JPWO2023008488A5 - - Google Patents
Download PDFInfo
- Publication number
- JPWO2023008488A5 JPWO2023008488A5 JP2023538599A JP2023538599A JPWO2023008488A5 JP WO2023008488 A5 JPWO2023008488 A5 JP WO2023008488A5 JP 2023538599 A JP2023538599 A JP 2023538599A JP 2023538599 A JP2023538599 A JP 2023538599A JP WO2023008488 A5 JPWO2023008488 A5 JP WO2023008488A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- carbon atoms
- independently
- single bond
- atoms
- Prior art date
- 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.)
- Pending
Links
- -1 biphenylyl group Chemical group 0.000 claims description 8
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims 30
- 229920000642 polymer Polymers 0.000 claims 15
- 125000000217 alkyl group Chemical group 0.000 claims 9
- 125000005843 halogen group Chemical group 0.000 claims 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 8
- 125000003545 alkoxy group Chemical group 0.000 claims 7
- 125000002947 alkylene group Chemical group 0.000 claims 7
- 125000004093 cyano group Chemical group *C#N 0.000 claims 7
- 125000002723 alicyclic group Chemical group 0.000 claims 4
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims 4
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 3
- 239000011248 coating agent Substances 0.000 claims 3
- 238000000576 coating method Methods 0.000 claims 3
- 125000002541 furyl group Chemical group 0.000 claims 3
- 125000000623 heterocyclic group Chemical group 0.000 claims 3
- 125000001624 naphthyl group Chemical group 0.000 claims 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- 239000003505 polymerization initiator Substances 0.000 claims 3
- 239000000463 material Substances 0.000 claims 2
- 125000004957 naphthylene group Chemical group 0.000 claims 2
- 229920001400 block copolymer Polymers 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 230000001747 exhibiting effect Effects 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 claims 1
- 230000001678 irradiating effect Effects 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 239000003960 organic solvent Substances 0.000 claims 1
- 238000011907 photodimerization Methods 0.000 claims 1
- 238000007699 photoisomerization reaction Methods 0.000 claims 1
- 239000002356 single layer Substances 0.000 claims 1
- 239000000758 substrate Substances 0.000 claims 1
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 8
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 4
- JNELGWHKGNBSMD-UHFFFAOYSA-N xanthone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3OC2=C1 JNELGWHKGNBSMD-UHFFFAOYSA-N 0.000 description 4
- HJIAMFHSAAEUKR-UHFFFAOYSA-N (2-hydroxyphenyl)-phenylmethanone Chemical compound OC1=CC=CC=C1C(=O)C1=CC=CC=C1 HJIAMFHSAAEUKR-UHFFFAOYSA-N 0.000 description 2
- MFGWMAAZYZSWMY-UHFFFAOYSA-N (2-naphthyl)methanol Chemical compound C1=CC=CC2=CC(CO)=CC=C21 MFGWMAAZYZSWMY-UHFFFAOYSA-N 0.000 description 2
- LXCJXYYYOPFEDH-UHFFFAOYSA-N 3-(2-oxochromene-3-carbonyl)chromen-2-one Chemical class C1=CC=C2OC(=O)C(C(C=3C(OC4=CC=CC=C4C=3)=O)=O)=CC2=C1 LXCJXYYYOPFEDH-UHFFFAOYSA-N 0.000 description 2
- HSHNITRMYYLLCV-UHFFFAOYSA-N 4-methylumbelliferone Chemical compound C1=C(O)C=CC2=C1OC(=O)C=C2C HSHNITRMYYLLCV-UHFFFAOYSA-N 0.000 description 2
- CDSULTPOCMWJCM-UHFFFAOYSA-N 4h-chromene-2,3-dione Chemical class C1=CC=C2OC(=O)C(=O)CC2=C1 CDSULTPOCMWJCM-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 2
- 150000004056 anthraquinones Chemical class 0.000 description 2
- ZCCUUQDIBDJBTK-UHFFFAOYSA-N psoralen Chemical compound C1=C2OC(=O)C=CC2=CC2=C1OC=C2 ZCCUUQDIBDJBTK-UHFFFAOYSA-N 0.000 description 2
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 2
- HSGLYHHOCKTAEL-UHFFFAOYSA-N 1-(6,6-dimethoxycyclohexa-2,4-dien-1-yl)ethanone Chemical compound COC1(OC)C=CC=CC1C(C)=O HSGLYHHOCKTAEL-UHFFFAOYSA-N 0.000 description 1
- AVAGDIXDPQCKCQ-UHFFFAOYSA-N 1-nitro-1,2-dihydroacenaphthylene Chemical compound C1=CC(C([N+](=O)[O-])C2)=C3C2=CC=CC3=C1 AVAGDIXDPQCKCQ-UHFFFAOYSA-N 0.000 description 1
- IAHOUQOWMXVMEH-UHFFFAOYSA-N 2,4,6-trinitroaniline Chemical compound NC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O IAHOUQOWMXVMEH-UHFFFAOYSA-N 0.000 description 1
- HQTQILOQZHGRIY-UHFFFAOYSA-N 2-(3-methyl-1,3-benzothiazol-2-ylidene)-1-naphthalen-1-ylethanone Chemical compound C1=CC=C2C(C(=O)C=C3N(C4=CC=CC=C4S3)C)=CC=CC2=C1 HQTQILOQZHGRIY-UHFFFAOYSA-N 0.000 description 1
- KUGJLFCEVQECCS-UHFFFAOYSA-N 2-(3-methyl-1,3-benzothiazol-2-ylidene)-1-naphthalen-2-ylethanone Chemical compound C1=CC=CC2=CC(C(=O)C=C3N(C4=CC=CC=C4S3)C)=CC=C21 KUGJLFCEVQECCS-UHFFFAOYSA-N 0.000 description 1
- SUXPIAIKCOXLDU-UHFFFAOYSA-N 2-(3-methyl-1,3-benzoxazol-2-ylidene)-1-naphthalen-1-ylethanone Chemical compound C1=CC=C2C(C(=O)C=C3N(C4=CC=CC=C4O3)C)=CC=CC2=C1 SUXPIAIKCOXLDU-UHFFFAOYSA-N 0.000 description 1
- DOEZUOKAUSRLHH-UHFFFAOYSA-N 2-(3-methyl-1,3-benzoxazol-2-ylidene)-1-naphthalen-2-ylethanone Chemical compound C1=CC=CC2=CC(C(=O)C=C3N(C4=CC=CC=C4O3)C)=CC=C21 DOEZUOKAUSRLHH-UHFFFAOYSA-N 0.000 description 1
- IMSODMZESSGVBE-UHFFFAOYSA-N 2-Oxazoline Chemical compound C1CN=CO1 IMSODMZESSGVBE-UHFFFAOYSA-N 0.000 description 1
- UOBYKYZJUGYBDK-UHFFFAOYSA-N 2-naphthoic acid Chemical compound C1=CC=CC2=CC(C(=O)O)=CC=C21 UOBYKYZJUGYBDK-UHFFFAOYSA-N 0.000 description 1
- GOLORTLGFDVFDW-UHFFFAOYSA-N 3-(1h-benzimidazol-2-yl)-7-(diethylamino)chromen-2-one Chemical compound C1=CC=C2NC(C3=CC4=CC=C(C=C4OC3=O)N(CC)CC)=NC2=C1 GOLORTLGFDVFDW-UHFFFAOYSA-N 0.000 description 1
- TYMLOMAKGOJONV-UHFFFAOYSA-N 4-nitroaniline Chemical compound NC1=CC=C([N+]([O-])=O)C=C1 TYMLOMAKGOJONV-UHFFFAOYSA-N 0.000 description 1
- CUARLQDWYSRQDF-UHFFFAOYSA-N 5-Nitroacenaphthene Chemical compound C1CC2=CC=CC3=C2C1=CC=C3[N+](=O)[O-] CUARLQDWYSRQDF-UHFFFAOYSA-N 0.000 description 1
- HUKPVYBUJRAUAG-UHFFFAOYSA-N 7-benzo[a]phenalenone Chemical compound C1=CC(C(=O)C=2C3=CC=CC=2)=C2C3=CC=CC2=C1 HUKPVYBUJRAUAG-UHFFFAOYSA-N 0.000 description 1
- XGWFJBFNAQHLEF-UHFFFAOYSA-N 9-anthroic acid Chemical compound C1=CC=C2C(C(=O)O)=C(C=CC=C3)C3=CC2=C1 XGWFJBFNAQHLEF-UHFFFAOYSA-N 0.000 description 1
- KYNSBQPICQTCGU-UHFFFAOYSA-N Benzopyrane Chemical compound C1=CC=C2C=CCOC2=C1 KYNSBQPICQTCGU-UHFFFAOYSA-N 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
- JCJNNHDZTLRSGN-UHFFFAOYSA-N anthracen-9-ylmethanol Chemical compound C1=CC=C2C(CO)=C(C=CC=C3)C3=CC2=C1 JCJNNHDZTLRSGN-UHFFFAOYSA-N 0.000 description 1
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N benzo-alpha-pyrone Natural products C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 1
- 229960002130 benzoin Drugs 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
- 235000001671 coumarin Nutrition 0.000 description 1
- AFYCEAFSNDLKSX-UHFFFAOYSA-N coumarin 460 Chemical compound CC1=CC(=O)OC2=CC(N(CC)CC)=CC=C21 AFYCEAFSNDLKSX-UHFFFAOYSA-N 0.000 description 1
- 150000004775 coumarins Chemical class 0.000 description 1
- ISAOCJYIOMOJEB-UHFFFAOYSA-N desyl alcohol Natural products C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- VBEGHXKAFSLLGE-UHFFFAOYSA-N n-phenylnitramide Chemical compound [O-][N+](=O)NC1=CC=CC=C1 VBEGHXKAFSLLGE-UHFFFAOYSA-N 0.000 description 1
- 239000003504 photosensitizing agent Substances 0.000 description 1
- 125000005504 styryl group Chemical group 0.000 description 1
- CBDKQYKMCICBOF-UHFFFAOYSA-N thiazoline Chemical compound C1CN=CS1 CBDKQYKMCICBOF-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2021123463 | 2021-07-28 | ||
| PCT/JP2022/028970 WO2023008488A1 (ja) | 2021-07-28 | 2022-07-27 | 重合体組成物及び単層位相差材 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPWO2023008488A1 JPWO2023008488A1 (https=) | 2023-02-02 |
| JPWO2023008488A5 true JPWO2023008488A5 (https=) | 2024-04-23 |
Family
ID=85086858
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2023538599A Pending JPWO2023008488A1 (https=) | 2021-07-28 | 2022-07-27 |
Country Status (5)
| Country | Link |
|---|---|
| JP (1) | JPWO2023008488A1 (https=) |
| KR (1) | KR20240037250A (https=) |
| CN (1) | CN117677669A (https=) |
| TW (1) | TW202313936A (https=) |
| WO (1) | WO2023008488A1 (https=) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN119866360A (zh) * | 2022-09-29 | 2025-04-22 | 日产化学株式会社 | 聚合物组合物和单层相位差材料 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH09208957A (ja) | 1996-01-31 | 1997-08-12 | Teijin Ltd | 光学異方体の製造方法 |
| JPH1095821A (ja) * | 1996-09-26 | 1998-04-14 | Dainippon Ink & Chem Inc | 液晶性ブロック共重合体及びその製造方法 |
| JP3945790B2 (ja) | 1997-12-25 | 2007-07-18 | 林テレンプ株式会社 | 複屈折フィルムとその製造方法 |
| JP4378786B2 (ja) * | 1998-04-30 | 2009-12-09 | Ｊｓｒ株式会社 | 反射防止膜 |
| KR101436795B1 (ko) | 2006-09-13 | 2014-09-03 | 롤리크 아게 | 체적 광-정렬 지연판 |
| JP2008164925A (ja) | 2006-12-28 | 2008-07-17 | Hayashi Telempu Co Ltd | 位相差フィルムおよびその製造方法 |
| CN100513449C (zh) * | 2007-03-09 | 2009-07-15 | 北京大学 | 一种主链含液晶高分子基元的嵌段共聚物及其自由基/正离子转化聚合法 |
| KR101090325B1 (ko) | 2009-03-18 | 2011-12-07 | 동방에프티엘(주) | 고순도 올메사탄 메독소밀의 제조방법 |
| JP6578919B2 (ja) * | 2015-12-07 | 2019-09-25 | 東洋インキＳｃホールディングス株式会社 | 細胞培養用部材 |
| WO2017170947A1 (ja) * | 2016-03-31 | 2017-10-05 | 日産化学工業株式会社 | 偏光層形成組成物 |
-
2022
- 2022-07-27 KR KR1020247002612A patent/KR20240037250A/ko active Pending
- 2022-07-27 JP JP2023538599A patent/JPWO2023008488A1/ja active Pending
- 2022-07-27 CN CN202280051122.6A patent/CN117677669A/zh active Pending
- 2022-07-27 WO PCT/JP2022/028970 patent/WO2023008488A1/ja not_active Ceased
- 2022-07-28 TW TW111128288A patent/TW202313936A/zh unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP7082021B2 (ja) | 偏光フィルム及びその製造方法 | |
| JP7390101B2 (ja) | 光学積層体および表示装置 | |
| US10941225B2 (en) | Photocurable electron deficient olefin-containing compositions | |
| US6153662A (en) | Aromatic maleimides and methods of using the same | |
| JP7082022B2 (ja) | 偏光フィルム及びその製造方法 | |
| JPS59142205A (ja) | 高感度光開始剤組成物 | |
| JP3766435B2 (ja) | Ｕｖ硬化性剥離被膜組成物、使用法及びその製品 | |
| EP0018672B1 (en) | U.v.-curable coating composition | |
| JPWO2023008488A5 (https=) | ||
| JP2018205341A (ja) | 光学異方性フィルム | |
| JP2015094801A (ja) | 光学異方素子およびその製造方法 | |
| JP6822062B2 (ja) | 側鎖型液晶ポリマー、液晶組成物、位相差フィルム、位相差フィルムの製造方法、転写用積層体、光学部材、及び表示装置 | |
| JP2017068019A (ja) | 光配向性を有する熱硬化性組成物、配向層、配向層付基板及びその製造方法、並びに、位相差板及びその製造方法 | |
| WO2022220083A1 (ja) | 光学積層体 | |
| JP2023081092A (ja) | 粘着剤層付き円偏光板 | |
| JP2021099482A (ja) | 重合性液晶組成物、偏光膜、偏光フィルムおよび偏光板 | |
| JP2022120662A (ja) | 光配向膜形成用組成物、光配向膜、積層体および偏光素子 | |
| JP7657064B2 (ja) | 偏光素子およびその製造方法 | |
| JP2019185044A (ja) | 重合性液晶組成物 | |
| JP5710517B2 (ja) | 重合・発色性組成物およびそれに用いる化合物 | |
| JPH02212502A (ja) | 光硬化性組成物 | |
| JP2024144145A (ja) | 偏光膜形成用組成物、偏光膜、偏光板およびその製造方法 | |
| JPS6026125B2 (ja) | 光増感剤 | |
| JP7140387B2 (ja) | 新規な重合性単量体及びこれを用いた歯科用重合硬化性組成物 | |
| JPH04132710A (ja) | 樹脂組成物及びその硬化物 |