WO2011019156A1 - Novel organic electroluminescent compounds and organic electroluminescent device using the same - Google Patents

Novel organic electroluminescent compounds and organic electroluminescent device using the same Download PDF

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WO2011019156A1
WO2011019156A1 PCT/KR2010/005092 KR2010005092W WO2011019156A1 WO 2011019156 A1 WO2011019156 A1 WO 2011019156A1 KR 2010005092 W KR2010005092 W KR 2010005092W WO 2011019156 A1 WO2011019156 A1 WO 2011019156A1
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Prior art keywords
substituent
alkyl
aryl
organic electroluminescent
group
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PCT/KR2010/005092
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French (fr)
Inventor
Soo Yong Lee
Young Jun Cho
Hyuck Joo Kwon
Bong Ok Kim
Sung Min Kim
Seung Soo Yoon
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Rohm And Haas Electronic Materials Korea Ltd.
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Priority to CN201080045750.0A priority Critical patent/CN102918134B/en
Priority to US13/389,750 priority patent/US20120235123A1/en
Publication of WO2011019156A1 publication Critical patent/WO2011019156A1/en
Priority to US14/624,921 priority patent/US20150171341A1/en

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Definitions

  • the present invention relates to novel organic electroluminescent compounds and an organic electroluminescent device using the same.
  • the organic electroluminescent compound according to the present invention is represented by Chemical Formula 1:
  • the organic EL device commonly has a configuration of anode/hole injection layer (HIL)/hole transport layer (HTL)/emission material layer (EML)/electron transport layer (ETL)/electron injection layer (EIL)/cathode.
  • HIL hole injection layer
  • HTL hole transport layer
  • EML emission material layer
  • ETL electron transport layer
  • EIL electron injection layer
  • CBP 4,4'-bis(carbazol-9-yl) biphenyl
  • BCP 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline
  • BAlq Bis(2-methyl-8-quinolinato)( ⁇ -phenyl-phenolato)aluminum(III) (BAlq)
  • BAlq Bis(2-methyl-8-quinolinato)( ⁇ -phenyl-phenolato)aluminum(III)
  • the OLED devices do not have satisfactory operation life. Therefore, development of more stable, higherperformance host materials is required.
  • an object of the present invention is to provide an organic electroluminescent compound having luminescence efficiency and device operation life improved over existing host materials and having superior backbone with appropriate color coordinates in order to solve the aforesaid problems.
  • Another object of the present invention is to provide a highly efficient and longlife organic electroluminescent device employing the organic electroluminescent compound as an electroluminescent material.
  • the present invention relates to organic electroluminescent compounds represented by Chemical Formula 1, and an organic electroluminescent device using the same.
  • the organic electroluminescent compounds according to the present invention exhibit high luminous efficiency, excellent color purity and life property of the material, so that OLED's with very excellent operation life can be manufactured therefrom.
  • a 1 through A 19 independently represent CR 1 or N
  • Ar 1 represents (C6-C40)arylene with or without substituent(s) or (C3-C40)heteroarylene with or without substituent(s), except for the case where m is 0, and A 15 through A 19 are CR 1 at the same time;
  • R 1 through R 9 independently represent hydrogen, deuterium, halogen, (C1-C30)alkyl with or without substituent(s), (C6-C30)aryl with or without substituent(s), substituted or unsubstituted (C6-C30)aryl fused with one or more (C3-C30)cycloalkyl(s) with or without substituent(s), (C3-C30)heteroaryl with or without substituent(s), 5- to 7-membered heterocycloalkyl with or without substituent(s), 5- to 7-membered heterocycloalkyl fused with one or more aromatic ring(s) with or without substituent(s), (C3-C30)cycloalkyl with or without substituent(s), (C3-C30)cycloalkyl fused with one or more aromatic ring(s) with or without substituent(s), cyano, trifluoromethyl, NR 21 R 22 , BR 23 R 24 , PR 25 R 26
  • R 21 through R 28 independently represent (C1-C30)alkyl with or without substituent(s), (C6-C30)aryl with or without substituent(s) or (C3-C30)heteroaryl with or without substituent(s),
  • R a , R b , and R c independently represent (C1-C30)alkyl with or without substituent(s) or (C6-C30)aryl with or without substituent(s)
  • Y represents S or O
  • R d represent (C1-C30)alkyl with or without substituent(s) or (C6-C30)aryl with or without substituent(s)
  • R e represent (C1-C30)alkyl with or without substituent(s), (C1-C30)alkoxy with or without substituent(s), (C6-C30)aryl with or without substituent(s) or (C6-C30)aryloxy with or without substituent(s)
  • R f represent (C1
  • n an integer 0 to 2;
  • l and n represent an integer 1 or 2.
  • alkyl in the present invention, “alkyl”, “alkoxy” and other substituents containing “alkyl” moiety include both linear and branched species.
  • cycloalkyl includes both adamantyl with or without substituent(s) and (C7-C30)bicycloalkyl with or without substituent(s).
  • aryl means an organic radical derived from an aromatic hydrocarbon by the removal of one hydrogen atom, and may include a 4- to 7-membered, particularly 5- or 6-membered, single ring or fused ring, including a plurality of aryls linked by chemical bond(s).
  • Specific examples include phenyl, naphthyl, biphenyl, anthryl, indenyl, fluorenyl, phenanthryl, triphenylenyl, pyrenyl, perylenyl, chrysenyl, naphthacenyl, fluoranthenyl, etc., but are not limited thereto.
  • monocyclic heteroaryl such as furyl, thienyl, pyrrolyl, imidazolyl, pyrazolyl, thiazolyl, thiadiazolyl, isothiazolyl, isoxazolyl, oxazolyl, oxadiazolyl, triazinyl, tetrazinyl, triazolyl, tetrazolyl, furazanyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, etc., polycyclic heteroaryl such as benzofuryl, benzothienyl, isobenzofuryl, benzimidazolyl, benzothiazolyl, benzoisothiazolyl, benzoisoxazolyl, benzoxazolyl, isoindolyl, indolyl, indazolyl, benzothiadiazolyl, quinolyl, isoquinolyl, c
  • the “(C1-C30)alkyl” groups described herein may include (C1-C20)alkyl or (C1-C10)alkyl and the “(C6-C30)aryl” groups include (C6-C20)aryl or (C6-C12)aryl.
  • the “(C3-C30)heteroaryl” groups include (C3-C20)heteroaryl or (C3-C12)heteroaryl and the “(C3-C30)cycloalkyl” groups include (C3-C20)cycloalkyl or (C3-C7)cycloalkyl.
  • the “(C2-C30)alkenyl or alkynyl” group include (C2-C20)alkenyl or alkynyl, (C2-C10)alkenyl or alkynyl.
  • substituent(s) is further substituted by one or more substituent(s) selected from the group consisting of deuterium, halogen, (C1-C30)alkyl with or without halogen substituent(s), (C6-C30)aryl, (C3-C30)heteroaryl with or without (C6-C30)aryl substituent(s), 5- to 7-membered heterocycloalkyl, 5- to 7-membered heterocycloalkyl fused with one or more aromatic ring(s), (C3-C30)cycloalkyl, (C3-C30)cycloalkyl fused with one or more aromatic ring(s), tri(C1-C30)alkylsilyl, di(C1-C30)alkyl(C6-C30)arylsilyl, tri(C6-C30)arylsilyl, (C2-C30)alkenyl, (C2-C30)alkynyl,
  • the R 1 through R 9 , R 21 through R 28 , R 51 through R 58 and R 61 through R 63 are independently selected from hydrogen, deuterium, halogen, alkyl such as methyl, ethyl, propyl, butyl, pentyl, hexyl, ethylhexyl, heptyl, octyl, etc., aryl such as phenyl, naphthyl, fluorenyl, biphenyl, phenanthryl, terphenyl, pyrenyl, perylenyl, spirobifluorenyl, fluoranthenyl, chrysenyl, triphenylenyl, etc., aryl fused with one or more cycloalkyl such as 1,2-dihydroacenaphthyl, heteroaryl such as dibenzothiophenyl, dibenzofuryl, carbazolyl, pyridyl, fu
  • heteroaryl such as dibenzothiophenyl, dibenzofuryl, carbazolyl, pyridyl, furyl, thienyl, quinolyl, triazinyl, pyrimidinyl, pyridazinyl, quinoxalinyl, phenanthrolinyl, etc., aryloxy such as biphenyloxy, etc., arylthio such as biphenylthio, etc., aralkyl such as biphenylmethyl, triphenylmethyl, etc., or , but are not limited thereto, and may be further substituted as shown in Chemical Formula 1.
  • R 1 through R 9 may be exemplified as following structures but are not limited thereto.
  • organic electroluminescent compound according to the present invention may be specifically exemplified as following compounds but is not limited thereto.
  • the organic electroluminescent compound according to the present invention may be prepared as shown in following Reaction Scheme 1.
  • a 1 through A 19 , X, Ar 1 and m are the same as defined in Chemical Formula 1.
  • an organic electroluminescent device which comprises a first electrode; a second electrode; and one or more organic layer(s) interposed between the first electrode and the second electrode, wherein the organic layer comprises one or more organic electroluminescent compound(s) represented by Chemical Formula 1.
  • the organic electroluminescent compound is used as a host material of the electroluminescent layer.
  • the organic layer may include the electroluminescent layer, and the electroluminescent layer may further include one or more dopants besides one or more organic electroluminescent compounds of Chemical Formula 1.
  • the dopant applied to the organic electroluminescent device of the present invention is not specifically limited.
  • the dopant applied to the organic electroluminescent device of the present invention is selected from following Chemical Formula 2.
  • M 1 is a metal selected from a group consisting of Group 7, Group 8, Group 9, Group 10, Group 11, Group 13, Group 14, Group 15 and Group 16 metals, and ligand L 101 , L 102 and L 103 are independently selected from the following structures;
  • R 201 through R 203 independently represent hydrogen, (C1-C30)alkyl with or without halogen substituent(s), (C6-C30)aryl with or without (C1-C30)alkyl substituent(s) or halogen;
  • R 204 through R 219 independently represent hydrogen, (C1-C30)alkyl with or without substituent(s), (C1-C30)alkoxy with or without substituent(s), (C3-C30)cycloalkyl with or without substituent(s), (C2-C30)alkenyl with or without substituent(s), (C6-C30)aryl with or without substituent(s), mono- or di-(C1-C30)alkylamino with or without substituent(s), mono- or di-(C6-C30)arylamino with or without substituent(s), SF 5 , tri(C1-C30)alkylsilyl with or without substituent(s), di(C1-C30)alkyl(C6-C30)arylsilyl with or without substituent(s), tri(C6-C30)arylsilyl with or without substituent(s), cyano or halogen;
  • R 220 through R 223 independently represent hydrogen, (C1-C30)alkyl with or without halogen substituent(s) or (C6-C30)aryl with or without (C1-C30)alkyl substituent(s);
  • R 224 and R 225 independently represent hydrogen, (C1-C30)alkyl with or without substituent(s), (C6-C30)aryl with or without substituent(s) or halogen, or R 224 and R 225 may be linked via (C3-C12)alkylene or (C3-C12)alkenylene with or without a fused ring to form an alicylic ring or a mono or polycyclic aromatic ring;
  • R 226 represents (C1-C30)alkyl with or without substituent(s), (C6-C30)aryl with or without substituent(s), (C5-C30)heteroaryl with or without substituent(s) or halogen;
  • R 227 through R 229 independently represent hydrogen, (C1-C30)alkyl with or without substituent(s), (C6-C30)aryl with or without substituent(s) or halogen;
  • Q represents , or , wherein R 231 through R 242 independently represent hydrogen, (C1-C30)alkyl with or without halogen substituent(s), (C1-C30)alkoxy, halogen, (C6-C30)aryl with or without substituent(s), cyano or (C5-C30)cycloalkyl with or without substituent(s), or each of them may be linked to an adjacent substituent via alkylene or alkenylene to form a spiro ring or a fused ring, or may be linked to R 207 or R 208 via alkylene or alkenylene to form a saturated or unsaturated fused ring.
  • the meaning of the electroluminescent layer may be a single layer as a layer where the light is emitted or may be a multiple layer where two or more layers are laminated.
  • the electroluminescent host of the present invention when hostdopant are used in mixture, it is confirmed that the luminous efficiency are remarkably improved by the electroluminescent host of the present invention. It may be configured at doping concentration of 0.5 to 10wt%.
  • the electroluminescent host of the present invention has superior conductivity with respect to the hole and electron and excellent stability in material, thereby showing a characteristic of remarkably increasing its life span as well as improving the luminous efficiency.
  • the M 1 is selected from a group consisting of Ir, Pt, Pd, Rh, Re, Os, Tl, Pb, Bi, In, Sn, Sb, Te, Au and Ag.
  • the dopant compounds of Chemical Formula 2 are exemplified by the compounds described in Korean Patent Application No. 10-2008-0112855, but are not limited thereto.
  • the organic layer may further include, in addition to the organic electroluminescent compound represented by Chemical Formula 1, one or more compound(s) selected from a group consisting of arylamine compounds and styrylarylamine compounds, at the same time.
  • the arylamine compounds or styrylarylamine compounds are exemplified in Korean Patent Application No. 10-2008-0123276, 10-2008-0107606 or 10-2008-0118428, but are not limited thereto.
  • the organic layer may further include, in addition to the organic electroluminescent compound represented by Chemical Formula 1, one or more metal(s) selected from a group consisting of organic metals of Group 1, Group 2, 4th period and 5th period transition metals, lanthanide metals and dtransition elements or complex compound(s).
  • the organic layer may include an electroluminescent layer and a charge generating layer.
  • the organic layer may include, in addition to the organic electroluminescent compound of Chemical Formula 1, one or more organic electroluminescent layer(s) emitting blue, green or red light at the same time in order to embody a whiteemitting organic electroluminescent device.
  • the compound emitting blue, green or red light may be exemplified by the compounds described in Korean Patent Application No. 10-2008-0123276, 10-2008-0107606 or 10-2008-0118428, but are not limited thereto.
  • a layer selected from a chalcogenide layer, a metal halide layer and a metal oxide layer may be placed on the inner surface of one or both electrode(s) among the pair of electrodes. More specifically, a metal chalcogenide (including oxide) layer of silicon or aluminum may be placed on the anode surface of the electroluminescent medium layer, and a metal halide layer or metal oxide layer may be placed on the cathode surface of the electroluminescent medium layer. Operation stability may be attained therefrom.
  • the chalcogenide may be, for example, SiO x (1 ⁇ x ⁇ 2), AlO x (1 ⁇ x ⁇ 1.5), SiON, SiAlON, etc.
  • the metal halide may be, for example, LiF, MgF 2 , CaF 2 , a rare earth metal fluoride, etc.
  • the metal oxide may be, for example, Cs 2 O, Li 2 O, MgO, SrO, BaO, CaO, etc.
  • the organic electroluminescent device it is also preferable to arrange on at least one surface of the pair of electrodes thus manufactured a mixed region of an electron transport compound and a reductive dopant, or a mixed region of a hole transport compound and an oxidative dopant.
  • a mixed region of an electron transport compound and a reductive dopant or a mixed region of a hole transport compound and an oxidative dopant.
  • the electron transport compound is reduced to an anion, injection and transport of electrons from the mixed region to an electroluminescent medium are facilitated.
  • the hole transport compound is oxidized to a cation, injection and transport of holes from the mixed region to an electroluminescent medium are facilitated.
  • Preferable oxidative dopants include various Lewis acids and acceptor compounds.
  • Preferable reductive dopants include alkali metals, alkali metal compounds, alkaline earth metals, rareearth metals, and mixtures thereof.
  • a white-emitting electroluminescent device having two or more electroluminescent layers may be manufactured by employing a reductive dopant layer as a charge generating layer.
  • the organic electroluminescent compound according to the present invention exhibits good luminous efficiency and excellent life property, it may be used to manufacture OLED devices having very superior operation life.
  • the 1-neck flask was filled with Compound 1-2 (8.5 g, 26.30 mmol), formed a vacuum and was filled with argon. After tetrahydrofuran (500 mL) was added, the mixture was stirred at 78°C for 10 minutes. n-BuLi(2.5M in hexane) (15.8 mL, 39.45 mmol) was added dropwise and stirred at -78°C for 1 hour and a half. Trimethylborate (4.85 mL, 39.45 mmol) was added at -78°C. The mixture was stirred at -78°C for 30 minutes and stirred at room temperature for 4 hours. Upon completion of the reaction, the product was extracted with distilled water and EA.
  • Compound 2-3 (5.7 g, 11.97 mmol, 80.9%) was obtained by combining Compound 2-2 (7 g, 14.78 mmol) in Preparation Example 1 according to the same method as the preparation of Compound 1-2.
  • Compound 2-4 (3.4 g, 7.70 mmol, 64.4%) was obtained by combining Compound 2-3 (5.7 g, 11.97 mmol) in Preparation Example 1 according to the same method as the preparation of Compound 1-3.
  • Compound 3-4 (7.2 g, 16.28 mmol, 53.2%) was obtained by combining Compound 3-3 (14.6 g, 30.59 mmol) in Preparation Example 2 according to the same method as the preparation of Compound 2-4.
  • Compound 51 (5.1 g, 8.63 mmol, 53%) was obtained by using Compound 3-4 (7.2 g, 16.28 mmol) and 2-bromo-9,9-dimethyl-9H-fluorene in Preparation Example 2 according to the same method as the preparation of Compound 49.
  • 1,3-dibromobenzene (28 g, 0.119 mol) was dissolved in THF (600 mL) and n-BuLi (47.5 mL) was slowly added dropwise at -78 o C. After reacting and stirring for 1 hour, Compound 3-1 (47.5 mL) was slowly added dropwise and slowly heated. The mixture was stirred at room temperature for 5 hours. Upon completion of the reaction, the product was extracted with EA and distilled water. Compound 4-1 (15.7 g, 40.43 mmol, 40.4%) was obtained via column separation.
  • Compound 4-2 (12.5 g, 26.34 mmol, 65.2%) was obtained by combining Compound 4-1 (15.7 g, 40.43 mmol) in Preparation Example 1 according to the same method as the preparation of Compound 1-1.
  • Compound 4-3 ( 9.8 g, 17.71 mmol, 67.3%) was obtained by combining Compound 4-2 (12.5 g, 26.34 mmol) in Preparation Example 1 according to the same method as the preparation of Compound 1-2.
  • Compound 4-5 ( 52.4 g, 162.63 mmol, 62.4%) was obtained by combining Compound 4-4 ( 63.4 g, 260.58 mmol) in Preparation Example 1 according to the same method as the preparation of Compound 1-2.
  • Compound 4-6 (20.3 g, 70.70 mmol, 43%) was obtained by combining Compound 4-5 (52.4 g, 162.63 mmol) in Preparation Example 1 according to the same method as the preparation of Compound 1-3.
  • Organic electroluminescent Compounds 1 to 68 were prepared according to Preparation Examples 1 to 4 and Table 1 shows 1 H NMR and MS/FAB of the prepared organic electroluminescent compounds.
  • An OLED device was manufactured using the electroluminescent material according to the present invention.
  • a transparent electrode ITO thin film (15 ⁇ / ⁇ ) obtained from a glass for OLED (produced by Samsung Corning) was subjected to ultrasonic washing with trichloroethylene, acetone, ethanol and distilled water, sequentially, and stored in isopropanol before use.
  • an ITO substrate was equipped in a substrate folder of a vacuum vapor deposition apparatus, and 4,4',4"-tris(N,N-(2-naphthyl)-phenylamino)triphenylamine (2-TNATA) was placed in a cell of the vacuum vapor deposition apparatus, which was then ventilated up to 10 -6 torr of vacuum in the chamber. Then, electric current was applied to the cell to evaporate 2-TNATA, thereby forming a hole injection layer having a thickness of 60 nm on the ITO substrate.
  • 2-TNATA 4,4',4"-tris(N,N-(2-naphthyl)-phenylamino)triphenylamine
  • NPB N,N' -bis( ⁇ -naphthyl) -N,N' -diphenyl-4,4'-diamine
  • an electroluminescent layer was formed thereon as follows.
  • Compound 49 was placed in a cell of a vacuum vapor deposition apparatus as host, and Ir(ppy) 3 [tris(2-phenylpyridine)iridium] was placed in another cell as a dopant.
  • the two materials were evaporated at different rates such that an electroluminescent layer having a thickness of 30 nm was vapordeposited on the hole transport layer at 4 to 10 wt%.
  • An OLED was manufactured as in Example 1 except that Compound 23 according to the present invention is used as host material on the electroluminescent layer and an organic iridium complex (piq) 2 Ir(acac)[bis-(1-phenylisoquinolyl)iridium(III)acetylacetonate] is used as electroluminescent dopant.
  • Compound 23 according to the present invention is used as host material on the electroluminescent layer and an organic iridium complex (piq) 2 Ir(acac)[bis-(1-phenylisoquinolyl)iridium(III)acetylacetonate] is used as electroluminescent dopant.
  • An OLED device was manufactured in the same manner as Examples 1 and 3 except that 4,4'-Bis(carbazol-9-yl)-biphenyl (CBP) instead of the compounds of the present invention was used as host material in a cell of the vacuum vapor deposition apparatus.
  • CBP 4,4'-Bis(carbazol-9-yl)-biphenyl
  • Luminous efficiency of the OLED devices including the organic electroluminescent compound according to the present invention manufactured in Examples 1 to 2 and Comparative Examples 1 and 2 and the conventional electroluminescent compound was measured at 1,000 cd/m 2 . The result is given in Table 2.
  • the organic electroluminescent compounds according to the present invention have excellent properties compared with the conventional material.
  • the device using the organic electroluminescent compound according to the present invention as host material for emitting red or green light has excellent electroluminescent properties and drops driving voltage, thereby increasing power efficiency and improving power consumption.

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Abstract

Provided are a novel organic electroluminescent compound and an organic electroluminescent device using the same. Since the organic electroluminescent compound disclosed herein exhibits good luminous efficiency and excellent life property, it may be used to manufacture OLED devices having very superior operation life.

Description

NOVEL ORGANIC ELECTROLUMINESCENT COMPOUNDS AND ORGANIC ELECTROLUMINESCENT DEVICE USING THE SAME
The present invention relates to novel organic electroluminescent compounds and an organic electroluminescent device using the same. The organic electroluminescent compound according to the present invention is represented by Chemical Formula 1:
[Chemical Formula 1]
Figure PCTKR2010005092-appb-I000001
In general, the organic EL device commonly has a configuration of anode/hole injection layer (HIL)/hole transport layer (HTL)/emission material layer (EML)/electron transport layer (ETL)/electron injection layer (EIL)/cathode. Organic electroluminescent devices emitting blue, green or red light may be created depending on how to form the emission material layer.
At present, 4,4'-bis(carbazol-9-yl) biphenyl (CBP) is the most widely known as a host material for a phosphorescent material. Highefficiency OLEDs using a hole blocking layer comprising 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP), Bis(2-methyl-8-quinolinato)(ρ-phenyl-phenolato)aluminum(III) (BAlq), etc. are reported. Highperformance OLEDs using BAlq derivatives as a host were reported by Pioneer (Japan) and others.
Although these materials provide good electroluminescence characteristics, they are disadvantageous in that degradation may occur during the hightemperature deposition process in vacuum because of low glass transition temperature and poor thermal stability. Since the power efficiency of an OLED is given by (π / voltage) × current efficiency, the power efficiency is inversely proportional to the voltage. High power efficiency is required to reduce the power consumption of an OLED. Actually, OLEDs using phosphorescent materials provide much better current efficiency (cd/A) than those using fluorescent materials. However, when the existing materials such as BAlq, CBP, etc. are used as a host of the phosphorescent material, there is no significant advantage in power efficiency (lm/W) over the OLEDs using fluorescent materials because of high driving voltage.
Further, the OLED devices do not have satisfactory operation life. Therefore, development of more stable, higherperformance host materials is required.
Accordingly, an object of the present invention is to provide an organic electroluminescent compound having luminescence efficiency and device operation life improved over existing host materials and having superior backbone with appropriate color coordinates in order to solve the aforesaid problems. Another object of the present invention is to provide a highly efficient and longlife organic electroluminescent device employing the organic electroluminescent compound as an electroluminescent material.
The present invention relates to organic electroluminescent compounds represented by Chemical Formula 1, and an organic electroluminescent device using the same. The organic electroluminescent compounds according to the present invention exhibit high luminous efficiency, excellent color purity and life property of the material, so that OLED's with very excellent operation life can be manufactured therefrom.
[Chemical Formula 1]
Figure PCTKR2010005092-appb-I000002
wherein
A1 through A19 independently represent CR1 or N, X represents -(CR2R3)l-, -N(R4)-, -S-, -O-, -Si(R5)(R6)-, -P(R7)-, -P(=O)(R8)- or -B(R9)-, and Ar1 represents (C6-C40)arylene with or without substituent(s) or (C3-C40)heteroarylene with or without substituent(s), except for the case where m is 0, and A15 through A19 are CR1 at the same time;
R1 through R9 independently represent hydrogen, deuterium, halogen, (C1-C30)alkyl with or without substituent(s), (C6-C30)aryl with or without substituent(s), substituted or unsubstituted (C6-C30)aryl fused with one or more (C3-C30)cycloalkyl(s) with or without substituent(s), (C3-C30)heteroaryl with or without substituent(s), 5- to 7-membered heterocycloalkyl with or without substituent(s), 5- to 7-membered heterocycloalkyl fused with one or more aromatic ring(s) with or without substituent(s), (C3-C30)cycloalkyl with or without substituent(s), (C3-C30)cycloalkyl fused with one or more aromatic ring(s) with or without substituent(s), cyano, trifluoromethyl, NR21R22, BR23R24, PR25R26, P(=O)R27R28, RaRbRcSi-, RdY-, ReC(=O)-, RfC(=O)O-, (C6-C30)ar(C1-C30)alkyl with or without substituent(s), (C2-C30)alkenyl with or without substituent(s), (C2-C30)alkynyl with or without substituent(s), carboxyl, nitro,
Figure PCTKR2010005092-appb-I000003
,
Figure PCTKR2010005092-appb-I000004
,or hydroxyl, or each of them may be linked to an adjacent substituent via (C3-C30)alkylene or (C3-C30)alkenylene with or without a fused ring to form an alicylic ring, a mono or polycyclic aromatic ring or a mono or polycyclic heteroaromatic ring;
W represents -(CR51R52)n-, -(R51)C=C(R52)-, -N(R53)-, -S-, -O-, -Si(R54)(R55)-, -P(R56)-, -P(=O)(R57)-, -C(=O)- or -B(R58)-, and R51 through R58 and R61 through R63 are the same as R1 through R9;
the heterocycloalkyl or heteroaryl may contain one or more heteroatom(s) selected from B, N, O, S, P(=O), Si and P;
R21 through R28 independently represent (C1-C30)alkyl with or without substituent(s), (C6-C30)aryl with or without substituent(s) or (C3-C30)heteroaryl with or without substituent(s), Ra, Rb, and Rc independently represent (C1-C30)alkyl with or without substituent(s) or (C6-C30)aryl with or without substituent(s), Y represents S or O, Rd represent (C1-C30)alkyl with or without substituent(s) or (C6-C30)aryl with or without substituent(s), Re represent (C1-C30)alkyl with or without substituent(s), (C1-C30)alkoxy with or without substituent(s), (C6-C30)aryl with or without substituent(s) or (C6-C30)aryloxy with or without substituent(s), Rf represent (C1-C30)alkyl with or without substituent(s), (C1-C30)alkoxy with or without substituent(s), (C6-C30)aryl with or without substituent(s) or (C6-C30)aryloxy with or without substituent(s);
m represents an integer 0 to 2; and
l and n represent an integer 1 or 2.
In the present invention, “alkyl”, “alkoxy” and other substituents containing “alkyl” moiety include both linear and branched species. In the present invention, “cycloalkyl” includes both adamantyl with or without substituent(s) and (C7-C30)bicycloalkyl with or without substituent(s).
In the present invention, “aryl” means an organic radical derived from an aromatic hydrocarbon by the removal of one hydrogen atom, and may include a 4- to 7-membered, particularly 5- or 6-membered, single ring or fused ring, including a plurality of aryls linked by chemical bond(s). Specific examples include phenyl, naphthyl, biphenyl, anthryl, indenyl, fluorenyl, phenanthryl, triphenylenyl, pyrenyl, perylenyl, chrysenyl, naphthacenyl, fluoranthenyl, etc., but are not limited thereto. “heteroaryl” means an aryl group containing 1 to 4 heteroatom(s) selected from B, N, O, S, P(=O), Si and P as aromatic ring backbone atom(s), other remaining aromatic ring backbone atoms being carbon. It may be 5- or 6-membered monocyclic heteroaryl or polycyclic heteroaryl resulting from condensation with a benzene ring, and may be partially saturated. Further, the heteroaryl includes more than one heteroaryls linked by chemical bond(s). The heteroaryl includes a divalent aryl group wherein the heteroatom(s) in the ring may be oxidized or quaternized to form, for example, an Noxide or a quaternary salt.
Specific examples include monocyclic heteroaryl such as furyl, thienyl, pyrrolyl, imidazolyl, pyrazolyl, thiazolyl, thiadiazolyl, isothiazolyl, isoxazolyl, oxazolyl, oxadiazolyl, triazinyl, tetrazinyl, triazolyl, tetrazolyl, furazanyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, etc., polycyclic heteroaryl such as benzofuryl, benzothienyl, isobenzofuryl, benzimidazolyl, benzothiazolyl, benzoisothiazolyl, benzoisoxazolyl, benzoxazolyl, isoindolyl, indolyl, indazolyl, benzothiadiazolyl, quinolyl, isoquinolyl, cinnolinyl, quinazolinyl, quinolizinyl, quinoxalinyl, carbazolyl, phenanthridinyl, benzodioxolyl, etc., an Noxide thereof (e.g., pyridyl Noxide, quinolyl Noxide, etc.), a quaternary salt thereof, etc., but are not limited thereto.
The “(C1-C30)alkyl” groups described herein may include (C1-C20)alkyl or (C1-C10)alkyl and the “(C6-C30)aryl” groups include (C6-C20)aryl or (C6-C12)aryl. The “(C3-C30)heteroaryl” groups include (C3-C20)heteroaryl or (C3-C12)heteroaryl and the “(C3-C30)cycloalkyl” groups include (C3-C20)cycloalkyl or (C3-C7)cycloalkyl. The “(C2-C30)alkenyl or alkynyl” group include (C2-C20)alkenyl or alkynyl, (C2-C10)alkenyl or alkynyl.
In “with or without substituent(s)”, the substituent is further substituted by one or more substituent(s) selected from the group consisting of deuterium, halogen, (C1-C30)alkyl with or without halogen substituent(s), (C6-C30)aryl, (C3-C30)heteroaryl with or without (C6-C30)aryl substituent(s), 5- to 7-membered heterocycloalkyl, 5- to 7-membered heterocycloalkyl fused with one or more aromatic ring(s), (C3-C30)cycloalkyl, (C3-C30)cycloalkyl fused with one or more aromatic ring(s), tri(C1-C30)alkylsilyl, di(C1-C30)alkyl(C6-C30)arylsilyl, tri(C6-C30)arylsilyl, (C2-C30)alkenyl, (C2-C30)alkynyl, cyano, carbazolyl, NR31R32, BR33R34, PR35R36, P(=O)R37R38, (C6-C30)ar(C1-C30)alkyl, (C1-C30)alkyl(C6-C30)aryl, (C1-C30)alkyloxy, (C1-C30)alkylthio, (C6-C30)aryloxy, (C6-C30)arylthio, (C1-C30)alkoxycarbonyl, (C1-C30)alkylcarbonyl, (C6-C30)arylcarbonyl, (C6-C30)aryloxycarbonyl, (C1-C30)alkoxycarbonyloxy, (C1-C30)alkylcarbonyloxy, (C6-C30)arylcarbonyloxy, (C6-C30)aryloxycarbonyloxy, carboxyl, nitro and hydroxyl, or is linked to an adjacent substituent to form a ring, wherein R31 through R38 independently represent (C1-C30)alkyl, (C6-C30)aryl or (C3-C30)heteroaryl.
The R1 through R9, R21 through R28, R51 through R58 and R61 through R63 are independently selected from hydrogen, deuterium, halogen, alkyl such as methyl, ethyl, propyl, butyl, pentyl, hexyl, ethylhexyl, heptyl, octyl, etc., aryl such as phenyl, naphthyl, fluorenyl, biphenyl, phenanthryl, terphenyl, pyrenyl, perylenyl, spirobifluorenyl, fluoranthenyl, chrysenyl, triphenylenyl, etc., aryl fused with one or more cycloalkyl such as 1,2-dihydroacenaphthyl, heteroaryl such as dibenzothiophenyl, dibenzofuryl, carbazolyl, pyridyl, furyl, thienyl, quinolyl, triazinyl, pyrimidinyl, pyridazinyl, quinoxalinyl, phenanthrolinyl, etc., heterocycloalkyl fused with one or more aromatic ring such as benzopyrrolidino, benzopiperidino, dibenzomorpholino, dibenzoazepino, etc., amino substituted by aryl such as phenyl, naphthyl, fluorenyl, biphenyl, phenanthryl, terphenyl, pyrenyl, perylenyl, spirobifluorenyl, fluoranthenyl, chrysenyl, triphenylenyl, etc. or heteroaryl such as dibenzothiophenyl, dibenzofuryl, carbazolyl, pyridyl, furyl, thienyl, quinolyl, triazinyl, pyrimidinyl, pyridazinyl, quinoxalinyl, phenanthrolinyl, etc., aryloxy such as biphenyloxy, etc., arylthio such as biphenylthio, etc., aralkyl such as biphenylmethyl, triphenylmethyl, etc.,
Figure PCTKR2010005092-appb-I000005
or
Figure PCTKR2010005092-appb-I000006
, but are not limited thereto, and may be further substituted as shown in Chemical Formula 1.
More specifically, the R1 through R9 may be exemplified as following structures but are not limited thereto.
Figure PCTKR2010005092-appb-I000007
Figure PCTKR2010005092-appb-I000008
Figure PCTKR2010005092-appb-I000009
wherein
R71 through R138 independently represent hydrogen, deuterium, halogen, (C1-C30)alkyl, (C6-C30)aryl, (C6-C30)aryl fused with one or more (C3-C30)cycloalkyl(s), (C3-C30)heteroaryl, 5- to 7-membered heterocycloalkyl, 5- to 7-membered heterocycloalkyl fused with one or more aromatic ring(s), (C3-C30)cycloalkyl, (C3-C30)cycloalkyl fused with one or more aromatic ring(s), cyano, amino, (C1-C30)alkylamino, (C6-C30)arylamino, NR41R42, BR43R44, PR45R46, P(=O)R47R48, tri(C1-C30)alkylsilyl, di(C1-C30)alkyl(C6-C30)arylsilyl, tri(C6-C30)arylsilyl, (C6-C30)ar(C1-C30)alkyl, (C1-C30)alkyloxy, (C1-C30)alkylthio, (C6-C30)aryloxy, (C6-C30)arylthio, (C1-C30)alkoxycarbonyl, (C1-C30)alkylcarbonyl, (C6-C30)arylcarbonyl, (C2-C30)alkenyl, (C2-C30)alkynyl, (C6-C30)aryloxycarbonyl, (C1-C30)alkoxycarbonyloxy, (C1-C30)alkylcarbonyloxy, (C6-C30)arylcarbonyloxy, (C6-C30)aryloxycarbonyloxy, carboxyl, nitro or hydroxyl, or each of them may be linked to an adjacent substituent via (C3-C30)alkylene or (C3-C30)alkenylene with or without a fused ring to form an alicylic ring or a mono or polycyclic aromatic ring, wherein R41 through R48 independently represent (C1-C30)alkyl, (C6-C30)aryl or (C3-C30)heteroaryl.
The
Figure PCTKR2010005092-appb-I000010
is exemplified as following structures but not limited thereto. m is the same as defined in Chemical Formula 1.
Figure PCTKR2010005092-appb-I000011
The organic electroluminescent compound according to the present invention may be specifically exemplified as following compounds but is not limited thereto.
Figure PCTKR2010005092-appb-I000012
Figure PCTKR2010005092-appb-I000013
Figure PCTKR2010005092-appb-I000014
Figure PCTKR2010005092-appb-I000015
Figure PCTKR2010005092-appb-I000016
Figure PCTKR2010005092-appb-I000017
Figure PCTKR2010005092-appb-I000018
Figure PCTKR2010005092-appb-I000019
Figure PCTKR2010005092-appb-I000020
Figure PCTKR2010005092-appb-I000021
The organic electroluminescent compound according to the present invention may be prepared as shown in following Reaction Scheme 1.
[Reaction Scheme 1]
Figure PCTKR2010005092-appb-I000022
wherein
A1 through A19, X, Ar1 and m are the same as defined in Chemical Formula 1.
Provided is an organic electroluminescent device, which comprises a first electrode; a second electrode; and one or more organic layer(s) interposed between the first electrode and the second electrode, wherein the organic layer comprises one or more organic electroluminescent compound(s) represented by Chemical Formula 1. The organic electroluminescent compound is used as a host material of the electroluminescent layer.
In addition, the organic layer may include the electroluminescent layer, and the electroluminescent layer may further include one or more dopants besides one or more organic electroluminescent compounds of Chemical Formula 1. The dopant applied to the organic electroluminescent device of the present invention is not specifically limited.
Preferably, the dopant applied to the organic electroluminescent device of the present invention is selected from following Chemical Formula 2.
[Chemical Formula 2]
M1L101L102L103
wherein
M1 is a metal selected from a group consisting of Group 7, Group 8, Group 9, Group 10, Group 11, Group 13, Group 14, Group 15 and Group 16 metals, and ligand L101, L102 and L103 are independently selected from the following structures;
Figure PCTKR2010005092-appb-I000023
Figure PCTKR2010005092-appb-I000024
Figure PCTKR2010005092-appb-I000025
Figure PCTKR2010005092-appb-I000026
wherein
R201 through R203 independently represent hydrogen, (C1-C30)alkyl with or without halogen substituent(s), (C6-C30)aryl with or without (C1-C30)alkyl substituent(s) or halogen;
R204 through R219 independently represent hydrogen, (C1-C30)alkyl with or without substituent(s), (C1-C30)alkoxy with or without substituent(s), (C3-C30)cycloalkyl with or without substituent(s), (C2-C30)alkenyl with or without substituent(s), (C6-C30)aryl with or without substituent(s), mono- or di-(C1-C30)alkylamino with or without substituent(s), mono- or di-(C6-C30)arylamino with or without substituent(s), SF5, tri(C1-C30)alkylsilyl with or without substituent(s), di(C1-C30)alkyl(C6-C30)arylsilyl with or without substituent(s), tri(C6-C30)arylsilyl with or without substituent(s), cyano or halogen;
R220 through R223 independently represent hydrogen, (C1-C30)alkyl with or without halogen substituent(s) or (C6-C30)aryl with or without (C1-C30)alkyl substituent(s);
R224 and R225 independently represent hydrogen, (C1-C30)alkyl with or without substituent(s), (C6-C30)aryl with or without substituent(s) or halogen, or R224 and R225 may be linked via (C3-C12)alkylene or (C3-C12)alkenylene with or without a fused ring to form an alicylic ring or a mono or polycyclic aromatic ring;
R226 represents (C1-C30)alkyl with or without substituent(s), (C6-C30)aryl with or without substituent(s), (C5-C30)heteroaryl with or without substituent(s) or halogen;
R227 through R229 independently represent hydrogen, (C1-C30)alkyl with or without substituent(s), (C6-C30)aryl with or without substituent(s) or halogen; and
Q represents
Figure PCTKR2010005092-appb-I000027
,
Figure PCTKR2010005092-appb-I000028
or
Figure PCTKR2010005092-appb-I000029
, wherein R231 through R242 independently represent hydrogen, (C1-C30)alkyl with or without halogen substituent(s), (C1-C30)alkoxy, halogen, (C6-C30)aryl with or without substituent(s), cyano or (C5-C30)cycloalkyl with or without substituent(s), or each of them may be linked to an adjacent substituent via alkylene or alkenylene to form a spiro ring or a fused ring, or may be linked to R207 or R208 via alkylene or alkenylene to form a saturated or unsaturated fused ring.
The meaning of the electroluminescent layer may be a single layer as a layer where the light is emitted or may be a multiple layer where two or more layers are laminated. In the configuration of the present invention, when hostdopant are used in mixture, it is confirmed that the luminous efficiency are remarkably improved by the electroluminescent host of the present invention. It may be configured at doping concentration of 0.5 to 10wt%. Compared to other host materials, the electroluminescent host of the present invention has superior conductivity with respect to the hole and electron and excellent stability in material, thereby showing a characteristic of remarkably increasing its life span as well as improving the luminous efficiency.
The M1 is selected from a group consisting of Ir, Pt, Pd, Rh, Re, Os, Tl, Pb, Bi, In, Sn, Sb, Te, Au and Ag. The dopant compounds of Chemical Formula 2 are exemplified by the compounds described in Korean Patent Application No. 10-2008-0112855, but are not limited thereto.
In the organic electronic device of the present invention, the organic layer may further include, in addition to the organic electroluminescent compound represented by Chemical Formula 1, one or more compound(s) selected from a group consisting of arylamine compounds and styrylarylamine compounds, at the same time. The arylamine compounds or styrylarylamine compounds are exemplified in Korean Patent Application No. 10-2008-0123276, 10-2008-0107606 or 10-2008-0118428, but are not limited thereto.
Further, in the organic electroluminescent device of the present invention, the organic layer may further include, in addition to the organic electroluminescent compound represented by Chemical Formula 1, one or more metal(s) selected from a group consisting of organic metals of Group 1, Group 2, 4th period and 5th period transition metals, lanthanide metals and dtransition elements or complex compound(s). The organic layer may include an electroluminescent layer and a charge generating layer.
Further, the organic layer may include, in addition to the organic electroluminescent compound of Chemical Formula 1, one or more organic electroluminescent layer(s) emitting blue, green or red light at the same time in order to embody a whiteemitting organic electroluminescent device. The compound emitting blue, green or red light may be exemplified by the compounds described in Korean Patent Application No. 10-2008-0123276, 10-2008-0107606 or 10-2008-0118428, but are not limited thereto.
In the organic electroluminescent device of the present invention, a layer (hereinafter referred to as “surface layer”) selected from a chalcogenide layer, a metal halide layer and a metal oxide layer may be placed on the inner surface of one or both electrode(s) among the pair of electrodes. More specifically, a metal chalcogenide (including oxide) layer of silicon or aluminum may be placed on the anode surface of the electroluminescent medium layer, and a metal halide layer or metal oxide layer may be placed on the cathode surface of the electroluminescent medium layer. Operation stability may be attained therefrom.
The chalcogenide may be, for example, SiOx (1 ≤ x ≤ 2), AlOx (1 ≤ x ≤ 1.5), SiON, SiAlON, etc. The metal halide may be, for example, LiF, MgF2, CaF2, a rare earth metal fluoride, etc. The metal oxide may be, for example, Cs2O, Li2O, MgO, SrO, BaO, CaO, etc.
In the organic electroluminescent device according to the present invention, it is also preferable to arrange on at least one surface of the pair of electrodes thus manufactured a mixed region of an electron transport compound and a reductive dopant, or a mixed region of a hole transport compound and an oxidative dopant. In that case, since the electron transport compound is reduced to an anion, injection and transport of electrons from the mixed region to an electroluminescent medium are facilitated. In addition, since the hole transport compound is oxidized to a cation, injection and transport of holes from the mixed region to an electroluminescent medium are facilitated. Preferable oxidative dopants include various Lewis acids and acceptor compounds. Preferable reductive dopants include alkali metals, alkali metal compounds, alkaline earth metals, rareearth metals, and mixtures thereof.
Further, a white-emitting electroluminescent device having two or more electroluminescent layers may be manufactured by employing a reductive dopant layer as a charge generating layer.
Since the organic electroluminescent compound according to the present invention exhibits good luminous efficiency and excellent life property, it may be used to manufacture OLED devices having very superior operation life.
The present invention is further described with respect to organic electroluminescent compounds according to the present invention, processes for preparing the same, and luminescence properties of devices employing the same. However, the following examples are provided for illustrative purposes only and they are not intended to limit the scope of the present invention.
[Preparation Example 1] Preparation of Compound 1
Figure PCTKR2010005092-appb-I000030
Preparation of Compound 1-1
9H-carbazole (10 g, 41.10 mmol), 2-chloropyridine (5.60 g, 49.32 mmol), Pd(OAc)2 (0.46 g), NaOt-bu (7.9 g, 82.20 mmol), toluene (100 mL), P(t-bu)3 (2 mL, 4.11 mmol, 50% in toluene) were added and stirred under reflux. 10 hours later, the mixture was cooled to room temperature and distilled water was added. Extracting with EA and drying with MgSO4, drying under reduce pressure was performed. Compound 1-1 (8.3 g, 33.98 mmol, 83%) was obtained via column separation.
Preparation of Compound 1-2
1-neck flask was filled with Compound 1-1 (8.3 g, 33.98 mmol), formed a vacuum and was filled with argon. After tetrahydrofuran (500 mL) was added, the mixture was stirred at 0℃ for 10 minutes. NBS (7.35 g, 40.78 mmol) was added thereto and stirred at room temperature for one day. Upon completion of the reaction, the product was extracted with distilled water and EA. After drying an organic layer with MgSO4 and removing solvent by a rotary type evaporator, Compound 1-2 (8.5 g, 26.30 mmol, 77%) was obtained via column chromatography using hexan and EA as developing solvent.
Preparation of Compound 1-3
The 1-neck flask was filled with Compound 1-2 (8.5 g, 26.30 mmol), formed a vacuum and was filled with argon. After tetrahydrofuran (500 mL) was added, the mixture was stirred at 78℃ for 10 minutes. n-BuLi(2.5M in hexane) (15.8 mL, 39.45 mmol) was added dropwise and stirred at -78℃ for 1 hour and a half. Trimethylborate (4.85 mL, 39.45 mmol) was added at -78℃. The mixture was stirred at -78℃ for 30 minutes and stirred at room temperature for 4 hours. Upon completion of the reaction, the product was extracted with distilled water and EA. After drying an organic layer with MgSO4 and removing solvent by a rotary type evaporator, Compound 1-3 (5.2 g, 18.05 mmol, 68.6%) was obtained via column chromatography using hexan and EA as developing solvent.
Preparation of Compound 1
Compound 1-3 (5.0 g, 17.4 mmol), 2-bromodibenzo[b,d]furan (5.2 g, 20.88 mmol), Pd(PPh3)4 (0.8 g, 0.7 mmol), 2M K2CO3 aqueous solution (20 mL), toluene (100 mL), and ethanol (50 mL) were added and stirred under reflux for 12 hours. After washing with distilled water, extracting with EA, and drying with MgSO4, distillation under reduced pressure followed by column separation yielded Compound 1 (4.3 g, 10.48 mmol, 60 %).
[Preparation Example 2] Preparation of Compound 49
Figure PCTKR2010005092-appb-I000031
Preparation of Compound 2-1
2,4,6-trichloropyrimidine (10 g, 54.51 mmol), phenylboronic acid (16.6 g, 136,29 mmol), Pd(PPh3)4 (3.15 g, 2.72 mmol), 2M K2CO3 (50 mL), toluene (100 mL), and ethanol (30 mL) were added and stirred under reflux. 4 hours later, the mixture was cooled to room temperature and distilled water was added thereto. After extracting with EA and drying with MgSO4, distillation under reduced pressure followed by column separation yielded Compound 2-1 (7 g, 26.24 mmol, 48.14%).
Preparation of Compound 2-2
NaH (1.57 g, 39.36 mmol, 60% in mineral oil) was mixed with DMF (70 mL) and Compound 2-1 (7 g, 26.24 mmol) was dissolved in DMF (60 mL). 1 hour later, Compound 9H-carbazole was dissolved in DMF (70 mL). The mixture was stirred for 10 hours. After adding distilled water, extracting with EA, and drying with MgSO4, distillation under reduced pressure followed by column separation yielded Compound 2-2 (7 g, 14.78 mmol, 56.33%).
Preparation of Compound 2-3
Compound 2-3 (5.7 g, 11.97 mmol, 80.9%) was obtained by combining Compound 2-2 (7 g, 14.78 mmol) in Preparation Example 1 according to the same method as the preparation of Compound 1-2.
Preparation of Compound 2-4
Compound 2-4 (3.4 g, 7.70 mmol, 64.4%) was obtained by combining Compound 2-3 (5.7 g, 11.97 mmol) in Preparation Example 1 according to the same method as the preparation of Compound 1-3.
Preparation of Compound 49
Compound 49 (3.2 g, 5.52 mmol, 72%) was obtained by using Compound 2-4 (3.4 g, 7.70 mmol) and 2-bromodibenzo[b,d]thiophene in Preparation Example 1 according to the same method as the preparation of Compound 1.
[Preparation Example 3] Preparation of Compound 51
Figure PCTKR2010005092-appb-I000032
Preparation of Compound 3-1
Compound 3-1 (13.2 g, 47.7 mmol, 87.5%) was obtained by combining 2,4,6-trichlorotriazine (10 g, 54.51 mmol) in Preparation Example 2 according to the same method as the preparation of Compound 2-1.
Preparation of Compound 3-2
Compound 3-2(14.5 g, 36.39 mmol, 76.3%) was obtained by combining Compound 3-1 (13.2 g, 47.7 mmol) in Preparation Example 2 according to the same method as the preparation of Compound 2-2.
Preparation of Compound 3-3
Compound 3-3 (14.6 g, 30.59 mmol, 84%) was obtained by combining Compound 3-2 (14.5 g, 36.39 mmol) in Preparation Example 2 according to the same method as the preparation of Compound 2-3.
Preparation of Compound 3-4
Compound 3-4 (7.2 g, 16.28 mmol, 53.2%) was obtained by combining Compound 3-3 (14.6 g, 30.59 mmol) in Preparation Example 2 according to the same method as the preparation of Compound 2-4.
Preparation of Compound 51
Compound 51 (5.1 g, 8.63 mmol, 53%) was obtained by using Compound 3-4 (7.2 g, 16.28 mmol) and 2-bromo-9,9-dimethyl-9H-fluorene in Preparation Example 2 according to the same method as the preparation of Compound 49.
[Preparation Example 4] Preparation of Compound 62
Figure PCTKR2010005092-appb-I000033
Figure PCTKR2010005092-appb-I000034
Preparation of Compound 4-1
1,3-dibromobenzene (28 g, 0.119 mol) was dissolved in THF (600 mL) and n-BuLi (47.5 mL) was slowly added dropwise at -78oC. After reacting and stirring for 1 hour, Compound 3-1 (47.5 mL) was slowly added dropwise and slowly heated. The mixture was stirred at room temperature for 5 hours. Upon completion of the reaction, the product was extracted with EA and distilled water. Compound 4-1 (15.7 g, 40.43 mmol, 40.4%) was obtained via column separation.
Preparation of Compound 4-2
Compound 4-2 (12.5 g, 26.34 mmol, 65.2%) was obtained by combining Compound 4-1 (15.7 g, 40.43 mmol) in Preparation Example 1 according to the same method as the preparation of Compound 1-1.
Preparation of Compound 4-3
Compound 4-3 (9.8 g, 17.71 mmol, 67.3%) was obtained by combining Compound 4-2 (12.5 g, 26.34 mmol) in Preparation Example 1 according to the same method as the preparation of Compound 1-2.
Preparation of Compound 4-4
9H-carbazole (70 g, 0.42 mmol), Iodobenzene (46 mL), cooper (40 g), potassiumcarbonate (174 g), 18-crown-6 (9 g), and 1,2-Dichlorobenzene (2 L) were added and stirred under reflux for 12 hours. Upon completion of the reaction, the product was extracted with EA and dried with MgSO4. Distillation under reduced pressure followed by column separation yielded Compound 4-4 (63.4 g, 260.58 mmol, 62%).
Preparation of Compound 4-5
Compound 4-5 (52.4 g, 162.63 mmol, 62.4%) was obtained by combining Compound 4-4 (63.4 g, 260.58 mmol) in Preparation Example 1 according to the same method as the preparation of Compound 1-2.
Preparation of Compound 4-6
Compound 4-6 (20.3 g, 70.70 mmol, 43%) was obtained by combining Compound 4-5 (52.4 g, 162.63 mmol) in Preparation Example 1 according to the same method as the preparation of Compound 1-3.
Preparation of Compound 62
Compound 62 (5.7 g, 7.96 mmol, 50%) was obtained by using Compound 4-3 (9.8 g, 17.71 mmol) and Compound 4-6 in Preparation Example 1 according to the same method as the preparation of Compound 1.
Organic electroluminescent Compounds 1 to 68 were prepared according to Preparation Examples 1 to 4 and Table 1 shows 1H NMR and MS/FAB of the prepared organic electroluminescent compounds.
[Table 1]
Figure PCTKR2010005092-appb-I000035
Figure PCTKR2010005092-appb-I000036
Figure PCTKR2010005092-appb-I000037
Figure PCTKR2010005092-appb-I000038
Figure PCTKR2010005092-appb-I000039
[Example 1] Manufacture of OLED device using the organic electroluminescent compound according to the present invention
An OLED device was manufactured using the electroluminescent material according to the present invention. First, a transparent electrode ITO thin film (15 Ω/□) obtained from a glass for OLED (produced by Samsung Corning) was subjected to ultrasonic washing with trichloroethylene, acetone, ethanol and distilled water, sequentially, and stored in isopropanol before use.
Then, an ITO substrate was equipped in a substrate folder of a vacuum vapor deposition apparatus, and 4,4',4"-tris(N,N-(2-naphthyl)-phenylamino)triphenylamine (2-TNATA) was placed in a cell of the vacuum vapor deposition apparatus, which was then ventilated up to 10-6 torr of vacuum in the chamber. Then, electric current was applied to the cell to evaporate 2-TNATA, thereby forming a hole injection layer having a thickness of 60 nm on the ITO substrate.
Then, N,N'-bis(α-naphthyl)-N,N'-diphenyl-4,4'-diamine (NPB) was placed in another cell of the vacuum vapor deposition apparatus, and electric current was applied to the cell to evaporate NPB, thereby forming a hole transport layer having a thickness of 20 nm on the hole injection layer.
After forming the hole injection layer and the hole transport layer, an electroluminescent layer was formed thereon as follows. Compound 49 was placed in a cell of a vacuum vapor deposition apparatus as host, and Ir(ppy)3[tris(2-phenylpyridine)iridium] was placed in another cell as a dopant. The two materials were evaporated at different rates such that an electroluminescent layer having a thickness of 30 nm was vapordeposited on the hole transport layer at 4 to 10 wt%.
Subsequently, tris(8-hydroxyquinoline)-aluminum(III) (Alq) was vapor-deposited with a thickness of 20 nm as an electron transport layer. Then, after vapor-depositing lithium quinolate (Liq) of a following structure with a thickness of 1 to 2 nm as an electron injection layer, an Al cathode having a thickness of 150 nm was formed using another vacuum vapor deposition apparatus to manufacture an OLED. Each compound used in the OLED was purified by vacuum sublimation at 10-6 torr.
[Example 2] Manufacture of OLED device using the organic electroluminescent compounds of the present invention
An OLED was manufactured as in Example 1 except that Compound 23 according to the present invention is used as host material on the electroluminescent layer and an organic iridium complex (piq)2Ir(acac)[bis-(1-phenylisoquinolyl)iridium(III)acetylacetonate] is used as electroluminescent dopant.
[Comparative Examples 1 and 2] Electroluminescent properties of the OLED device using conventional electroluminescent material
An OLED device was manufactured in the same manner as Examples 1 and 3 except that 4,4'-Bis(carbazol-9-yl)-biphenyl (CBP) instead of the compounds of the present invention was used as host material in a cell of the vacuum vapor deposition apparatus.
Luminous efficiency of the OLED devices including the organic electroluminescent compound according to the present invention manufactured in Examples 1 to 2 and Comparative Examples 1 and 2 and the conventional electroluminescent compound was measured at 1,000 cd/m2. The result is given in Table 2.
[Table 2]
Figure PCTKR2010005092-appb-I000040
As shown in Table 2, the organic electroluminescent compounds according to the present invention have excellent properties compared with the conventional material. In addition, the device using the organic electroluminescent compound according to the present invention as host material for emitting red or green light has excellent electroluminescent properties and drops driving voltage, thereby increasing power efficiency and improving power consumption.

Claims (10)

  1. An organic electroluminescent compound represented by Chemical Formula 1:
    [Chemical Formula 1]
    Figure PCTKR2010005092-appb-I000041
    wherein
    A1 through A19 independently represent CR1 or N, X represents -(CR2R3)l-, -N(R4)-, -S-, -O-, -Si(R5)(R6)-, -P(R7)-, -P(=O)(R8)- or -B(R9)-, and Ar1 represents (C6-C40)arylene with or without substituent(s) or (C3-C40)heteroarylene with or without substituent(s), except for the case where m is 0, and A15 through A19 are CR1 at the same time;
    R1 through R9 independently represent hydrogen, deuterium, halogen, (C1-C30)alkyl with or without substituent(s), (C6-C30)aryl with or without substituent(s), substituted or unsubstituted (C6-C30)aryl fused with one or more (C3-C30)cycloalkyl(s) with or without substituent(s), (C3-C30)heteroaryl with or without substituent(s), 5- to 7-membered heterocycloalkyl with or without substituent(s), 5- to 7-membered heterocycloalkyl fused with one or more aromatic ring(s) with or without substituent(s), (C3-C30)cycloalkyl with or without substituent(s), (C3-C30)cycloalkyl fused with one or more aromatic ring(s) with or without substituent(s), cyano, trifluoromethyl, NR21R22, BR23R24, PR25R26, P(=O)R27R28, RaRbRcSi-, RdY-, ReC(=O)-, RfC(=O)O-, (C6-C30)ar(C1-C30)alkyl with or without substituent(s), (C2-C30)alkenyl with or without substituent(s), (C2-C30)alkynyl with or without substituent(s), carboxyl, nitro,
    Figure PCTKR2010005092-appb-I000042
    ,
    Figure PCTKR2010005092-appb-I000043
    , or hydroxyl, or each of them may be linked to an adjacent substituent via (C3-C30)alkylene or (C3-C30)alkenylene with or without a fused ring to form an alicylic ring, a mono or polycyclic aromatic ring or a mono or polycyclic heteroaromatic ring;
    W represents -(CR51R52)n-, -(R51)C=C(R52)-, -N(R53)-, -S-, -O-, -Si(R54)(R55)-, -P(R56)-, -P(=O)(R57)-, -C(=O)- or -B(R58)-, and R51 through R58 and R61 through R63 are the same as R1 through R9;
    the heterocycloalkyl or heteroaryl may contain one or more heteroatom(s) selected from B, N, O, S, P(=O), Si and P;
    R21 through R28 independently represent (C1-C30)alkyl with or without substituent(s), (C6-C30)aryl with or without substituent(s) or (C3-C30)heteroaryl with or without substituent(s), Ra, Rb, and Rc independently represent (C1-C30)alkyl with or without substituent(s) or (C6-C30)aryl with or without substituent(s), Y represents S or O, Rd represent (C1-C30)alkyl with or without substituent(s) or (C6-C30)aryl with or without substituent(s), Re represent (C1-C30)alkyl with or without substituent(s), (C1-C30)alkoxy with or without substituent(s), (C6-C30)aryl with or without substituent(s) or (C6-C30)aryloxy with or without substituent(s), Rf represent (C1-C30)alkyl with or without substituent(s), (C1-C30)alkoxy with or without substituent(s), (C6-C30)aryl with or without substituent(s) or (C6-C30)aryloxy with or without substituent(s);
    m represents an integer 0 to 2; and
    l and n represent an integer 1 or 2.
  2. The organic electroluminescent compound according to claim 1, wherein the substituent of R1 through R9, R21 through R28, R51 through R58 and R61 through R63 is further substituted by one or more substituent(s) selected from a group consisting of deuterium, halogen, (C1-C30)alkyl with or without halogen substituent(s), (C6-C30)aryl, (C3-C30)heteroaryl with or without (C6-C30)aryl substituent(s), 5- to 7-membered heterocycloalkyl, 5- to 7-membered heterocycloalkyl fused with one or more aromatic ring(s), (C3-C30)cycloalkyl, (C3-C30)cycloalkyl fused with one or more aromatic ring(s), tri(C1-C30)alkylsilyl, di(C1-C30)alkyl(C6-C30)arylsilyl, tri(C6-C30)arylsilyl, adamantyl, (C7-C30)bicycloalkyl, (C2-C30)alkenyl, (C2-C30)alkynyl, cyano, carbazolyl, NR31R32, BR33R34, PR35R36, P(=O)R37R38, (C6-C30)ar(C1-C30)alkyl, (C1-C30)alkyl(C6-C30)aryl, (C1-C30)alkyloxy, (C1-C30)alkylthio, (C6-C30)aryloxy, (C6-C30)arylthio, (C1-C30)alkoxycarbonyl, (C1-C30)alkylcarbonyl, (C6-C30)arylcarbonyl, (C6-C30)aryloxycarbonyl, (C1-C30)alkoxycarbonyloxy, (C1-C30)alkylcarbonyloxy, (C6-C30)arylcarbonyloxy, (C6-C30)aryloxycarbonyloxy, carboxyl, nitro and hydroxyl, or is linked to an adjacent substituent to form a ring, wherein R31 through R38 independently represent (C1-C30)alkyl, (C6-C30)aryl or (C3-C30)heteroaryl.
  3. The organic electroluminescent compound according to claim 1, wherein R1 through R9 are selected from the following structures:
    Figure PCTKR2010005092-appb-I000044
    Figure PCTKR2010005092-appb-I000045
    Figure PCTKR2010005092-appb-I000046
    wherein
    R71 through R138 independently represent hydrogen, deuterium, halogen, (C1-C30)alkyl, (C6-C30)aryl, (C6-C30)aryl fused with one or more (C3-C30)cycloalkyl(s), (C3-C30)heteroaryl, 5- to 7-membered heterocycloalkyl, 5- to 7-membered heterocycloalkyl fused with one or more aromatic ring(s), (C3-C30)cycloalkyl, (C3-C30)cycloalkyl fused with one or more aromatic ring(s), cyano, amino, (C1-C30)alkylamino, (C6-C30)arylamino, NR41R42, BR43R44, PR45R46, P(=O)R47R48, tri(C1-C30)alkylsilyl, di(C1-C30)alkyl(C6-C30)arylsilyl, tri(C6-C30)arylsilyl, (C6-C30)ar(C1-C30)alkyl, (C1-C30)alkyloxy, (C1-C30)alkylthio, (C6-C30)aryloxy, (C6-C30)arylthio, (C1-C30)alkoxycarbonyl, (C1-C30)alkylcarbonyl, (C6-C30)arylcarbonyl, (C2-C30)alkenyl, (C2-C30)alkynyl, (C6-C30)aryloxycarbonyl, (C1-C30)alkoxycarbonyloxy, (C1-C30)alkylcarbonyloxy, (C6-C30)arylcarbonyloxy, (C6-C30)aryloxycarbonyloxy, carboxyl, nitro or hydroxyl, or each of them may be linked to an adjacent substituent via (C3-C30)alkylene or (C3-C30)alkenylene with or without a fused ring to form an alicylic ring or a mono or polycyclic aromatic ring, wherein R41 through R48 independently represent (C1-C30)alkyl, (C6-C30)aryl or (C3-C30)heteroaryl.
  4. The organic electroluminescent compound according to claim 1, wherein
    Figure PCTKR2010005092-appb-I000047
    is selected from the following structures:
    Figure PCTKR2010005092-appb-I000048
  5. The organic electroluminescent compound according to claim 1, which is selected from the following structures:
    Figure PCTKR2010005092-appb-I000049
    Figure PCTKR2010005092-appb-I000050
    Figure PCTKR2010005092-appb-I000051
    Figure PCTKR2010005092-appb-I000052
    Figure PCTKR2010005092-appb-I000053
    Figure PCTKR2010005092-appb-I000054
    Figure PCTKR2010005092-appb-I000055
    Figure PCTKR2010005092-appb-I000056
    Figure PCTKR2010005092-appb-I000057
    Figure PCTKR2010005092-appb-I000058
  6. An organic electroluminescent device comprising the organic electroluminescent compound according any of claims 1 to 5.
  7. The organic electroluminescent device according to claim 6, which comprises a first electrode; a second electrode; and one or more organic layer(s) interposed between the first electrode and the second electrode, wherein the organic layer comprises one or more organic electroluminescent compound(s) according to any of claims 1 to 5 and one or more dopant(s) represented by Chemical Formula 2:
    [Chemical Formula 2]
    M1L101L102L103
    wherein
    M1 is a metal selected from a group consisting of Group 7, Group 8, Group 9, Group 10, Group 11, Group 13, Group 14, Group 15 and Group 16 metals, and ligand L101, L102 and L103 are independently selected from the following structures:
    Figure PCTKR2010005092-appb-I000059
    Figure PCTKR2010005092-appb-I000060
    Figure PCTKR2010005092-appb-I000061
    Figure PCTKR2010005092-appb-I000062
    wherein
    R201 through R203 independently represent hydrogen, (C1-C30)alkyl with or without halogen substituent(s), (C6-C30)aryl with or without (C1-C30)alkyl substituent(s) or halogen;
    R204 through R219 independently represent hydrogen, (C1-C30)alkyl with or without substituent(s), (C1-C30)alkoxy with or without substituent(s), (C3-C30)cycloalkyl with or without substituent(s), (C2-C30)alkenyl with or without substituent(s), (C6-C30)aryl with or without substituent(s), mono- or di-(C1-C30)alkylamino with or without substituent(s), mono- or di-(C6-C30)arylamino with or without substituent(s), SF5, tri(C1-C30)alkylsilyl with or without substituent(s), di(C1-C30)alkyl(C6-C30)arylsilyl with or without substituent(s), tri(C6-C30)arylsilyl with or without substituent(s), cyano or halogen;
    R220 through R223 independently represent hydrogen, (C1-C30)alkyl with or without halogen substituent(s) or (C6-C30)aryl with or without (C1-C30)alkyl substituent(s);
    R224 and R225 independently represent hydrogen, (C1-C30)alkyl with or without substituent(s), (C6-C30)aryl with or without substituent(s) or halogen, or R224 and R225 may be linked via (C3-C12)alkylene or (C3-C12)alkenylene with or without a fused ring to form an alicylic ring or a mono or polycyclic aromatic ring;
    R226 represents (C1-C30)alkyl with or without substituent(s), (C6-C30)aryl with or without substituent(s), (C5-C30)heteroaryl with or without substituent(s) or halogen;
    R227 through R229 independently represent hydrogen, (C1-C30)alkyl with or without substituent(s), (C6-C30)aryl with or without substituent(s) or halogen; and
    Q represents
    Figure PCTKR2010005092-appb-I000063
    ,
    Figure PCTKR2010005092-appb-I000064
    or
    Figure PCTKR2010005092-appb-I000065
    , wherein R231 through R242 independently represent hydrogen, (C1-C30)alkyl with or without halogen substituent(s), (C1-C30)alkoxy, halogen, (C6-C30)aryl with or without substituent(s), cyano or (C5-C30)cycloalkyl with or without substituent(s), or each of them may be linked to an adjacent substituent via alkylene or alkenylene to form a spiro ring or a fused ring, or may be linked to R207 or R208 via alkylene or alkenylene to form a saturated or unsaturated fused ring.
  8. The organic electroluminescent device according to claim 7, wherein the organic layer further comprises one or more amine compound(s) selected from a group consisting of arylamine compounds and styrylarylamine compounds, or one or more metal(s) selected from a group consisting of organic metals of Group 1, Group 2, 4th period and 5th period transition metals, lanthanide metals and dtransition elements or complex compound(s).
  9. The organic electroluminescent device according to claim 7, wherein the organic layer comprises an electroluminescent layer and a charge generating layer.
  10. The organic electroluminescent device according to claim 7, which is a white lightemitting organic electroluminescent device wherein the organic layer comprises one or more organic compound layer(s) emitting red, green or blue light at the same time.
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