CN104177329A - Bipolar blue light phosphorescent host material, preparation method and organic electroluminescent device thereof - Google Patents
Bipolar blue light phosphorescent host material, preparation method and organic electroluminescent device thereof Download PDFInfo
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- CN104177329A CN104177329A CN201310204468.8A CN201310204468A CN104177329A CN 104177329 A CN104177329 A CN 104177329A CN 201310204468 A CN201310204468 A CN 201310204468A CN 104177329 A CN104177329 A CN 104177329A
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- 239000000463 material Substances 0.000 title claims abstract description 65
- 238000002360 preparation method Methods 0.000 title claims abstract description 20
- 238000000034 method Methods 0.000 claims abstract description 8
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 18
- 238000001035 drying Methods 0.000 claims description 18
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 15
- 239000000243 solution Substances 0.000 claims description 15
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 14
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 12
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims description 12
- -1 tris-argon benzyl acetone Chemical compound 0.000 claims description 12
- 239000003054 catalyst Substances 0.000 claims description 10
- 238000006243 chemical reaction Methods 0.000 claims description 9
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 8
- 238000006069 Suzuki reaction reaction Methods 0.000 claims description 8
- 239000012043 crude product Substances 0.000 claims description 8
- 239000013078 crystal Substances 0.000 claims description 8
- 239000012074 organic phase Substances 0.000 claims description 8
- 229940126062 Compound A Drugs 0.000 claims description 7
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 claims description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 7
- 229910052763 palladium Inorganic materials 0.000 claims description 7
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 claims description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 6
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 6
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims description 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- 238000001816 cooling Methods 0.000 claims description 6
- 239000003446 ligand Substances 0.000 claims description 6
- 239000003208 petroleum Substances 0.000 claims description 6
- 229910000073 phosphorus hydride Inorganic materials 0.000 claims description 6
- 239000000741 silica gel Substances 0.000 claims description 6
- 229910002027 silica gel Inorganic materials 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 5
- 239000003513 alkali Substances 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 4
- YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical group [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 claims description 3
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 claims description 3
- 229910000030 sodium bicarbonate Inorganic materials 0.000 claims description 3
- 235000017557 sodium bicarbonate Nutrition 0.000 claims description 3
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 3
- FIDLTJALOIOIEK-UHFFFAOYSA-N C(=O)[Ir+2].N1=CC=CC=C1 Chemical compound C(=O)[Ir+2].N1=CC=CC=C1 FIDLTJALOIOIEK-UHFFFAOYSA-N 0.000 claims description 2
- YXPUNWKYPJPPFC-UHFFFAOYSA-N COC1=C(C(=CC=C1)OC)C1=CC=CC=C1.P Chemical group COC1=C(C(=CC=C1)OC)C1=CC=CC=C1.P YXPUNWKYPJPPFC-UHFFFAOYSA-N 0.000 claims description 2
- 239000012670 alkaline solution Substances 0.000 claims description 2
- 239000012295 chemical reaction liquid Substances 0.000 claims description 2
- 238000005859 coupling reaction Methods 0.000 claims description 2
- 239000003480 eluent Substances 0.000 claims description 2
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 claims description 2
- 230000035484 reaction time Effects 0.000 claims description 2
- COIOYMYWGDAQPM-UHFFFAOYSA-N tris(2-methylphenyl)phosphane Chemical compound CC1=CC=CC=C1P(C=1C(=CC=CC=1)C)C1=CC=CC=C1C COIOYMYWGDAQPM-UHFFFAOYSA-N 0.000 claims description 2
- 230000005540 biological transmission Effects 0.000 abstract description 8
- 230000005525 hole transport Effects 0.000 abstract description 4
- 230000008569 process Effects 0.000 abstract description 3
- 239000004065 semiconductor Substances 0.000 abstract description 3
- 238000004020 luminiscence type Methods 0.000 abstract 2
- 239000010410 layer Substances 0.000 description 34
- 229910052757 nitrogen Inorganic materials 0.000 description 22
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 16
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 12
- 239000011521 glass Substances 0.000 description 11
- 230000000903 blocking effect Effects 0.000 description 8
- 238000002347 injection Methods 0.000 description 8
- 239000007924 injection Substances 0.000 description 8
- PQXKHYXIUOZZFA-UHFFFAOYSA-M lithium fluoride Chemical compound [Li+].[F-] PQXKHYXIUOZZFA-UHFFFAOYSA-M 0.000 description 7
- DHDHJYNTEFLIHY-UHFFFAOYSA-N 4,7-diphenyl-1,10-phenanthroline Chemical compound C1=CC=CC=C1C1=CC=NC2=C1C=CC1=C(C=3C=CC=CC=3)C=CN=C21 DHDHJYNTEFLIHY-UHFFFAOYSA-N 0.000 description 6
- 229910052786 argon Inorganic materials 0.000 description 6
- 239000000758 substrate Substances 0.000 description 6
- RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-naphthylamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 5
- OGGKVJMNFFSDEV-UHFFFAOYSA-N 3-methyl-n-[4-[4-(n-(3-methylphenyl)anilino)phenyl]phenyl]-n-phenylaniline Chemical group CC1=CC=CC(N(C=2C=CC=CC=2)C=2C=CC(=CC=2)C=2C=CC(=CC=2)N(C=2C=CC=CC=2)C=2C=C(C)C=CC=2)=C1 OGGKVJMNFFSDEV-UHFFFAOYSA-N 0.000 description 4
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- 238000002411 thermogravimetry Methods 0.000 description 4
- 239000007789 gas Substances 0.000 description 3
- YNHIGQDRGKUECZ-UHFFFAOYSA-N dichloropalladium;triphenylphosphanium Chemical group Cl[Pd]Cl.C1=CC=CC=C1[PH+](C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1[PH+](C=1C=CC=CC=1)C1=CC=CC=C1 YNHIGQDRGKUECZ-UHFFFAOYSA-N 0.000 description 2
- 239000002346 layers by function Substances 0.000 description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 description 2
- ZFGCKZCEDNBNMV-UHFFFAOYSA-N 2,8-dibromodibenzothiophene 5,5-dioxide Chemical compound BrC1=CC=C2S(=O)(=O)C3=CC=C(Br)C=C3C2=C1 ZFGCKZCEDNBNMV-UHFFFAOYSA-N 0.000 description 1
- SJXGROCZTVDNGT-UHFFFAOYSA-N N1=C(C=CC=C1)C(=O)[Ir+2] Chemical compound N1=C(C=CC=C1)C(=O)[Ir+2] SJXGROCZTVDNGT-UHFFFAOYSA-N 0.000 description 1
- CGMKCLNRCCHDMM-UHFFFAOYSA-N O=S(c(c(-c1c2)c3)ccc3-c(cc3)ccc3N(c3ccccc3)c3c(cccc4)c4ccc3)(c1ccc2-c(cc1)ccc1N(c1ccccc1)c1c(cccc2)c2ccc1)=O Chemical compound O=S(c(c(-c1c2)c3)ccc3-c(cc3)ccc3N(c3ccccc3)c3c(cccc4)c4ccc3)(c1ccc2-c(cc1)ccc1N(c1ccccc1)c1c(cccc2)c2ccc1)=O CGMKCLNRCCHDMM-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 1
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 238000001755 magnetron sputter deposition Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000001819 mass spectrum Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- IIOSDXGZLBPOHD-UHFFFAOYSA-N tris(2-methoxyphenyl)phosphane Chemical compound COC1=CC=CC=C1P(C=1C(=CC=CC=1)OC)C1=CC=CC=C1OC IIOSDXGZLBPOHD-UHFFFAOYSA-N 0.000 description 1
- 238000007738 vacuum evaporation Methods 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/50—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D333/76—Dibenzothiophenes
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
- H10K85/6576—Polycyclic condensed heteroaromatic hydrocarbons comprising only sulfur in the heteroaromatic polycondensed ring system, e.g. benzothiophene
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Electroluminescent Light Sources (AREA)
Abstract
Belonging to the field of organic semiconductor materials, the invention discloses a bipolar blue light phosphorescent host material, a preparation method and an organic electroluminescent device thereof. The host material has a structural formula shown as the specification. The bipolar blue light phosphorescent host material provided by the invention has bipolar carrier transport capacity, also has hole transport properties and electron transport properties at the same time, and enables balance transport of holes and electrons in a luminescent layer. With a high triplet state energy level, the host material can effectively prevent back transmission of energy to the host material in a luminescence process, thus greatly improving the luminescence efficiency.
Description
Technical Field
The invention relates to the field of organic semiconductor materials, in particular to a bipolar blue-light phosphorescent host material and a preparation method thereof. The invention also relates to an organic electroluminescent device, and the luminescent layer material of the organic electroluminescent device comprises a bipolar blue light phosphorescent host material.
Background
The organic electroluminescent device has the advantages of low driving voltage, high response speed, wide visual angle range, abundant colors due to the fact that the luminous performance can be changed through fine adjustment of a chemical structure, high resolution, light weight, large-area panel display and the like, is known as a panel display technology in the 21 st century, and becomes a hotspot of research in the fields of materials, information, physics and other subjects and panel display. Future efficient commercial organic light emitting diodes will likely contain organometallic phosphors because they can trap both singlet and triplet excitons, achieving 100% internal quantum efficiency. However, due to the relatively long excited exciton lifetime of the transition metal complexes, unwanted triplet-triplet (T) results1-T1) Quenching in the actual operation of the device. To overcome this problem, researchers often dope triplet emitters into organic host materials.
In recent years, green and red phosphorescent OLED devices have exhibited satisfactory electroluminescent efficiency. While highly efficient blue phosphorescent devices are rare, the main reason is the lack of a combination of good carrier transport properties and high triplet energy level (E)T) The host material of (1).
Disclosure of Invention
One of the problems to be solved by the present invention is to provide a semiconductor device having a good carrier transport property and a high triplet level (E)T) The ambipolar blue phosphorescent host material of (1).
The second problem to be solved by the present invention is to provide a method for preparing a bipolar blue-light phosphorescent host material.
The present invention provides an organic electroluminescent device, wherein the material of the light-emitting layer includes a bipolar blue-light phosphorescent host material.
The technical scheme of the invention is as follows:
a bipolar blue light phosphorescence host material has the following structural formula:
namely, N, N '- (4,4' -dibenzo [ b, d ]]thiophene-S, S-dioxo-2, 8-diyl) bis (4, 1-phenylene)) bis (N-phenylnaphthyl-1-amine).
The preparation method of the bipolar blue-light phosphorescent host material comprises the following steps:
compounds A and B are provided, respectively, represented by the following structural formulae,
i.e. 2, 8-dibromo-dibenzo [ b, d ]]thiophene-S, S-dioxygen;
namely N-phenyl-N- (4-pinacol borate) phenyl) naphthalen-1-amine;
adding a compound A and a compound B with a molar ratio of 1: 2-2.4 into an organic solvent containing a catalyst and an alkali solution in an oxygen-free environment for dissolving, carrying out Suzuki coupling reaction at 70-130 ℃ for 12-48 hours, stopping the reaction, cooling to room temperature, and separating and purifying the reaction solution to obtain the bipolar blue-light phosphorescent host material with the following structural formula:
the preparation method of the bipolar blue light phosphorescence host material comprises the step of forming an oxygen-free environment by at least one gas of nitrogen and argon.
The preparation method of the bipolar blue light phosphorescence host material comprises the following steps of (1) preparing a catalyst, wherein the catalyst is bis (triphenylphosphine) palladium dichloride or tetrakis (triphenylphosphine) palladium; or,
the catalyst is a mixture of organic palladium and an organic phosphine ligand, and in the mixture, the molar weight of the organic phosphine ligand is 4-8 times that of the organic palladium; the organic palladium is palladium acetate or tris-argon benzyl acetone dipalladium; the organic phosphine ligand is tri-o-tolylphosphine or 2-dicyclohexyl phosphine-2 ', 6' -dimethoxy biphenyl;
the molar ratio of the catalyst to the compound A is 1: 20-1: 100.
The preparation method of the bipolar blue-light phosphorescent host material comprises the following steps of selecting at least one of a sodium carbonate solution, a potassium carbonate solution and a sodium bicarbonate solution as the alkali solution; in the alkaline solution, the molar weight of the alkaline solute is 20 times of the molar weight of the compound A.
The preparation method of the bipolar blue-light phosphorescent host material comprises the step of preparing a bipolar blue-light phosphorescent host material, wherein the organic solvent is at least one of toluene, N-dimethylformamide and tetrahydrofuran.
The preparation method of the bipolar blue-light phosphorescent host material comprises the following steps of enabling the temperature of Suzuki coupling reaction to be 90-120 ℃, and enabling reaction time to be 24-36 hours.
The preparation method of the bipolar blue-light phosphorescent host material comprises the following steps of:
after the coupling reaction is stopped, extracting the reaction liquid for a plurality of times, preferably more than three times, combining organic phases, drying the organic phases by anhydrous magnesium sulfate, then carrying out spin drying to obtain a crude product, separating the crude product by using petroleum ether and ethyl acetate with the volume ratio of 10:1 as eluent through a silica gel chromatographic column to obtain a crystal, and drying the crystal at 50 ℃ in vacuum for 24 hours to obtain the bipolar blue-light phosphorescent host material.
An organic electroluminescent device comprises a substrate, an anode layer, a hole injection layer, a hole transmission/electron blocking layer, a light emitting layer, an electron transmission/hole blocking layer, an electron injection layer and a cathode layer which are sequentially stacked on one surface of the substrate; wherein, the material of each functional layer is as follows:
a substrate made of glass;
an anode layer made of Indium Tin Oxide (ITO) and combined with a glass substrate, which is generally called ITO glass or ITO;
a hole injection layer made of CuPc;
the material of the hole transport/electron blocking layer is N, N '-diphenyl-N, N' -di (3-methylphenyl) -1,1 '-biphenyl-4, 4' -diamine (TPD);
the material of the luminescent layer is a doped mixed material formed by adding bis (4, 6-difluorophenylpyridine-N, C2) pyridine formyl iridium (III) (FIrpic) into a bipolar blue light phosphorescence host material with the following structural formula according to the mass percentage of 10 percent:
an electron transport/hole blocking layer made of 4, 7-diphenyl-1, 10-phenanthroline (BPhen)
An electron injection layer of LiF, and
and the cathode layer is made of Al.
The bipolar blue light phosphorescence host material provided by the invention has bipolar carrier transmission capability, hole transmission property and electron transmission property, so that the transmission of holes and electrons in a light-emitting layer is balanced, and the high triplet state energy level can effectively prevent energy from being transmitted back to the host material in the light-emitting process, thereby greatly improving the light-emitting efficiency.
In addition, the preparation method of the bipolar blue-light phosphorescent host material adopts a simpler synthesis route, thereby reducing the process flow, and the raw materials are cheap and easy to obtain, so that the manufacturing cost is reduced.
Drawings
FIG. 1 is a thermogravimetric analysis chart of the ambipolar blue phosphorescent host material prepared in example 1;
fig. 2 is a schematic view of the structure of an organic electroluminescent device produced in example 5.
Detailed Description
For a better understanding of the contents of the present patent application, the following further illustrates the technical scheme of the present invention by specific examples and illustrations, including materials preparation and device preparation, but these examples do not limit the present invention, wherein compound a, compound B are commercially available.
Example 1
The bipolar blue-light phosphorescent host material of the embodiment has a structure of N, N '- (4,4' -dibenzo [ b, d ] thiophene-S, S-dioxo-2, 8-diyl) bis (4, 1-phenylene)) bis (N-phenylnaphthyl-1-amine), and is prepared by the following steps:
under the protection of argon, 2, 8-dibromo-dibenzo [ b, d ]]Adding thiophene-S, S-dioxy (75mg,0.2mmol) and N-phenyl-N- (4-pinacol borate) phenyl) naphthalene-1-amine (168mg,0.4mmol) into a flask containing 10mL of a toluene solvent, fully dissolving, adding a potassium carbonate (2mL,2mol/L) solution into the flask, vacuumizing to remove oxygen and filling argon, and then adding bis (triphenylphosphine) palladium dichloride (5.6 mg,0.008 mmol); the flask was heated to 100 ℃ for a Suzuki coupling reaction for 24 h. Stopping reaction, cooling to room temperature, extracting with dichloromethane for three times, combining organic phases, drying with anhydrous magnesium sulfate, then spin-drying, and separating the crude product with petroleum ether and ethyl acetate in a volume ratio of 10:1 as leacheate through a silica gel chromatographic column to obtain white crystals. And finally drying for 24h at 50 ℃ in vacuum to obtain the bipolar blue-light phosphorescent host material. The yield was 78%. Mass spectrum: m/z770.3 (M)++ 1); elemental analysis (%) C56H38N2S is a theoretical value: c87.24, H4.97, N3.63, S4.16; measured value: c87.31, H4.87, N3.5, S4.24.
FIG. 1 is a thermogravimetric analysis chart of the ambipolar blue phosphorescent host material prepared in example 1; thermogravimetric analysis was performed by a Perkin-Elmer Series7 thermogravimetric analysis system, all measurements performed in a room temperature atmosphere, 5% thermogravimetric temperature (T.sub.w.)d) Is 366 ℃.
Example 2
The bipolar blue-light phosphorescent host material of the embodiment has a structure of N, N '- (4,4' -dibenzo [ b, d ] thiophene-S, S-dioxo-2, 8-diyl) bis (4, 1-phenylene)) bis (N-phenylnaphthyl-1-amine), and is prepared by the following steps:
under the protection of a mixed gas of nitrogen and argon, 2, 8-dibromo-dibenzo [ b, d ] thiophene-S, S-dioxo (112mg,0.3mmol), N-phenyl-N- (4-pinacol borate) phenyl) naphthalene-1-amine (278mg,0.66mmol) and 15mL of tetrahydrofuran were added to a 50 mL-standard two-necked bottle, and after fully dissolving, a mixed gas of nitrogen and argon was introduced to evacuate air for about 20min, and then tetratriphenylphosphine palladium (4 mg,0.003 mmol) was added thereto, and after fully dissolving, a sodium bicarbonate (3mL,2mol/L) solution was added. After the mixture of nitrogen and argon was fully purged for about 10min, the two bottles were charged to 70 ℃ to conduct Suzuki coupling reaction for 48 hours. Stopping reaction, cooling to room temperature, extracting with dichloromethane for seven times, combining organic phases, drying with anhydrous magnesium sulfate, spin-drying, and separating the crude product with petroleum ether and ethyl acetate in a volume ratio of 10:1 as leacheate through a silica gel chromatographic column to obtain white crystals. And finally drying for 24h at 50 ℃ in vacuum to obtain the bipolar blue-light phosphorescent host material. The yield was 82%.
Example 3
The bipolar blue-light phosphorescent host material of the embodiment has a structure of N, N '- (4,4' -dibenzo [ b, d ] thiophene-S, S-dioxo-2, 8-diyl) bis (4, 1-phenylene)) bis (N-phenylnaphthyl-1-amine), and is prepared by the following steps:
under the protection of nitrogen, adding 2, 8-dibromo-dibenzo [ b, d ] thiophene-S, S-dioxide (112mg,0.3mmol), N-phenyl-N- (4-pinacol borate) phenyl) naphthalene-1-amine (303mg,0.72mmol), palladium acetate (3.5mg,0.015mmol) and tris (o-methoxyphenyl) phosphine (21mg, 0.06mmol) into a flask containing 12mL of N, N-dimethylformamide, fully dissolving, adding a potassium carbonate (3mL,2mol/L) solution, and then introducing nitrogen into the flask to exhaust air for about 30 min; the flask was heated to 130 ℃ for a Suzuki coupling reaction for 12 h. Stopping reaction, cooling to room temperature, extracting with dichloromethane five times, combining organic phases, drying with anhydrous magnesium sulfate, spin-drying, and separating the crude product with petroleum ether and ethyl acetate in a volume ratio of 10:1 as leacheate through a silica gel chromatographic column to obtain white crystals. And finally drying for 24h at 50 ℃ in vacuum to obtain the bipolar blue-light phosphorescent host material. The yield was 74%.
Example 4
The bipolar blue-light phosphorescent host material of the embodiment has a structure of N, N '- (4,4' -dibenzo [ b, d ] thiophene-S, S-dioxo-2, 8-diyl) bis (4, 1-phenylene)) bis (N-phenylnaphthyl-1-amine), and is prepared by the following steps:
under nitrogen, 2, 8-dibromo-dibenzo [ b, d ] thiophene-S, S-dioxo (112mg,0.3mmol), N-phenyl-N- (4-pinacol borate) phenyl) naphthalen-1-amine (303mg,0.72mmol), tris-argon benzylacetone dipalladium (9mg,0.009mmol), and 2-dicyclohexylphosphine-2 ', 6' -dimethoxybiphenyl (29mg, 0.072mmol) were added to a flask containing 12mL of N, N-dimethylformamide, and after sufficient dissolution, a solution of sodium carbonate (3mL,2mol/L) was added. Then introducing nitrogen into the flask to exhaust air for about 30 min; the flask was heated to 120 ℃ for a Suzuki coupling reaction for 36 h. Stopping reaction, cooling to room temperature, extracting with dichloromethane for three times, combining organic phases, drying with anhydrous magnesium sulfate, then spin-drying, and separating the crude product with petroleum ether and ethyl acetate in a volume ratio of 10:1 as leacheate through a silica gel chromatographic column to obtain white crystals. And finally drying for 24h at 50 ℃ in vacuum to obtain the bipolar blue-light phosphorescent host material. The yield was 79%.
Example 5
This example is an organic electroluminescent device using N, N '- (4,4' -dibenzo [ b, d ] thiophene-S, S-dioxo-2, 8-diyl) bis (4, 1-phenylene)) bis (N-phenylnaphthyl-1-amine) (represented by P) prepared in any one of examples 1 to 4 as a host material of a light-emitting layer.
The organic electroluminescent device, as shown in fig. 2, includes a sequentially stacked structure: substrate 1/anode layer 2/hole injection layer 3/(hole transport/electron blocking layer) 4/light emitting layer 5/(electron transport/hole blocking layer) 6/electron injection layer 7/cathode layer 8; wherein slashes "/" indicate a layered structure.
The functional layer of the organic electroluminescent device is made of the following materials and the thickness:
the substrate 1 is made of glass;
the anode layer 2 is made of ITO (indium tin oxide compound) with the thickness of 150 nm; after the ITO is prepared on the surface of the glass, the ITO glass is called as the ITO glass for short;
the hole injection layer 3 is made of copper phthalocyanine (CuPc) and has a thickness of 30 nm;
the hole transport/electron blocking layer 4 was made of N, N '-diphenyl-N, N' -bis (3-methylphenyl) -1,1 '-biphenyl-4, 4' -diamine (TPD) and had a thickness of 20 nm;
the material of the light-emitting layer 5 was bis (4, 6-difluorophenylpyridine-N, C2) picolinoyl iridium (III) (FIrpic) as a guest light-emitting material, and was doped with N, N '- (4,4' -dibenzo [ b, d ] thiophene-S, S-dioxo-2, 8-diyl) bis (4, 1-phenylene)) bis (N-phenylnaphthyl-1-amine) (represented by P) as a host material at a mass ratio of 10%, and was represented by P: FIrpic with a thickness of 20 nm;
the material of the electron transmission/hole blocking layer 6 is 4, 7-diphenyl-1, 10-phenanthroline (BPhen), and the thickness is 30 nm;
the electron injection layer 7 is made of lithium fluoride (LiF) and has a thickness of 1 nm;
the cathode layer 8 is made of aluminum (Al) and has a thickness of 100 nm.
The organic electroluminescent device described above may be represented as:
glass/ITO/CuPc/TPD/P FIrpic/BPhen/LiF/Al; wherein slashes "/" indicate a layered structure.
The preparation process of the organic electroluminescent device comprises the following steps:
firstly, preparing an ITO layer on the surface of cleaned glass through magnetron sputtering to obtain ITO glass;
secondly, moving the ITO glass into vacuum evaporation equipment, and sequentially laminating and evaporating CuPc, TPD, P, FIrpic, BPhen, LiF and Al on the surface of the ITO layer;
and after the process steps are completed, obtaining the organic electroluminescent device.
The current-luminance-voltage characteristics of the organic electroluminescent device were performed by a Keithley source measuring system (Keithley 2400Sourcemeter, Keithley2000 Cuirrentmeter) with a calibrated silicon photodiode.
The test result shows that the starting voltage of the organic electroluminescent device is 3.4V and is 1000cd/m2The lumen efficiency is 6.8 lm/W.
Claims (10)
1. A bipolar blue light phosphorescence host material is characterized in that the structural formula is as follows:
2. a preparation method of a bipolar blue-light phosphorescent host material is characterized by comprising the following steps:
compounds A and B are provided, respectively, represented by the following structural formulae,
A：B：
adding a compound A and a compound B with a molar ratio of 1: 2-2.4 into an organic solvent containing a catalyst and an alkali solution in an oxygen-free environment for dissolving, carrying out Suzuki coupling reaction at 70-130 ℃ for 12-48 hours, stopping the reaction, cooling to room temperature, and separating and purifying the reaction solution to obtain the bipolar blue-light phosphorescent host material with the following structural formula:
3. the preparation method of the bipolar blue-light phosphorescent host material according to claim 2, wherein the catalyst is bis-triphenylphosphine palladium dichloride or tetrakis-triphenylphosphine palladium; the molar ratio of the catalyst to the compound A is 1: 20-1: 100.
4. The preparation method of the bipolar blue-light phosphorescent host material according to claim 2, wherein the catalyst is a mixture of organic palladium and an organic phosphine ligand, and the molar amount of the organic phosphine ligand in the mixture is 4-8 times that of the organic palladium; the molar ratio of the catalyst to the compound A is 1: 20-1: 100.
5. The preparation method of the bipolar blue-light phosphorescent host material according to claim 4, wherein the organic palladium is palladium acetate or tris-argon benzyl acetone dipalladium; the organic phosphine ligand is tri-o-tolylphosphine or 2-dicyclohexyl phosphine-2 ', 6' -dimethoxy biphenyl.
6. The method of claim 2, wherein the alkali solution is at least one selected from sodium carbonate solution, potassium carbonate solution, and sodium bicarbonate solution; in the alkaline solution, the molar weight of the alkaline solute is 20 times of the molar weight of the compound A.
7. The method of claim 2, wherein the organic solvent is at least one of toluene, N-dimethylformamide, and tetrahydrofuran.
8. The preparation method of the bipolar blue-light phosphorescent host material according to claim 2, wherein the temperature of the Suzuki coupling reaction is 90-120 ℃, and the reaction time is 24-36 hours.
9. The method of claim 2, wherein the separating and purifying the reaction solution comprises:
after the coupling reaction is stopped, extracting the reaction liquid for multiple times by using dichloromethane, merging organic phases, drying the organic phases by using anhydrous magnesium sulfate, and then carrying out spin drying to obtain a crude product, separating the crude product by using petroleum ether and ethyl acetate with the volume ratio of 10:1 as eluent through a silica gel chromatographic column to obtain a crystal, and drying the crystal at 50 ℃ in vacuum for 24 hours to obtain the bipolar blue-light phosphorescence host material.
10. An organic electroluminescent device is characterized in that a luminescent layer of the organic electroluminescent device is a doped mixed material formed by adding bis (4, 6-difluorophenylpyridine-N, C2) pyridine formyl iridium (III) into a bipolar blue light phosphorescence host material with the following structural formula according to the proportion of 10% by mass:
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| CN114890981A (en) * | 2022-05-16 | 2022-08-12 | 内蒙古大学 | Preparation method of amino-substituted dibenzothiophene sulfoxide derivatives |
| CN114890984A (en) * | 2022-05-16 | 2022-08-12 | 内蒙古大学 | Preparation method and application of photosensitizer with aggregation-induced emission characteristic |
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| CN102775398A (en) * | 2012-07-25 | 2012-11-14 | 烟台万润精细化工股份有限公司 | Novel bipolar material and application thereof |
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| CN102775398A (en) * | 2012-07-25 | 2012-11-14 | 烟台万润精细化工股份有限公司 | Novel bipolar material and application thereof |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN114890981A (en) * | 2022-05-16 | 2022-08-12 | 内蒙古大学 | Preparation method of amino-substituted dibenzothiophene sulfoxide derivatives |
| CN114890984A (en) * | 2022-05-16 | 2022-08-12 | 内蒙古大学 | Preparation method and application of photosensitizer with aggregation-induced emission characteristic |
| CN114890984B (en) * | 2022-05-16 | 2023-08-29 | 内蒙古大学 | Preparation method and application of photosensitizer with aggregation-induced emission characteristic |
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