TWI396871B - 具改良之著色劑分布的彩色濾光片元件 - Google Patents
具改良之著色劑分布的彩色濾光片元件 Download PDFInfo
- Publication number
- TWI396871B TWI396871B TW098136529A TW98136529A TWI396871B TW I396871 B TWI396871 B TW I396871B TW 098136529 A TW098136529 A TW 098136529A TW 98136529 A TW98136529 A TW 98136529A TW I396871 B TWI396871 B TW I396871B
- Authority
- TW
- Taiwan
- Prior art keywords
- pigment
- color filter
- filter
- color
- transmittance
- Prior art date
Links
- 239000006185 dispersion Substances 0.000 title description 50
- 239000003086 colorant Substances 0.000 title description 12
- 239000000049 pigment Substances 0.000 claims description 127
- 238000002834 transmittance Methods 0.000 claims description 40
- 239000002245 particle Substances 0.000 claims description 39
- -1 aluminum fluoride anthraquinone Chemical compound 0.000 claims description 27
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 claims description 27
- 150000004056 anthraquinones Chemical class 0.000 claims description 27
- 238000010521 absorption reaction Methods 0.000 claims description 21
- 229910003849 O-Si Inorganic materials 0.000 claims description 16
- 229910003872 O—Si Inorganic materials 0.000 claims description 16
- 229910052731 fluorine Inorganic materials 0.000 claims description 15
- 239000011737 fluorine Substances 0.000 claims description 15
- RZVHIXYEVGDQDX-UHFFFAOYSA-N 9,10-anthraquinone Chemical group C1=CC=C2C(=O)C3=CC=CC=C3C(=O)C2=C1 RZVHIXYEVGDQDX-UHFFFAOYSA-N 0.000 claims description 9
- 150000004636 anthocyanins Chemical class 0.000 claims description 9
- 229930002877 anthocyanin Natural products 0.000 claims description 8
- 235000010208 anthocyanin Nutrition 0.000 claims description 8
- 239000004410 anthocyanin Substances 0.000 claims description 8
- 125000001153 fluoro group Chemical group F* 0.000 claims description 7
- 239000003446 ligand Substances 0.000 claims description 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 229910052782 aluminium Inorganic materials 0.000 claims description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical group [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 5
- 230000007935 neutral effect Effects 0.000 claims description 4
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims description 4
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 claims description 3
- 235000000177 Indigofera tinctoria Nutrition 0.000 claims description 2
- 229940097275 indigo Drugs 0.000 claims description 2
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 claims description 2
- 239000011356 non-aqueous organic solvent Substances 0.000 claims description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 1
- 238000003801 milling Methods 0.000 description 37
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 26
- 239000000203 mixture Substances 0.000 description 23
- 238000000034 method Methods 0.000 description 19
- 239000011248 coating agent Substances 0.000 description 17
- 238000000576 coating method Methods 0.000 description 17
- 239000002270 dispersing agent Substances 0.000 description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 15
- 229910052751 metal Inorganic materials 0.000 description 15
- 239000002184 metal Substances 0.000 description 15
- 238000002360 preparation method Methods 0.000 description 15
- 239000002609 medium Substances 0.000 description 14
- 239000000758 substrate Substances 0.000 description 14
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical group N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 12
- 239000002904 solvent Substances 0.000 description 12
- 239000011521 glass Substances 0.000 description 11
- 239000007787 solid Substances 0.000 description 11
- 239000000047 product Substances 0.000 description 10
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
- 238000009826 distribution Methods 0.000 description 9
- 238000002156 mixing Methods 0.000 description 9
- 239000002002 slurry Substances 0.000 description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 8
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 8
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 8
- 229920000642 polymer Polymers 0.000 description 7
- 230000008569 process Effects 0.000 description 7
- FOWDZVNRQHPXDO-UHFFFAOYSA-N propyl hydrogen carbonate Chemical compound CCCOC(O)=O FOWDZVNRQHPXDO-UHFFFAOYSA-N 0.000 description 7
- 230000003595 spectral effect Effects 0.000 description 7
- 238000001228 spectrum Methods 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 6
- 230000008901 benefit Effects 0.000 description 6
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 6
- 239000004973 liquid crystal related substance Substances 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000002952 polymeric resin Substances 0.000 description 6
- LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 125000001424 substituent group Chemical group 0.000 description 6
- 229920003002 synthetic resin Polymers 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 5
- 239000010408 film Substances 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000003960 organic solvent Substances 0.000 description 5
- 239000004094 surface-active agent Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 230000005540 biological transmission Effects 0.000 description 4
- 150000001768 cations Chemical class 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 239000010949 copper Substances 0.000 description 4
- 238000002347 injection Methods 0.000 description 4
- 239000007924 injection Substances 0.000 description 4
- 238000004020 luminiscence type Methods 0.000 description 4
- 238000009877 rendering Methods 0.000 description 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 4
- 238000001429 visible spectrum Methods 0.000 description 4
- XQLUSZJJMCMUDV-UHFFFAOYSA-N 2,3,5,6-tetraphenyl-1,4-dioxane Chemical compound O1C(C=2C=CC=CC=2)C(C=2C=CC=CC=2)OC(C=2C=CC=CC=2)C1C1=CC=CC=C1 XQLUSZJJMCMUDV-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000011149 active material Substances 0.000 description 3
- 125000000129 anionic group Chemical group 0.000 description 3
- AZYGCZIJFCZOOP-UHFFFAOYSA-N anthracene-9,10-dione copper Chemical compound C1=CC=CC=2C(C3=CC=CC=C3C(C12)=O)=O.[Cu] AZYGCZIJFCZOOP-UHFFFAOYSA-N 0.000 description 3
- 239000008365 aqueous carrier Substances 0.000 description 3
- 239000003125 aqueous solvent Substances 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 239000011324 bead Substances 0.000 description 3
- 239000000706 filtrate Substances 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 238000000227 grinding Methods 0.000 description 3
- 150000002576 ketones Chemical class 0.000 description 3
- 239000011159 matrix material Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000012860 organic pigment Substances 0.000 description 3
- 229920006391 phthalonitrile polymer Polymers 0.000 description 3
- 229920005862 polyol Polymers 0.000 description 3
- 150000003077 polyols Chemical class 0.000 description 3
- 239000011164 primary particle Substances 0.000 description 3
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 239000011877 solvent mixture Substances 0.000 description 3
- 238000004528 spin coating Methods 0.000 description 3
- 239000010409 thin film Substances 0.000 description 3
- DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- JTPNRXUCIXHOKM-UHFFFAOYSA-N 1-chloronaphthalene Chemical compound C1=CC=C2C(Cl)=CC=CC2=C1 JTPNRXUCIXHOKM-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
- BUEDBKYORKGOSS-UHFFFAOYSA-N C1(=CC=CC=C1)C(C(O)(O)C1=CC=CC=C1)CCCCCCCC Chemical compound C1(=CC=CC=C1)C(C(O)(O)C1=CC=CC=C1)CCCCCCCC BUEDBKYORKGOSS-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 229940045799 anthracyclines and related substance Drugs 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- LZCLXQDLBQLTDK-UHFFFAOYSA-N ethyl 2-hydroxypropanoate Chemical compound CCOC(=O)C(C)O LZCLXQDLBQLTDK-UHFFFAOYSA-N 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 229920002313 fluoropolymer Polymers 0.000 description 2
- 150000004820 halides Chemical class 0.000 description 2
- 230000005525 hole transport Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 238000003384 imaging method Methods 0.000 description 2
- 239000001023 inorganic pigment Substances 0.000 description 2
- 239000002198 insoluble material Substances 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 2
- 239000002105 nanoparticle Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 230000000737 periodic effect Effects 0.000 description 2
- XQZYPMVTSDWCCE-UHFFFAOYSA-N phthalonitrile Chemical class N#CC1=CC=CC=C1C#N XQZYPMVTSDWCCE-UHFFFAOYSA-N 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000011085 pressure filtration Methods 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 238000012216 screening Methods 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- BSYVTEYKTMYBMK-UHFFFAOYSA-N tetrahydrofurfuryl alcohol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 description 2
- RWRDLPDLKQPQOW-UHFFFAOYSA-N tetrahydropyrrole Natural products C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- 239000001052 yellow pigment Substances 0.000 description 2
- RTHCYVBBDHJXIQ-MRXNPFEDSA-N (R)-fluoxetine Chemical compound O([C@H](CCNC)C=1C=CC=CC=1)C1=CC=C(C(F)(F)F)C=C1 RTHCYVBBDHJXIQ-MRXNPFEDSA-N 0.000 description 1
- RHUYHJGZWVXEHW-UHFFFAOYSA-N 1,1-Dimethyhydrazine Chemical compound CN(C)N RHUYHJGZWVXEHW-UHFFFAOYSA-N 0.000 description 1
- ZWVMLYRJXORSEP-UHFFFAOYSA-N 1,2,6-Hexanetriol Chemical compound OCCCCC(O)CO ZWVMLYRJXORSEP-UHFFFAOYSA-N 0.000 description 1
- CYSGHNMQYZDMIA-UHFFFAOYSA-N 1,3-Dimethyl-2-imidazolidinon Chemical compound CN1CCN(C)C1=O CYSGHNMQYZDMIA-UHFFFAOYSA-N 0.000 description 1
- CAQYAZNFWDDMIT-UHFFFAOYSA-N 1-ethoxy-2-methoxyethane Chemical compound CCOCCOC CAQYAZNFWDDMIT-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- ZFQCFWRSIBGRFL-UHFFFAOYSA-B 2-hydroxypropane-1,2,3-tricarboxylate;zirconium(4+) Chemical compound [Zr+4].[Zr+4].[Zr+4].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O ZFQCFWRSIBGRFL-UHFFFAOYSA-B 0.000 description 1
- OLRPEJSOUYZNSN-UHFFFAOYSA-N 3,5-difluorobenzene-1,2-dicarbonitrile Chemical compound FC1=CC(F)=C(C#N)C(C#N)=C1 OLRPEJSOUYZNSN-UHFFFAOYSA-N 0.000 description 1
- QQEKYCCJLSRLEC-UHFFFAOYSA-N 4-fluorobenzene-1,2-dicarbonitrile Chemical compound FC1=CC=C(C#N)C(C#N)=C1 QQEKYCCJLSRLEC-UHFFFAOYSA-N 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N Caprylic acid Natural products CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- 229920005732 JONCRYL® 678 Polymers 0.000 description 1
- 229930194542 Keto Natural products 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical class OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 229920001311 Poly(hydroxyethyl acrylate) Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 229920002732 Polyanhydride Polymers 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 229920001710 Polyorthoester Polymers 0.000 description 1
- 229920002675 Polyoxyl Polymers 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 229930182558 Sterol Natural products 0.000 description 1
- 241000583281 Sugiura Species 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- UWHCKJMYHZGTIT-UHFFFAOYSA-N Tetraethylene glycol, Natural products OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
- 229910001315 Tool steel Inorganic materials 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000001089 [(2R)-oxolan-2-yl]methanol Substances 0.000 description 1
- 238000002835 absorbance Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- LSQZJLSUYDQPKJ-NJBDSQKTSA-N amoxicillin Chemical compound C1([C@@H](N)C(=O)N[C@H]2[C@H]3SC([C@@H](N3C2=O)C(O)=O)(C)C)=CC=C(O)C=C1 LSQZJLSUYDQPKJ-NJBDSQKTSA-N 0.000 description 1
- 229960003022 amoxicillin Drugs 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000003491 array Methods 0.000 description 1
- GONOPSZTUGRENK-UHFFFAOYSA-N benzyl(trichloro)silane Chemical compound Cl[Si](Cl)(Cl)CC1=CC=CC=C1 GONOPSZTUGRENK-UHFFFAOYSA-N 0.000 description 1
- 229920002988 biodegradable polymer Polymers 0.000 description 1
- 239000004621 biodegradable polymer Substances 0.000 description 1
- 150000003842 bromide salts Chemical class 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 229940112021 centrally acting muscle relaxants carbamic acid ester Drugs 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 235000019646 color tone Nutrition 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 239000006184 cosolvent Substances 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 230000001186 cumulative effect Effects 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 239000002612 dispersion medium Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000002296 dynamic light scattering Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- AEDZKIACDBYJLQ-UHFFFAOYSA-N ethane-1,2-diol;hydrate Chemical compound O.OCCO AEDZKIACDBYJLQ-UHFFFAOYSA-N 0.000 description 1
- 229940116333 ethyl lactate Drugs 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000007888 film coating Substances 0.000 description 1
- 238000009501 film coating Methods 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 239000004811 fluoropolymer Substances 0.000 description 1
- 229960002464 fluoxetine Drugs 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000007756 gravure coating Methods 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- OAKJQQAXSVQMHS-UHFFFAOYSA-N hydrazine Substances NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- MNUOZFHYBCRUOD-UHFFFAOYSA-N hydroxyphthalic acid Natural products OC(=O)C1=CC=CC(O)=C1C(O)=O MNUOZFHYBCRUOD-UHFFFAOYSA-N 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 125000003387 indolinyl group Chemical group N1(CCC2=CC=CC=C12)* 0.000 description 1
- JJTUDXZGHPGLLC-UHFFFAOYSA-N lactide Chemical compound CC1OC(=O)C(C)OC1=O JJTUDXZGHPGLLC-UHFFFAOYSA-N 0.000 description 1
- 239000006193 liquid solution Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000004949 mass spectrometry Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910001512 metal fluoride Inorganic materials 0.000 description 1
- CQDGTJPVBWZJAZ-UHFFFAOYSA-N monoethyl carbonate Chemical compound CCOC(O)=O CQDGTJPVBWZJAZ-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N n-hexanoic acid Natural products CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 229910052755 nonmetal Inorganic materials 0.000 description 1
- 230000005693 optoelectronics Effects 0.000 description 1
- LSQZJLSUYDQPKJ-UHFFFAOYSA-N p-Hydroxyampicillin Natural products O=C1N2C(C(O)=O)C(C)(C)SC2C1NC(=O)C(N)C1=CC=C(O)C=C1 LSQZJLSUYDQPKJ-UHFFFAOYSA-N 0.000 description 1
- 238000010951 particle size reduction Methods 0.000 description 1
- 239000011236 particulate material Substances 0.000 description 1
- 238000000059 patterning Methods 0.000 description 1
- 125000005062 perfluorophenyl group Chemical group FC1=C(C(=C(C(=C1F)F)F)F)* 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920002120 photoresistant polymer Polymers 0.000 description 1
- 229940067265 pigment yellow 138 Drugs 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920000747 poly(lactic acid) Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 239000002745 poly(ortho ester) Substances 0.000 description 1
- 229920002627 poly(phosphazenes) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001610 polycaprolactone Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920002338 polyhydroxyethylmethacrylate Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920003053 polystyrene-divinylbenzene Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000012925 reference material Substances 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000012798 spherical particle Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 150000003432 sterols Chemical class 0.000 description 1
- 235000003702 sterols Nutrition 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000010345 tape casting Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- LWRYDHOHXNQTSK-UHFFFAOYSA-N thiophene oxide Chemical class O=S1C=CC=C1 LWRYDHOHXNQTSK-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/20—Filters
- G02B5/22—Absorbing filters
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B47/00—Porphines; Azaporphines
- C09B47/04—Phthalocyanines abbreviation: Pc
- C09B47/06—Preparation from carboxylic acids or derivatives thereof, e.g. anhydrides, amides, mononitriles, phthalimide, o-cyanobenzamide
- C09B47/067—Preparation from carboxylic acids or derivatives thereof, e.g. anhydrides, amides, mononitriles, phthalimide, o-cyanobenzamide from phthalodinitriles naphthalenedinitriles, aromatic dinitriles prepared in situ, hydrogenated phthalodinitrile
- C09B47/0671—Preparation from carboxylic acids or derivatives thereof, e.g. anhydrides, amides, mononitriles, phthalimide, o-cyanobenzamide from phthalodinitriles naphthalenedinitriles, aromatic dinitriles prepared in situ, hydrogenated phthalodinitrile having halogen atoms linked directly to the Pc skeleton
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B47/00—Porphines; Azaporphines
- C09B47/04—Phthalocyanines abbreviation: Pc
- C09B47/06—Preparation from carboxylic acids or derivatives thereof, e.g. anhydrides, amides, mononitriles, phthalimide, o-cyanobenzamide
- C09B47/067—Preparation from carboxylic acids or derivatives thereof, e.g. anhydrides, amides, mononitriles, phthalimide, o-cyanobenzamide from phthalodinitriles naphthalenedinitriles, aromatic dinitriles prepared in situ, hydrogenated phthalodinitrile
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B47/00—Porphines; Azaporphines
- C09B47/04—Phthalocyanines abbreviation: Pc
- C09B47/08—Preparation from other phthalocyanine compounds, e.g. cobaltphthalocyanineamine complex
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B47/00—Porphines; Azaporphines
- C09B47/04—Phthalocyanines abbreviation: Pc
- C09B47/08—Preparation from other phthalocyanine compounds, e.g. cobaltphthalocyanineamine complex
- C09B47/085—Preparation from other phthalocyanine compounds, e.g. cobaltphthalocyanineamine complex substituting the central metal atom
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B47/00—Porphines; Azaporphines
- C09B47/04—Phthalocyanines abbreviation: Pc
- C09B47/08—Preparation from other phthalocyanine compounds, e.g. cobaltphthalocyanineamine complex
- C09B47/10—Obtaining compounds having halogen atoms directly bound to the phthalocyanine skeleton
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0033—Blends of pigments; Mixtured crystals; Solid solutions
- C09B67/0034—Mixtures of two or more pigments or dyes of the same type
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0033—Blends of pigments; Mixtured crystals; Solid solutions
- C09B67/0034—Mixtures of two or more pigments or dyes of the same type
- C09B67/0035—Mixtures of phthalocyanines
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B69/00—Dyes not provided for by a single group of this subclass
- C09B69/008—Dyes containing a substituent, which contains a silicium atom
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/20—Filters
- G02B5/201—Filters in the form of arrays
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/20—Filters
- G02B5/22—Absorbing filters
- G02B5/223—Absorbing filters containing organic substances, e.g. dyes, inks or pigments
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K59/00—Integrated devices, or assemblies of multiple devices, comprising at least one organic light-emitting element covered by group H10K50/00
- H10K59/30—Devices specially adapted for multicolour light emission
- H10K59/38—Devices specially adapted for multicolour light emission comprising colour filters or colour changing media [CCM]
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electroluminescent Light Sources (AREA)
- Optical Filters (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12/260,195 US8277697B2 (en) | 2008-10-29 | 2008-10-29 | Color filter element with improved colorant dispersion |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TW201027145A TW201027145A (en) | 2010-07-16 |
| TWI396871B true TWI396871B (zh) | 2013-05-21 |
Family
ID=42101899
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW098136529A TWI396871B (zh) | 2008-10-29 | 2009-10-28 | 具改良之著色劑分布的彩色濾光片元件 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US8277697B2 (enExample) |
| EP (1) | EP2361398B1 (enExample) |
| JP (1) | JP5117618B2 (enExample) |
| KR (1) | KR101256995B1 (enExample) |
| CN (1) | CN102227655B (enExample) |
| TW (1) | TWI396871B (enExample) |
| WO (1) | WO2010053503A2 (enExample) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5391998B2 (ja) * | 2009-10-22 | 2014-01-15 | 東洋インキＳｃホールディングス株式会社 | 緑色着色組成物、カラーフィルタおよびカラー表示装置 |
| JP5691634B2 (ja) * | 2011-02-25 | 2015-04-01 | 凸版印刷株式会社 | 有機ｅｌ表示装置用カラーフィルタ、及びそれを具備する有機ｅｌ表示装置 |
| WO2012128233A1 (ja) * | 2011-03-18 | 2012-09-27 | 東洋インキＳｃホールディングス株式会社 | カラーフィルタ用着色組成物及びカラーフィルタ |
| JP5779832B2 (ja) * | 2012-01-16 | 2015-09-16 | 東洋インキＳｃホールディングス株式会社 | カラーフィルタ用着色組成物、およびカラーフィルタ |
| JP5776122B2 (ja) * | 2012-01-30 | 2015-09-09 | 東洋インキＳｃホールディングス株式会社 | カラーフィルタ用着色組成物、およびカラーフィルタ |
| JP5834328B2 (ja) * | 2012-02-17 | 2015-12-16 | 東洋インキＳｃホールディングス株式会社 | カラーフィルタ用着色組成物、およびカラーフィルタ |
| JP5783086B2 (ja) * | 2012-02-29 | 2015-09-24 | 東洋インキＳｃホールディングス株式会社 | カラーフィルタ用緑色着色組成物、およびカラーフィルタ |
| ES2478693B1 (es) * | 2012-12-21 | 2015-04-29 | Universidad Complutense De Madrid | Elemento bloqueante de longitudes de onda corta en fuentes de iluminación de tipo led |
| CN103197462B (zh) * | 2013-03-26 | 2016-05-25 | 京东方科技集团股份有限公司 | 一种彩膜基板、显示面板及显示装置 |
| KR101801671B1 (ko) | 2014-01-31 | 2017-11-27 | 후지필름 가부시키가이샤 | 컬러 필터용 녹색 착색 조성물, 착색막, 컬러 필터, 고체 촬상 소자 |
| EP3125005B1 (en) * | 2015-07-29 | 2025-08-13 | Tecnología Sostenible y Responsable SL | Optical product comprising two pigments |
| TWI554816B (zh) | 2015-07-31 | 2016-10-21 | 元太科技工業股份有限公司 | 反射式顯示裝置 |
| KR102423430B1 (ko) * | 2015-08-10 | 2022-07-21 | 삼성디스플레이 주식회사 | 컬러필터 및 이를 포함하는 표시장치 |
| KR102432875B1 (ko) * | 2015-12-04 | 2022-08-16 | 에스케이씨하이테크앤마케팅(주) | 컬러필터용 안료배합물, 가공안료 및 가공안료 분산액 |
| JP6477977B2 (ja) * | 2016-08-31 | 2019-03-06 | Dic株式会社 | カラーフィルタ用顔料組成物及びカラーフィルタ |
| CN109863208B (zh) * | 2016-11-04 | 2022-02-08 | M技术株式会社 | 绿色滤光器用颜料组合物及其制造方法 |
| US20220045133A1 (en) * | 2020-08-05 | 2022-02-10 | Joled Inc. | Display panel and display device |
| JP7748216B2 (ja) * | 2020-08-05 | 2025-10-02 | 株式会社Magnolia Blue | 表示パネル及び表示装置 |
| CN112649992B (zh) * | 2020-12-25 | 2022-10-04 | Tcl华星光电技术有限公司 | 一种背光模组及显示装置 |
| CN113136112B (zh) * | 2021-04-16 | 2023-04-28 | 上海昀通电子科技有限公司 | 宽光谱带的近红外吸收染料 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20020117080A1 (en) * | 2000-12-22 | 2002-08-29 | Satoshi Okutsu | Colored composition for color filter and color filter |
| TW200829965A (en) * | 2006-11-08 | 2008-07-16 | Fujifilm Corp | Color filter, liquid crystal display device and CCD device |
Family Cites Families (79)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2227628A (en) | 1938-06-30 | 1941-01-07 | Du Pont | Fluorination of phthalocyanines |
| US2925423A (en) | 1958-01-24 | 1960-02-16 | Du Pont | Solvent-soluble metal phthalocyanine compounds and process of making the same |
| US4209458A (en) | 1979-04-04 | 1980-06-24 | The United States Of America As Represented By The Secretary Of The Navy | Fluorinated phthalonitriles |
| DE3115532A1 (de) | 1980-04-17 | 1982-01-28 | Canon K.K., Tokyo | Tintenstrahl-aufzeichnungsverfahren und aufzeichnungstinte fuer die aufzeichnung auf einem bildempfangsmaterial |
| US4382033A (en) | 1980-10-06 | 1983-05-03 | Eastman Kodak Company | Novel phthalocyanine pigments |
| US4311775A (en) * | 1980-10-06 | 1982-01-19 | Eastman Kodak Company | Novel phthalocyanine pigments and electrophotographic uses thereof |
| CH654121A5 (de) | 1983-03-25 | 1986-01-31 | Ciba Geigy Ag | Verfahren zur herstellung von festen photoaktivatorpraeparaten. |
| US4701396A (en) | 1986-05-06 | 1987-10-20 | Eastman Kodak Company | Photoconductive phthalocyanine pigments, electrophotographic elements containing them and a method of use |
| WO1987007267A1 (en) | 1986-05-19 | 1987-12-03 | Allied Corporation | Method of synthesizing tetrafluorophthalonitrile |
| US4892941A (en) | 1987-04-17 | 1990-01-09 | Dolphin David H | Porphyrins |
| US5085698A (en) | 1990-04-11 | 1992-02-04 | E. I. Du Pont De Nemours And Company | Aqueous pigmented inks for ink jet printers |
| JP2899088B2 (ja) | 1990-08-31 | 1999-06-02 | キヤノン株式会社 | インクジェット用インク及びその製造方法、かかるインクを用いたインクジェット記録方法 |
| US5145684A (en) | 1991-01-25 | 1992-09-08 | Sterling Drug Inc. | Surface modified drug nanoparticles |
| NL9100191A (nl) | 1991-02-04 | 1992-09-01 | Philips Nv | Werkwijze voor het vervaardigen van een magneetkop en magneetkop vervaardigd volgens de werkwijze. |
| GB9116240D0 (en) | 1991-07-27 | 1991-09-11 | Ciba Geigy Ag | Pigment compositions |
| SG48074A1 (en) | 1992-05-20 | 1998-04-17 | Seiko Epson Corp | Ink composition for ink jet printing |
| US5405709A (en) | 1993-09-13 | 1995-04-11 | Eastman Kodak Company | White light emitting internal junction organic electroluminescent device |
| US7083984B2 (en) | 1993-09-24 | 2006-08-01 | Biosite, Inc. | Hybrid phthalocyanine derivatives and their uses |
| US6964844B1 (en) | 1993-09-24 | 2005-11-15 | Biosite, Inc. | Hybrid phthalocyanine derivatives and their uses |
| US6238931B1 (en) | 1993-09-24 | 2001-05-29 | Biosite Diagnostics, Inc. | Fluorescence energy transfer in particles |
| JP3451680B2 (ja) | 1993-11-15 | 2003-09-29 | 三菱化学株式会社 | 有機電界発光素子 |
| US5466796A (en) | 1994-04-26 | 1995-11-14 | Xerox Corporation | Alkoxy-bridged metallophthalocyanine dimers |
| US5500331A (en) | 1994-05-25 | 1996-03-19 | Eastman Kodak Company | Comminution with small particle milling media |
| US5441837A (en) | 1994-07-29 | 1995-08-15 | Xerox Corporation | Photoconductive imaging members with acetoxymetal phthalocyanines |
| US5614342A (en) | 1995-05-02 | 1997-03-25 | Eastman Kodak Company | Methods for preparing cocrystals of titanyl fluorophthalocyanines and unsubstituted titanyl phthalocyanine, electrophotographic elements, and titanyl phthalocyanine compositions |
| US5773181A (en) | 1995-05-23 | 1998-06-30 | Eastman Kodak Company | Non-uniformly substituted phthalocyanine compositions preparation methods, and electrophotographic elements |
| CN1068029C (zh) | 1995-11-01 | 2001-07-04 | 中国科学院化学研究所 | 纳米级酞菁类有机光导材料及其制备方法和用途 |
| US5679138A (en) | 1995-11-30 | 1997-10-21 | Eastman Kodak Company | Ink jet inks containing nanoparticles of organic pigments |
| US5683823A (en) | 1996-01-26 | 1997-11-04 | Eastman Kodak Company | White light-emitting organic electroluminescent devices |
| US5738716A (en) | 1996-08-20 | 1998-04-14 | Eastman Kodak Company | Color pigmented ink jet ink set |
| US5679139A (en) | 1996-08-20 | 1997-10-21 | Eastman Kodak Company | Cyan and magenta pigment set |
| US5679142A (en) | 1996-08-20 | 1997-10-21 | Eastman Kodak Company | Cyan ink jet pigment set |
| KR100256392B1 (ko) | 1996-09-30 | 2000-05-15 | 겐지 아이다 | 칼라필터용 감광성 수지 착색 조성물 및 이로부터 형성된 칼라필터 및 그 제조방법 |
| EP0889097B1 (en) | 1996-10-14 | 2005-06-29 | Nippon Shokubai Co., Ltd. | Phthalocyanine compounds, process for preparing the same, and optical recording medium made using the same |
| DE69703874T2 (de) | 1996-12-13 | 2001-07-19 | Eastman Kodak Co., Rochester | Pigmentierte Tintenstrahl-Tinten, die phosphatierte Ester-Derivate enthalten |
| US5817805A (en) | 1997-02-21 | 1998-10-06 | Eastman Kodak Company | Synthesis of bis(phthalocyanylalumino)tetraphenyldisiloxanes |
| US6051702A (en) | 1997-05-08 | 2000-04-18 | Rutgers, The University Of New Jersey | Organic dyes for photovoltaic cells and for photoconductive electrophotography systems |
| JPH11174702A (ja) * | 1997-12-09 | 1999-07-02 | Fuji Xerox Co Ltd | 電子写真感光体 |
| JPH11251059A (ja) | 1998-02-27 | 1999-09-17 | Sanyo Electric Co Ltd | カラー表示装置 |
| US6511971B1 (en) | 1998-10-13 | 2003-01-28 | Brown University Research Foundation | Substituted perhalogenated phthalocyanines |
| US6152999A (en) | 1999-04-27 | 2000-11-28 | Eastman Kodak Company | Color pigmented ink jet set |
| US6153000A (en) | 1999-07-12 | 2000-11-28 | Eastman Kodak Company | Color pigmented ink jet ink set |
| WO2001042826A1 (en) | 1999-12-09 | 2001-06-14 | Toray Industries, Inc. | Color filter and liquid crystal display device |
| JP2002014221A (ja) | 2000-06-30 | 2002-01-18 | Sumitomo Chem Co Ltd | 緑色フィルタ層を有する色フィルタアレイおよびその製造方法 |
| JP4287030B2 (ja) | 2000-06-30 | 2009-07-01 | 住友化学株式会社 | 赤色フィルタ層を有する色フィルタアレイおよびその製造方法 |
| JP2002014222A (ja) | 2000-06-30 | 2002-01-18 | Sumitomo Chem Co Ltd | 青色フィルタ層を有する色フィルタアレイおよびその製造方法 |
| AU2001277782A1 (en) | 2000-08-17 | 2002-02-25 | Mitsubishi Chemical Corporation | Composition for color filters and color filters |
| JP4407097B2 (ja) * | 2001-02-23 | 2010-02-03 | Ｄｉｃ株式会社 | カラーフィルター |
| DE60212345T2 (de) | 2001-02-23 | 2007-05-24 | Dainippon Ink And Chemicals, Inc. | Farbfilter |
| US20030027893A1 (en) | 2001-06-28 | 2003-02-06 | Eastman Kodak Company | Ink jet printing method |
| US6726755B2 (en) | 2002-02-08 | 2004-04-27 | Xerox Corporation | Ink compositions containing phthalocyanines |
| US7382514B2 (en) | 2002-02-11 | 2008-06-03 | Sipix Imaging, Inc. | Core-shell particles for electrophoretic display |
| JP2003241374A (ja) | 2002-02-14 | 2003-08-27 | Dainippon Printing Co Ltd | アルカリ可溶性グラフトポリマーからなる有機溶剤系着色レジスト用バインダー、有機溶剤系着色レジスト用顔料分散液、感光性着色組成物及び、カラーフィルター |
| TWI329662B (en) | 2002-05-17 | 2010-09-01 | Sipix Imaging Inc | Novel fluorinated silicon (iv) phthalocyanines and naphthalocyanines for electrophoretic, magnetophoretic or electromagnetophoretic display |
| JP4321013B2 (ja) | 2002-06-25 | 2009-08-26 | セイコーエプソン株式会社 | アルミニウムフタロシアニン顔料組成物及びこれを用いた画像記録物質 |
| KR100708327B1 (ko) | 2002-07-24 | 2007-04-17 | 다이니폰 인사츠 가부시키가이샤 | 컬러 필터용 녹색 안료, 녹색 안료 분산체, 감광성 착색조성물, 컬러 필터 및 액정 패널 |
| JP2004145275A (ja) | 2002-08-27 | 2004-05-20 | Seiko Epson Corp | 着色層材料、カラーフィルタ基板、電気光学装置及び電子機器、カラーフィルタ基板の製造方法、並びに電気光学装置の製造方法 |
| US6715869B1 (en) | 2002-11-19 | 2004-04-06 | Eastman Kodak Company | Ink set for ink jet printing |
| US6949139B2 (en) | 2002-12-02 | 2005-09-27 | Eastman Kodak Company | Process for forming cocrystals containing chlorine-free titanyl phthalocyanines and low concentration of titanyl fluorophthalocyanine using organic milling aid |
| DE10257498A1 (de) | 2002-12-10 | 2004-07-01 | Clariant Gmbh | Verfahren zur Herstellung von Phthalocyaninpigmentzubereitungen |
| EP1652410A1 (de) * | 2003-08-05 | 2006-05-03 | Technische Universität Braunschweig | Verwendung einer schicht aus hydrophoben, linear oder zweidimensional polyzyklischen aromaten als sperrschicht oder kapselung und mit einer derartigen schicht aufgebaute elektrische bauelemente mit organischen polymeren |
| WO2005033110A1 (en) | 2003-10-07 | 2005-04-14 | York University | Processes for producing polysubstituted phythalocyanines |
| US7572394B2 (en) | 2003-11-04 | 2009-08-11 | Sipix Imaging, Inc. | Electrophoretic dispersions |
| US7008742B2 (en) | 2003-12-24 | 2006-03-07 | Eastman Kodak Company | Heat-induced formation of co-crystalline composition containing titanyl phthalocyanine and titanyl fluorophthalocyanine |
| US7473777B2 (en) | 2004-03-15 | 2009-01-06 | Nippon Shokubai Co., Ltd. | Method for production of halogen-containing phthalocyanine compound |
| JP2005298490A (ja) | 2004-03-19 | 2005-10-27 | Toyo Ink Mfg Co Ltd | フタロシアニン化合物及びこれを用いた有機色素、光記録媒体 |
| US7211359B2 (en) | 2004-04-30 | 2007-05-01 | Eastman Kodak Company | Coating solution containing cocrystals and or crystals of a charge-generation pigment or a mixture of charge-generation pigments |
| US20050272831A1 (en) | 2004-06-04 | 2005-12-08 | Eastman Kodak Company | Aqueous inkjet ink compositon |
| US20060014855A1 (en) | 2004-07-14 | 2006-01-19 | Eastman Kodak Company | Pigment dispersion with polymeric dispersant |
| KR100882503B1 (ko) | 2004-10-06 | 2009-02-06 | 한국과학기술연구원 | 염료감응 태양전지용 고효율 대향전극 및 그 제조방법 |
| TW200730587A (en) | 2006-02-01 | 2007-08-16 | Fujifilm Corp | Phthalocyanine based pigment fine particle, pigment dispersing photoresist, colour transcription material, color filter, and liquid crystal display device |
| JP2007321107A (ja) | 2006-06-02 | 2007-12-13 | Fujifilm Corp | ナノ顔料分散物の製造方法、それにより得られるナノ顔料分散物、それを含む着色感光性樹脂組成物および感光性樹脂転写材料、ならびにそれらを用いたカラーフィルタおよび液晶表示装置 |
| TW200811249A (en) | 2006-06-02 | 2008-03-01 | Fujifilm Corp | Organic pigment nano-particle dispersion, its producing method, and ink-jet ink, colored photosensitive resin composition, photosensitive resin transcription material containing it, and color filter, liquid crystal display device, CCD device using it |
| JP2007321110A (ja) | 2006-06-02 | 2007-12-13 | Fujifilm Corp | 顔料ナノ粒子分散物の製造方法、顔料ナノ粒子を含む着色感光性樹脂組成物及び感光性転写材料、それらを用いたカラーフィルタ、液晶表示装置、及びｃｃｄデバイス、並びにカラーフィルタ用インクジェットインクの製造方法 |
| JP2007321111A (ja) | 2006-06-02 | 2007-12-13 | Fujifilm Corp | 顔料ナノ粒子の製造方法、顔料ナノ粒子分散物の製造方法、顔料ナノ粒子を含む顔料ナノ粒子分散物、着色感光性樹脂組成物、及び感光性転写材料、それらを用いたカラーフィルタ、液晶表示装置、及びｃｃｄデバイス |
| US7837780B2 (en) * | 2006-11-10 | 2010-11-23 | Global Oled Technology Llc | Green color filter element |
| US7973902B2 (en) | 2006-11-10 | 2011-07-05 | Global Oled Technology Llc | Display with RGB color filter element sets |
| US7585363B1 (en) * | 2008-10-29 | 2009-09-08 | Eastman Kodak Company | Method for preparing nanodispersions of fluorinated phthalocyanine pigments |
| US7628849B1 (en) * | 2008-10-29 | 2009-12-08 | Eastman Kodak Company | Fluorinated bis-(phthalocyanylaluminoxy)silyl pigments |
-
2008
- 2008-10-29 US US12/260,195 patent/US8277697B2/en active Active
-
2009
- 2009-10-20 JP JP2011534489A patent/JP5117618B2/ja active Active
- 2009-10-20 EP EP09752508.3A patent/EP2361398B1/en active Active
- 2009-10-20 KR KR1020117010983A patent/KR101256995B1/ko active Active
- 2009-10-20 CN CN200980147840.8A patent/CN102227655B/zh active Active
- 2009-10-20 WO PCT/US2009/005706 patent/WO2010053503A2/en not_active Ceased
- 2009-10-28 TW TW098136529A patent/TWI396871B/zh active
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20020117080A1 (en) * | 2000-12-22 | 2002-08-29 | Satoshi Okutsu | Colored composition for color filter and color filter |
| TW200829965A (en) * | 2006-11-08 | 2008-07-16 | Fujifilm Corp | Color filter, liquid crystal display device and CCD device |
Also Published As
| Publication number | Publication date |
|---|---|
| EP2361398B1 (en) | 2015-07-08 |
| KR20110079721A (ko) | 2011-07-07 |
| JP2012507743A (ja) | 2012-03-29 |
| WO2010053503A2 (en) | 2010-05-14 |
| EP2361398A2 (en) | 2011-08-31 |
| WO2010053503A3 (en) | 2010-11-04 |
| US20100102283A1 (en) | 2010-04-29 |
| US8277697B2 (en) | 2012-10-02 |
| CN102227655A (zh) | 2011-10-26 |
| CN102227655B (zh) | 2014-10-22 |
| TW201027145A (en) | 2010-07-16 |
| JP5117618B2 (ja) | 2013-01-16 |
| KR101256995B1 (ko) | 2013-04-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| TWI396871B (zh) | 具改良之著色劑分布的彩色濾光片元件 | |
| TWI426328B (zh) | 具有紅綠藍彩色濾光片元件組之顯示器以及形成該顯示器之方法 | |
| JP5837563B2 (ja) | 緑色フィルターエレメント | |
| CN109642970B (zh) | 滤色器用颜料组合物和滤色器 | |
| JP5944954B2 (ja) | 青色フィルターエレメント | |
| TW200837396A (en) | Red color filter element | |
| TWI898037B (zh) | 濾色器用顏料、著色組成物、及濾色器 |