CN109765754A - 固化性组合物、固化膜形成方法、固化物、已被图案化的固化膜、及透明光学构件 - Google Patents
固化性组合物、固化膜形成方法、固化物、已被图案化的固化膜、及透明光学构件 Download PDFInfo
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- CN109765754A CN109765754A CN201811344055.9A CN201811344055A CN109765754A CN 109765754 A CN109765754 A CN 109765754A CN 201811344055 A CN201811344055 A CN 201811344055A CN 109765754 A CN109765754 A CN 109765754A
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- 150000001875 compounds Chemical class 0.000 title claims abstract description 165
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- 230000008023 solidification Effects 0.000 title claims abstract description 87
- 238000000034 method Methods 0.000 title claims abstract description 51
- 239000000463 material Substances 0.000 title claims abstract description 44
- 230000003287 optical effect Effects 0.000 title claims abstract description 14
- 125000001424 substituent group Chemical group 0.000 claims description 179
- -1 nitro, Cyano, sulfydryl Chemical group 0.000 claims description 160
- 125000000217 alkyl group Chemical group 0.000 claims description 124
- 229910052799 carbon Inorganic materials 0.000 claims description 78
- 125000003118 aryl group Chemical group 0.000 claims description 47
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 37
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 claims description 27
- 125000005843 halogen group Chemical group 0.000 claims description 24
- 239000000758 substrate Substances 0.000 claims description 24
- 125000003545 alkoxy group Chemical group 0.000 claims description 23
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 23
- 239000002904 solvent Substances 0.000 claims description 22
- 125000001118 alkylidene group Chemical group 0.000 claims description 21
- 125000002252 acyl group Chemical group 0.000 claims description 20
- 239000000126 substance Substances 0.000 claims description 19
- 230000008569 process Effects 0.000 claims description 18
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- 239000003505 polymerization initiator Substances 0.000 claims description 17
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 16
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- 125000004093 cyano group Chemical group *C#N 0.000 claims description 12
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- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 8
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- 125000000962 organic group Chemical group 0.000 description 43
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 33
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- 125000001931 aliphatic group Chemical group 0.000 description 8
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 8
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- 125000001231 benzoyloxy group Chemical group C(C1=CC=CC=C1)(=O)O* 0.000 description 6
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- 125000001309 chloro group Chemical group Cl* 0.000 description 6
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- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 5
- QZZJTWAHFMBFSX-UHFFFAOYSA-N 2,4-bis(trichloromethyl)-1,3,5-triazine Chemical compound ClC(Cl)(Cl)C1=NC=NC(C(Cl)(Cl)Cl)=N1 QZZJTWAHFMBFSX-UHFFFAOYSA-N 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Natural products CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 5
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- 125000002619 bicyclic group Chemical group 0.000 description 5
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- 125000003884 phenylalkyl group Chemical group 0.000 description 5
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- VVBLNCFGVYUYGU-UHFFFAOYSA-N 4,4'-Bis(dimethylamino)benzophenone Chemical compound C1=CC(N(C)C)=CC=C1C(=O)C1=CC=C(N(C)C)C=C1 VVBLNCFGVYUYGU-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
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- 239000002253 acid Substances 0.000 description 4
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
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- YPHQUSNPXDGUHL-UHFFFAOYSA-N n-methylprop-2-enamide Chemical compound CNC(=O)C=C YPHQUSNPXDGUHL-UHFFFAOYSA-N 0.000 description 4
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- RXELBMYKBFKHSM-UHFFFAOYSA-N 2-phenyl-1,3,5-triazine Chemical compound C1=CC=CC=C1C1=NC=NC=N1 RXELBMYKBFKHSM-UHFFFAOYSA-N 0.000 description 3
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- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 3
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- 125000004122 cyclic group Chemical group 0.000 description 3
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- ATUOYWHBWRKTHZ-UHFFFAOYSA-N dimethylmethane Natural products CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 3
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- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
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- MQDJYUACMFCOFT-UHFFFAOYSA-N bis[2-(1-hydroxycyclohexyl)phenyl]methanone Chemical compound C=1C=CC=C(C(=O)C=2C(=CC=CC=2)C2(O)CCCCC2)C=1C1(O)CCCCC1 MQDJYUACMFCOFT-UHFFFAOYSA-N 0.000 description 2
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- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
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- ZMIGMASIKSOYAM-UHFFFAOYSA-N cerium Chemical compound [Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce] ZMIGMASIKSOYAM-UHFFFAOYSA-N 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
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- 125000000000 cycloalkoxy group Chemical group 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
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- XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
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- CIBMHJPPKCXONB-UHFFFAOYSA-N propane-2,2-diol Chemical compound CC(C)(O)O CIBMHJPPKCXONB-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 150000003233 pyrroles Chemical class 0.000 description 1
- 229940107700 pyruvic acid Drugs 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 235000021003 saturated fats Nutrition 0.000 description 1
- 238000009738 saturating Methods 0.000 description 1
- 238000000790 scattering method Methods 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 239000003566 sealing material Substances 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 229920005573 silicon-containing polymer Polymers 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 125000005504 styryl group Chemical group 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 1
- UWHCKJMYHZGTIT-UHFFFAOYSA-N tetraethylene glycol Chemical compound OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 125000004001 thioalkyl group Chemical group 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 238000010023 transfer printing Methods 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- 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
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/26—Esters containing oxygen in addition to the carboxy oxygen
- C08F220/30—Esters containing oxygen in addition to the carboxy oxygen containing aromatic rings in the alcohol moiety
-
- 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
- C08F2/00—Processes of polymerisation
- C08F2/46—Polymerisation initiated by wave energy or particle radiation
- C08F2/48—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
- C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09D133/08—Homopolymers or copolymers of acrylic acid esters
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Materials For Photolithography (AREA)
- Polymerisation Methods In General (AREA)
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JP2017-217614 | 2017-11-10 | ||
JP2017217614A JP7028612B2 (ja) | 2017-11-10 | 2017-11-10 | 硬化性組成物、硬化膜形成方法、硬化物、パターン化されている硬化膜、及び透明光学部材 |
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CN201811344055.9A Pending CN109765754A (zh) | 2017-11-10 | 2018-11-12 | 固化性组合物、固化膜形成方法、固化物、已被图案化的固化膜、及透明光学构件 |
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JP (1) | JP7028612B2 (ja) |
KR (1) | KR20190053776A (ja) |
CN (1) | CN109765754A (ja) |
Cited By (1)
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CN116601244A (zh) * | 2020-12-15 | 2023-08-15 | 中央硝子株式会社 | 光学构件用涂布液、聚合物、固化膜、感光性涂布液、图案固化膜、光学构件、固体摄像元件、显示装置、聚硅氧烷化合物、涂布液中使用的稳定剂、固化膜的制造方法、图案固化膜的制造方法和聚合物的制造方法 |
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KR102148772B1 (ko) * | 2020-04-09 | 2020-08-27 | 로움하이텍 주식회사 | 신규한 중합체, 이를 포함하는 하층막 형성용 조성물 및 이를 이용한 방법 |
KR102679790B1 (ko) * | 2022-12-27 | 2024-07-02 | 인하대학교 산학협력단 | 포토리소그래피용 레지스트 화합물, 이의 제조방법 및 이를 이용한 반도체 소자의 제조방법 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2013033208A (ja) * | 2011-06-28 | 2013-02-14 | Mitsubishi Rayon Co Ltd | 光学シートおよび光学シートの製造方法 |
CN103059620A (zh) * | 2011-10-24 | 2013-04-24 | Jsr株式会社 | 热固性水分捕获体形成用组合物、水分捕获体以及电子设备 |
JP2015040224A (ja) * | 2013-08-20 | 2015-03-02 | 大阪ガスケミカル株式会社 | フルオレン骨格を有する多官能性(メタ)アクリレート |
US20160046552A1 (en) * | 2013-03-29 | 2016-02-18 | Tokyo Ohka Kogyo Co., Ltd. | Composition containing vinyl-group-containing compound |
JPWO2016031415A1 (ja) * | 2014-08-27 | 2017-06-15 | 富士フイルム株式会社 | 組成物、膜、光学機器、化合物 |
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Publication number | Priority date | Publication date | Assignee | Title |
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WO2014157676A1 (ja) * | 2013-03-29 | 2014-10-02 | 東京応化工業株式会社 | ビニル基含有フルオレン系化合物 |
JP6059754B2 (ja) * | 2014-03-20 | 2017-01-11 | 富士フイルム株式会社 | 組成物、硬化性組成物、透明膜、固体撮像素子および表示装置 |
JP6156671B2 (ja) | 2015-02-26 | 2017-07-05 | 大日本印刷株式会社 | 透過型スクリーン及びそれを用いたヘッドアップディスプレイ装置 |
WO2016140245A1 (ja) * | 2015-03-02 | 2016-09-09 | 富士フイルム株式会社 | 硬化性組成物、硬化物、光学部材、レンズ及び化合物 |
JP6118837B2 (ja) * | 2015-04-07 | 2017-04-19 | 株式会社三共 | 遊技機 |
JP2017015824A (ja) | 2015-06-29 | 2017-01-19 | Jxエネルギー株式会社 | シート状透明積層体、それを備えた透明スクリーン、およびそれを備えた画像投影装置 |
JP6631092B2 (ja) * | 2015-08-24 | 2020-01-15 | 三菱ケミカル株式会社 | 透明光学部材用硬化性樹脂組成物、硬化物、透明光学部材、レンズ及びカメラモジュール |
JP2016195917A (ja) * | 2016-08-30 | 2016-11-24 | シャープ株式会社 | 吸込口体およびそれを備えた電気掃除機 |
JP6882823B2 (ja) * | 2016-10-03 | 2021-06-02 | 大阪ガスケミカル株式会社 | 硬化性組成物及びその硬化物 |
JP6871667B2 (ja) * | 2016-10-06 | 2021-05-12 | 大阪ガスケミカル株式会社 | 硬化性組成物及びその硬化物 |
WO2019026889A1 (ja) * | 2017-08-01 | 2019-02-07 | 大阪ガスケミカル株式会社 | 単官能性(メタ)アクリレート及び硬化性組成物 |
-
2017
- 2017-11-10 JP JP2017217614A patent/JP7028612B2/ja active Active
-
2018
- 2018-10-19 KR KR1020180125175A patent/KR20190053776A/ko not_active Application Discontinuation
- 2018-11-12 CN CN201811344055.9A patent/CN109765754A/zh active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2013033208A (ja) * | 2011-06-28 | 2013-02-14 | Mitsubishi Rayon Co Ltd | 光学シートおよび光学シートの製造方法 |
CN103059620A (zh) * | 2011-10-24 | 2013-04-24 | Jsr株式会社 | 热固性水分捕获体形成用组合物、水分捕获体以及电子设备 |
US20160046552A1 (en) * | 2013-03-29 | 2016-02-18 | Tokyo Ohka Kogyo Co., Ltd. | Composition containing vinyl-group-containing compound |
JP2015040224A (ja) * | 2013-08-20 | 2015-03-02 | 大阪ガスケミカル株式会社 | フルオレン骨格を有する多官能性(メタ)アクリレート |
JPWO2016031415A1 (ja) * | 2014-08-27 | 2017-06-15 | 富士フイルム株式会社 | 組成物、膜、光学機器、化合物 |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN116601244A (zh) * | 2020-12-15 | 2023-08-15 | 中央硝子株式会社 | 光学构件用涂布液、聚合物、固化膜、感光性涂布液、图案固化膜、光学构件、固体摄像元件、显示装置、聚硅氧烷化合物、涂布液中使用的稳定剂、固化膜的制造方法、图案固化膜的制造方法和聚合物的制造方法 |
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JP2019089873A (ja) | 2019-06-13 |
KR20190053776A (ko) | 2019-05-20 |
JP7028612B2 (ja) | 2022-03-02 |
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