WO2009101932A1 - 感光性着色組成物、並びにカラーフィルタ及びその製造方法 - Google Patents
感光性着色組成物、並びにカラーフィルタ及びその製造方法 Download PDFInfo
- Publication number
- WO2009101932A1 WO2009101932A1 PCT/JP2009/052218 JP2009052218W WO2009101932A1 WO 2009101932 A1 WO2009101932 A1 WO 2009101932A1 JP 2009052218 W JP2009052218 W JP 2009052218W WO 2009101932 A1 WO2009101932 A1 WO 2009101932A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- group
- coloring composition
- pigment
- photosensitive coloring
- acid
- Prior art date
Links
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/0005—Production of optical devices or components in so far as characterised by the lithographic processes or materials used therefor
- G03F7/0007—Filters, e.g. additive colour filters; Components for display devices
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/20—Filters
-
- 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
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/0045—Photosensitive materials with organic non-macromolecular light-sensitive compounds not otherwise provided for, e.g. dissolution inhibitors
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
- G03F7/028—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with photosensitivity-increasing substances, e.g. photoinitiators
- G03F7/031—Organic compounds not covered by group G03F7/029
Definitions
- the present invention relates to a photosensitive coloring composition containing a pigment as a colorant, a color filter using the same, and a method for producing the same.
- Color filters used in liquid crystal display elements (LCD) and image sensors (CCD, CMOS, etc.) are generally red (R), green (G), blue (B), and in some cases, magenta (M), cyan. (C), yellow (Y), and black (K) fine colored patterns are regularly arranged on a glass substrate or a wafer.
- the pixels constituting the color filter are conventionally produced by a method such as a dyeing method, a printing method, a pigment dispersion method, or an electrodeposition method.
- pixels are sequentially formed one color at a time.
- the pigment dispersion method has high pattern accuracy and the manufacturing process is stable, many color filters are manufactured by this method. Has been.
- a photosensitive coloring composition containing a colorant, a polymerizable monomer, and a photopolymerization initiator is applied onto a substrate, pre-baked to form a film, and then irradiated with ultraviolet rays through a desired mask. Then, the irradiated portion is cured, the unirradiated portion is removed by a development process to form a colored pattern, and a heat treatment is further performed on this to obtain a cured film (colored pixel) formed in a desired pattern.
- This method is based on the principle that a photopolymerization initiator generates an active radical by irradiation with ultraviolet rays or the like, which attacks a polymerizable group such as a (meth) acryloyl group to induce a polymerization reaction. That is, the polymerization is not started until the presence of active radicals.
- the required product spec width has become stricter, and there is a need to reduce variations in line width, film thickness, spectral spectrum, and the like due to exposure illumination dependency. That is, when exposure is performed at low illuminance, there is a tendency that variations in the shape of the pattern to be formed tend to occur as compared to, for example, pattern formation by high illuminance exposure.
- the problem caused by the exposure illuminance dependency improves the exposure illuminance dependency which is difficult to be solved only by adjusting the type and amount of the photopolymerization initiator as described above, particularly for a color having a high i-line transmittance. In order to do this, measures are usually taken to increase the amount of photopolymerization initiation. When the amount of the photopolymerization initiator is increased, on the contrary, the line width becomes too thick or peripheral residues due to exposure halation are likely to occur.
- the present invention has been made in view of the above. Under the above circumstances, exposure illuminance dependency (particularly, variation in shape such as line width at low illuminance of 95% or less of high illuminance) is kept small, the remaining film ratio is high, the development residue is small, and the resolution is high. There is a need for a photosensitive coloring composition that can stably form a pattern having excellent properties. There is also a need for a color filter capable of displaying fine and high quality images and a method for manufacturing the same.
- a photosensitive coloring composition containing at least a pigment, a polymerizable monomer, a photopolymerization initiator, and a compound represented by the following general formula (I).
- R 1 and R 2 each independently represents a hydrogen atom, an alkyl group having 1 to 20 carbon atoms, or an aryl group having 6 to 20 carbon atoms.
- R 1 and R 2 may be the same or different from each other, but do not represent a hydrogen atom at the same time, and R 1 and R 2 may form a cyclic amino group together with a nitrogen atom.
- R 3 and R 4 each independently represents an electron withdrawing group.
- the photosensitive material according to ⁇ 1> wherein the content of the compound represented by the general formula (I) is 0.01 to 10% by mass in the solid content of the photosensitive coloring composition. It is a sex coloring composition.
- R 1 and R 2 are each independently a lower alkyl group having 1 to 8 carbon atoms. Or a substituted or unsubstituted phenyl group.
- the electron withdrawing group represented by R 3 or R 4 has a ⁇ p value of 0.30 or more. An electron-withdrawing group of 0.80 or less is preferable.
- R 3 is a cyano group, —COOR 5 , —CONHR 5 , —COR 5 , and —SO It is preferable that R 4 is a group selected from 2 R 5 , wherein R 4 is a group selected from a cyano group, —COOR 6 , —CONHR 6 , —COR 6 , and —SO 2 R 6 .
- R 5 and R 6 each independently represents an alkyl group having 1 to 20 carbon atoms or an aryl group having 6 to 20 carbon atoms.
- the photopolymerization initiator is preferably an oxime ester compound, more preferably 2- (O— Benzoyloxime) -1- [4- (phenylthio) phenyl] -1,2-octanedione and 1- (O-acetyloxime) -1- [9-ethyl-6- (2-methylbenzoyl) -9H- Carbazol-3-yl] ethanone.
- the pigment is a red pigment, and is preferably configured in a magenta or red color.
- Pattern formation by applying the photosensitive coloring composition according to any one of ⁇ 1> to ⁇ 8>, exposing the applied coating layer through a photomask, and developing the coating layer This is a method for manufacturing a color filter.
- exposure illuminance dependency (particularly, shape variation such as line width at a low illuminance of 95% or less of high illuminance) is suppressed to be small, the residual film ratio is high, the development residue is small, and the resolution is reduced.
- the photosensitive coloring composition which can form the pattern excellent in the property stably can be provided. Also, ADVANTAGE OF THE INVENTION According to this invention, the color filter which can display a fine and high quality image, and its manufacturing method can be provided.
- the photosensitive coloring composition of the present invention a color filter constituted using the photosensitive coloring composition, and a method for producing the same will be described in detail.
- the photosensitive coloring composition of the present invention is composed of at least a compound represented by the following general formula (I) as a pigment, a polymerizable monomer, a photopolymerization initiator, and an ultraviolet absorber.
- a solvent is used.
- the photosensitive coloring composition of this invention can be further comprised using other components, such as a pigment dispersant and / or a pigment derivative, alkali-soluble resin, as needed.
- a photosensitive composition containing a pigment as a colorant is formed using an ultraviolet absorber having a specific structure, so that the illuminance dependency during exposure, particularly low illuminance (for example, 95% or less of high illuminance). Since the development performance fluctuations when developing with pattern exposure with (illuminance) are suppressed, pattern variations such as residual film ratio after development, development residue fluctuations, pattern width variations, etc. are reduced, and the pattern has excellent resolution. Can be formed stably.
- each component which comprises the photosensitive coloring composition of this invention is explained in full detail.
- the photosensitive coloring composition of the present invention contains at least one pigment.
- the pigment conventionally known various inorganic pigments or organic pigments can be used. Regardless of whether the pigment is an inorganic pigment or an organic pigment, it is preferable to use a pigment having a small particle size and a small particle size as much as possible in consideration of handling properties.
- the pigment preferably has an average primary particle size of 0.01 to 0.3 ⁇ m, more preferably 0.01 to 0.15 ⁇ m. When the average primary particle diameter is within the above range, the transmittance is high, the color characteristics are good, and it is effective for forming a color filter with high contrast.
- the average primary particle diameter is obtained by observing with a scanning electron microscope (SEM) or a transmission electron microscope (TEM), measuring 100 particle sizes in a portion where the particles are not aggregated, and calculating the average value. It is done.
- the inorganic pigment examples include metal compounds such as metal oxides and metal complex salts. Specific examples include metal oxides such as iron, cobalt, aluminum, cadmium, lead, copper, titanium, magnesium, chromium, zinc, and antimony, and composite oxides of the above metals.
- Examples of the organic pigment include: C. I. Pigment Red 1, 2, 3, 4, 5, 6, 7, 9, 10, 14, 17, 22, 23, 31, 38, 41, 48: 1, 48: 2, 48: 3, 48: 4 49, 49: 1, 49: 2, 52: 1, 52: 2, 53: 1, 57: 1, 60: 1, 63: 1, 66, 67, 81: 1, 81: 2, 81: 3 83, 88, 90, 105, 112, 119, 122, 123, 144, 146, 149, 150, 155, 166, 168, 169, 170, 171, 172, 175, 176, 177, 178, 179, 184 185, 187, 188, 190, 200, 202, 206, 207, 208, 209, 210, 216, 220, 224, 226, 242, 246, 254, 255, 264, 270, 272, 279; C.
- preferable pigments include the following. However, the present invention is not limited to these.
- a fine and sized organic pigment can be used as necessary.
- the refinement of the pigment is a process of grinding as a highly viscous liquid composition together with the pigment, the water-soluble organic solvent, and the water-soluble inorganic salts. Specifically, it is described in paragraph numbers [0030] to [0032] of JP-A-2007-112934. Then, as described in paragraph [0034] of the same publication, the ground mixture is dissolved in warm water at 80 ° C. together with a water-soluble organic solvent and water-soluble inorganic salts, filtered, washed with water, and dried in an oven. A fine pigment can be obtained.
- the organic pigments can be used alone or in various combinations in order to increase color purity. Specific examples of combinations are shown below.
- red pigments anthraquinone pigments, perylene pigments, diketopyrrolopyrrole pigments alone or at least one of them, disazo yellow pigments, isoindoline yellow pigments, quinophthalone yellow pigments or perylene pigments
- a mixture of a red pigment, an anthraquinone red pigment, a diketopyrrolopyrrole red pigment, or the like can be used.
- an anthraquinone pigment C.I. I. Pigment Red 177
- perylene pigments include C.I. I. Pigment red 155, C.I. I.
- Pigment red 224, and diketopyrrolopyrrole pigments include C.I. I. Pigment Red 254, and C.I. I. Pigment yellow 83, C.I. I. Pigment yellow 139 or C.I. I. Mixing with Pigment Red 177 is preferred.
- the mass ratio of the red pigment to the other color pigment is preferably 100: 5 to 100: 80. When the mass ratio is 100: 5 or more, the light transmittance of 400 nm to 500 nm can be suppressed and the color purity can be increased, and when it is 100: 80 or less, the color developing power is good. In particular, the mass ratio is optimally in the range of 100: 10 to 100: 65. In addition, in the case of the combination of red pigments, it can adjust according to chromaticity.
- one kind of halogenated phthalocyanine pigment may be used alone or a mixture thereof with a disazo yellow pigment, a quinophthalone yellow pigment, an azomethine yellow pigment or an isoindoline yellow pigment may be used. it can.
- a disazo yellow pigment a quinophthalone yellow pigment, an azomethine yellow pigment or an isoindoline yellow pigment
- an isoindoline yellow pigment it can.
- C.I. I. Pigment Green 7, 36, 37 and C.I. I. Pigment yellow 83 C.I. I. Pigment yellow 138, C.I. I. Pigment yellow 139, C.I. I. Pigment yellow 150, C.I. I. Pigment yellow 180 or C.I. I. Mixing with Pigment Yellow 185 is preferred.
- the mass ratio of the green pigment to the yellow pigment is preferably 100: 5 to 100: 200.
- the mass ratio is 100: 5 or more, the light transmittance at 400 to 450 nm can be suppressed, and the color purity can be increased.
- the mass ratio is 100: 200 or less, the main wavelength is not deviated from the long wavelength and the NTSC target hue is not lost. Can be avoided.
- the mass ratio is particularly preferably in the range of 100: 20 to 100: 150.
- the blue pigment a single phthalocyanine pigment or a mixture of this and a dioxazine purple pigment can be used.
- C.I. I. Pigment blue 15: 6 and C.I. I. A mixture with pigment violet 23 can be mentioned.
- the mass ratio of the blue pigment to the violet pigment is preferably 100: 0 to 100: 100, more preferably 100: 70 or less.
- carbon black, graphite, titanium black, iron oxide, titanium oxide alone or a mixture thereof can be used, and a combination of carbon black and titanium black is preferable.
- the mass ratio of carbon black to titanium black is preferably in the range of 100: 0 to 100: 60. If it is 100: 61 or more, the dispersion stability may decrease.
- the content of the pigment in the photosensitive coloring composition is preferably 1 to 30% by mass and more preferably 3 to 20% by mass with respect to the total solid content (mass) of the composition.
- the color density is sufficient and it is effective to ensure excellent color characteristics.
- Pigment dispersant The photosensitive coloring composition of the present invention may contain at least one pigment dispersant for dispersing a pigment. By containing this pigment dispersant, the dispersibility of the pigment in the composition can be improved.
- pigment dispersant for example, a known pigment dispersant or surfactant can be appropriately selected and used. Specifically, many types of compounds can be used. For example, organosiloxane polymer KP341 (manufactured by Shin-Etsu Chemical Co., Ltd.), (meth) acrylic acid (co) polymer polyflow No. 75, no. 90, no.
- Cationic surfactants such as 95 (manufactured by Kyoeisha Chemical Industry Co., Ltd.) and W001 (manufactured by Yusho Co., Ltd.); polyoxyethylene lauryl ether, polyoxyethylene stearyl ether, polyoxyethylene oleyl ether, polyoxyethylene octyl Nonionic surfactants such as phenyl ether, polyoxyethylene nonyl phenyl ether, polyethylene glycol dilaurate, polyethylene glycol distearate, sorbitan fatty acid ester; anionic surfactants such as W004, W005, W017 (manufactured by Yusho Co., Ltd.) Agent: EFKA-46, EFKA-47, EFKA-47EA, EFKA polymer 100, EFKA polymer 400, EFKA polymer 401, EFKA polymer 450 (all manufactured by Ciba Specialty Chemicals) Polymer dispersants such as Disperse Aid 6, Disperse Aid 8,
- the content of the pigment dispersant in the photosensitive coloring composition is preferably 1 to 100% by mass and more preferably 3 to 70% by mass with respect to the mass of the pigment described above.
- the photosensitive coloring composition of the present invention may contain a pigment derivative together with the pigment dispersant, if necessary.
- a pigment derivative having an affinity for the pigment dispersant or a polar group introduced is adsorbed on the surface of the pigment, and this is used as an adsorption point for the pigment dispersant, whereby the pigment is formed into fine particles as a photosensitive coloring composition. It can be dispersed to prevent re-aggregation, and is effective in constructing a color filter having high contrast and excellent transparency.
- the pigment derivative is a compound in which an organic pigment is used as a base skeleton and an acidic group, a basic group, or an aromatic group is introduced as a substituent in the side chain.
- organic pigments include quinacridone pigments, phthalocyanine pigments, azo pigments, quinophthalone pigments, isoindoline pigments, isoindolinone pigments, quinoline pigments, diketopyrrolopyrrole pigments, benzimidazo And Ron pigments.
- light yellow aromatic polycyclic compounds such as naphthalene series, anthraquinone series, triazine series and quinoline series which are not called pigments are also included.
- Examples of the dye derivatives include JP-A-11-49974, JP-A-11-189732, JP-A-10-245501, JP-A-2006-265528, JP-A-8-295810, and JP-A-11-199796. JP-A-2005-234478, JP-A-2003-240938, JP-A-2001-356210, etc. can be used.
- the content of the pigment derivative in the photosensitive coloring composition is preferably 1 to 30% by mass and more preferably 3 to 20% by mass with respect to the mass of the pigment.
- the content is within the above range, it is possible to achieve good dispersion while keeping the viscosity low, improve the dispersion stability after dispersion, and obtain excellent color characteristics with high transmittance.
- it can be comprised by the high contrast which has a favorable color characteristic.
- the dispersion method is, for example, using a bead disperser using zirconia beads or the like (for example, a disperse mat made by GETZMANN Co., Ltd.), in which a pigment and a pigment dispersant are mixed in advance and dispersed in advance using a homogenizer or the like. Can be done by finely dispersing.
- the dispersion time is preferably about 3 to 6 hours.
- the photosensitive coloring composition of the present invention comprises at least one compound represented by the following general formula (I), which is a conjugated diene compound, as an ultraviolet absorber. contains.
- this conjugated diene compound suppresses subsequent development performance fluctuations particularly when low-illuminance exposure is performed, so it is related to pattern formability such as pattern line width, film thickness, and spectral spectrum. Dependence on exposure illuminance can be suppressed.
- R 1 and R 2 each independently represent a hydrogen atom, an alkyl group having 1 to 20 carbon atoms, or an aryl group having 6 to 20 carbon atoms, and R 1 and R 2 May be the same as or different from each other, but do not represent a hydrogen atom at the same time.
- Examples of the alkyl group having 1 to 20 carbon atoms represented by R 1 and R 2 include a methyl group, an ethyl group, a propyl group, an n-butyl group, an n-hexyl group, a cyclohexyl group, and n-decyl.
- the alkyl group represented by R 1 and R 2 may have a substituent, and examples of the substituent of the alkyl group having a substituent include an alkyl group, an aryl group, an alkoxy group, an aryloxy group, Acyloxy group, halogen atom, acylamino group, acyl group, alkylthio group, arylthio group, hydroxy group, cyano group, alkyloxycarbonyl group, aryloxycarbonyl group, substituted carbamoyl group, substituted sulfamoyl group, nitro group, substituted amino group, alkyl A sulfonyl group, an arylsulfonyl group, etc. are mentioned.
- the aryl group having 6 to 20 carbon atoms represented by R 1 and R 2 may be a monocyclic ring or a condensed ring, and may be a substituted aryl group having a substituent or an unsubstituted aryl group. There may be. Examples thereof include a phenyl group, a 1-naphthyl group, a 2-naphthyl group, an anthryl group, a phenanthryl group, an indenyl group, an acenaphthenyl group, a fluorenyl group, and the like.
- Examples of the substituent of the substituted aryl group having a substituent include an alkyl group, an aryl group, an alkoxy group, an aryloxy group, an acyloxy group, a halogen atom, an acylamino group, an acyl group, an alkylthio group, an arylthio group, and a hydroxy group.
- a substituted or unsubstituted phenyl group, 1-naphthyl group, and 2-naphthyl group are preferable.
- R 1 and R 2 may form a cyclic amino group together with the nitrogen atom.
- the cyclic amino group include piperidino group, morpholino group, pyrrolidino group, hexahydroazepino group, piperazino group and the like.
- R 1 and R 2 are lower alkyl groups having 1 to 8 carbon atoms (for example, methyl, ethyl, isopropyl, butyl, sec-butyl, tert-butyl, pentyl, tert-pentyl, hexyl, octyl) , 2-ethylhexyl, tert-octyl, etc.) or a substituted or unsubstituted phenyl group (for example, tolyl group, phenyl group, anisyl group, mesityl group, chlorophenyl group, 2,4-di-t-amylphenyl group, etc.) preferable. It is also preferred that R 1 and R 2 are combined to form a ring (for example, a piperidine ring, a pyrrolidine ring, a morpholine ring) containing the nitrogen atom represented by N in the formula.
- a ring for example, a pipe
- R 3 and R 4 represent an electron withdrawing group.
- the electron-withdrawing group is an electron-withdrawing group having a Hammett's substituent constant ⁇ p value (hereinafter simply referred to as “ ⁇ p value”) of 0.20 or more and 1.0 or less.
- ⁇ p value a Hammett's substituent constant
- ⁇ p value a Hammett's substituent constant
- it is an electron withdrawing group having a ⁇ p value of 0.30 or more and 0.80 or less.
- Hammett's rule is an empirical rule proposed by L. P. Hammett in 1935 to quantitatively discuss the effect of substituents on the reaction or equilibrium of benzene derivatives. This is widely accepted today.
- Substituent constants obtained by Hammett's rule include a ⁇ p value and a ⁇ m value, and these values are described in many general books. For example, the JA Dean edition “Lange's Handbook of Chemistry” “Twelfth edition, 1979 (Mc Graw-Hill)", “Chemical domain special issue”, 122, 96-103, 1979 (Nanedo), Chemical Reviews, 91, 165-195, 1991 detailed. In the present invention, it does not mean that the literature known values described in these documents are limited to only certain substituents, and even if the values are unknown to the literature, Of course, it is included in the electron withdrawing group as long as it falls within the range.
- the electron-withdrawing group having a ⁇ p value of 0.20 or more and 1.0 or less include an acyl group, an acyloxy group, a carbamoyl group, an alkyloxycarbonyl group, an aryloxycarbonyl group, a cyano group, a nitro group, Dialkylphosphono group, diarylphosphono group, diarylphosphinyl group, alkylsulfinyl group, arylsulfinyl group, alkylsulfonyl group, arylsulfonyl group, sulfonyloxy group, acylthio group, sulfamoyl group, thiocyanate group, thiocarbonyl group, at least An alkyl group substituted with two or more halogen atoms, an alkoxy group substituted with at least two halogen atoms, an aryloxy group substituted with at least two halogen atoms, or at least
- R 3 is preferably a cyano group, a group selected from —COOR 5 , —CONHR 5 , —COR 5 , —SO 2 R 5 , and R 4 is cyano.
- a group selected from the group, —COOR 6 , —CONHR 6 , —COR 6 , —SO 2 R 6 is preferred.
- R 5 and R 6 each independently represents an alkyl group having 1 to 20 carbon atoms or an aryl group having 6 to 20 carbon atoms.
- the alkyl group having 1 to 20 carbon atoms and the aryl group having 6 to 20 carbon atoms represented by R 5 and R 6 have the same meanings as in R 1 and R 2 , and the preferred embodiments are also the same.
- R 3 and R 4 acyl group, carbamoyl group, alkyloxycarbonyl group, aryloxycarbonyl group, cyano group, nitro group, alkylsulfonyl group, arylsulfonyl group, sulfonyloxy group, sulfamoyl group are preferable.
- an acyl group, a carbamoyl group, an alkyloxycarbonyl group, an aryloxycarbonyl group, a cyano group, an alkylsulfonyl group, an arylsulfonyl group, a sulfonyloxy group, and a sulfamoyl group are preferable.
- R 3 and R 4 may be bonded to each other to form a ring.
- R 1 , R 2 , R 3 , and R 4 may be in the form of a polymer derived from a monomer bonded to a vinyl group via a linking group.
- the copolymer with another monomer may be sufficient.
- examples of other monomers include acrylic acid, ⁇ -chloroacrylic acid, ⁇ -alacrylic acid (for example, esters derived from acrylic acids such as methacrylic acid, preferably lower alkyl esters).
- amides eg, acrylamide, methacrylamide, t-butyl acrylamide, methyl acrylate, methyl methacrylate, ethyl acrylate, ethyl methacrylate, n-propyl acrylate, n-butyl acrylate, 2-ethylhexyl acrylate, n-hexyl acrylate, Octyl methacrylate, lauryl methacrylate, methylene bisacrylamide, etc.)), vinyl esters (eg, vinyl acetate, vinyl propionate, vinyl laurate, etc.), acrylonitrile, meta Acrylonitrile, aromatic vinyl compounds (for example, styrene and its derivatives such as vinyl toluene, divinylbenzene, vinyl acetophenone, sulfostyrene, styrene sulfinic acid, etc.), itaconic acid, citraconic acid, crotonic acid, vinylidene chlor
- acrylic acid esters methacrylic acid esters, and aromatic vinyl compounds are particularly preferable.
- Two or more comonomer compounds can be used together.
- n-butyl acrylate and divinylbenzene, styrene and methyl methacrylate, methyl acrylate and methacrylate acid, and the like can be used.
- the compounds represented by the general formula (I) in the present invention are disclosed in JP-B-44-29620, JP-A-53-128333, JP-A-61-169831, JP-A-63-53543, They can be synthesized by the methods described in Japanese Utility Model Laid-Open Nos. 63-53544 and 63-56651.
- the content of the compound represented by the above general formula (I) (conjugated diene compound) in the photosensitive coloring composition of the present invention is 0.01% by mass to 10% with respect to the total solid content of the composition. % By mass is preferable, 0.01% by mass to 7.5% by mass is more preferable, and 0.01% by mass to 5% by mass is particularly preferable.
- the content of the conjugated diene compound (ultraviolet absorber) is 0.01% by mass or more, the light shielding ability at the time of exposure is good and the pattern line width is prevented from being increased due to excessive progress of polymerization. It is easy to obtain the line width and the generation of peripheral residues is further suppressed. Further, when the content of the conjugated diene compound is 10% by mass or less, the light shielding ability at the time of exposure is not too strong, and the polymerization proceeds better.
- the change in the pattern line width as described above becomes conspicuous in a magenta or red photosensitive coloring composition with little light absorption with respect to ultraviolet rays such as g-line, h-line and i-line as exposure light sources. Therefore, the compound represented by the general formula (I) (conjugated diene compound) is particularly effective when constituting a magenta or red photosensitive coloring composition.
- the photosensitive coloring composition of the present invention contains at least one photopolymerization initiator.
- the photopolymerization initiator include halomethyl oxadiazole described in JP-A-57-6096, halomethyl-s-triazine described in JP-B-59-1281, JP-A-53-133428, and the like.
- Aromatic ketone compounds such as benzophenones, (thio) xanthones or acridine compounds described in Fr-2456541, compounds such as coumarins or lophine dimers described in JP-A-10-62986, JP-A Sulfonium organoboron such as in Japanese Patent No. 8-015521 Body, etc., etc. can be mentioned.
- photopolymerization initiator examples include acetophenone, ketal, benzophenone, benzoin, benzoyl, xanthone, triazine, halomethyloxadiazole, acridine, coumarins, lophine dimers, biphenyl Imidazole type, oxime ester type and the like are preferable.
- acetophenone photopolymerization initiator examples include 2,2-diethoxyacetophenone, p-dimethylaminoacetophenone, 2-hydroxy-2-methyl-1-phenyl-propan-1-one, p-dimethylaminoacetophenone, Preferable examples include 4′-isopropyl-2-hydroxy-2-methyl-propiophenone.
- ketal photopolymerization initiator examples include benzyldimethyl ketal and benzyl- ⁇ -methoxyethyl acetal.
- benzophenone photopolymerization initiator examples include benzophenone, 4,4 ′-(bisdimethylamino) benzophenone, 4,4 ′-(bisdiethylamino) benzophenone, 4,4′-dichlorobenzophenone, and 1-hydroxy-cyclohexyl.
- Preferred examples include 2-methyl-1- [4- (methylthio) phenyl] -2-morpholinopropanone-1, and the like.
- benzoin-based or benzoyl-based photopolymerization initiator examples include benzoin isopropyl ether, benzoin isobutyl ether, benzoin methyl ether, methyl o-benzoyl bezoate, and the like.
- Preferred examples of the xanthone photopolymerization initiator include diethyl thioxanthone, diisopropyl thioxanthone, monoisopropyl thioxanthone, chlorothioxanthone, and the like.
- triazine photopolymerization initiator examples include 2,4-bis (trichloromethyl) -6-p-methoxyphenyl-s-triazine, 2,4-bis (trichloromethyl) -6-p-methoxystyryl- s-triazine, 2,4-bis (trichloromethyl) -6- (1-p-dimethylaminophenyl) -1,3-butadienyl-s-triazine, 2,4-bis (trichloromethyl) -6-biphenyl- s-triazine, 2,4-bis (trichloromethyl) -6- (p-methylbiphenyl) -s-triazine, p-hydroxyethoxystyryl-2,6-di (trichloromethyl) -s-triazine, methoxystyryl- 2,6-di (trichloromethyl-s-triazine, 3,4-dimethoxysty
- halomethyl oxadiazole photopolymerization initiator examples include 2-trichloromethyl-5-styryl-1,3,4-oxodiazole, 2-trichloromethyl-5- (cyanostyryl) -1,3. , 4-oxodiazole, 2-trichloromethyl-5- (naphth-1-yl) -1,3,4-oxodiazole, 2-trichloromethyl-5- (4-styryl) styryl-1,3
- a preferred example is 4-oxodiazole.
- Preferred examples of the acridine series photopolymerization initiator include 9-phenylacridine, 1,7-bis (9-acridinyl) heptane, and the like.
- Examples of the coumarin photopolymerization initiator include 3-methyl-5-amino-((s-triazin-2-yl) amino) -3-phenylcoumarin, 3-chloro-5-diethylamino-((s Preferred examples include -triazin-2-yl) amino) -3-phenylcoumarin, 3-butyl-5-dimethylamino-((s-triazin-2-yl) amino) -3-phenylcoumarin, and the like.
- lophine dimer-based photopolymerization initiator examples include 2- (o-chlorophenyl) -4,5-diphenylimidazolyl dimer and 2- (o-methoxyphenyl) -4,5-diphenylimidazolyl dimer.
- 2- (2,4-dimethoxyphenyl) -4,5-diphenylimidazolyl dimer and the like can be preferably exemplified.
- biimidazole photopolymerization initiator examples include 2-mercaptobenzimidazole, 2,2′-benzothiazolyl disulfide, and the like.
- Examples of the oxime ester photopolymerization initiator include 2- (O-benzoyloxime) -1- [4- (phenylthio) phenyl] -1,2-octanedione, 1- (O-acetyloxime) -1 -[9-ethyl-6- (2-methylbenzoyl) -9H-carbazol-3-yl] ethanone, 1-phenyl-1,2-propanedione-2- (o-ethoxycarbonyl) oxime, O-benzoyl- Preferable examples include 4 ′-(benzmercapto) benzoyl-hexyl-ketoxime.
- 2,4,6-trimethylphenylcarbonyl-diphenylphosphonyl oxide, hexafluorophospho-trialkylphenylphosphonium salt and the like can be mentioned.
- an oxime ester compound is preferable in that it can be highly sensitive by addition in a small amount when used in combination with the conjugated diene compound represented by the general formula (I).
- O-benzoyloxime) -1- [4- (phenylthio) phenyl] -1,2-octanedione, 1- (O-acetyloxime) -1- [9-ethyl-6- (2-methylbenzoyl) -9H -Carbazol-3-yl] ethanone is most preferred.
- the content of the photopolymerization initiator in the photosensitive coloring composition is preferably 0.1 to 10.0% by mass, more preferably 0.5 to 5.0%, based on the total solid content of the composition. % By mass.
- the content of the photopolymerization initiator is within the above range, the polymerization reaction can proceed well to form a film with good strength.
- thermal polymerization inhibitor examples include hydroquinone, p-methoxyphenol, di-t-butyl-p-cresol, pyrogallol, t-butylcatechol, benzoquinone, 4,4′-thiobis (3-methyl-6-t- Butylphenol), 2,2′-methylenebis (4-methyl-6-tert-butylphenol), 2-mercaptobenzimidazole, and the like are useful.
- the photosensitive coloring composition of the present invention contains at least one polymerizable monomer.
- a compound having at least one addition-polymerizable ethylenic double bond and having a boiling point of 100 ° C. or higher under normal pressure is preferable.
- the photosensitive coloring composition of the present invention can be constituted in a negative type.
- polymerizable monomers include monofunctional acrylates and methacrylates such as polyethylene glycol mono (meth) acrylate, polypropylene glycol mono (meth) acrylate, and phenoxyethyl (meth) acrylate; polyethylene glycol di (meth) acrylate, trimethylol Ethane tri (meth) acrylate, neopentyl glycol di (meth) acrylate, pentaerythritol tri (meth) acrylate, pentaerythritol tetra (meth) acrylate, dipentaerythritol penta (meth) acrylate, dipentaerythritol hexa (meth) acrylate, Hexanediol (meth) acrylate, trimethylolpropane tri (acryloyloxypropyl) ether, tri (acryloyloxye) (I) A polyfunctional alcohol such as isocyanurate, g
- the content of the polymerizable monomer in the photosensitive coloring composition is preferably 10 to 80% by mass and more preferably 10 to 40% by mass with respect to the total solid content of the composition.
- the content is within the above range, a sufficient degree of cure and elution of the unexposed area can be maintained, and the degree of cure of the exposed area can be sufficiently maintained, and the elution of the unexposed area is significantly reduced. Can be prevented.
- Alkali-soluble resin The photosensitive coloring composition of the present invention can be constituted using an alkali-soluble resin.
- the alkali-soluble resin is not particularly limited as long as it is alkali-soluble, but is preferably selected from the viewpoints of heat resistance, developability, availability, and the like.
- the alkali-soluble resin is preferably a linear organic polymer and is soluble in an organic solvent and can be developed with a weak alkaline aqueous solution.
- linear organic high molecular polymers include polymers having a carboxylic acid in the side chain, such as JP-A-59-44615, JP-B-54-34327, JP-B-58-12777, and JP-B-54-25957.
- examples thereof include a polymer, a maleic acid copolymer, and a partially esterified maleic acid copolymer.
- acidic cellulose derivatives having a carboxylic acid in the side chain are useful.
- alkali-soluble resins include those obtained by adding an acid anhydride to a polymer having a hydroxyl group, polyhydroxystyrene resins, polysiloxane resins, poly (2-hydroxyethyl (meth) acrylate), polyvinyl Pyrrolidone, polyethylene oxide, polyvinyl alcohol, etc. are also useful.
- the linear organic polymer may be a copolymer of hydrophilic monomers.
- examples include alkoxyalkyl (meth) acrylate, hydroxyalkyl (meth) acrylate, glycerol (meth) acrylate, (meth) acrylamide, N-methylol acrylamide, secondary or tertiary alkyl acrylamide, dialkylaminoalkyl (meth) Acrylate, morpholine (meth) acrylate, N-vinylpyrrolidone, N-vinylcaprolactam, vinylimidazole, vinyltriazole, methyl (meth) acrylate, ethyl (meth) acrylate, branched or linear propyl (meth) acrylate, branched or straight
- Examples include butyl (meth) acrylate of a chain, phenoxyhydroxypropyl (meth) acrylate, and the like.
- hydrophilic monomers include tetrahydrofurfuryl group, phosphoric acid group, phosphoric acid ester group, quaternary ammonium base, ethyleneoxy chain, propyleneoxy chain, sulfonic acid and groups derived from salts thereof, morpholinoethyl group, etc. Including monomers are also useful.
- the alkali-soluble resin may have a polymerizable group in the side chain in order to improve the crosslinking efficiency, and includes, for example, an allyl group, a (meth) acryl group, an allyloxyalkyl group, etc. in the side chain. Polymers and the like are also useful.
- polymer having a polymerizable group examples include commercially available KS resist-106 (manufactured by Osaka Organic Chemical Industry Co., Ltd.), cyclomer P series (manufactured by Daicel Chemical Industries, Ltd.), and the like.
- KS resist-106 manufactured by Osaka Organic Chemical Industry Co., Ltd.
- cyclomer P series manufactured by Daicel Chemical Industries, Ltd.
- alcohol-soluble nylon, polyether of 2,2-bis- (4-hydroxyphenyl) -propane and epichlorohydrin are also useful.
- polyhydroxystyrene resins, polysiloxane resins, acrylic resins, acrylamide resins, and acrylic / acrylamide copolymer resins are preferable, and from the viewpoint of development control.
- acrylic resins, acrylamide resins, and acrylic / acrylamide copolymer resins are preferable, and from the viewpoint of development control.
- acrylic resins, acrylamide resins, and acrylic / acrylamide copolymer resins are preferably acrylic resins, acrylamide resins, and acrylic / acrylamide copolymer resins.
- acrylic resin examples include a copolymer obtained by polymerization of a monomer selected from benzyl (meth) acrylate, (meth) acrylic acid, hydroxyethyl (meth) acrylate, and (meth) acrylamide, and a commercially available product.
- KS resist-106 manufactured by Osaka Organic Chemical Industry Co., Ltd.
- cyclomer P series manufactured by Daicel Chemical Industries, Ltd.
- the alkali-soluble resin a polymer having a weight average molecular weight (polystyrene equivalent value measured by GPC method) of 1000 to 2 ⁇ 10 5 is preferable from the viewpoint of developability, liquid viscosity and the like, and 2000 to 1 ⁇ 10 5 is preferable.
- a polymer is more preferred, and a polymer of 5000 to 5 ⁇ 10 4 is particularly preferred.
- the content of the alkali-soluble resin in the photosensitive coloring composition is preferably 10 to 90% by mass, more preferably 20 to 80% by mass with respect to the total solid content of the composition, from the viewpoint of developability and the like. ⁇ 70% by weight is particularly preferred.
- the photosensitive coloring composition of the present invention can generally be constituted using an organic solvent.
- the organic solvent is basically not particularly limited as long as the solubility of each component and the coating property of the photosensitive coloring composition are satisfied, but in particular, the solubility, coating property, and safety of the ultraviolet absorber and binder are taken into consideration. Are preferably selected.
- organic solvent examples include esters such as ethyl acetate, n-butyl acetate, isobutyl acetate, amyl formate, isoamyl acetate, isobutyl acetate, butyl propionate, isopropyl butyrate, ethyl butyrate, butyl butyrate, alkyl esters, and methyl lactate.
- esters such as ethyl acetate, n-butyl acetate, isobutyl acetate, amyl formate, isoamyl acetate, isobutyl acetate, butyl propionate, isopropyl butyrate, ethyl butyrate, butyl butyrate, alkyl esters, and methyl lactate.
- Ethyl lactate methyl oxyacetate, ethyl oxyacetate, butyl oxyacetate, methyl methoxyacetate, ethyl methoxyacetate, butyl methoxyacetate, methyl ethoxyacetate, ethyl ethoxyacetate, etc .;
- 3-oxypropionic acid alkyl esters such as methyl 3-oxypropionate and ethyl 3-oxypropionate, such as methyl 3-methoxypropionate, ethyl 3-methoxypropionate, methyl 3-ethoxypropionate, 3-ethoxy Ethyl propionate, etc .
- 2-oxypropionic acid alkyl esters such as methyl 2-oxypropionate, ethyl 2-oxypropionate, propyl 2-oxypropionate, such as methyl 2-methoxypropionate, 2-methoxypropionate Acid ethyl, propyl 2-methoxypropionate, methyl 2-ethoxypropionate, ethyl 2-ethoxypropionate, methyl 2-oxy-2-methylpropionate, ethyl 2-oxy-2-methylpropionate, 2-methoxy- 2-methylpropio Methyl acid, 2-ethoxy-2-methylpropionic acid ethyl, etc; methyl pyruvate,
- Ethers such as diethylene glycol dimethyl ether, tetrahydrofuran, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, methyl cellosolve acetate, ethyl cellosolve acetate, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, diethylene glycol monobutyl ether, propylene glycol monomethyl ether, propylene glycol monomethyl Ether acetate, propylene glycol monoethyl ether acetate, propylene glycol monopropyl ether acetate, etc .;
- Ketones such as methyl ethyl ketone, cyclohexanone, 2-heptanone, 3-heptanone, etc .; aromatic hydrocarbons such as toluene and xylene are preferred.
- these organic solvents may be used in combination of two or more from the viewpoints of solubility of the ultraviolet absorber and the alkali-soluble resin, improvement of the coating surface state, etc., in particular, methyl 3-ethoxypropionate, Ethyl 3-ethoxypropionate, ethyl cellosolve acetate, ethyl lactate, diethylene glycol dimethyl ether, butyl acetate, methyl 3-methoxypropionate, 2-heptanone, cyclohexanone, ethyl carbitol acetate, butyl carbitol acetate, propylene glycol methyl ether, and propylene
- a mixed solution composed of two or more selected from glycol methyl ether acetate is preferably used.
- the content of the organic solvent in the photosensitive coloring composition is preferably such that the total solid concentration of the composition is 5 to 80% by mass, and more preferably 5 to 60% by mass, from the viewpoint of applicability. 10 to 50% by mass is particularly preferable.
- additives such as a filler, a polymer compound other than the above, a surfactant, an adhesion promoter, an antioxidant are added as necessary. Further, an aggregation inhibitor and the like can be blended.
- additives include fillers such as glass and alumina; polymer compounds other than binder resins such as polyvinyl alcohol, polyacrylic acid, polyethylene glycol monoalkyl ether, and polyfluoroalkyl acrylate; nonionic, cationic And anionic surfactants: vinyltrimethoxysilane, vinyltriethoxysilane, vinyltris (2-methoxyethoxy) silane, N- (2-aminoethyl) -3-aminopropylmethyldimethoxysilane, N- (2 -Aminoethyl) -3-aminopropyltrimethoxysilane, 3-aminopropyltriethoxysilane, 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropylmethyldimethoxysilane, 2- (3,4-epoxycyclohexyl) ) Ethyltrimet Adhesion promoters such as silane, 3-chloro
- the photosensitive coloring composition of the present invention is an organic carboxylic acid, preferably a molecular weight of 1000, in order to promote alkali solubility in the UV-irradiated part of the photosensitive coloring composition and to further improve developability.
- organic carboxylic acids preferably a molecular weight of 1000, in order to promote alkali solubility in the UV-irradiated part of the photosensitive coloring composition and to further improve developability.
- the following low molecular weight organic carboxylic acids can be contained.
- organic carboxylic acid examples include aliphatic monocarboxylic acids such as formic acid, acetic acid, propionic acid, butyric acid, valeric acid, pivalic acid, caproic acid, diethyl acetic acid, enanthic acid, caprylic acid; oxalic acid, malonic acid, succinic acid Aliphatic dicarboxylic acids such as acid, glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, brassic acid, methylmalonic acid, ethylmalonic acid, dimethylmalonic acid, methylsuccinic acid, tetramethylsuccinic acid, citraconic acid Acid; Aliphatic tricarboxylic acid such as tricarballylic acid, aconitic acid, and camphoronic acid; Aromatic monocarboxylic acid such as benzoic acid, toluic acid, cumic acid, hemelitic acid, mesitylene
- the photosensitive coloring composition of the present invention is used for forming colored pixels such as color filters used in liquid crystal display devices (LCD) and solid-state imaging devices (for example, CCD, CMOS, etc.), electroluminescent color filters, etc. It can be suitably used as a production application for printing ink, inkjet ink, paint, and the like.
- LCD liquid crystal display devices
- solid-state imaging devices for example, CCD, CMOS, etc.
- electroluminescent color filters etc. It can be suitably used as a production application for printing ink, inkjet ink, paint, and the like.
- the color filter of the present invention is formed by arranging a plurality of colored or non-colored patterns on a substrate, and is produced using the above-described photosensitive colored composition of the present invention.
- the color filter of the present invention can be most preferably produced by the method for producing the color filter of the present invention using the photosensitive coloring composition of the present invention. It was applied directly or via another layer (preferably after drying) to form a coating layer (hereinafter sometimes referred to as “coating film forming step”), and the coating was formed.
- the coating layer is exposed imagewise through a photomask (for example, at least with ultraviolet rays) (hereinafter, this may be referred to as “exposure step”), and the exposed coating layer is developed with a developer (for example, an alkali developer).
- the pattern can be formed by developing the film (hereinafter, also referred to as “development process”).
- development process a coating layer after the development treatment, that is, a step of applying heat treatment to the pattern (hereinafter sometimes referred to as “post-baking step”) can be further provided.
- post-baking step a coating layer after the development treatment
- the hardening process hardened by further heating and / or exposing the pattern after exposure and image development as needed can further be provided.
- the photosensitive coloring composition is applied on a substrate by a coating method such as spin coating, casting coating, roll coating, slit coating, etc. (preferably dried afterwards).
- a colored composition layer (coating layer) is formed.
- the substrate examples include soda glass, Pyrex (registered trademark) glass, quartz glass used for liquid crystal display elements and the like, and those obtained by attaching a transparent conductive film to these, and photoelectric conversion element substrates used for imaging elements and the like.
- examples thereof include a silicon substrate and a complementary metal oxide semiconductor (CMOS).
- CMOS complementary metal oxide semiconductor
- a black matrix for isolating each pixel pattern constituting the color filter is formed on these substrates.
- an undercoat layer may be provided on these substrates, if necessary, in order to improve adhesion with a layer provided on the substrate, prevent diffusion of substances, or planarize the substrate surface.
- the coating layer formed in the coating film forming step is exposed by irradiating actinic rays or radiation in an image-like manner with a specific pattern through a photomask.
- actinic ray or radiation include infrared rays, visible rays, ultraviolet rays, far ultraviolet rays, X-rays, and electron beams, but at least ultraviolet rays are preferable, and ultraviolet rays such as g-rays, h-rays, and i-rays are particularly preferable. Is preferably used.
- the exposure is preferably exposure using mainly i-line in a stepper exposure machine.
- the exposure illuminance is preferably 10 mW / cm 2 or more, more preferably 20 mW / cm 2 or more, and more preferably 30 mW from the viewpoint of throughput in the proximity exposure apparatus and mirror projection exposure apparatus used for the production of color filters for liquid crystal display devices. / Cm 2 or more is particularly preferable.
- the stepper exposure machine used for manufacturing a color filter for a solid-state imaging device, also in view of the throughput is preferably 300 mW / cm 2 or more, more preferably 500 mW / cm 2 or more, 1000 mW / cm 2 or more is particularly preferable.
- the exposure amount is also from the viewpoint of throughput, generally preferably 1000 mJ / cm 2 or less, more preferably 500 mJ / cm 2 or less, particularly preferably 300 mJ / cm 2 or less.
- the exposed coating layer is developed with a developer to reveal a pattern.
- a developer Any developer can be used as long as it dissolves the unexposed portion of the photosensitive coloring composition and hardly dissolves the exposed portion (radiation irradiated portion).
- various organic solvents and combinations thereof, and alkaline aqueous solutions can be used.
- organic solvent examples include the above-described solvents that can be used when preparing a photosensitive coloring composition.
- alkaline aqueous solution examples include sodium hydroxide, potassium hydroxide, sodium carbonate, sodium oxalate, sodium metasuccinate, aqueous ammonia, ethylamine, diethylamine, dimethylethanolamine, tetramethylammonium hydroxide, tetraethylammonium hydroxide. , Choline, pyrrole, piperidine, 1,8-diazabicyclo- [5.4.0] -7-undecene, and the like.
- the developer it is preferable to use an alkaline aqueous solution in which the alkali concentration is preferably adjusted to pH 11 to 13, more preferably pH 11.5 to 12.5.
- the alkali concentration is pH 13 or less, pattern roughness, peeling, and reduction in the remaining film ratio can be avoided, and when the alkali concentration is pH 11 or more, the development speed is good and the generation of residues can be prevented.
- the development process is performed using a developer such as an alkaline aqueous solution.
- a developer such as an alkaline aqueous solution.
- Examples of the development method include a dipping method, a spray method, and a paddle method.
- the development temperature is preferably 15 to 40 ° C. Further, after development, washing is generally performed with running water.
- a heat treatment is performed by providing a post-baking step.
- the heating temperature in the post-baking step is preferably 100 to 300 ° C, more preferably 150 to 250 ° C.
- the heating time is preferably about 10 minutes to 1 hour, more preferably about 5 minutes to 30 minutes.
- the color filter of the present invention can have a plurality of patterns on the substrate, for example, a pattern in which colored pixels, a black matrix, and the like are regularly arranged.
- the colored pixels constituting the color filter are generally formed in a quadrilateral shape, and in this case, one side (maximum side) is generally formed in a range of 1.5 to 200 ⁇ m. Among these, 5 ⁇ m or less is preferable, 4 ⁇ m or less is more preferable, and 3 ⁇ m or less is particularly preferable from the viewpoint of effective use of a substrate such as a silicon wafer, miniaturization of a device using a solid-state image sensor, and high-speed operation of the solid-state image sensor.
- the thickness of the colored pixel in the color filter is not particularly limited, but it tends to be thin from the viewpoint of effective use of a substrate such as a silicon wafer and shading of a device using a solid-state image sensor. It is preferably 2 ⁇ m or less, more preferably 1.5 ⁇ m or less, and particularly preferably 1.0 ⁇ m or less.
- the pigment content in the colored pixels constituting the color filter is not particularly limited, but is preferably 25% by mass or more based on the total solid content of the composition from the viewpoint of color separation. More preferably, it is 30 mass% or more, and 40 mass% or more is especially preferable.
- the color filter of the present invention can be used as a color filter for a liquid crystal display device (LCD). However, it can be used as an image sensor such as a CCD or CMOS, particularly for a high-resolution CCD element or CMOS element exceeding 1 million pixels. It is preferable to use it.
- the color filter of the present invention is optimally used, for example, as a color filter disposed between a light receiving portion and a microlens for condensing light in each colored pixel constituting the CCD.
- the mixed solution obtained above was further subjected to a dispersion treatment for 6 hours using a bead disperser Dispermat (manufactured by GETZMANN) using 0.3 mm ⁇ zirconia beads. Thereafter, dispersion treatment was further performed at a flow rate of 500 g / min under a pressure of 2,000 kg / cm 3 using a high-pressure disperser NANO-3000-10 (manufactured by Nippon BEE Co., Ltd.) with a decompression mechanism. This dispersion treatment was repeated 10 times to obtain a magenta pigment dispersion composition R-1.
- red pigment dispersion composition R-2 (Preparation of red pigment dispersion composition R-2) Ingredients having the following composition were mixed, and the rotational speed was 3,000 r.m. using a homogenizer. p. m. And mixed for 3 hours to prepare a mixed solution containing the pigment.
- the mixed solution obtained above was further subjected to a dispersion treatment for 6 hours using a bead disperser Dispermat (manufactured by GETZMANN) using 0.3 mm ⁇ zirconia beads. Thereafter, dispersion treatment was further performed at a flow rate of 500 g / min under a pressure of 2,000 kg / cm 3 using a high-pressure disperser NANO-3000-10 (manufactured by Nippon BEE Co., Ltd.) with a decompression mechanism. This dispersion treatment was repeated 10 times to obtain a red pigment dispersion composition R-2.
- Example 1 Fabrication of color filter for solid-state imaging device -Preparation of resist solution for planarization film- The following components were mixed and stirred with a homogenizer stirrer to prepare a flattening film resist solution.
- the obtained flattening film resist solution was applied onto a 6-inch silicon wafer by spin coating. Next, heat treatment was performed on a hot plate at a surface temperature of 120 ° C. for 120 seconds on the surface of the coating film to obtain a uniform coating film having a thickness of about 2 ⁇ m on the silicon wafer. Next, the coating film was cured in an oven at 220 ° C. for 1 hour to form a flattened film.
- the surface temperature of the coating film surface is 100 ° C. for 120 seconds, and then heated and dried on a hot plate, A coating film having a thickness of about 1.0 ⁇ m after drying was formed.
- an i-line stepper (FPA-3000i5 + manufactured by Canon Inc.) is passed through a mask pattern in which 2.0 ⁇ m square pixels are arranged in a 4 mm ⁇ 3 mm region on the substrate with respect to the dried coating film. ) At an exposure amount of 100 mJ / cm 2 , exposure was performed at two levels of illuminance 1200 mW / cm 2 (high illuminance) and 600 mW / cm 2 (low illuminance).
- the pattern-exposed coating film was subjected to paddle development for 60 seconds at room temperature using a 60% aqueous solution of organic alkaline developer CD-2000 (Fuji Film Electronics Materials Co., Ltd.), and then spin shower for another 20 seconds. And rinsed with pure water. Thereafter, it was further washed with pure water. Thereafter, water droplets were blown off with high-pressure air, the substrate was naturally dried, and post-baked with a hot plate at 220 ° C. for 300 seconds to form a colored pattern (colored resin film) on the silicon wafer. As described above, a color filter for a solid-state imaging device was produced.
- organic alkaline developer CD-2000 Fluji Film Electronics Materials Co., Ltd.
- As described above, for each of the pixel patterns obtained by the exposure at the two levels (high illuminance: 1200 mW / cm 2 , low illuminance: 600 mW / cm 2 ), the evaluation of the “(1-3) remaining film ratio” is performed. The remaining film rate c (%) at low illuminance obtained in step 1 and the remaining film rate d (%) at high illuminance are compared, and the difference in the remaining film rate (
- Example 2 Preparation of color filter for solid-state imaging device
- Example 1 the composition of the photosensitive coloring composition was changed as shown in Table 1 below
- a photosensitive coloring composition was prepared to produce a color filter.
- the same evaluation as in Example 1 was performed.
- the results of evaluation and measurement are shown in Table 2 below.
- Example 6 Production of color filter for solid-state imaging device In Example 1, except that the composition of the photosensitive coloring composition was changed as shown in Table 1 below, A photosensitive coloring composition was prepared to produce a color filter. The same evaluation as in Example 1 was performed. The results of evaluation and measurement are shown in Table 2 below.
- the pattern shape was good, the residue was suppressed, and the exposure illuminance dependency was small.
- the line width and the remaining film ratio especially in low illumination exposure The fluctuation of the exposure illuminance was large and the exposure illuminance dependence could not be suppressed.
- the compound XII which is an antioxidant, although the dependency on exposure illuminance was small to some extent, the generation of development residue could not be suppressed.
- Example 13 to 24, Comparative Examples 7 to 12 Preparation of Color Filters for Liquid Crystal Display Elements
- the photosensitive coloring compositions used in Examples 1 to 12 and Comparative Examples 1 to 6 were prepared, and these were separately prepared.
- a coating film was formed by spin coating so as to have a film thickness of 1.5 ⁇ m.
- each Cr film-coated glass substrate on which the coating film was formed was dried in a 90 ° C. oven for 60 seconds (prebaked), and then a 100 ⁇ m stripe was formed on the entire surface of the coating film in a 4 mm ⁇ 3 mm region on the substrate.
- exposure was performed at two levels of illuminance of 20 mW / cm 2 (low illuminance) and 40 mW / cm 2 (high illuminance) using a high-pressure mercury lamp at an exposure amount of 100 mJ / cm 2 .
- the pattern shape was good, the residue was suppressed, and the exposure illuminance dependency was small.
- the pattern shape and the remaining film ratio particularly in low illumination exposure The fluctuation of the exposure illuminance was large and the exposure illuminance dependence could not be suppressed.
- the compound XII which is an antioxidant the generation of the development residue could not be suppressed.
Abstract
Description
<1> 顔料、重合性モノマー、光重合開始剤、及び下記一般式(I)で表される化合物を少なくとも含有する感光性着色組成物である。
<5> 前記<1>~前記<4>のいずれか1つに記載の感光性着色組成物において、前記R3又はR4で表される電子吸引基は、σp値が0.30以上0.80以下の電子吸引性基であることが好ましい。
<6> 前記<1>~前記<5>のいずれか1つに記載の感光性着色組成物において、前記R3が、シアノ基、-COOR5、-CONHR5、-COR5、及び-SO2R5より選択される基であって、前記R4が、シアノ基、-COOR6、-CONHR6、-COR6、及び-SO2R6より選択される基であることが好ましい。このとき、R5及びR6は、各々独立に、炭素原子数1~20のアルキル基、又は炭素原子数6~20のアリール基を表す。
<7> 前記<1>~前記<6>のいずれか1つに記載の感光性着色組成物において、前記光重合開始剤は、オキシムエステル系化合物が好ましく、さらに好ましくは、2-(O-ベンゾイルオキシム)-1-[4-(フェニルチオ)フェニル]-1,2-オクタンジオン、及び1-(O-アセチルオキシム)-1-[9-エチル-6-(2-メチルベンゾイル)-9H-カルバゾール-3-イル]エタノンの少なくとも一方である。
<8> 前記<1>~前記<7>のいずれか1つに記載の感光性着色組成物は、顔料が赤色用の顔料であり、マゼンタ色又は赤色に構成されている場合が好ましい。
<10> 前記<9>に記載のカラーフィルタの製造方法により作製されたカラーフィルタである。
本発明によれば、精細で高品質の画像表示が可能なカラーフィルタ及びその製造方法を提供することができる。
本発明の感光性着色組成物は、少なくとも、顔料、重合性モノマー、光重合開始剤、及び紫外線吸収剤として、以下に示す一般式(I)で表される化合物を用いて構成されたものであり、一般的には溶剤が用いられる。また、本発明の感光性着色組成物は、必要に応じて、更に顔料分散剤及び/又は顔料誘導体、アルカリ可溶性樹脂などの他の成分を用いて構成することができる。
以下、本発明の感光性着色組成物を構成する各成分について詳述する。
本発明の感光性着色組成物は、顔料の少なくとも1種を含有する。
顔料としては、従来公知の種々の無機顔料又は有機顔料を用いることができる。顔料は、無機顔料又は有機顔料を問わず、膜形成したときに高透過率が得られるものが好ましいことを考慮すると、できるだけ粒子径が小さく微少な粒子サイズの顔料が好ましく、ハンドリング性をも考慮すると、好ましくは平均一次粒子径0.01~0.3μm、より好ましくは0.01~0.15μmの顔料である。平均一次粒子径が前記範囲内であると、透過率が高く、色特性が良好であると共に、高いコントラストのカラーフィルタを形成するのに有効である。
平均一次粒子径は、走査型電子顕微鏡(SEM)あるいは透過型電子顕微鏡(TEM)で観察し、粒子が凝集していない部分で粒子サイズを100個計測し、その平均値を算出することによって求められる。
C.I.Pigment Red 1,2,3,4,5,6,7,9,10,14,17,22,23,31,38,41,48:1,48:2,48:3,48:4,49,49:1,49:2,52:1,52:2,53:1,57:1,60:1,63:1,66,67,81:1,81:2,81:3,83,88,90,105,112,119,122,123,144,146,149,150,155,166,168,169,170,171,172,175,176,177,178,179,184,185,187,188,190,200,202,206,207,208,209,210,216,220,224,226,242,246,254,255,264,270,272,279;
C.I.Pigment Yellow 1,2,3,4,5,6,10,11,12,13,14,15,16,17,18,20,24,31,32,34,35,35:1,36,36:1,37,37:1,40,42,43,53,55,60,61,62,63,65,73,74,77,81,83,86,93,94,95,97,98,100,101,104,106,108,109,110,113,114,115,116,117,118,119,120,123,125,126,127,128,129,137,138,139,147,148,150,151,152,153,154,155,156,161,162,164,166,167,168,169,170,171,172,173,174,175,176,177,179,180,181,182,185,187,188,193,194,199,213,214;
C.I.Pigment Orange 2,5,13,16,17:1,31,34,36,38,43,46,48,49,51,52,55,59,60,61,62,64,71,73;
C.I.Pigment Green 7,10,36,37;
C.I.Pigment Blue 1,2,15,15:1,15:2,15:3,15:4,15:6,16,22,60,64,66,79,79のCl置換基をOHに変更したもの,80;
C.I.Pigment Violet 1,19,23,27,32,37,42;
C.I.Pigment Brown 25,28;
C.I.Pigment Black 1,7;
等を挙げることができる。
C.I.Pigment Yellow 11,24,108,109,110,138,139,150,151,154,167,180,185;
C.I.Pigment Orange 36,71;
C.I.Pigment Red 122,150,171,175,177,209,224,242,254,255,264;
C.I.Pigment Violet 19,23,32;
C.I.Pigment Blue 15:1,15:3,15:6,16,22,60,66;
C.I.Pigment Green 7,36,37;
C.I.Pigment Black 1、7;
例えば、赤色用の顔料として、アントラキノン系顔料、ペリレン系顔料、ジケトピロロピロール系顔料の単独又はそれらの少なくとも1種と、ジスアゾ系黄色顔料、イソインドリン系黄色顔料、キノフタロン系黄色顔料又はペリレン系赤色顔料、アントラキノン系赤色顔料、ジケトピロロピロール系赤色顔料と、の混合などを用いることができる。例えば、アントラキノン系顔料としては、C.I.ピグメント・レッド177が挙げられ、ペリレン系顔料としては、C.I.ピグメント・レッド155、C.I.ピグメント・レッド224が挙げられ、ジケトピロロピロール系顔料としては、C.I.ピグメント・レッド254が挙げられ、色再現性の点でC.I.ピグメント・イエロー83、C.I.ピグメント・イエロー139又はC.I.ピグメント・レッド177との混合が好ましい。
また、赤色顔料と他色顔料との質量比は、100:5~100:80が好ましい。該質量比は、100:5以上であると、400nm~500nmの光透過率が抑えられ、色純度を上げることができ、100:80以下であると発色力が良好である。特に該質量比としては、100:10~100:65の範囲が最適である。なお、赤色顔料同士の組み合わせの場合は、色度に併せて調整することができる。
緑色顔料と黄色顔料との質量比は、100:5~100:200が好ましい。該質量比は、100:5以上であると400~450nmの光透過率が抑えられ、色純度を上げることができ、100:200以下であると主波長が長波長偏らずにNTSC目標色相からのズレを回避できる。該質量比としては、100:20~100:150の範囲が特に好ましい。
青色顔料と紫色顔料との質量比は、100:0~100:100が好ましく、より好ましくは100:70以下である。
また、カーボンブラックとチタンブラックとの質量比は、100:0~100:60の範囲が好ましい。100:61以上では、分散安定性が低下する場合がある。
本発明の感光性着色組成物は、顔料を分散するための顔料分散剤の少なくとも1種を含有することができる。この顔料分散剤を含有することにより、顔料の組成物中での分散性を向上させることができる。
本発明の感光性着色組成物は、必要に応じて、前記顔料分散剤と共に顔料誘導体を添加することができる。顔料分散剤と親和性のある部分あるいは極性基が導入された顔料誘導体を顔料表面に吸着させ、これを顔料分散剤の吸着点として用いることで、顔料を微細な粒子として感光性着色組成物に分散させ、その再凝集を防止することができ、コントラストが高く、透明性に優れたカラーフィルタを構成するのに有効である。
本発明の感光性着色組成物は、紫外線吸収剤として、共役ジエン系化合物である下記一般式(I)で表される化合物の少なくとも1種を含有する。本発明においては、この共役ジエン系化合物を用いることで、特に低照度露光を行なった際のその後の現像性能変動を抑えるので、パターンの線幅、膜厚、分光スペクトル等のパターン形成性に関係する露光照度依存性を抑制することができる。
R1、R2で表されるアルキル基は、置換基を有していてもよく、置換基を有するアルキル基の置換基としては、例えば、アルキル基、アリール基、アルコキシ基、アリールオキシ基、アシルオキシ基、ハロゲン原子、アシルアミノ基、アシル基、アルキルチオ基、アリールチオ基、ヒドロキシ基、シアノ基、アルキルオキシカルボニル基、アリールオキシカルボニル基、置換カルバモイル基、置換スルファモイル基、ニトロ基、置換アミノ基、アルキルスルホニル基、アリールスルホニル基等が挙げられる。
ハメット則は、ベンゼン誘導体の反応又は平衡に及ぼす置換基の影響を定量的に論ずるために、1935年にL. P. Hammettにより提唱された経験則である。これは、今日広く
妥当性が認められている。ハメット則により求められた置換基定数には、σp値とσm値とがあり、これらの値は多くの一般的な成書に記載があるが、例えば、J.A. Dean編「Lange’s Handbook of Chemistry」第12版、1979年(Mc Graw-Hill)や「化学の領域増刊」、122号、96~103頁、1979年(南江堂)、Chemical Reviews, 91巻、165頁~195頁、1991年に詳しい。本発明では、これらの成書に記載の文献既知の値がある置換基にのみ限定されるという意味ではなく、その値が文献未知であっても、ハメット則に基づいて測定した場合に上記の範囲内に含まれる限り、前記電子吸引基に包含されることは勿論である。
これらのうち、R3、R4としては、アシル基、カルバモイル基、アルキルオキシカルボニル基、アリールオキシカルボニル基、シアノ基、ニトロ基、アルキルスルホニル基、アリールスルホニル基、スルホニルオキシ基、スルファモイル基が好ましく、特にアシル基、カルバモイル基、アルキルオキシカルボニル基、アリールオキシカルボニル基、シアノ基、アルキルスルホニル基、アリールスルホニル基、スルホニルオキシ基、スルファモイル基が好ましい。
また、R3及びR4は、互いに結合して環を形成してもよい。
前記共重合体である場合、他のモノマーとしては、例えば、アクリル酸、α-クロロアクリル酸、α-アルアクリル酸(例えば、メタクリル酸などのアクリル酸類から誘導されるエステル、好ましくは低級アルキルエステル及びアミド(例えば、アクリルアミド、メタクリルアミド、t-ブチルアクリルアミド、メチルアクリレート、メチルメタクリレート、エチルアクリレート、エチルメタクリレート、n-プロピルアクリレート、n-ブチルアクリレート、2-エチルへキシルアクリレート、n-へキシルアクリレート、オクチルメタクリレート、及びラウリルメタクリレート、メチレンビスアクリルアミド等))、ビニルエステル(例えば、ビニルアセテート、ビニルプロピオネート及びビニルラウレート等)、アクリロニトリル、メタクリロニトリル、芳香族ビニル化合物(例えば、スチレン及びその誘導体、例えばビニルトルエン、ジビニルベンゼン、ビニルアセトフェノン、スルホスチレン、及びスチレンスルフィン酸等)、イタコン酸、シトラコン酸、クロトン酸、ビニリデンクロライド、ビニルアルキルエーテル(例えば、ビニルエチルエーテル等)、マレイン酸エステル、N-ビニル-2-ピロリドン、N-ビニルピリジン、2-及び4-ビニルピリジン等がある。
このうち、特にアクリル酸エステル、メタクリル酸エステル、芳香族ビニル化合物が好ましい。
コモノマー化合物の2種以上を一緒に使用することもできる。例えば、n-ブチルアクリレートとジビニルベンゼン、スチレンとメチルメタクリレート、メチルアクリレートとメタクリレート酸等を使用できる。
-例示化合物(1)の合成法-
3-アニリノアクロレインアニル(13.3g)と、エチルフェニルスルホニルアセテート(14.3g)を無水酢酸(40ml)中で85~90℃に2時間加熱する。減圧乾燥下に無水酢酸を除き、エタノール(40ml)とジ-n―へキシルアミン(24.1g)を加えて2時間還流する。エタノールを除去し、残渣をカラムクロマトにかけ、精製し、エタノールより再結晶すると目的物が得られる(融点=95~96℃)。
本発明の感光性着色組成物は、光重合開始剤の少なくとも1種を含有する。
光重合開始剤としては、例えば、特開平57-6096号公報に記載のハロメチルオキサジアゾール、特公昭59-1281号公報、特開昭53-133428号公報等に記載のハロメチル-s-トリアジン等活性ハロゲン化合物、米国特許USP-4318791、欧州特許公開EP-88050A等の各明細書に記載のケタール、アセタール、又はベンゾインアルキルエーテル類等の芳香族カルボニル化合物、米国特許USP-4199420明細書に記載のベンゾフェノン類等の芳香族ケトン化合物、Fr-2456741明細書に記載の(チオ)キサントン類又はアクリジン類化合物、特開平10-62986号公報に記載のクマリン類又はロフィンダイマー類等の化合物、特開平8-015521号公報等のスルホニウム有機硼素錯体等、等を挙げることができる。
スチリル-2,6-ジ(トリクロロメチル)-s-トリアジン、メトキシスチリル-2,6-ジ(トリクロロメチル-s-トリアジン、3,4-ジメトキシスチリル-2,6-ジ(トリクロロメチル)-s-トリアジン、4-ベンズオキソラン-2,6-ジ(トリクロロメチル)-s-トリアジン、4-(o-ブロモ-p-N,N-(ジエトキシカルボニルアミノ)-フェニル)-2,6-ジ(クロロメチル)-s-トリアジン、4-(p-N,N-(ジエトキシカルボニルアミノ)-フェニル)-2,6-ジ(クロロメチル)-s-トリアジン等を好適に挙げることができる。
上記以外に、2,4,6-トリメチルフェニルカルボニル-ジフェニルフォスフォニルオキサイド、ヘキサフルオロフォスフォロ-トリアルキルフェニルホスホニウム塩等が挙げられる。
また、これらの光重合開始剤を併用することもできる。
光重合開始剤の感光性着色組成物中における含有量としては、該組成物の全固形分に対して、0.1~10.0質量%が好ましく、より好ましくは0.5~5.0質量%である。光重合開始剤の含有量が前記範囲内であると、重合反応を良好に進行させて強度の良好な膜形成が可能である。
本発明の感光性着色組成物は、重合性モノマーの少なくとも1種を含有する。
重合性モノマーとしては、少なくとも1つの付加重合可能なエチレン性二重結合を有し、かつ常圧下で100℃以上の沸点を持つ化合物が好ましい。重合性モノマーは、前記光重合開始剤等と共に含有することにより、本発明の感光性着色組成物をネガ型に構成することができる。
更に、日本接着協会誌Vol.20、No.7、300~308頁に光硬化性モノマー及びオリゴマーとして紹介されているものも挙げることができる。中でも、重合性モノマーとしては、多官能(メタ)アクリル化合物が好ましい。
本発明の感光性着色組成物には、アルカリ可溶性樹脂を用いて構成することができる。アルカリ可溶性樹脂は、アルカリ可溶性であれば特に限定はないが、耐熱性、現像性、入手性等の観点から選ばれることが好ましい。
本発明の感光性着色組成物は、一般には、有機溶剤を用いて構成することができる。
有機溶剤は、各成分の溶解性や感光性着色組成物の塗布性を満足すれば基本的には特に制限はないが、特に紫外線吸収剤、バインダーの溶解性、塗布性、安全性を考慮して選ばれることが好ましい。また、本発明の感光性着色組成物を調製する際には、少なくとも2種類の有機溶剤を含むことが好ましい。
本発明の感光性着色組成物には、必要に応じて、各種添加物、例えば、充填剤、上記以外の高分子化合物、界面活性剤、密着促進剤、酸化防止剤、凝集防止剤等を配合することができる。
有機カルボン酸の具体例としては、ギ酸、酢酸、プロピオン酸、酪酸、吉草酸、ピバル酸、カプロン酸、ジエチル酢酸、エナント酸、カプリル酸等の脂肪族モノカルボン酸;シュウ酸、マロン酸、コハク酸、グルタル酸、アジピン酸、ピメリン酸、スベリン酸、アゼライン酸、セバシン酸、ブラシル酸、メチルマロン酸、エチルマロン酸、ジメチルマロン酸、メチルコハク酸、テトラメチルコハク酸、シトラコン酸等の脂肪族ジカルボン酸;トリカルバリル酸、アコニット酸、カンホロン酸等の脂肪族トリカルボン酸;安息香酸、トルイル酸、クミン酸、ヘメリト酸、メシチレン酸等の芳香族モノカルボン酸;フタル酸、イソフタル酸、テレフタル酸、トリメリト酸、トリメシン酸、メロファン酸、ピロメリト酸等の芳香族ポリカルボン酸;フェニル酢酸、ヒドロアトロパ酸、ヒドロケイ皮酸、マンデル酸、フェニルコハク酸、アトロパ酸、ケイ皮酸、ケイ皮酸メチル、ケイ皮酸ベンジル、シンナミリデン酢酸、クマル酸、ウンベル酸等のその他のカルボン酸が挙げられる。
本発明のカラーフィルタは、基板上に複数の着色もしくは非着色のパターンが配列形成されてなるものであり、既述の本発明の感光性着色組成物を用いて作製されたものである。本発明のカラーフィルタは、本発明の感光性着色組成物を用いた本発明のカラーフィルタの製造方法により最も好適に作製することができ、具体的には、感光性着色組成物を、例えば基板上に直接又は他の層を介して、塗布して(好ましくはその後に乾燥させて)塗布層を形成し(以下、これを「塗膜形成工程」ということがある。)、塗布形成された塗布層をフォトマスクを介して(例えば少なくとも紫外線で)画像様に露光し(以下、これを「露光工程」ということがある。)、露光された前記塗布層を現像液(例えばアルカリ現像液)で現像する(以下、「現像工程」ということがある。)ことによりパターンを形成して作製することができる。また、本発明においては、必要に応じて、現像処理した後の塗布層、つまりパターンに加熱処理を施す工程(以下、「ポストベーク工程」ということがある。)を更に設けることができる。
また、本発明のカラーフィルタの製造方法においては、必要に応じて露光・現像後のパターンを更に加熱及び/又は露光することによって硬化させる硬化工程を更に設けることができる。
また、これらの基板上には、必要により、基板の上に設けられる層との密着性改良、物質の拡散防止、あるいは基板表面の平坦化のために、下塗り層を設けてもよい。
現像液としては、感光性着色組成物の未露光部を溶解し、かつ露光部(放射線照射部)を溶解し難いものであれば、いかなるものも用いることができる。具体的には、種々の有機溶剤及びその組合せ、アルカリ性の水溶液を用いることができる。
(マゼンタ顔料分散組成物R-1の調製)
下記組成の成分を混合し、ホモジナイザーを用いて回転数3,000r.p.m.で3時間撹拌して混合し、顔料を含む混合溶液を調製した。
<組成>
・Pigment Red 122(顔料) ・・・10部
・Disperbyk-163(分散剤) ・・・2.3部
(ビックケミー社製、ブロック共重合体系分散剤)
・ベンジルメタクリレート/メタクリル酸(=70/30[モル比])共重合体のプロピレングリコールモノメチルエーテルアセテート溶液(45%、重量平均分子量30000、藤倉化成(株)製、製品名:アクリベースFF-187) ・・・4.4部
・プロピレングリコールモノメチルエーテルアセテート(ダイセル化学工業(株)製、製品名:MMPGAC) ・・・83.3部
下記組成の成分を混合し、ホモジナイザーを用いて回転数3,000r.p.m.で3時間撹拌して混合し、顔料を含む混合溶液を調製した。
<組成>
・Pigment Red 254(顔料) ・・・10部
・アジスパーPB821(味の素ファインテクノ社製;分散剤) ・・・2.3部
・ベンジルメタクリレート/メタクリル酸(=70/30[モル比])共重合体のプロピレングリコールモノメチルエーテルアセテート溶液(45%、重量平均分子量30000、藤倉化成(株)製、製品名:アクリベースFF-187) ・・・4.4部
・プロピレングリコールモノメチルエーテルアセテート(ダイセル化学工業(株)製、製品名:MMPGAC) ・・・83.3部
-平坦化膜用レジスト液の調製-
下記の各成分をホモジナイザー攪拌機で混合、攪拌して、平坦化膜用レジスト液を調製した。
<平坦化膜用レジスト液の組成>
・ベンジルメタクリレート/メタクリル酸(=70/30[モル比])共重合体のプロピレングリコールモノメチルエーテルアセテート溶液(45%、重量平均分子量30000、藤倉化成(株)製、製品名:アクリベースFF-187) ・・・22部
・ジペンタエリスリトールペンタアクリレート ・・・6.5部
(日本化薬社製、製品名:KAYARAD DPHA)
・プロピレングリコールモノメチルエーテルアセテート(ダイセル化学工業(株)製、製品名:MMPGAC) ・・・13.8部
・エチル-3-エトキシプロピオネート(長瀬産業(株)製、製品名:エチル-3エトキシプロピオネート) ・・・12.3部
・ハロメチルトリアジン化合物(下記化合物I)(PANCHIM社製、製品名:トリアジンPP) ・・・0.3部
得られた平坦化膜用レジスト液を、6インチのシリコンウエハ上にスピンコートを用いて塗布した。次いで、塗布膜面の表面温度120℃で120秒間、ホットプレート上で加熱処理し、シリコンウエハ上に約2μmの膜厚の均一な塗布膜を得た。次いで、220℃の条件下で1時間、オーブンにてその塗布膜を硬化処理して、平坦化膜を形成した。
次いで、前記マゼンタ顔料分散組成物R-1をサンドミル分散機で混練・分散して得られた顔料分散液を用い、下記組成の成分を混合して感光性着色組成物を調製した。
・樹脂A ・・・20.57部
(ベンジルメタクリレート/メタクリル酸(=70/30[モル比])共重合体のプロピレングリコールモノメチルエーテルアセテート溶液(30%、重量平均分子量30000、藤倉化成(株)製、製品名:アクリベースFF-187))
・モノマーA ・・・1.46部
(ジペンタエリスリトールペンタアクリレート;日本化薬社製、製品名:KAYARAD DPHA)
・前記マゼンタ顔料分散組成物R-1 ・・・55.80部
・溶剤A(有機溶剤) ・・・16.75部
(プロピレングリコールモノメチルエーテルアセテート;ダイセル化学工業(株)製、製品名:MMPGAC)
・開始剤A(下記化合物II;チバ・スペシャルティ・ケミカルズ(株)製、製品名:IRGACURE OXE01) ・・・0.314部
・下記化合物III(紫外線吸収剤) ・・・0.576部
・界面活性剤A ・・・0.36部
(フッ素系界面活性剤;大日本インキ化学工業(株)製、製品名:メガファックF-144)
・重合禁止剤A(p-メトキシフェノール;関東化学(株)製、製品名:p-メトキシフェノール) ・・・0.001部
上記より得られた感光性着色組成物を、前記シリコンウエハの平坦化膜上にスピンコートにより塗布した後、塗布膜面の表面温度100℃で120秒間、ホットプレートで加熱処理して乾燥させ、乾燥後の膜厚が約1.0μmの塗布膜を形成した。
次に、乾燥後の塗布膜に対して、2.0μmの正方ピクセルがそれぞれ基板上の4mm×3mmの領域に配列されたマスクパターンを介してi線ステッパー(キャノン(株)製のFPA-3000i5+)により、露光量100mJ/cm2にて照度1200mW/cm2(高照度)及び600mW/cm2(低照度)の各2水準で露光した。
以上のようにして、固体撮像素子用カラーフィルタを作製した。
上記より得られた固体撮像素子用カラーフィルタについて、下記の評価、測定を行なった。評価、測定の結果は、下記表2に示す。
得られたカラーフィルタの2.0μm四方の画素パターンの形状を、測長SEM(S-7800H、(株)日立製作所製)を用いて、シリコンウエハ上のカラーフィルタの更に上方から3万倍で観察し、角(カド)の形状を下記の評価基準にしたがって評価した。なお、角(カド)の形状が丸まっているものは、デバイス製造時に隣り合った他色のパターン形状と異なってしまい画像認識時に混色、ノイズとして計測されてしまい、デバイスの性能を悪化させる。
<評価基準>
A:角(カド)の丸みが小さく、良好な矩形が得られた。
B:角(カド)に丸みができたが、実用上許容できる程度であった。
C:角(カド)に扇状に丸みがついており、矩形が得られなかった。
ポストベーク後のカラーフィルタの画素パターンを、測長SEM(S-7800H、(株)日立製作所製)を用いて、シリコンウエハ上のカラーフィルタの更に上方から3万倍で観察し、目測で残渣の発生の有無を下記の評価基準にしたがって評価した。
<評価基準>
A:現像残渣はなかった。
B:現像残渣が僅かにみられたが、実用上許容できる程度であった。
C:残渣の発生が顕著であった。
ポストベーク後のカラーフィルタの画素パターンの膜厚D1と、露光後で現像前における膜厚D2とを触針式表面形状測定器(Dektak8、日本ビーコ社製)を用いて測定し、得られた膜厚D1を膜厚D2で除算して残膜率(%;=D1/D2×100)を求め、これを指標として下記の評価基準にしたがって評価した。なお、露光感度の点から残膜率は高い方が望ましい。
<評価基準>
A:露光感度は良好で、残膜率は70%以上であった。
B:露光感度は不充分であり、残膜率も70%未満であった。
600mW/cm2(低照度)及び1200mW/cm2(高照度)での露光後に現像、ポストベークを行なった後のカラーフィルタの画素パターンの形状を、測長SEM(S-7800H、(株)日立製作所製)を用いて、シリコンウエハ上のカラーフィルタの更に上方から3万倍で観察した。線幅は、マスクパターンの2.0μmの正方ピクセルと対比した適性寸法という観点から、下記の評価基準にしたがって評価した。
<評価基準>
A:線幅が、1.80μm以上2.20μm未満であった。
B:線幅が、1.80μm未満もしくは2.20μm以上であった。
~A.線幅|a-b|~
上記のように2水準(高照度:1200mW/cm2、低照度:600mW/cm2)での露光により得られた画素パターンの各々について、前記「(1-4)線幅」の評価で得られた低照度での線幅a(μm)と高照度での線幅b(μm)の双方を比較し、線幅差(=|a-b|)求めて指標とし、下記の評価基準にしたがって評価した。固体撮像素子用カラーフィルタでは、得られるパターンの線幅の一定性が重要であるため、0.05μmを閾値に評価した。なお、「| |」の表記は絶対値を表す。
<評価基準>
A:線幅差が0.05μm未満であった。
B:線幅差が0.05μm以上であった。
~B.残膜率|c-d|~
上記のように2水準(高照度:1200mW/cm2、低照度:600mW/cm2)での露光により得られた画素パターンの各々について、上記の「(1-3)残膜率」の評価で得られた低照度での残膜率c(%)と高照度での残膜率d(%)の双方を比較し、残膜率の差(=|c-d|)を求めて指標とし、下記の評価基準にしたがって評価した。固体撮像素子用カラーフィルタでは、得られるパターンの膜厚の一定性が重要であるため、1.0%を閾値に評価した。なお、「| |」の表記は絶対値を表す。
<評価基準>
A:残膜率の差が1.0%未満であった。
B:残膜率の差が1.0%以上であった。
実施例1において、感光性着色組成物の組成を下記表1に示すように変更したこと以外は、実施例1と同様にして、感光性着色組成物を調製し、カラーフィルタを作製した。また、実施例1と同様の評価を行なった。評価、測定の結果は下記表2に示す。
実施例1において、感光性着色組成物の組成を下記表1に示すように変更したこと以外は、実施例1と同様にして、感光性着色組成物を調製し、カラーフィルタを作製した。また、実施例1と同様の評価を行なった。評価、測定の結果は下記表2に示す。
これに対して、他種類の紫外線吸収剤であるトリアジン系、ベンゾトリアゾ-ル系の紫外線吸収剤(化合物X、化合物XI)を用いた比較例では、特に低照度露光での線幅、残膜率の変動が大きく、露光照度依存性を抑制することはできなかった。また、酸化防止剤である化合物XIIを用いた比較例では、ある程度は露光照度依存性は小さいものの、現像残渣の発生を抑制できなかった。
実施例1~12並びに比較例1~6で用いた感光性着色組成物を用意し、これらをそれぞれ、別々のCr膜付ガラス基板(1737、コーニング社製、100mm×100mm)のCrBM膜上に、スピンコートにより膜厚1.5μmになるように塗布し、塗布膜を形成した。
以上のようにして、18種類の液晶表示素子用カラーフィルタを作製した。
上記より得られた18種類の液晶表示素子用カラーフィルタの各々について、下記の評価を行なった。結果は下記表3に示す。
得られた各カラーフィルタの100μmストライプ状の画素パターンをカラーフィルタ面に直交する面で切断し、その切断面の形状をSEM(S-4800、(株)日立ハイテクノロジ―ズ製)を用いて3万倍で観察し、切断面の形状を下記の評価基準にしたがって評価した。なお、断面形状が逆テーパーであると、液晶表示素子用カラーフィルタに後付けされるITO電極が断線しやすく、液晶セルの電圧保持率が低くなって液晶表示装置での表示不良を招来することから望ましくない。
<評価基準>
A:切断面の形状が順テーパーであった。
B:切断面の形状が矩形であった。
C:切断面の形状が逆テーパーであった。
上記のように2水準(高照度:40mW/cm2、低照度:20mW/cm2)での露光により得られた画素パターンの各々について、ポストベーク後の各カラーフィルタの画素パターンの膜厚D1と、露光後で現像前における膜厚D2とを触針式表面形状測定器(Dektak8、日本ビーコ社製)を用いて測定して、得られた膜厚D1を膜厚D2で除算して残膜率(%;=D1/D2×100)を求め、これを指標として下記の評価基準にしたがって評価した。なお、露光感度の点から残膜率は高い方が望ましい。
<評価基準>
A:露光感度は良好で、残膜率は70%以上であった。
B:露光感度は不充分であり、残膜率も70%未満であった。
上記のように2水準(高照度:40mW/cm2、低照度:20mW/cm2)での露光により得られた画素パターンの各々について、上記の「(2-2)残膜率」の評価で得られた低照度での残膜率e(%)と高照度での残膜率f(%)の双方を比較し、残膜率の差(=|e-f|)を求めて指標とし、下記の評価基準にしたがって評価した。液晶表示素子用カラーフィルタでは、得られるパターンの膜厚の一定性が重要であるため、1.0%を閾値に評価した。
<評価基準>
A:残膜率の差が1.0%未満であった。
B:残膜率の差が1.0%以上であった。
ポストベーク後の各カラーフィルタの画素パターンの形状を、測長SEM(S-7800H、(株)日立製作所製)を用いて、CrBM膜付ガラス基板上のカラーフィルタの更に上方から3万倍で観察し、目測で残渣の発生の有無を下記の評価基準にしたがって評価した。
<評価基準>
A:現像残渣はなかった。
B:現像残渣が僅かにみられたが、実用上許容できる程度であった。
C:残渣の発生が顕著であった。
これに対して、他種類の紫外線吸収剤であるトリアジン系、ベンゾトリアゾ-ル系の紫外線吸収剤(化合物X、化合物XI)を用いた比較例では、特に低照度露光でのパターン形状、残膜率の変動が大きく、露光照度依存性を抑制することはできなかった。また、酸化防止剤である化合物XIIを用いた比較例では、現像残渣の発生を抑制できなかった。
本明細書に記載された全ての文献、特許出願、および技術規格は、個々の文献、特許出願、および技術規格が参照により取り込まれることが具体的かつ個々に記された場合と同程度に、本明細書中に参照により取り込まれる。
Claims (11)
- 前記一般式(I)で表される化合物の含有量が、感光性着色組成物の固形分中0.01~10質量%であることを特徴とする請求項1に記載の感光性着色組成物。
- 前記光重合開始剤の少なくとも1種が、オキシムエステル系化合物である請求項1又は請求項2に記載の感光性着色組成物。
- 前記R1及び前記R2が、各々独立に、炭素数1~8の低級のアルキル基、又は置換もしくは無置換のフェニル基を表す請求項1~請求項3のいずれか1項に記載の感光性着色組成物。
- 前記R3又はR4で表される電子吸引基は、σp値が0.30以上0.80以下の電子吸引性基である請求項1~請求項4のいずれか1項に記載の感光性着色組成物。
- 前記R3が、シアノ基、-COOR5、-CONHR5、-COR5、及び-SO2R5より選択される基であって、前記R4が、シアノ基、-COOR6、-CONHR6、-COR6、及び-SO2R6より選択される基である請求項1~請求項5のいずれか1項に記載の感光性着色組成物。
〔R5及びR6は、各々独立に、炭素原子数1~20のアルキル基、又は炭素原子数6~20のアリール基を表す。〕 - 前記光重合開始剤がオキシムエステル系化合物である請求項1~請求項6のいずれか1項に記載の感光性着色組成物。
- 前記光重合開始剤が、2-(O-ベンゾイルオキシム)-1-[4-(フェニルチオ)フェニル]-1,2-オクタンジオン、及び1-(O-アセチルオキシム)-1-[9-エチル-6-(2-メチルベンゾイル)-9H-カルバゾール-3-イル]エタノンの少なくとも一方である請求項1~請求項6のいずれか1項に記載の感光性着色組成物。
- 前記顔料が赤色用の顔料であり、マゼンタ色又は赤色に構成された請求項1~請求項8のいずれか1項に記載の感光性着色組成物。
- 請求項1~請求項9のいずれか1項に記載の感光性着色組成物を塗布し、塗布形成された塗布層をフォトマスクを介して露光し、現像することによりパターン形成するカラーフィルタの製造方法。
- 請求項10に記載のカラーフィルタの製造方法により作製されたカラーフィルタ。
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020107020304A KR101308504B1 (ko) | 2008-02-13 | 2009-02-10 | 감광성 착색 조성물, 컬러필터 및 그 제조방법 |
EP09710455A EP2246739B1 (en) | 2008-02-13 | 2009-02-10 | Photosensitive colored composition, color filter and method for producing the same |
US12/867,669 US8980505B2 (en) | 2008-02-13 | 2009-02-10 | Photosensitive colored composition, color filter and method for producing the same |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2008032220 | 2008-02-13 | ||
JP2008-032220 | 2008-02-13 | ||
JP2008-093839 | 2008-03-31 | ||
JP2008093839A JP5147499B2 (ja) | 2008-02-13 | 2008-03-31 | 感光性着色組成物、並びにカラーフィルタ及びその製造方法 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2009101932A1 true WO2009101932A1 (ja) | 2009-08-20 |
Family
ID=40956964
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2009/052218 WO2009101932A1 (ja) | 2008-02-13 | 2009-02-10 | 感光性着色組成物、並びにカラーフィルタ及びその製造方法 |
Country Status (6)
Country | Link |
---|---|
US (1) | US8980505B2 (ja) |
EP (1) | EP2246739B1 (ja) |
JP (1) | JP5147499B2 (ja) |
KR (1) | KR101308504B1 (ja) |
TW (1) | TWI397768B (ja) |
WO (1) | WO2009101932A1 (ja) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2022000700A (ja) * | 2017-03-24 | 2022-01-04 | 富士フイルム株式会社 | 感光性着色組成物、硬化膜、カラーフィルタ、固体撮像素子および画像表示装置 |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5155920B2 (ja) | 2008-03-31 | 2013-03-06 | 富士フイルム株式会社 | 感光性透明樹脂組成物、カラーフィルタの製造方法及びカラーフィルター |
JP5137662B2 (ja) * | 2008-03-31 | 2013-02-06 | 富士フイルム株式会社 | 硬化性組成物、カラーフィルタ及びその製造方法、並びに固体撮像素子 |
JP2011184414A (ja) * | 2010-03-11 | 2011-09-22 | Fujifilm Corp | ポリマーフィルム、紫外線吸収剤、メロシアニン系化合物、及びメロシアニン系化合物の製造方法 |
JP2013068814A (ja) * | 2011-09-22 | 2013-04-18 | Fujifilm Corp | 着色感放射線性組成物、カラーフィルタ及びそのカラーフィルタの製造方法、並びに、固体撮像素子 |
WO2014084147A1 (ja) * | 2012-11-29 | 2014-06-05 | 富士フイルム株式会社 | 組成物、赤外線透過フィルタ及びその製造方法、並びに赤外線センサー |
JP6049521B2 (ja) | 2013-03-29 | 2016-12-21 | 富士フイルム株式会社 | 感光性樹脂組成物、硬化膜、画像形成方法、固体撮像素子、カラーフィルタおよび紫外線吸収剤 |
JP2015052754A (ja) * | 2013-09-09 | 2015-03-19 | 富士フイルム株式会社 | 樹脂硬化物の製造方法、並びにこれを用いた固体撮像素子および液晶表示装置の製造方法 |
EP3431513B1 (en) | 2016-03-14 | 2020-12-23 | FUJIFILM Corporation | Composition, film, cured film, optical sensor and method for producing film |
KR20180124013A (ko) * | 2016-03-25 | 2018-11-20 | 도레이 카부시키가이샤 | 착색 수지 조성물, 컬러 필터 기판, 및 액정 표시 장치 |
TW202231641A (zh) | 2020-12-16 | 2022-08-16 | 日商富士軟片股份有限公司 | 組成物、膜、濾光器、固體攝像元件、圖像顯示裝置及紅外線感測器 |
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 |
EP4310556A1 (en) | 2021-03-19 | 2024-01-24 | FUJIFILM Corporation | Film and photosensor |
CN117916279A (zh) | 2021-09-29 | 2024-04-19 | 富士胶片株式会社 | 组合物、树脂、膜及光传感器 |
Citations (50)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2367670A (en) | 1941-12-31 | 1945-01-23 | Du Pont | Cementing process |
US2367660A (en) | 1941-12-31 | 1945-01-23 | Du Pont | Process of photopolymerization |
US2367661A (en) | 1941-12-31 | 1945-01-23 | Du Pont | Process of photopolymerization |
US2448828A (en) | 1946-09-04 | 1948-09-07 | Du Pont | Photopolymerization |
US2722512A (en) | 1952-10-23 | 1955-11-01 | Du Pont | Photopolymerization process |
US2951758A (en) | 1957-05-17 | 1960-09-06 | Du Pont | Photopolymerizable compositions and elements |
US3046127A (en) | 1957-10-07 | 1962-07-24 | Du Pont | Photopolymerizable compositions, elements and processes |
JPS4429620B1 (ja) | 1961-10-10 | 1969-12-02 | ||
JPS4841708B1 (ja) | 1970-01-13 | 1973-12-07 | ||
JPS4943191B1 (ja) | 1969-07-11 | 1974-11-19 | ||
JPS506034B1 (ja) | 1970-08-11 | 1975-03-10 | ||
JPS5137193A (ja) | 1974-09-25 | 1976-03-29 | Toyo Boseki | |
JPS5148516A (ja) | 1974-10-22 | 1976-04-26 | Nishimatsu Constr Co Ltd | Nanjakujibanokairyosuru hoho |
JPS5230490B2 (ja) | 1972-03-21 | 1977-08-09 | ||
JPS53128333A (en) | 1977-04-15 | 1978-11-09 | Fuji Photo Film Co Ltd | Prevention of influences of ultraviolet ray upon photosensitive material of silver halogenide |
JPS53133428A (en) | 1977-04-25 | 1978-11-21 | Hoechst Ag | Radiation sensitive copying constitute |
JPS5425957B2 (ja) | 1974-10-04 | 1979-08-31 | ||
JPS5434327B1 (ja) | 1970-12-28 | 1979-10-26 | ||
JPS576096A (en) | 1980-06-11 | 1982-01-12 | Tokyo Gas Co Ltd | Arc propelling method |
US4318791A (en) | 1977-12-22 | 1982-03-09 | Ciba-Geigy Corporation | Use of aromatic-aliphatic ketones as photo sensitizers |
JPS5812577B2 (ja) | 1973-12-21 | 1983-03-09 | ヘキスト アクチエンゲゼルシヤフト | 光重合可能な複写材料 |
EP0088050A2 (de) | 1982-02-26 | 1983-09-07 | Ciba-Geigy Ag | Photohärtbare gefärbte Massen |
JPS591281B2 (ja) | 1971-09-03 | 1984-01-11 | ミネソタ マイニング アンド マニュファクチュアリング コンパニ− | ヒカリジユウゴウカイシザイ |
JPS5944615A (ja) | 1982-09-07 | 1984-03-13 | Furuno Electric Co Ltd | ジヤイロ装置 |
JPS5953836A (ja) | 1982-09-21 | 1984-03-28 | Fuji Photo Film Co Ltd | 感光性平版印刷版 |
JPS5971048A (ja) | 1982-10-18 | 1984-04-21 | Mitsubishi Chem Ind Ltd | 光重合系感光性組成物 |
JPS6214149A (ja) * | 1985-07-11 | 1987-01-22 | ミネソタ マイニング アンド マニュファクチュアリング コンパニ− | 3−アミノアリリデンマロノニトリル化合物よりなる紫外線吸収剤を含有する写真材料 |
JPS6353544A (ja) | 1986-08-25 | 1988-03-07 | Konica Corp | 発汗現象及びスタチツクマ−ク発生を防止したハロゲン化銀写真感光材料 |
JPS6353543A (ja) | 1986-08-23 | 1988-03-07 | Konica Corp | 発汗現象及びスタチツクマ−ク発生を防止したハロゲン化銀写真感光材料 |
JPS6356651A (ja) | 1986-08-27 | 1988-03-11 | Konica Corp | 発汗現象及びスタチツクマ−ク発生を防止したハロゲン化銀写真感光材料 |
JPH06169831A (ja) | 1992-12-08 | 1994-06-21 | Okamura Corp | 冷蔵ショーケース |
JPH0815521A (ja) | 1994-07-01 | 1996-01-19 | Toyo Ink Mfg Co Ltd | カラーフィルタ用感光性着色組成物およびカラーフィルタ |
JPH08295810A (ja) | 1995-04-26 | 1996-11-12 | Toyo Ink Mfg Co Ltd | カラーフィルタ用顔料および着色組成物 |
JPH1062986A (ja) | 1996-08-21 | 1998-03-06 | Fuji Photo Film Co Ltd | 感放射線性着色組成物 |
JPH10245501A (ja) | 1997-03-03 | 1998-09-14 | Toyo Ink Mfg Co Ltd | 顔料組成物およびその製造方法 |
JPH11189732A (ja) | 1996-12-16 | 1999-07-13 | Dainichiseika Color & Chem Mfg Co Ltd | 顔料の分散剤、顔料分散液、カラーフイルター用顔料分散液 |
JPH11199796A (ja) | 1997-11-17 | 1999-07-27 | Toyo Ink Mfg Co Ltd | 顔料分散剤、及びそれを含有する顔料組成物 |
JP2000066385A (ja) | 1998-08-18 | 2000-03-03 | Ciba Specialty Chem Holding Inc | 高感度で高レジスト厚さのi線ホトレジスト用スルホニルオキシム類 |
JP2001356210A (ja) | 2000-06-14 | 2001-12-26 | Jsr Corp | カラーフィルタ用感放射線性組成物およびカラーフィルタ |
JP2003025524A (ja) | 2001-07-18 | 2003-01-29 | Gunze Ltd | 積層延伸フィルム |
JP2003025525A (ja) | 2001-07-17 | 2003-01-29 | Sumika Plastech Co Ltd | 印刷シート用基材 |
JP2003240938A (ja) | 2002-02-22 | 2003-08-27 | Toyo Ink Mfg Co Ltd | カラーフィルタ用着色組成物およびカラーフィルタ |
JP2005234478A (ja) | 2004-02-23 | 2005-09-02 | Toyo Ink Mfg Co Ltd | カラーフィルタ用着色組成物およびカラーフィルタ |
JP2006011397A (ja) | 2004-05-21 | 2006-01-12 | Nippon Kayaku Co Ltd | ネガ型着色感光性組成物 |
WO2006035807A1 (ja) * | 2004-09-28 | 2006-04-06 | Fujifilm Corporation | パターン形成材料、並びにパターン形成装置及びパターン形成方法 |
JP2006265528A (ja) | 2005-02-22 | 2006-10-05 | Dainichiseika Color & Chem Mfg Co Ltd | 顔料分散剤およびその使用 |
JP2007034119A (ja) * | 2005-07-29 | 2007-02-08 | Toray Ind Inc | カラーフィルター用感光性着色組成物、およびカラーフィルター |
JP2007108275A (ja) * | 2005-10-12 | 2007-04-26 | Toppan Printing Co Ltd | 感光性赤色着色組成物、それを用いたカラーフィルタ基板、および半透過型液晶表示装置 |
JP2007112934A (ja) | 2005-10-21 | 2007-05-10 | Toyo Ink Mfg Co Ltd | 微細顔料、その製造方法及びそれを用いた着色組成物 |
JP2007293127A (ja) * | 2006-04-26 | 2007-11-08 | Fujifilm Corp | 染料含有ネガ型硬化性組成物、カラーフィルタ及びその製造方法 |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1065180A (en) * | 1974-09-17 | 1979-10-30 | Eastman Kodak Company | Photographic element having 1-amino-4-cyano-1,3-butadiene derivative as ultraviolet filter |
IT1206995B (it) * | 1979-10-12 | 1989-05-17 | Minnesota Mining & Mfg | Assorbenti ultravioletti polimerici materiale fotografico che li contiene e metodo per introdurli in detto materiale fotografico |
JPS58178351A (ja) * | 1982-04-14 | 1983-10-19 | Fuji Photo Film Co Ltd | ハロゲン化銀写真感光材料 |
JPH08239509A (ja) * | 1995-03-06 | 1996-09-17 | Fuji Photo Film Co Ltd | ポリマーフィルム |
JP3627886B2 (ja) * | 1996-11-08 | 2005-03-09 | 富士写真フイルム株式会社 | 感放射線性着色組成物 |
JP2002323762A (ja) * | 2001-04-25 | 2002-11-08 | Nippon Kayaku Co Ltd | ネガ型着色感光性組成物 |
JP4089491B2 (ja) * | 2003-04-14 | 2008-05-28 | コニカミノルタホールディングス株式会社 | 重合開始剤、重合組成物、ラジカル発生方法、平版印刷版材料および平版印刷版の作製方法 |
TWI342983B (en) * | 2003-07-16 | 2011-06-01 | Sumitomo Chemical Co | Coloring photosensitive resin composition |
JP4839710B2 (ja) * | 2004-08-09 | 2011-12-21 | 三菱化学株式会社 | 感光性樹脂組成物、カラーフィルタ及び液晶表示装置 |
JP4742789B2 (ja) * | 2005-03-28 | 2011-08-10 | 東レ株式会社 | アルカリ現像用感光性透明樹脂組成物、および半透過型液晶表示装置 |
JP4661384B2 (ja) * | 2005-06-16 | 2011-03-30 | Jsr株式会社 | 着色層形成用感放射線性組成物およびカラーフィルタ |
EP1906242B1 (en) * | 2005-06-30 | 2015-07-15 | DIC Corporation | Photosensitive resin composition |
JP2007017814A (ja) * | 2005-07-08 | 2007-01-25 | Fujifilm Holdings Corp | パターン形成材料、並びにパターン形成装置及び永久パターン形成方法 |
JP2007065640A (ja) * | 2005-08-03 | 2007-03-15 | Fujifilm Electronic Materials Co Ltd | 光硬化性組成物及び液晶表示装置用フォトスペーサー |
JP2007072163A (ja) * | 2005-09-07 | 2007-03-22 | Fujifilm Corp | 光学補償素子及びその製造方法、液晶表示装置及び液晶プロジェクタ |
JP4745110B2 (ja) * | 2006-04-19 | 2011-08-10 | 東京応化工業株式会社 | 感光性組成物及びこの感光性組成物により形成されたカラーフィルタ |
TWI403840B (zh) * | 2006-04-26 | 2013-08-01 | Fujifilm Corp | 含染料之負型硬化性組成物、彩色濾光片及其製法 |
JP5137662B2 (ja) * | 2008-03-31 | 2013-02-06 | 富士フイルム株式会社 | 硬化性組成物、カラーフィルタ及びその製造方法、並びに固体撮像素子 |
-
2008
- 2008-03-31 JP JP2008093839A patent/JP5147499B2/ja active Active
-
2009
- 2009-02-10 EP EP09710455A patent/EP2246739B1/en active Active
- 2009-02-10 US US12/867,669 patent/US8980505B2/en not_active Expired - Fee Related
- 2009-02-10 WO PCT/JP2009/052218 patent/WO2009101932A1/ja active Application Filing
- 2009-02-10 KR KR1020107020304A patent/KR101308504B1/ko active IP Right Grant
- 2009-02-12 TW TW098104412A patent/TWI397768B/zh active
Patent Citations (50)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2367670A (en) | 1941-12-31 | 1945-01-23 | Du Pont | Cementing process |
US2367660A (en) | 1941-12-31 | 1945-01-23 | Du Pont | Process of photopolymerization |
US2367661A (en) | 1941-12-31 | 1945-01-23 | Du Pont | Process of photopolymerization |
US2448828A (en) | 1946-09-04 | 1948-09-07 | Du Pont | Photopolymerization |
US2722512A (en) | 1952-10-23 | 1955-11-01 | Du Pont | Photopolymerization process |
US2951758A (en) | 1957-05-17 | 1960-09-06 | Du Pont | Photopolymerizable compositions and elements |
US3046127A (en) | 1957-10-07 | 1962-07-24 | Du Pont | Photopolymerizable compositions, elements and processes |
JPS4429620B1 (ja) | 1961-10-10 | 1969-12-02 | ||
JPS4943191B1 (ja) | 1969-07-11 | 1974-11-19 | ||
JPS4841708B1 (ja) | 1970-01-13 | 1973-12-07 | ||
JPS506034B1 (ja) | 1970-08-11 | 1975-03-10 | ||
JPS5434327B1 (ja) | 1970-12-28 | 1979-10-26 | ||
JPS591281B2 (ja) | 1971-09-03 | 1984-01-11 | ミネソタ マイニング アンド マニュファクチュアリング コンパニ− | ヒカリジユウゴウカイシザイ |
JPS5230490B2 (ja) | 1972-03-21 | 1977-08-09 | ||
JPS5812577B2 (ja) | 1973-12-21 | 1983-03-09 | ヘキスト アクチエンゲゼルシヤフト | 光重合可能な複写材料 |
JPS5137193A (ja) | 1974-09-25 | 1976-03-29 | Toyo Boseki | |
JPS5425957B2 (ja) | 1974-10-04 | 1979-08-31 | ||
JPS5148516A (ja) | 1974-10-22 | 1976-04-26 | Nishimatsu Constr Co Ltd | Nanjakujibanokairyosuru hoho |
JPS53128333A (en) | 1977-04-15 | 1978-11-09 | Fuji Photo Film Co Ltd | Prevention of influences of ultraviolet ray upon photosensitive material of silver halogenide |
JPS53133428A (en) | 1977-04-25 | 1978-11-21 | Hoechst Ag | Radiation sensitive copying constitute |
US4318791A (en) | 1977-12-22 | 1982-03-09 | Ciba-Geigy Corporation | Use of aromatic-aliphatic ketones as photo sensitizers |
JPS576096A (en) | 1980-06-11 | 1982-01-12 | Tokyo Gas Co Ltd | Arc propelling method |
EP0088050A2 (de) | 1982-02-26 | 1983-09-07 | Ciba-Geigy Ag | Photohärtbare gefärbte Massen |
JPS5944615A (ja) | 1982-09-07 | 1984-03-13 | Furuno Electric Co Ltd | ジヤイロ装置 |
JPS5953836A (ja) | 1982-09-21 | 1984-03-28 | Fuji Photo Film Co Ltd | 感光性平版印刷版 |
JPS5971048A (ja) | 1982-10-18 | 1984-04-21 | Mitsubishi Chem Ind Ltd | 光重合系感光性組成物 |
JPS6214149A (ja) * | 1985-07-11 | 1987-01-22 | ミネソタ マイニング アンド マニュファクチュアリング コンパニ− | 3−アミノアリリデンマロノニトリル化合物よりなる紫外線吸収剤を含有する写真材料 |
JPS6353543A (ja) | 1986-08-23 | 1988-03-07 | Konica Corp | 発汗現象及びスタチツクマ−ク発生を防止したハロゲン化銀写真感光材料 |
JPS6353544A (ja) | 1986-08-25 | 1988-03-07 | Konica Corp | 発汗現象及びスタチツクマ−ク発生を防止したハロゲン化銀写真感光材料 |
JPS6356651A (ja) | 1986-08-27 | 1988-03-11 | Konica Corp | 発汗現象及びスタチツクマ−ク発生を防止したハロゲン化銀写真感光材料 |
JPH06169831A (ja) | 1992-12-08 | 1994-06-21 | Okamura Corp | 冷蔵ショーケース |
JPH0815521A (ja) | 1994-07-01 | 1996-01-19 | Toyo Ink Mfg Co Ltd | カラーフィルタ用感光性着色組成物およびカラーフィルタ |
JPH08295810A (ja) | 1995-04-26 | 1996-11-12 | Toyo Ink Mfg Co Ltd | カラーフィルタ用顔料および着色組成物 |
JPH1062986A (ja) | 1996-08-21 | 1998-03-06 | Fuji Photo Film Co Ltd | 感放射線性着色組成物 |
JPH11189732A (ja) | 1996-12-16 | 1999-07-13 | Dainichiseika Color & Chem Mfg Co Ltd | 顔料の分散剤、顔料分散液、カラーフイルター用顔料分散液 |
JPH10245501A (ja) | 1997-03-03 | 1998-09-14 | Toyo Ink Mfg Co Ltd | 顔料組成物およびその製造方法 |
JPH11199796A (ja) | 1997-11-17 | 1999-07-27 | Toyo Ink Mfg Co Ltd | 顔料分散剤、及びそれを含有する顔料組成物 |
JP2000066385A (ja) | 1998-08-18 | 2000-03-03 | Ciba Specialty Chem Holding Inc | 高感度で高レジスト厚さのi線ホトレジスト用スルホニルオキシム類 |
JP2001356210A (ja) | 2000-06-14 | 2001-12-26 | Jsr Corp | カラーフィルタ用感放射線性組成物およびカラーフィルタ |
JP2003025525A (ja) | 2001-07-17 | 2003-01-29 | Sumika Plastech Co Ltd | 印刷シート用基材 |
JP2003025524A (ja) | 2001-07-18 | 2003-01-29 | Gunze Ltd | 積層延伸フィルム |
JP2003240938A (ja) | 2002-02-22 | 2003-08-27 | Toyo Ink Mfg Co Ltd | カラーフィルタ用着色組成物およびカラーフィルタ |
JP2005234478A (ja) | 2004-02-23 | 2005-09-02 | Toyo Ink Mfg Co Ltd | カラーフィルタ用着色組成物およびカラーフィルタ |
JP2006011397A (ja) | 2004-05-21 | 2006-01-12 | Nippon Kayaku Co Ltd | ネガ型着色感光性組成物 |
WO2006035807A1 (ja) * | 2004-09-28 | 2006-04-06 | Fujifilm Corporation | パターン形成材料、並びにパターン形成装置及びパターン形成方法 |
JP2006265528A (ja) | 2005-02-22 | 2006-10-05 | Dainichiseika Color & Chem Mfg Co Ltd | 顔料分散剤およびその使用 |
JP2007034119A (ja) * | 2005-07-29 | 2007-02-08 | Toray Ind Inc | カラーフィルター用感光性着色組成物、およびカラーフィルター |
JP2007108275A (ja) * | 2005-10-12 | 2007-04-26 | Toppan Printing Co Ltd | 感光性赤色着色組成物、それを用いたカラーフィルタ基板、および半透過型液晶表示装置 |
JP2007112934A (ja) | 2005-10-21 | 2007-05-10 | Toyo Ink Mfg Co Ltd | 微細顔料、その製造方法及びそれを用いた着色組成物 |
JP2007293127A (ja) * | 2006-04-26 | 2007-11-08 | Fujifilm Corp | 染料含有ネガ型硬化性組成物、カラーフィルタ及びその製造方法 |
Non-Patent Citations (8)
Title |
---|
"Kagaku no Ryoiki", JOURNAL OF JAPANESE CHEMISTRY, vol. 122, 1979, pages 96 - 103 |
"Lange's Handbook of Chemistry 12th edition", 1979, MCGRAW HILL |
CHEMICAL REVIEWS, vol. 91, 1991, pages L65 - 195 |
J. C. S. PERKIN II, 1979, pages 156 - 162 |
J. C. S. PERKIN IL, 1979, pages 1653 - 1660 |
JOURNAL OF PHOTOPOLYMER SCIENCE AND TECHNOLOGY, 1995, pages 202 - 232 |
JOURNAL OF THE ADHESION SOCIETY OF JAPAN, vol. 20, no. 7, pages 300 - 308 |
See also references of EP2246739A4 |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2022000700A (ja) * | 2017-03-24 | 2022-01-04 | 富士フイルム株式会社 | 感光性着色組成物、硬化膜、カラーフィルタ、固体撮像素子および画像表示装置 |
JP7233499B2 (ja) | 2017-03-24 | 2023-03-06 | 富士フイルム株式会社 | 感光性着色組成物、硬化膜、カラーフィルタ、固体撮像素子および画像表示装置 |
Also Published As
Publication number | Publication date |
---|---|
TW200947120A (en) | 2009-11-16 |
JP5147499B2 (ja) | 2013-02-20 |
EP2246739A1 (en) | 2010-11-03 |
EP2246739A4 (en) | 2011-02-23 |
KR101308504B1 (ko) | 2013-09-17 |
TWI397768B (zh) | 2013-06-01 |
JP2009217221A (ja) | 2009-09-24 |
US8980505B2 (en) | 2015-03-17 |
EP2246739B1 (en) | 2012-07-04 |
KR20100112200A (ko) | 2010-10-18 |
US20100323285A1 (en) | 2010-12-23 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5147499B2 (ja) | 感光性着色組成物、並びにカラーフィルタ及びその製造方法 | |
JP5155920B2 (ja) | 感光性透明樹脂組成物、カラーフィルタの製造方法及びカラーフィルター | |
JP5371507B2 (ja) | 着色感光性組成物、カラーフィルタ、および液晶表示装置 | |
US6140016A (en) | Photosensitive colored composition for color filter | |
JP2010039475A (ja) | 紫外光レーザー露光用感光性樹脂組成物、パターン形成方法、その方法を用いて製造したカラーフィルタ、カラーフィルタの製造方法および液晶表示装置 | |
JP4393104B2 (ja) | Lcd用硬化性緑色組成物およびカラーフィルタ | |
JP4472287B2 (ja) | Lcd用カラーフィルタ | |
JP2010224308A (ja) | カラーフィルタ及びその製造方法 | |
JP4652213B2 (ja) | 顔料分散組成物、光硬化性組成物及びカラーフィルタ | |
JP5030375B2 (ja) | カラーフィルタ、固体撮像素子及びシアン色カラーフィルタ用光硬化性組成物 | |
JP3893443B2 (ja) | カラーフィルター用組成物 | |
JP5301596B2 (ja) | 青色感光性組成物、カラーフィルタ、カラーフィルタの製造方法、液晶表示装置、及び有機el表示装置 | |
JP2010134137A (ja) | カラーフィルタ及びその製造方法、並びに液晶表示装置 | |
JP2005062494A (ja) | 光硬化性組成物及びそれを用いたカラーフィルタ | |
JP2009244802A (ja) | 感光性着色組成物及びカラーフィルタの製造方法 | |
JP5192964B2 (ja) | 透明膜形成用組成物、透明膜、カラーフィルタ用下地透明膜及び固体撮像素子 | |
JP4717370B2 (ja) | カラーフィルター | |
JP4584009B2 (ja) | 光硬化性組成物およびそれを用いたカラーフィルタ | |
JP2010230841A (ja) | 感光性樹脂組成物、カラーフィルタの製造方法、及びカラーフィルタ | |
JP5554389B2 (ja) | シアン色カラーフィルタ作製用光硬化性組成物及びその製造方法 | |
JP5306291B2 (ja) | シアン色カラーフィルタ及びそれを用いた固体撮像素子 | |
JP2010048927A (ja) | 赤色着色硬化性組成物、赤色着色硬化性組成物の製造方法、カラーフィルタ、及び液晶表示装置 | |
JP2010224309A (ja) | カラーフィルタ用着色硬化性組成物、カラーフィルタ及びその製造方法、並びに固体撮像素子 | |
JP2009282426A (ja) | カラーフィルタの製造方法、カラーフィルタ、および画像表示装置 | |
KR20180020098A (ko) | 착색 조성물, 착색 경화막, 및 컬러 필터, 표시 소자 및 수광 소자 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 09710455 Country of ref document: EP Kind code of ref document: A1 |
|
WWE | Wipo information: entry into national phase |
Ref document number: 12867669 Country of ref document: US |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2009710455 Country of ref document: EP |
|
ENP | Entry into the national phase |
Ref document number: 20107020304 Country of ref document: KR Kind code of ref document: A |