JP2010248358A - Resin composition for optical material - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a resin composition for an optical material, which achieves a high refractive index, and simultaneously excels in adhesiveness and/or low curl. <P>SOLUTION: The resin composition for the optical material comprises (A) a bifunctional (meth)acrylate compound having a fluorene skeleton represented by formula (1), and (B) a monofunctional (meth)acrylate compound represented by formula (2), wherein R<SP>1</SP>and R<SP>2</SP>are identical or different, and a hydrogen atom or a methyl group; a and b are each an integer of 1 to 4; and c is an integer of 0 to 4. <P>COPYRIGHT: (C)2011,JPO&INPIT

Description

  The present invention relates to a resin composition for optical materials, and more particularly to a resin composition for optical materials suitable for a high refractive index coating material having excellent low curing shrinkage, adhesion, and transparency, and a cured product thereof.

High refractive index plastics are widely used for optical materials because of their ease of molding and light weight.
Examples of means for achieving a high refractive index include a method of introducing bromine atoms into the molecular structure of the resin composition and a method of blending a bifunctional (meth) acrylate having a fluorene skeleton (for example, Patent Document 1). : JP 2003-322706 A).
However, a resin into which a bromine atom is introduced has a drawback that it has a high refractive index but tends to be brittle, has a large specific gravity, and deteriorates light resistance.
Further, when the refractive index is increased by blending a bifunctional (meth) acrylate having a fluorene skeleton, the adhesion to the substrate is lowered. Furthermore, when thick film coating is applied, curing shrinkage is large and the coated sheet is likely to curl, which often impedes molding and processing.

Under such circumstances, a resin composition excellent in adhesion and / or low curl is desired as a coating material for optical applications while realizing a high refractive index.
This invention is made | formed in view of such a subject, and it aims at providing the resin composition for optical materials excellent in adhesiveness and / or low curl, implement | achieving high refractive index.

（式中、Ｒ^１及びＲ^２は、同一又は異なって、水素原子又はメチル基、ａ及びｂは、それぞれ１〜４の整数、ｃは０〜４の整数を表す。） The resin composition for optical materials of the present invention comprises a bifunctional (meth) acrylate compound (A) having a fluorene skeleton represented by formula (1) and a monofunctional (meth) acrylate compound represented by formula (2) ( B) is contained.

(In formula, R < ¹ > and R < ² > are the same or different, a hydrogen atom or a methyl group, a and b represent the integer of 1-4 respectively, and c represents the integer of 0-4.)

In such a resin composition for optical materials, a bifunctional (meth) acrylate compound (A) represented by the formula (1) and a monofunctional (meth) acrylate compound (B) represented by the formula (2) It is preferable to contain a (meth) acrylate compound (C) and / or a photopolymerization initiator (D) other than the component.
Moreover, it is preferable that a refractive index is 1.57 or more at 25 degreeC.
Furthermore, the cured product of the present invention is obtained by curing the above-described resin composition for optical materials.

  ADVANTAGE OF THE INVENTION According to this invention, the resin composition for optical materials excellent in adhesiveness and / or low curl can be provided, implement | achieving high refractive index.

  The resin composition for an optical material of the present invention (hereinafter sometimes simply referred to as “resin composition”) is a bifunctional (meth) acrylate compound (A) having a fluorene skeleton represented by the above formula (1). And a monofunctional (meth) acrylate compound (B) represented by the formula (2).

Specific examples of the compound of the formula (1) include the following compounds (a) to (h).

Of these, the compound (a) is preferable. This is because the refractive index of the cured product using this can be further improved and the curing rate by ultraviolet irradiation can be increased.
These compounds may be used alone or in combination of two or more.
The compound of the formula (1) can be obtained using a method known in the art, for example, a method described in JP-A-2008-94987, a commercially available product, and the like.

なかでも、化合物（ｉ）が好ましい。 Moreover, it does not specifically limit as a compound of Formula (2), For example, the (meth) acrylic-acid benzyl ester described in Unexamined-Japanese-Patent No. 2001-139518 etc. can be illustrated. Specific examples include the following compounds (i) to (l).

Of these, compound (i) is preferred.

The compound of the formula (2) can be produced by a method known in the art, for example, a method described in JP-A No. 2001-139518 or a method desired in accordance therewith.
In the resin composition of the present invention, the compound represented by the formula (1) and the compound represented by the formula (2) are used in a weight ratio of about 0.1: 1 to 10: 1, for example. A weight ratio of about 0.4: 1 to 8: 1 is preferred.

Moreover, the resin composition for optical materials of this invention may contain compounds other than the compound represented by Formula (1) and Formula (2) mentioned above.
Of these, the (meth) acrylate compound (C) is suitable.

  As monofunctional (meth) acrylate, for example, n-butyl (meth) acrylate, isobutyl (meth) acrylate, tert-butyl (meth) acrylate, n-pentyl (meth) acrylate, n-hexyl (meth) acrylate, n -Octyl (meth) acrylate, isooctyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, benzyl (meth) acrylate, phenoxyethyl (meth) acrylate, phenoxydiethylene glycol (meth) acrylate, glycidyl (meth) acrylate, morpholine (meta) ) Acrylate, 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 4-hydroxybutyl (meth) acrylate, diethylene glycol mono (meth) Chryrate, triethylene glycol mono (meth) acrylate, dipropylene glycol mono (meth) acrylate, 2-methoxyethyl (meth) acrylate, methoxydiethylene glycol (meth) acrylate, methoxytriethylene glycol (meth) acrylate, methoxypolyethylene glycol (meta ) Acrylate, 2-butoxyethyl (meth) acrylate, butoxytriethylene glycol (meth) acrylate, 2-ethoxyethyl (meth) acrylate, 2- (2-ethoxyethoxy) ethyl (meth) acrylate, ethoxy polyethylene glycol (meth) Acrylate, 4-nonylphenoxyethylene glycol (meth) acrylate, tetrahydrofurfuryl (meth) acrylate, caprolactone modified Trahydrofurfuryl (meth) acrylate, cyclohexyl (meth) acrylate, isobornyl (meth) acrylate, 2-hydroxy-3-phenoxypropyl (meth) acrylate, cyclohexyl (meth) acrylate, cyclohexylmethyl (meth) acrylate, cyclohexylethyl ( (Meth) acrylate, dicyclopentanyl (meth) acrylate, dicyclopentanyloxyethyl (meth) acrylate, dicyclopentenyl (meth) acrylate, dicyclopentenyloxyethyl (meth) acrylate, o-phenylphenoxyethyl (meth) ) Acrylate and the like.

  Examples of the bifunctional (meth) acrylate include ethylene glycol di (meth) acrylate, diethylene glycol di (meth) acrylate, triethylene glycol di (meth) acrylate, polyethylene glycol di (meth) acrylate, and propylene glycol di (meth) acrylate. , Dipropylene glycol di (meth) acrylate, tripropylene glycol di (meth) acrylate, butylene glycol di (meth) acrylate, tetrabutylene glycol di (meth) acrylate, 1,4-butanediol di (meth) acrylate, 1, 6-hexanediol di (meth) acrylate, 1,9-nonanediol di (meth) acrylate, neopentyl glycol di (meth) acrylate, ethylene oxide of bisphenol A Di (meth) acrylates of idoid adducts, di (meth) acrylates of propylene oxide adducts of bisphenol A, dicyclopentanyl di (meth) acrylates, glycerol di (meth) acrylates, neopentyl glycol hydroxypivalate esters ) Acrylate, caprolactone-modified hydroxypivalate neopentyl glycol di (meth) acrylate, tetrabromobisphenol A di (meth) acrylate, hydropivalaldehyde-modified trimethylolpropane di (meth) acrylate, 1,4-cyclohexanedimethanol di ( And (meth) acrylate.

  Examples of the polyfunctional (meth) acrylate include trimethylolpropane tri (meth) acrylate, tri (meth) acrylate of trimethylolpropane ethylene oxide adduct, tri (meth) acrylate of propylene oxide adduct of trimethylolpropane, Pentaerythritol tri (meth) acrylate, glycerol tri (meth) acrylate, tri (meth) acrylate of alkyl-modified dipentaerythritol, ditrimethylolpropane tetra (meth) acrylate, tetra (meth) of ethylene oxide adduct of ditrimethylolpropane Examples include acrylate and tetra (meth) acrylate of propylene oxide adduct of ditrimethylolpropane.

  Among them, as monofunctional (meth) acrylate, benzyl (meth) acrylate, phenoxyethyl (meth) acrylate, tetrahydrofurfuryl (meth) acrylate, caprolactone-modified tetrahydrofurfuryl (meth) acrylate, o-phenylphenoxyethyl (meth) ) Acrylate is preferred.

  Examples of the bifunctional (meth) acrylate include 1,6-hexanediol di (meth) acrylate, 1,9-nonanediol di (meth) acrylate, neopentyl glycol di (meth) acrylate, and an ethylene oxide adduct of bisphenol A. Di (meth) acrylate, neopentyl glycol hydroxypivalate ester di (meth) acrylate and the like are preferable.

As the polyfunctional (meth) acrylate, trimethylolpropane tri (meth) acrylate and the like are preferable.
These may be used alone or in combination of two or more.
When such a (meth) acrylate compound (C) is used, the component (A) is 30 to 80 parts by weight with respect to (A) + (B) + (C) component = 100 parts by weight, The component is suitably 10 to 70 parts by weight, and the component (C) is suitably 0 to 40 parts by weight. However, in this case, the total amount of the components (A) + (B) is suitably in the range of 40 to 100 parts by weight, preferably in the range of 50 to 100 parts by weight, More preferably, it is within the range of parts by weight. In other words, the compound (C) is preferably contained so as not to become the main component (the component with the largest content weight) of the resin component in the resin composition of the present invention, and the resin component in the resin composition of the present invention On the other hand, it is preferably contained in an amount of about 40% by weight or less.

The resin composition for optical materials of the present invention may further contain a photopolymerization initiator (D).
The photopolymerization initiator (D) is a polymerizable initiator that generates radicals with active energy rays such as ultraviolet rays. Examples of such photopolymerization initiator (D) include hydroxycyclohexyl phenyl ketone, 2,2-dimethoxy-2-phenylacetophenone, 2-hydroxy-2-methyl-1-phenylpropan-1-one, 2, Examples include 4,6-trimethylbenzoylphosphine oxide.
You may use these individually or in combination of 2 or more types.
When using such a photoinitiator (D), about 0.1 to 10 weight% is suitable with respect to the total weight of the resin composition for optical materials of this invention, 0.5 to 6 About 2 wt% is preferable, and 2 to 6 wt% is more preferable.

In addition to the above components, a polymerization inhibitor, a release agent, a leveling agent, and the like can be blended with the resin composition for an optical material of the present invention as necessary.
Examples of the polymerization inhibitor include hydroquinone, methylhydroquinone, 4-methoxyphenol (methoquinone) and the like.
Examples of the release agent include a fluorine-based nonionic surfactant, a silicone-based nonionic surfactant, an alkyl quaternary ammonium salt, a phosphate ester, and a phosphite ester.

Examples of the leveling agent include a copolymer of polyoxyalkylene and polydimethylsiloxane, a copolymer of polyoxyalkylene and fluorocarbon, and the like.
Etc.

  Furthermore, bis (1,2,2,6,6-pentamethyl-4-piperidyl) sebacate, bis (2,2,6,6-tetramethyl-4-piperidyl) sebacate, tetra (1,2,2,6) , 6-pentamethyl-4-piperidyl) -1,2,3,4-butanetetracarboxylic acid ester, etc., hindered amine light stabilizer having 1,2,2,6,6-pentamethyl-4-piperidyl residue,

Tetrakis [methylene-3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate] methane, n-octyl-3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate, Hindered phenols such as 4,4′-thiobis (3-methyl-6-tert-butylphenol), ditridecyl-3,3′-thiodipropionate, dilauryl-3,3′-thiodipropionate, bis [2-methyl-4- {3-n-alkyl _{(C 12} or _{C 14)} thio propionyloxy} -5-t-butylphenyl] sulfur system such as the sulfides 3,5 di t-butyl-4 An antioxidant having a hydroxyphenyl residue or a 3-methyl-6-tert-butylphenyl residue,

Phosphite-based decolorizing agent,
Antifoaming agent such as silicone oil,
Organic solvents such as alcohols, glycols, aliphatic cyclic ketones, acetate esters,
You may mix | blend well-known additives in the said fields, such as a silane coupling agent, a flame retardant, an antistatic agent, a filler, a matting agent, a photosensitizer, and an ultraviolet absorber.

  Especially, it is preferable to mix | blend the xylene resin whose number average molecular weight (polystyrene conversion value by a gel permeation chromatography) is 200-600, and the polyfunctional thiol compound which has a 2 or more thiol group in a molecule | numerator. By blending such a compound, the adhesion to the substrate can be improved.

  Examples of the polyfunctional thiol compound include trimethylolpropane-tris-3-mercaptopropionate, pentaerythritol tetrakis-3-mercaptopropionate, dipentaerythritol-hex-3-mercaptopropionate, 1,4-bis ( 3-mercaptobutyryloxy) butane, 1,3,5-tris (3-mercaptobutyloxyethyl) -1,3,5-triazine-2,4,6 (1H, 3H, 5H) -trione, pentaerythritol Examples include tetrakis-3-mercaptobutyrate. Among them, 1,4-bis (3-mercaptobutyryloxy) butane, 1,3,5-tris (3-lcaptobutyloxyethyl) -1,3,5-triazine-2,4,6 (1H , 3H, 5H) -trione, pentaerythritol tetrakis-3-mercaptobutyrate. These can also contribute to the improvement of transparency.

  Also, blue or purple dyes or pigments may be added to reduce the number of colors (APHA) of the cured product.

  The refractive index of the resin composition for an optical material of the present invention is suitably 1.55 or more at 25 ° C., and preferably 1.57 or more. The refractive index can be measured by, for example, an Abbe refractometer. By using such a refractive index, it is possible to further improve background reflection or front luminance. In addition, such adjustment of a refractive index can be arbitrarily adjusted with the compounding ratio of a raw material component, for example.

The resin composition for optical materials of the present invention can obtain a cured product by irradiation with active energy rays such as ultraviolet rays. Examples of the active energy ray light source include a xenon lamp, carbon arc, germicidal lamp, ultraviolet fluorescent lamp, high pressure mercury lamp for copying, medium pressure mercury lamp, high pressure mercury lamp, ultrahigh pressure mercury lamp, electrodeless lamp, metal halide lamp, scanning type or Examples thereof include an electron beam by a curtain type electron beam acceleration path.
In the case of curing using such a light source, the active energy ray dose is suitably about 300 to 3000 mJ / cm ² . In order to sufficiently cure the resin composition, it is desirable to irradiate active energy rays such as ultraviolet rays in an inert gas atmosphere such as nitrogen gas.

  The resin composition for optical materials of the present invention can be cured into a molded product such as a plastic lens. As a method for producing such a molded product, a resin composition is injected between a gasket made of polyvinyl chloride, an ethylene vinyl acetate copolymer, etc. and two molds having a desired shape, and then an active energy such as ultraviolet rays is used. Examples thereof include a method of curing the resin composition obtained in the present invention by irradiating a wire and peeling the cured product from the mold.

  Moreover, you may form the resin composition for optical materials of this invention as a coating layer with respect to a target object. Specifically, methods such as brush coating, bar coater, applicator, roll coater, roller brush, etc., spray coating using an air spray or airless spray coating machine, shower coater, curtain flow coater, etc. The film can be coated by a method of using a flow coating method (flow coating), a dipping method, a casting method, a method using a spin coating method, or the like. These coating methods are preferably selected as appropriate according to the material, shape or application of the object.

  Furthermore, you may shape | mold the resin composition for optical materials of this invention in a film form. The film is formed by a method known in the art, for example, extrusion molding or the like, or a method of forming a coating film on an appropriate base material using the above-described method and curing it, and then peeling the base material. Is exemplified.

The refractive index of the resin composition of the present invention and the cured product thereof can be arbitrarily adjusted. Therefore, it is particularly useful as a material for optical plastic lenses such as prism lens sheets, Fresnel lenses, spectacle lenses, and aspheric lenses. It can also be used for optical electronics, optical fibers, optical waveguides and other optoelectronic applications, printing inks, paints, clear coating agents, glossy varnishes, and the like.
EXAMPLES The present invention will be specifically described below with reference to examples of the resin composition for optical materials and the cured product of the present invention, but the present invention is not limited to these.

[Synthesis example of component A]
A four-necked flask was charged with 600 g of bisphenoxyethanol fluorene, 258 g of acrylic acid, 30 g of p-toluenesulfonic acid, 1350 g of toluene, 1 g of hydroquinone monomethyl ether and 0.03 g of hydroquinone, and a stirrer, thermometer, condenser and water separator were attached. Thereafter, while refluxing at 100 to 120 ° C., a dehydration esterification reaction was performed for about 5 to 6 hours until a theoretical dehydration amount was obtained. Subsequently, the reaction solution was neutralized with alkali and washed with 10% saline. After washing, toluene was removed by concentration under reduced pressure to obtain the compound (a) described above. The refractive index of this compound was 1.620 at 25 ° C.

[Example of synthesis of component B]
A 4-necked flask was charged with 360 g of 3-phenoxybenzyl alcohol, 160 g of acrylic acid, 5 g of sulfuric acid, 300 g of toluene, 0.4 g of hydroquinone monomethyl ether and 0.02 g of hydroquinone, and a stirrer, thermometer, condenser and water separator were attached. Thereafter, a dehydration esterification reaction was performed for about 5 to 6 hours while obtaining a theoretical dehydration amount while refluxing at 100 to 120 ° C. Subsequently, the reaction solution was neutralized with alkali and washed with 10% saline. After washing, toluene was removed by concentration under reduced pressure to obtain a compound.

As a result of analyzing this compound by FT-IR, vibration of a carbonyl attributed to an ester bond at 1727 cm ⁻¹ and a double bond attributed to an acryloyl group at 692 cm ⁻² was confirmed.
In addition, ¹ HNMR (CDCl ₃ ) was measured to be 6.92-7.36 ppm = 9H, 6.40-6.47 ppm = 1H, 6.10-6.20 ppm = 1H, 5.81-5.85 ppm. = 1H, 5.16 ppm = 2H peaks were obtained.
This confirmed that the obtained compound was compound (i).
The refractive index of this compound was 1.566 at 25 ° C.

Example 1
Compound (a) as component (A), Compound (i) as component (B), Irgacure 184 (hydroxycyclohexyl phenyl ketone; manufactured by Ciba Specialty Co., Ltd.) as component (D), (A) : (B): (D) = 40: 60: 3 (parts by weight) were mixed and stirred uniformly to obtain the resin composition of the present invention.
Table 1 shows the physical properties of the obtained resin solution and its cured product.

Example 2
Compound (a) as component (A), Compound (i) as component (B), Light acrylate PO-A (phenoxyethyl acrylate; manufactured by Kyoeisha Chemical Co., Ltd.) as component (C), Irgacure 184 as component (D) (Hydroxycyclohexyl phenyl ketone; manufactured by Ciba Specialty Co., Ltd.) was used in the same manner as in Example 1 in the weight ratio shown in Table 1.

Example 3
Compound (a) as component (A), Compound (i) as component (B), o-phenylphenoxyethyl acrylate as component (C), Irgacure 184 as component (D) (hydroxycyclohexyl phenyl ketone; Ciba Specialty Co., Ltd.) In the same manner as in Example 1, the weight ratio shown in Table 1 was used.

Comparative Examples 1 and 2
Compound (a) as component (A), Light acrylate PO-A (phenoxyethyl acrylate; manufactured by Kyoeisha Chemical Co., Ltd.) as component (C), Irgacure 184 (hydroxycyclohexyl phenyl ketone; Ciba Specialty Co., Ltd.) as component (D) In the same manner as in Example 1, the weight ratios shown in Table 1 were used.

note)
※ 1), ※ 2) refractive index: measured with an Abbe refractometer ※ 3) curling property: 100 [mu] m was coated in a thickness of 80μm to easy adhesion PET film, then cured by irradiation with ultraviolet rays of 600 mJ / cm ² A 6 cm square was cut out, and the average of the heights (mm) of the four corners was calculated.
* 4) Adhesiveness: 100 μm easy-adhesive PET film (A-4300 manufactured by Toyobo Co., Ltd.) coated at a film thickness of 80 μm, cured by irradiating with 600 mJ / cm ² of ultraviolet rays, and then laid according to JISK5400 An eye cellophane tape peel test was performed, and the peeled state of the grid was observed and evaluated at 0/100 to 100/100.

As shown in Table 1, in each of Examples 1 to 3, curling property was small, adhesion was good, and a high refractive index was obtained.
On the other hand, in Comparative Example 1, the refractive index was low, and in Comparative Example 2, warping due to curling was strongly expressed.

  The resin composition for optical materials and the cured product of the present invention are optical articles made of various plastic materials such as liquid crystal display panels, color filter protective films, spectacle lenses, Fresnel lenses, lenticular lenses, prism lens sheets, The present invention can be applied to various articles such as spherical lenses, optical disk coating agents and adhesives, optical fiber core materials and clad materials, optical fiber connection adhesives, optical waveguide core materials and clad materials.

JP 2003-322706 A

Claims (5)

An optical system comprising a bifunctional (meth) acrylate compound (A) having a fluorene skeleton represented by formula (1) and a monofunctional (meth) acrylate compound (B) represented by formula (2) Resin composition for materials.

(In formula, R < ¹ > and R < ² > are the same or different, a hydrogen atom or a methyl group, a and b represent the integer of 1-4 respectively, and c represents the integer of 0-4.)   Furthermore, (meth) acrylate compounds (C) other than the bifunctional (meth) acrylate compound (A) represented by formula (1) and the monofunctional (meth) acrylate compound (B) component represented by formula (2) The resin composition for optical materials according to claim 1, comprising:   Furthermore, the resin composition for optical materials of Claim 1 or 2 containing a photoinitiator (D).   The resin composition for optical materials according to any one of claims 1 to 3, wherein the refractive index is 1.57 or more at 25 ° C. Hardened | cured material obtained by hardening the resin composition for optical materials as described in any one of Claims 1-4.