JP2007101743A - Composition for optical recording, optical recording medium, optical recording method and optical recording apparatus - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a composition for hologram recording having high sensitivity and capable of high multiple recording, a hologram type optical recording medium capable of achieving high multiple recoding of interference figures formed by information light and reference light, and an optical recording method and an optical recording apparatus using the optical recording medium. <P>SOLUTION: The composition for optical recording contains a polymerizable monomer having a functional group capable of forming a hydrogen bond, and an ethylenic double bond, and a matrix polymer formed by mixing a prepolymer having terminal isocyanate groups and a polyol. <P>COPYRIGHT: (C)2007,JPO&INPIT

Description

  The present invention is an optical recording medium that is used for an optical recording medium that records information using holography, has high sensitivity, and is capable of high-multiplex recording, and an optical recording medium using the optical recording composition The present invention relates to an optical recording method and an optical recording apparatus.

  An optical recording medium is one of recording media capable of writing a large amount of information such as high-density image data. As this optical recording medium, for example, a rewritable optical recording medium such as a magneto-optical disk and a phase change optical disk and a write-once optical recording medium such as a CD-R have already been put into practical use. The demand for larger capacity is increasing. However, all conventionally proposed optical recording media are two-dimensional recording, and there is a limit to increasing the recording capacity. Therefore, recently, a hologram type optical recording medium capable of recording information three-dimensionally has attracted attention.

In the hologram type optical recording method, in general, information light provided with a two-dimensional intensity distribution and reference light having a substantially constant intensity are superimposed on a photosensitive recording layer to form them. Information is recorded by generating a distribution of optical characteristics inside the recording layer using the interference image. On the other hand, in reading (reproducing) the written information, the recording layer is irradiated with only the reference light in the same arrangement as in recording, and the reproducing light having an intensity distribution corresponding to the optical characteristic distribution formed inside the recording layer is used. This is done by emitting from the recording layer.
In this hologram type optical recording method, since the optical characteristic distribution is three-dimensionally formed in the recording layer, an area where information is written by one information light, an area where information is written by other information light, and Can be partially overlapped, that is, multiple recording is possible. When digital volume holography is used, the signal-to-noise ratio (S / N ratio) of one spot is extremely high, so that the original information can be faithfully reproduced even if the S / N ratio is somewhat lowered by overwriting. As a result, the number of times of multiple recording reaches several hundreds, and the recording capacity of the optical recording medium can be remarkably increased (see Patent Document 1).
As an optical recording composition used for such a hologram type optical recording medium, for example, a radical polymerization monomer, a binder polymer, a photo radical polymerization initiator, and a sensitizing dye are the main components. One using a difference in refractive index is known (see Patent Document 2). In this material, when the photosensitive composition formed into a film is subjected to interference exposure, radical polymerization is started in a portion where light is strong, and accordingly, a concentration gradient of radical polymerization monomer is formed, from a portion where light is weak to a portion where light is strong. The diffusion transfer of the radical polymerization monomer occurs. As a result, the density of the radical polymerization monomer can be increased or decreased according to the intensity of the interference light, which appears as a difference in refractive index.
Further, as other examples of photosensitive compositions for volume holograms, those containing polymer matrix precursors such as NCO-terminated prepolymers and polyols, or bifunctional epoxides and tetrafunctional mercaptans are known. In this case, these polymer matrix precursors are deposited at a predetermined thickness between two substrates, and then the precursors are reacted to form a polymer matrix to produce a hologram recording medium without using solvent coating. (See Patent Document 3). Hologram recording is achieved by subjecting the hologram recording medium thus produced to interference exposure.

As a feature of hologram recording, it has the property that it can be written twice or more by changing the incident angle, incident position, wavelength, etc. of one recording spot by coherent light such as laser light.
For such hologram recording, diffusion of the polymerizable monomer is important along with the polymerization reaction of the polymerizable monomer. Therefore, in order to diffuse the polymerizable monomer efficiently, the polymer matrix is designed to have a low Tg (see Non-Patent Document 1). However, when the Tg of the polymer matrix is lowered, there is a problem that the polymer of the polymerizable monomer tends to move and the hologram recording is easily lost over time.

On the other hand, it is known that a low molecular weight compound having either a sulfonamide group or a phenolic hydroxyl group plasticizes a urethane / urea matrix (Patent Document 4). However, this document does not disclose any optical recording composition.
Accordingly, a hologram recording composition having high sensitivity and capable of high multiplex recording, and a hologram type light capable of achieving high multiplex recording of interference images formed by information light and reference light with high sensitivity. At present, no satisfactory recording medium, optical recording method and optical recording apparatus using the optical recording medium have been provided.

JP 2002-123949 A JP-A-6-43634 US Pat. No. 6,482,551 Japanese Patent Publication No. 6-55546 J. et al. Appl. Phys. 81 (9), 5913 (1997)

  An object of the present invention is to solve the conventional problems and achieve the following objects. That is, the present invention is highly sensitive and capable of high multiplex recording, and is a composition for hologram recording, and is highly sensitive and can achieve high multiplex recording of interference images formed by information light and reference light. It is an object of the present invention to provide a hologram type optical recording medium, an optical recording method and an optical recording apparatus using the optical recording medium.

  As a result of intensive studies in view of the above problems, the present inventors have obtained the following knowledge. That is, a matrix having a high glass transition temperature (Tg) is originally used by introducing a polymerizable monomer having a functional group capable of forming a hydrogen bond into a matrix polymer composed of a prepolymer having an isocyanate group at its terminal and a polyol. However, it is a finding that diffusion of the polymerizable monomer is likely to occur, and high sensitivity and high multiplex recording are possible.

Means for solving the problems are as follows. That is,
<1> A functional group capable of forming a hydrogen bond, a polymerizable monomer having an ethylenic double bond, a prepolymer having an isocyanate group at the terminal, and a matrix polymer formed by mixing a polyol, This is an optical recording composition.
<2> The optical recording composition according to <1>, wherein the functional group capable of forming a hydrogen bond and the polymerizable monomer having an ethylenic double bond are represented by the following general formula (1).

(PX) _m -G- (A) _n General formula (1)

In Formula (1), P _{is, CH 2 = CH-, CH 2} = C (CH 3) -, CH 2 = CH-COO-L-, CH 2 = C (CH 3) -COO-L- _{, CH 2 = CH-CONHR-} L-, and CH ₂ = C (CH ₃₎ represents either -CONHR-L-a. L represents any one of an alkylene group, an arylene group, and an aralkylene group. R represents a hydrogen atom, an alkyl group, or an aryl group. X represents one of a single bond, —O—, —COO—, —O—CO—, —CONH—, and —NHCO—. A represents a functional group that forms a hydrogen bond. m and n may be the same as or different from each other, and represent an integer of 1 to 3. G represents an m + n-valent organic group having 1 to 50 carbon atoms.
<3> Functional groups capable of forming hydrogen bonds include hydroxyl group, sulfonylamide group, sulfamoyl group, acylamino group, carbamoyl group, alkoxycarbonylamino group, aryloxycarbonylamino group, aminocarbonyloxy group, ureido group, amino group, carboxyl The composition for optical recording according to any one of <1> to <2>, wherein the composition is any one of a group and a sulfo group.
<4> The above-mentioned <1, wherein the content of the polymerizable monomer having a functional group capable of forming a hydrogen bond and an ethylenic double bond is 3 to 45% by mass with respect to the total solid content of the optical recording composition. > To <3>, the optical recording composition.

<5> An optical recording medium comprising a recording layer containing the optical recording composition according to any one of <1> to <4>.
<6> The optical recording medium according to <5>, including a first substrate, a recording layer, a filter layer, and a second substrate in this order.
<7> The optical recording medium according to any one of <5> to <6>, wherein the filter layer transmits the first light and reflects the second light.

<8> Irradiating the optical recording medium according to any one of <5> to <7> with information light and reference light having coherence, and forming an interference image with the information light and the reference light, An interference recording image is recorded on the optical recording medium.
<9> An optical recording medium is irradiated with the information light and the reference light so that the optical axis of the information light and the optical axis of the reference light are coaxial, and is generated by interference between the information light and the reference light. The optical recording method according to <8>, wherein the interference image is recorded on the optical recording medium.

<10> Irradiating the coherent information light and reference light to the optical recording medium according to any one of <5> to <7>, and forming an interference image by the information light and the reference light, An interference recording image is recorded on the optical recording medium.

  ADVANTAGE OF THE INVENTION According to the present invention, various problems in the prior art can be solved, the composition for hologram recording is highly sensitive and capable of high multiplex recording, and the highly sensitive interference image formed by information light and reference light is highly multiplexed. It is possible to provide a hologram type optical recording medium capable of recording, an optical recording method and an optical recording apparatus using the optical recording medium. The principle of the present invention can be used not only for high multiplex recording but also for a single type optical recording medium.

(Optical recording composition)
The optical recording composition of the present invention is a matrix polymer formed by mixing a functional group capable of forming a hydrogen bond and a polymerizable monomer having an ethylenic double bond, a prepolymer having an isocyanate group at its terminal, and a polyol. The composition for optical recording characterized by including these. The optical recording composition of the present invention may contain a polymerizable monomer, a photopolymerization initiator, and other compounds as necessary.
The optical recording of the present invention is optical recording using multiplex recording. However, the principle of the present invention can also be used for single-recording optical recording.

<Polymerizable monomer having a functional group capable of forming a hydrogen bond and having an ethylenic double bond>
The functional group capable of forming a hydrogen bond is preferably a functional group having a hydrogen bond donating ability, a functional group having a hydrogen bond accepting ability, or a functional group having both of them. There may be one functional group capable of forming a hydrogen bond in the molecule of the polymerizable monomer, or two or more functional groups.
It is preferable that the functional group having hydrogen bond donating ability mainly donates hydrogen to the carbonyl oxygen atom of the urethane bond, and the functional group having hydrogen bond accepting ability mainly accepts the N—H hydrogen atom of the urethane bond. It is preferable.
The hydrogen bond donating ability is determined by R.I. W. Parameter α and hydrogen bond acceptability determined by Taft et al. Can be expressed by parameter β.
The parameter α is preferably 0.4 to 1.51, and more preferably 0.7 to 1.2.
The parameter β is preferably 0.3 to 1.05, and more preferably 0.5 to 0.9.

  Examples of functional groups capable of forming hydrogen bonds include hydroxyl groups, sulfonylamide groups, sulfamoyl groups, acylamino groups, carbamoyl groups, alkoxycarbonylamino groups, aryloxycarbonylamino groups, aminocarbonyloxy groups, ureido groups, amino groups, and carboxyl groups. Group, sulfo group and the like. Among these, a hydroxyl group, a sulfonylamide group, a sulfamoyl group, an acylamino group, a carbamoyl group, an alkoxycarbonylamino group, an aryloxycarbonylamino group, an aminocarbonyloxy group, and a ureido group are preferable.

Examples of the sulfonylamide group include an N-alkylsulfonylamide group and an N-arylsulfonylamide group.
The alkyl group of the N-alkylsulfonylamide group may have a substituent, and examples of the substituent include a halogen atom, an aryl group, an alkoxy group, an alkylthio group, an acyl group, and a cyano group. .
The aryl group of the N-arylsulfonylamide group may have a substituent, and examples of the substituent include a halogen atom, an alkyl group, an alkoxy group, an alkylthio group, an acyl group, and a cyano group.
As the sulfonylamide, an N-alkylsulfonylamide group having 1 to 20 carbon atoms, an N-arylsulfonyl group having 6 to 30 carbon atoms, and the like are preferable.
Examples of the N-alkylsulfonylamide group having 1 to 20 carbon atoms include a methylsulfonylamide group, an ethylsulfonylamide group, a propylsulfonylamide group, an isopropylsulfonylamide group, a butylsulfonylamide group, a hexylsulfonylamide group, and a cyclohexylsulfonyl group. Examples include an amide group, an octylsulfonylamide group, a 2-ethylhexylsulfonylamide group, a decanoylsulfonylamide group, a dodecanoylsulfonylamide group, an octadecanoylsulfonylamide group, a cyanomethylsulfonylamide group, and a trifluoromethanesulfonylamide group.
Examples of the arylsulfonyl group having 6 to 30 carbon atoms include phenylsulfonyl group, 1-naphthylsulfonyl group, 2-naphthylsulfonyl group, 2-chlorophenylsulfonyl group, 2-methylphenylsulfonyl group, and 2-methoxyphenylsulfonyl. Group, 2-butoxyphenylsulfonyl group, 3-bromophenylsulfonyl group, 2,4-dibromophenylsulfonyl group, 3-trifluoromethylphenylsulfonyl group, 3-cyanophenylsulfonyl group, 3- (2-ethylhexyloxy) phenyl Sulfonyl group, 3-nitrophenylsulfonyl group, 4-fluorophenylsulfonyl group, 4-cyanophenylsulfonyl group, 4-butoxyphenylsulfonyl group, 4- (2-ethylhexyloxy) phenylsulfonyl group, 4-octade Le phenylsulfonyl group and the like.

Examples of the sulfamoyl group include a sulfamoyl group, an N-alkylsulfamoyl group, an N-arylsulfamoyl group, an N, N-dialkylsulfamoyl group, an N, N-diarylsulfamoyl group, and an N-alkyl. -N-arylsulfamoyl group etc. are mentioned.
The sulfamoyl group having a substituent preferably has 1 to 30 carbon atoms.
Examples of the sulfamoyl group having a substituent having 1 to 30 carbon atoms include N-methylsulfamoyl group, N-ethylsulfamoyl group, N-propylsulfamoyl group, N-butylsulfamoyl group, N -Hexylsulfamoyl group, N-cyclohexylsulfamoyl group, N-octylsulfamoyl group, N- (2-ethylhexyl) sulfamoyl group, N-decylsulfamoyl group, N-octadecylsulfamoyl group, N -Phenylsulfamoyl group, N- (2-methylphenyl) sulfamoyl group, N- (2-chlorophenyl) sulfamoyl group, N- (2-methoxyphenyl) sulfamoyl group, N- (2-isopropoxyphenyl) sulfamoyl group , N- (2- (2-ethylhexyloxy) phenyl) sulfamoyl group, N- 3-chlorophenyl) sulfamoyl group, N- (3-nitrophenyl) sulfamoyl group, N- (3-cyanophenyl) sulfamoyl group, N- (4-methoxyphenyl) sulfamoyl group, N- (4- (2-ethylhexyloxy) ) Phenyl) sulfamoyl group, N- (4-cyanophenyl) sulfamoyl group, N-methyl-N-phenylsulfamoyl group, N, N-dimethylsulfamoyl group, N, N-dibutylsulfamoyl group, N , N-diphenylsulfamoyl group, N, N-di (2-ethylhexyl) sulfamoyl group and the like.

The acylamino group is a branched or straight chain acylamino group, may be substituted with a substituent, may be aliphatic, or may be aromatic. 2-30 are preferable and, as for carbon number of the said acylamino group, 2-20 are more preferable.
As the substituent, for example, a halogen atom, an alkyl group, an aryl group, an alkenyl group, an alkoxy group, an alkoxycarbonyl group, and a carbamoyl group are preferable. Such acylamino groups include acetylamino, 2-ethylhexanoylamino, benzoylamino, trifluoroacetylamino, 4-fluorobenzoylamino, 4-bromobenzoylamino, biphenylcarbonylamino, butenoylamino, methoxyacetylamino, 4-octyl Examples include oxybenzoylamino, 4-methoxycarbonylbenzoylamino, 4-N-butylcarbamoylbenzoylamino, N-methyl-N-acetylamino and the like.

Examples of the carbamoyl group include a carbamoyl group, an N-alkylcarbamoyl group, an N-arylcarbamoyl group, an N, N-dialkylcarbamoyl group, an N, N-diarylcarbamoyl group, and an N-alkyl-N-arylcarbamoyl group. Can be mentioned.
The carbamoyl group having a substituent preferably has 2 to 30 carbon atoms.
Examples of the carbamoyl group having a substituent having 2 to 30 carbon atoms include N-methylcarbamoyl group, N-ethylcarbamoyl group, N-propylcarbamoyl group, N-butylcarbamoyl group, N-hexylcarbamoyl group, and N-cyclohexyl. Carbamoyl group, N-octylcarbamoyl group, N-2-ethylhexylcarbamoyl group, N-decylcarbamoyl group, N-octadecylcarbamoyl group, N-phenylcarbamoyl group, N- (2-methylphenyl) carbamoyl group, N- (2 -Chlorophenyl) carbamoyl group, N- (2-methoxyphenyl) carbamoyl group, N- (2-isopropoxyphenyl) carbamoyl group, N- (2- (2-ethylhexyloxy) phenyl) carbamoyl group, N- (3- Chlorophenyl) carbamoyl group, -(3-nitrophenyl) carbamoyl group, N- (3-cyanophenyl) carbamoyl group, N- (4-methoxyphenyl) carbamoyl group, N- (4- (2-ethylhexyloxy) phenyl) carbamoyl group, N- (4-cyanophenyl) carbamoyl group, N-methyl-N-phenylcarbamoyl group, N, N-dimethylcarbamoyl group, N, N-dibutylcarbamoyl group, N, N-diphenylcarbamoyl group, N-toluenesulfonylcarbamoyl group, N-hexylsulfonylcarbamoyl group etc. are mentioned.

The alkoxycarbonylamino group may have a substituent, and examples of the substituent include a halogen atom, an aryl group, an alkoxy group, and an alkylthio group.
The alkoxycarbonylamino group preferably has 2 to 20 carbon atoms.
Examples of the alkoxycarbonylamino group having 2 to 20 carbon atoms include methoxycarbonylamino group, ethoxycarbonylamino group, propoxycarbonylamino group, butoxycarbonylamino group, hexyloxycarbonylamino group, 2-ethylhexyloxycarbonylamino group, octyl Oxycarbonylamino group, decyloxycarbonylamino group, octadecyloxycarbonylamino group, phenyloxyethyloxycarbonylamino group, phenyloxypropyloxycarbonylamino group, 2,4-di-t-amylphenyloxyethylcarbonylamino group, 2 , 6-di-t-butyl-4-methylcyclohexyloxycarbonylamino group, isostearyloxycarbonylamino group, and the like.

  The aryloxycarbonylamino group may have a substituent, and examples of the substituent include a halogen atom, an alkyl group, an alkoxy group, and an alkylthio group. In addition, an aryloxycarbonylamino group having 7 to 30 carbon atoms is preferable, for example, 2-methylphenyloxycarbonylamino group, 2-chlorophenyloxycarbonylamino group, 2,6-dimethylphenyloxycarbonylamino group, 2,4 , 6-trimethylphenyloxycarbonylamino group, 2-methoxyphenyloxycarbonylamino group, 2-butoxyphenyloxycarbonylamino group, 3-cyanophenyloxycarbonylamino group, 3-nitrophenyloxycarbonylamino group, 2- (2 -Ethylhexyl) phenyloxycarbonylamino group, 3- (2-ethylhexyloxy) phenyloxycarbonylamino group, 4-fluorophenyloxycarbonylamino group, 4-chlorophenyloxycarbonylamino group 3,4-dibromophenyl aryloxycarbonylamino group, 4-cyanophenyl aryloxycarbonylamino group, such as 4-butoxy phenyloxycarbonylamino group.

Examples of the aminocarbonyloxy group include an aminocarbonyloxy group, an N-alkylaminocarbonyloxy group, an N-arylaminocarbonyloxy group, an N, N-dialkylaminocarbonyloxy group, and an N, N-diarylaminocarbonyloxy group. , N-alkyl-N-arylaminocarbonyloxy group.
The aminocarbonyloxy group having a substituent preferably has 1 to 30 carbon atoms.
Examples of the aminocarbonyloxy group having a substituent having 1 to 30 carbon atoms include an N-propylaminocarbonyloxy group, an N-isopropylaminocarbonyloxy group, an N-butylaminocarbonyloxy group, and an N-hexylaminocarbonyloxy group. N-cyclohexylaminocarbonyloxy group, N-octylaminocarbonyloxy group, N- (2-ethylhexyl) aminocarbonyloxy group, N-benzylaminocarbonyloxy group, N-phenylaminocarbonyloxy group, N- (2- Methylphenyl) aminocarbonyloxy group, N- (2-chlorophenyl) aminocarbonyloxy group, N- (2-methoxyphenyl) aminocarbonyloxy group, N- (2-isopropoxyphenyl) aminocarbonyloxy group, N- ( 3-ku Rofeniru) aminocarbonyl group, N-(4-methoxyphenyl) aminocarbonyl group, N-(4-cyanophenyl) amino carbonyl group, and the like.

Examples of the ureido group include ureido group, N′-alkylureido group, N′-arylureido group, N, N′-dialkylureido group, N, N′-diarylureido group, N-alkyl-N′-. An arylureido group and an N-aryl-N′-alkylureido group can be mentioned.
The ureido group having a substituent preferably has 1 to 30 carbon atoms.
Examples of the ureido group having a substituent having 1 to 30 carbon atoms include N′-propylureido group, N′-isopropylureido group, N′-butylureido group, N′-cyclohexylureido group, and N′-octylureido. Group, N ′-(2-ethylhexyl) ureido group, N′-benzylureido group, N′-propylureido group, N′-propylureido group, N′-propylureido group, N′-propylureido group, N ′ -Phenylureido group, N '-(2-methylphenyl) ureido group, N'-(2-chlorophenyl) ureido group, N '-(3-bromophenyl) ureido group, N'-(2-methoxyphenyl) ureido Group, N ′-(4-cyanophenyl) ureido group, N, N′-dibutylureido group, N-butyl-N′-methylureido group, N, N′-diphenylureido group, - phenyl -N '- (2-bromophenyl) ureido group, N- cyclohexyl -N'- phenylureido group, etc. N- phenyl -N'- methylureido group.

Examples of the amino group include an amino group, an N-alkylamino group, an N-arylamino group, an N, N-dialkylamino group, an N, N-diarylamino group, and an N-alkyl-N-arylamino group. It is done.
The amino group having a substituent preferably has 1 to 30 carbon atoms.
Examples of the amino group having a substituent having 1 to 30 carbon atoms include N-methylamino group, N-ethylamino group, N-propylamino group, N-isopropylamino group, N-tert-butylamino group, N -Hexylamino group, N-cyclohexylamino group, N-octylamino group, N- (2-ethylhexyl) amino group, N-decylamino group, N-octadecylamino group, N-benzylamino group, N-phenylamino group, N- (2-methylphenyl) amino group, N- (2-chlorophenyl) amino group, N- (2-methoxyphenyl) amino group, N- (2-isopropoxyphenyl) amino group, N- (2- ( 2-ethylhexyloxy) phenyl) amino group, N- (3-chlorophenyl) amino group, N- (3-nitrophenyl) amino group, N- (3- Anophenyl) amino group, N- (4-methoxyphenyl) amino group, N- (4- (2-ethylhexyloxy) phenyl) amino group, N- (4-cyanophenyl) amino group, N-methyl-N-phenyl Amino group, N, N-dimethylamino group, N, N-dibutylamino group, N, N-diphenylamino group and the like can be mentioned.

  The ethylenic double bond is not particularly limited and may be appropriately selected depending on the purpose. For example, the ethylenic double bond may be monofunctional or polyfunctional. The polyfunctional means that having at least two polymerizable ethylenic double bonds in the molecule of the polymerizable monomer.

The polymerizable monomer having a functional group capable of forming a hydrogen bond and having an ethylenic double bond has a functional group capable of forming a hydrogen bond and an ethylenic double bond as described above. Other portions are not particularly limited, but for example, those having a structure represented by the following general formula (1) are preferable.

(PX) _m -G- (A) _n General formula (1)

In Formula (1), P _{is, CH 2 = CH-, CH 2} = C (CH 3) -, CH 2 = CH-COO-L-, CH 2 = C (CH 3) -COO-L- _{, CH 2 = CH-CONHR-} L-, and CH ₂ = C (CH ₃₎ represents either -CONHR-L-a. L represents any one of an alkylene group, an arylene group, and an aralkylene group. R represents a hydrogen atom, an alkyl group, or an aryl group. X represents one of a single bond, —O—, —COO—, —O—CO—, —CONH—, and —NHCO—. A represents a functional group that forms a hydrogen bond. m and n may be the same as or different from each other, and represent an integer of 1 to 3. G represents an m + n-valent organic group having 1 to 50 carbon atoms.

The P is preferably CH ₂ = CH-, CH ₂ = CH-COO-L-, CH ₂ = C (CH ₃ ) -COO-L-, CH ₂ = CH-CONHR-L-, and among these, _{CH 2 = CH-, CH 2 =} CH-COO-L-, CH 2 = CH-CONHR-L- is more preferable.

When R is an alkyl group, the alkyl group is preferably an alkyl group having 1 to 20 carbon atoms, and more preferably an alkyl group having 1 to 12 carbon atoms. These may be substituted with a substituent. Examples of the substituent include a halogen atom, an aryl group, an alkoxy group, and an alkylthio group.
When R is an aryl group, an aryl group having 6 to 20 carbon atoms is preferable, and an alkyl group having 6 to 12 carbon atoms is more preferable. These may be substituted with a substituent. Examples of the substituent include a halogen atom, an alkyl group, an alkoxy group, and an alkylthio group.
R is preferably a hydrogen atom or an alkyl group.

式（１） When said L is an alkylene group, a C1-C20 alkylene group is preferable and a C1-C8 alkylene group is more preferable. These may be substituted with a substituent. Examples of the substituent include a halogen atom, an alkoxy group, an aryl group, and an alkenyl group.
One carbon atom or two or more carbon atoms not adjacent to each other in the alkylene group may be replaced with an oxygen atom or a sulfur atom. Examples of such an alkylene group include a methylene group, an ethylene group, a butylene group, a 1-methyl-ethylene group, — (CH ₂ ) ₂ O (CH ₂ ) ₂ — and the like.
When L is an arylene group, an arylene group having 6 to 20 carbon atoms is preferable, and an arylene group having 6 to 12 carbon atoms is more preferable. These may be substituted with a substituent. Examples of the substituent include a halogen atom, an alkyl group, an alkoxy group, and an alkylthio group.
Examples of the arylene group include 1,4-phenylene group, 1,3-phenylene group, 2-bromo-1,4-phenylene group, 2,6-dibromo-1,4-phenylene group, 4-butoxy- 1,2-phenylene group, 3-methylthio-1,5-phenylene group, naphthalene-2,6-di-yl group and the like can be mentioned.
When L is an aralkylene group, an aralkylene group having 8 to 20 carbon atoms is preferable, and an aralkylene group having 8 to 15 carbon atoms is more preferable. These may be substituted with a substituent. Examples of the substituent include a halogen atom, an alkoxy group, and an alkylthio group.
As the aralkylene group, for example, an aralkylene group represented by the following formula (1) is preferable.

Formula (1)

  L is preferably an alkylene group or an arylene group, and more preferably an alkylene group.

  X is preferably a single bond, —O—, —COO—, or —CONH—, and more preferably a single bond or —O—.

  A is preferably a hydroxyl group, a sulfonamide group, a sulfamoyl group, an acylamino group, a carbamoyl group, an amino group, a carboxyl group or a sulfo group, more preferably a hydroxyl group, a sulfonamide group, a sulfamoyl group, an acylamino group or a carbamoyl group. The explanation of these substituents is the same as the explanation of the functional group capable of forming a hydrogen bond.

The value of m is preferably 1. When the value of m is 2 or more, P-L-X may represent different groups.
The value of n is preferably 1. When the value of n is 2 or more, A may represent a different group.
The value of m + n is preferably 4 or less, and more preferably 2.

式（２）
Examples of the organic group having 1 to 50 carbon atoms of G include a divalent organic group, a trivalent organic group, and a tetravalent organic group. In these, a C1-C30 bivalent organic group, a trivalent organic group, and a tetravalent organic group are preferable.
The divalent organic group is preferably an alkylene group or an arylene group, and more preferably an arylene group.
The trivalent organic group is preferably an alkanetriyl group or an arenetriyl group, and more preferably an arenetriyl group.
The tetravalent organic group is preferably an alkanetetrayl group or an arenetetrayl group, and more preferably an arenetetrayl group.
The alkylene group is a linear or branched alkylene group, and may be substituted with a substituent. As the substituent, a halogen atom, an aryl group, an alkenyl group, an alkoxy group, an aryloxy, an alkoxycarbonyl group, and an aryloxycarbonyl group are preferable. Among these, a halogen atom and an aryl group are more preferable.
The alkylene group preferably has 1 to 30 carbon atoms, and more preferably 1 to 20 carbon atoms.
The alkylene chain of the alkylene group may have divalent functional groups so as not to be adjacent to each other. The divalent functional group is preferably —O—, —S—, —COO—, or —O—CO—, and more preferably —O—.
Either an arylene group or an alkenylene group may be present in the alkylene chain of the alkyl group or at one end of the alkylene chain, and among these, an arylene group is preferable.
As said alkylene group, the alkylene group of following formula (2) is mentioned, for example.

Formula (2)

式（３）
The arylene group preferably has 6 to 30 carbon atoms, and more preferably 6 to 20 carbon atoms. These may be substituted with a substituent. The substituent is preferably a halogen atom, an alkyl group, an alkenyl group, an alkoxy group, an aryloxy, an alkylthio group, an alkoxycarbonyl group, or an aryloxycarbonyl group. Among these, a halogen atom, an alkoxy group, or an alkylthio group is more preferable.
The arylene chain of the arylene group may have a divalent functional group so as not to be adjacent to each other. The divalent functional group is preferably —O—, —S—, —COO—, or —O—CO—, and more preferably —O—.
As said arylene group, the arylene group of following formula (3) is mentioned, for example.

Formula (3)

式（４）
The alkanetriyl group is a linear or branched alkanetriyl group and may be substituted with a substituent. As the substituent, a halogen atom, an aryl group, an alkenyl group, an alkoxy group, an aryloxy, an alkoxycarbonyl group, and an aryloxycarbonyl group are preferable. Among these, a halogen atom and an aryl group are more preferable.
The alkanetriyl group preferably has 1 to 30 carbon atoms, and more preferably 1 to 20 carbon atoms.
In the alkanetriyl chain of the alkanetriyl group, divalent functional groups may be provided so as not to be adjacent to each other. The divalent functional group is preferably —O—, —S—, —COO—, or —O—CO—, and more preferably —O—.
Either an arylene group or an alkenylene group may be present in either the alkanetriyl chain of the alkanetriyl group or one end of the alkanetriyl chain, and among these, an arylene group may be present. preferable.
As said alkanetriyl group, the alkanetriyl group represented by following formula (4) is mentioned, for example.

Formula (4)

式（５）
The arenetriyl group may be substituted with a substituent. As the substituent, a halogen atom, an alkyl group, an alkenyl group, an alkoxy group, an aryloxy group, an alkylthio group, an alkoxycarbonyl group, and an aryloxycarbonyl group are preferable, and among these, a halogen atom, an alkoxy group, and an alkylthio group are more preferable. .
The arenetriyl group preferably has 6 to 30 carbon atoms, and more preferably 6 to 20 carbon atoms.
In the arenetriyl chain of the arenetriyl group, divalent functional groups may be provided so as not to be adjacent to each other. The divalent functional group is preferably —O—, —S—, —COO—, or —O—CO—, and more preferably —O—.
Examples of the arenetriyl group include an arenetriyl group represented by the following formula (5).

Formula (5)

式（６）
The alkanetetrayl group is a linear or branched alkanetetrayl group and may be substituted with a substituent. As the substituent, a halogen atom, an aryl group, an alkenyl group, an alkoxy group, an aryloxy, an alkoxycarbonyl group, and an aryloxycarbonyl group are preferable, and among these, a halogen atom and an aryl group are more preferable.
The alkanetetrayl group preferably has 1 to 20 carbon atoms.
The alkanetetrayl chain of the alkanetetrayl group may have divalent functional groups so as not to be adjacent to each other. The divalent functional group is preferably —O—, —S—, —COO—, or —O—CO—, and more preferably —O—.
Either an arylene group or an alkenylene group may be present in either the alkanetetrayl chain of the alkanetetrayl group or one end of the alkanetetrayl chain, and among these, an arylene group is preferred. .
As said alkanetetrayl group, the alkanetetrayl group represented by following formula (6) is mentioned, for example.

Formula (6)

式（７）
The arenetetrayl group may be substituted with a substituent. As the substituent, a halogen atom, an alkyl group, an alkenyl group, an alkoxy group, an aryloxy, an alkylthio group, an alkoxycarbonyl group, and an aryloxycarbonyl group are preferable. Among these, a halogen atom, an alkoxy group, and an alkylthio group are more preferable. .
The arenetetrayl group preferably has 6 to 30 carbon atoms, and more preferably 6 to 20 carbon atoms.
In the arenetetrayl chain of the arenetetrayl group, divalent functional groups may be provided so as not to be adjacent to each other. The divalent functional group is preferably —O—, —S—, —COO—, or —O—CO—, and more preferably —O—.
Examples of the arenetetrayl group include an arenetetrayl group represented by the following formula (7).

Formula (7)

式（８）

式（９）

式（１０） Examples of the polymerizable monomer having a functional group capable of forming a hydrogen bond and having an ethylenic double bond include 3-chloro-4-hydroxybenzoate vinylphenethyl ester, 3-chloro-4-hydroxy Benzoic acid- (2-acryloyloxyethyl) ester, 3-chloro-4-hydroxybenzoic acid- (2-methacryloyloxyethyl) ester, 3-chloro-4-hydroxybenzoic acid- (4-acryloyloxybutyl) ester, Examples include 3-chloro-4-hydroxybenzoic acid- (6-acryloyloxyhexyl) ester, β-acryloxyethoxyphenol, hydroxystyrenesulfonic acid-N-ethylamide, methacrylamidepropanesulfonylamide, acrylamidepropanesulfonylamide, and the like. Moreover, what is shown to the following formula | equation (8)-(10) (No.1-1 to 1-22, No.2-1 to 2-6, No.3-1 to 3-4) is also mentioned.

Formula (8)

Formula (9)

Formula (10)

  The content of the functional group capable of forming a hydrogen bond and the polymerizable monomer having an ethylenic double bond in the optical recording composition is preferably 3 to 45% by mass in the solid content of the total recording composition, 4-25 mass% is more preferable. When the content of the polymerizable monomer is less than 3% by mass, sufficient sensitivity may not be obtained. When the content exceeds 45% by mass, the Tg of the matrix is too low to obtain a sufficient recorded image. Sometimes.

<Matrix polymer formed by mixing prepolymer having terminal isocyanate group and polyol>
-Prepolymer having an isocyanate group at the end-
The prepolymer having an isocyanate group at the end is a polyfunctional isocyanate having two or more isocyanate groups in the molecule.
As a prepolymer which has the said isocyanate group at the terminal, the compound which has two isocyanate groups in the molecule | numerator of a prepolymer is mentioned, for example.
Examples of the compound having two isocyanate groups include m-phenylene diisocyanate, p-phenylene diisocyanate, 2,6-tolylene diisocyanate, 2,4-tolylene diisocyanate, naphthalene-1,4-diisocyanate, diphenylmethane- 4,4′-diisocyanate, 3,3′-dimethoxy-biphenyl diisocyanate, 3,3′-dimethyldiphenylmethane-4,4′-diisocyanate, xylylene-1,4-diisocyanate, xylylene-1,3-diisocyanate, 4- Chloroxylylene-1,3-diisocyanate, 2-methylxylylene-1,3-diisocyanate, 4,4′-diphenylpropane diisocyanate, 4,4′-diphenylhexafluoropropane diisocyanate, trimethyl Diisocyanate, hexamethylene diisocyanate, propylene-1,2-diisocyanate, butylene-1,2-diisocyanate, cyclohexylene-1,2-diisocyanate, cyclohexylene-1,3-diisocyanate, cyclohexylene-1,4-diisocyanate, Examples include dicyclohexylmethane-4,4′-diisocyanate, 1,4-bis (isocyanatemethyl) cyclohexane and 1,3-bis (isocyanatemethyl) cyclohexane, isophorone diisocyanate, and lysine diisocyanate.
In addition, examples of the prepolymer having an isocyanate group at the terminal include an addition reaction product of the compound having the two isocyanate groups, a bifunctional alcohol such as ethylene glycols and bisphenols, and a phenol. .
Moreover, as a prepolymer which has the said isocyanate group at the terminal, the compound which has a 3 or more polyfunctional isocyanate group is mentioned, for example.
Moreover, as a prepolymer which has the said isocyanate group at the terminal, the compound which has a polyfunctional isocyanate group other than the compound which has the said two isocyanate groups is mentioned.
Examples of the compound having a polyfunctional isocyanate group include, for example, a trimer (burette or isocyanurate) using a compound having two isocyanate groups as a main raw material, a polyol such as trimethylolpropane, and the bifunctional compound. Examples include adducts with isocyanate compounds, formalin condensates of benzene isocyanate, polymers of isocyanate compounds having a polymerizable group such as methacryloyloxyethyl isocyanate, and lysine triisocyanate. Specifically, xylene diisocyanate and its hydrogenated product, hexamethylene diisocyanate, tolylene diisocyanate and its hydrogenated product are trimer compounds (burette or isosinurate), or trimethylolpropane and 2 A polyfunctional compound which is an adduct with a functional isocyanate compound is preferred. These compounds are described in “Polyurethane Resin Handbook” (edited by Keiji Iwata, published by Nikkan Kogyo Shimbun (1987)).

-Polyol-
A polyol is a compound having a bifunctional or higher functional hydroxyl group having at least one of an alkylene chain, an arylene chain, a polyether chain, a polyester chain, and a polysiloxane chain.
As the polyol, a diol, triol or tetraol having a molecular weight of 60 to 10,000 is preferable, and a diol or triol having a molecular weight of 100 to 5,000 is more preferable.
Examples of the alkylene chain include ethylene, hexamethylene, decamethylene, and the like.
Examples of the polyether chain include polyethylene oxide, polypropylene oxide, polytetramethylene oxide, polystyrene oxide, polycyclohexylene oxide, poly (ethylene thioglycol), and copolymers thereof.
As said polyester chain, the polyester which has a hydroxyl group at the terminal is mentioned, for example. Examples of the polyester having a hydroxyl group at the terminal include compounds represented by the following general formula (3) or (4).

H— (O—R ⁶ —OCO—R ⁷ —CO) n —R ⁶ —OH General Formula (3)

In the general formula (3), R ⁶ represents a diol residue. R ⁷ represents a dicarboxylic acid residue. n represents a positive integer.

HO— (R ⁸ —CO—O) m —R ⁹ — (O—CO—R ⁸ ) 1 —OH General formula (4)

In the general formula (4), R ⁸ represents any of a cyclic ester residue, a hydroxycarboxylic acid residue, and a hydroxyester residue. R ⁹ represents a diol residue. The values of m and l may be the same or different from each other, and represent a positive integer.
As said polysiloxane, the polydimethylsiloxane derivative etc. which have a hydroxyl group at the terminal are mentioned, for example.
Examples of the polyol include polyethylene oxide, polypropylene oxide, polytetramethylene oxide diol, triol, tetraol, polyester in which R ⁶ is alkylene and R ⁷ is alkylene in the general formula (3), and the general formula (4). In which R ⁸ is alkylene (for example, polycaprolactone) is preferred.
It is preferable that the polyol does not contain moisture. An additive such as a high-temperature vacuum distillation treatment or a water removing agent can be used to prevent water from remaining in the polyol before use.

The matrix polymer is formed by a polymerization reaction of a material containing the isocyanate-terminated prepolymer and the polyol.
When a catalyst is used for the polymerization reaction, examples of the catalyst include a tin catalyst, a nitrogen-containing heterocycle, and an amine.
Examples of the tin catalyst include dimethyl dilaurate tin, dibutyl dilactate tin, stannous octoate, and the like.
Examples of the nitrogen-containing heterocycle include imidazole, pyridine, pyrazole and the like.
Examples of the amine include triethylamine, trioctylamine, N-methylmorpholine, and the like.

  The matrix polymer can be used by appropriately selecting an appropriate compound according to the purpose, in addition to a polymer formed by a polymerization reaction of a material containing the isocyanate-terminated prepolymer and the polyol, For example, a copolymer of an unsaturated acid such as (meth) acrylic acid or itaconic acid and an alkyl (meth) acrylate, phenyl (meth) acrylate, benzyl (meth) acrylate, styrene, α-methylstyrene, etc. Polymer of alkyl methacrylate and alkyl acrylate represented by polymethyl methacrylate; copolymer of alkyl (meth) acrylate and acrylonitrile, vinyl chloride, vinylidene chloride, styrene, etc .; acrylonitrile and vinyl chloride or vinylidene chloride Copolymers with: Cellulos having a carboxyl group in the side chain Polyethylene oxide; Polyvinyl pyrrolidone; Novolak resin obtained by condensation reaction of any one selected from phenol, o-cresol, m-cresol, p-cresol and xylenol with any one of aldehyde and acetone A polyether of epichlorohydroline and bisphenol A; a soluble nylon; a polyvinylidene chloride; a chlorinated polyolefin; a copolymer of vinyl chloride and vinyl acetate; a polymer of vinyl acetate; a copolymer of acrylonitrile and styrene; Copolymer of acrylonitrile and butadiene and styrene; polyvinyl alkyl ether; polyvinyl alkyl ketone; polystyrene; polyurethane; polyethylene terephthalate isophthalate; acetyl cellulose; Scan; acetyl butoxy cellulose; nitrocellulose; celluloid, polyvinyl butyral, epoxy resins, melamine resins, formalin resins; organosiloxane polymers. These may be used alone or in combination of two or more.

  The content of the matrix polymer in the optical recording composition is preferably 50 to 97% by mass, and more preferably 70 to 95% by mass in the solid content of the entire recording composition.

-Analysis-
The method for analyzing the polymerizable monomer having a functional group capable of forming a hydrogen bond and having an ethylenic double bond and the polymer matrix is not particularly limited and can be appropriately selected depending on the purpose. For example, mass spectrometry by various gas chromatography (GC), mass analysis by liquid chromatography, mass analysis by gel permeation chromatography, Fourier transform infrared spectroscopic analysis, micro Raman spectroscopic analysis, organic trace element analysis (C, H, N) ), Micro-infrared spectroscopic analysis, nuclear magnetic resonance spectrum, gas chromatography, ultraviolet-visible spectroscopic spectrum and the like. Among these, analysis of a polymerizable monomer having a functional group capable of forming a hydrogen bond and having an ethylenic double bond is preferably performed by nuclear magnetic resonance spectrum or gas chromatography, and analysis of a polymer matrix is performed. It is preferably carried out by Fourier transform infrared spectroscopy.

<Polymerizable monomer>
As the polymerizable monomer, in addition to the functional group capable of forming a hydrogen bond and a polymerizable polymer having an ethylenic double bond, polymerization having no functional group capable of forming an appropriate hydrogen bond depending on the purpose For example, phenoxyethyl acrylate, isobornyl acrylate, 2-ethylhexyl acrylate, 1,6-hexanediol acrylate, neopentyl glycol PO-modified diacrylate, 1,9-nonanediol acrylate, EO-modified bisphenol A diacrylate, polyethylene glycol diacrylate, pentaerythritol tetraacrylate, EO-modified glycerol triacrylate, EO-modified trimethylolpropane triacrylate, 2-naphth-1-oxyethyl acrylate, (Trimethylsilyloxy) dimethylsilylpropyl acrylate, vinyl-1-naphthoate, N-vinylcarbazole, 2,4,6-tribromophenyl acrylate, pentabromophenyl acrylate, phenylthioethyl acrylate, tetrahydrofurfuryl acrylate, styrene, etc. It is done. These monomers may be monofunctional or polyfunctional. Moreover, what utilized the photocrosslinking reaction may be used.
When the polymerizable monomer having no functional group capable of forming a hydrogen bond is used, the content in the recording composition is preferably 3 to 40% by mass in the solid content of the total polymerizable monomer, and 5 to 20%. The mass% is more preferable.

<Photopolymerization initiator>
The photopolymerization initiator is not particularly limited as long as it has sensitivity to recording light and causes a radical polymerization reaction by light irradiation, and can be appropriately selected according to the purpose. , 2′-bis (o-chlorophenyl) -4,4′5,5′-tetraphenyl-1,1′-biimidazole, 2,4,6-tris (trichloromethyl) -1,3,5-triazine 2,4-bis (trichloromethyl) -6- (p-methoxyphenylvinyl) -1,3,5-triazine, benzoin, 2-hydroxy-2-methyl-1-phenylpropan-2-one, benzophenone, Thioxanthone, 2,4,6-trimethylbenzoyldiphenylacylphosphine oxide, triphenylbutyl borate tetratyl ammonium, bis (η-5-2,4-cyclope Ntadien-1-yl) bis [2,6-difluoro-3- (1H-pyrrol-1-yl)] phenyltitanium, a light-absorbing part described in JP-A-2005-49608 and an active part that generates free radicals. Examples thereof include compounds possessed in the molecule. Among these, 2,2′-bis (o-chlorophenyl) -4,4′5,5′-tetraphenyl-1,1′-biimidazole, triphenylbutyl borate tetratyl ammonium, bis (η-5 2,4-cyclopentadien-1-yl) bis [2,6-difluoro-3- (1H-pyrrol-1-yl)] phenyltitanium is preferred. These may be used alone or in combination of two or more. Moreover, you may use a sensitizing dye together as a sensitizer according to the wavelength of the light to irradiate. The content of the photopolymerization initiator in the recording composition is preferably 0.3 to 4% by mass and more preferably 0.5 to 3% by mass in the solid content of the entire recording composition.

Examples of the sensitizing dye include “Research Disclosure, Vol. 200, December 1980, Item 20036” and “sensitizer” (p.160-p.163, Kodansha; Katsumi Tokumaru, Nobu Okawara, edited by 1987. ) And the like can be used.
Specific examples of the spectral sensitizing dyes include 3-ketocoumarin compounds described in JP-A No. 58-15603, thiopyrylium salts described in JP-A No. 58-40302, JP-B No. 59-28328, The naphthothiazole merocyanine compound described in JP-A-60-53300, the merocyanine compound described in JP-B-61-9621, JP-A-62-2842, JP-A-59-89303, and JP-A-60-60104 Can be mentioned.
Further, the dyes described in “Chemicals of Functional Dyes” (1981, CMC Publishing Co., p.393 to p.416), “Coloring Materials” (60 [4] 212-224 (1987)), and the like are also included. Specific examples include cationic methine dyes, cationic carbonium dyes, cationic quinoneimine dyes, cationic indoline dyes, and cationic styryl dyes.
Further, coumarin (including ketocoumarin or sulfonocoumarin) dyes, melostyryl dyes, oxonol dyes, hemioxonol dyes, and other keto dyes; non-ketopolymethine dyes, triarylmethane dyes, xanthene dyes, anthracene dyes, rhodamine dyes, acridine dyes Non-keto dyes such as dyes, aniline dyes, azo dyes; non-ketopolymethine dyes such as azomethine dyes, cyanine dyes, carbocyanine dyes, dicarbocyanine dyes, tricarbocyanine dyes, hemicyanine dyes, styryl dyes; azine dyes, oxazine dyes, Quinoneimine dyes such as thiazine dyes, quinoline dyes, and thiazole dyes are also included in the spectral sensitizing dyes. The spectral sensitizing dyes may be used alone or in combination of two or more.
The content of the sensitizing dye in the recording composition is preferably 0.3 to 4% by mass, and more preferably 0.5 to 3% by mass in the solid content of the entire recording composition.

Examples of sensitizing dyes include “Research Disclosure, Vol. 200, December 1980, Item 20036” and “sensitizer” (p.160-p.163, Kodansha; Katsumi Tokumaru and Nobu Okawara, edited by 1987). The known compounds described in the above can be used.
Specific examples of the spectral sensitizing dyes include 3-ketocoumarin compounds described in JP-A No. 58-15603, thiopyrylium salts described in JP-A No. 58-40302, JP-B No. 59-28328, The naphthothiazole merocyanine compound described in JP-A-60-53300, the merocyanine compound described in JP-B-61-9621, JP-A-62-2842, JP-A-59-89303, and JP-A-60-60104 Can be mentioned.
Further, the dyes described in “Functional dye chemistry” (1981, CMC Publishing Co., p.393 to p.416), “Coloring materials” (60 [4] 212-224 (1987)), and the like are also included. Specific examples include cationic methine dyes, cationic carbonium dyes, cationic quinoneimine dyes, cationic indoline dyes, and cationic styryl dyes.
In addition, coumarin (including ketocoumarin or sulfonocoumarin) dyes, melostyryl dyes, oxonol dyes, hemioxonol dyes and other keto dyes; non-ketopolymethine dyes, triarylmethane dyes, xanthene dyes, anthracene dyes, rhodamine dyes, acridine dyes Non-keto dyes such as dyes, aniline dyes, azo dyes; non-ketopolymethine dyes such as azomethine dyes, cyanine dyes, carbocyanine dyes, dicarbocyanine dyes, tricarbocyanine dyes, hemicyanine dyes, styryl dyes; azine dyes, oxazine dyes, Quinoneimine dyes such as thiazine dyes, quinoline dyes and thiazole dyes are also included in the spectral sensitizing dyes. The spectral sensitizing dyes may be used alone or in combination of two or more. These sensitizers may also be bonded to a part of the binder.
The content of the sensitizing dye in the recording composition is preferably 0.3 to 4% by mass, and more preferably 0.5 to 3% by mass in the solid content of the entire recording composition.

<Other compounds>
The other compound is not particularly limited and may be appropriately selected depending on the purpose. For example, a photopolymerization inhibitor and an antioxidant may be added to improve storage stability. .
The polymerization inhibitor and the antioxidant are not particularly limited and may be appropriately selected depending on the intended purpose. Examples thereof include hydroquinone, p-benzoquinone, hydroquinone monomethyl ether, 2,6-ditertiary-butyl-p-cresol. 2,2′-methylenebis (4-methyl-6-tert-butylphenol), trifel phosphite, trisnonylphenyl phosphite, phenothiazine, N-isopropyl-N′-phenyl-p-phenylenediamine, and the like. Among these, 2,6-ditertiary-butyl-p-cresol and 2,2′-methylenebis (4-methyl-6-tertiary-butylphenol) are preferable. These may be used alone or in combination of two or more.
As the usage-amount of the said polymerization inhibitor and antioxidant, within 3 mass% is preferable with respect to the whole quantity of the monomer used for a composition. When the amount used exceeds 3% by mass, the polymerization reaction may be slow, and in some cases, the polymerization may not be performed.
Moreover, a photothermal conversion material can also be contained for the purpose of improving the sensitivity of the optical recording composition. As the photothermal conversion material, the description in Japanese Patent Application No. 2005-84780 can be referred to.
Furthermore, in order to relieve the volume change during polymerization, a component that diffuses in the direction opposite to the polymerization component may be added, or a compound having an acid cleavage structure may be added separately in addition to the polymer.

(Optical recording medium, optical recording method, and optical recording apparatus)
The optical recording medium of the present invention is an optical recording medium having, on a support, the recording layer of the present invention for recording information using holography and other layers appropriately selected as necessary.
The optical recording medium of the present invention may be a relatively thin planar hologram for recording information such as two dimensions, or a volume hologram for recording a large amount of information such as a three-dimensional image, and is either a transmission type or a reflection type. Also good. The hologram recording method may be any, for example, an amplitude hologram, a phase hologram, a blazed hologram, a complex amplitude hologram, or the like.
The optical recording method and optical recording apparatus of the present invention are a method and apparatus for recording and reproducing the optical recording medium of the present invention.
The optical recording method and optical recording apparatus of the present invention are not particularly limited and may be appropriately selected depending on the intended purpose. For example, U.S. Pat. Nos. 5,719,691 and 5,838,467 are applicable. No. 6,163,391, 6,414,296, U.S. Patent Application Publication No. 2002-136143, JP-A-2000-98862, 2000-2988837 No. 2001, No. 2001-23169, No. 2002-83431, No. 2002-123949, No. 2002-123948, No. 2003-43904, No. 2004-171611, International Publication No. 99 / Optical recordings described in the 57719 pamphlet, the 02/05270 pamphlet, the 02/75727 pamphlet, etc. Method, such as an optical recording apparatus.

  The optical recording medium of the present invention comprises a first mode used for recording a general hologram in which a recording layer is laminated on at least one support and information light and reference light are irradiated from different directions, and information Irradiation of light and reference light is used in a collinear method in which the optical axis of the information light and the optical axis of the reference light are coaxial, a first substrate, a second substrate, and the Examples thereof include a second form having a recording layer on the second substrate and a filter layer between the second substrate and the recording layer. Hereinafter, the first embodiment and the second embodiment will be described in order.

≪First form≫
The first embodiment is used for a general hologram recording method, and the layer structure is not particularly limited and can be appropriately selected according to the purpose. For example, the recording layer is a single layer on a support. Alternatively, as shown in FIG. 1, the recording layer 41 is sandwiched between the supports 42 and 43, and the antireflection layers 44 and 45 are formed on the outermost layers of the supports 42 and 43, respectively. Examples include layer structure.
Further, a gas barrier layer or the like may be formed between the recording layer 41 and the support 42 and between the recording layer 41 and the support 43. Further, a protective layer or the like may be provided on the surfaces of the antireflection layers 44 and 45.

-Information light and reference light-
The information light and the reference light are not particularly limited and may be appropriately selected according to the purpose. For example, a coherent laser beam emitted from a light source is preferable.
There is no restriction | limiting in particular as said laser beam, According to the objective, it can select suitably, For example, the laser beam etc. which consist of 1 or more types of wavelengths selected from 360-850 nm are mentioned. The wavelength is preferably 380 to 800 nm, more preferably 400 to 750 nm, and most preferably 500 to 600 nm where the center of the visible region is most visible.
When the wavelength is less than 360 nm, a clear stereoscopic image may not be obtained. When the wavelength is greater than 850 nm, the interference fringes may be fine, and a corresponding photosensitive material may not be obtained.

  The light source of the laser light is not particularly limited and may be appropriately selected depending on the intended purpose. For example, a solid-state laser light oscillator, a blue region semiconductor laser light oscillator, a liquid laser light oscillator, a gas laser light such as argon Examples thereof include an oscillator, a He-Cd laser oscillator, a frequency doubled YAG laser oscillator, a He-Ne laser oscillator, and a Kr laser oscillator. Among these, a gas laser light oscillator, a semiconductor laser light oscillator in the blue region, and the like are preferable.

The irradiation method of the information light and the reference light is not particularly limited and can be appropriately selected depending on the purpose. For example, the information light is divided by dividing one laser light emitted from the same light source. The light and the reference light may be irradiated, or two laser beams emitted from different light sources may be irradiated.
There is no restriction | limiting in particular as an irradiation direction of the said information light and the said reference light, According to the objective, it can select suitably, For example, the said information light and the said reference light may be irradiated from a different direction, and are the same It may be irradiated in the direction. Further, it may be irradiated so as to be coaxial with the optical axis of the information light and the optical axis of the reference light.

-Fixing light-
The fixing light irradiation area is not particularly limited and may be appropriately selected depending on the purpose. For example, the fixing light irradiation area may be the same area as the recording target portion by the information light and the reference light at an arbitrary position of the recording layer. It is preferable that the region is wider than the outer extension of the portion to be recorded and extends at least 1 μm outside from the outer extension. When the fixing light is irradiated to the area exceeding 1 μm from the outside of the recording target portion, the adjacent recording area is also irradiated, resulting in excessive irradiation energy and inefficiency.

There is no restriction | limiting in particular as the irradiation time of the said fixing light, According to the objective, it can select suitably, For example, 1 ns-100 ms are preferable in the arbitrary locations of the said recording layer, and 1 ns-80 ms are more preferable. If the irradiation time is less than 1 ns, fixing may be insufficient, and if it exceeds 100 ms, irradiation with excessive energy occurs.
The irradiation direction of the fixing light is not particularly limited and may be appropriately selected depending on the purpose. For example, the direction may be the same as the information light and the reference light at any location of the recording layer, and may be different. Direction may be used. The irradiation angle is preferably 0 to 60 °, more preferably 0 to 40 ° with respect to the layer surface of the recording layer. If the irradiation angle is an angle other than the above, fixing may be inefficient.
There is no restriction | limiting in particular as a wavelength of the said fixing light, According to the objective, it can select suitably, For example, it is preferable that it is 350-850 nm in arbitrary places of the said recording layer, and is 400-600 nm. Is more preferable.
If the wavelength is less than 350 nm, the material may be decomposed, and if it exceeds 850 nm, the temperature may increase and the material may deteriorate.

The light source for the fixing light is not particularly limited and may be appropriately selected depending on the purpose. For example, it is preferable to irradiate incoherent light, such as a fluorescent lamp, a high-pressure mercury lamp, a xenon lamp, a light emitting diode, a coherent light. The light etc. which performed operation (for example, putting frosted glass in an optical path) which changes a phase to light at random are mentioned. Among these, light emitting diodes, light that has been subjected to an operation of randomly changing the phase to coherent light (for example, putting ground glass into the optical path), and the like are preferable.
There is no restriction | limiting in particular as irradiation amount of the said fixing light, According to the objective, it can select suitably, For example, it is preferable that it is 0.001-1J / cm < ² > in the arbitrary locations of the said recording layer, More preferably, it is 0.01-300 mJ / cm < ² >.

  The method for irradiating the fixing light is not particularly limited and may be appropriately selected depending on the purpose. For example, the fixing light is emitted from the same light source as the information light and the reference light at an arbitrary position of the recording layer You may irradiate light and you may irradiate the light radiate | emitted from a different light source.

<Recording layer>
The recording layer contains the recording composition of the present invention.

The recording layer includes at least a step of mixing the matrix precursor and the photoreactive monomer, a step of curing the mixture in the system to form a matrix, and further including other steps as necessary. Manufactured by the method.
The recording layer can be formed according to a known method depending on the material. For example, a vapor deposition method, a wet film formation method, an MBE (molecular beam epitaxy) method, a cluster ion beam method, a molecular lamination method, LB It can be suitably formed by a method, a printing method, a transfer method, or the like. Alternatively, the two-component urethane matrix forming method described in US Pat. No. 6,743,552 may be used.

  Formation of the recording layer by the wet film formation method can be suitably performed by using (coating and drying) a solution (coating liquid) in which the recording layer material is dissolved or dispersed in a solvent. The wet film forming method is not particularly limited and can be appropriately selected from known ones according to the purpose. For example, an ink jet method, a spin coating method, a kneader coating method, a bar coating method, a blade coating method, Examples thereof include a casting method, a dip method, and a curtain coating method.

There is no restriction | limiting in particular as thickness of the said recording layer, According to the objective, it can select suitably, 1-1,500 micrometers is preferable and 100-700 micrometers is more preferable.
When the thickness of the recording layer is within the preferable numerical range, a sufficient S / N ratio can be obtained even when 10-300 multiple shift multiplex recording is performed, and when the thickness is within the more preferable numerical range, this is remarkable. This is advantageous.

<Support>
The support is not particularly limited in shape, structure, size, etc., and can be appropriately selected according to the purpose. Examples of the shape include a disk shape, a card shape, a plate shape, and a sheet shape. The structure may be a single layer structure or a laminated structure, and the size may be appropriately selected according to the size of the optical recording medium. .

The material for the support is not particularly limited, and any of inorganic materials and organic materials can be suitably used. However, the optical strength of the optical recording medium can be ensured, and the light used for recording and reproduction can be used. In the case of the transmissive type in which the light enters through the substrate, it is necessary to be sufficiently transparent in the wavelength region of the light used.
Examples of the inorganic material include glass, quartz, silicon, and the like.
Examples of the organic material include acetate resins such as triacetyl cellulose, polyester resins, polyethersulfone resins, polysulfone resins, polycarbonate resins, polyamide resins, polyimide resins, polyolefin resins, and acrylic resins. Polynorbornene resin, cellulose resin, polyarylate resin, polystyrene resin, polyvinyl alcohol resin, polyvinyl chloride resin, polyvinylidene chloride resin, polyacrylic resin, polylactic acid resin, plastic film laminated paper And synthetic paper. These may be used alone or in combination of two or more. Among these, polycarbonate resins and acrylic resins are preferable from the viewpoints of moldability, optical characteristics, and cost.

As said support body, what was synthesize | combined suitably may be used and a commercial item may be used.
There is no restriction | limiting in particular as thickness of the said support body, According to the objective, it can select suitably, 0.1-5 mm is preferable and 0.3-2 mm is more preferable. If the thickness of the substrate is less than 0.1 mm, distortion of the shape during storage of the disk may not be suppressed. If the thickness exceeds 5 mm, the weight of the entire disk increases and is rotated by a drive motor or the like. In some cases, an excessive load may be applied.

≪Second form≫
The second form is an optical recording medium used in a collinear method in which the information light and the reference light are irradiated so that the optical axis of the information light and the optical axis of the reference light are coaxial. An optical recording medium having a first substrate, a second substrate, a recording layer of the present invention on the second substrate, and a filter layer between the second substrate and the recording layer. Can be mentioned.

-Optical recording method and reproduction method in the second embodiment-
In the optical recording method according to the second aspect, the optical recording medium is irradiated with information light and reference light as a coaxial light beam, and information is recorded on a recording layer by an interference pattern due to interference between the information light and the reference light. This is an optical recording method based on the method.

  The reproduction method is not particularly limited and can be appropriately selected depending on the purpose. For example, the interference image formed on the recording layer by the optical recording method is irradiated with the same light as the reference light to cause the interference. Record information corresponding to the image can be reproduced.

In the optical recording method and the reproducing method of the second embodiment, the information light provided with a two-dimensional intensity distribution and the information light and the reference light having a substantially constant intensity are superposed inside the photosensitive recording layer. Information is recorded by generating a distribution of optical characteristics inside the recording layer using an interference pattern formed by them. On the other hand, when reading (reproducing) written information, the recording layer is irradiated with only the reference light in the same arrangement as during recording, and the reproduction has an intensity distribution corresponding to the optical characteristic distribution formed inside the recording layer. Light is emitted from the recording layer as light.
Here, the optical recording method and the reproducing method according to the second embodiment are performed using an optical recording / reproducing apparatus described below.

An optical recording / reproducing apparatus used in the optical recording method and reproducing method will be described with reference to FIG.
FIG. 6 is an overall configuration diagram of the optical recording / reproducing apparatus according to the second embodiment. The optical recording / reproducing apparatus includes an optical recording apparatus and a reproducing apparatus.
The optical recording / reproducing apparatus 100 controls a spindle 81 to which the optical recording medium 22 is attached, a spindle motor 82 for rotating the spindle 81, and the spindle motor 82 so as to keep the rotational speed of the optical recording medium 22 at a predetermined value. A spindle servo circuit 83.
The optical recording / reproducing apparatus 100 records information by irradiating the optical recording medium 22 with information light and recording reference light, and irradiates the optical recording medium 22 with reproduction reference light to reproduce information. A pickup 31 for detecting light and reproducing information recorded on the optical recording medium 22 and a drive device 84 that enables the pickup 31 to move in the radial direction of the optical recording medium 22 are provided.

  The optical recording / reproducing apparatus 100 uses a detection circuit 85 for detecting a focus error signal FE, a tracking error signal TE, and a reproduction signal RF from an output signal of the pickup 31, and a focus error signal FE detected by the detection circuit 85. Based on this, the actuator in the pickup 31 is driven to move the objective lens (not shown) in the thickness direction of the optical recording medium 20 to perform focus servo, and the tracking error signal detected by the detection circuit 85. Based on TE, a tracking servo circuit 87 that drives the actuator in the pickup 31 to move the objective lens in the radial direction of the optical recording medium 22 to perform tracking servo, a tracking error signal TE, and a command from a controller to be described later. Drive 84 pickup 31 controls to move in the radial direction of the optical recording medium 22 and and a slide servo circuit 88 for performing slide servo.

The optical recording / reproducing apparatus 100 further decodes output data of a later-described CMOS or CCD array in the pickup 31 to reproduce data recorded in the data area of the optical recording medium 22 or reproduce from the detection circuit 85. A signal processing circuit 89 that reproduces a basic clock and discriminates an address from the signal RF, a controller 90 that controls the entire optical recording / reproducing apparatus 100, and an operation unit 91 that gives various instructions to the controller 90; It has.
The controller 90 inputs the basic clock and address information output from the signal processing circuit 89, and controls the pickup 31, spindle servo circuit 83, slide servo circuit 88, and the like. The spindle servo circuit 83 receives the basic clock output from the signal processing circuit 89. The controller 90 includes a CPU (Central Processing Unit), a ROM (Read Only Memory), and a RAM (Random Access Memory), and the CPU executes a program stored in the ROM using the RAM as a work area. The function of the controller 90 is realized.

  The optical recording / reproducing apparatus used in the optical recording method and reproducing method of the second aspect uses the optical recording medium of the present invention, and after recording interference fringes by information light and reference light, any recording layer Fixing exposure is performed at the spot, other means appropriately selected as necessary and sufficient fixing is performed, and an optical recording medium having a high density and high diffraction efficiency is obtained without affecting the sensitivity of the unrecorded portion. .

<Recording layer>
The recording layer contains the recording composition of the present invention.

<Filter layer>
The filter layer has a function of preventing the occurrence of noise by preventing irregular reflection from the reflection film of the optical recording medium by information light and reference light without causing a shift in the selective reflection wavelength even when the incident angle changes. . By laminating the filter layer on the optical recording medium, optical recording with high resolution and excellent diffraction efficiency can be obtained.
The function of the filter layer is preferably to transmit light having a first wavelength and reflect light having a second wavelength different from the light having the first wavelength, and the light having the first wavelength is 350 to 600 nm. It is preferable that the light of the second wavelength is 600 to 900 nm. For that purpose, it is preferable that the optical recording medium has a structure in which a recording layer, a filter layer, and a servo bit pattern are laminated in this order as viewed from the optical system side.
The filter layer has a light transmittance at 655 nm of 50% or more, preferably 80% or more, and a light reflectance at 532 nm of 30% or more and 40% or more at an incident angle of ± 40 °. Is preferred.
There is no restriction | limiting in particular as said filter layer, According to the objective, it can select suitably, For example, lamination | stacking of a dielectric vapor deposition layer, a single layer or two or more cholesteric liquid crystal layers, and also other layers as needed Formed by the body. Moreover, you may have a color material content layer. Japanese Patent Application No. 2004-352084 can be referred to for the color material-containing layer.
The filter layer may be laminated together with a direct recording layer or the like on the support by coating or the like, and is laminated on a substrate such as a film to produce an optical recording medium filter, and the optical recording medium filter May be laminated on a support.

-Dielectric deposition layer-
The dielectric vapor deposition layer is formed by laminating a plurality of dielectric thin films having different refractive indexes. In order to obtain a wavelength selective reflection film, a dielectric thin film having a high refractive index and a dielectric thin film having a low refractive index are used. Although it is preferable to laminate a plurality of layers alternately, it is not limited to two or more types, and may be more types. Moreover, when providing a color material content layer, it forms under a dielectric material vapor deposition layer.
The number of stacked layers is preferably 2 to 20 layers, more preferably 2 to 12 layers, still more preferably 4 to 10 layers, and particularly preferably 6 to 8 layers. If the number of stacked layers exceeds 20, the production efficiency may decrease due to multi-layer deposition, and the objects and effects of the present invention may not be achieved.

  The order of lamination of the dielectric thin films is not particularly limited and can be appropriately selected according to the purpose. For example, when the refractive index of an adjacent film is high, a film having a lower refractive index is first laminated. To do. Conversely, when the refractive index of the adjacent layer is low, a film having a higher refractive index is first laminated. The threshold value for determining whether the refractive index is high or low is preferably 1.8. Note that whether the refractive index is high or low is not absolute. Among high-refractive-index materials, there may be a material with a relatively high refractive index and a material with a relatively low refractive index, which are used alternately. May be.

The material for the high refractive index dielectric thin film is not particularly limited and may be appropriately selected depending on the intended purpose. For example, Sb ₂ O ₃ , Sb ₂ S ₃ , Bi ₂ O ₃ , CeO ₂ , CeF _{3, HfO 2, La 2 O} 3, Nd 2 O 3, Pr 6 O 11, Sc 2 O 3, SiO, Ta 2 O 5, TiO 2, TlCl, Y 2 O 3, ZnSe, ZnS, ZrO 2 , etc. Can be mentioned. Among these, Bi ₂ O ₃ , CeO ₂ , CeF ₃ , HfO ₂ , SiO, Ta ₂ O ₅ , TiO ₂ , Y ₂ O ₃ , ZnSe, ZnS, ZrO ₂ are preferable, and among these, SiO, Ta ₂ O ₅ , TiO ₂ , Y ₂ O ₃ , ZnSe, ZnS, and ZrO ₂ are more preferable.

The material for the low refractive index dielectric thin film is not particularly limited and may be appropriately selected depending on the intended purpose. For example, Al ₂ O ₃ , BiF ₃ , CaF ₂ , LaF ₃ , PbCl ₂ , PbF ₂ , LiF, MgF ₂ , MgO, NdF ₃ , SiO ₂ , Si ₂ O ₃ , NaF, ThO ₂ , ThF _{4 and the} like. Among these, Al ₂ O ₃ , BiF ₃ , CaF ₂ , MgF ₂ , MgO, SiO ₂ , Si ₂ O ₃ are preferable, and among these, Al ₂ O ₃ , CaF ₂ , MgF ₂ , MgO, SiO ₂ , Si ₂ O ₃ is more preferable.
In the dielectric thin film material, the atomic ratio is not particularly limited and can be appropriately selected depending on the purpose. The atomic ratio can be adjusted by changing the atmospheric gas concentration during film formation. .

The method for forming the dielectric thin film is not particularly limited and may be appropriately selected depending on the purpose. For example, a physical vapor deposition method such as ion plating, vacuum deposition using an ion beam, sputtering, or the like. (PVD method), chemical vapor deposition method (CVD method) and the like. Among these, vacuum deposition and sputtering are preferable, and sputtering is more preferable.
As the sputtering, a DC sputtering method having a high film formation rate is preferable. In the DC sputtering method, it is preferable to use a material having high conductivity.
In addition, as a method for forming a multilayer film by sputtering, for example, (1) a one-chamber method in which a plurality of targets are alternately or sequentially formed in one chamber, and (2) continuous film formation in a plurality of chambers. There is a multi-chamber method. Among these, the multi-chamber method is particularly preferable from the viewpoint of preventing productivity and material contamination.
The thickness of the dielectric thin film is preferably λ / 16 to λ, more preferably λ / 8 to 3λ / 4, and more preferably λ / 6 to 3λ / 8 in the order of the optical wavelength.

-Cholesteric liquid crystal layer-
The cholesteric liquid crystal layer contains at least a cholesterol derivative, or a nematic liquid crystal compound and a chiral compound, and further contains a polymerizable monomer and, if necessary, other components.
The cholesteric liquid crystal layer may be either a single-layer cholesteric liquid crystal layer or two or more cholesteric liquid crystal layers.

  The cholesteric liquid crystal layer preferably has a circularly polarized light separation function. The cholesteric liquid crystal layer having the function of separating circularly polarized light has only a circularly polarized light component in which the rotation direction (clockwise or counterclockwise) of the liquid crystal is coincident with the circular polarization direction and the wavelength is the helical pitch of the liquid crystal. Has a selective reflection characteristic of reflecting the light. Using the selective reflection characteristics of the cholesteric liquid crystal layer, only circularly polarized light having a specific wavelength is transmitted and separated from natural light in a certain wavelength band, and the rest is reflected.

In the filter for optical recording medium, the normal incidence 0 ° and to ± 20 ° range at which λ ₀ ~λ _{0 /} cos20 ° (but, lambda ₀ represents a wavelength of the irradiated light) in the light reflectance of 40% or more preferably there, lambda ₀ to [lambda] a perpendicular incidence in the range of ± 40 ° and ₀ ° 0 _/ cos40 ° (However, lambda ₀ represents a wavelength of the irradiated light) that light reflectance at not less than 40% Particularly preferred. Wherein λ ₀ ~λ ₀ / cos20 °, especially λ ₀ ~λ ₀ / cos40 ° (However, lambda ₀ represents a wavelength of the irradiated light) If the light reflectance is 40% or more at the angular dependence of the irradiation light reflected The lens optical system used for a normal optical recording medium can be employed. For this purpose, it is preferable that the selective reflection wavelength width of the cholesteric liquid crystal layer is large.
Specifically, in the case of a single-layer cholesteric liquid crystal layer, the selective reflection wavelength region width Δλ of the cholesteric liquid crystal layer is expressed by the following formula 1, and therefore it is preferable to use a liquid crystal having a large (ne-no). .
<Formula 1>
Δλ = 2λ (ne−no) / (ne + no)
In Equation 1, no represents the refractive index of nematic liquid crystal molecules contained in the cholesteric liquid crystal layer with respect to normal light. ne represents the refractive index of the nematic liquid crystal molecules with respect to extraordinary light. λ represents the center wavelength of selective reflection.
In addition, as described in Japanese Patent Application No. 2004-352081, a photoreactive chiral compound having photosensitivity as a chiral compound and capable of greatly changing the helical pitch of liquid crystal by light is used. It is preferable to use a filter for an optical recording medium in which the helical pitch is continuously changed in the thickness direction of the liquid crystal layer by adjusting the compound content and the UV irradiation time.

In the case of (2) a plurality of cholesteric liquid crystal layers, it is preferable to stack cholesteric liquid crystal layers having different selective reflection center wavelengths and having the same rotational direction of the spirals of the cholesteric liquid crystal layers.
The cholesteric liquid crystal layer is not particularly limited as long as it satisfies the above characteristics, and can be appropriately selected depending on the purpose.As described above, the cholesteric liquid crystal layer contains a nematic liquid crystal compound and a chiral compound. Further, it contains other components as required.

-Nematic liquid crystal compounds-
The nematic liquid crystal compound is characterized in that the liquid crystal phase is fixed below the liquid crystal transition temperature, the liquid crystal compound having a refractive index anisotropy Δn of 0.10 to 0.40, a polymer liquid crystal compound, and polymerization The liquid crystal compound can be appropriately selected according to the purpose. While it is in the liquid crystal state at the time of melting, it can be used as a solid phase by, for example, aligning by using an alignment substrate subjected to alignment treatment such as rubbing, and then cooling and fixing as it is.

  The nematic liquid crystal compound is not particularly limited and may be appropriately selected depending on the purpose. From the viewpoint of ensuring sufficient curability, a nematic liquid crystal compound having a polymerizable group in the molecule is preferable, and among these, Ultraviolet (UV) polymerizable liquid crystals are preferred. Commercially available products can be used as the UV polymerizable liquid crystal, for example, trade name PALIOCOLOR LC242 manufactured by BASF; trade name E7 manufactured by Merck; trade name LC-Slicon-CC3767 manufactured by Wacker-Chem; Takasago Examples include trade names L35, L42, L55, L59, L63, L79, and L83 manufactured by Perfume Co., Ltd.

  As content of the said nematic liquid crystal compound, 30-99 mass% is preferable with respect to the total solid content mass of each said cholesteric liquid crystal layer, and 50-99 mass% is more preferable. When the content is less than 30% by mass, the alignment of the nematic liquid crystal compound may be insufficient.

-Chiral compounds-
The chiral compound is not particularly limited in the case of a multi-layer cholesteric liquid crystal layer, and can be appropriately selected from known ones according to the purpose. From the viewpoint of improving the hue and color purity of the liquid crystal compound, , Isomannide compounds, catechin compounds, isosorbide compounds, fencon compounds, carboxylic compounds, and the like. These may be used alone or in combination of two or more.
Moreover, a commercial item can be used as said chiral compound, As this commercial item, the brand name S101, R811, CB15 by Merck, and the brand name PALIOCOLOR LC756 by BASF are mentioned, for example.

  The chiral compound content in each liquid crystal layer of the multi-layer cholesteric liquid crystal layer is preferably 0 to 30% by mass and more preferably 0 to 20% by mass with respect to the total solid mass of each cholesteric liquid crystal layer. When the content exceeds 30% by mass, the orientation of the cholesteric liquid crystal layer may be insufficient.

-Polymerizable monomer-
In the cholesteric liquid crystal layer, for example, a polymerizable monomer can be used in combination for the purpose of improving the degree of curing such as film strength. When the polymerizable monomer is used in combination, after changing the twisting force of the liquid crystal by light irradiation (patterning) (for example, after forming a selective reflection wavelength distribution), the helical structure (selective reflectivity) is fixed, The strength of the cholesteric liquid crystal layer after fixation can be further improved. However, when the liquid crystal compound has a polymerizable group in the same molecule, it is not necessarily added.
The polymerizable monomer is not particularly limited and may be appropriately selected from known ones according to the purpose. Examples thereof include monomers having an ethylenically unsaturated bond, and specifically, pentaerythritol. And polyfunctional monomers such as tetraacrylate and dipentaerythritol hexaacrylate. These may be used alone or in combination of two or more.
As addition amount of the said polymerizable monomer, 0-50 mass% is preferable with respect to the total solid content mass of the said cholesteric liquid crystal layer, and 1-20 mass% is more preferable. When the addition amount exceeds 50% by mass, the orientation of the cholesteric liquid crystal layer may be inhibited.

-Other ingredients-
The other components are not particularly limited and may be appropriately selected depending on the purpose. For example, photopolymerization initiator, sensitizer, binder resin, polymerization inhibitor, solvent, surfactant, thickener , Dyes, pigments, ultraviolet absorbers, gelling agents and the like.

There is no restriction | limiting in particular as said photoinitiator, According to the objective, it can select suitably according to the objective, For example, p-methoxyphenyl-2,4-bis (trichloromethyl) -s-triazine, 2- (p-butoxystyryl) -5-trichloromethyl 1,3,4-oxadiazole, 9-phenylacridine, 9,10-dimethylbenzphenazine, benzophenone / Michler's ketone, hexaarylbiimidazole / mercaptobenzimidazole, benzyl Examples include dimethyl ketal, acylphosphine derivatives, and thioxanthone / amine. These may be used alone or in combination of two or more.
As the photopolymerization initiator, commercially available products can be used. Examples of the commercially available products include trade names of Irgacure 907, Irgacure 369, Irgacure 784, and Irgacure 814 manufactured by Ciba Specialty Chemicals; Examples include lucillin TPO.

  The addition amount of the photopolymerization initiator is preferably 0.1 to 20% by mass, and more preferably 0.5 to 5% by mass with respect to the total solid mass of the cholesteric liquid crystal layer. When the addition amount is less than 0.1% by mass, it may take a long time because the curing efficiency at the time of light irradiation is low, and when it exceeds 20% by mass, the light transmittance from the ultraviolet region to the visible light region is increased. May be inferior.

The sensitizer is added as necessary to increase the degree of cure of the cholesteric liquid crystal layer.
There is no restriction | limiting in particular as said sensitizer, According to the objective, it can select suitably according to the objective, For example, diethyl thioxanthone, isopropyl thioxanthone, etc. are mentioned.
The addition amount of the sensitizer is preferably 0.001 to 1.0 mass% with respect to the total solid mass of the cholesteric liquid crystal layer.

There is no restriction | limiting in particular as said binder resin, According to the objective, it can select suitably according to the objective, For example, Polyvinyl alcohol; Polystyrene compounds, such as a polystyrene and poly-alpha-methylstyrene; Methylcellulose, ethylcellulose, acetyl Cellulose resins such as cellulose; acidic cellulose derivatives having a carboxyl group in the side chain; acetal resins such as polyvinyl formal and polyvinyl butyral; methacrylic acid copolymer, acrylic acid copolymer, itaconic acid copolymer, crotonic acid copolymer Examples thereof include a polymer, a maleic acid copolymer, a partially esterified maleic acid copolymer; a homopolymer of acrylic acid alkyl ester or a homopolymer of alkyl methacrylic acid; other polymer having a hydroxyl group. These may be used alone or in combination of two or more.
Examples of the alkyl group in the homopolymer of acrylic acid alkyl ester or homopolymer of methacrylic acid alkyl ester include, for example, methyl group, ethyl group, n-propyl group, n-butyl group, iso-butyl group, and n-hexyl group. , A cyclohexyl group, a 2-ethylhexyl group, and the like.
Examples of the other polymer having a hydroxyl group include benzyl (meth) acrylate / (homopolymer of methacrylic acid) acrylic acid copolymer, benzyl (meth) acrylate / (meth) acrylic acid / multiple monomers of other monomers. A polymer etc. are mentioned.

  As addition amount of the said binder resin, 0-80 mass% is preferable with respect to the total solid mass of the said cholesteric liquid crystal layer, and 0-50 mass% is more preferable. When the addition amount exceeds 80% by mass, the orientation of the cholesteric liquid crystal layer may be insufficient.

There is no restriction | limiting in particular as said polymerization inhibitor, According to the objective, it can select suitably, For example, hydroquinone, hydroquinone monomethyl ether, phenothiazine, benzoquinone, or these derivatives etc. are mentioned.
As addition amount of the said polymerization inhibitor, 0-10 mass% is preferable with respect to solid content of the said polymerizable monomer, and 100 ppm-1 mass% is more preferable.

  The solvent is not particularly limited and may be appropriately selected from known solvents according to the purpose. For example, 3-methoxypropionic acid methyl ester, 3-methoxypropionic acid ethyl ester, 3-methoxypropionic acid propyl Esters, alkoxypropionic acid esters such as 3-ethoxypropionic acid methyl ester, 3-ethoxypropionic acid ethyl ester, 3-ethoxypropionic acid propyl ester; 2-methoxypropyl acetate, 2-ethoxypropyl acetate, 3-methoxybutyl acetate Esters of alkoxy alcohols such as: Lactic acid esters such as methyl lactate and ethyl lactate; Ketones such as methyl ethyl ketone, cyclohexanone and methylcyclohexanone; γ-butyrolactone, N-methylpyrrolidone, di Sulfoxide, chloroform, tetrahydrofuran, and the like. These may be used individually by 1 type and may use 2 or more types together.

As a method for forming the cholesteric liquid crystal layer, for example, a coating solution for a cholesteric liquid crystal layer prepared using the solvent (in the case of a plurality of layers, a coating solution for each cholesteric liquid crystal layer) is applied onto the substrate and dried. For example, a cholesteric liquid crystal layer can be formed by irradiating with ultraviolet rays.
The most suitable method for mass production is to prepare the base material in a roll form, and apply a coating solution for the cholesteric liquid crystal layer on the base material such as bar coat, die coat, blade coat, curtain coat, etc. A type in which coating is performed with a long continuous coater is preferable.

Examples of the coating method include spin coating, casting, roll coating, flow coating, printing, dip coating, casting film formation, bar coating, and gravure printing.
There is no restriction | limiting in particular as conditions for the said ultraviolet irradiation, According to the objective, it can select suitably, For example, 160-380 nm is preferable and, as for irradiation ultraviolet rays, 250-380 nm is more preferable. For example, the irradiation time is preferably 0.1 to 600 seconds, and more preferably 0.3 to 300 seconds. By adjusting the conditions of ultraviolet irradiation, the helical pitch in the optical cholesteric liquid crystal layer using the reactive chiral agent can be continuously changed along the thickness direction of the liquid crystal layer.

  In order to adjust the conditions of the ultraviolet irradiation, an ultraviolet absorber may be added to the cholesteric liquid crystal layer. There is no restriction | limiting in particular as this ultraviolet absorber, According to the objective, it can select suitably, For example, a benzophenone type ultraviolet absorber, a benzotriazole type ultraviolet absorber, a salicylic acid type ultraviolet absorber, a cyanoacrylate type ultraviolet absorber Preferable examples include oxalic acid anilide-based ultraviolet absorbers. Specific examples of these ultraviolet absorbers include JP-A Nos. 47-10537, 58-111942, 58-212844, 59-19945, 59-46646, 59. No. -109055, No. 63-53544, No. 36-10466, No. 42-26187, No. 48-30492, No. 48-31255, No. 48-41572, No. 48. -54965, 50-10726, U.S. Pat. Nos. 2,719,086, 3,707,375, 3,754,919, 4, No. 220,711 and the like.

In the case of the plural layers, the thickness of each cholesteric liquid crystal layer is preferably, for example, 1 to 10 μm, and more preferably 2 to 7 μm. When the thickness is less than 1 μm, the selective reflectance is not sufficient, and when it exceeds 10 μm, the uniform alignment of the liquid crystal layer may be disturbed.
Further, the total thickness of each cholesteric liquid crystal layer (in the case of a single layer, the thickness of the cholesteric liquid crystal layer) is, for example, preferably 1 to 30 μm, and more preferably 3 to 10 μm.

<Method for Producing Filter for Optical Recording Medium Having Cholesteric Layer>
There is no restriction | limiting in particular as a manufacturing method of the said filter for optical recording media, According to the objective, it can select suitably.
The optical recording medium filter is not particularly limited and may be appropriately selected depending on the purpose. However, the entire base material is processed into a disk shape (for example, punching) and is applied onto the second substrate of the optical recording medium. Preferably it is arranged. Moreover, when using for the filter layer of an optical recording medium, it can also provide directly on a 2nd board | substrate not via a base material.

-Base material-
There is no restriction | limiting in particular as said base material, According to the objective, it can select suitably, For example, the same material as the support body used for said 1st form can be used.

As said base material, what was synthesize | combined suitably may be used and a commercial item may be used.
There is no restriction | limiting in particular as thickness of the said base material, According to the objective, it can select suitably, 10-500 micrometers is preferable and 50-300 micrometers is more preferable. When the thickness of the base material is less than 10 μm, the adhesion may be lowered due to the bending of the substrate. On the other hand, if it exceeds 500 μm, the focal positions of the information light and the reference light must be greatly shifted, and the optical system size becomes large.
For laminating the wavelength selective films, known adhesives can be used in any combination.
There is no restriction | limiting in particular as said adhesive, According to the objective, it can select suitably, For example, a rubber adhesive, an acrylic adhesive, a silicone adhesive, a urethane adhesive, a vinyl alkyl ether adhesive , Polyvinyl alcohol pressure sensitive adhesive, polyvinyl pyrrolidone pressure sensitive adhesive, polyacrylamide pressure sensitive adhesive, and cellulose pressure sensitive adhesive.
The application thickness of the adhesive or the pressure-sensitive adhesive is not particularly limited and can be appropriately selected according to the purpose. From the viewpoint of optical properties and thinning, 0.1 to 10 μm is preferable in the case of an adhesive, 0.1-5 micrometers is more preferable. Moreover, in the case of an adhesive, 1-50 micrometers is preferable and 2-30 micrometers is more preferable.

  In some cases, the filter layer can be formed directly on the substrate.

-Optical recording medium having reflective film, first and second gap layers-
The optical recording medium includes a first substrate, a second substrate, the recording layer on the second substrate, and the filter layer between the second substrate and the recording layer. It may be configured to have a reflective film, a first gap layer, a second gap layer, and other layers as necessary.

-Board-
The shape, structure, size and the like of the substrate are not particularly limited and can be appropriately selected according to the purpose. Examples of the shape include a disk shape and a card shape. It is necessary to select a material that can ensure the mechanical strength of the medium. In addition, when light used for recording and reproduction enters through the substrate, it is necessary to be sufficiently transparent in the wavelength region of the light used.
As the substrate material, glass, ceramics, resin, and the like are usually used, but resin is particularly preferable from the viewpoint of moldability and cost.
Examples of the resin include polycarbonate resin, acrylic resin, epoxy resin, polystyrene resin, acrylonitrile-styrene copolymer, polyethylene resin, polypropylene resin, silicone resin, fluorine resin, ABS resin, and urethane resin. Among these, polycarbonate resin and acrylic resin are particularly preferable from the viewpoints of moldability, optical characteristics, and cost.
As said board | substrate, what was synthesize | combined suitably may be used and a commercial item may be used.

  The substrate is provided with a plurality of address-servo areas serving as positioning areas extending linearly in the radial direction at predetermined angular intervals, and a sector-shaped section between adjacent address-servo areas is a data area. In the address-servo area, information for performing focus servo and tracking servo by the sampled servo method and address information are recorded in advance by embossed pits (servo pits) (preformat). Note that the focus servo can be performed using the reflective surface of the reflective film. As information for performing the tracking servo, for example, a wobble pit can be used. If the optical recording medium has a card shape, the servo pit pattern may be omitted.

  There is no restriction | limiting in particular as thickness of the said board | substrate, According to the objective, it can select suitably, 0.1-5 mm is preferable and 0.3-2 mm is more preferable. If the thickness of the substrate is less than 0.1 mm, distortion of the shape during storage of the disk may not be suppressed. If the thickness exceeds 5 mm, the weight of the entire disk increases and an excessive load is applied to the drive motor. Sometimes.

-Reflective film-
The reflective film is formed on the surface of the servo pit pattern of the substrate.
As the material of the reflective film, a material having a high reflectance with respect to recording light or reference light is preferably used. When the wavelength of light to be used is 400 to 780 nm, for example, Al, Al alloy, Ag, Ag alloy, etc. are preferably used. When the wavelength of light to be used is 650 nm or more, it is preferable to use Al, Al alloy, Ag, Ag alloy, Au, Cu alloy, TiN, or the like.
As the reflective film, an optical recording medium that reflects light and can be written or erased, such as a DVD (digital video disk), is used. It is also possible to add and rewrite directory information such as information on which part has an error and how replacement processing is performed without affecting the hologram.

There is no restriction | limiting in particular as a formation method of the said reflecting film, According to the objective, it can select suitably, Various vapor phase growth methods, for example, a vacuum evaporation method, sputtering method, plasma CVD method, photo-CVD method, ion plate method. A ting method, an electron beam evaporation method, or the like is used. Among these, the sputtering method is excellent in terms of mass productivity and film quality.
The thickness of the reflective film is preferably 50 nm or more, and more preferably 100 nm or more so that sufficient reflectance can be realized.

-First gap layer-
The first gap layer is provided between the filter layer and the reflective film as necessary, and is formed for the purpose of smoothing the second substrate surface. It is also effective for adjusting the size of the hologram generated in the recording layer. That is, since it is necessary for the recording layer to form an interference region for recording reference light and information light to a certain size, it is effective to provide a gap between the recording layer and the servo pit pattern.
The first gap layer can be formed, for example, by applying a material such as an ultraviolet curable resin on the servo pit pattern by spin coating or the like and curing it. Moreover, when using what apply | coated and formed on the transparent base material as a filter layer, this transparent base material will work | function also as a 1st gap layer.
There is no restriction | limiting in particular as thickness of said 1st gap layer, According to the objective, it can select suitably, 1-200 micrometers is preferable.

-Second gap layer-
The second gap layer is provided between the recording layer and the filter layer as necessary.
There is no restriction | limiting in particular as a material of said 2nd gap layer, According to the objective, it can select suitably, For example, a triacetyl cellulose (TAC), a polycarbonate (PC), a polyethylene terephthalate (PET), polystyrene (PS) ), Transparent resin films such as polysulfone (PSF), polyvinyl alcohol (PVA), polymethyl methacrylate-polymethyl methacrylate (PMMA), etc., or JSR brand name ARTON film or Nippon Zeon brand name ZEONOR And norbornene-based resin films. Among these, those having high isotropic properties are preferred, and TAC, PC, trade name ARTON, and trade name ZEONOR are particularly preferred.
There is no restriction | limiting in particular as thickness of said 2nd gap layer, According to the objective, it can select suitably, 1-200 micrometers is preferable.

  Here, specific examples of the optical recording medium having the reflective film, the first and second gap layers of the present invention will be described in more detail with reference to the drawings.

<Specific examples of optical recording media>
FIG. 4 is a schematic cross-sectional view showing the structure of an optical recording medium in a specific example of the present invention. In the optical recording medium 22 according to the specific example 1, the servo pit pattern 3 is formed on the second substrate 1 made of polycarbonate resin or glass, and the servo pit pattern 3 is coated with aluminum, gold, platinum, etc. 2 is provided. In FIG. 4, the servo pit pattern 3 is formed on the entire surface of the second substrate 1, but it may be formed periodically as shown in FIG. The height of the servo pit pattern 3 is normally 1750 mm (175 nm), which is sufficiently smaller than the thicknesses of the substrate and other layers.

The first gap layer 8 is formed by applying a material such as an ultraviolet curable resin on the reflective film 2 of the second substrate 1 by spin coating or the like. The first gap layer 8 is effective for protecting the reflective film 2 and adjusting the size of the hologram generated in the recording layer 4. That is, since it is necessary to form an interference area between the recording reference light and the information light in a certain size in the recording layer 4, it is effective to provide a gap between the recording layer 4 and the servo pit pattern 3.
A filter layer 6 is provided on the first gap layer 8, a second gap layer 7 is provided between the filter layer 6 and the first substrate 5 (polycarbonate resin substrate or glass substrate), and the recording layer 4 is sandwiched between them. Thus, the optical recording medium 22 is configured.

  In FIG. 4, the filter layer 6 transmits only red light and does not transmit light of other colors. Therefore, since the information light, the recording and reproduction reference light are green or blue light, the light does not pass through the filter layer 6 and does not reach the reflection film 2 and becomes return light, which is emitted from the incident / exit surface A. Become.

  The optical recording medium 22 in the specific example may be disk-shaped or card-shaped. In the case of a card shape, there is no need for the servo pit pattern. Further, in this optical recording medium 21, the second substrate 1 is 0.6 mm, the first gap layer 8 is 100 μm, the filter layer 6 is 2 to 3 μm, the second gap layer 7 is 50 μm, and the recording layer 4 is 0.6 mm. The first substrate 5 has a thickness of 0.6 mm, and the total thickness is about 1.9 mm.

  Next, the optical operation around the optical recording medium 22 will be described with reference to FIG. First, light (red light) emitted from the servo laser is reflected almost 100% by the dichroic mirror 13 and passes through the objective lens 12. Servo light is applied to the optical recording medium 22 by the objective lens 12 so as to be focused on the reflective film 2. That is, the dichroic mirror 13 transmits light having a wavelength of green or blue, and reflects light having a wavelength of red almost 100%. The servo light incident from the light incident / exit surface A of the optical recording medium 22 passes through the first substrate 5, the recording layer 4, the second gap layer 7, the filter layer 6, and the first gap layer 8 and is reflected. The light is reflected by the film 2, passes through the first gap layer 8, the filter layer 6, the second gap layer 7, the recording layer 4, and the first substrate 5 and is emitted from the incident / exit surface A again. The returned return light passes through the objective lens 12, is reflected almost 100% by the dichroic mirror 13, and servo information is detected by a servo information detector (not shown). The detected servo information is used for focus servo, tracking servo, slide servo, and the like. Since the hologram material constituting the recording layer 4 is not sensitive to red light, even if the servo light passes through the recording layer 4 or the servo light is irregularly reflected by the reflective film 2, the recording layer 4 is not affected. In addition, since the return light of the servo light reflected by the reflective film 2 is reflected almost 100% by the dichroic mirror 13, the servo light is detected by the CMOS sensor or the CCD 14 for detecting the reproduced image. In addition, there is no noise with respect to the reproduction light.

  In addition, the information light and the recording reference light generated from the recording / reproducing laser pass through the polarizing plate 16 to become linearly polarized light, pass through the half mirror 17 and pass through the quarter-wave plate 15 at a time. Become polarized. The optical recording medium 22 is irradiated with information light and recording reference light through the dichroic mirror 13 so as to generate an interference pattern in the recording layer 4 by the objective lens 12. The information light and the recording reference light enter from the incident / exit surface A, interfere with each other at the recording layer 4 to generate an interference pattern there, and record the interference pattern. Thereafter, the information light and the recording reference light pass through the recording layer 4 and enter the filter layer 6, but are reflected between the bottom of the filter layer 6 and become return light. That is, the information light and the recording reference light do not reach the reflective film 2. This is because the filter layer 6 has a property of transmitting only red light. Alternatively, if light leaking through the filter layer is suppressed to 20% or less of the incident light intensity, even if the leaked light reaches the bottom surface and becomes return light, it is reflected again by the filter layer and reproduced. The light intensity mixed into the light is 20% × 20% = 4% or less, which is not substantially a problem.

(Method for producing optical recording medium)
The method for producing an optical recording medium of the present invention includes at least a recording layer forming step, and further includes a filter layer forming step, a reflective film forming step, and other steps as necessary.

The recording layer forming step includes at least a step of adjusting a mixture by mixing a matrix precursor and a photoreactive monomer, and a step of curing the mixture to form a matrix, and further, if necessary It is a manufacturing method including these processes.
The step of mixing the matrix precursor and the photoreactive monomer is a step of mixing the matrix precursor, the photoreactive monomer, the photopolymerization initiator, and other components.
The matrix precursor is a material of the matrix polymer, and includes a prepolymer having an isocyanate group at the terminal, a polyol, and other compounds as required.
Examples of the photoreactive monomer include a polymerizable monomer having a functional group capable of forming a hydrogen bond and an ethylenic double bond, and, if necessary, the other polymerizable monomer.
Examples of the photopolymerization initiator include the same photopolymerization initiators as those contained in the optical recording composition.
Examples of the other components include those similar to other compounds contained in the optical recording composition.
There is no restriction | limiting in particular in the said mixing, For example, it is performed by stirring.

  The step of curing the mixture to form a matrix is a step of curing the mixture obtained in the step of mixing the matrix precursor and a photoreactive monomer to form a matrix. The curing reaction is performed at room temperature or by heating.

  There is no restriction | limiting in particular as said other process, According to the objective, it can select suitably, For example, application | coating, drying, etc. of a recording layer are mentioned. The recording layer is applied and dried as described in the method for forming the recording layer.

The filter layer forming step is a step of processing the optical recording medium filter of the present invention into an optical recording medium shape, and bonding the processed filter to the second substrate to form a filter layer.
Here, the method for producing the optical recording medium filter of the present invention is as described above.
Examples of the optical recording medium shape include a disk shape and a card shape.
There is no restriction | limiting in particular as said process, According to the objective, it can select suitably, For example, the cutting process by a press cutter, the punching process by a punch cutter, etc. are mentioned.
In the bonding, for example, an adhesive, a pressure-sensitive adhesive, or the like is used to attach a filter to the substrate so that bubbles do not enter.
The adhesive is not particularly limited and may be appropriately selected depending on the intended purpose. Examples thereof include various adhesives such as a UV curable type, an emulsion type, a one-component curable type, and a two-component curable type, Known adhesives can be used in any combination.
There is no restriction | limiting in particular as said adhesive, According to the objective, it can select suitably, For example, a rubber adhesive, an acrylic adhesive, a silicone adhesive, a urethane adhesive, a vinyl alkyl ether adhesive , Polyvinyl alcohol pressure sensitive adhesive, polyvinyl pyrrolidone pressure sensitive adhesive, polyacrylamide pressure sensitive adhesive, cellulose pressure sensitive adhesive, and the like.
The application thickness of the adhesive or the pressure-sensitive adhesive is not particularly limited and can be appropriately selected according to the purpose. From the viewpoint of optical properties and thinning, 0.1 to 10 μm is preferable in the case of an adhesive, 0.1-5 micrometers is more preferable. Moreover, in the case of an adhesive, 1-50 micrometers is preferable and 2-30 micrometers is more preferable.

  In some cases, the filter layer can be formed directly on the substrate. For example, a method of forming a color material-containing layer by applying a coating material for a color material-containing layer on a substrate and forming a dielectric vapor deposition film on the color material-containing layer by a sputtering method may be mentioned.

<Optical recording and playback method>
The optical recording / reproducing method is not particularly limited and may be appropriately selected depending on the purpose. For example, the optical recording medium recorded by the optical recording method of the present invention is irradiated with reference light during recording. And a method of reproducing by irradiating the same light from the same direction. When the interference image formed on the recording layer of the optical recording medium is irradiated with the light, diffracted light as recording information corresponding to the interference image is generated and can be reproduced by receiving the diffracted light.

Example 1
The optical recording composition of the present invention was prepared, an optical recording medium having a recording layer containing the optical recording composition was prepared, recorded on the optical recording medium as follows, and evaluated.

<Preparation of optical recording composition>
The following compositions were mixed under a nitrogen stream to prepare an optical recording composition. Content (mass%) of each component of the following composition is the quantity of a solid component.
------------------------------------
・ Biscyclohexylmethane diisocyanate 31.5% by mass
Polypropylene oxide triol (molecular weight 1000) 61.2% by mass
・ Tetramethylene glycol 2.5% by mass
-Specific compound examples 1-9 3.1% by mass
Photopolymerization initiator [Ciba Special Chemical Co., Irgacure 784] 0.69% by mass
・ Dibutyl dilaurate tin 1.01% by mass
------------------------------------

<Preparation of optical recording medium>
A first substrate is produced by applying an antireflection treatment so that the reflectance of incident light perpendicular to a wavelength of 532 nm is 0.1% on one surface of a glass having a thickness of 0.5 mm. One side of the glass was subjected to aluminum vapor deposition so that the reflectance by incident light perpendicular to the wavelength of 532 nm was 90%, and a second substrate was produced.
Next, a transparent polyethylene terephthalate sheet having a thickness of 500 μm was used as a spacer on the surface of the first substrate that was not subjected to antireflection treatment, and the optical recording composition was applied to the first substrate. Next, the surface of the second substrate subjected to aluminum vapor deposition is brought into contact with the optical recording composition side of the first substrate and bonded so as not to entrain the air layer, and the first substrate is interposed via a spacer. The substrate and the second substrate were bonded together. Finally, it was allowed to stand at 45 ° C. for 24 hours to produce an optical recording medium.

<Recording on optical recording media and evaluation>
Using the collinear hologram recording / reproduction tester SHOT-1000 manufactured by Pulstec Industrial Co., Ltd., the optical recording medium produced as described above was subjected to a series of multiplexing with a recording spot size of 200 μm in diameter at the focal point of the recording hologram. A hologram was written, and the sensitivity (recording energy) and multiplex number were measured and evaluated.

(Measurement of sensitivity)
The irradiation light energy (mJ / cm ² ) at the time of recording was changed, and the change in the error probability (BER: Bit Error Rate) of the reproduction signal was measured. Usually, the luminance of the reproduction signal increases with the increase of irradiation light energy, and the BER of the reproduction signal tends to gradually decrease. Here, the lowest irradiation light energy at which a substantially good reproduced image (BER <10-3) is obtained is defined as the recording sensitivity of the optical recording medium. The results are shown in Table 1.

(Evaluation of multiple number)
As a method for evaluating the number of multiplexed optical recording media obtained, ISO'04, Th-J-06, pp. 184-185, Oct. In 2004, the recording spot was shifted in a spiral shape and evaluated. Here, the number of recorded holograms was 13 × 13 = 169 holograms, and the recording pitch was 28.5 μm. The multiplicity when recording the last 169th hologram is 49. Since the multiplicity increases as the number of recording holograms increases, the BER increases as the number of recordings increases if the multiplexing characteristics of the optical recording medium are insufficient. Here, the number of recording holograms satisfying BER> 10-3 is defined as the multiple characteristic M of the optical recording medium. The results are shown in Table 1.

(Example 2)
In Example 1, specific compound examples No. Instead of 1-9, specific compound examples No. 1-9 The optical recording medium of Example 2 was produced in the same manner as in Example 1 except that 1% by mass of 1-6 was added, and the sensitivity and multiplex number were evaluated. The results are shown in Table 1.

(Example 3)
In Example 1, specific compound examples No. Instead of 1-9, specific compound examples No. 1-9 The optical recording medium of Example 3 was prepared in the same manner as in Example 1 except that 1 to 14% by mass of 1-14 was added, and the sensitivity and the multiplex number were evaluated. The results are shown in Table 1.

Example 4
In Example 1, specific compound examples No. Instead of 1-9, specific compound examples No. 1-9 The optical recording medium of Example 4 was produced in the same manner as in Example 1 except that 1 to 12% by mass of 1-12 was added, and the sensitivity and multiplex number were evaluated. The results are shown in Table 1.

(Example 5)
In Example 1, specific compound examples No. Instead of 1-9, specific compound examples No. 1-9 The optical recording medium of Example 5 was produced in the same manner as in Example 1 except that 3.1% by mass of 2-3 was added, and the sensitivity and multiplex number were evaluated. The results are shown in Table 1.

(Example 6)
In Example 1, specific compound examples No. Instead of 1-9, specific compound examples No. The optical recording medium of Example 6 was produced in the same manner as in Example 1 except that 3.1% by mass of 3-1 was added, and the sensitivity and multiplex number were evaluated. The results are shown in Table 1.

(Comparative Example 1)
In Example 1, specific compound examples No. An optical recording medium of Comparative Example 1 was prepared in the same manner as in Example 1 except that 3.1% by mass of 2,4,6-tribromophenyl acrylate was added instead of 1-9, and the sensitivity and multiple number were evaluated. The results are shown in Table 1.

  From the results of Table 1, it can be seen that the optical recording compositions of Examples 1 to 6 have good recording sensitivity and multiple characteristics when the compounds used in the present invention are used.

The hologram recording composition of the present invention can provide a hologram recording composition capable of high sensitivity and high multiplex recording, and can achieve high multiplex recording of interference images formed by information light and reference light. It is suitably used as a photosensitive material.
The optical recording medium of the present invention can provide a hologram recording composition capable of high multiplex recording, and various holographic light beams capable of achieving high multiplex recording of interference images formed by information light and reference light. Widely used as a recording medium.

FIG. 1 is a partial cross-sectional view of an optical recording medium. FIG. 2 is a partial cross-sectional view of a disk-type optical recording medium. FIG. 3 is a schematic cross-sectional view showing an example of an optical recording medium. FIG. 4 is a schematic sectional view showing an example of an optical recording medium according to the embodiment of the present invention. FIG. 5 is an explanatory diagram showing an example of an optical system around the optical recording medium. FIG. 6 is a block diagram showing an example of the overall configuration of the optical recording / reproducing apparatus according to the second embodiment.

Explanation of symbols

DESCRIPTION OF SYMBOLS 1 2nd board | substrate 2 Reflecting film 3 Servo pit pattern 4 Recording layer 5 1st board | substrate 6 Filter layer 7 2nd gap layer 8 1st gap layer 12 Objective lens 13 Dichroic mirror 14 Detector 15 1/4 wavelength plate 16 Polarization Element 17 Half mirror 22 Optical recording medium 31 Pickup 41 Recording layer 42 Support body 43 Support body 44 Antireflection layer 45 Antireflection layer 81 Spindle 82 Spindle motor 83 Spindle servo circuit 84 Drive device 85 Detection circuit 86 Focus servo circuit 87 Tracking servo circuit 88 Slide servo circuit 89 Signal processing circuit 90 Controller 91 Operation unit 100 Optical recording / reproducing device A Input / output surface FE Focus error signal TE Tracking error signal RF reproduction signal

Claims (10)

  An optical recording comprising a polymerizable monomer having a functional group capable of forming a hydrogen bond and an ethylenic double bond, a prepolymer having an isocyanate group at its terminal, and a matrix polymer formed by mixing a polyol. Composition. The optical recording composition according to claim 1, wherein the functional group capable of forming a hydrogen bond and the polymerizable monomer having an ethylenic double bond are represented by the following general formula (1).

(PX) _m -G- (A) _n General formula (1)

In Formula (1), P _{is, CH 2 = CH-, CH 2} = C (CH 3) -, CH 2 = CH-COO-L-, CH 2 = C (CH 3) -COO-L- _{, CH 2 = CH-CONHR-} L-, and CH ₂ = C (CH ₃₎ represents either -CONHR-L-a. L represents any one of an alkylene group, an arylene group, and an aralkylene group. R represents a hydrogen atom, an alkyl group, or an aryl group. X represents one of a single bond, —O—, —COO—, —O—CO—, —CONH—, and —NHCO—. A represents a functional group that forms a hydrogen bond. m and n may be the same as or different from each other, and represent an integer of 1 to 3. G represents an m + n-valent organic group having 1 to 50 carbon atoms.   The functional group capable of forming a hydrogen bond is a hydroxyl group, sulfonylamide group, sulfamoyl group, acylamino group, carbamoyl group, alkoxycarbonylamino group, aryloxycarbonylamino group, aminocarbonyloxy group, ureido group, amino group, carboxyl group, and The optical recording composition according to claim 1, which is a sulfo group.   The content of the polymerizable group having a functional group capable of forming a hydrogen bond and an ethylenic double bond is 3 to 45% by mass based on the total solid content of the optical recording composition. The composition for optical recording in any one.   An optical recording medium comprising a recording layer comprising the optical recording composition according to claim 1.   The optical recording medium according to claim 5, comprising a first substrate, a recording layer, a filter layer, and a second substrate in this order.   The optical recording medium according to claim 5, wherein the filter layer transmits the first light and reflects the second light.   The information light and the reference light having coherence are irradiated on the optical recording medium according to any one of claims 5 to 7, an interference image is formed by the information light and the reference light, and the interference image is converted into the light. An optical recording method comprising recording on a recording medium.   An interference image generated by irradiating the optical recording medium with the information light and the reference light so that the optical axis of the information light and the optical axis of the reference light are coaxial, and generated by interference between the information light and the reference light The optical recording method according to claim 8, wherein the data is recorded on the optical recording medium. The information light and the reference light having coherence are irradiated on the optical recording medium according to any one of claims 5 to 7, an interference image is formed by the information light and the reference light, and the interference image is converted into the light. An optical recording apparatus for recording on a recording medium.

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