JP6346539B2 - Resin, resist composition and method for producing resist pattern - Google Patents

Description

  The present invention relates to a resin, a resist composition, and a method for producing a resist pattern.

特許文献２には、下記構造単位の組合せからなる樹脂と、酸発生剤とからなるレジスト
組成物が記載されている。

Patent Document 1 describes a resist composition comprising a resin comprising a combination of the following structural units and an acid generator.

Patent Document 2 describes a resist composition comprising a resin comprising a combination of the following structural units and an acid generator.

JP 2012-41523 A JP2011-237477A

In the resist pattern formed by the above resist composition, the focus margin may not be satisfied.

［式（Ｉ）中、
Ｒ^I1は、水素原子、ハロゲン原子又はハロゲン原子を有してもよい炭素数１〜６のアル
キル基を表す。
Ｒ^I2は、ハロゲン原子、ヒドロキシ基、炭素数１〜６のアルキル基、炭素数１〜６のア
ルコキシ基、炭素数２〜４のアシル基、炭素数２〜４のアシルオキシ基、アクリロイルオ
キシ基又はメタクリロイルオキシ基を表す。
Ａ¹は、単結合又は^＊−Ａ²−Ｘ¹−（Ａ³−Ｘ²）_a−を表す。
Ａ²及びＡ³は、それぞれ独立に、炭素数１〜６のアルカンジイル基を表す。
Ｘ¹及びＸ²は、それぞれ独立に、−Ｏ−、−ＣＯ−Ｏ−又は−Ｏ−ＣＯ−を表す。
ａは、０又は１を表す。
Ｗは、炭素数４〜１８の脂環式炭化水素を表す。
ｍｃは０〜４の整数を表し、ｍｃが２以上の整数である場合、複数のＲ^I2は互いに同一
であっても異なってもよい。］

［式（ａ２−２）中、
Ｒ^a50は、水素原子、ハロゲン原子又はハロゲン原子を有してもよい炭素数１〜６のア
ルキル基を表す。
Ｒ^a51は、ハロゲン原子、ヒドロキシ基、炭素数１〜６のアルキル基、炭素数１〜６の
アルコキシ基、炭素数２〜４のアシル基、炭素数２〜４のアシルオキシ基、アクリロイル
オキシ基又はメタクリロイルオキシ基を表す。
Ａ^a50は、単結合又は^＊−Ａ^a51−Ｘ^a51−（Ａ^a52−Ｘ^a52）_na−を表す。
Ａ^a51及びＡ^a52は、それぞれ独立に、炭素数１〜６のアルカンジイル基を表す。
Ｘ^a51及びＸ^a52は、それぞれ独立に、−Ｏ−、−ＣＯ−Ｏ−又は−Ｏ−ＣＯ−を表す。
ｎａは、０又は１を表す。
ｍｂは０〜４の整数を表し、ｍｂが２以上の整数である場合、複数のＲ^a51は互いに同
一であっても異なってもよい。］
〔２〕さらに、酸不安定基を有する構造単位を含む〔１〕記載の樹脂。
〔３〕酸不安定基を有する構造単位が、式（ａ１−１）で表される構造単位である〔２
〕記載の樹脂。

［式（ａ１−１）中、
Ｌ^a1は、−Ｏ−又は^＊−Ｏ−（ＣＨ₂）_k1−ＣＯ−Ｏ−を表し、ｋ１は１〜７の整数を
表し、＊は−ＣＯ−との結合手を表す。
Ｒ^a4は、水素原子又はメチル基を表す。
Ｒ^a6は、炭素数１〜８のアルキル基、炭素数３〜１８の脂環式炭化水素基又はこれらを
組み合わせた基を表す。
ｍ１は０〜１４の整数を表す。］
〔４〕〔１〕〜〔３〕のいずれかに記載の樹脂と、酸発生剤とを含むレジスト組成物。
〔５〕酸発生剤から発生する酸よりも酸性度の弱い塩をさらに含有する〔４〕に記載の
レジスト組成物。
〔６〕（１）〔４〕又は〔５〕記載のレジスト組成物を基板上に塗布する工程、
（２）塗布後の組成物を乾燥させて組成物層を形成する工程、
（３）組成物層に露光する工程、
（４）露光後の組成物層を加熱する工程、及び
（５）加熱後の組成物層を現像する工程、
を含むレジストパターンの製造方法。 The present invention includes the following inventions.
[1] A resin containing a structural unit represented by formula (I) and a structural unit represented by formula (a2-2).

[In the formula (I),
R ^I1 represents a hydrogen atom, a halogen atom or an alkyl group having 1 to 6 carbon atoms which may have a halogen atom.
R ^I2 represents a halogen atom, a hydroxy group, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, an acyl group having 2 to 4 carbon atoms, an acyloxy group having 2 to 4 carbon atoms, an acryloyloxy group, or Represents a methacryloyloxy group.
A ¹ represents a single bond or ^{* -A 2 -X 1 - (A} 3 -X 2) a - represents a.
A ² and A ³ each independently represents an alkanediyl group having 1 to 6 carbon atoms.
X ¹ and X ² each independently represent —O—, —CO—O— or —O—CO—.
a represents 0 or 1.
W represents an alicyclic hydrocarbon having 4 to 18 carbon atoms.
mc represents an integer of 0 to 4, and when mc is an integer of 2 or more, the plurality of R ^I2 may be the same as or different from each other. ]

[In the formula (a2-2),
R ^a50 represents a hydrogen atom, a halogen atom or an alkyl group having 1 to 6 carbon atoms which may have a halogen atom.
R ^a51 is a halogen atom, a hydroxy group, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, an acyl group having 2 to 4 carbon atoms, an acyloxy group having 2 to 4 carbon atoms, an acryloyloxy group, or Represents a methacryloyloxy group.
A ^a50 represents a single bond or ^{* -A a51 -X a51 - (A} a52 -X a52) na - represents a.
A ^a51 and A ^a52 each independently represent an alkanediyl group having 1 to 6 carbon atoms.
X ^a51 and X ^a52 each independently represent —O—, ^—CO —O— or —O—CO—.
na represents 0 or 1.
mb represents an integer of 0 to 4, and when mb is an integer of 2 or more, the plurality of ^Ra51s may be the same as or different from each other. ]
[2] The resin according to [1], further comprising a structural unit having an acid labile group.
[3] The structural unit having an acid labile group is a structural unit represented by the formula (a1-1) [2
] Resin of description.

[In the formula (a1-1),
L ^a1 represents —O— or ^* —O— (CH ₂ ) _k1 —CO—O—, k1 represents an integer of 1 to 7, and * represents a bond to —CO—.
R ^a4 represents a hydrogen atom or a methyl group.
R ^a6 represents an alkyl group having 1 to 8 carbon atoms, an alicyclic hydrocarbon group having 3 to 18 carbon atoms, or a group obtained by combining these.
m1 represents the integer of 0-14. ]
[4] A resist composition comprising the resin according to any one of [1] to [3] and an acid generator.
[5] The resist composition according to [4], further comprising a salt having a lower acidity than the acid generated from the acid generator.
[6] A step of applying the resist composition according to (1) [4] or [5] on a substrate,
(2) The process of drying the composition after application | coating and forming a composition layer,
(3) a step of exposing the composition layer;
(4) a step of heating the composition layer after exposure, and (5) a step of developing the composition layer after heating,
A method for producing a resist pattern including:

According to the resist composition containing the resin of the present invention, a resist pattern can be produced with a good focus margin.

In the present specification, unless otherwise specified, in the description of the structural formula of a compound, “aliphatic hydrocarbon group” means a linear or branched hydrocarbon group, and “alicyclic hydrocarbon group” means an aliphatic group. A group obtained by removing a number of hydrogen atoms corresponding to the valence from the ring of a cyclic hydrocarbon. "Aromatic hydrocarbon group"
Includes a group in which a hydrocarbon group is bonded to an aromatic ring. When stereoisomers exist, all stereoisomers are included.

In this specification, “(meth) acrylic monomer” means “CH ₂ ═CH—CO—”.
Or it means at least one monomer having a structure of _{"CH 2 = C (CH 3)} -CO- ". Similarly, “(meth) acrylate” and “(meth) acrylic acid” mean “at least one of acrylate and methacrylate” and “at least one of acrylic acid and methacrylic acid”, respectively. Moreover, in the group described in the present specification, any group that can take both a linear structure and a branched structure may be used.

［式（Ｉ）中、
Ｒ^I1は、水素原子、ハロゲン原子又はハロゲン原子を有してもよい炭素数１〜６のアル
キル基を表す。
Ｒ^I2は、ハロゲン原子、ヒドロキシ基、炭素数１〜６のアルキル基、炭素数１〜６のア
ルコキシ基、炭素数２〜４のアシル基、炭素数２〜４のアシルオキシ基、アクリロイルオ
キシ基又はメタクリロイルオキシ基を表す。
Ａ¹は、単結合又は^＊−Ａ²−Ｘ¹−（Ａ³−Ｘ²）_a−を表す。
Ａ²及びＡ³は、それぞれ独立に、炭素数１〜６のアルカンジイル基を表す。
Ｘ¹及びＸ²は、それぞれ独立に、−Ｏ−、−ＣＯ−Ｏ−又は−Ｏ−ＣＯ−を表す。
ａは、０又は１を表す。
Ｗは、炭素数４〜１８の脂環式炭化水素を表す。
ｍｃは０〜４の整数を表し、ｍｃが２以上の整数である場合、複数のＲ^I2は互いに同一
であっても異なってもよい。］ <Resin (A)>
The resin of the present invention comprises a structural unit represented by formula (I) (hereinafter sometimes referred to as “structural unit (I)”) and a structural unit represented by formula (a2-2) (hereinafter referred to as “structural unit ( a2-2) "in some cases) (hereinafter also referred to as" resin (A) ").

[In the formula (I),
R ^I1 represents a hydrogen atom, a halogen atom or an alkyl group having 1 to 6 carbon atoms which may have a halogen atom.
R ^I2 represents a halogen atom, a hydroxy group, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, an acyl group having 2 to 4 carbon atoms, an acyloxy group having 2 to 4 carbon atoms, an acryloyloxy group, or Represents a methacryloyloxy group.
A ¹ represents a single bond or ^{* -A 2 -X 1 - (A} 3 -X 2) a - represents a.
A ² and A ³ each independently represents an alkanediyl group having 1 to 6 carbon atoms.
X ¹ and X ² each independently represent —O—, —CO—O— or —O—CO—.
a represents 0 or 1.
W represents an alicyclic hydrocarbon having 4 to 18 carbon atoms.
mc represents an integer of 0 to 4, and when mc is an integer of 2 or more, the plurality of R ^I2 may be the same as or different from each other. ]

Examples of the halogen atom in R ^I1 include a fluorine atom, a chlorine atom and a bromine atom.
Examples of the alkyl group having 1 to 6 carbon atoms which may have a halogen atom in R ^I1 include a trifluoromethyl group, a difluoromethyl group, a methyl group, a perfluoroethyl group, 1,1,1-
Trifluoroethyl group, 1,1,2,2-tetrafluoroethyl group, ethyl group, perfluoropropyl group, 1,1,1,2,2-pentafluoropropyl group, propyl group, perfluorobutyl group, 1,1 , 2,2,3,3,4,4-octafluorobutyl group, butyl group, perfluoropentyl group, 1,1,1,2,2,3,4,4-nonafluoropentyl group, n- A pentyl group, n-hexyl group, and n-perfluorohexyl group are mentioned.
R ^I1 is preferably a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, more preferably a hydrogen atom, a methyl group or an ethyl group, and even more preferably a hydrogen atom or a methyl group.
As the alkyl group for R ^I2 , a methyl group, an ethyl group, an n-propyl group, an isopropyl group,
Examples include an n-butyl group, a sec-butyl group, a tert-butyl group, an n-pentyl group, and an n-hexyl group, and a methyl group is preferable.
^Examples of the alkoxy group of R ^I2 include a methoxy group, an ethoxy group, an n-propoxy group, an isopropoxy group, an n-butoxy group, a sec-butoxy group, and a tert-butoxy group.
A C1-C4 alkoxy group is preferable, a methoxy group or an ethoxy group is more preferable, and a methoxy group is more preferable.
^Examples of the acyl group of R ^I2 include an acetyl group, a propionyl group, and a butyryl group.
^Examples of the acyloxy group for R ^I2 include an acetyloxy group, a propionyloxy group, and a butyryloxy group.

^* -A ² -X ^1- (A ³ -X ² ) _a- includes ^* -A ² -O-, ^* -A ² -CO-O-, ^{*
-A 2 -O-CO-, * -A} 2 -CO-O-A 3 -CO-O-, * -A 2 -O-CO-A 3 -
^{O-, * -A 2 -O-A} 3 -CO-O-, * -A 2 -CO-O-A 3 -O-CO-, * -A 2
^{-O-CO-A 3 -O-} CO-, and the like. Among ^{them, * -A 2 -O-, * -A} 3 -C
O—O—, ^* —A ² —CO—O—A ³ —CO—O— or ^* —A ² —O—A ³ —CO—O— is preferred.

A ² and A ³ are preferably a methylene group or an ethylene group.

A ¹ is preferably a single bond or ^* —A ² —CO—O—, and is a single bond, —CH ₂ —C
More preferably, it is O—O— or —C ₂ H ₄ —CO—O—, a single bond or —CH ₂ —C
More preferably, it is O—O—.

mc is preferably 0, 1 or 2, more preferably 0 or 1, and particularly preferably 0.
The hydroxyl group is preferably bonded to the o-position or p-position of the benzene ring, and more preferably bonded to the p-position.

Examples of the alicyclic hydrocarbon of W include a cyclopentane ring, a cyclohexane ring, an adamantane ring, and a norbornane ring. Of these, a cyclohexane ring and a norbornane ring are preferable, and a norbornane ring is more preferable.

Examples of the structural unit (I) include structural units represented by formulas (I-1) to (I-12), and are represented by formulas (I-1) to (I-8), respectively. A structural unit is preferred,
The structural unit represented by the formula (I-1) to the formula (I-4) is more preferable, and the formula (I-3) or the formula (
The structural unit represented by I-4) is more preferable.

Examples of the monomer for deriving the structural unit (I) include monomers described in JP 2012-41523 A.
The content of the structural unit (I) in the resin (A) is the resin (A) in terms of the shape of the resist pattern.
) Is preferably 5 to 50 mol%, more preferably 5 to 40 mol%,
10-30 mol% is more preferable.

［式（ａ２−２）中、
Ｒ^a50は、水素原子、ハロゲン原子又はハロゲン原子を有してもよい炭素数１〜６のア
ルキル基を表す。
Ｒ^a51は、ハロゲン原子、ヒドロキシ基、炭素数１〜６のアルキル基、炭素数１〜６の
アルコキシ基、炭素数２〜４のアシル基、炭素数２〜４のアシルオキシ基、アクリロイル
オキシ基又はメタクリロイルオキシ基を表す。
Ａ^a50は、単結合又は^＊−Ａ^a51−Ｘ^a51−（Ａ^a52−Ｘ^a52）_na−を表す。
Ａ^a51及びＡ^a52は、それぞれ独立に、炭素数１〜６のアルカンジイル基を表す。
Ｘ^a51及びＸ^a52は、それぞれ独立に、−Ｏ−、−ＣＯ−Ｏ−又は−Ｏ−ＣＯ−を表す。
ｎａは、０又は１を表す。
ｍｂは０〜４の整数を表し、ｍｂが２以上の整数である場合、複数のＲ^a51は互いに同
一であっても異なってもよい。］ The structural unit (a2-2) is represented below.

[In the formula (a2-2),
R ^a50 represents a hydrogen atom, a halogen atom or an alkyl group having 1 to 6 carbon atoms which may have a halogen atom.
R ^a51 is a halogen atom, a hydroxy group, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, an acyl group having 2 to 4 carbon atoms, an acyloxy group having 2 to 4 carbon atoms, an acryloyloxy group, or Represents a methacryloyloxy group.
A ^a50 represents a single bond or ^{* -A a51 -X a51 - (A} a52 -X a52) na - represents a.
A ^a51 and A ^a52 each independently represent an alkanediyl group having 1 to 6 carbon atoms.
X ^a51 and X ^a52 each independently represent —O—, ^—CO —O— or —O—CO—.
na represents 0 or 1.
mb represents an integer of 0 to 4, and when mb is an integer of 2 or more, the plurality of ^Ra51s may be the same as or different from each other. ]

^Examples of the halogen atom of R ^a50 and the alkyl group having 1 to 6 carbon atoms which may have a halogen atom include those equivalent to those in R ^I1 .
R ^a50 is preferably a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, more preferably a hydrogen atom, a methyl group or an ethyl group, and even more preferably a hydrogen atom or a methyl group.
^Examples of the alkyl group, alkoxy group, acyl group, and acyloxy group for R ^a51 include those equivalent to those for R ^I2 .
R ^a51 is preferably a methyl group.

^* -A ^a51 -X ^a51- (A ^a52 -X ^a52 ) _na- includes ^* -A ^a51 -O-, ^* -A ^a51 -C
O—O—, ^* —A ^a51 —O—CO—, ^* —A ^a51 —CO—O—A ^a52 —CO—O—, ^* —A ^a
51 —O—CO—A ^a52 —O—, ^* —A ^a51 —O—A ^a52 —CO—O—, ^* —A ^a51 —CO—O
-A ^a52 -O-CO-, ^* -A ^a51 -O-CO-A ^a52 -O-CO-. Among them, ^{* -Aa51-} O-, ^{* -Aa51-} CO-O-, ^{* -Aa51-} CO-O- ^Aa52 - ^CO-
O— or ^* —A ^a51 —O—A ^a52 —CO—O— is preferred.

A ^a51 and A ^a52 are preferably a methylene group or an ethylene group.

A ^a50 is preferably a single bond or ^* -A ^a51 —CO—O—, and is a single bond, —CH _2.
It is more preferably —CO—O— or —C ₂ H ₄ —CO—O—, a single bond or —CH ₂
More preferably, it is —CO—O—.

mb is preferably 0, 1 or 2, more preferably 0 or 1, and particularly preferably 0.
The hydroxyl group is preferably bonded to the o-position or p-position, and more preferably bonded to the p-position.

As the structural unit (a2-2), the formula (a2-2-1), the formula (a2-2-2), the formula (a2)
-2-3) and structural units represented by the formula (a2-2-4) are preferable, respectively,
The structural unit represented by 2-1) or formula (a2-2-2) is more preferable.

Examples of the monomer for deriving the structural unit (a2-2) include monomers described in JP2012-12577A.

The content of the structural unit (a2-2) in the resin (A) is preferably 5 to 50 mol% with respect to the total structural units of the resin (A) in terms of the shape of the resist pattern, and preferably 5 to 40 mol. % Is more preferable, and 10 to 30 mol% is more preferable.
When the content ratio of the structural unit (I) and the structural unit (a2-2) is within the above range, a resist pattern having a better focus margin can be manufactured.

<Structural unit (a)>
The resin (A) preferably further contains an acid labile group, and is preferably a resin having a structural unit having an acid labile group (hereinafter sometimes referred to as “structural unit (a)”). Here, the acid labile group means a group having a leaving group and forming a hydrophilic group (for example, a hydroxy group or a carboxy group) by leaving the leaving group by contact with an acid.

［式（１）中、Ｒ^a1〜Ｒ^a3は、それぞれ独立に、炭素数１〜８のアルキル基、炭素数３
〜２０の脂環式炭化水素基又はこれらを組み合わせた基を表すか、Ｒ^a1及びＲ^a2は互いに
結合してそれらが結合する炭素原子とともに炭素数３〜２０の２価の脂環式炭化水素基を
形成する。
ｎａは、０又は１を表す。
＊は結合手を表す。］

［式（２）中、Ｒ^a1’及びＲ^a2’は、それぞれ独立に、水素原子又は炭素数１〜１２の
炭化水素基を表し、Ｒ^a3’は、炭素数１〜２０の炭化水素基を表すか、Ｒ^a2’及びＲ^a3’
は互いに結合してそれらが結合する炭素原子とともに炭素数３〜２０の２価の脂環式炭化
水素基を形成し、該炭化水素基及び該２価の脂環式炭化水素基に含まれる−ＣＨ₂−は、
−Ｏ−又は−Ｓ−で置き換わってもよい。
Ｘは、酸素原子又は硫黄原子を表す。
＊は結合手を表す。］ The structural unit (a) is derived from a monomer having an acid labile group (hereinafter sometimes referred to as “monomer (a)”). Examples of the acid labile group contained in the structural unit (a) include the following formula (1):
And a group represented by the formula (2).

[In Formula (1), R ^<a1 > -R < ^a3 > is respectively independently a C1-C8 alkyl group, C3
Represents a group of -20 alicyclic hydrocarbons or a combination thereof, or R ^a1 and R ^a2 are bonded to each other and the divalent alicyclic hydrocarbon having 3 to 20 carbon atoms together with the carbon atom to which they are bonded. Form a group.
na represents 0 or 1.
* Represents a bond. ]

[In Formula (2), R ^{a1 ′} and R ^{a2 ′} each independently represent a hydrogen atom or a hydrocarbon group having 1 to 12 carbon atoms, and R ^{a3 ′} represents a hydrocarbon group having 1 to 20 carbon atoms. R ^{a2 ′} and R ^{a3 ′}
Form a divalent alicyclic hydrocarbon group having 3 to 20 carbon atoms together with the carbon atoms to which they are bonded, and are contained in the hydrocarbon group and the divalent alicyclic hydrocarbon group- CH ₂ -is
-O- or -S- may be substituted.
X represents an oxygen atom or a sulfur atom.
* Represents a bond. ]

アルキル基と脂環式炭化水素基とを組み合わせた基としては、メチルシクロヘキシル基
、ジメチルシクロへキシル基、メチルノルボルニル基、シクロヘキシルメチル基、アダマ
ンチルメチル基、ノルボルニルエチル基等が挙げられる。
ｎａは、好ましくは０である。 ^Examples of the alkyl group for R ^{a1 to} R ^a3 include a methyl group, an ethyl group, a propyl group, an n-butyl group,
An n-pentyl group, an n-hexyl group, an n-heptyl group, and an n-octyl group are exemplified.
The alicyclic hydrocarbon group for R ^{a1 to} R ^a3 may be monocyclic or polycyclic. Examples of the monocyclic alicyclic hydrocarbon group include cycloalkyl groups such as a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, and a cyclooctyl group. Examples of the polycyclic alicyclic hydrocarbon group include a decahydronaphthyl group, an adamantyl group, a norbornyl group, and the following group (* represents a bond). The alicyclic hydrocarbon group represented by R ^{a1 to} R ^a3 preferably has 3 to 3 carbon atoms.
16.

Examples of the group in which the alkyl group and the alicyclic hydrocarbon group are combined include a methylcyclohexyl group, a dimethylcyclohexyl group, a methylnorbornyl group, a cyclohexylmethyl group, an adamantylmethyl group, and a norbornylethyl group. .
na is preferably 0.

—C (R ^a1 ) in the case where R ^a1 and R ^a2 are bonded to each other to form a divalent alicyclic hydrocarbon group.
^{Examples of} (R ^a2 ) (R ^a3 ) include the following groups. The divalent alicyclic hydrocarbon group preferably has 3 to 12 carbon atoms. * Represents a bond with -O-.

Examples of the group represented by the formula (1) include a 1,1-dialkylalkoxycarbonyl group (formula (1
) In which R ^{a1 to} R ^a3 are alkyl groups, preferably tert-butoxycarbonyl group), 2-alkyladamantan-2-yloxycarbonyl groups (in formula (1), R ^a1 ,
R ^a2 and the carbon atom to which they are bonded form an adamantyl group, and R ^a3 is an alkyl group) and 1- (adamantan-1-yl) -1-alkylalkoxycarbonyl group (formula (
In 1), R ^a1 and R ^a2 are alkyl groups, and R ^a3 is an adamantyl group).

Examples of the hydrocarbon group of R ^{a1 ′ to} R ^{a3 ′} include an alkyl group, an alicyclic hydrocarbon group, an aromatic hydrocarbon group, and a group formed by combining these.
Examples of the alkyl group and alicyclic hydrocarbon group are the same as those described above.
Aromatic hydrocarbon groups include phenyl, naphthyl, anthryl, p-methylphenyl, p-tert-butylphenyl, p-adamantylphenyl, tolyl, xylyl, cumenyl, mesityl, biphenyl Groups, phenanthryl groups, 2,6-diethylphenyl groups, aryl groups such as 2-methyl-6-ethylphenyl, and the like.
Examples of the divalent hydrocarbon group formed by combining R ^{a2 ′} and R ^{a3 ′} include R ^{a1 ′}
And a group obtained by removing one hydrogen atom from a hydrocarbon group represented by ^{-Ra3 '} .
At least one of R ^{a1 ′} and R ^{a2 ′} is preferably a hydrogen atom.

Specific examples of the group represented by the formula (2) include the following groups. * Represents a bond.

The monomer (a) is preferably a monomer having an acid labile group and an ethylenically unsaturated bond, more preferably a (meth) acrylic monomer having an acid labile group.

Of the (meth) acrylic monomers having an acid labile group, preferably 5 to 20 carbon atoms.
And those having an alicyclic hydrocarbon group. If a resin having a structural unit (a) having a bulky structure such as an alicyclic hydrocarbon group is used in the resist composition, the resolution of the resist pattern can be improved.

In the resin (A), the content of the structural unit (a) is based on the total structural unit of the resin (A).
Preferably it is 30-90 mol%, More preferably, it is 35-85 mol%, More preferably, it is 40-80 mol%.

As a structural unit derived from a (meth) acrylic monomer having a group represented by the formula (1), a structural unit represented by the formula (a1-0) is preferably represented by the formula (a1-1). The structural unit represented by a structural unit or a formula (a1-2) is mentioned. These may be used alone,
Two or more kinds may be used in combination. In this specification, the structural unit represented by the formula (a1-0), the formula (a
The structural unit represented by 1-1) and the structural unit represented by the formula (a1-2) are respectively the structural unit (a1-0), the structural unit (a1-1), and the structural unit (a1-2). , Structural unit (a1-
0) -derived monomer, structural unit (a1-1) -derived monomer and structural unit (a1)
-2) may be referred to as monomer (a1-0), monomer (a1-1) and monomer (a1-2), respectively.

［式（ａ１−０）中、
Ｌ^a01は、酸素原子又は^＊−Ｏ−（ＣＨ₂）_k01−ＣＯ−Ｏ−を表し、ｋ０１は１〜７の
整数を表し、＊はカルボニル基との結合手を表す。
Ｒ^a01は、水素原子又はメチル基を表す。
Ｒ^a02、Ｒ^a03及びＲ^a04は、それぞれ独立に、炭素数１〜８のアルキル基、炭素数３〜
１８の脂環式炭化水素基又はこれらを組み合わせた基を表す。］

[In the formula (a1-0),
L ^a01 represents an oxygen atom or ^* —O— (CH ₂ ) _k01 —CO—O—, k01 represents an integer of 1 to 7, and * represents a bond to a carbonyl group.
R ^a01 represents a hydrogen atom or a methyl group.
R ^a02 , R ^a03 and R ^a04 are each independently an alkyl group having 1 to 8 carbon atoms,
It represents 18 alicyclic hydrocarbon groups or a combination thereof. ]

［式（ａ１−１）及び式（ａ１−２）中、
Ｌ^a1及びＬ^a2は、それぞれ独立に、−Ｏ−又は^＊−Ｏ−（ＣＨ₂）_k1−ＣＯ−Ｏ−を表
し、ｋ１は１〜７の整数を表し、＊は−ＣＯ−との結合手を表す。
Ｒ^a4及びＲ^a5は、それぞれ独立に、水素原子又はメチル基を表す。
Ｒ^a6及びＲ^a7は、それぞれ独立に、炭素数１〜８のアルキル基、炭素数３〜１８の脂環
式炭化水素基又はこれらを組み合わせた基を表す。
ｍ１は０〜１４の整数を表す。
ｎ１は０〜１０の整数を表す。
ｎ１’は０〜３の整数を表す。］

[In Formula (a1-1) and Formula (a1-2),
L ^a1 and L ^a2 each independently represent —O— or ^* —O— (CH ₂ ) _k1 —CO—O—, k1 represents an integer of 1 to 7, and * represents a bond to —CO—. Represents a hand.
R ^a4 and R ^a5 each independently represent a hydrogen atom or a methyl group.
R ^a6 and R ^a7 each independently represent an alkyl group having 1 to 8 carbon atoms, an alicyclic hydrocarbon group having 3 to 18 carbon atoms, or a group obtained by combining these.
m1 represents the integer of 0-14.
n1 represents an integer of 0 to 10.
n1 ′ represents an integer of 0 to 3. ]

L ^a01 is preferably an oxygen atom or ^* —O— (CH ₂ ) _k01 —CO—O—, and more preferably an oxygen atom. k01 is preferably an integer of 1 to 4, more preferably 1.
Examples of the alkyl group of R ^a02 , R ^a03, and R ^a04 , the alicyclic hydrocarbon group, and a group obtained by combining these include the same groups as those described for R ^{a1 to} R ^a3 in formula (1).
The alkyl group for R ^a02 , R ^a03 and R ^a04 preferably has 6 or less carbon atoms.
The alicyclic hydrocarbon group ^{represented by} R ^a02 , R ^a03 and R ^a04 preferably has 8 or less carbon atoms, more preferably 6 or less.
The group combining the alkyl group and the alicyclic hydrocarbon group preferably has a total carbon number of 18 or less, combining the alkyl group and the alicyclic hydrocarbon group. Examples of such a group include a methylcyclohexyl group, a dimethylcyclohexyl group, and a methylnorbornyl group.
R ^a02 and R ^a03 are preferably an alkyl group having 1 to 6 carbon atoms, more preferably a methyl group or an ethyl group.
R ^a04 is preferably an alkyl group having 1 to 6 carbon atoms or an alicyclic hydrocarbon group having 5 to 12 carbon atoms, and more preferably a methyl group, an ethyl group, a cyclohexyl group, or an adamantyl group.

L ^a1 and L ^a2 are preferably —O— or ^* —O— (CH ₂ ) _k1 —CO—O—,
More preferably, it is -O-. k1 is preferably an integer of 1 to 4, more preferably 1.
R ^a4 and R ^a5 are preferably methyl groups.
Examples of the alkyl group represented by R ^a6 and R ^a7 , the alicyclic hydrocarbon group, and a combination thereof include
^Examples thereof include the same groups as those described for R ^{a1 to} R ^a3 in formula (1).
The alkyl group for R ^a6 and R ^a7 preferably has 6 or less carbon atoms.
The alicyclic hydrocarbon group of R ^a6 and R ^a7 preferably has 8 or less carbon atoms, more preferably 6 or less.
m1 is preferably an integer of 0 to 3, more preferably 0 or 1.
n1 is preferably an integer of 0 to 3, more preferably 0 or 1.
n1 ′ is preferably 0 or 1.

Examples of the monomer (a1-0) include those represented by the formula (a1-0-1) to the formula (a1-0-12)
A monomer represented by any one of formulas (a1-0-1) to (a1-0-10) is preferred.
A monomer represented by any of the above is more preferred.

In the above structural unit, a structural unit in which a methyl group corresponding to R ^a01 is replaced with a hydrogen atom can also be given as a specific example of the structural unit (a1-0).

The content of the structural unit represented by the formula (a1-0) is preferably 3 to 60 mol%, more preferably 4 to 55 mol% with respect to all the structural units of the resin (A).

As a monomer (a1-1), the monomer described in Unexamined-Japanese-Patent No. 2010-204646 is mentioned. Among these, a monomer represented by any one of formula (a1-1-1) to formula (a1-1-8) is preferable, and any one of formula (a1-1-1) to formula (a1-1-4) is preferable. The monomer represented by is more preferable.

As the monomer (a1-2), 1-methylcyclopentan-1-yl (meth) acrylate, 1-ethylcyclopentan-1-yl (meth) acrylate, 1-methylcyclohexane-1-yl (meth) acrylate, 1-ethylcyclohexane-1-yl (meth) acrylate, 1-ethylcycloheptan-1-yl (meth) acrylate, 1-methylcyclopentan-1-yl (meth) acrylate, 1-methylcyclohexane-1-yl ( And (meth) acrylate, 1-isopropylcyclopentan-1-yl (meth) acrylate, 1-isopropylcyclohexane-1-yl (meth) acrylate, and the like. Monomers represented by the formula (a1-2-1) to the formula (a1-2-12) are preferred, and the formula (a1
-2-3) to the formula (a1-2-4) or the formula (a1-2-9) to the formula (a1-2-10) are more preferable, and the formula (a1-2-3) or The monomer represented by the formula (a1-2-9) is more preferable.

When the resin (A) includes the structural unit (a1-0) and / or the structural unit (a1-1) and / or the structural unit (a1-2), the total content thereof is the total structure of the resin (A). For units
Usually, it is 10-95 mol%, Preferably it is 15-90 mol%, More preferably, it is 20
-85 mol%.

式（ａ１−３）中、
Ｒ^a9は、ヒドロキシ基を有していてもよい炭素数１〜３の脂肪族炭化水素基、カルボキ
シ基、シアノ基、水素原子又は−ＣＯＯＲ^a13を表す。
Ｒ^a13は、炭素数１〜８の脂肪族炭化水素基、炭素数３〜２０の脂環式炭化水素基、又
はこれらを組み合わせることにより形成される基を表し、該脂肪族炭化水素基及び該脂環
式炭化水素基に含まれる水素原子は、ヒドロキシ基で置換されていてもよく、該脂肪族炭
化水素基及び該脂環式炭化水素基に含まれる−ＣＨ₂−は、−Ｏ−又は−ＣＯ−に置き換
わっていてもよい。
Ｒ^a10、Ｒ^a11及びＲ^a12は、それぞれ独立に、炭素数１〜８のアルキル基、炭素数３〜
２０の脂環式炭化水素基又はこれらを組み合わせることにより形成される基を表すか、Ｒ
^a10及びＲ^a11は互いに結合して、それらが結合する炭素原子とともに炭素数２〜２０の２
価の炭化水素基を形成する。 Further, examples of the structural unit (a) having the group (1) include a structural unit represented by the formula (a1-3). The structural unit represented by the formula (a1-3) may be referred to as a structural unit (a1-3). Moreover, the monomer which derives the structural unit (a1-3) may be referred to as a monomer (a1-3).

In formula (a1-3),
R ^a9 represents an aliphatic hydrocarbon group having 1 to 3 carbon atoms which may have a hydroxy group, a carboxy group, a cyano group, a hydrogen atom, or —COOR ^a13 .
R ^a13 represents an aliphatic hydrocarbon group having 1 to 8 carbon atoms, an alicyclic hydrocarbon group having 3 to 20 carbon atoms, or a group formed by a combination thereof, the aliphatic hydrocarbon group and the The hydrogen atom contained in the alicyclic hydrocarbon group may be substituted with a hydroxy group, and —CH ₂ — contained in the aliphatic hydrocarbon group and the alicyclic hydrocarbon group is —O— or -CO- may be substituted.
R ^a10 , R ^a11 and R ^a12 each independently represent an alkyl group having 1 to 8 carbon atoms,
Represents 20 alicyclic hydrocarbon groups or groups formed by combining these, or R
^a10 and R ^a11 are bonded to each other, together with the carbon atom to which they are bonded, 2 to 2 carbon atoms.
A valent hydrocarbon group is formed.

Here, -COOR ^a13 includes a group in which a carbonyl group is bonded to an alkoxy group such as a methoxycarbonyl group and an ethoxycarbonyl group.

Examples of the aliphatic hydrocarbon group which may have a hydroxy group of R ^a9 include a methyl group, an ethyl group, a propyl group, a hydroxymethyl group and a 2-hydroxyethyl group.
^Examples of the aliphatic hydrocarbon group having 1 to 8 carbon atoms represented by R ^a13 include methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, sec-butyl group, tert-butyl group, n-pentyl group, n -Hexyl group, n-heptyl group, 2-ethylhexyl group, n-octyl group, etc. are mentioned.
^Examples of the alicyclic hydrocarbon group having 3 to 20 carbon atoms represented by R ^a13 include a cyclopentyl group, a cyclopropyl group, an adamantyl group, an adamantylmethyl group, a 1-adamantyl-1-methylethyl group, and 2-oxo-oxolane-3- Yl group and 2-oxo-oxolan-4-yl group.
^Examples of the alkyl group represented by R ^{a10 to} R ^a12 include methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, sec-butyl group, tert-butyl group, n-pentyl group, n-
A hexyl group, n-heptyl group, 2-ethylhexyl group, n-octyl group, etc. are mentioned.
The alicyclic hydrocarbon group for R ^{a10 to} R ^a12 may be either monocyclic or polycyclic, and the monocyclic alicyclic hydrocarbon group may be a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, Examples thereof include cycloalkyl groups such as a cyclohexyl group, a methylcyclohexyl group, a dimethylcyclohexyl group, a cycloheptyl group, a cyclooctyl group, a cycloheptyl group, and a cyclodecyl group. Examples of the polycyclic alicyclic hydrocarbon group include decahydronaphthyl group, adamantyl group, 2-alkyladamantan-2-yl group, 1- (adamantan-1-yl) alkane-1-yl group, norbornyl group, Examples thereof include a methylnorbornyl group and an isobornyl group.
-C (R ^a10 ) (R ^a11 ) (R ^a12 ) in the case where R ^a10 and R ^a11 are bonded to each other to form a divalent hydrocarbon group together with the carbon atom to which they are bonded, Groups are preferred.

Specifically, the monomer (a1-3) is 5-norbornene-2-carboxylic acid-tert.
-Butyl, 1-cyclohexyl-1-methylethyl 5-norbornene-2-carboxylate,
1-methylcyclohexyl 5-norbornene-2-carboxylate, 5-norbornene-2-
2-methyl-2-adamantyl carboxylate, 2-ethyl-2-adamantyl 5-norbornene-2-carboxylate, 1- (4-methylcyclohexyl) -1-methylethyl 5-norbornene-2-carboxylate, 5- 1- (4-Hydroxycyclohexyl) -1-methylethyl norbornene-2-carboxylic acid, 1-methyl-1 5-norbornene-2-carboxylic acid
-(4-Oxocyclohexyl) ethyl and 5-norbornene-2-carboxylic acid 1- (1
-Adamantyl) -1-methylethyl and the like.

Since the resin (A) containing the structural unit (a1-3) includes a sterically bulky structural unit, the resist composition of the present invention containing such a resin (A) is more expensive. A resist pattern can be obtained with resolution. Further, since a rigid norbornane ring is introduced into the main chain, the resulting resist pattern tends to be excellent in dry etching resistance.

When the resin (A) contains the structural unit (a1-3), the content thereof is preferably 10 to 95 mol%, more preferably 15 to 90 mol%, based on all the structural units of the resin (A). 20-8
5 mol% is more preferable.

［式（ａ１−４）中、
Ｒ^a32は、水素原子、ハロゲン原子、又は、ハロゲン原子を有してもよい炭素数１〜６
のアルキル基を表す。
Ｒ^a33は、ハロゲン原子、ヒドロキシ基、炭素数１〜６のアルキル基、炭素数１〜６の
アルコキシ基、炭素数２〜４のアシル基、炭素数２〜４のアシルオキシ基、アクリロイル
オキシ基又はメタクリロイルオキシ基を表す。
ｌａは０〜４の整数を表す。ｌａが２以上である場合、複数のＲ^a33は互いに同一であ
っても異なってもよい。
Ｒ^a34及びＲ^a35はそれぞれ独立に、水素原子又は炭素数１〜１２の炭化水素基を表し、
Ｒ^a36は、炭素数１〜２０の炭化水素基を表すか、Ｒ^a35及びＲ^a36は互いに結合してそれ
らが結合するＣ−Ｏとともに炭素数２〜２０の２価の炭化水素基を形成し、該炭化水素基
及び該２価の炭化水素基に含まれる−ＣＨ₂−は、−Ｏ−又は−Ｓ−で置き換わってもよ
い。］ As the structural unit (a) having a group represented by the group (2), a structural unit represented by the formula (a1-4) (hereinafter sometimes referred to as “structural unit (a1-4)”). Can be mentioned.

[In the formula (a1-4),
R ^a32 is a hydrogen atom, a halogen atom, or a C 1-6 which may have a halogen atom.
Represents an alkyl group.
R ^a33 is a halogen atom, a hydroxy group, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, an acyl group having 2 to 4 carbon atoms, an acyloxy group having 2 to 4 carbon atoms, an acryloyloxy group, or Represents a methacryloyloxy group.
la represents an integer of 0 to 4. When la is 2 or more, the plurality of R ^a33 may be the same as or different from each other.
R ^a34 and R ^a35 each independently represent a hydrogen atom or a hydrocarbon group having 1 to 12 carbon atoms,
R ^a36 is either a hydrocarbon group having 1 to 20 carbon atoms, R ^a35 and R ^a36 is a divalent hydrocarbon group having 2 to 20 carbon atoms to form together with the C-O to which they are attached, The —CH ₂ — contained in the hydrocarbon group and the divalent hydrocarbon group may be replaced by —O— or —S—. ]

^Examples of the alkyl group for R ^a32 and R ^a33 include a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, a pentyl group, and a hexyl group. The alkyl group has 1 carbon atom.
-4 alkyl groups are preferable, a methyl group or an ethyl group is more preferable, and a methyl group is more preferable.
Examples of the halogen atom for R ^a32 and R ^a33 include a fluorine atom, a chlorine atom, and a bromine atom.
The R ^a34 and R ^a35, include the same groups as R ^{a1 'and} R ^a2' of formula (2).
As R ^a36 , an alkyl group having 1 to 18 carbon atoms, an alicyclic hydrocarbon group having 3 to 18 carbon atoms,
Examples thereof include aromatic hydrocarbon groups having 6 to 18 carbon atoms or groups formed by combining these.

In formula (a1-4), R ^a32 is preferably a hydrogen atom.
R ^a33 is preferably an alkoxy group having 1 to 4 carbon atoms, more preferably a methoxy group or an ethoxy group, and further preferably a methoxy group.
la is preferably 0 or 1, more preferably 0.
R ^a34 is preferably a hydrogen atom.
R ^a35 is preferably a hydrocarbon group having 1 to 12 carbon atoms, more preferably a methyl group or an ethyl group.
The hydrocarbon group for R ^a36 is preferably an alkyl group having 1 to 18 carbon atoms, an alicyclic hydrocarbon group having 3 to 18 carbon atoms, an aromatic hydrocarbon group having 6 to 18 carbon atoms, or a combination thereof. A group to be formed, more preferably an alkyl group having 1 to 18 carbon atoms, 3 to 1 carbon atoms.
8 alicyclic aliphatic hydrocarbon groups or aralkyl groups having 7 to 18 carbon atoms. The alkyl group in R ^a36 and the alicyclic hydrocarbon group are preferably unsubstituted. When the aromatic hydrocarbon group in R ^a36 has a substituent, the substituent is preferably an aryloxy group having 6 to 10 carbon atoms.

Examples of the monomer that leads to the structural unit (a1-4) include, for example, JP 2010-204646 A.
And the monomers described in the Japanese Patent Publication. Among them, the formula (a1-4-1) to the formula (a1-4)
-8) are preferable, and the monomers represented by formula (a1-4-1) to formula (a1-4-5) are preferable.
And monomers represented by formula (a1-4-8), respectively.

When resin (A) has a structural unit (a1-4), the content rate is preferable with respect to all the structural units of resin (A), and 10-95 mol% is preferable, and 15-90 mol% is more preferable. , 20
More preferred is ~ 85 mol%.

式（ａ１−５）中、
Ｒ^a8は、ハロゲン原子を有してもよい炭素数１〜６のアルキル基、水素原子又はハロゲ
ン原子を表す。
Ｚ^a1は、単結合又は＊−（ＣＨ₂）_h3−ＣＯ−Ｌ⁵⁴−を表し、ｈ３は１〜４の整数を表
し、＊は、Ｌ⁵¹との結合手を表す。
Ｌ⁵¹、Ｌ⁵²、Ｌ⁵³及びＬ⁵⁴は、それぞれ独立に、−Ｏ−又は−Ｓ−を表す。
ｓ１は、１〜３の整数を表す。
ｓ１’は、０〜３の整数を表す。 As a structural unit derived from a (meth) acrylic monomer having a group represented by the formula (2), a structural unit represented by the formula (a1-5) (hereinafter referred to as “structural unit (a1-5)”) Is also included).

In formula (a1-5),
R ^a8 represents a C 1-6 alkyl group optionally having a halogen atom, a hydrogen atom, or a halogen atom.
Z ^a1 represents a single bond or * — (CH ₂ ) _h3 —CO—L ⁵⁴ —, h3 represents an integer of 1 to 4, and * represents a bond to L ⁵¹ .
L ⁵¹ , L ⁵² , L ⁵³ and L ⁵⁴ each independently represent —O— or —S—.
s1 represents an integer of 1 to 3.
s1 ′ represents an integer of 0 to 3.

In formula (a1-5), R ^a8 is preferably a hydrogen atom, a methyl group or a trifluoromethyl group.
L ⁵¹ is preferably an oxygen atom.
One of L ⁵² and L ⁵³ is preferably —O— and the other is —S—.
s1 is preferably 1.
s1 ′ is preferably an integer of 0 to 2.
Z ^a1 is preferably a single bond or * —CH ₂ —CO—O—.

As a monomer which introduce | transduces structural unit (a1-5), the monomer described in Unexamined-Japanese-Patent No. 2010-61117 is mentioned, for example. Among these, the formula (a1-5-1) to the formula (a1-5)
4) is preferably a monomer represented by formula (a1-5-1) or formula (a1-5-2).
) Is more preferable.

When resin (A) has a structural unit (a1-5), the content rate is preferable 1-50 mol% with respect to all the structural units of resin (A), and 3-45 mol% is more preferable. 5-40
More preferred is mol%.

As the structural unit (a) having an acid labile group in the resin (A), the structural unit (a1-0),
One or more types selected from the group consisting of the structural unit (a1-1), the structural unit (a1-2) and the structural unit (a1-5) are preferable, two or more types are more preferable, and the structural unit (a1-1) and the structure Combination of unit (a1-2), combination of structural unit (a1-1) and structural unit (a1-5), combination of structural unit (a1-1) and structural unit (a1-0), structural unit (a1)
-2) and the structural unit (a1-0), the structural unit (a1-5) and the structural unit (a
1-0), structural unit (a1-0), structural unit (a1-1) and structural unit (a
1-2), structural unit (a1-0), structural unit (a1-1) and structural unit (a
1-5) is more preferable, and the structural unit (a1-1) and the structural unit (a1-2)
) Is particularly preferred.

<Structural unit without acid labile group>
A monomer (hereinafter also referred to as “monomer (s)”) that leads to a structural unit having no acid labile group (hereinafter sometimes referred to as “structural unit (s)”) is structural unit (I) or structural unit. (
The monomer is not particularly limited as long as it is a monomer having no acid labile group other than the monomer leading to a2-2), and a known monomer in the resist field can be used.
As the structural unit (s), a structural unit having a hydroxy group or a lactone ring and having no acid labile group is preferable. A structure having a hydroxy group and having no acid labile group (hereinafter sometimes referred to as “structural unit (a2)”) and / or a lactone ring and having no acid labile group If a resin having a unit (hereinafter sometimes referred to as “structural unit (a3)”) is used for the resist composition, the resolution of the resist pattern and the adhesion to the substrate can be improved.

<Structural unit (a2)>
The hydroxy group contained in the structural unit (a2) may be an alcoholic hydroxy group or a phenolic hydroxy group.
When producing a resist pattern from the resist composition of the present invention, KrF is used as an exposure light source.
In the case of using a high energy beam such as an excimer laser (248 nm), an electron beam or EUV (ultra-ultraviolet light), a structural unit having a phenolic hydroxy group (a2)
It is preferable to use a2), and it is more preferable to use a structural unit represented by formula (a2-0) or formula (a2-2) described later. In the case of using an ArF excimer laser (193 nm) or the like, the structural unit (a2) having an alcoholic hydroxy group is preferable as the structural unit (a2), and the structural unit represented by the formula (a2-1) described later It is more preferable to use As a structural unit (a2), 1 type may be included independently and 2 or more types may be included.

When the resin (A) has a structural unit (a2) having a phenolic hydroxy group, the content is preferably from 5 to 95 mol%, preferably from 10 to 80 mol%, based on all structural units of the resin (A). Is more preferable, and 15-80 mol% is further more preferable.

［式（ａ２−０）中、
Ｒ^a30は、水素原子、ハロゲン原子又はハロゲン原子を有してもよい炭素数１〜６のア
ルキル基を表す。
Ｒ^a31は、ハロゲン原子、ヒドロキシ基、炭素数１〜６のアルキル基、炭素数１〜６の
アルコキシ基、炭素数２〜４のアシル基、炭素数２〜４のアシルオキシ基、アクリロイル
オキシ基又はメタクリロイルオキシ基を表す。
ｍａは０〜４の整数を表す。ｍａが２以上の整数である場合、複数のＲ^a31は互いに同
一であっても異なってもよい。］ Examples of the structural unit (a2) having a phenolic hydroxy group include a structural unit represented by the formula (a2-0) (hereinafter sometimes referred to as “structural unit (a2-0)”).

[In the formula (a2-0),
R ^a30 represents a hydrogen atom, a halogen atom or an alkyl group having 1 to 6 carbon atoms which may have a halogen atom.
R ^a31 is a halogen atom, a hydroxy group, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, an acyl group having 2 to 4 carbon atoms, an acyloxy group having 2 to 4 carbon atoms, an acryloyloxy group, or Represents a methacryloyloxy group.
ma represents an integer of 0 to 4. When ma is an integer of 2 or more, the plurality of R ^a31 may be the same as or different from each other. ]

^Examples of the alkyl group having 1 to 6 carbon atoms which may have a halogen atom of R ^a30 include a trifluoromethyl group, a difluoromethyl group, a methyl group, a perfluoroethyl group, a 1,1,1-trifluoroethyl group, 1 , 1,2,2-tetrafluoroethyl group, ethyl group, perfluoropropyl group, 1,1,1,2,2-pentafluoropropyl group, propyl group, perfluorobutyl group, 1,1,2,2,3 , 3,4,4-octafluorobutyl group, butyl group, perfluoropentyl group, 1,1,1,2,2,3,3,4,4-nonafluoropentyl group, n-pentyl group, n-hexyl Group, n-perfluorohexyl group and the like. R ^a3
0 is preferably a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, more preferably a hydrogen atom, a methyl group or an ethyl group, and even more preferably a hydrogen atom or a methyl group.
The alkoxy group of R ^a31 is preferably an alkoxy group having 1 to 4 carbon atoms, more preferably a methoxy group or an ethoxy group, and further preferably a methoxy group.
ma is preferably 0, 1 or 2, more preferably 0 or 1, and particularly preferably 0.

構造単位（ａ２−０）を誘導するモノマーとしては、例えば、特開２０１０−２０４６
３４号公報に記載されているモノマーが挙げられる。 Among them, as the structural unit (a2-0) having a phenolic hydroxy group, the following formula (
a2-0-1), formula (a2-0-2), formula (a2-0-3) and formula (a2-0-4) are preferred respectively, and formula (a2-0-1) Or the structural unit represented by a formula (a2-0-2) is more preferable.

Examples of the monomer for deriving the structural unit (a2-0) include, for example, JP 2010-2046 A.
And monomers described in Japanese Patent No. 34.

The resin (A) containing the structural unit (a2-0) is subjected to a polymerization reaction using a monomer in which the phenolic hydroxy group of the monomer that derives the structural unit (a2-0) is protected with a protective group, and then deprotected. It can be manufactured by processing. However, when the deprotection treatment is performed, the acid labile group of the structural unit (a) needs to be not significantly impaired. Examples of such protecting groups include acetyl groups.

When the resin (A) has a structural unit (a2-0) having a phenolic hydroxy group, the content is preferably from 5 to 95 mol% with respect to all the structural units of the resin (A).
80 mol% is more preferable, and 15-80 mol% is further more preferable.

式（ａ２−１）中、
Ｌ^a3は、−Ｏ−又は^＊−Ｏ−（ＣＨ₂）_k2−ＣＯ−Ｏ−を表し、
ｋ２は１〜７の整数を表す。＊は−ＣＯ−との結合手を表す。
Ｒ^a14は、水素原子又はメチル基を表す。
Ｒ^a15及びＲ^a16は、それぞれ独立に、水素原子、メチル基又はヒドロキシ基を表す。
ｏ１は、０〜１０の整数を表す。 Examples of the structural unit (a2) having an alcoholic hydroxy group include a structural unit represented by the formula (a2-1) (hereinafter sometimes referred to as “structural unit (a2-1)”).

In formula (a2-1),
L ^a3 represents —O— or ^* —O— (CH ₂ ) _k2 —CO—O—,
k2 represents an integer of 1 to 7. * Represents a bond with -CO-.
R ^a14 represents a hydrogen atom or a methyl group.
R ^a15 and R ^a16 each independently represent a hydrogen atom, a methyl group or a hydroxy group.
o1 represents an integer of 0 to 10.

In formula (a2-1), L ^a3 is preferably —O—, —O— (CH ₂ ) _f1 —CO—O—.
(Wherein the f1 is an integer of 1 to 4), more preferably —O—.
R ^a14 is preferably a methyl group.
R ^a15 is preferably a hydrogen atom.
R ^a16 is preferably a hydrogen atom or a hydroxy group.
o1 is preferably an integer of 0 to 3, more preferably 0 or 1.

式（ａ２−１−１）〜式（ａ２−１−４）のいずれかで表される構造単位が好ましく、
式式（ａ２−１−１）又は式（ａ２−１−３）で表される構造単位がより好ましい。
アルコール性ヒドロキシ基を有する構造単位（ａ２）を誘導するモノマーとしては、例
えば、特開２０１０−２０４６４６号公報に記載されたモノマーが挙げられる。 As the structural unit (a2-1) having an alcoholic hydroxy group, the following formula (a2-
1-1) to a structural unit represented by any one of formulas (a2-1-6).

A structural unit represented by any one of formula (a2-1-1) to formula (a2-1-4) is preferred,
The structural unit represented by formula (a2-1-1) or formula (a2-1-3) is more preferable.
Examples of the monomer for deriving the structural unit (a2) having an alcoholic hydroxy group include monomers described in JP2010-204646A.

When resin (A) contains a structural unit (a2-1), the content rate is 1-45 mol% normally with respect to all the structural units of resin (A), Preferably it is 1-40 mol%. More preferably, it is 1-35 mol%, More preferably, it is 2-20 mol%.

<Structural unit (a3)>
The lactone ring of the structural unit (a3) may be a monocycle such as a β-propiolactone ring, γ-butyrolactone ring, or δ-valerolactone ring, or a condensed ring of a monocyclic lactone ring and another ring. But you can. Preferably, a γ-butyrolactone ring or a bridged ring containing a γ-butyrolactone ring structure is used. The structural unit (a3) may contain two or more kinds. Structural unit (
Examples of a3) include the following structural units.

Examples of the monomer for deriving the structural unit (a3) include monomers described in JP 2010-204646 A, monomers described in JP 2000-122294 A, and JP 201
The monomer described in 2-41274 gazette is mentioned. As the structural unit (a3),
Formula (a3-1-1) to Formula (a3-1-6), Formula (a3-2-1) to Formula (a3-2-4),
Formula (a3-3-1) to Formula (a3-3-4) and Formula (a3-4-1) to Formula (a3-4-6)
A structural unit represented by any one of formulas (a3-1-1), (a3-1-2) and (a3-2-3) to (a3-2-4) is preferred. Is more preferable, and the structural unit represented by the formula (a3-1-1) or the formula (a3-2-3) is more preferable.
When the resin (A) includes the structural unit (a3), the content is usually 5 to 70 mol%, preferably 10 to 65 mol%, based on all the structural units of the resin (A). More preferably, it is 10-60 mol%.

<Other structural units (t)>
The resin (A) may contain another structural unit (t) as a structural unit other than the structural unit (I), the structural unit (a2-2), the structural unit (a), and the structural unit (s). . Structural unit (
t) is a structural unit having a fluorine atom in addition to the structural unit (a2) and the structural unit (a3) (hereinafter sometimes referred to as “structural unit (a4)”) and a structural unit having a non-elimination hydrocarbon group. (S) (hereinafter sometimes referred to as “structural unit (a5)”), structural units well known in the art, and the like.

［式（ａ４−０）中、
Ｒ⁵は、水素原子又はメチル基を表す。
Ｌ⁴は、炭素数１〜４の脂肪族飽和炭化水素基を表す。
Ｌ³は、炭素数１〜８のペルフルオロアルカンジイル基を表す。
Ｒ⁶は、水素原子又はフッ素原子を表す。］ As the structural unit (a4), a structural unit represented by the formula (a4-0) (hereinafter “structural unit (a
4-0) ").

[In the formula (a4-0),
R ⁵ represents a hydrogen atom or a methyl group.
L ⁴ represents an aliphatic saturated hydrocarbon group having 1 to 4 carbon atoms.
L ³ represents a C 1-8 perfluoroalkanediyl group.
R ⁶ represents a hydrogen atom or a fluorine atom. ]

As the perfluoroalkanediyl group of L ³ , a difluoromethylene group, a perfluoroethylene group, a perfluoroethylfluoromethylene group, a perfluoropropane-1,3-
Diyl group, perfluoropropane-1,2-diyl group, perfluorobutane-1,4-diyl group, perfluoropentane-1,5-diyl group, perfluorohexane-1,6-diyl group, perfluoroheptane-1,7- Diyl group and perfluorooctane-1,8-
A diyl group is mentioned.

L ⁴ is preferably a methylene group or an ethylene group, and more preferably a methylene group.
L ³ is preferably a C 1-6 perfluoroalkanediyl group, more preferably a C 1-3 perfluoroalkanediyl group.

Examples of the structural unit (a4-0) include the structural units shown below and structural units in which a methyl group corresponding to R ⁵ in the following structural units is replaced with a hydrogen atom.

［式（ａ４−１）中、
Ｒ^a41は、水素原子又はメチル基を表す。
Ａ^a41は、置換基を有していてもよい炭素数１〜６のアルカンジイル基又は式（ａ−ｇ
１）で表される基を表す。

〔式（ａ−ｇ１）中、
ｓは０又は１を表す。
Ａ^a42及びＡ^a44は、それぞれ独立に、置換基を有していてもよい炭素数１〜５の脂肪族
炭化水素基を表す。
Ａ^a43は、置換基を有していてもよい炭素数１〜５の脂肪族炭化水素基又は単結合を表
す。
Ｘ^a41及びＸ^a42は、それぞれ独立に、−Ｏ−、−ＣＯ−、−ＣＯ−Ｏ−又は−Ｏ−ＣＯ
−を表す。
ただし、Ａ^a42、Ａ^a43、Ａ^a44、Ｘ^a41及びＸ^a42の炭素数の合計は７以下である。〕
Ｒ^a42は、置換基を有していてもよい炭素数１〜２０の炭化水素基を表し、該炭化水素
基に含まれる−ＣＨ₂−は、−Ｏ−又は−ＣＯ−に置き換わっていてもよい。ただし、Ａ^a
41及びＲ^a42のうち少なくとも一方は、置換基としてハロゲン原子を有する基である。］ As the structural unit (a4), a structural unit represented by formula (a4-1) can be given.

[In the formula (a4-1),
R ^a41 represents a hydrogen atom or a methyl group.
A ^a41 is an alkanediyl group having 1 to 6 carbon atoms which may have a substituent or a compound represented by the formula ( ^ag
The group represented by 1) is represented.

[In the formula (a-g1),
s represents 0 or 1.
A ^a42 and A ^a44 each independently represent an ^optionally substituted aliphatic hydrocarbon group having 1 to 5 carbon atoms.
A ^a43 represents an aliphatic hydrocarbon group having 1 to 5 carbon atoms which may have a substituent or a single bond.
X ^a41 and X ^a42 each independently represent —O—, ^—CO— , ^—CO —O— or —O—CO.
-Represents.
However, the total number of carbon atoms of A ^a42 , A ^a43 , A ^a44 , X ^a41 and X ^a42 is 7 or less. ]
R ^a42 represents an ^optionally substituted hydrocarbon group having 1 to 20 carbon atoms, and —CH ₂ — contained in the hydrocarbon group may be replaced by —O— or —CO—. Good. However, A ^a
At least one of ⁴¹ and R ^a42 is a group having a halogen atom as a substituent. ]

Examples of the halogen atom include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom.
Preferred is a fluorine atom.
The aliphatic hydrocarbon group may have a carbon-carbon unsaturated bond, but is preferably an aliphatic saturated hydrocarbon group. As the aliphatic saturated hydrocarbon group, an alkyl group (the alkyl group may be linear or branched) and an alicyclic hydrocarbon group, and an alkyl group and an alicyclic hydrocarbon group are combined. Examples thereof include aliphatic hydrocarbon groups that are formed.

芳香族炭化水素基としては、フェニル基、ナフチル基、アントリル基、ビフェニリル基
、フェナントリル基及びフルオレニル基が挙げられる。 ^Examples of the hydrocarbon group for R ^a42 include chain and cyclic aliphatic hydrocarbon groups, aromatic hydrocarbon groups,
And groups formed by combining them. Examples of the chain aliphatic hydrocarbon group include a methyl group, an ethyl group, an n-propyl group, an n-butyl group, an n-pentyl group,
n-hexyl group, n-heptyl group, n-octyl group, n-decyl group, n-dodecyl group, n
-Pentadecyl group, n-hexadecyl group, n-heptadecyl group and n-octadecyl group are mentioned. Examples of the cyclic aliphatic hydrocarbon group include a cyclopentyl group, a cyclohexyl group,
Cycloalkyl groups such as cycloheptyl group and cyclooctyl group; polycyclic alicyclic hydrocarbon groups such as decahydronaphthyl group, adamantyl group, norbornyl group and the following groups (* represents a bond) And cyclic alicyclic hydrocarbon groups.

Examples of the aromatic hydrocarbon group include a phenyl group, a naphthyl group, an anthryl group, a biphenylyl group, a phenanthryl group, and a fluorenyl group.

［式（ａ−ｇ３）中、
Ｘ^a43は、酸素原子、カルボニル基、カルボニルオキシ基又はオキシカルボニル基を表
す。
Ａ^a45は、少なくとも１つのハロゲン原子を有する炭素数３〜１７の脂肪族炭化水素基
を表す。
＊はカルボニル基との結合手を表す。］
Ｒ^a42が、式（ａ−ｇ３）で表される基を有する脂肪族炭化水素基である場合、式（ａ
−ｇ３）で表される基に含まれる炭素数を含めて、脂肪族炭化水素基の総炭素数は、１５
以下が好ましく、１２以下がより好ましい。式（ａ−ｇ３）で表される基を置換基として
有する場合、その数は１個が好ましい。 The hydrocarbon group for R ^a42 is preferably a chain or cyclic aliphatic hydrocarbon group or a group formed by a combination thereof, and may have a carbon-carbon unsaturated bond. And a cyclic aliphatic saturated hydrocarbon group and a group formed by combining these are more preferable.
As the aliphatic hydrocarbon group, an alkyl group and an alicyclic hydrocarbon group are preferable.
Examples of the alkyl group include methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, sec-butyl group, tert-butyl group, n-pentyl group, n-hexyl group, n
-An octyl group and 2-ethylhexyl group are mentioned.
The alicyclic hydrocarbon group may be monocyclic or polycyclic. Monocyclic alicyclic hydrocarbon groups include cyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohexyl group, methylcyclohexyl group, dimethylcyclohexyl group, cycloheptyl group,
Examples thereof include a cycloalkyl group such as a cyclooctyl group, a cycloheptyl group, and a cyclodecyl group. Examples of the polycyclic alicyclic hydrocarbon group include decahydronaphthyl group, adamantyl group, 2-
Examples thereof include an alkyladamantan-2-yl group, a 1- (adamantan-1-yl) alkane-1-yl group, a norbornyl group, a methylnorbornyl group, and an isobornyl group.
R ^a42 is preferably an aliphatic hydrocarbon group which may have a halogen atom, more preferably an alkyl group having a halogen atom and / or an aliphatic hydrocarbon group having a group represented by the formula (a-g3). .

[In the formula (a-g3),
X ^a43 represents an oxygen atom, a carbonyl group, a carbonyloxy group or an oxycarbonyl group.
A ^a45 represents a C ^3-17 aliphatic hydrocarbon group having at least one halogen atom.
* Represents a bond with a carbonyl group. ]
When R ^a42 is an aliphatic hydrocarbon group having a group represented by the formula (a-g3), the formula (a
-The carbon number of the aliphatic hydrocarbon group including the carbon number contained in the group represented by -g3) is 15
The following is preferable, and 12 or less is more preferable. When it has a group represented by the formula (a-g3) as a substituent, the number is preferably 1.

［式（ａ−ｇ２）中、
Ａ^a46は、ハロゲン原子を有していてもよい炭素数３〜１５の脂肪族炭化水素基を表す
。
Ｘ^a44は、カルボニルオキシ基又はオキシカルボニル基を表す。
Ａ^a47は、ハロゲン原子を有していてもよい炭素数３〜１５の脂肪族炭化水素基を表す
。
ただし、Ａ^a46、Ａ^a47及びＸ^a44の炭素数の合計は１８以下であり、Ａ^a46及びＡ^a47の
うち、少なくとも一方は、少なくとも１つのハロゲン原子を有する。
＊はカルボニル基との結合手を表す。］ The aliphatic hydrocarbon having a group represented by the formula (a-g3) is more preferably a formula (a-g
It is group represented by 2).

[In the formula (a-g2),
A ^a46 represents an aliphatic hydrocarbon group having 3 to 15 carbon atoms which may have a halogen atom.
X ^a44 represents a carbonyloxy group or an oxycarbonyl group.
A ^a47 represents an aliphatic hydrocarbon group having 3 to 15 carbon atoms which may have a halogen atom.
However, the total number of carbon atoms of A ^a46 , A ^a47, and X ^a44 is 18 or less, and at least one of A ^a46 and A ^a47 has at least one halogen atom.
* Represents a bond with a carbonyl group. ]

When R ^a42 is an aliphatic hydrocarbon group having a halogen atom, it is preferably an aliphatic hydrocarbon group having a fluorine atom, more preferably a perfluoroalkyl group or a perfluorocycloalkyl group, and still more preferably a carbon number. It is a 1-6 perfluoroalkyl group, Most preferably, it is a C1-C3 perfluoroalkyl group. Examples of the perfluoroalkyl group include a perfluoromethyl group, a perfluoroethyl group, a perfluoropropyl group, a perfluorobutyl group, a perfluoropentyl group, a perfluorohexyl group, a perfluoroheptyl group, and a perfluorooctyl group. Examples of the perfluorocycloalkyl group include a perfluorocyclohexyl group.

1-6 are preferable and, as for carbon number of the aliphatic hydrocarbon group of ^Aa46 , 1-3 are more preferable.
4-15 are preferable, as for carbon number of the aliphatic hydrocarbon group of ^Aa47 , 5-12 are more preferable,
A ^a47 is more preferably a cyclohexyl group or an adamantyl group.

* -A ^a46 -X ^a44 -A ^a47 Partial structure (* is a bond to a carbonyl group)
The more preferable structure of is the following structure.

^As the alkanediyl group of ^Aa41 , a methylene group, an ethylene group, a propane-1,3-diyl group, a butane-1,4-diyl group, a pentane-1,5-diyl group, hexane-1,6-
Linear alkanediyl group such as diyl group; propane-1,2-diyl group, butane-1,3-
Examples thereof include branched alkanediyl groups such as diyl group, 2-methylpropane-1,2-diyl group, 1-methylbutane-1,4-diyl group, and 2-methylbutane-1,4-diyl group.
^Examples of the substituent in the alkanediyl group of A ^a41 include a hydroxy group and an alkoxy group having 1 to 6 carbon atoms.
A ^a41 is preferably an alkanediyl group having 1 to 4 carbon atoms, more preferably an alkanediyl group having 2 to 4 carbon atoms, and still more preferably an ethylene group.

A group represented by the formula (a-g1) of A ^a41 (hereinafter referred to as “group (a-g1)” in some cases.
), A ^a44 is ^bonded to —O—CO—R ^a42 .
As the aliphatic hydrocarbon group for A ^a42 , A ^a43 and A ^{a44 in} the group (a-g1), a methylene group, an ethylene group, a propane-1,3-diyl group, a propane-1,2-diyl group, a butane- 1,4-diyl group, 1-methylpropane-1,3-diyl group, 2-methylpropane-1
, 3-diyl group, 2-methylpropane-1,2-diyl group and the like. Examples of these substituents include a hydroxy group and an alkoxy group having 1 to 6 carbon atoms.

^Examples of the group ( ^{ag1) in} which X ^a42 represents an oxygen atom, a carbonyl group, a carbonyloxy group or an oxycarbonyl group include the following groups. In the following examples, * and ** each represent a bond, and ** is a bond with —O—CO—R ^a42 .

［式（ａ４−２）中、
Ｒ^f1は、水素原子又はメチル基を表す。
Ａ^f1は、炭素数１〜６のアルカンジイル基を表す。
Ｒ^f2は、フッ素原子を有する炭素数１〜１０の炭化水素基を表す。］ As the structural unit represented by the formula (a4-1), structural units represented by the formula (a4-2) and the formula (a4-3) are preferable.

[In the formula (a4-2),
R ^f1 represents a hydrogen atom or a methyl group.
A ^f1 represents an alkanediyl group having 1 to 6 carbon atoms.
R ^f2 represents a C 1-10 hydrocarbon group having a fluorine atom. ]

As the alkanediyl group of A ^f1 , a methylene group, an ethylene group, a propane-1,3-diyl group, a propane-1,2-diyl group, a butane-1,4-diyl group, a pentane-1,5-diyl group , A straight-chain alkanediyl group such as hexane-1,6-diyl group; 1-methylpropane-1,3-diyl group, 2-methylpropane-1,3-diyl group, 2-methylpropane-1
, 2-diyl group, 1-methylbutane-1,4-diyl group, 2-methylbutane-1,4-diyl group and the like branched alkanediyl groups.

The hydrocarbon group of R ^f2 includes an aliphatic hydrocarbon group and an aromatic hydrocarbon group, and the aliphatic hydrocarbon group includes a chain, a cyclic group, and a group formed by a combination thereof. As the aliphatic hydrocarbon group, an alkyl group and an alicyclic hydrocarbon group are preferable.
Examples of the alkyl group include methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, sec-butyl group, tert-butyl group, n-pentyl group, n-hexyl group, n
-An octyl group and 2-ethylhexyl group are mentioned.
The alicyclic hydrocarbon group may be monocyclic or polycyclic. Monocyclic alicyclic hydrocarbon groups include cyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohexyl group, methylcyclohexyl group, dimethylcyclohexyl group, cycloheptyl group,
Examples thereof include a cycloalkyl group such as a cyclooctyl group, a cycloheptyl group, and a cyclodecyl group. Examples of the polycyclic alicyclic hydrocarbon group include decahydronaphthyl group, adamantyl group, 2-
Examples thereof include an alkyladamantan-2-yl group, a 1- (adamantan-1-yl) alkane-1-yl group, a norbornyl group, a methylnorbornyl group, and an isobornyl group.

Examples of the hydrocarbon group having a fluorine atom for R ^f2 include an alkyl group having a fluorine atom and an alicyclic hydrocarbon group having a fluorine atom.
Examples of the alkyl group having a fluorine atom include a difluoromethyl group, a trifluoromethyl group, a 1,1-difluoroethyl group, a 2,2-difluoroethyl group, a 2,2,2-trifluoroethyl group, a perfluoroethyl group, 1 , 1,2,2-tetrafluoropropyl group, 1,
1,2,2,3,3-hexafluoropropyl group, perfluoroethylmethyl group, 1- (
(Trifluoromethyl) -1,2,2,2-tetrafluoroethyl group, perfluoropropyl group, 1,1,2,2-tetrafluorobutyl group, 1,1,2,2,3,3-hexafluorobutyl 1,1,2,2,3,3,4,4-octafluorobutyl group, perfluorobutyl group, 1,1-bis (trifluoro) methyl-2,2,2-trifluoroethyl group, 2 -(Perfluoropropyl) ethyl group, 1,1,2,2,3,3,4,4-octafluoropentyl group, perfluoropentyl group, 1,1,2,2,3,3,4,4,5 , 5
-Decafluoropentyl group, 1,1-bis (trifluoromethyl) -2,2,3,3,3
-Pentafluoropropyl group, perfluoropentyl group, 2- (perfluorobutyl) ethyl group, 1,1,2,2,3,3,4,4,5,5-decafluorohexyl group, 1,1,
Fluorinated alkyl groups such as 2,2,3,3,4,5,5,6,6-dodecafluorohexyl group, perfluoropentylmethyl group, and perfluorohexyl group can be mentioned.
Examples of the alicyclic hydrocarbon group having a fluorine atom include fluorinated cycloalkyl groups such as a perfluorocyclohexyl group and a perfluoroadamantyl group.

A ^f1 in formula (a4-2) is preferably an alkanediyl group having 2 to 4 carbon atoms, and more preferably an ethylene group.
R ^f2 is preferably a fluorinated alkyl group having 1 to 6 carbon atoms.

［式（ａ４−３）中、
Ｒ^f11は、水素原子又はメチル基を表す。
Ａ^f11は、炭素数１〜６のアルカンジイル基を表す。
Ａ^f13は、フッ素原子を有していてもよい炭素数１〜１８の脂肪族炭化水素基を表す。
Ｘ^f12は、カルボニルオキシ基又はオキシカルボニル基を表す。
Ａ^f14は、フッ素原子を有していてもよい炭素数１〜１７の脂肪族炭化水素基を表す。
ただし、Ａ^f13及びＡ^f14の少なくとも１つは、フッ素原子を有する脂肪族炭化水素基を
表す。］

[In the formula (a4-3),
R ^f11 represents a hydrogen atom or a methyl group.
A ^f11 represents an alkanediyl group having 1 to 6 carbon atoms.
A ^f13 represents an aliphatic hydrocarbon group having 1 to 18 carbon atoms which may have a fluorine atom.
X ^f12 represents a carbonyloxy group or an oxycarbonyl group.
A ^f14 represents an aliphatic hydrocarbon group having 1 to 17 carbon atoms which may have a fluorine atom.
However, at least one of A ^f13 and A ^f14 represents an aliphatic hydrocarbon group having a fluorine atom. ]

^Examples of the alkanediyl group for A ^f11 include the same groups as the alkanediyl group for A ^f1 .

The aliphatic hydrocarbon group for A ^f13 includes chain and cyclic aliphatic hydrocarbon groups, and divalent aliphatic hydrocarbon groups formed by combining them. The aliphatic hydrocarbon may have a carbon-carbon unsaturated bond, but is preferably a saturated aliphatic hydrocarbon group.
The aliphatic hydrocarbon group which may have a fluorine atom of A ^f13 is preferably an aliphatic saturated hydrocarbon group which may have a fluorine atom, and more preferably a perfluoroalkanediyl group.
Examples of the divalent chain aliphatic hydrocarbon group which may have a fluorine atom include a methylene group,
Alkanediyl groups such as ethylene group, propanediyl group, butanediyl group and pentanediyl group; and perfluoroalkanediyl groups such as difluoromethylene group, perfluoroethylene group, perfluoropropanediyl group, perfluorobutanediyl group and perfluoropentanediyl group .
The divalent cyclic aliphatic hydrocarbon group which may have a fluorine atom may be either monocyclic or polycyclic. Examples of the monocyclic divalent aliphatic hydrocarbon group include a cyclohexanediyl group and a perfluorocyclohexanediyl group. Examples of the polycyclic divalent aliphatic hydrocarbon group include an adamantanediyl group, a norbornanediyl group, a perfluoroadamantanediyl group, and the like.

As the aliphatic hydrocarbon group for A ^f14 , one of chain and cyclic groups and an aliphatic hydrocarbon group formed by combining them are included. This aliphatic hydrocarbon
Although it may have a carbon-carbon unsaturated bond, it is preferably a saturated aliphatic hydrocarbon group.
The aliphatic hydrocarbon group which may have a fluorine atom of A ^f14 is preferably an aliphatic saturated hydrocarbon group which may have a fluorine atom.
Examples of the chain aliphatic hydrocarbon group which may have a fluorine atom include a trifluoromethyl group, a difluoromethyl group, a methyl group, a perfluoroethyl group, a 1,1,1-trifluoroethyl group, 1,1 , 2,2-tetrafluoroethyl group, ethyl group, perfluoropropyl group, 1,1,1,2,2-pentafluoropropyl group, propyl group, perfluorobutyl group, 1,1,2,2,3,3 , 4,4-octafluorobutyl group, butyl group, perfluoropentyl group, 1,1,1,2,2,3,3,4,4-nonafluoropentyl group, pentyl group, hexyl group, perfluorohexyl group, A heptyl group, a perfluoro heptyl group, an octyl group, a perfluorooctyl group, etc. are mentioned.
The cyclic aliphatic hydrocarbon group which may have a fluorine atom may be monocyclic or polycyclic. Examples of the group containing a monocyclic aliphatic hydrocarbon group include a cyclopropylmethyl group, a cyclopropyl group, a cyclobutylmethyl group, a cyclopentyl group, a cyclohexyl group, and a perfluorocyclohexyl group. Examples of the group containing a polycyclic aliphatic hydrocarbon group include an adamantyl group, an adamantylmethyl group, a norbornyl group, a norbornylmethyl group, a perfluoroadamantyl group, and a perfluoroadamantylmethyl group.

In the formula (a4-3), A ^f11 is an ethylene group is preferred.
The aliphatic hydrocarbon group for A ^f13 is preferably an aliphatic hydrocarbon group having 1 to 6 carbon atoms, and has 2 carbon atoms.
Even more preferred are ~ 3 aliphatic hydrocarbon groups.
The aliphatic hydrocarbon group for A ^f14 is preferably an aliphatic hydrocarbon group having 3 to 12 carbon atoms, and more preferably an aliphatic hydrocarbon group having 3 to 10 carbon atoms. Among them, A ^f14 is preferably a group containing an alicyclic hydrocarbon group having 3 to 12 carbon atoms, and more preferably a cyclopropylmethyl group, a cyclopentyl group, a cyclohexyl group, a norbornyl group, and an adamantyl group.

As a monomer for deriving the structural unit represented by formula (a4-2), formula (a4-1-1)
To a monomer represented by Formula (a4-1-22).

Examples of the monomer for deriving the structural unit represented by the formula (a4-3) include the formula (a4-1′-1).
) To monomers represented by formula (a4-1′-22).

［式（ａ４−４）中、
Ｒ^f21は、水素原子又はメチル基を表す。
Ａ^f21は、−（ＣＨ₂）_j1−、−（ＣＨ₂）_j2−Ｏ−（ＣＨ₂）_j3−又は−（ＣＨ₂）_j4−
ＣＯ−Ｏ−（ＣＨ₂）_j5−を表す。
ｊ１〜ｊ５は、それぞれ独立に、１〜６の整数を表す。
Ｒ^f22は、フッ素原子を有する炭素数１〜１０の炭化水素基を表す。］ Examples of the structural unit (a4) include a structural unit represented by the formula (a4-4).

[In the formula (a4-4),
R ^f21 represents a hydrogen atom or a methyl group.
A ^f21 represents — (CH ₂ ) _j1 —, — (CH ₂ ) _j2 —O— (CH ₂ ) _j3 — or — (CH ₂ ) _j4 —.
CO—O— (CH ₂ ) _j5 — is represented.
j1 to j5 each independently represents an integer of 1 to 6.
R ^f22 represents a C 1-10 hydrocarbon group having a fluorine atom. ]

^Examples of the hydrocarbon group having a fluorine atom of R ^f22 include the same hydrocarbon groups as R ^f2 in formula (a4-2). R ^f22 is preferably a ^C 1-10 alkyl group having a fluorine atom or a C 1-10 alicyclic hydrocarbon group having a fluorine atom, more preferably a C 1-10 alkyl group having a fluorine atom. Preferably, it has 1 to 6 carbon atoms having a fluorine atom
The alkyl group is more preferable.

In formula (a4-4), A ^f21 is preferably — (CH ₂ ) _j1 —, more preferably an ethylene group or a methylene group, and still more preferably a methylene group.

Examples of the monomer for deriving the structural unit represented by the formula (a4-4) include the following monomers.

When the resin (A1) has the structural unit (a4), the content is preferably from 1 to 20 mol%, more preferably from 2 to 15 mol%, based on all structural units of the resin (A1). -10
More preferred is mol%.

Examples of the non-leaving hydrocarbon group that the structural unit (a5) has include a linear, branched, or cyclic hydrocarbon group. Especially, it is preferable that a structural unit (a5) has an alicyclic hydrocarbon group. Examples of the structural unit (a5) include structural units represented by the following formulas (a5-1-1) to (a5-1-18).

When the resin (A) has the structural unit (a5), the content is preferably 1 to 30 mol%, more preferably 2 to 20 mol%, based on all structural units of the resin (A). More preferred is ˜15 mol%.

The resin (A) may have a structural unit other than the above. Examples of such structural units include structural units derived from carboxy group-containing monomers such as acrylic acid and methacrylic acid, structural units derived from styrene, structural units derived from alkoxystyrene, structural units derived from acyloxystyrene, and the like. It is done.

The structural unit derived from the alkoxystyrene is a structural unit in which the hydroxy group of the structural unit (a2-0) is substituted with an alkoxy group. Monomers that lead to the structural unit include methoxystyrene, ethoxystyrene, isopropoxystyrene, and tert-butoxystyrene.
The structural unit derived from the acyloxystyrene is a structural unit in which the hydroxy group of the structural unit (a2-0) is substituted with an acyloxy group. Examples of the monomer for deriving the structural unit include benzoyloxystyrene, acetyloxystyrene, and pivaloyloxystyrene.

When resin (A) contains another structural unit, the content rate is preferable 1-50 mol% with respect to all the structural units of resin (A), and 3-30 mol% is more preferable.

The resin (A) contains at least the structural unit (I) and the structural unit (a2-2), and is preferably a resin containing the structural unit (a) and the structural unit (s).
The structural unit (a) is preferably at least one of the structural unit (a1-1) and the structural unit (a1-2) (preferably the structural unit having a cyclohexyl group or a cyclopentyl group), more preferably the structural unit (a1- 1).
The structural unit (s) is preferably at least one of the structural unit (a2) and the structural unit (a3). The structural unit (a2) is preferably the structural unit (a2-1). Structural unit (a
3) is preferably at least one of the structural unit (a3-1) and the structural unit (a3-2).

The resin (A) preferably contains 15 mol% or more of structural units derived from the monomer having an adamantyl group (particularly the structural unit (a1-1)) with respect to the total structural units (a). When the content of the structural unit having an adamantyl group is large, the dry etching resistance of the resist pattern is improved.

Each structural unit constituting the resin (A) may be used alone or in combination of two or more, and is produced by a known polymerization method (for example, radical polymerization method) using a monomer that derives these structural units. can do.
The weight average molecular weight of the resin (A) is preferably 2,500 or more (more preferably 3,0
00 or more, more preferably 4,000 or more), 50,000 or less (more preferably 30)
15,000 or less, more preferably 15,000 or less).

<Resist composition>
The resist composition of the present invention contains a resin (A), may further contain a resin other than the resin (A), and is a known acid generator (hereinafter referred to as “acid generator (B)” in the resist field. May be included).
The resist composition of the present invention preferably contains a basic compound (hereinafter sometimes referred to as “basic compound (C)”) and contains a solvent (hereinafter sometimes referred to as “solvent (E)”). It is preferable.
The resist composition of the present invention preferably further contains a salt with weak acidity such as a weak acid inner salt (hereinafter sometimes referred to as “weak acid inner salt (D)”).

<Resin (A)>
In the resist composition of the present invention, the content of the resin (A) is preferably 80% by mass or more and 99.9% by mass or less in the solid content of the resist composition. In the present specification, the “solid content of the composition” means the total of the components of the resist composition excluding the solvent (E) described later from the resist composition of the present invention. The solid content and the content of the resin (A) relative thereto can be measured by a known analysis means such as liquid chromatography or gas chromatography.

<Resin other than resin (A)>
The resist composition of the present invention may contain a resin other than the resin (A) described above. Such a resin may be any resin that does not have the structural unit (I) and the structural unit (a2-2). For example, the structural unit derived from the monomer (a) having the acid labile group described above, It may contain a resin having at least one selected from a structural unit derived from an acid-stable monomer and a structural unit derived from a known monomer used in the field, or may be a structural unit (a) and a structural unit (s ) (Hereinafter sometimes referred to as “resin (A1)”), a resin having a structural unit (a4) (hereinafter sometimes referred to as “resin (X)”), and a structural unit (s).
You may contain resin which consists only of.

As the resin other than the resin (A), the resin (A1) is preferable. In the resin (A1), the content of the structural unit (a) is preferably 1 to 80 mol%, more preferably 1 to 75 mol%, and more preferably 3 to 70 mol% with respect to all the structural units of the resin (A1). Is more preferable.
The structural unit (a) in the resin (A1) is preferably the structural unit (a1-1) and the structural unit (a1-2) (preferably the structural unit having a cyclohexyl group or a cyclopentyl group).
Is at least one kind.
The structural unit (s) in the resin (A1) is preferably the structural unit (a2) and the structural unit (
It is at least one of a3). The structural unit (a2) is preferably a structural unit represented by the formula (a2-1). The structural unit (a3) is preferably at least one of a structural unit represented by the formula (a3-1) and a structural unit represented by the formula (a3-2).
The weight average molecular weight of the resin (A1) is preferably 2,500 or more (more preferably 3,
000 or more, more preferably 4,000 or more), 50,000 or less (more preferably 3
Or less, more preferably 15,000 or less.

As the resin other than the resin (A), the resin (X) is also preferable. In the resin (X), the content of the structural unit (a4) is preferably 40 mol% or more based on the total structural units of the resin (X).
45 mol% or more is more preferable, and 50 mol% or more is further more preferable.
Examples of the structural unit that the resin (X) may further include a structural unit derived from the structural unit (a2), the structural unit (a3), and other known monomers.
The weight average molecular weight of the resin (X) is preferably 8,000 or more (more preferably 10,
000 or more), 80,000 or less (more preferably 60,000 or less). The means for measuring the weight average molecular weight of the resin (X) is the same as that for the resin (A).
When the resist composition of this invention contains resin other than resin (A), these content rates are 0.1-50 mass% normally with respect to the total amount of resin (A), Preferably it is 0. It is 5-30 mass%, More preferably, it is 1-20 mass%.

<Acid generator (B)>
As the acid generator (B), a known acid generator can be used, and it may be a nonionic acid generator or an ionic acid generator. Preferably, it is an ionic acid generator. Examples of the ionic acid generator include an ionic acid generator composed of a combination of a known cation and a known anion.
Nonionic acid generators include organic halides and sulfonate esters (for example, 2
-Nitrobenzyl ester, aromatic sulfonate, oxime sulfonate, N-sulfonyloxyimide, N-sulfonyloxyimide, sulfonyloxyketone, diazonaphthoquinone 4-sulfonate), and sulfones (eg, disulfone, ketosulfone, sulfonyldiazomethane). . Examples of the ionic acid generator include onium salts containing onium cations (for example, diazonium salts, phosphonium salts, sulfonium salts, iodonium salts) and the like. Examples of the anion of the onium salt include a sulfonate anion, a sulfonylimide anion, and a sulfonylmethide anion.
The acid generator (B) is preferably an acid generator that generates sulfonic acid or an acid generator that does not have a fluorine atom.
The acid generator (B) is more preferably an acid generator that generates a sulfonic acid having no fluorine atom.

As the acid generator (B), JP-A 63-26653, JP-A 55-164824,
JP-A-62-269263, JP-A-63-146038, JP-A-63-163452, JP-A-62-153853, JP-A-63-146029, US Pat. No. 3,779,
No. 778, U.S. Pat. No. 3,849,137, German Patent No. 3914407, European Patent No. 126,712, and the like can be used.

The acid generated from the acid generator is preferably a sulfonic acid, more preferably a sulfonic acid containing no fluorine atom.
Two or more acid generators (B) may be used. When the acid generator (B) includes an acid generator that generates a sulfonic acid containing no fluorine atom, the content of the acid generator is determined by the acid generator (B).
The total amount is preferably 50% by mass or more, more preferably 60% by mass or more, and still more preferably 90% by mass or more.

式（Ｂ１）中、
Ｒ^b1及びＲ^b2は、互いに独立に、炭素数１〜１０の炭化水素基を表す。 Nonionic acid generators that generate sulfonic acids that do not contain fluorine atoms include those represented by the formula (B
The compound represented by 1) is preferred.

In formula (B1),
R ^b1 and R ^b2 each independently represent a hydrocarbon group having 1 to 10 carbon atoms.

Examples of the hydrocarbon group in R ^b1 and R ^b2 include an alkyl group, an alicyclic hydrocarbon group, an aromatic hydrocarbon group, and a group obtained by combining them. Examples of the alkyl group include a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, a hexyl group, a heptyl group, and an octyl group.
The alicyclic hydrocarbon group may be monocyclic or polycyclic. Examples of the monocyclic alicyclic hydrocarbon group include cycloalkyl groups such as a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, and a cyclooctyl group. Examples of the polycyclic alicyclic hydrocarbon group include an adamantyl group and a norbornyl group.
Aromatic hydrocarbon groups include phenyl, naphthyl, p-methylphenyl, pt
ert-butylphenyl group, tolyl group, xylyl group, cumenyl group, mesityl group, 2,6-
Examples thereof include an aryl group such as a diethylphenyl group and 2-methyl-6-ethylphenyl.
Examples of the group in which an alkyl group and an alicyclic hydrocarbon group are combined include a methylcyclohexyl group, a dimethylcyclohexyl group, a methylnorbornyl group, and an isobornyl group.
Examples of the group in which an alkyl group and an aromatic hydrocarbon group are combined include a benzyl group, a phenethyl group, a phenylpropyl group, a naphthylmethyl group, and a naphthylethyl group.
R ^b1 and R ^b2 are preferably a butyl group, a cyclohexyl group, a methylcyclohexyl group, and a butylcyclohexyl group.
R ^b1 and R ^b2 are preferably the same group.

Specific examples of the compound represented by the formula (B1) include the following compounds.

式（Ｂ２）中、
Ｒ^b3は、炭素数１〜２４の炭化水素基を表し、該炭化水素基に含まれる水素原子は、ヒ
ドロキシ基又はカルボキシ基に置換されていてもよく、該炭化水素基に含まれるメチレン
基は、酸素原子又はカルボニル基に置き換わっていてもよい。
Ａ^＋は有機カチオンを表す。 As an ionic acid generator that generates a sulfonic acid that does not contain a fluorine atom, formula (B2)
The salt represented by these is preferable.

In formula (B2),
R ^b3 represents a hydrocarbon group having 1 to 24 carbon atoms, the hydrogen atom contained in the hydrocarbon group may be substituted with a hydroxy group or a carboxy group, and the methylene group contained in the hydrocarbon group is , Oxygen atom or carbonyl group may be substituted.
A ⁺ represents an organic cation.

The hydrocarbon group of R ^b3 is an aliphatic hydrocarbon group having 1 to 24 carbon atoms, an alicyclic hydrocarbon group having 3 to 24 carbon atoms, an aromatic hydrocarbon group having 6 to 24 carbon atoms, or a combination of these. It is a group of formula 24 or less.
Aliphatic hydrocarbon groups include methyl, ethyl, propyl, isopropyl, butyl, pentyl, hexyl, heptyl, octyl, decyl, dodecyl, hexadecyl, pentadecyl, hexyldecyl And alkyl groups such as a heptadecyl group, an octadecyl group and an icosyl group.
As the alicyclic hydrocarbon group, a cyclopropyl group, a cyclobutyl group, a cyclopentyl group,
Monocyclic alicyclic hydrocarbon groups such as cyclohexyl group, cycloheptyl group, cyclooctyl group, and cyclodecyl group; polycyclic alicyclic hydrocarbons such as bicyclo [2.2.1] heptyl group and adamantyl group Groups.
Aromatic hydrocarbon groups include phenyl, naphthyl, anthryl, p-methylphenyl, p-tert-butylphenyl, p-adamantylphenyl, tolyl, xylyl, cumenyl, biphenyl, phenanthryl Group, 2,6-diethylphenyl group, 2-methyl-6-ethylphenyl group, 2,4,6-trimethylphenyl group, 2,4,6
-An aryl group such as a triisopropylphenyl group.
Examples of the group obtained by combining an aliphatic hydrocarbon group and an alicyclic hydrocarbon group include a methylcyclohexyl group, a dimethylcyclohexyl group, a methylnorbornyl group, and an isobornyl group.
Examples of the group obtained by combining an aliphatic hydrocarbon group and an aromatic hydrocarbon group include a benzyl group, a phenethyl group, a phenylpropyl group, a naphthylmethyl group, and a naphthylethyl group.

Examples of the group in which the hydrogen atom contained in the hydrocarbon group is substituted with a hydroxy group or a carboxy group include the following groups. * Represents a bond with SO ₃ ^— .

Examples of the group in which the methylene group contained in the hydrocarbon group is replaced with an oxygen atom or a carbonyl group include the following groups. * Represents a bond with SO ₃ ^— .

式（Ｂ３）中、
Ｒ^b30は、ヒドロキシ基、カルボキシ基又は炭素数１〜８の炭化水素基を表し、該炭化
水素基に含まれるメチレン基は、酸素原子又はカルボニル基に置き換わっていてもよい。
ｍｘは、０〜５の整数を表す。ｍｘが２以上のとき、複数のＲ^b30は同一又は相異なり
、さらに複数のＲ^b30が炭素数１〜８の炭化水素基を表す場合、その合計炭素数は１８以
下である。
＊は、ＳＯ₃ ⁻との結合手を表す。 R ^b3 is preferably an aromatic hydrocarbon group having 6 to 24 carbon atoms or an alicyclic hydrocarbon group having 3 to 24 carbon atoms, and the hydrogen atom contained in the aromatic hydrocarbon group is a hydroxy group or a carboxy group. The methylene group contained in the aromatic hydrocarbon group and the alicyclic hydrocarbon group may be replaced with an oxygen atom or a carbonyl group.
R ^b3 is more preferably a group represented by the formula (B3).

In formula (B3),
R ^b30 represents a hydroxy group, a carboxy group, or a hydrocarbon group having 1 to 8 carbon atoms, and the methylene group contained in the hydrocarbon group may be replaced with an oxygen atom or a carbonyl group.
mx represents an integer of 0 to 5. When mx is 2 or more, the plurality of R ^b30 are the same or different, and when the plurality of R ^b30 represent a hydrocarbon group having 1 to 8 carbon atoms, the total carbon number is 18 or less.
* Represents a bond with SO ₃ ^— .

Examples of the hydrocarbon group having 1 to 8 carbon atoms in R ^b30 include an aliphatic hydrocarbon group having 1 to 8 carbon atoms, an alicyclic hydrocarbon group having 3 to 8 carbon atoms, and an aromatic hydrocarbon having 6 to 8 carbon atoms. And groups having 8 or less carbon atoms in combination with these groups. Preferably, it is a C1-C8 aliphatic hydrocarbon group. Specifically, the same thing as ^Rb1 is mentioned.
R ^b30 is preferably a hydroxy group, a carboxy group or an aliphatic hydrocarbon group having 1 to 8 carbon atoms, and the methylene group contained in the hydrocarbon group may be replaced by an oxygen atom or a carbonyl group, More preferably, it is a C1-C8 aliphatic hydrocarbon group.
mx is preferably an integer of 0 to 3.
When mx is 2 or more, the plurality of R ^b30 are preferably the same group.

The group represented by the formula (B3) is preferably a phenyl group, a 2,4,6-trimethylphenyl group or a 2,4,6-triisopropylphenyl group.

As the sulfonate anion of the formula (B2), the formula (B2-a-1) to the formula (B2-a-19)
And an anion represented by any one of the formulas (B2-a-8) to (B)
2-a-16), and more preferably an anion represented by the formula (B2-a-
8) to an anion represented by any one of the formulas (B2-a-11), (B2-a-15) and (B2-a-16).

A ⁺ is preferably a cation represented by any one of formulas (b2-1) to (b2-4).

In formula (b2-1) to formula (b2-4),
R ^b4 , R ^b5 and R ^b6 are each independently an alkyl group having 1 to 30 carbon atoms, 3 to 18 carbon atoms,
The alicyclic hydrocarbon group or the aromatic hydrocarbon group having 6 to 36 carbon atoms, or R ^b4 and R ^b5 together with a sulfur atom containing a 3-membered ring to a 12-membered ring (preferably a 3-membered ring) Ring to 7-membered ring).
The hydrogen atom contained in the alkyl group is substituted with a hydroxy group, an alkoxy group having 1 to 12 carbon atoms, an alicyclic saturated hydrocarbon group having 3 to 12 carbon atoms, or an aromatic hydrocarbon group having 6 to 18 carbon atoms. The hydrogen atom contained in the alicyclic hydrocarbon group may be a halogen atom or a carbon number of 1 to 1.
8 may be substituted with an alkyl group, an acyl group having 2 to 4 carbon atoms, or a glycidyloxy group, and the hydrogen atom contained in the aromatic hydrocarbon group may be a halogen atom, a hydroxy group, or a carbon atom having 1 to 12 carbon atoms. It may be substituted with an alkoxy group.
R ^b7 and R ^b8 each independently represent a hydroxy group, an alkyl group having 1 to 12 carbon atoms, or an alkoxy group having 1 to 12 carbon atoms.
m2 and n2 represent the integer of 0-5 independently of each other. When m2 is 2 or more, a plurality of R
^b7 is the same or different, and when n2 is 2 or more, a plurality of ^Rb8 are the same or different.
R ^b9 and R ^b10 each independently represent an alkyl group having 1 to 18 carbon atoms or an alicyclic hydrocarbon group having 3 to 18 carbon atoms, or R ^b9 and R ^b10 are They are bonded to each other together with the sulfur atom to be bonded to form a 3- to 12-membered ring (preferably a 3- to 7-membered ring). The methylene group contained in the ring may be replaced with an oxygen atom, a sulfur atom or a carbonyl group.
R ^b11 represents a hydrogen atom, an alkyl group having 1 to 18 carbon atoms, an alicyclic hydrocarbon group having 3 to 18 carbon atoms, or an aromatic hydrocarbon group having 6 to 18 carbon atoms.
R ^b12 represents an alkyl group having 1 to 12 carbon atoms, an alicyclic hydrocarbon group having 3 to 18 carbon atoms, or an aromatic hydrocarbon group having 6 to 18 carbon atoms. The hydrogen atom contained in the alkyl group has 6 carbon atoms.
The hydrogen atom contained in the aromatic hydrocarbon group which may be substituted with -18 aromatic hydrocarbon groups is substituted with an alkoxy group having 1 to 12 carbon atoms or an alkylcarbonyloxy group having 1 to 12 carbon atoms. May be.
R ^b11 and R ^b12 together with —CH—CO—, to which they are bonded, are 3-membered rings to 12
A member ring (preferably a 3-membered ring to a 7-membered ring) may be formed, and a methylene group contained in the ring may be replaced with an oxygen atom, a sulfur atom or a carbonyl group.
R ^{b13 to} R ^b18 each independently represent a hydroxy group, an alkyl group having 1 to 12 carbon atoms, or an alkoxy group having 1 to 12 carbon atoms.
L ^b11 represents an oxygen atom or a sulfur atom.
o2, p2, s2, and t2 each independently represent an integer of 0 to 5.
q2 and r2 each independently represents an integer of 0 to 4.
u2 represents 0 or 1.
When o2 is 2 or more, multiple R ^b13 are the same or different, when p2 is 2 or more, multiple R ^b14 are the same or different, and when q2 is 2 or more, multiple R ^b15 are the same or different , R2
When is 2 or more, plural R ^b16 same or different, when s2 is 2 or more, plural R ^b17 same or different, when t2 is 2 or more, plural R ^b18 same or different.

特に、Ｒ^b9〜Ｒ^b11の脂環式炭化水素基は、好ましくは炭素数３〜１８、より好ましく
は炭素数４〜１２である。 Examples of the alkyl group include methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, sec-butyl group, tert-butyl group, pentyl group, hexyl group, octyl group and 2-ethylhexyl group. . The alkyl group of R ^{b9 to} R ^b12 preferably has 1 to 12 carbon atoms.
Examples of the alkyl group in which a hydrogen atom is substituted with an alicyclic hydrocarbon group include 1- (adamantane-
1-yl) alkane-1-yl group and the like.
The alicyclic hydrocarbon group may be monocyclic or polycyclic, and the hydrogen atom contained in the alicyclic hydrocarbon group may be substituted with an alkyl group. In this case, the carbon number of the alicyclic hydrocarbon group is 20 or less including the carbon number of the alkyl group. Examples of the monocyclic alicyclic hydrocarbon group include cycloalkyl groups such as a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclooctyl group, and a cyclodecyl group. Examples of the polycyclic alicyclic hydrocarbon group include decahydronaphthyl group, adamantyl group, norbornyl group, and the following groups.

In particular, the alicyclic hydrocarbon group of R ^{b9 to} R ^b11 preferably has 3 to 18 carbon atoms, more preferably 4 to 12 carbon atoms.

Examples of the alicyclic hydrocarbon group in which a hydrogen atom is substituted with an alkyl group include a methylcyclohexyl group, a dimethylcyclohexyl group, a 2-alkyladamantan-2-yl group, a methylnorbornyl group, and an isobornyl group. Can be mentioned. In the alicyclic hydrocarbon group in which the hydrogen atom is substituted with an alkyl group, the total number of carbon atoms of the monovalent alicyclic hydrocarbon group and the monovalent aliphatic hydrocarbon group is preferably 20 or less.

Examples of the aromatic hydrocarbon group include phenyl group, tolyl group, xylyl group, cumenyl group, mesityl group, 4-ethylphenyl group, 4-tert-butylphenyl group, 4-cyclohexylphenyl group, 4-adamantyl group. Substituted or unsubstituted phenyl groups such as phenyl group, 2,6-diethylphenyl group, 2-methyl-6-ethylphenyl group; biphenylyl group, naphthyl group, phenanthryl group and the like.
Examples of the aromatic hydrocarbon group in which a hydrogen atom is substituted with an alkoxy group include a 4-methoxyphenyl group.
Examples of the alkyl group in which a hydrogen atom is substituted with an aromatic hydrocarbon group, that is, an aralkyl group, include a benzyl group, a phenethyl group, a phenylpropyl group, a trityl group, a naphthylmethyl group, and a naphthylethyl group.
In addition, when an alkyl group or an alicyclic hydrocarbon group is contained in an aromatic hydrocarbon group, a C1-C12 alkyl group and a C3-C18 alicyclic hydrocarbon group are preferable.

Examples of the alkoxy group include methoxy group, ethoxy group, propoxy group, butoxy group, pentyloxy group, hexyloxy group, heptyloxy group, octyloxy group, decyloxy group and dodecyloxy group.
Examples of the acyl group include an acetyl group, a propionyl group, and a butyryl group.
Examples of the halogen atom include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom.
Examples of the alkylcarbonyloxy group include a methylcarbonyloxy group, an ethylcarbonyloxy group, an n-propylcarbonyloxy group, an isopropylcarbonyloxy group, an n-butylcarbonyloxy group, a sec-butylcarbonyloxy group, a tert-butylcarbonyloxy group, Examples include a pentylcarbonyloxy group, a hexylcarbonyloxy group, an octylcarbonyloxy group, and a 2-ethylhexylcarbonyloxy group.

The ring containing a sulfur atom which may be formed by combining R ^b4 and R ^b5 is any of monocyclic, polycyclic, aromatic, non-aromatic, saturated and unsaturated rings. There may be 1 sulfur atom
As long as it contains the above, it may further contain one or more oxygen atoms. The ring is preferably a ring having 3 to 18 carbon atoms, more preferably a ring having 4 to 18 carbon atoms, and examples thereof include the following rings.

The hydrocarbon groups for R ^b4 , R ^b5 and R ^b6 are preferably independently of each other having 1 to 3 carbon atoms.
An alkyl group having 0, an alicyclic hydrocarbon group having 3 to 18 carbon atoms, or an aromatic hydrocarbon group having 6 to 18 carbon atoms, and the hydrogen atom contained in the alkyl group includes a hydroxy group and 1 to 12 carbon atoms. And the hydrogen atom contained in the alicyclic hydrocarbon group may be a halogen atom, an acyl group having 2 to 4 carbon atoms, or glycidyl. The aromatic hydrocarbon group may be substituted with an oxy group, and the aromatic hydrocarbon group may be substituted with a halogen atom, a hydroxy group, or an alkoxy group having 1 to 12 carbon atoms.

Examples of the ring formed together with the sulfur atom to which R ^b9 and R ^b10 are bonded include a thiolane-1-ium ring (tetrahydrothiophenium ring), a thian-1-ium ring, and a 1,4-oxathian-4-ium ring. Is mentioned.
Examples of the ring formed with —CH—CO— in which R ^b11 and R ^b12 are bonded include an oxocycloheptane ring, an oxocyclohexane ring, an oxonorbornane ring, and an oxoadamantane ring.

Examples of cations represented by formula (b2-1) to formula (b2-4) include, for example, JP-A-20102010.
-204646 is mentioned.

Preferred examples of the salt represented by the formula (B2) include the following compounds.

The acid generator (B) is preferably an acid generator containing a compound represented by the formula (B1) and a salt represented by the formula (B2). The content ratio of the compound represented by the formula (B1) and the salt represented by the formula (B2) is based on mass, preferably represented by the compound represented by the formula (B1): Formula (B2). Compound = 50: 50 to 95: 5, more preferably 60:40 to 90:10.

<Solvent (E)>
The content of the solvent (E) is 90% by mass or more, preferably 92% by mass or more, more preferably 94% by mass or more, and 99.9% by mass or less, preferably 99% by mass or less in the resist composition. . The content rate of a solvent (E) can be measured by well-known analysis means, such as a liquid chromatography or a gas chromatography, for example.

Solvents (E) include glycol ether esters such as ethyl cellosolve acetate, methyl cellosolve acetate and propylene glycol monomethyl ether acetate; glycol ethers such as propylene glycol monomethyl ether; ethyl lactate, butyl acetate, amyl acetate and pyruvic acid Esters such as ethyl; ketones such as acetone, methyl isobutyl ketone, 2-heptanone and cyclohexanone; cyclic esters such as γ-butyrolactone; A solvent (E) may contain 1 type independently, and may contain 2 or more types.

<Basic compound (C)>
Examples of the basic compound (C) include a salt having a lower acidity than an acid generated from a basic nitrogen-containing organic compound or an acid generator (B).
Examples of the basic nitrogen-containing organic compound include amines and ammonium salts. Examples of amines include aliphatic amines and aromatic amines. Aliphatic amines include primary amines, secondary amines and tertiary amines.

The basic compound (C) includes 1-naphthylamine, 2-naphthylamine, aniline,
Diisopropylaniline, 2-, 3- or 4-methylaniline, 4-nitroaniline, N
-Methylaniline, N, N-dimethylaniline, diphenylamine, hexylamine, heptylamine, octylamine, nonylamine, decylamine, dibutylamine, dipentylamine, dihexylamine, diheptylamine, dioctylamine, dinonylamine, didecylamine, triethylamine, trimethylamine, Tripropylamine, tributylamine, tripentylamine, trihexylamine, triheptylamine, trioctylamine, trinonylamine, tridecylamine, methyldibutylamine, methyldipentylamine, methyldihexylamine, methyldicyclohexylamine, methyldiheptyl Amine, methyl dioctyl amine, methyl dinonyl amine, methyl didecyl amine,
Ethyldibutylamine, ethyldipentylamine, ethyldihexylamine, ethyldiheptylamine, ethyldioctylamine, ethyldinonylamine, ethyldidecylamine, dicyclohexylmethylamine, tris [2- (2-methoxyethoxy) ethyl] amine, tri Isopropanolamine, ethylenediamine, tetramethylenediamine, hexamethylenediamine, 4,4′-diamino-1,2-diphenylethane, 4,4′-diamino-3,3′-dimethyldiphenylmethane, 4,4′-diamino-3 , 3′-diethyldiphenylmethane, 2,2′-methylenebisaniline, imidazole, 4-methylimidazole, pyridine, 4-methylpyridine, 1,2-di (2-pyridyl) ethane, 1,2-di (4- Pyridyl) ethane, 1,2-di 2-pyridyl) ethene, 1,2-di (4-pyridyl) ethene, 1,3-di (4-pyridyl) propane, 1,2-di (4-pyridyloxy)
Examples include ethane, di (2-pyridyl) ketone, 4,4′-dipyridyl sulfide, 4,4′-dipyridyl disulfide, 2,2′-dipyridylamine, 2,2′-dipicolylamine, bipyridine, and the like. Includes diisopropylaniline, particularly preferably 2
, 6-diisopropylaniline.

As ammonium salts, tetramethylammonium hydroxide, tetraisopropylammonium hydroxide, tetrabutylammonium hydroxide, tetrahexylammonium hydroxide, tetraoctylammonium hydroxide, phenyltrimethylammonium hydroxide, 3- (trifluoromethyl) phenyltrimethyl Ammonium hydroxide, tetra-n-butylammonium salicylate, choline and the like can be mentioned.

<Slightly acidic salt>
The acidity in the salt having a lower acidity than the acid generated from the acid generator (B) is the acid dissociation constant (p
Ka). The salt having a lower acidity than the acid generated from the acid generator (B) is a salt in which the acid dissociation constant of the acid generated from the salt is usually -3 <pKa, preferably -1 <pKa <7. A salt, more preferably a salt of 0 <pKa <5.
As the salt having a lower acidity than the acid generated from the acid generator (B), a salt represented by the following formula,
Weak acid inner salt represented by formula (D), JP 2012-229206 A, JP 20
Examples thereof include salts described in JP-A Nos. 12-6908, 2012-72109, 2011-39502, and 2011-191745.

［式（Ｄ）中、
Ｒ^D1及びＲ^D2は、それぞれ独立に、炭素数１〜１２の１価の炭化水素基、炭素数１〜６
のアルコキシ基、炭素数２〜７のアシル基、炭素数２〜７のアシルオキシ基、炭素数２〜
７のアルコキシカルボニル基、ニトロ基又はハロゲン原子を表す。
ｍ’及びｎ’は、それぞれ独立に、０〜４の整数を表し、ｍ’が２以上の場合、複数の
Ｒ^D1は同一又は相異なり、ｎ’が２以上の場合、複数のＲ^D2は同一又は相異なる。］ <Weak acid inner salt (D)>
The weak acid inner salt (D) is a compound represented by the formula (D).

[In the formula (D),
R ^D1 and R ^D2 each independently represent a monovalent hydrocarbon group having 1 to 12 carbon atoms, or 1 to 6 carbon atoms.
An alkoxy group having 2 to 7 carbon atoms, an acyloxy group having 2 to 7 carbon atoms, and 2 to 2 carbon atoms.
7 represents an alkoxycarbonyl group, a nitro group, or a halogen atom.
m ′ and n ′ each independently represents an integer of 0 to 4, and when m ′ is 2 or more, the plurality of R ^D1 are the same or different, and when n ′ is 2 or more, the plurality of R ^D2 are Same or different. ]

Examples of the hydrocarbon group represented by R ^D1 and R ^D2 in the compound represented by the formula (D) include a monovalent aliphatic hydrocarbon group, a monovalent alicyclic hydrocarbon group, a monovalent aromatic hydrocarbon group, and Examples include groups formed by combining these.
Examples of the monovalent aliphatic hydrocarbon group include alkyl groups such as methyl group, ethyl group, propyl group, isopropyl group, butyl group, isobutyl group, t-butyl group, pentyl group, hexyl group, and nonyl group.
The monovalent alicyclic hydrocarbon group may be monocyclic or polycyclic, and may be either saturated or unsaturated. For example, cyclopropyl group, cyclobutyl group, cyclopentyl group,
Examples thereof include a cycloalkyl group such as a cyclohexyl group, a cyclononyl group, and a cyclododecyl group, a norbornyl group, an adamantyl group, and the like.
Monovalent aromatic hydrocarbon groups include phenyl, 1-naphthyl, 2-naphthyl, and 2
-Methylphenyl group, 3-methylphenyl group, 4-methylphenyl group, 4-ethylphenyl group, 4-propylphenyl group, 4-isopropylphenyl group, 4-butylphenyl group,
4-t-butylphenyl group, 4-hexylphenyl group, 4-cyclohexylphenyl group,
Anthryl group, p-adamantylphenyl group, tolyl group, xylyl group, cumenyl group, mesityl group, biphenyl group, phenanthryl group, 2,6-diethylphenyl group, 2-methyl-
Examples include aryl groups such as 6-ethylphenyl.
Examples of the group formed by combining these include an alkyl-cycloalkyl group, a cycloalkyl-alkyl group, an aralkyl group (for example, phenylmethyl group, 1-phenylethyl group, 2-phenylethyl group, 1-phenyl-1 -Propyl group, 1-phenyl-2
-Propyl group, 2-phenyl-2-propyl group, 3-phenyl-1-propyl group, 4-phenyl-1-butyl group, 5-phenyl-1-pentyl group, 6-phenyl-1-hexyl group, etc.) Etc.

Examples of the alkoxy group include a methoxy group and an ethoxy group.
Examples of the acyl group include an acetyl group, a propanoyl group, a benzoyl group, and a cyclohexanecarbonyl group.
Examples of the acyloxy group include a group in which an oxy group (—O—) is bonded to the acyl group.
Examples of the alkoxycarbonyl group include a group in which a carbonyl group (—CO—) is bonded to the above alkoxy group.
Examples of the halogen atom include a fluorine atom, a chlorine atom, and a bromine atom.

In the formula (D), R ^D1 and R ^D2 are each independently an alkyl group having 1 to 8 carbon atoms,
A cycloalkyl group having 3 to 10 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, an acyl group having 2 to 4 carbon atoms, an acyloxy group having 2 to 4 carbon atoms, an alkoxycarbonyl group having 2 to 4 carbon atoms, a nitro group, or A halogen atom is preferred.
m ′ and n ′ are each independently preferably an integer of 0 to 2, and more preferably 0. m '
Is 2 or more, the plurality of R ^D1 are the same or different, and when n ′ is 2 or more, the plurality of R ^D2 are the same or different.

Examples of the weak acid inner salt (D) include the following compounds.

The weak acid inner salt (D) can be produced by the method described in “Tetrahedron Vol. 45, No. 19, p6281-6296”. A commercially available compound can be used as the weak acid inner salt (D).

The content of the weak acid salt, particularly the weak acid intramolecular salt (D), is preferably 0.01 to 5% by mass, more preferably 0.01 to 3% by mass in the solid content of the resist composition. is there.

<Other ingredients>
The resist composition of the present invention may contain other components (hereinafter sometimes referred to as “other components (F)”) other than the above-described components, if necessary. The other component (F) is not particularly limited, and additives known in the resist field, such as sensitizers, dissolution inhibitors, surfactants, stabilizers, dyes, and the like can be used.

<Preparation of resist composition>
The resist composition of the present invention comprises a resin (A) and an acid generator (B) of the present invention, and, if necessary, a solvent (E), a basic compound (C), a resin (X), a salt with low acidity In particular, it can be prepared by mixing the weak acid inner salt (D) and the other component (F). The mixing order is arbitrary and is not particularly limited. The temperature at the time of mixing can select the suitable temperature range from the range of 10-40 degreeC according to the solubility with respect to the solvent (E), such as a kind, etc. of resin. An appropriate mixing time can be selected from 0.5 to 24 hours depending on the mixing temperature. The mixing means is not particularly limited, and stirring and mixing can be used.
After mixing each component, it is preferable to filter using a filter having a pore size of about 0.003 to 0.2 μm.

<Method for producing resist pattern>
The method for producing a resist pattern of the present invention comprises:
(1) The process of apply | coating the resist composition of this invention on a board | substrate,
(2) The process of drying the composition after application | coating and forming a composition layer,
(3) a step of exposing the composition layer,
(4) The process of heating the composition layer after exposure, (5) The process of developing the composition layer after a heating is included.

The resist composition can be applied onto the substrate by a commonly used apparatus such as a spin coater. Examples of the substrate include an inorganic substrate such as a silicon wafer. Before applying the resist composition, the substrate may be washed, or an antireflection film or the like may be formed on the substrate.

By drying the composition after coating, the solvent is removed and a composition layer is formed. Drying is
For example, it is performed by evaporating the solvent using a heating device such as a hot plate (so-called pre-baking), or using a decompression device. The heating temperature is preferably 50 to 200 ° C., and the heating time is preferably 10 to 180 seconds. The pressure when drying under reduced pressure is 1 to
About 1.0 × 10 ⁵ Pa is preferable.

The obtained composition layer is usually exposed using an exposure machine. The exposure machine may be an immersion exposure machine. Exposure light sources include those that emit laser light in the ultraviolet region such as KrF excimer laser (wavelength 248 nm), ArF excimer laser (wavelength 193 nm), F ₂ excimer laser (wavelength 157 nm), solid-state laser light source (YAG or semiconductor laser) Etc.) Using various lasers such as those that convert wavelength of laser light from the laser and emit harmonic laser light in the far-ultraviolet region or vacuum ultraviolet region, those that irradiate electron beams or extreme ultraviolet light (EUV), etc. Can do. In this specification, the irradiation of these radiations may be collectively referred to as “exposure”. At the time of exposure, exposure is usually performed through a mask corresponding to a required pattern. When the exposure light source is an electron beam, exposure may be performed by direct drawing without using a mask.

The composition layer after exposure is subjected to heat treatment (so-called post-exposure baking) in order to promote the deprotection reaction in the acid labile group. The heating temperature is usually about 50 to 200 ° C, preferably about 70 to 150 ° C.

The heated composition layer is usually developed using a developer using a developing device. Examples of the developing method include a dipping method, a paddle method, a spray method, and a dynamic dispensing method. The development temperature is preferably 5 to 60 ° C., for example, and the development time is preferably 5 to 300 seconds, for example. A positive resist pattern or a negative resist pattern can be produced by selecting the type of developer as follows.

When producing a positive resist pattern from the resist composition of the present invention, an alkaline developer is used as the developer. The alkaline developer may be various alkaline aqueous solutions used in this field. Examples thereof include an aqueous solution of tetramethylammonium hydroxide and (2-hydroxyethyl) trimethylammonium hydroxide (commonly called choline).
The alkali developer may contain a surfactant.
It is preferable to wash the resist pattern with ultrapure water after development, and then remove the water remaining on the substrate and the pattern.

In the case of producing a negative resist pattern from the resist composition of the present invention, a developer containing an organic solvent as a developer (hereinafter sometimes referred to as “organic developer”) is used.
Organic solvents contained in the organic developer include ketone solvents such as 2-hexanone and 2-heptanone; glycol ether ester solvents such as propylene glycol monomethyl ether acetate; ester solvents such as butyl acetate; glycols such as propylene glycol monomethyl ether Examples include ether solvents; amide solvents such as N, N-dimethylacetamide; aromatic hydrocarbon solvents such as anisole.
In the organic developer, the content of the organic solvent is preferably 90% by mass to 100% by mass,
More preferably, it is 95 mass% or more and 100 mass% or less, and it is still more preferable that it is substantially only an organic solvent.
Among them, the organic developer is preferably a developer containing butyl acetate and / or 2-heptanone. The total content of butyl acetate and 2-heptanone in the organic developer is 50% by mass.
The content is preferably 100% by mass or less, more preferably 90% by mass or more and 100% by mass or less, and still more preferably substantially only butyl acetate and / or 2-heptanone.
The organic developer may contain a surfactant. The organic developer may contain a trace amount of water.
At the time of development, the development may be stopped by substituting a solvent of a different type from the organic developer.

It is preferable to wash the developed resist pattern with a rinse solution. As a rinse liquid,
There is no particular limitation as long as it does not dissolve the resist pattern, and a solution containing a general organic solvent can be used, and an alcohol solvent or an ester solvent is preferable.
After the cleaning, it is preferable to remove the rinse solution remaining on the substrate and the pattern.

<Application>
The resist composition of the present invention includes a resist composition for KrF excimer laser exposure, a resist composition for ArF excimer laser exposure, a resist composition for electron beam (EB) exposure, or an EU.
It is suitable as a resist composition for V exposure, particularly as a resist composition for electron beam (EB) exposure or a resist composition for EUV exposure, and is useful for fine processing of semiconductors.

The present invention will be described more specifically with reference to examples. In the examples, “%” and “parts” representing the content or amount used are based on mass unless otherwise specified.
The structure of the compound is MASS (LC: Agilent 1100 type, MASS: Agil.
ent LC / MSD type or LC / MSD TOF type).
The weight average molecular weight is a value determined by gel permeation chromatography under the following conditions.
Apparatus: HLC-8120GPC type (manufactured by Tosoh Corporation)
Column: TSKgel Multipore HXL-M x 3 + guardcolumn (manufactured by Tosoh Corporation)
Eluent: Tetrahydrofuran Flow rate: 1.0 mL / min
Detector: RI detector Column temperature: 40 ° C
Injection volume: 100 μl
Molecular weight standard: Standard polystyrene (manufactured by Tosoh Corporation)

Resin Synthesis The compounds (monomers) used in the resin synthesis are shown below.

  Hereinafter, these monomers are referred to as “monomer (a1-1-2)” or the like according to the formula number.

Example 1 [Synthesis of Resin A1]
As the monomer, monomer (I-3), monomer (a2-2-1), monomer (a1-
1-2) and monomer (a3-1-1), and the molar ratio [monomer (I-3): monomer (a2-2-1): monomer (a1-1-2): monomer (a3-1) -1)] is 15
: 15: 50: 20, and 1.5 mass times the total monomer amount of propylene glycol monomethyl ether acetate was added to prepare a solution. To this solution, azobisisobutyronitrile and azobis (2,4-dimethylvaleronitrile) as initiators were added in an amount of 1.1 mol% and 3.3 mol%, respectively, with respect to the total monomer amount, and these were added at 75 ° C. Heated for about 5 hours. The obtained reaction mixture was poured into a large amount of methanol / water mixed solvent to precipitate the resin, and this resin was filtered. The obtained resin was again dissolved in propylene glycol monomethyl ether acetate, and the resulting solution was poured into a methanol / water mixed solvent to precipitate the resin, followed by reprecipitation operation of filtering the resin twice. Molecular weight 5.5 × 10
³ resin A1 (copolymer) was obtained with a yield of 66%. This resin A1 has the following structural units.

Example 2 [Synthesis of Resin A2]
As the monomer, monomer (I-3), monomer (a2-2-1), monomer (a1-
1-2) and monomer (a3-1-1), and the molar ratio [monomer (I-3): monomer (a2-2-1): monomer (a1-1-2): monomer (a3-1) -1)] is 20
: 10: 50: 20, and 1.5 mass times the total monomer amount of propylene glycol monomethyl ether acetate was added to prepare a solution. To this solution, azobisisobutyronitrile and azobis (2,4-dimethylvaleronitrile) as initiators were added in an amount of 1.1 mol% and 3.3 mol%, respectively, with respect to the total monomer amount, and these were added at 75 ° C. Heated for about 5 hours. The obtained reaction mixture was poured into a large amount of methanol / water mixed solvent to precipitate the resin, and this resin was filtered. The obtained resin was again dissolved in propylene glycol monomethyl ether acetate, and the resulting solution was poured into a methanol / water mixed solvent to precipitate the resin, followed by reprecipitation operation of filtering the resin twice. Molecular weight 5.5 × 10
³ resin A2 (copolymer) was obtained with a yield of 68%. This resin A2 has the following structural units.

Example 3 [Synthesis of Resin A3]
As the monomer, monomer (I-3), monomer (a2-2-1), monomer (a1-
1-2) and monomer (a3-1-1), and the molar ratio [monomer (I-3): monomer (a2-2-1): monomer (a1-1-2): monomer (a3-1) -1)] is 10
: 20: 50: 20, and propylene glycol monomethyl ether acetate of 1.5 mass times the total monomer amount was added to obtain a solution. To this solution, azobisisobutyronitrile and azobis (2,4-dimethylvaleronitrile) as initiators were added in an amount of 1.1 mol% and 3.3 mol%, respectively, with respect to the total monomer amount, and these were added at 75 ° C. Heated for about 5 hours. The obtained reaction mixture was poured into a large amount of methanol / water mixed solvent to precipitate the resin, and this resin was filtered. The obtained resin was again dissolved in propylene glycol monomethyl ether acetate, and the resulting solution was poured into a methanol / water mixed solvent to precipitate the resin, followed by reprecipitation operation of filtering the resin twice. Molecular weight 5.6 × 10
³ resin A3 (copolymer) was obtained with a yield of 62%. This resin A3 has the following structural units.

Synthesis Example 1 [Synthesis of Resin AX1]
As the monomer, monomer (I-3), monomer (a1-4-2), monomer (a1-1-2) and monomer (a2-1-1) were used, and the molar ratio [monomer (I-3): Monomer (a1-4-2): monomer (a1-1-2): monomer (a2-1-1)] is mixed so as to be 10: 40: 40: 10, and the total monomer amount is 1.5 mass. Doubled propylene glycol monomethyl ether acetate was added to make a solution. To this solution, azobisisobutyronitrile and azobis (2,4-dimethylvaleronitrile) as initiators were added in an amount of 1.1 mol% and 3.3 mol%, respectively, with respect to the total monomer amount, and these were added at 75 ° C. Heated for about 5 hours. The obtained reaction mixture was poured into a large amount of methanol / water mixed solvent to precipitate the resin, and this resin was filtered. The obtained resin was again dissolved in propylene glycol monomethyl ether acetate, an aqueous p-toluenesulfonic acid solution was added, and the mixture was stirred for about 6 hours, and then separated to recover the organic layer. The recovered organic layer was poured into a methanol / water mixed solvent to precipitate a resin, and this resin was filtered to obtain a resin AX1 (copolymer) having a weight average molecular weight of 4.9 × 10 ^{3 in} a yield of 42%. Obtained. This resin AX1 has the following structural units.

Synthesis Example 2 [Synthesis of Resin AX2]
Monomer (IX) and monomer (a2-2-1) are used as monomers and mixed so that the molar ratio [monomer (IX): monomer (a2-2-1)] is 70:30. An amount of 1.5 mass times propylene glycol monomethyl ether acetate was added to prepare a solution. To this solution, 1 mol% and 3 mol% of azobisisobutyronitrile and azobis (2,4-dimethylvaleronitrile) as initiators were added to the total monomer amount, respectively, and these were heated at 75 ° C. for about 5 hours. did. The obtained reaction mixture was poured into a large amount of methanol / water mixed solvent to precipitate the resin, and this resin was filtered. The obtained resin was again dissolved in propylene glycol monomethyl ether acetate, and the resulting solution was poured into a methanol / water mixed solvent to precipitate the resin, followed by reprecipitation operation of filtering the resin twice. Resin AX2 (copolymer) having a molecular weight of 8.1 × 10 ³ was obtained in a yield of 65%. This resin AX2 has the following structural units.

<Preparation of resist composition>
A mixture obtained by mixing and dissolving the components shown in Table 1 was filtered through a fluororesin filter having a pore size of 0.2 μm to prepare a resist composition.

<Resin>
A1: Resin A1
A2: Resin A2
A3: Resin A3
AX1: Resin AX1
AX2: Resin AX2

Ｂ２：ジフェニルトリルスルホニウム ｐ−トルエンスルホナート（和光純薬工業（株
）製）

<Acid generator (B)>
B1: Bis (tert-butanesulfonyl) diazomethane; trade name “WPAG-170
(Wako Pure Chemical Industries, Ltd.)

B2: Diphenyltolylsulfonium p-toluenesulfonate (manufactured by Wako Pure Chemical Industries, Ltd.)

Ｃ２：ジイソプロピルアニリン（東京化成工業（株）製）
＜弱酸分子内塩＞
Ｄ１：（東京化成工業（株）製）

<Basic compound: Quencher>
C1: Synthesis according to the examples of JP2012-197261A

C2: Diisopropylaniline (manufactured by Tokyo Chemical Industry Co., Ltd.)
<Weak acid inner salt>
D1: (Tokyo Chemical Industry Co., Ltd.)

<Solvent>
Propylene glycol monomethyl ether acetate 180 parts Propylene glycol monomethyl ether 20 parts γ-butyrolactone 1 part

(Manufacture of resist pattern)
A silicon wafer is coated with a composition for organic antireflection film (DUV-42P; manufactured by Nissan Chemical Co., Ltd.) and baked at 205 ° C. for 60 seconds to form a film thickness of 60 nm on the wafer.
An organic antireflection film was formed. Next, the resist composition was applied (spin coated) on the organic antireflection film so that the film thickness after drying was 490 nm.
Thereafter, the composition layer was formed by prebaking on a direct hot plate for 60 seconds at the temperature shown in the column “PB” in Table 1. A KrF excimer laser stepper [NSR-2205EX12B NA0.55 2/3 Ann.
The line and space pattern was exposed by changing the exposure amount stepwise.
After exposure, perform post-exposure baking for 60 seconds at the temperature shown in the column of “PEB” in Table 1 on the hot plate, and then perform paddle development for 60 seconds with a 2.38% tetramethylammonium hydroxide aqueous solution. Thus, a resist pattern was obtained.

In each resist film, the exposure amount at which the 180 nm line and space pattern becomes an exposure amount of 1: 1 was defined as the effective sensitivity.

Focus margin evaluation (DOF): When the focus is shaken with an exposure amount at which the line width of a line-and-space pattern with a mask size of 180 nm is 180 nm, the line width is 180
A range having a width of nm ± 5% (about 171 to 189 nm) was used as a line width index. The results are shown in Table 2.
Shown in

From the results shown in Table 2, it is apparent that a resist pattern having a good focus margin can be produced according to the resist composition of the present invention.

Claims (6)

Resin containing the structural unit represented by Formula (I) and the structural unit represented by Formula (a2-2).

[In the formula (I),
R ^I1 represents a hydrogen atom, a halogen atom or an alkyl group having 1 to 6 carbon atoms which may have a halogen atom.
R ^I2 represents a halogen atom, a hydroxy group, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, an acyl group having 2 to 4 carbon atoms, an acyloxy group having 2 to 4 carbon atoms, an acryloyloxy group, or Represents a methacryloyloxy group.
A ¹ represents a single bond or ^{* -A 2 -X 1 - (A} 3 -X 2) a - represents a.
A ² and A ³ each independently represents an alkanediyl group having 1 to 6 carbon atoms.
X ¹ and X ² each independently represent —O—, —CO—O— or —O—CO—.
a represents 0 or 1.
W represents an alicyclic hydrocarbon having 4 to 18 carbon atoms.
mc represents an integer of 0 to 4, and when mc is an integer of 2 or more, the plurality of R ^I2 may be the same as or different from each other. ]

[In the formula (a2-2),
R ^a50 represents a hydrogen atom, a halogen atom or an alkyl group having 1 to 6 carbon atoms which may have a halogen atom.
R ^a51 is a halogen atom, a hydroxy group, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, an acyl group having 2 to 4 carbon atoms, an acyloxy group having 2 to 4 carbon atoms, an acryloyloxy group, or Represents a methacryloyloxy group.
A ^a50 represents a single bond or ^{* -A a51 -X a51 - (A} a52 -X a52) na - represents a.
A ^a51 and A ^a52 each independently represent an alkanediyl group having 1 to 6 carbon atoms.
X ^a51 and X ^a52 each independently represent —O—, ^—CO —O— or —O—CO—.
na represents 0 or 1.
mb represents an integer of 0 to 4, and when mb is an integer of 2 or more, the plurality of ^Ra51s may be the same as or different from each other. ]   The resin according to claim 1, further comprising a structural unit having an acid labile group. The resin according to claim 2, wherein the structural unit having an acid labile group is a structural unit represented by the formula (a1-1).

[In the formula (a1-1),
L ^a1 represents —O— or ^* —O— (CH ₂ ) _k1 —CO—O—, k1 represents an integer of 1 to 7, and * represents a bond to —CO—.
R ^a4 represents a hydrogen atom or a methyl group.
R ^a6 represents an alkyl group having 1 to 8 carbon atoms, an alicyclic hydrocarbon group having 3 to 18 carbon atoms, or a group obtained by combining these.
m1 represents the integer of 0-14. ]   A resist composition comprising the resin according to claim 1 and an acid generator. The resist composition according to claim 4, further comprising a salt having a lower acidity than the acid generated from the acid generator. (1) The process of apply | coating the resist composition of Claim 4 or 5 on a board | substrate,
(2) The process of drying the composition after application | coating and forming a composition layer,
(3) a step of exposing the composition layer;
(4) a step of heating the composition layer after exposure, and (5) a step of developing the composition layer after heating,
A method for producing a resist pattern including: