JP2001013686A5 - - Google Patents
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- JP2001013686A5 JP2001013686A5 JP1999186607A JP18660799A JP2001013686A5 JP 2001013686 A5 JP2001013686 A5 JP 2001013686A5 JP 1999186607 A JP1999186607 A JP 1999186607A JP 18660799 A JP18660799 A JP 18660799A JP 2001013686 A5 JP2001013686 A5 JP 2001013686A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- alkyl group
- alicyclic hydrocarbon
- carbon atoms
- linear
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 125000000217 alkyl group Chemical group 0.000 claims 9
- 125000002723 alicyclic group Chemical group 0.000 claims 7
- 125000004432 carbon atoms Chemical group C* 0.000 claims 7
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 6
- 229920002120 photoresistant polymer Polymers 0.000 claims 6
- 125000002947 alkylene group Chemical group 0.000 claims 4
- 125000003710 aryl alkyl group Chemical group 0.000 claims 3
- 125000003118 aryl group Chemical group 0.000 claims 3
- 125000000732 arylene group Chemical group 0.000 claims 3
- 125000006165 cyclic alkyl group Chemical group 0.000 claims 3
- 125000001424 substituent group Chemical group 0.000 claims 3
- 239000002253 acid Substances 0.000 claims 2
- 125000003368 amide group Chemical group 0.000 claims 2
- 125000004185 ester group Chemical group 0.000 claims 2
- 125000001033 ether group Chemical group 0.000 claims 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 claims 1
- DOVZUKKPYKRVIK-UHFFFAOYSA-N 1-methoxypropan-2-yl propanoate Chemical compound CCC(=O)OC(C)COC DOVZUKKPYKRVIK-UHFFFAOYSA-N 0.000 claims 1
- BYVKCQBOHJQWIO-UHFFFAOYSA-N 2-ethoxyethyl propanoate Chemical compound CCOCCOC(=O)CC BYVKCQBOHJQWIO-UHFFFAOYSA-N 0.000 claims 1
- LZCLXQDLBQLTDK-UHFFFAOYSA-N Ethyl lactate Chemical compound CCOC(=O)C(C)O LZCLXQDLBQLTDK-UHFFFAOYSA-N 0.000 claims 1
- LLHKCFNBLRBOGN-UHFFFAOYSA-N Propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 claims 1
- 239000003513 alkali Substances 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 150000007514 bases Chemical class 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 125000004122 cyclic group Chemical group 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 235000014113 dietary fatty acids Nutrition 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 229940116333 ethyl lactate Drugs 0.000 claims 1
- 239000000194 fatty acid Substances 0.000 claims 1
- 150000004665 fatty acids Chemical class 0.000 claims 1
- 229910052731 fluorine Inorganic materials 0.000 claims 1
- 239000011737 fluorine Substances 0.000 claims 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims 1
- 125000000524 functional group Chemical group 0.000 claims 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 125000000686 lactone group Chemical group 0.000 claims 1
- 125000005647 linker group Chemical group 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 239000012046 mixed solvent Substances 0.000 claims 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 239000011347 resin Substances 0.000 claims 1
- 229920005989 resin Polymers 0.000 claims 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims 1
- 229910052710 silicon Inorganic materials 0.000 claims 1
- 239000010703 silicon Substances 0.000 claims 1
- 125000000547 substituted alkyl group Chemical group 0.000 claims 1
- 125000005156 substituted alkylene group Chemical group 0.000 claims 1
- 125000000565 sulfonamide group Chemical group 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 125000000101 thioether group Chemical group 0.000 claims 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims 1
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims 1
Claims (4)
(ロ)(a)下記一般式(pI)〜(pVI)で表される脂環式炭化水素構造を含む基のうちの少なくとも1種の基で保護されたアルカリ可溶性基を有する繰り返し単位、(b)下記一般式(II)で表される繰り返し単位、および(c)下記一般式(III-a)〜(III-d)で表される繰り返し単位のうち少なくとも1種を含み、かつ酸の作用により分解しアルカリに対する溶解性が増加する樹脂
並びに
(ハ)(1)プロピレングリコールモノメチルエーテルアセテート又はプロピレングリコールモノメチルエーテルプロピオネートと、
(2)乳酸エチル、プロピレングリコールモノメチルエーテル及びエトキシエチ
ルプロピオネートのうち少なくとも1種
とを含有する混合溶剤
を含有することを特徴とする遠紫外線露光用ポジ型フォトレジスト組成物。
R11は、メチル基、エチル基、n−プロピル基、イソプロピル基、n−ブチル基、イソブチル基またはsec−ブチル基を表し、Zは、炭素原子とともに脂環式炭化水素基を形成するのに必要な原子団を表す。
R12〜R16は、各々独立に、炭素数1〜4個の、直鎖もしくは分岐のアルキル基または脂環式炭化水素基を表し、但し、R12〜R14のうち少なくとも1つ、もしくはR15、R16のいずれかは脂環式炭化水素基を表す。
R17〜R21は、各々独立に、水素原子、炭素数1〜4個の、直鎖もしくは分岐のアルキル基または脂環式炭化水素基を表し、但し、R17〜R21のうち少なくとも1つは脂環式炭化水素基を表す。また、R19、R21のいずれかは炭素数1〜4個の、直鎖もしくは分岐のアルキル基または脂環式炭化水素基を表す。
R22〜R25は、各々独立に、炭素数1〜4個の、直鎖もしくは分岐のアルキル基または
脂環式炭化水素基を表し、但し、R22〜R25のうち少なくとも1つは脂環式炭化水素基を表す。
R1は、水素原子、ハロゲン原子または1〜4個の炭素原子を有する直鎖もしくは分岐のアルキル基を表す。X1は、2価の連結基を表す。
Lcは、ラクトン基を表す。
Rは、水素原子あるいは、置換基を有していてもよい、アルキル基、環状アルキル基、アリール基又はアラルキル基を表す。mは、1〜10の整数を表す。
X2は、単結合又は、置換基を有していてもよい、アルキレン基、環状アルキレン基、アリーレン基あるいは、エーテル基、チオエーテル基、カルボニル基、エステル基、アミド基、スルフォンアミド基、ウレタン基、ウレア基からなる群から選択される単独、あるいはこれらの基の少なくとも2つ以上が組み合わされ、酸の作用により分解しない2価の基
を表す。
Z1は、単結合、エーテル基、エステル基、アミド基、アルキレン基、又はこれらを組み合わせた2価の基を表す。R38は、単結合、アルキレン基、アリーレン基、又はこれらを組み合わせた2価の基を表す。R40は、アルキレン基、アリーレン基、又はこれらを組み合わせた2価の基を表す。R39は置換基を有していてもよい、アルキル基、環状アルキル基、アリール基又はアラルキル基を表す。R41は、水素原子あるいは、置換基を有していてもよい、アルキル基、環状アルキル基、アルケニル基、アリール基又はアラルキル基を表す。
Aは、下記に示す官能基のいずれかを表す。
(B) (a) a repeating unit having an alkali-soluble group protected with at least one group selected from groups containing an alicyclic hydrocarbon structure represented by the following general formulas (pI) to (pVI); b) a repeating unit represented by the following general formula (II), and (c) at least one of repeating units represented by the following general formulas (III-a) to (III-d), A resin which decomposes by action and increases the solubility in alkali, and (c) (1) propylene glycol monomethyl ether acetate or propylene glycol monomethyl ether propionate;
(2) A positive photoresist composition for far ultraviolet exposure, comprising a mixed solvent containing at least one of ethyl lactate, propylene glycol monomethyl ether and ethoxyethyl propionate.
R 11 represents a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group or a sec-butyl group, and Z forms an alicyclic hydrocarbon group together with a carbon atom. Represents the necessary atomic group.
R 12 to R 16 each independently represents a linear or branched alkyl group or alicyclic hydrocarbon group having 1 to 4 carbon atoms, provided that at least one of R 12 to R 14 , or Either R 15 or R 16 represents an alicyclic hydrocarbon group.
R 17 to R 21 each independently represents a hydrogen atom, a linear or branched alkyl group having 1 to 4 carbon atoms, or an alicyclic hydrocarbon group, provided that at least one of R 17 to R 21 Represents an alicyclic hydrocarbon group. Further, either R 19 or R 21 represents a linear or branched alkyl group or alicyclic hydrocarbon group having 1 to 4 carbon atoms.
R 22 to R 25 each independently represents a linear or branched alkyl group or alicyclic hydrocarbon group having 1 to 4 carbon atoms, provided that at least one of R 22 to R 25 is a fatty acid. Represents a cyclic hydrocarbon group.
R1 represents a hydrogen atom, a halogen atom or a linear or branched alkyl group having 1 to 4 carbon atoms. X1 represents a divalent linking group.
Lc represents a lactone group.
R represents a hydrogen atom or an alkyl group, cyclic alkyl group, aryl group or aralkyl group which may have a substituent. m represents an integer of 1 to 10.
X2 is a single bond or an optionally substituted alkylene group, cyclic alkylene group, arylene group or ether group, thioether group, carbonyl group, ester group, amide group, sulfonamide group, urethane group, The divalent group selected from the group consisting of urea groups alone or a combination of at least two of these groups and not decomposed by the action of an acid.
Z1 represents a single bond, an ether group, an ester group, an amide group, an alkylene group, or a divalent group obtained by combining these. R38 represents a single bond, an alkylene group, an arylene group, or a divalent group obtained by combining these. R40 represents an alkylene group, an arylene group, or a divalent group obtained by combining these. R39 represents an alkyl group, cyclic alkyl group, aryl group or aralkyl group which may have a substituent. R41 represents a hydrogen atom or an optionally substituted alkyl group, cyclic alkyl group, alkenyl group, aryl group or aralkyl group.
A represents any of the functional groups shown below.
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18660799A JP3976109B2 (en) | 1999-06-30 | 1999-06-30 | Positive photoresist composition for deep ultraviolet exposure |
US09/563,436 US6596458B1 (en) | 1999-05-07 | 2000-05-03 | Positive-working photoresist composition |
TW089108532A TW546548B (en) | 1999-05-07 | 2000-05-04 | Positive-working photoresist composition |
KR1020000025558A KR100645847B1 (en) | 1999-05-07 | 2000-05-08 | Positive-working photoresist composi tion |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18660799A JP3976109B2 (en) | 1999-06-30 | 1999-06-30 | Positive photoresist composition for deep ultraviolet exposure |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2001013686A JP2001013686A (en) | 2001-01-19 |
JP2001013686A5 true JP2001013686A5 (en) | 2005-07-07 |
JP3976109B2 JP3976109B2 (en) | 2007-09-12 |
Family
ID=16191541
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP18660799A Expired - Fee Related JP3976109B2 (en) | 1999-05-07 | 1999-06-30 | Positive photoresist composition for deep ultraviolet exposure |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3976109B2 (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4102032B2 (en) * | 2001-03-12 | 2008-06-18 | 富士フイルム株式会社 | Positive resist composition |
JP4186497B2 (en) * | 2001-04-12 | 2008-11-26 | 東レ株式会社 | Positive radiation-sensitive composition and method for producing resist pattern using the same |
JP3912767B2 (en) * | 2001-06-21 | 2007-05-09 | 富士フイルム株式会社 | Positive photosensitive composition |
JP4494161B2 (en) * | 2004-10-14 | 2010-06-30 | 東京応化工業株式会社 | POLYMER COMPOUND, POSITIVE RESIST COMPOSITION AND METHOD FOR FORMING RESIST PATTERN |
JP4684740B2 (en) * | 2005-05-19 | 2011-05-18 | 東京応化工業株式会社 | Positive resist composition and resist pattern forming method |
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1999
- 1999-06-30 JP JP18660799A patent/JP3976109B2/en not_active Expired - Fee Related