JP2008074917A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2008074917A5 JP2008074917A5 JP2006253962A JP2006253962A JP2008074917A5 JP 2008074917 A5 JP2008074917 A5 JP 2008074917A5 JP 2006253962 A JP2006253962 A JP 2006253962A JP 2006253962 A JP2006253962 A JP 2006253962A JP 2008074917 A5 JP2008074917 A5 JP 2008074917A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- electrode
- polymer
- hours
- energy level
- 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.)
- Granted
Links
- -1 tetrabutyl ammonium tetrafluoroborate Chemical compound 0.000 description 18
- 229920000642 polymer Polymers 0.000 description 15
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 12
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 11
- 239000000243 solution Substances 0.000 description 10
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 8
- 238000004770 highest occupied molecular orbital Methods 0.000 description 6
- 238000004768 lowest unoccupied molecular orbital Methods 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- 229910052697 platinum Inorganic materials 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 238000005259 measurement Methods 0.000 description 5
- 230000003647 oxidation Effects 0.000 description 5
- 238000007254 oxidation reaction Methods 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- 125000005103 alkyl silyl group Chemical group 0.000 description 4
- 239000012044 organic layer Substances 0.000 description 4
- 229910052709 silver Inorganic materials 0.000 description 4
- 239000004332 silver Substances 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 3
- 230000005587 bubbling Effects 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- 229940126062 Compound A Drugs 0.000 description 2
- 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 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 2
- 229910021607 Silver chloride Inorganic materials 0.000 description 2
- FOIXSVOLVBLSDH-UHFFFAOYSA-N Silver ion Chemical compound [Ag+] FOIXSVOLVBLSDH-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 235000011114 ammonium hydroxide Nutrition 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 238000002484 cyclic voltammetry Methods 0.000 description 2
- 229910021397 glassy carbon Inorganic materials 0.000 description 2
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- JRTIUDXYIUKIIE-KZUMESAESA-N (1z,5z)-cycloocta-1,5-diene;nickel Chemical compound [Ni].C\1C\C=C/CC\C=C/1.C\1C\C=C/CC\C=C/1 JRTIUDXYIUKIIE-KZUMESAESA-N 0.000 description 1
- 239000004912 1,5-cyclooctadiene Substances 0.000 description 1
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 description 1
- WNEXSUAHKVAPFK-UHFFFAOYSA-N 2,8-dibromodibenzothiophene Chemical compound C1=C(Br)C=C2C3=CC(Br)=CC=C3SC2=C1 WNEXSUAHKVAPFK-UHFFFAOYSA-N 0.000 description 1
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 description 1
- ROFVEXUMMXZLPA-UHFFFAOYSA-N Bipyridyl Chemical group N1=CC=CC=C1C1=CC=CC=N1 ROFVEXUMMXZLPA-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 125000005036 alkoxyphenyl group Chemical group 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- UQNVLAAMEYKKJO-UHFFFAOYSA-N dimethoxy methyl borate Chemical compound COOB(OC)OOC UQNVLAAMEYKKJO-UHFFFAOYSA-N 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- IMBKASBLAKCLEM-UHFFFAOYSA-L ferrous ammonium sulfate (anhydrous) Chemical compound [NH4+].[NH4+].[Fe+2].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O IMBKASBLAKCLEM-UHFFFAOYSA-L 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2006253962A JP5162868B2 (ja) | 2006-09-20 | 2006-09-20 | 高分子発光素子及び有機トランジスタ並びにそれらに有用な組成物 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2006253962A JP5162868B2 (ja) | 2006-09-20 | 2006-09-20 | 高分子発光素子及び有機トランジスタ並びにそれらに有用な組成物 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2008074917A JP2008074917A (ja) | 2008-04-03 |
| JP2008074917A5 true JP2008074917A5 (https=) | 2009-07-23 |
| JP5162868B2 JP5162868B2 (ja) | 2013-03-13 |
Family
ID=39347305
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006253962A Expired - Fee Related JP5162868B2 (ja) | 2006-09-20 | 2006-09-20 | 高分子発光素子及び有機トランジスタ並びにそれらに有用な組成物 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP5162868B2 (https=) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101626994B1 (ko) | 2008-03-07 | 2016-06-03 | 스미또모 가가꾸 가부시끼가이샤 | 적층 구조체 |
| JP5415035B2 (ja) * | 2008-07-24 | 2014-02-12 | 株式会社船井電機新応用技術研究所 | 発光性組成物及び有機エレクトロルミネッセンス素子の製造方法 |
| WO2012011510A1 (ja) | 2010-07-21 | 2012-01-26 | 住友化学株式会社 | 有機ｅｌ素子 |
| CN103120019B (zh) | 2010-07-21 | 2015-09-16 | 住友化学株式会社 | 有机el元件的制造方法 |
| EP2597933B1 (en) | 2010-07-21 | 2019-06-12 | Sumitomo Chemical Company, Limited | Manufacturing method for organic electroluminescence element |
| JP5653122B2 (ja) | 2010-08-10 | 2015-01-14 | 住友化学株式会社 | 有機エレクトロルミネッセンス素子およびその製造方法 |
| CN103385036B (zh) | 2011-02-21 | 2017-02-08 | 住友化学株式会社 | 有机电致发光元件的制造方法 |
| CN104093689A (zh) * | 2012-01-31 | 2014-10-08 | 剑桥显示技术有限公司 | 聚合物 |
| JP6724294B2 (ja) * | 2015-05-08 | 2020-07-15 | 三菱ケミカル株式会社 | 有機電界発光素子用組成物、有機電界発光素子、表示装置及び照明装置 |
| CN114106295B (zh) * | 2020-12-29 | 2023-06-16 | 广东聚华印刷显示技术有限公司 | 可交联型聚合物及其制备方法和应用 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2360644A1 (en) * | 1999-02-04 | 2000-08-10 | The Dow Chemical Company | Fluorene copolymers and devices made therefrom |
| JP2003077673A (ja) * | 2001-06-19 | 2003-03-14 | Honda Motor Co Ltd | 有機エレクトロルミネッセンス素子 |
| JP2003253258A (ja) * | 2002-02-28 | 2003-09-10 | Jsr Corp | 燐光発光剤、その製造方法および発光性組成物 |
| US7138483B2 (en) * | 2003-02-12 | 2006-11-21 | E.I. Du Pont De Nemours And Company | Monomers, conjugated polymers and electronic devices using such polymers |
| JP2004323823A (ja) * | 2003-04-08 | 2004-11-18 | Jsr Corp | 有機エレクトロルミネッセンス素子形成用重合体材料および重合体組成物並びに有機エレクトロルミネッセンス素子 |
| JP4736471B2 (ja) * | 2004-02-26 | 2011-07-27 | 住友化学株式会社 | 高分子化合物およびそれを用いた高分子発光素子 |
| WO2008024379A2 (en) * | 2006-08-24 | 2008-02-28 | E. I. Du Pont De Nemours And Company | Crosslinkable hole transport polymers |
-
2006
- 2006-09-20 JP JP2006253962A patent/JP5162868B2/ja not_active Expired - Fee Related
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR101710043B1 (ko) | 하이드로실릴화 촉매 | |
| Plenio et al. | Optically and Redox‐Active Ferroceneacetylene Polymers and Oligomers | |
| US20020156223A1 (en) | Method of preparing aminofunctional alkoxy polysiloxanes | |
| JP5959171B2 (ja) | π共役有機ホウ素化合物及びその製造方法 | |
| Karagollu et al. | Phosphate ion sensors based on triazole connected ferrocene moieties | |
| JP2008074917A5 (https=) | ||
| US4005117A (en) | Organosilane compounds | |
| JP2862753B2 (ja) | チオフェン−シロ−ル共重合体およびその製造方法 | |
| JP2008031337A5 (https=) | ||
| Dexheimer et al. | Acetyldi-t-butylsilane and acetyldi-t-butylfluorosilane: Synthesis of functionalized acylsilanes | |
| Plenio et al. | Synthesis of Soluble 1, 3‐Bridged Ferrocene‐Acetylene Polymers and the Divergent‐Convergent Synthesis of Defined Oligomers | |
| Chakraborty et al. | Windmill-shaped octanuclear Zn II4/Ln III4 (Ln III= Dy, Tb, Ho) heterometallic ensembles supported by a tetraferrocene scaffold | |
| JP2001247576A (ja) | チオフェン誘導体およびその重合体 | |
| JP6944141B2 (ja) | アルコキシアルキル基を有するイソシアヌル酸誘導体及びその製造方法 | |
| JPS6245894B2 (https=) | ||
| Ma et al. | A geminal dithallated bis (iminodiphenylphosphorano) methine carbon bridged dimer bound by Tl–Tl interactions | |
| Takimiya et al. | Improved Synthesis of Double‐Bridged Tetraselenafulvalenophanes and Formation of Their Conductive Radical Cation Salts | |
| CN103665018A (zh) | 硅烷类化合物及其制备方法 | |
| JPWO2006009123A1 (ja) | ポリカルボシラン及びその製造方法 | |
| JP4505568B2 (ja) | 被覆型ヘテロ芳香環化合物 | |
| JP5980659B2 (ja) | カルバゾール基を有するポリマー、カルバゾール基を有するモノマー及び化合物 | |
| JP2773362B2 (ja) | キノキサリン―パラジウム錯体およびその製造方法 | |
| DE2250921A1 (de) | Neue silane von sulfon- und phosphorsaeureamiden | |
| Kostenko et al. | A Synthetic Route to Quaternary Pyridinium Salt‐Functionalized Silsesquioxanes | |
| JP3602725B2 (ja) | カルボラン含有ケイ素系重合体 |