TWI425047B - 可聚合型配向組成物,以此組成物製得之配向層,配向層之製造方法、包含其之光學膜及顯示裝置 - Google Patents
可聚合型配向組成物,以此組成物製得之配向層,配向層之製造方法、包含其之光學膜及顯示裝置 Download PDFInfo
- Publication number
- TWI425047B TWI425047B TW099111051A TW99111051A TWI425047B TW I425047 B TWI425047 B TW I425047B TW 099111051 A TW099111051 A TW 099111051A TW 99111051 A TW99111051 A TW 99111051A TW I425047 B TWI425047 B TW I425047B
- Authority
- TW
- Taiwan
- Prior art keywords
- liquid crystal
- alignment layer
- group
- alignment
- optical film
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 103
- 239000012788 optical film Substances 0.000 title claims description 82
- 238000000034 method Methods 0.000 title description 32
- 239000004973 liquid crystal related substance Substances 0.000 claims description 266
- 239000000758 substrate Substances 0.000 claims description 67
- 239000002904 solvent Substances 0.000 claims description 43
- -1 amine compound Chemical class 0.000 claims description 31
- 239000007822 coupling agent Substances 0.000 claims description 30
- 238000000576 coating method Methods 0.000 claims description 21
- 239000011347 resin Substances 0.000 claims description 18
- 229920005989 resin Polymers 0.000 claims description 18
- 239000011230 binding agent Substances 0.000 claims description 16
- 125000002947 alkylene group Chemical group 0.000 claims description 15
- 150000001412 amines Chemical class 0.000 claims description 15
- 239000011248 coating agent Substances 0.000 claims description 10
- 150000003335 secondary amines Chemical class 0.000 claims description 10
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 6
- 125000002993 cycloalkylene group Chemical group 0.000 claims description 6
- 229920000728 polyester Polymers 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 125000002924 primary amino group Chemical class [H]N([H])* 0.000 claims description 5
- 239000012956 1-hydroxycyclohexylphenyl-ketone Substances 0.000 claims description 4
- MQDJYUACMFCOFT-UHFFFAOYSA-N bis[2-(1-hydroxycyclohexyl)phenyl]methanone Chemical compound C=1C=CC=C(C(=O)C=2C(=CC=CC=2)C2(O)CCCCC2)C=1C1(O)CCCCC1 MQDJYUACMFCOFT-UHFFFAOYSA-N 0.000 claims description 4
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- LANMLKBTRDDCOD-UHFFFAOYSA-N 1-[diethoxy(propyl)silyl]oxy-n-methylethanamine Chemical compound CCC[Si](OCC)(OCC)OC(C)NC LANMLKBTRDDCOD-UHFFFAOYSA-N 0.000 claims description 3
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical group OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 claims description 3
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 3
- ZCZFEIZSYJAXKS-UHFFFAOYSA-N [3-hydroxy-2,2-bis(hydroxymethyl)propyl] prop-2-enoate Chemical compound OCC(CO)(CO)COC(=O)C=C ZCZFEIZSYJAXKS-UHFFFAOYSA-N 0.000 claims description 3
- 125000003282 alkyl amino group Chemical group 0.000 claims description 3
- VFHVQBAGLAREND-UHFFFAOYSA-N diphenylphosphoryl-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C)=C1C(=O)P(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 VFHVQBAGLAREND-UHFFFAOYSA-N 0.000 claims description 3
- 229920000570 polyether Polymers 0.000 claims description 3
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 claims description 2
- FDSUVTROAWLVJA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol;prop-2-enoic acid Chemical compound OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OCC(CO)(CO)COCC(CO)(CO)CO FDSUVTROAWLVJA-UHFFFAOYSA-N 0.000 claims description 2
- QZPSOSOOLFHYRR-UHFFFAOYSA-N 3-hydroxypropyl prop-2-enoate Chemical compound OCCCOC(=O)C=C QZPSOSOOLFHYRR-UHFFFAOYSA-N 0.000 claims description 2
- TZZGHGKTHXIOMN-UHFFFAOYSA-N 3-trimethoxysilyl-n-(3-trimethoxysilylpropyl)propan-1-amine Chemical compound CO[Si](OC)(OC)CCCNCCC[Si](OC)(OC)OC TZZGHGKTHXIOMN-UHFFFAOYSA-N 0.000 claims description 2
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 claims description 2
- 239000002202 Polyethylene glycol Substances 0.000 claims description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims description 2
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 claims description 2
- CQHKDHVZYZUZMJ-UHFFFAOYSA-N [2,2-bis(hydroxymethyl)-3-prop-2-enoyloxypropyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(CO)COC(=O)C=C CQHKDHVZYZUZMJ-UHFFFAOYSA-N 0.000 claims description 2
- HVVWZTWDBSEWIH-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(COC(=O)C=C)COC(=O)C=C HVVWZTWDBSEWIH-UHFFFAOYSA-N 0.000 claims description 2
- 125000003277 amino group Chemical group 0.000 claims description 2
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 claims description 2
- 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 claims description 2
- 229920001223 polyethylene glycol Polymers 0.000 claims description 2
- KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 claims description 2
- XFCMNSHQOZQILR-UHFFFAOYSA-N 2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOC(=O)C(C)=C XFCMNSHQOZQILR-UHFFFAOYSA-N 0.000 claims 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims 2
- KFOZMMAXUUCIKU-UHFFFAOYSA-N n-(3-triethoxysilylpropyl)butan-1-amine Chemical compound CCCCNCCC[Si](OCC)(OCC)OCC KFOZMMAXUUCIKU-UHFFFAOYSA-N 0.000 claims 1
- DVYVMJLSUSGYMH-UHFFFAOYSA-N n-methyl-3-trimethoxysilylpropan-1-amine Chemical compound CNCCC[Si](OC)(OC)OC DVYVMJLSUSGYMH-UHFFFAOYSA-N 0.000 claims 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 claims 1
- 239000010410 layer Substances 0.000 description 245
- 239000010408 film Substances 0.000 description 57
- 238000002360 preparation method Methods 0.000 description 39
- 239000000243 solution Substances 0.000 description 30
- 238000001035 drying Methods 0.000 description 14
- 239000000178 monomer Substances 0.000 description 14
- 230000003287 optical effect Effects 0.000 description 13
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 11
- 230000007547 defect Effects 0.000 description 11
- 239000004094 surface-active agent Substances 0.000 description 11
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 9
- 239000004033 plastic Substances 0.000 description 9
- 229920003023 plastic Polymers 0.000 description 9
- 239000000463 material Substances 0.000 description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 7
- 238000001723 curing Methods 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 5
- 239000011259 mixed solution Substances 0.000 description 5
- 230000000704 physical effect Effects 0.000 description 5
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 5
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 4
- VATRWWPJWVCZTA-UHFFFAOYSA-N 3-oxo-n-[2-(trifluoromethyl)phenyl]butanamide Chemical compound CC(=O)CC(=O)NC1=CC=CC=C1C(F)(F)F VATRWWPJWVCZTA-UHFFFAOYSA-N 0.000 description 4
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- 230000002411 adverse Effects 0.000 description 4
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 4
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 4
- BGTOWKSIORTVQH-UHFFFAOYSA-N cyclopentanone Chemical compound O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 0.000 description 4
- 238000007756 gravure coating Methods 0.000 description 4
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 4
- 229910052753 mercury Inorganic materials 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 4
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 4
- ABDKAPXRBAPSQN-UHFFFAOYSA-N veratrole Chemical compound COC1=CC=CC=C1OC ABDKAPXRBAPSQN-UHFFFAOYSA-N 0.000 description 4
- QNODIIQQMGDSEF-UHFFFAOYSA-N (1-hydroxycyclohexyl)-phenylmethanone Chemical compound C=1C=CC=CC=1C(=O)C1(O)CCCCC1 QNODIIQQMGDSEF-UHFFFAOYSA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- 239000004322 Butylated hydroxytoluene Substances 0.000 description 3
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 3
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 3
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 150000003141 primary amines Chemical class 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
- KWVGIHKZDCUPEU-UHFFFAOYSA-N 2,2-dimethoxy-2-phenylacetophenone Chemical compound C=1C=CC=CC=1C(OC)(OC)C(=O)C1=CC=CC=C1 KWVGIHKZDCUPEU-UHFFFAOYSA-N 0.000 description 2
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 2
- LWRBVKNFOYUCNP-UHFFFAOYSA-N 2-methyl-1-(4-methylsulfanylphenyl)-2-morpholin-4-ylpropan-1-one Chemical compound C1=CC(SC)=CC=C1C(=O)C(C)(C)N1CCOCC1 LWRBVKNFOYUCNP-UHFFFAOYSA-N 0.000 description 2
- PZLZYIGQAMXMGH-UHFFFAOYSA-N 2-methyl-1-[4-(2-methyl-1H-inden-1-yl)phenyl]-2-morpholin-4-ylpropan-1-one Chemical compound CC(C(=O)C1=CC=C(C=C1)C1C(=CC2=CC=CC=C12)C)(C)N1CCOCC1 PZLZYIGQAMXMGH-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 2
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- 238000003848 UV Light-Curing Methods 0.000 description 2
- 229960005164 acesulfame Drugs 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- 235000006708 antioxidants Nutrition 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 229940095259 butylated hydroxytoluene Drugs 0.000 description 2
- 235000012000 cholesterol Nutrition 0.000 description 2
- 238000003851 corona treatment Methods 0.000 description 2
- VEVZSMAEJFVWIL-UHFFFAOYSA-O cyanidin Natural products [O+]=1C2=CC(O)=CC(O)=C2C=C(O)C=1C1=CC=C(O)C(O)=C1 VEVZSMAEJFVWIL-UHFFFAOYSA-O 0.000 description 2
- 235000007336 cyanidin Nutrition 0.000 description 2
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 150000008282 halocarbons Chemical class 0.000 description 2
- 238000007603 infrared drying Methods 0.000 description 2
- 229910001507 metal halide Inorganic materials 0.000 description 2
- 150000005309 metal halides Chemical class 0.000 description 2
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 238000000016 photochemical curing Methods 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 238000003847 radiation curing Methods 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 239000011342 resin composition Substances 0.000 description 2
- 238000004528 spin coating Methods 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 238000001029 thermal curing Methods 0.000 description 2
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical compound C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 1
- REPVLJRCJUVQFA-UHFFFAOYSA-N (-)-isopinocampheol Natural products C1C(O)C(C)C2C(C)(C)C1C2 REPVLJRCJUVQFA-UHFFFAOYSA-N 0.000 description 1
- NAMDIHYPBYVYAP-UHFFFAOYSA-N 1-methoxy-2-(2-methoxyethoxy)ethane Chemical compound COCCOCCOC.COCCOCCOC NAMDIHYPBYVYAP-UHFFFAOYSA-N 0.000 description 1
- FWWXYLGCHHIKNY-UHFFFAOYSA-N 2-ethoxyethyl prop-2-enoate Chemical compound CCOCCOC(=O)C=C FWWXYLGCHHIKNY-UHFFFAOYSA-N 0.000 description 1
- RWLDCNACDPTRMY-UHFFFAOYSA-N 3-triethoxysilyl-n-(3-triethoxysilylpropyl)propan-1-amine Chemical compound CCO[Si](OCC)(OCC)CCCNCCC[Si](OCC)(OCC)OCC RWLDCNACDPTRMY-UHFFFAOYSA-N 0.000 description 1
- GWIQFKROZGQFNQ-UHFFFAOYSA-N C(C)OC(CCCCCCCCCCCCNCCCCCCCCCCCCC(OCC)(OCC)OCC)(OCC)OCC Chemical compound C(C)OC(CCCCCCCCCCCCNCCCCCCCCCCCCC(OCC)(OCC)OCC)(OCC)OCC GWIQFKROZGQFNQ-UHFFFAOYSA-N 0.000 description 1
- NGLCNAVWWQWSPV-UHFFFAOYSA-N C(CCC)NCCCC(C(OC)(OC)OC)CCCCCCCC Chemical compound C(CCC)NCCCC(C(OC)(OC)OC)CCCCCCCC NGLCNAVWWQWSPV-UHFFFAOYSA-N 0.000 description 1
- 229920002284 Cellulose triacetate Polymers 0.000 description 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
- HTJDQJBWANPRPF-UHFFFAOYSA-N Cyclopropylamine Chemical compound NC1CC1 HTJDQJBWANPRPF-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- HONIICLYMWZJFZ-UHFFFAOYSA-N azetidine Chemical compound C1CNC1 HONIICLYMWZJFZ-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229940116229 borneol Drugs 0.000 description 1
- CKDOCTFBFTVPSN-UHFFFAOYSA-N borneol Natural products C1CC2(C)C(C)CC1C2(C)C CKDOCTFBFTVPSN-UHFFFAOYSA-N 0.000 description 1
- GVOAXUUMYXAKOB-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN.CCCCN GVOAXUUMYXAKOB-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000012295 chemical reaction liquid Substances 0.000 description 1
- 230000003098 cholesteric effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- KZZKOVLJUKWSKX-UHFFFAOYSA-N cyclobutanamine Chemical compound NC1CCC1 KZZKOVLJUKWSKX-UHFFFAOYSA-N 0.000 description 1
- NISGSNTVMOOSJQ-UHFFFAOYSA-N cyclopentanamine Chemical compound NC1CCCC1 NISGSNTVMOOSJQ-UHFFFAOYSA-N 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- IUNMPGNGSSIWFP-UHFFFAOYSA-N dimethylaminopropylamine Chemical compound CN(C)CCCN IUNMPGNGSSIWFP-UHFFFAOYSA-N 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- WEHWNAOGRSTTBQ-UHFFFAOYSA-N dipropylamine Chemical compound CCCNCCC WEHWNAOGRSTTBQ-UHFFFAOYSA-N 0.000 description 1
- DTGKSKDOIYIVQL-UHFFFAOYSA-N dl-isoborneol Natural products C1CC2(C)C(O)CC1C2(C)C DTGKSKDOIYIVQL-UHFFFAOYSA-N 0.000 description 1
- 201000003373 familial cold autoinflammatory syndrome 3 Diseases 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
- 239000011254 layer-forming composition Substances 0.000 description 1
- 239000006193 liquid solution Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 239000000693 micelle Substances 0.000 description 1
- XCOASYLMDUQBHW-UHFFFAOYSA-N n-(3-trimethoxysilylpropyl)butan-1-amine Chemical compound CCCCNCCC[Si](OC)(OC)OC XCOASYLMDUQBHW-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000003518 norbornenyl group Chemical class C12(C=CC(CC1)C2)* 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 229960005222 phenazone Drugs 0.000 description 1
- XUWHAWMETYGRKB-UHFFFAOYSA-N piperidin-2-one Chemical compound O=C1CCCCN1 XUWHAWMETYGRKB-UHFFFAOYSA-N 0.000 description 1
- 238000009832 plasma treatment Methods 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- BHRZNVHARXXAHW-UHFFFAOYSA-N sec-butylamine Chemical compound CCC(C)N BHRZNVHARXXAHW-UHFFFAOYSA-N 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 125000005409 triarylsulfonium group Chemical group 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- 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
- G02F1/1335—Structural association of cells with optical devices, e.g. polarisers or reflectors
- G02F1/13363—Birefringent elements, e.g. for optical compensation
- G02F1/133636—Birefringent elements, e.g. for optical compensation with twisted orientation, e.g. comprising helically oriented LC-molecules or a plurality of twisted birefringent sublayers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F222/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
- C08F222/10—Esters
- C08F222/1006—Esters of polyhydric alcohols or polyhydric phenols
- C08F222/103—Esters of polyhydric alcohols or polyhydric phenols of trialcohols, e.g. trimethylolpropane tri(meth)acrylate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
- C08F290/02—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated end groups
- C08F290/06—Polymers provided for in subclass C08G
- C08F290/067—Polyurethanes; Polyureas
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/67—Unsaturated compounds having active hydrogen
- C08G18/671—Unsaturated compounds having only one group containing active hydrogen
- C08G18/672—Esters of acrylic or alkyl acrylic acid having only one group containing active hydrogen
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
- C09D167/06—Unsaturated polyesters having carbon-to-carbon unsaturation
- C09D167/07—Unsaturated polyesters having carbon-to-carbon unsaturation having terminal carbon-to-carbon unsaturated bonds
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/30—Polarising elements
- G02B5/3016—Polarising elements involving passive liquid crystal elements
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/30—Polarising elements
- G02B5/3083—Birefringent or phase retarding elements
-
- 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
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0025—Crosslinking or vulcanising agents; including accelerators
-
- 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/17—Amines; Quaternary ammonium 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
- C08K5/54—Silicon-containing compounds
- C08K5/544—Silicon-containing compounds containing nitrogen
-
- 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
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Health & Medical Sciences (AREA)
- Nonlinear Science (AREA)
- Crystallography & Structural Chemistry (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Mathematical Physics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Liquid Crystal (AREA)
- Polarising Elements (AREA)
- Polymerisation Methods In General (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR20090030940 | 2009-04-09 | ||
| KR1020100030369A KR101042214B1 (ko) | 2009-04-09 | 2010-04-02 | 배향막 조성물, 이로 제조된 배향막, 배향막 제조방법, 이를 포함하는 광학필름 및 광학필름을 포함하는 디스플레이 장치 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TW201041967A TW201041967A (en) | 2010-12-01 |
| TWI425047B true TWI425047B (zh) | 2014-02-01 |
Family
ID=43132445
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW099111051A TWI425047B (zh) | 2009-04-09 | 2010-04-09 | 可聚合型配向組成物,以此組成物製得之配向層,配向層之製造方法、包含其之光學膜及顯示裝置 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US20120021142A1 (enExample) |
| JP (1) | JP5948655B2 (enExample) |
| KR (1) | KR101042214B1 (enExample) |
| CN (1) | CN102459457B (enExample) |
| TW (1) | TWI425047B (enExample) |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2700698B1 (en) | 2011-04-21 | 2020-03-25 | LG Chem, Ltd. | Liquid crystal composition |
| WO2013051831A2 (ko) * | 2011-10-07 | 2013-04-11 | 동우화인켐 주식회사 | 배향막 형성용 조성물, 그로부터 제조된 배향막 및 위상차 필름 |
| TW201329585A (zh) * | 2011-12-20 | 2013-07-16 | Dongwoo Fine Chem Co Ltd | 偏光板及具此偏光板之影像顯示裝置 |
| WO2013119066A1 (ko) * | 2012-02-07 | 2013-08-15 | 주식회사 엘지화학 | 액정 렌즈 |
| WO2015005122A1 (ja) * | 2013-07-08 | 2015-01-15 | 富士フイルム株式会社 | 光学フィルム、偏光板、画像表示装置および光学フィルムの製造方法 |
| CN104342172B (zh) * | 2013-08-09 | 2019-01-18 | 住友化学株式会社 | 取向膜形成用组合物 |
| KR102368381B1 (ko) * | 2013-08-09 | 2022-02-28 | 스미또모 가가꾸 가부시키가이샤 | 광학 필름 |
| KR101582007B1 (ko) * | 2013-09-30 | 2015-12-31 | 주식회사 엘지화학 | 오버코팅 조성물, 오버코팅막의 제조방법, 이를 포함하는 광학 필름 및 상기 광학 필름을 포함하는 디스플레이 장치 |
| JP2015106060A (ja) * | 2013-11-29 | 2015-06-08 | 大日本印刷株式会社 | 位相差フィルム及び位相差フィルムの製造方法、並びに光学フィルム |
| JP6667983B2 (ja) * | 2014-05-30 | 2020-03-18 | 富士フイルム株式会社 | 積層体およびその製造方法、偏光板、液晶表示装置、有機el表示装置 |
| US20160146995A1 (en) * | 2014-11-26 | 2016-05-26 | Sumitomo Chemical Company, Limited | Optical film |
| US9880421B2 (en) | 2014-12-10 | 2018-01-30 | Samsung Display Co., Ltd | Curved liquid crystal display |
| CN104536210B (zh) * | 2015-02-03 | 2017-09-29 | 京东方科技集团股份有限公司 | 一种配向膜印刷板的制备方法 |
| US9902906B2 (en) | 2015-04-21 | 2018-02-27 | The United States Of America As Represented By The Secretary Of The Air Force | Voxelated liquid crystal elastomers |
| WO2017001039A1 (en) * | 2015-06-30 | 2017-01-05 | Merck Patent Gmbh | Polymerisable liquid crystal material and polymerised liquid crystal film |
| KR101990286B1 (ko) * | 2015-12-18 | 2019-06-18 | 주식회사 엘지화학 | 수직 배향막 |
| KR101959515B1 (ko) * | 2016-08-19 | 2019-03-18 | 주식회사 엘지화학 | 액정 배향막의 제조 방법 |
| EP3407127B1 (en) * | 2016-08-31 | 2020-08-12 | LG Chem, Ltd. | Method for manufacturing multilayer liquid crystal film |
| WO2018155581A1 (ja) * | 2017-02-22 | 2018-08-30 | 日産化学株式会社 | 硬化膜形成組成物、配向材および位相差材 |
| CN107501894A (zh) * | 2017-09-03 | 2017-12-22 | 苏建 | 一种用于延迟膜的共混树脂 |
| KR102280864B1 (ko) * | 2018-01-25 | 2021-07-22 | 주식회사 엘지화학 | 다층 액정 필름, 편광판 및 편광판의 제조방법 |
| KR102383293B1 (ko) * | 2018-01-25 | 2022-04-05 | 주식회사 엘지화학 | 다층 액정 필름, 편광판 및 편광판의 제조방법 |
| KR102555870B1 (ko) | 2018-02-22 | 2023-07-14 | 삼성전자주식회사 | 폴리머, 상기 폴리머를 포함하는 필름, 및 상기 필름을 포함하는 표시 장치 |
| WO2021060371A1 (ja) * | 2019-09-27 | 2021-04-01 | 富士フイルム株式会社 | 光学素子 |
| CN111367127B (zh) * | 2020-03-16 | 2023-03-28 | Tcl华星光电技术有限公司 | 一种液晶膜结构及其制备方法、液晶显示面板 |
| CN114269094A (zh) * | 2020-09-16 | 2022-04-01 | Oppo广东移动通信有限公司 | 壳体组件及其制作方法、电子设备 |
| CN112099125B (zh) * | 2020-09-28 | 2022-05-17 | 北京瑞波科技术有限公司 | 一种液晶高分子多方向薄膜的制作方法 |
| KR102788596B1 (ko) * | 2021-11-22 | 2025-03-31 | 주식회사 엘지화학 | 액정셀의 제조방법 |
| CN116120616A (zh) * | 2022-12-30 | 2023-05-16 | 成都瑞波科材料科技有限公司 | 能够实现液晶聚合物配向的树脂薄膜及其制备方法 |
| CN116559990A (zh) * | 2023-04-24 | 2023-08-08 | 成都瑞波科材料科技有限公司 | 视角补偿膜、视角补偿膜制备方法以及液晶显示面板 |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1593991A1 (en) * | 2003-02-12 | 2005-11-09 | Nippon Kayaku Kabushiki Kaisha | Substrate for vertical alignment and process for producing vertically aligned liquid crystal retardation film |
| TW200628309A (en) * | 2004-10-21 | 2006-08-16 | Nitto Denko Corp | Antistatic adhesion type optical film and image display |
| EP1813972A2 (en) * | 2001-02-23 | 2007-08-01 | Nippon Kayaku Kabushiki Kaisha | Alignment Film |
| TW200819509A (en) * | 2006-07-18 | 2008-05-01 | Nissan Chemical Ind Ltd | Liquid crystal orienting agent and liquid crystal oriented film and liquid crystal display element using the same |
| TW200831589A (en) * | 2006-11-16 | 2008-08-01 | Lg Chemical Ltd | Composition for alignment film having excellent adhesiveness |
Family Cites Families (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US588744A (en) * | 1897-08-24 | Nail-puller | ||
| US4390401A (en) * | 1981-02-23 | 1983-06-28 | Celanese Corporation | Acrylate or methacrylate esters of alkylene oxide adducts of alkyl/aryl phenols as wetting agents for ultraviolet curable coating compositions |
| JPS6244439A (ja) * | 1985-08-22 | 1987-02-26 | 新日本製鐵株式会社 | ポリオレフイン被覆金属管 |
| JPH02238440A (ja) * | 1989-03-10 | 1990-09-20 | Seiko Epson Corp | 電気光学装置 |
| JPH0429117A (ja) * | 1990-05-24 | 1992-01-31 | Sanyo Chem Ind Ltd | 液晶表示素子および液晶配向膜の製法 |
| JPH0458224A (ja) * | 1990-06-28 | 1992-02-25 | Asahi Chem Ind Co Ltd | 液晶セル |
| JPH08194227A (ja) * | 1995-01-20 | 1996-07-30 | Fuji Photo Film Co Ltd | 配向膜の形成方法及び液晶表示素子 |
| JPH09165445A (ja) * | 1995-12-18 | 1997-06-24 | Toyo Ink Mfg Co Ltd | 硬化性樹脂組成物、およびその硬化物の製造方法 |
| JP3988267B2 (ja) * | 1998-08-20 | 2007-10-10 | Jsr株式会社 | 光ディスク用接着剤 |
| EP1391484B1 (en) * | 2001-04-19 | 2006-08-30 | Kaneka Corporation | Curable composition |
| JP2004206100A (ja) * | 2002-12-12 | 2004-07-22 | Dainippon Printing Co Ltd | 配向膜用組成物、配向膜の製造方法、及び光学素子の製造方法 |
| JP4223927B2 (ja) | 2003-11-17 | 2009-02-12 | 日東電工株式会社 | 垂直配向膜、液晶配向膜及びその製造方法、光学フィルム並びに画像表示装置 |
| JP4595498B2 (ja) * | 2003-12-12 | 2010-12-08 | チッソ株式会社 | 有機ケイ素化合物含有重合性液晶組成物 |
| WO2005076059A1 (ja) * | 2004-02-10 | 2005-08-18 | Dai Nippon Printing Co., Ltd. | 液晶表示素子 |
| JP2005326439A (ja) * | 2004-05-12 | 2005-11-24 | Fuji Photo Film Co Ltd | 位相差板材料、重合体、位相差板および画像表示装置 |
| JP4895343B2 (ja) * | 2004-09-22 | 2012-03-14 | 富士フイルム株式会社 | 反射防止フィルム、その製造方法、偏光板、及び画像表示装置 |
| KR101202635B1 (ko) * | 2004-09-22 | 2012-11-20 | 후지필름 가부시키가이샤 | 경화성 조성물, 반사방지 필름, 이의 제조 방법, 편광판 및영상 표시 장치 |
| KR100845534B1 (ko) * | 2004-12-31 | 2008-07-10 | 엘지전자 주식회사 | 전도성 금속 도금 폴리이미드 기판 및 그 제조 방법 |
| JP2006276061A (ja) * | 2005-03-25 | 2006-10-12 | Dainippon Printing Co Ltd | 光学素子 |
| KR101362827B1 (ko) | 2005-06-09 | 2014-02-14 | 제이엔씨 석유 화학 주식회사 | 중합성 액정 조성물 및 그 중합체 |
| TWI305287B (en) * | 2005-09-22 | 2009-01-11 | Lg Chemical Ltd | Multi-functional monomer having a photoreactive group, alignment film for lcd using the monomer, and lcd comprising the alignment film |
| KR100822142B1 (ko) * | 2005-10-20 | 2008-04-14 | 주식회사 엘지화학 | 신규한 유기 실란 화합물 |
| JP2007148099A (ja) * | 2005-11-29 | 2007-06-14 | Nitto Denko Corp | ポジティブcプレートの製造方法及びポジティブcプレート、そのポジティブcプレートを用いた液晶パネル及び液晶表示装置 |
| JP2008019434A (ja) * | 2006-06-14 | 2008-01-31 | Dainippon Printing Co Ltd | 液晶組成物、これを用いたカラーフィルタ及び液晶表示装置 |
| KR100927467B1 (ko) * | 2006-11-16 | 2009-11-19 | 주식회사 엘지화학 | 내구성이 우수한 o-플레이트 및 이를 포함하는 일체형편광판 |
| JP2009040984A (ja) * | 2007-08-13 | 2009-02-26 | Dainippon Printing Co Ltd | 液晶組成物、該液晶組成物を用いた位相差制御部材、及び、液晶表示装置 |
| JP5446864B2 (ja) * | 2007-08-28 | 2014-03-19 | 住友ベークライト株式会社 | 多層プリント配線板用絶縁樹脂組成物、基材付き絶縁樹脂シート、多層プリント配線板及び半導体装置 |
| JP2009098636A (ja) * | 2007-09-27 | 2009-05-07 | Fujifilm Corp | 光学フィルム、偏光板、及び液晶表示装置 |
| WO2009066947A2 (en) * | 2007-11-23 | 2009-05-28 | Lg Chem, Ltd. | Polymerizable liquid crystal composition, homeotropic alignment liquid crystal film made from the compostion and method for preparing the same |
-
2010
- 2010-04-02 KR KR1020100030369A patent/KR101042214B1/ko active Active
- 2010-04-08 JP JP2012504619A patent/JP5948655B2/ja active Active
- 2010-04-08 US US13/259,946 patent/US20120021142A1/en not_active Abandoned
- 2010-04-08 CN CN201080025687.4A patent/CN102459457B/zh active Active
- 2010-04-09 TW TW099111051A patent/TWI425047B/zh active
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1813972A2 (en) * | 2001-02-23 | 2007-08-01 | Nippon Kayaku Kabushiki Kaisha | Alignment Film |
| EP1593991A1 (en) * | 2003-02-12 | 2005-11-09 | Nippon Kayaku Kabushiki Kaisha | Substrate for vertical alignment and process for producing vertically aligned liquid crystal retardation film |
| TW200628309A (en) * | 2004-10-21 | 2006-08-16 | Nitto Denko Corp | Antistatic adhesion type optical film and image display |
| TW200819509A (en) * | 2006-07-18 | 2008-05-01 | Nissan Chemical Ind Ltd | Liquid crystal orienting agent and liquid crystal oriented film and liquid crystal display element using the same |
| TW200831589A (en) * | 2006-11-16 | 2008-08-01 | Lg Chemical Ltd | Composition for alignment film having excellent adhesiveness |
Also Published As
| Publication number | Publication date |
|---|---|
| CN102459457B (zh) | 2015-04-15 |
| CN102459457A (zh) | 2012-05-16 |
| TW201041967A (en) | 2010-12-01 |
| KR20100112525A (ko) | 2010-10-19 |
| JP5948655B2 (ja) | 2016-07-06 |
| KR101042214B1 (ko) | 2011-06-20 |
| US20120021142A1 (en) | 2012-01-26 |
| JP2012523581A (ja) | 2012-10-04 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| TWI425047B (zh) | 可聚合型配向組成物,以此組成物製得之配向層,配向層之製造方法、包含其之光學膜及顯示裝置 | |
| JP5250635B2 (ja) | 重合性液晶組成物、これを用いた垂直配向液晶フィルムおよびその製造方法 | |
| JP5076810B2 (ja) | 光配向膜用組成物、光配向膜、及び光学異方体 | |
| CN100405093C (zh) | 液晶化合物及使用其的相位差膜 | |
| US8867002B2 (en) | Polymer composition having photoalignable group, liquid crystal alignment film formed of the polymer composition, and liquid crystal display device having phase difference plate formed of the liquid crystal alignment film | |
| TWI356246B (en) | Retardation film having a homeotropic alignment li | |
| US9388259B2 (en) | Photosensitive polymer and photoalignable phase difference film | |
| JP4227680B2 (ja) | 液晶フィルムおよびその製造方法 | |
| EP1693690A1 (en) | Composition for liquid crystal film formation, optically anisotropic film and process for producing them | |
| KR101560040B1 (ko) | 액정 조성물 | |
| JP4008246B2 (ja) | 複合体組成物、及びこれを架橋させてなる成形硬化物 | |
| JP5504601B2 (ja) | 配向膜用組成物、配向膜の製造方法、及び光学異方体 | |
| CN108983343A (zh) | 光学各向异性膜、椭圆偏振片及有机电致发光显示器 | |
| CN106324911A (zh) | 视角补偿膜用聚合物组合物、视角补偿膜、视角补偿膜的制造方法及其应用 | |
| CN113167957B (zh) | 液晶取向剂、液晶取向膜及相位差材 | |
| JP2010175931A (ja) | 光配向膜用組成物、光配向膜、及び光学異方体 | |
| JP2006249318A (ja) | ディスプレイ用光学フィルム | |
| WO2019017181A1 (ja) | 積層体、液晶配向剤及び液晶表示素子 | |
| JP4289604B2 (ja) | 配向膜用紫外線硬化型樹脂組成物及びこれを用いた配向板、位相差板 | |
| JP3674236B2 (ja) | 液晶表示素子 | |
| JP2019095613A (ja) | 感光性モノマー、光配向性ポリマー、およびこれを用いたフィルム | |
| JP2020177217A (ja) | 積層体及び積層体の製造方法 | |
| WO2024235529A1 (en) | Polymerizable liquid crystal composition | |
| KR102068868B1 (ko) | 위상차 보상 필름 및 이를 포함하는 액정 표시 장치 | |
| JP2004300433A (ja) | 透明複合体組成物およびこれを用いた表示素子用基板 |