Indenotriphenylene-based amine derivative for organic electroluminescent device

Abstract

The present invention discloses an indenotriphenylene-based amine derivative represented by the following formula (A): ##STR00001##
wherein R.sub.1 to R.sub.5, m, n, p, L and Ar are the same definition as described in the present invention. The present invention also discloses an organic EL device employing the indenotriphenylene-based amine derivative as a hole transport material or an electron blocking material, which can lower driving voltage and power consumption and increase efficiency and half-life time.

Claims

1. An indenotriphenylene-based amine derivative with a general formula (A) as following: ##STR00035## wherein L represents a single bond, a substituted or unsubstituted divalent arylene group having 6 to 30 carbon atoms; m represents an integer of 0 to 10; n represents an integer of 0 to 3; p represents an integer of 0 to 7; X is absent or represents a divalent bridge selected from the atom or group consisting from O, S, C(R.sub.6)(R.sub.7), and NR.sub.8; R.sub.1 to R.sub.8 are independently selected from the group consisting of a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted aryl group having 6 to 30 carbon atoms, and a substituted or unsubstituted heteroaryl group having 3 to 30 carbon atoms; Ar is selected from the group consisting of a substituted or unsubstituted aryl group having 6 to 50 carbon atoms, and a substituted or unsubstituted heteroaryl group having 3 to 50 carbon atoms.

2. The indenotriphenylene-based amine derivative according to claim 1, wherein L represents one of the following: ##STR00036##

3. The indenotriphenylene-based amine derivative according to claim 1, wherein Ar represents one of the following: ##STR00037## ##STR00038## ##STR00039##

4. The indenotriphenylene-based amine derivative according to claim 1, wherein the indenotriphenylene-based amine derivative is selected from the group consisting of ##STR00040## ##STR00041## ##STR00042## ##STR00043## ##STR00044## ##STR00045##

5. An organic electroluminescent device comprising a pair of electrodes consisting of a cathode and an anode and between the pairs of electrodes comprising at least a layer of the indenotriphenylene-based amine derivative with a general formula (A) according to claim 1.

6. The organic electroluminescent device according to claim 5, wherein the layer of the indenotriphenylene-based amine derivative with a general formula (A) is a hole transport layer.

7. The organic electroluminescent device according to claim 5, wherein the layer of the indenotriphenylene-based amine derivative with a general formula (A) is an electron blocking layer.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 show one example of organic EL device in the present invention. 6 is transparent electrode, 13 is metal electrode, 7 is hole injection layer which is deposited onto 6, 8 is hole transport layer which is deposited onto 7, 9 is electron blocking layer which is deposited onto 8, 10 is fluorescent or phosphorescent emitting layer which is deposited onto 9, 11 is electron transport layer which is deposited onto 10, 12 is electron injection layer which is deposited on to 11.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

(2) What probed into the invention is the indenotriphenylene-based amine derivative and organic EL device using the indenotriphenylene-based amine derivative. Detailed descriptions of the production, structure and elements will be provided in the following to make the invention thoroughly understood. Obviously, the application of the invention is not confined to specific details familiar to those who are skilled in the art. On the other hand, the common elements and procedures that are known to everyone are not described in details to avoid unnecessary limits of the invention. Some preferred embodiments of the present invention will now be described in greater detail in the following. However, it should be recognized that the present invention can be practiced in a wide range of other embodiments besides those explicitly described, that is, this invention can also be applied extensively to other embodiments, and the scope of the present invention is expressly not limited except as specified in the accompanying claims.

(3) In a first embodiment of the present invention, the indenotriphenylene-based amine derivative which can be used as hole transport material, electron blocking material for organic EL device are disclosed. The mentioned derivative is represented by the following formula (A):

(4) ##STR00003##
wherein L represents a single bond, a substituted or unsubstituted divalent arylene group having 6 to 30 carbon atoms; m represents an integer of 0 to 10; n represents an integer of 0 to 3; p represents an integer of 0 to 7; X is absent or represents a divalent bridge selected from the atom or group consisting from O, S, C(R.sub.6)(R.sub.7), and NR.sub.8; R.sub.1 to R.sub.8 are independently selected from the group consisting of a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted aryl group having 6 to 30 carbon atoms, and a substituted or unsubstituted heteroaryl group having 3 to 30 carbon atoms; Ar is selected from the group consisting of a substituted or unsubstituted aryl group having 6 to 50 carbon atoms, and a substituted or unsubstituted heteroaryl group having 3 to 50 carbon atoms.

(5) According to the above-mentioned formula (A) wherein L is represented the following:

(6) ##STR00004##

(7) According to the above-mentioned formula (A) wherein Ar is represented the following:

(8) ##STR00005## ##STR00006## ##STR00007##

(9) In this embodiment, some specific derivatives are shown below:

(10) ##STR00008## ##STR00009## ##STR00010## ##STR00011## ##STR00012## ##STR00013##

(11) Detailed preparation for the indenotriphenylene-based amine derivative in the present invention could be clarified by exemplary embodiments, but the present invention is not limited to exemplary embodiments. EXAMPLE 1˜6 show the preparation for some EXAMPLES of the derivative in the present invention. EXAMPLE 7˜8 show the fabrication of organic EL device and I-V-B, half-life time of organic EL device testing report.

EXAMPLE 1

Synthesis of Derivative A1

Synthesis of 2-(biphenyl-2-yl)-7-bromo-9,9-dimethyl-9H-fluorene

(12) ##STR00014##

(13) A mixture of 35.2 g (100 mmol) of 2,7-dibromo-9,9-dimethyl-9H-fluorene, 21.8 g (110 mmol) of biphenyl-2-ylboronic acid, 2.31 g (2 mmol) of Pd(PPh.sub.3).sub.4, 75 ml of 2M Na2CO3, 150 ml of EtOH and 300 ml toluene was degassed and placed under nitrogen, and then heated at 100° C. for 12 h. After finishing the reaction, the mixture was allowed to cool to room temperature. The organic layer was extracted with ethyl acetate and water, dried with anhydrous magnesium sulfate, the solvent was removed and the residue was purified by column chromatography on silica to give product (26.8 g, 63.0 mmol, 63%) as a white solid.

Synthesis of 12-bromo-10,10-dimethyl-10H-indeno[2,1-b]triphenylene

(14) ##STR00015##

(15) In a 3000 ml three-necked flask that had been degassed and filled with nitrogen, 26.8 g (60 mmol) of 2-(biphenyl-2-yl)-7-bromo-9,9-dimethyl-9H-fluorene was dissolved in anhydrous dichloromethane (1500 ml), 97.5 g (600 mmol) Iron(III)chloride was then added, and the mixture was stirred one hour. Methanol 500 ml were added to the mixture and the organic layer was separated and the solvent removed in vacuo. The residue was purified by column chromatography on silica (hexane-dichloromethane) afforded a white solid (10.7 g, 25.3 mmol, 40%). .sup.1H NMR (CDCl3, 400 MHz): chemical shift (ppm) 8.95 (s, 1H), 8.79˜8.74 (m, 2H), 8.69˜8.68 (m, 3H), 7.84 (d, J=8.0 Hz, 1H), 7.72˜7.65 (m, 5H), 7.57 (d, J=8.0 Hz, 1H), 1.66 (s, 6H).

Synthesis of N-(biphenyl-4-yl)-9,9′-spirobifluorene-2-amine

(16) ##STR00016##

(17) A mixture of 30 g (75.8 mmol) 2-bromo-9,9′-spirobifluorene, 15.3 g (90.9 mmol) of biphenyl-4-amine, 0.17 g (0.76 mmol) of palladium(II) acetate, 0.26 g (0.76 mmol) of 2-(dicyclohexylphosphino)biphenyl, 9.5 g (98.5 mmol) of sodium tert-butoxide and 300 ml of toluene was refluxed under nitrogen overnight. After finishing the reaction, than cooled to room temperature. The organic layer was extracted with dichloromethane and water, dried with anhydrous magnesium sulfate, the solvent was removed and the residue was purified by column chromatography on silica(hexane-dichloromethane) to give product 21.9 g (yield 60%) as a white solid.

Synthesis of N-(biphenyl-4-yl)-N-(4-bromophenyl)-9,9′-spirobifluorene-2-amine

(18) ##STR00017##

(19) A mixture of 20 g (41.3 mmol) N-(biphenyl-4-yl)-9,9′-spiro bifluorene-2-amine, 14 g (49.5 mmol) of 1-bromo-4-iodobenzene, 2.4 g (12.4 mmol) of copper iodide, 17.1 g (123.9 mmol) of potassium carbonate and 300 ml of DMF was refluxed under nitrogen overnight. After finishing the reaction, than cooled to room temperature. The organic layer was extracted with ethyl acetate and water, dried with anhydrous magnesium sulfate, the solvent was removed and the residue was purified by column chromatography on silica (hexane-dichloromethane) to give product 26.3 g (yield 43%) as a white solid.

Synthesis of intermediate of N-(biphenyl-4-yl)-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-9,9′-spirobi[fluoren]-2-amine

(20) ##STR00018##

(21) A mixture of 10 g (15.6 mmol) of N-(biphenyl-4-yl)-N-(4-bromophenyl)-9,9′-spirobi[fluoren]-2-amine, 4.75 g (18.72 mmol) of bis(pinacolato)diboron, 0.18 g (0.156 mmol) of tetrakis(triphenylphosphine)palladium, 2 g (20.28 mmol) of potassium acetate, and 300 ml of 1,4-dioxane was degassed and placed under nitrogen, and then heated at 90° C. for 16 h. After finishing the reaction, the mixture was allowed to cool to room temperature. The organic layer was extracted with ethyl acetate and water, dried with anhydrous magnesium sulfate, the solvent was removed and the product was purified by column using a mixture of hexanes and ethyl as eluent to get 8.77 g of light yellow product (yield 82%).

Synthesis of N-(biphenyl-4-yl)-N-(4-(10,10-dimethyl-10H-indeno[1,2-b]triphenylen-12-yl)phenyl)-9,9′-spirobi[fluoren]-2-amine

(22) ##STR00019##

(23) A mixture of 15 g (35.43 mmol) of 12-bromo-10,10-dimethyl-10H-indeno[1,2-b]triphenylene, 29.1 g (42.51 mmol) of N-(biphenyl-4-yl)-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-9,9′-spirobifluorene-2-amine, 0.41 g (0.35 mmol) of tetrakis(triphenylphosphine)palladium, 23 ml of 2M Na.sub.2CO.sub.3, 100 ml of EtOH and 200 ml toluene was degassed and placed under nitrogen, and then heated at 100° C. for 8 hours. After finishing the reaction, the mixture was allowed to cool to room temperature. The organic layer was extracted with dichloromethane and water, dried with anhydrous magnesium sulfate, the solvent was removed and the residue was purified by column chromatography on silica (hexane-dichloromethane) to give product 17.5 g (yield 55%) as a yellow solid. MS (m/z, FAB.sup.+): 902.3; .sup.1H NMR (CDCl.sub.3, 500 MHz): chemical shift (ppm) 8.97 (s, 1H), 8.80 (d, J=8.0 Hz, 1H), 8.75 (d, J=8.0 Hz, 1H), 8.68 (s, 1H), 8.67 (d, J=8.0 Hz, 2H), 7.98 (d, J=8.0 Hz, 1H), 7.77˜7.63 (m, 9H), 7.59 (d, J=8 Hz, 1H), 7.52 (d, J=7.5 Hz, 2H), 7.47˜7.41 (d, 2H), 7.41˜7.28 (m, 8H), 7.16˜7.05 (m, 8H), 6.84 (d, J=7.5 Hz, 2H), 6.68 (d, J=7.5 Hz, 2H), 1.59 (s, 6H)

EXAMPLE 2

Synthesis of Derivative A8

Synthesis of N-(9,9′-spirobifluorene-2-yl)-N-(biphenyl-4-yl)-10,10-dimethyl-10H-indeno[1,2-b]triphenylen-12-amine

(24) ##STR00020##

(25) A mixture of 5 g (11.8 mmol) 12-bromo-10,10-dimethyl-10H-indeno[1,2-b]triphenylene, 6.8 g (14.1 mmol) of N-(biphenyl-4-yl)-9,9′-spirobi fluorene-2-amine, 0.03 g (0.11 mmol) of palladium(II)acetate, 0.04 g (0.11 mmol) of 2-(dicyclohexylphosphino)biphenyl, 1.7 g (17.7 mmol) of sodium tert-butoxide and 100 ml of toluene was refluxed under nitrogen overnight. After finishing the reaction, than cooled to room temperature. The organic layer was extracted with dichloromethane and water, dried with anhydrous magnesium sulfate, the solvent was removed and the residue was purified by column chromatography on silica (hexane-dichloromethane) to give product 5.8 g (yield 60%) as a yellow solid. MS (m/z, FAB.sup.+): 826.3; .sup.1H NMR (CDCl.sub.3, 500 MHz): chemical shift (ppm) 8.78 (s, 1H), 8.73 (d, J=8.0 Hz, 2H), 8.70 (d, J=8.0 Hz, 2H), 8.78 (s, 1H), 7.77˜7.61 (m, 9H), 7.56 (d, J=7.5 Hz, 2H), 7.44˜7.39 (m, 4H), 7.34˜7.26 (m, 4H), 7.15˜6.97 (m, 8H), 6.85 (d, J=7.5 Hz, 2H), 6.67˜6.64 (m, 2H), 1.35 (s, 6H)

EXAMPLE 3

Synthesis of Derivative A14

Synthesis of N-(biphenyl-4-yl)-9,9′-spirobifluorene-4-amine

(26) ##STR00021##

(27) A mixture of 30 g (75.8 mmol) 4-bromo-9,9′-spirobi[fluorene], 15.3 g (90.9 mmol) of biphenyl-4-amine, 0.17 g (0.76 mmol) of palladium(II) acetate, 0.26 g (0.76 mmol) of 2-(dicyclohexylphosphino)biphenyl, 9.5 g (98.5 mmol) of sodium tert-butoxide and 300 ml of toluene was refluxed under nitrogen overnight. After finishing the reaction, than cooled to room temperature. The organic layer was extracted with dichloromethane and water, dried with anhydrous magnesium sulfate, the solvent was removed and the residue was purified by column chromatography on silica (hexane-dichloromethane) to give product 19.0 g (yield 52%) as a white solid.

Synthesis of N-(9,9′-spirobifluorene-4-yl)-N-(biphenyl-4-yl)-10,10-dimethyl-10H-indeno[1,2-b]triphenylen-13-amine

(28) ##STR00022##

(29) A mixture of 4.5 g (10.6 mmol) 13-bromo-10,10-dimethyl-10H-indeno[1,2-b]triphenylene, 6.1 g (12.7 mmol) of N-(biphenyl-4-yl)-9,9′-spirobifluorene-4-amine, 0.03 g (0.11 mmol) of palladium(II)acetate, 0.04 g (0.11 mmol) of 2-(dicyclohexylphosphino)biphenyl, 1.3 g (13.8 mmol) of sodium tert-butoxide and 100 ml of toluene was refluxed under nitrogen overnight. After finishing the reaction, than cooled to room temperature. The organic layer was extracted with dichloromethane and water, dried with anhydrous magnesium sulfate, the solvent was removed and the residue was purified by column chromatography on silica (hexane-dichloromethane) to give product 4.8 g (yield 55%) as a yellow solid. MS (m/z, FAB.sup.+): 826.5; .sup.1H NMR (CDCl.sub.3, 500 MHz): chemical shift (ppm) 8.81 (s, 1H), 8.75 (d, J=8.0 Hz, 1H), 8.67˜8.65 (m, 3H), 7.89˜7.83 (m, 4H), 7.67˜7.54 (m, 8H), 7.44˜7.25 (m, 8H), 7.21˜7.10 (m, 6H), 7.01 (t, 1H), 6.83 (b, 2H), 6.69 (d, J=7.0 Hz, 1H), 1.65 (s, 6H)

EXAMPLE 4

Synthesis of Derivative A18

Synthesis of N,N-di(biphenyl-4-yl)-10,10-dimethyl-10H-indeno[2,1-b]triphenylen-12-amine

(30) ##STR00023##

(31) A mixture of 4.3 g (10.1 mmol) 12-bromo-10,10-dimethyl-10H-indeno[2,1-b]triphenylene, 3.9 g (12.1 mmol) of dibiphenyl-4-ylamine, 0.05 g (0.2 mmol) of palladium(II)acetate, 0.15 g (0.4 mmol) of 2-(dicyclohexyl phosphine)biphenyl, 2 g (20 mmol) of sodium tert-butoxide and 50 ml of o-xylene was refluxed under nitrogen overnight. After finishing the reaction, the solution was filtered at 100° C., to receive the filtrate, and the filtrate was added to 500 ml MeOH, while stirring and the precipitated product was filtered off with suction. The product was purified by sublimation to get 2.9 g of product (yield 37%). MS (m/z, FAB.sup.+): 663.1; .sup.1H NMR (CDCl.sub.3, 500 MHz): chemical shift (ppm) 8.88 (s, 1H), 8.79 (d, J=8.0 Hz, 1H), 8.72 (d, J=8.0 Hz, 1H), 8.66 (d, J=5.0 Hz, 2H), 8.63 (s, 1H), 7.85 (d, J=8.0 Hz, 1H), 7.69˜7.63 (m, 4H), 7.61 (d, J=7.5 Hz, 4H), 7.54 (d, J=8.5 Hz, 4H), 7.44˜7.41 (t, 4H), 7.33˜7.26 (m, 7H), 7.20 (d, J=8.0 Hz, 1H), 1.59 (s, 6H)

EXAMPLE 5

Synthesis of Derivative A19

Synthesis of 3-bromo-N-(4-bromophenyl)aniline

(32) ##STR00024##

(33) A mixture of 32.5 g (114.9 mmol) of 1-bronco-3-iodobenzene, 14.1 g (81.9 mmol) of 4-bromoaniline, 23.6 g (245.8 mmol) of sodium t-butoxide and 2 ml (8.2 mmol) of tri-t-butylphosphine were dissolved in 400 ml of toluene, 1.5 g (1.64 mmol) of Pd.sub.2 (dba).sub.3 was added thereto, and then the mixture was stirred while refluxing overnight. After finishing the reaction, the mixture was allowed to cool to room temperature. The organic layer was extracted with ethyl acetate and water, dried with anhydrous magnesium sulfate, the solvent was removed and the product was purified by column using a mixture of hexanes and ethyl acetate as eluent to get 12.6 g (yield 47%) of product.

Synthesis of 3-(dibenzo[b,d]furan-4-yl)-N-(4-(dibenzo[b,d]furan-4-yl)phenyl) aniline

(34) ##STR00025##

(35) A mixture of 9.8 g (30 mmol) of 3-bromo-N-(4-bromophenyl) aniline, 14 g (66 mmol) of dibenzo[b,d]furan-4-ylboronic acid, 0.69 g (0.6 mmol) of tetrakis(triphenylphosphine)palladium, 60 ml of 2M Na.sub.2CO.sub.3, 60 ml of EtOH and 150 ml toluene was degassed and placed under nitrogen, and then heated at 110° C. overnight. After finishing the reaction, the mixture was allowed to cool to room temperature. Than 100 ml of MeOH was added, while stirring and the precipitated product was filtered off with suction. To give 9.8 g (yield 65%) of yellow product which was recrystallized from ethyl acetate.

Synthesis of N-(3-(dibenzo[b,d]furan-4-yl)phenyl)-N-(4-(dibenzo[b,d]furan-4-yl)phenyl)-10,10-dimethyl-10H-indeno[2,1-b]triphenylen-12-amine

(36) ##STR00026##

(37) A mixture of 4.3 g (10.1 mmol) 12-bromo-10,10-dimethyl-10H-indeno[2,1-b]triphenylene, 6.1 g (12.1 mmol) of 3-(dibenzo[b,d]furan-4-yl)-N-(4-(dibenzo[b,d]furan-4-yl)phenyl)aniline, 0.05 g (0.2 mmol) of palladium(II) acetate, 0.15 g (0.4 mmol) of 2-(dicyclohexylphosphino)biphenyl, 2 g (20 mmol) of sodium tert-butoxide and 50 ml of o-xylene was refluxed under nitrogen overnight. After finishing the reaction, the solution was filtered at 100° C., to receive the filtrate, and the filtrate was added to 500 ml MeOH, while stirring and the precipitated product was filtered off with suction. The product was purified by sublimation to get 4.0 g of product (yield 47%). MS (m/z, FAB.sup.+): 843.3; .sup.1H NMR (CDCl.sub.3, 500 MHz): chemical shift (ppm) 8.90 (s, 1H), 8.81 (d, J=8.0 Hz, 1H), 8.74 (d, J=8.0 Hz, 1H), 8.68 (d, J=5.0 Hz, 2H), 8.61 (s, 1H), 8.1˜7.94 (m, 3H), 7.69˜7.54 (m, 12H), 7.44˜7.38 (m, 6H), 7.33˜7.26 (m, 7H), 7.20 (d, J=8.0 Hz, 1H), 1.61 (s, 6H)

EXAMPLE 6

Synthesis of Derivative A21

Synthesis of N-(4-bromophenyl)biphenyl-4-amine

(38) ##STR00027##

(39) A mixture of 14.7 g (45 mmol) of bis(4-bromophenyl)amine, 5.5 g (45 mmol) of phenylboronic acid, 0.51 g (0.45 mmol) of tetrakis(triphenyl-phosphine)palladium, 45 ml of 2M Na.sub.2CO.sub.3, 45 ml of EtOH and 90 ml toluene was degassed and placed under nitrogen, and then heated at 90° C. overnight. After finishing the reaction, the mixture was allowed to cool to room temperature. The organic layer was extracted with ethyl acetate and water, dried with anhydrous magnesium sulfate, the solvent was removed and the product was purified by column using a mixture of hexanes and ethyl acetate as eluent to get 5.2 g (yield 36%) of product.

Synthesis of N-(4-(9-phenyl-9H-carbazol-3-yl)phenyl)biphenyl-4-amine

(40) ##STR00028##

(41) A mixture of 5.2 g (16 mmol) of N-(4-bromophenyl)biphenyl-4-amine, 6.6 g (18 mmol) of 9-phenyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole, 0.37 g (0.32 mmol) of tetrakis(triphenyl-phosphine) palladium, 16 ml of 2M Na.sub.2CO.sub.3, 20 ml of EtOH and 50 ml toluene was degassed and placed under nitrogen, and then heated at 90° C. overnight. After finishing the reaction, the mixture was allowed to cool to room temperature. The organic layer was extracted with ethyl acetate and water, dried with anhydrous magnesium sulfate, the solvent was removed and the product was purified by column using a mixture of hexanes and ethyl acetate as eluent to get 5.0 g (yield 64%) of product.

Synthesis of N-(biphenyl-4-yl)-10,10-dimethyl-N-(4-(9-phenyl-9H-carbazol-3-yl)phenyl)-10H-indeno[2,1-b]triphenylen-12-amine

(42) ##STR00029##

(43) A mixture of 4.3 g (10.1 mmol) 12-bromo-10,10-dimethyl-10H-indeno[2,1-b]triphenylene, 5.0 g (10.2 mmol) of 3-(dibenzo[b,d]furan-4-yl)-N-(4-(dibenzo[b,d]furan-4-yl)phenyl)aniline, 0.05 g (0.2 mmol) of palladium(II) acetate, 0.15 g (0.4 mmol) of 2-(dicyclohexylphosphino)biphenyl, 2 g (20 mmol) of sodium tert-butoxide and 50 ml of o-xylene was refluxed under nitrogen overnight. After finishing the reaction, 500 ml MeOH was added, while stirring and the precipitated product was filtered off with suction. The product was purified by sublimation to get 5.1 g of product (yield 61%). MS (m/z, FAB.sup.+): 828.6; .sup.1H NMR (CDCl.sub.3, 500 MHz): chemical shift (ppm) 8.86 (s, 1H), 8.81 (d, J=8.0 Hz, 1H), 8.72 (d, J=8.0 Hz, 1H), 8.66 (d, J=5.0 Hz, 2H), 8.59 (s, 1H), 8.37 (s, 1H), 8.11˜7.94 (m, 4H), 7.74˜7.47 (m, 12H), 7.44˜7.38 (m, 6H), 7.31˜7.23 (m, 8H), 7.20 (d, J=8.0 Hz, 1H), 1.61 (s, 6H)

General Method of Producing Organic EL Device

(44) ITO-coated glasses with 9˜12 ohm/square in resistance and 120˜160 nm in thickness are provided (hereinafter ITO substrate) and cleaned in a number of cleaning steps in an ultrasonic bath (e.g. detergent, deionized water). Before vapor deposition of the organic layers, cleaned ITO substrates are further treated by UV and ozone. All pre-treatment processes for ITO substrate are under clean room (class 100).

(45) These organic layers are applied onto the ITO substrate in order by vapor deposition in a high-vacuum unit (10.sup.−7 Torr), such as: resistively heated quartz boats. The thickness of the respective layer and the vapor deposition rate (0.1˜0.3 nm/sec) are precisely monitored or set with the aid of a quartz-crystal monitor. It is also possible, as described above, for individual layers to consist of more than one compound, i.e. in general a host material doped with a dopant material. This is achieved by co-vaporization from two or more sources.

(46) Dipyrazino[2,3-f:2,3-]quinoxaline-2,3,6,7,10,11-hexacarbonitrile (HAT-CN) is used as hole injection layer in this organic EL device. N,N-Bis(naphthalene-1-yl)-N,N-bis(phenyl)-benzidine (NPB) is most widely used as the hole transporting layer. 10,10-Dimethyl-12-(4-(pyren-1-yl)phenyl)-10H-indeno[1,2-b]triphenylene (PT-312, US20140175384) is used as blue emitting host in organic EL device, and N1,N1,N6,N6-tetram-tolylpyrene-1,6-diamine (D1) is used as blue guest. 2-(10,10-dimethyl-10H-indeno[2,1-b]triphenylen-13-yl)-4,6-bis-5-phenylbiphenyl-3-yl)-1,3,5-triazine (ET3) is used as electron transporting material to co-deposit with 8-hydroxyquinolato-lithium (LiQ) in organic EL device. Tris(2-phenylpyridinato)iridium(III) (D2) is used as phosphorescent dopant. H2 (US 20140166988A1, see the below chemical structure) is used as phosphorescent host for organic EL device. The prior art of OLED materials for producing standard organic EL device control and comparable material in this invention shown its chemical structure as following:

(47) ##STR00030## ##STR00031## ##STR00032## ##STR00033##

(48) A typical organic EL device consists of low work function metals, such as Al, Mg, Ca, Li and K, as the cathode by thermal evaporation, and the low work function metals can help electrons injecting the electron transporting layer from cathode. In addition, for reducing the electron injection barrier and improving the organic EL device performance, a thin-film electron injecting layer is introduced between the cathode and the electron transporting layer. Conventional materials of electron injecting layer are metal halide or metal oxide with low work function, such as: LiF, LiQ, MgO, or Li.sub.2O. On the other hand, after the organic EL device fabrication, EL spectra and CIE coordination are measured by using a PR650 spectra scan spectrometer. Furthermore, the current/voltage, luminescence/voltage and yield/voltage characteristics are taken with a Keithley 2400 programmable voltage-current source. The above-mentioned apparatuses are operated at room temperature (about 25° C.) and under atmospheric pressure.

EXAMPLE 7

(49) Using a procedure analogous to the above mentioned general method, fluorescent blue-emitting organic EL device having the following device structure I was produced (See FIG. 1). Device I: ITO/HAT-CN (20 nm)/hole transport material (HTM) (110 nm)/electron blocking material (EBM) (5 nm)/PT-312 doped 5% D1 (30 nm)/ET3 co-deposit 50% LiQ (40 nm)/LiF (0.5 nm)/Al (160 nm). The I-V-B (at 1000 nits) and half-life time of fluorescent blue-emitting organic EL device testing report as Table 1. The half-life time is defined that the initial luminance of 1000 cd/m.sup.2 has dropped to half.

(50) TABLE-US-00001 TABLE 1 Voltage Efficiency CIE Half-life time HTM EBM (V) (cd/A) (y) (hour) NPB — 5.0 4.3 0.172 180 A21 — 5.0 4.8 0.175 260 NPB A1 5.2 4.9 0.175 350 NPB A8 5.2 5.3 0.175 380 NPB A14 5.0 5.0 0.174 350 A21 A18 4.8 5.4 0.175 280 NPB A19 4.8 5.1 0.174 450

EXAMPLE 8

(51) Using a procedure analogous to the above mentioned general method, phosphorescent emitting organic EL device having the following device structures are produced (See FIG. 1.): Device I: ITO/HAT-CN (20 nm)/hole transport material (HTM) (110 nm)/electron blocking material (EBM) (5 nm)/H2 doped 12% D2 (35 nm)/ET3 co-deposit 50% LiQ (40 nm)/LiF (0.5 nm)/Al (160 nm). The I-V-B (at 1000 nits) and half-life time of phosphorescent emitting organic EL device testing report as Table 2. The half-life time is defined that the initial luminance of 3000 cd/m.sup.2 has dropped to half.

(52) TABLE-US-00002 TABLE 2 Voltage Efficiency CIE Half-life time HTM EBM (V) (cd/A) (x, y) (hour) NPB — 3.8 42 0.352, 0.612 620 A21 — 3.2 48 0.353, 0.613 810 NPB A1 3.2 49 0.352, 0.613 850 NPB A8 3.2 53 0.352, 0.613 880 NPB A14 3.5 50 0.353, 0.612 860 NPB A18 3.0 48 0.353, 0.612 700 NPB A19 3.2 51 0.353, 0.612 715 NPB A21 3.3 46 0.352, 0.613 960

(53) In the above preferred embodiments for organic EL device test report (see Table 1 and Table 2), we show that with a general formula (A) in the present invention display good performance and shown lower power consumption, higher efficiency and longer half-life time.

(54) To sum up, the present invention discloses an indenotriphenylene-based amine derivative which can be used for organic EL device. More specifically, an organic EL device employing the derivative as a hole transport material or an electron blocking material is disclosed. The mentioned derivative is represented by the following formula (A):

(55) ##STR00034##
wherein L represent a single bond, a substituted or unsubstituted divalent arylene group having 6 to 30 carbon atoms; m represents an integer of 0 to 10; n represents an integer of 0 to 3; p represents an integer of 0 to 7; X is absent or represents a divalent bridge selected from the atom or group consisting from O, S, C(R.sub.6)(R.sub.7), and NR.sub.8; R.sub.1 to R.sub.8 are independently selected from the group consisting of a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted aryl group having 6 to 30 carbon atoms, and a substituted or unsubstituted heteroaryl group having 3 to 30 carbon atoms; Ar is selected from the group consisting of a substituted or unsubstituted aryl group having 6 to 50 carbon atoms, and a substituted or unsubstituted heteroaryl group having 3 to 50 carbon atoms.