Thermally activated delayed fluorescence material having red, green, or blue color, synthesis method thereof, and application thereof

Abstract

The present disclosure relates to the field of organic light-emitting materials, and more particularly, to a thermally activated delayed fluorescence material having red, green, or blue color, a synthesis method thereof, and application thereof. The thermally activated delayed fluorescence material having red, green, or blue color has the following structural formula: ##STR00001## the present disclosure provides a novel thermally activated delayed fluorescence material having red, green, or blue color which has a lower singlet triplet energy level difference, a high RISC rate constant (kRISC), and a high photoluminescence quantum yield (PLQY). It has significant characteristics of a thermally activated delayed fluorescence material and a long service life that can be used in an electroluminescent display and a light-emitting equipment structure which are mass produced.

Claims

1. A thermally activated delayed fluorescence material having red, green, or blue color, having the following structural formula: ##STR00008## wherein, R is one of the following structural formulas: ##STR00009##

2. A synthesis method of the thermally activated delayed fluorescence material having red, green, or blue color according to claim 1, comprising: under an inert gas protective environment, performing a Buchwald-Hartwig coupling reaction between a raw material 1 and a raw material 2 under an effect of a palladium catalyst to obtain the thermally activated delayed fluorescence material having red, green, or blue color; wherein, the raw material 1 has the following structural formula: ##STR00010## the raw material 2 is one of carbazole, phenoxazine, or dimethyldiphenylamine, and a molar ratio of the raw material 1 to the raw material 2 ranges from 1:1 to 1:3.

3. The synthesis method of the thermally activated delayed fluorescence material having red, green, or blue color according to claim 2, wherein a reaction temperature of the Buchwald-Hartwig coupling reaction ranges from 80° C. to 160° C., and a reaction time thereof ranges from 12 hours to 48 hours.

4. The synthesis method of the thermally activated delayed fluorescence material having red, green, or blue color according to claim 2, wherein a reaction solvent of the Buchwald-Hartwig coupling reaction is dehydrated and deoxygenated toluene, and the palladium catalyst is at least one selected from the group consisting of palladium acetate, palladium nitrate, palladium sulfate, or palladium chloride.

5. The synthesis method of the thermally activated delayed fluorescence material having red, green, or blue color according to claim 2, wherein, after finishing the Buchwald-Hartwig coupling reaction, a reaction product is subjected to cooling, extraction, and column chromatography separation in sequence to obtain the thermally activated delayed fluorescence material having red, green, or blue color.

6. A light-emitting device, comprising an electrothermally activated delayed fluorescent device comprising the thermally activated delayed fluorescence material having red, green, or blue color according to claim 1.

7. The light-emitting device according to claim 6, wherein the electrothermally activated delayed fluorescent device comprises a substrate layer, a light-emitting layer, and a cathode layer in a stack, and a light-emitting material of the light-emitting layer is the thermally activated delayed fluorescence material having red, green, or blue color.

Description

DESCRIPTION OF DRAWINGS

(1) The accompanying figures to be used in the description of embodiments of the present disclosure or prior art will be described in brief to more clearly illustrate the technical solutions of the embodiments or the prior art. The accompanying figures described below are only part of the embodiments of the present disclosure, from which those skilled in the art can derive further figures without making any inventive efforts.

(2) FIG. 1 is a schematic molecular orbital diagram of compound 1 to compound 3 obtained according to embodiment 1 to embodiment 3 of the present disclosure.

(3) FIG. 2 is photoluminescence spectrums of compound 1 to compound 3 in a n-hexane solution at room temperature obtained according to embodiment 1 to embodiment 3 of the present disclosure.

(4) FIG. 3 is a schematic structural diagram of an electrothermally activated delayed fluorescent device according to an application embodiment of the present disclosure.

DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS

(5) The present disclosure will be further described below in conjunction with embodiments 1 to 3 and application embodiments 1 to 3.

Embodiment 1: Synthesis of a Thermally Activated Delayed Fluorescence Material Having Red, Green, or Blue Color

(6) The reaction formula is as follows:

(7) ##STR00005##

(8) Add raw material 1 (1.47 g, 5 mmol), carbazole (1.00 g, 6 mmol), palladium acetate (45 mg, 0.2 mmol), and tri-tert-butylphosphine tetrafluoroborate (0.17 g, 0.6 mmol) to a 100 mL two-necked flask, then add NaOt-Bu (0.58 g, 6 mmol) in the glove box, then inject 40 mL of toluene which is dehydrated and deoxygenated under an argon atmosphere, and then react at 120° C. for 24 hours. Cool to room temperature, the reaction solution is poured into 200 mL of ice water, and is extracted three times with dichloromethane. Combine the organic phase to spin to a silica gel column chromatography (volume of dichloromethane:volume of n-hexane, 2:1) to separate and purify to obtain 1.6 g of white blue powders. The yield is 84%.

(9) The nuclear magnetic resonance spectrum of the obtained product (compound 1) is: 1H NMR (300 MHz, CD2Cl2, δ): 8.55 (d, J=6.9 Hz, 2H), 7.93 (d, J=6.0 Hz, 2H), 7.35-7.18 (m, 4H), 2.50 (s, 6H). MS (EI) m/z: [M]+ calcd for C22H14F3NO2, 381.10; found, 381.08.

Embodiment 2: Synthesis of a Thermally Activated Delayed Fluorescence Material Having Red, Green, or Blue Color

(10) The reaction formula is as follows:

(11) ##STR00006##

(12) Add raw material 1 (1.47 g, 5 mmol), phenoxazine (1.01 g, 6 mmol), palladium acetate (45 mg, 0.2 mmol), and tri-tert-butylphosphine tetrafluoroborate (0.17 g, 0.6 mmol) to a 100 mL two-necked flask, then add NaOt-Bu (0.58 g, 6 mmol) in the glove box, then inject 40 mL of toluene which is dehydrated and deoxygenated under an argon atmosphere, and then react at 120° C. for 24 hours. Cool to room temperature, the reaction solution is poured into 200 mL of ice water, and is extracted three times with dichloromethane. Combine the organic phase to spin to a silica gel column chromatography (volume of dichloromethane:volume of n-hexane, 2:1) to separate and purify to obtain 1.5 g of green powders. The yield is 76%.

(13) The nuclear magnetic resonance spectrum of the obtained product (compound 2) is: 1H NMR (300 MHz, CD2Cl2, δ): 7.14 (d, J=6.3 Hz, 2H), 7.05-6.96 (m, 6H), 2.50 (s, 6H). MS (EI) m/z: [M]+ calcd for C22H14F3NO3, 397.09; found, 397.08.

Embodiment 3: Synthesis of a Thermally Activated Delayed Fluorescence Material Having Red, Green, or Blue Color

(14) ##STR00007##

(15) The reaction formula is as follows:

(16) Add raw material 1 (1.47 g, 5 mmol), dimethyldiphenylamine (1.10 g, 6 mmol), palladium acetate (45 mg, 0.2 mmol), and tri-tert-butylphosphine tetrafluoroborate (0.17 g, 0.6 mmol) to a 100 mL two-necked flask, then add NaOt-Bu (0.58 g, 6 mmol) in the glove box, then inject 40 mL of toluene which is dehydrated and deoxygenated under an argon atmosphere, and then react at 120° C. for 24 hours. Cool to room temperature, the reaction solution is poured into 200 mL of ice water, and is extracted three times with dichloromethane. Combine the organic phase to spin to a silica gel column chromatography (volume of dichloromethane:volume of n-hexane, 2:1) to separate and purify to obtain 1.6 g of red powders. The yield is 76%.

(17) The nuclear magnetic resonance spectrum of the obtained product (compound 2) is: 1H NMR (300 MHz, CD2Cl2, δ): 7.15 (d, J=6.9 Hz, 4H), 7.09 (d, J=6.6 Hz, 2H), 2.50 (s, 6H), 2.32 (s, 6H). MS (EI) m/z: [M]+ calcd for C22H20F3NO2, 381.10; found, 381.08.

(18) The molecular orbital diagram of compound 1 to compound 3 obtained according to embodiment 1 to embodiment 3 of the present disclosure is as shown in FIG. 1. The distribution of HOMO and LUMO of compound 1 to compound 3 can be seen from FIG. 1. Specifically, HOMO is distributed on electron donors, LUMO is distributed on electron acceptors, and there is great HOMO-LUMO separation, thereby ensuring molecules have a lower singlet triplet energy level difference.

(19) Electrochemical energy levels and other parameters of compounds 1 to 3 obtained according to embodiments 1 to 3 are tested, the result are as shown in the following table 1: S1 was determined by a room temperature fluorescence spectroscopy, T1 was determined by a low temperature (77K) phosphorescence spectrometer, and HOMO and LUMO were determined by electrochemical redox.

(20) TABLE-US-00001 TABLE 1 the lowest singlet state (S1), the lowest triplet state (T1), and electrochemical energy levels of compound 1 to compound 3. PL Peak S.sub.1 T.sub.1 □E.sub.ST HOMO LUMO (nm) (eV) (eV) (eV) (eV) (eV) Compound 1 460 2.70 2.62 0.08 −6.11 −2.48 Compound 2 543 2.29 2.18 0.11 −5.62 −2.48 Compound 3 638 1.95 1.76 0.19 −5.43 −2.48

(21) Results of photoluminescence spectrums of compound 1 to compound 3 in a n-hexane solution at room temperature obtained according to embodiment 1 to embodiment 3 are as shown in FIG. 2. In FIG. 2, waveforms from left to right are respectively photoluminescence spectrums of compound 1, compound 2, and compound 3. It can be known from FIG. 2: as the electron donating ability of the electron donor increases, the charge-transfer state energy of the luminescent molecule is lower and the corresponding spectrum is gradually red-shifted.

Application Embodiment 1: An Electrothermally Activated Delayed Fluorescent Device 1

(22) An electrothermally activated delayed fluorescent device can be prepared according to methods known in the art, such as a method disclosed in the reference of Adv. Mater. 2003, 15, 277. The specific method is: vapor depositing HATCN, TCTA, host material: TADF guest, TmPyPB, 1 nm of LiF, and 100 nm of Al on a cleaned conductive glass substrate (ITO) under a high vacuum condition in sequence.

(23) A structure of the electrothermally activated delayed fluorescent device is as shown in FIG. 3, which comprises: a substrate layer 1, a hole injection layer 2 disposed on the substrate layer 1, a transport layer 3 disposed on the hole injection layer 2, a light-emitting layer 4 disposed on the transport layer 3, an electron transport layer 5 disposed on the light-emitting layer 4, and a cathode layer 6 disposed on the electron transport layer 5. The substrate layer 1 is a glass or a conductive glass (ITO), the hole injection layer 2 is made of HATCN, the transport layer 3 is made of Tris(4-carbazoyl-9-ylphenyl)amine (TCTA), the light-emitting layer 4 is made of the compound 1 obtained according to embodiment 1, the transport layer 5 is made of 1,3,5-tris(3-(3-pyridyl)phenyl)benzene (TmPyPB), and the cathode layer 6 is made of lithium fluoride/aluminum. The structure of formed device 1 is: ITO/HATCN (2 nm)/TCTA (35 nm)/DPEPO: compound 1 (2%, 20 nm)/TmPyPB (40 nm)/LiF (1 nm)/Al (100 nm).

Application Embodiment 2: An Electrothermally Activated Delayed Fluorescent Device 2

(24) Application embodiment 2 uses the same method as application embodiment 1. The difference is that the light-emitting layer 4 is made of the compound 2 obtained according to embodiment 2. A structure of formed device 2 is: ITO/HATCN (2 nm)/TCTA (35 nm)/mCBP: compound 2 (6%, 40 nm)/TmPyPB (40 nm)/LiF (1 nm)/Al (100 nm).

Application Embodiment 3: An Electrothermally Activated Delayed Fluorescent Device 3

(25) Application embodiment 3 uses the same method as application embodiment 1. The difference is that the light-emitting layer 4 is made of the compound 3 obtained according to embodiment 3. A structure of formed device 3 is: ITO/HATCN (2 nm)/TCTA (35 nm)/CBP: compound 3 (10%, 40 nm)/TmPyPB (40 nm)/LiF (1 nm)/Al (100 nm).

(26) Performances of the devices 1 to 3 obtained according to application embodiments 1 to 3 are tested. Current-brightness-voltage characteristics of the device are measured by Keithley source measurement system with a calibrated silicon photodiode (Keithley 2400 Sourcemeter, Keithley 2000 Currentmeter). Electroluminescence spectrums are measured by SPEX CCD3000 spectrometer (from JY company, French) at room temperature under atmospheric environment. The test results are as shown in table 2.

(27) TABLE-US-00002 TABLE 2 tested performances of devices. Maximum current Maximum external Device efficiency (cd/A) CIEy&CIEx quantum efficiency (%) Device 1 17.3 0.10 18.3% Device 2 65.3 0.26 30.7% Device 3 17.8 0.68 21.6%

(28) Industrial applicability: The subject matter of the present disclosure can be manufactured and used in the industry, thereby having industrial applicability.