KR102604339B1 - 액정 배향제, 액정 배향막, 및 액정 표시 소자 - Google Patents
액정 배향제, 액정 배향막, 및 액정 표시 소자 Download PDFInfo
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- KR102604339B1 KR102604339B1 KR1020197021828A KR20197021828A KR102604339B1 KR 102604339 B1 KR102604339 B1 KR 102604339B1 KR 1020197021828 A KR1020197021828 A KR 1020197021828A KR 20197021828 A KR20197021828 A KR 20197021828A KR 102604339 B1 KR102604339 B1 KR 102604339B1
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Classifications
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- 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
- C09K19/00—Liquid crystal materials
- C09K19/52—Liquid crystal materials characterised by components which are not liquid crystals, e.g. additives with special physical aspect: solvents, solid particles
- C09K19/54—Additives having no specific mesophase characterised by their chemical composition
- C09K19/56—Aligning agents
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
- C08J3/09—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in organic liquids
- C08J3/091—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in organic liquids characterised by the chemical constitution of the organic liquid
- C08J3/095—Oxygen containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L79/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen or carbon only, not provided for in groups C08L61/00 - C08L77/00
- C08L79/04—Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors
- C08L79/08—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
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- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2379/00—Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen, or carbon only, not provided for in groups C08J2361/00 - C08J2377/00
- C08J2379/04—Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors
- C08J2379/08—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
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- Physics & Mathematics (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
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- Health & Medical Sciences (AREA)
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- Optics & Photonics (AREA)
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- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Liquid Crystal (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Compositions Of Macromolecular Compounds (AREA)
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PCT/JP2017/046854 WO2018124167A1 (ja) | 2016-12-28 | 2017-12-27 | 液晶配向剤、液晶配向膜、及び液晶表示素子 |
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CN117280277A (zh) | 2021-05-06 | 2023-12-22 | 日产化学株式会社 | 液晶取向剂、液晶取向膜以及液晶显示元件 |
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JP2011237755A (ja) * | 2009-09-18 | 2011-11-24 | Jnc Corp | 液晶配向剤、液晶配向膜、液晶配向膜の製造方法および液晶表示素子 |
CN106167709A (zh) * | 2015-05-22 | 2016-11-30 | 奇美实业股份有限公司 | 液晶配向剂及其应用 |
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JP5057074B2 (ja) * | 2008-02-21 | 2012-10-24 | Jsr株式会社 | 液晶配向剤および液晶表示素子 |
JP5699543B2 (ja) * | 2010-11-02 | 2015-04-15 | Jsr株式会社 | 液晶配向剤、液晶配向膜及び液晶表示素子 |
JP5874646B2 (ja) * | 2010-12-28 | 2016-03-02 | 日産化学工業株式会社 | 液晶配向処理剤、液晶配向膜および液晶表示素子 |
KR101878522B1 (ko) | 2011-03-07 | 2018-07-13 | 닛산 가가쿠 고교 가부시키 가이샤 | 조성물, 액정 배향 처리제, 액정 배향막, 및 액정 표시 소자 |
WO2013157463A1 (ja) * | 2012-04-16 | 2013-10-24 | Jnc株式会社 | 光配向用液晶配向膜を形成するための液晶配向剤、液晶配向膜およびこれを用いた液晶表示素子 |
JP6146077B2 (ja) * | 2012-06-29 | 2017-06-14 | Jsr株式会社 | 液晶配向膜の製造方法 |
TWI605091B (zh) * | 2012-08-29 | 2017-11-11 | Nissan Chemical Ind Ltd | Liquid crystal alignment agent, liquid crystal alignment film and liquid crystal display element |
JP6127721B2 (ja) * | 2012-09-14 | 2017-05-17 | Jsr株式会社 | 液晶配向剤、液晶配向膜及び液晶表示素子 |
TWI649411B (zh) * | 2013-02-01 | 2019-02-01 | 日產化學工業股份有限公司 | Liquid crystal alignment treatment agent, liquid crystal alignment film, and liquid crystal display element |
BR112015018967A2 (pt) | 2013-02-08 | 2017-07-18 | 3M Innovative Properties Co | construção óptica |
WO2014133042A1 (ja) * | 2013-02-28 | 2014-09-04 | 日産化学工業株式会社 | 重合体、液晶配向処理剤、液晶配向膜および液晶表示素子 |
KR102159410B1 (ko) * | 2013-03-14 | 2020-09-23 | 제이엔씨 주식회사 | 액정 배향제 및 액정 표시 소자 |
KR102135493B1 (ko) * | 2013-05-01 | 2020-08-26 | 닛산 가가쿠 가부시키가이샤 | 액정 배향 처리제, 액정 배향막 및 액정 표시 소자 |
WO2014178406A1 (ja) * | 2013-05-01 | 2014-11-06 | 日産化学工業株式会社 | 液晶配向処理剤、液晶配向膜及び液晶表示素子 |
JP6597307B2 (ja) * | 2013-10-23 | 2019-10-30 | 日産化学株式会社 | 液晶配向剤、液晶配向膜、及び液晶表示素子 |
CN107077031B (zh) * | 2014-11-21 | 2020-11-06 | Jnc株式会社 | 包含聚酰胺酸或其衍生物的液晶取向剂、液晶取向膜和液晶显示元件 |
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Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2011237755A (ja) * | 2009-09-18 | 2011-11-24 | Jnc Corp | 液晶配向剤、液晶配向膜、液晶配向膜の製造方法および液晶表示素子 |
CN106167709A (zh) * | 2015-05-22 | 2016-11-30 | 奇美实业股份有限公司 | 液晶配向剂及其应用 |
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