TWI842879B
Provided is a liquid crystal aligning agent in which there is little occurrence of after-images derived from residual DC voltage and AC after-images, which can be easily reworked and which can form a liquid crystal alignment film having high transmittance. This liquid crystal alignment agent is char...
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creator | NIITSU, SHINPEI BEPPU, KOICHIRO NAKAI, TAKASHI NAKAHARA, SHOICHIRO TOMOE, KOJI |
description | Provided is a liquid crystal aligning agent in which there is little occurrence of after-images derived from residual DC voltage and AC after-images, which can be easily reworked and which can form a liquid crystal alignment film having high transmittance. This liquid crystal alignment agent is characterized by containing a component (A) and a component (B). Component (A): A polymer (A) having a repeating unit represented by formula (1). Component (B): A polymer (B) having a repeating unit represented by formula (2) and a repeating unit represented by formula (3). (X1 is a tetravalent organic group; Y1 is a divalent organic group; X2 and X3 are each a tetravalent organic group derived from a tetravalent alicyclic tetracarboxylic acid dianhydride or alicyclic aliphatic tetracarboxylic acid dianhydride; R2 is a hydrogen atom or the like; Z21, Z22, Z31 and Z32 are hydrogen atoms or the like; Y3 is a divalent organic group having a partial structure represented by formula (n); R3 is a hydrogen atom or the like; Q |
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This liquid crystal alignment agent is characterized by containing a component (A) and a component (B). Component (A): A polymer (A) having a repeating unit represented by formula (1). Component (B): A polymer (B) having a repeating unit represented by formula (2) and a repeating unit represented by formula (3). (X1 is a tetravalent organic group; Y1 is a divalent organic group; X2 and X3 are each a tetravalent organic group derived from a tetravalent alicyclic tetracarboxylic acid dianhydride or alicyclic aliphatic tetracarboxylic acid dianhydride; R2 is a hydrogen atom or the like; Z21, Z22, Z31 and Z32 are hydrogen atoms or the like; Y3 is a divalent organic group having a partial structure represented by formula (n); R3 is a hydrogen atom or the like; Q</description><language>chi</language><subject>CHEMISTRY ; COMPOSITIONS BASED THEREON ; DEVICES OR ARRANGEMENTS, THE OPTICAL OPERATION OF WHICH ISMODIFIED BY CHANGING THE OPTICAL PROPERTIES OF THE MEDIUM OF THEDEVICES OR ARRANGEMENTS FOR THE CONTROL OF THE INTENSITY,COLOUR, PHASE, POLARISATION OR DIRECTION OF LIGHT, e.g.SWITCHING, GATING, MODULATING OR DEMODULATING ; FREQUENCY-CHANGING ; MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS ; METALLURGY ; NON-LINEAR OPTICS ; OPTICAL ANALOGUE/DIGITAL CONVERTERS ; OPTICAL LOGIC ELEMENTS ; OPTICS ; ORGANIC MACROMOLECULAR COMPOUNDS ; PHYSICS ; TECHNIQUES OR PROCEDURES FOR THE OPERATION THEREOF ; THEIR PREPARATION OR CHEMICAL WORKING-UP</subject><creationdate>2024</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20240521&DB=EPODOC&CC=TW&NR=I842879B$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76289</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20240521&DB=EPODOC&CC=TW&NR=I842879B$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>NIITSU, SHINPEI</creatorcontrib><creatorcontrib>BEPPU, KOICHIRO</creatorcontrib><creatorcontrib>NAKAI, TAKASHI</creatorcontrib><creatorcontrib>NAKAHARA, SHOICHIRO</creatorcontrib><creatorcontrib>TOMOE, KOJI</creatorcontrib><title>TWI842879B</title><description>Provided is a liquid crystal aligning agent in which there is little occurrence of after-images derived from residual DC voltage and AC after-images, which can be easily reworked and which can form a liquid crystal alignment film having high transmittance. This liquid crystal alignment agent is characterized by containing a component (A) and a component (B). Component (A): A polymer (A) having a repeating unit represented by formula (1). Component (B): A polymer (B) having a repeating unit represented by formula (2) and a repeating unit represented by formula (3). (X1 is a tetravalent organic group; Y1 is a divalent organic group; X2 and X3 are each a tetravalent organic group derived from a tetravalent alicyclic tetracarboxylic acid dianhydride or alicyclic aliphatic tetracarboxylic acid dianhydride; R2 is a hydrogen atom or the like; Z21, Z22, Z31 and Z32 are hydrogen atoms or the like; Y3 is a divalent organic group having a partial structure represented by formula (n); R3 is a hydrogen atom or the like; Q</description><subject>CHEMISTRY</subject><subject>COMPOSITIONS BASED THEREON</subject><subject>DEVICES OR ARRANGEMENTS, THE OPTICAL OPERATION OF WHICH ISMODIFIED BY CHANGING THE OPTICAL PROPERTIES OF THE MEDIUM OF THEDEVICES OR ARRANGEMENTS FOR THE CONTROL OF THE INTENSITY,COLOUR, PHASE, POLARISATION OR DIRECTION OF LIGHT, e.g.SWITCHING, GATING, MODULATING OR DEMODULATING</subject><subject>FREQUENCY-CHANGING</subject><subject>MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS</subject><subject>METALLURGY</subject><subject>NON-LINEAR OPTICS</subject><subject>OPTICAL ANALOGUE/DIGITAL CONVERTERS</subject><subject>OPTICAL LOGIC ELEMENTS</subject><subject>OPTICS</subject><subject>ORGANIC MACROMOLECULAR COMPOUNDS</subject><subject>PHYSICS</subject><subject>TECHNIQUES OR PROCEDURES FOR THE OPERATION THEREOF</subject><subject>THEIR PREPARATION OR CHEMICAL WORKING-UP</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2024</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZOAKCfe0MDGyMLd04mFgTUvMKU7lhdLcDApuriHOHrqpBfnxqcUFicmpeakl8QgNTsZEKAEAEG4bow</recordid><startdate>20240521</startdate><enddate>20240521</enddate><creator>NIITSU, SHINPEI</creator><creator>BEPPU, KOICHIRO</creator><creator>NAKAI, TAKASHI</creator><creator>NAKAHARA, SHOICHIRO</creator><creator>TOMOE, KOJI</creator><scope>EVB</scope></search><sort><creationdate>20240521</creationdate><title>TWI842879B</title><author>NIITSU, SHINPEI ; BEPPU, KOICHIRO ; NAKAI, TAKASHI ; NAKAHARA, SHOICHIRO ; TOMOE, KOJI</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_TWI842879BB3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>chi</language><creationdate>2024</creationdate><topic>CHEMISTRY</topic><topic>COMPOSITIONS BASED THEREON</topic><topic>DEVICES OR ARRANGEMENTS, THE OPTICAL OPERATION OF WHICH ISMODIFIED BY CHANGING THE OPTICAL PROPERTIES OF THE MEDIUM OF THEDEVICES OR ARRANGEMENTS FOR THE CONTROL OF THE INTENSITY,COLOUR, PHASE, POLARISATION OR DIRECTION OF LIGHT, e.g.SWITCHING, GATING, MODULATING OR DEMODULATING</topic><topic>FREQUENCY-CHANGING</topic><topic>MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS</topic><topic>METALLURGY</topic><topic>NON-LINEAR OPTICS</topic><topic>OPTICAL ANALOGUE/DIGITAL CONVERTERS</topic><topic>OPTICAL LOGIC ELEMENTS</topic><topic>OPTICS</topic><topic>ORGANIC MACROMOLECULAR COMPOUNDS</topic><topic>PHYSICS</topic><topic>TECHNIQUES OR PROCEDURES FOR THE OPERATION THEREOF</topic><topic>THEIR PREPARATION OR CHEMICAL WORKING-UP</topic><toplevel>online_resources</toplevel><creatorcontrib>NIITSU, SHINPEI</creatorcontrib><creatorcontrib>BEPPU, KOICHIRO</creatorcontrib><creatorcontrib>NAKAI, TAKASHI</creatorcontrib><creatorcontrib>NAKAHARA, SHOICHIRO</creatorcontrib><creatorcontrib>TOMOE, KOJI</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>NIITSU, SHINPEI</au><au>BEPPU, KOICHIRO</au><au>NAKAI, TAKASHI</au><au>NAKAHARA, SHOICHIRO</au><au>TOMOE, KOJI</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>TWI842879B</title><date>2024-05-21</date><risdate>2024</risdate><abstract>Provided is a liquid crystal aligning agent in which there is little occurrence of after-images derived from residual DC voltage and AC after-images, which can be easily reworked and which can form a liquid crystal alignment film having high transmittance. This liquid crystal alignment agent is characterized by containing a component (A) and a component (B). Component (A): A polymer (A) having a repeating unit represented by formula (1). Component (B): A polymer (B) having a repeating unit represented by formula (2) and a repeating unit represented by formula (3). (X1 is a tetravalent organic group; Y1 is a divalent organic group; X2 and X3 are each a tetravalent organic group derived from a tetravalent alicyclic tetracarboxylic acid dianhydride or alicyclic aliphatic tetracarboxylic acid dianhydride; R2 is a hydrogen atom or the like; Z21, Z22, Z31 and Z32 are hydrogen atoms or the like; Y3 is a divalent organic group having a partial structure represented by formula (n); R3 is a hydrogen atom or the like; Q</abstract><oa>free_for_read</oa></addata></record> |
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subjects | CHEMISTRY COMPOSITIONS BASED THEREON DEVICES OR ARRANGEMENTS, THE OPTICAL OPERATION OF WHICH ISMODIFIED BY CHANGING THE OPTICAL PROPERTIES OF THE MEDIUM OF THEDEVICES OR ARRANGEMENTS FOR THE CONTROL OF THE INTENSITY,COLOUR, PHASE, POLARISATION OR DIRECTION OF LIGHT, e.g.SWITCHING, GATING, MODULATING OR DEMODULATING FREQUENCY-CHANGING MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS METALLURGY NON-LINEAR OPTICS OPTICAL ANALOGUE/DIGITAL CONVERTERS OPTICAL LOGIC ELEMENTS OPTICS ORGANIC MACROMOLECULAR COMPOUNDS PHYSICS TECHNIQUES OR PROCEDURES FOR THE OPERATION THEREOF THEIR PREPARATION OR CHEMICAL WORKING-UP |
title | TWI842879B |
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