Ultraviolet-ray-curable organopolysiloxane composition, and method for producing printing material

Abstract

The present invention pertains to an ultraviolet-ray-curable organopolysiloxane composition containing: (A) (A-1) a straight-chain organopolysiloxane containing an alkenyl group, and (A-2) a three-dimensional-network-shaped organopolysiloxane resin containing an R.sup.1.sub.2R.sup.2SiO.sub.1/2 unit, an R.sup.1.sub.3SiO.sub.1/2 unit, an SiO.sub.2 unit, and an alkenyl group; (B) an organohydrogenpolysiloxane; (C) a photoactive platinum complex curing catalyst; and (D) an organopolysiloxane oligomer containing an R.sup.1.sub.2R.sup.2SiO.sub.1/2 unit or the R.sup.1.sub.2R.sup.2SiO.sub.1/2 unit and an R.sup.1.sub.3R.sup.2SiO.sub.1/2 unit, also containing an R.sup.1SiO.sub.3/2 unit, not containing an SiO.sub.2 unit, and also containing an alkenyl group. As a result, this ultraviolet-ray-curable organopolysiloxane composition retains high strength and does extremely well suppressing heat-induced expansion or contraction; hence, it is possible to transfer a pattern and print with high dimensional accuracy.

Claims

1. A UV-curable organopolysiloxane composition comprising: (A) 100 parts by weight of (A-1) 50 to 90% by weight, based on component (A), of a linear organopolysiloxane containing at least two silicon atom-bonded alkenyl groups per molecule, and (A-2) 10 to 50% by weight, based on component (A), of a three-dimensional network-type organopolysiloxane resin comprising R.sup.1.sub.2R.sup.2SiO.sub.1/2 units, R.sup.1.sub.3SiO.sub.1/2 units and SiO.sub.2 units (wherein R.sup.1 is an unsubstituted or halogen-substituted monovalent hydrocarbon group exclusive of alkenyl, and R.sup.2 is an alkenyl group) in a molar ratio of the sum of R.sup.1.sub.2R.sup.2SiO.sub.1/2 units and R.sup.1.sub.3SiO.sub.1/2 units to SiO.sub.2 units, expressed as (R.sup.1.sub.2R.sup.2SiO.sub.1/2+R.sup.1.sub.3SiO.sub.1/2)/SiO.sub.2, of from 0.5 to 1.5, and containing from 110.sup.4 to 5010.sup.4 mol/g of alkenyl groups, the sum of components (A-1) and (A-2) being 100% by weight; (B) an organohydrogenpolysiloxane containing at least two silicon atom-bonded hydrogen atoms per molecule but no alkoxy groups, in an amount that gives a molar ratio of silicon atom-bonded hydrogen atoms in component (B) to the sum of alkenyl groups in components (A) and (D) of from 0.5 to 6.0; (C) an effective amount of a photoactive platinum complex curing catalyst; and (D) an alkenyl group-containing organopolysiloxane oligomer comprising R.sup.1.sub.2R.sup.2SiO.sub.1/2 or R.sup.1.sub.2R.sup.2SiO.sub.1/2 and R.sup.1.sub.3SiO.sub.1/2 units, and R.sup.1SiO.sub.3/2 units (wherein R.sup.1 is an unsubstituted or halogen-substituted monovalent hydrocarbon group exclusive of alkenyl, and R.sup.2 is an alkenyl group) but no SiO.sub.2 units, in an amount that gives a molar ratio of alkenyl groups in component (D) to the sum of alkenyl groups in components (A) and (D) of from 0.01 to 0.6.

2. The UV-curable organopolysiloxane composition of claim 1, wherein the photoactive platinum complex catalyst is a -diketone platinum complex or a platinum complex having a cyclic diene compound as a ligand.

3. The UV-curable organopolysiloxane composition of claim 2, wherein the photoactive platinum complex catalyst is one or more selected from the group consisting of trimethyl(acetylacetonato)platinum complex, trimethyl(2,4-pentanedionate)platinum complex, trimethyl(3,5-heptanedionate)platinum complex, trimethyl(methylacetoacetate)platinum complex, bis(2,4-pentanedionato)platinum complex, bis(2,4-hexanedionato)platinum complex, bis(2,4-heptanedionato)platinum complex, bis(3,5-heptanedionato)platinum complex, bis(1-phenyl-1,3-butanedionato)platinum complex, bis(1,3-diphenyl-1,3-propanedionato)platinum complex, (1,5-cyclooctadienyl)dimethyl platinum complex, (1,5-cyclooctadienyl)diphenyl platinum complex, (1,5-cyclooctadienyl)dipropyl platinum complexes, (2,5-norbornadiene)dimethyl platinum complex, (2,5-norbornadiene)diphenyl platinum complex, (cyclopentadienyl)dimethyl platinum complex, (methylcyclopentadienyl)diethyl platinum complex, (trimethylsilylcyclopentadienyl)diphenyl platinum complex, (methylcycloocta-1,5-dienyl)diethyl platinum complex, (cyclopentadienyl)trimethyl platinum complex, (cyclopentadienyl)ethyldimethyl platinum complex, (cyclopentadienyl)acetyldimethyl platinum complex, (methylcyclopentadienyl)trimethyl platinum complex, (methylcyclopentadienyl)trihexyl platinum complex, (trimethylsilylcyclopentadienyl)trimethyl platinum complex, (dimethylphenylsilylcyclopentadienyl)triphenyl platinum complex and (cyclopentadienyl)dimethyltrimethylsilylmethyl platinum complex.

4. The UV-curable organopolysiloxane composition of claim 1 which is for use in forming a master material for nanoimprinting, a pad material for printing on a curved surface, a blanket material for offset printing or a shape-forming material for 3D printing.

5. A method for producing a plate material selected from the group consisting of a master material for nanoimprinting, a pad material for printing on a curved surface, a blanket material for offset printing and a shape-forming material for 3D printing, the method comprising the steps of applying the UV-curable organopolysiloxane composition of claim 1 to a matrix on which is formed a fine pattern to be inverted; irradiating the applied organopolysiloxane composition with UV radiation to effect curing by a stereolithographic process; and removing the cured composition from the matrix, thereby inverting and forming the fine pattern of the matrix on the surface of the cured composition.

6. A plate material selected from the group consisting of a master material for nanoimprinting, a pad material for printing on a curved surface, a blanket material for offset printing and a shape-forming material for 3D printing, wherein the plate material comprises the UV-curable organopolysiloxane of claim 1 in a cured form having a linear shrinkage of not more than 0.5%.

Description

EMBODIMENT FOR CARRYING OUT THE INVENTION

(1) The invention is described more fully below.

(2) [Component (A)]

(3) Component (A) is an alkenyl group-containing organopolysiloxane consisting of (A-1) an alkenyl group-containing linear diorganopolysiloxane and (A-2) an alkenyl group-containing organopolysiloxane resin.

(4) Component (A-1), an organopolysiloxane serving as the base polymer of the composition, is a linear organopolysiloxane having at least 2 (generally from 2 to 50), and especially about 2 to 20, silicon atom-bonded alkenyl groups per molecule. This is typically a linear diorganopolysiloxane in which the backbone is composed of repeating diorganopolysiloxane units and both ends of the molecular chain are capped with triorganosiloxy groups.

(5) Component (A-2) is a three-dimensional network-type organopolysiloxane resin comprising R.sup.1.sub.2R.sup.2SiO.sub.1/2 units, R.sup.1.sub.3SiO.sub.1/2 units and SiO.sub.2 units (wherein R.sup.1 is an unsubstituted or halogen-substituted monovalent hydrocarbon group exclusive of alkenyl, and R.sup.2 is an alkenyl group) in a molar ratio of the sum of R.sup.1.sub.2R.sup.2SiO.sub.1/2 units and R.sup.1.sub.3SiO.sub.1/2 units to SiO.sub.2 units, expressed as (R.sup.1.sub.2R.sup.2SiO.sub.1/2+R.sup.1.sub.3SiO.sub.1/2)/SiO.sub.2, of from 0.5 to 1.5, and preferably 0.7 to 1.0, and containing from 110.sup.4 to 5010.sup.4 mol/g of alkenyl groups. In general, the organopolysiloxane resin having a three-dimensional network structure that serves as component (A-2) preferably contains no trifunctional siloxane units on the molecule, although it is clearly differentiated from the branched organopolysiloxane oligomer serving as the subsequently described component (D) in that it must contain SiO.sub.2 units on the molecule.

(6) In addition to the above units, the organopolysiloxane resin of component (A-2) may also contain R.sup.1.sub.2SiO units, R.sup.1R.sup.2SiO units, R.sup.2.sub.2SiO units, R.sup.1SiO.sub.3/2 units and R.sup.2SiO.sub.3/2 units, the content of such units being preferably not more than 30% by weight (0 to 30% by weight), and especially not more than 20% by weight (0 to 20% by weight) of the organopolysiloxane resin of component (A-2). In order for the resin to be able to stably reinforce the cured product, it is preferable for the polystyrene-equivalent weight-average molecular weight, as determined by gel permeation chromatography, to be from 400 to 100,000, and especially from 500 to 30,000. When the weight-average molecular weight is too small, there may be no cured product reinforcing effect; when it is too large, stable production may not be possible.

(7) The silicon atom-bonded alkenyl groups included in component (A) (that is, components (A-1) and (A-2)) are typically alkenyl groups having 2 to 8 carbon atoms, such as vinyl, allyl, butenyl, pentenyl, hexenyl or heptenyl, and preferably alkenyl groups having 2 to 6 carbon atoms. Vinyl is especially preferred.

(8) With respect to the bonding positions of the alkenyl groups in component (A-1), that is, the positions of the silicon atom-bonded alkenyl groups in the molecule, alkenyl groups bonded to terminal silicon atoms and/or non-terminal silicon atoms on the molecular chain may be included, although it is preferable for at least alkenyl groups bonded to silicon atoms at both ends of the molecular weight to be included.

(9) Examples of silicon atom-bonded organic groups other than alkenyl groups (e.g., unsubstituted or halogen-substituted monovalent hydrocarbon groups) in component (A) include unsubstituted or halogen-substituted monovalent hydrocarbon groups of generally about 1 to 10 carbon atoms, and preferably about 1 to 8 carbon atoms, including alkyl groups such as methyl, ethyl, propyl, butyl, pentyl, hexyl and heptyl; aryl groups such as phenyl, tolyl, xylyl and naphthyl; aralkyl groups such as benzyl and phenethyl; and halogenated alkyl groups such as chloromethyl, 3-chloropropyl and 3,3,3-trifluoropropyl. Methyl and phenyl are preferred.

(10) Component (A-1) has a viscosity at 25 C. which is preferably in the range of 10 to 500,000 mPa.Math.s, and especially 100 to 100,000 mPa.Math.s, in order for the composition to be easy to handle and work (e.g., it has sufficient flowability) and for the resulting cured product to have good physical properties (e.g., hardness (flexibility), strength, elongation). In this invention, the viscosity can generally be measured with a rotational viscometer such as a BL, BH, BS or cone-and-plate type viscometer.

(11) Examples of the organopolysiloxane serving as component (A-1) include dimethylsiloxane-methylvinylsiloxane copolymers capped at both ends of the molecular chain with trimethylsiloxy groups, methylvinylpolysiloxane capped at both ends of the molecular chain with trimethylsiloxy groups, dimethylsiloxane-methylvinylsiloxane-methylphenylsiloxane copolymers capped at both ends of the molecular chain with trimethylsiloxy groups, dimethylsiloxane-methylvinylsiloxane-diphenylsiloxane copolymers capped at both ends of the molecular chain with trimethylsiloxy groups, dimethylpolysiloxane-methylvinylpolysiloxane copolymers capped at one end of the molecular chain with a dimethylvinylsiloxy group and capped at the other end of the molecular chain with a trimethylsiloxy group, dimethylsiloxane-methylvinylpolysiloxane copolymers capped at both ends of the molecular chain with dimethylvinylsiloxy groups, dimethylsiloxane-methylvinylsiloxane-methylphenylsiloxane copolymers capped at both ends of the molecular chain with dimethylvinylsiloxy groups, dimethylsiloxane-methylvinylsiloxane-diphenylsiloxane copolymers capped at both ends of the molecular chain with dimethylvinylsiloxy groups, dimethylpolysiloxane capped at both ends of the molecular chain with divinylmethylsiloxy groups, dimethylpolysiloxane capped at both ends of the molecular chain with trivinylsiloxy groups, and mixtures of two or more of these organopolysiloxanes.

(12) Examples of the organopolysiloxane resin serving as component (A-2) include organopolysiloxane copolymers consisting essentially of siloxane units of the formula R.sup.1.sub.3SiO.sub.1/2, siloxane units of the formula R.sup.1.sub.2R.sup.2SiO.sub.1/2, units of the formula R.sup.1.sub.2SiO, and siloxane units of the formula SiO.sub.2, organopolysiloxane copolymers consisting essentially of siloxane units of the formula R.sup.1.sub.3SiO.sub.1/2, siloxane units of the formula R.sup.1.sub.2R.sup.2SiO.sub.1/2 and siloxane units of the formula SiO.sub.2, organopolysiloxane copolymers consisting essentially of siloxane units of the formula R.sup.1.sub.2R.sup.2SiO.sub.1/2, siloxane units of the formula R.sup.1.sub.2SiO and siloxane units of the formula SiO.sub.2, and mixtures of two or more of these organopolysiloxanes.

(13) In the above formulas, R.sup.1 is an unsubstituted or halogen-substituted monovalent hydrocarbon group exclusive of alkenyl which is the same as described above. Examples include alkyl groups such as methyl, ethyl, propyl, butyl, pentyl, hexyl and heptyl; aryl groups such as phenyl, tolyl, xylyl and naphthyl; aralkyl groups such as benzyl and phenethyl; and halogenated alkyl groups such as chloromethyl, 3-chloropropyl and 3,3,3-trifluoropropyl. R.sup.2 is an alkenyl group, examples of which include vinyl, allyl, butenyl, pentenyl, hexenyl and heptenyl. The compounding ratio of component (A-1) and (A-2), expressed as the weight ratio component (A-1)/component (A-2), is about 90/10 to 50/50, and preferably about 85/15 to 60/40. Within this range, the composition is easy to handle and work (e.g., it has sufficient flowability), and the cured product has optimal physical properties (e.g., hardness (flexibility), strength, elongation). Outside of this range, the composition is not easy to handle and work and the cured product does not have the desired physical properties, making accurate pattern transfer impossible.

(14) [Component (B)]

(15) Component (B) is an organohydrogenpolysiloxane having at least two silicon atom-bonded hydrogen atoms per molecule and containing no alkoxy groups on the molecule. In this composition, it acts as a crosslinking agent.

(16) The organohydrogenpolysiloxane included as component (B) serves as a crosslinking agent by reacting with component (A) (i.e., components (A-1) and (A-2)). The molecular structure is not particularly limited. That is, use may be made of organohydrogenpolysiloxanes manufactured in the prior art that have a structure which is linear, linear with some branching, cyclic or a three-dimensional network (resinous). The organohydrogenpolysiloxane must have at least two, and preferably has three or more, silicon atom-bonded hydrogen atoms (hydrosilyl groups denoted as SiH) on the molecule. It is desirable for the molecule to have generally from 2 to 300, preferably from 3 to 200, and more preferably from 4 to 100, SiH groups. The organohydrogenpolysiloxane used may be one having the average compositional formula (1) below.
R.sup.4.sub.bHcSiO.sub.(4-b-c)/2(1)

(17) In formula (1) above, R.sup.4 is a silicon-bonded substituted or unsubstituted monovalent hydrocarbon group of preferably 1 to 10 carbon atoms that is free of aliphatic unsaturation. Illustrative examples of this substituted or unsubstituted monovalent hydrocarbon group R.sup.4 include alkyl groups such as methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl, pentyl, neopentyl, hexyl, cyclohexyl, octyl, nonyl and decyl; aryl groups such as phenyl, tolyl, xylyl and naphthyl; aralkyl groups such as benzyl, phenylethyl and phenylpropyl; and any of these groups in which some or all of the hydrogen atoms are substituted with halogen atoms such as fluorine, bromine or chlorine, such as chloromethyl, chloropropyl, bromoethyl and trifluoropropyl. This substituted or unsubstituted monovalent hydrocarbon group R.sup.4 is preferably an alkyl group or aryl group, and more preferably methyl or phenyl. Also, b is a positive number from 0.7 to 2.1, c is a positive number from 0.001 to 1.0, and b+c is a positive number of from 0.8 to 3.0. Preferably, b is 1.0 to 2.0, c is 0.01 to 1.0, and b+c is 1.5 to 2.5.

(18) The at least two, and preferably 3 or more, SiH groups included per molecule may be positioned at the ends of the molecular chain, positioned partway along the molecular chain, or positioned at both the ends of and partway along the molecular chain. The molecular structure of the organohydrogenpolysiloxane may be linear, linear with some branching, cyclic, branched, or a three-dimensional network. It is desirable for the number of silicon atoms on the molecule (or the degree of polymerization) to be generally about 2 to 300, preferably 3 to 200, and more preferably 4 to 100. In order for the composition to be easy to handle and work (such as having sufficient flowability) and for the resulting cured product to have good physical properties (e.g., hardness (flexibility), heat resistance), the use of an organohydrogenpolysiloxane which is liquid at room temperature (25 C.) and has a viscosity at 25 C. of generally about 1 to 1,000 mPa.Math.s, and especially 5 to 500 mPa.Math.s, is preferred.

(19) In this invention, the degree of polymerization (or molecular weight) can be determined as, for example, the weight-average degree of polymerization (or weight-average molecular weight) in gel permeation chromatography (GPC) using toluene, for example, as the developing solvent. The viscosity can be measured at 25 C. with a rotational viscometer such as a BL, BH, BS or cone-and-plate type viscometer.

(20) Illustrative examples of the organohydrogenpolysiloxane of component (B) having formula (1) include 1,1,3,3-tetramethyldisiloxane, 1,3,5,7-tetramethylcyclotetrasiloxane, tris(hydrogendimethylsiloxy)methylsilane, tris(hydrogendimethylsiloxy)phenylsilane, methylhydrogencyclopolysiloxane, methylhydrogensiloxane-dimethylsiloxane cyclic copolymers, methylhydrogenpolysiloxane capped at both ends with trimethylsiloxy groups, dimethylsiloxane-methylhydrogensiloxane copolymers capped at both ends with trimethylsiloxy groups, dimethylpolysiloxane capped at both ends with dimethylhydrogensiloxy groups, dimethylsiloxane-methylhydrogensiloxane copolymers capped at both ends with dimethylhydrogensiloxy groups, methylhydrogensiloxane-diphenylsiloxane copolymers capped at both ends with trimethylsiloxy groups, methylhydrogensiloxane-diphenylsiloxane-dimethylsiloxane copolymers capped at both ends with trimethylsiloxy groups, methylhydrogensiloxane-methylphenylsiloxane-dimethylsiloxane copolymers capped at both ends with trimethylsiloxy groups, methylhydrogensiloxane-dimethylsiloxane-diphenylsiloxane copolymers capped at both ends with dimethylhydrogensiloxy groups, methylhydrogensiloxane-dimethylsiloxane-methylphenylsiloxane copolymers capped at both ends with dimethylhydrogensiloxy groups, copolymers consisting essentially of (CH.sub.3).sub.2HSiO.sub.1/2 units, (CH.sub.3).sub.3SiO.sub.1/2 units and SiO.sub.4/2 units, copolymers consisting essentially of (CH.sub.3).sub.2HSiO.sub.1/2 units and SiO.sub.4/2 units, copolymers consisting essentially of (CH.sub.3).sub.2HSiO.sub.1/2 units, SiO.sub.4/2 units and (C.sub.6H.sub.5).sub.3SiO.sub.1/2 units, and any of these example compounds in which some or all methyl groups are replaced with another alkyl, phenyl or the like. Organohydrogenpolysiloxanes of molecular formula (2) below are especially preferred

(21) ##STR00001##
(wherein R is a hydrogen atom or methyl, m and n are integers such that 0m and 1n, and m+n is an integer of from 1 to 299).

(22) Component (B) may be prepared by a known method. For example, in one general method, component (B) can easily be obtained by equilibrating octamethylcyclotetrasiloxane and/or tetramethylcyclodisiloxane with a compound containing a hexamethyldisiloxane or 1,1-dihydro-2,2,3,3-tetramethyldisiloxane unit capable of becoming an end group in the presence of a catalyst such as sulfuric acid, trifluoromethanesulfonic acid or methanesulfonic acid and at a temperature of about 10 to +40 C.

(23) Component (B) is used in an amount such that the molar ratio of silicon atom-bonded hydrogen atoms in component (B) to the sum of alkenyl groups in the organopolysiloxanes of components (A) and (D) is from 0.5 to 6.0, and preferably from 1.0 to 5.0. At a molar ratio below 0.5 or above 6.0, the composition does not fully cure.

(24) [Component (C)]

(25) Component (C) used in the invention is a photoactive platinum complex catalyst. When activated by irradiation with light, it has a catalytic action that promotes addition reactions between components (A), (B) and (D). In this invention, the compound that serves as the photoactive platinum complex catalyst of component (C) is preferably a -diketone platinum complex or a platinum complex having a cyclic diene compound as a ligand.

(26) Illustrative examples of -diketone platinum complexes include trimethyl(acetylacetonato)platinum complex, trimethyl(2,4-pentanedionate)platinum complex, trimethyl(3,5-heptanedionate)platinum complex, trimethyl(methylacetoacetate)platinum complex, bis(2,4-pentanedionato)platinum complex, bis(2,4-hexanedionato)platinum complex, bis(2,4-heptanedionato)platinum complex, bis(3,5-heptanedionato)platinum complex, bis(1-phenyl-1,3-butanedionato)platinum complex and bis(1,3-diphenyl-1,3-propanedionato)platinum complex. Illustrative examples of platinum complexes having a cyclic diene compound as a ligand include (1,5-cyclooctadienyl)dimethyl platinum complex, (1,5-cyclooctadienyl)diphenyl platinum complex, (1,5-cyclooctadienyl)dipropyl platinum complex, (2,5-norbornadiene)dimethyl platinum complex, (2,5-norbornadiene)diphenyl platinum complex, (cyclopentadienyl)dimethyl platinum complex, (methylcyclopentadienyl)diethyl platinum complex, (trimethylsilylcyclopentadienyl)diphenyl platinum complex, (methylcycloocta-1,5-dienyl)diethyl platinum complex, (cyclopentadienyl)trimethyl platinum complex, (cyclopentadienyl)ethyldimethyl platinum complex, (cyclopentadienyl)acetyldimethyl platinum complex, (methylcyclopentadienyl)trimethyl platinum complex, (methylcyclopentadienyl)trihexyl platinum complex, (trimethylsilylcyclopentadienyl)trimethyl platinum complex, (dimethylphenylsilylcyclopentadienyl)triphenyl platinum complex and (cyclopentadienyl)dimethyltrimethylsilylmethyl platinum complex.

(27) Component (C) should be included in an amount that is effective as a catalyst. For example, component (C) may be used in an amount, expressed in terms of the platinum metal with respect to the weight of component (A), of 1 to 5,000 ppm, and preferably 10 to 500 ppm. When less than 1 ppm is included, the addition reaction may be substantially retarded or curing may not occur.

(28) [Component (D)]

(29) The branched organopolysiloxane oligomer included as component (D) serves as a reinforcement in the inventive composition. It is an alkenyl group-containing branched organopolysiloxane oligomer comprising R.sup.1SiO.sub.3/2 units and either R.sup.1.sub.2R.sup.2SiO.sub.1/2 units or both R.sup.1.sub.2R.sup.2SiO.sub.1/2 and R.sup.1.sub.3SiO.sub.1/2 units (wherein R.sup.1 is an unsubstituted or halogen-substituted monovalent hydrocarbon atom exclusive of alkenyl, and R.sup.2 is an alkenyl group), and preferably having two or more alkenyl groups per molecule. Component (D) is clearly differentiated from the three-dimensional network-type organopolysiloxane resin of component (A-2) above in that the molecule is free of SiO.sub.2 units.

(30) The proportion (molar ratio) of R.sup.1.sub.2R.sup.2SiO.sub.1/2 units or both R.sup.1.sub.2R.sup.2SiO.sub.1/2 units and R.sup.1.sub.3SiO.sub.1/2 units with respect to R.sup.1SiO.sub.3/2 units, expressed as (R.sup.1.sub.2R.sup.2SiO.sub.1/2)/(R.sup.1SiO.sub.3/2) or (R.sup.1.sub.2R.sup.2SiO.sub.1/2+R.sup.1.sub.3SiO.sub.1/2)/(R.sup.1SiO.sub.3/2), is preferably from 0.1 to 10, and more preferably from 0.5 to 5. The amount of alkenyl groups included in component (D) is preferably from 0.0001 to 0.05 mol/g, and more preferably form 0.0002 to 0.02 mol/g. When the amount of alkenyl groups is too small, the cured product reinforcing effect may weaken; when the amount is too large, the composition may not sufficiently cure. The viscosity as determined with a rotational viscometer at 25 C. is preferably in the range of 1 to 1,000 mPa.Math.s, and more preferably in the range of 10 to 100 mPa.Math.s.

(31) Component (D) may be prepared by a known method. For example, in one general method, component (D) can easily be prepared by stirring a hydrolyzate of methyltrichlorosilane obtained with the aid of water or methanol with a hexamethyldisiloxane and/or tetramethyldivinyldisiloxane-containing compound in the presence of a catalyst such as sulfuric acid, trifluoromethanesulfonic acid or methanesulfonic acid and at a temperature of not above +50 C., and then adding water dropwise at a temperature of not above +65 C. to effect cohydrolysis.

(32) Component (D) is included in an amount such that the molar ratio of alkenyl groups on component (D) to the sum of alkenyl groups on components (A) and (D) is from 0.01 to 0.6. At a molar ratio below 0.01, there may be no cured product reinforcing effect, whereas at more than 0.6 of the composition, the composition may not fully cure. The compounding ratio of components (A) and (D), expressed as the weight ratio component (A)/component (D), is preferably from 99.99/0.01 to 50/50, and more preferably from 99.95/0.05 to 60/40.

(33) [Other Compounding Ingredients]

(34) The inventive composition may include, as optional ingredients other than above components (A) to (D), a compound having an addition curing reaction suppressing and regulating effect (hydrosilylation reaction regulator). Examples of such compounds include phosphorus-containing compounds such as triphenylphosphine, nitrogen-containing compounds such as tributylamine, tetramethylethylenediamine and benzotriazole, sulfur-containing compounds, acetylene compounds, compounds having two or more alkenyl groups, hydroperoxy compounds and maleic acid derivatives. The degree of the cure-retarding effect by this compound varies greatly with the chemical structure. Accordingly, the amount of addition thereof should be adjusted to the optimal amount for the particular compound used. In general, however, when the amount of addition is too small, long-term storage stability at room temperature may not be obtained, whereas adding too much may inhibit the cure.

(35) Other optional ingredients that may be used to an extent that does not detract from the transparency include inorganic fillers such as fumed silica and polyorganosilsesquioxane, and fillers obtained by surface-treating the foregoing fillers with an organosilicon compound such as an organoalkoxysilane compound, an organochlorosilane compound, an organosilazane compound or a low-molecular-weight siloxane compound.

(36) In addition, agents that impart, for example, heat resistance or flame retardance may also be optionally included in the inventive composition.

(37) [UV Cure]

(38) It is desirable for the organopolysiloxane composition of the invention to be cured by exposure to 200 to 500 nm wavelength light. The lamp used for UV exposure is not particularly limited, provided that it emits UV radiation in a wavelength range of 200 to 500 nm. Examples of suitable lamps include low-pressure mercury vapor lamps, medium-pressure mercury vapor lamps, high-pressure mercury vapor lamps, xenon lamps, metal halide lamps and UV LED lamps. The exposure dose of UV light varies with the type and amount of the photoactive platinum complex used, but should be sufficient to activate the photoactive platinum complex. Exposure at a UV intensity of 10 to 1,000 mW/cm.sup.2, and especially 20 to 400 mW/cm.sup.2, for a period of 0.1 second to 5 minutes, and especially 0.5 second to about 1 minute, is preferred.

(39) The resulting silicone cured product which is used as a master material for nanoimprinting, a pad material for printing on a curved surface, a blanket material for offset printing or a shape-forming material for 3D printing has a hardness, as measured with a Type A durometer, of generally at least 40, and especially at least 50, and has a tear strength (crescent type) of at least 1 kN/m, and especially at least 2 kN/m. The hardness upper limit should generally be no more than about 80, and especially no more than about 75, and the tear strength upper limit should generally be no more than about 10 kN/m, and especially no more than about 8 kN/m. The hardness and tear strength can be measured by the method described in JIS-K6249.

(40) The ability to prevent expansion of the silicone cured product used as a master material for nanoimprinting, a pad material for printing on a curved surface, a blanket material for offset printing or a shape-forming material for 3D printing is determined by measuring the linear shrinkage after the cure relative to before the cure, with a smaller linear shrinkage being preferred. For the inventive composition, the linear shrinkage measured according to JIS-K6294 is generally not more than 0.5% (0 to 0.5%), and especially not more than 0.3% (0 to 0.3%).

EXAMPLES

(41) The invention is illustrated more fully below by way of Working Examples and Comparative Examples, although these Examples are not intended to limit the invention. The viscosity results are measured values obtained with a rotational viscometer at 25 C., and the weight-average molecular weights are polystyrene-equivalent values obtained by gel permeation chromatography using toluene as the developing solvent. Parts are indicated by weight.

(42) Details on and abbreviations for components (A) to (D) used in the Examples are given below. Vi stands for vinyl and Me for methyl.

(43) Component (A-1):

(44) a-1: Dimethylpolysiloxane capped at both ends of the molecular chain with dimethylvinylsiloxy groups and having a viscosity of 1,000 mPa.Math.s. Vinyl group content, 0.000125 mol/g. a-2: Dimethylpolysiloxane capped at both ends of the molecular chain with trivinylsiloxy groups and having a viscosity of 5,000 mPa.Math.s. Vinyl group content, 0.00006 mol/g.
Component (A-2): a-3: Resinous copolymer consisting essentially of Me.sub.3SiO.sub.1/2 units, ViMe.sub.2SiO.sub.1/2 units and SiO.sub.2 units (Me.sub.3SiO.sub.1/2 units+ViMe.sub.2SiO.sub.1/2 units)/SiO.sub.2 units=0.85 (molar ratio). Vinyl group content, 0.0009 mol/g; weight-average molecular weight, 3,800.
Component (B):

(45) Methylhydrogenpolysiloxane having SiH groups at both ends and on side chains (degree of polymerization, 64; SiH group content, 0.0112 mol/g),

(46) Component (C):

(47) 2-(2-Butoxyethoxy)ethyl acetate solution of bis(2,4-pentanedionato)platinum complex (concentration, 1 wt %).

(48) Component (D):

(49) Organopolysiloxane oligomer consisting essentially of MeSiO.sub.3/2 units and Me.sub.2ViSiO.sub.1/2 units, containing 0.0054 mol/g of vinyl groups, having a weight-average molecular weight of 2,000, containing an average of about 12.5 vinyl groups per molecule, and having a viscosity of 24 mPa.Math.s. (Me.sub.2ViSiO.sub.1/2 units)/(MeSiO.sub.3/2 units)=1/1 (molar ratio).

Working Example 1

(50) A UV-curable organopolysiloxane composition was prepared by uniformly mixing: 14 parts of component (a-1), 60 parts of component (a-2) and 26 parts of component (a-3) as component (A), and also 7.9 parts of component (B), 0.48 part of component (C), and 0.61 part of component (D). In the composition, the molar ratio of SiH groups in component (B) to the sum of the alkenyl groups in components (A) and (D), expressed as H/Vi, was about 2.7; and the molar ratio of alkenyl groups in component (D) to the sum of the alkenyl groups in components (A) and (D) was about 0.10. The viscosity of the composition at 25 C., as measured with a BL-type viscometer at 60 rpm and using a No. 4 rotor, was 2.6 Pa.Math.s.

(51) This composition was poured into a mold and cured at room temperature (25 C.) under UV exposure conditions of 120 mW/cm.sup.2 and 1.7 seconds (=200 mW/cm.sup.2). Following UV exposure, the cured composition was cooled 1 hour at room temperature (25 C.) and then demolded. The linear shrinkage was determined in accordance with JIS-K6249.

(52) In a separate procedure, the above composition was cast into a frame and cured under UV exposure conditions of 120 mW/cm.sup.2 and 1.7 seconds to produce a 2 mm thick cured sheet. The hardness and tear strength (crescent) were measured in accordance with JIS-K6249. The results are shown in Table 1.

Comparative Example 1

(53) A UV-curable silicone composition was prepared by uniformly mixing, as component (A), 17.4 parts of component (a-1), 62.3 parts of component (a-2) and 24.9 parts of component (a-3), and also, as component (B), 5 parts of a resinous copolymer consisting essentially of HMe.sub.2SiO.sub.1/2 units and SiO.sub.2 units (HMe.sub.2SiO.sub.1/2 units/SiO.sub.2 units=1.6 (molar ratio), Sill group content, 0.00915 mol/g; weight-average molecular weight, 1,230), 0.3 part of a cyclic organopolysiloxane oligomer consisting essentially of MeViSiO units (alkenyl group content, 0.0116 mol/g; viscosity, 3.45 mPa.Math.s) as a regulator, and 0.05 part of a 2-ethylhexanol solution of chloroplatinic acid (Pt concentration, 2 wt %). In the composition, the molar ratio H/Vi of SiH groups in component (B) to alkenyl groups in component (A) was about 1.6. The viscosity of the composition at 25 C., as measured with a BL-type viscometer at 60 rpm and using a No. 4 rotor, was 3.5 Pa.Math.s.

(54) This composition was poured into a mold and cured under heating conditions of 150 C. and 30 minutes. The cured composition was left at rest for one hour at room temperature (25 C.) and then demolded. The linear shrinkage was determined in accordance with JIS-K6249.

(55) In a separate procedure, the above composition was poured into a frame and cured under heating conditions of 150 C. and 30 minutes to produce a 2 mm thick cured sheet. The hardness and tear strength (crescent) were measured in accordance with JIS-K6249. The results are shown in Table 1.

(56) TABLE-US-00001 TABLE 1 Working Example 1 Comparative Example 1 Hardness (Durometer A) 54 50 Tear strength (kN/m) 2.8 3.0 Linear shrinkage (%) 0.1 2.6