474 results about "Cyclopentadiene" patented technology

The invention provides a preparation method and application of an asymmetric dicyclopentadienyl dialkoxy zirconium compound, and the preparation method comprises the following steps: (1) mixing a solvent with ZrCl4 and sodium cyclopentadienyl CpNa, and carrying out a reaction to obtain CpZrCl3; (2) the CpZrCl3 obtained in the step (1) and R1 substituted sodium cyclopentadienyl R1CpNa are subjected to a mixed reaction, and (R1Cp) CpZrCl2 is obtained; and (3) mixing the (R1Cp) CpZrCl2 obtained in the step (2) with alkoxy sodium salt R2Na, and carrying out a reaction so as to obtain the asymmetric dicyclopentadiene dialkoxy zirconium compound. According to the method, the substitution reaction of three sodium salts is used for replacing the ligand replacement reaction in the prior art, so that the reaction steps are shortened, the use of unnecessary raw materials is avoided, the production cost is reduced, and the obtained target product is high in yield and high in purity.

The invention discloses a carbon fiber modified sizing agent as well as a preparation method and application thereof. The preparation method of the carbon fiber modified sizing agent comprises the following steps: (1) reacting 5-norbornene-2-methylamine with monofunctional epoxy resin to obtain slurry; and (2) dissolving the slurry prepared in the step (1) in an organic solvent to prepare the modified sizing agent. And then obtaining the modified carbon fiber through a dipping and sizing process. The method is simple in process, and the interface bonding strength of the carbon fibers and the polydicyclopentadiene can be greatly improved.

The invention provides dicyclopentadiene phenol resin and a preparation method thereof, dicyclopentadiene phenol epoxy resin and a preparation method and application thereof. Compared with common dicyclopentadiene phenol resin, the dicyclopentadiene phenol resin has unsaturated cycloolefin active functional groups at the tail ends of molecular chains, so that the reactivity of the resin can be improved, and the application field of the dicyclopentadiene phenol resin is expanded.

The invention discloses a dicarbonyl cyclopentadienyl cobalt complex as well as a preparation method and application thereof, and belongs to the technical field of organic metal synthesis. The preparation method of the dicarbonyl cyclopentadienyl cobalt complex specifically comprises the following steps: (1) dissolving cobalt octacarbonyl in carbon monoxide pre-saturated dichloromethane, and continuously introducing carbon monoxide gas for protection to obtain a reaction system; (2) dissolving cyclopentadiene in dichloromethane, and continuously introducing carbon monoxide gas for protection to obtain a cyclopentadiene solution; (3) adding a cyclopentadiene solution into the reaction system, heating and stirring for reaction; and (4) carrying out pressurized distillation and rectification on the reaction system. According to the invention, the carbon monoxide protective gas is introduced and the cyclopentadiene solution is prepared in the whole process to reduce the decomposition of the raw materials and reduce the generation of byproducts, so that the subsequent purification difficulty is reduced, and the reaction yield and the economic benefit of the product are improved.

The invention discloses a packaging material as well as a preparation method and application thereof. The packaging material comprises the following components in parts by mass: 40-85 parts of matrix resin, 5-30 parts of phase change PCM particles, 3-20 parts of self-repairing microcapsules, 1-8 parts of an interface compatilizer and 10-20 parts of a heat-conducting network reinforcing material, the melting point of the phase change PCM particles is not more than 80 DEG C; a core layer of the self-repairing microcapsule comprises dicyclopentadiene and a ruthenium catalyst, and a shell layer of the self-repairing microcapsule comprises polyurea or polyurethane; the PCBA packaging material with the intelligent response function is formed by combining the low-melting-point phase-change PCM particles with the self-repairing microcapsule system, when the PCBA temperature is too high, the low-melting-point phase-change PCM particles are molten, junction temperature suddenly rising is restrained through melting heat absorption, meanwhile, the adjacent microcapsules are triggered to be broken through volume expansion, DCPD monomers are released and subjected to in-situ polymerization under the action of a catalyst, and the PCBA packaging material with the intelligent response function is obtained. Microcracks generated by thermal stress are rapidly repaired, and the heat dissipation stability and the electrical insulation reliability of the material in long-term thermal circulation are remarkably improved.

The present invention provides a method for manufacturing an adhesive member, comprising the steps of applying an ultraviolet-curable silicone composition containing (A) an organopolysiloxane containing an unsaturated group, (B) an organohydrogenpolysiloxane, and (C) an ultraviolet-activated hydrosilylated platinum catalyst having a cyclopentadienyl group to which a condensed aromatic hydrocarbon group is bonded as a ligand, to a first substrate layer, and including in any order: (i) bonding the first substrate layer to which the ultraviolet-curable silicone composition has been applied to a second substrate layer via a layer of ultraviolet-curable silicone composition; (ii) depressurizing the ultraviolet-curable silicone composition applied to the first substrate layer under a pressure below atmospheric pressure; and (iii) irradiating the ultraviolet-curable silicone composition applied to the first substrate layer with ultraviolet light. The invention also provides an adhesive made of a silicone composition with excellent curability, and an adhesive member with high adhesiveness and high reliability as a component.

A method of rapidly forming an elastomer with tunable properties is described herein. The method includes preparing a monomer solution comprising a catalyst and one or more monomers including 1,5-cyclooctadiene (COD). The one or more monomers may further include dicyclopentadiene (DCPD), and each of the COD and the DCPD may be present in the monomer solution at a predetermined volume percentage. A region of the monomer solution is activated to initiate an exothermic polymerization reaction and generate a self-propagating polymerization front, which moves through the monomer solution and polymerizes the one or more monomers. Thus, an elastomer having predetermined properties is rapidly formed.

The invention relates to the technical field of electronic materials, in particular to a copper-clad plate resin composition with an ultralow-loss medium and a preparation method of the copper-clad plate resin composition. The composition comprises the following components: modified polyphenyl ether, dicyclopentadiene epoxy resin, trifunctional epoxy resin, active ester, cyanate ester, DMAP, spherical silicon dioxide and a POSS-silicon dioxide compound, the preparation method comprises the following steps: carrying out surface norbornenylation modification on bimodal spherical silicon dioxide, and carrying out click reaction on the bimodal spherical silicon dioxide and octa-aminophenyl polysilsesquioxane with tetrazinyl at the tail end to prepare a POSS-silicon dioxide compound, so as to construct an interface transition layer with gradient modulus. According to the invention, collaborative optimization of dielectric loss, thermal mechanical properties and interface bonding strength is realized, and the material has excellent properties of low dielectric loss, high thermal stability, high peel strength and the like, and is suitable for the fields of 5G communication, high-frequency electronic equipment and the like.

According to the modified water-based alkyd resin based on dicyclopentadiene and the preparation method of the modified water-based alkyd resin, the water-based alkyd resin is modified by combining diacrylic acid, cyclopentadiene modification and tung oil, and the rigidity of cyclopentadiene modification and the flexibility of tung oil achieve the modification effect of combining rigidity and softness; the problems of poor storage stability, low paint film hardness and insufficient water resistance of traditional water-based alkyd resin are successfully solved, the storage period of the water-based alkyd resin water-based paint is greatly prolonged, the formed paint film is high in drying speed and high in hardness and has good adhesive force, impact resistance, weather resistance and corrosion resistance, the production process is stable and controllable, and the production cost is low. Wide application prospects and economic values are realized.

The application belongs to the technical field of organic compound synthesis and the field of polymer preparation, and discloses a method for directly preparing a cycloolefin copolymer from dicyclopentadiene and ethylene based on a continuous flow reactor; the continuous flow reactor is used to efficiently prepare norbornene and derivatives thereof from ethylene and dicyclopentadiene, and then the norbornene and derivatives thereof are used to prepare a cycloolefin copolymer from excessive ethylene. The application uses dicyclopentadiene and ethylene as raw materials, realizes a continuous process from the synthesis of a cycloolefin monomer to the preparation of a cycloolefin copolymer, and the cycloolefin monomer does not need to be separated and stored and can directly participate in the polymerization reaction, so that the original complicated process is effectively simplified, energy consumption is reduced, the catalyst in the polymerization stage is not easy to be deactivated even at high temperature, the catalytic efficiency is high, and a high polymer yield can be obtained in a very short time.

The invention discloses a water-soluble near-infrared two-region aggregation-induced emission material and a preparation method and application thereof, and belongs to the technical field of aggregation-induced emission materials.Benzobithiadiazole is used as an electron acceptor group, dithieno-cyclopentadiene and derivatives thereof are used as electron donor units, and benzobithiadiazole and dithieno-cyclopentadiene and derivatives thereof are coupled to form the water-soluble near-infrared two-region aggregation-induced emission material. The organic near-infrared second-region molecule with the intramolecular charge transfer characteristic is constructed. According to the invention, the positively charged quaternary ammonium salt group is introduced into the electron donor group, and the positively charged quaternary ammonium salt group has good hydrophilicity, so that the water solubility of molecules can be effectively improved. Moreover, the water-soluble near-infrared two-region aggregation-induced emission material has excellent photodynamic and photothermal activity, and realizes efficient killing of bacteria (especially propionibacterium acnes) through the synergistic effect of photodynamic and photothermal effects.

The present application relates to the technical field of deep processing of petroleum chemical carbon five fraction oil, and particularly relates to a petroleum cracking carbon five fraction oil hydrofining method, wherein a polar competitive adsorbent is added into raw oil before the raw oil enters a main hydrogenation reaction, so that enrichment and deposition of cyclopentadiene (CPD) / dicyclopentadiene (DCPD) and chain double bond components in the catalyst are reduced; meanwhile, a low-acid hole-expanding Ni catalyst is used to reduce the polymerization deposition risk and maintain an effective hydrogenation rate, so that the problems of colloid deposition and pressure drop increase in the front section of the catalyst bed are relieved, and the problem that a Ni-based catalyst in the prior art cannot effectively inhibit the deposition of CPD components for a long time when hydrofining the CPD-containing carbon five fraction oil is solved.

To provide a tire which can improve total performance of anti-wear performance, snow grip performance, and wet grip performance.SOLUTION: A tire has a tread part, wherein the tread part is composed of a rubber composition containing a rubber component, silica, a resin component, and vegetable oil, the rubber component contains 20 mass% or more and 90 mass% or less of styrene-butadiene rubber, the rubber composition contains more than 50 pts.mass and 150 pts.mass or less of silica with respect to 100 pts.mass of the rubber component, the resin component contains at least one selected from the group consisting of a terpene-based resin, a C5C9-based resin, and a dicyclopentadiene-based resin, a glass transition temperature of the rubber composition is -30°C or lower, and when a thickness of a thickest part of the tread part is represented by t (mm), and a styrene content of the styrene butadiene rubber is represented by S (mass%), t×S is less than 300.SELECTED DRAWING: Figure 1

The application provides a polydicyclopentadiene / glass fiber felt composite material and a preparation method thereof. The method comprises the following steps: step (1): laying a glass fiber felt on a glass plate, sequentially laying a release cloth, a flow guide net and a vacuum bag, and performing vacuum pumping and pressure maintaining; step (2): pouring a cyclic olefin liquid into the vacuum bag in step (1), performing stage temperature rising and curing, and releasing a polydicyclopentadiene / glass fiber felt composite material. The cyclic olefin liquid is configured as follows: A1, uniformly mixing 100 parts by mass of DCPD and 5-20 parts by mass of a TCPD system to prepare a mixed solution; wherein the TCPD system comprises 10wt% of TCPD and 90wt% of DCPD; A2, dissolving 0.02-0.06 parts by mass of a Grubbs second-generation catalyst and 0.002-0.006 parts by mass of a retarder in 1-2 parts by mass of a high-boiling-point silane coupling agent, and adding the mixture into the mixed solution in step A1 to prepare a liquid. The method adopts a vacuum-assisted resin infusion molding (VARI) technology, has the characteristics of simple operation and rapid reaction, and the obtained composite material has high mechanical properties.

The invention relates to the field of photocuring adhesives, and mainly relates to a UV adhesive for wig connection and a preparation method thereof. The UV adhesive for wig connection is prepared from the following components in parts by weight: 30 to 50 parts of urethane acrylate, 45 to 70 parts of first reactive diluent, 2 to 4 parts of photoinitiator and 2 to 4 parts of fumed silica, the first active diluent is prepared from two or a mixture of more than two of acryloyl morphine, 2-acrylic acid-2-(2-phenoxy ethyoxyl) ethyl ester, dicyclopentadiene acrylate and ethylene glycol dicyclopentenyl ether methacrylate. The preparation method comprises the following steps: mixing the components, heating in a water bath, and stirring to obtain the UV adhesive for wig connection. The UV adhesive for wig connection provided by the invention is low in odor, good in durability and good in matte effect.

Catalyst systems comprising a metal-ligand complex having a structure according to Formula (I): Y and Z are independently a monodentate or bidentate ligand selected from the group consisting of (C1−C30)hydrocarbyl, (C1−C30)heterohydrocarbyl, (C6-C30)aryl, (C3-C30)heteroaryl, halogen and –H. R1, R2, R3, and R4 are independently selected from the group consisting of (C1−C30)hydrocarbyl, (C1−C30)heterohydrocarbyl, (C6-C30)aryl, (C3-C30)heteroaryl, −ORC, −Si(RC)3, −Ge(RC)3, halogen, and –H; R5, R6, R7, and R8 are independently selected from the group consisting of (C1−C30)hydrocarbyl, (C1−C30)heterohydrocarbyl, (C6-C30)aryl, (C3-C30)heteroaryl, −ORC, −Si(RC)3, −Ge(RC)3, halogen, and –H; R9 and R10 are independently selected from the group consisting of (C1−C30)hydrocarbyl, (C1−C30)heterohydrocarbyl, (C6-C30)aryl, (C3-C30)heteroaryl, −ORC, −Si(RC)3, −Ge(RC)3, halogen, and –H; and each RC is independently selected from the group consisting of (C1−C30)hydrocarbyl, (C1−C30)heterohydrocarbyl, (C6-C30)aryl, (C3-C30)heteroaryl, and –H.

The invention provides an anti-interference control method for the concentration of a main reactant in a continuous stirring reaction kettle process, belongs to the technical field of chemical process control, and solves the problem that in the chemical process of producing cyclopentanol by catalyzing electrophilic water with cyclopentadienoic acid, the concentration of the main reactant is not influenced. The technical problem that the concentration of a main reactant is difficult to track a set value without steady-state errors under the conditions of fluctuation of feeding concentration, uncertainty and external disturbance of the continuous stirring reaction kettle is solved. According to the technical scheme, the method comprises the steps of constructing a model pre-estimation compensator and an anti-interference control structure, designing a four-dimensional decision model, carrying out parameter collaborative optimization by adopting a multi-target genetic optimization algorithm, and carrying out optimal solution selection based on a TOPSIS method. Under the condition of feed concentration fluctuation, the dynamic response speed and the anti-interference capability of the system can be remarkably improved, and faster adjustment time, smaller overshoot and stronger robustness can be realized in linear and nonlinear models.

The application relates to a weather-resistant color master batch for modified polypropylene cable protection pipes, which is composed of a carrier resin, a photo-thermal stable color powder, a filler and a grafting compatibility modifier; the photo-thermal stable color powder is composed of zinc dicyclopentadiene dimethylate, orange yellow, bright red, an antioxidant, an ultraviolet absorber and a dispersant; the dicyclopentadiene in the zinc dicyclopentadiene dimethylate has heat-reversible crosslinking properties, is disdimerized during heat processing, has good processing fluidity, is re-cyclized and addition-dimerized to be crosslinked after temperature reduction, so that the decomposition of the orange yellow and the bright red caused by cable heating is reduced; meanwhile, the antioxidant and the ultraviolet absorber have a compound synergistic effect, so that the weather resistance of the color master batch can be better improved; the modified polypropylene cable protection pipe prepared by using the color master batch has the advantages of color stability, reduced processing toxicity, good processing fluidity, low price and the like, and is more suitable for power cable protection pipe use.

Embodiments of the present disclosure are directed towards polyolefin compositions, useful for films, made with asymmetrical hafnium metallocenes having an n-propyl cyclopentadienyl ligand, processes utilizing the polyolefin compositions, and products made with the compositions.

The application belongs to the technical field of metal surface treatment, and particularly relates to a passivation agent for a conversion film of die-cast aluminum and aluminum alloy and a preparation method thereof, which comprises gamma-aminopropyl triethoxysilane, cyclopentadienyl dibutoxy titanium chloride, fatty alcohol polyoxyethylene ether sodium carboxylate, zirconium isooctoate, aluminum coupling agent AL-M and water. The passivation agent for the conversion film of the die-cast aluminum provided by the application does not contain strong acid, strong base and phosphorus components, is friendly to the environment, is safe to operate in production and use, has a simple operation process, does not have obvious corrosion or discoloration on a metal substrate, and can reach 120 hours in neutral salt spray.

The application relates to a preparation method of a crosslinked polymer and belongs to the technical field of polymer preparation. The preparation method of the crosslinked polymer provided by the application comprises the following steps: (1) mixing reactant A and reactant B to perform an esterification reaction to obtain an esterification product; (2) dissolving a crosslinking agent in the obtained esterification product and standing for solidification, so that the crosslinked polymer is obtained; the reactant A is a polyether polyol containing at least three hydroxyl groups; the reactant B is 4-(cyclopenta-2,4-dien-1-ylidene) pentanoic acid; and the crosslinking agent contains a maleimide group. The application constructs a fulvene-maleimide D-A reaction system capable of being rapidly crosslinked under low-temperature conditions by end-capping fulvene at the end of a polyether polyol and then adding a crosslinking agent with a maleimide group.

The invention relates to the field of polyacrylate photoresists, in particular to a photoresist film-forming resin raw material and a preparation method thereof.The preparation method comprises the steps that cyclopentadiene is dropwise added into a mixed solution of alpha-bromomethyl acrylate and a solvent, the temperature is controlled, a reaction is conducted for 4 h, and 5-bromodicyclohept-2-ene-5-carboxylic acid methyl ester is prepared; the preparation method comprises the following steps: adding alkali into 5-bromo dicycloheptyl-2-ene-5-carboxylic acid methyl ester, and hydrolyzing at 20-30 DEG C for 2 hours to obtain a hydrolysis product; the hydrolysis product is subjected to epoxidation and hydrolysis with hydrogen peroxide under the condition of glacial acetic acid, and 1-bromine-5-hydroxy-3-oxa-tricyclic nonyl-2-ketone is obtained; according to the method, 1-bromo-5-hydroxy-3-oxa-tricyclic nonyl-2-ketone is cyanided by cuprous cyanide to prepare the 1-cyano-5-hydroxy-3-oxa-tricyclic nonyl-2-ketone monomer, and the method has the advantages that the raw materials are convenient and easy to obtain, the route is short, the reaction conditions are relatively mild, the operation safety is relatively high, the total yield is remarkably improved, and the like.

The invention relates to a method for preparing (cyclopentadienyl) tris (dimethylamino) hafnium by using nuclear magnetic control, which comprises the following steps: S1, carrying out heating reflux reaction on hafnium tetrachloride, cyclopentadiene and dimethylamine in the presence of n-butyllithium and n-hexane, and after reacting for a certain time, taking supernate to detect a nuclear magnetic hydrogen spectrum; s2, calculating the ratio a of the integral area of the characteristic peak A to the integral area of the characteristic peak B according to the nuclear magnetic hydrogen spectrum, judging whether a is in a target range or not, if a is in the target range, terminating the reaction, separating a liquid phase, distilling and collecting a crude product; and if a value is greater than the maximum value of the target range, adding cyclopentadiene into the reaction system to continue the reaction, and if a value is less than the minimum value of the target range, continuing the reaction until the ratio of the integral area of the characteristic peak A to the integral area of the characteristic peak B in the nuclear magnetic hydrogen spectrum of the reaction supernatant is within the target range, terminating the reaction, separating the liquid phase, distilling and collecting a crude product. The method can effectively improve the safety of the production process, the raw material conversion rate and the product purity.

Processes of polymerizing olefin monomers and catalyst systems. The catalyst systems include a non-hydrogen-generating post-metallocene procatalyst; a co-catalyst; and a hydrogenation procatalyst having the formula Cp2TiXnTiCp2 or Cp2TiXn, in which each Cp is cyclopentadienyl substituted with at least one (C1-C10)alkyl; each X is independently monoanionic or neutral, wherein each X is independently (C1-C40)hydrocarbon, (C1-C40)heterohydrocarbon, (C1-C40)hydrocarbyl, (C1-C40)heterohydrocarbyl, or a halogen atom; and n is 1 or 2.

The invention discloses a HUSY molecular sieve pretreatment method, a HUSY catalyst, a hanging type tetrahydrodicyclopentadiene preparation process and hanging type tetrahydrodicyclopentadiene prepared by the hanging type tetrahydrodicyclopentadiene preparation process. The HUSY molecular sieve pretreatment method comprises the following steps: taking an acidified HUSY molecular sieve, putting into a heating reaction device, calcining, heating to 500 DEG C at a heating rate of 5 DEG C / min, maintaining the constant temperature of 500 DEG C, reacting for 5 hours, naturally cooling to 80 DEG C, and taking out. According to the method, the yield of exo-tetrahydrodicyclopentadiene is increased by improving the pretreatment conditions of the catalyst, the temperature required by the isomerization reaction and the dosage of the catalyst.

The invention relates to the technical field of engineering plastics, and discloses a polydicyclopentadiene / carbon fiber felt composite material and a preparation method and application thereof, and the preparation method comprises the following steps: dispersing nanoparticles and norbornene dicarboxylic acid in a methanol solution to prepare a dispersion liquid; immersing the carboxylated modified carbon fiber felt into the dispersion liquid to obtain a modified carbon fiber felt; and mixing dicyclopentadiene, ethylidene norbornene and a Grubbs second-generation catalyst, immersing the mixture into the modified carbon fiber felt, and carrying out hot-pressing curing molding to obtain the composite material. By constructing an HCFF-NPA-PDCPD covalent interface system, a synergistic modification strategy of a physical effect (NP increases the surface roughness and provides reaction sites) and chemical bonding (NDA serves as a bridge to connect fibers and a matrix) is realized; the production process of the obtained composite material has the characteristic of being green and environment-friendly, waste water, waste gas or dust emission is avoided, the energy consumption is relatively low, and the requirement of the modern industry for sustainable development is met.

Catalyst systems comprising a metal-ligand complex having a structure according to Formula (I): where M is a metal chosen from scandium or yttrium; X is chosen from silicon or germanium; L is a monodentate or bidentate ligand selected from the group consisting of (C1−C30) hydrocarbyl, (C1−C30) heterohydrocarbyl, (C6−C30)aryl, (C3−C30) heteroaryl, halogen and –H; and Z is a Lewis base. R1, R2, R3, and R4 are independently selected from the group consisting of (C1−C30) hydrocarbyl, (C1−C30) heterohydrocarbyl, (C6−C30)aryl, (C3−C30) heteroaryl, −ORC, −Si(RC)3, −Ge(RC)3, halogen, and –H; R5, R6, R7, and R8 are independently selected from the group consisting of (C1−C30) hydrocarbyl, (C1−C30) heterohydrocarbyl, (C6−C30)aryl, (C3−C30) heteroaryl, −ORC, −Si(RC)3, −Ge(RC)3, halogen, and –H; R9 and R10 are independently selected from the group consisting of (C1−C30)hydrocarbyl, (C1−C30) heterohydrocarbyl, (C6−C30)aryl, (C3−C30) heteroaryl, −ORC, −Si(RC)3, −Ge(RC)3, halogen, and –H; and each RC is independently selected from the group consisting of (C1−C30) hydrocarbyl, (C1−C30) heterohydrocarbyl, (C6−C30)aryl, (C3−C30) heteroaryl, and –H.

The present invention provides a photocurable thermosetting resin composition, a dry film, a cured product, and an electronic component. Namely, a photocurable thermosetting resin composition having excellent printability, a dry film having a resin layer formed of the resin composition, which is excellent in crack resistance and adhesion, a cured product formed of the resin composition, which is excellent in crack resistance and adhesion, and an electronic component are provided. The photocurable thermosetting resin composition comprises a carboxyl group-containing resin, a photopolymerization initiator, an epoxy resin comprising an epoxy resin containing a dicyclopentadiene skeleton, a stress relaxing agent, and an inorganic filler, the stress relaxing agent being any one or more of an elastomer having two or more Tgs apart by 50°C or more at 200°C and a rubber particle having a shell layer and a core layer, the content of the stress relaxing agent being 1 to 13% by weight of the solid content of the composition, the inorganic filler comprising talc, the content of the inorganic filler being 5 to 20% by weight of the solid content of the composition.

The invention discloses a synthesis method of halauxifen-methyl. The halauxifen-methyl is obtained by carrying out Suzuki coupling reaction on 4-amino-6-bromo-3-chloro-5-fluoropyridine carboxylic acid benzyl ester and 4-chloro-2-fluoro-3-methoxyphenylboronic acid, a catalytic system adopted by the Suzuki coupling reaction is a palladium catalyst, a phosphine ligand and a phase transfer catalyst; wherein the phosphine ligand is 4-(anthracene-9-yl)-3-(tert-butyl)-2, 3-dihydrobenzo [d] [1, 3] oxaphosphorus pentadiene, and the phosphine ligand is 4-(anthracene-9-yl)-3-(tert-butyl)-2, 3-dihydrobenzo [d] [1, 3] The molar use amount of the palladium catalyst is 0.1 to 0.5 mol percent of the molar use amount of the 4-amino-6-bromo-3-chloro-5-fluoropyridine benzyl formate. According to the invention, AntPhos is used as a phosphine ligand to form a catalytic system together with the palladium catalyst and the phase transfer catalyst, so that higher reaction yield and product purity can be obtained with very low dosage of the palladium catalyst, the synthesis cost of the halauxifen-methyl can be greatly reduced, the reaction condition is mild, the energy consumption is lower, and the method is suitable for industrial production.

The present disclosure relates to a composition comprising: (a) a cationic polymerization initiator; and (b) an indene based or cyclopentadiene based resin; wherein the cationic polymerization initiator is selected from the group consisting of (i) an aromatic sulfonium salt-based cationic polymerization initiator; (ii) a phosphonium salt-based cationic polymerization initiator; (iii) a quaternary ammonium salt-based cationic polymerization initiator; (iv) an aluminum complex-based cationic polymerization initiator; (v) an aromatic iodonium salt-based cationic polymerization initiator; (vi) an aromatic diazonium salt-based cationic polymerization initiator; (vii) a pyridinium-based cationic polymerization initiator and (viii) a mixture thereof. Also described are varnishes and coatings formed from said composition.