JPWO2020080206A5 - - Google Patents
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- JPWO2020080206A5 JPWO2020080206A5 JP2020553099A JP2020553099A JPWO2020080206A5 JP WO2020080206 A5 JPWO2020080206 A5 JP WO2020080206A5 JP 2020553099 A JP2020553099 A JP 2020553099A JP 2020553099 A JP2020553099 A JP 2020553099A JP WO2020080206 A5 JPWO2020080206 A5 JP WO2020080206A5
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- -1 amino, imino Chemical group 0.000 claims 7
- 239000011342 resin composition Substances 0.000 claims 7
- 239000004642 Polyimide Substances 0.000 claims 6
- 150000002148 esters Chemical class 0.000 claims 6
- 229920005575 poly(amic acid) Polymers 0.000 claims 6
- 229920001721 polyimide Polymers 0.000 claims 6
- 239000002243 precursor Substances 0.000 claims 6
- 125000004432 carbon atom Chemical group C* 0.000 claims 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 4
- 239000011347 resin Substances 0.000 claims 4
- 229920005989 resin Polymers 0.000 claims 4
- 239000000758 substrate Substances 0.000 claims 4
- 125000000217 alkyl group Chemical group 0.000 claims 3
- 150000001875 compounds Chemical class 0.000 claims 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 3
- 125000000962 organic group Chemical group 0.000 claims 3
- 239000004065 semiconductor Substances 0.000 claims 3
- 125000003342 alkenyl group Chemical group 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 2
- 125000000304 alkynyl group Chemical group 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims 2
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 2
- 125000005067 haloformyl group Chemical group 0.000 claims 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- 125000005842 heteroatom Chemical group 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
- 125000000018 nitroso group Chemical group N(=O)* 0.000 claims 2
- 125000004043 oxo group Chemical group O=* 0.000 claims 2
- 229920000642 polymer Polymers 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 claims 2
- 125000003396 thiol group Chemical group [H]S* 0.000 claims 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical group O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 claims 1
- 239000011248 coating agent Substances 0.000 claims 1
- 238000000576 coating method Methods 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims 1
Claims (9)
[式中、X1は、4価の有機基であり、Y1は、2価の有機基であり、R1及びR2は、それぞれ独立に、1価の有機基である。]で表される単位構造を有するポリイミド前駆体;
及び
(B)下記一般式(30):
[式中、Z1及びZ2は、それぞれ独立に、
水素原子、ハロゲン原子、ヒドロキシ基、メルカプト基、カルボキシ基、シアノ基、ホルミル基、ハロホルミル基、スルホ基、ニトロ基、ニトロソ基、オキソ基、チオキシ基、
置換されていてもよい炭素原子数1~10のアルキル、アルコキシ、もしくはアルキルスルファニル基、
置換されていてもよい炭素原子数2~10のアルケニル、アルキニル、もしくはアルコキシカルボニル基、又は
置換されていてもよいアミノ、イミノ、もしくはカルバモイル基を表し、
Z1及びZ2は、相互に結合して、ヘテロ原子を含んでもよく、置換基を有していてもよく、縮合していてもよい環を形成してもよく、当該環が芳香族環であるとき、
はHOOCがCOOHに対してオルト位にある共役二重結合を示し、当該環が芳香族環であるとき以外の場合、
はHOOCとCOOHについてのシス型二重結合を示す。]
で表されるカルボン酸化合物
を含み、
任意選択的に(P)前記ポリイミド前駆体(A)以外の高分子化合物を含み、
前記カルボン酸化合物(B)はZ1又はZ2を介して前記ポリイミド前駆体(A)及び/又は前記ポリイミド前駆体(A)以外の高分子化合物(P)に化学結合していてもよい、
ポリアミック酸エステル樹脂組成物。 (A) The following general formula (1):
[In the formula, X 1 is a tetravalent organic group, Y 1 is a divalent organic group, and R 1 and R 2 are independently monovalent organic groups. ] A polyimide precursor having a unit structure represented by;
And (B) the following general formula (30):
[In the formula, Z 1 and Z 2 are independent of each other.
Hydrogen atom, halogen atom, hydroxy group, mercapto group, carboxy group, cyano group, formyl group, haloformyl group, sulfo group, nitro group, nitroso group, oxo group, tioxy group,
An alkyl, alkoxy, or alkylsulfanil group having 1 to 10 carbon atoms which may be substituted,
Represents an alkenyl, alkynyl, or alkoxycarbonyl group having 2 to 10 carbon atoms which may be substituted, or an amino, imino, or carbamoyl group which may be substituted.
Z 1 and Z 2 may be bonded to each other to form a ring that may contain a heteroatom, may have a substituent, or may be fused, and the ring may be an aromatic ring. When
Indicates a conjugated double bond in which the HOOC is in the ortho position with respect to COOH, except when the ring is an aromatic ring.
Shows a cis-type double bond for HOOC and COOH. ]
Carboxylic acid compound represented by
Including
Optionally, (P) contains a polymer compound other than the polyimide precursor (A).
The carboxylic acid compound ( B) may be chemically bonded to a polymer compound (P) other than the polyimide precursor (A) and / or the polyimide precursor (A) via Z 1 or Z 2 . ,
Polyamic acid ester resin composition.
[式中、R33~R36は、それぞれ独立に、
水素原子、ハロゲン原子、ヒドロキシ基、メルカプト基、カルボキシ基、シアノ基、ホルミル基、ハロホルミル基、
スルホ基、ニトロ基、ニトロソ基、オキソ基、チオキシ基、
置換されていてもよい炭素原子数1~6のアルキル、アルコキシ、もしくはアルキルスルファニル基、
置換されていてもよい炭素原子数2~6のアルケニル、アルキニル、もしくはアルコキシカルボニル基、又は
置換されていてもよいアミノ、イミノ、もしくはカルバモイル基を表し、
R33とR34、R34とR35、もしくはR35とR36は、相互に結合して、ヘテロ原子を含んでもよく、置換基を有していてもよく、縮合していてもよい環を形成してもよい。]
で表されるカルボン酸化合物である、請求項1に記載の樹脂組成物。 The carboxylic acid compound ( B) has the following general formula (31):
[In the formula, R 33 to R 36 are independent of each other.
Hydrogen atom, halogen atom, hydroxy group, mercapto group, carboxy group, cyano group, formyl group, haloformyl group,
Sulfon group, nitro group, nitroso group, oxo group, tioxy group,
An alkyl, alkoxy, or alkylsulfanil group having 1 to 6 carbon atoms which may be substituted,
Represents an alkenyl, alkynyl, or alkoxycarbonyl group having 2 to 6 carbon atoms which may be substituted, or an amino, imino, or carbamoyl group which may be substituted.
R 33 and R 34 , R 34 and R 35 , or R 35 and R 36 may be bonded to each other and contain a heteroatom, may have a substituent, or may be fused. May be formed. ]
The resin composition according to claim 1 , which is a carboxylic acid compound represented by.
(1)請求項1~請求項5のいずれか1項に記載のポリアミック酸エステル樹脂組成物を基板上に塗布して、ポリアミック酸エステル樹脂層を該基板上に形成する工程と、
(2)該ポリアミック酸エステル樹脂層を露光する工程と、
(3)該露光後のポリアミック酸エステル樹脂層を現像して、レリーフパターンを形成する工程と、
(4)該レリーフパターンを加熱処理して、硬化レリーフパターンを形成する工程と
を含む硬化レリーフパターン付き基板の製造方法。 The following steps:
(1) A step of applying the polyamic acid ester resin composition according to any one of claims 1 to 5 onto a substrate to form a polyamic acid ester resin layer on the substrate.
(2) A step of exposing the polyamic acid ester resin layer and
(3) A step of developing the polyamic acid ester resin layer after the exposure to form a relief pattern, and
(4) A method for manufacturing a substrate with a cured relief pattern, which comprises a step of heat-treating the relief pattern to form a cured relief pattern.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2018194129 | 2018-10-15 | ||
JP2018194129 | 2018-10-15 | ||
PCT/JP2019/039733 WO2020080206A1 (en) | 2018-10-15 | 2019-10-09 | Polyamic acid ester resin composition |
Publications (3)
Publication Number | Publication Date |
---|---|
JPWO2020080206A1 JPWO2020080206A1 (en) | 2021-10-07 |
JPWO2020080206A5 true JPWO2020080206A5 (en) | 2022-07-08 |
JP7327410B2 JP7327410B2 (en) | 2023-08-16 |
Family
ID=70284628
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2020553099A Active JP7327410B2 (en) | 2018-10-15 | 2019-10-09 | Polyamic acid ester resin composition |
Country Status (3)
Country | Link |
---|---|
JP (1) | JP7327410B2 (en) |
TW (1) | TW202028303A (en) |
WO (1) | WO2020080206A1 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2024033021A (en) * | 2021-01-14 | 2024-03-13 | 日産化学株式会社 | Metal removing method using metal removing filter for removing metal impurity in photosensitive resin composition |
TW202307085A (en) | 2021-03-30 | 2023-02-16 | 日商富士軟片股份有限公司 | Resin composition, cured product, laminated body, cured product manufacturing method, semiconductor device, and polyimide precursor |
JPWO2022210532A1 (en) | 2021-03-30 | 2022-10-06 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0920865A (en) * | 1995-07-06 | 1997-01-21 | Toray Ind Inc | Color paste, paste for resin black matrix and color filter |
JPH09184912A (en) * | 1995-12-28 | 1997-07-15 | Toray Ind Inc | Resin black matrix and paste for resin black matrix |
JP5092426B2 (en) * | 2006-07-21 | 2012-12-05 | 東レ株式会社 | RESIN COMPOSITION FOR retardation film, color filter substrate for liquid crystal display device, liquid crystal display device, and method for producing color filter substrate for liquid crystal display device with retardation film |
JP6151475B2 (en) * | 2010-09-30 | 2017-06-21 | 大日本印刷株式会社 | Photosensitive resin composition, pattern forming material, and pattern forming method |
KR20160147712A (en) * | 2014-04-18 | 2016-12-23 | 나가세케무텍쿠스가부시키가이샤 | Resist resin and manufacturing method for same |
EP3000837B1 (en) * | 2014-09-23 | 2017-06-07 | Lotte Advanced Materials Co., Ltd. | Polyamide ester resin, method for preparing the same, and molded article including the same |
KR20180089487A (en) * | 2015-12-03 | 2018-08-08 | 닛산 가가쿠 가부시키가이샤 | Liquid crystal aligning agent, liquid crystal alignment film and liquid crystal display element using same |
-
2019
- 2019-10-09 TW TW108136532A patent/TW202028303A/en unknown
- 2019-10-09 JP JP2020553099A patent/JP7327410B2/en active Active
- 2019-10-09 WO PCT/JP2019/039733 patent/WO2020080206A1/en active Application Filing
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