JP5619201B2 - Multilayer optical recording medium manufacturing sheet and multilayer optical recording medium - Google Patents

Description

  The present invention relates to a multilayer optical recording medium manufacturing sheet and a multilayer optical recording medium, and in particular, a multilayer optical recording medium manufacturing sheet capable of easily manufacturing a multilayer optical recording medium having high recording density and good recording characteristics. And a multilayer optical recording medium manufactured using the same.

 In recent years, optical recording media have attracted attention because they can record a large amount of recording data, and are used in various applications. Recently, a method for recording data three-dimensionally (hereinafter, also referred to as “multilayer optical recording method”) has been proposed with the aim of further improving the recording density. For example, Y. Kawata et al. Have reported a technique for performing multi-layer optical recording on a photopolymer material having a photopolymerizable photoreactive component (see, for example, Non-Patent Document 1). However, in the multilayer optical recording medium for performing such a multilayer optical recording method, there has conventionally been a problem that data crosstalk occurs during multilayer recording / reproduction. As a countermeasure against such crosstalk, it is conceivable to increase the distance between the optical recording layers. In this case, however, a decrease in recording density is unavoidable, and light used for reading and writing of the recording is absorbed in the middle. In addition, there is a problem that the number of optical recording layers is unavoidable.

 Therefore, in order to reduce the crosstalk, for example, an optical recording medium having two or more recording layers, and optical information is recorded on a part or all of the layers of the two or more recording layers by recording light. There has been proposed an optical recording medium (see, for example, Patent Document 1) in which a non-recording layer made of a material that is not recorded is interposed. For forming the recording layer and the non-recording layer constituting this optical recording medium, a method is generally used in which each layer is formed by spin coating and laminated. However, the lamination method by spin coating has a problem that it is difficult to increase the area, the productivity is low, and the thickness accuracy of each layer and the whole layer is low.

 As a means for solving such a problem, a method of obtaining a multilayer structure by sequentially laminating a sheet material in which an optical recording layer containing a photosensitive material and a pressure-sensitive adhesive layer are laminated has been proposed (for example, Patent Document 2). The multilayer optical recording medium having this multilayer structure has high thickness accuracy of each layer and the whole, and can have a large area. However, if an attempt is made to make the optical recording layer thinner (1000 nm or less) in the production method by the sheet method using the pressure-sensitive adhesive, the film strength of the optical recording layer is reduced, and the optical recording layer is removed when the process film is peeled off. It may break. On the other hand, if the amount of the matrix material (binder) in the optical recording layer is increased in order to increase the film strength, there is a problem that the recording sensitivity of the optical recording layer is lowered even if peeling is possible. .

JP-A-11-250496 JP 2005-209328 A

Appl. Opt., 35, 2466 (1996)

 The present invention has been made under such circumstances, and a multilayer optical recording medium manufacturing sheet capable of easily peeling a process film from an optical recording layer and transferring the optical recording layer, and using the same An object of the present invention is to provide a multilayer optical recording medium having a high recording density and good recording characteristics.

 As a result of intensive studies to achieve the above object, the present inventors have a unit including at least a peeling auxiliary layer, an optical recording layer, and a pressure sensitive adhesive layer on the process film, and the above peeling auxiliary. A layer is provided on the surface of the process film, a pressure-sensitive adhesive layer is disposed on the outermost layer, and the refractive index difference between the peeling assist layer and the pressure-sensitive adhesive layer at a wavelength of 660 nm. It has been found that the object can be achieved by a sheet for producing an optical recording medium having an absolute value equal to or less than a certain value. The present invention has been completed based on such findings.

That is, the present invention
(1) A sheet for producing a multilayer optical recording medium having a repetitive structure in which a plurality of optical recording layers are laminated, on a process film having releasability with respect to the separation assisting layer, While having a unit including an optical recording layer having a thickness of 1-1000 nm and a pressure-sensitive adhesive layer, the above-mentioned peeling auxiliary layer was provided on the surface of the process film, and a pressure-sensitive adhesive layer was disposed on the outermost layer. A multilayer optical recording medium manufacturing sheet having a structure and having an absolute value of a refractive index difference between the peeling assist layer and the pressure-sensitive adhesive layer of 0.11 or less at a wavelength of 660 nm;
(2) The sheet for producing a multilayer optical recording medium according to (1), wherein the absolute value of the difference in refractive index between the peeling assist layer and the pressure-sensitive adhesive layer at a wavelength of 405 nm is 0.11 or less,
(3) The multilayer optical recording medium production sheet according to (1) or (2), wherein the refractive index of the peeling assist layer is 1.42 to 1.60 at a wavelength of 660 nm,
(4) The multilayer optical recording medium manufacturing sheet according to any one of (1) to (3), wherein the optical recording layer has a thickness of 1 to 80 nm ,
(5) The sheet for producing a multilayer optical recording medium according to any one of (1) to (4), wherein the material constituting the peeling assist layer contains a cured product of an energy curable compound.
(6) The energy curable compound is at least one selected from an energy curable oligomer, an energy curable monomer, or an energy ray curable polymer having a polymerizable double bond in a side chain ( A multilayer optical recording medium manufacturing sheet according to 5),
( 7 ) The multilayer optical recording medium manufacturing sheet according to any one of (1) to ( 6 ), wherein the optical recording layer is a multiphoton absorbing material, and ( 8 ) the above (1) to ( 7 ). A multilayer optical recording medium obtained by using the multilayer optical recording medium manufacturing sheet according to any one of
Is to provide.

 According to the present invention, an optical recording medium manufacturing sheet capable of easily producing a multilayer optical recording medium having an optical recording layer having a thickness of 1000 nm or less, and reflected light intensity from a deep part manufactured using the sheet. Is sufficiently large, the recording density is high, and a multilayer optical recording medium having good recording characteristics can be provided.

It is a cross-sectional schematic diagram which shows the structure of one example of the sheet | seat for multilayer optical recording medium manufacture of this invention. It is a cross-sectional schematic diagram which shows the structure of the example from which the sheet | seat for multilayer optical recording media manufacture of this invention differs. It is a cross-sectional schematic diagram which shows an example of a structure of the multilayer optical recording medium of this invention.

First, the multilayer optical recording medium manufacturing sheet of the present invention will be described.
The multilayer optical recording medium production sheet of the present invention (hereinafter sometimes simply referred to as “recording medium production sheet”) produces a multilayer optical recording medium having a repeating structure in which a plurality of optical recording layers are laminated. And a unit including at least a peeling auxiliary layer, an optical recording layer having a thickness of 1 to 1000 nm and a pressure-sensitive adhesive layer on the process film, and the peeling auxiliary layer is provided on the surface of the process film. The pressure-sensitive adhesive layer is disposed on the outermost layer.

[Process film]
The process film in the recording medium manufacturing sheet of the present invention has releasability with respect to the peeling auxiliary layer provided thereon. As this process film, what has peelability with respect to a peeling auxiliary | assistant layer should just be used, and various synthetic resin films can be used.
Specifically, polyester films such as polyethylene terephthalate, polybutylene terephthalate, polyethylene naphthalate, polyethylene film, polypropylene film, polyvinyl chloride film, polyvinylidene chloride film, polyvinyl alcohol film, ethylene-vinyl acetate copolymer film, polystyrene Film, polycarbonate film, polymethylpentene film, polysulfone film, polyetheretherketone film, polyethersulfone film, polyphenylene sulfide film, polyetherimide film, polyimide film, fluororesin film, polyamide film, acrylic resin film, norbornene resin Film, cycloolefin resin film, cellulose acetate Mention may be made of the butter, and the like. Although the thickness of a process film is not specifically limited, Usually, 5-500 micrometers, Preferably, it is 10-200 micrometers.

In addition, the process film may be one in which a peeling treatment is performed on the surface on which the peeling auxiliary layer is provided. Examples of the release treatment include a method in which a known release agent such as a silicone release agent, a polybutadiene release agent, a fluororesin release agent, and an alkyd release agent is applied to the film. The thickness of the release agent layer obtained by applying the release agent is not particularly limited and may be set as desired, but is usually 0.05 to 50 μm. In addition, in order to improve the adhesion with the release agent layer on the film before applying the release agent, for example, corona discharge treatment, plasma discharge treatment, chromic acid treatment, flame treatment, hot air treatment, ozone / ultraviolet irradiation treatment Etc. may be given.
The peel strength of the process film is preferably 10 to 700 mN / 25 mm. When the peeling force is within this range, the transfer workability of the unit including the peeling auxiliary layer, the optical recording layer, and the pressure-sensitive adhesive layer provided on the process film is good. A more preferable peeling force is 30 to 500 mN / 25 mm.
Moreover, it is preferable that the surface in which the peeling assistance layer of the said process film is formed is a thing which does not contain a filler. The method for measuring the peeling force will be described later.

[Peeling auxiliary layer]
In the recording medium manufacturing sheet of the present invention, the peeling auxiliary layer laminated on the process film is a layer peeled from the process film together with the optical recording layer, and an ultrathin optical recording layer (thickness of 1 to 1000 nm) is formed. There is an effect of reinforcing, and the optical recording layer can be easily peeled off.
The material for the peeling auxiliary layer should be a material that has transparency and can effectively exhibit the above-mentioned peeling properties and reinforcing properties, and does not impair the optical properties of the recording medium manufacturing sheet of the present invention. There are no particular restrictions. Examples of such materials include cured products of energy curable compounds (energy curable resins), cellulose resins such as triacetyl cellulose, polycarbonate resins, cycloolefin resins, modified acrylic resins, polyvinyl alcohol, polyvinyl acetal, polystyrene, Resin materials such as polyimide, polyetherimide, polysulfone, polyethersulfone, polyarylate, and polyester are suitable. In addition, an energy curable compound means the compound hardened | cured by energy ray irradiation or a heating.

(Energy curable compound)
As the energy curable compound used as the raw material for the energy curable resin, energy ray curable oligomers and monomers, thermosetting oligomers and monomers, and energy curable functional groups having a polymerizable double bond in the side chain are introduced. And the like.
<Energy curable oligomer>
Examples of energy curable oligomers include polyester acrylate, epoxy acrylate, urethane acrylate, polyether acrylate, polybutadiene acrylate, and silicone acrylate oligomers. Here, examples of the polyester acrylate oligomer include esterification of hydroxyl groups of a polyester oligomer having hydroxyl groups at both ends obtained by condensation of polyvalent carboxylic acid and polyhydric alcohol with (meth) acrylic acid, It can be obtained by esterifying the terminal hydroxyl group of an oligomer obtained by adding an alkylene oxide to a carboxylic acid with (meth) acrylic acid. The epoxy acrylate oligomer can be obtained, for example, by reacting (meth) acrylic acid with an oxirane ring of a relatively low molecular weight bisphenol type epoxy resin or novolak type epoxy resin and esterifying it. A carboxyl-modified epoxy acrylate oligomer obtained by partially modifying this epoxy acrylate oligomer with a dibasic carboxylic acid anhydride can also be used. The urethane acrylate oligomer can be obtained, for example, by esterifying a polyurethane oligomer obtained by the reaction of polyether polyol or polyester polyol and polyisocyanate with (meth) acrylic acid. It can be obtained by esterifying the hydroxyl group of ether polyol with (meth) acrylic acid.
The weight average molecular weight of the oligomer is a value in terms of standard polymethyl methacrylate measured by gel permeation chromatography (GPC) method, preferably 500 to 100,000, more preferably 1,000 to 70,000, still more preferably. Is selected in the range of 3,000 to 40,000. This oligomer may be used individually by 1 type, and may be used in combination of 2 or more type.

<Energy curable monomer>
On the other hand, examples of the energy curable monomer include monofunctional acrylates such as cyclohexyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, lauryl (meth) acrylate, stearyl (meth) acrylate, and isobornyl (meth) acrylate. 1,4-butanediol di (meth) acrylate, 1,6-hexanediol di (meth) acrylate, 1,9-nonanediol di (meth) acrylate, 1,10-decanediol di (meth) acrylate, neopentyl glycol Di (meth) acrylate, polyethylene glycol di (meth) acrylate, neopentyl glycol adipate di (meth) acrylate, hydroxypivalate neopentyl glycol di (meth) acrylate, dicyclopentanyl di (meth) ) Acrylate, caprolactone-modified dicyclopentenyl di (meth) acrylate, ethylene oxide-modified phosphoric acid di (meth) acrylate, allylated cyclohexyl di (meth) acrylate, isocyanurate di (meth) acrylate, trimethylolpropane tri (meth) acrylate, Dipentaerythritol tri (meth) acrylate, propionic acid modified dipentaerythritol tri (meth) acrylate, pentaerythritol tri (meth) acrylate, propylene oxide modified trimethylolpropane tri (meth) acrylate, tris (acryloxyethyl) isocyanurate, Propionic acid modified dipentaerythritol penta (meth) acrylate, dipentaerythritol hexa (meth) acrylate, caprolactone modified Dipentaerythritol hexa (meth) acrylate, tri Julio ii ethyl (meth) acrylate, tetrafluoropropyl (meth) acrylate, octafluoropentyl (meth) acrylate. These monomers may be used alone or in combination of two or more.

<Energy curable polymer having a polymerizable double bond in the side chain>
Examples of the energy curable polymer having a polymerizable double bond in the side chain include, for example, —COOH, —NCO, and an epoxy group in the polymer chain of an acrylic polymer mainly composed of (meth) acrylic acid ester as a constituent monomer. , -OH, -NH2 and the like, an energy curing type having a polymerizable double bond in the side chain of the acrylic polymer by reacting a compound having a polymerizable double bond with this active site The thing formed by introduce | transducing a functional group can be mentioned. In order to introduce the active site into the acrylic polymer, when the acrylic polymer is produced, a functional group such as —COOH, —NCO, epoxy group, —OH, —NH ₂ and polymerizable double A monomer or oligomer having a bond may be present in the reaction system.
Specifically, when producing an acrylic polymer, (meth) acrylic acid or the like is introduced when a -COOH group is introduced, and (meth) acryloxyethyl isocyanate or the like is introduced when an -NCO group is introduced. In the case of introducing an epoxy group, glycidyl (meth) acrylate, etc., in the case of introducing an —OH group, 2-hydroxyethyl (meth) acrylate, 1,6-hexanediol mono (meth) acrylate, etc. In the case of introducing an —NH ₂ group, (meth) acrylamide or the like may be used.
Examples of the compound having a polymerizable double bond to be reacted with these active sites include (meth) acryloxyethyl isocyanate, glycidyl (meth) acrylate, pentaerythritol mono (meth) acrylate, dipentaerythritol mono (meth) acrylate, The trimethylolpropane mono (meth) acrylate can be appropriately selected and used depending on the type of active site.

<Polymerization initiator>
For curing the energy curable compound, a polymerization initiator may be used as desired. As the polymerization initiator, when the energy curable compound is a thermosetting type, an organic peroxide or an azo compound is used. Examples of the organic peroxide include dialkyl peroxides such as di-t-butyl peroxide, t-butyl cumyl peroxide, and dicumyl peroxide, and diacyl peroxides such as acetyl peroxide, lauroyl peroxide, and benzoyl peroxide. , Ketone peroxides such as methyl ethyl ketone peroxide, cyclohexanone peroxide, 3,3,5-trimethylcyclohexanone peroxide, methylcyclohexanone peroxide, and peroxyketals such as 1,1-bis (t-butylperoxy) cyclohexane , T-butyl hydroperoxide, cumene hydroperoxide, 1,1,3,3-tetramethylbutyl hydroperoxide, p-menthane hydroperoxide, diisopropyl base Hydroperoxides such as zenhydroperoxide, 2,5-dimethylhexane-2,5-dihydroperoxide, t-butylperoxyacetate, t-butylperoxy-2-ethylhexanoate, t-butylperoxide Examples thereof include peroxyesters such as oxybenzoate and t-butylperoxyisopropyl carbonate. As the azo compound, 2,2′-azobis (4-methoxy-2,4-dimethylvaleronitrile), 2,2′-azobis (2-cyclopropylpropionitrile), 2,2′-azobis (2,4-dimethylvaleronitrile), azobisisobutyronitrile, 2,2′-azobis (2-methylbutyronitrile), 1,1′-azobis (cyclohexane-1-carbonitrile), 2- ( Carbamoylazo) isobutyronitrile, 2-phenylazo-4-methoxy-2,4-dimethylvaleronitrile and the like. These polymerization initiators may be used individually by 1 type, and may be used in combination of 2 or more type.

 On the other hand, when the energy curable compound is an energy ray curable compound, the energy ray is usually irradiated with ultraviolet rays or electron beams. When irradiating with ultraviolet rays, a photopolymerization initiator is used as a polymerization initiator. Can be used. Examples of this photopolymerization initiator include benzoin, benzoin methyl ether, benzoin ethyl ether, benzoin isopropyl ether, benzoin-n-butyl ether, benzoin isobutyl ether, acetophenone, dimethylaminoacetophenone, 2,2-dimethoxy-2-phenylacetophenone, 2,2-diethoxy-2-phenylacetophenone, 2-hydroxy-2-methyl-1-phenylpropan-1-one, 1-hydroxycyclohexyl phenyl ketone, 2-methyl-1- [4- (methylthio) phenyl]- 2-morpholino-propan-1-one, 4- (2-hydroxyethoxy) phenyl-2 (hydroxy-2-propyl) ketone, benzophenone, p-phenylbenzophenone, 4,4′-diethylaminobenzo Enone, dichlorobenzophenone, 2-methylanthraquinone, 2-ethylanthraquinone, 2-tert-butylanthraquinone, 2-aminoanthraquinone, 2-methylthioxanthone, 2-ethylthioxanthone, 2-chlorothioxanthone, 2,4-dimethylthioxanthone, 2 , 4-diethylthioxanthone, benzyldimethyl ketal, acetophenone dimethyl ketal, p-dimethylamine benzoate, oligo (2-hydroxy-2-methyl-1- [4- (1-propenyl) phenyl] propane) and the like. . These may be used alone or in combination of two or more.

(Energy curing resin)
An energy curable resin comprising a cured product of the above-mentioned energy curable compound includes, as desired, the above-described polymerization initiator, crosslinking agent, tackifier, antioxidant, ultraviolet absorber, and light stabilizer. It can be obtained by adding a softener, a filler or the like and curing.
As the material constituting the peeling auxiliary layer, when the optical recording layer is laminated on the peeling auxiliary layer, a solution of the optical recording material can be applied to the peeling auxiliary layer to form the optical recording layer, so that the solvent resistance is high. Further, a cured product of energy curable oligomer or monomer, or triacetyl cellulose is preferable. Among these, a cured product of an energy curable oligomer or monomer is particularly preferable from the viewpoint of easily adjusting the refractive index. The resin material preferably has a glass transition temperature of 50 ° C. or higher from the viewpoint of peelability, reinforcing effect, and reliability as an optical recording medium. The thickness of the peeling auxiliary layer has a peeling effect and a reinforcing effect, and is preferably 0.2 to 25 μm, more preferably 0 from the viewpoint of effectively peeling the optical recording layer and obtaining a practical recording density. .3 to 23 μm, more preferably 0.4 to 20 μm.

In the present invention, as described later, the absolute value of the difference in refractive index between the peeling assist layer and the pressure sensitive adhesive layer at a wavelength of 660 nm needs to be 0.11 or less. As a material constituting the peeling assisting layer, a material containing a fluorine atom is preferable. Examples of such a material containing a fluorine atom include a cured product such as trifluoroethyl (meth) acrylate, tetrafluoropropyl (meth) acrylate, and octafluoropentyl (meth) acrylate, and a polyvinyl fluoride copolymer. . The peeling assist layer uses a coating solution containing the above-mentioned materials, and is coated by a bar coating method, a reverse roll coating method, a knife coating method, a roll knife coating method, a gravure coating method, an air doctor coating method, a doctor blade coating method, or the like. It can be applied by the method, and can be formed by heating and drying at a temperature of about 80 to 150 ° C. for several tens of seconds to several minutes if necessary.
The peeling auxiliary layer may be subjected to a surface treatment as desired for the purpose of improving the adhesion with the optical recording layer provided thereon. Examples of the surface treatment method include corona discharge treatment, plasma treatment, chromic acid treatment (wet), flame treatment, hot air treatment, ozone / ultraviolet irradiation treatment, and the like. These surface treatment methods are appropriately selected depending on the type of the auxiliary peeling layer, but in general, the corona discharge treatment method is preferably used from the viewpoints of effects and operability.

[Optical recording layer]
As the optical recording layer in the multilayer optical recording medium manufacturing sheet of the present invention, any material known as a constituent material of the optical recording layer can be appropriately selected and used, but the recording density can be improved. From the point of view, a multiphoton absorbing material is preferably used. A multiphoton absorbing material means a compound having the property of simultaneously absorbing two or more photons and transitioning to an excited state. Among these, from the viewpoint of obtaining recording sensitivity sufficient for practical use, those containing a two-photon absorbing material having a two-photon absorption cross-sectional area of 0.1 GM or more are preferable, and particularly those containing a two-photon absorbing material of 100 GM or more are further included. preferable. As such a material, for example, a multiphoton absorbing material constituted alone, or a multiphoton absorbing material, for example, and other reactive compounds that change due to energy transfer from the excited multiphoton absorbing material. You may comprise with the material comprised by these, and the material which mix | blended these with the matrix as needed.

The “GM” means 10 ⁻⁵⁰ cm ⁴ · s · molecule ⁻¹ · photon ⁻¹ . The material constituting the matrix may be an inorganic material or an organic material. However, from the viewpoints of simplicity of manufacturing the recording medium manufacturing sheet of the present invention and many choices of materials, organic materials are used. The polymer material is preferable. The polymer material may be a homopolymer or a copolymer, and there are no particular restrictions on the type of monomer, molecular weight, polymerization form, and the like, and examples thereof include polymethyl methacrylate.
The multiphoton absorbing material may be chemically bonded to the matrix as a main chain or side chain component, or may be simply dispersed or dissolved in the matrix. The multiphoton absorbing material is not particularly limited, and various compounds can be used. For example, cyanine dye, styryl dye, pyrylium dye, thiapyrylium dye, merocyanine dye, arylidene dye, oxonol dye, squalium dye, azurenium dye, coumarin dye, pyran dye, quinone dye, anthraquinone dye, triphenylmethane dye, diphenylmethane dye, xanthene Dyes, thioxanthene dyes, phenothiazine dyes, azo dyes, azomethine dyes, fluorenone dyes, diarylethene dyes, spiropyran dyes, fulgide dyes, perylene dyes, polyene dyes, diphenylamine dyes, quinacdrine dyes, azurenium dyes, porphyrin dyes, phthalocyanine dyes, styrene series Examples thereof include compounds such as dyes, phenylene vinylene dyes, triphenylamine dyes, and carbazole dyes.

As a recording method using such a multiphoton absorbing compound, for example, a material isomerized by light such as an azo group, a C═C group, or a C═N group-containing compound, or a (meth) acrylate compound For example, a material that causes a polymerization reaction by light, a material that causes a reversible structural change by light, such as an organic photochromic material, a method that reads refractive index modulation using an organic refractory material in which charge distribution is caused by light, A method of reading fluorescence using a material whose fluorescence characteristics change, a combination of a material that generates acid by light and an acid coloring dye, or a combination of a decoloring agent and a decoloring dye to perform absorption rate modulation or refractive index modulation. Examples include reading methods. In these recording methods, the multiphoton absorbing compound itself may have such photoreactivity, or from the multiphoton absorbing compound excited by multiphoton absorption to another reactive compound. The reaction may be caused by energy transfer.
In the optical recording medium manufacturing sheet of the present invention, the thickness of the optical recording layer is 1-1000 nm, preferably 10-800 nm.

[Pressure sensitive adhesive layer]
In the multilayer optical recording medium manufacturing sheet of the present invention, a pressure-sensitive adhesive layer having adhesiveness at room temperature is disposed on the outermost layer. By using the sheet for producing a multilayer optical recording medium having this pressure-sensitive adhesive layer, the multilayer optical recording medium can be easily produced. As the pressure-sensitive adhesive constituting the pressure-sensitive adhesive layer, an acrylic pressure-sensitive adhesive is particularly preferable because of its high transparency.
As this acrylic pressure-sensitive adhesive, for example, an adhesive containing a (meth) acrylic acid ester copolymer and a crosslinking agent can be used.

((Meth) acrylic acid ester copolymer)
As the (meth) acrylic acid ester-based copolymer, a (meth) acrylic acid ester having 1 to 20 carbon atoms of an alkyl group bonded to a non-carbonyl oxygen atom of the ester portion, and a functional group having active hydrogen. The copolymer of the monomer which has and the other monomer used depending on necessity can be mentioned preferably.
Examples of the (meth) acrylic acid ester having 1 to 20 carbon atoms in the alkyl group bonded to the non-carbonyl oxygen atom of the ester moiety include methyl (meth) acrylate, ethyl (meth) acrylate, and propyl (meth) acrylate. , Isopropyl (meth) acrylate, n-butyl (meth) acrylate, isobutyl (meth) acrylate, t-butyl (meth) acrylate, pentyl (meth) acrylate, hexyl (meth) acrylate, cyclohexyl (meth) acrylate, 2-ethylhexyl (Meth) acrylate, isooctyl (meth) acrylate, decyl (meth) acrylate, dodecyl (meth) acrylate, myristyl (meth) acrylate, palmityl (meth) acrylate, stearyl (meth) acrylate, etc. It is. These may be used alone or in combination of two or more.

 On the other hand, examples of monomers having a functional group having active hydrogen include 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 3-hydroxypropyl (meth) acrylate, and 2-hydroxybutyl (meth). Acrylate, hydroxyalkyl (meth) acrylate such as 3-hydroxybutyl (meth) acrylate, 4-hydroxybutyl (meth) acrylate, monomethylaminoethyl (meth) acrylate, monoethylaminoethyl (meth) acrylate, monomethylaminopropyl (meth) ) Monoalkylaminoalkyl (meth) acrylates such as acrylate and monoethylaminopropyl (meth) acrylate; acrylic acid, methacrylic acid, crotonic acid, maleic acid, itaconic acid, citraconic acid, etc. Such as ethylenically unsaturated carboxylic acids. These monomers may be used independently and may be used in combination of 2 or more type.

 Examples of other monomers used as desired include vinyl esters such as vinyl acetate and vinyl propionate; olefins such as ethylene, propylene and isobutylene; halogenated olefins such as vinyl chloride and vinylidene chloride; styrene, α -Styrene monomers such as methylstyrene; Diene monomers such as butadiene, isoprene and chloroprene; Nitrile monomers such as acrylonitrile and methacrylonitrile; Acrylamides such as acrylamide, N-methylacrylamide and N, N-dimethylacrylamide, Phenoxy Ethyl (meth) acrylate, phenoxydiethylene glycol (meth) acrylate, phenoxypolyethylene glycol (meth) acrylate, hydroxyethylated o-phenyl phen Lumpur (meth) acrylate, isobornyl (meth) acrylate and benzyl (meth) acrylate. These may be used alone or in combination of two or more.

 The (meth) acrylic acid ester-based copolymer is not particularly limited as to its copolymerization form, and may be any of random, block, and graft copolymers. The molecular weight is preferably in the range of 300,000 to 2,000,000 in terms of weight average molecular weight. In addition, the said weight average molecular weight is the value of polystyrene conversion measured by the gel permeation chromatography (GPC) method. In the present invention, this (meth) acrylic ester copolymer may be used alone or in combination of two or more.

(Crosslinking agent)
The crosslinking agent in the acrylic pressure-sensitive adhesive is not particularly limited, and those conventionally used as a crosslinking agent in acrylic pressure-sensitive adhesives such as polyisocyanate compounds, epoxy compounds, aziridine compounds, melamine resins, urea It can be appropriately selected from resins, dialdehydes, metal chelate compounds, metal alkoxides, metal salts, etc., but it does not easily change the light transmittance due to discoloration (yellowing) of the pressure-sensitive adhesive layer. , Cycloaliphatic polyisocyanate compounds, aliphatic polyisocyanate compounds, xylene polyisocyanate compounds, alicyclic epoxy compounds, aliphatic epoxy compounds that are unlikely to be altered by laser irradiation during recording or playback A metal chelate compound or an aliphatic aziridine compound is preferred.

<Alicyclic and aliphatic polyisocyanate compounds>
Examples of the alicyclic polyisocyanate compounds include isophorone diisocyanate, bicycloheptane triisocyanate, cyclopentylene diisocyanate, cyclohexylene diisocyanate, methylcyclohexylene diisocyanate, hydrogenated diphenylmethane diisocyanate, and the like. And biuret bodies, isocyanurate bodies, and adduct bodies that are reaction products with low molecular active hydrogen-containing compounds such as ethylene glycol, propylene glycol, neopentyl glycol, trimethylolpropane, and castor oil. Examples of the aliphatic polyisocyanate compounds include hexamethylene diisocyanate, trimethylhexamethylene diisocyanate, lysine diisocyanate, and the like, biurets, isocyanurates, ethylene glycol, propylene glycol, and neopentyl glycol. And adduct bodies which are reaction products with low molecular active hydrogen-containing compounds such as trimethylolpropane and castor oil.

<Alicyclic and aliphatic epoxy compounds>
Examples of the alicyclic epoxy compounds include 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexylcarboxylate, 1,3-bis (N, N′-diglycidylaminomethyl) cyclohexane, hydrogenated bisphenol A diester. Examples of the aliphatic epoxy compound include polyethylene glycol diglycidyl ether, polypropylene glycol diglycidyl ether, 1,6-hexanediol glycidyl ester, adipic acid glycidyl ester, and sebacic acid glycidyl ester. .

<Metal chelate compound>
Examples of the metal chelate compound include chelate compounds whose metal atoms are aluminum, zirconium, titanium, zinc, iron, tin and the like, and aluminum chelate compounds are preferable.
Examples of the aluminum chelate compound include diisopropoxy aluminum monooleyl acetoacetate, monoisopropoxy aluminum bis oleyl acetoacetate, monoisopropoxy aluminum monooleate monoethyl acetoacetate, diisopropoxy aluminum monolauryl acetoacetate, diisopropoxy aluminum Monostearyl acetoacetate, diisopropoxyaluminum monoisostearyl acetoacetate, monoisopropoxyaluminum mono-N-lauroyl-β-alanate monolauryl acetoacetate, aluminum trisacetylacetonate, monoacetylacetonate aluminum bis (isobutylacetoacetate ) Chelate, monoacetylacetonate aluminum Scan (2-ethylhexyl acetoacetate) chelate, monoacetylacetonate aluminum bis (dodecyl acetoacetate) chelate, monoacetylacetonate aluminum bis (oleyl acetoacetate) and a chelating the like.

 Examples of the aliphatic aziridine compounds include trimethylolpropane tri (2-methyl-1-aziridinepropionate), tetramethylolmethane-tri-β-aziridinylpropionate, and 2,2′-bishydroxymethylbutanol. -Tris [3- (1-aziridinyl) propionate], 1,6-hexamethylenediethylene urea and the like.

In the pressure-sensitive adhesive in the present invention, the crosslinking agent may be used alone or in combination of two or more. Moreover, the content is 0.01-5.0 mass parts normally with respect to 100 mass parts of said (meth) acrylic acid ester-type copolymers from a viewpoint of the performance as a pressure sensitive adhesive, Preferably it is 0.00. It is selected in the range of 05 to 3.0 parts by mass, more preferably 0.1 to 1.0 parts by mass.
In the pressure-sensitive adhesive, a tackifier, an antioxidant, an ultraviolet absorber, a light stabilizer, a softener, a filler, and the like can be added as desired as long as the effects of the present invention are not impaired. .
The thickness of the pressure-sensitive adhesive layer in the sheet of the present invention is not particularly limited, but is usually about 1 to 100 μm, preferably 1 to 30 μm.

[Refractive index difference between peeling auxiliary layer and pressure-sensitive adhesive layer]
In a multilayer optical recording medium having a recording layer and a non-recording layer (peeling auxiliary layer and pressure-sensitive adhesive layer), the focus servo during recording utilizes reflected light from the laminated interface. If the difference in refractive index between the recording layer and the non-recording layer is large, the reflected light intensity is large, and if it is small, the reflected light intensity is also small. When the reflected light intensity is higher, it is easier to apply focus servo to the interface. On the other hand, if you want to use the reflected light from the deep part of the multilayer optical recording medium, if the reflected light at each layer is too large, As a result, most of the light is reflected and the intensity of reflected light from the deepest interface becomes extremely small. Also, the greater the number of interfaces, the greater the attenuation factor, and the focus servo to the deepest part becomes difficult. Therefore, by eliminating the difference in refractive index between the peeling assisting layer and the pressure sensitive adhesive layer at the wavelength of the laser used, it becomes possible to eliminate the reflected light at the interface between the peeling assisting layer and the pressure sensitive adhesive. It is possible to reduce the loss of (reflected light).

The laser wavelength used in the multilayer optical recording medium is 660 nm or 405 nm, and the refractive index of the substance has wavelength dependency. This means that the material properties must be designed with a design suitable for each wavelength.
In the multilayer optical recording medium manufacturing sheet of the present invention, the absolute value of the refractive index difference between the peeling assist layer and the pressure-sensitive adhesive layer at a wavelength of 660 nm is required to be 0.11 or less. When the difference in refractive index exceeds 0.11, the reflected light at the interface becomes so large that it cannot be ignored, and it becomes difficult to use the reflected light from the deep part of the multilayer body, so that the recording characteristics are deteriorated.
The absolute value of the difference in refractive index between the peeling assist layer and the pressure sensitive adhesive layer at a wavelength of 405 nm is preferably 0.11 or less for the same reason as described above.
Since the refractive index of the pressure-sensitive adhesive layer at a wavelength of 660 nm is usually about 1.32 to 1.60, the refractive index of the peeling assist layer at a wavelength of 660 nm is about 1.21 to 1.71. It is preferable that it is 42-1.60.
Moreover, since the refractive index of the pressure-sensitive adhesive layer at a wavelength of 405 nm is usually about 1.35 to 1.65, the refractive index of the peeling assist layer at a wavelength of 405 nm is usually 1.24 to 1.76, preferably 1.42-1.60. A method for measuring the refractive index will be described later.

[Layer structure of multilayer optical recording medium manufacturing sheet]
The layer structure of the multilayer optical recording medium manufacturing sheet of the present invention has a unit including at least the above-described release auxiliary layer, optical recording layer, and pressure-sensitive adhesive layer on the process film, and the release auxiliary layer. Is provided on the surface of the process film, and has a layer structure in which a pressure-sensitive adhesive layer is disposed on the outermost layer. The unit has at least a peeling auxiliary layer, an optical recording layer, and a pressure sensitive adhesive layer, and the peeling auxiliary layer is disposed on the process film side, and the pressure sensitive adhesive layer is disposed on the outermost layer. For example, the configuration and the number of layers are not particularly limited.

Specific examples of the recording medium manufacturing sheet of the present invention include a laminated sheet having the structure shown in FIGS.
FIG. 1 is a schematic cross-sectional view showing the structure of an example of a multilayer optical recording medium manufacturing sheet according to the present invention. The multilayer optical recording medium manufacturing sheet 15 includes a peeling assist layer 2, an optical recording layer 1, and a pressure sensitive layer. The unit 10a having a three-layer structure in which the adhesive layer 3 is sequentially laminated has a structure provided on the process film 4, and the peeling auxiliary layer 2 is in contact with the surface of the process film 4, and the pressure sensitive A release film 5 is stuck on the adhesive layer 3.
FIG. 2 is a schematic cross-sectional view showing the structure of a different example of the multilayer optical recording medium manufacturing sheet of the present invention. The multilayer optical recording medium manufacturing sheet 20 includes a peeling assist layer 2a, an optical recording layer 1a, and a peeling assist. A unit 10b having a five-layer structure in which a layer 2b, an optical recording layer 1b, and a pressure-sensitive adhesive layer 3 are sequentially laminated is provided on the process film 4, and is peeled off from the surface of the process film 4 While the auxiliary layer 2 a is in contact, a release film 5 is stuck on the pressure-sensitive adhesive layer 3.
The laminated sheet having the configuration shown in FIGS. 1 and 2 can be produced by sequentially forming each layer on the process film 4 by various conventionally known coating methods. At this time, when an optical recording layer is formed on the peeling auxiliary layer, depending on the type of the peeling auxiliary layer, for the purpose of protecting the peeling auxiliary layer, a barrier layer is provided on the peeling auxiliary layer as necessary, and an optical recording layer is formed. A recording layer may be formed.

As said peeling film 5, the well-known peeling film conventionally used for the pressure sensitive adhesive layer can be used.
Although there is no restriction | limiting in particular as said peeling film, The thing etc. which apply | coated peeling agents, such as silicone resin, etc. to polyolefin films, such as a polyethylene film and a polypropylene film, and polyester films, such as a polyethylene terephthalate, provided the release agent layer. It is done. Moreover, although there is no restriction | limiting in particular about the thickness of these peeling films, Usually, it is about 20-150 micrometers.
Since it is preferable that the maximum height roughness (Rz) of the pressure-sensitive adhesive layer surface is small, Rz of the release-treated surface of the release film is preferably 500 nm or less. Rz is measured according to JIS B0601.

Next, the multilayer optical recording medium of the present invention will be described.
[Multilayer optical recording medium]
The multilayer optical recording medium of the present invention is obtained by using the above-described sheet for producing a multilayer optical recording medium of the present invention.
The multilayer optical recording medium has a structure in which a plurality of the recording medium manufacturing sheets are laminated via a pressure-sensitive adhesive layer disposed on the outermost side. Specifically, a unit having a three-layer structure in which a peeling auxiliary layer, an optical recording layer, and a pressure-sensitive adhesive layer are sequentially laminated as shown in FIG. 1, or a peeling auxiliary layer and an optical recording layer as shown in FIG. A unit having a five-layer structure in which a peeling auxiliary layer, an optical recording layer, and a pressure-sensitive adhesive layer are sequentially stacked has a structure in which a plurality of units are stacked via a pressure-sensitive adhesive layer.

The number of units stacked in the multilayer optical recording medium of the present invention is not particularly limited, but from the viewpoint of recording density, the optical recording layer is about 5 to 100 layers, preferably 8 to 80 layers. If the optical recording layer is less than five layers, a sufficient recording density cannot be obtained. If the optical recording layer exceeds 100 layers, there is a possibility that information may be written or read due to absorption of light in each layer or reflection of light between layers. .
FIG. 3 is a schematic cross-sectional view showing an example of the configuration of the multilayer optical recording medium of the present invention. The multilayer optical recording medium 30 is formed by laminating n layers of a three-layer unit composed of a pressure sensitive adhesive layer, an optical recording layer, and a peeling auxiliary layer on a substrate 6 such as a polymethyl methacrylate film. Layer 3-1, optical recording layer 1-1, peeling auxiliary layer 2-1, pressure sensitive adhesive layer 3-2, optical recording layer 1-2, peeling auxiliary layer 2-2, pressure sensitive adhesive layer 3-3 , Optical recording layer 1-3, peeling auxiliary layer 2-3,... Having a structure provided with pressure sensitive adhesive layer 3-n, optical recording layer 1-n, peeling auxiliary layer 2-n. .
The multilayer optical recording medium 30 having such a structure can be manufactured, for example, as follows. First, a plurality of sheets 15 shown in FIG. 1 are prepared, the release film 5 of the first sheet 15 is peeled off, and the exposed pressure-sensitive adhesive layer 3 and the base material 6 shown in FIG. And the process film 4 is peeled off. At this stage, the peeling assist layer 2-1 in FIG. 3 is exposed. Next, the release film 5 is peeled off from the second sheet 15, and the exposed pressure-sensitive adhesive layer 3 and the peeling assisting layer 2-1 in FIG. Thereafter, the multilayer optical recording medium 30 in which n optical recording layers are laminated is obtained by sequentially repeating the lamination in the same procedure.
A protective film 7 such as a polyvinyl alcohol film can be provided on the peeling assist layer 2-n via the pressure sensitive adhesive layer 3a.

Although there is no restriction | limiting in particular in the thickness of the said base material 6, Usually, about 5-1000 micrometers, Preferably it is 5-100 micrometers. Examples of the material for the substrate 6 include polymethyl methacrylate, polycarbonate, polyethylene terephthalate, polyolefin, and glasses.
The information recording / reproducing method in the multilayer optical recording medium of the present invention is not particularly limited, and can be appropriately selected from conventionally known methods as the information recording / reproducing method in the multilayer optical recording medium.
There is no restriction | limiting in particular about the form of the multilayer optical recording medium of this invention, Either a disk shape and a roll shape may be sufficient.

EXAMPLES Next, although an Example demonstrates this invention further in detail, this invention is not limited at all by these examples.
In addition, the various characteristics in each example were calculated | required according to the method shown below.
(1) Peeling force The peeling film of the multilayer optical recording medium production sheet obtained in Reference Examples 1 to 6, Examples 1 and 2 and Comparative Examples 1 and 2 was peeled off, and the glass plate [Matsunami Glass Industry Co., Ltd. Manufactured, product name “MICRO SLIDE GLASS S-112”], which is pasted through an exposed pressure-sensitive adhesive layer, and then processed in a 25 ° C. and 50% relative humidity environment using a tensile tester. The peeling force was measured by peeling off at a peeling angle of 180 ° and a peeling speed of 300 mm / min.
(2) Refractive index The refractive index of the peeling assist layer of the multilayer optical recording medium production sheets of Reference Examples 1 to 6, Examples 1 and 2 and Comparative Example 2 is the same as that of the process film used in Reference Example 5. The preparation coating solution was applied and dried to form a 20 μm-thick peeling auxiliary layer, and the process film was peeled off and measured using an Abbe refractometer [manufactured by Atago Co., Ltd.]. The refractive index of the pressure-sensitive adhesive layer of the sheets for producing multilayer optical recording media of Reference Examples 1 to 6, Examples 1 and 2 and Comparative Examples 1 and 2 is the same as that of the release film used in Reference Example 1. The layer-forming coating solution was applied and dried to form a pressure-sensitive adhesive layer having a thickness of 20 μm, and the release film was peeled off and measured using an Abbe refractometer [manufactured by Atago Co., Ltd.]. The refractive index of the optical recording layer of the multilayer optical recording medium manufacturing sheet of Reference Examples 1 to 6, Examples 1 and 2 and Comparative Examples 1 and 2 is the surface of the peeling assist layer or the process in the manufacturing process of the optical recording medium manufacturing sheet. When an optical recording layer was formed on the film, the measurement was performed using an ellipsometer [manufactured by JA Woollam Japan Co., Ltd., trade name “Spectroscopic Ellipsometry 2000U”].
(3) Layer Thickness Auxiliary peeling layer and pressure-sensitive adhesive layer of the multilayer optical recording medium production sheets of Reference Examples 1 to 6, Examples 1 and 2, and Comparative Example 2 and production of the multilayer optical recording medium of Comparative Example 1 The thickness of the pressure-sensitive adhesive layer of the sheet for use in the manufacturing process of the optical recording medium manufacturing sheet is a pressure type thickness meter [trade name “PG-02” manufactured by Teclock Co., Ltd. ] Was used to measure and calculate the total thickness before and after forming each layer. The thickness of the optical recording layer of the multilayer optical recording medium production sheet of Reference Examples 1 to 6, Examples 1 and 2 and Comparative Examples 1 and 2 is the surface of the peeling assist layer or the process in the production process of the optical recording medium production sheet When an optical recording layer was formed on the film, the measurement was performed using an ellipsometer [manufactured by JA Woollam Japan Co., Ltd., trade name “Spectroscopic Ellipsometry 2000U”].

(4) Reflected Light Intensity For the multilayer optical recording media obtained in Examples 3 to 10 and Comparative Example 3, the reflected light intensity was confirmed as follows.
A semiconductor laser with a wavelength of 405 nm [manufactured by TOPICA, product name “CUBE405-100C”] or a semiconductor laser with a wavelength of 660 nm [manufactured by TOPICA, product name “iPulse 660”] is incorporated into a confocal optical system, and a protective film for a multilayer recording medium (I) reflected light intensity at the interface between the first peeling auxiliary layer and the pressure-sensitive adhesive layer adjacent to the first peeling auxiliary layer counted from the protective film side, (ii) Examples 3 to 9 and In Comparative Example 3, the reflected light intensity at the interface between the first optical recording layer and the pressure-sensitive adhesive layer adjacent thereto counted from the protective film side, and in Example 10, the second optical recording layer counted from the protective film side And the reflected light intensity at the pressure-sensitive adhesive layer interface adjacent thereto, and (iii) the 20th optical recording layer counted from the protective film side, and The reflected light intensity at the adjacent pressure-sensitive adhesive layer interface is measured, and the ratio of the reflected light intensity of (ii) to the reflected light intensity of (i) (intensity ratio 1), (iii) with respect to the reflected light intensity of (ii) The ratio of the intensity of reflected light (intensity ratio 2) was calculated. Here, the intensity ratio 1 is an index of whether or not the reflected light from the interface between the optical recording layer and the pressure-sensitive adhesive layer can be discriminated, and if it is 1.5 or more, it is good (the position of the optical recording layer can be recognized). is there. The intensity ratio 2 indicates the degree of attenuation of the reflected light in the deep optical recording layer of the multilayer optical recording medium, and is preferably 0.1 to 1 (the reflected light from the deep optical recording layer can be recognized). It is.
(5) Recording characteristics Using the multilayer optical recording media obtained in Examples 3 to 10 and Comparative Example 3, recording experiments were performed under the following conditions.
In a confocal optical system using a titanium sapphire femtosecond laser (wavelength 780 nm) as a light source, the 20th optical recording layer counted from the protective film side was irradiated with laser light 25 times. The average intensity of the laser beam was 60 (mW), and the irradiation time was 128 milliseconds, 64 milliseconds, 32 milliseconds, 16 milliseconds, and 8 milliseconds, and 5 points each (25 points in total) were recorded. Next, using a semiconductor laser with a wavelength of 405 nm [trade name “CUBE405-100C” manufactured by TOPICA Co., Ltd.] in the same confocal system, the number of recorded spots observed in 25 points was investigated.

Example 1
(1) Preparation of coating liquid for preparing peeling auxiliary layer As an ultraviolet curable compound (energy curable compound), neopentyl glycol diacrylate [manufactured by Shin-Nakamura Chemical Co., Ltd., trade name “NK Ester A-NPG”, 503.5 g of solid content] is mixed with 463.5 g of methyl ethyl ketone as a solvent and 1.5 g of 1-hydroxycyclohexyl phenyl ketone [trade name “Irgacure 184” manufactured by Ciba Specialty Chemicals Co., Ltd.] as a photopolymerization initiator. Then, a coating solution having a solid content concentration of 10% by mass was prepared.
(2) Preparation of coating solution for producing optical recording layer 1,1-bis- [4- [N, N-di (p-tolyl) amino] phenyl] cyclohexane [Tokyo Chemical Industry Co., Ltd.] as a multiphoton absorbing material Manufactured] 5 g and 95 g of toluene as a solvent were mixed to prepare a coating solution having a solid content concentration of 5% by mass.
(3) Preparation of coating solution for preparing pressure-sensitive adhesive layer n-butyl acrylate, phenoxyethyl acrylate and hydroxyethyl acrylate (n-butyl acrylate / phenoxyethyl acrylate / hydroxyethyl acrylate = 60: 35: 5 (mass ratio) ) To 100 g of an ethyl acetate solution (solid content concentration 30 mass%) of an acrylic ester copolymer (weight average molecular weight 600000) consisting of xylylene diisocyanate-based crosslinker [trade name “TD- 75 ", solid content concentration 75 mass%] 1 g was added and stirred to prepare a coating solution having a solid content concentration of 30 mass%.
(4) Production of sheet for optical recording medium production As a process film, on one side of a 50 μm thick polyethylene terephthalate film [manufactured by Toyobo Co., Ltd., trade name “PET50A-4100”] Was coated by a gravure coating method, dried at 90 ° C. for 1 minute, and a polyethylene terephthalate film [trade name “PET50A-4100” manufactured by Toyobo Co., Ltd.] having a thickness of 50 μm was used thereon with two rubber rollers. crimp Te, ultraviolet irradiation device [(Ltd.) GS Yuasa Lighting Ltd., trade name "UVSYSTEM CSN2-40"] under a nitrogen atmosphere by using a light intensity 500mJ / cm ^2, the ultraviolet rays under the conditions of illuminance of 120mW / cm ² Irradiation was performed to form a peeling auxiliary layer having a thickness of 6.2 μm. In addition, the light quantity and illuminance of ultraviolet rays were measured using a light quantity illuminometer [manufactured by GS Yuasa Lighting Co., Ltd., trade name “UVR-N1”] (the same applies hereinafter). The pressure-bonded polyethylene terephthalate film was peeled off, and a coating liquid for producing an optical recording layer was applied to the surface of the obtained peeling auxiliary layer by a gravure coating method and dried at 90 ° C. for 1 minute to form an optical recording layer. The thickness of the obtained optical recording layer was 110 nm. Next, the pressure-sensitive adhesive layer preparation coating solution was applied to the release surface of the release film [manufactured by Lintec Corporation, trade name “PET381031”] by the knife coat method and dried at 90 ° C. for 1 minute. A pressure sensitive adhesive sheet was prepared. The thickness of this pressure sensitive adhesive layer was 5.1 μm. The pressure-sensitive adhesive layer of the obtained pressure-sensitive adhesive sheet was pressure-bonded onto the optical recording layer using two rubber rollers to obtain a sheet for producing an optical recording medium.

Example 2
The preparation of the peeling assisting layer preparation coating solution was changed as follows, and the optical recording layer preparation coating solution and the pressure sensitive adhesive layer preparation coating solution were the same as in Example 1 for optical recording. A sheet for producing a medium was produced.
<Preparation of a coating liquid for preparing a peeling assist layer>
Purified water (95 g) was mixed as a solvent with 5 g of polyvinyl alcohol [manufactured by Nippon Synthetic Chemical Industry Co., Ltd., trade name “GOHSENOL T-350”] to prepare a coating solution having a solid content concentration of 5 mass%.
<Preparation of optical recording medium manufacturing sheet>
As a process film, a coating liquid for preparing a peeling assist layer was applied to one side of a polyethylene terephthalate film having a thickness of 50 μm [trade name “PET50A-4100” manufactured by Toyobo Co., Ltd.] by a gravure coating method at 90 ° C. for 1 minute. By drying, a peeling auxiliary layer having a thickness of 0.4 μm was formed. A coating liquid for producing an optical recording layer was applied to the surface of the obtained peeling assist layer by a gravure coating method and dried at 90 ° C. for 1 minute to form an optical recording layer. The thickness of the obtained optical recording layer was 80 nm. Next, the pressure-sensitive adhesive layer preparation coating solution was applied to the release surface of the release film [manufactured by Lintec Corporation, trade name “PET381031”] by the knife coating method and dried at 90 ° C. for 1 minute. A pressure sensitive adhesive sheet was prepared. The thickness of this pressure sensitive adhesive layer was 10.5 μm. The pressure-sensitive adhesive layer of the obtained pressure-sensitive adhesive sheet was pressure-bonded onto the optical recording layer using two rubber rollers to obtain a sheet for producing an optical recording medium.

Example 3
The preparation of the peeling assisting layer preparation coating solution was changed as follows, and the optical recording layer preparation coating solution and the pressure sensitive adhesive layer preparation coating solution were the same as in Example 1 for optical recording. A sheet for producing a medium was produced.
<Preparation of a coating liquid for preparing a peeling assist layer>
95 g of xylene as a solvent was mixed with 5 g of cycloolefin resin [manufactured by Polyplastic Co., Ltd., trade name “Topas 5013”] to prepare a coating solution having a solid content concentration of 5 mass%.
<Preparation of optical recording medium manufacturing sheet>
As a process film, a coating liquid for preparing a peeling assist layer was applied to one side of a polyethylene terephthalate film having a thickness of 50 μm [trade name “PET50A-4100” manufactured by Toyobo Co., Ltd.] by a gravure coating method at 90 ° C. for 1 minute. By drying, a peeling auxiliary layer having a thickness of 1 μm was formed. A coating liquid for producing an optical recording layer was applied to the surface of the obtained peeling assist layer by a gravure coating method and dried at 90 ° C. for 1 minute to form an optical recording layer. The thickness of the obtained optical recording layer was 600 nm. Next, the pressure-sensitive adhesive layer preparation coating solution was applied to the release surface of the release film [manufactured by Lintec Corporation, trade name “PET381031”] by the knife coating method and dried at 90 ° C. for 1 minute. A pressure sensitive adhesive sheet was prepared. The thickness of this pressure sensitive adhesive layer was 10.5 μm. The pressure-sensitive adhesive layer of the obtained pressure-sensitive adhesive sheet was pressure-bonded onto the optical recording layer using two rubber rollers to obtain a sheet for producing an optical recording medium.

Example 4
The preparation of the peeling assisting layer preparation coating solution and the pressure-sensitive adhesive layer preparation coating solution was changed as follows, and the optical recording layer preparation coating solution was the same as in Example 1 for optical recording. A sheet for producing a medium was produced.
<Preparation of a coating liquid for preparing a peeling assist layer>
To 3 g of triacetylcellulose [manufactured by Daicel Chemical Industries, Ltd., trade name “LT-105”], 97 g of dichloromethane was mixed as a solvent to prepare a coating solution having a solid content concentration of 3 mass%.
<Preparation of coating solution for pressure-sensitive adhesive layer preparation>
Ethyl acetate solution (solid content concentration: 30% by mass) of acrylic acid ester copolymer (weight average molecular weight 1000000) consisting of n-butyl acrylate and acrylic acid (n-butyl acrylate / acrylic acid = 95: 5 (mass ratio)) To 100 g, 2 g of an aluminum chelate-based cross-linking agent [manufactured by Soken Chemical Co., Ltd., trade name “M-5A”, solid content concentration 5 mass%] was added and stirred to obtain a coating solution.
<Preparation of optical recording medium manufacturing sheet>
As a process film, a coating liquid for preparing a peeling assist layer was applied to one side of a polyethylene terephthalate film having a thickness of 50 μm [trade name “PET50A-4100” manufactured by Toyobo Co., Ltd.] by a gravure coating method at 90 ° C. for 1 minute. Drying was performed to form a 2 μm-thick peeling auxiliary layer. A coating liquid for producing an optical recording layer was applied to the surface of the obtained peeling assist layer by a gravure coating method and dried at 90 ° C. for 1 minute to form an optical recording layer. The thickness of the obtained optical recording layer was 400 nm. Next, the pressure-sensitive adhesive layer preparation coating solution was applied to the release surface of the release film [manufactured by Lintec Corporation, trade name “PET381031”] by the knife coating method and dried at 90 ° C. for 1 minute. A pressure sensitive adhesive sheet was prepared. The thickness of this pressure sensitive adhesive layer was 3.2 μm. The pressure-sensitive adhesive layer of the obtained pressure-sensitive adhesive sheet was pressure-bonded onto the optical recording layer using two rubber rollers to obtain a sheet for producing an optical recording medium.

Example 5
The preparation of the peeling assisting layer preparation coating solution was changed as follows, and the optical recording layer preparation coating solution and the pressure sensitive adhesive layer preparation coating solution were the same as in Example 1 for optical recording. A sheet for producing a medium was produced.
<Preparation of a coating liquid for preparing a peeling assist layer>
100 g of methyl ethyl ketone and xylylene diisocyanate cross-linking agent for 100 g of acrylic thermosetting resin having fluorine atoms [trade name “FA-300G-EA”, solid content 30% by mass, manufactured by Sanwa Laboratory Co., Ltd.] [Soken Chemical Co., Ltd., trade name “TD-75”, solid content concentration 75 mass%] 4 g was added and stirred to obtain a coating solution.
<Sheet for optical recording medium production>
As a process film, a release auxiliary layer preparation coating solution is applied to one side of a release film [trade name “PET38AL-5” manufactured by Lintec Corporation] having an alkyd release agent layer by a gravure coating method, 90 Heat curing was performed at 1 ° C. for 1 minute to form a peeling auxiliary layer having a thickness of 3.5 μm. A coating liquid for producing an optical recording layer was applied to the surface of the obtained peeling assist layer by a gravure coating method and dried at 90 ° C. for 1 minute to form an optical recording layer. The thickness of the obtained optical recording layer was 600 nm. Next, the pressure-sensitive adhesive layer preparation coating solution was applied to the release surface of the release film [manufactured by Lintec Corporation, trade name “PET381031”] by the knife coating method and dried at 90 ° C. for 1 minute. A pressure sensitive adhesive sheet was prepared. The thickness of this pressure sensitive adhesive layer was 10.5 μm. The pressure-sensitive adhesive layer of the obtained pressure-sensitive adhesive sheet was pressure-bonded onto the optical recording layer using two rubber rollers to obtain a sheet for producing an optical recording medium.

Example 6
The preparation of the peeling assisting layer preparation coating liquid was changed as follows, and the optical recording layer preparation coating liquid and the pressure sensitive adhesive layer preparation coating liquid were the same as those used in Example 4 for optical recording. A sheet for producing a medium was produced.
<Preparation of a coating liquid for preparing a peeling assist layer>
Acryloxyethyl isocyanate is added (2-hydroxy) to an acrylate ester copolymer composed of trifluoroethyl methacrylate and 2-hydroxyethyl methacrylate (trifluoroethyl methacrylate: 2-hydroxyethyl methacrylate = 95: 5 (mass ratio)). 25 g of an ultraviolet curable compound (weight average molecular weight 20000) having a polymerizable double bond in the side chain obtained by adding to 90 mol% of the hydroxyl group of ethyl methacrylate), an ultraviolet curable polyfunctional acrylate compound [Shin Nakamura Chemical Co., Ltd. ( Co., Ltd., trade name “NK Ester A-TMMT”] 25 g, solvent, methyl ethyl ketone 50 g, photopolymerization initiator 1-hydroxycyclohexyl phenyl ketone [Ciba Specialty Chemicals, trade name “Irgacure 184” ]] 1.5g was mixed and the coating liquid with a solid content concentration of 50 mass% was prepared.
<Preparation of optical recording medium manufacturing sheet>
As a process film, a 50 μm thick polyethylene terephthalate film [manufactured by Toyobo Co., Ltd., trade name “PET50A-4100”] is coated with a coating liquid for preparing a peeling assist layer by a gravure coating method, and 90 ° C. The film was dried for 1 minute, and a polyethylene terephthalate film [trade name “PET50A-4100” manufactured by Toyobo Co., Ltd.] having a thickness of 50 μm was pressure-bonded thereon using two rubber rollers, and an ultraviolet irradiation device [GS Yuasa Co., Ltd.]. Lighting Co., Ltd., trade name "UVSYSTEM CSN2-40"] quantity 500 mJ / cm ² in a nitrogen atmosphere using a peeling assist layer illuminance 120 mW / cm thickness was irradiated with ultraviolet in ^two conditions 6.6μm Formed. The pressure-bonded polyethylene terephthalate film was peeled off, and a coating liquid for producing an optical recording layer was applied to the surface of the obtained peeling auxiliary layer by a gravure coating method and dried at 90 ° C. for 1 minute. The thickness of the obtained optical recording layer was 50 nm. Next, the pressure-sensitive adhesive layer preparation coating solution was applied to the release surface of the release film [manufactured by Lintec Corporation, trade name “PET381031”] by the knife coating method and dried at 90 ° C. for 1 minute. A pressure sensitive adhesive sheet was prepared. The thickness of this pressure sensitive adhesive layer was 3.2 μm. The pressure-sensitive adhesive layer of the obtained pressure-sensitive adhesive sheet was pressure-bonded onto the optical recording layer using two rubber rollers to obtain a sheet for producing an optical recording medium.

Example 7
The preparation of the peeling assisting layer preparation coating liquid was changed as follows, and the optical recording layer preparation coating liquid and the pressure sensitive adhesive layer preparation coating liquid were the same as those used in Example 4 for optical recording. A sheet for producing a medium was produced.
<Preparation of a coating liquid for preparing a peeling assist layer>
40 g of an ultraviolet curable compound having a bisphenol A skeleton [manufactured by Shin-Nakamura Chemical Co., Ltd., trade name “NK Ester A-BPE-4”] and an ultraviolet curable compound [manufactured by Shin-Nakamura Chemical Co., Ltd., trade name "NK ester A-GLY-3EO"] 10 g, methyl ethyl ketone 50 g as a solvent, [Ciba Specialty Chemicals, trade name "Irgacure 184"] 1.5 g as a photopolymerization initiator, and a solid content concentration of 50 g are mixed. A mass% coating solution was prepared.
<Preparation of optical recording medium manufacturing sheet>
As a process film, a 50 μm thick polyethylene terephthalate film [manufactured by Toyobo Co., Ltd., trade name “PET50A-4100”] is coated with a coating liquid for preparing a peeling assist layer by a gravure coating method, and 90 ° C. For 1 minute, and then pressure-bonded using a polyethylene terephthalate film having a thickness of 50 μm (trade name “PET50A-4100” manufactured by Toyobo Co., Ltd.) with two rubber rollers, and an ultraviolet irradiation device [GS Yuasa Co., Ltd.]. Lighting Co., Ltd., trade name "UVSYSTEM CSN2-40"] quantity 500 mJ / cm ² in a nitrogen atmosphere using a peeling assist layer illuminance 120 mW / cm thickness was irradiated with ultraviolet in ^two conditions 6.1μm Formed. The pressure-bonded polyethylene terephthalate film was peeled off, and a coating liquid for producing an optical recording layer was applied to the surface of the obtained peeling auxiliary layer by a gravure coating method and dried at 90 ° C. for 1 minute. The thickness of the obtained optical recording layer was 100 nm. Next, the pressure-sensitive adhesive layer preparation coating solution was applied to the release surface of the release film [manufactured by Lintec Corporation, trade name “PET381031”] by the knife coating method and dried at 90 ° C. for 1 minute. A pressure sensitive adhesive sheet was prepared. The thickness of this pressure sensitive adhesive layer was 3.2 μm. The pressure-sensitive adhesive layer of the obtained pressure-sensitive adhesive sheet was pressure-bonded onto the optical recording layer using two rubber rollers to obtain an optical recording medium manufacturing sheet.

Example 8
Using the same coating solution as in Example 2, an optical recording medium production sheet was produced as follows.
<Preparation of optical recording medium manufacturing sheet>
As a process film, a 50 μm thick polyethylene terephthalate film [manufactured by Toyobo Co., Ltd., trade name “PET50A-4100”] is coated with a coating liquid for preparing a peeling assist layer by a gravure coating method, and 1 at 90 ° C. The film was dried for 4 minutes to form a peeling auxiliary layer having a thickness of 0.4 μm. A coating liquid for producing an optical recording layer was applied to the surface of the obtained peeling assist layer by a gravure coating method and dried at 90 ° C. for 1 minute to form an optical recording layer. The thickness of the obtained optical recording layer was 80 nm. On the surface of the obtained optical recording layer, a coating liquid for preparing a peeling auxiliary layer is applied by a gravure coating method and dried at 90 ° C. for 1 minute to form a peeling auxiliary layer having a thickness of 0.4 μm. A coating solution for preparing an optical recording layer was applied to the surface of the auxiliary layer by a gravure coating method and dried at 90 ° C. for 1 minute to form an optical recording layer. The thickness of the obtained optical recording layer was 80 nm. Next, the pressure-sensitive adhesive layer preparation coating solution was applied to the release surface of the release film [manufactured by Lintec Corporation, trade name “PET381031”] by the knife coating method and dried at 90 ° C. for 1 minute. A pressure sensitive adhesive sheet was prepared. The thickness of this pressure sensitive adhesive layer was 10.5 μm. The pressure-sensitive adhesive layer of the obtained pressure-sensitive adhesive sheet is pressure-bonded onto the optical recording layer using two rubber rollers, and on the process film, a peeling auxiliary layer, an optical recording layer, a peeling auxiliary layer, an optical recording A multilayer optical recording medium manufacturing sheet having a structure in which a layer and a pressure-sensitive adhesive were laminated was obtained.

Comparative Example 1
A sheet for producing an optical recording medium was produced in the same manner as in Example 4 except that the optical recording layer was directly formed on the process film without forming the peeling assist layer.

Comparative Example 2
The preparation of the peeling assisting layer preparation coating liquid was changed as follows, and the optical recording layer preparation coating liquid and the pressure sensitive adhesive layer preparation coating liquid were the same as those used in Example 4 for optical recording. A sheet for producing a medium was produced.
<Preparation of a coating liquid for preparing a peeling assist layer>
An ultraviolet curable compound having a fluorene skeleton [manufactured by Osaka Gas Chemical Co., Ltd., trade name “Ogsol EA-F5003”] 45 g, and an ultraviolet curable compound [Shin Nakamura Chemical Co., Ltd., trade name “NK Ester A-GLY” -3EO "] 5 g, 50 g of methyl ethyl ketone as a solvent, 1.5 g of 1-hydroxycyclohexyl phenyl ketone [manufactured by Ciba Specialty Chemicals, Inc., trade name" Irgacure 184 "] as a photopolymerization initiator, and a solid content concentration of 50 g A mass% coating solution was prepared.
<Preparation of optical recording medium manufacturing sheet>
As a process film, a coating solution for preparing a peeling assist layer was applied on one side of a polyethylene terephthalate film having a thickness of 50 μm [trade name “PET50A-4100” manufactured by Toyobo Co., Ltd.] by a gravure coating method. For 1 minute, and then pressure-bonded using a polyethylene terephthalate film having a thickness of 50 μm (trade name “PET50A-4100” manufactured by Toyobo Co., Ltd.) with two rubber rollers, and an ultraviolet irradiation device [GS Yuasa Co., Ltd. Lighting Co., forming a trade name "UVSYSTEM CSN2-40"] peeling auxiliary layer having a thickness of 7.0μm light quantity 500 mJ / cm ^2, the ultraviolet under the conditions of illuminance of 120 mW / cm ² was irradiated under a nitrogen atmosphere using a did. One polyethylene terephthalate film was peeled off, and a coating liquid for preparing an optical recording layer was applied to the surface of the obtained peeling auxiliary layer by a gravure coating method and dried at 90 ° C. for 1 minute. The thickness of the obtained optical recording layer was 200 nm. The pressure-sensitive adhesive layer preparation coating solution is applied to the release surface of the release film [manufactured by Lintec Corporation, trade name “PET381031”] by the knife coat method, and dried at 90 ° C. for 1 minute to make pressure-sensitive adhesive. A sheet was produced. The thickness of this pressure sensitive adhesive layer was 3.2 μm. The pressure-sensitive adhesive layer of the obtained pressure-sensitive adhesive sheet was pressure-bonded onto the optical recording layer using two rubber rollers to obtain a sheet for producing an optical recording medium.
Regarding the optical recording medium manufacturing sheets obtained in Examples 1 to 8 and Comparative Examples 1 and 2, the material type of each layer is shown in Table 1, and the thickness and refractive index of each layer are shown in Table 2.

[note]
1) UV curable compound: “NK Ester A-NPG” manufactured by Shin-Nakamura Chemical Co., Ltd.
2) Polyvinyl alcohol: “GOHSENOL T-350” manufactured by Nippon Synthetic Chemical Industry Co., Ltd.
3) Cycloolefin resin: “Topass 5013” manufactured by Polyplastics Co., Ltd.
4) Triacetylcellulose: “LT-105” manufactured by Daicel Chemical Industries, Ltd.
5) Fluorine-based thermosetting resin: “FA-300G-EA” manufactured by Sanwa Laboratory Co., Ltd.
6) Fluorine-based UV-curable compound: UV-curing having a polymerizable double bond in the side chain obtained by adding acryloxyethyl isocyanate to an acrylate copolymer comprising trifluoroethyl methacrylate and 2-hydroxyethyl methacrylate 7) UV curable compound: Shin-Nakamura Chemical Co., Ltd., trade name “NK Ester A-BPE-4” and new Nakamura Chemical Co., Ltd., trade name “NK Ester A-GLY-3EO” 8) UV curable compound: Osaka Gas Chemical Co., Ltd., trade name “Ogsol EA-F5003” and Shin-Nakamura Chemical ( 9) Dye material A: 1,1-bis [4- [N, N-di (P-tolyl)], a mixture of trade name “NK ester A-GLY-3EO” Mino] phenyl] cyclohexane 10) BA: n-butyl acrylate 11) PEA: phenoxyethyl acrylate 12) HEA: hydroxyethyl acrylate 13) AA: Acrylic acid

Examples 9 to 16 and Comparative Example 3
The optical recording medium production sheets obtained in Examples 1 to 8 and Comparative Example 2 were laminated by the following methods to produce multilayer optical recording media of Examples 9 to 16 and Comparative Example 3. The optical recording medium manufacturing sheet of Comparative Example 1 was unable to produce a multilayer optical recording medium because the optical recording layer was broken when the process film was peeled from the optical recording layer.
(1) The release film of the optical recording medium production sheet is peeled off and attached to a glass substrate as a support through the exposed pressure-sensitive adhesive layer.
(2) The process film is peeled off to expose the peeling auxiliary layer.
(3) The release film of another optical recording medium production sheet is peeled off, and laminated on the auxiliary peeling layer exposed in (2) above via a pressure sensitive adhesive layer.
(4) The above operations (2) and (3) are repeated to produce a laminate having 20 optical recording layers.
(5) A light-transmitting protective film made of a polyvinyl alcohol film (thickness: 10 μm) is laminated on the peeling auxiliary layer exposed by peeling off the final process film via an adhesive layer (thickness: 20 μm), and 20 A multilayer optical recording medium having a single optical recording layer. In addition, the polyvinyl alcohol film apply | coats the aqueous solution (concentration 10 mass%) of polyvinyl alcohol [The Nippon Gosei Chemical Co., Ltd. make, brand name "Gosenol T-350"] to the process film used in Example 2, and is 100 degreeC. And prepared by drying for 2 minutes. Moreover, the same thing as the adhesive used in order to manufacture the sheet | seat for optical recording medium manufacture of each Example or a comparative example was used for the adhesive which forms an adhesive layer.
Various characteristics of the multilayer optical recording medium thus obtained were determined. The peel strength of the used optical recording medium manufacturing sheet is shown in Table 3, and the absolute value (Δn) of the refractive index difference between the peeling auxiliary layer and the pressure-sensitive adhesive layer of the multilayer optical recording medium, the reflected light intensity ratio, and the recording The characteristics are shown in Table 4.

As shown in Table 3, the sheets for producing multilayer optical recording media of Examples 1 to 8 had an appropriate peeling force. On the other hand, in the multilayer optical recording medium manufacturing sheet of Comparative Example 1, when the process film was peeled off, the optical recording layer was broken.
As shown in Table 4, the multilayer optical recording media of Examples 9 to 16 have a large intensity ratio of 1, and it is easy to determine the reflected light from the interface between the optical recording layer and the pressure-sensitive adhesive layer. . Further, the value of the intensity ratio 2 is 0.2 to 0.9, and the reflected light from the optical recording layer in the deep part of the optical recording medium can be sufficiently recognized.

 The multilayer optical recording medium manufacturing sheet of the present invention can easily produce a multilayer optical recording medium having an optical recording layer having a thickness of 1000 nm or less, has high reflection strength, high recording density, and good It is possible to provide a multilayer optical recording medium having excellent recording characteristics.

1, 1a, 1b, 1-1, 1-2, 1-3, 1-n optical recording layer 2, 2a, 2b, 2-1, 2-2, 2-3, 2-n peeling auxiliary layer 3, 3a, 3-1, 3-2, 3-3, 3-n Pressure sensitive adhesive layer 4 Process film 5 Release film 6 Base material 7 Protective film 15 Sheet for multilayer optical recording medium production 20 Sheet for multilayer optical recording medium production 30 Multilayer optical recording medium

Claims (8)

A sheet for producing a multilayer optical recording medium having a repetitive structure in which a plurality of optical recording layers are laminated , and having at least a peeling auxiliary layer and a thickness of 1 on a process film having peeling properties with respect to the peeling auxiliary layer It has a unit including an optical recording layer of ~ 1000 nm and a pressure sensitive adhesive layer, the peeling assisting layer is provided on the surface of the process film, and the pressure sensitive adhesive layer is disposed on the outermost layer. and, and multilayer optical recording medium-producing sheet, characterized in that at a wavelength of 660 nm, the absolute value of the refractive index difference between said peeling auxiliary layer and the pressure-sensitive adhesive layer is 0.11 or less.   The sheet for producing a multilayer optical recording medium according to claim 1, wherein the absolute value of the difference in refractive index between the peeling assist layer and the pressure-sensitive adhesive layer at a wavelength of 405 nm is 0.11 or less.   The sheet for producing a multilayer optical recording medium according to claim 1, wherein the peeling assist layer has a refractive index of 1.42 to 1.60 at a wavelength of 660 nm. The multilayer optical recording medium manufacturing sheet according to any one of claims 1 to 3, wherein the optical recording layer has a thickness of 1 to 80 nm . The multilayer optical recording medium manufacturing sheet according to any one of claims 1 to 4, wherein the material constituting the peeling assisting layer contains a cured product of an energy curable compound. 6. The energy curable compound is at least one selected from an energy curable oligomer, an energy curable monomer, or an energy ray curable polymer having a polymerizable double bond in a side chain. A multilayer optical recording medium manufacturing sheet. The sheet for producing a multilayer optical recording medium according to any one of claims 1 to 6 , wherein the optical recording layer is a multiphoton absorbing material. Multilayer optical recording medium, characterized in that obtained by using the multilayer optical recording medium-producing sheet according to any one of claims 1-7.

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