CN112679503B - 一种p型掺杂剂及其中间体和应用 - Google Patents
一种p型掺杂剂及其中间体和应用 Download PDFInfo
- Publication number
- CN112679503B CN112679503B CN202011476127.2A CN202011476127A CN112679503B CN 112679503 B CN112679503 B CN 112679503B CN 202011476127 A CN202011476127 A CN 202011476127A CN 112679503 B CN112679503 B CN 112679503B
- Authority
- CN
- China
- Prior art keywords
- type dopant
- layer
- organic electroluminescent
- added
- group
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 239000002019 doping agent Substances 0.000 title claims abstract description 39
- 239000010410 layer Substances 0.000 claims description 29
- 239000000463 material Substances 0.000 claims description 12
- 238000002347 injection Methods 0.000 claims description 11
- 239000007924 injection Substances 0.000 claims description 11
- 230000005525 hole transport Effects 0.000 claims description 8
- 239000000758 substrate Substances 0.000 claims description 6
- 239000002346 layers by function Substances 0.000 claims description 4
- 230000000903 blocking effect Effects 0.000 claims description 3
- 238000005401 electroluminescence Methods 0.000 abstract description 2
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 18
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 15
- -1 cyanomethylene group Chemical group 0.000 description 15
- 125000003118 aryl group Chemical group 0.000 description 11
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 8
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 7
- 125000001072 heteroaryl group Chemical group 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 6
- 238000003786 synthesis reaction Methods 0.000 description 6
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 5
- 238000001514 detection method Methods 0.000 description 5
- 238000001819 mass spectrum Methods 0.000 description 5
- 239000012046 mixed solvent Substances 0.000 description 5
- 230000007935 neutral effect Effects 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
- 125000006413 ring segment Chemical group 0.000 description 4
- 125000001424 substituent group Chemical group 0.000 description 4
- IXHWGNYCZPISET-UHFFFAOYSA-N 2-[4-(dicyanomethylidene)-2,3,5,6-tetrafluorocyclohexa-2,5-dien-1-ylidene]propanedinitrile Chemical compound FC1=C(F)C(=C(C#N)C#N)C(F)=C(F)C1=C(C#N)C#N IXHWGNYCZPISET-UHFFFAOYSA-N 0.000 description 3
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 description 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
- 150000005840 aryl radicals Chemical class 0.000 description 2
- 125000002619 bicyclic group Chemical group 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 229910052805 deuterium Inorganic materials 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- 239000004973 liquid crystal related substance Substances 0.000 description 2
- 125000002950 monocyclic group Chemical group 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 125000006745 (C2-C60) alkynyl group Chemical group 0.000 description 1
- 125000006751 (C6-C60) aryloxy group Chemical group 0.000 description 1
- PXLYGWXKAVCTPX-UHFFFAOYSA-N 1,2,3,4,5,6-hexamethylidenecyclohexane Chemical class C=C1C(=C)C(=C)C(=C)C(=C)C1=C PXLYGWXKAVCTPX-UHFFFAOYSA-N 0.000 description 1
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
- BAXOFTOLAUCFNW-UHFFFAOYSA-N 1H-indazole Chemical compound C1=CC=C2C=NNC2=C1 BAXOFTOLAUCFNW-UHFFFAOYSA-N 0.000 description 1
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 1
- DPZSNGJNFHWQDC-UHFFFAOYSA-N 2,3-diaminobut-2-enedinitrile Chemical compound N#CC(N)=C(N)C#N DPZSNGJNFHWQDC-UHFFFAOYSA-N 0.000 description 1
- DEJPYROXSVVWIE-UHFFFAOYSA-N 2-(3-fluorophenyl)acetonitrile Chemical compound FC1=CC=CC(CC#N)=C1 DEJPYROXSVVWIE-UHFFFAOYSA-N 0.000 description 1
- UUZLADCDKJUECN-UHFFFAOYSA-N 4-(cyanomethyl)-2,3,5,6-tetrafluorobenzonitrile Chemical compound FC1=C(F)C(C#N)=C(F)C(F)=C1CC#N UUZLADCDKJUECN-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 241000854350 Enicospilus group Species 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- JMYCOQCPLILNOM-UHFFFAOYSA-N N#CCC(C(F)=C(C(C#N)=C1C(F)(F)F)F)=C1F Chemical compound N#CCC(C(F)=C(C(C#N)=C1C(F)(F)F)F)=C1F JMYCOQCPLILNOM-UHFFFAOYSA-N 0.000 description 1
- PEANDNKFMZIVCN-UHFFFAOYSA-N N#CCC(C(F)=C1C(F)(F)F)=C(C(F)(F)F)C(F)=C1F Chemical compound N#CCC(C(F)=C1C(F)(F)F)=C(C(F)(F)F)C(F)=C1F PEANDNKFMZIVCN-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical group OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
- 125000000304 alkynyl group Chemical group 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
- 239000004411 aluminium Substances 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 150000004832 aryl thioethers Chemical group 0.000 description 1
- 125000000732 arylene group Chemical group 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 125000003739 carbamimidoyl group Chemical group C(N)(=N)* 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000012769 display material Substances 0.000 description 1
- 238000001194 electroluminescence spectrum Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 125000005549 heteroarylene group Chemical group 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- OAKJQQAXSVQMHS-UHFFFAOYSA-N hydrazine group Chemical group NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 1
- 125000005597 hydrazone group Chemical group 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 description 1
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 description 1
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 1
- QNLOWBMKUIXCOW-UHFFFAOYSA-N indol-2-one Chemical compound C1=CC=CC2=NC(=O)C=C21 QNLOWBMKUIXCOW-UHFFFAOYSA-N 0.000 description 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 1
- FGFUBBNNYLNVLJ-UHFFFAOYSA-N indolone Natural products C1=CC=C2C(=O)C=NC2=C1 FGFUBBNNYLNVLJ-UHFFFAOYSA-N 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 238000004020 luminiscence type Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 125000002560 nitrile group Chemical group 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 230000005693 optoelectronics Effects 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 description 1
- UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical compound OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- SBYHFKPVCBCYGV-UHFFFAOYSA-N quinuclidine Chemical compound C1CC2CCN1CC2 SBYHFKPVCBCYGV-UHFFFAOYSA-N 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 125000005942 tetrahydropyridyl group Chemical group 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- GBXQPDCOMJJCMJ-UHFFFAOYSA-M trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;bromide Chemical compound [Br-].C[N+](C)(C)CCCCCC[N+](C)(C)C GBXQPDCOMJJCMJ-UHFFFAOYSA-M 0.000 description 1
Landscapes
- Electroluminescent Light Sources (AREA)
Abstract
Description
Claims (5)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202011476127.2A CN112679503B (zh) | 2020-12-14 | 2020-12-14 | 一种p型掺杂剂及其中间体和应用 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202011476127.2A CN112679503B (zh) | 2020-12-14 | 2020-12-14 | 一种p型掺杂剂及其中间体和应用 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN112679503A CN112679503A (zh) | 2021-04-20 |
CN112679503B true CN112679503B (zh) | 2022-08-23 |
Family
ID=75447842
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202011476127.2A Active CN112679503B (zh) | 2020-12-14 | 2020-12-14 | 一种p型掺杂剂及其中间体和应用 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN112679503B (zh) |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108947925B (zh) * | 2018-08-22 | 2020-12-01 | 石家庄诚志永华显示材料有限公司 | 1,3,4-噁二唑衍生物、材料和有机电致发光器件 |
CN114560789B (zh) * | 2018-10-09 | 2023-12-19 | 宁波卢米蓝新材料有限公司 | 一种含有多元环的化合物、应用及有机电致发光器件 |
CN110437103B (zh) * | 2019-08-01 | 2021-01-26 | 宁波卢米蓝新材料有限公司 | 一种环状化合物及其用途和电子器件 |
CN111704605B (zh) * | 2020-06-28 | 2023-09-22 | 宁波卢米蓝新材料有限公司 | 一种咔唑衍生物及其制备方法和用途 |
-
2020
- 2020-12-14 CN CN202011476127.2A patent/CN112679503B/zh active Active
Also Published As
Publication number | Publication date |
---|---|
CN112679503A (zh) | 2021-04-20 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP6880120B2 (ja) | 新規なヘテロレプティックイリジウム錯体 | |
JP2020084189A (ja) | インドロカルバゾール誘導体及びこれを用いた有機発光素子 | |
CN104342126B (zh) | 有机电致发光材料和有机电致发光器件 | |
TWI415921B (zh) | 藍色螢光化合物及使用該化合物之有機電致發光裝置 | |
JP2017098556A (ja) | 有機セレン材料および有機発光デバイス内でのその使用 | |
JP2012229195A (ja) | 新規スピロ化合物およびそれを有する有機発光素子 | |
US20140183485A1 (en) | Blue fluorescent compounds and organic light emitting diode devices using the same | |
CN110835318B (zh) | 一种以氮杂芴为核心的有机化合物及其制备方法与应用 | |
CN110563746A (zh) | 一种新型含so2螺环结构化合物及其在oled器件中的应用 | |
JP2023511161A (ja) | 多環芳香族誘導体化合物及びこれを用いた有機発光素子 | |
KR20130121516A (ko) | 신규한 아릴아민을 사용한 정공 수송 물질 및 이를 포함한 유기 전계 발광 소자 | |
CN110835351A (zh) | 一种以吡咯亚甲基硼络合物为核心的有机化合物及其制备和应用 | |
Grigalevicius et al. | 9, 9′-bis (2, 2-diphenylvinyl)[3, 3′] bicarbazole as low cost efficient hole transporting material for application in red PhOLEDs | |
WO2024078287A1 (zh) | 有机化合物、有机电致发光器件和电子装置 | |
KR20140080322A (ko) | 유기전기 소자용 화합물, 이를 이용한 유기전기소자 및 그 전자 장치 | |
CN113121544A (zh) | 一种有机电致发光化合物及其制备方法和应用 | |
JP6940887B2 (ja) | ケイ素含有電子輸送材料およびその使用 | |
CN112707908B (zh) | 一种有机电子材料及其应用 | |
CN112679503B (zh) | 一种p型掺杂剂及其中间体和应用 | |
CN106831766B (zh) | 一种双极性发光主体材料及其合成方法与应用 | |
TWI612047B (zh) | 有機電子傳輸材料 | |
KR101922050B1 (ko) | 인광 화합물 및 이를 이용한 유기전계발광소자 | |
KR20150114658A (ko) | 유기발광 화합물 및 이를 포함하는 유기전계발광소자 | |
KR102175379B1 (ko) | 유기 전기 발광 소자용 발광 재료, 이를 이용한 유기 전기 발광 소자 및 유기 전기 발광 소자용 재료 | |
KR20230132040A (ko) | 코팅 조성물, 이를 포함하는 유기 발광 소자 및 이의 제조 방법 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant | ||
TR01 | Transfer of patent right | ||
TR01 | Transfer of patent right |
Effective date of registration: 20231012 Address after: 236000 No.1 Tianzhushan Road, Hefei modern industrial park, Yingzhou District, Fuyang City, Anhui Province Patentee after: FUYANG SINEVA MATERIAL TECHNOLOGY Co.,Ltd. Patentee after: Beijing xinyihua Material Technology Co.,Ltd. Address before: 236000 No.1 Tianzhushan Road, Hefei modern industrial park, Yingzhou District, Fuyang City, Anhui Province Patentee before: FUYANG SINEVA MATERIAL TECHNOLOGY Co.,Ltd. Patentee before: BEIJING SINEVA TECHNOLOGY Co.,Ltd. Patentee before: Beijing xinyihua Material Technology Co.,Ltd. |
|
CP03 | Change of name, title or address | ||
CP03 | Change of name, title or address |
Address after: 236000 No.1 Tianzhushan Road, Hefei modern industrial park, Yingzhou District, Fuyang City, Anhui Province Patentee after: Fuyang Xinyihua New Material Technology Co.,Ltd. Country or region after: China Patentee after: Beijing xinyihua Material Technology Co.,Ltd. Address before: 236000 No.1 Tianzhushan Road, Hefei modern industrial park, Yingzhou District, Fuyang City, Anhui Province Patentee before: FUYANG SINEVA MATERIAL TECHNOLOGY Co.,Ltd. Country or region before: China Patentee before: Beijing xinyihua Material Technology Co.,Ltd. |