DE69708721T2 - Pigmentzusammensetzungen - Google Patents
PigmentzusammensetzungenInfo
- Publication number
- DE69708721T2 DE69708721T2 DE69708721T DE69708721T DE69708721T2 DE 69708721 T2 DE69708721 T2 DE 69708721T2 DE 69708721 T DE69708721 T DE 69708721T DE 69708721 T DE69708721 T DE 69708721T DE 69708721 T2 DE69708721 T2 DE 69708721T2
- Authority
- DE
- Germany
- Prior art keywords
- quinacridone
- pigment
- halogen
- alkyl
- derivative
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000049 pigment Substances 0.000 title claims description 91
- 239000000203 mixture Substances 0.000 title claims description 58
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 claims description 82
- 229910052739 hydrogen Inorganic materials 0.000 claims description 38
- 239000001257 hydrogen Substances 0.000 claims description 38
- 229910052736 halogen Inorganic materials 0.000 claims description 33
- 150000002367 halogens Chemical group 0.000 claims description 33
- 150000002431 hydrogen Chemical group 0.000 claims description 31
- 125000006702 (C1-C18) alkyl group Chemical group 0.000 claims description 24
- 239000008199 coating composition Substances 0.000 claims description 21
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 16
- 125000000041 C6-C10 aryl group Chemical group 0.000 claims description 16
- 239000006104 solid solution Substances 0.000 claims description 13
- 239000006185 dispersion Substances 0.000 claims description 11
- 238000000576 coating method Methods 0.000 claims description 10
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 9
- 230000007062 hydrolysis Effects 0.000 claims description 9
- 238000006460 hydrolysis reaction Methods 0.000 claims description 9
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 9
- XTBAPWCYTNCZTO-UHFFFAOYSA-N 1H-isoindolone Natural products C1=CC=C2C(=O)N=CC2=C1 XTBAPWCYTNCZTO-UHFFFAOYSA-N 0.000 claims description 8
- 125000002723 alicyclic group Chemical group 0.000 claims description 8
- 125000003118 aryl group Chemical group 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 150000001768 cations Chemical class 0.000 claims description 8
- 125000000623 heterocyclic group Chemical group 0.000 claims description 8
- 229910052751 metal Inorganic materials 0.000 claims description 8
- 239000002184 metal Substances 0.000 claims description 8
- 238000002156 mixing Methods 0.000 claims description 8
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 8
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 8
- 125000001453 quaternary ammonium group Chemical group 0.000 claims description 8
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 5
- 229910052801 chlorine Inorganic materials 0.000 claims description 5
- 239000000460 chlorine Substances 0.000 claims description 5
- 239000011248 coating agent Substances 0.000 claims description 5
- -1 flavanthrone Chemical compound 0.000 claims description 5
- 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 4
- 150000004056 anthraquinones Chemical class 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 235000019239 indanthrene blue RS Nutrition 0.000 claims description 4
- UHOKSCJSTAHBSO-UHFFFAOYSA-N indanthrone blue Chemical compound C1=CC=C2C(=O)C3=CC=C4NC5=C6C(=O)C7=CC=CC=C7C(=O)C6=CC=C5NC4=C3C(=O)C2=C1 UHOKSCJSTAHBSO-UHFFFAOYSA-N 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 claims description 4
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 claims description 4
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound 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 claims description 4
- 230000000485 pigmenting effect Effects 0.000 claims description 4
- LLBIOIRWAYBCKK-UHFFFAOYSA-N pyranthrene-8,16-dione Chemical compound C12=CC=CC=C2C(=O)C2=CC=C3C=C4C5=CC=CC=C5C(=O)C5=C4C4=C3C2=C1C=C4C=C5 LLBIOIRWAYBCKK-UHFFFAOYSA-N 0.000 claims description 4
- JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical compound S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-N 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- GWVMLCQWXVFZCN-UHFFFAOYSA-N isoindoline Chemical compound C1=CC=C2CNCC2=C1 GWVMLCQWXVFZCN-UHFFFAOYSA-N 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 239000003973 paint Substances 0.000 description 11
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 7
- 229920005989 resin Polymers 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- XPZQBGDNVOHQIS-UHFFFAOYSA-N 2,9-dichloro-5,12-dihydroquinolino[2,3-b]acridine-7,14-dione Chemical compound N1C2=CC=C(Cl)C=C2C(=O)C2=C1C=C(C(=O)C=1C(=CC=C(C=1)Cl)N1)C1=C2 XPZQBGDNVOHQIS-UHFFFAOYSA-N 0.000 description 6
- 229910052782 aluminium Inorganic materials 0.000 description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- 239000010445 mica Substances 0.000 description 5
- 229910052618 mica group Inorganic materials 0.000 description 5
- IWCLHLSTAOEFCW-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-3-hydroxy-2H-pyrrolo[3,4-c]pyrrol-6-one Chemical compound Oc1[nH]c(c2C(=O)N=C(c12)c1ccc(Cl)cc1)-c1ccc(Cl)cc1 IWCLHLSTAOEFCW-UHFFFAOYSA-N 0.000 description 4
- 229920000178 Acrylic resin Polymers 0.000 description 4
- 229920000877 Melamine resin Polymers 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 239000002987 primer (paints) Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 4
- IGPFDBHTWKTPFD-UHFFFAOYSA-N 1,4-diphenylpyrrolo[3,4-c]pyrrole-3,6-dione Chemical compound C=1C=CC=CC=1C1=NC(=O)C2=C1C(=O)N=C2C1=CC=CC=C1 IGPFDBHTWKTPFD-UHFFFAOYSA-N 0.000 description 3
- TXWSZJSDZKWQAU-UHFFFAOYSA-N 2,9-dimethyl-5,12-dihydroquinolino[2,3-b]acridine-7,14-dione Chemical compound N1C2=CC=C(C)C=C2C(=O)C2=C1C=C(C(=O)C=1C(=CC=C(C=1)C)N1)C1=C2 TXWSZJSDZKWQAU-UHFFFAOYSA-N 0.000 description 3
- BFEJTCHFLJECJN-UHFFFAOYSA-N 4,11-Dichloro-5,12-dihydroquino[2,3-b]acridine-7,14-dione Chemical compound N1C2=C(Cl)C=CC=C2C(=O)C2=C1C=C(C(C=1C=CC=C(C=1N1)Cl)=O)C1=C2 BFEJTCHFLJECJN-UHFFFAOYSA-N 0.000 description 3
- DGWVTMBLTSNMFN-UHFFFAOYSA-N 4,11-dimethyl-5,12-dihydroquinolino[2,3-b]acridine-7,14-dione Chemical compound N1C2=C(C)C=CC=C2C(=O)C2=C1C=C(C(C=1C=CC=C(C=1N1)C)=O)C1=C2 DGWVTMBLTSNMFN-UHFFFAOYSA-N 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000000227 grinding Methods 0.000 description 3
- 238000000518 rheometry Methods 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- CEQCYBQBUDDHCB-UHFFFAOYSA-N 1,4-bis(2-tert-butylphenyl)pyrrolo[3,4-c]pyrrole-3,6-dione Chemical compound CC(C)(C)C1=CC=CC=C1C1=NC(=O)C2=C1C(=O)N=C2C1=CC=CC=C1C(C)(C)C CEQCYBQBUDDHCB-UHFFFAOYSA-N 0.000 description 2
- WOYGPBPSFPLCAJ-UHFFFAOYSA-N 1,4-bis(3,4-dichlorophenyl)pyrrolo[3,4-c]pyrrole-3,6-dione Chemical compound C1=C(Cl)C(Cl)=CC=C1C1=NC(=O)C2=C1C(=O)N=C2C1=CC=C(Cl)C(Cl)=C1 WOYGPBPSFPLCAJ-UHFFFAOYSA-N 0.000 description 2
- IGKHBMWUGKPAGT-UHFFFAOYSA-N 1,4-bis(4-methylphenyl)pyrrolo[3,4-c]pyrrole-3,6-dione Chemical compound C1=CC(C)=CC=C1C1=NC(=O)C2=C1C(=O)N=C2C1=CC=C(C)C=C1 IGKHBMWUGKPAGT-UHFFFAOYSA-N 0.000 description 2
- VTGOVLRDTGCTMT-UHFFFAOYSA-N 2,9-difluoro-5,12-dihydroquinolino[2,3-b]acridine-7,14-dione Chemical compound N1C2=CC=C(F)C=C2C(=O)C2=C1C=C(C(=O)C=1C(=CC=C(C=1)F)N1)C1=C2 VTGOVLRDTGCTMT-UHFFFAOYSA-N 0.000 description 2
- PBEFQMYEANTVGS-UHFFFAOYSA-N 3-hydroxy-1,4-bis(4-phenylphenyl)-2H-pyrrolo[3,4-c]pyrrol-6-one Chemical compound Oc1[nH]c(c2C(=O)N=C(c12)c1ccc(cc1)-c1ccccc1)-c1ccc(cc1)-c1ccccc1 PBEFQMYEANTVGS-UHFFFAOYSA-N 0.000 description 2
- 125000004801 4-cyanophenyl group Chemical group [H]C1=C([H])C(C#N)=C([H])C([H])=C1* 0.000 description 2
- 239000004640 Melamine resin Substances 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- 239000004411 aluminium Substances 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 2
- 238000003801 milling Methods 0.000 description 2
- YKPJEYXZEBLYCI-UHFFFAOYSA-N pyrrolo[3,4-c]pyrrole Chemical compound C1=NC=C2C=NC=C21 YKPJEYXZEBLYCI-UHFFFAOYSA-N 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- KSLLMGLKCVSKFF-UHFFFAOYSA-N 5,12-dihydroquinolino[2,3-b]acridine-6,7,13,14-tetrone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C(=O)C(C(=O)C1=CC=CC=C1N1)=C1C2=O KSLLMGLKCVSKFF-UHFFFAOYSA-N 0.000 description 1
- BUGUFPOZAOTHBP-UHFFFAOYSA-N C=12C(=O)C3=CC=CC=C3NC2=CC=CC=1NC1=CC=CC=C1 Chemical compound C=12C(=O)C3=CC=CC=C3NC2=CC=CC=1NC1=CC=CC=C1 BUGUFPOZAOTHBP-UHFFFAOYSA-N 0.000 description 1
- 239000004129 EU approved improving agent Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- XTDYIOOONNVFMA-UHFFFAOYSA-N dimethyl pentanedioate Chemical compound COC(=O)CCCC(=O)OC XTDYIOOONNVFMA-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000003966 growth inhibitor Substances 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000001935 peptisation Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- RQGPLDBZHMVWCH-UHFFFAOYSA-N pyrrolo[3,2-b]pyrrole Chemical compound C1=NC2=CC=NC2=C1 RQGPLDBZHMVWCH-UHFFFAOYSA-N 0.000 description 1
- FYNROBRQIVCIQF-UHFFFAOYSA-N pyrrolo[3,2-b]pyrrole-5,6-dione Chemical compound C1=CN=C2C(=O)C(=O)N=C21 FYNROBRQIVCIQF-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- C09B48/00—Quinacridones
-
- 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
-
- 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
- C09B67/0036—Mixtures of quinacridones
-
- 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
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/41—Organic pigments; Organic dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Paints Or Removers (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US1156696P | 1996-02-13 | 1996-02-13 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE69708721D1 DE69708721D1 (de) | 2002-01-17 |
| DE69708721T2 true DE69708721T2 (de) | 2002-08-22 |
Family
ID=21750960
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE69708721T Expired - Lifetime DE69708721T2 (de) | 1996-02-13 | 1997-02-04 | Pigmentzusammensetzungen |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US5827364A (https=) |
| EP (1) | EP0790281B1 (https=) |
| JP (1) | JP3865849B2 (https=) |
| CA (1) | CA2197275A1 (https=) |
| DE (1) | DE69708721T2 (https=) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001515942A (ja) | 1997-09-10 | 2001-09-25 | チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド | 着色剤として有用なイソキシンジゴ及びそれらの製造 |
| US6057449A (en) | 1998-06-02 | 2000-05-02 | Ciba Specialty Chemicals Corporation | Direct preparation of pyrrolo[3,4-c]pyrroles |
| DE60026133T2 (de) * | 1999-02-02 | 2006-08-03 | Ciba Speciality Chemicals Holding Inc. | Verbindungen zur Kontrolle des Teilchenwachstums und /oder der Kristallphase von Pigmenten |
| US6264733B1 (en) * | 1999-02-02 | 2001-07-24 | Ciba Specialty Chemicals Corporation | Pigment particle growth and/or crystal phase directors |
| US20010015154A1 (en) | 2000-01-27 | 2001-08-23 | Roman Lenz | Ternary pigment compositions |
| AU2003303819A1 (en) * | 2003-01-28 | 2004-08-23 | Ciba Specialty Chemicals Holding Inc. | Synthesis of small particle size quinacridone of beta crystal phase |
| JP4385210B2 (ja) * | 2003-07-31 | 2009-12-16 | Ｄｉｃ株式会社 | インクジェット記録用水性インキ組成物、該インク組成物を製造するためのインクジェットインク用水性顔料分散液、及びインクジェットインク用着色混練物及びこれらの製造方法。 |
| CA2542519A1 (en) | 2003-10-23 | 2005-05-06 | Ciba Specialty Chemicals Holding Inc. | Heat-stable diketopyrrolopyrrole pigment mixtures |
| US8273269B2 (en) | 2008-05-28 | 2012-09-25 | Basf Se | Red colour filter composition |
| EP2471876B1 (en) | 2009-08-27 | 2014-12-10 | FUJIFILM Corporation | Dichlorodiketopyrrolopyrrole pigment, coloring material dispersion containing the pigment, and process for production of the coloring material dispersion |
| KR101130651B1 (ko) | 2009-12-24 | 2012-04-02 | (주)경인양행 | 디스플레이의 컬러 필터용 피라졸 함유 안료 유도체 |
| WO2019054281A1 (ja) | 2017-09-15 | 2019-03-21 | 富士フイルム株式会社 | 組成物、膜、積層体、赤外線透過フィルタ、固体撮像素子および赤外線センサ |
| JP7114724B2 (ja) | 2018-09-20 | 2022-08-08 | 富士フイルム株式会社 | 硬化性組成物、硬化膜、赤外線透過フィルタ、積層体、固体撮像素子、センサ、及び、パターン形成方法 |
| WO2021039205A1 (ja) | 2019-08-29 | 2021-03-04 | 富士フイルム株式会社 | 組成物、膜、近赤外線カットフィルタ、パターン形成方法、積層体、固体撮像素子、赤外線センサ、画像表示装置、カメラモジュール、及び、化合物 |
| WO2022131191A1 (ja) | 2020-12-16 | 2022-06-23 | 富士フイルム株式会社 | 組成物、膜、光学フィルタ、固体撮像素子、画像表示装置および赤外線センサ |
| WO2022130773A1 (ja) | 2020-12-17 | 2022-06-23 | 富士フイルム株式会社 | 組成物、膜、光学フィルタ、固体撮像素子、画像表示装置および赤外線センサ |
| EP4535432A4 (en) | 2022-06-01 | 2025-10-29 | Fujifilm Corp | PHOTOSENSING ELEMENT, IMAGE SENSOR AND METHOD FOR MANUFACTURING PHOTOSENSING ELEMENT |
| WO2023234094A1 (ja) | 2022-06-01 | 2023-12-07 | 富士フイルム株式会社 | 光検出素子、イメージセンサおよび光検出素子の製造方法 |
| EP4535047A4 (en) | 2022-06-01 | 2025-10-08 | Fujifilm Corp | LIGHT DETECTION ELEMENT, IMAGE SENSOR, AND METHOD FOR PRODUCING LIGHT DETECTION ELEMENT |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3275637A (en) * | 1965-11-18 | 1966-09-27 | Du Pont | Modified quinacridones |
| DE2905114C2 (de) * | 1979-02-10 | 1981-03-19 | Basf Ag, 6700 Ludwigshafen | Pigmentzubereitungen |
| DE3164935D1 (en) * | 1980-02-18 | 1984-08-30 | Basf Ag | Dyestuffs containing imidazolylethylene groups and their use |
| JPS61168666A (ja) * | 1985-01-21 | 1986-07-30 | Dainippon Ink & Chem Inc | 顔料組成物 |
| DE3833422A1 (de) * | 1988-10-01 | 1990-04-05 | Hoechst Ag | Chinacridone mit gezielt eingestellten triboelektrischen effekten |
| EP0485337B1 (en) * | 1990-11-08 | 1995-04-19 | Ciba-Geigy Ag | Pyrazole-containing pigment derivatives |
| US5145524A (en) * | 1991-02-20 | 1992-09-08 | Ciba-Geigy Corporation | Surface modified pigment compositions |
| JPH06212088A (ja) * | 1993-01-20 | 1994-08-02 | Dainippon Ink & Chem Inc | 顔料組成物及び塗料 |
-
1997
- 1997-02-04 EP EP97810053A patent/EP0790281B1/en not_active Expired - Lifetime
- 1997-02-04 DE DE69708721T patent/DE69708721T2/de not_active Expired - Lifetime
- 1997-02-11 CA CA002197275A patent/CA2197275A1/en not_active Abandoned
- 1997-02-13 JP JP02857897A patent/JP3865849B2/ja not_active Expired - Fee Related
- 1997-02-21 US US08/804,306 patent/US5827364A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JP3865849B2 (ja) | 2007-01-10 |
| US5827364A (en) | 1998-10-27 |
| JPH1030063A (ja) | 1998-02-03 |
| DE69708721D1 (de) | 2002-01-17 |
| EP0790281B1 (en) | 2001-12-05 |
| CA2197275A1 (en) | 1997-08-14 |
| EP0790281A2 (en) | 1997-08-20 |
| EP0790281A3 (en) | 1997-12-17 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8364 | No opposition during term of opposition | ||
| 8328 | Change in the person/name/address of the agent |
Representative=s name: PFENNING MEINIG & PARTNER GBR, 80339 MUENCHEN |
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| 8327 | Change in the person/name/address of the patent owner |
Owner name: CIBA HOLDING INC., BASEL, CH |
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| 8328 | Change in the person/name/address of the agent |
Representative=s name: MAIWALD PATENTANWALTSGESELLSCHAFT MBH, 80335 MUENC |