WO2024005141A1 - ホログラム記録媒体用組成物 - Google Patents

ホログラム記録媒体用組成物 Download PDF

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Publication number
WO2024005141A1
WO2024005141A1 PCT/JP2023/024171 JP2023024171W WO2024005141A1 WO 2024005141 A1 WO2024005141 A1 WO 2024005141A1 JP 2023024171 W JP2023024171 W JP 2023024171W WO 2024005141 A1 WO2024005141 A1 WO 2024005141A1
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Prior art keywords
component
recording medium
composition
isocyanate
compound
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English (en)
French (fr)
Japanese (ja)
Inventor
一真 井上
憲 佐藤
麻人 田中
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Mitsubishi Chemical Corp
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Mitsubishi Chemical Corp
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Priority to JP2024530963A priority Critical patent/JPWO2024005141A1/ja
Priority to EP23831580.8A priority patent/EP4550330A4/en
Priority to CN202380047858.0A priority patent/CN119422198A/zh
Publication of WO2024005141A1 publication Critical patent/WO2024005141A1/ja
Priority to US18/999,485 priority patent/US20250122326A1/en
Anticipated expiration legal-status Critical
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
    • C08G18/4266—Polycondensates having carboxylic or carbonic ester groups in the main chain prepared from hydroxycarboxylic acids and/or lactones
    • C08G18/4269—Lactones
    • C08G18/4277—Caprolactone and/or substituted caprolactone
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/67—Unsaturated compounds having active hydrogen
    • C08G18/675—Low-molecular-weight compounds
    • C08G18/677—Low-molecular-weight compounds containing heteroatoms other than oxygen and the nitrogen of primary or secondary amino groups
    • C08G18/678—Low-molecular-weight compounds containing heteroatoms other than oxygen and the nitrogen of primary or secondary amino groups containing nitrogen
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
    • C08F283/006—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polymers provided for in C08G18/00
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08—Processes
    • C08G18/16—Catalysts
    • C08G18/22—Catalysts containing metal compounds
    • C08G18/227—Catalysts containing metal compounds of antimony, bismuth or arsenic
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/2805—Compounds having only one group containing active hydrogen
    • C08G18/285—Nitrogen containing compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72—Polyisocyanates or polyisothiocyanates
    • C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
    • C08G18/75—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic
    • C08G18/751—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring
    • C08G18/752—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group
    • C08G18/753—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group containing one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group having a primary carbon atom next to the isocyanate or isothiocyanate group
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72—Polyisocyanates or polyisothiocyanates
    • C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
    • C08G18/78—Nitrogen
    • C08G18/7806—Nitrogen containing -N-C=0 groups
    • C08G18/7818—Nitrogen containing -N-C=0 groups containing ureum or ureum derivative groups
    • C08G18/7837—Nitrogen containing -N-C=0 groups containing ureum or ureum derivative groups containing allophanate groups
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72—Polyisocyanates or polyisothiocyanates
    • C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
    • C08G18/78—Nitrogen
    • C08G18/79—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates
    • C08G18/791—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72—Polyisocyanates or polyisothiocyanates
    • C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
    • C08G18/78—Nitrogen
    • C08G18/79—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates
    • C08G18/791—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups
    • C08G18/792—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups formed by oligomerisation of aliphatic and/or cycloaliphatic isocyanates or isothiocyanates
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72—Polyisocyanates or polyisothiocyanates
    • C08G18/80—Masked polyisocyanates
    • C08G18/8061—Masked polyisocyanates masked with compounds having only one group containing active hydrogen
    • C08G18/8064—Masked polyisocyanates masked with compounds having only one group containing active hydrogen with monohydroxy compounds
    • G—PHYSICS
    • G02—OPTICS
    • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B5/00—Optical elements other than lenses
    • G02B5/32—Holograms used as optical elements
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03H—HOLOGRAPHIC PROCESSES OR APPARATUS
    • G03H1/00—Holographic processes or apparatus using light, infrared or ultraviolet waves for obtaining holograms or for obtaining an image from them; Details peculiar thereto
    • G03H1/02—Details of features involved during the holographic process; Replication of holograms without interference recording
    • G—PHYSICS
    • G02—OPTICS
    • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B27/00—Optical systems or apparatus not provided for by any of the groups G02B1/00 - G02B26/00, G02B30/00
    • G02B27/01—Head-up displays
    • G02B27/017—Head mounted
    • G02B27/0172—Head mounted characterised by optical features
    • G02B2027/0174—Head mounted characterised by optical features holographic
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03H—HOLOGRAPHIC PROCESSES OR APPARATUS
    • G03H1/00—Holographic processes or apparatus using light, infrared or ultraviolet waves for obtaining holograms or for obtaining an image from them; Details peculiar thereto
    • G03H1/02—Details of features involved during the holographic process; Replication of holograms without interference recording
    • G03H1/0252—Laminate comprising a hologram layer
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03H—HOLOGRAPHIC PROCESSES OR APPARATUS
    • G03H1/00—Holographic processes or apparatus using light, infrared or ultraviolet waves for obtaining holograms or for obtaining an image from them; Details peculiar thereto
    • G03H1/04—Processes or apparatus for producing holograms
    • G03H1/0402—Recording geometries or arrangements
    • G03H1/0408—Total internal reflection [TIR] holograms, e.g. edge lit or substrate mode holograms
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03H—HOLOGRAPHIC PROCESSES OR APPARATUS
    • G03H1/00—Holographic processes or apparatus using light, infrared or ultraviolet waves for obtaining holograms or for obtaining an image from them; Details peculiar thereto
    • G03H1/02—Details of features involved during the holographic process; Replication of holograms without interference recording
    • G03H2001/026—Recording materials or recording processes
    • G03H2001/0264—Organic recording material

Definitions

  • the present invention relates to a composition for holographic recording media, a cured product for holographic recording media obtained by curing this composition for holographic recording media, and a holographic recording medium using this composition for holographic recording media.
  • Holographic recording media which have been attracting attention in recent years, are recording media that utilize light interference and diffraction phenomena.
  • a hologram is a recording method that three-dimensionally records an interference pattern created by the interference fringes of two lights called a reference light and an object light (also called information light or signal light) (these are called recording lights) inside a recording medium. It is.
  • a hologram recording medium includes a photosensitive material in its recording layer, and the photosensitive material chemically changes in accordance with the interference pattern, thereby recording the interference pattern by locally changing its optical properties.
  • Holographic recording media were being developed for memory applications. As another use of the hologram recording medium, studies are being conducted to apply it to optical elements such as AR glass light guide plates. In the case of AR glasses (AR glasses) applications, the hologram-recorded optical element used in the light guide plate is required to have a wide viewing angle, high diffraction efficiency for light in the visible region, and high transparency of the medium.
  • AR glasses AR glasses
  • Hologram recording media can be divided into several types depending on what kind of optical properties are changed.
  • Volume hologram media which performs recording by creating a refractive index difference within a recording layer with a certain thickness or more, are advantageous for AR glass light guide plate applications because they can save space and achieve high diffraction efficiency and wavelength selectivity. It is believed that.
  • An example of a volume hologram recording medium is a write-once format that does not require wet processing or bleaching.
  • the composition of the recording layer is generally one in which a photoactive compound is dissolved in a matrix resin.
  • a photopolymer in which a matrix resin is combined with a photopolymerization initiator and a polymerizable reactive compound capable of radical polymerization or cationic polymerization as a recording layer (Patent Document 1-4).
  • the photopolymerization initiator When recording a hologram, if there is a recording layer made of photopolymer in the area where the reference beam and object beam intersect to form an interference pattern, the photopolymerization initiator will undergo a chemical reaction in the areas of the interference pattern where the light intensity is high.
  • the active substance acts on the polymerizable compound and the polymerizable compound polymerizes. At this time, if there is a difference in refractive index between the matrix resin and the polymer produced from the polymerizable compound, the interference pattern becomes a refractive index difference and is fixed in the recording layer.
  • the process of changing the optical characteristics of the recording layer by exposing the recording layer of the medium under predetermined conditions as described above will be referred to as “recording exposure.”
  • the process of repeatedly recording and exposing different interference patterns at the same position by changing the intersection angle of the reference beam and the object beam or by changing their respective incident angles is called “multiple recording exposure.”
  • the number of times of multiplex recording exposure is called the “total multiplex number”.
  • the interval between interference patterns (grating pitch) formed in a medium is not constant, and generally the grating pitch ranges from narrow to wide. At this time, it is desirable that the polymerization reaction proceeds equally whether the grating pitch is narrow or wide, and a hologram is formed. However, as a result of studies conducted by the present inventors, it has been found that, depending on the medium, the performance of the formed hologram changes depending on the grating pitch.
  • An object of the present invention is to provide a hologram recording medium whose hologram recording performance does not depend on the grating pitch.
  • the present inventors have discovered that by using a recording material containing a certain amount or more of allophanate binding units, it is possible to produce a hologram recording medium with excellent recording performance stability in which the hologram recording performance does not depend on the grating pitch. This makes it possible to reduce color unevenness and improve brightness of the hologram. That is, the gist of the present invention is as follows.
  • [1] Contains the following components (a) to (d), and the amount of allophanate binding units contained in component (a) relative to the total weight of component (a) and component (b) is 6.5 ⁇ 10 - 4 mol/g or more.
  • a composition for a holographic recording medium Component (a): Compound having an isocyanate group
  • the content of the component (c) in the composition is 0.1% by weight or more and 80% by weight or less, and the content of the component (d) is 0.1% by weight relative to the component (c).
  • the composition for a holographic recording medium according to any one of [1] to [3], which has a content of % by weight or more and 20% by weight or less.
  • composition for a holographic recording medium according to any one of [1] to [4], further comprising the following component (e).
  • component (e) Compound having a nitroxyl radical group
  • the molar ratio of the component (e) and the component (d) in the composition (component (e)/component (d)) is 0.1 or more and 10 or less, [5] to [7] The composition for a holographic recording medium according to any one of the above.
  • the total content of the component (a) and the component (b) in the composition is 0.1% by weight or more and 99.9% by weight or less, and the number of isocyanate groups contained in the component (a) is The composition for a holographic recording medium according to any one of [1] to [8], wherein the ratio of the number of isocyanate-reactive functional groups contained in the component (b) to the number of isocyanate-reactive functional groups is 0.1 or more and 10.0 or less.
  • composition for a holographic recording medium according to any one of [1] to [9], further comprising the following component (f).
  • a cured product for a hologram recording medium obtained by curing the composition for a hologram recording medium according to any one of [1] to [10].
  • a laminate for a holographic recording medium comprising a recording layer made of the cured product for a holographic recording medium according to [11] and a support.
  • a hologram recording medium obtained by exposing the cured product for a hologram recording medium according to [11] or the laminate for a hologram recording medium according to [12].
  • the present invention by using a recording material containing a certain amount or more of allophanate binding units, it is possible to produce a hologram recording medium whose hologram recording performance does not depend on the grating pitch. This makes it possible to reduce color unevenness and improve brightness of the hologram.
  • FIG. 1 is a configuration diagram showing an outline of an apparatus used for transmission hologram recording in an example.
  • FIG. 2 is a configuration diagram showing an outline of an apparatus used for holographic recording of reflections in the example.
  • composition for a hologram recording medium of the present invention contains the following components (a) to (d), and the presence of allophanate binding units contained in component (a) relative to the total weight of component (a) and component (b). It is characterized in that the amount is 6.5 ⁇ 10 ⁇ 4 mol/g or more.
  • Component (a) a compound having an isocyanate group, reacts with a compound having an isocyanate-reactive functional group (component (b)), preferably in the presence of a curing catalyst (component (f)) described below, to form a resin matrix. It is a constituent component.
  • the proportion of isocyanate groups in the molecule of the compound having isocyanate groups is preferably 50% by weight or less, more preferably 47% by weight or less, still more preferably 45% by weight or less.
  • This lower limit is usually 0.1% by weight or more, preferably 1% by weight or more.
  • turbidity is less likely to occur when a hologram recording medium is produced, and optical uniformity can be obtained. If the proportion of isocyanate groups is equal to or higher than the above lower limit, the hardness and glass transition temperature of the resin matrix will increase, and loss of recording can be prevented.
  • the proportion of isocyanate groups in the present invention indicates the proportion of isocyanate groups in the entire compound having isocyanate groups to be used, and the proportion of isocyanate groups in the compound having isocyanate groups is determined from the following formula.
  • the molecular weight of the isocyanate group is 42. (42 x number of isocyanate groups/molecular weight of compound having isocyanate groups) x 100
  • the type of compound having an isocyanate group is not particularly limited, and may have, for example, an aromatic, araliphatic, aliphatic, or alicyclic skeleton. Further, the compound having an isocyanate group may have one isocyanate group or two or more isocyanate groups in the molecule, but preferably has two or more isocyanate groups. This is a compound that has two or more isocyanate groups in the molecule (component (a)), a compound that has three or more isocyanate-reactive functional groups in the molecule (component (b)), or a compound that has three or more isocyanate-reactive functional groups in the molecule (component (b)).
  • Examples of compounds having an isocyanate group include isocyanic acid, butyl isocyanate, octyl isocyanate, butyl diisocyanate, hexamethylene diisocyanate (HMDI), isophorone diisocyanate (IPDI), 1,8-diisocyanato-4-(isocyanatomethyl ) octane, 2,2,4- or 2,4,4-trimethylhexamethylene diisocyanate, the isomers bis(4,4'-isocyanatocyclohexyl)methane and mixtures thereof with any desired isomer content, isocyanates Methyl-1,8-octane diisocyanate, 1,4-cyclohexylene diisocyanate, isomer cyclohexane dimethylene diisocyanate, 1,4-phenylene diisocyanate, 2,4- or 2,6-toluene diisocyanate, 1,5-naflethylene di
  • isocyanate derivatives having a urethane, urea, carbodiimied, acrylurea, isocyanurate, allophanate, biuret, oxadiazinetrione, uretdione and/or iminooxadiazinedione structure.
  • composition for a holographic recording medium of the present invention uses a compound having an isocyanate group having an allophanate bonding unit represented by the following formula (I) as the compound having an isocyanate group as such component (a).
  • the allophanate bond unit is generated by the reaction of a urethane bond with an isocyanate group. Therefore, a compound having an isocyanate group having an allophanate bonding unit represented by the above formula (I) can be obtained by, for example, obtaining a urethane compound of a polyfunctional isocyanate by subjecting a polyfunctional isocyanate and an alcohol to a urethanization reaction, and It can be obtained by reacting a compound having an isocyanate group.
  • polyfunctional isocyanate used in this reaction examples include hexamethylene diisocyanate (HMDI), isophorone diisocyanate (IPDI), 1,8-diisocyanato-4-(isocyanatomethyl)octane, 2,2,4- or 2 , 4,4-trimethylhexamethylene diisocyanate, isomer bis(4,4'-isocyanatocyclohexyl)methane and mixtures thereof with any desired isomer content, isocyanatomethyl-1,8-octane diisocyanate, 1, 4-Cyclohexylene diisocyanate, isomer cyclohexane dimethylene diisocyanate, 1,4-phenylene diisocyanate, 2,4- or 2,6-toluene diisocyanate, 1,5-naflethylene diisocyanate, 2,4'- or 4,4' -diphenylmethane diisocyanate, triphenylmethane
  • Examples of the alcohol include linear monovalent aliphatic alcohols and branched monovalent aliphatic alcohols.
  • Examples of the linear monohydric aliphatic alcohol include linear monohydric aliphatic alcohols having 1 to 20 carbon atoms.
  • Examples of linear monohydric aliphatic alcohols having 1 to 20 carbon atoms include methanol, ethanol, n-propanol, n-butanol, n-pentanol, n-hexanol, n-heptanol, n-octanol, n- Nonanol, n-decanol, n-undecanol, n-dodecanol (lauryl alcohol), n-tridecanol, n-tetradecanol, n-pentadecanol, n-hexadecanol, n-heptadecanol, n-octadecanol Nol (stearyl alcohol
  • a compound having an isocyanate group containing an allophanate bonding unit as described above is used in the following abundance amount.
  • the amount of allophanate binding units is within the following range, only compounds having isocyanate groups containing allophanate binding units may be used as compounds having isocyanate groups, and compounds having isocyanate groups containing allophanate binding units and It may be used in combination with a compound having an isocyanate group that does not contain an allophanate bonding unit.
  • allophanate bond units have a weaker intermolecular force than urethane bonds, so their interaction with polymerizable monomers is small and the diffusion coefficient of the polymerizable monomer within the composition can be maintained, making it ideal for gratings in hologram recording. By suppressing pitch dependence, color unevenness can be reduced and brightness can be improved.
  • the amount of allophanate bonding units contained in the compound having an isocyanate group as component (a) is 2.0 ⁇ 10 ⁇ 3 mol/g as a molar ratio to the total weight of component (a) and component (b).
  • the amount of allophanate bonding units present is determined by the total weight of the compound having an isocyanate group used as component (a) and the compound having an isocyanate-reactive functional group used as component (b) and the allophanate bonding unit in component (a). It can be determined by calculation from the molar amount of . The calculation method will be explained in the Examples section below.
  • the compound having an isocyanate-reactive functional group as component (b) is a compound having an active hydrogen (isocyanate-reactive functional group) that participates in a chain extension reaction with the compound having an isocyanate group as component (a).
  • the isocyanate-reactive functional group include a hydroxyl group, an amino group, and a mercapto group.
  • the compound having an isocyanate-reactive functional group may have one or more isocyanate-reactive functional groups in the molecule, but preferably has two or more. In addition, when it has two or more isocyanate-reactive functional groups, the number of isocyanate-reactive functional groups contained in one molecule may be one type, or may be plural types.
  • the number average molecular weight of the compound having an isocyanate-reactive functional group is usually 50 or more, preferably 100 or more, and more preferably 150 or more. Moreover, it is usually 50,000 or less, 10,000 or less, and more preferably 5,000 or less.
  • the number average molecular weight of the compound having an isocyanate-reactive functional group is equal to or higher than the above lower limit, the crosslink density decreases, and a decrease in recording speed can be prevented.
  • the number average molecular weight of the compound having an isocyanate-reactive functional group is below the above upper limit, loss of recorded content can be prevented due to improved compatibility with other components and increased crosslinking density. .
  • the number average molecular weight of component (b) is a value measured by gel permeation chromatography (GPC).
  • the compound having a hydroxyl group as an isocyanate-reactive functional group may have one or more hydroxyl groups in one molecule, but compounds having two or more hydroxyl groups are preferred.
  • examples include glycols such as ethylene glycol, triethylene glycol, diethylene glycol, polyethylene glycol, propylene glycol, polypropylene glycol (PPG), and neopentyl glycol; butanediol, pentanediol, hexanediol, heptanediol, and tetramethylene glycol (TMG).
  • diols such as polytetramethylene glycol (PTMG); bisphenols; triols such as glycerin, trimethylolpropane, butanetriol, pentanetriol, hexanetriol, and decanetriol;
  • PTMG polytetramethylene glycol
  • triols such as glycerin, trimethylolpropane, butanetriol, pentanetriol, hexanetriol, and decanetriol
  • examples include compounds modified with oxy chains; polyfunctional polyoxybutylene; polyfunctional polycaprolactone; polyfunctional polyester; polyfunctional polycarbonate; polyfunctional polypropylene glycol. Any one of these may be used alone, or two or more may be used in combination in any combination and ratio.
  • the number average molecular weight of the compound having a hydroxyl group is usually 50 or more, preferably 100 or more, and more preferably 150 or more. Moreover, it is usually 50,000 or less, 10,000 or less, and more preferably 5,000 or less.
  • the number average molecular weight of the compound having a hydroxyl group is equal to or higher than the above lower limit, the crosslink density decreases, and a decrease in recording speed can be prevented.
  • the number average molecular weight of the compound having a hydroxyl group is less than or equal to the above upper limit, the recorded content can be prevented from disappearing due to improved compatibility with other components and increased crosslinking density.
  • the compound having an amino group as an isocyanate-reactive functional group may be one having one or more amino groups in one molecule, but preferably one having two or more amino groups.
  • Examples include aliphatic amines such as ethylenediamine, diethylenetriamine, triethylenetetramine, hexamethylenediamine; alicyclic amines such as isophoronediamine, menthanediamine, 4,4'-diaminodicyclohexylmethane; m-xylylenediamine, diaminodiamine, etc.
  • Aromatic amines such as diphenylmethane and m-phenylenediamine; and the like. Any one of these may be used alone, or two or more may be used in combination in any combination and ratio.
  • the number average molecular weight of the compound having an amino group is usually 50 or more, preferably 100 or more, and more preferably 150 or more. Moreover, it is usually 50,000 or less, 10,000 or less, and more preferably 5,000 or less.
  • the number average molecular weight of the compound having an amino group is equal to or higher than the above lower limit, the crosslink density decreases, and a decrease in recording speed can be prevented.
  • the number average molecular weight of the compound having an amino group is less than or equal to the above upper limit, the recorded content can be prevented from disappearing due to improved compatibility with other components and increased crosslinking density.
  • the compound having a mercapto group as an isocyanate-reactive functional group may have one or more mercapto groups in one molecule, but compounds having two or more mercapto groups are preferred. Examples include 1,3-butanedithiol, 1,4-butanedithiol, 2,3-butanedithiol, 1,2-benzenedithiol, 1,3-benzenedithiol, 1,4-benzenedithiol, 1,10 -Decanedithiol, 1,2-ethanedithiol, 1,6-hexanedithiol, 1,9-nonanedithiol, pentaerythritol tetrakis (3-mercaptopropionate), pentaerythritol tetrakis (2-mercaptoacetate), pentaerythritol tetrakis (3-mercaptobutyrate), trimethylolpropane tris (3-mercapto
  • the number average molecular weight of the compound having a mercapto group is usually 50 or more, preferably 100 or more, and more preferably 150 or more. Moreover, it is usually 50,000 or less, 10,000 or less, and more preferably 5,000 or less.
  • the number average molecular weight of the compound having a mercapto group is equal to or higher than the above lower limit, the crosslink density decreases, and a decrease in recording speed can be prevented.
  • the number average molecular weight of the compound having a mercapto group is less than or equal to the above upper limit, the recorded content can be prevented from disappearing due to improved compatibility with other components and increased crosslinking density.
  • polycaprolactones As component (b), it is preferable to use polycaprolactones from the viewpoint of stability as a material and flexibility of structure.
  • polycaprolactones used as component (b) include ethylene glycol, diethylene glycol, triethylene glycol, propylene glycol, dipropylene glycol, 1,3-butanediol, 1,4-butanediol, hexamethylene glycol, and methylpentane.
  • the polymerizable monomer of component (c) is a compound that can be polymerized by the photopolymerization initiator of component (d) described below, and is a monomer compound that is polymerized during recording and/or during post-exposure.
  • the type of polymerizable monomer used in the composition for a holographic recording medium of the present invention is not particularly limited, and can be appropriately selected from known compounds.
  • Examples of polymerizable monomers include cationically polymerizable monomers, anionically polymerizable monomers, radically polymerizable monomers, and the like. Any of these may be used, or two or more types may be used in combination.
  • cationically polymerizable monomers examples include epoxy compounds, oxetane compounds, oxolane compounds, cyclic acetal compounds, cyclic lactone compounds, thiirane compounds, thietane compounds, vinyl ether compounds, spiro-orthoester compounds, ethylenically unsaturated bond compounds, and cyclic ether compounds. , cyclic thioether compounds, vinyl compounds, etc. Any one of the above cationically polymerizable monomers may be used alone, or two or more may be used in combination in any combination and ratio.
  • anionically polymerizable monomers examples include hydrocarbon monomers, polar monomers, and the like.
  • hydrocarbon monomers include styrene, ⁇ -methylstyrene, butadiene, isoprene, vinylpyridine, vinylanthracene, and derivatives thereof.
  • polar monomers include methacrylic esters, acrylic esters, vinyl ketones, isopropenyl ketones, and other polar monomers. Any one of the anionic polymerizable monomers exemplified above may be used alone, or two or more may be used in combination in any combination and ratio.
  • radically polymerizable monomers examples include compounds having (meth)acryloyl groups, (meth)acrylamides, vinyl esters, vinyl compounds, styrenes, spiro ring-containing compounds, and the like.
  • the radically polymerizable monomers exemplified above may be used alone or in combination of two or more in any desired ratio.
  • the polymerizable monomer used in the composition for a holographic recording medium of the present invention usually has a molecular weight of 80 or more, preferably 150 or more, and more preferably 300 or more. Moreover, it is usually 3000 or less, preferably 2500 or less, and more preferably 2000 or less.
  • the molecular weight is at least the above lower limit, it is possible to reduce the shrinkage rate due to polymerization of light irradiation during information recording of the hologram.
  • the molecular weight is below the above upper limit, the mobility of the polymerizable monomer in the recording layer using the composition for holographic recording media is high, diffusion occurs easily, and sufficient diffraction efficiency can be obtained. .
  • the polymerizable monomer has a refractive index of usually 1.50 or more, preferably 1.52 or more, more preferably 1.55 or more, and usually 1.80 or more at the wavelength of light irradiated onto the hologram recording medium (recording wavelength, etc.). It is preferably 1.78 or less. If the refractive index is too small, the diffraction efficiency may not be sufficient and the multiplicity may not be sufficient. If the refractive index is too large, the difference in refractive index with the resin matrix will become too large and scattering will increase, resulting in a decrease in transmittance and a need for greater energy during recording and reproduction.
  • the refractive index shows a large value when evaluated at short wavelengths, but a sample that shows a relatively large refractive index at short wavelengths also shows a relatively large refractive index at long wavelengths, and this relationship is never reversed. Therefore, it is also possible to evaluate the refractive index at a wavelength other than the recording wavelength and predict the refractive index at the recording wavelength.
  • the refractive index of the polymerizable monomer can be measured by the minimum deviation angle method, critical angle method, V-block method, etc.
  • the sample is a solid, the compound is dissolved in a suitable solvent to form a solution, the refractive index of this solution is measured, and the refractive index when the compound is 100% can be determined by extrapolation.
  • halogen atom iodine, chlorine, bromine, etc.
  • hetero atom nitrogen, sulfur, oxygen, etc.
  • the polymerizable monomer preferably has a molar absorption coefficient of 100 L ⁇ mol ⁇ 1 ⁇ cm ⁇ 1 or less at the recording wavelength of the hologram.
  • a molar extinction coefficient of 100 L ⁇ mol ⁇ 1 ⁇ cm ⁇ 1 or less it is possible to prevent the transmittance of the medium from becoming low and to obtain sufficient diffraction efficiency for the thickness.
  • a photopolymerization initiator is one that generates cations, anions, and radicals that cause chemical reactions when exposed to light, and contributes to the polymerization of the above-mentioned polymerizable monomers.
  • the type of photopolymerization initiator is not particularly limited, and can be appropriately selected depending on the type of polymerizable monomer.
  • Any known cationic photopolymerization initiator can be used as the cationic photopolymerization initiator.
  • aromatic onium salts include aromatic onium salts. Specific examples include anion components such as SbF 6 - , BF 4 - , AsF 6 - , PF 6 - , CF 3 SO 3 - , B(C 6 F 5 ) 4 - , and iodine, sulfur, nitrogen, phosphorus, etc. Examples include compounds consisting of an aromatic cation component containing an atom of Among these, diaryliodonium salts, triarylsulfonium salts, and the like are preferred. Any one of the above-exemplified cationic photopolymerization initiators may be used alone, or two or more may be used in combination in any combination and ratio.
  • anionic photopolymerization initiator can be used as the anionic photopolymerization initiator.
  • examples include amines.
  • amines include dimethylbenzylamine, dimethylaminomethylphenol, amino group-containing compounds such as 1,8-diazabicyclo[5.4.0]undecene-7, and derivatives thereof; imidazole, 2-methylimidazole, Examples include imidazole compounds such as 2-ethyl-4-methylimidazole, and derivatives thereof.
  • Any one of the anionic photopolymerization initiators exemplified above may be used alone, or two or more may be used in combination in any combination and ratio.
  • radical photopolymerization initiator can be used as the radical photopolymerization initiator.
  • examples include phosphine oxide compounds, azo compounds, azide compounds, organic peroxides, organic borates, onium salts, bisimidazole derivatives, titanocene compounds, iodonium salts, organic thiol compounds, halogenated hydrocarbon derivatives, oxime ester compounds. etc. are used. Any one of the radical photopolymerization initiators exemplified above may be used alone, or two or more may be used in combination in any combination and ratio.
  • photopolymerization initiators include imidazole derivatives, oxadiazole derivatives, naphthalene, perylene, pyrene, anthracene, coumarin, chrysene, p-bis(2-phenylethenyl)benzene and their derivatives, quinacridone derivatives, Coumarin derivatives, aluminum complexes such as Al( C9H6NO ) 3 , rubrene, perimidone derivatives, benzopyran derivatives, rhodamine derivatives, benzothioxanthene derivatives, azabenzothioxanthene, phenylpyridine complexes, porphyrin complexes, polyphenylene vinylene materials, etc. can be mentioned. .
  • a compound having a molar absorption coefficient of 1000 L ⁇ mol ⁇ 1 ⁇ cm ⁇ 1 or less at the recording wavelength is particularly preferred.
  • a molar extinction coefficient of 1000 L ⁇ mol ⁇ 1 ⁇ cm ⁇ 1 or less it is possible to suppress a decrease in the transmittance of the hologram recording medium at the recording wavelength, which occurs when mixing in an amount sufficient to obtain sufficient diffraction efficiency. can.
  • the composition for a holographic recording medium of the present invention preferably contains component (e), which is a compound having a nitroxyl radical group, as an optional component.
  • component (e) a compound having a nitroxyl radical group, a compound having an isocyanate-reactive functional group and a nitroxyl radical group is preferably used. Since the composition for a hologram recording medium of the present invention contains such component (e), the isocyanate-reactive functional group of component (e) reacts with the isocyanate group of component (a) and is immobilized in the resin matrix.
  • recording sensitivity can be improved and a high ⁇ n can be realized.
  • Examples of the isocyanate-reactive functional group contained in component (e) include those similar to the isocyanate-reactive functional group contained in component (b).
  • component (e) is not particularly limited, but specific examples include 4-hydroxy-2,2,6,6-tetramethylpiperidin-1-oxyl (TEMPOL), 4-sulfanyl-2,2 , 6,6-tetramethylpiperidine-1-oxyl, 4-amino-2,2,6,6-tetramethylpiperidine-1-oxyl, 4-mercapto-2,2,6,6-tetramethylpiperidine-1 -oxyl, 4-carboxy-2,2,6,6-tetramethylpiperidine-1-oxyl, 4-carbamoyl-2,2,6,6-tetramethylpiperidine-1-oxyl, 4-(2,3- epoxypropoxy)-2,2,6,6-tetramethylpiperidine-1-oxyl, 3-hydroxy-2,2,5,5-tetramethylpyrrolidine-1-oxyl, 3-sulfanyl-2,2,5, 5-tetramethylpyrrolidine-1-oxyl, 3-amino-2,2,5,5-tetramethylpyrrolidine-1-oxyl, 3-mercapto-2
  • TEMPOL 4-sulfanyl-2,2,6,6-tetramethylpiperidine-1-oxyl, 4-amino-2,2,6 , 6-tetramethylpiperidin-1-oxyl, and 4-mercapto-2,2,6,6-tetramethylpiperidin-1-oxyl, and particularly preferably TEMPOL.
  • composition for a hologram recording medium of the present invention further includes a curing catalyst as a component (f) that promotes the reaction between the compound having an isocyanate group as the component (a) and the compound having an isocyanate-reactive functional group as the component (b). It is preferable to include.
  • a curing catalyst for component (f) it is preferable to use a bismuth-based catalyst that acts as a Lewis acid.
  • bismuth-based catalysts include tris(2-ethylhexanate) bismuth, tribenzoyloxybismuth, bismuth triacetate, tris(dimethyldiocarbamic acid) bismuth, bismuth hydroxide, triphenylbismuth(V) bis(trichloroarate). ), tris(4-methylphenyl)oxobismuth (V), triphenylbis(3-chlorobenzoyloxy)bismuth (V), and the like.
  • trivalent bismuth compounds are preferred from the viewpoint of catalytic activity, such as bismuth carboxylate, general formula Bi(OCOR) 3 (R is a linear or branched alkyl group, a cycloalkyl group, or a substituted or unsubstituted aromatic group).
  • R is a linear or branched alkyl group, a cycloalkyl group, or a substituted or unsubstituted aromatic group.
  • the one represented by is more preferable.
  • Any one type of bismuth-based catalyst may be used alone, or two or more types may be used in combination in any combination and ratio.
  • the curing catalyst other curing catalysts can be used in combination with the above-mentioned bismuth-based catalyst in order to adjust the reaction rate.
  • the catalyst there are no particular restrictions on the catalyst that can be used in combination, as long as it does not go against the gist of the present invention, but in order to obtain a synergistic effect of the catalyst, it is preferable to use a compound having an amino group as part of its structure.
  • TAA triethylamine
  • DMEDA N,N-dimethylcyclohexylamine
  • TEDA N,N,N',N'-tetramethylethylenediamine
  • TMPDA N,N,N',N'-tetramethyl Propane-1,3-diamine
  • TMHMDA N,N,N',N'-tetramethylhexane-1,6-diamine
  • TMHMDA N,N,N',N",N"-pentamethyldiethylenetriamine
  • PMDETA N,N,N',N",N"-pentamethyldipropylene-triamine
  • TDA triethylenediamine
  • DMP N,N'-dimethylpiperazine
  • TMNAEP N-methylmorpholine
  • NMMO N.(N',N'-dimethylaminoethyl)-morpholine
  • NMMO N.(N',N'-dimethylaminoeth
  • composition for a holographic recording medium of the present invention may contain other components as long as they do not go against the gist of the present invention.
  • Other components include solvents, plasticizers, dispersants, leveling agents, antifoaming agents, adhesion promoters, etc. for preparing the recording layer of hologram recording media, and chain transfer agents for controlling recording reactions. , a polymerization terminator, a compatibilizer, a reaction aid, a sensitizer, an antioxidant, and the like. Any one type of these components may be used alone, or two or more types may be used in combination in any combination and ratio.
  • composition ratio of each component in the composition for hologram recording medium The content of each component in the composition for a holographic recording medium of the present invention is arbitrary as long as it does not go against the gist of the present invention, but the content of each component is preferably within the following ranges.
  • the total content of component (a) and component (b) in the composition for holographic recording media of the present invention is usually 0.1% by weight or more, preferably 10% by weight or more, and more preferably 35% by weight or more. It is. Further, it is usually 99.9% by weight or less, preferably 99% by weight or less, and more preferably 98% by weight or less.
  • this content By setting this content to the above lower limit value or more, it becomes easy to form the recording layer. By keeping this content below the above upper limit, the content of other essential components can be ensured.
  • the ratio of the number of isocyanate-reactive functional groups of component (b) to the number of isocyanate groups of component (a) is 0.1 or more, while satisfying the above-mentioned amount of allophanate bonding units present. It is preferably 0.5 or more, more preferably 0.5 or more. Moreover, this ratio is usually 10.0 or less, preferably 2.0 or less. When this ratio is within the above range, there are fewer unreacted functional groups and storage stability is improved.
  • the content of component (c) in the composition for a holographic recording medium of the present invention is usually 0.1% by weight or more, preferably 1% by weight or more, and more preferably 2% by weight or more. Further, it is usually 80% by weight or less, preferably 50% by weight or less, and more preferably 30% by weight or less. Sufficient diffraction efficiency can be obtained because the amount of component (c) is at least the above lower limit. The compatibility of the recording layer is maintained because the amount of component (c) is below the above upper limit.
  • the content of component (d) in the composition for a holographic recording medium of the present invention is usually 0.1% by weight or more, preferably 0.2% by weight or more, and more preferably 0.1% by weight or more relative to the content of component (c). .3% by weight or more. Further, it is usually 20% by weight or less, preferably 18% by weight or less, and more preferably 16% by weight or less. Sufficient recording sensitivity can be obtained when the proportion of component (d) is at least the above lower limit. When the proportion of component (d) is at most the above upper limit, it is possible to suppress a decrease in sensitivity due to bimolecular termination reaction due to generation of excessive radicals.
  • the content of component (e) is the molar ratio of component (e) to component (d) (component (e)/component (d)). is usually 0.1 or more, particularly 0.2 or more, particularly 0.3 or more, and usually 10 or less, particularly 8 or less, especially 6 or less. If the ratio of component (e)/component (d) is at least the above lower limit, the effect of improving ⁇ n by containing component (e) can be effectively obtained.
  • component (e)/component (d) is below the above upper limit, a radical polymerization reaction is allowed to proceed during exposure for recording purposes to obtain the degree of refractive index modulation necessary for forming a diffraction grating and to obtain sufficient recording sensitivity. be able to.
  • the content of component (f) in the composition for hologram recording media of the present invention is preferably determined by taking into account the reaction rate of component (a) and component (b), and is usually 5% by weight or less, preferably 4% by weight. % or less, more preferably 1% by weight or less, and preferably 0.001% by weight or more.
  • the total amount of other components other than components (a) to (f) in the composition for holographic recording media of the present invention is usually 30% by weight or less, preferably 15% by weight or less, and more preferably 5% by weight. .
  • composition for hologram recording medium and cured product for hologram recording medium In producing the composition for holographic recording media of the present invention, components (a) to (d), preferably components (a) to (e), more preferably components (a) to (f) are used in any combination, They may be mixed in this order, or at that time, other components may be mixed in combination.
  • the cured product for holographic recording media of the present invention By curing the obtained composition for holographic recording media, the cured product for holographic recording media of the present invention can be obtained. At this time, it may be heated at 30 to 100° C. for about 1 to 72 hours to accelerate the curing reaction.
  • composition for hologram recording media and the cured product for hologram recording media of the present invention can also be produced according to the method for forming a recording layer in the method for producing a hologram recording medium of the present invention, which will be described later.
  • the hologram recording medium of the present invention can be obtained by subjecting the cured product for hologram recording media of the present invention to interference exposure.
  • the hologram recording medium of the present invention includes a recording layer and, if necessary, a support and other layers.
  • a hologram recording medium has a support, and a recording layer and other layers are laminated on this support to constitute the hologram recording medium.
  • the recording layer or other layers have the strength and durability necessary for the medium, the hologram recording medium does not need to have a support.
  • other layers include a protective layer, a reflective layer, an antireflection layer (antireflection film), and the like.
  • the recording layer of the holographic recording medium of the present invention is preferably formed from the composition for holographic recording media of the present invention.
  • the recording layer of the holographic recording medium of the present invention is a layer formed from the composition for a holographic recording medium of the present invention, and is a layer on which information is recorded. Information is usually recorded as a hologram.
  • a part of the polymerizable monomer contained in the recording layer undergoes a chemical change such as polymerization during hologram recording or the like. Therefore, in the hologram recording medium after recording, a part of the polymerizable monomer is consumed and exists as a reacted compound such as a polymer.
  • the thickness of the recording layer is not particularly limited and may be determined as appropriate in consideration of the recording method, etc., but generally it is usually in the range of 1 ⁇ m or more, preferably 10 ⁇ m or more, and usually 3000 ⁇ m or less, preferably 2000 ⁇ m or less. It is.
  • the thickness of the recording layer By setting the thickness of the recording layer to the above lower limit or more, the selectivity of each hologram becomes high during multiple recording in a hologram recording medium, and the degree of multiple recording can be increased.
  • By setting the thickness of the recording layer to the above upper limit or less it becomes possible to uniformly mold the entire recording layer, and it is possible to perform multiple recording with uniform diffraction efficiency of each hologram and a high S/N ratio. .
  • the shrinkage rate of the recording layer due to exposure during recording and reproduction of information is preferably 0.5% or less.
  • ⁇ Support> There are no particular restrictions on the details of the support, and any support can be used as long as it has the strength and durability required for the medium. There are no restrictions on the shape of the support, but it is usually formed into a flat plate or film shape. There are no restrictions on the material constituting the support, and it may be transparent or opaque.
  • transparent materials for the support include organic materials such as acrylic, polyethylene terephthalate, polyethylene naphthoate, polycarbonate, polyethylene, polypropylene, amorphous polyolefin, polystyrene, and cellulose acetate; and inorganic materials such as glass, silicon, and quartz. It will be done. Among these, polycarbonate, acrylic, polyester, amorphous polyolefin, glass, etc. are preferred, and polycarbonate, acrylic, amorphous polyolefin, and glass are particularly preferred.
  • opaque support materials include metals such as aluminum; transparent supports coated with metals such as gold, silver, aluminum, or dielectrics such as magnesium fluoride and zirconium oxide; can be mentioned.
  • the thickness of the support is usually preferably in the range of 0.05 mm or more and 1 mm or less.
  • the thickness of the support is equal to or greater than the above lower limit, mechanical strength of the hologram recording medium can be obtained and warping of the substrate can be prevented. If the thickness of the support is equal to or less than the above upper limit, the amount of light transmitted can be maintained and an increase in cost can be suppressed.
  • the surface of the support may be subjected to surface treatment.
  • This surface treatment is usually performed to improve the adhesion between the support and the recording layer.
  • Examples of surface treatments include subjecting the support to corona discharge treatment and forming an undercoat layer on the support in advance.
  • examples of the composition of the undercoat layer include halogenated phenol, partially hydrolyzed vinyl chloride-vinyl acetate copolymer, polyurethane resin, and the like.
  • the surface treatment may be performed for purposes other than improving adhesion.
  • Examples include reflective coating treatment that forms a reflective coating layer made of metal such as gold, silver, or aluminum; dielectric coating treatment that forms a dielectric layer such as magnesium fluoride or zirconium oxide, etc. It will be done. These layers may be formed as a single layer, or may be formed as two or more layers.
  • These surface treatments may be performed for the purpose of controlling the gas and moisture permeability of the substrate. For example, the reliability of the medium can be further improved by providing the supports that sandwich the recording layer with the function of suppressing gas and moisture permeability.
  • the support may be provided only on either the upper side or the lower side of the recording layer of the holographic recording medium of the present invention, or may be provided on both sides. However, when supports are provided on both the upper and lower sides of the recording layer, at least one of the supports is configured to be transparent so as to transmit active energy rays (excitation light, reference light, reproduction light, etc.). In the case of a hologram recording medium having a support on one or both sides of the recording layer, a transmission type or reflection type hologram can be recorded. When a support having reflective properties is used on one side of the recording layer, a reflective hologram can be recorded.
  • the support may be provided with patterning for data addressing.
  • patterning method there are no restrictions on the patterning method in this case, but for example, unevenness may be formed on the support itself, a pattern may be formed on the reflective layer described below, or a combination of these methods may be used.
  • the protective layer is a layer for preventing the effects of oxygen and moisture on the recording layer, such as a decrease in sensitivity and deterioration of storage stability.
  • the protective layer is a layer for preventing the effects of oxygen and moisture on the recording layer, such as a decrease in sensitivity and deterioration of storage stability.
  • a layer made of a water-soluble polymer, an organic/inorganic material, etc. can be formed as a protective layer.
  • the formation position of the protective layer is not particularly limited, and may be formed, for example, on the surface of the recording layer or between the recording layer and the support.
  • the protective layer may be formed on the outer surface of the support.
  • a protective layer may be formed between the support and other layers.
  • the reflective layer is formed when the medium is configured as a reflective hologram recording medium.
  • the reflective layer may be formed between the support and the recording layer, or on the outer surface of the support. Usually, it is preferable that the reflective layer is between the support and the recording layer. Any known reflective layer can be used as the reflective layer. For example, a thin metal film or the like can be used.
  • an anti-reflection layer is provided on the side where the object light and readout light enter and exit, or between the recording layer and the support.
  • a membrane may also be provided.
  • the antireflection film functions to improve light utilization efficiency and suppress the generation of ghost images. Any known antireflection film can be used.
  • ⁇ Method for manufacturing hologram recording medium There are no limitations to the method of manufacturing the hologram recording medium of the present invention. For example, it can be manufactured by coating the composition for a holographic recording medium of the present invention on a support without a solvent to form a recording layer. Any method can be used to apply the composition for holographic recording media. Specific examples include a spray method, a spin coating method, a wire bar method, a dip method, an air knife coating method, a roll coating method, a blade coating method, and a doctor roll coating method.
  • composition for hologram recording media of the present invention when forming a recording layer, especially when forming a thick recording layer, there are methods in which the composition for hologram recording media of the present invention is placed in a mold and molded, or it is coated on a release film and molded. A punching method may also be used.
  • a coating solution may be prepared by mixing the composition for a holographic recording medium of the present invention with a solvent or an additive, and this may be coated onto a support and dried to form a recording layer.
  • any method can be used as the coating method, for example, the same method as described above can be employed.
  • solvents include ketone solvents such as acetone and methyl ethyl ketone; aromatic solvents such as toluene and xylene; alcohol solvents such as methanol and ethanol; ketone alcohol solvents such as diacetone alcohol; and ether solvents such as tetrahydrofuran.
  • Solvents Halogenated solvents such as dichloromethane and chloroform; Cellosolved solvents such as methyl cellosolve and ethylcellosolve; Propylene glycol solvents such as propylene glycol monomethyl ether and propylene glycol monoethyl ether; Ethyl acetate, methyl 3-methoxypropionate, etc.
  • Ester solvents include Perfluoroalkyl alcohol solvents such as tetrafluoropropanol; Highly polar solvents such as dimethylformamide and dimethyl sulfoxide; Chain hydrocarbon solvents such as n-hexane; Cyclic hydrocarbon solvents such as cyclohexane and cyclooctane ; or a mixed solvent thereof.
  • one type of solvent may be used alone, or two or more types may be used in combination in any combination and ratio.
  • the hologram recording of the present invention can be performed by, for example, an injection molding method, a sheet molding method, a hot press method, etc.
  • the recording layer can be formed by molding the medium composition.
  • the resin matrix consisting of components (a) and (b) is photocurable or thermosetting with few volatile components
  • the composition for holographic recording media of the present invention can be prepared by, for example, reaction injection molding or liquid injection molding.
  • the recording layer can be formed by molding. In this case, if the molded body has sufficient thickness, rigidity, strength, etc., the molded body can be used as a hologram recording medium as it is.
  • methods for producing hologram recording media include, for example, a method in which a composition for a hologram recording medium melted by heat is coated on a support, and the composition is cooled and solidified to form a recording layer; A method of manufacturing a recording layer by applying a composition for media to a support and curing it by thermal polymerization, and a method of manufacturing by applying a liquid composition for hologram recording media to a support and curing by photopolymerizing. There is also a method of manufacturing the recording layer by forming the recording layer.
  • the holographic recording medium thus produced can take the form of a free-standing slab or disk, and can be used in three-dimensional image display devices, diffractive optical elements, large-capacity memories, and more.
  • the hologram recording medium of the present invention using the composition for a hologram recording medium of the present invention has a high ⁇ n, can reduce color unevenness, and can improve brightness, and can be used as a light guide plate for AR glasses. It is useful as
  • Writing (recording) and reading (reproducing) information to the hologram recording medium of the present invention are both performed by irradiation with light.
  • the object light and the reference light are irradiated onto the recording layer so that the object light and the reference light interfere in the recording layer.
  • the interference light causes polymerization and concentration change of the polymerizable monomer in the recording layer, and as a result, interference fringes cause a refractive index difference in the recording layer, resulting in interference recorded in the recording layer.
  • the stripes are recorded as a hologram in the recording layer.
  • the recording layer is irradiated with a predetermined reproduction light (usually a reference light).
  • the irradiated reproduction light is diffracted according to the interference fringes. Since this diffracted light contains the same information as that of the recording layer, the information recorded on the recording layer can be reproduced by reading the diffracted light with an appropriate detection means.
  • the wavelength regions of the object light, reproduction light, and reference light are arbitrary depending on their respective uses, and may be in the visible light region or the ultraviolet region.
  • suitable ones include, for example, solid lasers such as ruby, glass, Nd-YAG, and Nd- YVO4 ; diode lasers such as GaAs, InGaAs, and GaN; helium-neon, argon, krypton, excimer, Examples include gas lasers such as CO2 ; lasers with excellent monochromaticity and directivity, such as dye lasers having dyes; and the like.
  • the irradiation amount of the object light, reproduction light, and reference light there is no limit to the irradiation amount of the object light, reproduction light, and reference light, and the irradiation amount is arbitrary as long as recording and reproduction are possible.
  • the irradiation dose is extremely small, the chemical change of the polymerizable monomer may be too incomplete and the heat resistance and mechanical properties of the recording layer may not be sufficiently developed.
  • the irradiation dose is extremely large, the components of the recording layer (components of the composition for a holographic recording medium of the present invention) may deteriorate.
  • the object beam, the reproduction beam, and the reference beam are usually 0.00, depending on the composition of the holographic recording medium composition of the present invention used to form the recording layer, the type and amount of the photopolymerization initiator, etc. Irradiation is performed in a range of 1 J/cm 2 or more and 20 J/cm 2 or less.
  • Examples of the hologram recording method include a polarized collinear hologram recording method and a reference beam incident angle multiplexed hologram recording method.
  • the hologram recording medium of the present invention is used as a recording medium, it is possible to provide good recording quality with any recording method.
  • a volume hologram is recorded on the hologram recording medium of the present invention in the same manner as in the aforementioned large-capacity memory application.
  • a predetermined reproduction light is irradiated onto the recording layer.
  • the irradiated reproduction light is diffracted according to the interference fringes.
  • the corresponding interference fringes are recorded according to the wavelength and incidence angle of the reproduced light to be diffracted, it is possible to cause diffraction for the reproduced light in a wide wavelength range, and the display color gamut of AR glasses can be increased. Can be expanded.
  • the wavelength range of the object light and the reproduction light is arbitrary depending on the respective uses, and may be in the visible light range or the ultraviolet range. Among these lights, the above-mentioned laser and the like are preferable.
  • the reproduction light is not limited to lasers and the like, and display devices such as liquid crystal displays (LCDs) and organic electroluminescent displays (OLEDs) are also suitable.
  • the irradiation amount of the object light, reproduction light, and reference light there is no limit to the irradiation amount of the object light, reproduction light, and reference light, and the irradiation amount is arbitrary as long as recording and reproduction are possible.
  • the irradiation dose is extremely small, the chemical change of the polymerizable monomer may be too incomplete and the heat resistance and mechanical properties of the recording layer may not be sufficiently developed.
  • the irradiation dose is extremely large, the components of the recording layer (components of the composition for a holographic recording medium of the present invention) may deteriorate.
  • the object beam, the reproduction beam, and the reference beam are usually 0.00, depending on the composition of the holographic recording medium composition of the present invention used to form the recording layer, the type and amount of the photopolymerization initiator, etc. Irradiation is performed in a range of 1 J/cm 2 or more and 20 J/cm 2 or less.
  • PCL-204HGT Polycaprolactone diol (molecular weight 400) (manufactured by Daicel)
  • PCL-205U Polycaprolactone diol (molecular weight 530) (manufactured by Daicel)
  • PCL-305 Polycaprolactone triol (molecular weight 550) (manufactured by Daicel)
  • HHM303 2-[[2,2-bis[(2-dibenzothiophen-4-ylphenyl)sulfanylmethyl]-3-(1,3-benzothiazo-2-lylsulfanylmethyl)propoxy]carbonylamino]ethyl acrylate (molecular weight 975)
  • Photopolymerization initiator/HLI02 1-(9-ethyl-6-cyclohexanoyl-9H-carbazol-3-yl)-1-(O-acetyloxime) methyl glutarate (molecular weight 505)
  • Component (e) Compound having an isocyanate-reactive functional group and a nitroxyl radical group - 4-hydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl free radical (TEMPOL): Manufactured by Tokyo Kasei Co., Ltd.
  • Component (f) Octylic acid solution of curing catalyst/tris(2-ethylhexanoate) bismuth (active ingredient amount 56% by weight)
  • Example 1 0.8541 g of polymerizable monomer HLM303, 0.0274 g of photoinitiator HLI02, and 0.0103 g of TEMPOL were dissolved in 0.8470 g of Duranate TM TSS-100 and 1.9764 g of Duranate TM A201H. Thereto, 0.7618 g of PCL-204HGT and 1.4148 g of PCL-305 were mixed, and 0.0005 g of an octylic acid solution of tris(2-ethylhexanoate) bismuth was dissolved and mixed with stirring.
  • a sample for evaluating a composition for a holographic recording medium was prepared by heating.
  • a recording layer with a thickness of 0.5 mm was formed between slide glasses serving as covers.
  • Example 2 Polymerizable monomer HLM201: 0.6306 g, photoinitiator HLI02: 0.0227 g, and TEMPOL: 0.0085 g were dissolved in 1.7661 g of Duranate TM TSS-100 and 1.1774 g of Tronate XFLO100. Thereto, 0.2057 g of PCL-205U and 1.8509 g of PCL-305 were mixed with stirring. An evaluation sample was prepared in the same manner as in Example 1 using the mixed solution.
  • DuranateTM TSS-100 is a mixture of difunctional and trifunctional isocyanate compounds, it cannot be determined by calculation from the NCO value. Therefore, the amount of allophanate binding units (mol/g) was calculated using the procedure described below. Benzylamine: 10 mg/1 mL (acetonitrile) was added to DuranateTM TSS-100: 5 mg/1 mL (acetonitrile), and the mixture was reacted at room temperature for 30 minutes. DMF (3 mL) was added to this to dissolve the precipitated components and a sample was analyzed by LC/MS. The LC/MS conditions are as shown in Table 1 below. From the obtained spectrum, the amount of allophanate binding units present (mol/g) was determined from the ratio of the peak area of all components to the peak area of the allophanate binding unit-containing structure.
  • Duranate TM TUL-100 and Takenate 600 are isocyanate compounds that do not contain allophanate linking units.
  • hologram recording and evaluation method Using the composition evaluation samples for hologram recording media produced in Examples and Comparative Examples, hologram recording and evaluation of the hologram recording performance of the hologram recording medium were performed according to the procedure described below.
  • the hologram recording was performed using a semiconductor laser with a wavelength of 405 nm and an exposure apparatus shown in FIG. 1 with an exposure power density of 10 mW/cm 2 per beam to perform two-beam plane wave hologram recording. This will be explained in detail below.
  • FIG. 1 is a block diagram showing an outline of an apparatus used for transmission hologram recording.
  • FIG. 2 is a block diagram showing an outline of the apparatus used for recording the reflection hologram.
  • S is a sample of a hologram recording medium.
  • M1, M2 and M3 all represent mirrors.
  • CS is an exposure time control shutter.
  • BS is a beam shutter.
  • PBS is a polarizing beam splitter.
  • the LED is a light source for post-exposure (LED with a center wavelength of 405 nm manufactured by THORLAB).
  • LD indicates a recording laser light source that emits light with a wavelength of 405 nm (a single mode laser manufactured by TOPTICA Photonics that can obtain light around a wavelength of 405 nm).
  • PD1 and PD2 indicate photodetectors.
  • Transmission hologram recording exposure the light with a wavelength of 405 nm generated from the LD is split by the PBS, and these are considered as object light (M1 side) and reference light (M2 side), and the angle between the two beams is 59.
  • the irradiation was performed so as to cross the recording surface at an angle of 3°.
  • the bisector of the angle formed by the two beams (hereinafter referred to as the optical axis) is made perpendicular to the recording surface of the recording layer of the hologram recording medium S, and the The plane of vibration of the electric field vectors of the two beams was made perpendicular to the plane containing the two intersecting beams.
  • the sample rotation angle was set to 0°, and 181 multiple recording exposures were performed on the same location while changing the sample rotation angle by 0.2° from ⁇ 18° to +18°. At this time, recording exposure was carried out equally so that the total recording energy was 2 J/cm 2 in all Examples and Comparative Examples so that the amounts of polymerizable monomer and photopolymerization initiator consumed for recording were equal. Ta.
  • Reflectid hologram recording exposure the light with a wavelength of 405 nm generated from the LD is split by the PBS, and these are regarded as the object light (M1-M3 side) and the reference light (M2 side), and the angle between the two beams is The light was irradiated so as to cross the recording surface at an angle of 127°.
  • the sample rotation angle of 0° was the same as that used in the transmission hologram recording exposure device, and 161 multiple recording exposures were performed on the same location while changing the orientation of the hologram recording medium S from -24° to +29°. .
  • recording exposure was carried out equally so that the total recording energy was 2 J/cm 2 in all Examples and Comparative Examples. Ta.

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JP2012504665A (ja) * 2008-10-01 2012-02-23 バイエル・マテリアルサイエンス・アクチェンゲゼルシャフト ホログラフィック媒体製造用のプレポリマー系ポリウレタン配合物
JP2016517450A (ja) * 2013-03-14 2016-06-16 ヴェンコレックス・フランス ポリアクリレートアロファネート
JP2016145352A (ja) * 2009-11-03 2016-08-12 コベストロ、ドイチュラント、アクチエンゲゼルシャフトＣｏｖｅｓｔｒｏ Ｄｅｕｔｓｃｈｌａｎｄ Ａｇ 感光性ポリマー組成物における添加剤としてのフルオロウレタン
WO2020032167A1 (ja) * 2018-08-09 2020-02-13 三菱ケミカル株式会社 ホログラム記録媒体用組成物及びホログラム記録媒体
JP2022106253A (ja) 2021-01-06 2022-07-19 アウル株式会社 プログラム、方法、情報処理装置、システム

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JP2012504665A (ja) * 2008-10-01 2012-02-23 バイエル・マテリアルサイエンス・アクチェンゲゼルシャフト ホログラフィック媒体製造用のプレポリマー系ポリウレタン配合物
JP2016145352A (ja) * 2009-11-03 2016-08-12 コベストロ、ドイチュラント、アクチエンゲゼルシャフトＣｏｖｅｓｔｒｏ Ｄｅｕｔｓｃｈｌａｎｄ Ａｇ 感光性ポリマー組成物における添加剤としてのフルオロウレタン
JP2016517450A (ja) * 2013-03-14 2016-06-16 ヴェンコレックス・フランス ポリアクリレートアロファネート
WO2020032167A1 (ja) * 2018-08-09 2020-02-13 三菱ケミカル株式会社 ホログラム記録媒体用組成物及びホログラム記録媒体
JP2022106253A (ja) 2021-01-06 2022-07-19 アウル株式会社 プログラム、方法、情報処理装置、システム

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