KR101603616B1 - 임프린트용 조성물, 패턴 및 패터닝 방법 - Google Patents
임프린트용 조성물, 패턴 및 패터닝 방법 Download PDFInfo
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- KR101603616B1 KR101603616B1 KR1020117008668A KR20117008668A KR101603616B1 KR 101603616 B1 KR101603616 B1 KR 101603616B1 KR 1020117008668 A KR1020117008668 A KR 1020117008668A KR 20117008668 A KR20117008668 A KR 20117008668A KR 101603616 B1 KR101603616 B1 KR 101603616B1
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Classifications
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
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- Y10T428/3154—Of fluorinated addition polymer from unsaturated monomers
-
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- Y10T428/31855—Of addition polymer from unsaturated monomers
- Y10T428/31935—Ester, halide or nitrile of addition polymer
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31855—Of addition polymer from unsaturated monomers
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Abstract
Description
Claims (16)
- 중합성 모노머,
광중합 개시제, 및
측쇄에 불소 원자 또는 규소 원자 중 하나 이상을 가진 관능기를 갖는 (메타)아크릴레이트 반복단위 및 측쇄에 중합성 관능기를 갖는 (메타)아크릴레이트 반복단위를 포함하는 폴리머를 포함하는 임프린트용 조성물로서:
상기 폴리머는 2000 이상의 중량평균 분자량을 갖고, 상기 폴리머의 양은 상기 중합성 모노머에 대하여 0.01∼20질량%인 것을 특징으로 하는 임프린트용 조성물. - 삭제
- 제 1 항에 있어서,
상기 불소 원자 또는 규소 원자 중 하나 이상을 가진 관능기는 트리플루오로메틸기, 트리메틸실릴기 및 디메틸실록산 구조 함유기로 이루어지는 군으로부터 선택된 하나 이상의 구조를 갖는 것을 특징으로 하는 임프린트용 조성물. - 제 1 항에 있어서,
상기 중합성 관능기는 (메타)아크릴레이트기인 것을 특징으로 하는 임프린트용 조성물. - 삭제
- 제 1 항에 있어서,
상기 폴리머는 측쇄에 방향족기, 4개 이상의 탄소 원자를 갖는 비환상 알킬기 또는 6개 이상의 탄소 원자를 갖는 환상 알킬기를 갖는 반복단위를 더 포함하는 것을 특징으로 하는 임프린트용 조성물. - 제 1 항에 있어서,
상기 폴리머의 분산도는 1.0∼4.0인 것을 특징으로 하는 임프린트용 조성물. - 제 1 항에 있어서,
상기 중합성 모노머는 방향족기, 4개 이상의 탄소 원자를 갖는 비환상 알킬기 또는 6개 이상의 탄소 원자를 갖는 환상 알킬기를 갖는 (메타)아크릴레이트 구조를 포함하는 것을 특징으로 하는 임프린트용 조성물. - 제 1 항에 있어서,
용제를 더 포함하는 것을 특징으로 하는 임프린트용 조성물. - 제 11 항에 있어서,
상기 용제는 에스테르기, 에테르기, 카르보닐기 및 히드록실기로 이루어지는 군으로부터 선택된 하나 이상을 갖는 것을 특징으로 하는 임프린트용 조성물. - 제 1 항에 있어서,
비이온성 계면활성제를 더 포함하는 것을 특징으로 하는 임프린트용 조성물. - 제 1 항, 제 3 항 내지 제 6 항, 및 제 8 항 내지 제 10 항 중 어느 한 항에 기재된 임프린트용 조성물을 기판 상에 도포하여 패터닝층을 형성하는 공정, 및
상기 패터닝층의 표면에 대해 몰드를 가압하는 공정을 포함하는 것을 특징으로 하는 패터닝 방법. - 제 14 항에 기재된 패터닝 방법에 의해 형성되는 것을 특징으로 하는 패턴.
- 제 1 항에 있어서,
상기 폴리머는 측쇄에 불소 원자 또는 규소 원자 중 하나 이상을 가진 관능기를 갖는 (메타)아크릴레이트 반복단위 1∼99몰% 및 측쇄에 중합성 관능기를 갖는 (메타)아크릴레이트 반복단위 1∼99몰%를 포함하는 것을 특징으로 하는 임프린트용 조성물.
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Families Citing this family (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5671302B2 (ja) | 2009-11-10 | 2015-02-18 | 富士フイルム株式会社 | インプリント用硬化性組成物、パターン形成方法およびパターン |
US20130049255A1 (en) * | 2010-03-10 | 2013-02-28 | Asahi Kasei Kabushiki Kaisha | Resin mold |
JPWO2011125800A1 (ja) * | 2010-03-31 | 2013-07-11 | Jsr株式会社 | ナノインプリント用硬化性組成物、半導体素子及びナノインプリント方法 |
WO2012017530A1 (ja) * | 2010-08-04 | 2012-02-09 | 旭硝子株式会社 | 光硬化性組成物および表面に微細パターンを有する成形体の製造方法 |
TWI480324B (zh) * | 2010-08-04 | 2015-04-11 | Asahi Glass Co Ltd | A photohardenable composition, and a molded article having a fine pattern on its surface |
SG187701A1 (en) | 2010-08-06 | 2013-03-28 | Soken Kagaku Kk | Resin mold for nanoimprinting |
JP2012093708A (ja) * | 2010-09-30 | 2012-05-17 | Hitachi Chem Co Ltd | 可視光導光路用感光性樹脂組成物、その硬化物及び可視光導光路 |
JP2012079865A (ja) * | 2010-09-30 | 2012-04-19 | Jsr Corp | ナノインプリント用硬化性組成物およびナノインプリント方法 |
JP2012216682A (ja) * | 2011-03-31 | 2012-11-08 | Jsr Corp | ナノインプリント用感放射線性組成物、及びパターン形成方法 |
WO2012148359A1 (en) * | 2011-04-28 | 2012-11-01 | National University Of Singapore | A highly hydrophilic and highly oleophobic membrane for oil-water separation |
JP5829177B2 (ja) * | 2011-07-12 | 2015-12-09 | 富士フイルム株式会社 | インプリント用硬化性組成物、パターン形成方法およびパターン |
JP5806903B2 (ja) * | 2011-09-30 | 2015-11-10 | 富士フイルム株式会社 | ナノインプリント方法およびそれに用いられるレジスト組成物 |
JP6082237B2 (ja) * | 2011-12-09 | 2017-02-15 | 株式会社トクヤマ | テクスチャー構造を有するシリコン基板の製法 |
JP5794387B2 (ja) * | 2012-04-10 | 2015-10-14 | ダイキン工業株式会社 | インプリント用樹脂モールド材料組成物 |
JP5827180B2 (ja) * | 2012-06-18 | 2015-12-02 | 富士フイルム株式会社 | インプリント用硬化性組成物と基板の密着用組成物およびこれを用いた半導体デバイス |
JP6307258B2 (ja) * | 2012-12-21 | 2018-04-04 | 旭化成株式会社 | 微細パタン形成用積層体 |
JP2014210865A (ja) * | 2013-04-19 | 2014-11-13 | Jsr株式会社 | マイクロ流路形成用放射線硬化性樹脂組成物およびマイクロ流路 |
JP2015009171A (ja) * | 2013-06-27 | 2015-01-19 | 富士フイルム株式会社 | インクジェット吐出方法、パターン形成方法、および、パターン |
JP6080813B2 (ja) | 2013-08-30 | 2017-02-15 | キヤノン株式会社 | 光インプリント用組成物、これを用いた、膜の製造方法、光学部品の製造方法、回路基板の製造方法、電子部品の製造方法 |
WO2016136240A1 (en) * | 2015-02-27 | 2016-09-01 | Canon Kabushiki Kaisha | Nanonimprint liquid material, method for manufacturing nanoimprint liquid material, method for manufacturing cured product pattern, method for manufacturing optical component, and method for manufacturing circuit board |
WO2016176129A1 (en) | 2015-04-29 | 2016-11-03 | 3M Innovative Properties Company | Swellable film forming compositions and methods of nanoimprint lithography employing same |
JP6324429B2 (ja) * | 2016-03-30 | 2018-05-16 | Jsr株式会社 | ラインパターン、光制御部材および光学結像部材の製造方法 |
JP6332717B2 (ja) * | 2016-05-11 | 2018-05-30 | Dic株式会社 | 光インプリント用硬化性組成物及びそれを用いたパターン転写方法 |
EP3564276B1 (en) * | 2016-12-27 | 2023-04-19 | Zeon Corporation | Polymer, positive resist composition, and method of forming resist pattern |
US20220246984A1 (en) * | 2019-08-08 | 2022-08-04 | Lg Energy Solution, Ltd. | Copolymer for polymer electrolyte, and gel polymer electrolyte and lithium secondary battery which include the same |
JP7442004B1 (ja) | 2023-03-01 | 2024-03-01 | artience株式会社 | 感光性組成物、それを用いた膜、光学フィルタ、固体撮像素子、画像表示装置、及び赤外線センサ |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005221721A (ja) * | 2004-02-05 | 2005-08-18 | Fuji Photo Film Co Ltd | 感光性組成物及び該感光性組成物を用いたパターン形成方法 |
JP2006114882A (ja) * | 2004-09-16 | 2006-04-27 | Asahi Glass Co Ltd | パターンの形成方法およびパターンを有する物品 |
Family Cites Families (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0243605B1 (en) * | 1986-02-27 | 1993-06-16 | Dainippon Ink And Chemicals, Inc. | Fluorine-containing resin composition having a low refractive index |
JPH0580530A (ja) * | 1991-09-24 | 1993-04-02 | Hitachi Ltd | 薄膜パターン製造方法 |
US5820769A (en) * | 1995-05-24 | 1998-10-13 | Regents Of The University Of Minnesota | Method for making magnetic storage having discrete elements with quantized magnetic moments |
US5772905A (en) * | 1995-11-15 | 1998-06-30 | Regents Of The University Of Minnesota | Nanoimprint lithography |
JP2004240241A (ja) | 2003-02-07 | 2004-08-26 | Jsr Corp | 感光性樹脂組成物、表示パネル用スペーサーおよび表示パネル |
JP2005084561A (ja) | 2003-09-11 | 2005-03-31 | Dainippon Printing Co Ltd | 微細パターン形成体およびその製造方法 |
KR101050292B1 (ko) | 2003-12-27 | 2011-07-19 | 엘지디스플레이 주식회사 | 박막트랜지스터 어레이 기판의 제조방법 |
KR101086476B1 (ko) | 2004-04-14 | 2011-11-25 | 엘지디스플레이 주식회사 | 액정표시패널 및 그 제조방법 |
JP4742665B2 (ja) | 2005-04-28 | 2011-08-10 | 旭硝子株式会社 | エッチング処理された処理基板の製造方法 |
US7507525B2 (en) * | 2005-05-10 | 2009-03-24 | Fujifilm Corporation | Polymerizable composition and lithographic printing plate precursor |
JP2007001250A (ja) * | 2005-06-27 | 2007-01-11 | Asahi Glass Co Ltd | 微細パターン形成体の製造方法 |
US20090304992A1 (en) * | 2005-08-08 | 2009-12-10 | Desimone Joseph M | Micro and Nano-Structure Metrology |
JP2007178724A (ja) * | 2005-12-28 | 2007-07-12 | Mitsubishi Rayon Co Ltd | 表面に微細凹凸構造を有する成形体の製造方法および反射防止物品 |
JP4929722B2 (ja) * | 2006-01-12 | 2012-05-09 | 日立化成工業株式会社 | 光硬化型ナノプリント用レジスト材及びパターン形成法 |
JP4793010B2 (ja) * | 2006-02-13 | 2011-10-12 | 大日本印刷株式会社 | 光回折構造賦型用の複製版及びその複製版の製造方法並びに複製版を用いた光回折構造転写用複製物の製造方法 |
US7468330B2 (en) * | 2006-04-05 | 2008-12-23 | International Business Machines Corporation | Imprint process using polyhedral oligomeric silsesquioxane based imprint materials |
JP2008084984A (ja) * | 2006-09-26 | 2008-04-10 | Fujifilm Corp | 光ナノインプリントリソグラフィ用光硬化性組成物およびそれを用いたパターン形成方法 |
-
2008
- 2008-10-29 JP JP2008278680A patent/JP5611519B2/ja not_active Expired - Fee Related
-
2009
- 2009-10-29 WO PCT/JP2009/068935 patent/WO2010050614A1/en active Application Filing
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- 2009-10-29 US US13/122,510 patent/US8980404B2/en not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005221721A (ja) * | 2004-02-05 | 2005-08-18 | Fuji Photo Film Co Ltd | 感光性組成物及び該感光性組成物を用いたパターン形成方法 |
JP2006114882A (ja) * | 2004-09-16 | 2006-04-27 | Asahi Glass Co Ltd | パターンの形成方法およびパターンを有する物品 |
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