US20210057655A1 - Organic light emitting compound and organic light emitting diode including the same - Google Patents
Organic light emitting compound and organic light emitting diode including the same Download PDFInfo
- Publication number
- US20210057655A1 US20210057655A1 US17/083,644 US202017083644A US2021057655A1 US 20210057655 A1 US20210057655 A1 US 20210057655A1 US 202017083644 A US202017083644 A US 202017083644A US 2021057655 A1 US2021057655 A1 US 2021057655A1
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- United States
- Prior art keywords
- groups
- substituted
- unsubstituted
- light emitting
- organic light
- Prior art date
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- 150000001875 compounds Chemical class 0.000 title claims abstract description 89
- 239000010410 layer Substances 0.000 claims description 72
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- 125000001072 heteroaryl group Chemical group 0.000 claims description 10
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- 125000005843 halogen group Chemical group 0.000 claims description 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 7
- 229910052805 deuterium Inorganic materials 0.000 claims description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 7
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 7
- 125000006686 (C1-C24) alkyl group Chemical group 0.000 claims description 5
- 125000003545 alkoxy group Chemical group 0.000 claims description 5
- 125000003282 alkyl amino group Chemical group 0.000 claims description 5
- 125000003277 amino group Chemical group 0.000 claims description 5
- 125000004104 aryloxy group Chemical group 0.000 claims description 5
- 150000001975 deuterium Chemical group 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 5
- 125000000923 (C1-C30) alkyl group Chemical group 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 125000005842 heteroatom Chemical group 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- 125000000739 C2-C30 alkenyl group Chemical group 0.000 claims description 3
- 125000005377 alkyl thioxy group Chemical group 0.000 claims description 3
- 125000000304 alkynyl group Chemical group 0.000 claims description 3
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- 238000001840 matrix-assisted laser desorption--ionisation time-of-flight mass spectrometry Methods 0.000 description 19
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- 235000019270 ammonium chloride Nutrition 0.000 description 4
- ILAHWRKJUDSMFH-UHFFFAOYSA-N boron tribromide Chemical compound BrB(Br)Br ILAHWRKJUDSMFH-UHFFFAOYSA-N 0.000 description 4
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- AYHGAQGOMUQMTR-UHFFFAOYSA-N 2-(4-bromophenyl)-4,6-diphenyl-1,3,5-triazine Chemical compound C1=CC(Br)=CC=C1C1=NC(C=2C=CC=CC=2)=NC(C=2C=CC=CC=2)=N1 AYHGAQGOMUQMTR-UHFFFAOYSA-N 0.000 description 3
- OGGKVJMNFFSDEV-UHFFFAOYSA-N 3-methyl-n-[4-[4-(n-(3-methylphenyl)anilino)phenyl]phenyl]-n-phenylaniline Chemical compound 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 3
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- 229910001887 tin oxide Inorganic materials 0.000 description 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
- PZJJKWKADRNWSW-UHFFFAOYSA-N trimethoxysilicon Chemical group CO[Si](OC)OC PZJJKWKADRNWSW-UHFFFAOYSA-N 0.000 description 1
- WRECIMRULFAWHA-UHFFFAOYSA-N trimethyl borate Chemical compound COB(OC)OC WRECIMRULFAWHA-UHFFFAOYSA-N 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- YVTHLONGBIQYBO-UHFFFAOYSA-N zinc indium(3+) oxygen(2-) Chemical compound [O--].[Zn++].[In+3] YVTHLONGBIQYBO-UHFFFAOYSA-N 0.000 description 1
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Definitions
- the present invention relates to an organic light emitting compound. More specifically, the present invention relates to an organic light emitting compound that has a specific structure for an electron transport layer and can be used to achieve long lifetime, low voltage and high-efficiency luminescence, and an organic light emitting diode including the organic light emitting compound.
- Organic light emitting diodes are self-luminous display devices and have the advantage of large viewing angle. Organic light emitting diodes can be reduced in weight, thickness, and size and have short response time compared to liquid crystal display devices. Due to these advantages, the application of organic light emitting diodes to full-color displays or lighting systems is expected.
- organic electroluminescence refers to the phenomenon in which electrical energy is converted into light energy using an organic material.
- a typical organic light emitting diode based on organic electroluminescence has a structure including an anode, a cathode, and an organic layer therebetween.
- the organic layer usually consists of one or more layers, for example, a hole injecting layer, a hole transport layer, a light emitting layer, an electron transport layer, and an electron injecting layer that are composed of different materials to increase the efficiency and stability of the organic light emitting diode.
- Such an organic light emitting diode When a voltage is applied between the two electrodes of the organic light emitting diode, holes from the anode and electrons from the cathode are injected into the organic layer. As a result of recombination of the holes and the electrons, excitons are formed which return back to the ground state to emit light.
- Such an organic light emitting diode is known to have excellent characteristics, such as self-luminescence, high luminance, high efficiency, low driving voltage, large viewing angle, high contrast, and fast response speed.
- Organic layers of organic light emitting diodes can be divided into light emitting materials and charge transport materials, for example, hole injecting materials, hole transport materials, electron transport materials, and electron injecting materials, by their functions.
- Organic layers of organic light emitting diodes may further include one or more layers, for example, an electron blocking layer or a hole blocking layer.
- Korean Patent Publication No. 10-2012-0104204 (Sep. 20, 2012) describes an organic compound in which a pyridoindole derivative is bonded to a substituted anthracene ring structures.
- Japanese Patent Publication No. 2010-168363 (Aug. 5, 2010) describes an anthracene derivative having a pyridylnaphthyl group that is excellent in terms of external quantum efficiency and driving voltage.
- the present invention has been made in an effort to solve the above problems and is directed to providing an organic light emitting compound having a specific structure that can be introduced into an electron transport layer to fabricate an organic light emitting diode with long lifetime, low voltage, and high efficiency.
- the present invention is also directed to providing an organic light emitting diode that employs the organic light emitting compound as a light emitting material to achieve low driving voltage, high efficiency, and long lifetime.
- One aspect of the present invention provides an organic light emitting compound represented by Formula I:
- a further aspect of the present invention provides an organic light emitting diode including the organic light emitting compound.
- the organic light emitting diode of the present invention employs the organic light emitting compound, particularly, as a material for electron injection and transport.
- the organic light emitting diode of the present invention exhibits low driving voltage, long lifetime, and high efficiency compared to conventional organic light emitting diodes. Due to these advantages, the organic light emitting diode of the present invention is useful in a variety of industrial applications, including displays and lighting systems.
- the present invention is directed to an organic light emitting compound represented by Formula I:
- L represents a linker and is a single bond or is selected from substituted or unsubstituted C 1 -C 30 alkylene groups, substituted or unsubstituted C 2 -C 30 alkenylene groups, substituted or unsubstituted C 2 -C 30 alkynylene groups, substituted or unsubstituted C 3 -C 30 cycloalkylene groups, substituted or unsubstituted C 2 -C 30 heterocycloalkylene groups, substituted or unsubstituted C 6 -C 30 arylene groups, and substituted or unsubstituted C 2 -C 30 heteroarylene groups, n is an integer from 1 to 3, provided that when n is equal to or greater than 2, the plurality of L groups are identical to or different from each other, HAr 1 is a substituted or unsubstituted C 6 -C 30 aryl group or a substituted or unsubstituted C 2 -C 30 heteroaryl group, and
- X 1 is CR 11 or N
- X 2 is CR 12 or N
- X 3 is CR 13 or N
- X 4 is CR 14 or N
- X 5 is CR 15 or N
- X 6 is CR 16 or N
- X 7 is CR 17 or N
- X 8 is CR 18 or N
- X 9 is CR 19 or N
- X 10 is CR 20 or N, with the proviso that at least two of X 1 to X 4 are selected from CR 11 to CR 14 , at least three of X 5 to X 10 are selected from CR 15 to CR 20
- one of X 1 to X 10 is a carbon atom linked to L
- R 1 , R 2 , and R 11 to R 20 are identical to or different from each other and are each independently selected from a hydrogen atom, a deuterium atom, substituted or unsubstituted C 1 -C 30 alkyl groups, substituted or unsubstituted C 2
- L may be a single bond or may be selected from the following structures 1 to 9:
- R 11 to R 20 is bonded to L and the remainders of R 11 to R 20 may be hydrogen or deuterium atoms. Only one of X 1 to X 10 may be a nitrogen atom or none of X 1 to X 10 may be nitrogen atoms.
- the organic light emitting compound of the present invention can be employed as an electron injecting or transport material for an organic layer of an organic light emitting diode to improve the efficiency, life characteristics, and driving voltage characteristics of the diode.
- the compound of Formula I is characterized by the presence of one of Structures A to E.
- Structures A to E have an indenodibenzofuran structure consisting of a 6-membered aromatic ring containing X 1 to X 4 , a 5-membered ring containing a carbon atom linked to R 1 and R 2 , a 6-membered aromatic carbocyclic ring containing X 5 and X 10 , X 5 and X 6 or X 9 and X 10 , a 5-membered ring containing an oxygen atom, and a 6-membered aromatic ring containing X 6 to X 9 , X 7 to X 10 or X 5 to X 8 , which are fused to each other, and optionally including at least one nitrogen atom in the ring structure.
- One of X 1 to X 10 in these fused rings is linked to L.
- HAr 1 is preferably a substituted or unsubstituted C 2 -C 30 heteroaryl group.
- HAr 1 is selected from the following structures E1 to E33:
- Z 1 to Z 8 are identical to or different from each other and each independently have the same meanings as R 1 , R 2 , and R 11 to R 20 , and each of Z 1 to Z 8 and substituents thereof may optionally form an aliphatic, aromatic, heteroaliphatic or heteroaromatic fused ring with the adjacent group.
- substituted in the definition of “substituted or unsubstituted” used herein refers to substitution with at least one substituent selected from the group consisting of deuterium, a cyano group, halogen groups, a hydroxyl group, a nitro group, C 1 -C 24 alkyl groups, C 1 -C 24 halogenated alkyl groups, C 2 -C 24 alkenyl groups, C 2 -C 24 alkynyl groups, C 1 -C 24 heteroalkyl groups, C 6 -C 24 aryl groups, C 7 -C 24 arylalkyl groups, C 2 -C 24 heteroaryl groups, C 2 -C 24 heteroarylalkyl groups, C 1 -C 24 alkoxy groups, C 1 -C 24 alkylamino groups, C 1 -C 24 arylamino groups, C 1 -C 24 heteroarylamino groups, C 1 -C 24 alkylsilyl groups, C 6
- the number of carbon atoms in each alkyl or aryl group is considered as the number of carbon atoms constituting the unsubstituted alkyl or aryl moiety and the number of carbon atoms in the substituent(s) is excluded therefrom.
- a phenyl group substituted with a butyl group at the para-position corresponds to a C 6 aryl group substituted with a C 4 butyl group.
- alkyl groups used in the present invention include methyl, ethyl, propyl, isobutyl, sec-butyl, tert-butyl, pentyl, iso-amyl, hexyl, heptyl, octyl, stearyl, trichloromethyl, and trifluoromethyl groups.
- At least one hydrogen atom of each alkyl group may be substituted with a deuterium atom, a halogen atom, a hydroxyl group, a nitro group, a cyano group, a trifluoromethyl group, a silyl group (herein referred to as an “alkylsilyl group”), a substituted or unsubstituted amino group (—NH 2 , —NH(R) or —N(R′)(R′′), in which R, R′, and R′′ are each independently a C 1 -C 24 alkyl group (the —NH(R) and —N(R′)(R′′) are referred to as “alkylamino groups”), an amidino group, a hydrazine group, a hydrazone group, a carboxyl group, a sulfonic acid group, a phosphoric acid group, a C 1 -C 24 alkyl group, a C 1 -C 24 halogen
- alkoxy groups used in the present invention include methoxy, ethoxy, propoxy, isobutyloxy, sec-butyloxy, pentyloxy, iso-amyloxy, and hexyloxy groups.
- the alkoxy groups may be substituted with the same substituents as in the alkyl groups.
- aryloxy groups used in the present invention refer to —O-aryl radicals in which the aryl group is as defined above.
- Specific examples of the aryloxy groups include phenoxy, naphthoxy, anthracenyloxy, phenanthrenyloxy, fluorenyloxy, and indenyloxy. At least one hydrogen atom of each aryloxy group may be substituted.
- silyl groups used in the present invention include trimethylsilyl, triethylsilyl, triphenylsilyl, trimethoxysilyl, dimethoxyphenylsilyl, diphenylmethylsilyl, diphenylvinylsilyl, methylcyclobutylsilyl, and dimethylfurylsilyl.
- aryl groups used in the present invention are organic radicals derived from aromatic hydrocarbons by removal of a hydrogen atom.
- Such aryl groups include 5- to 7-membered, preferably 5- or 6-membered single or fused ring systems.
- the substituent may be fused with an adjacent substituent to form a ring.
- aryl groups include aromatic groups, such as phenyl, o-biphenyl, m-biphenyl, p-biphenyl, o-terphenyl, m-terphenyl, p-terphenyl, naphthyl, anthryl, phenanthryl, pyrenyl, indenyl, fluorenyl, tetrahydronaphthyl, perylenyl, crycenyl, naphthacenyl, and fluoranthenyl groups.
- aromatic groups such as phenyl, o-biphenyl, m-biphenyl, p-biphenyl, o-terphenyl, m-terphenyl, p-terphenyl, naphthyl, anthryl, phenanthryl, pyrenyl, indenyl, fluorenyl, tetrahydronaphthyl, peryleny
- Each aryl group may also be substituted with at least one substituent. More specifically, at least one hydrogen atom of each aryl group may be substituted with a deuterium atom, a halogen atom, a hydroxyl group, a nitro group, a cyano group, a silyl group, an amino group (—NH 2 , —NH(R), —N(R′)(R′′) in which R, R′ and R′′ are each independently a C 1 -C 10 alkyl group (the —NH(R) and —N(R′)(R′′) are referred to as “alkylamino groups”)), an amidino group, a hydrazine group, a hydrazone group, a carboxyl group, a sulfonic acid group, a phosphoric acid group, a C 1 -C 24 alkyl group, a C 1 -C 24 halogenated alkyl group, a C 1 -C 24 alkenyl
- heteroaryl groups used in the present invention refer to C 2 -C 24 cyclic aromatic systems including one to three heteroatoms selected from N, O, P, Si, S, Ge, Se, and Te, with the remaining ring atoms being carbon.
- the rings may be fused together.
- One or more hydrogen atoms of each heteroaryl group may be substituted with the same substituents as in the aryl groups.
- heteroaromatic rings refer to aromatic hydrocarbon rings in which one or more aromatic carbon atoms are replaced with one or more heteroatoms selected from N, O, P, Si, S, Ge, Se, and Te.
- the organic light emitting compound represented by Formula I may be selected from Compounds 1 to 564:
- the present invention is also directed to an organic light emitting diode including the organic light emitting compound of Formula I.
- the organic light emitting diode of the present invention includes a first electrode, a second electrode opposite to the first electrode, and an organic layer interposed between the first and second electrodes.
- the organic layer includes one or more layers selected from a light emitting layer, an electron transport layer, a hole transport layer, an electron injecting layer, a hole injecting layer, a hole blocking layer, and an electron blocking layer.
- the electron transport layer or the electron injecting layer includes the organic light emitting compound of Formula I.
- organic layer may include the organic light emitting compound of Formula I or two or more different compounds falling within the scope of Formula I.
- the organic light emitting diode of the present invention includes an anode, a hole transport layer, a light emitting layer, an electron transport layer, and a cathode.
- the organic light emitting diode of the present invention may optionally further include a hole injecting layer and an electron injecting layer.
- One or more intermediate layers may be further formed in the organic light emitting diode.
- a hole blocking layer or an electron blocking layer may be further formed in the organic light emitting diode.
- the diode may further include one or more organic layers with various functions depending on the desired characteristics thereof.
- an electrode material for the anode is coated on a substrate to form the anode.
- the substrate may be any of those used in general organic light emitting diodes.
- the substrate is preferably an organic substrate or a transparent plastic substrate that is excellent in transparency, surface smoothness, ease of handling, and waterproofness.
- a highly transparent and conductive metal oxide such as indium tin oxide (ITO), indium zinc oxide (IZO), tin oxide (SnO 2 ) or zinc oxide (ZnO), is used as the anode material.
- a material for the hole injecting layer is coated on the anode by vacuum thermal evaporation or spin coating to form the hole injecting layer. Then, a material for the hole transport layer is coated on the hole injecting layer by vacuum thermal evaporation or spin coating to form the hole transport layer.
- the material for the hole injecting layer is not specially limited so long as it is usually used in the art.
- Example of such materials include 4,4′,4′′-tris(2-naphthyl(phenyl)amino)triphenylamine (2-TNATA), N,N′-di(1-naphthyl)-N,N′-diphenylbenzidine) (NPD), N,N′-diphenyl-N,N′-bis(3-methylphenyl)-1,1′-biphenyl-4,4′-diamine (TPD), and N,N′-diphenyl-N,N′-bis[4-(phenyl-m-tolylamino)phenyl]biphenyl-4,4′-diamine (DNTPD).
- the material for the hole transport layer is not specially limited so long as it is commonly used in the art.
- Example of such materials include N,N′-bis(3-methylphenyl)-N,N′-diphenyl-[1,1-biphenyl]-4,4′-diamine (TPD) and N,N′-di(naphthalen-1-yl)-N,N′-diphenylbenzidine ( ⁇ -NPD).
- a hole blocking layer may be optionally formed on the organic light emitting layer by vacuum thermal evaporation or spin coating.
- the hole blocking layer blocks holes from entering the cathode through the organic light emitting layer. This role of the hole blocking layer prevents the lifetime and efficiency of the diode from deteriorating.
- a material having a very low highest occupied molecular orbital (HOMO) energy level is used for the hole blocking layer.
- the hole blocking material is not particularly limited so long as it has the ability to transport electrons and a higher ionization potential than the light emitting compound. Representative examples of suitable hole blocking materials include BAIq, BCP, and TPBI.
- the electron transport layer is deposited on the hole blocking layer by vacuum thermal evaporation or spin coating, and the electron injecting layer is formed thereon.
- a metal for the cathode is deposited on the electron injecting layer by vacuum thermal evaporation to form the cathode, completing the fabrication of the organic light emitting diode.
- the metal for the cathode there may be used, for example, lithium (Li), magnesium (Mg), aluminum (Al), aluminum-lithium (Al—Li), calcium (Ca), magnesium-indium (Mg—In) or magnesium-silver (Mg—Ag).
- the organic light emitting diode may be of top emission type. In this case, a transmissive material, such as ITO or IZO, may be used for the cathode.
- the material for the electron transport layer functions to stably transport electrons injected from the electron injecting electrode (i.e. the cathode).
- the organic light emitting compound of Formula I is used as the material for the electron transport layer.
- One or more layers selected from the hole injecting layer, the hole transport layer, the electron blocking layer, the light emitting layer, the hole blocking layer, the electron transport layer, and the electron injecting layer may be formed by a monomolecular deposition or solution process.
- the material for each layer is evaporated under heat and vacuum or reduced pressure to form the layer in the form of a thin film.
- the solution process the material for each layer is mixed with a suitable solvent, and then the mixture is formed into a thin film by a suitable method, such as ink-jet printing, roll-to-roll coating, screen printing, spray coating, dip coating or spin coating.
- the organic light emitting diode of the present invention can be used in a variety of systems, such as flat panel displays, flexible displays, monochromatic flat panel lighting systems, white flat panel lighting systems, flexible monochromatic lighting systems, and flexible white lighting systems.
- Compound 5 (yield 72%) was synthesized in the same manner as in Synthesis Example 1-5, except that Intermediate 2-a was used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine.
- Compound 72 (yield 46%) was synthesized in the same manner as in Synthesis Example 1-5, except that 2-(3-bromophenyl)-4,6-diphenyl-1,3,5-triazine and Intermediate 3-g were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.
- Compound 234 (yield 52%) was synthesized in the same manner as in Synthesis Example 1-5, except that 2-(3-bromophenyl)-4,6-diphenyl-1,3,5-triazine and Intermediate 9-i were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.
- Compound 313 (yield 54%) was synthesized in the same manner as in Synthesis Example 1-5, except that Intermediate 12-b and Intermediate 3-g were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.
- Compound 414 (yield 54%) was synthesized in the same manner as in Synthesis Example 1-5, except that Intermediate 12-b and Intermediate 17-a were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.
- ITO glass was patterned to have a light emitting area of 2 mm ⁇ 2 mm, followed by cleaning. After the cleaned ITO glass was mounted in a vacuum chamber, the base pressure was adjusted to 1 ⁇ 10 ⁇ 6 torr. HATCN (50 ⁇ ), NPD (650 ⁇ ), [BH]+ Blue dopant (BD) 5% (200 ⁇ ), the corresponding compound shown in Table 1 (300 ⁇ ), Liq (10 ⁇ ), and Al (1,000 ⁇ ) were deposited in this order on the ITO glass to fabricate an organic light emitting diode. The luminescent properties of the organic light emitting diode were measured at 0.4 mA.
- An organic light emitting diode was fabricated in the same manner as in Examples 1-19, except that ET was used instead of the compounds shown in Table 1.
- ET is widely used as an electron transport material and its structure is as follows.
- the organic electroluminescence diodes fabricated in Examples 1-19 and Comparative Example 1 were measured for voltage, luminance, color coordinates, and lifetime. The results are shown in Table 1. T 95 indicates the time at which the luminance of each diode was decreased to 95% of the initial luminance (2000 cd/m 2 ).
- inventive organic compounds had higher efficiencies, lower driving voltages, and longer lifetimes than ET, which is widely used as an electron transport material. Therefore, it can be concluded that the inventive compounds are suitable for the fabrication of organic light emitting diodes with improved characteristics.
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Abstract
Disclosed is an organic light emitting compound represented by Formula I:
HAr1-(L)n-HAr2 (I)
Also disclosed is an organic light emitting diode including the organic light emitting compound. Particularly, the organic light emitting diode employs the organic light emitting compound as a material for electron injection and transport. The organic light emitting diode can be driven at a low voltage and has improved life characteristics compared to conventional organic light emitting diodes. Due to these advantages, the organic light emitting diode is useful in a variety of industrial applications, including displays and lighting systems.
Description
- This application is a continuation of U.S. patent application Ser. No. 15/660,388 filed Jul. 26, 2017 which claims the benefit under 35 USC § 119(a) of Korean Patent Application No. 10-2016-0095499 filed on Jul. 27, 2016, Korean Patent Application No. 10-2016-0128791 filed on Oct. 6, 2016, and Korean Patent Application No. 10-2017-0085283 filed on Jul. 5, 2017, in the Korean Intellectual Property Office, the entire disclosure of which is incorporated herein by reference for all purposes.
- The present invention relates to an organic light emitting compound. More specifically, the present invention relates to an organic light emitting compound that has a specific structure for an electron transport layer and can be used to achieve long lifetime, low voltage and high-efficiency luminescence, and an organic light emitting diode including the organic light emitting compound.
- Organic light emitting diodes (OLEDs) are self-luminous display devices and have the advantage of large viewing angle. Organic light emitting diodes can be reduced in weight, thickness, and size and have short response time compared to liquid crystal display devices. Due to these advantages, the application of organic light emitting diodes to full-color displays or lighting systems is expected.
- Generally, organic electroluminescence refers to the phenomenon in which electrical energy is converted into light energy using an organic material. A typical organic light emitting diode based on organic electroluminescence has a structure including an anode, a cathode, and an organic layer therebetween.
- The organic layer usually consists of one or more layers, for example, a hole injecting layer, a hole transport layer, a light emitting layer, an electron transport layer, and an electron injecting layer that are composed of different materials to increase the efficiency and stability of the organic light emitting diode.
- When a voltage is applied between the two electrodes of the organic light emitting diode, holes from the anode and electrons from the cathode are injected into the organic layer. As a result of recombination of the holes and the electrons, excitons are formed which return back to the ground state to emit light. Such an organic light emitting diode is known to have excellent characteristics, such as self-luminescence, high luminance, high efficiency, low driving voltage, large viewing angle, high contrast, and fast response speed.
- Materials for organic layers of organic light emitting diodes can be divided into light emitting materials and charge transport materials, for example, hole injecting materials, hole transport materials, electron transport materials, and electron injecting materials, by their functions. Organic layers of organic light emitting diodes may further include one or more layers, for example, an electron blocking layer or a hole blocking layer.
- Many materials for electron transport layers are known that possess an outstanding ability to transport electrons and block holes, have high luminance efficiency and can be formed into highly stable thin films. For example, Korean Patent Publication No. 10-2012-0104204 (Sep. 20, 2012) describes an organic compound in which a pyridoindole derivative is bonded to a substituted anthracene ring structures. Further, Japanese Patent Publication No. 2010-168363 (Aug. 5, 2010) describes an anthracene derivative having a pyridylnaphthyl group that is excellent in terms of external quantum efficiency and driving voltage.
- Despite numerous attempts to develop methods for fabricating organic light emitting diodes with efficient luminescent properties in the prior art, including the above patent publications, there is still a continued need to develop organic light emitting diodes with long lifetime, low voltage, and high efficiency.
- Therefore, the present invention has been made in an effort to solve the above problems and is directed to providing an organic light emitting compound having a specific structure that can be introduced into an electron transport layer to fabricate an organic light emitting diode with long lifetime, low voltage, and high efficiency.
- The present invention is also directed to providing an organic light emitting diode that employs the organic light emitting compound as a light emitting material to achieve low driving voltage, high efficiency, and long lifetime.
- One aspect of the present invention provides an organic light emitting compound represented by Formula I:
-
HAr1-(L)n-HAr2 (I) - The structure and specific substituents of the compound of Formula 1 are described below.
- A further aspect of the present invention provides an organic light emitting diode including the organic light emitting compound.
- The organic light emitting diode of the present invention employs the organic light emitting compound, particularly, as a material for electron injection and transport. The organic light emitting diode of the present invention exhibits low driving voltage, long lifetime, and high efficiency compared to conventional organic light emitting diodes. Due to these advantages, the organic light emitting diode of the present invention is useful in a variety of industrial applications, including displays and lighting systems.
- The present invention will now be described in more detail.
- The present invention is directed to an organic light emitting compound represented by Formula I:
-
HAr1-(L)n-HAr2 (I) - wherein L represents a linker and is a single bond or is selected from substituted or unsubstituted C1-C30 alkylene groups, substituted or unsubstituted C2-C30 alkenylene groups, substituted or unsubstituted C2-C30 alkynylene groups, substituted or unsubstituted C3-C30 cycloalkylene groups, substituted or unsubstituted C2-C30 heterocycloalkylene groups, substituted or unsubstituted C6-C30 arylene groups, and substituted or unsubstituted C2-C30 heteroarylene groups, n is an integer from 1 to 3, provided that when n is equal to or greater than 2, the plurality of L groups are identical to or different from each other, HAr1 is a substituted or unsubstituted C6-C30 aryl group or a substituted or unsubstituted C2-C30 heteroaryl group, and HAr2 is selected from the following structures A to E:
- wherein X1 is CR11 or N, X2 is CR12 or N, X3 is CR13 or N, X4 is CR14 or N, X5 is CR15 or N, X6 is CR16 or N, X7 is CR17 or N, X8 is CR18 or N, X9 is CR19 or N, and X10 is CR20 or N, with the proviso that at least two of X1 to X4 are selected from CR11 to CR14, at least three of X5 to X10 are selected from CR15 to CR20, and one of X1 to X10 is a carbon atom linked to L, R1, R2, and R11 to R20 are identical to or different from each other and are each independently selected from a hydrogen atom, a deuterium atom, substituted or unsubstituted C1-C30 alkyl groups, substituted or unsubstituted C2-C30 alkenyl groups, substituted or unsubstituted C2-C30 alkynyl groups, substituted or unsubstituted C3-C30 cycloalkyl groups, substituted or unsubstituted C2-C30 heterocycloalkyl groups, substituted or unsubstituted C5-C30 cycloalkenyl groups, substituted or unsubstituted C1-C30 alkoxy groups, substituted or unsubstituted C6-C30 aryloxy groups, substituted or unsubstituted C1-C30 alkylthioxy groups, substituted or unsubstituted C6-C30 arylthioxy groups, substituted or unsubstituted C1-C30 alkylamine groups, substituted or unsubstituted C6-C30 arylamine groups, substituted or unsubstituted C6-C50 aryl groups, substituted or unsubstituted C2-C50 heteroaryl groups containing O, N or S as a heteroatom, substituted or unsubstituted C1-C24 alkylsilyl groups, substituted or unsubstituted C6-C24 arylsilyl groups, an amino group, a thiol group, a cyano group, a hydroxyl group, a nitro group, and halogen groups.
- According to one embodiment, L may be a single bond or may be selected from the following structures 1 to 9:
- wherein hydrogen or deuterium atoms are bonded to the carbon atoms of the aromatic rings.
- One of R11 to R20 is bonded to L and the remainders of R11 to R20 may be hydrogen or deuterium atoms. Only one of X1 to X10 may be a nitrogen atom or none of X1 to X10 may be nitrogen atoms.
- The organic light emitting compound of the present invention can be employed as an electron injecting or transport material for an organic layer of an organic light emitting diode to improve the efficiency, life characteristics, and driving voltage characteristics of the diode.
- The compound of Formula I is characterized by the presence of one of Structures A to E. A more detailed description will be given of Structures A to E. Each of Structures A to E has an indenodibenzofuran structure consisting of a 6-membered aromatic ring containing X1 to X4, a 5-membered ring containing a carbon atom linked to R1 and R2, a 6-membered aromatic carbocyclic ring containing X5 and X10, X5 and X6 or X9 and X10, a 5-membered ring containing an oxygen atom, and a 6-membered aromatic ring containing X6 to X9, X7 to X10 or X5 to X8, which are fused to each other, and optionally including at least one nitrogen atom in the ring structure. One of X1 to X10 in these fused rings is linked to L.
- HAr1 is preferably a substituted or unsubstituted C2-C30 heteroaryl group.
- According to a preferred embodiment of the present invention, HAr1 is selected from the following structures E1 to E33:
- wherein Z1 to Z8 are identical to or different from each other and each independently have the same meanings as R1, R2, and R11 to R20, and each of Z1 to Z8 and substituents thereof may optionally form an aliphatic, aromatic, heteroaliphatic or heteroaromatic fused ring with the adjacent group.
- The term “substituted” in the definition of “substituted or unsubstituted” used herein refers to substitution with at least one substituent selected from the group consisting of deuterium, a cyano group, halogen groups, a hydroxyl group, a nitro group, C1-C24 alkyl groups, C1-C24 halogenated alkyl groups, C2-C24 alkenyl groups, C2-C24 alkynyl groups, C1-C24 heteroalkyl groups, C6-C24 aryl groups, C7-C24 arylalkyl groups, C2-C24 heteroaryl groups, C2-C24 heteroarylalkyl groups, C1-C24 alkoxy groups, C1-C24 alkylamino groups, C1-C24 arylamino groups, C1-C24 heteroarylamino groups, C1-C24 alkylsilyl groups, C6-C24 arylsilyl groups, and C6-C24 aryloxy groups.
- In the “substituted or unsubstituted C1-C30 alkyl groups”, “substituted or unsubstituted C6-C30 aryl groups”, etc., the number of carbon atoms in each alkyl or aryl group is considered as the number of carbon atoms constituting the unsubstituted alkyl or aryl moiety and the number of carbon atoms in the substituent(s) is excluded therefrom. For example, a phenyl group substituted with a butyl group at the para-position corresponds to a C6 aryl group substituted with a C4 butyl group.
- Specific examples of the alkyl groups used in the present invention include methyl, ethyl, propyl, isobutyl, sec-butyl, tert-butyl, pentyl, iso-amyl, hexyl, heptyl, octyl, stearyl, trichloromethyl, and trifluoromethyl groups. At least one hydrogen atom of each alkyl group may be substituted with a deuterium atom, a halogen atom, a hydroxyl group, a nitro group, a cyano group, a trifluoromethyl group, a silyl group (herein referred to as an “alkylsilyl group”), a substituted or unsubstituted amino group (—NH2, —NH(R) or —N(R′)(R″), in which R, R′, and R″ are each independently a C1-C24 alkyl group (the —NH(R) and —N(R′)(R″) are referred to as “alkylamino groups”), an amidino group, a hydrazine group, a hydrazone group, a carboxyl group, a sulfonic acid group, a phosphoric acid group, a C1-C24 alkyl group, a C1-C24 halogenated alkyl group, a C2-C24 alkenyl group, a C2-C24 alkynyl group, a C1-C24 heteroalkyl group, a C5-C24 aryl group, a C6-C24 arylalkyl group, a C3-C24 heteroaryl group or a C3-C24 heteroarylalkyl group.
- Specific examples of the alkoxy groups used in the present invention include methoxy, ethoxy, propoxy, isobutyloxy, sec-butyloxy, pentyloxy, iso-amyloxy, and hexyloxy groups. The alkoxy groups may be substituted with the same substituents as in the alkyl groups.
- Specific examples of the halogen groups used in the present invention include fluoro (F), chloro (Cl), bromo (Br), and iodo (I) groups.
- The aryloxy groups used in the present invention refer to —O-aryl radicals in which the aryl group is as defined above. Specific examples of the aryloxy groups include phenoxy, naphthoxy, anthracenyloxy, phenanthrenyloxy, fluorenyloxy, and indenyloxy. At least one hydrogen atom of each aryloxy group may be substituted.
- Specific examples of the silyl groups used in the present invention include trimethylsilyl, triethylsilyl, triphenylsilyl, trimethoxysilyl, dimethoxyphenylsilyl, diphenylmethylsilyl, diphenylvinylsilyl, methylcyclobutylsilyl, and dimethylfurylsilyl.
- The aryl groups used in the present invention are organic radicals derived from aromatic hydrocarbons by removal of a hydrogen atom. Such aryl groups include 5- to 7-membered, preferably 5- or 6-membered single or fused ring systems. When the aryl group is substituted, the substituent may be fused with an adjacent substituent to form a ring.
- Specific examples of the aryl groups include aromatic groups, such as phenyl, o-biphenyl, m-biphenyl, p-biphenyl, o-terphenyl, m-terphenyl, p-terphenyl, naphthyl, anthryl, phenanthryl, pyrenyl, indenyl, fluorenyl, tetrahydronaphthyl, perylenyl, crycenyl, naphthacenyl, and fluoranthenyl groups.
- Each aryl group may also be substituted with at least one substituent. More specifically, at least one hydrogen atom of each aryl group may be substituted with a deuterium atom, a halogen atom, a hydroxyl group, a nitro group, a cyano group, a silyl group, an amino group (—NH2, —NH(R), —N(R′)(R″) in which R, R′ and R″ are each independently a C1-C10 alkyl group (the —NH(R) and —N(R′)(R″) are referred to as “alkylamino groups”)), an amidino group, a hydrazine group, a hydrazone group, a carboxyl group, a sulfonic acid group, a phosphoric acid group, a C1-C24 alkyl group, a C1-C24 halogenated alkyl group, a C1-C24 alkenyl group, a C1-C24 alkynyl group, a C1-C24 heteroalkyl group, a C6-C24 aryl group, a C6-C24 arylalkyl group, a C2-C24 heteroaryl group or a C2-C24 heteroarylalkyl group.
- The heteroaryl groups used in the present invention refer to C2-C24 cyclic aromatic systems including one to three heteroatoms selected from N, O, P, Si, S, Ge, Se, and Te, with the remaining ring atoms being carbon. The rings may be fused together. One or more hydrogen atoms of each heteroaryl group may be substituted with the same substituents as in the aryl groups.
- The heteroaromatic rings refer to aromatic hydrocarbon rings in which one or more aromatic carbon atoms are replaced with one or more heteroatoms selected from N, O, P, Si, S, Ge, Se, and Te.
- The organic light emitting compound represented by Formula I may be selected from Compounds 1 to 564:
- However, it is noted that the scope of Formula I is not limited to Compounds 1 to 564.
- The present invention is also directed to an organic light emitting diode including the organic light emitting compound of Formula I. The organic light emitting diode of the present invention includes a first electrode, a second electrode opposite to the first electrode, and an organic layer interposed between the first and second electrodes. The organic layer includes one or more layers selected from a light emitting layer, an electron transport layer, a hole transport layer, an electron injecting layer, a hole injecting layer, a hole blocking layer, and an electron blocking layer. Particularly, the electron transport layer or the electron injecting layer includes the organic light emitting compound of Formula I.
- The expression “including the organic light emitting compound” can be interpreted to mean that the organic layer may include the organic light emitting compound of Formula I or two or more different compounds falling within the scope of Formula I.
- A more detailed description will be given concerning the organic light emitting diode of the present invention.
- The organic light emitting diode of the present invention includes an anode, a hole transport layer, a light emitting layer, an electron transport layer, and a cathode. The organic light emitting diode of the present invention may optionally further include a hole injecting layer and an electron injecting layer. One or more intermediate layers may be further formed in the organic light emitting diode. A hole blocking layer or an electron blocking layer may be further formed in the organic light emitting diode. The diode may further include one or more organic layers with various functions depending on the desired characteristics thereof.
- A description will be given concerning a method for fabricating the organic light emitting diode of the present invention. First, an electrode material for the anode is coated on a substrate to form the anode. The substrate may be any of those used in general organic light emitting diodes. The substrate is preferably an organic substrate or a transparent plastic substrate that is excellent in transparency, surface smoothness, ease of handling, and waterproofness. A highly transparent and conductive metal oxide, such as indium tin oxide (ITO), indium zinc oxide (IZO), tin oxide (SnO2) or zinc oxide (ZnO), is used as the anode material.
- A material for the hole injecting layer is coated on the anode by vacuum thermal evaporation or spin coating to form the hole injecting layer. Then, a material for the hole transport layer is coated on the hole injecting layer by vacuum thermal evaporation or spin coating to form the hole transport layer.
- The material for the hole injecting layer is not specially limited so long as it is usually used in the art. Example of such materials include 4,4′,4″-tris(2-naphthyl(phenyl)amino)triphenylamine (2-TNATA), N,N′-di(1-naphthyl)-N,N′-diphenylbenzidine) (NPD), N,N′-diphenyl-N,N′-bis(3-methylphenyl)-1,1′-biphenyl-4,4′-diamine (TPD), and N,N′-diphenyl-N,N′-bis[4-(phenyl-m-tolylamino)phenyl]biphenyl-4,4′-diamine (DNTPD).
- The material for the hole transport layer is not specially limited so long as it is commonly used in the art. Example of such materials include N,N′-bis(3-methylphenyl)-N,N′-diphenyl-[1,1-biphenyl]-4,4′-diamine (TPD) and N,N′-di(naphthalen-1-yl)-N,N′-diphenylbenzidine (α-NPD).
- Subsequently, the organic light emitting layer is laminated on the hole transport layer. A hole blocking layer may be optionally formed on the organic light emitting layer by vacuum thermal evaporation or spin coating. The hole blocking layer blocks holes from entering the cathode through the organic light emitting layer. This role of the hole blocking layer prevents the lifetime and efficiency of the diode from deteriorating. A material having a very low highest occupied molecular orbital (HOMO) energy level is used for the hole blocking layer. The hole blocking material is not particularly limited so long as it has the ability to transport electrons and a higher ionization potential than the light emitting compound. Representative examples of suitable hole blocking materials include BAIq, BCP, and TPBI.
- The electron transport layer is deposited on the hole blocking layer by vacuum thermal evaporation or spin coating, and the electron injecting layer is formed thereon. A metal for the cathode is deposited on the electron injecting layer by vacuum thermal evaporation to form the cathode, completing the fabrication of the organic light emitting diode. As the metal for the cathode, there may be used, for example, lithium (Li), magnesium (Mg), aluminum (Al), aluminum-lithium (Al—Li), calcium (Ca), magnesium-indium (Mg—In) or magnesium-silver (Mg—Ag). The organic light emitting diode may be of top emission type. In this case, a transmissive material, such as ITO or IZO, may be used for the cathode.
- The material for the electron transport layer functions to stably transport electrons injected from the electron injecting electrode (i.e. the cathode). The organic light emitting compound of Formula I is used as the material for the electron transport layer.
- One or more layers selected from the hole injecting layer, the hole transport layer, the electron blocking layer, the light emitting layer, the hole blocking layer, the electron transport layer, and the electron injecting layer may be formed by a monomolecular deposition or solution process. According to the monomolecular deposition process, the material for each layer is evaporated under heat and vacuum or reduced pressure to form the layer in the form of a thin film. According to the solution process, the material for each layer is mixed with a suitable solvent, and then the mixture is formed into a thin film by a suitable method, such as ink-jet printing, roll-to-roll coating, screen printing, spray coating, dip coating or spin coating.
- The organic light emitting diode of the present invention can be used in a variety of systems, such as flat panel displays, flexible displays, monochromatic flat panel lighting systems, white flat panel lighting systems, flexible monochromatic lighting systems, and flexible white lighting systems.
- The present invention will be explained in more detail with reference to the following specific examples, including synthesis examples for synthesizing dye compounds, and examples and a comparative example for fabricating organic light emitting diodes. However, these examples are provided for illustrative purposes only and are not intended to limit the scope of the invention.
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- 25 g (118 mmol) of dibenzofuran-1-boronic acid, 40.5 g (118 mmol) of methyl-5-bromo-2-iodobenzoate, 2.7 g (2.3 mmol) of tetrakis(triphenylphosphine)palladium, 33 g (237 mmol) of potassium carbonate, 200 ml of toluene, 200 ml of 1,4-dioxane, and 100 ml of water were placed in a round bottom flask under a nitrogen atmosphere. The mixture was refluxed for 12 h. After completion of the reaction, the reaction mixture was allowed to stand for phase separation. The organic layer was concentrated under reduced pressure and the resulting residue was purified by column chromatography to give Intermediate 1-a (33.5 g, yield 74%).
-
- 33.5 g (110 mmol) of Intermediate 1-a was added to 150 ml of tetrahydrofuran in a round bottom flask. After cooling to −10° C., 85 ml (254 mmol) of 3 M methylmagnesium bromide was slowly added dropwise to the flask. The mixture was heated to 40° C., followed by stirring for 4 h. Thereafter, the temperature was lowered to −10° C. 70 ml of 2 N hydrochloric acid was slowly added dropwise to the flask and 70 ml of an aqueous ammonium chloride solution was then added thereto. The temperature was allowed to rise to room temperature. After completion of the reaction, the reaction mixture was washed with water and concentrated under reduced pressure. The resulting residue was purified by column chromatography to give Intermediate 1-b (27 g, yield 80%).
-
- 27 g (89.2 mmol) of Intermediate 1-b and 70 ml of phosphoric acid were placed in a round bottom flask under a nitrogen atmosphere. The mixture was stirred at room temperature for 12 h. After completion of the reaction, the reaction mixture was extracted and concentrated. The resulting residue was purified by column chromatography to give Intermediate 1-c (17.6 g, yield 70%).
-
- 17.6 g (48.4 mmol) of Intermediate 1-c was placed in a round bottom flask and 200 ml of tetrahydrofuran was then added thereto under a nitrogen atmosphere. After cooling to −78° C., 36.3 ml (58.1 mmol) of 1.6 M butyllithium was slowly added dropwise to the flask. 1 h after the addition, 7.0 ml (62.9 mmol) of trimethyl borate was slowly added to the flask while maintaining the same temperature. Thereafter, the resulting mixture was stirred at room temperature. After completion of the reaction, the organic layer was concentrated under reduced pressure and recrystallized from hexane to give Intermediate 1-d (13 g, yield 82%).
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- 5 g (15.2 mmol) of Intermediate 1-d, 6.5 g (16.7 mmol) of 2-chloro-4,6-diphenyl-1,3,5-triazine, 0.3 g (0.3 mmol) of tetrakis(triphenylphosphine)palladium, 4.2 g (30.4 mmol) of potassium carbonate, 25 ml of toluene, 25 ml of 1,4-dioxane, and 15 ml of water were placed in a round bottom flask under a nitrogen atmosphere. The mixture was refluxed for 12 h. After completion of the reaction, the organic layer was concentrated under reduced pressure and the resulting residue was purified by column chromatography to give Compound 1 (6.8 g, yield 76%).
- MS (MALDI-TOF): m/z 515.20 [M]+
-
- Intermediate 2-a (yield 42%) was synthesized in the same manner as in Synthesis Example 1-5, except that 2,4-dichloro-6-phenyl-1,3,5-triazine and 1-naphthaleneboronic acid were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.
-
- Compound 5 (yield 72%) was synthesized in the same manner as in Synthesis Example 1-5, except that Intermediate 2-a was used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine.
- MS (MALDI-TOF): m/z 565.22 [M]+
-
- 50 g (183 mmol) of 2-bromo-9,9-dimethylfluorene, 59.3 g (1098 mmol) of an aqueous sodium methoxide solution, 10.4 g (54.9 mmol) of copper iodide, and 200 ml of methanol were placed in a round bottom flask under a nitrogen atmosphere. The mixture was refluxed for 12 h. After completion of the reaction, the organic layer was concentrated under reduced pressure and the resulting residue was purified by column chromatography to give Intermediate 3-a (33.2 g, yield 81%).
-
- 30 g (133 mmol) of Intermediate 3-a, 23.8 g (133 mmol) of N-bromosuccinimide, and 600 ml of dimethylformamide were placed in a round bottom flask under a nitrogen atmosphere. The mixture was stirred at 50° C. for 12 h. After completion of the reaction, the organic layer was concentrated under reduced pressure and the resulting residue was purified by column chromatography to give Intermediate 3-b (28 g, yield 70%).
-
- Intermediate 3-c (yield 77%) was synthesized in the same manner as in Synthesis Example 1-4, except that Intermediate 3-b was used instead of Intermediate 1-c.
-
- Intermediate 3-d (yield 52%) was synthesized in the same manner as in Synthesis Example 1-5, except that 1-bromo-3-chloro-2-fluorobenzene and Intermediate 3-c were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.
-
- 30 g (85 mmol) of Intermediate 3-d and 300 ml of dichloromethane were placed in a round bottom flask under a nitrogen atmosphere. After cooling to 0° C., a dilute solution of 63.9 g (255 mmol) of boron tribromide in 150 ml of dichloromethane was slowly added dropwise to the flask. The temperature was allowed to rise to room temperature. The mixture was stirred for 6 h. After completion of the reaction, the organic layer was concentrated under reduced pressure and the resulting residue was purified by column chromatography to give Intermediate 3-e (21.3 g, yield 74%).
-
- 20 g (59 mmol) of Intermediate 3-e, 13 g (94.5 mmol) of potassium carbonate, and 200 ml of 1-methyl-2-pyrrolidinone were placed in a round bottom flask under a nitrogen atmosphere. The mixture was stirred at 150° C. for 12 h. After completion of the reaction, the organic layer was concentrated under reduced pressure and the resulting residue was purified by column chromatography to give Intermediate 3-f (13.5 g, yield 72%).
-
- 13 g (40.8 mmol) of Intermediate 3-f, 12.4 g (48.9 mmol) of bis(pinacolato)diborane, 2 g (2.4 mmol) of tris(dibenzylideneacetone)palladium, 11.6 g (122 mmol) of potassium acetate, 2.7 g (9.8 mmol) of tricyclohexylphosphine, and 150 ml of N-dimethylformamide were placed in a round bottom flask under a nitrogen atmosphere. The mixture was refluxed. After completion of the reaction, the organic layer was concentrated under reduced pressure and the resulting residue was purified by column chromatography to give Intermediate 3-g (10.8 g, yield 65%).
-
- Compound 71 (yield 69%) was synthesized in the same manner as in Synthesis Example 1-5, except that Intermediate 3-g was used instead of Intermediate 1-d.
- MS (MALDI-TOF): m/z 515.20 [M]+
-
- Compound 72 (yield 46%) was synthesized in the same manner as in Synthesis Example 1-5, except that 2-(3-bromophenyl)-4,6-diphenyl-1,3,5-triazine and Intermediate 3-g were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.
- MS (MALDI-TOF): m/z 591.23 [M]+
-
- Intermediate 5-a (yield 76%) was synthesized in the same manner as in Synthesis Example 1-5, except that 3-bromodibenzofuran and phenylboronic acid were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.
-
- 50 g (204 mmol) of Intermediate 5-a and 500 ml of tetrahydrofuran were placed in a round bottom flask under a nitrogen atmosphere. After cooling to −78° C., 128 ml (204 mmol) of 1.6 M butyllithium was slowly added dropwise to the flask. The mixture was stirred for 1 h. To the mixture slowly added dropwise 14.3 g (245 mmol) of acetone. The resulting mixture was stirred at room temperature for 6 h. After completion of the reaction, 50 ml of an aqueous ammonium chloride solution was added for phase separation. The organic layer was concentrated under reduced pressure and the resulting residue was purified by column chromatography to give Intermediate 5-b (38.3 g, yield 62%).
-
- Intermediate 5-c (yield 69%) was synthesized in the same manner as in Synthesis Example 1-3, except that Intermediate 5-b was used instead of Intermediate 1-b.
-
- 14.5 g (50.9 mmol) of Intermediate 5-c and 150 ml of dichloromethane were stirred in a 1 L reactor. To the mixture was slowly added dropwise 8.9 g (56 mmol) at room temperature. The resulting mixture was stirred for 5 h. After completion of the reaction, the reaction mixture was precipitated by adding methanol. Filtration of the precipitate gave Intermediate 5-d (9.4 g, yield 51%).
-
- Intermediate 5-e (yield 65%) was synthesized in the same manner as in Synthesis Example 1-4, except that Intermediate 5-d was used instead of Intermediate 1-c.
-
- Compound 164 (yield 73%) was synthesized in the same manner as in Synthesis Example 1-5, except that Intermediate 5-e was used instead of Intermediate 1-d.
- MS (MALDI-TOF): m/z 515.20 [M]+
-
- Compound 167 (yield 48%) was synthesized in the same manner as in Synthesis Example 1-5, except that 2-(4-bromophenyl)-4,6-diphenyl-1,3,5-triazine and Intermediate 5-e were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.
- MS (MALDI-TOF): m/z 591.23 [M]+
-
- Intermediate 7-a (yield 66%) was synthesized in the same manner as in Synthesis Examples 1-1 to 1-4, except that dibenzofuran-3-boronic acid and methyl-5-bromo-1-iodobenzoate were used instead of dibenzofuran-1-boronic acid and methyl-5-bromo-2-iodobenzoate in Synthesis Example 1-1, respectively.
-
- Compound 197 (yield 63%) was synthesized in the same manner as in Synthesis Example 1-5, except that Intermediate 7-a was used instead of Intermediate 1-d.
- MS (MALDI-TOF): m/z 515.20 [M]+
-
- Compound 200 (yield 68%) was synthesized in the same manner as in Synthesis Example 1-5, except that 2-(4-bromophenyl)-4,6-diphenyl-1,3,5-triazine and Intermediate 7-a were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.
- MS (MALDI-TOF): m/z 591.23 [M]+
-
- 50 g (202 mmol) of 3-bromodibenzofuran, 54.6 g (1214 mmol) of an aqueous sodium methoxide solution, 11.5 g (60.7 mmol) of copper iodide, and 200 ml of methanol were placed in a round bottom flask under a nitrogen atmosphere. The mixture was refluxed for 12 h. After completion of the reaction, the organic layer was concentrated under reduced pressure and the resulting residue was purified by column chromatography to give Intermediate 9-a (36 g, yield 90%).
-
- 36 g (181 mmol) of Intermediate 9-a, 32.3 g (181 mmol) of N-bromosuccinimide, and 700 ml of dimethylformamide were placed in a round bottom flask under a nitrogen atmosphere. The mixture was stirred at 50° C. for 12 h. After completion of the reaction, the organic layer was concentrated under reduced pressure and the resulting residue was purified by column chromatography to give Intermediate 9-b (35 g, yield 70%).
-
- Intermediate 9-c (yield 71%) was synthesized in the same manner as in Synthesis Example 1-4, except that Intermediate 9-b was used instead of Intermediate 1-c.
-
- Intermediate 9-d (yield 64%) was synthesized in the same manner as in Synthesis Example 1-5, except that methyl-2-bromobenzoate and Intermediate 9-c were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.
-
- Intermediate 9-e (yield 77%) was synthesized in the same manner as in Synthesis Example 1-2, except that Intermediate 9-d was used instead of Intermediate 1-a.
-
- Intermediate 9-f was synthesized in a yield of 67% in the same manner as in Synthesis Example 1-3, except that Intermediate 9-e was used instead of Intermediate 1-b.
-
- 30 g (95.4 mmol) of Intermediate 9-f and 200 ml of dichloromethane were placed in a round bottom flask under a nitrogen atmosphere. The temperature was lowered to 0° C. A dilute solution of 120 g (143 mmol) of boron tribromide in 300 ml of dichloromethane was slowly added dropwise to the flask. The mixture was stirred at room temperature for 3 h. After completion of the reaction, the reaction solution was added to 1 L of distilled water. The organic layer was concentrated under reduced pressure and the resulting residue was purified by column chromatography to give Intermediate 9-g (19.2 g, yield 67%).
-
- 10 g (33.2 mmol) of Intermediate 9-g was placed in a round bottom flask under a nitrogen atmosphere. The temperature was lowered to 0° C. 3.2 ml (39.9 mmol) of pyridine and 7.3 ml (43.2 mmol) of trifluoromethanesulfonic anhydride were slowly added dropwise to the flask. The mixture was stirred at room temperature for 2 h. After completion of the reaction, the organic layer was concentrated under reduced pressure and the resulting residue was purified by column chromatography to give Intermediate 9-h (12.2 g, yield 85%).
-
- 8.5 g (26.7 mmol) of Intermediate 9-h, 8.8 g (34.7 mmol) of bis(pinacolato)diborane, 1 g (1.3 mmol) of (diphenylphosphinoferrocene)palladium dichloride, 7.6 g (80 mmol) of potassium acetate, and 90 ml of toluene were placed in a round bottom flask under a nitrogen atmosphere. The mixture was refluxed for 12 h. After completion of the reaction, the organic layer was concentrated under reduced pressure and the resulting residue was purified by column chromatography to give Intermediate 9-i (8 g, yield 75%).
-
- Compound 233 (yield 78%) was synthesized in the same manner as in Synthesis Example 1-5, except that Intermediate 9-i was used instead of Intermediate 1-d.
- MS (MALDI-TOF): m/z 515.20 [M]+
-
- Compound 234 (yield 52%) was synthesized in the same manner as in Synthesis Example 1-5, except that 2-(3-bromophenyl)-4,6-diphenyl-1,3,5-triazine and Intermediate 9-i were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.
- MS (MALDI-TOF): m/z 591.23 [M]+
-
- 37 g (156 mmol) of (3-amino-benzofuran-2-yl)-phenylmethanone, 16.9 g (281 mmol) of urea, and 185 mL of acetic acid were placed in a 500 mL reactor. The mixture was refluxed with stirring for 12 h. After completion of the reaction, the reaction mixture was precipitated by adding excess water. The precipitate was collected by filtration, slurried with hot methanol, filtered, slurried with hot toluene, filtered, and dried to obtain Intermediate 11-a (24 g, yield 59%).
-
- 15 g (44 mmol) of Intermediate 11-a and 150 mL of phosphorus oxychloride were placed in a 500 mL reactor. The mixture was refluxed with stirring for 3 h. After completion of the reaction, the reaction mixture was precipitated by slowly adding excess water at 0° C. The precipitate was collected by filtration and purified by column chromatography to give 21 g (yield 81%) of Intermediate 11-b.
-
- Compound 293 (yield 57%) was synthesized in the same manner as in Synthesis Example 1-5, except that Intermediate 11-b and Intermediate 5-e were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.
- MS (MALDI-TOF): m/z 528.18 [M]+
-
- 27.4 g (232 mmol) of 2-aminobenzonitrile and 300 mL of tetrahydrofuran were stirred in a 1 L reactor. After cooling to 0° C., 88.2 mL (487 mmol) of 3 M phenylmagnesium bromide was added dropwise to the flask. The mixture was refluxed for 3 h. After cooling to 0° C., a solution of 44.3 g (732 mmol) of ethyl chloroformate in 200 mL of tetrahydrofuran was added dropwise to the reaction mixture. The resulting mixture was refluxed for 2 h. After cooling to 0° C., to the reaction mixture was added a saturated aqueous solution of ammonium chloride. The organic layer was extracted and concentrated under reduced pressure. The resulting residue was purified by column chromatography to give Intermediate 12-a (40 g, yield 78%).
-
- 40 g (181 mmol) of Intermediate 12-a and 400 mL of phosphorus oxychloride were placed in a 1 L reactor. The mixture was refluxed for 5 h. After cooling to 0° C., distilled water was added dropwise to the reactor. The reaction mixture was filtered and the resulting residue was purified by column chromatography to give Intermediate 12-b (29.5 g, yield 68%).
-
- Compound 313 (yield 54%) was synthesized in the same manner as in Synthesis Example 1-5, except that Intermediate 12-b and Intermediate 3-g were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.
- MS (MALDI-TOF): m/z 488.19 [M]+
-
- 90 g (676 mmol) of 2-hydroxyphenylacetonitrile, 68.8 g (338 mmol) of 4-dimethylaminopyridine, 137 g (1352 mmol) of triethylamine, and 900 mL of methylene chloride were placed in a 2 L reactor and 82.4 g (676 mmol) of benzoyl chloride was then added dropwise thereto at 0° C. Thereafter, the mixture was stirred at room temperature for 4 h. After completion of the reaction, the reaction mixture was concentrated and the resulting residue was purified by column chromatography to give Intermediate 13-a (40 g, yield 61%).
-
- 40 g (169 mmol) of Intermediate 13-a, 9.5 g (34 mmol) of tricyclohexylphosphine, 1.9 g (17 mmol) of zinc, 3.8 g (17 mmol) of palladium acetate, and 400 mL of dimethylformamide were placed in a 1 L reactor. The mixture was refluxed with stirring under a nitrogen atmosphere for 12 h. After completion of the reaction, the reaction mixture was added to excess water at room temperature. The resulting brown crystal was collected by filtration and purified by column chromatography to give Intermediate 13-b (20 g, yield 52%).
-
- Intermediate 13-c (10 g, yield 62%) was synthesized in the same manner as in Synthesis Example 11-1, except that Intermediate 13-b was used instead of (3-amino-benzofuran-2-yl)-phenylmethanone.
-
- Intermediate 13-d (yield 77%) was synthesized in the same manner as in Synthesis Example 11-2, except that Intermediate 13-c was used instead of Intermediate 11-a.
-
- Compound 329 (yield 54%) was synthesized in the same manner as in Synthesis Example 1-5, except that Intermediate 13-d was used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine.
- MS (MALDI-TOF): m/z 528.18 [M]+
-
- Compound 341 (yield 58%) was synthesized in the same manner as in Synthesis Example 1-5, except that Intermediate 12-b and Intermediate 9-i were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.
- MS (MALDI-TOF): m/z 488.19 [M]+
-
- Ethyl cyanoacetate (139.8 g, 1.236 mol), potassium cyanide (29.5 g, 0.453 mol), and potassium hydroxide (46.2 g, 0.824 mol) were dissolved in 920 mL of dimethylformamide in a 2 L round bottom flask under a nitrogen atmosphere. The solution was stirred at 10° C. for 20 min. Thereafter, the solution was added with 1-nitronaphthalene (92 g, 531 mol), followed by stirring at 60° C. for 4 h. After completion of the reaction, the reaction mixture was concentrated and 600 mL of a 10% aqueous sodium hydroxide solution was added thereto. The resulting mixture was refluxed with stirring. The solid was collected by filtration and purified by column chromatography to give Intermediate 15-a (50 g, yield 56%).
-
- Intermediate 15-a (20.0 g, 169 mmol) and tetrahydrofuran (200 mL) were placed in a 1 L round bottom flask filled with nitrogen and 3 M phenylmagnesium bromide (113 mL, 623 mmol) was slowly added dropwise thereto at 0° C. The mixture was refluxed with stirring for 3 h. When the starting material disappeared, the temperature was again lowered. A solution of 3-bromobenzoyl chloride (44.58 g, 0.203 mmol) in 200 mL of tetrahydrofuran was slowly added dropwise to the flask. The resulting mixture was refluxed with stirring for 2 h. The reaction was quenched with an aqueous ammonium chloride solution. The reaction mixture was extracted with ethyl acetate and water. The organic layer was concentrated under reduced pressure and the resulting residue was purified by column chromatography to give Intermediate 15-b (37 g, yield 30%).
-
- Compound 370 (yield 57%) was synthesized in the same manner as in Synthesis Example 1-5, except that Intermediate 15-b and Intermediate 7-a were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.
- MS (MALDI-TOF): m/z 614.24 [M]+
-
- Intermediate 16-a (yield 42%) was synthesized in the same manner as in Synthesis Example 1-5, except that 2,4-dichloro-6-phenyl-1,3,5-triazine and benzofuran-1-boronic acid were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.
-
- Intermediate 16-b (yield 55%) was synthesized in the same manner as in Synthesis Examples 1-2 to 1-4, except that 3 M ethylmagnesium bromide was used instead of 3 M methylmagnesium bromide in Synthesis Example 1-2.
-
- Compound 375 (yield 55%) was synthesized in the same manner as in Synthesis Example 1-5, except that Intermediate 16-a and Intermediate 16-b were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.
- MS (MALDI-TOF): m/z 633.24 [M]+
-
- Intermediate 17-a (yield 57%) was synthesized in the same manner as in Synthesis Examples 3-1 to 3-7, except that 2-bromo-9,9-diethylfluorene was used instead of 2-bromo-9,9-dimethylfluorene in Synthesis Example 3-1.
-
- Compound 414 (yield 54%) was synthesized in the same manner as in Synthesis Example 1-5, except that Intermediate 12-b and Intermediate 17-a were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.
- MS (MALDI-TOF): m/z 516.22 [M]+
-
- Intermediate 18-a (yield 52%) was synthesized in the same manner as in Synthesis Examples 5-2 to 5-5, except that 2,4-dimethyl-3-pentanone was used instead of acetone in Synthesis Example 5-2.
-
- Compound 443 (yield 55%) was synthesized in the same manner as in Synthesis Example 1-5, except that 2-(4-bromophenyl)-4,6-diphenyl-1,3,5-triazine and Intermediate 18-a were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.
- MS (MALDI-TOF): m/z 647.29 [M]+
-
- Intermediate 19-a (yield 55%) was synthesized in the same manner as in Synthesis Examples 1-2 and 1-3, except that 3 M ethylmagnesium bromide and Intermediate 9-d were used instead of 3 M methylmagnesium bromide and Intermediate 1-a in Synthesis Example 1-2, respectively.
-
- Intermediate 19-b (yield 67%) was synthesized in the same manner as in Synthesis Examples 9-7 to 9-9, except that Intermediate 19-a was used instead of Intermediate 9-f in Synthesis Example 9-7.
-
- Compound 474 (yield 60%) was synthesized in the same manner as in Synthesis Example 1-5, except that Intermediate 11-b and Intermediate 19-b were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.
- MS (MALDI-TOF): m/z 556.22 [M]+
- ITO glass was patterned to have a light emitting area of 2 mm×2 mm, followed by cleaning. After the cleaned ITO glass was mounted in a vacuum chamber, the base pressure was adjusted to 1×10−6 torr. HATCN (50 Å), NPD (650 Å), [BH]+ Blue dopant (BD) 5% (200 Å), the corresponding compound shown in Table 1 (300 Å), Liq (10 Å), and Al (1,000 Å) were deposited in this order on the ITO glass to fabricate an organic light emitting diode. The luminescent properties of the organic light emitting diode were measured at 0.4 mA.
- The structures of HATCN, NPD, BD, BH, and Liq are as follows:
- An organic light emitting diode was fabricated in the same manner as in Examples 1-19, except that ET was used instead of the compounds shown in Table 1. ET is widely used as an electron transport material and its structure is as follows.
- The organic electroluminescence diodes fabricated in Examples 1-19 and Comparative Example 1 were measured for voltage, luminance, color coordinates, and lifetime. The results are shown in Table 1. T95 indicates the time at which the luminance of each diode was decreased to 95% of the initial luminance (2000 cd/m2).
-
TABLE 1 Properties ETL V Cd/A CIEx CIEy T95 (Hrs) Comparative ET 4.2 6.4 0.133 0.129 16 Example 1 Example 1 Compound 1 3.6 8.0 0.132 0.130 35 Example 2 Compound 5 3.6 7.9 0.133 0.128 43 Example 3 Compound 71 3.4 8.0 0.132 0.126 40 Example 4 Compound 72 3.8 7.9 0.133 0.125 36 Example 5 Compound 164 3.3 7.6 0.132 0.126 34 Example 6 Compound 167 3.9 7.6 0.133 0.125 45 Example 7 Compound 197 4.0 7.5 0.133 0.125 42 Example 8 Compound 200 3.6 8.1 0.132 0.130 37 Example 9 Compound 233 3.4 8.0 0.133 0.128 37 Example 10 Compound 234 3.6 7.8 0.133 0.127 34 Example 11 Compound 293 3.6 8.0 0.132 0.130 45 Example 12 Compound 313 3.6 7.9 0.133 0.128 42 Example 13 Compound 329 3.4 8.0 0.132 0.126 40 Example 14 Compound 341 3.8 7.9 0.133 0.125 34 Example 15 Compound 370 3.3 8.0 0.132 0.126 38 Example 16 Compound 375 3.9 7.9 0.133 0.125 40 Example 17 Compound 414 4.0 7.6 0.132 0.126 33 Example 18 Compound 443 3.6 7.6 0.133 0.125 37 Example 19 Compound 474 3.7 7.5 0.133 0.125 41 - As can be seen from the results in Table 1, the inventive organic compounds had higher efficiencies, lower driving voltages, and longer lifetimes than ET, which is widely used as an electron transport material. Therefore, it can be concluded that the inventive compounds are suitable for the fabrication of organic light emitting diodes with improved characteristics.
Claims (6)
1. An organic light emitting compound represented by Formula I:
HAr1-(L)n-HAr2 (I)
HAr1-(L)n-HAr2 (I)
wherein L represents a linker and is a single bond or is selected from substituted or unsubstituted C1-C30 alkylene groups, substituted or unsubstituted C2-C30 alkenylene groups, substituted or unsubstituted C2-C30 alkynylene groups, substituted or unsubstituted C3-C30 cycloalkylene groups, substituted or unsubstituted C2-C30 heterocycloalkylene groups, substituted or unsubstituted C6-C30 arylene groups, and substituted or unsubstituted C2-C30 heteroarylene groups, n is an integer from 1 to 3, provided that when n is equal to or greater than 2, the plurality of L groups are identical to or different from each other;
wherein HAr1 is a substituted or unsubstituted C6-C30 aryl group or a substituted or unsubstituted C2-C30 heteroaryl group; and
wherein HAr2 is selected from the following structures A to E:
where X1 is CR11 or N, X2 is CR12 or N, X3 is CR13 or N, X4 is CR14 or N, X5 is CR15 or N, X6 is CR16 or N, X7 is CR17 or N, X8 is CR18 or N, X9 is CR19 or N, and X10 is CR20 or N, with the proviso that at least two of X1 to X4 are selected from CR11 to CR14, at least three of X5 to X10 are selected from CR15 to CR20, and one of X1 to X10 is a carbon atom linked to L,
where R1 and R2 are identical to or different from each other and are each independently selected from a hydrogen atom, a deuterium atom, substituted or unsubstituted C1-C30 alkyl groups, substituted or unsubstituted C2-C30 alkenyl groups, substituted or unsubstituted C2-C30 alkynyl groups, substituted or unsubstituted C1-C30 alkoxy groups, substituted or unsubstituted C1-C30 alkylthioxy groups, substituted or unsubstituted C1-C30 alkylamine groups, substituted or unsubstituted C1-C24 alkylsilyl groups, an amino group, a thiol group, a cyano group, a hydroxyl group, a nitro group, and halogen groups, and
where R11 to R20 are identical to or different from each other and are each independently selected from a hydrogen atom, a deuterium atom, substituted or unsubstituted C1-C30 alkyl groups, substituted or unsubstituted C2-C30 alkenyl groups, substituted or unsubstituted C2-C30 alkynyl groups, substituted or unsubstituted C3-C30 cycloalkyl groups, substituted or unsubstituted C2-C30 heterocycloalkyl groups, substituted or unsubstituted C5-C30 cycloalkenyl groups, substituted or unsubstituted C1-C30 alkoxy groups, substituted or unsubstituted C6-C30 aryloxy groups, substituted or unsubstituted C1-C30 alkylthioxy groups, substituted or unsubstituted C6-C30 arylthioxy groups, substituted or unsubstituted C1-C30 alkylamine groups, substituted or unsubstituted C6-C30 arylamine groups, substituted or unsubstituted C6-C50 aryl groups, substituted or unsubstituted C2-C50 heteroaryl groups containing O, N or S as a heteroatom, substituted or unsubstituted C1-C24 alkylsilyl groups, substituted or unsubstituted C6-C24 arylsilyl groups, an amino group, a thiol group, a cyano group, a hydroxyl group, a nitro group, and halogen groups.
2. The organic light emitting compound according to claim 1 , wherein the “substituted” in the definition of “substituted or unsubstituted” indicates substitution with at least one substituent selected from the group consisting of deuterium, a cyano group, halogen groups, a hydroxyl group, a nitro group, C1-C24 alkyl groups, C1-C24 halogenated alkyl groups, C2-C24 alkenyl groups, C2-C24 alkynyl groups, C1-C24 heteroalkyl groups, C6-C24 aryl groups, C7-C24 arylalkyl groups, C2-C24 heteroaryl groups, C2-C24 heteroarylalkyl groups, C1-C24 alkoxy groups, C1-C24 alkylamino groups, C1-C24 arylamino groups, C1-C24 heteroarylamino groups, C1-C24 alkylsilyl groups, C6-C24 arylsilyl groups, and C6-C24 aryloxy groups.
3. The organic light emitting compound according to claim 1 , wherein HAr1 is selected from the following structures E1 to E33:
4. An organic light emitting diode comprising a first electrode, a second electrode opposite to the first electrode, and an organic layer interposed between the first and second electrodes wherein the organic layer comprises the compound represented by Formula I according to claim 1 .
5. The organic light emitting diode according to claim 5 , wherein the organic layer comprises one or more layers selected from a light emitting layer, an electron transport layer, a hole transport layer, an electron injecting layer, a hole injecting layer, a hole blocking layer, and an electron blocking layer.
6. The organic light emitting diode according to claim 6 , wherein the electron transport layer or the electron injecting layer comprises the compound represented by Formula I.
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KR102506419B1 (en) * | 2017-07-13 | 2023-03-07 | 솔루스첨단소재 주식회사 | Organic compound and organic electroluminescent device comprising the same |
KR102341241B1 (en) * | 2018-11-23 | 2021-12-20 | 주식회사 엘지화학 | Novel compound and organic light emitting device comprising the same |
CN110128458A (en) * | 2019-05-31 | 2019-08-16 | 浙江京合信新材料科技有限公司 | A kind of preparation method of 9,9- dimethyl fluorene 2- methoxyl group -3- boric acid |
CN112279844B (en) * | 2019-07-24 | 2022-04-19 | 南京高光半导体材料有限公司 | Green light main body material, organic electroluminescent device and electronic display equipment |
CN112390789B (en) * | 2019-08-16 | 2022-05-13 | 南京高光半导体材料有限公司 | Electron transport material and organic electroluminescent device using same |
CN110845483B (en) * | 2019-11-29 | 2021-11-16 | 武汉天马微电子有限公司 | Compound and application thereof |
CN111848588B (en) * | 2020-07-17 | 2021-11-16 | 陕西莱特光电材料股份有限公司 | Organic compound, and electronic element and electronic device using same |
CN114456155B (en) * | 2020-11-09 | 2024-04-12 | 江苏三月科技股份有限公司 | Compound with azabenzene as core and application thereof |
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- 2017-07-27 CN CN201710622977.0A patent/CN107663197A/en active Pending
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US10957865B2 (en) | 2021-03-23 |
CN107663197A (en) | 2018-02-06 |
US20180040834A1 (en) | 2018-02-08 |
EP3275970B1 (en) | 2019-05-22 |
EP3275970A1 (en) | 2018-01-31 |
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