JP2002251013A5 - - Google Patents

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JP2002251013A5
JP2002251013A5 JP2001048880A JP2001048880A JP2002251013A5 JP 2002251013 A5 JP2002251013 A5 JP 2002251013A5 JP 2001048880 A JP2001048880 A JP 2001048880A JP 2001048880 A JP2001048880 A JP 2001048880A JP 2002251013 A5 JP2002251013 A5 JP 2002251013A5
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group
substituent
hydrocarbon group
alkyl group
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JP4208422B2 (en
JP2002251013A (en
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Priority to JP2001048880A priority Critical patent/JP4208422B2/en
Priority claimed from JP2001048880A external-priority patent/JP4208422B2/en
Priority to KR1020020009638A priority patent/KR100795109B1/en
Priority to US10/079,414 priority patent/US6858370B2/en
Priority to TW91103178A priority patent/TW548523B/en
Publication of JP2002251013A publication Critical patent/JP2002251013A/en
Publication of JP2002251013A5 publication Critical patent/JP2002251013A5/ja
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【特許請求の範囲】
【請求項1】 (A)下記一般式(V−1)〜(V−4)のいずれかで表される基を有する繰り返し単位、及び他に脂肪族環状炭化水素基を有し、酸の作用によりアルカリ現像液に対する溶解速度が増加する樹脂、
(B)活性光線又は放射線の照射により酸を発生する化合物
を含有し、且つ(B)酸発生剤が、トリアリールスルフォニウム塩、フェナシルスルフォニウム塩構造を有する化合物及び芳香環を有さないスルホニウム塩の群から選択される少なくとも2種含有する混合物であることを特徴とするポジ型レジスト組成物。
【化1】

Figure 2002251013
一般式(V−1)〜(V−4)において、R1b〜R5bは、各々独立に水素原子、置換基を有していてもよい、アルキル基、シクロアルキル基又はアルケニル基を表す。R1b〜R5bの内の2つは、結合して環を形成してもよい。
【請求項2】 (A)の樹脂が、下記一般式(pI)〜一般式(pVI)で示される脂環式炭化水素を含む部分構造を有する繰り返し単位及び下記一般式(II)で示される繰り返し単位の群から選択される少なくとも1種を含有することを特徴とする請求項1に記載のポジ型レジスト組成物。
【化2】
Figure 2002251013
(式中、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、イソブチル基又は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。
12〜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又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。
17〜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又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又は脂環式炭化水素基を表す。
22〜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又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。また、R23とR24は、互いに結合して環を形成していてもよい。)
【化3】
Figure 2002251013
式(II)中:
11',R12'は、各々独立に、水素原子、シアノ基、ハロゲン原子、又は置換基を有していてもよいアルキル基を表す。
Z'は、結合した2つの炭素原子(C−C)を含み、置換基を有していてもよい脂環式構造を形成するための原子団を表す。
【請求項3】 前記一般式(II)におけるZ'が、結合した2つの炭素原子(C−C)を含み、置換基を有していてもよい有橋式脂環式構造を形成するための原子団を表すことを特徴とする請求項2に記載のポジ型レジスト組成物。
【請求項4】 前記一般式(II)が、下記一般式(II−A)又は一般式(II−B)であることを特徴とする請求項2に記載のポジ型レジスト組成物。
【化4】
Figure 2002251013
式(II−A)、(II−B)中:
13'〜R16'は、各々独立に、水素原子、ハロゲン原子、シアノ基、−COOH、−COOR5、酸の作用により分解する基、−C(=O)−X−A'−R17'、又は置換基を有していてもよいアルキル基あるいは環状炭化水素基を表す。
ここで、R5は、置換基を有していてもよい、アルキル基、環状炭化水素基又は下記の−Y基を表す。
Xは、酸素原子、硫黄原子、−NH−、−NHSO2−又は−NHSO2NH−を表す。
A'は単結合又は2価の連結基を表す。
また、Rl3'〜R16'のうち少なくとも2つが結合して環を形成してもよい。nは0又は1を表す。
17'は、−COOH、−COOR5、−CN、水酸基、置換基を有していてもよいアルコキシ基、−CO−NH−R6、−CO−NH−SO2−R6又は下記の−Y基を表す。
6は、置換基を有していてもよい、アルキル基又は環状炭化水素基を表す。
−Y基;
【化5】
Figure 2002251013
(−Y基中、R21'〜R30'は、各々独立に、水素原子又は置換基を有していてもよいアルキル基を表す。a,bは1又は2を表す。)
【請求項5】 請求項1〜4のいずれかに記載のポジ型レジスト組成物によりレジスト膜を形成し、当該レジスト膜を露光、現像することを特徴とするパターン形成方法。 [Claims]
(A) a repeating unit having a group represented by any of the following formulas (V-1) to (V-4), and an aliphatic cyclic hydrocarbon group, A resin whose action increases the dissolution rate in an alkali developer,
(B) It contains a compound that generates an acid upon irradiation with actinic rays or radiation, and (B) the acid generator does not have a compound having a triarylsulfonium salt or phenacylsulfonium salt structure or an aromatic ring. A positive resist composition comprising a mixture containing at least two members selected from the group of sulfonium salts.
Embedded image
Figure 2002251013
In formulas (V-1) to (V-4), R 1b to R 5b each independently represent a hydrogen atom, an alkyl group, a cycloalkyl group or an alkenyl group which may have a substituent. Two of R 1b to R 5b may combine to form a ring.
2. The resin of (A) is a repeating unit having a partial structure containing an alicyclic hydrocarbon represented by the following general formulas (pI) to (pVI) and represented by the following general formula (II) The positive resist composition according to claim 1, comprising at least one selected from the group consisting of repeating units.
Embedded image
Figure 2002251013
(Wherein, 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 represents an alicyclic hydrocarbon group together with a carbon atom. Represents the atomic groups required to form.
R 12 to R 16 each independently represent a linear or branched alkyl group or an 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 represent a hydrogen atom, a linear or branched alkyl group or an alicyclic hydrocarbon group having 1 to 4 carbon atoms, provided that at least one of R 17 to R 21 One represents an alicyclic hydrocarbon group. Further, either R 19 or R 21 represents a linear or branched alkyl group or an alicyclic hydrocarbon group having 1 to 4 carbon atoms.
R 22 to R 25 each independently represent a linear or branched alkyl group or an alicyclic hydrocarbon group having 1 to 4 carbon atoms, provided that at least one of R 22 to R 25 is an aliphatic group; Represents a cyclic hydrocarbon group. R 23 and R 24 may be bonded to each other to form a ring. )
Embedded image
Figure 2002251013
In formula (II):
R 11 ′ and R 12 ′ each independently represent a hydrogen atom, a cyano group, a halogen atom, or an alkyl group which may have a substituent.
Z ′ represents an atomic group for forming an alicyclic structure which may have a substituent and has two bonded carbon atoms (C—C).
3. The method according to claim 2, wherein Z ′ in the general formula (II) contains two bonded carbon atoms (CC) and forms a bridged alicyclic structure which may have a substituent. 3. The positive resist composition according to claim 2, wherein
4. The positive resist composition according to claim 2, wherein the general formula (II) is the following general formula (II-A) or general formula (II-B).
Embedded image
Figure 2002251013
In the formulas (II-A) and (II-B):
R 13 ′ to R 16 ′ each independently represent a hydrogen atom, a halogen atom, a cyano group, —COOH, —COOR 5 , a group decomposed by the action of an acid, —C (= O) —XA′-R 17 ′ represents an alkyl group or a cyclic hydrocarbon group which may have a substituent.
Here, R 5 represents an alkyl group, a cyclic hydrocarbon group or the following —Y group which may have a substituent.
X represents an oxygen atom, a sulfur atom, -NH -, - NHSO 2 - or an -NHSO 2 NH-.
A ′ represents a single bond or a divalent linking group.
Further, at least two of R 13 ′ to R 16 ′ may combine to form a ring. n represents 0 or 1.
R 17 ′ is —COOH, —COOR 5 , —CN, a hydroxyl group, an optionally substituted alkoxy group, —CO—NH—R 6 , —CO—NH—SO 2 —R 6 or Represents a -Y group.
R 6 represents an alkyl group or a cyclic hydrocarbon group which may have a substituent.
A —Y group;
Embedded image
Figure 2002251013
(In the —Y group, R 21 ′ to R 30 ′ each independently represent a hydrogen atom or an alkyl group which may have a substituent. A and b represent 1 or 2.)
5. A pattern forming method, comprising: forming a resist film from the positive resist composition according to claim 1, exposing and developing the resist film.

JP2001048880A 2001-02-23 2001-02-23 Positive resist composition Expired - Fee Related JP4208422B2 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP2001048880A JP4208422B2 (en) 2001-02-23 2001-02-23 Positive resist composition
KR1020020009638A KR100795109B1 (en) 2001-02-23 2002-02-22 Positive Photosensitive Composition
US10/079,414 US6858370B2 (en) 2001-02-23 2002-02-22 Positive photosensitive composition
TW91103178A TW548523B (en) 2001-02-23 2002-02-22 Positive photosensitive composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2001048880A JP4208422B2 (en) 2001-02-23 2001-02-23 Positive resist composition

Publications (3)

Publication Number Publication Date
JP2002251013A JP2002251013A (en) 2002-09-06
JP2002251013A5 true JP2002251013A5 (en) 2006-01-19
JP4208422B2 JP4208422B2 (en) 2009-01-14

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Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100382960B1 (en) 1998-07-03 2003-05-09 닛뽕덴끼 가부시끼가이샤 (meth)acrylate derivatives bearing lactone structure, polymers, photoresist compositions and process of forming patterns with the same
US7452655B2 (en) * 2002-11-05 2008-11-18 Jsr Corporation Acrylic copolymer and radiation-sensitive resin composition
US7279265B2 (en) * 2003-03-27 2007-10-09 Fujifilm Corporation Positive resist composition and pattern formation method using the same
WO2016051985A1 (en) * 2014-09-29 2016-04-07 富士フイルム株式会社 Active ray-sensitive or radiation-sensitive resin composition, pattern forming method, and method for producing electronic device

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