Hole transporting material using ethylene bisacridine as core and organic light emitting diode

Abstract

A hole transporting material using ethylene bisacridine as a core is provided, having a following structural formula (I) and suitable migration rates under highest occupied molecular orbital (HOMO) energy levels and lowest unoccupied molecular orbital (LUMO) energy levels. Moreover, an organic light emitting diode is disclosed, including an anode, a cathode, and a light emitting structure located between the anode and the cathode, wherein the light emitting structure includes the hole transporting material using ethylene bisacridine as the core which is represented by the following structural formula (I) ##STR00001##

Claims

1. A hole transporting material using ethylene bisacridine as a core, wherein the hole transporting material has a following structural formula (I): ##STR00022## wherein R1 and R2 are selected from ##STR00023## ##STR00024## or any combination thereof.

2. The hole transporting material according to claim 1, wherein the hole transporting material has the following structural formula: ##STR00025##

3. The hole transporting material according to claim 2, wherein the hole transporting material has the following structural formula: ##STR00026## and is synthesized by a following, synthesis route: ##STR00027##

4. The hole transporting material according to claim 2, wherein the hole transporting material has the following structural formula: ##STR00028## and is synthesized by the following synthesis route: ##STR00029##

5. The hole transporting material according to claim 2, wherein the hole transporting material has the following structural formula: ##STR00030## and is synthesized by a following synthesis route: ##STR00031##

6. An organic light emitting diode, wherein a material of a hole transport layer in the organic light emitting diode is a hole transporting material using ethylene bisacridine as a core and has a following structural formula (I): ##STR00032## wherein R1 and R2 are selected from ##STR00033## ##STR00034## or any combination thereof.

7. The organic light emitting diode according to claim 6, wherein the hole transporting material has a following structural formula: ##STR00035##

8. The organic light emitting diode according to claim 7, wherein the hole transporting material has the following structural formula: ##STR00036## and is synthesized by a following synthesis route: ##STR00037##

9. The organic light emitting diode according to claim 7, wherein the hole transporting material has the following structural formula: ##STR00038## and is synthesized by the following synthesis route: ##STR00039##

10. The organic light emitting diode according to claim 7, wherein the hole transporting material has the following structural formula: ##STR00040## and is synthesized by a following synthesis route: ##STR00041##

11. The organic light emitting diode according to claim 6, wherein the organic light emitting diode further comprises an anode, a cathode, and a light emitting structure located between the anode and the cathode, wherein the light emitting structure comprises the hole transporting layer according to claim 6.

12. The organic light emitting diode according to claim 11, wherein the light emitting structure comprises a hole injecting layer, the hole transporting layer, an electron blocking layer, a light emitting layer, and a hole blocking layer, an electron transporting layer, and an electron injecting layer which are sequentially formed.

Description

BRIEF DESCRIPTION OF DRAWINGS

(1) FIG. 1 is a schematic diagram of an organic light emitting diode according to an embodiment of the present invention.

DETAILED DESCRIPTION

(2) In response to urgent needs of high-performance hole transporting materials, hole transporting materials using ethylene bisacridine as a core with suitable mobilities under highest occupied molecular orbital (HOMO) energy levels and the lowest unoccupied molecular orbital (LUMO) energy levels are synthesized by the present invention on a structural basis using ethylene bisacridine as the core to incorporate different functional groups, which have the effect of effectively increasing the luminous efficiency of a light emitting structure, while a synthetic route also has improved material synthesis efficiency, which is conducive to the fabrication of organic light emitting diodes with long lifespan and high efficiency.

(3) In order to achieve the above-mentioned effects, a hole transporting material using ethylene bisacridine as a core is provided by the present invention, having the following structural formula (I):

(4) ##STR00012##
wherein R1 and R2 are selected from

(5) ##STR00013## ##STR00014##
or any combination thereof.

(6) In one embodiment of the present invention, the hole transporting material has the following structural formula:

(7) ##STR00015##

(8) The following further describes the present invention in detail with reference to the embodiments and drawings for purposes of better understanding of the content of the present invention, but the protection scope of the present invention is not limited to these embodiments.

(9) Embodiment 1: fabrication of a hole transporting material having the following structural formula:

(10) ##STR00016##
and it is synthesized by the following synthesis route:

(11) ##STR00017##

(12) Synthesis of Compound 1

(13) First, 3.61 grams or 5 mmol of raw material 1, 2.00 grams or 12 mmol of carbazole, 0.18 grams or 0.8 mmol palladium acetate, and 0.68 grams or 2.4 mmol of tri-tert-butylphosphine tetrafluoroborate were added to a 250 mL two-necked flask. The two-necked flask was next placed into a glove box and 1.17 grams or 12 mmol of NaOt-Bu were added. Next, 100 mL of toluene which was previously dehydrated and deoxygenated were injected under an argon atmosphere and were then reacted at 120° C. for 24 hours. A reaction solution was obtained after it was cooled to room temperature. Subsequently, the reaction solution was introduced into 200 mL of ice water and extracted three times with dichloromethane. The organic phases obtained in each extraction were collected and combined to spin thereof into silica gel, and the silica gel was then subjected to column chromatography (using dichloromethane:n-hexane, v:v, 1:5) for isolation and purification. Finally, 3.0 grams of compound 1 (white powder) were obtained with a yield of 67% and MS (EI) m/z: [M]+: 896.32.

(14) Embodiment 2: fabrication of a hole transporting material having the following structural formula

(15) ##STR00018##
and it is synthesized by the following synthesis route:

(16) ##STR00019##

(17) Synthesis of Compound 2

(18) First, 3.61 grams or 5 mmol of raw material 1, 2.03 grams or 12 mmol of diphenylamine, 0.18 grams or 0.8 mmol palladium acetate, and 0.68 grams or 2.4 mmol of tri-tert-butylphosphine tetrafluoroborate were added to a 250 mL two-necked flask. The two-necked flask was next placed into a glove box and 1.17 grams or 12 mmol of NaOt-Bu were added. Next, 100 mL of toluene which was previously dehydrated and deoxygenated were injected under an argon atmosphere and were then reacted at 120° C. for 24 hours. A reaction solution was obtained after it was cooled to room temperature. Subsequently, the reaction solution was introduced into 200 mL of ice water and extracted three times with dichloromethane. The organic phases obtained in each extraction were collected and combined to spin thereof into silica gel, and the silica gel was then subjected to column chromatography (using dichloromethane:n-hexane, v:v, 1:5) for isolation and purification. Finally, 2.9 grams of compound 2 (white powder) were obtained with a yield of 64% and MS (EI) m/z: [M]+: 900.42.

(19) Embodiment 3: fabrication of a hole transporting material having the following structural formula

(20) ##STR00020##
and it is synthesized by the following synthesis route:

(21) ##STR00021##

(22) Synthesis of Compound 3

(23) First, 3.61 grams or 5 mmol of raw material 1, 2.51 grams or 12 mmol of 9,9-dimethylacridine, 0.18 grams or 0.8 mmol palladium acetate, and 0.68 grams or 2.4 mmol of tri-tert-butylphosphine tetrafluoroborate were added in a 250 mL two-necked flask. The two-necked flask was next placed into a glove box and 1.17 grams or 12 mmol of NaOt-Bu were added. Next, 100 mL of toluene which was previously dehydrated and deoxygenated were injected under an argon atmosphere and were then reacted at 120° C. for 24 hours. A reaction solution was obtained after it was cooled to room temperature. Subsequently, the reaction solution was introduced into 200 mL of ice water and extracted three times with dichloromethane. The organic phases obtained in each extraction were collected and combined to spin thereof into silica gel, and the silica gel was then subjected to column chromatography (using dichloromethane:n-hexane, v:v, 1:5) for isolation and purification. Finally, 2.6 grams of compound 3 (white powder) were obtained with a yield of 53% and MS (EI) m/z: [M]+: 980.42.

(24) Physical Properties of Compounds 1-3:

(25) The highest occupied molecular orbital (HOMO) energy levels and the lowest unoccupied molecular orbital (LUMO) energy levels of the above compounds 1-3 are shown in the following Table 1:

(26) TABLE-US-00001 TABLE 1 HOMO (eV) LUMO (eV) Compound 1 −5.66 −2.41 Compound 2 −5.69 −2.47 Compound 3 −5.56 −2.44

(27) The HOMO and LUMO energy levels of the above compounds 1-3 were estimated using the cyclic voltammetry combined with the optical energy gap (Eg) of the molecule in the thin film state according to the following calculation formula:
HOMO=−([Eonset]ox+4.8) eV,
Eg=LUMO−HOMO,

(28) wherein [Eonset] ox refers to the redox starting potential value of ferrocene under testing.

(29) Embodiments 4-6: fabrication of an organic light emitting diode:

(30) Referring to FIG. 1, an organic light emitting diode of the present invention comprises a conductive anode glass layer S, a semi-transparent cathode layer 8 and a light coupling output layer 9, and a light emitting structure formed between the conductive anode glass layer S and the semi-transparent cathode layer 8. Specifically, the light emitting structure comprises a hole injecting layer 1, a hole transporting layer 2, an electron blocking layer 3, a light emitting layer 4, a hole blocking layer 5, and an electron transporting layer 6, and an electron injection layer 7, which are sequentially formed on the conductive anode glass layer S. Specifically, the conductive anode glass layer S was formed by plating a glass substrate with a total reflection substrate layer made of a conductive reflective indium tin oxide (ITO)/silver (Ag)/indium tin oxide (ITO). The hole injection layer 1 was composed of 2,3,6,7,10,11-hexacyano-1,4,5,8,9,12-hexaazabenzophenanthrene (HATCN). The hole transporting layer 2 was composed of a hole transporting material using ethylene bisacridine as a core according to the present invention, which is, for example, compounds 1-3. The electron blocking layer 3 was composed of 4-[1-[4-[bis (4-methylphenyl) amino] phenyl] cyclohexyl]-N-(3-methylphenyl)-N-(4-methyl Phenyl) aniline (TAPC). The light emitting layer 4 was composed of 4,4′-bis (9-carbazole) biphenyl (CBP) and tris (2-phenylpyridine) iridium (III) (Ir (PPy) 3). The hole blocking layer 5 was composed of 3,3′-[5′-[3-(3-pyridyl) phenyl] [1,1′:3′,1″-terphenyl]-3,3″-diyl] dipyridine (TMPyPb). The electron transport layer 6 was composed of 1,3,5-tris [3-(3-pyridyl) phenyl] benzene (TmPyPB) and lithium octahydroxyquinoline (LiQ). The electron injection layer 7 was composed of lithium fluoride (LiF). The semi-transparent cathode layer 8 was composed of magnesium and silver. The light-coupling output layer 9 was composed of 4,4′, 4″-tris (carbazole-9-yl) triphenylamine (TCTA). The hole injection layer 1, the hole transport layer 2, the electron blocking layer 3, the light emitting layer 4, the hole blocking layer 5, the electron transport layer 6, and the electron injection layer 7 constitute the light emitting structure of the organic light emitting diode of the present invention. The organic light emitting diode can be completed according to a method known in the technical field of the present invention, for example, the method disclosed in the reference “Adv. Mater. 2003, 15, 277”. The specific method is described as follows: under high vacuum conditions, the aforementioned materials containing the hole transporting material (compounds 1-3) of the present invention were sequentially formed on a conductive glass by evaporation to complete the process. Here, the compounds 1-3 of the present invention were used to prepare the organic light emitting diodes I-III of Examples 4-6. The structure of the organic light emitting diode I-III from the conductive glass anode layer S to the light coupling output layer 9 are provided as follows:

(31) Organic light emitting diode (OLED) I: ITO/Ag/ITO (15 nm/140 nm/15 nm)/HATCN (100 nm)/Compound 1 (130 nm)/TAPC (5 nm)/CBP: (Ir (PPy) 3 (38 nm: 2 nm)/TMPyPb (15 nm)/TmPyPB: LiQ (15 nm: 15 nm)/LiF (1 nm)/Mg: Ag (1 nm: 10 nm)/TCTA (100 nm).

(32) OLED II: ITO/Ag/ITO (15 nm/140 nm/15 nm)/HATCN (100 nm)/Compound 2 (130 nm)/TAPC (5 nm)/CBP: (Ir (PPy) 3 (38 nm: 2 nm)/TMPyPb (15 nm)/TmPyPB: LiQ (15 nm: 15 nm)/LiF (1 nm)/Mg: Ag (1 nm: 10 nm)/TCTA (100 nm).

(33) OLED III: ITO/Ag/ITO (15 nm/140 nm/15 nm)/HATCN (100 nm)/Compound 3 (130 nm)/TAPC (5 nm)/CBP: (Ir (PPy) 3 (38 nm: 2 nm)/TMPyPb (15 nm)/TmPyPB: LiQ (15 nm: 15 nm)/LiF (1 nm)/Mg: Ag (1 nm: 10 nm)/TCTA (100 nm).

(34) Data of performance the organic light emitting diodes I-III of Examples 4-6 are shown in the following Table 2. Current, brightness and voltage of the organic light emitting diodes were measured by a Keithley source measurement system (Keithley 2400 Source-meter, Keithley 2000 Current-meter) with a calibrated silicon photodiode. The electroluminescence spectrum of the organic light emitting diodes were measured by SPEX CCD3000 spectrometer of the French company JY. All measurements were made and done at room temperature.

(35) TABLE-US-00002 TABLE 2 Hole Max current chromaticity Max external transporting efficiency coordinate quantum OLED material (cd/A) (CIEx, CIEy) efficiency (%) I Compound 1 40 (0.68, 0.29) 36.9% II Compound 2 43 (0.68, 0.29) 38.0% III Compound 3 41 (0.68, 0.29) 37.2%

(36) In the hole transporting material using ethylene bisacridine as the core provided by the present invention, the hole transporting materials using ethylene bisacridine as a core with suitable mobilities under highest occupied molecular orbital (HOMO) energy levels and the lowest unoccupied molecular orbital (LUMO) energy levels are synthesized on a structural basis using ethylene bisacridine as the core to incorporate different functional groups, which have the effect of effectively increasing the luminous efficiency of a light emitting structure. In addition, a synthetic route of the hole transporting materials using ethylene bisacridine as a core of the present invention is also provided with improved material synthesis efficiency. At last, an organic light emitting diode adopting the hole transporting material using ethylene bisacridine as a core in the embodiment of the present invention as a light emitting structure has high light emitting efficiency, thereby facilitating the production of a long-life, high efficiency organic light emitting diode, which can be applied and used in various display devices and electronic devices.

(37) While the present disclosure has been described with the aforementioned preferred embodiments, it is preferable that the above embodiments should not be construed as limiting of the present disclosure. Anyone having ordinary skill in the art can make a variety of modifications and variations without departing from the spirit and scope of the present disclosure as defined by the following claims.