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US4383903A Expired / Lapsed US ⏱️ 0.0 years remaining

Curable resin composition

Assignee: Mitsubishi Gas Chemical Co Inc
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Filing: 1981-04-03
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Granted: 1983-05-17
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Expires: 2001-04-03
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Abstract

Abstract A photo-curable resin composition is disclosed comprising (i) a mixture and/or a preliminary reaction product of (a) at least one cyanate compound selected from the group consisting of polyfunctional cyanate esters, prepolymers of the cyanate esters, coprepolymers of the cyanate esters and an amine and mixtures thereof, (b) at least one compound selected from the group consisting of monomers having at least one olefinically double bond prepolymers of the monomers, liquid rubbers having one or more acryloyl or methacryloyl groups and mixtures thereof and optionally (c) at least one maleimide compound selected from the group consisting of polyfunctional maleimides, prepolymers of the maleimides, coprepolymers of the maleimides and an amine and mixtures thereof and (ii) a photo polymerization initiator or a photo sensitizer.

Inventors

  • 👤 Satoshi Ayano
  • 👤 Morio Gaku
  • 👤 Nobuyuki Ikeguchi
  • 👤 Hidenori Kinbara
  • 👤 Yasunari Osaki

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-24 17:17
CPC Classifications
C; C08; C08F; C08F2/00; C08F2/12; C08F2/16; C08F2/18; C08F2/20; C08F283/00; C08F299/00; C08F299/02; C08F299/022; C08F299/024; Y; Y10; Y10S; Y10S430/00; Y10S430/1053; Y10S430/1055; Y10S430/114; Y10S430/12; Y10S430/128

Claims Analysis

Total Claims: 8
Claim 1
Independent Claim 433 words
A photo-curable resin composition comprising: (i)(a) at least one cyanate ester compound selected from the group consisting of: (1) a polyfunctional aromatic cyanate ester monomer having the formula: R--O--C.tbd.N).sub.m wherein m is 2 to 5 and R is an aromatic organic group, the cyanate groups being bonded to an aromatic ring of said aromatic organic group, (2) a homoprepolymer of one or more cyanate esters of (1), and (3) a coprepolymer of (1) and an amine; (b) at least one compound selected from the group consisting of: (1) a monomer having one to six olefinic double bonds selected from the group consisting of compounds represented by the formula: ##STR18## wherein R 1 is an organic group comprising a main chain or carbon ring, or a main chain or carbon ring which contains O or N or a combination of O and N, or a main chain or carbon ring which is substituted by a pendant hydroxy or halogen or a combination of hydroxy and halogen, provided that when R contains an aromatic group R 1 has 6-35 carbon atoms, and when R 1 contains no benzene ring R 1 has 1-15 carbon atoms, X is hydrogen or methyl, n is an integer of 1, 2, 3, 4, 5 or 6 and the valency of R 1 is the same as n, (2) a homoprepolymer of one or more monomers of (1), and (3) a liquid rubber of (1) or (2) having one to six acryloyl or methacryloyl groups; and (c) at least one compound selected from the group consisting of: (1) a polyfunctional maleimide represented by the following general formula ##STR19## wherein R represents divalent to pentavalent aromatic or alicyclic organic group, each of X 1 and X 2 represents a hydrogen atom, halogen atom or alkyl group, and n represents an integer of 2-5, (2) a homoprepolymer of one or more maleimides of (1), and (3) a coprepolymer of (1) and an amine, said composition including a mixture of components (a), (b) and (c), a preliminary reaction product of components (a), (b) and (c), the combination of said mixture and said preliminary reaction product, the combination of (a) and the preliminary reaction product of (b) and (c), the combination of (b) and the preliminary reaction product of (a) and (c), or the combination of (c) and the preliminary reaction product of (a) and (b); (ii) a photo polymerization initiator or a photo sensitizer present in an amount of 0.01 to 10% by weight of combined weight of components (a), (b) and (c); and (iii) a heat curable catalyst or a curing agent.
Claim 2
Dependent Claim 433 words
A photo-curable resin composition comprising: (i)(a) at least one cyanate ester compound selected from the group consisting of: (1) a polyfunctional aromatic cyanate ester monomer having the formula: R--O--C.tbd.N).sub.m wherein m is 2 to 5 and R is an aromatic organic group, the cyanate groups being bonded to an aromatic ring of said aromatic organic group, (2) a homoprepolymer of one or more cyanate esters of (1), and (3) a coprepolymer of (1) and an amine; (b) at least one compound selected from the group consisting of: (1) a monomer having one to six olefinic double bonds selected from the group consisting of compounds represented by the formula: ##STR18## wherein R 1 is an organic group comprising a main chain or carbon ring, or a main chain or carbon ring which contains O or N or a combination of O and N, or a main chain or carbon ring which is substituted by a pendant hydroxy or halogen or a combination of hydroxy and halogen, provided that when R contains an aromatic group R 1 has 6-35 carbon atoms, and when R 1 contains no benzene ring R 1 has 1-15 carbon atoms, X is hydrogen or methyl, n is an integer of 1, 2, 3, 4, 5 or 6 and the valency of R 1 is the same as n, (2) a homoprepolymer of one or more monomers of (1), and (3) a liquid rubber of (1) or (2) having one to six acryloyl or methacryloyl groups; and (c) at least one compound selected from the group consisting of: (1) a polyfunctional maleimide represented by the following general formula ##STR19## wherein R represents divalent to pentavalent aromatic or alicyclic organic group, each of X 1 and X 2 represents a hydrogen atom, halogen atom or alkyl group, and n represents an integer of 2-5, (2) a homoprepolymer of one or more maleimides of (1), and (3) a coprepolymer of (1) and an amine, said composition including a mixture of components (a), (b) and (c), a preliminary reaction product of components (a), (b) and (c), the combination of said mixture and said preliminary reaction product, the combination of (a) and the preliminary reaction product of (b) and (c), the combination of (b) and the preliminary reaction product of (a) and (c), or the combination of (c) and the preliminary reaction product of (a) and (b); (ii) a photo polymerization initiator or a photo sensitizer present in an amount of 0.01 to 10% by weight of combined weight of components (a), (b) and (c); and (iii) a heat curable catalyst or a curing agent.
Claim 3
Dependent Claim 67 words
The composition as defined in claim 1 wherein the cyanate ester is selected from the group consisting of 1,3-, 1,4-dicyanatobenzene; 1,3,5-tricyanatobenzene; 1,3-, 1,4-, 1,6-, 1,8-, 2,6- or 2,7-dicyanatonaphthalene; 1,3,6-tricyanatonaphthalene; 4,4'-dicyanatobiphenyl; bis(4-cyanatophenyl)methane; 2,2-bis(4-cyanatophenyl)propane; 2,2-bis(3,5-dichloro-4-cyanatophenyl)propane; 2,2-bis(3,5-dibromo-4-dicyanatophenyl)propane; bis(4-cyanatophenyl)ether; bis(4-cyanatophenyl)thioether; bis(4-cyanatophenyl)sulfone; tris(4-cyanatophenyl)phosphite; tris(4-cyanatophenyl)phosphate; bis(3-chloro-4-cyanatophenyl)methane; cyanated novolak produced by reacting a novolak with cyanogen halide; cyanated bisphenoL polycarbonate oligomer produced by reacting a bisphenol polycarbonate oligomer with cyanogen halide; and mixtures thereof.
Claim 4
Dependent Claim 525 words
The composition as defined in claim 1 wherein the monomer is selected from the group consisting of compounds having one or more acryloyl or methacryloyl group represented by the following formulas (i), (ii), (iii), (iv), (v), (vi), (vii) and (viii) ##STR20## wherein R 5 is aliphatic hydrocarbon having 6-35 carbon atoms, or hydroxy or halogen-substituted hydrocarbon having 1-15 carbon atoms, X and n are defined above and valency of R 5 is the same as n; (ii) compounds represented by the formula ##STR21## wherein R 6 is aliphatic hdyrocarbon or hydroxy or halogen-substituted hydrocarbon, R 7 is alkylene or hydroxy or halogen-substituted alkylene, R 6 , R 7 , p and k are selected so that (the number of carbon atoms of R 6 )+(the number of carbon atoms of R 7 )×(p)×(k) is 15 or less, X is as defined above and valency of R 6 is the same as k, and k is 1, 2, 3, 4, 5 or 6. (iii) compounds represented by the formula ##STR22## wherein R 8 is alkylene, or hydroxy or halogen-substituted alkylene, R 8 and q are selected so that (the number of carbon atoms of R 8 )×(q) is 15 or less, X is as defined above: (iv) compounds represented by the formula ##STR23## wherein R 9 is aliphatic hydrocarbon or hydroxy or halogen-substituted hydrocarbon, R 10 is alkylene or hydroxy or halogen-substituted alkylene, l+p is 2, 3, 4, 5 or 6, (the number of carbon atoms of R 9 )+(the number of carbon atoms of R 10 )×(s)×(p) is 15 or less, X is as defined above, and valency of R 9 is the same as l+p, and each of l and p is at least one, (v) compounds represented by the formula ##STR24## wherein R 11 and R 12 are the same or different, and independently alkylene having 2-3 carbon atoms, or hydroxy or halogen-substituted alkylene having 2-3 carbon atoms, A is --O--, --CH 2 --, --C 2 H 5 --, or --C 3 H 7 --, t and w are independently 0 or 1, v and z are independently 1 or 2, and u and h are independently 0 or integer 1-7, and X is as defined above, (vi) compounds represented by the formula ##STR25## wherein y is 1, 2, or 3 and at least two of B groups on the benzene rings are ##STR26## wherein X is as defined above and the remainder of B groups are hydroxy and (vii) compounds represented by the formula ##STR27## wherein X is as defined above, (viii) compounds represented by the formula ##STR28## wherein R 13 is hydrogen or organic group comprising as member constituting a main chain or ring C and optionally O and/or N and optionally as a pendant hydroxy and/or halogen, when R 13 contains aromatic group R 13 has 6-35 carbon atoms; and when R 13 contains no benzene ring, R 13 has 1-15 carbon atoms, X is hydrogen or methyl, r is integer of 1, 2, 3, 4, 5 or 6 and valency of R 13 is the same as r, and liquid rubbers having one or more acryloyl or methacryloyl groups.
Claim 5
Dependent Claim 74 words
The composition as defined in claim 1 wherein the polyfunctional maleimide is selected from the group consisting of 1,3- or 1,4-dimaleimide benzene, 1,3- or 1,4-bis(maleimide methylene)benzene, 1,3- or 1,4-dimaleimide cyclohexane, 1,3- or 1,4-bis(maleimide methylene)cyclohexane, 4,4'-dimaleimide biphenyl, bis(4-maleimidephenyl)methane, bis(4-maleimidephenyl)ether, bis(4-maleimidephenyl sulfone, bis(4-maleimide-3-methylphenyl)methane, bis(4-maleimide-3-chlorophenyl)methane, bis(4-maleimide-3,5-dimethylphenyl)methane, 2,2-bis(4-maleimide-3-methylphenyl)propane, 2,2-bis(4-maleimide-3,5-dibromophenyl)propane, bis(4-maleimidephenyl)phenylmethane, 3,4-dimaleimidephenyl-4'-maleimidephenylmethane, 1,1-bis(4-maleimidephenyl)-1-phenylmethane, and maleimide derived from melamine and, addition product of formalin and an aniline in which benzene rings of two or more aniline bond through methylene group.
Claim 6
Dependent Claim 84 words
The composition as defined in claim 1 wherein the photo polymerization initiator or the photo sensitizer is selected from the group consisting of azidobenzene, 4-azidobenzoic acid, 4-diazidobiphenyl, 1,2-bis(4-azidophenyl)ethylene, 4-aminophenyl-4'-azidophenylmethane, 4,4'-diazidobenzophenone, 2,6-di(4'-azidobenzal)cyclohexanone, sodium 4,4'-diazidostilben-2,2'-disulfonate, benzophenone, benzophenoneoxime, benzoin, benzoin methyl ether, benzoin ethyl ether, benzoin isopropyl ether, acetophenone, α-haloketone, ω-bromoacetophenone, cyclohexanone, diphenylmonosulfide, dibenzothiazoyldisulfide, s-acyl-dithiocarbamate, m,m'-azoxystyrene, azoisobutylnitrile, benzoyl peroxide, di-t-butyl peroxide Fe 3+ X 3 - wherein X is halogen, Sb 4+ Cl 4 - , benzophenoneoxime, stearic dialkyl, dithiocarbamate, t-butyl anthraquinone, 2-mercaptobenzothiazole, 7-diethylamino-4-methylcumarin and diphenyl iodonium.
Claim 7
Dependent Claim 24 words
The composition as defined in claim 1 wherein the proportion of component (a) to component (b) is in the range of 85:15 to 1:99.
Claim 8
Dependent Claim 35 words
The composition as defined in claim 1 wherein the heat curing catalyst or the curing agent is used in an amount 0.01 to 5% by weight of combined weight of components (a), (b) and (c).

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USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1986-05-16 1986-11-15 1987-05-17 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1990-05-16 1990-11-15 1991-05-17 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1994-05-16 1994-11-15 1995-05-17 $7700.00 Window Closed / Lapsed

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