JP4786104B2 - 側鎖の光架橋性基を有する光活性ポリイミド、ポリアミド酸又はエステル - Google Patents
側鎖の光架橋性基を有する光活性ポリイミド、ポリアミド酸又はエステル Download PDFInfo
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- JP4786104B2 JP4786104B2 JP2001553849A JP2001553849A JP4786104B2 JP 4786104 B2 JP4786104 B2 JP 4786104B2 JP 2001553849 A JP2001553849 A JP 2001553849A JP 2001553849 A JP2001553849 A JP 2001553849A JP 4786104 B2 JP4786104 B2 JP 4786104B2
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- UENRXLSRMCSUSN-UHFFFAOYSA-N 3,5-diaminobenzoic acid Chemical compound NC1=CC(N)=CC(C(O)=O)=C1 UENRXLSRMCSUSN-UHFFFAOYSA-N 0.000 description 3
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- 238000004528 spin coating Methods 0.000 description 3
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- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 description 2
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- AUJXJFHANFIVKH-UHFFFAOYSA-N methyl cis-ferulate Natural products COC(=O)C=CC1=CC=C(O)C(OC)=C1 AUJXJFHANFIVKH-UHFFFAOYSA-N 0.000 description 1
- CLCWCGOCHZSFQE-UHFFFAOYSA-N n,n-bis(oxiran-2-ylmethyl)cyclohexanamine Chemical compound C1OC1CN(C1CCCCC1)CC1CO1 CLCWCGOCHZSFQE-UHFFFAOYSA-N 0.000 description 1
- KQSABULTKYLFEV-UHFFFAOYSA-N naphthalene-1,5-diamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1N KQSABULTKYLFEV-UHFFFAOYSA-N 0.000 description 1
- DOBFTMLCEYUAQC-UHFFFAOYSA-N naphthalene-2,3,6,7-tetracarboxylic acid Chemical compound OC(=O)C1=C(C(O)=O)C=C2C=C(C(O)=O)C(C(=O)O)=CC2=C1 DOBFTMLCEYUAQC-UHFFFAOYSA-N 0.000 description 1
- YTVNOVQHSGMMOV-UHFFFAOYSA-N naphthalenetetracarboxylic dianhydride Chemical compound C1=CC(C(=O)OC2=O)=C3C2=CC=C2C(=O)OC(=O)C1=C32 YTVNOVQHSGMMOV-UHFFFAOYSA-N 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 150000002829 nitrogen Chemical group 0.000 description 1
- SXJVFQLYZSNZBT-UHFFFAOYSA-N nonane-1,9-diamine Chemical compound NCCCCCCCCCN SXJVFQLYZSNZBT-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000007645 offset printing Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000004043 oxo group Chemical group O=* 0.000 description 1
- UFOIOXZLTXNHQH-UHFFFAOYSA-N oxolane-2,3,4,5-tetracarboxylic acid Chemical compound OC(=O)C1OC(C(O)=O)C(C(O)=O)C1C(O)=O UFOIOXZLTXNHQH-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- FZUGPQWGEGAKET-UHFFFAOYSA-N parbenate Chemical compound CCOC(=O)C1=CC=C(N(C)C)C=C1 FZUGPQWGEGAKET-UHFFFAOYSA-N 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 125000004675 pentylcarbonyl group Chemical group C(CCCC)C(=O)* 0.000 description 1
- 125000001148 pentyloxycarbonyl group Chemical group 0.000 description 1
- 125000005981 pentynyl group Chemical group 0.000 description 1
- 125000005003 perfluorobutyl group Chemical group FC(F)(F)C(F)(F)C(F)(F)C(F)(F)* 0.000 description 1
- 125000005007 perfluorooctyl group Chemical group FC(C(C(C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)* 0.000 description 1
- 125000005009 perfluoropropyl group Chemical group FC(C(C(F)(F)F)(F)F)(F)* 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- CLNCMEVPMGQWTB-UHFFFAOYSA-N propan-2-yl 3,5-diaminobenzoate Chemical compound CC(C)OC(=O)C1=CC(N)=CC(N)=C1 CLNCMEVPMGQWTB-UHFFFAOYSA-N 0.000 description 1
- WYVAMUWZEOHJOQ-UHFFFAOYSA-N propionic anhydride Chemical compound CCC(=O)OC(=O)CC WYVAMUWZEOHJOQ-UHFFFAOYSA-N 0.000 description 1
- 125000004673 propylcarbonyl group Chemical group 0.000 description 1
- 125000004742 propyloxycarbonyl group Chemical group 0.000 description 1
- 125000002568 propynyl group Chemical group [*]C#CC([H])([H])[H] 0.000 description 1
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 125000006413 ring segment Chemical group 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000005930 sec-butyloxycarbonyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(OC(*)=O)C([H])([H])[H] 0.000 description 1
- 239000005266 side chain polymer Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- GFYHSKONPJXCDE-UHFFFAOYSA-N sym-collidine Natural products CC1=CN=C(C)C(C)=C1 GFYHSKONPJXCDE-UHFFFAOYSA-N 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- DPKBAXPHAYBPRL-UHFFFAOYSA-M tetrabutylazanium;iodide Chemical compound [I-].CCCC[N+](CCCC)(CCCC)CCCC DPKBAXPHAYBPRL-UHFFFAOYSA-M 0.000 description 1
- 125000005329 tetralinyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- 125000005409 triarylsulfonium group Chemical group 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- KLNPWTHGTVSSEU-UHFFFAOYSA-N undecane-1,11-diamine Chemical compound NCCCCCCCCCCCN KLNPWTHGTVSSEU-UHFFFAOYSA-N 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 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
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
Classifications
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- 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
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/48—Polymers modified by chemical after-treatment
-
- 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
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/10—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
- C08G73/1003—Preparatory processes
- C08G73/1007—Preparatory processes from tetracarboxylic acids or derivatives and diamines
- C08G73/1025—Preparatory processes from tetracarboxylic acids or derivatives and diamines polymerised by radiations
-
- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
- G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
- G02F1/1333—Constructional arrangements; Manufacturing methods
- G02F1/1337—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers
- G02F1/133711—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers by organic films, e.g. polymeric films
- G02F1/133723—Polyimide, polyamide-imide
-
- 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
- C09K2323/00—Functional layers of liquid crystal optical display excluding electroactive liquid crystal layer characterised by chemical composition
- C09K2323/02—Alignment layer characterised by chemical composition
-
- 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
- C09K2323/00—Functional layers of liquid crystal optical display excluding electroactive liquid crystal layer characterised by chemical composition
- C09K2323/02—Alignment layer characterised by chemical composition
- C09K2323/027—Polyimide
-
- 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
- C09K2323/00—Functional layers of liquid crystal optical display excluding electroactive liquid crystal layer characterised by chemical composition
- C09K2323/02—Alignment layer characterised by chemical composition
- C09K2323/027—Polyimide
- C09K2323/0271—Polyimidfluoride
-
- 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
- C09K2323/00—Functional layers of liquid crystal optical display excluding electroactive liquid crystal layer characterised by chemical composition
- C09K2323/03—Viewing layer characterised by chemical composition
-
- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
- G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
- G02F1/1333—Constructional arrangements; Manufacturing methods
- G02F1/1337—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers
- G02F1/13378—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers by treatment of the surface, e.g. embossing, rubbing or light irradiation
- G02F1/133788—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers by treatment of the surface, e.g. embossing, rubbing or light irradiation by light irradiation, e.g. linearly polarised light photo-polymerisation
-
- 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]
- Y10T428/31721—Of polyimide
Landscapes
- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Nonlinear Science (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Mathematical Physics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- General Chemical & Material Sciences (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Polyamides (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Liquid Crystal (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0001543.8 | 2000-01-24 | ||
| GB0001543A GB0001543D0 (en) | 2000-01-24 | 2000-01-24 | Photoactive polymers |
| GB0005383A GB0005383D0 (en) | 2000-03-06 | 2000-03-06 | Photoactive polymers |
| GB0005383.5 | 2000-03-06 | ||
| PCT/CH2001/000044 WO2001053384A1 (en) | 2000-01-24 | 2001-01-22 | Photoactive polyimides, polyamide acids or esters with side chain photocrosslinkable groups |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2003520878A JP2003520878A (ja) | 2003-07-08 |
| JP2003520878A5 JP2003520878A5 (enExample) | 2008-02-07 |
| JP4786104B2 true JP4786104B2 (ja) | 2011-10-05 |
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| JP2001553849A Expired - Fee Related JP4786104B2 (ja) | 2000-01-24 | 2001-01-22 | 側鎖の光架橋性基を有する光活性ポリイミド、ポリアミド酸又はエステル |
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| Country | Link |
|---|---|
| US (1) | US6831148B2 (enExample) |
| EP (1) | EP1261659B1 (enExample) |
| JP (1) | JP4786104B2 (enExample) |
| KR (1) | KR100663661B1 (enExample) |
| CN (1) | CN1152906C (enExample) |
| AT (1) | ATE278731T1 (enExample) |
| AU (1) | AU2001224973A1 (enExample) |
| DE (1) | DE60106213T2 (enExample) |
| HK (1) | HK1048644B (enExample) |
| TW (1) | TW552282B (enExample) |
| WO (1) | WO2001053384A1 (enExample) |
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| JP4513191B2 (ja) * | 2000-08-30 | 2010-07-28 | チッソ株式会社 | ポリアミド酸、ポリイミド、該ポリイミド膜を用いた液晶配向膜、および該配向膜を用いた液晶表示素子 |
| EP1326138B1 (en) * | 2000-09-12 | 2014-11-05 | PI R & D Co., Ltd. | Negative photosensitive polyimide composition and method of forming image from the same |
| KR100673265B1 (ko) * | 2000-10-04 | 2007-01-22 | 엘지.필립스 엘시디 주식회사 | 액정표시장치 |
| EP1229066A1 (en) * | 2001-02-05 | 2002-08-07 | Rolic AG | Photoactive polymer |
| EP1277770A1 (en) * | 2001-07-17 | 2003-01-22 | Rolic AG | Photoactive materials |
| EP1353217A1 (en) | 2002-03-29 | 2003-10-15 | JSR Corporation | Optical alignment method and liquid crystal display element |
| US6900271B2 (en) | 2002-05-31 | 2005-05-31 | Elsicon, Inc | Hybrid polymer materials for liquid crystal alignment layers |
| WO2003102045A1 (en) | 2002-05-31 | 2003-12-11 | Elsicon, Inc. | Hybrid polymer materials for liquid crystal alignment layers |
| US6919404B2 (en) | 2002-05-31 | 2005-07-19 | Elsicon, Inc. | Hybrid polymer materials for liquid crystal alignment layers |
| EP1386910A1 (en) | 2002-07-30 | 2004-02-04 | Rolic AG | Photoactive materials |
| KR20040046229A (ko) * | 2002-11-26 | 2004-06-05 | 한국화학연구원 | 감광성 투명 폴리아믹산 유도체와 폴리이미드계 수지 |
| WO2005014677A1 (en) * | 2003-07-16 | 2005-02-17 | Rolic Ag | Polymerizable copolymers for alignment layers |
| KR100562524B1 (ko) * | 2003-10-21 | 2006-03-23 | 한국화학연구원 | 평탄화 특성이 우수한 감광성 투명 폴리아믹산 올리고머와이를 경화하여 제조된 폴리이미드 수지 |
| KR100552990B1 (ko) * | 2004-02-12 | 2006-02-17 | 한국화학연구원 | 전유기 박막트랜지스터 절연체용 저온경화형 감광성폴리이미드 수지 |
| WO2005096041A1 (ja) * | 2004-03-30 | 2005-10-13 | National Institute Of Advanced Industrial Science And Technology | マイクロパターン位相差素子 |
| CN101040028B (zh) * | 2004-10-13 | 2012-03-28 | 罗利克有限公司 | 光可交联材料 |
| EP1764405A1 (en) | 2005-09-20 | 2007-03-21 | Rolic AG | Functionalized photoreactive compounds |
| EP2305631A1 (en) * | 2005-12-23 | 2011-04-06 | Rolic AG | Photocrosslinkable materials |
| EP1860094A1 (en) * | 2006-05-23 | 2007-11-28 | Rolic AG | Photocrosslinkable materials |
| EP1801097A1 (en) * | 2005-12-23 | 2007-06-27 | Rolic AG | Photocrosslinkable materials |
| TWI358006B (en) * | 2006-09-11 | 2012-02-11 | Jsr Corp | Liquid crystal alignment agent and liquid crystal |
| JP4995267B2 (ja) | 2007-03-26 | 2012-08-08 | シャープ株式会社 | 液晶表示装置及び配向膜材料用重合体 |
| US20110065859A1 (en) * | 2007-05-02 | 2011-03-17 | Rolic Ag | Thermally stable alignment materials |
| EP2152660B1 (en) * | 2007-05-25 | 2016-05-11 | Rolic AG | Photocrosslinkable materials comprising alicyclic group |
| JP4458305B2 (ja) | 2007-08-21 | 2010-04-28 | Ｊｓｒ株式会社 | 液晶配向剤、液晶配向膜の製造方法および液晶表示素子 |
| EP2182406B1 (en) | 2007-08-21 | 2013-10-16 | JSR Corporation | Liquid crystal aligning agent, method for forming liquid crystal alignment film, and liquid crystal display device |
| KR100970831B1 (ko) | 2007-08-21 | 2010-07-16 | 제이에스알 가부시끼가이샤 | 액정 배향제, 액정 배향막의 제조 방법 및 액정 표시 소자 |
| KR101443216B1 (ko) * | 2007-09-05 | 2014-09-24 | 삼성전자주식회사 | 광 반응성 재료를 이용한 유기발광소자 및 그 제조 방법 |
| US9499649B2 (en) | 2007-12-21 | 2016-11-22 | Rolic Ag | Functionalized photoreactive compounds |
| CN105733606B (zh) | 2007-12-21 | 2018-04-03 | 罗利克有限公司 | 光校准组合物 |
| CN102077134B (zh) * | 2008-06-27 | 2013-11-27 | 夏普株式会社 | 液晶显示装置及其制造方法 |
| KR20110055637A (ko) * | 2008-09-03 | 2011-05-25 | 샤프 가부시키가이샤 | 배향막, 배향막 재료 및 배향막을 갖는 액정 표시 장치, 및 그 제조 방법 |
| RU2011126145A (ru) * | 2008-11-27 | 2013-01-10 | Шарп Кабусики Кайся | Ориентирующая пленка, жидкокристаллический дисплей, имеющий ориентирующую пленку, и способ получения ориентирующей пленки |
| KR101541018B1 (ko) * | 2008-12-08 | 2015-07-31 | 삼성디스플레이 주식회사 | 광배향 화합물, 광배향 조성물, 배향막을 포함하는 표시 기판 및 이의 제조 방법 |
| JP5630013B2 (ja) * | 2009-01-30 | 2014-11-26 | ソニー株式会社 | 液晶表示装置の製造方法 |
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- 2001-01-22 CN CNB018040470A patent/CN1152906C/zh not_active Expired - Lifetime
- 2001-01-22 WO PCT/CH2001/000044 patent/WO2001053384A1/en not_active Ceased
- 2001-01-22 EP EP01900356A patent/EP1261659B1/en not_active Expired - Lifetime
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- 2001-01-22 US US10/181,265 patent/US6831148B2/en not_active Expired - Lifetime
- 2001-01-22 AU AU2001224973A patent/AU2001224973A1/en not_active Abandoned
- 2001-01-22 KR KR1020027009486A patent/KR100663661B1/ko not_active Expired - Fee Related
- 2001-01-22 DE DE2001606213 patent/DE60106213T2/de not_active Expired - Lifetime
- 2001-01-22 AT AT01900356T patent/ATE278731T1/de not_active IP Right Cessation
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Also Published As
| Publication number | Publication date |
|---|---|
| TW552282B (en) | 2003-09-11 |
| HK1048644B (en) | 2005-03-18 |
| DE60106213D1 (de) | 2004-11-11 |
| KR100663661B1 (ko) | 2007-01-03 |
| WO2001053384A1 (en) | 2001-07-26 |
| KR20020069019A (ko) | 2002-08-28 |
| US20030039768A1 (en) | 2003-02-27 |
| CN1152906C (zh) | 2004-06-09 |
| EP1261659B1 (en) | 2004-10-06 |
| ATE278731T1 (de) | 2004-10-15 |
| US6831148B2 (en) | 2004-12-14 |
| AU2001224973A1 (en) | 2001-07-31 |
| EP1261659A1 (en) | 2002-12-04 |
| JP2003520878A (ja) | 2003-07-08 |
| CN1395593A (zh) | 2003-02-05 |
| HK1048644A1 (en) | 2003-04-11 |
| DE60106213T2 (de) | 2006-03-02 |
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