TW201817722A - 化合物、樹脂、組成物及圖型形成方法 - Google Patents
化合物、樹脂、組成物及圖型形成方法 Download PDFInfo
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- TW201817722A TW201817722A TW106124617A TW106124617A TW201817722A TW 201817722 A TW201817722 A TW 201817722A TW 106124617 A TW106124617 A TW 106124617A TW 106124617 A TW106124617 A TW 106124617A TW 201817722 A TW201817722 A TW 201817722A
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- NMOALOSNPWTWRH-UHFFFAOYSA-N tert-butyl 7,7-dimethyloctaneperoxoate Chemical compound CC(C)(C)CCCCCC(=O)OOC(C)(C)C NMOALOSNPWTWRH-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/20—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
- C07C43/215—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring having unsaturation outside the six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/20—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
- C07C43/23—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing hydroxy or O-metal groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/52—Esters of acyclic unsaturated carboxylic acids having the esterified carboxyl group bound to an acyclic carbon atom
- C07C69/533—Monocarboxylic acid esters having only one carbon-to-carbon double bond
- C07C69/54—Acrylic acid esters; Methacrylic acid esters
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/78—Ring systems having three or more relevant rings
- C07D311/80—Dibenzopyrans; Hydrogenated dibenzopyrans
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/78—Ring systems having three or more relevant rings
- C07D311/80—Dibenzopyrans; Hydrogenated dibenzopyrans
- C07D311/82—Xanthenes
- C07D311/90—Xanthenes with hydrocarbon radicals, substituted by amino radicals, directly attached in position 9
-
- 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
- C08F216/00—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 an alcohol, ether, aldehydo, ketonic, acetal or ketal radical
- C08F216/02—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 an alcohol, ether, aldehydo, ketonic, acetal or ketal radical by an alcohol radical
- C08F216/10—Carbocyclic compounds
-
- 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
- C08F224/00—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 a heterocyclic ring containing oxygen
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- G—PHYSICS
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- 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
- G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
- G03F7/028—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with photosensitivity-increasing substances, e.g. photoinitiators
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- 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
- G03F7/09—Photosensitive materials characterised by structural details, e.g. supports, auxiliary layers
- G03F7/11—Photosensitive materials characterised by structural details, e.g. supports, auxiliary layers having cover layers or intermediate layers, e.g. subbing layers
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- G03F7/20—Exposure; Apparatus therefor
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- G03F7/26—Processing photosensitive materials; Apparatus therefor
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/027—Making masks on semiconductor bodies for further photolithographic processing not provided for in group H01L21/18 or H01L21/34
- H01L21/0271—Making masks on semiconductor bodies for further photolithographic processing not provided for in group H01L21/18 or H01L21/34 comprising organic layers
- H01L21/0273—Making masks on semiconductor bodies for further photolithographic processing not provided for in group H01L21/18 or H01L21/34 comprising organic layers characterised by the treatment of photoresist layers
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/31—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to form insulating layers thereon, e.g. for masking or by using photolithographic techniques; After treatment of these layers; Selection of materials for these layers
- H01L21/3105—After-treatment
- H01L21/311—Etching the insulating layers by chemical or physical means
- H01L21/31144—Etching the insulating layers by chemical or physical means using masks
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Computer Hardware Design (AREA)
- Power Engineering (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Manufacturing & Machinery (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- Architecture (AREA)
- Structural Engineering (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Materials For Photolithography (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyrane Compounds (AREA)
- Phenolic Resins Or Amino Resins (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Photosensitive Polymer And Photoresist Processing (AREA)
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JP2016143659 | 2016-07-21 | ||
JP2016-143659 | 2016-07-21 |
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JP (1) | JP7194355B2 (ko) |
KR (1) | KR20190034213A (ko) |
CN (1) | CN109415286A (ko) |
TW (1) | TW201817722A (ko) |
WO (1) | WO2018016614A1 (ko) |
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TWI716141B (zh) * | 2018-10-08 | 2021-01-11 | 台灣積體電路製造股份有限公司 | 光阻組成物及在光阻劑中形成圖案的方法 |
CN112513737A (zh) * | 2018-07-31 | 2021-03-16 | 三菱瓦斯化学株式会社 | 下层膜形成组合物 |
US11215928B2 (en) | 2016-09-16 | 2022-01-04 | Jsr Corporation | Composition for resist underlayer film formation, resist underlayer film and method for forming the same, and production method of a patterned substrate |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20190034149A (ko) * | 2016-07-21 | 2019-04-01 | 미쯔비시 가스 케미칼 컴파니, 인코포레이티드 | 화합물, 수지 및 조성물, 그리고 레지스트패턴 형성방법 및 회로패턴 형성방법 |
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Family Cites Families (43)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3223104A1 (de) * | 1982-06-21 | 1983-12-22 | Hoechst Ag, 6230 Frankfurt | Photopolymerisierbares gemisch und damit hergestelltes photopolymerisierbares kopiermaterial |
JPH04253716A (ja) * | 1991-02-05 | 1992-09-09 | Dainippon Ink & Chem Inc | 新規なエネルギー線硬化型樹脂組成物 |
JP4365494B2 (ja) * | 1999-10-27 | 2009-11-18 | 日本ペイント株式会社 | 体積ホログラム記録用感光組成物およびこれから得られるホログラム |
DE60135154D1 (de) * | 2000-12-13 | 2008-09-11 | Tokuyama Corp | Photochrome härtbare zusammensetzung und gehärtete gegenstände daraus |
JP3774668B2 (ja) | 2001-02-07 | 2006-05-17 | 東京エレクトロン株式会社 | シリコン窒化膜形成装置の洗浄前処理方法 |
JP2003012660A (ja) * | 2001-06-28 | 2003-01-15 | Sumitomo Bakelite Co Ltd | エポキシアクリレート化合物およびその製造方法 |
US7553544B2 (en) * | 2001-11-30 | 2009-06-30 | Nikon Corporation | Precursor composition for optical resin, resin for optical use, optical element, and optical article |
JP3914493B2 (ja) | 2002-11-27 | 2007-05-16 | 東京応化工業株式会社 | 多層レジストプロセス用下層膜形成材料およびこれを用いた配線形成方法 |
EP1592051A4 (en) | 2003-01-24 | 2012-02-22 | Tokyo Electron Ltd | CHEMICAL VAPOR DEPOSITION METHOD FOR FORMING SILICON NITRIDE FILM ON A SUBSTRATE |
JP3981030B2 (ja) | 2003-03-07 | 2007-09-26 | 信越化学工業株式会社 | レジスト下層膜材料ならびにパターン形成方法 |
JP4388429B2 (ja) | 2004-02-04 | 2009-12-24 | 信越化学工業株式会社 | レジスト下層膜材料ならびにパターン形成方法 |
CN1942825B (zh) | 2004-04-15 | 2010-05-12 | 三菱瓦斯化学株式会社 | 抗蚀剂组合物 |
JP4630806B2 (ja) * | 2005-12-09 | 2011-02-09 | キヤノン株式会社 | 電子写真感光体、プロセスカートリッジ及び電子写真装置 |
JP4781280B2 (ja) | 2006-01-25 | 2011-09-28 | 信越化学工業株式会社 | 反射防止膜材料、基板、及びパターン形成方法 |
JP4638380B2 (ja) | 2006-01-27 | 2011-02-23 | 信越化学工業株式会社 | 反射防止膜材料、反射防止膜を有する基板及びパターン形成方法 |
JP4858136B2 (ja) | 2006-12-06 | 2012-01-18 | 三菱瓦斯化学株式会社 | 感放射線性レジスト組成物 |
US8586154B2 (en) * | 2007-03-09 | 2013-11-19 | 3M Innovative Properties Company | Triphenyl monomers suitable for microstructured optical films |
JP5446118B2 (ja) | 2007-04-23 | 2014-03-19 | 三菱瓦斯化学株式会社 | 感放射線性組成物 |
TW200906873A (en) * | 2007-05-30 | 2009-02-16 | Toagosei Co Ltd | Active energy ray curable composition, coating composition, coating member, and optical material |
TW200906869A (en) * | 2007-05-30 | 2009-02-16 | Toagosei Co Ltd | Active energy ray curable composition and optical material |
JP5251523B2 (ja) * | 2008-07-08 | 2013-07-31 | 日立化成株式会社 | 感光性樹脂組成物、並びにこれを用いた感光性エレメント、レジストパターンの形成方法及びプリント配線板の製造方法 |
JP2010138393A (ja) | 2008-11-13 | 2010-06-24 | Nippon Kayaku Co Ltd | 光学レンズシート用エネルギー線硬化型樹脂組成物及びその硬化物 |
JP5423004B2 (ja) * | 2009-01-08 | 2014-02-19 | 東レ株式会社 | ネガ型感光性樹脂組成物およびそれを用いたタッチパネル用材料 |
EP2567269A1 (en) * | 2010-05-07 | 2013-03-13 | 3M Innovative Properties Company | Antireflective films comprising microstructured surface |
JP5778462B2 (ja) * | 2011-04-18 | 2015-09-16 | 旭有機材工業株式会社 | アントラセン誘導体及びこの製造方法、硬化性組成物並びに硬化物 |
KR101986346B1 (ko) * | 2011-08-12 | 2019-06-05 | 미쯔비시 가스 케미칼 컴파니, 인코포레이티드 | 레지스트 조성물, 레지스트 패턴 형성방법, 이에 이용되는 폴리페놀 화합물 및 이로부터 유도될 수 있는 알코올 화합물 |
KR101907481B1 (ko) | 2011-08-12 | 2018-10-12 | 미쯔비시 가스 케미칼 컴파니, 인코포레이티드 | 리소그래피용 하층막 형성재료, 리소그래피용 하층막 및 패턴형성방법 |
CN102778814B (zh) * | 2012-07-05 | 2014-04-23 | 常州强力先端电子材料有限公司 | 一种含有酮肟酯类光引发剂的感光性组合物及其应用 |
EP2955169B1 (en) | 2013-02-08 | 2017-03-15 | Mitsubishi Gas Chemical Company, Inc. | Novel allyl compound and method for producing the same |
WO2015137486A1 (ja) * | 2014-03-13 | 2015-09-17 | 三菱瓦斯化学株式会社 | 化合物、樹脂、リソグラフィー用下層膜形成材料、リソグラフィー用下層膜、パターン形成方法、及び化合物又は樹脂の精製方法 |
JP2015174877A (ja) | 2014-03-13 | 2015-10-05 | 日産化学工業株式会社 | 特定の硬化促進触媒を含む樹脂組成物 |
JP7026439B2 (ja) * | 2014-12-25 | 2022-02-28 | 三菱瓦斯化学株式会社 | 化合物、樹脂、リソグラフィー用下層膜形成材料、リソグラフィー用下層膜、パターン形成方法及び精製方法 |
KR20180030847A (ko) * | 2015-07-23 | 2018-03-26 | 미쯔비시 가스 케미칼 컴파니, 인코포레이티드 | 신규 화합물 및 그 제조방법 |
CN107848946A (zh) * | 2015-07-23 | 2018-03-27 | 三菱瓦斯化学株式会社 | 新型(甲基)丙烯酰基化合物及其制造方法 |
KR20180048733A (ko) * | 2015-08-31 | 2018-05-10 | 미쯔비시 가스 케미칼 컴파니, 인코포레이티드 | 리소그래피용 하층막 형성재료, 리소그래피용 하층막 형성용 조성물, 리소그래피용 하층막 및 그 제조방법, 패턴형성방법, 수지, 그리고 정제방법 |
EP3346334B1 (en) * | 2015-08-31 | 2020-08-12 | Mitsubishi Gas Chemical Company, Inc. | Use of a composition for forming a photoresist underlayer film for lithography, photoresist underlayer film for lithography and method for producing same, and resist pattern forming method |
JP7212449B2 (ja) * | 2015-09-03 | 2023-01-25 | 三菱瓦斯化学株式会社 | 化合物及びその製造方法、並びに、組成物、光学部品形成用組成物、リソグラフィー用膜形成組成物、レジスト組成物、レジストパターンの形成方法、感放射線性組成物、アモルファス膜の製造方法、リソグラフィー用下層膜形成材料、リソグラフィー用下層膜形成用組成物、リソグラフィー用下層膜の製造方法、レジストパターン形成方法、回路パターン形成方法、及び、精製方法 |
JP6848869B2 (ja) * | 2015-09-10 | 2021-03-24 | 三菱瓦斯化学株式会社 | 化合物、樹脂、レジスト組成物又は感放射線性組成物、レジストパターン形成方法、アモルファス膜の製造方法、リソグラフィー用下層膜形成材料、リソグラフィー用下層膜形成用組成物、回路パターンの形成方法、及び、精製方法 |
WO2017111165A1 (ja) * | 2015-12-25 | 2017-06-29 | 三菱瓦斯化学株式会社 | 化合物、樹脂、組成物、レジストパターン形成方法、及び、回路パターン形成方法 |
JP7194355B2 (ja) * | 2016-07-21 | 2022-12-22 | 三菱瓦斯化学株式会社 | 化合物、樹脂、組成物及びパターン形成方法 |
JP7069530B2 (ja) * | 2016-07-21 | 2022-05-18 | 三菱瓦斯化学株式会社 | 化合物、樹脂、組成物及びパターン形成方法 |
KR20190033536A (ko) * | 2016-07-21 | 2019-03-29 | 미쯔비시 가스 케미칼 컴파니, 인코포레이티드 | 화합물, 수지, 조성물 그리고 레지스트패턴 형성방법 및 회로패턴 형성방법 |
CN109476575A (zh) * | 2016-07-21 | 2019-03-15 | 三菱瓦斯化学株式会社 | 化合物、树脂、组合物以及抗蚀图案形成方法及电路图案形成方法 |
-
2017
- 2017-07-21 JP JP2018528886A patent/JP7194355B2/ja active Active
- 2017-07-21 TW TW106124617A patent/TW201817722A/zh unknown
- 2017-07-21 KR KR1020197002640A patent/KR20190034213A/ko not_active Application Discontinuation
- 2017-07-21 CN CN201780041706.4A patent/CN109415286A/zh not_active Withdrawn
- 2017-07-21 WO PCT/JP2017/026412 patent/WO2018016614A1/ja active Application Filing
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11215928B2 (en) | 2016-09-16 | 2022-01-04 | Jsr Corporation | Composition for resist underlayer film formation, resist underlayer film and method for forming the same, and production method of a patterned substrate |
TWI765910B (zh) * | 2016-09-16 | 2022-06-01 | 日商Jsr股份有限公司 | 抗蝕劑底層膜形成用組成物、抗蝕劑底層膜及其形成方法以及圖案化基板的製造方法 |
CN112513737A (zh) * | 2018-07-31 | 2021-03-16 | 三菱瓦斯化学株式会社 | 下层膜形成组合物 |
TWI716141B (zh) * | 2018-10-08 | 2021-01-11 | 台灣積體電路製造股份有限公司 | 光阻組成物及在光阻劑中形成圖案的方法 |
US11971659B2 (en) | 2018-10-08 | 2024-04-30 | Taiwan Semiconductor Manufacturing Co., Ltd. | Photoresist composition and method of forming photoresist pattern |
Also Published As
Publication number | Publication date |
---|---|
KR20190034213A (ko) | 2019-04-01 |
JPWO2018016614A1 (ja) | 2019-05-09 |
CN109415286A (zh) | 2019-03-01 |
WO2018016614A1 (ja) | 2018-01-25 |
JP7194355B2 (ja) | 2022-12-22 |
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