TWI682921B - 肟酯化合物、含有肟酯化合物之光聚合起始劑及可光聚合的組成物、模製物件及顯示器裝置 - Google Patents
肟酯化合物、含有肟酯化合物之光聚合起始劑及可光聚合的組成物、模製物件及顯示器裝置 Download PDFInfo
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- TWI682921B TWI682921B TW105103739A TW105103739A TWI682921B TW I682921 B TWI682921 B TW I682921B TW 105103739 A TW105103739 A TW 105103739A TW 105103739 A TW105103739 A TW 105103739A TW I682921 B TWI682921 B TW I682921B
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- diethyl
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- oxime
- fusel
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- 0 *C(*)(c1cc(C(C(*)=NOC(*)=O)=NOC(*)=O)ccc1C1=CC2)C1=C[C@@]2C(C(*)=NOC(*)=O)=NOC(*)=O Chemical compound *C(*)(c1cc(C(C(*)=NOC(*)=O)=NOC(*)=O)ccc1C1=CC2)C1=C[C@@]2C(C(*)=NOC(*)=O)=NOC(*)=O 0.000 description 3
- CSFJGYCKSXSTSG-DWGHPKEWSA-N CC(C)(c1c2)c3cc(/C(/C)=N/OC(C)=O)cc([N+]([O-])=O)c3-c1ccc2/C(/C)=N/OC(C)=O Chemical compound CC(C)(c1c2)c3cc(/C(/C)=N/OC(C)=O)cc([N+]([O-])=O)c3-c1ccc2/C(/C)=N/OC(C)=O CSFJGYCKSXSTSG-DWGHPKEWSA-N 0.000 description 1
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- HVHFCWHRDUEMHE-UTMVNRITSA-N CC1(C)c2cc(/C(/c3ccccc3)=N/OC(C)=O)cc([N+]([O-])=O)c2-c(cc2)c1cc2/C(/c1ccccc1)=N/OC(C)=O Chemical compound CC1(C)c2cc(/C(/c3ccccc3)=N/OC(C)=O)cc([N+]([O-])=O)c2-c(cc2)c1cc2/C(/c1ccccc1)=N/OC(C)=O HVHFCWHRDUEMHE-UTMVNRITSA-N 0.000 description 1
- SWCGFJKACUGNRJ-UHFFFAOYSA-N CC1C(C(Cl)=O)=CC=CC1 Chemical compound CC1C(C(Cl)=O)=CC=CC1 SWCGFJKACUGNRJ-UHFFFAOYSA-N 0.000 description 1
- NJJGURSLXFGWFA-CIOBDNPFSA-N CCC(CC)(c1c2)c3cc(/C(/C)=N/OC(C)O)cc([N+]([O-])=O)c3-c1ccc2/C(/C)=N/OC(C)O Chemical compound CCC(CC)(c1c2)c3cc(/C(/C)=N/OC(C)O)cc([N+]([O-])=O)c3-c1ccc2/C(/C)=N/OC(C)O NJJGURSLXFGWFA-CIOBDNPFSA-N 0.000 description 1
- MLVFFTJYCXZTLK-UHFFFAOYSA-N CCC(CC)(c1cc(C(CC)=O)ccc1-1)c2c-1c([N+]([O-])=O)cc(C(CC)=O)c2 Chemical compound CCC(CC)(c1cc(C(CC)=O)ccc1-1)c2c-1c([N+]([O-])=O)cc(C(CC)=O)c2 MLVFFTJYCXZTLK-UHFFFAOYSA-N 0.000 description 1
- CGMFGAPLOGHVRC-NYOGSRRGSA-N CCC1(CC)c2cc(/C(/C(/C)=N/O)=N\O)ccc2-c2ccccc12 Chemical compound CCC1(CC)c2cc(/C(/C(/C)=N/O)=N\O)ccc2-c2ccccc12 CGMFGAPLOGHVRC-NYOGSRRGSA-N 0.000 description 1
- SDRZRFFTGGYYPK-BRYJUMNTSA-N CCC1(CC)c2cc(/C(/C(/C)=N/OC(C)=O)=N\OC(C)=O)ccc2-c2c1cccc2 Chemical compound CCC1(CC)c2cc(/C(/C(/C)=N/OC(C)=O)=N\OC(C)=O)ccc2-c2c1cccc2 SDRZRFFTGGYYPK-BRYJUMNTSA-N 0.000 description 1
- CGAZHUUFZGCCGP-CJRSFPGISA-N CCC1(CC)c2cc(/C(/CC)=N/OC(C)=O)cc([N+]([O-])=O)c2-c(cc2)c1cc2/C(/CC)=N/OC(C)=O Chemical compound CCC1(CC)c2cc(/C(/CC)=N/OC(C)=O)cc([N+]([O-])=O)c2-c(cc2)c1cc2/C(/CC)=N/OC(C)=O CGAZHUUFZGCCGP-CJRSFPGISA-N 0.000 description 1
- FRPLOAPAJWIFFE-UXOHLBSUSA-N CCC1(CC)c2cc(/C(/CC/C(/C)=N/OC(C3CCCCC3)=O)=N/OC(C3CCCCC3)=O)ccc2-c2c1cccc2 Chemical compound CCC1(CC)c2cc(/C(/CC/C(/C)=N/OC(C3CCCCC3)=O)=N/OC(C3CCCCC3)=O)ccc2-c2c1cccc2 FRPLOAPAJWIFFE-UXOHLBSUSA-N 0.000 description 1
- MNVHGIYLMOALLL-VHKBNUNLSA-N CCC1(CC)c2cc(/C(/c3ccccc3)=N/OC(C)=O)cc([N+]([O-])=O)c2-c(cc2)c1cc2/C(/c1ccccc1)=N/OC(C)=O Chemical compound CCC1(CC)c2cc(/C(/c3ccccc3)=N/OC(C)=O)cc([N+]([O-])=O)c2-c(cc2)c1cc2/C(/c1ccccc1)=N/OC(C)=O MNVHGIYLMOALLL-VHKBNUNLSA-N 0.000 description 1
- AZJCYNYSFUUUKE-RABJZLPGSA-N CCC1(CC)c2cc(C(/C(/C)=N/OC(C)=O)=O)cc([N+]([O-])=O)c2-c(cc2)c1cc2C(/C(/C)=N/OC(C)=O)=O Chemical compound CCC1(CC)c2cc(C(/C(/C)=N/OC(C)=O)=O)cc([N+]([O-])=O)c2-c(cc2)c1cc2C(/C(/C)=N/OC(C)=O)=O AZJCYNYSFUUUKE-RABJZLPGSA-N 0.000 description 1
- BOCNMKNSLVBIDK-UHFFFAOYSA-N CCC1(CC)c2cccc([N+]([O-])=O)c2-c2c1cccc2 Chemical compound CCC1(CC)c2cccc([N+]([O-])=O)c2-c2c1cccc2 BOCNMKNSLVBIDK-UHFFFAOYSA-N 0.000 description 1
- XBAATQNHWCDJIK-INQZDMBFSA-N CCCCC(CCCC)(c1c2)c(cc(cc3)[N+]([O-])=O)c3-c1ccc2/C(/C(C)/C(/C)=N/OC(C)=O)=N\OC(C)=O Chemical compound CCCCC(CCCC)(c1c2)c(cc(cc3)[N+]([O-])=O)c3-c1ccc2/C(/C(C)/C(/C)=N/OC(C)=O)=N\OC(C)=O XBAATQNHWCDJIK-INQZDMBFSA-N 0.000 description 1
- CBIKJAUQUXAXCH-UHFFFAOYSA-N CCCCC(CCCC)(c1c2)c3cc([N+]([O-])=O)ccc3-c1ccc2C(CC)=O Chemical compound CCCCC(CCCC)(c1c2)c3cc([N+]([O-])=O)ccc3-c1ccc2C(CC)=O CBIKJAUQUXAXCH-UHFFFAOYSA-N 0.000 description 1
- WKDMDVBEVSPBFE-LLUBJRRCSA-N CCCCC/C(/C(c(cc1)cc(C(CC)(C[O]=C)c2c3)c1-c2ccc3C(/C(/C)=N/OC(c1ccccc1)=O)=O)=O)=N\OC(c1ccccc1)=O Chemical compound CCCCC/C(/C(c(cc1)cc(C(CC)(C[O]=C)c2c3)c1-c2ccc3C(/C(/C)=N/OC(c1ccccc1)=O)=O)=O)=N\OC(c1ccccc1)=O WKDMDVBEVSPBFE-LLUBJRRCSA-N 0.000 description 1
- VCPWFFATCCGJFR-UHFFFAOYSA-N CCCCC1(CCCC)c2cc([N+]([O-])=O)ccc2-c2ccccc12 Chemical compound CCCCC1(CCCC)c2cc([N+]([O-])=O)ccc2-c2ccccc12 VCPWFFATCCGJFR-UHFFFAOYSA-N 0.000 description 1
- OVPKKRRBGKUHLY-HXVZTMQTSA-N CCCCCC(C(C)c1c2)c(cc(cc3)C(/C(/C)=N/O)=O)c3-c1ccc2C(/C(/CCCCC)=N/O)=O Chemical compound CCCCCC(C(C)c1c2)c(cc(cc3)C(/C(/C)=N/O)=O)c3-c1ccc2C(/C(/CCCCC)=N/O)=O OVPKKRRBGKUHLY-HXVZTMQTSA-N 0.000 description 1
- LOCXTTRLSIDGPS-AZPGRJICSA-N CCCCCC/C(/C(c(cc1)ccc1Sc1ccccc1)=O)=N\OC(c1ccccc1)=O Chemical compound CCCCCC/C(/C(c(cc1)ccc1Sc1ccccc1)=O)=N\OC(c1ccccc1)=O LOCXTTRLSIDGPS-AZPGRJICSA-N 0.000 description 1
- LSLQQWGQZQAUOO-SVIREBAHSA-N CCCCCC/C(/c(cc1)cc(C(C)(C)c2cc(/C(/C)=N/OC(C)=O)c3)c1-c2c3[N+]([O-])=O)=N\OC(C)O Chemical compound CCCCCC/C(/c(cc1)cc(C(C)(C)c2cc(/C(/C)=N/OC(C)=O)c3)c1-c2c3[N+]([O-])=O)=N\OC(C)O LSLQQWGQZQAUOO-SVIREBAHSA-N 0.000 description 1
- IYIJXBHTUVRGAU-DDYRMXSUSA-N CCCCCC/C(/c(cc1)cc(C(CC)(CC)c2cc(/C(/C)=N/OC(C)=O)c3)c1-c2c3[N+]([O-])=O)=N\OC(C)=O Chemical compound CCCCCC/C(/c(cc1)cc(C(CC)(CC)c2cc(/C(/C)=N/OC(C)=O)c3)c1-c2c3[N+]([O-])=O)=N\OC(C)=O IYIJXBHTUVRGAU-DDYRMXSUSA-N 0.000 description 1
- XIYATWBVQHWJPH-UHFFFAOYSA-N CCCc1ccccc1C=C Chemical compound CCCc1ccccc1C=C XIYATWBVQHWJPH-UHFFFAOYSA-N 0.000 description 1
- INRITZRWAQHXJU-UHFFFAOYSA-N OC(C1CCCCC1)Cl Chemical compound OC(C1CCCCC1)Cl INRITZRWAQHXJU-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C251/32—Oximes
- C07C251/62—Oximes having oxygen atoms of oxyimino groups esterified
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C251/32—Oximes
- C07C251/62—Oximes having oxygen atoms of oxyimino groups esterified
- C07C251/64—Oximes having oxygen atoms of oxyimino groups esterified by carboxylic acids
- C07C251/66—Oximes having oxygen atoms of oxyimino groups esterified by carboxylic acids with the esterifying carboxyl groups bound to hydrogen atoms, to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C251/32—Oximes
- C07C251/62—Oximes having oxygen atoms of oxyimino groups esterified
- C07C251/64—Oximes having oxygen atoms of oxyimino groups esterified by carboxylic acids
- C07C251/68—Oximes having oxygen atoms of oxyimino groups esterified by carboxylic acids with at least one of the esterifying carboxyl groups bound to a carbon atom of a six-membered aromatic ring
-
- 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
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Materials For Photolithography (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (4)
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KR10-2015-0018698 | 2015-02-06 | ||
KR1020150018698A KR101828927B1 (ko) | 2015-02-06 | 2015-02-06 | 신규한 옥심에스테르 화합물, 이를 포함하는 광중합 개시제 및 포토레지스트 조성물 |
KR10-2015-0050017 | 2015-04-09 | ||
KR1020150050017A KR101824443B1 (ko) | 2015-04-09 | 2015-04-09 | 신규한 플루오렌일 옥심 에스테르 화합물, 이를 포함하는 광중합 개시제 및 포토레지스트 조성물 |
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TW201634444A TW201634444A (zh) | 2016-10-01 |
TWI682921B true TWI682921B (zh) | 2020-01-21 |
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TW105103739A TWI682921B (zh) | 2015-02-06 | 2016-02-04 | 肟酯化合物、含有肟酯化合物之光聚合起始劑及可光聚合的組成物、模製物件及顯示器裝置 |
Country Status (4)
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JP (1) | JP6408715B2 (ko) |
CN (1) | CN107250105B (ko) |
TW (1) | TWI682921B (ko) |
WO (1) | WO2016126070A1 (ko) |
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KR101834209B1 (ko) * | 2016-11-25 | 2018-03-06 | 주식회사 삼양사 | 광중합 개시제 및 이를 포함하는 차광용 감광성 수지 조성물 |
KR101840584B1 (ko) * | 2017-01-17 | 2018-03-20 | 동우 화인켐 주식회사 | 착색 감광성 수지 조성물, 컬러필터 및 화상표시장치 |
CN106831487B (zh) * | 2017-01-22 | 2018-12-07 | 苏州楚凯药业有限公司 | 有机电子产品中间体芴类衍生物的制备方法 |
JP7032416B2 (ja) * | 2017-02-17 | 2022-03-08 | 常州強力先端電子材料有限公司 | フルオレニルアミノケトン類光開始剤、その調製方法及びフルオレニルアミノケトン類光開始剤を含有するuv光硬化性組成物 |
JP7051321B2 (ja) * | 2017-07-21 | 2022-04-11 | 東京応化工業株式会社 | 感光性組成物、パターン形成方法、硬化物、及び表示装置 |
CN107445861A (zh) * | 2017-08-04 | 2017-12-08 | 吴赣药业(苏州)有限公司 | 一种2‑硝基‑7‑乙酰肟基‑9,9‑二丁基芴的制备方法 |
KR20200135308A (ko) * | 2018-03-27 | 2020-12-02 | 가부시키가이샤 아데카 | 화합물, 라디칼 중합 개시제, 조성물, 경화물 및 경화물의 제조 방법 |
JP7460288B2 (ja) * | 2018-08-07 | 2024-04-02 | 株式会社Adeka | カルバモイルオキシム化合物並びに該化合物を含有する重合開始剤及び重合性組成物 |
CN112010788B (zh) * | 2019-05-31 | 2022-10-21 | 常州强力先端电子材料有限公司 | 一种非离子型肟酯类光产酸剂 |
CN110668971A (zh) * | 2019-10-24 | 2020-01-10 | 重庆沃肯精细化工有限公司 | 一种不对称芴肟酯化合物及其制备方法和光敏性组合物 |
CN112851547B (zh) * | 2019-11-12 | 2024-06-07 | 常州强力先端电子材料有限公司 | 芴肟酯类化合物及其制备方法、感光性树脂组合物 |
JP2021167905A (ja) * | 2020-04-10 | 2021-10-21 | 東京応化工業株式会社 | 感光性組成物、パターン化された硬化膜の製造方法、及びパターン化された硬化膜 |
JP2021167906A (ja) * | 2020-04-10 | 2021-10-21 | 東京応化工業株式会社 | 感光性組成物、パターン化された硬化膜の製造方法、及びパターン化された硬化膜 |
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TW201345882A (zh) * | 2012-05-03 | 2013-11-16 | Korea Res Inst Chem Tech | 新穎茀肟酯化合物、含彼之光聚合起始劑及光阻組合物 |
TW201425283A (zh) * | 2012-09-28 | 2014-07-01 | Daito Chemix Corp | 茀系化合物、含有該茀系化合物之光聚合起始劑及含有該光聚合起始劑之感光性組成物 |
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NL1016815C2 (nl) * | 1999-12-15 | 2002-05-14 | Ciba Sc Holding Ag | Oximester-fotoinitiatoren. |
KR100523295B1 (ko) * | 2003-01-10 | 2005-10-24 | 한국화학연구원 | 광중합성 조성물 및 이로부터 제조된 광중합성 막 |
JP2010156879A (ja) * | 2008-12-29 | 2010-07-15 | Fujifilm Corp | 感光性組成物、カラーフィルタ、及び液晶表示装置 |
JP6065596B2 (ja) * | 2013-01-16 | 2017-01-25 | Jsr株式会社 | 感放射線性着色組成物、着色硬化膜及び表示素子 |
KR101567837B1 (ko) * | 2013-06-11 | 2015-11-11 | 애경화학 주식회사 | 플루오렌 구조를 갖는 신규한 광개시제 및 이를 포함하는 반응성 액정 조성물 및 감광성 조성물 |
JP2015011095A (ja) * | 2013-06-27 | 2015-01-19 | 凸版印刷株式会社 | フォトスペーサー形成用感光性樹脂組成物及びカラーフィルタ |
KR101435652B1 (ko) * | 2014-01-17 | 2014-08-28 | 주식회사 삼양사 | 신규한 β-옥심에스테르 플루오렌 화합물, 이를 포함하는 광중합 개시제 및 포토레지스트 조성물 |
CN103819583B (zh) * | 2014-03-18 | 2016-05-18 | 常州强力电子新材料股份有限公司 | 一种含硝基双肟酯类光引发剂及其制备方法和应用 |
CN103833872B (zh) * | 2014-03-18 | 2016-04-06 | 常州强力先端电子材料有限公司 | 一种双肟酯类光引发剂及其制备方法和应用 |
CN104076606B (zh) * | 2014-07-15 | 2019-12-03 | 常州强力电子新材料股份有限公司 | 一种含肟酯类光引发剂的感光性组合物及其应用 |
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2016
- 2016-02-02 JP JP2017541678A patent/JP6408715B2/ja active Active
- 2016-02-02 WO PCT/KR2016/001103 patent/WO2016126070A1/ko active Application Filing
- 2016-02-02 CN CN201680008616.0A patent/CN107250105B/zh active Active
- 2016-02-04 TW TW105103739A patent/TWI682921B/zh active
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW201345882A (zh) * | 2012-05-03 | 2013-11-16 | Korea Res Inst Chem Tech | 新穎茀肟酯化合物、含彼之光聚合起始劑及光阻組合物 |
TW201425283A (zh) * | 2012-09-28 | 2014-07-01 | Daito Chemix Corp | 茀系化合物、含有該茀系化合物之光聚合起始劑及含有該光聚合起始劑之感光性組成物 |
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Publication number | Publication date |
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CN107250105B (zh) | 2019-08-20 |
TW201634444A (zh) | 2016-10-01 |
WO2016126070A1 (ko) | 2016-08-11 |
JP2018506532A (ja) | 2018-03-08 |
JP6408715B2 (ja) | 2018-10-17 |
CN107250105A (zh) | 2017-10-13 |
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