JP6370909B2 - 白色発光ダイオード用のポリ(チエノチオフェニルボラン)類及びポリ(ジチエノチオフェニルボラン)類 - Google Patents
白色発光ダイオード用のポリ(チエノチオフェニルボラン)類及びポリ(ジチエノチオフェニルボラン)類 Download PDFInfo
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- JP6370909B2 JP6370909B2 JP2016539641A JP2016539641A JP6370909B2 JP 6370909 B2 JP6370909 B2 JP 6370909B2 JP 2016539641 A JP2016539641 A JP 2016539641A JP 2016539641 A JP2016539641 A JP 2016539641A JP 6370909 B2 JP6370909 B2 JP 6370909B2
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- 229920000642 polymer Polymers 0.000 claims description 20
- 239000000463 material Substances 0.000 claims description 12
- 125000004429 atom Chemical group 0.000 claims description 10
- 150000001875 compounds Chemical class 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 125000003118 aryl group Chemical group 0.000 claims description 8
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 3
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 238000006138 lithiation reaction Methods 0.000 claims 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 6
- VJYJJHQEVLEOFL-UHFFFAOYSA-N thieno[3,2-b]thiophene Chemical compound S1C=CC2=C1C=CS2 VJYJJHQEVLEOFL-UHFFFAOYSA-N 0.000 description 6
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 5
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 5
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 5
- 125000003342 alkenyl group Chemical group 0.000 description 5
- 125000000304 alkynyl group Chemical group 0.000 description 5
- 150000001412 amines Chemical class 0.000 description 5
- 229910052796 boron Inorganic materials 0.000 description 5
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- 239000011368 organic material Substances 0.000 description 5
- 150000001282 organosilanes Chemical class 0.000 description 5
- 150000007944 thiolates Chemical class 0.000 description 5
- HKNRNTYTYUWGLN-UHFFFAOYSA-N dithieno[3,2-a:2',3'-d]thiophene Chemical compound C1=CSC2=C1SC1=C2C=CS1 HKNRNTYTYUWGLN-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000010409 thin film Substances 0.000 description 4
- 229930192474 thiophene Natural products 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- NCEUIABFEQHUQB-UHFFFAOYSA-N dimethoxy-(2,4,6-trimethylphenyl)borane Chemical compound COB(OC)C1=C(C)C=C(C)C=C1C NCEUIABFEQHUQB-UHFFFAOYSA-N 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 150000003577 thiophenes Chemical class 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- UORVGPXVDQYIDP-UHFFFAOYSA-N borane Chemical compound B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 description 2
- DLEDOFVPSDKWEF-UHFFFAOYSA-N lithium butane Chemical compound [Li+].CCC[CH2-] DLEDOFVPSDKWEF-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 230000005693 optoelectronics Effects 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 1
- UQRONKZLYKUEMO-UHFFFAOYSA-N 4-methyl-1-(2,4,6-trimethylphenyl)pent-4-en-2-one Chemical group CC(=C)CC(=O)Cc1c(C)cc(C)cc1C UQRONKZLYKUEMO-UHFFFAOYSA-N 0.000 description 1
- JBRZTFJDHDCESZ-UHFFFAOYSA-N AsGa Chemical compound [As]#[Ga] JBRZTFJDHDCESZ-UHFFFAOYSA-N 0.000 description 1
- 229910001218 Gallium arsenide Inorganic materials 0.000 description 1
- 229920000144 PEDOT:PSS Polymers 0.000 description 1
- 229920001609 Poly(3,4-ethylenedioxythiophene) Polymers 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
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910000085 borane Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 229940117389 dichlorobenzene Drugs 0.000 description 1
- 239000012776 electronic material Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000005669 field effect Effects 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 238000002189 fluorescence spectrum Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 150000002642 lithium compounds Chemical class 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 238000013086 organic photovoltaic Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000002211 ultraviolet spectrum Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G79/00—Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule
- C08G79/08—Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule a linkage containing boron
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
- C07F5/027—Organoboranes and organoborohydrides
-
- 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
-
- 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
- H10K85/10—Organic polymers or oligomers
- H10K85/111—Organic polymers or oligomers comprising aromatic, heteroaromatic, or aryl chains, e.g. polyaniline, polyphenylene or polyphenylene vinylene
- H10K85/113—Heteroaromatic compounds comprising sulfur or selene, e.g. polythiophene
-
- 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
- H10K85/10—Organic polymers or oligomers
- H10K85/151—Copolymers
-
- 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
- H10K85/30—Coordination compounds
- H10K85/321—Metal complexes comprising a group IIIA element, e.g. Tris (8-hydroxyquinoline) gallium [Gaq3]
- H10K85/322—Metal complexes comprising a group IIIA element, e.g. Tris (8-hydroxyquinoline) gallium [Gaq3] comprising boron
-
- 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
- C09K2211/14—Macromolecular compounds
- C09K2211/1441—Heterocyclic
- C09K2211/1458—Heterocyclic containing sulfur as the only heteroatom
-
- 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
- C09K2211/14—Macromolecular compounds
- C09K2211/1441—Heterocyclic
- C09K2211/1491—Heterocyclic containing other combinations of heteroatoms
-
- 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
- C09K2211/18—Metal complexes
-
- 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
-
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02B—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO BUILDINGS, e.g. HOUSING, HOUSE APPLIANCES OR RELATED END-USER APPLICATIONS
- Y02B20/00—Energy efficient lighting technologies, e.g. halogen lamps or gas discharge lamps
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Inorganic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Electroluminescent Light Sources (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Description
N2下で乾燥THF(30mL)に溶解させたチエノチオフェン(TT)(XLV、R4=H)(0.2g、0.44mmol)の溶液に、n−BuLi(0.8mL、3.3mmol、1.9M)を−78°Cで滴下し、この混合物を1時間半の間攪拌した。前記滴下は、−78〜+30°Cの任意の温度で行うことができる。次いで、温度を室温まで上昇させて、この温度で前記混合物を20分間攪拌した。乾燥THF(5mL)に溶解させたジメトキシメシチルボラン(MesB(OMe)2)(0.170g、0.88mmol)を窒素雰囲気下で添加した。この反応物を一晩の間攪拌し、溶媒を減圧下で除去した。前記攪拌は、1分間〜一晩以上行うことができ、ジメトキシメシチルボランは、ジメトキシメシチルボランと反応しない任意の有機溶媒に溶解させることができる。残留物を最小量のTHFに溶解させ、メタノール中に沈殿させた。この沈殿物をろ過して、メタノールで洗浄した。Mw:146600、Mn:102800、Mw/Mn:1.43、dn/dc:0.16mL/g(THF、25°C)。
ポリマー類をそれらの溶液から導電性基板に塗布して、有機発光デバイスを製造した。ポリマー(VIII)をトルエン/ジクロロベンゼン(8mg/mL)の混合物に溶解させた。アノード電極として、ガラスに塗布した酸化インジウムスズ(ITO)(15Ω/□)を用いた。ホール注入層として、PEDOT:PSSをITO上にスピン塗布し、これを110°Cで10分間乾燥させた。その後、活性層としてポリマー膜をスピン塗布で塗布した。最後に、LiF(1nm)及びアルミニウム(Al、100nm)を真空下(約10−6ミリバール)で加熱蒸着法により堆積させて、カソード電極を作製した。
Claims (5)
- 化学式(I)、(II)、(IV)、(V)、(VII)、(VIII)、(IX)又は(X)のポリマー化合物であって、
R、R1、R2、R3及びR4は、独立して又は等しく、1原子〜60原子の基であり、水素、アルキル及びアリールよりなる群から選択されることを特徴とするポリマー化合物。 - 化学式(XI)、(XII)、(XIV)又は(XV)のポリマー化合物であって、
R、R1、R2及びR3は、独立して又は等しく、1原子〜60原子の基であり、水素、アルキル、及びアリールよりなる群から選択されることを特徴とするポリマー化合物。 - 請求項1に記載のポリマー化合物を製造するための方法であって、
化学式(XXXVIII)、(XXXIX)、(XLI)、(XLII)、(XLIV)、(XLV)、(XLVI)又は(XLVII)で表されるブロモ化合物:
- 請求項1又は2に記載のポリマー化合物からなる、白色発光材料。
- 請求項1又は2に記載のポリマー化合物からなる、電荷輸送材料。
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/IB2013/058311 WO2015033187A1 (en) | 2013-09-05 | 2013-09-05 | Poly(thienothiophenylborane)s and poly(dithienothiophenylborane)s for white light emitting diodes |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2016530383A JP2016530383A (ja) | 2016-09-29 |
JP6370909B2 true JP6370909B2 (ja) | 2018-08-08 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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JP2016539641A Active JP6370909B2 (ja) | 2013-09-05 | 2013-09-05 | 白色発光ダイオード用のポリ(チエノチオフェニルボラン)類及びポリ(ジチエノチオフェニルボラン)類 |
Country Status (6)
Country | Link |
---|---|
US (1) | US9944761B2 (ja) |
EP (1) | EP3041848B1 (ja) |
JP (1) | JP6370909B2 (ja) |
KR (1) | KR101902841B1 (ja) |
CA (1) | CA2923125C (ja) |
WO (1) | WO2015033187A1 (ja) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
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FR3041148A1 (fr) * | 2015-09-14 | 2017-03-17 | Valeo Vision | Source lumineuse led comprenant un circuit electronique |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4356429A (en) | 1980-07-17 | 1982-10-26 | Eastman Kodak Company | Organic electroluminescent cell |
GB8909011D0 (en) * | 1989-04-20 | 1989-06-07 | Friend Richard H | Electroluminescent devices |
DE60116330T2 (de) | 2001-11-09 | 2006-12-14 | Simonazzi S.P.A. | Abfüllventil für Abfüllmaschine |
CN101111497B (zh) * | 2004-09-14 | 2013-10-30 | 康宁股份有限公司 | 稠合噻吩及其制备方法和用途 |
US20070215864A1 (en) * | 2006-03-17 | 2007-09-20 | Luebben Silvia D | Use of pi-conjugated organoboron polymers in thin-film organic polymer electronic devices |
WO2007134285A2 (en) | 2006-05-12 | 2007-11-22 | University Of Utah | π-CONJUGATED HEAVY-METAL POLYMERS PARTICULARLY SUITED TO HYDROPONIC APPLICATIONS |
ATE554122T1 (de) | 2006-12-22 | 2012-05-15 | Merck Patent Gmbh | Polymere mit kondensiertem selenophen |
-
2013
- 2013-09-05 KR KR1020167008068A patent/KR101902841B1/ko active IP Right Grant
- 2013-09-05 EP EP13798734.3A patent/EP3041848B1/en active Active
- 2013-09-05 CA CA2923125A patent/CA2923125C/en active Active
- 2013-09-05 US US14/916,571 patent/US9944761B2/en active Active
- 2013-09-05 JP JP2016539641A patent/JP6370909B2/ja active Active
- 2013-09-05 WO PCT/IB2013/058311 patent/WO2015033187A1/en active Application Filing
Also Published As
Publication number | Publication date |
---|---|
EP3041848B1 (en) | 2020-03-18 |
CA2923125C (en) | 2018-08-28 |
US20160194458A1 (en) | 2016-07-07 |
KR101902841B1 (ko) | 2018-10-01 |
JP2016530383A (ja) | 2016-09-29 |
US9944761B2 (en) | 2018-04-17 |
CA2923125A1 (en) | 2015-03-12 |
EP3041848A1 (en) | 2016-07-13 |
WO2015033187A1 (en) | 2015-03-12 |
KR20160051815A (ko) | 2016-05-11 |
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