METAL IRIDIUM COMPLEX AND USE THEREOF

Abstract

The present invention relates to a metal iridium complex and application thereof. The metal iridium complex has a structure as shown in the following formula (I). The compound provided in the present invention has the advantages of low sublimation temperature, great optical and electrical stability, high luminescence efficiency, long service life, and high color saturation, and can be used in organic light-emitting devices. In particular, the complex has the potential for application in the AMOLED industry as a red light-emitting phosphorescent material.

##STR00001##

Claims

1. A metal iridium complex, having a structure formula as shown in the following formula (I): ##STR00128## wherein A is CR.sub.0 or N; the number of R.sub.1, R.sub.2, and R.sub.3 ranges from a single substitution number to a maximum possible substitution number; R.sub.1 and R.sub.4 are independently selected from substituted or unsubstituted C.sub.1-C.sub.10 alkyl, substituted or unsubstituted C.sub.3-C.sub.20 cycloalkyl, substituted or unsubstituted C.sub.2-C.sub.10 alkenyl, substituted or unsubstituted C.sub.1-C.sub.10 heteroalkyl, substituted or unsubstituted C.sub.6-C.sub.30 aralkyl, substituted or unsubstituted C.sub.6-C.sub.30 aryl, or substituted or unsubstituted C.sub.1-C.sub.8 heteroaryl; R.sub.0, R.sub.2, and R.sub.3 are independently selected from hydrogen, deuterium, halogen, substituted or unsubstituted C.sub.1-C.sub.10 alkyl, substituted or unsubstituted C.sub.3-C.sub.20 cycloalkyl, substituted or unsubstituted C.sub.2-C.sub.10 alkenyl, substituted or unsubstituted C.sub.1-C.sub.10 heteroalkyl, substituted or unsubstituted C.sub.6-C.sub.30 aralkyl, substituted or unsubstituted C.sub.6-C.sub.30 aryl, or substituted or unsubstituted C.sub.1-C.sub.8 heteroaryl; or any two adjacent groups of the R.sub.0, the R.sub.1, the R.sub.2, and the R.sub.3 are capable of being connected to each other to form a ring structure or a fused ring structure; when the R.sub.3 exists and is located adjacent to the A, the R.sub.3 is not F; Rx-Rz are independently selected from hydrogen, deuterium, substituted or unsubstituted C.sub.1-C.sub.10 alkyl, substituted or unsubstituted C.sub.3-C.sub.20 cycloalkyl, substituted or unsubstituted C.sub.2-C.sub.10 alkenyl, or substituted or unsubstituted C.sub.1-C.sub.10 heteroalkyl; the Z is independently selected from O, S, C(R).sub.2, or NR; the R is independently selected from substituted or unsubstituted C.sub.1-C.sub.10 alkyl or alkoxy, substituted or unsubstituted C.sub.2-C.sub.30 cycloalkyl, substituted or unsubstituted C.sub.6-C.sub.30 aryl, or substituted or unsubstituted C.sub.1-C.sub.18 heteroaryl; the “substituted” refers to substitution with deuterium, F, Cl, Br, C.sub.1-C.sub.5 alkyl, or C.sub.3-C.sub.6 cycloalkyl; and a heteroatom in the heteroalkyl or heteroaryl comprises one or more of N, S, and O.

2. The metal iridium complex according to claim 1, wherein the number of the R.sub.1, the R.sub.2, and the R.sub.3 is a single substitution number; the R.sub.1 and the R.sub.4 are substituted or unsubstituted C.sub.1-C.sub.6 alkyl or substituted or unsubstituted C.sub.3-C.sub.6 cycloalkyl; and the R.sub.0, the R.sub.2, and the R.sub.3 are independently selected from hydrogen, deuterium, halogen, substituted or unsubstituted C.sub.1-C.sub.6 alkyl, or substituted or unsubstituted C.sub.3-C.sub.6 cycloalkyl.

3. The metal iridium complex according to claim 2, having a structural formula as shown in the following formula (II): ##STR00129## wherein R.sub.1 and R.sub.4 are substituted or unsubstituted C.sub.3-C.sub.6 branched alkyl, substituted C.sub.3-C.sub.6 linear alkyl, or substituted or unsubstituted C.sub.3-C.sub.6 cycloalkyl; R.sub.0, R.sub.2, and R.sub.3 are independently selected from hydrogen, deuterium, substituted or unsubstituted C.sub.1-C.sub.6 alkyl, or substituted or unsubstituted C.sub.3-C.sub.6 cycloalkyl; and the “substituted” refers to substitution with deuterium, F, C.sub.1-C.sub.5 alkyl, or C.sub.3-C.sub.6 cycloalkyl.

4. The metal iridium complex according to claim 3, wherein the “substituted” refers to substitution with D, F, C.sub.1-C.sub.5 alkyl partially or completely substituted with D or F, or C.sub.3-C.sub.6 cycloalkyl partially or completely substituted with D or F.

5. The metal iridium complex according to claim 4, wherein A is CH or N.

6. The metal iridium complex according to claim 5, wherein the A is N, and the R.sub.3 is not H.

7. The metal iridium complex according to any one of claims 1 to 5, wherein a structure of ##STR00130## in the right side of the formula I is one of the following structures, or corresponding parts or complete deuterides thereof, or corresponding parts or complete fluorides thereof, and a dotted line refers to a metal connection position. ##STR00131## ##STR00132## ##STR00133##

8. The metal iridium complex according to claim 1, having one of the following structural formulas, or corresponding parts or complete deuterides thereof, or corresponding parts or complete fluorides thereof. ##STR00134## ##STR00135## ##STR00136## ##STR00137## ##STR00138## ##STR00139## ##STR00140## ##STR00141## ##STR00142## ##STR00143## ##STR00144## ##STR00145## ##STR00146## ##STR00147## ##STR00148## ##STR00149## ##STR00150## ##STR00151## ##STR00152## ##STR00153## ##STR00154## ##STR00155## ##STR00156## ##STR00157## ##STR00158## ##STR00159## ##STR00160## ##STR00161## ##STR00162## ##STR00163## ##STR00164## ##STR00165## ##STR00166## ##STR00167## ##STR00168## ##STR00169## ##STR00170## ##STR00171## ##STR00172## ##STR00173## ##STR00174## ##STR00175## ##STR00176## ##STR00177## ##STR00178## ##STR00179## ##STR00180## ##STR00181## ##STR00182## ##STR00183## ##STR00184## ##STR00185## ##STR00186## ##STR00187## ##STR00188## ##STR00189## ##STR00190## ##STR00191## ##STR00192## ##STR00193## ##STR00194## ##STR00195## ##STR00196## ##STR00197## ##STR00198## ##STR00199## ##STR00200## ##STR00201## ##STR00202## ##STR00203## ##STR00204## ##STR00205##

9. An electroluminescent device, comprising a cathode, an anode, and an organic layer arranged between the cathode and the anode, wherein the organic layer comprises the metal iridium complex according to any one of claims 1 to 8.

10. The electroluminescent device according to claim 9, wherein the organic layer comprises a light-emitting layer, and the metal iridium complex according to any one of claims 1 to 9 is used as a red light-emitting doping material for the light-emitting layer; or the organic layer comprises a hole injection layer, and the metal iridium complex according to any one of claims 1 to 9 is used as a hole injection material for the hole injection layer.

Description

BRIEF DESCRIPTION OF DRAWINGS

[0033] FIG. 1 is a diagram showing the 1HNMR spectrum of a compound L12 of the present invention in a deuterated chloroform solution.

[0034] FIG. 2 is a diagram showing the 1HNMR spectrum of a compound CPD 93 of the present invention in a deuterated chloroform solution.

[0035] FIG. 3 is a diagram showing the 1HNMR spectrum of a compound L14 of the present invention in a deuterated chloroform solution.

[0036] FIG. 4 is a diagram showing the 1HNMR spectrum of a compound CPD 123 of the present invention in a deuterated chloroform solution.

[0037] FIG. 5 is a diagram showing the 1HNMR spectrum of a compound L17 of the present invention in a deuterated chloroform solution.

[0038] FIG. 6 is a diagram showing the 1HNMR spectrum of a compound CPD 249 of the present invention in a deuterated chloroform solution.

[0039] FIG. 7 shows the ultraviolet absorption spectrum and emission spectrum of the compounds CPD 93/CPD 123/CPD 249 of the present invention in a dichloromethane solution.

DETAILED DESCRIPTION OF EMBODIMENTS

[0040] The compound of the present invention is as shown in the following formula (I):

##STR00085##

[0041] where

[0042] A is CR.sub.0 or N;

[0043] the number of R.sub.1, R.sub.2, and R.sub.3 ranges from a single substitution number to a maximum possible substitution number;

[0044] R.sub.1 and R.sub.4 are independently selected from substituted or unsubstituted C.sub.1-C.sub.10 alkyl, substituted or unsubstituted C.sub.3-C.sub.20 cycloalkyl, substituted or unsubstituted C.sub.2-C.sub.10 alkenyl, substituted or unsubstituted C.sub.1-C.sub.10 heteroalkyl, substituted or unsubstituted C.sub.6-C.sub.30 aralkyl, substituted or unsubstituted C.sub.6-C.sub.30 aryl, or substituted or unsubstituted C.sub.1-C.sub.8 heteroaryl;

[0045] R.sub.0, R.sub.2, and R.sub.3 are independently selected from hydrogen, deuterium, halogen, substituted or unsubstituted C.sub.1-C.sub.10 alkyl, substituted or unsubstituted C.sub.3-C.sub.20 cycloalkyl, substituted or unsubstituted C.sub.2-C.sub.10 alkenyl, substituted or unsubstituted C.sub.1-C.sub.10 heteroalkyl, substituted or unsubstituted C.sub.6-C.sub.30 aralkyl, substituted or unsubstituted C.sub.6-C.sub.30 aryl, or substituted or unsubstituted C.sub.1-C.sub.8 heteroaryl;

[0046] or any two adjacent groups of the R.sub.0, the R.sub.1, the R.sub.2, and the R.sub.3 are capable of being connected to each other to form a ring structure or a fused ring structure;

[0047] when the R.sub.3 exists and is located adjacent to the A, the R.sub.3 is not F; Rx-Rz are independently selected from hydrogen, deuterium, substituted or unsubstituted C.sub.1-C.sub.10 alkyl, substituted or unsubstituted C.sub.3-C.sub.20 cycloalkyl, substituted or unsubstituted C.sub.2-C.sub.10 alkenyl, or substituted or unsubstituted C.sub.1-C.sub.10 heteroalkyl;

[0048] the Z is independently selected from O, S, C(R).sub.2, or NR; the R is independently selected from substituted or unsubstituted C.sub.1-C.sub.10 alkyl or alkoxy, substituted or unsubstituted C.sub.2-C.sub.30 cycloalkyl, substituted or unsubstituted C.sub.6-C.sub.30 aryl, or substituted or unsubstituted C.sub.1-C.sub.18 heteroaryl;

[0049] the “substituted” refers to substitution with deuterium, F, Cl, Br, C.sub.1-C.sub.5 alkyl, or C.sub.3-C.sub.6 cycloalkyl;

[0050] and a heteroatom in the heteroalkyl or heteroaryl includes one or more of N, S, and O.

[0051] In the formula (I), when more than two R.sub.3 exist, a plurality of the R.sub.3 may be separately identical or different.

[0052] In the formula (I), when more than two substituents exist, a plurality of the substituents may be separately identical or different.

[0053] Preferably, the number of the R.sub.1, the R.sub.2, and the R.sub.3 is a single substitution number.

[0054] More preferably, the compound has the following structure:

##STR00086##

[0055] Examples of groups of the compound as shown in the formula (I) are described below.

[0056] It should be noted that in the specification, “C.sub.a-C.sub.b” in the term “substituted or unsubstituted C.sub.a-C.sub.b X group” refers to the number of carbons when the X group is unsubstituted, excluding the number of carbons of a substituent when the X group is substituted.

[0057] As a linear or branched alkyl, the C.sub.1-C.sub.10 alkyl specifically includes methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl and isomers thereof, n-hexyl and isomers thereof, n-heptyl and isomers thereof, n-octyl and isomers thereof, n-nonyl and isomers thereof, and n-decyl and isomers thereof, preferably methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, sec-butyl, and tert-butyl, and more preferably propyl, isopropyl, isobutyl, sec-butyl, and tert-butyl.

[0058] The C.sub.3-C.sub.20 cycloalkyl may include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, 1-adamantyl, 2-adamantyl, 1-norbornyl, and 2-norbornyl, preferably cyclopentyl and cyclohexyl.

[0059] The C.sub.2-C.sub.10 alkenyl may include vinyl, propenyl, allyl, 1-butadienyl, 2-butadienyl, 1-hexatrienyl, 2-hexatrienyl, and 3-hexatrienyl, preferably propenyl and allyl.

[0060] As a linear or branched alkyl consisting of atoms other than carbon and hydrogen, the C.sub.1-C.sub.10 heteroalkyl may include mercaptomethyl methyl, methoxymethyl, ethoxymethyl, tert-butoxyl methyl, N,N-dimethyl methyl, epoxy butyl, epoxy pentyl, and epoxy hexyl, preferably methoxymethyl and epoxy pentyl.

[0061] Specific examples of the aryl include phenyl, naphthyl, anthracyl, phenanthryl, tetracenyl, pyrenyl, chrysenyl, benzo[c]phenanthryl, benzo[g]chrysenyl, fluorenyl, benzofluorenyl, dibenzofluorenyl, biphenyl, triphenyl, tetraphenyl, and fluoranthracyl, preferably phenyl and naphthyl.

[0062] Specific examples of the heteroaryl may include pyrrolyl, pyrazinyl, pyridyl, pyrimidinyl, triazinyl, indolyl, isoindolyl, imidazolyl, furyl, benzofuryl, isobenzofuryl, dibenzofuryl, dibenzothienyl, azodibenzofuryl, azodibenzothienyl, diazodibenzofuryl, diazodibenzothienyl, quinolyl, isoquinolyl, quinoxalinyl, carbazolyl, phenanthridinyl, acridinyl, phenanthrolinyl, phenazinyl, phenothiazinyl, phenoxazinyl, oxazolinyl, oxadiazolyl, furzanyl, thienyl, benzothienyl, dihydroacridinyl, azocarbazolyl, diazocarbazolyl, and quinazolinyl, preferably pyridyl, pyrimidinyl, triazinyl, dibenzofuryl, dibenzothienyl, azodibenzofuryl, azodibenzothienyl, diazodibenzofuryl, diazodibenzothienyl, carbazolyl, azocarbazolyl, and diazocarbazolyl.

[0063] The following embodiments are merely described to facilitate the understanding of the technical invention, and should not be considered as specific limitations of the present invention.

[0064] All raw materials, solvents and the like involved in the synthesis of compounds in the present invention were purchased from Alfa, Acros, and other suppliers known to persons skilled in the art.

Example 1 Synthesis of a Compound CPD 1

[0065] Synthesis of a Common Intermediate Compound B1:

##STR00087##

[0066] A compound B1-1 (49.0 g, 169.4 mmol, 1.0 eq), bis(pinacolato)diboron (51.6 g, 203.3 mmol, 1.2 eq), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (2.48 g, 3.39 mmol, 0.02 eq), potassium acetate (33.2 g, 338.9 mmol, 2.0 eq), and dioxane (500 ml) were sequentially added into a 1 L three-mouth flask under vacuumization and the replacement of nitrogen for 3 times. A mixture obtained was heated to about 100° C. in an oil bath, stirred for 16 hours, and then sampled. According to monitoring by TLC, the raw material B1-1 was reacted completely. The mixture was cooled to room temperature, transferred into a 1 L one-mouth flask in batches, and subjected to rotary evaporation to remove most of the dioxane. Then, toluene (300 ml) was added, and heated for dissolution, and deionized water was added for water washing for 3 times (100 ml/time). After liquid separation, an organic phase was filtered with silica gel (200-300 mesh, 30 g), and washed with toluene (100 ml). The organic phase was concentrated to about 80 ml, and n-hexane (160 ml) was added, and stirred at room temperature for crystallization for 4 hours. After filtration was conducted, a filter cake was rinsed with n-hexane (40 ml) to obtain a product. The product obtained was dried to obtain 44.7 g of a white-like solid compound B1 with a yield of 78.5%. Mass spectrometry was as follows: 337.2 (M+H).

[0067] Synthesis of a Common Ligand Compound L1:

##STR00088##

[0068] Synthesis of a Compound L1-3:

[0069] A compound L1-1 (42.1 g, 173.61 mmol, 1.0 eq), a compound L1-2 (27.21 g, 243.05 mmol, 1.4 eq), dichlorobis[di-tert-butyl(4-dimethylaminophenyl)phosphino]palladium(II) (1.23 g, 1.74 mmol, 0.01 eq), anhydrous K.sub.3PO.sub.4 (73.7 g, 347.22 mmol, 2.0 eq), and toluene (505 ml) were sequentially added into a 1 L three-mouth flask under vacuumization and the replacement of nitrogen for 3 times. A mixture obtained was heated to about 80° C. in an oil bath, stirred for 16 hours, and then sampled. According to monitoring by TLC, the raw material L1-1 was basically reacted completely. The mixture was cooled to room temperature. Ethyl acetate (250 ml) was added into the reaction flask, and deionized water was added for water washing for 3 times (150 ml/time). After liquid separation, an organic phase was concentrated under reduced pressure to obtain a solid. A crude product was separated by column chromatography (with a mixture of EA and Hex at a ratio of 1:10) to obtain a product. The product obtained was dried to obtain 27.4 g of a white-like solid compound L1-3 with a yield of 68.71%. Mass spectrometry was as follows: 230.7 (M+H)

[0070] Synthesis of a Compound L1-4:

[0071] The compound L1-3 (25.5 g, 111.01 mmol, 1.0 eq), the compound B1 (41.06 g, 122.11 mmol, 1.1 eq), dichlorobis[di-tert-butyl(4-dimethylaminophenyl)phosphino]palladium(II) (0.78 g, 1.11 mmol, 0.01 eq), sodium carbonate (23.53 g, 222.02 mmol, 2.0 eq), tetrahydrofuran (250 ml), and deionized water (62 ml) were sequentially added into a 500 ml three-mouth flask under vacuumization and the replacement of nitrogen for 3 times. A mixture obtained was heated to about 60° C. in an oil bath, stirred for 2 hours, and then sampled. According to monitoring by TLC, the raw material L1-3 was basically reacted completely. The mixture was cooled to room temperature. A reaction solution was transferred into a 1 L one-mouth flask. Ethyl acetate (300 ml) was added, and deionized water was added for water washing for 3 times (150 ml/time). After liquid separation, an organic phase was concentrated under reduced pressure to obtain a solid. A crude product was recrystallized with toluene and methanol (a ratio of the crude product to the toluene to the methanol was 1:5:20) to obtain a product. The product obtained was dried to obtain 35.97 g of a white solid compound L1-4 with a yield of 80.3%. Mass spectrometry was as follows: 404.5 (M+H)

[0072] Synthesis of a Compound L1:

[0073] The compound L1-4 (32.0 g, 79.3 mmol, 1.0 eq), 10% palladium carbon (8.44 g, 7.93 mmol, 0.1 eq), and a mixed solvent of tetrahydrofuran (64 ml) and ethanol (96 ml) were sequentially added into a 250 ml one-mouth flask. H.sub.2 was introduced into the reaction flask. A mixture obtained was heated to about 40° C. in an oil bath, stirred for 24 hours, and then sampled. According to monitoring by TLC, the raw material L1-4 was basically reacted completely. The mixture was cooled to room temperature. After a reaction solution was directly filtered, a filtrate was collected, concentrated, and dried. A crude product was separated by column chromatography (with a mixture of EA and Hex at a ratio of 1:8) to obtain a product. The product obtained was dried to obtain 25.47 g of a white-like solid compound L1 with a yield of 79.2%. Mass spectrometry was as follows: 406.5 (M+H). .sup.1HNMR (400 MHz, CDCl.sub.3) δ8.64 (d, J=5.7 Hz, 1H), 7.93 (d, J=7.4 Hz, 1H), 7.85 (s, 1H), 7.70 (d, J=7.9 Hz, 2H), 7.68-7.55 (m, 2H), 7.51 (s, 1H), 7.43-7.24 (m, 3H), 2.94 (s, 1H), δ2.87 (s, 1H), 2.00 (m, 2H), 1.71 (m, J=25.0 Hz, 6H), 1.20 (d, 6H).

[0074] Synthesis of a Compound CPD 1:

##STR00089##

[0075] Synthesis of a Common Intermediate Compound CPD1-1:

[0076] The compound L1 (24.7 g, 60.91 mmol, 3.0 eq) and IrCl.sub.3.Math.3H.sub.2O (6.83 g, 20.3 mmol, 1.0 eq) were put into a 500 ml three-mouth flask, and then 2-ethoxyethanol (247 ml) and deionized water (82.3 ml) were added. A mixture obtained was stirred for reflux at 110° C. for 16 hours under the protection of Na. The mixture was cooled to room temperature, and filtered. A filter residue was sequentially washed with methanol (100 ml*3) and n-hexane (100 ml*3), and then dried to obtain 22.03 g of a compound CPD1-1 with a yield of 88.3%. The obtained compound was directly used in the next step without purification.

[0077] Synthesis of a Compound CPD 1:

[0078] The compound CPD1-1 (8.75 g, 7.12 mmol, 1.0 eq) was dissolved in 2-ethoxyethanol (87.5 ml), and then anhydrous sodium carbonate (7.55 g, 71.2 mmol, 10.0 eq) and a compound A1 (3.65 g, 35.6 mmol, 5.0 eq) were sequentially added. After the addition was completed, a mixture obtained was stirred at 40° C. for 16 hours under the protection of N.sub.2, and then cooled to room temperature. Sampling was conducted. According to monitoring by TLC, a red product point was produced. Methanol (87.5 ml) was added into a reaction solution, and stirred to precipitate out a red solid. After filtration was conducted, a solid was collected. The solid was dissolved in dichloromethane (150 ml) for clarification, and filtered with silica gel. A filter cake was rinsed with a small amount of dichloromethane. A filtrate was collected. Deionized water was added for water washing for 3 times (60 ml/time). After liquid separation, an organic phase was concentrated under reduced pressure to obtain a solid. The solid was recrystallized with tetrahydrofuran and methanol (a ratio of the crude product to the tetrahydrofuran to the methanol was 1:5:7) for 3 times to obtain a product. The product obtained was dried to obtain 4.83 g of a target compound CPD 1 with a yield of 61.7%. 4.83 g of the crude product CPD 1 was sublimated and purified to obtain 3.32 g of a sublimated pure product CPD 1 with a yield of 68.73%. Mass spectrometry was as follows: 1101.37 (M+H).

Example 2 Synthesis of a Compound CPD 3

[0079] ##STR00090##

[0080] With reference to the synthesis process and post-treatment and purification methods of the compound CPD 1, only the corresponding raw materials were required to be changed, and 4.64 g of a target compound CPD 3 with a yield of 58.81% was obtained. 4.64 g of the crude product CPD 3 was sublimated and purified to obtain 3.26 g of a sublimated pure product CPD 3 with a yield of 70.25%. Mass spectrometry was as follows: 1213.5 (M+H).

Example 3 Synthesis of a Compound CPD 8

[0081] Synthesis of a Common Ligand Compound L4:

##STR00091##

[0082] Synthesis of a Compound B2:

[0083] With reference to the synthesis process and post-treatment and purification methods of the compound B1, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 351.3 (M+H).

[0084] Synthesis of a Compound L4-2:

[0085] With reference to the synthesis process and post-treatment and purification methods of the compound L1-4, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 418.5 (M+H).

[0086] Synthesis of a Compound L4:

[0087] With reference to the synthesis process and post-treatment and purification methods of the compound L1, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 420.6 (M+H). .sup.1HNMR (400 MHz, CDCl.sub.3) δ8.64 (d, J=5.7 Hz, 1H), 7.94 (d, J=7.4 Hz, 1H), 7.86 (s, 1H), 7.70 (d, J=7.9 Hz, 2H), 7.68-7.55 (m, 2H), 7.51 (s, 1H), 7.43-7.24 (m, 3H), 2.92 (s, 1H), 1.98 (d, J=7.0 Hz, 2H), 1.72 (dd, J=28.5, 21.5 Hz, 6H), 1.32 (s, 9H).

[0088] Synthesis of a Compound CPD 8:

##STR00092##

[0089] Synthesis of a Compound CPD8-1:

[0090] With reference to the synthesis process and post-treatment and purification methods of the compound CPD1-1, only the corresponding raw materials were required to be changed. The obtained compound was directly used in the next step without purification.

[0091] Synthesis of a Compound CPD 8:

[0092] With reference to the synthesis process and post-treatment and purification methods of the compound CPD 1, only the corresponding raw materials were required to be changed, and 3.77 g of a target compound CPD 8 with a yield of 60.3% was obtained. 3.77 g of the crude product CPD 8 was sublimated and purified to obtain 2.87 g of a sublimated pure product CPD 8 with a yield of 76.12%. Mass spectrometry was as follows: 1185.5 (M+H).

Example 4 Synthesis of a Compound CPD 21

[0093] Synthesis of a Common Ligand Compound L6:

##STR00093##

[0094] Synthesis of a Compound B3:

[0095] With reference to the synthesis process and post-treatment and purification methods of the compound B1, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 351.3 (M+H).

[0096] Synthesis of a Compound L6-1:

[0097] With reference to the synthesis process and post-treatment and purification methods of the compound L1-4, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 418.5 (M+H).

[0098] Synthesis of a Compound L6:

[0099] With reference to the synthesis process and post-treatment and purification methods of the compound L1, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 420.6 (M+H). .sup.1HNMR (400 MHz, CDCl.sub.3) δ8.65 (d, J=5.7 Hz, 1H), 7.95 (d, J=7.4 Hz, 1H), 7.86 (s, 1H), 7.70 (d, J=7.9 Hz, 2H), 7.68-7.55 (m, 2H), 7.51 (s, 1H), 7.43-7.24 (m, 3H), 2.85 (dt, 1H), 2.43 (d, 2H), 2.00 (m, 2H), 1.82 (dq, 1H), 1.79-1.60 (m, 6H), 0.87 (d, 6H).

[0100] Synthesis of a Compound CPD 21:

##STR00094##

[0101] Synthesis of a Compound CPD21-1:

[0102] With reference to the synthesis process and post-treatment and purification methods of the compound CPD1-1, only the corresponding raw materials were required to be changed. The obtained compound was directly used in the next step without purification.

[0103] Synthesis of a Compound CPD 21:

[0104] With reference to the synthesis process and post-treatment and purification methods of the compound CPD 1, only the corresponding raw materials were required to be changed, and 4.11 g of a target compound CPD 21 with a yield of 62.3% was obtained. 4.11 g of the crude product CPD 21 was sublimated and purified to obtain 2.94 g of a sublimated pure product CPD 21 with a yield of 71.53%. Mass spectrometry was as follows: 1241.6 (M+H).

Example 5 Synthesis of a Compound CPD 27

[0105] Synthesis of a Common Intermediate Compound B4:

##STR00095##

[0106] With reference to the synthesis process and post-treatment and purification methods of the compound B1, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 337.2 (M+H).

[0107] Synthesis of a Common Intermediate Compound L4:

##STR00096##

[0108] Synthesis of a Compound L7-2:

[0109] With reference to the synthesis process and post-treatment and purification methods of the compound L1-3, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 206.7 (M+H).

[0110] Synthesis of a Compound L7:

[0111] With reference to the synthesis process and post-treatment and purification methods of the compound L1-4, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 380.5 (M+H). .sup.1HNMR (400 MHz, CDCl3) δ8.66 (d, J=5.7 Hz, 1H), 7.98 (d, J=7.4 Hz, 1H), 7.89 (s, 1H), 7.80-7.67 (m, 3H), 7.50 (s, 1H), 7.37 (dq, J=13.9, 6.2 Hz, 4H), 3.11 (dt, J=13.7, 6.8 Hz, 1H), 2.87 (dt, 1H), 2.60 (s, 3H), 1.36 (d, J=6.9 Hz, 6H), 1.20 (d, 6H).

[0112] Synthesis of a Compound CPD 27:

##STR00097##

[0113] Synthesis of a Compound CPD27-1:

[0114] With reference to the synthesis process and post-treatment and purification methods of the compound CPD1-1, only the corresponding raw materials were required to be changed. The obtained compound was directly used in the next step without purification.

[0115] Synthesis of a Compound CPD 27:

[0116] With reference to the synthesis process and post-treatment and purification methods of the compound CPD 1, only the corresponding raw materials were required to be changed, and 4.35 g of a target compound CPD 27 with a yield of 57.6% was obtained. 4.35 g of the crude product CPD 27 was sublimated and purified to obtain 3.01 g of a sublimated pure product CPD 27 with a yield of 69.19%. Mass spectrometry was as follows: 1161.5 (M+H).

Example 6 Synthesis of a Compound CPD 28

[0117] ##STR00098##

[0118] With reference to the synthesis process and post-treatment and purification methods of the compound CPD 1, only the corresponding raw materials were required to be changed, and 3.52 g of a target compound CPD 28 with a yield of 54.71% was obtained. 3.52 g of the crude product CPD 28 was sublimated and purified to obtain 2.47 g of a sublimated pure product CPD 28 with a yield of 70.17%. Mass spectrometry was as follows: 1133.5 (M+H).

Example 7 Synthesis of a Compound CPD 33

[0119] Synthesis of a Common Intermediate Compound L9:

##STR00099##

[0120] Synthesis of a Compound L9-2:

[0121] With reference to the synthesis process and post-treatment and purification methods of the compound L1-3, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 220.7 (M+H).

[0122] Synthesis of a Compound L9:

[0123] With reference to the synthesis process and post-treatment and purification methods of the compound L1-4, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 394.5 (M+H). .sup.1HNMR (400 MHz, CDCl3) δ8.67 (d, J=5.7 Hz, 1H), 7.99 (d, J=7.4 Hz, 1H), 7.89 (s, 1H), 7.75 (d, J=8.6 Hz, 1H), 7.72-7.63 (m, 2H), 7.52 (s, 1H), 7.40 (d J=5.4 Hz, 2H), 7.36-7.27 (m, 2H), 2.87 (m, 1H), 2.68 (d, J=7.2 Hz, 2H), 2.01 (m, 1H), 1.20 (d, 6H), 0.97 (d, J=6.6 Hz, 6H).

[0124] Synthesis of a Compound CPD 33:

##STR00100##

[0125] Synthesis of a Compound CPD33-1:

[0126] With reference to the synthesis process and post-treatment and purification methods of the compound CPD1-1, only the corresponding raw materials were required to be changed. The obtained compound was directly used in the next step without purification.

[0127] Synthesis of a Compound CPD 33:

[0128] With reference to the synthesis process and post-treatment and purification methods of the compound CPD 1, only the corresponding raw materials were required to be changed, and 3.77 g of a target compound CPD 33 with a yield of 57.6% was obtained. 3.77 g of the crude product CPD 33 was sublimated and purified to obtain 2.69 g of a sublimated pure product CPD 33 with a yield of 71.35%. Mass spectrometry was as follows: 1189.6 (M+H).

Example 8 Synthesis of a Compound CPD 39

[0129] Synthesis of a Common Intermediate Compound L10:

##STR00101##

[0130] Synthesis of a Compound B5:

[0131] With reference to the synthesis process and post-treatment and purification methods of the compound B1, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 361.3 (M+H).

[0132] Synthesis of a Compound L10-1:

[0133] With reference to the synthesis process and post-treatment and purification methods of the compound L1-4, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 428.5 (M+H).

[0134] Synthesis of a Compound L10:

[0135] With reference to the synthesis process and post-treatment and purification methods of the compound L1, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 432.6 (M+H). .sup.1HNMR (400 MHz, CDCl.sub.3) δ8.67 (d, J=5.7 Hz, 1H), 7.99 (d, J=7.4 Hz, 1H), 7.89 (s, 1H), 7.75 (d, J=8.6 Hz, 1H), 7.72-7.63 (m, 2H), 7.52 (s, 1H), 7.40 (d J=5.4 Hz, 2H), 7.36-7.27 (m, 2H), 2.87 (m, 1H), 3.00 (m, 1H), 2.84 (m, 1H), 2.14-1.88 (m, 4H), 1.86-1.56 (m, 12H).

[0136] Synthesis of a Compound CPD 39:

##STR00102##

[0137] Synthesis of a Compound CPD39-1:

[0138] With reference to the synthesis process and post-treatment and purification methods of the compound CPD1-1, only the corresponding raw materials were required to be changed. The obtained compound was directly used in the next step without purification.

[0139] Synthesis of a Compound CPD 39:

[0140] With reference to the synthesis process and post-treatment and purification methods of the compound CPD 1, only the corresponding raw materials were required to be changed, and 3.96 g of a target compound CPD 39 with a yield of 60.71% was obtained. 3.96 g of the crude product CPD 39 was sublimated and purified to obtain 3.74 g of a sublimated pure product CPD 39 with a yield of 69.19%. Mass spectrometry was as follows: 1265.6 (M+H).

Example 9 Synthesis of a Compound CPD 75

[0141] Synthesis of a Common Intermediate Compound L11:

##STR00103##

[0142] Synthesis of a Compound L11-2:

[0143] With reference to the synthesis process and post-treatment and purification methods of the compound L1-3, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 262.8 (M+H).

[0144] Synthesis of a Compound L11:

[0145] With reference to the synthesis process and post-treatment and purification methods of the compound L1-4, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 436.6 (M+H). .sup.1HNMR (400 MHz, CDCl3) δ8.68 (d, J=5.7 Hz, 1H), 7.98 (d, J=7.4 Hz, 1H), 7.89 (s, 1H), 7.76 (d, J=8.6 Hz, 1H), 7.72-7.63 (m, 2H), 7.52 (s, 1H), 7.40 (d J=5.4 Hz, 2H), 7.36-7.27 (m, 2H), 2.97 (m, 1H), 2.87 (m, 1H), 2.68 (d, J=7.2 Hz, 2H), 2.01 (m, 1H), 1.20 (m, 12H), 0.97 (d, J=6.6 Hz, 6H).

[0146] Synthesis of a Compound CPD 75:

##STR00104##

[0147] Synthesis of a Compound CPD75-1:

[0148] With reference to the synthesis process and post-treatment and purification methods of the compound CPD1-1, only the corresponding raw materials were required to be changed. The obtained compound was directly used in the next step without purification.

[0149] Synthesis of a Compound CPD 75:

[0150] With reference to the synthesis process and post-treatment and purification methods of the compound CPD 1, only the corresponding raw materials were required to be changed, and 4.17 g of a target compound CPD 75 with a yield of 61.81% was obtained. 4.17 g of the crude product CPD 75 was sublimated and purified to obtain 2.94 g of a sublimated pure product CPD 75 with a yield of 70.5%. Mass spectrometry was as follows: 1273.6 (M+H).

Example 10 Synthesis of a Compound CPD 93

[0151] Synthesis of a Common Intermediate Compound L12:

##STR00105##

[0152] Synthesis of a Compound B6:

[0153] With reference to the synthesis process and post-treatment and purification methods of the compound B1, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 309.2 (M+H).

[0154] Synthesis of a Compound L12:

[0155] With reference to the synthesis process and post-treatment and purification methods of the compound L1-4, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 366.5 (M+H). .sup.1HNMR (400 MHz, CDCl.sub.3) δ8.67 (d, J=5.7 Hz, 1H), 7.99 (d, J=7.4 Hz, 1H), 7.89 (s, 1H), 7.75 (d, J=8.6 Hz, 1H), 7.72-7.63 (m, 2H), 7.52 (s, 1H), 7.40 (d J=5.4 Hz, 2H), 7.36-7.27 (m, 2H), 2.68 (d, J=7.2 Hz, 2H), 2.60 (s, 3H), 2.01 (m, 1H), 0.97 (d, J=6.6 Hz, 6H). The compound is as shown in FIG. 1.

[0156] Synthesis of a Compound CPD 93:

##STR00106##

[0157] Synthesis of a Compound CPD93-1:

[0158] With reference to the synthesis process and post-treatment and purification methods of the compound CPD1-1, only the corresponding raw materials were required to be changed. The obtained compound was directly used in the next step without purification.

[0159] Synthesis of a Compound CPD 93:

[0160] With reference to the synthesis process and post-treatment and purification methods of the compound CPD 1, only the corresponding raw materials were required to be changed, and 3.55 g of a target compound CPD 93 with a yield of 54.8% was obtained. 3.55 g of the crude product CPD 93 was sublimated and purified to obtain 2.23 g of a sublimated pure product CPD 93 with a yield of 62.81%. Mass spectrometry was as follows: 1133.5 (M+H). As shown in FIG. 2, .sup.1HNMR (400 MHz, CDCl.sub.3) δ8.89 (d, J=8.8 Hz, 2H), 8.26 (d, J=6.4 Hz, 2H), 7.80 (d, J=7.5 Hz, 2H), 7.58 (s, 2H), 7.48 (dd, J=15.7, 8.5 Hz, 4H), 7.39-7.31 (m, 3H), 7.31-7.19 (m, 5H), 4.81 (s, 1H), 2.76 (dd, J=14.3, 7.1 Hz, 5H), 2.21-2.01 (m, 4H), 1.76-1.41 (m, 12H), 1.20-0.92 (m, 11H), 0.78 (dd, J=17.0, 9.6 Hz, 3H), 0.47 (t, J=7.4 Hz, 5H), 0.01 (s, 2H), −0.16 (t, J=7.4 Hz, 4H).

Example 11 Synthesis of a Compound CPD 99

[0161] Synthesis of a Common Intermediate Compound L13:

##STR00107##

[0162] Synthesis of a Compound L13-2:

[0163] With reference to the synthesis process and post-treatment and purification methods of the compound L1-3, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 260.7 (M+H).

[0164] Synthesis of a Compound L13:

[0165] With reference to the synthesis process and post-treatment and purification methods of the compound L1-4, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 406.4 (M+H). .sup.1HNMR (400 MHz, CDCl3) δ8.69 (d, J=5.7 Hz, 1H), 8.01 (d, J=7.4 Hz, 1H), 7.90 (s, 1H), 7.76 (d, J=8.6 Hz, 1H), 7.73-7.64 (m, 2H), 7.52 (s, 1H), 7.41 (d, J=5.4 Hz, 2H), 7.38-7.28 (m, 2H), 2.93 (t, 3H), 2.46 (t, 3H), 2.31 (s, 3H).

[0166] Synthesis of a Compound CPD 99:

##STR00108##

[0167] Synthesis of a Compound CPD99-1:

[0168] With reference to the synthesis process and post-treatment and purification methods of the compound CPD1-1, only the corresponding raw materials were required to be changed. The obtained compound was directly used in the next step without purification.

[0169] Synthesis of a Compound CPD 99:

[0170] With reference to the synthesis process and post-treatment and purification methods of the compound CPD 1, only the corresponding raw materials were required to be changed, and 3.79 g of a target compound CPD 99 with a yield of 57.8% was obtained. 3.79 g of the crude product CPD 99 was sublimated and purified to obtain 2.44 g of a sublimated pure product CPD 99 with a yield of 64.37%. Mass spectrometry was as follows: 1213.4 (M+H).

Example 12 Synthesis of a Compound CPD 121

[0171] Synthesis of a Common Intermediate Compound L14:

##STR00109##

[0172] Synthesis of a Compound L14-1:

[0173] With reference to the synthesis process and post-treatment and purification methods of the compound L1-4, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 376.5 (M+H).

[0174] Synthesis of a Compound L14:

[0175] With reference to the synthesis process and post-treatment and purification methods of the compound L1, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 378.5 (M+H). .sup.1HNMR (400 MHz, CDCl.sub.3) δ8.65 (d, J=5.7 Hz, 1H), 7.94 (d, J=7.4 Hz, 1H), 7.86 (s, 1H), 7.72 (d, J=7.9 Hz, 2H), 7.69-7.56 (m, 2H), 7.52 (s, 1H), 7.44-7.25 (m, 3H), 2.96 (s, 1H), 2.31 (s, 3H), 1.96 (s, 2H), 1.72 (t, J=25.0 Hz, 6H). The compound is as shown in FIG. 3.

[0176] Synthesis of a Compound CPD 121:

##STR00110##

[0177] Synthesis of a Compound CPD121-1:

[0178] With reference to the synthesis process and post-treatment and purification methods of the compound CPD1-1, only the corresponding raw materials were required to be changed. The obtained compound was directly used in the next step without purification.

[0179] Synthesis of a Compound CPD 121:

[0180] With reference to the synthesis process and post-treatment and purification methods of the compound CPD 1, only the corresponding raw materials were required to be changed, and 4.05 g of a target compound CPD 121 with a yield of 59.3% was obtained. 4.05 g of the crude product CPD 121 was sublimated and purified to obtain 2.71 g of a sublimated pure product CPD 121 with a yield of 66.91%. Mass spectrometry was as follows: 1045.3 (M+H).

Example 13 Synthesis of a Compound CPD 123

[0181] ##STR00111##

[0182] With reference to the synthesis process and post-treatment and purification methods of the compound CPD 1, only the corresponding raw materials were required to be changed, and 3.97 g of a target compound CPD 123 with a yield of 61.1% was obtained. 3.97 g of the crude product CPD 123 was sublimated and purified to obtain 2.66 g of a sublimated pure product CPD 123 with a yield of 67.0%. Mass spectrometry was as follows: 1157.5 (M+H). As shown in FIG. 4, .sup.1HNMR (400 MHz, CDCl.sub.3) δ8.93 (d, J=8.9 Hz, 2H), 8.28 (d, J=6.3 Hz, 2H), 7.82 (d, J=7.5 Hz, 2H), 7.67 (s, 2H), 7.60 (dd, J=8.9, 1.6 Hz, 2H), 7.50 (d, J=8.0 Hz, 2H), 7.36 (d, J=7.5 Hz, 3H), 7.34-7.22 (m, 5H), 4.82 (s, 1H), 3.4-3.18 (m, 2H), 2.24 (s, 4H), 1.86 (dd, J=34.0, 16.9 Hz, 11H), 1.66 (s, 5H), 1.61-1.46 (m, 3H), 1.36-1.19 (m, 3H), 1.11 (dd, J=15.2, 9.7 Hz, 3H), 0.91-0.65 (m, 4H), 0.49 (t, J=7.4 Hz, 6H), −0.15 (t, J=7.4 Hz, 5H).

Example 14 Synthesis of a Compound CPD 145

[0183] ##STR00112##

[0184] Synthesis of a Compound L15:

[0185] The compound L14 (14.3 g, 37.88 mmol, 1.0 eq), sodium tert-butoxide (10.92 g, 113.65 mmol, 3 eq), and DMSO-d.sub.6 (172 ml) were sequentially added into a 250 ml one-mouth flask under vacuumization and the replacement of nitrogen for 3 times. A mixture obtained was heated to 75° C. in an oil bath, and stirred for 24 hours. The mixture was cooled to room temperature. Heavy water (35 ml) was added, and stirred for 10 minutes until a yellow solid was precipitated out, and then deionized water (350 ml) was added, and stirred for 10 minutes. After suction filtration was conducted, a yellow solid was collected. The solid was dissolved in ethyl acetate (450 ml), and deionized water was added for water washing for 3 times (200 ml/time). After liquid separation, aqueous phases were combined, and extracted with a small amount of ethyl acetate for one time. Organic phases were combined, concentrated, and dried. A crude product was separated by column chromatography (with a mixture of EA and Hex at a ratio of 1:8) to obtain a product. The product obtained was dried to obtain 12.8 g of a white solid compound L15 with a yield of 88.6%. Mass spectrometry was as follows: 382.5 (M+H). .sup.1HNMR (400 MHz, CDCl.sub.3) δ8.65 (d, J=5.7 Hz, 1H), 7.94 (d, J=7.4 Hz, 1H), 7.86 (s, 1H), 7.72 (d, J=7.9 Hz, 2H), 7.69-7.56 (m, 2H), 7.52 (s, 1H), 7.44-7.25 (m, 3H), 1.99 (m, 2H), 1.89-1.58 (m, 6H).

[0186] Synthesis of a Compound CPD145-1:

[0187] With reference to the synthesis process and post-treatment and purification methods of the compound CPD1-1, only the corresponding raw materials were required to be changed. The obtained compound was directly used in the next step without purification.

[0188] Synthesis of a Compound CPD 145:

[0189] With reference to the synthesis process and post-treatment and purification methods of the compound CPD 1, only the corresponding raw materials were required to be changed, and 3.62 g of a target compound CPD 145 with a yield of 53.7% was obtained. 3.62 g of the crude product CPD 145 was sublimated and purified to obtain 2.25 g of a sublimated pure product CPD 145 with a yield of 62.15%. Mass spectrometry was as follows: 1053.3 (M+H).

Example 15 Synthesis of a Compound CPD 147

[0190] ##STR00113##

[0191] With reference to the synthesis process and post-treatment and purification methods of the compound CPD 1, only the corresponding raw materials were required to be changed, and 3.55 g of a target compound CPD 147 with a yield of 54.4% was obtained. 3.55 g of the crude product CPD 147 was sublimated and purified to obtain 2.12 g of a sublimated pure product CPD 147 with a yield of 59.71%. Mass spectrometry was as follows: 1165.5 (M+H).

[0192] Synthesis of a Common Intermediate Compound L16:

##STR00114## ##STR00115##

[0193] Synthesis of a Compound L16-2:

[0194] With reference to the synthesis process and post-treatment and purification methods of the compound L1-3, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 244.7 (M+H).

[0195] Synthesis of a Compound L16-3:

[0196] With reference to the synthesis process and post-treatment and purification methods of the compound L1-4, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 390.4 (M+H).

[0197] Synthesis of a Compound L16-4:

[0198] The compound L16-3 (25 g, 64.19 mmol, 1.0 eq) and dichloromethane (150 ml) were sequentially added into a 500 ml one-mouth flask. The reaction system was cooled to about 0° C., and [bis(2-methoxyethyl)amino]sulfur trifluoride (BAST, 35.51 ml, 192.58 mmol, 3.0 eq) was slowly dropped. After the dropping was completed, a mixture obtained was stirred at room temperature for 16 hours, and then sampled. According to monitoring by TLC, the raw material L16-3 was basically reacted completely. A reaction solution was added into a saturated sodium carbonate solution (450 ml), stirred for 0.5 hour, and subjected to standing for liquid separation. Dichloromethane (150 ml) was added into an aqueous layer for extraction for 1 time, and organic phases were combined. Deionized water was added for water washing for 3 times (100 ml/time). After liquid separation, an organic phase was concentrated, and dried. A crude product was separated by column chromatography (with a mixture of EA and Hex at a ratio of 1:10) to obtain a product. The product obtained was dried to obtain 19.28 g of a white solid compound L16-4 with a yield of 73%. Mass spectrometry was as follows: 412.4 (M+H).

[0199] Synthesis of a Compound L16:

[0200] With reference to the synthesis process and post-treatment and purification methods of the compound L1, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 414.5 (M+H). .sup.1HNMR (400 MHz, CDCl3) δ8.65 (d, J=5.7 Hz, 1H), 7.94 (d, J=7.4 Hz, 1H), 7.86 (s, 1H), 7.72 (d, J=7.9 Hz, 2H), 7.69-7.56 (m, 2H), 7.52 (s, 1H), 7.44-7.25 (m, 3H), 3.26 (d, 1H), 2.44 (m, 1H), 2.32 (s, 3H), 2.03 (m, J=28.1, 24.1 Hz, 4H), 1.76 (m, 1H).

Example 16 Synthesis of a Compound CPD 175

[0201] ##STR00116##

[0202] Synthesis of a Compound CPD175-1:

[0203] With reference to the synthesis process and post-treatment and purification methods of the compound CPD1-1, only the corresponding raw materials were required to be changed. The obtained compound was directly used in the next step without purification.

[0204] Synthesis of a Compound CPD 175:

[0205] With reference to the synthesis process and post-treatment and purification methods of the compound CPD 1, only the corresponding raw materials were required to be changed, and 3.77 g of a target compound CPD 175 with a yield of 51.5% was obtained. 3.77 g of the crude product CPD 175 was sublimated and purified to obtain 2.44 g of a sublimated pure product CPD 175 with a yield of 64.72%. Mass spectrometry was as follows: 1117.3 (M+H).

Example 17 Synthesis of a Compound CPD 177

[0206] ##STR00117##

[0207] With reference to the synthesis process and post-treatment and purification methods of the compound CPD 1, only the corresponding raw materials were required to be changed, and 3.61 g of a target compound CPD 177 with a yield of 52.7% was obtained. 3.61 g of the crude product CPD 177 was sublimated and purified to obtain 2.37 g of a sublimated pure product CPD 177 with a yield of 65.65%. Mass spectrometry was as follows: 1229.4 (M+H).

Example 18 Synthesis of a Compound CPD 247

[0208] ##STR00118##

[0209] Synthesis of a Compound L17:

[0210] With reference to the synthesis process and post-treatment and purification methods of the compound L1-4, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 352.4 (M+H). .sup.1HNMR (400 MHz, CDCl3) δ8.66 (d, J=5.7 Hz, 1H), 7.98 (d, J=7.4 Hz, 1H), 7.89 (s, 1H), 7.80-7.67 (m, 3H), 7.50 (s, 1H), 7.37 (dq, J=13.9, 6.2 Hz, 4H), 3.11 (dt, J=13.7, 6.8 Hz, 1H), 2.60 (s, 3H), 1.36 (d, J=6.9 Hz, 6H). The compound is as shown in FIG. 5.

[0211] Synthesis of a Compound CPD247-1:

[0212] With reference to the synthesis process and post-treatment and purification methods of the compound CPD1-1, only the corresponding raw materials were required to be changed. The obtained compound was directly used in the next step without purification.

[0213] Synthesis of a Compound CPD 247:

[0214] With reference to the synthesis process and post-treatment and purification methods of the compound CPD 1, only the corresponding raw materials were required to be changed, and 3.23 g of a target compound CPD 247 with a yield of 48.9% was obtained. 3.23 g of the crude product CPD 247 was sublimated and purified to obtain 2.03 g of a sublimated pure product CPD 247 with a yield of 62.84%. Mass spectrometry was as follows: 993.2 (M+H).

Example 19 Synthesis of a Compound CPD 249

[0215] ##STR00119##

[0216] With reference to the synthesis process and post-treatment and purification methods of the compound CPD 1, only the corresponding raw materials were required to be changed, and 3.51 g of a target compound CPD 249 with a yield of 50.7% was obtained. 3.51 g of the crude product CPD 249 was sublimated and purified to obtain 2.17 g of a sublimated pure product CPD 249 with a yield of 61.82%. Mass spectrometry was as follows: 1105.4 (M+H). As shown in FIG. 6, .sup.1HNMR (400 MHz, CDCl3) δ8.89 (d, J=8.8 Hz, 2H), 8.26 (d, J=6.4 Hz, 2H), 7.79 (d, J=7.5 Hz, 2H), 7.58 (s, 2H), 7.48 (dd, J=15.7, 8.5 Hz, 5H), 7.37-7.30 (m, 4H), 7.28 (d, J=5.8 Hz, 2H), 4.80 (s, 1H), 2.75 (qd, J=13.2, 7.2 Hz, 4H), 2.10 (dt, J=13.5, 6.7 Hz, 2H), 1.63 (s, 6H), 1.61-1.48 (m, 12H), 1.09-0.98 (m, 12H), 0.46 (t, J=7.4 Hz, 6H).

[0217] Synthesis of a Common Intermediate Compound L18:

##STR00120##

[0218] Synthesis of a Compound B7:

[0219] With reference to the synthesis process and post-treatment and purification methods of the compound B1, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 324.2 (M+H).

[0220] Synthesis of a Compound L18:

[0221] With reference to the synthesis process and post-treatment and purification methods of the compound L1-4, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 367.5 (M+H). .sup.1HNMR (400 MHz, CDCl3) δ8.4 (d, 1H), 7.81 (dd, 1H), 7.74 (dd, 1H), 7.71 (s, 1H), 7.50 (s, 1H), 7.27-7.36 (m, 3H), 7.1 (d, 1H), 3.12 (q, 1H), 2.55 (s, 3H), 2.35 (s, 3H), 1.29 (d, 6H).

Example 20 Synthesis of a Compound CPD 253

[0222] ##STR00121##

[0223] Synthesis of a Compound CPD253-1:

[0224] With reference to the synthesis process and post-treatment and purification methods of the compound CPD1-1, only the corresponding raw materials were required to be changed. The obtained compound was directly used in the next step without purification.

[0225] Synthesis of a Compound CPD 253:

[0226] With reference to the synthesis process and post-treatment and purification methods of the compound CPD 1, only the corresponding raw materials were required to be changed, and 4.13 g of a target compound CPD 253 with a yield of 56.3% was obtained. 4.13 g of the crude product CPD 253 was sublimated and purified to obtain 2.78 g of a sublimated pure product CPD 253 with a yield of 67.3%. Mass spectrometry was as follows: 1023.3 (M+H).

Example 21 Synthesis of a Compound CPD 256

[0227] ##STR00122##

[0228] With reference to the synthesis process and post-treatment and purification methods of the compound CPD 1, only the corresponding raw materials were required to be changed, and 4.02 g of a target compound CPD 256 with a yield of 58.1% was obtained. 4.02 g of the crude product CPD 256 was sublimated and purified to obtain 2.67 g of a sublimated pure product CPD 256 with a yield of 66.41%. Mass spectrometry was as follows: 1107.4 (M+H).

Example 22 Synthesis of a Compound CPD 309

[0229] ##STR00123##

[0230] Synthesis of a Compound L19:

[0231] With reference to the synthesis process and post-treatment and purification methods of the compound L1-4, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 366.5 (M+H). .sup.1HNMR (400 MHz, CDCl3) δ8.65 (d, J=5.7 Hz, 1H), 7.97 (d, J=7.4 Hz, 1H), 7.88 (s, 1H), 7.80-7.67 (m, 3H), 7.50 (s, 1H), 7.37 (dq, J=13.9, 6.2 Hz, 4H), 2.60 (s, 3H), 1.43 (s, 9H).

[0232] Synthesis of a Compound CPD309-1:

[0233] With reference to the synthesis process and post-treatment and purification methods of the compound CPD1-1, only the corresponding raw materials were required to be changed. The obtained compound was directly used in the next step without purification.

[0234] Synthesis of a Compound CPD 309:

[0235] With reference to the synthesis process and post-treatment and purification methods of the compound CPD 1, only the corresponding raw materials were required to be changed, and 3.08 g of a target compound CPD 309 with a yield of 47.8% was obtained. 3.08 g of the crude product CPD 309 was sublimated and purified to obtain 1.89 g of a sublimated pure product CPD 309 with a yield of 61.36%. Mass spectrometry was as follows: 1133.5 (M+H).

Example 23 Synthesis of a Compound CPD 315

[0236] ##STR00124##

[0237] Synthesis of a Compound L20:

[0238] With reference to the synthesis process and post-treatment and purification methods of the compound L1-4, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 394.5 (M+H). .sup.1HNMR (400 MHz, CDCl3) δ8.65 (d, J=5.7 Hz, 1H), 7.99 (d, J=7.4 Hz, 1H), 7.88 (s, 1H), 7.80-7.67 (m, 3H), 7.50 (s, 1H), 7.37 (dq, J=13.9, 6.2 Hz, 4H), 2.60 (s, 3H), 1.78 (m, J=4.6 Hz, 4H), 1.35 (s, 3H), 0.89 (t, 6H).

[0239] Synthesis of a Compound CPD315-1:

[0240] With reference to the synthesis process and post-treatment and purification methods of the compound CPD1-1, only the corresponding raw materials were required to be changed. The obtained compound was directly used in the next step without purification.

[0241] Synthesis of a Compound CPD 315:

[0242] With reference to the synthesis process and post-treatment and purification methods of the compound CPD 1, only the corresponding raw materials were required to be changed, and 3.44 g of a target compound CPD 315 with a yield of 52.2% was obtained. 3.44 g of the crude product CPD 315 was sublimated and purified to obtain 2.24 g of a sublimated pure product CPD 315 with a yield of 65.11%. Mass spectrometry was as follows: 1189.5 (M+H).

Example 24 Synthesis of a Compound CPD 321

[0243] ##STR00125##

[0244] Synthesis of a Compound L21:

[0245] With reference to the synthesis process and post-treatment and purification methods of the compound L1-4, only the corresponding raw materials were required to be changed. Mass spectrometry was as follows: 380.5 (M+H). .sup.1HNMR (400 MHz, CDCl3) δ8.66 (d, J=5.7 Hz, 1H), 7.98 (d, J=7.4 Hz, 1H), 7.89 (s, 1H), 7.80-7.67 (m, 3H), 7.50 (s, 1H), 7.37 (dq, J=13.9, 6.2 Hz, 4H), 2.60 (s, 3H), 1.78 (t, 2H), 0.90 (d, J=10.0 Hz, 9H).

[0246] Synthesis of a Compound CPD321-1:

[0247] With reference to the synthesis process and post-treatment and purification methods of the compound CPD1-1, only the corresponding raw materials were required to be changed. The obtained compound was directly used in the next step without purification.

[0248] Synthesis of a Compound CPD 321:

[0249] With reference to the synthesis process and post-treatment and purification methods of the compound CPD 1, only the corresponding raw materials were required to be changed, and 3.21 g of a target compound CPD 321 with a yield of 51.1% was obtained. 3.21 g of the crude product CPD 321 was sublimated and purified to obtain 2.16 g of a sublimated pure product CPD 321 with a yield of 67.28%. Mass spectrometry was as follows: 1161.5 (M+H).

[0250] Other compounds can be synthesized and sublimated by using corresponding materials according to same or similar methods.

[0251] The ultraviolet absorption spectrum and emission spectrum of the compounds CPD 93/CPD 123/CPD 249 of the present invention in a dichloromethane solution are as shown in FIG. 7. All the compounds of the present invention have more saturated red luminescence and narrow half-peak width, so that the realization of high luminescence efficiency is facilitated.

Application Example: Manufacture of an Organic Electroluminescent Device

[0252] A glass substrate with a size of 50 mm*50 mm*1.0 mm including an ITO (100 nm) transparent electrode was ultrasonically cleaned in ethanol for 10 minutes, dried at 150° C., and then treated with N.sub.2 plasma for 30 minutes. The washed glass substrate was installed on a substrate support of a vacuum evaporation device. At first, a compound HATCN for covering the transparent electrode was evaporated on the surface of the side having a transparent electrode line to form a thin film with a thickness of 5 nm. Next, a layer of HTM1 was evaporated to form a thin film with a thickness of 60 nm. Then, a layer of HTM2 was evaporated on the HTM1 thin film to form a thin film with a thickness of 10 nm. After that, a main material CBP and a doping compound (including reference compounds X and CPD X) were co-evaporated on the HTM2 film layer to obtain a film with a thickness of 30 nm, where a ratio of the main material to the doping material was 90%:10%. An AlQ.sub.3 film layer (25 nm) and a LiF film layer (1 nm) were evaporated on a light-emitting layer in sequence. At last, a layer of metal A1 (100 nm) was evaporated to serve as an electrode.

##STR00126## ##STR00127##

[0253] Evaluation: Properties of a device obtained above were tested. In various examples and comparative examples, a constant-current power supply (Keithley 2400) was used, a current at a fixed density was used for flowing through light-emitting elements, and a spectroradiometer (CS 2000) was used for testing the light-emitting spectrum. Meanwhile, the voltage value was measured, and the time (LT90) when the brightness was reduced to 90% of an initial brightness was tested. Results are shown as follows.

TABLE-US-00001 Starting Current Power Peak Doping voltage efficiency efficiency wavelength LT90 @ material V Cd/A lm/W nm 3000 nits Example 1 CPD 1 4.21 30.3 22.0 616 192 Example 2 CPD 3 4.18 32.9 24.6 616 233 Example 3 CPD 8 4.17 29.9 22.5 615 212 Example 4 CPD 21 4.18 33.1 24.6 617 225 Example 5 CPD 27 4.16 30.6 22.9 616 218 Example 6 CPD 28 4.17 29.3 22.1 615 201 Example 7 CPD 33 4.15 31.2 23.6 616 219 Example 8 CPD 39 4.20 32.6 24.4 617 239 Example 9 CPD 75 4.19 31.6 23.7 618 218 Example 10 CPD 93 4.16 31.3 23.6 616 232 Example 11 CPD 99 4.13 30.9 23.5 615 189 Example 12 CPD 121 4.18 29.3 22.0 616 186 Example 13 CPD 123 4.15 32.5 24.6 617 225 Example 14 CPD 145 4.16 29.6 22.4 616 203 Example 15 CPD 147 4.16 33.2 25.1 618 229 Example 16 CPD 175 4.25 30.2 22.3 620 178 Example 17 CPD 177 4.26 29.9 22.1 620 192 Example 18 CPD 247 4.18 29.1 21.8 615 201 Example 19 CPD 249 4.16 30.3 22.9 616 222 Example 20 CPD 253 4.05 31.0 24.03 620 211 Example 21 CPD 256 3.99 33.1 25.97 626 232 Example 22 CPD 309 4.14 30.9 23.4 616 229 Example 23 CPD 315 4.15 31.6 23.9 617 220 Example 24 CPD 321 4.15 31.3 23.7 617 219 Comparative Reference 4.56 21 14.46 610 102 Example 1 compound 1 Comparative Reference 4.41 20 14.24 612 116 Example 2 compound 2 Comparative Reference 4.64 21 14.21 611 94 Example 3 compound 3 Comparative Reference 4.88 18 11.58 608 82 Example 4 compound 4

[0254] Through comparison of the data in the above table, it can be seen that compared with reference compounds, the compound of the present invention used as a dopant in an organic electroluminescent device has the advantages that more excellent properties, such as driving voltage, luminescence efficiency, and device service life, are achieved.

[0255] Comparison of the sublimation temperature is as follows. The sublimation temperature is defined as the temperature corresponding to an evaporation rate of 1 AA at a vacuum degree of 10.sup.−7 Torr. Test results are shown as follows.

TABLE-US-00002 Doping material Sublimation temperature CPD 1 263 CPD 75 262 CPD 93 265 CPD 99 258 CPD 123 269 CPD 249 268 Reference compound 1 280 Reference compound 2 288 Reference compound 3 286 Reference compound 4 276

[0256] Through comparison of the data in the above table, it can be seen that the metal iridium complex of the present invention has low sublimation temperature, and industrial application is facilitated.

[0257] According to the present invention, through special combinations of substituents, better device luminescence efficiency and improved service life are achieved unexpectedly. Meanwhile, compared with the prior art, low sublimation temperature is achieved unexpectedly. According to the above results, it is indicated that the compound of the present invention has the advantages of low sublimation temperature, high optical and electrochemical stability, high color saturation, high luminescence efficiency, and long device service life, and can be used in organic electroluminescent devices. In particular, the complex has the potential for application in the OLED industry as a red light-emitting dopant.