629 results about "Carbazole" patented technology

The application provides a process method for preparing (2-(3,6-dimethoxy-9H-carbazol-9-yl)ethyl) phosphonic acid, and particularly relates to the technical field of organic synthesis. The process method is that, under alkaline conditions, a halogenated phosphonate compound is added into a 3,6-dimethoxy-9H-carbazole solution to perform a reaction, hydrochloric acid aqueous solution is added after the reaction to perform acidolysis degreasing, and finally (2-(3,6-dimethoxy-9H-carbazol-9-yl)ethyl) phosphonic acid is obtained through extraction, reflux adsorption and beating purification. The process method uses 3,6-dimethoxy-9H-carbazole as a starting material, realizes the synthesis of the target product through one-pot reaction, has mild reaction conditions, uses non-toxic raw materials which are easy to obtain, has simple synthesis process, is convenient to operate, and has high separation yield.

The invention provides a preparation method and application of a quantum dot light-emitting diode based on interface modification, and belongs to the technical field of quantum dot materials. The preparation method comprises the following steps: (1) spin-coating PEDOT: PSS-4083 on ITO (Indium Tin Oxide) to obtain a hole injection layer; (2) spin-coating polyvinyl carbazole on the hole injection layer in the step (1) to obtain a hole transport layer; (3) spin-coating pyridine on the hole transport layer in the step (2) to obtain a modification layer; (4) spin-coating ZnCdS / ZnS quantum dot normal octane on the modification layer in the step (3) to obtain a quantum dot film; and (5) spin-coating an Mg-doped ZnO ethanol solution on the quantum dot film in the step (4), and performing high-vacuum evaporation to obtain the quantum dot light-emitting diode. Compared with an original device, the EQE of the prepared quantum dot light emitting diode is improved by 16.5%, and the highest brightness is improved by 12.5%.

The invention provides a carbazole-containing heterocyclic compound and an organic electroluminescent device thereof, and relates to the technical field of organic electroluminescent materials. The carbazole-containing heterocyclic compound provided by the invention has relatively high polarizability, is beneficial to improving the refractive index, and can reduce the total reflection phenomenon during light emission of the device and effectively improve the light extraction efficiency of the device when being applied to a covering layer of the organic electroluminescent device; and meanwhile, the compound has relatively high glass transition temperature and good film-forming property, and can isolate moisture and oxygen, so that the luminous efficiency and the service life of the organic electroluminescent device are further improved and prolonged. The preparation method of the compound is simple, raw materials are easy to obtain, and the compound can be widely applied to the fields of organic thin film transistors, panel display and the like and has good application effects and industrialization prospects.

The invention provides a tritium radiation volt isotope battery. The tritium radiation volt isotope battery comprises a shell and a stacking structure, the shell is provided with an accommodating cavity; the stacked structure is arranged in the containing cavity and comprises a positive pole piece, a semiconductor transduction layer and a negative pole piece which are arranged in a stacked mode, the semiconductor transduction layer is arranged to be an array formed by columnar nano particles, liquid tritides are distributed on the surfaces of the columnar nano particles, and the liquid tritides comprise all-tritiated N-ethyl carbazole and / or all-tritiated N-ethyl carbazole and / or all-tritiated N-ethyl carbazole and / or all-tritiated N-ethyl carbazole and / or all-tritiated N-ethyl carbazole and / or all-tritiated N-ethyl carbazole. And part of tritiated N-ethyl carbazole. The radiation volt isotope battery has improved energy conversion efficiency.

The invention discloses a phenanthridine-6-formaldehyde derivative and a preparation method and application thereof.The preparation method comprises the steps that 2, 4, 5, 6-tetra (9-carbazolyl)-isophthalonitrile serves as a photocatalyst, 1-azabicyclo [2.2. 2] octane serves as a hydrogen atom transfer catalyst, a biphenyl isocyanide compound, the photocatalyst, the hydrogen atom transfer catalyst and an alkali additive are jointly dissolved in 1, 3-dioxolane, the mixture is stirred to be uniform, and the phenanthridine-6-formaldehyde derivative is obtained. And carrying out free radical tandem cyclization and acid-catalyzed hydrolysis reaction to obtain the phenanthridine-6-formaldehyde derivative. The invention also provides a specific reaction equation. According to the developed synthesis method of the phenanthridine-6-formaldehyde derivative, the compound can be efficiently and conveniently prepared, the technical bottlenecks of harsh reaction conditions and tedious steps in a traditional process are successfully overcome, raw materials which are low in price and easy to obtain are adopted, operation is carried out under mild conditions, the synthesis method has the outstanding advantages of being high in yield, safe and simple to operate, environmentally friendly and the like, and the method is suitable for industrial production. Good industrial application potential is shown.

The invention discloses an indolocarbazole compound, a perovskite solar cell and a preparation method, and belongs to the technical field of perovskite solar cells, the indolocarbazole compound provided by the invention is an organic small molecule material and has an asymmetric molecular structure, and an asymmetric conjugated structure system of the indolocarbazole compound enhances the molecular dipole moment and improves the photoelectric conversion efficiency. And the energy level matching is optimized. Meanwhile, benzene ring groups on side chains of molecules of the organic hole transport layer can further inhibit excessive aggregation of the molecules, uniform coverage is achieved, and efficient transport of carriers is achieved. Therefore, when the indolocarbazole compound organic small molecule material is used as a hole transport layer material for a perovskite solar cell, the energy levels of the highest occupied molecular orbital HOMO and the lowest unoccupied molecular orbital LUMO of the indolocarbazole compound organic small molecule material provided by the invention can be well matched with the energy level of an active layer material; therefore, the collection efficiency of current carriers is greatly improved, and the filling factor and the photoelectric conversion efficiency are improved.

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 discloses a polymeric dispersant, a preparation method, a pigment paste and a photocuring composition, the polymeric dispersant is characterized in that the polymeric dispersant is a terpolymer formed by controllable free radical polymerization of a structural unit A, a structural unit B and a structural unit C. The structural unit A is derived from alkyl (meth) acrylate; the structural unit B is derived from polyethylene glycol (methyl) acrylate; and the structural unit C is derived from an N-acryloyl carbazole monomer. The polymeric dispersant aims to overcome the defect that the flexibility of the anchoring group connection mode in the existing carbazole dispersant is too large, and the N-acryloyl carbazole monomer with an optimized structure and a ternary polymerization framework are adopted to realize more efficient and lasting anchoring with the pigment surface, so that the flocculation problem is solved, and the super-stable dispersion is realized.

Disclosed herein is an organic light emitting diode device. The organic light emitting diode device includes an anode, a cathode and a light emitting layer. The light emitting layer has a structure where a blue light emitter and a red / green simultaneous light emitter are stacked. The red / green simultaneous light emitter has a structure where a red light emitter and a green light emitter are stacked. The red light emitter includes a red host compound, and in some embodiments, the red host compound includes a spirobisfluorene-based compound where an aryl amino group is substituted. The green light emitter includes a green host compound, and the green host compound includes a mixture of a first green host compound and a second green host compound. In some embodiments, the first green host compound includes a biscarbazole-based compound and the second green host compound includes an indolocarbazole-based compound.

The invention discloses a hydrogenation device scale inhibitor for heavy high-sulfur raw oil and a preparation method of the hydrogenation device scale inhibitor, and relates to the technical field of scale inhibitors. The scale inhibitor is prepared from a polyisobutylene succinimide dispersing agent, a high-temperature-resistant scale inhibition dispersing agent, an anti-rust agent, an imidazoline corrosion inhibitor, an antioxidant, a sulfide chelating agent, a clearing agent, cup carbazole alkylbenzene sulfonate and a solvent in specific parts by weight. The preparation method comprises the following steps: heating the solvent to 80-100 DEG C, sequentially adding the other components, and stirring for 30-40 minutes. Aiming at the characteristics of heavy high-sulfur raw oil, the scale inhibitor realizes high scale inhibition rate, excellent high-temperature stability and strong sulfur corrosion resistance through a multi-component synergistic effect, effectively solves the problems of scaling and corrosion of a hydrogenation device, prolongs the operation cycle of the device, and is suitable for a hydrogenation process of high-sulfur and high-asphaltene raw oil.

The invention relates to the technical field of hydrogen storage of organic aromatic hydrocarbon molecules, in particular to a derivative of a benzopyrrole compound, a preparation method and application of the derivative, a hydrogen storage method and a hydrogen release method. The chemical structural formula of the derivative is selected from one of M1, M2, M3, M4, M5R and M5S, wherein when the chemical structural formula of the derivative is M1, M2, M3, M5R or M5S, A is selected from a saturated alkyl chain with the carbon number of 1-6 or an unsaturated alkyl chain with the carbon number of 2-6; when the chemical structural formula of the derivative is M4, A is selected from a saturated alkyl chain with the carbon number of 1-6, an unsaturated alkyl chain with the carbon number of 2-6 or boron. Compared with azacyclo-organic molecular materials (carbazoles and indoles) which exist in the field of organic hydrogen storage and are massively researched, the azacyclo-aromatic organic molecular material containing the double nitrogen atoms, which can generate a bridging structure between the double nitrogen atoms and can be used for hydrogen storage, is provided for the first time; and the material is large in hydrogen storage capacity and low in melting point.

The invention discloses a tetrahydrocarbazole enhanced fluorescent probe for detecting hydrosulfite as well as a preparation method and application of the tetrahydrocarbazole enhanced fluorescent probe. The fluorescent probe is a 2-(2-(5-(2, 2-dimethyl-2, 3, 4, 9-tetrahydro-1H-1, 3-methyl carbazole-6-yl) furan-2-yl) vinyl)-3-ethyl benzothiazole-3-onium iodised salt compound, namely, TC-FV-BT, and the fluorescent probe can be applied to the field of fluorescence detection. The probe TC-FV-BT can be used for specifically recognizing the hydrosulfite. Under sunlight, after bisulfite is added into a DMF / H2O (2: 8, v / v) solution of the probe TC-FV-BT, the color of the solution is changed from dark pink to white, under irradiation of ultraviolet light with the wavelength of 365 nm, the solution emits orange fluorescence at the emission wavelength of 605 nm, the fluorescence color of the solution is changed from colorless to orange, the response time is 4 min, the detection limit of the bisulfite reaches 77.27 nM, and the detection limit of the bisulfite reaches 77.27 nM. The fluorescent probe shows good selectivity and anti-interference performance, and has a good application prospect in the fields of environmental analysis, food and the like as a fluorescent probe for detecting hydrosulfite.

The invention discloses a molecular assembly method of a D-A type blending system, which comprises the following steps: by taking indolo [3, 2-B] carbazole as an electron donor (D) and N, N '-bis (4-pyridyl)-1, 4, 5, 8-naphthalene tetraformyl diimide as an electron acceptor (A), dispersing the electron donor (D) and the electron acceptor (A) in an organic solvent, heating, and carrying out ultrasonic treatment to dissolve the electron donor (D) and the electron acceptor (A) to obtain clear and transparent D-A type blending system assembly liquid; vertically inserting a cleaned conductive substrate into the D-A type blending system assembly liquid, soaking for a period of time, lifting the conductive substrate at a constant speed by using a lifting instrument until the conductive substrate is completely separated from the liquid level, horizontally placing, and naturally volatilizing the solvent until the conductive substrate is completely dried to obtain a completely assembled D-A type assembly film; the invention also provides an application of the D-A type assembled film as multi-system information storage. The micromolecule blending assembly system provided by the invention can realize an ultrahigh-density information storage function.

The invention discloses a novel fused heterocyclic compound and application thereof, and an organic electroluminescent device comprising the compound, relates to the technical field of organic electroluminescence, and provides a high-efficiency and long-life green light-emitting material based on a boron-nitrogen skeleton and application of the high-efficiency and long-life green light-emitting material. The compound is designed on the basis of a single-spiro structure material FBN (CAS: 3018116-98-5), a benzene ring on a carbazole unit connected with a spiro ring is replaced with a naphthalene, quinoline or fused ring structure, and substituent groups can be introduced into other fragments for modification. According to the design, the luminous nuclear rigidity is improved, non-radiative vibration is inhibited, the spectrum is narrowed, and the color purity and efficiency are improved; the single-spiro structure is beneficial to control of molecular weight and enhancement of evaporation stability; the HOMO / LUMO delocalization range is expanded by molecular conjugation enhancement, the stability is improved, and the service life of the device is prolonged.

This invention relates to the use of compounds of formula (I), or pharmaceutically acceptable salts or solvates thereof, in the treatment or prevention of mycobacterial infections, wherein: one of R2 and R3 is H, and the other is (CR) a R b ) n Y; Y is selected from CO2R c CN and CONR e R f R4 is selected from H, halogens, CN, alkyl and alkoxy groups; R6 is selected from H, F, Br, I, COOH, CN, COR. d CO2R d Alkyl, haloalkyl, alkoxy, haloalkoxy, nitro, OH, SR d SOR d SO2R d SO2NR d R d NHSO2R d aryl and heteroaryl groups, wherein the aryl or heteroaryl group is optionally substituted by one or more substituents selected from alkyl, alkoxy, halogen, haloalkyl, and haloalkoxy groups; R7 is selected from H, halogen, alkyl, and alkoxy groups; R9 is selected from H, COR... d Alkyl, haloalkyl, aryl, CO-aryl, CO-haloaryl, aralkyl and haloaralkyl; R1, R5 and R8 are H; each R a R b R c R d R e and R f The compounds are independently selected from H, alkyl, and haloalkyl groups; n is 1 to 6. Other aspects of the invention relate to subgroups of compounds of formula (Ia), pharmaceutical compositions comprising such subgroups, and their use in the treatment or prevention of mycobacterial infections.

An organic electroluminescent device having high efficiency and high driving stability, and a material suitable for the organic electroluminescent device are provided. The material for organic electroluminescent devices comprises an indolocarbazole compound represented by a general formula (1). In the formula, the ring a is represented by a formula (1a), X is NR, S, O or CR2, and Ar1 and Ar2 are an aromatic heterocyclic group represented by a formula (1b). Y is N or CR, and at least one is N. L1 is an aromatic hydrocarbon group. The material for the organic electroluminescent devices is suitable as material for the host of the light emitting layer or the hole blocking layer of organic EL devices.

The invention discloses an extraction head and a method for detecting organochlorine pesticides in water by using the extraction head. According to the preparation method, 4-hydroxycarbazole is taken as a functional monomer for electro-polymerization, (benzotriazole-1-yloxy) dipyrrolidine carbon hexafluorophosphate ionic liquid (IL) is taken as a doping medium, and the composite extraction coating is obtained in an electrochemical co-deposition mode. The polymerization 4-Hydroxycarbazole-IL (HBPyU) with the ionic liquid concentration of 25 mu g / mL, the salt solution of 35% saturated sodium chloride solution, the stirring rate of 600 r / min, the extraction temperature of 50 DEG C and the extraction time of 30 min is used as an optimal extraction head, and organochlorine pesticides Hepache and Quintozene in water are analyzed and detected. Therefore, according to the technical scheme, compared with an extraction head only provided with a monomer, the coating material added with the ionic liquid has the best extraction capacity on an analyte, and the beneficial effects of high efficiency and high sensitivity are achieved.

The present invention relates to specific deuterated spirocarbazole-triazine derivatives, mixtures and formulations comprising the same, and to electronic devices comprising these compounds, in particular organic electroluminescent devices comprising these compounds as matrix material, electron transport material or hole blocking material.

The invention belongs to the technical field of photoelectric materials, and particularly relates to a preparation method of a perovskite solar cell. The preparation method of the perovskite solar cell comprises the following steps: soaking an ITO substrate in carbazole phosphonic acid dispersion liquid to spontaneously form a hole modification layer on the surface of the ITO substrate; and sequentially overlapping a perovskite layer, an electron transport layer and an electrode layer on the surface of the hole modification layer to obtain the perovskite solar cell. The beneficial effects of the invention are that the preparation method of the perovskite solar cell achieves the uniform preparation of the hole modification layer through the regulation and control of the inclination angle, temperature and humidity, and improves the efficiency of the cell.

A compound having a structure represented by general formula (1). In general formula (1), R101 to R121 are each independently a hydrogen atom or a substituent, where R101 to R121 are not a substituted or unsubstituted N-carbazolyl group. The structure represented by general formula (1) has at least one group represented by general formula (2). In general formula (2), at least one of X1-X5 is represented by a nitrogen atom.

The present application relates to fluorescent material technical field, especially based on benzopentacyclic / septacyclic structure's carbonyl nitrogen type fluorescent material and its preparation method, the present application provides the preparation method with carbazole as raw material, in the synthesis process, the aldehyde group precursor is directly oxidized to acid by using strong oxidant, then the intermediate is made to occur intramolecular Friedel-Crafts reaction by acid catalyst, finally the carbonyl / nitrogen type fluorescent material of inlaid non-benzene structure is synthesized.This structure inhibits molecular relaxation through multiple resonance effect, and then realizes narrow band emission characteristics.At the same time, the structure retains higher photoluminescence quantum yield.The carbonyl nitrogen type fluorescent material based on benzopentacyclic / septacyclic structure provided by the present application is different from the existing all benzene type polycyclic aromatic hydrocarbons, so as to effectively widen the molecular system of carbonyl / nitrogen type narrow band light emitting material.

The application discloses a pinacine alkyl tetrahydrocarbazole fluorescent probe capable of detecting cell lysosome polarity and a preparation method and application thereof. 9-(3-(dimethylamino)propyl)-3,3-dimethyl-2,3,4,9-tetrahydro-1H-2,4-bridged methylene carbazole-6-formaldehyde is used as raw material, and condensation reaction is carried out with 1,3-indan dione to obtain compound 2-(2-(9-(3-(dimethylamino)propyl)-3,3-dimethyl-2,3,4,9-tetrahydro-1H-2,4-bridged methylene carbazole-6-yl)vinyl)-1-indene-1,3(2H)-dione (TC-AP-ID), and the probe can specifically detect the polarity of cell lysosomes. In a mixed system of 1,4-dioxane and water, with the increase of the polarity of the system, the fluorescence color of the probe gradually changes from orange to red, and the fluorescence intensity significantly decreases. The probe has the advantages of simple synthesis, good selectivity, high sensitivity, good biocompatibility, low toxicity and the like, can be applied to targeted detection of the polarity of cell lysosomes, and has a good application prospect.

The invention discloses a photostimulation response material which is characterized in that a < 7 > H-benzo [c] carbazole group or a < 7 > H-dibenzo [c, g] carbazole group is connected to the site 2 of 9-thioxanthone to construct a thioxanthone derivative, and the thioxanthone derivative is doped in a polymethyl methacrylate matrix to form a composite film, so that the photostimulation response material has a remarkable photostimulation response characteristic; the light color of the film is changed after the film is subjected to ultraviolet radiation for 10 seconds, afterglow emission of s level appears, and the film can be applied to the technical field of information encryption and security anti-counterfeiting.

The application discloses a blue fluorescent molecule, which has a D-pi-A structure, contains an oxadiazole as an acceptor group and a phenyl carbazole as a donor group, and connects the acceptor group and the donor group with an aromatic ring having a thermal excitation energy level arrangement characteristic as a pi bridge. The application also provides a preparation method and application of the blue fluorescent molecule. The application uses the aromatic ring having the thermal excitation energy level arrangement characteristic as the pi bridge, reasonably regulates a high-energy excited state of the acceptor by introducing the donor, activates a thermal excitation channel of the molecule, breaks through a limitation of 25% of an excitation utilization rate of a fluorescent material, and thus improves the excitation utilization rate.

The invention relates to the technical field of solar cells, in particular to a self-assembled monomolecular hole transport material, a preparation method and application thereof, a perovskite solar cell, a preparation method thereof and a photovoltaic module. The self-assembled monomolecular hole transport material provided by the invention has a structure as shown in a formula I. In the formula I, A1, A2 and A3 are respectively and independently anchor groups or hydrogen atoms; the anchoring groups are independently selected from phosphate groups respectively; g is selected from a substituted or unsubstituted carbazolyl group, a substituted or unsubstituted acridinyl group, a substituted or unsubstituted phenothiazinyl group, and a substituted or unsubstituted phenoxazinyl group. The self-assembled monomolecular hole transport material provided by the invention has stronger anchoring binding capacity, conjugation in molecules is enhanced through the aromatic connection unit, and transport of carriers is facilitated; polyphosphonic acid anchoring in the self-assembled monomolecular hole transport material provided by the invention can enhance adsorption and uniformity of molecules, and a formed hole transport interface has better charge transport and defect passivation effects.

The invention belongs to the technical field of sodium-ion batteries, and particularly relates to an iron-manganese-based sodium-ion battery positive electrode material as well as a preparation method and application thereof. The preparation method of the iron-manganese-based sodium ion battery positive electrode material comprises the following steps: adding ferric nitrate and manganese nitrate into water for dissolving, performing spray pyrolysis to obtain an iron-manganese oxide precursor, performing ball-milling mixing on sodium carbonate, the iron-manganese oxide precursor and lanthanum telluride, and calcining in an inert gas atmosphere to obtain a composite material; and adding Ni4O4 cubic alkane modified carbazole, the composite material and manganese dioxide into dilute sulphuric acid for ultrasonic dispersion, stirring for reaction, centrifuging, washing and drying to obtain the iron-manganese-based sodium ion positive electrode material. The iron-manganese-based sodium ion battery positive electrode material provided by the invention has the advantages of stable rate cycle, high specific capacity and excellent capacity retention rate.

The invention belongs to the technical field of carboxylic ester preparation, and particularly relates to a preparation method of dioctyl terephthalate, which comprises the following steps: under the catalysis of acid, modifying mesoporous silica by using OTES and a carbazole silane solution to obtain modified silica; under the protection of inert atmosphere, uniformly mixing TBT and methylbenzene, adding absolute ethyl alcohol for reaction, adding modified silicon dioxide for dispersion, adding water-containing mixed liquid for reaction, and aging, filtering, washing and drying to obtain the titanium-based catalyst. The preparation method comprises the following steps: uniformly mixing PTA, 2-ethylhexanol and a titanium-based catalyst, carrying out heating reaction, filtering, and carrying out reduced pressure distillation to obtain the dioctyl terephthalate. The method can inhibit hydrolysis failure of a titanium active center in the catalytic esterification reaction process, and improves the yield and purity of dioctyl terephthalate.

This invention relates to a method for preparing and applying polyamides from a monomer containing 7-methyldibenzo[c,g]carbazole and triphenylamine: 4-({9-[(4-aminophenyl)(4-methoxyphenyl)amino]-7-methyldibenzo[c,g]carbazole-5-yl}(4-methoxyphenyl)amino)aniline. To address the problems of low solubility, difficulty in film formation, poor cycling stability, narrow color change range, and limited functionality in polyamide materials, this invention constructs two triphenylamine groups on 7-methyldibenzo[c,g]carbazole and introduces a methoxy group onto the triphenylamine to increase the polymer's solubility and stability. The polymer of this invention exhibits excellent electrochromic properties, including excellent cycling stability, fast switching time, and high optical contrast. Furthermore, to address the material's multifunctionality, a naphthalene unit is added to the molecular structure, resulting in a polymer with fluorescent emission. This invention can be applied to displays, rearview mirrors, camouflage applications, and the fluorescence detection of p-trinitrophenol.

Provided is a blue light emitting organic EL device having high emission efficiency and a long lifetime. This organic EL device includes one or more light emitting layers between an anode and a cathode opposite to each other, wherein at least one of the light emitting layers includes a first host selected from indolocarbazole compounds, a second host selected from the compounds represented by the following general formula (2), and, as a light emitting dopant, a polycyclic aromatic compound represented by the following general formula (3) or a polycyclic aromatic compound represented by the general formula (3) as a substructure, wherein Y4 is B, P, P═O, P═S, Al, Ga, As, Si—R4 or Ge—R5, and X4 is O, N—Ar4, S or Se.

The invention discloses a TADF luminescent material and a preparation method thereof, and relates to the technical field of organic optoelectronics, the molecular structure of the material comprises a phenyl triazine derivative electron-deficient core as an electron acceptor and a carbazole or tert-butyl carbazole electron-rich group as an electron donor; an aggregation-induced emission mechanism is introduced into the thermally activated delayed fluorescence material, so that the aggregation-induced quenching problem of a traditional thermally activated delayed fluorescence material and the exciton annihilation effect under high brightness are effectively solved, and meanwhile, the defect that a traditional aggregation-induced emission molecule is low in electroluminescence efficiency is overcome; the material can be used for preparing a non-doped organic electroluminescent device, the process is simplified, the cost is reduced, and the material has application potential in the field of intelligent response materials.