ORGANIC COMPOUND AND APPLICATION THEREOF

Abstract

Provided are an organic compound and an application thereof. The compound has a relatively deep LUMO energy level and can reduce a potential barrier of electron transport, improve an electron injection ability, and effectively reduce the voltage of an OLED device. Such compounds all have relatively deep HOMO energy levels and can effectively block holes so that more holes and electrons are recombined in a light-emitting region, achieving higher luminescence efficiency. Materials of an electron transport layer and/or a hole blocking layer suitable for the OLED device can reduce the voltage and power consumption, improve the luminescence efficiency, and extend the service life of the device so that the OLED device has better comprehensive performance.

Claims

1. An organic compound having a structure represented by Formula I: ##STR00144## wherein the ring A is selected from a substituted or unsubstituted C6-C20 aromatic ring, or a substituted or unsubstituted C5-C30 aromatic heterocycle; wherein Y.sub.1 and Y.sub.2 are independently selected from a C atom or a N atom; wherein L is selected from substituted or unsubstituted C6-C20 aryl, or substituted or unsubstituted C5-C30 heteroaryl; wherein X.sub.1 to X.sub.3 are independently selected from the C atom or the N atom, and at least one of X.sub.1 to X.sub.3 is N; wherein R.sub.1 and R.sub.2 are independently selected from substituted or unsubstituted C6-C30 aryl or substituted or unsubstituted C5-C30 heteroaryl; and wherein n.sub.1 is an integer from 0 to 3, for example, may be 0, 1, 2 or 3.

2. The organic compound according to claim 1, wherein the organic compound has a structure represented by Formula II: ##STR00145##

3. The organic compound according to claim 1, wherein when the substituted or unsubstituted C6-C20 aromatic ring, substituted or unsubstituted C5-C30 aromatic heterocycle, substituted or unsubstituted C6-C20 aryl, substituted or unsubstituted C5-C30 heteroaryl, substituted or unsubstituted C6-C30 aryl or substituted or unsubstituted C5-C30 heteroaryl contains a substituent, the substituent is selected from at least one of deuterium, cyano, halogen, unsubstituted or halogenated C1-C10 linear or branched alkyl, unsubstituted or halogenated C1-C10 alkoxy, C1-C10 alkylthio, C6-C20 aryl, C5-C20 heteroaryl or C6-C18 arylamine.

4. The organic compound according to claim 1, wherein the ring A is any one of phenylene, biphenylene, naphthylene, terphenylene, pyridylene and phenylene-naphthylene.

5. The organic compound according to claim 1, wherein L is selected from any one of phenylene, biphenylene, naphthylene, terphenylene and pyridylene.

6. The organic compound according to claim 1, wherein two of X.sub.1 to X.sub.3 are N or all of X.sub.1 to X.sub.3 are N.

7. The organic compound according to claim 1, wherein both Y.sub.1 and Y.sub.2 are selected from the C atom, and n.sub.1 is an integer from 1 to 3.

8. The organic compound according to claim 1, wherein at least one of Y.sub.1 and Y.sub.2 is selected from the N atom, and n.sub.1 is an integer from 0 to 3.

9. The organic compound according to claim 1, wherein R.sub.1 and R.sub.2 are independently selected from any one of the following groups: ##STR00146## ##STR00147## wherein the dashed line represents a linkage site of the group; wherein L.sub.1 is selected from any one of a single bond or substituted or unsubstituted C6-C20 arylene; wherein X.sub.4 is selected from 0, S or NR.sub.N1; wherein X.sub.5 is selected from O, S, NR.sub.N2 or CR.sub.C3R.sub.C4; wherein R.sub.N1, R.sub.N2, R.sub.C3 and R.sub.C4 are each independently selected from any one of hydrogen, substituted or unsubstituted C1-C20 linear or branched alkyl, substituted or unsubstituted C6-C20 aryl or substituted or unsubstituted C5-C20 heteroaryl; wherein R.sub.11 and R.sub.12 are each independently selected from any one of deuterium, cyano, halogen, unsubstituted or halogenated C1-C10 linear or branched alkyl, unsubstituted or halogenated C1-C10 alkoxy, C1-C10 alkylthio, C6-C20 aryl, C5-C20 heteroaryl or C6-C18 arylamine; wherein m.sub.1 is selected from an integer from 0 to 5; wherein m.sub.2 is selected from an integer from 0 to 6; wherein m.sub.3 is selected from an integer from 0 to 9; wherein m.sub.4 and m.sub.6 are each independently selected from an integer from 0 to 4; and wherein m.sub.5 is selected from an integer from 0 to 3.

10. The organic compound according to claim 9, wherein R.sub.1 and R.sub.2 are independently selected from any one of the following substituted or unsubstituted groups: ##STR00148## ##STR00149## ##STR00150## wherein the dashed line represents a linkage site of the group; wherein the substituted substituents are each independently selected from at least one of deuterium, cyano, halogen, unsubstituted or halogenated C1-C10 linear or branched alkyl, unsubstituted or halogenated C1-C10 alkoxy, C1-C10 alkylthio, C6-C20 aryl, C2-C20 heteroaryl or C6-C18 arylamine.

11. The organic compound according to claim 1, wherein the organic compound is any one of the following compounds: ##STR00151## ##STR00152## ##STR00153## ##STR00154## ##STR00155## ##STR00156## ##STR00157## ##STR00158## ##STR00159## ##STR00160## ##STR00161## ##STR00162## ##STR00163## ##STR00164## ##STR00165## ##STR00166## ##STR00167## ##STR00168## ##STR00169## ##STR00170## ##STR00171## ##STR00172## ##STR00173## ##STR00174## ##STR00175## ##STR00176## ##STR00177## ##STR00178## ##STR00179## ##STR00180## ##STR00181## ##STR00182## ##STR00183## ##STR00184## ##STR00185## ##STR00186## ##STR00187## ##STR00188## ##STR00189## ##STR00190## ##STR00191## ##STR00192## ##STR00193## ##STR00194## ##STR00195## ##STR00196## ##STR00197## ##STR00198## ##STR00199## ##STR00200## ##STR00201## ##STR00202## ##STR00203## ##STR00204## ##STR00205## ##STR00206## ##STR00207## ##STR00208## ##STR00209## ##STR00210## ##STR00211## ##STR00212##

12. A material of an electron transport layer, comprising the organic compound according to claim 1.

13. A material of a hole blocking layer, comprising the organic compound according to claim 1.

14. An OLED device, comprising an anode, a cathode and an organic thin film layer disposed between the anode and the cathode, wherein a material of the organic thin film layer comprises the organic compound according to claim 1.

15. The OLED device according to claim 14, wherein the organic thin film layer comprises an electron transport layer whose material comprises the organic compound.

16. The OLED device according to claim 14, wherein the organic thin film layer comprises a hole blocking layer whose material comprises the organic compound.

17. A display panel, comprising the OLED device, wherein the OLED device comprises the anode, the cathode and the organic thin film layer disposed between the anode and the cathode, wherein the material of the organic thin film layer comprises the organic compound.

18. An electronic apparatus, comprising the display panel, wherein the display panel comprises the OLED device which comprises the anode, the cathode and the organic thin film layer disposed between the anode and the cathode, wherein the material of the organic thin film layer comprises the organic compound.

Description

BRIEF DESCRIPTION OF DRAWINGS

[0029] FIG. 1 is a structure diagram of an OLED device according to the present disclosure.

REFERENCE LIST

[0030] 101 anode [0031] 102 cathode [0032] 103 light-emitting layer [0033] 104 first organic thin film layer [0034] 105 second organic thin film layer

DETAILED DESCRIPTION

[0035] Technical solutions of the present disclosure are further described below through embodiments. It is to be understood by those skilled in the art that the embodiments described herein are used for a better understanding of the present disclosure and are not to be construed as specific limitations to the present disclosure.

[0036] A first aspect of the present disclosure is to provide an organic compound, where the organic compound has a structure represented by Formula I:

##STR00002##

[0037] The ring A is selected from a substituted or unsubstituted C6-C20 aromatic ring, or a substituted or unsubstituted C5-C30 aromatic heterocycle.

[0038] Y.sub.1 and Y.sub.2 are independently selected from a C atom or a N atom.

[0039] L is selected from substituted or unsubstituted C6-C20 aryl, or substituted or unsubstituted C5-C30 heteroaryl.

[0040] X.sub.1 to X.sub.3 are independently selected from the C atom or the N atom, and at least one of X.sub.1 to X.sub.3 is N.

[0041] R.sub.1 and R.sub.2 are independently selected from substituted or unsubstituted C6-C30 aryl, or substituted or unsubstituted C5-C30 heteroaryl.

[0042] n.sub.1 is an integer from 0 to 3.

[0043] In the present disclosure, C6-C20 may each independently be C6, C9, C10, C12, C13, C14, C15, C16, C18, C19 or the like.

[0044] C5-C30 may each independently be C6, C7, C8, C9, C10, C12, C13, C14, C15, C16, C18, C20, C22, C24, C26, C28, C29 or the like.

[0045] C6-C30 may each independently be C7, C8, C9, C10, C12, C13, C14, C15, C16, C18, C20, C22, C24, C26, C28, C29 or the like.

[0046] C6-C30 aryl involved in the present disclosure exemplarily includes, but is not limited to, phenyl, biphenyl, terphenyl, naphthyl, anthryl, phenanthryl, pyrenyl, fluorenyl and derivatives thereof (dimethylfluorenyl, diphenylfluorenyl), indenyl, perylenyl, triphenylene or the like.

[0047] C5-C30 heteroaryl involved in the present disclosure exemplarily includes, but is not limited to, pyridyl, pyrazinyl, pyridazinyl, pyrimidyl, triazinyl, quinolyl, isoquinolyl, quinoxalinyl, quinazolinyl, pyridopyridyl, an o-phenanthroline group, acridinyl, phenazinyl, benzimidazolyl, benzothiazolyl, benzoxazolyl, indolyl, furyl, thienyl, pyrrolyl, dibenzofuryl, dibenzothienyl, carbazolyl, N-phenylcarbazolyl or the like.

[0048] C1-C20 linear or branched alkyl involved in the present disclosure exemplarily includes, but is not limited to, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, t-butyl, n-pentyl, t-pentyl, isopentyl, neopentyl, n-hexyl, n-heptyl, n-octyl or the like.

[0049] In the structure of the organic compound provided by the present disclosure,

##STR00003##

cooperates with the ring A and L cooperates with

##STR00004##

so that the organic compound achieves the purpose of electron transport, has a sufficiently high reduction potential, facilitates electron transport, reduces a potential barrier of electron injection, and further reduces device voltage. The suitable HOMO energy level and LUMO energy level of the organic compound are conducive to energy level matching of adjacent layers. The organic compound has a hole blocking ability due to a relatively deep HOMO energy level so that more holes and electrons are recombined in a light-emitting region, which can achieve higher luminescence efficiency.

[0050] An NC group contained in the compound of the present disclosure enhances an electron withdrawing ability of the compound, which means a deeper LUMO energy level, so that the potential barrier of electron injection is reduced, which is conducive to electron injection and reducing device voltage.

[0051] The compound of the present disclosure is suitable for use as materials of an electron transport layer and/or a hole blocking layer and can reduce voltage and power consumption, improve the luminescence efficiency, and extend the service life of a device.

[0052] In an embodiment, the organic compound has a structure represented by Formula II:

##STR00005##

[0053] The groups in Formula II are defined within the same ranges as in Formula I.

[0054] In an embodiment, when the substituted or unsubstituted C6-C20 aromatic ring, substituted or unsubstituted C5-C30 aromatic heterocycle, substituted or unsubstituted C6-C20 aryl, substituted or unsubstituted C5-C30 heteroaryl, substituted or unsubstituted C6-C30 aryl or substituted or unsubstituted C5-C30 heteroaryl contains a substituent, the substituent is selected from at least one of deuterium, cyano, halogen, unsubstituted or halogenated C1-C10 (for example, C1, C2, C3, C4, C5, C6, C7, C8, C9 or C10) linear or branched alkyl, unsubstituted or halogenated C1-C10 (for example, C1, C2, C3, C4, C5, C6, C7, C8, C9 or C10) alkoxy, C1-C10 (for example, C1, C2, C3, C4, C5, C6, C7, C8, C9 or C10) alkylthio, C6-C20 (for example, C6, C9, C10, C12, C14, C16, C18 or the like) aryl, C5-C20 (for example, C6, C8, C10, C12, C14, C16, C18 or the like) heteroaryl, or C6-C18 (for example, C6, C9, C10, C12, C14, C16, C18 or the like) arylamine.

[0055] In an embodiment, the ring A is any one of phenylene, biphenylene, naphthylene, terphenylene, pyridylene and phenylene-naphthylene.

[0056] In an embodiment, L is selected from any one of phenylene, biphenylene, naphthylene, terphenylene and pyridylene.

[0057] In an embodiment, two of X.sub.1 to X.sub.3 are N or all of X.sub.1 to X.sub.3 are N.

[0058] In an embodiment, both Y.sub.1 and Y.sub.2 are selected from the C atom, and n.sub.1 is an integer from 1 to 3, for example, 1, 2 or 3.

[0059] In an embodiment, at least one of Y.sub.1 and Y.sub.2 is selected from the N atom, and n.sub.1 is an integer from 0 to 3, for example, 0, 1, 2 or 3.

[0060] In an embodiment, R.sub.1 and R.sub.2 are independently selected from any one of the following groups:

##STR00006## ##STR00007##

[0061] The dashed line represents a linkage site of the group.

[0062] L.sub.1 is selected from any one of a single bond or substituted or unsubstituted C6-C20 (for example, C6, C9, C10, C12, C14, C16, C18 or the like) arylene.

[0063] X.sub.4 is selected from O, S or NR.sub.N1.

[0064] X.sub.5 is selected from O, S, NR.sub.N2 or CR.sub.C3R.sub.C4.

[0065] R.sub.N1, R.sub.N2, R.sub.C3 and R.sub.C4 are each independently selected from any one of hydrogen, substituted or unsubstituted C1-C20 (for example, C2, C3, C4, C5, C6, C8, C10, C12, C14, C16, C18, C19 or the like) linear or branched alkyl, substituted or unsubstituted C6-C20 (for example, C6, C9, C10, C12, C14, C16, C18 or the like) aryl, or substituted or unsubstituted C5-C20 (for example, C6, C8, C10, C12, C14, C16, C18 or the like) heteroaryl.

[0066] R.sub.11 and R.sub.12 are each independently selected from any one of deuterium, cyano, halogen, unsubstituted or halogenated C1-C10 (for example, C1, C2, C3, C4, C5, C6, C7, C8, C9 or C10) linear or branched alkyl, unsubstituted or halogenated C1-C10 (for example, C1, C2, C3, C4, C5, C6, C7, C8, C9 or C10) alkoxy, C1-C10 (for example, C1, C2, C3, C4, C5, C6, C7, C8, C9 or C10) alkylthio, C6-C20 (for example, C6, C8, C10, C12, C14, C16, C18 or the like) aryl, C5-C20 (for example, C6, C8, C10, C12, C14, C16, C18 or the like) heteroaryl, or C6-C18 arylamine.

[0067] m.sub.1 is selected from an integer from 0 to 5, for example, may be 0, 1, 2, 3, 4 or 5.

[0068] m.sub.2 is selected from an integer from 0 to 6, for example, may be 0, 1, 2, 3, 4, 5 or 6.

[0069] m.sub.3 is selected from an integer from 0 to 9, for example, may be 0, 1, 2, 3, 4, 5, 6, 7, 8 or 9.

[0070] m.sub.4 and m.sub.6 are each independently selected from an integer from 0 to 4, for example, may be 0, 1, 2, 3 or 4.

[0071] m.sub.5 is selected from an integer from 0 to 3, for example, may be 0, 1, 2 or 3.

[0072] In an embodiment, R.sub.1 and R.sub.2 are independently selected from any one of the following substituted or unsubstituted groups:

##STR00008## ##STR00009## ##STR00010##

[0073] The dashed line represents a linkage site of the group.

[0074] The substituted substituents are each independently selected from at least one of deuterium, cyano, halogen, unsubstituted or halogenated C1-C10 (for example, C1, C2, C3, C4, C5, C6, C7, C8, C9 or C10) linear or branched alkyl, unsubstituted or halogenated C1-C10 (for example, C1, C2, C3, C4, C5, C6, C7, C8, C9 or C10) alkoxy, C1-C10 (for example, C1, C2, C3, C4, C5, C6, C7, C8, C9 or C10) alkylthio, C6-C20 (for example, C6, C9, C10, C12, C14, C16, C18 or the like) aryl, C5-C20 (for example, C6, C9, C10, C12, C14, C16, C18 or the like) heteroaryl, or C6-C18 (for example, C6, C9, C10, C12, C14, C16, C18 or the like) arylamine.

[0075] In an embodiment, the organic compound is selected from any one of the following compounds:

##STR00011## ##STR00012## ##STR00013## ##STR00014## ##STR00015## ##STR00016## ##STR00017## ##STR00018## ##STR00019## ##STR00020## ##STR00021## ##STR00022## ##STR00023## ##STR00024## ##STR00025## ##STR00026## ##STR00027## ##STR00028## ##STR00029## ##STR00030## ##STR00031## ##STR00032## ##STR00033## ##STR00034## ##STR00035## ##STR00036## ##STR00037## ##STR00038## ##STR00039## ##STR00040## ##STR00041## ##STR00042## ##STR00043## ##STR00044## ##STR00045## ##STR00046## ##STR00047## ##STR00048## ##STR00049## ##STR00050## ##STR00051## ##STR00052## ##STR00053## ##STR00054## ##STR00055## ##STR00056## ##STR00057## ##STR00058## ##STR00059## ##STR00060## ##STR00061## ##STR00062## ##STR00063## ##STR00064## ##STR00065## ##STR00066## ##STR00067## ##STR00068## ##STR00069## ##STR00070## ##STR00071## ##STR00072##

[0076] A second aspect of the present disclosure is to provide a material of an electron transport layer, wherein the material of the electron transport layer includes the organic compound as described in the first aspect.

[0077] A third aspect of the present disclosure is to provide a material of a hole blocking layer, wherein the material of the hole blocking layer includes the organic compound as described in the first aspect.

[0078] A fourth aspect of the present disclosure is to provide an OLED device. The OLED device includes an anode, a cathode and an organic thin film layer disposed between the anode and the cathode, wherein a material of the organic thin film layer includes the organic compound as described in the first aspect.

[0079] In an embodiment, the organic thin film layer includes an electron transport layer whose material includes at least one of the organic compound as described in the first object.

[0080] In an embodiment, the organic thin film layer includes an electron transport layer whose material includes at least one of the organic compound as described in the first object.

[0081] In an embodiment, the organic thin film layer includes a hole blocking layer whose material includes the organic compound as described in the first object.

[0082] In the OLED device provided by the present disclosure, a material of the anode may be a metal, a metal oxide or a conductive polymer, where the metal includes copper, gold, silver, iron, chromium, nickel, manganese, palladium, platinum and the like as well as alloys thereof, the metal oxide includes indium tin oxide (ITO), indium zinc oxide (IZO), zinc oxide, indium gallium zinc oxide (IGZO) and the like, and the conductive polymer includes polyaniline, polypyrrole, poly(3-methylthiophene) and the like. In addition to the above materials that facilitate hole injection and combinations thereof, the material of the anode further includes known materials suitable for use as the anode.

[0083] In the OLED device, a material of the cathode may be a metal or a multilayer metal material, where the metal includes aluminum, magnesium, silver, indium, tin, titanium and the like as well as alloys thereof, and the multilayer metal material includes LiF/Al, LiO.sub.2/Al, BaF.sub.2/Al and the like. In addition to the above materials that facilitate electron injection and combinations thereof, the material of the cathode further includes known materials suitable for use as the cathode.

[0084] In the OLED device, the organic thin film layer includes at least one emissive layer (EML) and any one or a combination of at least two of a hole injection layer (HIL), a hole transport layer (HTL), an electron blocking layer (EBL), a hole blocking layer (HBL), an electron transport layer (ETL) or an electron injection layer (EIL) that are arranged on two sides of the emissive layer. In addition to the organic compound as described in the first object of the present disclosure, the hole/electron injection and transport layers may also include carbazole compounds, arylamine compounds, benzimidazole compounds, metal compounds and the like. The OLED device may further be optionally provided with a capping layer (CPL) disposed on the cathode (on a side of the cathode facing away from the anode).

[0085] As shown in FIG. 1 which is a schematic diagram of the OLED device, the OLED device includes an anode 101, a cathode 102 and an emissive layer 103 disposed between the anode 101 and the cathode 102, where a first organic thin film layer 104 and a second organic thin film layer 105 are disposed on two sides of the emissive layer 103. The first organic thin film layer 104 is any one or a combination of at least two of a hole injection layer (HIL), a hole transport layer (HTL) or an electron blocking layer (EBL), and the second organic thin film layer 105 includes any one or a combination of at least two of a hole blocking layer (HBL), an electron transport layer (ETL) or an electron injection layer (EIL). A capping layer (CPL) may further be optionally disposed on the cathode 102 (on a side of the cathode 102 facing away from 105).

[0086] The OLED device may be prepared by the following method: forming the anode on a transparent or opaque smooth substrate, forming the organic thin film layer on the anode, and forming the cathode on the organic thin film layer. The organic thin film layer may be formed by using known film forming methods such as evaporation, sputtering, spin coating, impregnation and ion plating.

[0087] A fifth aspect of the present disclosure is to provide a display panel. The display panel includes the OLED device as described in the fourth aspect.

[0088] A sixth aspect of the present disclosure is to provide an electronic apparatus. The electronic apparatus includes the display panel as described in the fifth aspect.

[0089] In the present disclosure, the organic compound having the structure represented by Formula I may be prepared according to the following synthesis route:

##STR00073##

[0090] wherein, X.sub.1, X.sub.2, X.sub.3, Y.sub.1, Y.sub.2, L, R.sub.1, R.sub.2, A and n.sub.1 are defined within the same ranges as in Formula I, and X is selected from halogen (for example, chlorine, bromine or iodine).

[0091] Preparation examples of the organic compound of the present disclosure are exemplarily described below.

Preparation Example: Preparation of Compound 1-18

[0092] ##STR00074##

[0093] In a nitrogen atmosphere, reaction solvents, toluene, ethanol and water, were added to the reaction flask at a ratio of 7:2:1, and then K.sub.2CO.sub.3 (10 mmol) aq, Reactant A1 (5 mmol), Reactant a-1 (5 mmol) and Pd(PPh.sub.3).sub.4 (0.25 mmol) were added in sequence. The system was warmed to 80° C. and reacted overnight. After the reaction was finished, the system was cooled to room temperature, dichloromethane/H.sub.2O were added for extraction, and the collected organic phases were dried over anhydrous Na.sub.2SO.sub.4 and suction filtered. The filtrate was collected, the solvents were removed through rotary evaporation, and the product was purified through column chromatography to obtain Intermediate B1 (with a yield of 70%).

[0094] MALDI-TOF (m/z): C39H24ClN3: calculated value: 569.17, measured value: 569.38.

##STR00075##

[0095] In a nitrogen atmosphere, 1,4-dioxane was added to the reaction flask, and then K.sub.2CO.sub.3 (8 mmol) aq, Intermediate B1 (4 mmol), Reactant b-1 (4 mmol) and Pd(PPh.sub.3).sub.4 (0.2 mmol) were added in sequence. The system was warmed to 100° C. and reacted overnight. After the reaction was finished, the system was cooled to room temperature, dichloromethane/H.sub.2O were added for extraction, and the collected organic phases were dried over anhydrous Na.sub.2SO.sub.4 and suction filtered. The filtrate was collected, the solvent was removed through rotary evaporation, and the product was purified through column chromatography to obtain Compound 1 (with a yield of 71%).

[0096] MALDI-TOF (m/z): C46H28N4: calculated value: 636.23, measured value: 636.45.

[0097] Elemental analysis (%): C46H28N4: calculated value: C 86.77, H 4.43, N 8.80; measured value: C 86.78, H 4.42, N 8.82.

[0098] The following intermediates/products were synthesized by methods similar to the preceding method.

TABLE-US-00001 (1) MALDI-TOF Raw Raw Yield (m/z) Material/Intermediate Material/Intermediate Intermediate/Product (%) (2) EA (%) [00076] [00077] [00078] 75 C56H34N4: (1) calculated value: 762.28, measured value: 762.50; (2) b-2 calculated B1 Compound 2 value: C 88.16, H 4.49, N 7.34; measured value: C 88.17, H 4.47, N 7.36. [00079] [00080] [00081] 72 C53H31N5: (1) calculated value: 737.26, measured value: 737.47; (2) b-3 calculated B1 Compound 3 value: C 86.27, H 4.23, N 9.49; measured value: C 86.28, H 4.22, N 9.51. [00082]

[0099] The following intermediates/products were synthesized by methods similar to the preceding method.

TABLE-US-00002 Reaction 2 (1) MALDI- TOF Reaction 1 (m/z) Raw Raw Raw Yield (2) EA Material 1 Material 2 Material 3 Intermediate/Product (%) (%) [00083] [00084] [00085] [00086] 72 C52H32 N4: (1) calculated value: 712.26, measured value: 712.56; (2) calculated value: A1 b-1 Compound 4 C 87.62, a-2 H 4.52, N 7.86; measured value: C 87.64, H 4.51, N 7.87. [00087] [00088] [00089] [00090] 71 C52H30 N4O: (1) calculated value: 726.24, measured value: 726.44; (2) calculated value: A1 b-1 C 85.93, a-3 Compound 5 H 4.16, N 7.71; measured value: C 85.94, H 4.15, N 7.73. [00091] [00092] [00093] [00094] 70 C52H30 N4S: (1) calculated value: 742.22, measured value: 742.52; (2) calculated value: A1 b-1 C 84.07, a-4 Compound 6 H 4.07, N 7.54; measured value: C 84.08, H 4.06, N 7.56. [00095]

[0100] The following intermediates/products were synthesized by methods similar to the preceding method.

TABLE-US-00003 Raw Raw Material/ Material/ Yield (1) MALDI-TOF (m/z) Intermediate Intermediate Intermediate/Product (%) (2) EA (%) [00096] [00097] [00098] 72 C38H23ClN4: (1) calculated value: 570.16, measured value: 570.36. A2 a-1 B2 [00099] [00100] [00101] 78 C44H28N4: (1) calculated value: 612.23, measured value: 612.45; (2) calculated value: C 86.25, H 4.61, N 9.14; measured value: C 86.26, H 4.60, N 9.16. B2 c-1 Compound 7 [00102] [00103] [00104] 74 C45H27N5: (1) calculated value: 637.23, measured value: 637.51; (2) calculated value: C 84.75, H 4.27, N 10.98; measured value: C 84.76, H 4.26, N 11.00. B2 b-1 Compound 8 [00105] [00106] [00107] 76 C55H33N5: (1) calculated value: 763.27, measured value: 763.57; (2) calculated value: C 86.48, H 4.35, N 9.17; measured value: C 86.49, H 4.34, N 9.19. B2 b-2 Compound 9 [00108] [00109] [00110] 72 C51H29N5O: (1) calculated value: 727.24, measured value: 727.46; (2) calculated value: C 84.16, H 4.02, N 9.62; measured value: C 84.17, H 4.01, N 9.64. A2 Compound 10

[0101] The following intermediates/products were synthesized by methods similar to the preceding method.

TABLE-US-00004 Raw Raw Material/ Material/ Yield (1) MALDI-TOF (m/z) Intermediate Intermediate Intermediate/Product (%) (2) EA (%) [00111] [00112] [00113] 73 C38H23ClN4: (1) calculated value: 570.16, measured value: 570.46. A3 a-1 B3 [00114] [00115] [00116] 79 C44H28N4: (1) calculated value: 612.23, measured value: 612.43; (2) calculated value: C 86.25, H 4.61, N 9.14; measured value: C 86.26, H 4.60, N 9.16. B3 c-1 Compound 11 [00117] [00118] [00119] 75 C45H27N5: (1) calculated value: 637.23, measured value: 637.50; (2) calculated value: C 84.75, H 4.27, N 10.98; measured value: C 84.76, H 4.26, N 10.99. B3 b-1 Compound 12 [00120] [00121] [00122] 77 C55H33N5: (1) calculated value: 763.27, measured value: 763.57; (2) calculated value: C 86.48, H 4.35, N 9.17; measured value: C 86.49, H 4.34, N 9.19. B3 b-2 Compound 13 [00123] [00124] [00125] 73 C51H29N5O: (1) calculated value: 727.24, measured value: 727.54; (2) calculated value: C 84.16, H 4.02, N 9.62; measured value: C 84.17, H 4.01, N 9.64. A3 Compound 14 [00126]

[0102] The following intermediates/products were synthesized by methods similar to the preceding method.

TABLE-US-00005 Raw Raw Material/ Material/ Yield (1) MALDI-TOF (m/z) Intermediate Intermediate Intermediate/Product (%) (2) EA (%) [00127] [00128] [00129] 72 C37H22ClN5: (1) calculated value: 571.16, measured value: 571.45. A4 a-1 B4 [00130] [00131] [00132] 79 C43H27N5: (1) calculated value: 613.23, measured value: 613.43; (2) calculated value: C 84.15, H 4.43, N 11.41; measured value: C 84.16, H 4.42, N 11.43. B4 c-1 Compound 15 [00133] [00134] [00135] 75 C44H26N6: (1) calculated value: 638.22, measured value: 638.50; (2) calculated value: C 82.74, H 4.10, N 13.16; measured value: C 82.75, H 4.09, N 13.18. B4 b-1 Compound 16 [00136] [00137] [00138] 77 C54H32N6: (1) calculated value: 764.27, measured value: 764.47; (2) calculated value: C 84.80, H 4.22, N 10.99; measured value: C 84.81, H 4.21, N 11.01. B4 b-2 Compound 17 [00139] [00140] [00141] 74 C50H28N6O: (1) calculated value: 728.23, measured value: 728.53; (2) calculated value: C 82.40, H 3.87, N 11.53; measured value: C 82.41, H 3.86, N 11.55. A4 Compound 18

[0103] Simulated Calculations of Energy Levels of Compounds

[0104] By use of a density-functional theory (DFT), the distribution of molecular frontier orbital HOMO and LUMO was optimized and calculated for the organic compounds provided in the examples of the present disclosure using a Guassian 09 package (Guassian Inc.) at a calculation level of B3LYP/6-31G(d). Meanwhile, based on a time-dependent density-functional theory (TDDFT), the lowest singlet energy level S1 and the lowest triplet energy level T1 of molecules of the compounds were simulated and calculated. Results are shown in Table 1.

TABLE-US-00006 TABLE 1 Compound HOMO (eV) LUMO (eV) E.sub.S1 (eV) E.sub.T1 (eV) Compound 1 −5.62 −1.94 3.27 2.34 Compound 2 −5.55 −1.92 3.26 2.34 Compound 3 −5.51 −1.98 3.23 2.34 Compound 4 −5.60 −1.93 3.27 2.34 Compound 5 −5.61 −1.98 3.27 2.34 Compound 6 −5.60 −1.98 3.27 2.34 Compound 7 −5.50 −1.76 3.33 2.33 Compound 8 −5.66 −1.96 3.29 2.33 Compound 9 −5.62 −1.94 3.28 2.33 Compound −5.67 −1.98 3.28 2.33 10 Compound −5.51 −1.78 3.33 2.33 11 Compound −5.64 −1.98 3.27 2.32 12 Compound −5.61 −1.96 3.26 2.32 13 Compound −5.65 −1.99 3.26 2.32 14 Compound −5.53 −1.80 3.33 2.34 15 Compound −5.78 −1.98 3.24 2.30 16 Compound −5.76 −1.97 3.23 2.30 17 Compound −5.79 −1.99 3.23 2.30 18

[0105] As can be seen from Table 1, the compounds provided by the present disclosure have relatively deep LUMO energy levels (−1.76 to −1.99 eV) and can reduce a potential barrier of electron transport, improve an electron injection ability, and effectively reduce the voltage of an OLED device. Such compounds all have relatively deep HOMO energy levels (−5.50 to −5.79 eV) and can effectively block holes so that more holes and electrons are recombined in a light-emitting region, which can achieve higher luminescence efficiency.

[0106] Application examples in which the organic compounds of the present disclosure are applied to the OLED device are described below.

Application Example 1

[0107] This application example provides an OLED device whose structure is shown in FIG. 1. The OLED device includes a substrate 1, an anode 2, a hole injection layer 3, a hole transport layer 4, an electron blocking layer 5, an emissive layer 6, a hole blocking layer 7, an electron transport layer 8, an electron injection layer 9 and a cathode 10 which are stacked in sequence. An arrow in FIG. 1 represents a light-emitting direction of the device.

[0108] The OLED device was prepared by specific steps described below.

[0109] (1) A glass substrate 1 having an indium tin oxide (ITO) anode 2 (with a thickness of 100 nm) was sonicated in isopropyl alcohol and deionized water for 30 minutes separately and cleaned under ozone for about 10 minutes. The cleaned glass substrate was installed onto a vacuum deposition apparatus.

[0110] (2) On the ITO anode 2, Compound a was deposited through vacuum evaporation as the hole injection layer 3 with a thickness of 10 nm.

[0111] (3) On the hole injection layer 3, Compound b was deposited through vacuum evaporation as the hole transport layer 4 with a thickness of 40 nm.

[0112] (4) On the hole transport layer 4, Compound c was deposited through vacuum evaporation as the electron blocking layer 5 with a thickness of 10 nm.

[0113] (5) On the electron blocking layer 5, Compound d and Compound e were co-deposited through vacuum evaporation at a doping proportion of 5% (mass ratio) as the emissive layer 6 with a thickness of 20 nm.

[0114] (6) On the emissive layer 6, Compound f was deposited through vacuum evaporation as the hole blocking layer 7 with a thickness of 10 nm.

[0115] (7) On the hole blocking layer 7, Compound 1 in Preparation Example 1 was deposited through vacuum evaporation as the electron transport layer 8 with a thickness of 30 nm.

[0116] (8) On the electron transport layer 8, Compound LiF was deposited through vacuum evaporation as the electron injection layer 9 with a thickness of 2 nm.

[0117] (9) On the electron injection layer 9, an aluminum electrode was deposited through vacuum evaporation as the cathode 10 with a thickness of 100 nm.

[0118] The compounds used for preparing the OLED device are as follows:

##STR00142## ##STR00143##

[0119] Performance Evaluation of the OLED Device

[0120] According to the current densities and brightness of the OLED device under different voltages, the operating voltage V and current efficiency CE (cd/A) of the OLED device at a current density (10 mA/cm.sup.2) were obtained. The lifetime LT95 (h) was obtained by measuring the time taken for the OLED device to reach 95% of its initial brightness (at 50 mA/cm.sup.2). Measured data is shown in Table 2.

TABLE-US-00007 TABLE 2 Electron OLED Transport V CE LT95 Device Layer (V) (cd/A) (h) Application 1 4.06 15.9 67 Example 1 Application 2 4.07 16.1 68 Example 2 Application 3 4.03 15.6 64 Example 3 Application 4 4.08 15.7 65 Example 4 Application 5 4.02 15.9 66 Example 5 Application 6 4.04 15.8 64 Example 6 Application 7 4.13 14.8 58 Example 7 Application 8 4.05 15.8 65 Example 8 Application 9 4.06 15.9 66 Example 9 Application 10 4.04 15.7 62 Example 10 Application 11 4.12 14.9 58 Example 11 Application 12 4.05 15.8 65 Example 12 Application 13 4.06 15.9 66 Example 13 Application 14 4.04 15.7 62 Example 14 Application 15 4.10 15.0 59 Example 15 Application 16 4.04 15.9 66 Example 16 Application 17 4.05 16.0 67 Example 17 Application 18 4.03 15.8 64 Example 18 Comparative Comparative 4.19 14.1 52 Example 1 Compound 1 Comparative Comparative 4.27 13.7 50 Example 2 Compound 2

[0121] As can be seen from Table 2, the OLED devices provided by the present disclosure have relatively low driving voltage, relatively high luminescence efficiency and relatively long lifetimes, where the operating voltage is less than or equal to 4.13 V, the current efficiency CE is greater than or equal to 14.8 cd/A, and the lifetime LT95 is greater than or equal to 58 h. Compared with those in Comparative Examples 1 and 2, the OLED devices using the compounds of the present disclosure have reduced operating voltage and improved efficiency and lifetimes for the following reasons: the organic compounds of the present disclosure have relatively deep LUMO energy levels so that more smooth electron injection is achieved and the operating voltage of the device is reduced; the organic compounds have relatively deep HOMO values and can effectively block holes and restrict the holes in the light-emitting region to be recombined with electrons, which is conducive to widening a light-emitting recombination region and improving the luminescence efficiency of the device. Meanwhile, the organic compounds provided by the present disclosure have good thermal stability and a good film-forming property, which is conducive to the stability of the device and improves the lifetime of the device.

[0122] The applicant has stated that although the organic compound and the application thereof in the present disclosure are described through the preceding embodiments, the present disclosure is not limited to the preceding embodiments, which means that the implementation of the present disclosure does not necessarily depend on the preceding embodiments. It should be apparent to those skilled in the art that any improvements made to the present disclosure, equivalent replacements of raw materials selected in the present disclosure and additions of adjuvant ingredients thereof and selections of specific methods, etc., all fall within the protection scope and the disclosure scope of the present disclosure.