Photosensitive resin composition, resist laminate, and cured product thereof (2)
US-9684239-B2 · Jun 20, 2017 · US
US10012901B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10012901-B2 |
| Application number | US-201314443669-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 21, 2013 |
| Priority date | Nov 22, 2012 |
| Publication date | Jul 3, 2018 |
| Grant date | Jul 3, 2018 |
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The purpose of the present invention is to provide the following: a photosensitive epoxy resin composition that, via photolithography, can form a high-resolution, low-stress image that has vertical side walls and resists moisture and heat, and/or a resist laminate using said photosensitive epoxy resin composition; and an article or articles obtained by curing said photosensitive epoxy resin composition and/or resist laminate. The present invention is a photosensitive resin composition containing the following: an epoxy resin (A), a polyol compound (B) having a specific structure, a cationic-polymerization photoinitiator (C), a silane compound (D) containing an epoxy group, and a reactive epoxy monomer (E) having a specific structure. The epoxy resin (A) contains the phenol derivative represented by formula (1), an epoxy resin (a) obtained via a reaction with epihalohydrin, and an epoxy resin (b) that can be represented by formula (2).
Opening claim text (preview).
The invention claimed is: 1. A photosensitive resin composition comprising: an epoxy resin (A), a polyol compound (B), a cationic photopolymerization initiator (C), an epoxy group-containing silane compound (D), and a reactive epoxy monomer (E); the epoxy resin (A) comprising an epoxy resin (a) obtained from reaction of a phenol derivative represented by the following Formula (1) and epihalohydrin: and an epoxy resin (b) represented by the following Formula (2): wherein m is an average value, representing a real number in the range from 2 to 30, R 1 and R 2 each independently represent a hydrogen atom, an alkyl group having 1 to 4 carbon atoms, or a trifluoromethyl group, X each independently represents a hydrogen atom or a glycidyl group, and at least one of a plurality of X present is a glycidyl group; the polyol compound (B) comprising a polyester polyol represented by the following Formula (3): wherein x is an average value, representing a real number in the range from 1 to 9, and R 3 represents a divalent aliphatic hydrocarbon group which may contain at least one ether bond within a carbon chain; and/or a polyester polyol represented by the following Formula (4): wherein y is an average value, representing a real number in the range from 1 to 6, and R 4 represents a trivalent aliphatic hydrocarbon group which may contain at least one ether bond within a carbon chain; and the reactive epoxy monomer (E) comprising an epoxy compound represented by the following Formula (10) and/or an epoxy compound represented by the following Formula (11): wherein R 5 represents a divalent aliphatic hydrocarbon group having 1 to 11 carbon atoms; wherein R 6 represents a trivalent aliphatic hydrocarbon group having 1 to 11 carbon atoms; wherein a blending ratio of the reactive epoxy monomer (E) is 3 to 10 mass % relative to a total mass of the epoxy resin (A) and the polyol compound (B); wherein a blending ratio of the polyol compound (B) is 5 to 15 mass % relative to a total mass of the epoxy resin (A); wherein a blending ratio of the cationic photopolymerization initiator (C) is 3 to 8 mass % relative to a total mass of the epoxy resin (A), the polyol compound (B), and the reactive epoxy monomer (E); wherein a blending ratio of the epoxy group-containing silane compound (D) is 3 to 8 mass % relative to a total mass of the epoxy resin (A), the polyol compound (B), the cationic photopolymerization initiator (C), and the reactive epoxy monomer (E); and wherein the ratio of the amount of the epoxy resin (b) to the amount of the epoxy resin (a) ranges from 10 to 20 mass %. 2. The photosensitive resin composition according to claim 1 , wherein the reactive epoxy monomer (E) comprises trimethylolpropane triglycidyl ether. 3. The photosensitive resin composition according to claim 1 , wherein the epoxy group-containing silane compound (D) is an epoxy group-containing alkoxysilane compound. 4. The photosensitive resin composition according to claim 1 , further comprising a solvent (F). 5. The photosensitive resin composition according to claim 4 , wherein a blending ratio of the solvent (F) is 5 to 95 mass % relative to a total mass of the photosensitive resin composition including the solvent (F). 6. A cured product of the photosensitive resin composition according to any one of claims 1 , 2 , 3 , 4 and 5 . 7. A resist laminate comprising the photosensitive resin composition according to any one of claim 1 , 2 , 3 , 4 and 5 sandwiched between two substrates. 8. A cured product of a dry film resist obtained from the resist laminate according to claim 7 .
Non-macromolecular compounds containing Si-O, Si-C or Si-N bonds (G03F7/0752 takes precedence) · CPC title
used as adhesion-promoting additives or as means to improve adhesion · CPC title
Macromolecular compounds which are rendered insoluble or differentially wettable (G03F7/075 takes precedence; macromolecular azides G03F7/012; macromolecular diazonium compounds G03F7/021) · CPC title
together with di-epoxy compounds · CPC title
aromatic · CPC title
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