JP4717703B2 - 化合物および有機el素子 - Google Patents
化合物および有機el素子 Download PDFInfo
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- JP4717703B2 JP4717703B2 JP2006120806A JP2006120806A JP4717703B2 JP 4717703 B2 JP4717703 B2 JP 4717703B2 JP 2006120806 A JP2006120806 A JP 2006120806A JP 2006120806 A JP2006120806 A JP 2006120806A JP 4717703 B2 JP4717703 B2 JP 4717703B2
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- 150000001875 compounds Chemical class 0.000 title claims description 36
- 150000002894 organic compounds Chemical group 0.000 claims description 22
- 125000000217 alkyl group Chemical group 0.000 claims description 16
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 11
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 11
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- 239000010410 layer Substances 0.000 description 58
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 30
- 125000001424 substituent group Chemical group 0.000 description 22
- 239000000463 material Substances 0.000 description 11
- 238000000034 method Methods 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- 125000000623 heterocyclic group Chemical group 0.000 description 8
- 230000005525 hole transport Effects 0.000 description 8
- -1 aluminum quinolinol Chemical compound 0.000 description 7
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- 125000003118 aryl group Chemical group 0.000 description 6
- GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthene Chemical compound C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 description 6
- 125000005843 halogen group Chemical group 0.000 description 6
- 239000012044 organic layer Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 4
- 125000003277 amino group Chemical group 0.000 description 4
- 230000000903 blocking effect Effects 0.000 description 4
- 239000013078 crystal Substances 0.000 description 4
- 230000006866 deterioration Effects 0.000 description 4
- 238000002347 injection Methods 0.000 description 4
- 239000007924 injection Substances 0.000 description 4
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000010408 film Substances 0.000 description 3
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 101100030361 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) pph-3 gene Proteins 0.000 description 2
- 235000002597 Solanum melongena Nutrition 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 125000000732 arylene group Chemical group 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 229920000547 conjugated polymer Polymers 0.000 description 2
- 230000021615 conjugation Effects 0.000 description 2
- 238000005401 electroluminescence Methods 0.000 description 2
- 230000005284 excitation Effects 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 125000001153 fluoro group Chemical group F* 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229920000553 poly(phenylenevinylene) Polymers 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 238000001771 vacuum deposition Methods 0.000 description 2
- 238000001291 vacuum drying Methods 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 229910001316 Ag alloy Inorganic materials 0.000 description 1
- 229940126062 Compound A Drugs 0.000 description 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- ZEEBGORNQSEQBE-UHFFFAOYSA-N [2-(3-phenylphenoxy)-6-(trifluoromethyl)pyridin-4-yl]methanamine Chemical compound C1(=CC(=CC=C1)OC1=NC(=CC(=C1)CN)C(F)(F)F)C1=CC=CC=C1 ZEEBGORNQSEQBE-UHFFFAOYSA-N 0.000 description 1
- ABRVLXLNVJHDRQ-UHFFFAOYSA-N [2-pyridin-3-yl-6-(trifluoromethyl)pyridin-4-yl]methanamine Chemical compound FC(C1=CC(=CC(=N1)C=1C=NC=CC=1)CN)(F)F ABRVLXLNVJHDRQ-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 230000009849 deactivation Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000007850 fluorescent dye Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000005283 ground state Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000004020 luminiscence type Methods 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- SJCKRGFTWFGHGZ-UHFFFAOYSA-N magnesium silver Chemical compound [Mg].[Ag] SJCKRGFTWFGHGZ-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000001840 matrix-assisted laser desorption--ionisation time-of-flight mass spectrometry Methods 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- DCZNSJVFOQPSRV-UHFFFAOYSA-N n,n-diphenyl-4-[4-(n-phenylanilino)phenyl]aniline Chemical class C1=CC=CC=C1N(C=1C=CC(=CC=1)C=1C=CC(=CC=1)N(C=1C=CC=CC=1)C=1C=CC=CC=1)C1=CC=CC=C1 DCZNSJVFOQPSRV-UHFFFAOYSA-N 0.000 description 1
- IBHBKWKFFTZAHE-UHFFFAOYSA-N n-[4-[4-(n-naphthalen-1-ylanilino)phenyl]phenyl]-n-phenylnaphthalen-1-amine Chemical compound C1=CC=CC=C1N(C=1C2=CC=CC=C2C=CC=1)C1=CC=C(C=2C=CC(=CC=2)N(C=2C=CC=CC=2)C=2C3=CC=CC=C3C=CC=2)C=C1 IBHBKWKFFTZAHE-UHFFFAOYSA-N 0.000 description 1
- 150000004866 oxadiazoles Chemical class 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 238000006862 quantum yield reaction Methods 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 238000005215 recombination Methods 0.000 description 1
- 230000006798 recombination Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 238000009751 slip forming Methods 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000001269 time-of-flight mass spectrometry Methods 0.000 description 1
- 125000006617 triphenylamine group Chemical group 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C4/00—Preparation of hydrocarbons from hydrocarbons containing a larger number of carbon atoms
- C07C4/26—Preparation of hydrocarbons from hydrocarbons containing a larger number of carbon atoms by splitting polyaryl compounds at a bond between uncondensed six-membered aromatic rings, e.g. biphenyl to benzene
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C13/00—Cyclic hydrocarbons containing rings other than, or in addition to, six-membered aromatic rings
- C07C13/28—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof
- C07C13/32—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings
- C07C13/62—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings with more than three condensed rings
- C07C13/66—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings with more than three condensed rings the condensed ring system contains only four rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C15/00—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts
- C07C15/12—Polycyclic non-condensed hydrocarbons
- C07C15/14—Polycyclic non-condensed hydrocarbons all phenyl groups being directly linked
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C15/00—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts
- C07C15/12—Polycyclic non-condensed hydrocarbons
- C07C15/16—Polycyclic non-condensed hydrocarbons containing at least two phenyl groups linked by one single acyclic carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/01—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms
- C07C211/02—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C211/14—Amines containing amino groups bound to at least two aminoalkyl groups, e.g. diethylenetriamines
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B33/00—Electroluminescent light sources
- H05B33/12—Light sources with substantially two-dimensional radiating surfaces
- H05B33/14—Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of the electroluminescent material, or by the simultaneous addition of the electroluminescent material in or onto the light source
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
- H10K50/12—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers comprising dopants
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/80—Constructional details
- H10K50/805—Electrodes
- H10K50/81—Anodes
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
- H10K85/622—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene containing four rings, e.g. pyrene
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/02—Ortho- or ortho- and peri-condensed systems
- C07C2603/40—Ortho- or ortho- and peri-condensed systems containing four condensed rings
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
- C09K2211/1007—Non-condensed systems
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- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
- C09K2211/1011—Condensed systems
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/917—Electroluminescent
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/26—Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension
- Y10T428/263—Coating layer not in excess of 5 mils thick or equivalent
- Y10T428/264—Up to 3 mils
- Y10T428/265—1 mil or less
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
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- Spectroscopy & Molecular Physics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Electroluminescent Light Sources (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
このように有機発光素子における最近の進歩は著しく、その特徴は低印加電圧で高輝度、発光波長の多様性、高速応答性、薄型、軽量の発光デバイス化が可能であることから、広汎な用途への可能性を示唆している。
下記一般式(1)で示されることを特徴とする化合物を提供する。
R3乃至R5はそれぞれ独立して水素原子である。
R6は水素原子あるいは炭素原子数1から5の直鎖状または分岐状のアルキル基を有するフェニル基のいずれかである。]
下記一般式(2)で示されることを特徴とする上記(1)に記載の化合物を提供する。
R9乃至R11はいずれも水素原子である。]
一対の電極間に、少なくとも一層の有機化合物を含む層からなる有機EL素子において、前記少なくとも一層の有機化合物を含む層は一般式(1)乃至(2)のいずれかの有機化合物を含む層であることを特徴とする有機EL素子。
前記層が発光層であることを特徴とする有機EL素子を提供する。
前記発光層が少なくともホストとゲストからなり、前記ホストが前記有機化合物であることを特徴とする有機EL素子を提供する。
前記発光層が少なくともホストとゲストからなり、ゲストが前記有機化合物であることを特徴とする有機EL素子を提供する。
前記発光層が少なくともホストとゲストからなり、前記ホストおよび前記ゲストが共に夫々独立に前記有機化合物である特徴とする有機EL素子を提供する。
前記ゲストからの発光が蛍光発光であることを特徴とする有機EL素子を提供する。
下記一般式(5)で示されることを特徴とする化合物である。
または、下記一般式(6)で示されることを特徴とする上記(5)の一般式に記載の化合物である。
または、下記一般式(7)で示されることを特徴とする一般式(5)に記載の化合物である。
一対の電極間に、少なくとも一層の有機化合物を含む層からなる有機EL素子(有機エレクトロルミネッセンス素子)において、前記有機化合物を含む層を有することを特徴とする有機EL素子である。
前記有機化合物を含む層は発光層であることを特徴とする有機EL素子である。
前記有機化合物を含む層は発光層であり、発光層が少なくともホストとゲストの化合物からなる有機エレクトロルミネッセンス素子においてホストとゲストの少なくとも一方が、上記有機化合物であることを特徴とする有機EL素子である。
ゲストからの発光が蛍光発光であることを特徴とする有機EL素子である。
1.発光層内での電子・ホールの輸送
2.ホストの励起子生成
3.ホスト分子間の励起エネルギー伝達
4.ホストからゲストへの励起エネルギー移動
それぞれの過程における所望のエネルギー移動や、発光はさまざまな失活過程と競争でおこる。
トルエン中での発光特性を図2においてグラフで示す。
本実施例では、素子構成として、図1に示す有機層が3層の素子を使用した。ガラス基板上に100nmのITOをパターニングした。そのITO基板上に、以下の有機層と電極層を10−5Paの真空チャンバー内で抵抗加熱による真空蒸着して連続製膜し、対向する電極面積が3mm2になるようにした。
素子A
ホール輸送層(20nm):化合物A
発光層(25nm):例示化合物No.F−28(重量比5%):化合物B
電子輸送層(40nm):Bphen
金属電極層1(1nm):KF
金属電極層2(100nm):Al
Claims (8)
- 下記一般式(1)で示されることを特徴とする化合物。
[R1、R2は同じで、炭素原子数1から5の直鎖状または分岐状のアルキル基、フェニル基のいずれかである。
R3乃至R5はそれぞれ独立して水素原子である。
R6は水素原子あるいは炭素原子数1から5の直鎖状または分岐状のアルキル基を有するフェニル基のいずれかである。] - 下記一般式(2)で示されることを特徴とする請求項1に記載の化合物。
[R7、R8は同じで、炭素原子数1から5の直鎖状または分岐状のアルキル基のいずれかである。
R9乃至R11はいずれも水素原子である。] - 一対の電極間に、少なくとも一層の有機化合物を含む層からなる有機EL素子において、前記少なくとも一層の有機化合物を含む層は、請求項1乃至2の何れか1項に記載の有機化合物を含む層であることを特徴とする有機EL素子。
- 請求項3記載の前記層が発光層であることを特徴とする有機EL素子。
- 前記発光層が少なくともホストとゲストからなり、前記ホストが前記有機化合物であることを特徴とする請求項4に記載の有機EL素子。
- 前記発光層が少なくともホストとゲストからなり、該ゲストが前記有機化合物であることを特徴とする請求項4に記載の有機EL素子。
- 前記発光層が少なくともホストとゲストからなり、前記ホストおよび前記ゲストが共に夫々独立に前記有機化合物である特徴とする請求項4に記載の有機EL素子。
- 前記ゲストからの発光が蛍光発光であることを特徴とする請求項5乃至7のいずれか1項に記載の有機EL素子。
Priority Applications (5)
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JP2006120806A JP4717703B2 (ja) | 2006-04-25 | 2006-04-25 | 化合物および有機el素子 |
PCT/JP2007/059000 WO2007125976A1 (en) | 2006-04-25 | 2007-04-19 | Compound and organic el device |
CNA2007800147860A CN101432250A (zh) | 2006-04-25 | 2007-04-19 | 化合物和有机el器件 |
US12/298,300 US8808875B2 (en) | 2006-04-25 | 2007-04-19 | Compound and organic EL device |
KR1020087028748A KR101077720B1 (ko) | 2006-04-25 | 2007-04-19 | 화합물 및 유기 전계발광 소자 |
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JP2006120806A JP4717703B2 (ja) | 2006-04-25 | 2006-04-25 | 化合物および有機el素子 |
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JP2007291013A JP2007291013A (ja) | 2007-11-08 |
JP4717703B2 true JP4717703B2 (ja) | 2011-07-06 |
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US (1) | US8808875B2 (ja) |
JP (1) | JP4717703B2 (ja) |
KR (1) | KR101077720B1 (ja) |
CN (1) | CN101432250A (ja) |
WO (1) | WO2007125976A1 (ja) |
Cited By (1)
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WO2018124304A1 (ja) | 2016-12-28 | 2018-07-05 | 株式会社クラレ | 1,3,7-オクタトリエン重合体およびその水素化物、並びに該重合体の製造方法 |
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JP5241256B2 (ja) * | 2007-03-09 | 2013-07-17 | キヤノン株式会社 | 縮合環芳香族化合物及びこれを用いた有機発光素子 |
US8330350B2 (en) * | 2007-07-07 | 2012-12-11 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device and material for organic electroluminescence device |
US8779655B2 (en) | 2007-07-07 | 2014-07-15 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device and material for organic electroluminescence device |
US8900724B2 (en) * | 2007-11-19 | 2014-12-02 | Idemitsu Kosan Co., Ltd. | Monobenzochrysene derivative, a material for an organic electroluminescence device containing the same, and an organic electroluminescence device using the material |
JP5562549B2 (ja) * | 2007-11-26 | 2014-07-30 | 双葉電子工業株式会社 | 有機el素子用化合物及び有機el素子 |
JP4721475B2 (ja) * | 2009-10-01 | 2011-07-13 | キヤノン株式会社 | ジインデノピセン化合物及びこれを使用した有機発光素子 |
JP4781474B1 (ja) * | 2010-03-31 | 2011-09-28 | キヤノン株式会社 | 有機発光素子 |
JP5721491B2 (ja) | 2010-06-30 | 2015-05-20 | キヤノン株式会社 | 新規有機化合物およびそれを有するエレクトロクロミック素子 |
TW201213502A (en) | 2010-08-05 | 2012-04-01 | Idemitsu Kosan Co | Organic electroluminescent element |
EP2719702B1 (en) | 2011-06-07 | 2016-05-11 | Canon Kabushiki Kaisha | Electrochromic element |
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JP3853042B2 (ja) | 1996-11-07 | 2006-12-06 | 三井化学株式会社 | 有機電界発光素子 |
JP4041583B2 (ja) | 1998-06-17 | 2008-01-30 | 三井化学株式会社 | ベンゾ〔k〕フルオランテン誘導体 |
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JP2007314511A (ja) | 2006-04-24 | 2007-12-06 | Canon Inc | 化合物および有機発光素子 |
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JP4827775B2 (ja) | 2007-03-13 | 2011-11-30 | キヤノン株式会社 | 電界発光素子 |
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- 2007-04-19 KR KR1020087028748A patent/KR101077720B1/ko active IP Right Grant
- 2007-04-19 CN CNA2007800147860A patent/CN101432250A/zh active Pending
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JPH10189248A (ja) * | 1996-11-07 | 1998-07-21 | Mitsui Chem Inc | 有機電界発光素子 |
JP2002043058A (ja) * | 2000-07-25 | 2002-02-08 | Nec Corp | 有機エレクトロルミネッセンス素子 |
JP2004107326A (ja) * | 2002-08-27 | 2004-04-08 | Canon Inc | 縮合多環化合物及びそれを用いた有機発光素子 |
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WO2018124304A1 (ja) | 2016-12-28 | 2018-07-05 | 株式会社クラレ | 1,3,7-オクタトリエン重合体およびその水素化物、並びに該重合体の製造方法 |
Also Published As
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WO2007125976A1 (en) | 2007-11-08 |
KR20090009906A (ko) | 2009-01-23 |
JP2007291013A (ja) | 2007-11-08 |
KR101077720B1 (ko) | 2011-10-27 |
CN101432250A (zh) | 2009-05-13 |
US20090096368A1 (en) | 2009-04-16 |
US8808875B2 (en) | 2014-08-19 |
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