JP7594534B2 - 化合物、酸発生剤、組成物、硬化物及びパターン、並びに硬化物及びパターンの製造方法 - Google Patents
化合物、酸発生剤、組成物、硬化物及びパターン、並びに硬化物及びパターンの製造方法 Download PDFInfo
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- JP7594534B2 JP7594534B2 JP2021545535A JP2021545535A JP7594534B2 JP 7594534 B2 JP7594534 B2 JP 7594534B2 JP 2021545535 A JP2021545535 A JP 2021545535A JP 2021545535 A JP2021545535 A JP 2021545535A JP 7594534 B2 JP7594534 B2 JP 7594534B2
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- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical group C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
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- 239000013307 optical fiber Substances 0.000 description 1
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- 125000002958 pentadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
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- NQQWFVUVBGSGQN-UHFFFAOYSA-N phosphoric acid;piperazine Chemical compound OP(O)(O)=O.C1CNCCN1 NQQWFVUVBGSGQN-UHFFFAOYSA-N 0.000 description 1
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- 239000000049 pigment Substances 0.000 description 1
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- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 229910001415 sodium ion Chemical group 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
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- 125000001544 thienyl group Chemical group 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- BRNULMACUQOKMR-UHFFFAOYSA-N thiomorpholine Chemical group C1CSCCN1 BRNULMACUQOKMR-UHFFFAOYSA-N 0.000 description 1
- NBOMNTLFRHMDEZ-UHFFFAOYSA-N thiosalicylic acid Chemical compound OC(=O)C1=CC=CC=C1S NBOMNTLFRHMDEZ-UHFFFAOYSA-N 0.000 description 1
- 229940103494 thiosalicylic acid Drugs 0.000 description 1
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- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- GRGCWBWNLSTIEN-UHFFFAOYSA-N trifluoromethanesulfonyl chloride Chemical compound FC(F)(F)S(Cl)(=O)=O GRGCWBWNLSTIEN-UHFFFAOYSA-N 0.000 description 1
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- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/64—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and sulfur atoms, not being part of thio groups, bound to the same carbon skeleton
- C07C323/66—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and sulfur atoms, not being part of thio groups, bound to the same carbon skeleton containing sulfur atoms of sulfo, esterified sulfo or halosulfonyl groups, bound to the carbon skeleton
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- C07D335/10—Dibenzothiopyrans; Hydrogenated dibenzothiopyrans
- C07D335/12—Thioxanthenes
- C07D335/14—Thioxanthenes with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 9
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Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005319758A (ja) | 2004-05-11 | 2005-11-17 | Fuji Photo Film Co Ltd | 平版印刷方法及びそれに用いる平版印刷版原版 |
JP2006517950A (ja) | 2003-02-19 | 2006-08-03 | チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド | ハロゲン化オキシム誘導体及び潜在的酸としてのそれらの使用 |
JP2008506749A (ja) | 2004-07-20 | 2008-03-06 | チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド | オキシム誘導体および潜在酸としてのそれらの使用 |
JP2010164964A (ja) | 2008-12-19 | 2010-07-29 | Fujifilm Corp | 感光性組成物、カラーフィルタ、および液晶表示装置 |
CN103389621A (zh) | 2013-07-26 | 2013-11-13 | 常州强力先端电子材料有限公司 | 一种磺酸肟酯类光产酸剂 |
KR101491973B1 (ko) | 2014-03-12 | 2015-02-11 | (주)휴넷플러스 | 화학 증폭형 포지티브형 포토레지스트 조성물 및 이를 이용한 tft 레지스트 패턴 형성방법 |
KR101491975B1 (ko) | 2014-03-14 | 2015-02-11 | (주)휴넷플러스 | 화학 증폭형 포지티브 감광성 경화 수지 조성물, 이를 이용한 경화막의 제조 방법 및 경화막을 포함하는 전자소자 |
CN107163169A (zh) | 2017-05-25 | 2017-09-15 | 同济大学 | 一类香豆素并咔唑型肟酯类化合物及其制备方法和应用 |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SG78412A1 (en) * | 1999-03-31 | 2001-02-20 | Ciba Sc Holding Ag | Oxime derivatives and the use thereof as latent acids |
JP6605820B2 (ja) | 2015-03-11 | 2019-11-13 | 株式会社Adeka | オキシムスルホネート化合物、光酸発生剤、レジスト組成物、カチオン重合開始剤、およびカチオン重合性組成物 |
CN108603094A (zh) | 2016-01-26 | 2018-09-28 | 株式会社Adeka | 热产酸剂及使用其的抗蚀剂组合物 |
CN110806677A (zh) * | 2018-08-06 | 2020-02-18 | 常州强力先端电子材料有限公司 | 光致抗蚀剂组合物、其图案形成方法及应用 |
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Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006517950A (ja) | 2003-02-19 | 2006-08-03 | チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド | ハロゲン化オキシム誘導体及び潜在的酸としてのそれらの使用 |
JP2005319758A (ja) | 2004-05-11 | 2005-11-17 | Fuji Photo Film Co Ltd | 平版印刷方法及びそれに用いる平版印刷版原版 |
JP2008506749A (ja) | 2004-07-20 | 2008-03-06 | チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド | オキシム誘導体および潜在酸としてのそれらの使用 |
JP2010164964A (ja) | 2008-12-19 | 2010-07-29 | Fujifilm Corp | 感光性組成物、カラーフィルタ、および液晶表示装置 |
CN103389621A (zh) | 2013-07-26 | 2013-11-13 | 常州强力先端电子材料有限公司 | 一种磺酸肟酯类光产酸剂 |
KR101491973B1 (ko) | 2014-03-12 | 2015-02-11 | (주)휴넷플러스 | 화학 증폭형 포지티브형 포토레지스트 조성물 및 이를 이용한 tft 레지스트 패턴 형성방법 |
KR101491975B1 (ko) | 2014-03-14 | 2015-02-11 | (주)휴넷플러스 | 화학 증폭형 포지티브 감광성 경화 수지 조성물, 이를 이용한 경화막의 제조 방법 및 경화막을 포함하는 전자소자 |
CN107163169A (zh) | 2017-05-25 | 2017-09-15 | 同济大学 | 一类香豆素并咔唑型肟酯类化合物及其制备方法和应用 |
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