrane, and cell behaviors are regulated and controlled by inducing signal transduction through a cytoskeleton, so that skin microcirculation can be effectively improved, and a skin barrier can be repaired; the hydrogel dressing matrix has the effects of resisting inflammation, resisting oxidation, resisting bacteria, promoting healing and the like, the biological performance of the dressing is remarkably improved, and a better curative effect is achieved.

The invention relates to a hyaluronic acid-polyurethane composite material based on a double dynamic network and a preparation method and application thereof, and the preparation method comprises the following steps: carrying out hydrophobic modification reaction on hyaluronic acid and aminophenylboronic acid to obtain aminophenylboronic acid modified hyaluronic acid; the preparation method comprises the following steps: mixing polytetrahydrofuran ether glycol, polyethylene glycol and isophorone diisocyanate, carrying out a primary reaction, adding trimethylolpropane tri (3-mercaptopropionic acid) ester, carrying out a secondary reaction, adding tannic acid, and carrying out a third reaction to obtain tannic acid-terminated dynamic thionocarbamate polyurethane; and mixing the amino phenylboronic acid modified hyaluronic acid with the tannic acid terminated dynamic thionocarbamate polyurethane for reaction to obtain the hyaluronic acid-polyurethane composite material with the double dynamic networks. Compared with the prior art, by introducing a'thionocarbamate-borate 'double-dynamic network, high toughness, high strength, good self-repairability and repeatable processability in an extreme environment are realized, and the material is particularly suitable for manufacturing and repairing of key components in an LNG ship body and a heat insulation system thereof.

The invention discloses a dynamic borate bond-based self-healing polyacrylic acid binder and a preparation method thereof. The dynamic borate bond-based self-healing polyacrylic acid binder comprises a polymer main chain and a dynamic cross-linking agent, the dynamic cross-linking agent is a polyol compound containing at least two pairs of ortho-hydroxyl groups; the polymer main chain is formed by copolymerizing the following monomers: an acrylic structural monomer, the molar fraction of which accounts for 85-94% of the total monomer; a functional monomer containing a boric acid group, wherein the molar fraction of the functional monomer accounts for 3-8% of the total monomer; the mole fraction of the flexible monomer containing the acrylate group accounts for 3-8% of the total monomer. Various stresses generated by different negative electrode materials in circulation can be effectively adapted and buffered through a network formed by dynamic boric acid ester bonds and reversible fracture and combination of the boric acid ester bonds, so that the service life of the battery is generally prolonged, the working temperature range of the battery can be remarkably widened, the low-temperature discharge capacity can be remarkably increased, and the high-temperature cycle life can be prolonged.

The invention discloses a reprocessable solid-solid phase change material based on dynamic borate bonds and a preparation method of the reprocessable solid-solid phase change material. Based on the mechanism that boric acid ester is subjected to ester exchange during thermal stimulation, a dynamic cross-linking agent containing boric acid ester is adopted for cross-linking a polyurethane prepolymer, polyethylene glycol is cross-linked through chemical bonds, the tensile strength and the elongation at break of the phase change material are improved, and the problem that the phase change material is prone to leakage in the phase change process is solved; besides, borate bonds belong to associated dynamic covalent bonds and can keep the crosslinking density of the material unchanged when ester exchange occurs under thermal stimulation, so that the thermal stability of the material is relatively good; the solid-solid phase change material disclosed by the invention is excellent in mechanical property, has a relatively high enthalpy value, can be reprocessed, and has an application prospect in the fields of thermal management, energy storage, infrared stealth and the like.

The invention discloses a baicalin and boric acid antibacterial peptide assembly and a preparation method and application thereof, belongs to the technical field of biological medicine, and provides a baicalin and boric acid antibacterial peptide assembly which comprises baicalin and boric acid antibacterial peptide. The amino acid sequence of the boric acid antibacterial peptide is one of SEQ ID NO. 1, SEQ ID NO. 2, SEQ ID NO. 3, SEQ ID NO. 4, SEQ ID NO. 5 or SEQ ID NO. 6. According to the baicalin and boric acid antibacterial peptide assembly, phenylboronic acid molecules introduced to the C end of boric acid antibacterial peptide polypeptide can form boric acid ester bonds with the baicalin, the water solubility and membrane permeability of the baicalin can be improved, the baicalin can enter bacterial cells more easily to play a role, and the baicalin and the boric acid antibacterial peptide can form a multi-target synergistic antibacterial effect; therefore, the antibacterial effect is obviously improved.

The invention discloses an antibacterial material rich in a bismuth metal organic framework and a preparation method thereof, the method comprises the following steps: adding an indole monomer and an alcohol monomer into a solvent, and then adding nitrosalicylaldehyde into the solvent to obtain a spiropyran compound; the preparation method comprises the following steps: adding humic acid into a binary solvent consisting of dioxane and butanol to obtain a mixed solution; the ratio of the mass of the humic acid to the volume of the binary solvent is (2-3): (20-40) g / ml; sequentially adding a bismuth source, 2-bromo-5-(trifluoromethyl) pyridine and 4-(trifluoromethyl) phenylboronic acid into the mixed solution to obtain a bismuth metal organic framework; and adding the spiropyran compound into the bismuth metal organic framework to obtain the antibacterial material rich in the bismuth metal organic framework. The antibacterial capability of the antibacterial material is improved.

The invention discloses a modified organic silicon marine antifouling paint and coating based on dynamic crosslinking of boric acid ester, and the modified organic silicon marine antifouling paint based on dynamic crosslinking of boric acid ester comprises the following components in parts by weight: 20-40 parts of a component A; 4-10 parts of a component B; 1-3 parts of a component C; wherein the component A comprises hydroxyl-terminated polydimethylsiloxane, borate modified polysiloxane, an auxiliary agent, a pigment filler and a first solvent, the component B comprises a curing agent and a second solvent, and the component C comprises a catalyst and a third solvent. Hydrolysis of boric acid ester bonds increases the hydrogen-bond interaction between the coating and a base material, and meanwhile, ether groups are introduced to strengthen the hydrogen-bond interaction effect, so that the coating can be firmly adhered to the intermediate paint in a seawater soaking environment.

The invention relates to the field of copper-clad plates, and discloses a high-performance flame-retardant low-dielectric-loss copper-clad plate and a preparation method thereof.The copper-clad plate comprises epoxy resin, benzoxazine resin, composite filler, carboxyl-terminated nitrile rubber, an active diluent, a curing agent and the like; the composite filler is prepared by compounding flame-retardant modifier grafted graphene oxide and epoxy silane modified silicon dioxide hollow spheres; according to the flame-retardant modifier, boric acid and pentaerythritol are used for preparing a double-terminal hydroxyl boron-containing intermediate, then dichlorodiphenyl silane and phenylphosphonic dichloride react with hydroxyl groups at the two ends of the intermediate to prepare a flame-retardant intermediate, and amino silane and vanillic aldehyde react with chlorine atoms at the two ends of the intermediate to prepare an aldehyde modified flame-retardant intermediate; the copper-clad plate prepared by the preparation method disclosed by the invention is low in dielectric constant and dielectric loss, high in heat conductivity coefficient and good in flexibility, and also has excellent heat resistance and flame retardance.

The invention relates to the field of oral cavities, and particularly discloses a lasting antibacterial type composite tooth socket for medicine carrying and a preparation method thereof.The lasting antibacterial type composite tooth socket comprises an adsorption layer and an antibacterial membrane layer, the adsorption layer is used for adsorbing oral cavity treatment liquid medicine, and the antibacterial membrane layer comprises a nano-silver antibacterial layer and a chitosan antibacterial layer; the preparation method comprises the following steps: mixing a tea polyphenol-polylactic acid composite solution, a nano-silver-carboxylation modified cellulose compound and a polyvinyl alcohol solution, and carrying out electrostatic spinning to prepare a nano-silver antibacterial fiber membrane, so as to form the nano-silver antibacterial layer; mixing chitosan with hot water, adding cinnamyl aldehyde, glycerol and boric acid, stirring to obtain a mixed solution, coating one side of the nano-silver antibacterial layer with the mixed solution, and curing to form a chitosan antibacterial layer; the adsorption layer is attached to the side, away from the chitosan antibacterial layer, of the nano-silver antibacterial layer, and then the lasting antibacterial type composite tooth socket for carrying the medicine is prepared through hot-pressing compounding. The drug-loaded composite tooth socket has the characteristic of further improving the antibacterial property and the antibacterial durability of the drug-loaded composite tooth socket.

The invention discloses an anti-collision protection lining and an ice hockey helmet, and relates to the field of safety protection buffer functional materials, the anti-collision protection lining comprises an outer layer high microsphere density area, a middle layer fiber reinforcement area, an inner layer low density opening area and an inner layer composite antibacterial foaming polypropylene foam layer; the preparation of the anti-collision protection lining comprises the following steps: adding polyvinyl alcohol and polyethylene glycol into hot water for dissolving, adding silicon dioxide aerogel powder for stirring, and carrying out boric acid crosslinking, alkali treatment, polyurethane prepolymer coating and high-pressure hot air dispersion drying; performing plasma activation and maleic anhydride grafting; the preparation method comprises the following steps: mixing a component A containing nano colloid microspheres and grafted fibers with a polyisocyanate component B according to a ratio of 1: 1, and carrying out foaming molding to form a microsphere gradient enrichment layer; antibacterial foamed polypropylene foam is attached to the perforated layer in a hot-pressing mode and cut; through molecular flexible modification, microsphere elastic coating and interface strengthening and gradient energy distribution, the use reliability and impact resistance of the ice hockey helmet are improved.

The invention discloses an antifouling waterborne polyurethane coating for ships, and relates to the technical field of waterborne polyurethane coatings, and the antifouling waterborne polyurethane coating is prepared from the following raw materials in parts by weight: 5 to 8 parts of polytetrahydrofuran, 3 to 5 parts of diphenylmethane diisocyanate, 4 to 5.2 parts of chain extender and 0.45 to 0.7 part of functional filler. According to the antifouling waterborne polyurethane coating for the ship, the chain extender I tends to be distributed on a coating-water interface through the hydrophilicity of triethanolamine in the chain extender I, meanwhile, boric acid groups are preferentially in contact with seawater and are distributed on the surface layer of a coating, the water solubility is high, boric acid ions are rapidly released at the initial stage, and the antifouling waterborne polyurethane coating is good in antifouling property. The initial adhesion of marine microorganisms is inhibited through ion repulsion; an MDI fragment in the chain extender II provides an extra-NCO reaction site, and chemical crosslinking is generated between the MDI fragment and a network formed by the chain extender I, so that the overall crosslinking density is improved, and the toughness and weather resistance of a coating film are improved.

The invention relates to the technical field of soil improvement, and discloses a soil improvement repairing agent and a preparation method thereof. The preparation method comprises the following steps: adding biochar, modified eugenol, modified benzothiazolyl pyridine, bacillus licheniformis and diatomite into a mixer, mixing and stirring, extruding and granulating in a granulator, and drying to obtain the soil improvement repairing agent. Eugenol can destroy a membrane structure and denature protein, so that a bacteriostatic effect is achieved, and a healthy soil microenvironment is provided for crops; the quaternary ammonium salt can destroy the membrane structure of pathogenic microorganisms, plays a role in killing the microorganisms, can improve the antibacterial effect of the remediation agent, and prevents and treats spread diseases of soil; nitrogen atoms and sulfur atoms in benzothiazolyl pyridine molecules can coordinate with free heavy metal ions in the soil, the heavy metal adsorption effect of the remediation agent is improved, the production value of the soil is gradually restored, meanwhile, boric acid capable of being absorbed by plants can be released through hydrolysis of pinacol ester, and the fertility of the soil is improved.

The invention discloses resin composite liquid with dual self-repairing and high ethanol solvent wiping resistance as well as a preparation method and application of the resin composite liquid, and belongs to the technical field of polyurethane emulsion coatings. Aiming at the problems that an existing waterborne polyurethane coating is poor in ethanol resistance due to residual carboxyl / hydroxyl of a hydrophilic chain extender and the self-repairing efficiency of a single dynamic bond is low, a metal ion buffer solution is added into a hydroxyl-terminated polyurethane emulsion to coordinate with the carboxyl of the hydrophilic chain extender, so that a hydrophilic group is closed, and the crosslinking density is increased; meanwhile, a boric acid compound is introduced to form dynamic boric acid ester bonds with residual hydroxyl groups of the system, and hydrophilic groups in the system are consumed while a dual self-repairing network is constructed. The coating prepared by the invention has good self-repairing and ethanol wiping resistance.

The invention provides a preparation method of a shape-adaptive hydrogel material for tissue repair. The method comprises the following steps: S1, preparing HPC (Hydroxypropyl Chitosan); s2, preparation of phenylboronic acid functional chitosan PHPC (Polyhydroxyalkanoate); s3, preparing a PHPC solution; s4, preparing a polyvinyl alcohol (PVA) solution; and S5, preparing the dynamic covalent bond hydrogel. According to the invention, a dynamic covalent bond-boric acid ester bond with stimulation response capability is introduced on the basis of common dual-network CS-PVA hydrogel; on the premise of not changing the biocompatibility and biodegradability of the original dual-network hydrogel, the hydrogel is endowed with response capability under physical and chemical stimulation, and the diversity of application scenes is expanded; the dynamic mechanical behavior changes of the PCA hydrogel at four different strain rates of 0.05 mm / s, 0.5 mm / s, 5 mm / s and 50 mm / s are explored, and the passive shape adaptability of the PCA hydrogel along with tissue growth is studied; meanwhile, changes of hydrogel creep deformation and stress relaxation caused by addition of dynamic covalent bonds are researched.

The invention discloses an anti-corrosion self-repairing super-amphiphobic coating film and a preparation method thereof, and belongs to the technical field of polymer coating materials. The coating film sequentially comprises a nano particle skeleton layer, a dynamic borate bond layer and a super-amphiphobic functional layer from inside to outside, and the three-layer gradient design synergistically realizes micro / nano structure stability, self-repairing and super-amphiphobic functions. The framework layer takes SiO2-TiO2 composite nanoparticles as a substrate and provides support; the dynamic boric acid ester bond layer forms a dynamic network through polycondensation of an organic boron compound, endows the self-repairing capability and enhances interface bonding; the super-amphiphobic functional layer is formed by grafting a fluorine-containing organosilicon compound and has hydrophobic and oleophobic properties. A multi-layer structure is constructed step by step, the reaction condition is mild, the operation is simple, the cost is low, the method is suitable for large-scale industrial preparation, the coating film has excellent super-amphiphobic performance and interface adhesion performance, the super-amphiphobic performance of the coating film can still be kept stable in long-term use or a complex environment, and the problem that an existing super-amphiphobic material is prone to damage is effectively solved.

The present invention relates to a fluxapyroxad intermediate trifluoronitrobiphenyl synthesis method, and belongs to the technical field of organic synthesis, the method comprises the following steps: Step 1: under nitrogen protection, adding 3, 4, 5-bromotrifluorobenzene, o-nitrophenylboronic acid, a catalyst, a promoter, an alkali and a solvent into a reaction flask, and after addition, carrying out a heat preservation reaction; and Step 2: after the reaction is finished, carrying out phase splitting and organic phase concentration to obtain the 3 ', 4', 5 '-trifluoro-2-nitrobiphenyl. Compared with a traditional synthetic method of the trifluoro-nitrobiphenyl, the synthetic method of the trifluoro-nitrobiphenyl has the advantages that the 3, 4, 5-trifluoro-bromobenzene and the o-nitrophenylboronic acid are directly used as raw materials, the production step of preparing the 3, 4, 5-trifluoro-phenylboronic acid from the 3, 4, 5-trifluoro-bromobenzene through a multi-step reaction is avoided, the yield can be effectively improved, the utilization rate of the raw materials is high, and the method is suitable for industrial production. And the o-nitrophenylboronic acid preparation method is simple, the reaction cost can be effectively reduced, the reaction route is shorter, simpler and more efficient, the reaction conditions are mild, and the method has higher industrial application value.

The invention relates to the technical field of fertilizers and pesticides for agricultural production, and discloses a liquid pesticide fertilizer for preventing and treating root-knot nematodes in a water-fertilizer integrated system and application thereof, and the liquid pesticide fertilizer is prepared from the following components: a plant source nematicide, a biocontrol inoculant, a macroelement and medium trace element fertilizer, a boron cross-linking agent, a modified polycarboxylic acid dispersing agent, a microbial protective agent and the like. The preparation method comprises the steps of biological phase pretreatment, matrix phase construction, oil phase micro-emulsification, multiphase fusion and dynamic crosslinking. Through trehalose gradient permeation pretreatment, the survival rate of biocontrol bacteria in a high-salt matrix is increased; a boric acid ester bond dynamic cross-linked network is constructed by using a variable pH adjusting process, so that the system is endowed with shear thinning characteristics, and the contradiction between suspension stability and drip irrigation fluidity is solved; and the chelating dispersion effect of the modified polycarboxylic acid dispersing agent is matched, so that the generation of precipitates is effectively inhibited, and stable coexistence and synergistic interaction of the pesticide, the fertilizer and the bacteria are realized.

The invention discloses a preparation method and application of a sulfonylurea structure thermosensitive color developing agent, and relates to the technical field of color developing agents. The core of the thermosensitive color developing agent is a # imgabs0 # compound in a formula 1 containing a sulfonylurea structure. The preparation method comprises the following three steps: synthesizing an intermediate 1 through esterification of raw materials, obtaining an intermediate 2 through boric acidification, and synthesizing a target compound through Suzuki reaction. Through the synergistic effect of sulfonyl and ureido, hydrogen bond network regulation and electron transfer efficiency optimization are realized, and the technical bottlenecks of high-temperature activation requirements and insufficient color development stability of a traditional thermosensitive color developing agent are solved.

The invention discloses a slow-release hydrophobic microcapsule and a preparation method of a cement-based material thereof. Wherein the microcapsule wall structure is mainly an interpenetrating network structure formed by polyvinyl alcohol and sodium alginate, the polyvinyl alcohol is cross-linked by boric acid, the sodium alginate is cross-linked by calcium ions, and the cross-linked polyvinyl alcohol and sodium alginate are linked through hydrogen-bond interaction to form an interpenetrating network system. And meanwhile, the carboxymethyl cellulose serving as a thickening agent and a stabilizing agent can promote the formation of the microspheres and increase the strength of the microspheres in the process of synthesizing the microcapsule wall material. Hydroxyl-terminated polydimethylsiloxane is wrapped in the microcapsule, and a hydroxyl group of the hydroxyl-terminated polydimethylsiloxane reacts with a carboxyl group in sodium alginate, so that the hydroxyl-terminated polydimethylsiloxane is wrapped in the microcapsule. The microcapsule is doped into a neat paste test block to prepare a cement-based material, the cement-based material can be normally hydrated to ensure the strength, and meanwhile, the cement-based material has a hydrophobic characteristic in the service period to prevent invasion of water and corrosive ions and adhesion of inorganic matters and microorganisms.

The invention provides an imidazo [1, 2-alpha] pyridine stimuli-responsive molecule with a D-A twisted structure as well as a preparation method and application of the imidazo [1, 2-alpha] pyridine stimuli-responsive molecule, belongs to the technical field of intelligent materials, and is used for solving the technical problem that intelligent materials for developing stimuli-responsive molecules for data encryption and information anti-counterfeiting are insufficient. The preparation method of the compounds N1 and N3 comprises the following steps: 2-aminopyridine and 2, 4 '-dibromoacetophenone are subjected to an amphiphilic reaction to obtain a compound a; the compound a and POCl3 are subjected to a Vilsmeier-Haack reaction, and a compound b is obtained; carrying out Suzuki coupling reaction on the compound a or the compound b and triphenylamine boric acid to obtain a compound N1 or N2; the compound N2 and malononitrile are subjected to a Knovenagel condensation reaction, and a compound N3 is obtained. The compound prepared in the invention has good fluorescence emission capability in a solution and a solid state and a grinding solvent acid / alkali stimulated fluorescence discoloration behavior, and can realize good data encryption and information anti-counterfeiting.

The invention relates to the technical field of enzyme-linked immunosorbent assay, and discloses a quality control serum diluent as well as a preparation method and application thereof, and the quality control serum diluent is prepared from the following raw materials: boric acid, borax, sodium caseinate, liquid gelatin, aminopyrine, an osmotic pressure stabilizer and bovine serum. The quality control serum diluent prepared by adopting the formula has no potential interfering substances (such as formaldehyde and thiomersalate), has excellent thermal stability and long-term stability, is applied to quality control serum dilution, is beneficial to improving the detection accuracy, ensures that the characteristics of the diluent meet the requirements when the diluent is used every time, and provides stable reference data for the detection process.

The invention discloses a staged delayed coagulation and viscosity reduction type iron aluminate cement water reducing agent and a preparation method thereof. The iron aluminate cement water reducing agent is obtained by copolymerizing prepared isopentenol polyoxyethylene ether borate, hydroxyethyl methylacrylate glucolactone and methacrylic acid. The boric acid ester is rapidly hydrolyzed in the initial stage of hydration (9 < pH < 12) to obtain boric acid, and first-stage delayed coagulation is performed on the aluminoferrite cement. When delayed coagulation fails, the cement continues to be hydrated to reach the middle stage of hydration (pH > 12), glucolactone is hydrolyzed to generate gluconate for further delayed coagulation of the cement, meanwhile, hydroxyethyl methylacrylate is hydrolyzed to release more adsorption sites, and hydration products are further dispersed to reduce the viscosity of the system. And stage release enables the aluminoferrite cement to be hydrated stage by stage, so that the problem of poor bleeding cohesiveness caused by non-hydration of the cement after one-time doping of the retarder is solved, the problem of slurry tackifying caused by large hydration of the cement in the later stage is also avoided, and engineering application of the aluminoferrite cement is further promoted.

Disclosed herein is a compound that is (R)-(2-(3-((((2-ethylbutanoyl)oxy)methoxy)carbonyl)-2-hydroxyphenyl)-1-propionamidoethyl)boronic acid citrate coordination complex, or a pharmaceutically acceptable salt or solvate thereof. Also disclosed herein are methods of treating a bacterial with a compound that is (R)-(2-(3-((((2-ethylbutanoyl)oxy)methoxy)carbonyl)-2-hydroxyphenyl)-1-propionamidoethyl)boronic acid citrate coordination complex, or a pharmaceutically acceptable salt or solvate thereof in combination with ceftibuten.

The invention discloses a C60-BODIPY triplet photosensitizer as well as a preparation method and photodynamic antibacterial application thereof. In the preparation process, a fullerene pyrrole ring compound and a BODIPY molecule are connected together through a benzene bridge group, and two ends of a bridge bond are respectively connected to a C atom on a fullerene pyrrole ring and a 6th site of the BODIPY molecule; a BODIPY-C60 binary molecule is formed; the preparation method comprises the following steps: reacting 9-anthracene formaldehyde with 2, 4-dimethyl pyrrole to generate a boron-dipyrromethene molecule of which the meso position is substituted by 9-anthryl, brominating the boron-dipyrromethene molecule at the 6 position by N-bromosuccinimide, coupling the boron-dipyrromethene molecule with p-formylphenylboronic acid, and carrying out Prato reaction on the coupled boron-dipyrromethene molecule with C60 and N-methylglycine to prepare the BODIPY-C60 binary triplet photosensitizer. The triplet photosensitizer has excellent photodynamic activity and relatively high reactive oxygen quantum yield, and can effectively kill bacteria.