JP2012149245A - 反応性化合物及びそれを用いた高分子化合物の製造方法 - Google Patents
反応性化合物及びそれを用いた高分子化合物の製造方法 Download PDFInfo
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- 125000001626 borono group Chemical group [H]OB([*])O[H] 0.000 description 1
- AQNQQHJNRPDOQV-UHFFFAOYSA-N bromocyclohexane Chemical compound BrC1CCCCC1 AQNQQHJNRPDOQV-UHFFFAOYSA-N 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- WVIIMZNLDWSIRH-UHFFFAOYSA-N cyclohexylcyclohexane Chemical group C1CCCCC1C1CCCCC1 WVIIMZNLDWSIRH-UHFFFAOYSA-N 0.000 description 1
- 238000003795 desorption Methods 0.000 description 1
- 229940117389 dichlorobenzene Drugs 0.000 description 1
- LMBWSYZSUOEYSN-UHFFFAOYSA-N diethyldithiocarbamic acid Chemical compound CCN(CC)C(S)=S LMBWSYZSUOEYSN-UHFFFAOYSA-N 0.000 description 1
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- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
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- XKBGEWXEAPTVCK-UHFFFAOYSA-M methyltrioctylammonium chloride Chemical compound [Cl-].CCCCCCCC[N+](C)(CCCCCCCC)CCCCCCCC XKBGEWXEAPTVCK-UHFFFAOYSA-M 0.000 description 1
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- 238000007645 offset printing Methods 0.000 description 1
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- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
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- HXITXNWTGFUOAU-UHFFFAOYSA-N phenylboronic acid Chemical compound OB(O)C1=CC=CC=C1 HXITXNWTGFUOAU-UHFFFAOYSA-N 0.000 description 1
- NIXKBAZVOQAHGC-UHFFFAOYSA-N phenylmethanesulfonic acid Chemical group OS(=O)(=O)CC1=CC=CC=C1 NIXKBAZVOQAHGC-UHFFFAOYSA-N 0.000 description 1
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- 239000000843 powder Substances 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- ZJMWRROPUADPEA-UHFFFAOYSA-N sec-butylbenzene Chemical compound CCC(C)C1=CC=CC=C1 ZJMWRROPUADPEA-UHFFFAOYSA-N 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical group CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- FMYXZXAKZWIOHO-UHFFFAOYSA-N trichloro(2-phenylethyl)silane Chemical compound Cl[Si](Cl)(Cl)CCC1=CC=CC=C1 FMYXZXAKZWIOHO-UHFFFAOYSA-N 0.000 description 1
- 125000002827 triflate group Chemical group FC(S(=O)(=O)O*)(F)F 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
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- C07F5/02—Boron compounds
- C07F5/04—Esters of boric acids
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- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/02—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes
- C08G61/10—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aromatic carbon atoms, e.g. polyphenylenes
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- C08G61/122—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides
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- C08G61/126—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds with a five-membered ring containing one sulfur atom in the ring
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- C08G2261/1426—Side-chains containing oxygen containing carboxy groups (COOH) and/or -C(=O)O-moieties
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- C08G2261/3223—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain non-condensed containing one or more sulfur atoms as the only heteroatom, e.g. thiophene
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- C08G2261/324—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain condensed
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- C08G2261/3424—Monomer units or repeat units incorporating structural elements in the main chain incorporating partially-aromatic structural elements in the main chain containing only carbon atoms non-conjugated, e.g. paracyclophanes or xylenes
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- C08G2261/30—Monomer units or repeat units incorporating structural elements in the main chain
- C08G2261/36—Oligomers, i.e. comprising up to 10 repeat units
- C08G2261/364—Oligomers, i.e. comprising up to 10 repeat units containing hetero atoms
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- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
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- C08G2261/411—Suzuki reactions
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- C08G2261/70—Post-treatment
- C08G2261/80—Functional group cleavage, e.g. removal of side-chains or protective groups
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- C08G2261/95—Use in organic luminescent diodes
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| JP2011284988A JP2012149245A (ja) | 2010-12-27 | 2011-12-27 | 反応性化合物及びそれを用いた高分子化合物の製造方法 |
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| JP2011284988A JP2012149245A (ja) | 2010-12-27 | 2011-12-27 | 反応性化合物及びそれを用いた高分子化合物の製造方法 |
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| WO (1) | WO2012090972A1 (fr) |
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| CN112661939B (zh) * | 2020-12-17 | 2024-05-31 | 广东聚华印刷显示技术有限公司 | 聚合物及其制备方法和应用 |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001515909A (ja) * | 1997-09-08 | 2001-09-25 | コモンウエルス サイエンティフィック アンド インダストリアル リサーチ オーガナイゼーション | ジボロン酸を使用する有機ボロン酸誘導体の製造方法 |
| JP2005232136A (ja) * | 2004-02-23 | 2005-09-02 | Asahi Kasei Corp | ポリアセン化合物前駆体及びポリアセン化合物の合成方法 |
| JP2007273938A (ja) * | 2005-09-06 | 2007-10-18 | Canon Inc | 半導体素子の製造方法 |
| JP2008505239A (ja) * | 2004-07-06 | 2008-02-21 | メルク パテント ゲーエムベーハー | エレクトロルミネセンスポリマー |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19806037A1 (de) * | 1998-02-13 | 1999-08-19 | Aventis Res & Tech Gmbh & Co | Triptycen-Polymere und -Copolymere |
| EP1165648B1 (fr) * | 1999-03-05 | 2007-08-15 | Cambridge Display Technology Limited | Preparation de polymere |
| US6638644B2 (en) * | 2001-08-28 | 2003-10-28 | Eastman Kodak Company | Electroluminescent devices having diarylanthracene polymers |
| JP3915757B2 (ja) * | 2003-08-14 | 2007-05-16 | ソニーケミカル＆インフォメーションデバイス株式会社 | エレクトロルミネスセンスポリマー、有機ｅｌ素子及びディスプレイ装置 |
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- 2011-12-20 WO PCT/JP2011/080139 patent/WO2012090972A1/fr active Application Filing
- 2011-12-23 TW TW100148256A patent/TW201237043A/zh unknown
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Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001515909A (ja) * | 1997-09-08 | 2001-09-25 | コモンウエルス サイエンティフィック アンド インダストリアル リサーチ オーガナイゼーション | ジボロン酸を使用する有機ボロン酸誘導体の製造方法 |
| JP2005232136A (ja) * | 2004-02-23 | 2005-09-02 | Asahi Kasei Corp | ポリアセン化合物前駆体及びポリアセン化合物の合成方法 |
| JP2008505239A (ja) * | 2004-07-06 | 2008-02-21 | メルク パテント ゲーエムベーハー | エレクトロルミネセンスポリマー |
| JP2007273938A (ja) * | 2005-09-06 | 2007-10-18 | Canon Inc | 半導体素子の製造方法 |
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| Title |
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| JPN6015042240; Ｐ．Ｈｏｄｇｅ， Ｇ．Ａ．Ｐｏｗｅｒ ａｎｄ Ｍ．Ａ．Ｒａｂｊｏｈｎｓ: 'Ｓｙｎｔｈｅｓｉｓ ｏｆ ｐｏｌｙ（ａｎｔｈｒａｃｅｎｅ-２，６-ｄｉｙｌ） ａｎｄ ａ ｃｏｐｏｌｙｍｅｒ ｃｏｎｔａｉｎｉｎｇ ａｌｔｅｒｎａｔｅｌｙ ａｎｔｈｒａｃｅｎｅ-２，６-ｄｉｙｌ ａｎ' Ｃｈｅｍｉｃａｌ Ｃｏｍｍｕｎｉｃａｔｉｏｎｓ Ｎｏ．１, 1997, ７３-７４ * |
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| WO2012090972A1 (fr) | 2012-07-05 |
| TW201237043A (en) | 2012-09-16 |
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