JP6026550B2 - 積層体 - Google Patents

積層体 Download PDF

Info

Publication number: JP6026550B2
Authority: JP; Japan
Prior art keywords: compound; group; laminate; chiral agent; liquid crystal
Prior art date: 2013-12-18
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired - Fee Related

Application number

JP2014540255A

Other languages

English (en)

Japanese (ja)

Other versions

JPWO2015093093A1 (ja

Inventor

裕一松木

丈章齋木

山本　正樹

正樹山本

成之青野

依慶米山

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Yokohama Rubber Co Ltd

Original Assignee

Yokohama Rubber Co Ltd

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2013-12-18

Filing date

2014-08-12

Publication date

2016-11-16

2014-08-12 Application filed by Yokohama Rubber Co Ltd filed Critical Yokohama Rubber Co Ltd

2016-11-16 Application granted granted Critical

2016-11-16 Publication of JP6026550B2 publication Critical patent/JP6026550B2/ja

2017-03-16 Publication of JPWO2015093093A1 publication Critical patent/JPWO2015093093A1/ja

Status Expired - Fee Related legal-status Critical Current

2034-08-12 Anticipated expiration legal-status Critical

Links

150000001875 compounds Chemical class 0.000 claims description 108
UWCWUCKPEYNDNV-LBPRGKRZSA-N 2,6-dimethyl-n-[[(2s)-pyrrolidin-2-yl]methyl]aniline Chemical compound CC1=CC=CC(C)=C1NC[C@H]1NCCC1 UWCWUCKPEYNDNV-LBPRGKRZSA-N 0.000 claims description 40
239000004988 Nematic liquid crystal Substances 0.000 claims description 29
239000000758 substrate Substances 0.000 claims description 23
239000011347 resin Substances 0.000 claims description 22
229920005989 resin Polymers 0.000 claims description 22
125000000524 functional group Chemical group 0.000 claims description 21
239000003999 initiator Substances 0.000 claims description 17
239000011342 resin composition Substances 0.000 claims description 15
239000004925 Acrylic resin Substances 0.000 claims description 12
229920000178 Acrylic resin Polymers 0.000 claims description 12
125000005842 heteroatom Chemical group 0.000 claims description 12
125000000962 organic group Chemical group 0.000 claims description 11
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 10
VMRIVYANZGSGRV-UHFFFAOYSA-N 4-phenyl-2h-triazin-5-one Chemical group OC1=CN=NN=C1C1=CC=CC=C1 VMRIVYANZGSGRV-UHFFFAOYSA-N 0.000 claims description 9
125000003354 benzotriazolyl group Chemical group N1N=NC2=C1C=CC=C2* 0.000 claims description 8
238000000576 coating method Methods 0.000 claims description 8
239000011248 coating agent Substances 0.000 claims description 7
XJHABGPPCLHLLV-UHFFFAOYSA-N benzo[de]isoquinoline-1,3-dione Chemical group C1=CC(C(=O)NC2=O)=C3C2=CC=CC3=C1 XJHABGPPCLHLLV-UHFFFAOYSA-N 0.000 claims description 6
125000001183 hydrocarbyl group Chemical group 0.000 claims 1
239000000203 mixture Substances 0.000 description 38
239000003795 chemical substances by application Substances 0.000 description 28
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 22
150000002430 hydrocarbons Chemical group 0.000 description 21
-1 acryloyloxy group Chemical group 0.000 description 20
230000006870 function Effects 0.000 description 20
125000001931 aliphatic group Chemical group 0.000 description 11
238000000034 method Methods 0.000 description 11
238000001035 drying Methods 0.000 description 9
238000004519 manufacturing process Methods 0.000 description 9
125000002029 aromatic hydrocarbon group Chemical group 0.000 description 8
239000000463 material Substances 0.000 description 8
229920000139 polyethylene terephthalate Polymers 0.000 description 8
239000005020 polyethylene terephthalate Substances 0.000 description 8
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 7
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 7
125000002723 alicyclic group Chemical group 0.000 description 7
230000000052 comparative effect Effects 0.000 description 7
125000002887 hydroxy group Chemical group [H]O* 0.000 description 7
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
239000007788 liquid Substances 0.000 description 6
239000002904 solvent Substances 0.000 description 6
238000009281 ultraviolet germicidal irradiation Methods 0.000 description 6
PTJWCLYPVFJWMP-UHFFFAOYSA-N 2-[[3-hydroxy-2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)COCC(CO)(CO)CO PTJWCLYPVFJWMP-UHFFFAOYSA-N 0.000 description 5
229920000089 Cyclic olefin copolymer Polymers 0.000 description 5
JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 5
125000000217 alkyl group Chemical group 0.000 description 5
238000002156 mixing Methods 0.000 description 5
239000005056 polyisocyanate Substances 0.000 description 5
229920001228 polyisocyanate Polymers 0.000 description 5
150000005846 sugar alcohols Polymers 0.000 description 5
TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 4
125000003277 amino group Chemical group 0.000 description 4
125000004432 carbon atom Chemical group C* 0.000 description 4
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
239000004973 liquid crystal related substance Substances 0.000 description 4
238000002834 transmittance Methods 0.000 description 4
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 4
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 3
UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 3
238000000862 absorption spectrum Methods 0.000 description 3
239000000654 additive Substances 0.000 description 3
229920001577 copolymer Polymers 0.000 description 3
239000004744 fabric Substances 0.000 description 3
229910052731 fluorine Inorganic materials 0.000 description 3
238000005286 illumination Methods 0.000 description 3
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 3
229910052753 mercury Inorganic materials 0.000 description 3
230000003287 optical effect Effects 0.000 description 3
239000012956 1-hydroxycyclohexylphenyl-ketone Substances 0.000 description 2
ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 2
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
ROWKJAVDOGWPAT-UHFFFAOYSA-N Acetoin Chemical compound CC(O)C(C)=O ROWKJAVDOGWPAT-UHFFFAOYSA-N 0.000 description 2
229920002799 BoPET Polymers 0.000 description 2
XMWRBQBLMFGWIX-UHFFFAOYSA-N C60 fullerene Chemical class C12=C3C(C4=C56)=C7C8=C5C5=C9C%10=C6C6=C4C1=C1C4=C6C6=C%10C%10=C9C9=C%11C5=C8C5=C8C7=C3C3=C7C2=C1C1=C2C4=C6C4=C%10C6=C9C9=C%11C5=C5C8=C3C3=C7C1=C1C2=C4C6=C2C9=C5C3=C12 XMWRBQBLMFGWIX-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
239000005057 Hexamethylene diisocyanate Substances 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
MPIAGWXWVAHQBB-UHFFFAOYSA-N [3-prop-2-enoyloxy-2-[[3-prop-2-enoyloxy-2,2-bis(prop-2-enoyloxymethyl)propoxy]methyl]-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(COC(=O)C=C)(COC(=O)C=C)COCC(COC(=O)C=C)(COC(=O)C=C)COC(=O)C=C MPIAGWXWVAHQBB-UHFFFAOYSA-N 0.000 description 2
125000003545 alkoxy group Chemical group 0.000 description 2
230000003712 anti-aging effect Effects 0.000 description 2
239000003963 antioxidant agent Substances 0.000 description 2
239000002216 antistatic agent Substances 0.000 description 2
ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 2
QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 2
239000012964 benzotriazole Substances 0.000 description 2
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
238000003851 corona treatment Methods 0.000 description 2
150000001925 cycloalkenes Chemical class 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
239000000975 dye Substances 0.000 description 2
229920001971 elastomer Polymers 0.000 description 2
238000011156 evaluation Methods 0.000 description 2
239000000945 filler Substances 0.000 description 2
239000003063 flame retardant Substances 0.000 description 2
239000011737 fluorine Substances 0.000 description 2
229910003472 fullerene Inorganic materials 0.000 description 2
239000011521 glass Substances 0.000 description 2
RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 2
229930195733 hydrocarbon Chemical group 0.000 description 2
238000005984 hydrogenation reaction Methods 0.000 description 2
230000001771 impaired effect Effects 0.000 description 2
230000001678 irradiating effect Effects 0.000 description 2
230000031700 light absorption Effects 0.000 description 2
239000004611 light stabiliser Substances 0.000 description 2
239000006224 matting agent Substances 0.000 description 2
238000005259 measurement Methods 0.000 description 2
125000004430 oxygen atom Chemical group O* 0.000 description 2
238000010422 painting Methods 0.000 description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
239000000049 pigment Substances 0.000 description 2
229920003023 plastic Polymers 0.000 description 2
239000004033 plastic Substances 0.000 description 2
229920003229 poly(methyl methacrylate) Polymers 0.000 description 2
239000004926 polymethyl methacrylate Substances 0.000 description 2
229920001296 polysiloxane Polymers 0.000 description 2
150000003464 sulfur compounds Chemical class 0.000 description 2
229920002554 vinyl polymer Polymers 0.000 description 2
QNODIIQQMGDSEF-UHFFFAOYSA-N (1-hydroxycyclohexyl)-phenylmethanone Chemical compound C=1C=CC=CC=1C(=O)C1(O)CCCCC1 QNODIIQQMGDSEF-UHFFFAOYSA-N 0.000 description 1
SWFHGTMLYIBPPA-UHFFFAOYSA-N (4-methoxyphenyl)-phenylmethanone Chemical compound C1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 SWFHGTMLYIBPPA-UHFFFAOYSA-N 0.000 description 1
NNOZGCICXAYKLW-UHFFFAOYSA-N 1,2-bis(2-isocyanatopropan-2-yl)benzene Chemical compound O=C=NC(C)(C)C1=CC=CC=C1C(C)(C)N=C=O NNOZGCICXAYKLW-UHFFFAOYSA-N 0.000 description 1
FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 description 1
MTZUIIAIAKMWLI-UHFFFAOYSA-N 1,2-diisocyanatobenzene Chemical compound O=C=NC1=CC=CC=C1N=C=O MTZUIIAIAKMWLI-UHFFFAOYSA-N 0.000 description 1
MSAHTMIQULFMRG-UHFFFAOYSA-N 1,2-diphenyl-2-propan-2-yloxyethanone Chemical compound C=1C=CC=CC=1C(OC(C)C)C(=O)C1=CC=CC=C1 MSAHTMIQULFMRG-UHFFFAOYSA-N 0.000 description 1
125000004955 1,4-cyclohexylene group Chemical group [H]C1([H])C([H])([H])C([H])([*:1])C([H])([H])C([H])([H])C1([H])[*:2] 0.000 description 1
CDMDQYCEEKCBGR-UHFFFAOYSA-N 1,4-diisocyanatocyclohexane Chemical compound O=C=NC1CCC(N=C=O)CC1 CDMDQYCEEKCBGR-UHFFFAOYSA-N 0.000 description 1
VZXPHDGHQXLXJC-UHFFFAOYSA-N 1,6-diisocyanato-5,6-dimethylheptane Chemical compound O=C=NC(C)(C)C(C)CCCCN=C=O VZXPHDGHQXLXJC-UHFFFAOYSA-N 0.000 description 1
AUXIEQKHXAYAHG-UHFFFAOYSA-N 1-phenylcyclohexane-1-carbonitrile Chemical class C=1C=CC=CC=1C1(C#N)CCCCC1 AUXIEQKHXAYAHG-UHFFFAOYSA-N 0.000 description 1
RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
PIZHFBODNLEQBL-UHFFFAOYSA-N 2,2-diethoxy-1-phenylethanone Chemical compound CCOC(OCC)C(=O)C1=CC=CC=C1 PIZHFBODNLEQBL-UHFFFAOYSA-N 0.000 description 1
KWVGIHKZDCUPEU-UHFFFAOYSA-N 2,2-dimethoxy-2-phenylacetophenone Chemical compound C=1C=CC=CC=1C(OC)(OC)C(=O)C1=CC=CC=C1 KWVGIHKZDCUPEU-UHFFFAOYSA-N 0.000 description 1
GJKGAPPUXSSCFI-UHFFFAOYSA-N 2-Hydroxy-4'-(2-hydroxyethoxy)-2-methylpropiophenone Chemical compound CC(C)(O)C(=O)C1=CC=C(OCCO)C=C1 GJKGAPPUXSSCFI-UHFFFAOYSA-N 0.000 description 1
SITYOOWCYAYOKL-UHFFFAOYSA-N 2-[4,6-bis(2,4-dimethylphenyl)-1,3,5-triazin-2-yl]-5-(3-dodecoxy-2-hydroxypropoxy)phenol Chemical compound OC1=CC(OCC(O)COCCCCCCCCCCCC)=CC=C1C1=NC(C=2C(=CC(C)=CC=2)C)=NC(C=2C(=CC(C)=CC=2)C)=N1 SITYOOWCYAYOKL-UHFFFAOYSA-N 0.000 description 1
KMNCBSZOIQAUFX-UHFFFAOYSA-N 2-ethoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OCC)C(=O)C1=CC=CC=C1 KMNCBSZOIQAUFX-UHFFFAOYSA-N 0.000 description 1
NLGDWWCZQDIASO-UHFFFAOYSA-N 2-hydroxy-1-(7-oxabicyclo[4.1.0]hepta-1,3,5-trien-2-yl)-2-phenylethanone Chemical class OC(C(=O)c1cccc2Oc12)c1ccccc1 NLGDWWCZQDIASO-UHFFFAOYSA-N 0.000 description 1
XMLYCEVDHLAQEL-UHFFFAOYSA-N 2-hydroxy-2-methyl-1-phenylpropan-1-one Chemical compound CC(C)(O)C(=O)C1=CC=CC=C1 XMLYCEVDHLAQEL-UHFFFAOYSA-N 0.000 description 1
BQZJOQXSCSZQPS-UHFFFAOYSA-N 2-methoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OC)C(=O)C1=CC=CC=C1 BQZJOQXSCSZQPS-UHFFFAOYSA-N 0.000 description 1
125000003504 2-oxazolinyl group Chemical group O1C(=NCC1)* 0.000 description 1
WLNDDIWESXCXHM-UHFFFAOYSA-N 2-phenyl-1,4-dioxane Chemical class C1OCCOC1C1=CC=CC=C1 WLNDDIWESXCXHM-UHFFFAOYSA-N 0.000 description 1
OXPDQFOKSZYEMJ-UHFFFAOYSA-N 2-phenylpyrimidine Chemical class C1=CC=CC=C1C1=NC=CC=N1 OXPDQFOKSZYEMJ-UHFFFAOYSA-N 0.000 description 1
BUZICZZQJDLXJN-UHFFFAOYSA-N 3-azaniumyl-4-hydroxybutanoate Chemical compound OCC(N)CC(O)=O BUZICZZQJDLXJN-UHFFFAOYSA-N 0.000 description 1
UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
BVEYJWQCMOVMAR-UHFFFAOYSA-N 5-Hydroxy-4-octanone Chemical compound CCCC(O)C(=O)CCC BVEYJWQCMOVMAR-UHFFFAOYSA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
239000004342 Benzoyl peroxide Substances 0.000 description 1
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
229920000298 Cellophane Polymers 0.000 description 1
208000003556 Dry Eye Syndromes Diseases 0.000 description 1
206010013774 Dry eye Diseases 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical group OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 1
239000005058 Isophorone diisocyanate Substances 0.000 description 1
KLDXJTOLSGUMSJ-JGWLITMVSA-N Isosorbide Chemical group O[C@@H]1CO[C@@H]2[C@@H](O)CO[C@@H]21 KLDXJTOLSGUMSJ-JGWLITMVSA-N 0.000 description 1
YJPIGAIKUZMOQA-UHFFFAOYSA-N Melatonin Natural products COC1=CC=C2N(C(C)=O)C=C(CCN)C2=C1 YJPIGAIKUZMOQA-UHFFFAOYSA-N 0.000 description 1
QORUGOXNWQUALA-UHFFFAOYSA-N N=C=O.N=C=O.N=C=O.C1=CC=C(C(C2=CC=CC=C2)C2=CC=CC=C2)C=C1 Chemical compound N=C=O.N=C=O.N=C=O.C1=CC=C(C(C2=CC=CC=C2)C2=CC=CC=C2)C=C1 QORUGOXNWQUALA-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
241001234580 Palio Species 0.000 description 1
229920000265 Polyparaphenylene Polymers 0.000 description 1
244000028419 Styrax benzoin Species 0.000 description 1
235000000126 Styrax benzoin Nutrition 0.000 description 1
235000008411 Sumatra benzointree Nutrition 0.000 description 1
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
RVWADWOERKNWRY-UHFFFAOYSA-N [2-(dimethylamino)phenyl]-phenylmethanone Chemical compound CN(C)C1=CC=CC=C1C(=O)C1=CC=CC=C1 RVWADWOERKNWRY-UHFFFAOYSA-N 0.000 description 1
KXBFLNPZHXDQLV-UHFFFAOYSA-N [cyclohexyl(diisocyanato)methyl]cyclohexane Chemical compound C1CCCCC1C(N=C=O)(N=C=O)C1CCCCC1 KXBFLNPZHXDQLV-UHFFFAOYSA-N 0.000 description 1
239000006096 absorbing agent Substances 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
150000008062 acetophenones Chemical class 0.000 description 1
150000001252 acrylic acid derivatives Chemical class 0.000 description 1
229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
230000002411 adverse Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
125000005370 alkoxysilyl group Chemical group 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
150000001454 anthracenes Chemical class 0.000 description 1
239000002518 antifoaming agent Substances 0.000 description 1
230000003078 antioxidant effect Effects 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
208000003464 asthenopia Diseases 0.000 description 1
125000004069 aziridinyl group Chemical group 0.000 description 1
125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
125000005337 azoxy group Chemical group [N+]([O-])(=N*)* 0.000 description 1
150000001558 benzoic acid derivatives Chemical class 0.000 description 1
229960002130 benzoin Drugs 0.000 description 1
150000008359 benzonitriles Chemical class 0.000 description 1
RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
239000012965 benzophenone Substances 0.000 description 1
150000008366 benzophenones Chemical class 0.000 description 1
235000019400 benzoyl peroxide Nutrition 0.000 description 1
235000019445 benzyl alcohol Nutrition 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
JGCWKVKYRNXTMD-UHFFFAOYSA-N bicyclo[2.2.1]heptane;isocyanic acid Chemical compound N=C=O.N=C=O.C1CC2CCC1C2 JGCWKVKYRNXTMD-UHFFFAOYSA-N 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
235000010290 biphenyl Nutrition 0.000 description 1
150000004074 biphenyls Chemical class 0.000 description 1
OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
150000001728 carbonyl compounds Chemical class 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
239000000919 ceramic Substances 0.000 description 1
229920006026 co-polymeric resin Polymers 0.000 description 1
239000000470 constituent Substances 0.000 description 1
238000005520 cutting process Methods 0.000 description 1
150000001924 cycloalkanes Chemical class 0.000 description 1
VGHOWOWLIXPTOA-UHFFFAOYSA-N cyclohexane;toluene Chemical compound C1CCCCC1.CC1=CC=CC=C1 VGHOWOWLIXPTOA-UHFFFAOYSA-N 0.000 description 1
LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
238000009792 diffusion process Methods 0.000 description 1
125000005442 diisocyanate group Chemical group 0.000 description 1
238000003618 dip coating Methods 0.000 description 1
230000009982 effect on human Effects 0.000 description 1
230000000694 effects Effects 0.000 description 1
125000003700 epoxy group Chemical group 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
QKLCQKPAECHXCQ-UHFFFAOYSA-N ethyl phenylglyoxylate Chemical compound CCOC(=O)C(=O)C1=CC=CC=C1 QKLCQKPAECHXCQ-UHFFFAOYSA-N 0.000 description 1
230000001747 exhibiting effect Effects 0.000 description 1
125000001153 fluoro group Chemical group F* 0.000 description 1
239000004088 foaming agent Substances 0.000 description 1
235000019382 gum benzoic Nutrition 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
GFAZHVHNLUBROE-UHFFFAOYSA-N hydroxymethyl propionaldehyde Natural products CCC(=O)CO GFAZHVHNLUBROE-UHFFFAOYSA-N 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
YPQKTLPPOXNDMC-UHFFFAOYSA-N isocyanic acid;methylcyclohexane Chemical compound N=C=O.CC1CCCCC1 YPQKTLPPOXNDMC-UHFFFAOYSA-N 0.000 description 1
ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
125000005647 linker group Chemical group 0.000 description 1
DRLFMBDRBRZALE-UHFFFAOYSA-N melatonin Chemical compound COC1=CC=C2NC=C(CCNC(C)=O)C2=C1 DRLFMBDRBRZALE-UHFFFAOYSA-N 0.000 description 1
229960003987 melatonin Drugs 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
AYLRODJJLADBOB-QMMMGPOBSA-N methyl (2s)-2,6-diisocyanatohexanoate Chemical compound COC(=O)[C@@H](N=C=O)CCCCN=C=O AYLRODJJLADBOB-QMMMGPOBSA-N 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
YLHXLHGIAMFFBU-UHFFFAOYSA-N methyl phenylglyoxalate Chemical compound COC(=O)C(=O)C1=CC=CC=C1 YLHXLHGIAMFFBU-UHFFFAOYSA-N 0.000 description 1
150000002790 naphthalenes Chemical class 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
150000002848 norbornenes Chemical class 0.000 description 1
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
125000003566 oxetanyl group Chemical group 0.000 description 1
MPQXHAGKBWFSNV-UHFFFAOYSA-N oxidophosphanium Chemical class [PH3]=O MPQXHAGKBWFSNV-UHFFFAOYSA-N 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
OPYYWWIJPHKUDZ-UHFFFAOYSA-N phenyl cyclohexanecarboxylate Chemical class C1CCCCC1C(=O)OC1=CC=CC=C1 OPYYWWIJPHKUDZ-UHFFFAOYSA-N 0.000 description 1
125000005543 phthalimide group Chemical group 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
229920006122 polyamide resin Polymers 0.000 description 1
229920005668 polycarbonate resin Polymers 0.000 description 1
239000004431 polycarbonate resin Substances 0.000 description 1
239000004645 polyester resin Substances 0.000 description 1
229920001225 polyester resin Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
229920005990 polystyrene resin Polymers 0.000 description 1
239000004800 polyvinyl chloride Substances 0.000 description 1
229920000915 polyvinyl chloride Polymers 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
125000000168 pyrrolyl group Chemical group 0.000 description 1
239000000376 reactant Substances 0.000 description 1
230000004243 retinal function Effects 0.000 description 1
238000007151 ring opening polymerisation reaction Methods 0.000 description 1
239000005268 rod-like liquid crystal Substances 0.000 description 1
239000005060 rubber Substances 0.000 description 1
230000028327 secretion Effects 0.000 description 1
239000007787 solid Substances 0.000 description 1
238000004528 spin coating Methods 0.000 description 1
238000005507 spraying Methods 0.000 description 1
125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
125000004434 sulfur atom Chemical group 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
208000024891 symptom Diseases 0.000 description 1
150000001911 terphenyls Chemical class 0.000 description 1
XBFJAVXCNXDMBH-UHFFFAOYSA-N tetracyclo[6.2.1.1(3,6).0(2,7)]dodec-4-ene Chemical compound C1C(C23)C=CC1C3C1CC2CC1 XBFJAVXCNXDMBH-UHFFFAOYSA-N 0.000 description 1
229920005992 thermoplastic resin Polymers 0.000 description 1
229920001187 thermosetting polymer Polymers 0.000 description 1
125000002053 thietanyl group Chemical group 0.000 description 1
125000003396 thiol group Chemical group [H]S* 0.000 description 1
KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
229960002447 thiram Drugs 0.000 description 1
DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
239000006097 ultraviolet radiation absorber Substances 0.000 description 1
239000008096 xylene 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
- 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
- C08F2/50—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light with sensitising agents
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B17/00—Layered products essentially comprising sheet glass, or glass, slag, or like fibres
- B32B17/06—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
- B32B17/10—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/30—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
- 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
- C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
- C08G64/04—Aromatic polycarbonates
- C08G64/045—Aromatic polycarbonates containing aliphatic unsaturation
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3472—Five-membered rings
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3477—Six-membered rings
- C08K5/3492—Triazines
- C08K5/34922—Melamine; Derivatives thereof
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/20—Filters
- G02B5/22—Absorbing filters
- G02B5/223—Absorbing filters containing organic substances, e.g. dyes, inks or pigments
- G—PHYSICS
- G02—OPTICS
- G02C—SPECTACLES; SUNGLASSES OR GOGGLES INSOFAR AS THEY HAVE THE SAME FEATURES AS SPECTACLES; CONTACT LENSES
- G02C7/00—Optical parts
- G02C7/02—Lenses; Lens systems ; Methods of designing lenses
- 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
- C08F220/303—Esters containing oxygen in addition to the carboxy oxygen containing aromatic rings in the alcohol moiety and one or more carboxylic moieties in the chain

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Physics & Mathematics (AREA)
Optics & Photonics (AREA)
General Physics & Mathematics (AREA)
Ophthalmology & Optometry (AREA)
General Health & Medical Sciences (AREA)
Laminated Bodies (AREA)
Paints Or Removers (AREA)
Polymerisation Methods In General (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Optical Filters (AREA)
Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
Compositions Of Macromolecular Compounds (AREA)
Eyeglasses (AREA)

JP2014540255A 2013-12-18 2014-08-12 積層体 Expired - Fee Related JP6026550B2 (ja)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
JP2013261569		2013-12-18
JP2013261569		2013-12-18
PCT/JP2014/071302 WO2015093093A1 (ja)	2013-12-18	2014-08-12	紫外線硬化型樹脂組成物および積層体

Related Child Applications (1)

Application Number	Title	Priority Date	Filing Date
JP2015135171A Division JP6481530B2 (ja)	2013-12-18	2015-07-06	紫外線硬化型樹脂組成物および積層体

Publications (2)

Publication Number	Publication Date
JP6026550B2 true JP6026550B2 (ja)	2016-11-16
JPWO2015093093A1 JPWO2015093093A1 (ja)	2017-03-16

Family

ID=53402450

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
JP2014540255A Expired - Fee Related JP6026550B2 (ja)	2013-12-18	2014-08-12	積層体
JP2015135171A Active JP6481530B2 (ja)	2013-12-18	2015-07-06	紫外線硬化型樹脂組成物および積層体

Family Applications After (1)

Application Number	Title	Priority Date	Filing Date
JP2015135171A Active JP6481530B2 (ja)	2013-12-18	2015-07-06	紫外線硬化型樹脂組成物および積層体

Country Status (5)

Country	Link
JP (2)	JP6026550B2 (zh)
KR (1)	KR20160100908A (zh)
CN (1)	CN105793362A (zh)
TW (1)	TWI626279B (zh)
WO (1)	WO2015093093A1 (zh)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP6387651B2 (ja) *	2014-03-31	2018-09-12	大日本印刷株式会社	ブルーライトカットフィルム、表示装置、及び、ブルーライトカットフィルム用樹脂組成物
WO2016002670A1 (ja) *	2014-06-30	2016-01-07	横浜ゴム株式会社	紫外線硬化性樹脂組成物及びこれを用いる積層体
JP6229802B2 (ja) *	2014-12-16	2017-11-15	横浜ゴム株式会社	紫外線硬化型樹脂組成物および積層体
JP6786614B2 (ja)	2015-11-06	2020-11-18	エシロールアンテルナショナルＥｓｓｉｌｏｒＩｎｔｅｒｎａｔｉｏｎａｌ	青色光から保護する光学物品
WO2018021486A1 (ja) *	2016-07-28	2018-02-01	富士フイルム株式会社	眼鏡用レンズおよび眼鏡
JP6632730B2 (ja) *	2016-07-28	2020-01-22	富士フイルム株式会社	ブルーライトカットフィルムおよび光源
US11073638B2 (en)	2016-09-07	2021-07-27	Largan Precision Co., Ltd.	Optical image lens assembly and plastic material thereof, image capturing apparatus and electronic device
ES2935514T3 (es)	2016-11-23	2023-03-07	Ppg Ind Ohio Inc	Transparencia protectora ultravioleta
CN106800376A (zh) *	2016-12-29	2017-06-06	武汉华星光电技术有限公司	一种滤蓝光抗眩手机盖板及其制备方法
WO2018186369A1 (ja) *	2017-04-06	2018-10-11	日本化薬株式会社	遮光機能付きアイウェア用光学フィルム、並びにこれを用いた光学積層体および遮光機能付きアイウェア
KR20190141000A (ko) *	2017-05-11	2019-12-20	니폰 가야꾸 가부시끼가이샤	블루 라이트 차단 필름용 자외선 경화형 수지 조성물 및 이것을 이용한 블루 라이트 차단 필름
KR102378356B1 (ko)	2017-08-09	2022-03-25	삼성디스플레이 주식회사	유기 발광 소자 및 이를 포함한 전자 장치
KR102346673B1 (ko) *	2017-08-09	2022-01-04	삼성디스플레이 주식회사	유기 발광 표시 장치
CN109553792A (zh) *	2017-09-25	2019-04-02	安徽屹珹新材料科技有限公司	一种双光学涂层的防蓝光薄膜及其制备方法
EP3474063A1 (en) *	2017-10-19	2019-04-24	Essilor International	Optical lens
CN109694488A (zh) *	2017-10-23	2019-04-30	苏州艾科迪新材料科技有限公司	一种反射型镜片近紫外截止膜
JP2021534284A (ja) *	2018-08-13	2021-12-09	メルクパテントゲゼルシャフトミットベシュレンクテルハフツングMerck Patent Gesellschaft mit beschraenkter Haftung	重合性液晶材料および重合された液晶フィルム
JP7038028B2 (ja)	2018-08-31	2022-03-17	サントリーホールディングス株式会社	選択的光透過抑制容器入りアルコール飲料
CN114846085B (zh) *	2019-12-24	2023-09-08	东洋油墨Sc控股株式会社	树脂组合物、及成形体

Citations (16)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH075440A (ja) *	1993-06-16	1995-01-10	Ajinomoto Co Inc	調光液晶素子用液晶樹脂配合物
JPH08286033A (ja) *	1995-02-13	1996-11-01	Idemitsu Kosan Co Ltd	赤色蛍光変換膜及びそれを用いた赤色発光素子
JPH09171248A (ja) *	1995-12-19	1997-06-30	Mitsubishi Chem Corp	感放射線性塗布組成物及びそれを使用する半導体製造方法
JP3180287B2 (ja) *	1995-07-28	2001-06-25	関西ペイント株式会社	多彩模様塗料組成物
JP2001172329A (ja) *	1999-08-27	2001-06-26	Basf Ag	改善された色彩印象を有するコレステリック層材料およびその製造方法
JP2002533742A (ja) *	1998-12-22	2002-10-08	ビーエーエスエフアクチェンゲゼルシャフト	光学素子を製造するための重合性液晶物質の使用
JP2002536529A (ja) *	1999-02-10	2002-10-29	ビーエーエスエフアクチェンゲゼルシャフト	液晶性物質混合物
JP2004233988A (ja) *	2003-01-10	2004-08-19	Nitto Denko Corp	広帯域コレステリック液晶フィルム、その製造方法、円偏光板、直線偏光子、照明装置および液晶表示装置
WO2006137454A1 (ja) *	2005-06-21	2006-12-28	Nippon Sheet Glass Company, Limited	透明物品およびその製造方法
JP2007093927A (ja) *	2005-09-28	2007-04-12	Yamamoto Kogaku Co Ltd	光学物品
JP2007286189A (ja) *	2006-04-13	2007-11-01	Adeka Corp	光学フィルター
EP2113807A2 (en) *	2008-04-30	2009-11-04	Fujifilm Corporation	Optical material having a colored optically anisotropic layer
JP2010217356A (ja) *	2009-03-16	2010-09-30	Fujifilm Corp	光学異方性膜、液晶セル用基板、及び液晶表示装置
JP2013054275A (ja) *	2011-09-06	2013-03-21	Nikon-Essilor Co Ltd	染色レンズおよびその製造方法
JP2013514396A (ja) *	2009-12-17	2013-04-25	ビーエーエスエフソシエタス・ヨーロピア	液晶混合物
JP5459446B1 (ja) *	2013-04-30	2014-04-02	横浜ゴム株式会社	紫外線硬化型樹脂組成物及びこれを用いる積層体

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP3188050B2 (ja) *	1993-05-17	2001-07-16	ダイセル網干産業株式会社	メガネレンズ
US6221517B1 (en) *	1996-02-09	2001-04-24	Idemitsu Kosan Co., Ltd.	Fluorescence-reddening membrane and red-emitting device
JPH11228953A (ja) *	1998-02-17	1999-08-24	Toshiba Corp	蛍光体
US6773766B2 (en) *	1998-12-22	2004-08-10	Basf Aktiengesellschaft	Utilization of polymerizable liquid crystal substances for the production of optical components
CN100375910C (zh) *	2003-01-10	2008-03-19	日东电工株式会社	宽带胆甾醇型液晶薄膜、其制造方法、圆偏振片、直线偏振镜、照明装置及液晶显示装置
DE102005012056A1 (de) *	2005-03-16	2006-09-28	Basf Coatings Ag	Mehrschichtlackierungen, Verfahren zu ihrer Herstellung und deren Verwendung im Automobilbau
JP2007019487A (ja) *	2005-06-09	2007-01-25	Semiconductor Energy Lab Co Ltd	発光装置及び電子機器
JP2008134579A (ja) *	2006-10-24	2008-06-12	Nippon Zeon Co Ltd	光学フィルタ、偏光板、照明装置、および液晶表示装置
JP5325608B2 (ja) *	2008-05-22	2013-10-23	リンテック株式会社	発光性組成物、それを用いる電界発光シート及びその製造方法
JP3180287U (ja) *	2012-09-28	2012-12-13	李季洋	紫色光及び青色光を遮断するコンピュータ用ディスプレイ及びテレビ画面の保護カバー構造

2014
- 2014-08-12 WO PCT/JP2014/071302 patent/WO2015093093A1/ja active Application Filing
- 2014-08-12 CN CN201480065593.8A patent/CN105793362A/zh active Pending
- 2014-08-12 JP JP2014540255A patent/JP6026550B2/ja not_active Expired - Fee Related
- 2014-08-12 KR KR1020167009793A patent/KR20160100908A/ko not_active Application Discontinuation
- 2014-08-21 TW TW103128798A patent/TWI626279B/zh active
2015
- 2015-07-06 JP JP2015135171A patent/JP6481530B2/ja active Active

Patent Citations (16)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH075440A (ja) *	1993-06-16	1995-01-10	Ajinomoto Co Inc	調光液晶素子用液晶樹脂配合物
JPH08286033A (ja) *	1995-02-13	1996-11-01	Idemitsu Kosan Co Ltd	赤色蛍光変換膜及びそれを用いた赤色発光素子
JP3180287B2 (ja) *	1995-07-28	2001-06-25	関西ペイント株式会社	多彩模様塗料組成物
JPH09171248A (ja) *	1995-12-19	1997-06-30	Mitsubishi Chem Corp	感放射線性塗布組成物及びそれを使用する半導体製造方法
JP2002533742A (ja) *	1998-12-22	2002-10-08	ビーエーエスエフアクチェンゲゼルシャフト	光学素子を製造するための重合性液晶物質の使用
JP2002536529A (ja) *	1999-02-10	2002-10-29	ビーエーエスエフアクチェンゲゼルシャフト	液晶性物質混合物
JP2001172329A (ja) *	1999-08-27	2001-06-26	Basf Ag	改善された色彩印象を有するコレステリック層材料およびその製造方法
JP2004233988A (ja) *	2003-01-10	2004-08-19	Nitto Denko Corp	広帯域コレステリック液晶フィルム、その製造方法、円偏光板、直線偏光子、照明装置および液晶表示装置
WO2006137454A1 (ja) *	2005-06-21	2006-12-28	Nippon Sheet Glass Company, Limited	透明物品およびその製造方法
JP2007093927A (ja) *	2005-09-28	2007-04-12	Yamamoto Kogaku Co Ltd	光学物品
JP2007286189A (ja) *	2006-04-13	2007-11-01	Adeka Corp	光学フィルター
EP2113807A2 (en) *	2008-04-30	2009-11-04	Fujifilm Corporation	Optical material having a colored optically anisotropic layer
JP2010217356A (ja) *	2009-03-16	2010-09-30	Fujifilm Corp	光学異方性膜、液晶セル用基板、及び液晶表示装置
JP2013514396A (ja) *	2009-12-17	2013-04-25	ビーエーエスエフソシエタス・ヨーロピア	液晶混合物
JP2013054275A (ja) *	2011-09-06	2013-03-21	Nikon-Essilor Co Ltd	染色レンズおよびその製造方法
JP5459446B1 (ja) *	2013-04-30	2014-04-02	横浜ゴム株式会社	紫外線硬化型樹脂組成物及びこれを用いる積層体

Also Published As

Publication number	Publication date
TWI626279B (zh)	2018-06-11
KR20160100908A (ko)	2016-08-24
WO2015093093A1 (ja)	2015-06-25
JPWO2015093093A1 (ja)	2017-03-16
JP2016006184A (ja)	2016-01-14
TW201525082A (zh)	2015-07-01
JP6481530B2 (ja)	2019-03-13
CN105793362A (zh)	2016-07-20

Legal Events

Date	Code	Title	Description
2015-04-08	A02	Decision of refusal	Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20150407
2016-08-10	A521	Request for written amendment filed	Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20160810
2016-10-20	A61	First payment of annual fees (during grant procedure)	Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20161012
2016-10-21	R150	Certificate of patent or registration of utility model	Ref document number: 6026550 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150
2019-09-24	R250	Receipt of annual fees	Free format text: JAPANESE INTERMEDIATE CODE: R250
2020-09-23	R250	Receipt of annual fees	Free format text: JAPANESE INTERMEDIATE CODE: R250
2021-09-22	R250	Receipt of annual fees	Free format text: JAPANESE INTERMEDIATE CODE: R250
2021-11-22	S111	Request for change of ownership or part of ownership	Free format text: JAPANESE INTERMEDIATE CODE: R313111
2021-12-10	R350	Written notification of registration of transfer	Free format text: JAPANESE INTERMEDIATE CODE: R350
2022-09-12	R250	Receipt of annual fees	Free format text: JAPANESE INTERMEDIATE CODE: R250
2023-10-21	LAPS	Cancellation because of no payment of annual fees

Publication	Publication Date	Title
JP6026550B2 (ja)	2016-11-16	積層体
JP6597310B2 (ja)	2019-10-30	紫外線硬化型樹脂組成物および積層体
TWI613266B (zh)	2018-02-01	紫外線硬化型樹脂組成物及使用其之層合體
JP7176409B2 (ja)	2022-11-22	光学積層体、及び、画像表示装置
JP6708126B2 (ja)	2020-06-10	紫外線硬化性樹脂組成物及びこれを用いる積層体
JPWO2014178148A1 (ja)	2017-02-23	紫外線硬化型樹脂組成物及びこれを用いる積層体
JP6731486B2 (ja)	2020-07-29	防曇性積層体
TW200837160A (en)	2008-09-16	Anti-glare hard coating solution and hard coating film with high hardness using the same
JP2014174321A (ja)	2014-09-22	表面形状を有する光学フィルムの製造方法、重合性液晶フィルム、および表面形状を有する重合性液晶フィルム
TW201610027A (zh)	2016-03-16	紫外線硬化性樹脂組成物以及使用其之層合體
CN107108819B (zh)	2020-04-21	紫外线固化型树脂组合物及叠层体
TW201514259A (zh)	2015-04-16	折射率調整用塗覆材料組成物及其層合體
JPWO2014208749A1 (ja)	2017-02-23	紫外線硬化型ハードコート樹脂組成物
TWI753980B (zh)	2022-02-01	構成體以及其製造方法、顯示體以及光學用黏著板片
JP6631523B2 (ja)	2020-01-15	紫外線硬化性樹脂組成物及びこれを用いる積層体
JP2022045341A (ja)	2022-03-18	ウレタン（メタ）アクリレート、活性エネルギー線硬化型樹脂組成物、硬化物、積層体及び成型物
JP7108505B2 (ja)	2022-07-28	機械加工性向上フィルム、積層体、及び機械加工性向上フィルムの使用方法
JP7367316B2 (ja)	2023-10-24	高滑水性活性エネルギー線硬化性組成物及び樹脂成形品