阅读说明：本技术 一种化合物、包含其的有机电子发光器件及其应用 (Compound, organic electronic light-emitting device comprising compound and application of compound ) 是由 黄金华 曾礼昌 于 2019-04-30 设计创作，主要内容包括：本发明提供一种化合物、包含该化合物的有机电子发光器件及其应用,所述化合物具有式I所示结构,在本发明中化合物结构中萘2-位同另外一个萘环相连,而1-位则同二芳胺基相连,使得本发明化合物具有大π平面结构,同时能有效改变分子空间结构,有利于改善膜内分子堆积,由于邻位取代限制了N原子上芳环的转动,从而增强了该类材料的稳定性,本发明的化合物可用作有机电致发光器件的空穴传输层材料或者电子阻挡层材料。使用本发明的化合物的有机电致发光器件亮度达到5000cd/m<Sup>2</Sup>时,驱动电压低至3.8V以下,电流效率高达12.7cd/A以上,LT95达到165h以上。(The invention provides a compound, an organic electronic luminescent device containing the compound and application thereof, wherein the compound has a structure shown in formula I, in the structure of the compound, a naphthalene 2-position is connected with another naphthalene ring, and a naphthalene 1-position is connected with the other naphthalene ringThe diarylamine groups are connected, so that the compound has a large pi plane structure, the molecular space structure can be effectively changed, the improvement of intra-film molecular accumulation is facilitated, the rotation of an aromatic ring on an N atom is limited by ortho-position substitution, and the stability of the material is enhanced. The organic electroluminescent device using the compound of the invention has a luminance of 5000cd/m 2 When the voltage is low, the driving voltage is below 3.8V, the current efficiency is higher than 12.7cd/A, and LT95 is higher than 165 h.)

1. A compound having the structure shown in formula I:

wherein L is¹And L²The same or different, each independently is a single bond, C₆-C₅₀Substituted or unsubstituted arylene of, C₃-C₃₀Substituted or unsubstituted heteroarylene of (a);

Ar¹and Ar²Same or different, each independently H, C ₆-C₅₀Substituted or unsubstituted aryl of (1), C₆-C₅₀Substituted or unsubstituted fused aryl, C₃-C₃₀Substituted or unsubstituted heteroaryl, C₃-C₃₀Substituted or unsubstituted fused heteroaryl of (a);

and Ar¹When it is H, L¹Is not a single bond; ar (Ar)²When it is H, L²Is not a single bond;

R¹and R²Identical or different, each independently H, halogen, C₁-C₂₀Alkyl of (C)₁-C₁₂Alkoxy group of (C)₃-C₂₀Cycloalkyl of, C₂-C₁₂Alkenyl of, C₂-C₁₂Alkynyl, carbonyl, carboxyl, cyano, amino, C₆-C₅₀Substituted or unsubstituted aryl of (1), C₃-C₃₀Substituted or unsubstituted heteroaryl of (A), C₆-C₅₀A fused aryl group of (a), and R¹And R²Is connected to the naphthalene ring in a single bond mode;

m is an integer of 0 to 6, n is an integer of 0 to 7;

when the above groups have substituents, the substituents are respectively and independently selected from halogen and C₁-C₁₀Alkyl of (C)₃-C₁₀Cycloalkyl of, C₂-C₁₀Alkenyl radical, C₁-C₆Alkoxy group of (C)₁-C₆Thioalkoxy, carbonyl, carboxyl, cyano, amino, C₆-C₃₀Monocyclic aromatic hydrocarbon or condensed ring aromatic hydrocarbon group of (A), C₃-C₃₀One or more of the monocyclic or fused ring heteroaromatic groups of (a).

2. The compound of claim 1, wherein Ar is Ar¹And Ar²Each independently selected from C₆-C₃₀Aryl of (C)₆-C₃₀Condensed aryl of, C₃-C₃₀Heteroaryl of (A), C₃-C₃₀A fused heteroaryl group of (a); l is ¹And L²Independently selected from single bonds; r¹And R²Independently selected from hydrogen.

3. The compound of claim 2, wherein Ar is Ar¹And Ar²Is independently selected from

Wherein

4. The compound of claim 1, wherein the compound has a structure according to formula II or formula III:

wherein L is¹、L²、Ar¹、Ar²、R¹、R²M and n are as defined in claim 1.

5. The compound of claim 1, wherein the compound of formula (I)

6. An organic electroluminescent device comprising a first electrode, a second electrode and an organic layer interposed between the first electrode and the second electrode, wherein the organic layer comprises the compound according to any one of claims 1 to 5.

7. The organic electroluminescent device according to claim 6, wherein the organic layer comprises a hole transport region comprising the compound according to any one of claims 1 to 5.

8. The organic electroluminescent device according to claim 7, wherein the hole transport region comprises a hole transport layer and/or an electron blocking layer, wherein at least one of the hole transport layer and the electron blocking layer comprises the compound according to any one of claims 1 to 5.

9. Use of a compound according to any one of claims 1 to 5 as a hole transport layer and/or an electron blocking layer in an organic electronic light emitting device.

Technical Field

The invention relates to the field of organic light-emitting compounds and organic electronic light-emitting devices, in particular to a compound, an organic electronic light-emitting device containing the compound and application of the compound.

Background

Organic Light Emission Diodes (OLED) devices are a kind of devices with sandwich-like structure, which includes positive and negative electrode films and Organic functional material layers sandwiched between the electrode films. And applying voltage to the electrodes of the OLED device, injecting positive charges from the positive electrode and injecting negative charges from the negative electrode, and transferring the positive charges and the negative charges in the organic layer under the action of an electric field to meet for composite luminescence. Because the OLED device has the advantages of high brightness, fast response, wide viewing angle, simple process, flexibility and the like, the OLED device is concerned in the field of novel display technology and novel illumination technology. At present, the technology is widely applied to display panels of products such as novel lighting lamps, smart phones and tablet computers, and further expands the application field of large-size display products such as televisions, and is a novel display technology with fast development and high technical requirements.

With the continuous advance of OLEDs in both lighting and display areas, much attention has been paid to the research on their core materials. This is because an efficient, long-lived OLED device is generally the result of an optimized configuration of the device structure and various organic materials, which provides great opportunities and challenges for chemists to design and develop functional materials with various structures. Common functionalized organic materials are: hole injection materials, hole transport materials, hole blocking materials, electron injection materials, electron transport materials, electron blocking materials, and light emitting host materials and light emitting objects (dyes), and the like.

In order to prepare an OLED light-emitting device with lower driving voltage, better light-emitting efficiency and longer service life, the performance of the OLED device is continuously improved, the structure and the manufacturing process of the OLED device need to be innovated, and photoelectric functional materials in the OLED device need to be continuously researched and innovated, so that functional materials with higher performance can be prepared. Based on this, the OLED material industry has been working on developing new organic electroluminescent materials to achieve low starting voltage, high luminous efficiency and better lifetime of the device.

So far, the development of the existing OLED photoelectric functional material is far behind the requirements of panel manufacturing enterprises on the OLED material, so it is very urgent to develop an organic functional material with better performance to meet the development requirements of the current industry.

The application of the compound with the binaphthyl structure in the OLED is explored, and a material capable of improving the performance of the device is expected to be found. Korean patent application KR1020140096227A discloses a binaphthyl compound containing diarylamine, which has the following general formula:

the invention patents (applications) of US9178001B2, US8829783B2, KR1020160080420A, CN108084091A and the like also disclose several organic electroluminescent materials containing binaphthyl structure.

However, the performance requirements of OLED devices still cannot be met by these compounds. As described above, the conventional organic electroluminescent materials have room for improvement in light-emitting properties, and development of new organic electroluminescent materials is urgently required.

Disclosure of Invention

In view of the defects of the prior art, the invention aims to provide a novel compound, an organic electronic light-emitting device containing the compound and application thereof, and an OLED device based on the compound has low starting voltage, high light-emitting efficiency and better service life and can meet the requirements of panel manufacturing enterprises on high-performance materials at present.

In order to achieve the purpose, the invention adopts the following technical scheme:

in one aspect, the present invention provides a compound having the structure shown in formula I below:

wherein L is¹And L²The same or different, each independently is a single bond, C₆-C₅₀Substituted or unsubstituted arylene of, C₃-C₃₀Substituted or unsubstituted heteroarylene of (a);

Ar¹and Ar²Same or different, each independently H, C₆-C₅₀Substituted or unsubstituted aryl, C₆-C₅₀Substituted or unsubstituted fused aryl, C₃-C₃₀Substituted or unsubstituted heteroaryl, C₃-C₃₀Substituted or unsubstituted fused heteroaryl;

And Ar¹When it is H, L¹Is not a single bond; ar (Ar)²When it is H, L²Is not a single bond;

R¹and R²Identical or different, each independently H, halogen, C₁-C₂₀Alkyl of (C)₁-C₁₂Alkoxy group of (C)₃-C₂₀Cycloalkyl of, C₂-C₁₂Alkenyl of, C₂-C₁₂Alkynyl, carbonyl, carboxyl, cyano, amino, C₆-C₅₀Substituted or unsubstituted aryl of (1), C₃-C₃₀Substituted or unsubstituted heteroaryl of (A), C₆-C₅₀A fused aryl group of (a), and R¹And R²A single bond rather than a fused bond to the naphthalene ring;

m is an integer of 0 to 6, n is an integer of 0 to 7;

when the above groups have substituents, the substituents are respectively and independently selected from halogen and C₁-C₁₀Alkyl of (C)₃-C₁₀Cycloalkyl of, C₂-C₁₀Alkenyl radical, C₁-C₆Alkoxy group of (C)₁-C₆Thioalkoxy, carbonyl, carboxyl, cyano, amino, C₆-C₃₀Monocyclic aromatic hydrocarbon or condensed ring aromatic hydrocarbon group of (A), C₃-C₃₀One or more of the monocyclic or fused ring heteroaromatic groups of (a).

In the invention, when the compound is used as an electron blocking layer in a hole transport layer of an organic electroluminescent device, compared with the prior art, the driving voltage can be further reduced, the luminous efficiency can be improved, and the service life can be prolonged.

In the compounds of the invention, the 2-position of the naphthalene is linked to another naphthalene ring and the 1-position is linked to a diarylamine group, and the other substituents on the two naphthalene rings are not amine or arylamine substituents, i.e. R ¹And R²And is not an amine or arylamine substituent.

In the present invention, said C₆-C₅₀Substituted or unsubstituted arylene of and C₆-C₅₀C in substituted or unsubstituted aryl₆-C₅₀Represents the number of carbon atoms in the group and can be, for example, 6, 8, 10, 15, 18, 20, 23, 25, 30, 33, 35, 38, 40, 45, 50 carbon atoms; in the same way, C₃-C₃₀Substituted or unsubstituted heteroarylene of (1) and C₃-C₃₀The number of carbon atoms in the substituted or unsubstituted heteroaryl group can be 3, 5, 8, 10, 12, 15, 18, 20, 23, 25, 28, or 30; c₁-C₂₀The number of carbon atoms in the alkyl group of (a) may be 1, 3, 5, 8, 10, 12, 15, 18 or 20, and as such other limitation of the range of carbon atoms indicates that the number of carbon atoms in the group may take any integer within the recited range of values.

In the present invention, said m may be 0, 1, 2, 3, 4, 5 or 6; the n may be 0, 1, 2, 3, 4, 5, 6 or 7.

In the structure represented by formula I, the expression "connecting bond" - "crossing a ring structure of a substituent means that the connecting site is located at an arbitrary position on the ring structure where the bond can be formed.

Preferably, said L¹And L²Is a single bond.

Preferably, R¹And R²Selected from hydrogen.

Preferably, Ar is¹And Ar ²Independently selected from C₆-C₃₀Aryl of (C)₆-C₃₀Condensed aryl of, C₃-C₃₀Heteroaryl of (A), C₃-C₃₀The fused heteroaryl group of (1).

Preferably, Ar is¹And Ar²Is independently selected from

WhereinRepresents the access position of the group. Preferably, the compound has a structure as shown in formula II or formula III:

wherein L is¹、L²、Ar¹、Ar²、R¹、R²M and n are as defined for formula I.

Preferably, the compound is any one of the following compounds P1-P356:

in the present invention, the compound is any one of P1 to P356, but is not limited to these exemplary compounds.

In the present invention, a method for synthesizing the compound is briefly described, and a representative synthetic route of the compound is as follows:

based on the synthetic route and thought of the above compounds, the skilled person can obtain the substituent Ar¹、Ar²、R¹And R²A compound of formula I.

In another aspect, the present invention provides the use of a compound as described above as a hole transport material or an electron blocking material in an organic electroluminescent device.

In another aspect, the present invention provides an organic electroluminescent device comprising a first electrode, a second electrode and one or more organic layers interposed between the first electrode and the second electrode, wherein the organic layers comprise a compound as described above.

In the present invention, the one or more layers mean at least one layer.

Preferably, the organic layer between the first electrode and the second electrode includes at least a light emitting layer.

Preferably, the organic layer comprises a hole transport region comprising a compound as described above.

Preferably, the hole transport region comprises a hole transport layer and/or an electron blocking layer, wherein at least one of the hole transport layer and the electron blocking layer comprises a compound as described above.

In the present invention, the organic layer containing the compound of the present invention can be used as, but not limited to, a hole transport layer and an electron blocking layer.

The compound of the present invention can be applied to organic electronic devices, for example, organic electroluminescent devices, lighting devices, organic thin-film transistors, organic field-effect transistors, organic thin-film solar cells, large-area sensors such as information labels, electronic artificial skin sheets and sheet scanners, electronic paper, organic EL panels, and the like.

Next, the organic electroluminescent device will be explained in detail.

The organic electroluminescent device includes first and second electrodes, and an organic material layer between the electrodes. The organic material layer may be divided into a plurality of regions. For example, the organic material layer may include a hole transport region, a light emitting layer, and an electron transport region.

In a specific embodiment, a substrate may be used below the first electrode or above the second electrode. The substrate is a glass or polymer material having excellent mechanical strength, thermal stability, water resistance, and transparency. In addition, a Thin Film Transistor (TFT) may be provided on a substrate for a display.

The first electrode may be formed by sputtering or depositing a material used as the first electrode on the substrate. When the first electrode is used as an anode, an oxide transparent conductive material such as Indium Tin Oxide (ITO), Indium Zinc Oxide (IZO), tin dioxide (SnO2), zinc oxide (ZnO), or any combination thereof may be used. When the first electrode is used as a cathode, a metal or an alloy such as magnesium (Mg), silver (Ag), aluminum (Al), aluminum-lithium (Al-Li), calcium (Ca), magnesium-indium (Mg-In), magnesium-silver (Mg-Ag), or any combination thereof can be used.

The organic material layer may be formed on the electrode by vacuum thermal evaporation, spin coating, printing, or the like. The compound used as the organic material layer may be an organic small molecule, an organic large molecule, and a polymer, and a combination thereof.

The hole transport region is located between the anode and the light emitting layer. The hole transport region may be a Hole Transport Layer (HTL) of a single layer structure including a single layer containing only one compound and a single layer containing a plurality of compounds. The hole transport region may also be a multilayer structure including at least one of a Hole Injection Layer (HIL), a Hole Transport Layer (HTL), and an Electron Blocking Layer (EBL).

A hole transport region, wherein when the hole transport layer of the hole transport region is selected from one or any combination of the above-mentioned compounds, the electron blocking layer of the hole transport region may be absent, or may be present and selected from, but not limited to, phthalocyanine derivatives such as CuPc, conductive polymers or polymers containing conductive dopants such as polyphenylenevinylene, polyaniline/dodecylbenzenesulfonic acid (Pani/DBSA), poly (3, 4-ethylenedioxythiophene)/poly (4-styrenesulfonate) (PEDOT/PSS), polyaniline/camphorsulfonic acid (Pani/CSA), polyaniline/poly (4-styrenesulfonate) (Pani/PSS), aromatic amine derivatives such as compounds represented by HT-1 to HT-34 below; or any combination thereof; when the hole transport layer of the hole transport region is selected from, but not limited to, phthalocyanine derivatives such as CuPc, conductive polymers or polymers containing conductive dopants such as polyphenylenevinylene, polyaniline/dodecylbenzenesulfonic acid (Pani/DBSA), poly (3, 4-ethylenedioxythiophene)/poly (4-styrenesulfonate) (PEDOT/PSS), polyaniline/camphorsulfonic acid (Pani/CSA), polyaniline/poly (4-styrenesulfonate) (Pani/PSS), aromatic amine derivatives such as the compounds shown below as HT-1 to HT-34, or any combination thereof; the electron blocking layer of the hole transport region is selected from one or any combination of the compounds described above.

The materials for the hole transport region and the hole injection region may be selected from, but not limited to, the compounds of the present invention and the above-mentioned compounds; or any combination thereof. The hole injection layer may be a single compound material or a combination of a plurality of compounds. For example, the hole injection layer may employ one or more of the compounds of the present invention described above, or employ one or more of the compounds of HI1-HI3 described below; one or more of the compounds may also be used to dope one or more of the compounds described below as HI1-HI 3.

The light-emitting layer includes a light-emitting dye (i.e., dopant) that can emit different wavelength spectra, and may also include a Host material (Host). The light emitting layer may be a single color light emitting layer emitting a single color of red, green, blue, or the like. The single color light emitting layers of a plurality of different colors may be arranged in a planar manner in accordance with a pixel pattern, or may be stacked to form a color light emitting layer. When the light emitting layers of different colors are stacked together, they may be spaced apart from each other or may be connected to each other. The light-emitting layer may be a single color light-emitting layer capable of emitting red, green, blue, or the like at the same time.

According to different technologies, the luminescent layer material can be different materials such as fluorescent electroluminescent material, phosphorescent electroluminescent material, thermal activation delayed fluorescent luminescent material, and the like. In an OLED device, a single light emitting technology may be used, or a combination of a plurality of different light emitting technologies may be used. These technically classified different luminescent materials may emit light of the same color or of different colors.

In one aspect of the invention, the light-emitting layer employs phosphorescent electroluminescent technology. The host material of the light emitting layer is selected from, but not limited to, one or more of GPH-1 to GPH-80.

In one aspect of the invention, the light-emitting layer employs phosphorescent electroluminescent technology. The phosphorescent dopant of the light emitting layer can be selected from, but is not limited to, one or more of GPD-1 to GPD-47 listed below.

Wherein D is deuterium.

In one aspect of the invention, the light-emitting layer employs phosphorescent electroluminescent technology. The phosphorescent dopant of the light emitting layer thereof may be selected from, but not limited to, a combination of one or more of RPD-1 to RPD-28 listed below.

In one aspect of the invention, the light-emitting layer employs phosphorescent electroluminescent technology. The phosphorescent dopant of the light-emitting layer can be selected from, but is not limited to, one or more of YPD-1-YPD-11 listed below.

The OLED organic material layer may further include an electron transport region between the light emitting layer and the cathode. The electron transport region may be an Electron Transport Layer (ETL) of a single-layer structure including a single-layer electron transport layer containing only one compound and a single-layer electron transport layer containing a plurality of compounds. The electron transport region may also be a multilayer structure including at least one of an Electron Injection Layer (EIL), an Electron Transport Layer (ETL), and a Hole Blocking Layer (HBL).

In one aspect of the invention, the electron transport layer material may be selected from, but is not limited to, the combination of one or more of ET-1 through ET-57 listed below.

An electron injection layer may also be included in the device between the electron transport layer and the cathode, the electron injection layer material including, but not limited to, combinations of one or more of the following: LiQ, LiF, NaCl, CsF, Li₂O、Cs₂CO₃BaO, Na, Li or Ca.

Compared with the prior art, the invention has the following beneficial effects:

in the structure of the compound, the 2-position of naphthalene is connected with another naphthalene ring, and the 1-position is connected with a diarylamine group, so that the compound has a large-pi plane structure, the molecular space structure can be effectively changed, the improvement of intra-membrane molecular accumulation is facilitated, the rotation of an aromatic ring on an N atom is limited by ortho-position substitution, and the stability of the material is enhanced, so that when the compound is used as a hole transport layer material or an electron blocking layer of an organic electroluminescent device, the luminous efficiency can be improved, the starting voltage can be reduced, and the device has longer service life. The organic electroluminescent device using the compound of the invention has a luminance of 5000cd/m²When the voltage is low, the driving voltage is below 3.8V, the current efficiency is higher than 12.7cd/A, and LT95 is higher than 165 h.

Drawings

FIG. 1 is a molecular structure model diagram of compound P1 according to the present invention;

FIG. 2 is a molecular structure model diagram of compound P144 according to the present invention;

FIG. 3 is a molecular structure model diagram of a comparative example compound EMT-3;

FIG. 4 is a molecular structure model diagram of a comparative example compound EMT-4;

FIG. 5 is a molecular structure model diagram of a comparative example compound EMT-5.

Detailed Description

The technical solution of the present invention is further explained by the following embodiments. It should be understood by those skilled in the art that the examples are only for the understanding of the present invention and should not be construed as the specific limitations of the present invention.

The solvents and reagents used in the following synthesis examples in the present invention, for example, aniline, 1-naphthylamine, 2-bromo-9, 9' -dimethylfluorene, 2-bromodibenzofuran, 2-bromodibenzothiophene, 2-aminobiphenyl, 2-amino-4-methoxy-5 ' -methoxy-1, 2' -binaphthyl, 2-amino-4-methoxy-5 ' -methoxy-1, 1' -binaphthyl, 2-amino-1, 1' -binaphthyl, 4-bromobiphenyl, [1,1' -bis (diphenylphosphino) ferrocene ] dichloropalladium, tris (dibenzylideneacetone) dipalladium, toluene, petroleum ether, and the like, Chemical reagents such as n-hexane, dichloromethane, acetone, sodium sulfate, ethyl acetate, ethanol, triphenylphosphine, potassium/sodium tert-butoxide, etc. can be purchased or customized from the national chemical product market, for example, from national drug group reagents, Sigma-Aldrich, and Bailingwei reagents. In addition, they can be synthesized by a known method by those skilled in the art.

Synthesis example 1: synthesis of Compound P1

In a 1000ml single-neck flask, 13.5g (50mmol) of 1-amino-2, 1' -binaphthyl, 15.7g (100mmol) of bromobenzene, 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium (i.e., Pd)₂(dba)₃) 0.5mL of tributylphosphine ((t-Bu)₃P), 500ml of Toluene (Toluene), 14.4g (150mmol) of sodium tert-butoxide (NaOBu-t), vacuumizing and changing nitrogen for 3 times, and heating the reaction to 110 ℃ for 5 h. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction liquid, concentrating the organic phase, adding methanol, stirring for 1h, and performing suction filtration to obtain light yellow powder P1, wherein the theoretical value of M/Z is 421, and the actual value of M/Z is 422.

Synthesis example 2: synthesis of Compound P7

In a 1000ml single-neck flask, 13.5g (50mmol) of 1-amino-2, 1' -binaphthyl, 18.7g (100mmol) of 4-methoxybromobenzene, 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium (i.e., Pd)₂(dba)₃) 0.5mL of tributylphosphine ((t-Bu)₃P), 500ml of Toluene (Toluene), 14.4g (150mmol) of sodium tert-butoxide (NaOBu-t), and evacuation is carried outChanging nitrogen for 3 times, and heating the reaction to 110 ℃ for 5 hours. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction solution, concentrating the organic phase, adding methanol, stirring for 1h, and performing suction filtration to obtain light yellow powder P7, wherein the theoretical value of M/Z is 481, and the actual value of M/Z is 482.

Synthesis example 3: synthesis of Compound P39

In a 1000ml single-neck flask, 13.5g (50mmol) of 1-amino-2, 1' -binaphthyl, 23.1g (100mmol) of 4-phenylbromide, 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium (i.e., Pd)₂(dba)₃) 0.5mL of tributylphosphine ((t-Bu)₃P), 500ml Toluene (Toluene), 14.4g (150mmol) sodium tert-butoxide (NaOBu-t), vacuumizing and changing nitrogen for 3 times, and heating the reaction to 110 ℃ for 5 h. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction liquid, concentrating the organic phase, adding methanol, stirring for 1h, and performing suction filtration to obtain light yellow powder P39, wherein the theoretical value of M/Z is 573, and the actual value of M/Z is 574.

Synthesis example 4: synthesis of Compound P59

Into a 1000ml single-necked flask were charged 13.5g (50mmol) of 1-amino-2, 1 '-binaphthyl, 27g (100mmol) of 2-bromo-9, 9' -dimethylfluorene, and 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium (i.e., Pd)₂(dba)₃) 0.5mL of tributylphosphine ((t-Bu)₃P), 500ml Toluene (Toluene), 14.4g (150mmol) sodium tert-butoxide (NaOBu-t), vacuumizing and changing nitrogen for 3 times, and heating the reaction to 110 ℃ for 5 h. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction liquid, concentrating the organic phase, adding methanol, stirring for 1h, and performing suction filtration to obtain light yellow powder P59, wherein the theoretical value of M/Z is 653, and the actual value of M/Z is 654.

Synthesis example 5: synthesis of Compound P65

Into a 1000ml single-neck flask were charged 13.5g (50mmol) of 1-amino-2, 1' -binaphthyl, 13.5g (50mmol) of 2-bromo-9, 9' -dimethylfluorene, and 0.7g (1mmol) of [1,1' -bis (diphenylphosphino) ferrocene]Palladium dichloride (Pd (dppf) Cl₂) 0.5g of 2-dicyclohexylphosphine-2 ',6' -dimethoxybiphenyl (spos), 500ml of toluene, 14.4g (150mmol) of sodium tert-butoxide, vacuumizing and nitrogen exchange for 3 times, and heating to 90 ℃ for reaction for 5 hours. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction liquid, concentrating the organic phase, adding methanol, stirring for 1h, and filtering to obtain light yellow powder M1.

In a 1000mL single-neck flask, 23g (50mmol) of M1, 13.5g (50mmol) of 3-bromo-9, 9' -dimethylfluorene, 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium and 500mL of toluene were added, the atmosphere was evacuated and purged with nitrogen 3 times, and 0.5mL of tritylphosphine ((t-Bu) was added₃P) toluene solution, heating to 110 ℃ for reaction for 12h, evaporating the solvent after the reaction is finished, and carrying out silica gel column chromatography to obtain P65, wherein the theoretical value of M/Z is 653, and the measured value of M/Z is 654.

Synthesis example 6: synthesis of Compound P124

In a 1000ml single-neck flask, 13.5g (50mmol) of 1-amino-2, 1' -binaphthyl, 13.5g (50mmol) of 2-bromo-9, 9' -dimethylfluorene, 0.7g (1mmol) of [1,1' -bis (diphenylphosphino) ferrocene ] dichloropalladium, 0.5g of 2-dicyclohexylphosphine-2 ',6' -dimethoxybiphenyl, 500ml of toluene, 14.4g (150mmol) of sodium tert-butoxide, evacuating and changing nitrogen gas for 3 times, heating the reaction to 90 ℃ and reacting for 5 hours. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction liquid, concentrating the organic phase, adding methanol, stirring for 1h, and filtering to obtain light yellow powder M1.

In a 1000mL single-neck flask, 23g (50mmol) of M1, 12.3g (50mmol) of 1-bromo-dibenzofuran, 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium and 500mL of toluene are added, nitrogen is exchanged for 3 times by vacuumizing, 0.5mL of a tributylphosphine toluene solution is added, the temperature is raised to 110 ℃ for reaction for 12 hours, after the reaction is finished, the solvent is distilled off, and silica gel column chromatography is carried out, so that P124 is obtained, the theoretical value of M/Z is 627, and the actual value of M/Z is 628.

Synthesis example 7: synthesis of Compound P138

In a 1000ml single-neck flask, 13.5g (50mmol) of 1-amino-2, 1' -binaphthyl, 13.5g (50mmol) of 2-bromo-9, 9' -dimethylfluorene, 0.7g (1mmol) of [1,1' -bis (diphenylphosphino) ferrocene ] dichloropalladium, 0.5g of 2-dicyclohexylphosphine-2 ',6' -dimethoxybiphenyl, 500ml of toluene, 14.4g (150mmol) of sodium tert-butoxide, evacuating and changing nitrogen gas for 3 times, heating the reaction to 90 ℃ and reacting for 5 hours. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction liquid, concentrating the organic phase, adding methanol, stirring for 1h, and filtering to obtain light yellow powder M1.

In a 1000mL single-neck flask, 23g (50mmol) of M1, 12.3g (50mmol) of 2-bromo-dibenzofuran, 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium and 500mL of toluene are added, nitrogen is exchanged for 3 times by vacuum pumping, 0.5mL of tert-butylphosphine toluene solution is added, the temperature is raised to 110 ℃ for reaction for 12 hours, after the reaction is finished, the solvent is distilled off, and silica gel column chromatography is carried out, so that P138 is obtained, the theoretical value of M/Z is 627, and the measured value of M/Z is 628.

Synthesis example 8: synthesis of Compound P139

In a 1000ml single-neck flask, 13.5g (50mmol) of 1-amino-2, 1' -binaphthyl, 13.5g (50mmol) of 2-bromo-9, 9' -dimethylfluorene, 0.7g (1mmol) of [1,1' -bis (diphenylphosphino) ferrocene ] dichloropalladium, 0.5g of 2-dicyclohexylphosphine-2 ',6' -dimethoxybiphenyl, 500ml of toluene, 14.4g (150mmol) of sodium tert-butoxide, evacuating and changing nitrogen gas for 3 times, heating the reaction to 90 ℃ and reacting for 5 hours. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction liquid, concentrating the organic phase, adding methanol, stirring for 1h, and filtering to obtain light yellow powder M1.

In a 1000mL single-neck flask, 23g (50mmol) of M1, 12.3g (50mmol) of 2-bromo-dibenzofuran, 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium and 500mL of toluene are added, nitrogen is exchanged for 3 times by vacuumizing, 0.5mL of a tributylphosphine toluene solution is added, the temperature is raised to 110 ℃ for reaction for 12 hours, after the reaction is finished, the solvent is distilled off, and silica gel column chromatography is carried out, so that P139 is obtained, the theoretical value of M/Z is 627, and the actual value of M/Z is 628.

Synthesis example 9: synthesis of Compound P140

In a 1000ml single-neck flask, 13.5g (50mmol) of 1-amino-2, 1' -binaphthyl, 13.5g (50mmol) of 2-bromo-9, 9' -dimethylfluorene, 0.7g (1mmol) of [1,1' -bis (diphenylphosphino) ferrocene ] dichloropalladium, 0.5g of 2-dicyclohexylphosphine-2 ',6' -dimethoxybiphenyl, 500ml of toluene, 14.4g (150mmol) of sodium tert-butoxide, evacuating and changing nitrogen gas for 3 times, heating the reaction to 90 ℃ and reacting for 5 hours. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction liquid, concentrating the organic phase, adding methanol, stirring for 1h, and filtering to obtain light yellow powder M1.

In a 1000mL single-neck flask, 23g (50mmol) of M1, 12.3g (50mmol) of 2-bromo-dibenzofuran, 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium and 500mL of toluene are added, nitrogen is exchanged for 3 times by vacuum pumping, 0.5mL of a tributylphosphine toluene solution is added, the temperature is raised to 110 ℃ for reaction for 12 hours, after the reaction is finished, the solvent is distilled off, and silica gel column chromatography is carried out, so that P140 is obtained, the theoretical value of M/Z is 627, and the actual value of M/Z is 628.

Synthesis example 10: synthesis of Compound P141

In a 1000ml single-neck flask, 13.5g (50mmol) of 1-amino-2, 1' -binaphthyl, 13.5g (50mmol) of 2-bromo-9, 9' -dimethylfluorene, 0.7g (1mmol) of [1,1' -bis (diphenylphosphino) ferrocene ] dichloropalladium, 0.5g of 2-dicyclohexylphosphine-2 ',6' -dimethoxybiphenyl, 500ml of toluene, 14.4g (150mmol) of sodium tert-butoxide, evacuating and changing nitrogen gas for 3 times, heating the reaction to 90 ℃ and reacting for 5 hours. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction liquid, concentrating the organic phase, adding methanol, stirring for 1h, and filtering to obtain light yellow powder M1.

In a 1000mL single-neck flask, 23g (50mmol) of M1, 16.1g (50mmol) of 4- (4-bromophenyl) -dibenzofuran, 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium and 500mL of toluene are added, nitrogen is exchanged for 3 times by vacuumizing, 0.5mL of a tributylphosphine toluene solution is added, the temperature is raised to 110 ℃ for reaction for 12 hours, after the reaction is finished, the solvent is distilled off, and silica gel column chromatography is carried out, so that P141, the theoretical value of M/Z: 703 and the actual value of M/Z: 704 are obtained.

Synthesis example 11: synthesis of Compound P142

In a 1000ml single-neck flask, 13.5g (50mmol) of 1-amino-2, 1' -binaphthyl, 13.5g (50mmol) of 2-bromo-9, 9' -dimethylfluorene, 0.7g (1mmol) of [1,1' -bis (diphenylphosphino) ferrocene ] dichloropalladium, 0.5g of 2-dicyclohexylphosphine-2 ',6' -dimethoxybiphenyl, 500ml of toluene, 14.4g (150mmol) of sodium tert-butoxide, evacuating and changing nitrogen gas for 3 times, heating the reaction to 90 ℃ and reacting for 5 hours. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction liquid, concentrating the organic phase, adding methanol, stirring for 1h, and filtering to obtain light yellow powder M1.

In a 1000mL single-neck bottle, 23g (50mmol) of M1, 16g (50mmol) of 9- (4-bromophenyl) carbazole, 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium and 500mL of toluene are added, nitrogen is exchanged for 3 times by vacuumizing, 0.5mL of tributylphosphine toluene solution is added, the temperature is raised to 110 ℃ for reaction for 12 hours, after the reaction is finished, the solvent is distilled off, and silica gel column chromatography is carried out, thus obtaining P142, the theoretical value of M/Z is 702, and the actual value of M/Z is 703.

Synthesis example 12: synthesis of Compound P143

In a 1000ml single-neck flask, 13.5g (50mmol) of 1-amino-2, 1' -binaphthyl, 13.5g (50mmol) of 2-bromo-9, 9' -dimethylfluorene, 0.7g (1mmol) of [1,1' -bis (diphenylphosphino) ferrocene ] dichloropalladium, 0.52-dicyclohexylphosphine-2 ',6' -dimethoxybiphenyl, 500ml of toluene, 14.4g (150mmol) of sodium tert-butoxide, evacuating and changing nitrogen gas for 3 times, and raising the temperature to 90 ℃ for reaction for 5 hours. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction liquid, concentrating the organic phase, adding methanol, stirring for 1h, and filtering to obtain light yellow powder M1.

In a 1000mL single-neck flask, 23g (50mmol) of M1, 13.1g (50mmol) of 2-bromo-dibenzothiophene, 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium and 500mL of toluene are added, nitrogen is exchanged for 3 times by vacuum pumping, 0.5mL of a tributylphosphine toluene solution is added, the temperature is raised to 110 ℃ for reaction for 12 hours, after the reaction is finished, the solvent is distilled off, and silica gel column chromatography is carried out, so that P143 is obtained, the theoretical value of M/Z is 643, and the actual value of M/Z is 644.

Synthesis example 13: synthesis of compound P144

Into a 1000mL single-neck flask were charged 13.5g (50mmol) of 1-amino-2, 2' -binaphthyl, 15.7g (100mmol) of bromobenzene, 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium, 0.5mL of tributylphosphine, 500mL of toluene, and 14.4g (150mmol) of sodium tert-butoxide, and the reaction was evacuated and purged with nitrogen 3 times, and the reaction was heated to 110 ℃ for 5 hours. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction liquid, concentrating the organic phase, adding methanol, stirring for 1h, and performing suction filtration to obtain light yellow powder P144, wherein the theoretical value of M/Z is 421, and the actual value of M/Z is 422.

Synthesis example 14: synthesis of Compound P173

Into a 1000mL single-neck flask were charged 13.5g (50mmol) of 1-amino-2, 2 '-binaphthyl, 27g (100mmol) of 2-bromo-9, 9' -dimethylfluorene, 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium, 0.5mL of tributylphosphine, 500mL of toluene, 14.4g (150mmol) of sodium tert-butoxide, and the reaction was evacuated and purged with nitrogen 3 times, and the temperature was raised to 110 ℃ for 5 hours. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction liquid, concentrating the organic phase, adding methanol, stirring for 1h, and performing suction filtration to obtain light yellow powder P173, wherein the theoretical value of M/Z is 653, and the actual value of M/Z is 654.

Synthesis example 15: synthesis of Compound P206

In a 1000ml single-neck flask, 13.5g (50mmol) of 1-amino-2, 2' -binaphthyl, 13.5g (50mmol) of 2-bromo-9, 9' -dimethylfluorene, 0.7g (1mmol) of [1,1' -bis (diphenylphosphino) ferrocene ] dichloropalladium, 0.5g of 2-dicyclohexylphosphine-2 ',6' -dimethoxybiphenyl, 500ml of toluene, 14.4g (150mmol) of sodium tert-butoxide, evacuating and changing nitrogen gas for 3 times, heating the reaction to 90 ℃ and reacting for 5 hours. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction liquid, concentrating the organic phase, adding methanol, stirring for 1h, and filtering to obtain light yellow powder M2.

In a 1000mL single-neck flask, 23g (50mmol) of M1, 13.5g (50mmol) of 3-bromo-9, 9' -dimethylfluorene, 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium and 500mL of toluene are added, the mixture is vacuumized and nitrogen-exchanged for 3 times, 0.5mL of a tributylphosphine toluene solution is added, the temperature is raised to 110 ℃ for reaction for 12 hours, after the reaction is finished, the solvent is distilled off, and silica gel column chromatography is carried out, so that P206 is obtained, the theoretical value of M/Z is 653, and the actual value of M/Z is 654.

Synthesis example 16: synthesis of Compound P207

In a 1000ml single-neck flask, 13.5g (50mmol) of 1-amino-2, 2' -binaphthyl, 13.5g (50mmol) of 2-bromo-9, 9' -dimethylfluorene, 0.7g (1mmol) of [1,1' -bis (diphenylphosphino) ferrocene ] dichloropalladium, 0.5g of 2-dicyclohexylphosphine-2 ',6' -dimethoxybiphenyl, 500ml of toluene, 14.4g (150mmol) of sodium tert-butoxide, evacuating and changing nitrogen gas for 3 times, heating the reaction to 90 ℃ and reacting for 5 hours. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction liquid, concentrating the organic phase, adding methanol, stirring for 1h, and filtering to obtain light yellow powder M2.

In a 1000mL single-neck flask, 23g (50mmol) of M1, 12.3g (50mmol) of 1-bromo-dibenzofuran, 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium and 500mL of toluene are added, nitrogen is exchanged for 3 times by vacuumizing, 0.5mL of a tributylphosphine toluene solution is added, the temperature is raised to 110 ℃ for reaction for 12 hours, after the reaction is finished, the solvent is distilled off, and silica gel column chromatography is carried out, so that P207 is obtained, the theoretical value of M/Z is 627, and the actual value of M/Z is 628.

Synthesis example 17: synthesis of Compound P210

In a 1000ml single-neck flask, 13.5g (50mmol) of 1-amino-2, 2' -binaphthyl, 13.5g (50mmol) of 2-bromo-9, 9' -dimethylfluorene, 0.7g (1mmol) of [1,1' -bis (diphenylphosphino) ferrocene ] dichloropalladium, 0.5g of 2-dicyclohexylphosphine-2 ',6' -dimethoxybiphenyl, 500ml of toluene, 14.4g (150mmol) of sodium tert-butoxide, evacuating and changing nitrogen gas for 3 times, heating the reaction to 90 ℃ and reacting for 5 hours. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction liquid, concentrating the organic phase, adding methanol, stirring for 1h, and filtering to obtain light yellow powder M2.

In a 1000mL single-neck flask, 23g (50mmol) of M1, 12.3g (50mmol) of 2-bromo-dibenzofuran, 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium and 500mL of toluene are added, nitrogen is exchanged for 3 times by vacuumizing, 0.5mL of a tributylphosphine toluene solution is added, the temperature is raised to 110 ℃ for reaction for 12 hours, after the reaction is finished, the solvent is distilled off, and silica gel column chromatography is carried out, so that P210 is obtained, the theoretical value of M/Z is 627, and the actual value of M/Z is 628.

Synthesis example 18: synthesis of Compound P211

In a 1000ml single-neck flask, 13.5g (50mmol) of 1-amino-2, 2' -binaphthyl, 13.5g (50mmol) of 2-bromo-9, 9' -dimethylfluorene, 0.7g (1mmol) of [1,1' -bis (diphenylphosphino) ferrocene ] dichloropalladium, 0.5g of 2-dicyclohexylphosphine-2 ',6' -dimethoxybiphenyl, 500ml of toluene, 14.4g (150mmol) of sodium tert-butoxide, evacuating and changing nitrogen gas for 3 times, heating the reaction to 90 ℃ and reacting for 5 hours. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction liquid, concentrating the organic phase, adding methanol, stirring for 1h, and filtering to obtain light yellow powder M2.

In a 1000mL single-neck flask, 23g (50mmol) of M1, 12.3g (50mmol) of 2-bromo-dibenzofuran, 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium and 500mL of toluene are added, nitrogen is exchanged for 3 times by vacuum pumping, 0.5mL of a tributylphosphine toluene solution is added, the temperature is raised to 110 ℃ for reaction for 12 hours, after the reaction is finished, the solvent is distilled off, and silica gel column chromatography is carried out, so that P211 is obtained, the theoretical value of M/Z is 627, and the actual value of M/Z is 628.

Synthesis example 19: synthesis of Compound P216

In a 1000ml single-neck flask, 13.5g (50mmol) of 1-amino-2, 2' -binaphthyl, 13.5g (50mmol) of 2-bromo-9, 9' -dimethylfluorene, 0.7g (1mmol) of [1,1' -bis (diphenylphosphino) ferrocene ] dichloropalladium, 0.5g of 2-dicyclohexylphosphine-2 ',6' -dimethoxybiphenyl, 500ml of toluene, 14.4g (150mmol) of sodium tert-butoxide, evacuating and changing nitrogen gas for 3 times, heating the reaction to 90 ℃ and reacting for 5 hours. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction liquid, concentrating the organic phase, adding methanol, stirring for 1h, and filtering to obtain light yellow powder M2.

In a 1000mL single-neck flask, 23g (50mmol) of M1, 12.3g (50mmol) of 2-bromo-dibenzofuran, 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium and 500mL of toluene are added, nitrogen is exchanged for 3 times by vacuum pumping, 0.5mL of a tributylphosphine toluene solution is added, the temperature is raised to 110 ℃ for reaction for 12 hours, after the reaction is finished, the solvent is distilled off, and silica gel column chromatography is carried out, so that P216 is obtained, the theoretical value of M/Z is 627, and the actual value of M/Z is 628.

Synthesis example 20: synthesis of Compound P220

In a 1000ml single-neck flask, 13.5g (50mmol) of 1-amino-2, 2' -binaphthyl, 13.5g (50mmol) of 2-bromo-9, 9' -dimethylfluorene, 0.7g (1mmol) of [1,1' -bis (diphenylphosphino) ferrocene ] dichloropalladium, 0.5g of 2-dicyclohexylphosphine-2 ',6' -dimethoxybiphenyl, 500ml of toluene, 14.4g (150mmol) of sodium tert-butoxide, evacuating and changing nitrogen gas for 3 times, heating the reaction to 90 ℃ and reacting for 5 hours. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction liquid, concentrating the organic phase, adding methanol, stirring for 1h, and filtering to obtain light yellow powder M2.

In a 1000mL single-neck flask, 23g (50mmol) of M1, 16.1g (50mmol) of 4- (4-bromophenyl) -dibenzofuran, 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium and 500mL of toluene are added, nitrogen is exchanged for 3 times by vacuumizing, 0.5mL of a tributylphosphine toluene solution is added, the temperature is raised to 110 ℃ for reaction for 12 hours, after the reaction is finished, the solvent is distilled off, and silica gel column chromatography is carried out, so that P220 is obtained, the theoretical value of M/Z is 703, and the actual value of M/Z is 704.

Synthesis example 21: synthesis of Compound P241

In a 1000ml single-neck flask, 13.5g (50mmol) of 1-amino-2, 2' -binaphthyl, 13.5g (50mmol) of 2-bromo-9, 9' -dimethylfluorene, 0.7g (1mmol) of [1,1' -bis (diphenylphosphino) ferrocene ] dichloropalladium, 0.5g of 2-dicyclohexylphosphine-2 ',6' -dimethoxybiphenyl, 500ml of toluene, 14.4g (150mmol) of sodium tert-butoxide, evacuating and changing nitrogen gas for 3 times, heating the reaction to 90 ℃ and reacting for 5 hours. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction liquid, concentrating the organic phase, adding methanol, stirring for 1h, and filtering to obtain light yellow powder M2.

In a 1000mL single-neck bottle, 23g (50mmol) of M1, 16g (50mmol) of 9- (4-bromophenyl) carbazole, 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium and 500mL of toluene are added, nitrogen is exchanged for 3 times by vacuumizing, 0.5mL of tributylphosphine toluene solution is added, the temperature is raised to 110 ℃ for reaction for 12 hours, after the reaction is finished, the solvent is distilled off, and silica gel column chromatography is carried out, thus obtaining P241, the theoretical value of M/Z is 702, and the actual value of M/Z is 703.

Synthesis example 22: synthesis of compound P292

In a 1000ml single-neck flask, 13.5g (50mmol) of 1-amino-2, 2' -binaphthyl, 13.5g (50mmol) of 2-bromo-9, 9' -dimethylfluorene, 0.7g (1mmol) of [1,1' -bis (diphenylphosphino) ferrocene ] dichloropalladium, 0.5g of 2-dicyclohexylphosphine-2 ',6' -dimethoxybiphenyl, 500ml of toluene, 14.4g (150mmol) of sodium tert-butoxide, evacuating and changing nitrogen gas for 3 times, heating the reaction to 90 ℃ and reacting for 5 hours. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction liquid, concentrating the organic phase, adding methanol, stirring for 1h, and filtering to obtain light yellow powder M2.

In a 1000mL single-neck flask, 23g (50mmol) of M1, 13.1g (50mmol) of 2-bromo-dibenzothiophene, 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium and 500mL of toluene are added, nitrogen is exchanged for 3 times by vacuum pumping, 0.5mL of a tributylphosphine toluene solution is added, the temperature is raised to 110 ℃ for reaction for 12 hours, after the reaction is finished, the solvent is distilled off, and silica gel column chromatography is carried out, so that P292 is obtained, the theoretical value of M/Z is 643, and the actual value of M/Z is 644.

Synthesis example 23: synthesis of Compound P330

In a 1000mL single-neck flask, 16.4g (50mmol) of 2- [2'- (5-methoxy) naphthyl ] -4-methoxy-1-naphthylamine, 27g (100mmol) of 3-bromo-9, 9' -dimethylfluorene, 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium, 0.5mL of tributylphosphine, 500mL of toluene, 14.4g (150mmol) of sodium tert-butoxide, nitrogen gas exchange for 3 times by evacuation, and the reaction is heated to 110 ℃ for 5 hours. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction liquid, concentrating the organic phase, adding methanol, stirring for 1h, and performing suction filtration to obtain light yellow powder P330, wherein the theoretical value of M/Z is 713, and the actual value of M/Z is 714.

Synthesis example 24: synthesis of Compound P331

In a 1000mL single-neck flask, 16.4g (50mmol) of 2- [2'- (5-methoxy) naphthyl ] -4-methoxy-1-naphthylamine, 27g (100mmol) of 2-bromo-9, 9' -dimethylfluorene, 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium, 0.5mL of tributylphosphine, 500mL of toluene, 14.4g (150mmol) of sodium tert-butoxide, nitrogen gas exchange for 3 times by evacuation, and the reaction is heated to 110 ℃ for 5 hours. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction liquid, concentrating the organic phase, adding methanol, stirring for 1h, and performing suction filtration to obtain light yellow powder P331, wherein the theoretical value of M/Z is 713, and the actual value of M/Z is 714.

Synthesis example 25: synthesis of compound P263

In a 1000ml single-neck flask, 13.5g (50mmol) of 1-amino-2, 2 '-binaphthyl, 12.5g (50mmol) of 9-bromo-phenanthrene, 0.7g (1mmol) of [1,1' -bis (diphenylphosphino) ferrocene ] dichloropalladium, 0.5g of 2-dicyclohexylphosphine-2 ',6' -dimethoxybiphenyl, 500ml of toluene, 14.4g (150mmol) of sodium tert-butoxide, vacuumizing and changing nitrogen for 3 times, and heating to 90 ℃ for reaction for 5 h. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction liquid, concentrating the organic phase, adding methanol, stirring for 1h, and filtering to obtain light yellow powder M3.

22g (50mmol) of M3, 15g (70mmol) of 2-bromobiphenyl, 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium and 500mL of toluene are added into a 1000mL single-neck bottle, nitrogen is exchanged for 3 times by vacuumizing, 0.5mL of tributylphosphine toluene solution is added, the temperature is increased to 110 ℃ for reaction for 12 hours, after the reaction is finished, the solvent is distilled off, and silica gel column chromatography is carried out, thus obtaining P263, the theoretical value of M/Z is 597, and the measured value of M/Z is 598.

Synthesis example 26: synthesis of Compound P314

Into a 1000ml single-neck flask were charged 13.5g (50mmol) of 1-amino-2, 2 '-binaphthyl, 17.5g (50mmol) of 2- (1-naphthyl) -4-phenylborobenzene, 0.7g (1mmol) of [1,1' -bis (diphenylphosphino) ferrocene ] dichloropalladium, 0.5g of 2-dicyclohexylphosphine-2 ',6' -dimethoxybiphenyl, 500ml of toluene, 14.4g (150mmol) of sodium tert-butoxide, and the reaction was evacuated to remove nitrogen and warmed to 90 ℃ for 5 hours. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction liquid, concentrating the organic phase, adding methanol, stirring for 1h, and filtering to obtain light yellow powder M4.

27g (50mmol) of M4, 13g (50mmol) of 1-bromodibenzofuran, 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium and 500mL of toluene are added into a 1000mL single-neck flask, nitrogen is exchanged for 3 times by vacuumizing, 0.5mL of tributylphosphine toluene solution is added, the temperature is raised to 110 ℃ for reaction for 12 hours, after the reaction is finished, the solvent is distilled off, and silica gel column chromatography is carried out, thus obtaining P314, the theoretical value of M/Z is 713, and the measured value of M/Z is 714.

Synthesis example 27: synthesis of Compound P329

In a 1000ml single-neck flask, 13.5g (50mmol) of 1-amino-2, 2 '-binaphthyl, 15.4g (50mmol) of 4-bromoterphenyl, 0.7g (1mmol) of [1,1' -bis (diphenylphosphino) ferrocene ] dichloropalladium, 0.5g of 2-dicyclohexylphosphine-2 ',6' -dimethoxybiphenyl, 500ml of toluene and 14.4g (150mmol) of sodium tert-butoxide are added, the nitrogen is exchanged for 3 times by vacuum pumping, and the reaction is heated to 90 ℃ for 5 hours. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction liquid, concentrating the organic phase, adding methanol, stirring for 1h, and filtering to obtain light yellow powder M5.

In a 1000mL single-neck flask, 25g (50mmol) of M5, 20g (50mmol) of 3-bromoRobifluorene, 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium and 500mL of toluene are added, nitrogen is exchanged for 3 times by vacuum pumping, 0.5mL of tert-butylphosphine toluene solution is added, the temperature is raised to 110 ℃ for reaction for 12 hours, after the reaction is finished, the solvent is distilled off, and silica gel column chromatography is carried out, thus obtaining P29, the theoretical value of M/Z is 811, and the actual value of M/Z is 812.

Synthesis example 28: synthesis of Compound P336

In a 1000ml single-neck flask, 13.5g (50mmol) of 1-amino-2, 1' -binaphthyl, 13.5g (50mmol) of 3-bromo-9, 9' -dimethylfluorene, 0.7g (1mmol) of [1,1' -bis (diphenylphosphino) ferrocene ] dichloropalladium, 0.5g of 2-dicyclohexylphosphine-2 ',6' -dimethoxybiphenyl, 500ml of toluene, 14.4g (150mmol) of sodium tert-butoxide, evacuating and changing nitrogen gas for 3 times, heating the reaction to 90 ℃ and reacting for 5 hours. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction liquid, concentrating the organic phase, adding methanol, stirring for 1h, and filtering to obtain light yellow powder M6.

In a 1000mL single-neck flask, 23g (50mmol) of M6, 10g (50mmol) of 2-bromonaphthalene, 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium and 500mL of toluene are added, nitrogen is exchanged for 3 times by vacuumizing, 0.5mL of tributylphosphine toluene solution is added, the temperature is raised to 110 ℃ for reaction for 12 hours, after the reaction is finished, the solvent is distilled off, and silica gel column chromatography is carried out, thus obtaining P336, the theoretical value of M/Z is 587, and the actual value of M/Z is 588.

Synthesis example 29: synthesis of Compound P343

In a 1000ml single-neck flask, 13.5g (50mmol) of 1-amino-2, 1' -binaphthyl, 13.5g (50mmol) of 3-bromo-9, 9' -dimethylfluorene, 0.7g (1mmol) of [1,1' -bis (diphenylphosphino) ferrocene ] dichloropalladium, 0.5g of 2-dicyclohexylphosphine-2 ',6' -dimethoxybiphenyl, 500ml of toluene, 14.4g (150mmol) of sodium tert-butoxide, evacuating and changing nitrogen gas for 3 times, heating the reaction to 90 ℃ and reacting for 5 hours. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction liquid, concentrating the organic phase, adding methanol, stirring for 1h, and filtering to obtain light yellow powder M6.

In a 1000mL single-neck flask, 23g (50mmol) of M6, 13.5g (50mmol) of 2-bromo-9, 9-dimethylfluorene, 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium and 500mL of toluene are added, the mixture is vacuumized and nitrogen-exchanged for 3 times, 0.5mL of a tributylphosphine toluene solution is added, the temperature is raised to 110 ℃ for reaction for 12 hours, after the reaction is finished, the solvent is distilled off, and silica gel column chromatography is carried out, so that P343, the theoretical value of M/Z: 653, and the actual value of M/Z: 654 are obtained.

Synthesis example 30: synthesis of Compound P348

In a 1000ml single-neck flask, 13.5g (50mmol) of 1-amino-2, 2' -binaphthyl, 13.5g (50mmol) of 3-bromo-9, 9' -dimethylfluorene, 0.7g (1mmol) of [1,1' -bis (diphenylphosphino) ferrocene ] dichloropalladium, 0.5g of 2-dicyclohexylphosphine-2 ',6' -dimethoxybiphenyl, 500ml of toluene, 14.4g (150mmol) of sodium tert-butoxide, evacuating and changing nitrogen gas for 3 times, heating the reaction to 90 ℃ and reacting for 5 hours. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction liquid, concentrating the organic phase, adding methanol, stirring for 1h, and filtering to obtain light yellow powder M7.

In a 1000mL single-neck flask, 23g (50mmol) of M7, 10g (50mmol) of 2-bromonaphthalene, 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium and 500mL of toluene are added, nitrogen is exchanged for 3 times by vacuumizing, 0.5mL of tributylphosphine toluene solution is added, the temperature is raised to 110 ℃ for reaction for 12 hours, after the reaction is finished, the solvent is distilled off, and silica gel column chromatography is carried out, thus obtaining P348, the theoretical value of M/Z is 587, and the actual value of M/Z is 588.

Synthesis example 31: synthesis of Compound P355

In a 1000ml single-neck flask, 13.5g (50mmol) of 1-amino-2, 2' -binaphthyl, 13.5g (50mmol) of 3-bromo-9, 9' -dimethylfluorene, 0.7g (1mmol) of [1,1' -bis (diphenylphosphino) ferrocene ] dichloropalladium, 0.5g of 2-dicyclohexylphosphine-2 ',6' -dimethoxybiphenyl, 500ml of toluene, 14.4g (150mmol) of sodium tert-butoxide, evacuating and changing nitrogen gas for 3 times, heating the reaction to 90 ℃ and reacting for 5 hours. And stopping the reaction after the reaction is finished. Cooling to room temperature, separating the reaction liquid, concentrating the organic phase, adding methanol, stirring for 1h, and filtering to obtain light yellow powder M7.

In a 1000mL single-neck flask, 23g (50mmol) of M7, 13.5g (50mmol) of 2-bromo-9, 9-dimethylfluorene, 0.9g (1mmol) of tris (dibenzylideneacetone) dipalladium and 500mL of toluene are added, the mixture is vacuumized and nitrogen-exchanged for 3 times, 0.5mL of a tributylphosphine toluene solution is added, the temperature is raised to 110 ℃ for reaction for 12 hours, after the reaction is finished, the solvent is distilled off, and silica gel column chromatography is carried out, so that P355 is obtained, the theoretical value of M/Z is 653, and the actual value of M/Z is 654.