JP5803401B2 - ホログラム記録材料及びホログラム記録媒体 - Google Patents
ホログラム記録材料及びホログラム記録媒体 Download PDFInfo
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- JP5803401B2 JP5803401B2 JP2011171895A JP2011171895A JP5803401B2 JP 5803401 B2 JP5803401 B2 JP 5803401B2 JP 2011171895 A JP2011171895 A JP 2011171895A JP 2011171895 A JP2011171895 A JP 2011171895A JP 5803401 B2 JP5803401 B2 JP 5803401B2
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- Prior art keywords
- polymerizable monomer
- hologram recording
- recording material
- refractive index
- monomer
- Prior art date
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- 239000000463 material Substances 0.000 title claims description 87
- 239000000178 monomer Substances 0.000 claims description 193
- 239000003999 initiator Substances 0.000 claims description 69
- 150000001875 compounds Chemical class 0.000 claims description 41
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- 230000037048 polymerization activity Effects 0.000 claims description 30
- 150000001768 cations Chemical class 0.000 claims description 25
- 238000010526 radical polymerization reaction Methods 0.000 claims description 25
- 238000010538 cationic polymerization reaction Methods 0.000 claims description 22
- 229920005596 polymer binder Polymers 0.000 claims description 15
- 239000002491 polymer binding agent Substances 0.000 claims description 15
- 125000003118 aryl group Chemical group 0.000 claims description 12
- 125000003566 oxetanyl group Chemical group 0.000 claims description 11
- 125000002091 cationic group Chemical group 0.000 claims description 10
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- 125000003700 epoxy group Chemical group 0.000 claims description 9
- 238000010438 heat treatment Methods 0.000 claims description 9
- 239000007788 liquid Substances 0.000 claims description 8
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- 150000007517 lewis acids Chemical class 0.000 claims description 5
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- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
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- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 3
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- KSCKTBJJRVPGKM-UHFFFAOYSA-N octan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCCCCCC[O-].CCCCCCCC[O-].CCCCCCCC[O-].CCCCCCCC[O-] KSCKTBJJRVPGKM-UHFFFAOYSA-N 0.000 description 3
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- WPZJSWWEEJJSIZ-UHFFFAOYSA-N tetrabromobisphenol-F Natural products C1=C(Br)C(O)=C(Br)C=C1CC1=CC(Br)=C(O)C(Br)=C1 WPZJSWWEEJJSIZ-UHFFFAOYSA-N 0.000 description 3
- 238000012546 transfer Methods 0.000 description 3
- LWNGJAHMBMVCJR-UHFFFAOYSA-N (2,3,4,5,6-pentafluorophenoxy)boronic acid Chemical compound OB(O)OC1=C(F)C(F)=C(F)C(F)=C1F LWNGJAHMBMVCJR-UHFFFAOYSA-N 0.000 description 2
- LJWZDTGRJUXOCE-UHFFFAOYSA-N 2-(2-ethylhexyl)oxetane Chemical compound CCCCC(CC)CC1CCO1 LJWZDTGRJUXOCE-UHFFFAOYSA-N 0.000 description 2
- QNYBOILAKBSWFG-UHFFFAOYSA-N 2-(phenylmethoxymethyl)oxirane Chemical compound C1OC1COCC1=CC=CC=C1 QNYBOILAKBSWFG-UHFFFAOYSA-N 0.000 description 2
- YCPMSWJCWKUXRH-UHFFFAOYSA-N 2-[4-[9-[4-(2-prop-2-enoyloxyethoxy)phenyl]fluoren-9-yl]phenoxy]ethyl prop-2-enoate Chemical compound C1=CC(OCCOC(=O)C=C)=CC=C1C1(C=2C=CC(OCCOC(=O)C=C)=CC=2)C2=CC=CC=C2C2=CC=CC=C21 YCPMSWJCWKUXRH-UHFFFAOYSA-N 0.000 description 2
- KUAUJXBLDYVELT-UHFFFAOYSA-N 2-[[2,2-dimethyl-3-(oxiran-2-ylmethoxy)propoxy]methyl]oxirane Chemical compound C1OC1COCC(C)(C)COCC1CO1 KUAUJXBLDYVELT-UHFFFAOYSA-N 0.000 description 2
- VEORPZCZECFIRK-UHFFFAOYSA-N 3,3',5,5'-tetrabromobisphenol A Chemical compound C=1C(Br)=C(O)C(Br)=CC=1C(C)(C)C1=CC(Br)=C(O)C(Br)=C1 VEORPZCZECFIRK-UHFFFAOYSA-N 0.000 description 2
- FNYWFRSQRHGKJT-UHFFFAOYSA-N 3-ethyl-3-[(3-ethyloxetan-3-yl)methoxymethyl]oxetane Chemical compound C1OCC1(CC)COCC1(CC)COC1 FNYWFRSQRHGKJT-UHFFFAOYSA-N 0.000 description 2
- NZGQHKSLKRFZFL-UHFFFAOYSA-N 4-(4-hydroxyphenoxy)phenol Chemical compound C1=CC(O)=CC=C1OC1=CC=C(O)C=C1 NZGQHKSLKRFZFL-UHFFFAOYSA-N 0.000 description 2
- QEQQAFXMPDXVSV-UHFFFAOYSA-N 4-[1,2,2,3,3,3-hexafluoro-1-(4-hydroxyphenyl)propyl]phenol Chemical compound C1=CC(O)=CC=C1C(F)(C(F)(F)C(F)(F)F)C1=CC=C(O)C=C1 QEQQAFXMPDXVSV-UHFFFAOYSA-N 0.000 description 2
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- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 2
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- OZLBDYMWFAHSOQ-UHFFFAOYSA-N diphenyliodanium Chemical compound C=1C=CC=CC=1[I+]C1=CC=CC=C1 OZLBDYMWFAHSOQ-UHFFFAOYSA-N 0.000 description 2
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- NFLOWLFQCMNSRE-UHFFFAOYSA-N methyl 2-tert-butylperoxycarbonyl-4-(3-tert-butylperoxycarbonyl-4-methoxycarbonylbenzoyl)benzoate Chemical compound C1=C(C(=O)OOC(C)(C)C)C(C(=O)OC)=CC=C1C(=O)C1=CC=C(C(=O)OC)C(C(=O)OOC(C)(C)C)=C1 NFLOWLFQCMNSRE-UHFFFAOYSA-N 0.000 description 2
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- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 150000004032 porphyrins Chemical class 0.000 description 1
- 125000006238 prop-1-en-1-yl group Chemical group [H]\C(*)=C(/[H])C([H])([H])[H] 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 239000007870 radical polymerization initiator Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 150000003459 sulfonic acid esters Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical compound CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 150000004897 thiazines Chemical class 0.000 description 1
- OKYDCMQQLGECPI-UHFFFAOYSA-N thiopyrylium Chemical class C1=CC=[S+]C=C1 OKYDCMQQLGECPI-UHFFFAOYSA-N 0.000 description 1
- 238000006276 transfer reaction Methods 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- LGQXXHMEBUOXRP-UHFFFAOYSA-N tributyl borate Chemical compound CCCCOB(OCCCC)OCCCC LGQXXHMEBUOXRP-UHFFFAOYSA-N 0.000 description 1
- WILBTFWIBAOWLN-UHFFFAOYSA-N triethyl(triethylsilyloxy)silane Chemical compound CC[Si](CC)(CC)O[Si](CC)(CC)CC WILBTFWIBAOWLN-UHFFFAOYSA-N 0.000 description 1
- WLOQLWBIJZDHET-UHFFFAOYSA-N triphenylsulfonium Chemical compound C1=CC=CC=C1[S+](C=1C=CC=CC=1)C1=CC=CC=C1 WLOQLWBIJZDHET-UHFFFAOYSA-N 0.000 description 1
- 239000012953 triphenylsulfonium Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/0005—Production of optical devices or components in so far as characterised by the lithographic processes or materials used therefor
- G03F7/001—Phase modulating patterns, e.g. refractive index patterns
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
- G03F7/032—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with binders
- G03F7/033—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with binders the binders being polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. vinyl polymers
-
- 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
- G03H1/024—Hologram nature or properties
- G03H1/0244—Surface relief holograms
-
- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B7/00—Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
- G11B7/24—Record carriers characterised by shape, structure or physical properties, or by the selection of the material
- G11B7/2403—Layers; Shape, structure or physical properties thereof
- G11B7/24035—Recording layers
- G11B7/24044—Recording layers for storing optical interference patterns, e.g. holograms; for storing data in three dimensions, e.g. volume storage
-
- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B7/00—Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
- G11B7/24—Record carriers characterised by shape, structure or physical properties, or by the selection of the material
- G11B7/241—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
- G11B7/242—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers
- G11B7/244—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only
- G11B7/245—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only containing a polymeric component
-
- 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
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03H—HOLOGRAPHIC PROCESSES OR APPARATUS
- G03H2260/00—Recording materials or recording processes
- G03H2260/12—Photopolymer
Description
画像記録に用いられる反射型ホログラムでは、回折効率(回折スペクトルのピーク値)は屈折率変調度(Δn)の上昇に伴って急速に100%に漸近する一方、半値全幅はΔnに対してほぼ線形的に増加する。すなわち、回折効率だけでなく半値全幅の拡大も図ろうとすると、より高いΔnが必要になる。
同公報における成分(a)の平均屈折率は成分(b)の平均屈折率より低い。すなわち、成分(a)は前記可塑剤(III)に相当する。室温で液状の可塑剤にカチオン重合性を付与することにより、記録時には光重合性モノマー(I)の拡散を促す可塑剤として作用させる一方、記録後に例えば紫外光でカチオン重合させることにより硬化できる。このため、紫外光照射(ポストキュアと呼ぶ)後の記録膜に液状成分が残ることがなく、記録信号の安定性が高い。
(1)ラジカル重合活性を有し、且つカチオン重合に対して実質的に不活性である重合性モノマー(A)、カチオン重合活性を有し、且つラジカル重合に対して実質的に不活性である重合性モノマー(B)、及び、光照射により少なくとも重合性モノマー(A)又は重合性モノマー(B)のいずれかを重合させる開始剤系(C)を含み、重合性モノマー(A)及び重合性モノマー(B)がともに、芳香環、フッ素以外のハロゲン原子、及び、環状スルフィド及びメルカプト基以外に由来する硫黄原子、からなる群から選ばれる部位をその構造中に有するホログラム記録材料。
等が挙げられる。
前記重合性モノマー(A) 10〜40重量部、
前記重合性モノマー(B) 10〜40重量部、
前記光重合開始剤系(C) 0.1〜10重量部、
前記可塑剤(D) 5〜50重量部、
前記高分子結合剤(E) 5〜50重量部、
とすることが好ましく、
前記重合性モノマー(A) 10〜30重量部、
前記重合性モノマー(B) 10〜30重量部、
前記光重合開始剤系(C) 0.5〜5重量部、
前記可塑剤(D) 10〜40重量部、
前記高分子結合剤(E) 10〜40重量部、
とすることがより好ましい。
ただし、高分子結合剤(E)を用いない場合には、
前記重合性モノマー(A) 10〜40重量部、
前記重合性モノマー(B) 10〜40重量部、
前記光重合開始剤系(C) 0.1〜10重量部、
前記可塑剤(D) 20〜80重量部
とすることが好ましく、
前記重合性モノマー(A) 10〜30重量部、
前記重合性モノマー(B) 10〜30重量部、
前記光重合開始剤系(C) 0.5〜5重量部、
前記可塑剤(D) 35〜60重量部、
とすることがより好ましい。
また、上記の各成分以外に、界面活性剤、重合禁止剤、連鎖移動剤、ラジカル重合反応及び/又はカチオン重合反応を促進するための助触媒、紫外線吸収剤などの各種添加剤を添加してもよい。
(ホログラム記録媒体サンプルの作製)
以下の手順に従って、表1に示す配合組成の記録材料組成物溶液を調製した。
重合性モノマー(A)として9,9−ビス[4−(2−アクリロイルオキシエトキシ)フェニル]フルオレン(新中村化学工業(株)製NKエステルA−BPEF、n20/D=1.62)2.0g、及び重合性モノマー(B)として1,2−エポキシエチル基を有し、且つ9,9−ジアリールフルオレン骨格を有するフルオレンモノマー(大阪ガスケミカル(株)製オグソールEG−250、n20/D=1.58)2.0g、可塑剤(D)としてセバシン酸ジエチル(東京化成工業(株)製、n20/D=1.44)0.5g、カチオン反応性可塑剤(Dc)としてネオペンチルグリコールジグリシジルエーテル(シグマ・アルドリッチ社製、n20/D=1.46)1.0g、及び高分子結合剤(E)として酢酸ビニルポリマー(シグマ・アルドリッチ社製、重量平均分子量Mw=100,000、n20/D=1.47)2.0gを混合し、次いで光ラジカル開始剤(C−1r)として3,3’−ジ(tert−ブチルパーオキシカルボニル)−4,4’−ジ(メトキシカルボニル)ベンゾフェノンほか位置異性体混合物(チッソ(株)製BT−2、40%アニソール溶液)0.25g、光カチオン開始剤(C−1c)として、トリアリールスルホニウムヘキサフルオロアンチモネート(三新化学工業(株)製サンエイドSI−100L)0.1g、及び20mgの増感色素(C−2)(Dye−1: 3−ブチル−2−[3−(3−ブチル−5−フェニル−1,3−ベンゾオキサゾール−2(3H)−イリデン)プロパ−1−エン−1−イル]−5−フェニル−1,3−ベンゾオキサゾール−1−イウム=ヘキサフルオロ−λ5−ホスファヌイド)を溶解させた10.37gのアセトン溶液(アセトンとして10.0g)を添加し、撹拌して溶解させた。なお、前記増感色素は、光ラジカル開始剤(C−1r)を分光増感する作用を有する。このようにして記録材料組成物を得た。
実施例1のホログラム記録媒体サンプルについて、図1に示すようなホログラム記録光学系を用いて、特性評価を行った。図1の紙面の方向を便宜的に水平方向とする。
回折効率η(%)=[(T0−Tp)/T0]×100
各構成成分を、表1〜2に示すような化合物及び配合組成とした以外は、実施例1と同様にしてホログラム記録媒体サンプルをそれぞれ作製し、その特性評価を行った。ただし、実施例4の記録媒体サンプルについてのみ、実施例1と同様の手順に従って反射型ホログラムの記録及び光ポストキュアを行った後、さらに80℃で1時間の熱ポストキュアを行った。結果を表3に示す。また、開始剤系(C)及び希釈溶媒を除く各成分の屈折率(n20/D)を併せて表1〜2に付記した。
重合性モノマー(A)
・A−BPEF: 9,9−ビス[4−(2−アクリロイルオキシエトキシ)フェニル]フルオレン (新中村化学工業(株)製)
・2−フェノキシエチルアクリレート (シグマ・アルドリッチ社製)
・A−DCP: トリシクロデカンメタノール ジアクリレート (新中村化学工業(株)製)
・EG−250: 1,2−エポキシ基を有し、且つ9,9−ジアリールフルオレン骨格を有するフルオレンモノマー (大阪ガスケミカル(株)製、エポキシ当量:393g/eq)
・ベンジルグリシジルエーテル (シグマ・アルドリッチ社製)
・CHDC−DG: 1,2−シクロヘキサンジカルボン酸ジグリシジル (シグマ・アルドリッチ社製)
・セバシン酸ジエチル (東京化成工業(株)製)
・ジ(エチレングリコール)ジベンゾエート (シグマ・アルドリッチ社製)
・りん酸トリクレジル (和光純薬工業(株)製)
カチオン反応性可塑剤(Dc)
・ネオペンチルグリコールジグリシジルエーテル (シグマ・アルドリッチ社製)
・OXT−212: 2−エチルヘキシルオキセタン (東亞合成(株)製)
・2,4,7,9−テトラメチル−5−デシン−4,7−ジオール エトキシレート (シグマ・アルドリッチ社製、Mw=395、淡黄色粘稠液体、下記式(1)の化合物)
・酢酸ビニルポリマー (シグマ・アルドリッチ社製、Mw=100,000)
・ポリ(メタクリル酸メチル) (シグマ・アルドリッチ社製、Mw=23,800)
・BT−2: 3,3’−ジ(tert−ブチルパーオキシカルボニル)−4,4’−ジ(メトキシカルボニル)ベンゾフェノンほか位置異性体混合物 (チッソ(株)製、40%アニソール溶液)
光カチオン開始剤(C−1c)
・SI−100L: トリアリールスルホニウム ヘキサフルオロアンチモネート (三新化学工業(株)製)
・DAI−B: 4−イソプロピル−4’−メチルジフェニルヨードニウム テトラキス(ペンタフルオロフェニル)ボレート (東京化成工業(株)製)
増感色素(C−2)
・Dye−1: 3−ブチル−2−[3−(3−ブチル−5−フェニル−1,3−ベンゾオキサゾール−2(3H)−イリデン)プロパ−1−エン−1−イル]−5−フェニル−1,3−ベンゾオキサゾール−1−イウム=ヘキサフルオロ−λ5−ホスファヌイド (下記式(2)の化合物)
・Dye−2: 2,5−ビス(4−ジブチルアミノベンジリデン)シクロペンタノン (下記式(3)の化合物)
・CP−77: 1−(3−メチル−2−ブテニル)テトラヒドロチオフェニウム ヘキサフルオロアンチモネート ((株)ADEKA製、66%プロピレンカーボネート溶液、下記式(4)の化合物)
一方、比較例1〜2では、ラジカル重合活性を有する重合性モノマー(A)と、カチオン重合活性を有する重合性モノマー(B)のいずれか一方しか用いていない。また、比較例3では、重合性モノマー(A)と重合性モノマー(B)が、芳香環、フッ素以外のハロゲン原子、及び、環状スルフィド及びメルカプト基以外に由来する硫黄原子、からなる群から選ばれる部位のいずれも有していない。その結果、回折ピークの半値全幅、若しくは半値全幅と回折効率の両方が、実施例1〜4、参考例1〜5に比べて大きく劣っていた。
(11):光源
(12):シャッター
(13),(15):凸レンズ
(14):ピンホール
(16),(19),(20):ミラー
(17):1/2波長板
(18):ビームスプリッタ
(21),(22):アパーチャ
Claims (6)
- ラジカル重合活性を有し、且つカチオン重合に対して実質的に不活性である重合性モノマー(A)、カチオン重合活性を有し、且つラジカル重合に対して実質的に不活性である重合性モノマー(B)、光照射により少なくとも前記重合性モノマー(A)又は前記重合性モノマー(B)のいずれかを重合させる開始剤系(C)、室温で液状である可塑剤(D)と高分子結合剤(E)との少なくとも一方、及び、加熱によりブレンステッド酸またはルイス酸を発生する熱カチオン開始剤(F)を含み、
前記重合性モノマー(A)及び前記重合性モノマー(B)がともに、芳香環をその構造中に有し、
前記開始剤系(C)が、可視光の照射により前記重合性モノマー(A)を重合させる光ラジカル開始剤系であり、
前記熱カチオン開始剤(F)が、トリアルキルスルホニウム塩類であるホログラム記録材料であって、
前記重合性モノマー(A)と前記重合性モノマー(B)とを同質量含み、
前記可塑剤(D)は、前記重合性モノマー(A)及び前記重合性モノマー(B)のいずれの平均屈折率よりも0.05以上低い屈折率を有し、
前記高分子結合剤(E)は、前記重合性モノマー(A)及び前記重合性モノマー(B)のいずれの平均屈折率よりも0.05以上低い屈折率を有する
ことを特徴とするホログラム記録材料。 - 前記重合性モノマー(A)が(メタ)アクリロイル基を有する化合物であって、且つ前記重合性モノマー(B)が、少なくともエポキシ基又はオキセタニル基のいずれかを有する化合物である、請求項1に記載のホログラム記録材料。
- 前記重合性モノマー(A)の少なくとも一部と、前記重合性モノマー(B)の少なくとも一部とが、ともに9,9−ジアリールフルオレン骨格を有するものである、請求項1または2に記載のホログラム記録材料。
- 前記可塑剤(D)の少なくとも一部が、カチオン反応性可塑剤(Dc)である、請求項1〜3のいずれか1項に記載のホログラム記録材料。
- 前記開始剤系(C)がさらに、光照射によりブレンステッド酸又はルイス酸を発生するものである、請求項1〜4のいずれか1項に記載のホログラム記録材料。
- 基材と、前記基材上に形成された請求項1〜5のいずれか1項に記載のホログラム記録材料からなるホログラム記録層とを有するホログラム記録媒体。
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US13/566,371 US8900775B2 (en) | 2011-08-05 | 2012-08-03 | Hologram recording material and hologram recording medium |
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JP6130122B2 (ja) * | 2012-10-15 | 2017-05-17 | 株式会社ダイセル | 体積ホログラム記録層形成用感光性組成物 |
KR101724616B1 (ko) * | 2014-09-18 | 2017-04-07 | 주식회사 엘지화학 | 유리 대체용 경화성 조성물 |
CN107533318B (zh) * | 2015-04-27 | 2021-06-29 | 索尼公司 | 全息记录组合物、全息记录介质和全息记录介质的制造方法 |
US20180180994A1 (en) | 2015-06-23 | 2018-06-28 | Covestro Deutschland Ag | Substituted triazines |
EP3327472B1 (en) * | 2015-07-23 | 2019-10-30 | Konica Minolta, Inc. | Holographic optical element and production method therefor |
US11299430B2 (en) * | 2016-11-30 | 2022-04-12 | Hrl Laboratories, Llc | Formulations with active functional additives for 3D printing of preceramic polymers, and methods of 3D-printing the formulations |
KR20210102237A (ko) * | 2018-12-11 | 2021-08-19 | 소니그룹주식회사 | 홀로그램 기록용 조성물, 홀로그램 기록 매체, 회절 광학 소자, 및 이를 사용한 광학 장치, 광학 부품, 화상 표시 장치 |
WO2020158300A1 (ja) * | 2019-01-31 | 2020-08-06 | ソニー株式会社 | ホログラム記録用組成物、ホログラム記録媒体、ホログラム光学素子、及びこれを用いた光学装置、光学部品並びにホログラム回折格子の形成方法 |
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US4942112A (en) * | 1988-01-15 | 1990-07-17 | E. I. Du Pont De Nemours And Company | Photopolymerizable compositions and elements for refractive index imaging |
JP3058929B2 (ja) | 1991-03-15 | 2000-07-04 | セントラル硝子株式会社 | ホログラフィック光学素子の評価方法およびその装置 |
JP2873126B2 (ja) | 1991-04-17 | 1999-03-24 | 日本ペイント株式会社 | 体積ホログラム記録用感光性組成物 |
JP2859761B2 (ja) * | 1991-07-03 | 1999-02-24 | 日本化薬株式会社 | 放射線硬化性樹脂組成物及びその硬化物 |
JP2849021B2 (ja) * | 1993-04-12 | 1999-01-20 | 日本ペイント株式会社 | 体積ホログラム記録用感光性組成物 |
JP3370762B2 (ja) | 1993-11-04 | 2003-01-27 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | フィルム組成物およびその組成物を含む積層構造 |
JPH1135611A (ja) * | 1997-07-15 | 1999-02-09 | Denki Kagaku Kogyo Kk | 樹脂組成物、活性エネルギー線硬化性樹脂組成物及びその硬化物 |
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JP2001282082A (ja) | 2000-01-25 | 2001-10-12 | Natl Inst Of Advanced Industrial Science & Technology Meti | ホログラム記録材料組成物、ホログラム記録媒体およびその製法 |
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JP4142396B2 (ja) * | 2002-10-18 | 2008-09-03 | 大日本印刷株式会社 | 体積型ホログラム記録用感光性組成物およびそれを用いた体積型ホログラム記録用感光性媒体 |
JP4525042B2 (ja) * | 2003-10-01 | 2010-08-18 | コニカミノルタエムジー株式会社 | ホログラフィック記録用組成物、ホログラフィック記録メディア、およびホログラフィック記録方法 |
JP2005181954A (ja) * | 2003-11-28 | 2005-07-07 | Konica Minolta Medical & Graphic Inc | ホログラフィック記録メディア、ホログラフィック記録方法およびホログラフィック情報メディア |
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JP2006003388A (ja) * | 2004-06-15 | 2006-01-05 | Daiso Co Ltd | 体積位相型ホログラム記録用感光性組成物、ホログラム記録媒体とその製法、およびホログラム記録法 |
JP4632101B2 (ja) * | 2008-07-02 | 2011-02-16 | ソニー株式会社 | 光情報記録媒体 |
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