Photo-curable resin composition and photo-curable dry film using the same
US-2016357105-A1 · Dec 8, 2016 · US
US10604654B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10604654-B2 |
| Application number | US-201815951577-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 12, 2018 |
| Priority date | Apr 13, 2017 |
| Publication date | Mar 31, 2020 |
| Grant date | Mar 31, 2020 |
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One of the purposes of the present invention is to provide a curable resin composition which has good curability and provides a cured product having a sufficient hardness, in particular an addition-curable organic silicon resin composition. The present invention provides a curable resin composition comprising the following components (A) to (C): (A) an organic-silicon compound having at least two alkenyl groups in a molecule, (B) an organic silicon compound which is represented by the formula (I) and has at least three hydrosilyl groups each bonded to the carbon atom of the benzene ring in an amount such that a ratio of the number of the hydrosilyl group in component (B) to the number of the alkenyl group in component (A) is 0.4 to 4, and (C) a hydrosilylation catalyst in a catalytic amount.
Opening claim text (preview).
The invention claimed is: 1. A curable resin composition comprising the following components (A) to (C): (A) an organic silicon compound having at least two alkenyl groups in a molecule, (B) an organic silicon compound represented by the following formula (1) in an amount such that a ratio of the number of the hydrosilyl groups in component (B) to the number of the alkenyl groups in component (A) is 0.4 to 4, wherein R 2 is, independently of each other, a hydrogen atom or a monovalent hydrocarbon group having 1 to 12 carbon atoms and all of the X 1 to X 4 and X 9 are a group represented by the following formula (1′), wherein R 2 is as defined above, and (C) a hydrosilylation catalyst in a catalytic amount. 2. The curable resin composition according to claim 1 , wherein component (A) is an organic silicon compound represented by the following formula (4): (R 4 3 SiO 1/2 ) a (R 4 2 SiO 2/2 ) b (R 4 SiO 3/2 ) c (SiO 4/2 ) d (Y) e (O 1/2 R 3 ) f (4), wherein R 4 is, independently of each other, a monovalent hydrocarbon group having 1 to 12 carbon atoms and optionally having an unsaturated bond, provided that at least two of R 4 are an alkenyl group, R 3 is a hydrogen atom or a monovalent hydrocarbon group having 1 to 6 carbon atoms, a is an integer of from 0 to 100, b is an integer of from 0 to 1,000, c is an integer of from 0 to 500, d is an integer of from 0 to 500, e is an integer of from 0 to 500, f is an integer of from 0 to 50, a total of a, b, c, d and e is 2 to 1,000, and Y is a silphenylene unit which has a valance of 1 to 26 and is represented by the following formula (II), wherein r is 0 or 1, k is an integer of from 1 to 3, a bonding marked with ** in the formula (II) bonds to a silicon atom of another siloxane in the formula (4), R 4 is as defined above, Z 1 to Z 9 are, independently of each other, a hydrogen atom, a monovalent hydrocarbon group having 1 to 6 carbon atoms, a divalent, trivalent or tetravalent group represented by the following formula (5′), a monovalent group represented by the following formula (5″), or a group having a valance of 1 to 16 and represented by the following formula (7′), R 6 is, independently of each other, selected from the groups defined for R 4 or a group which has a valance of 1 to 16 and is represented by the following formula (6′), wherein a bonding marked with * in the formulas (5′) and (5″) bonds to a carbon atom of the benzene ring, a bonding marked with ** in the formula (5′) bonds to a silicon atom of another siloxane in the formula (4), k is an integer of from 1 to 3, k′ is an integer of from 1 to 3, R 4 is as defined above, and R 5 is a monovalent hydrocarbon group having 1 to 6 carbon atoms, wherein Z′ is, independently of each other, a hydrogen atom, a monovalent hydrocarbon group having 1 to 6 carbon atoms or the group represented by the formula (5′) or (5″), R 4 is as defined above, a bonding marked with * in the formula (7′) bonds to a carbon atom of the benzene ring and a bonding marked with *** in the formula (6′) bonds to a silicon atom of another siloxane in the formula (4). 3. A curable resin composition comprising the following components (A) to (C): (A) an organic silicon compound having at least two alkenyl groups in a molecule, (B) an organic silicon compound represented by the following formula (2) in an amount such that a ratio of the number of the hydrosilyl groups in component (B) to the number of the alkenyl groups in component (A) is 0.4 to 4; wherein R 1 is, independently of each other, a hydrogen atom, a monovalent hydrocarbon group having 1 to 12 carbon atoms or the group represented by the formula (4′), R 2 is independently of each other, a hydrogen atom or a monovalent hydrocarbon group having 1 to 12 carbon atoms, X 1 to X 9 and X′ are, independently of each other, a hydrogen atom, a monovalent hydrocarbon group having 1 to 6 carbon atoms or the group represented by the formula (1′), and at least two of X 1 to X 9 and X′ are the group represented by the formula (1′), and (C) a hydrosilylation catalyst in a catalytic amount. 4. A curable resin composition comprising the following components (A) to (C): (A) an organic silicon compound having at least two alkenyl groups in a molecule, (B) an organic silicon compound represented by the following formula (3) in an amount such that a ratio of the number of the hydrosilyl groups in component (B) to the number of the alkenyl groups in component (A) is 0.4 to 4; wherein R 2 is, independently of each other, a hydrogen atom or a monovalent hydrocarbon group having 1 to 12 carbon atoms, X 1 to X 4 and X 9 are, independently of each other, a hydrogen atom, a monovalent hydrocarbon group having 1 to 6 carbon atoms or the group represented by the formula (1′) or (3′), X′ is, independently of each other, a hydrogen atom, a monovalent hydrocarbon group having 1 to 6 carbon atoms or the group represented by the formula (1′), at least two of X 1 to X 4 and X 9 are the group represented by the formula (3′) and at least two of X 1 to X 4 , X 9 and X′ are the group represented by the formula (1′), and (C) a hydrosilylation catalyst in a catalytic amount. 5. A semiconductor device provided with a cured product obtained by curing the curable resin composition according to claim 1 or 2 . 6. The curable resin composition according to claim 3 , wherein component (A) is an organic silicon compound represented by the following formula (4): (R 4 3 SiO 1/2 ) a (R 4 2 SiO 2/2 ) b (R 4 SiO 3/2 ) c (SiO 4/2 ) d (Y) e (O 1/2 R 3 ) f (4), wherein R 4 is, independently of each other, a monovalent hydrocarbon group having 1 to 12 carbon atoms and optionally having an unsaturated bond, provided that at least two of R 4 are an alkenyl group, R 3 is a hydrogen atom or a monovalent hydrocarbon group having 1 to 6 carbon atoms, a is an integer of from 0 to 100, b is an integer of from 0 to 1,000, c is an integer of from 0 to 500, d is an integer of from 0 to 500, e is an integer of from 0 to 500, f is an integer of from 0 to 50, a total of a, b, c, d and e is 2 to 1,000, and Y is a silphenylene unit which has a valance of 1 to 26 and is represented by the following formula (II), wherein r is 0 or 1, k is an integer of from 1 to 3, a bonding marked with ** in the formula (II) bonds to a silicon atom of another siloxane in the formula (4), R 4 is as defined above, Z 1 to Z 9 are, independently of each other, a hydrogen atom, a monovalent hydrocarbon group having 1 to 6 carbon atoms, a divalent, trivalent or tetravalent group represented by the following formula (5′), a monovalent group represented by the following formula (5″), or a group having a valance of 1 to 16 and represented by the following formula (7′), R 6 is, independently of each other, sele
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in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms (C08L83/10 takes precedence) · CPC title
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