JP6948880B2 - Method for producing salt, acid generator, resist composition and resist pattern - Google Patents

Description

The present invention relates to a salt, an acid generator, a resist composition, a method for producing a resist pattern using the resist composition, and the like.

Patent Document 1 describes a resist composition containing a salt represented by the following formula as an acid generator.

US2013 / 35503 Gazette

An object of the present invention is to improve the CD uniformity (CDU) of a resist pattern.

［式（Ｉ）中、
Ｒ^１は、置換基を有してもよい炭素数６〜１８の芳香族炭化水素基を表す。
Ｒ^２は、置換基を有してもよい炭素数１〜１８の炭化水素基を表す。
Ｘ^１は、炭素数１〜１２の２価の脂肪族飽和炭化水素基を表し、該２価の脂肪族飽和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。
Ｘ^２及びＸ^３は、それぞれ独立に、フッ素原子又は炭素数１〜６のペルフルオロアルキル基を表す。
Ｌ^ｂ１は、炭素数１〜２４の２価の飽和炭化水素基を表し、該飽和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く、該飽和炭化水素基に含まれる水素原子は、フッ素原子又はヒドロキシ基で置換されていてもよい。
Ａ⁻は、有機アニオンを表す。
Ｚ^＋は、有機カチオンを表す。］
〔２〕Ｘ^１が、炭素数１〜６のアルカンジイル基である〔１〕に記載の塩。
〔３〕Ｒ^１及びＲ^２が、それぞれ独立に、置換基を有してもよいフェニル基である〔１〕又は〔２〕に記載の塩。
〔４〕〔１〕〜〔３〕のいずれかに記載の塩を含有する酸発生剤。
〔５〕〔４〕に記載の酸発生剤と酸不安定基を有する構造単位を含む樹脂とを含有するレジスト組成物。
〔６〕酸発生剤から発生する酸よりも酸性度の低い酸を発生する塩をさらに含有する〔５〕に記載のレジスト組成物。
〔７〕（１）〔５〕又は〔６〕に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）組成物層を露光する工程、
（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 salt represented by the formula (I).

[In formula (I),
R ¹ represents an aromatic hydrocarbon group having 6 to 18 carbon atoms which may have a substituent.
R ² represents a hydrocarbon group having 1 to 18 carbon atoms which may have a substituent.
X ¹ represents a divalent aliphatic saturated hydrocarbon group having 1 to 12 carbon atoms, and the methylene group contained in the divalent aliphatic saturated hydrocarbon group may be replaced with an oxygen atom or a carbonyl group. ..
X ² and X ³ independently represent a fluorine atom or a perfluoroalkyl group having 1 to 6 carbon atoms.
L ^b1 represents a divalent saturated hydrocarbon group having 1 to 24 carbon atoms, and the methylene group contained in the saturated hydrocarbon group may be replaced with an oxygen atom or a carbonyl group, and the saturated hydrocarbon group may be used. The contained hydrogen atom may be substituted with a fluorine atom or a hydroxy group.
A ⁻ represents an organic anion.
Z ⁺ represents an organic cation. ]
[2] ^{The salt according to [1], wherein X 1} is an alkanediyl group having 1 to 6 carbon atoms.
[3] The salt according to [1] or [2], wherein ^{R 1} and R ^{2 are phenyl groups which may independently have a substituent.}
[4] An acid generator containing the salt according to any one of [1] to [3].
[5] A resist composition containing the acid generator according to [4] and a resin containing a structural unit having an acid unstable group.
[6] The resist composition according to [5], which further contains a salt that generates an acid having a lower acidity than the acid generated from the acid generator.
[7] (1) A step of applying the resist composition according to [5] or [6] onto a substrate.
(2) A step of drying the applied composition to form a composition layer,
(3) 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 present invention, a resist pattern can be produced with good CD uniformity (CDU).

In the present specification, the "(meth) acrylic monomer" has a structure of "CH ₂ = CH-C (= O)-" or "CH ₂ = C (CH ₃ ) -C (= O)-". It means at least one kind of monomer having. 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.
In the present specification, the "solid content of the resist composition" means the total amount of the components excluding the solvent (E) described later from the total amount of the resist composition.

［式（Ｉ）中、
Ｒ^１は、置換基を有してもよい炭素数６〜１８の芳香族炭化水素基を表す。
Ｒ^２は、置換基を有してもよい炭素数１〜１８の炭化水素基を表す。
Ｘ^１は、炭素数１〜１２の２価の脂肪族飽和炭化水素基を表し、該２価の脂肪族飽和炭化水素基に含まれるメチレン基（−ＣＨ_２−）は、酸素原子（−Ｏ−）又はカルボニル基（−Ｃ（＝Ｏ）−）に置き換わっていてもよい。
Ｘ^２及びＸ^３は、それぞれ独立に、フッ素原子又は炭素数１〜６のペルフルオロアルキル基を表す。
Ｌ^ｂ１は、炭素数１〜２４の２価の飽和炭化水素基を表し、該飽和炭化水素基に含まれる−ＣＨ_２−は、−Ｏ−又は−Ｃ（＝Ｏ）−に置き換わっていてもよく、該飽和炭化水素基に含まれる水素原子は、フッ素原子又はヒドロキシ基で置換されていてもよい。
Ａ⁻は、有機アニオンを表す。
Ｚ^＋は、有機カチオンを表す。］ <Salt represented by formula (I)>
The salt of the present invention is a salt represented by the formula (I) (hereinafter, in some cases, referred to as "salt (I)").

[In formula (I),
R ¹ represents an aromatic hydrocarbon group having 6 to 18 carbon atoms which may have a substituent.
R ² represents a hydrocarbon group having 1 to 18 carbon atoms which may have a substituent.
X ¹ represents a divalent aliphatic saturated hydrocarbon group having 1 to 12 carbon atoms, and the methylene group (-CH _2- ) contained in the divalent aliphatic saturated hydrocarbon group is an oxygen atom (-O). It may be replaced with a −) or a carbonyl group (−C (= O) −).
X ² and X ³ independently represent a fluorine atom or a perfluoroalkyl group having 1 to 6 carbon atoms.
L ^b1 represents a divalent saturated hydrocarbon group having 1 to 24 carbon atoms, and -CH _2- contained in the saturated hydrocarbon group may be replaced with -O- or -C (= O)-. Often, the hydrogen atom contained in the saturated hydrocarbon group may be substituted with a fluorine atom or a hydroxy group.
A ⁻ represents an organic anion.
Z ⁺ represents an organic cation. ]

置換基は、ヒドロキシ基、炭素数１〜１２のアルキル基又は炭素数１〜１２のアルコキシ基であることが好ましく、ヒドロキシ基又は炭素数１〜１２のアルキル基であることがより好ましく、炭素数１〜１２のアルキル基であることがさらに好ましく、炭素数１〜６のアルキル基であることがさらにより好ましい。
Ｒ^１で表される、置換基を有していてもよい炭素数６〜１８の芳香族炭化水素基は、フェニル基又は置換基を有するフェニル基が好ましく、フェニル基又は炭素数１〜６のアルキル基を有するフェニル基がより好ましい。 Examples of the aromatic hydrocarbon group having 6 to 18 carbon atoms of R ¹ include aryl groups such as phenyl group, naphthyl group, anthryl group, biphenyl group, phenanthryl group and fluorenyl group, and phenyl group, naphthyl group and anthryl group. Is preferable, a phenyl group and a naphthyl group are more preferable, and a phenyl group is further preferable.
The substituents that the aromatic hydrocarbon group having 6 to 18 carbon atoms may have include a hydroxy group, a carboxyl group, an alkyl group having 1 to 12 carbon atoms, an alkoxy group having 1 to 12 carbon atoms, and 3 to 12 carbon atoms. Examples thereof include 12 alicyclic hydrocarbon groups and groups combining these groups.
Examples of the alkyl group having 1 to 12 carbon atoms include a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, a hexyl group, a heptyl group, an octyl group, a nonyl group, a decyl group, an undecyl group and a dodecyl group. ..
The alkoxy group having 1 to 12 carbon atoms includes a methoxy group, an ethoxy group, a propoxy group, a butoxy group, a pentyloxy group, a hexyloxy group, an octyloxy group, a 2-ethylhexyloxy group, a nonyloxy group, a decyloxy group and an undecyloxy group. Groups, dodecyloxy groups and the like can be mentioned.
Examples of the alicyclic hydrocarbon group having 3 to 12 carbon atoms include the groups shown below. * Is a bond with an aromatic hydrocarbon group.

The substituent is preferably a hydroxy group, an alkyl group having 1 to 12 carbon atoms or an alkoxy group having 1 to 12 carbon atoms, and more preferably a hydroxy group or an alkyl group having 1 to 12 carbon atoms. It is more preferably an alkyl group of 1 to 12, and even more preferably an alkyl group having 1 to 6 carbon atoms.
Represented by R ^1, an aromatic hydrocarbon group having 6 to 18 carbon atoms which may have a substituent, preferably a phenyl group having a phenyl group or a substituted group, a phenyl group or 1 to 6 carbon atoms A phenyl group having an alkyl group is more preferable.

Examples of the hydrocarbon group having 1 to 18 carbon atoms R ^2, an alkyl group, an alicyclic hydrocarbon group include groups formed by combining an aromatic hydrocarbon group, and these.
Alkyl groups include methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, sec-butyl group, tert-butyl group, pentyl group, hexyl group, heptyl group, 2-ethylhexyl group and octyl group. , Nonyl group, decyl group, undecyl group, dodecyl group and the like.
The alicyclic hydrocarbon group may be either a monocyclic group or a polycyclic group, and the monocyclic alicyclic hydrocarbon group includes a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group and a methylcyclohexyl group. , Cycloalkyl groups such as dimethylcyclohexyl group, cycloheptyl group, cyclooctyl group, cyclodecyl group and the like. Examples of the polycyclic alicyclic hydrocarbon group include a decahydronaphthyl group, an adamantyl group, a 2-alkyladamantan-2-yl group, a 1- (adamantan-1-yl) alkane-1-yl group, and a norbornyl group. Examples thereof include a methylnorbornyl group and an isobornyl group.
Examples of the aromatic hydrocarbon group include a phenyl group and a naphthyl group.
Examples of the group formed by combining these include an aralkyl group, a benzyl group, a phenethyl group and the like.
The R ^2, an alkyl group having 1 to 6 carbon atoms, a phenyl group and a naphthyl group, more preferably an alkyl group and a phenyl group having 1 to 4 carbon atoms, more preferably a phenyl group.
Examples of the substituent that the hydrocarbon group having 1 to 18 carbon atoms may have include ^{a substituent similar to R 1,} which is a hydroxy group, an alkyl group having 1 to 12 carbon atoms, or an alkyl group having 1 to 12 carbon atoms. It is preferably an alkoxy group, more preferably a hydroxy group or an alkyl group having 1 to 12 carbon atoms, further preferably an alkyl group having 1 to 12 carbon atoms, and an alkyl group having 1 to 6 carbon atoms. It is even more preferable to have.

Examples of the divalent aliphatic saturated hydrocarbon group having 1 to 12 carbon atoms represented by X ^{1 include an alkanediyl group, a monocyclic or polycyclic divalent alicyclic saturated hydrocarbon group.} A combination of two or more of these groups may be used.
Specifically, methylene group, ethylene group, propane-1,3-diyl group, butane-1,4-diyl group, pentane-1,5-diyl group, hexane-1,6-diyl group, heptane-1 , 7-Diyl group, Octane-1,8-Diyl group, Nonan-1,9-Diyl group, Decane-1,10-Diyl group, Undecane-1,11-Diyl group, Dodecane-1,12-Diyl group Linear alkanediyl groups such as;
Ethane-1,1-diyl group, propane-1,1-diyl group, propane-1,2-diyl group, propane-2,2-diyl group, pentane-2,4-diyl group, 2-methylpropane- Branched alkanediyl groups such as 1,3-diyl group, 2-methylpropane-1,2-diyl group, pentane-1,4-diyl group, 2-methylbutane-1,4-diyl group;
Monocyclic 2 which is a cycloalkanediyl group such as cyclobutane-1,3-diyl group, cyclopentane-1,3-diyl group, cyclohexane-1,4-diyl group, cyclooctane-1,5-diyl group, etc. Valuable alicyclic saturated hydrocarbon group;
Polycyclic divalent alicyclic saturated hydrocarbons such as norbornane-1,4-diyl group, norbornane-2,5-diyl group, adamantane-1,5-diyl group, and adamantane-2,6-diyl group. The group etc. can be mentioned.
The ^{divalent aliphatic saturated hydrocarbon group represented by X 1} is preferably an alkanediyl group (linear alkanediyl group or branched alkanediyl group), and is an alkanediyl group having 1 to 6 carbon atoms. It is more preferable to have an alkanediyl group having 1 to 4 carbon atoms, and even more preferably a linear alkanediyl group having 1 to 4 carbon atoms.

The _{methylene group (-CH 2-} ) contained in the aliphatic saturated hydrocarbon group of ^{X 1} may be replaced with an oxygen atom (-O-) or a carbonyl group (-C (= O)-). Further, the −CH ₂₋ may be replaced with a group consisting of a combination of two or more groups selected from −O− and −C (= O) −. For example, aliphatic saturated hydrocarbon groups are ether bonds, carbonyl bonds, ester bonds (-C (= O) -O- or -OC (= O)-) or -OC (= O) -O. It may be an aliphatic saturated hydrocarbon group replaced by − or the like. _{When -CH 2-} constituting the aliphatic saturated hydrocarbon group is replaced with a group consisting of -O-, -C (= O)-or the above combination, the number of carbon atoms before the replacement is the aliphatic saturated hydrocarbon group. The number of carbon atoms in.

The perfluoroalkyl groups of X ² and X ³ include trifluoromethyl group, perfluoroethyl group, perfluoropropyl group, perfluoroisopropyl group, perfluorobutyl group, perfluorosec-butyl group, perfluorotert-butyl group, perfluoropentyl group and perfluoro. Hexyl groups and the like can be mentioned.
It is preferable that X ² and X ³ are independently fluorine atoms or trifluoromethyl groups, and it is more preferable that both are fluorine atoms.

Examples of the divalent saturated hydrocarbon group having 1 to 24 carbon atoms represented by L ^b1 include a linear or branched alkanediyl group and a monocyclic or polycyclic divalent alicyclic saturated hydrocarbon group. However, it may be a group formed by combining two or more of these groups.
Specifically, methylene group, ethylene group, propane-1,3-diyl group, butane-1,4-diyl group, pentane-1,5-diyl group, hexane-1,6-diyl group, heptane-1 , 7-Diyl Group, Octane-1,8-Diyl Group, Nonan-1,9-Diyl Group, Decane-1,10-Diyl Group, Undecane-1,11-Diyl Group, Dodecane-1,12-Diyl Group , Tridecane-1,13-diyl group, tetradecane-1,14-diyl group, pentadecane-1,15-diyl group, hexadecane-1,16-diyl group, heptadecane-1,17-diyl group, etc. Alcandiyl group;
Ethane-1,1-diyl group, propane-1,1-diyl group, propane-1,2-diyl group, propane-2,2-diyl group, pentane-2,4-diyl group, 2-methylpropane- Branched alkanediyl groups such as 1,3-diyl group, 2-methylpropane-1,2-diyl group, pentane-1,4-diyl group, 2-methylbutane-1,4-diyl group;
Monocyclic 2 which is a cycloalkanediyl group such as cyclobutane-1,3-diyl group, cyclopentane-1,3-diyl group, cyclohexane-1,4-diyl group, cyclooctane-1,5-diyl group, etc. Valuable alicyclic saturated hydrocarbon group;
Polycyclic divalent alicyclic saturated hydrocarbons such as norbornane-1,4-diyl group, norbornane-2,5-diyl group, adamantane-1,5-diyl group, and adamantane-2,6-diyl group. The group etc. can be mentioned.

［式（ｂ１−１）中、
Ｌ^ｂ２は、単結合又は炭素数１〜２２の２価の飽和炭化水素基を表し、該飽和炭化水素基に含まれる水素原子は、フッ素原子に置換されていてもよい。
Ｌ^ｂ３は、単結合又は炭素数１〜２２の２価の飽和炭化水素基を表し、該飽和炭化水素基に含まれる水素原子は、フッ素原子又はヒドロキシ基に置換されていてもよく、該飽和炭化水素基に含まれる−ＣＨ_２−は、−Ｏ−又は−Ｃ（＝Ｏ）−に置き換わっていてもよい。
ただし、Ｌ^ｂ２とＬ^ｂ３との合計炭素数は、２２以下である。
式（ｂ１−２）中、
Ｌ^ｂ４は、単結合又は炭素数１〜２２の２価の飽和炭化水素基を表し、該飽和炭化水素基に含まれる水素原子は、フッ素原子に置換されていてもよい。
Ｌ^ｂ５は、単結合又は炭素数１〜２２の２価の飽和炭化水素基を表し、該飽和炭化水素基に含まれる水素原子は、フッ素原子又はヒドロキシ基に置換されていてもよく、該飽和炭化水素基に含まれる−ＣＨ_２−は、−Ｏ−又は−Ｃ（＝Ｏ）−に置き換わっていてもよい。
ただし、Ｌ^ｂ４とＬ^ｂ５との合計炭素数は、２２以下である。
式（ｂ１−３）中、
Ｌ^ｂ６は、単結合又は炭素数１〜２３の２価の飽和炭化水素基を表し、該飽和炭化水素基に含まれる水素原子は、フッ素原子又はヒドロキシ基に置換されていてもよい。
Ｌ^ｂ７は、単結合又は炭素数１〜２３の２価の飽和炭化水素基を表し、該飽和炭化水素基に含まれる水素原子は、フッ素原子又はヒドロキシ基に置換されていてもよく、該飽和炭化水素基に含まれる−ＣＨ_２−は、−Ｏ−又は−Ｃ（＝Ｏ）−に置き換わっていてもよい。
ただし、Ｌ^ｂ６とＬ^ｂ７との合計炭素数は、２３以下である。］ _{Examples of the group in which −CH 2} − contained in the divalent saturated hydrocarbon group of L ^b1 is replaced by −O− or −C (= O) − include formulas (b1-1) to (b1-3). ) Can be mentioned. Incidentally, in the embodiment wherein (b1-1) ~ formula (b1-3) and below, * represents a bond to ^{X 1.}

[In equation (b1-1),
L ^b2 represents a single bond or a divalent saturated hydrocarbon group having 1 to 22 carbon atoms, and the hydrogen atom contained in the saturated hydrocarbon group may be substituted with a fluorine atom.
L ^b3 represents a single bond or a divalent saturated hydrocarbon group having 1 to 22 carbon atoms, and the hydrogen atom contained in the saturated hydrocarbon group may be substituted with a fluorine atom or a hydroxy group, and the saturated hydrocarbon group may be substituted. _{-CH 2−} contained in the hydrocarbon group may be replaced with −O− or −C (= O) −.
However, the total number of carbon atoms of ^{L b2} and L ^{b3 is 22 or less.}
In equation (b1-2),
L ^b4 represents a single bond or a divalent saturated hydrocarbon group having 1 to 22 carbon atoms, and the hydrogen atom contained in the saturated hydrocarbon group may be substituted with a fluorine atom.
L ^b5 represents a single bond or a divalent saturated hydrocarbon group having 1 to 22 carbon atoms, and the hydrogen atom contained in the saturated hydrocarbon group may be substituted with a fluorine atom or a hydroxy group, and the saturated hydrocarbon group may be substituted. _{-CH 2−} contained in the hydrocarbon group may be replaced with −O− or −C (= O) −.
However, the total number of carbon atoms of ^{L b4} and L ^{b5 is 22 or less.}
In equation (b1-3),
L ^b6 represents a single bond or a divalent saturated hydrocarbon group having 1 to 23 carbon atoms, and the hydrogen atom contained in the saturated hydrocarbon group may be substituted with a fluorine atom or a hydroxy group.
L ^b7 represents a single bond or a divalent saturated hydrocarbon group having 1 to 23 carbon atoms, and the hydrogen atom contained in the saturated hydrocarbon group may be substituted with a fluorine atom or a hydroxy group, and the saturated hydrocarbon group may be substituted. _{-CH 2−} contained in the hydrocarbon group may be replaced with −O− or −C (= O) −.
However, the total number of carbon atoms of ^{L b6} and L ^{b7 is 23 or less.} ]

In formulas (b1-1) to (b1-3), when −CH ₂ − contained in the saturated hydrocarbon group is replaced with −O− or −C (= O) −, the number of carbon atoms before the replacement Is the number of carbon atoms of the saturated hydrocarbon group.
The divalent saturated hydrocarbon group and the groups in which -CH _2- and hydrogen atoms contained in the saturated hydrocarbon group may be substituted as described above are the same as those of the divalent saturated hydrocarbon group of ^{L b1.} Can be mentioned.

L ^b2 is preferably a single bond.
L ^b3 is preferably a divalent saturated hydrocarbon group having 1 to 4 carbon atoms.
L ^b4 is preferably a divalent saturated hydrocarbon group having 1 to 8 carbon atoms, and the hydrogen atom contained in the divalent saturated hydrocarbon group may be substituted with a fluorine atom.
L ^b5 is preferably a single bond or a divalent saturated hydrocarbon group having 1 to 8 carbon atoms.
L ^b6 is preferably a single bond or a divalent saturated hydrocarbon group having 1 to 4 carbon atoms, and the hydrogen atom contained in the saturated hydrocarbon group may be substituted with a fluorine atom.
L ^b7 is preferably a single bond or a divalent saturated hydrocarbon group having 1 to 18 carbon atoms, and the hydrogen atom contained in the saturated hydrocarbon group may be substituted with a fluorine atom or a hydroxy group. _{-CH 2-} contained in the divalent saturated hydrocarbon group may be replaced with -O- or -C (= O)-.
The _{group in which -CH 2-} contained in the divalent saturated hydrocarbon group of ^{L b1} is replaced by -O- or -C (= O)-is represented by the formula (b1-1) or the formula (b1-3). The group represented is preferred. Among these ^groups, divalent -CH ₂ - contained in the saturated hydrocarbon group of ^{L b1} - is -O- or -C (= O) - Preferred groups replaced by, binding to ^{X 1} -O- Can be mentioned as a group containing. In this case, X ¹ is preferably a divalent aliphatic saturated hydrocarbon group in which the methylene group is not replaced with —O— or −C (= O) −.

［式（ｂ１−４）中、
Ｌ^ｂ８は、単結合又は炭素数１〜２２の２価の飽和炭化水素基を表し、該飽和炭化水素基に含まれる水素原子は、フッ素原子又はヒドロキシ基に置換されていてもよい。
式（ｂ１−５）中、
Ｌ^ｂ９は、炭素数１〜２０の２価の飽和炭化水素基を表す。
Ｌ^ｂ１０は、単結合又は炭素数１〜１９の２価の飽和炭化水素基を表し、該２価の飽和炭化水素基に含まれる水素原子は、フッ素原子又はヒドロキシ基に置換されていてもよい。
ただし、Ｌ^ｂ９及びＬ^ｂ１０の合計炭素数は２０以下である。
式（ｂ１−６）中、
Ｌ^ｂ１１は、炭素数１〜２１の２価の飽和炭化水素基を表す。
Ｌ^ｂ１２は、単結合又は炭素数１〜２０の２価の飽和炭化水素基を表し、該２価の飽和炭化水素基に含まれる水素原子は、フッ素原子又はヒドロキシ基に置換されていてもよい。
ただし、Ｌ^ｂ１１及びＬ^ｂ１２の合計炭素数は２１以下である。
式（ｂ１−７）中、
Ｌ^ｂ１３は、炭素数１〜１９の２価の飽和炭化水素基を表す。
Ｌ^ｂ１４は、単結合又は炭素数１〜１８の２価の飽和炭化水素基を表す。
Ｌ^ｂ１５は、単結合又は炭素数１〜１８の２価の飽和炭化水素基を表し、該２価の飽和炭化水素基に含まれる水素原子は、フッ素原子又はヒドロキシ基に置換されていてもよい。
ただし、Ｌ^ｂ１３〜Ｌ^ｂ１５の合計炭素数は１９以下である。
式（ｂ１−８）中、
Ｌ^ｂ１６は、炭素数１〜１８の２価の飽和炭化水素基を表す。
Ｌ^ｂ１７は、炭素数１〜１８の２価の飽和炭化水素基を表す。
Ｌ^ｂ１８は、単結合又は炭素数１〜１７の２価の飽和炭化水素基を表し、該２価の飽和炭化水素基に含まれる水素原子は、フッ素原子又はヒドロキシ基に置換されていてもよい。
ただし、Ｌ^ｂ１６〜Ｌ^ｂ１８の合計炭素数は１９以下である。］ Examples of the formula (b1-1) include groups represented by the formulas (b1-4) to (b1-8).

[In equation (b1-4),
L ^b8 represents a single bond or a divalent saturated hydrocarbon group having 1 to 22 carbon atoms, and the hydrogen atom contained in the saturated hydrocarbon group may be substituted with a fluorine atom or a hydroxy group.
In equation (b1-5),
L ^b9 represents a divalent saturated hydrocarbon group having 1 to 20 carbon atoms.
L ^b10 represents a single bond or a divalent saturated hydrocarbon group having 1 to 19 carbon atoms, and the hydrogen atom contained in the divalent saturated hydrocarbon group may be substituted with a fluorine atom or a hydroxy group. ..
However, the total number of carbon atoms of ^{L b9} and L ^{b10 is 20 or less.}
In equation (b1-6),
L ^b11 represents a divalent saturated hydrocarbon group having 1 to 21 carbon atoms.
L ^b12 represents a single bond or a divalent saturated hydrocarbon group having 1 to 20 carbon atoms, and the hydrogen atom contained in the divalent saturated hydrocarbon group may be substituted with a fluorine atom or a hydroxy group. ..
However, the total number of carbon atoms of ^{L b11} and L ^{b12 is 21 or less.}
In equation (b1-7),
L ^b13 represents a divalent saturated hydrocarbon group having 1 to 19 carbon atoms.
L ^b14 represents a single bond or a divalent saturated hydrocarbon group having 1 to 18 carbon atoms.
L ^b15 represents a single bond or a divalent saturated hydrocarbon group having 1 to 18 carbon atoms, and the hydrogen atom contained in the divalent saturated hydrocarbon group may be substituted with a fluorine atom or a hydroxy group. ..
However, the total number of carbon atoms of ^{L b13 to} L ^{b15 is 19 or less.}
In equation (b1-8),
L ^b16 represents a divalent saturated hydrocarbon group having 1 to 18 carbon atoms.
L ^b17 represents a divalent saturated hydrocarbon group having 1 to 18 carbon atoms.
L ^b18 represents a single bond or a divalent saturated hydrocarbon group having 1 to 17 carbon atoms, and the hydrogen atom contained in the divalent saturated hydrocarbon group may be substituted with a fluorine atom or a hydroxy group. ..
However, the total number of carbon atoms of ^{L b16 to} L ^{b18 is 19 or less.} ]

L ^b8 is preferably a divalent saturated hydrocarbon group having 1 to 4 carbon atoms.
L ^b9 is preferably a divalent saturated hydrocarbon group having 1 to 8 carbon atoms.
L ^b10 is preferably a single bond or a divalent saturated hydrocarbon group having 1 to 19 carbon atoms, and more preferably a single bond or a divalent saturated hydrocarbon group having 1 to 8 carbon atoms.
L ^b11 is preferably a divalent saturated hydrocarbon group having 1 to 8 carbon atoms.
L ^b12 is preferably a single bond or a divalent saturated hydrocarbon group having 1 to 8 carbon atoms.
L ^b13 is preferably a divalent saturated hydrocarbon group having 1 to 12 carbon atoms.
L ^b14 is preferably a single bond or a divalent saturated hydrocarbon group having 1 to 6 carbon atoms.
L ^b15 is preferably a single bond or a divalent saturated hydrocarbon group having 1 to 18 carbon atoms, and more preferably a single bond or a divalent saturated hydrocarbon group having 1 to 8 carbon atoms.
L ^b16 is preferably a divalent saturated hydrocarbon group having 1 to 12 carbon atoms.
L ^b17 is preferably a divalent saturated hydrocarbon group having 1 to 6 carbon atoms.
L ^b18 is preferably a single bond or a divalent saturated hydrocarbon group having 1 to 17 carbon atoms, and more preferably a single bond or a divalent saturated hydrocarbon group having 1 to 4 carbon atoms.

［式（ｂ１−９）中、
Ｌ^ｂ１９は、単結合又は炭素数１〜２３の２価の飽和炭化水素基を表し、該２価の飽和炭化水素基に含まれる水素原子は、フッ素原子に置換されていてもよい。
Ｌ^ｂ２０は、単結合又は炭素数１〜２３の２価の飽和炭化水素基を表し、該２価の飽和炭化水素基に含まれる水素原子はフッ素原子、ヒドロキシ基又はアルキルカルボニルオキシ基に置換されていてもよい。該アルキルカルボニルオキシ基に含まれる−ＣＨ_２−は、−Ｏ−又は−Ｃ（＝Ｏ）−に置き換わっていてもよく、該アルキルカルボニルオキシ基に含まれる水素原子は、ヒドロキシ基に置換されていてもよい。
ただし、Ｌ^ｂ１９及びＬ^ｂ２０の合計炭素数は２３以下である。
式（ｂ１−１０）中、
Ｌ^ｂ２１は、単結合又は炭素数１〜２１の２価の飽和炭化水素基を表し、該２価の飽和炭化水素基に含まれる水素原子は、フッ素原子に置換されていてもよい。
Ｌ^ｂ２２は、単結合又は炭素数１〜２１の２価の飽和炭化水素基を表し、該２価の飽和炭化水素基に含まれる水素原子はフッ素原子、ヒドロキシ基又はアルキルカルボニルオキシ基に置換されていてもよい。該アルキルカルボニルオキシ基に含まれる−ＣＨ_２−は、−Ｏ−又は−ＣＯ−に置き換わっていてもよく、該アルキルカルボニルオキシ基に含まれる水素原子は、ヒドロキシ基に置換されていてもよい。
Ｌ^ｂ２３は、単結合又は炭素数１〜２１の２価の飽和炭化水素基を表し、該２価の飽和炭化水素基に含まれる水素原子は、フッ素原子、ヒドロキシ基又はアルキルカルボニルオキシ基に置換されていてもよい。該アルキルカルボニルオキシ基に含まれる−ＣＨ_２−は、−Ｏ−又は−Ｃ（＝Ｏ）−に置き換わっていてもよく、該アルキルカルボニルオキシ基に含まれる水素原子は、ヒドロキシ基に置換されていてもよい。
ただし、Ｌ^ｂ２１〜Ｌ^ｂ２３の合計炭素数は２１以下である。
式（ｂ１−１１）中、
Ｌ^ｂ２４は、単結合又は炭素数１〜２０の２価の飽和炭化水素基を表し、該２価の飽和炭化水素基に含まれる水素原子は、フッ素原子に置換されていてもよい。
Ｌ^ｂ２５は、炭素数１〜２１の２価の飽和炭化水素基を表し、該２価の飽和炭化水素基に含まれる水素原子はフッ素原子、ヒドロキシ基又はアルキルカルボニルオキシ基に置換されていてもよい。該アルキルカルボニルオキシ基に含まれる−ＣＨ_２−は、−Ｏ−又は−ＣＯ−に置き換わっていてもよく、該アルキルカルボニルオキシ基に含まれる水素原子は、ヒドロキシ基に置換されていてもよい。
Ｌ^ｂ２６は、単結合又は炭素数１〜２０の２価の飽和炭化水素基を表し、該２価の飽和炭化水素基に含まれる水素原子は、フッ素原子、ヒドロキシ基又はアルキルカルボニルオキシ基に置換されていてもよい。該アルキルカルボニルオキシ基に含まれる−ＣＨ_２−は、−Ｏ−又は−Ｃ（＝Ｏ）−に置き換わっていてもよく、該アルキルカルボニルオキシ基に含まれる水素原子は、ヒドロキシ基に置換されていてもよい。
ただし、Ｌ^ｂ２４〜Ｌ^ｂ２６の合計炭素数は２１以下である。］ Examples of the formula (b1-3) include groups represented by the formulas (b1-9) to (b1-11).

[In equation (b1-9),
L ^b19 represents a single bond or a divalent saturated hydrocarbon group having 1 to 23 carbon atoms, and the hydrogen atom contained in the divalent saturated hydrocarbon group may be substituted with a fluorine atom.
L ^b20 represents a single bond or a divalent saturated hydrocarbon group having 1 to 23 carbon atoms, and the hydrogen atom contained in the divalent saturated hydrocarbon group is replaced with a fluorine atom, a hydroxy group or an alkylcarbonyloxy group. May be. _{The −CH 2} − contained in the alkylcarbonyloxy group may be replaced with −O− or −C (= O) −, and the hydrogen atom contained in the alkylcarbonyloxy group is substituted with a hydroxy group. May be.
However, the total number of carbon atoms of ^{L b19} and L ^{b20 is 23 or less.}
In equation (b1-10),
L ^b21 represents a single bond or a divalent saturated hydrocarbon group having 1 to 21 carbon atoms, and the hydrogen atom contained in the divalent saturated hydrocarbon group may be substituted with a fluorine atom.
L ^b22 represents a single bond or a divalent saturated hydrocarbon group having 1 to 21 carbon atoms, and the hydrogen atom contained in the divalent saturated hydrocarbon group is replaced with a fluorine atom, a hydroxy group or an alkylcarbonyloxy group. May be. _{-CH 2-} contained in the alkylcarbonyloxy group may be replaced with -O- or -CO-, and the hydrogen atom contained in the alkylcarbonyloxy group may be replaced with a hydroxy group.
L ^b23 represents a single bond or a divalent saturated hydrocarbon group having 1 to 21 carbon atoms, and the hydrogen atom contained in the divalent saturated hydrocarbon group is replaced with a fluorine atom, a hydroxy group or an alkylcarbonyloxy group. It may have been. _{The −CH 2} − contained in the alkylcarbonyloxy group may be replaced with −O− or −C (= O) −, and the hydrogen atom contained in the alkylcarbonyloxy group is substituted with a hydroxy group. May be.
However, the total number of carbon atoms of ^{L b21 to} L ^{b23 is 21 or less.}
In equation (b1-11),
L ^b24 represents a single bond or a divalent saturated hydrocarbon group having 1 to 20 carbon atoms, and the hydrogen atom contained in the divalent saturated hydrocarbon group may be substituted with a fluorine atom.
L ^b25 represents a divalent saturated hydrocarbon group having 1 to 21 carbon atoms, and even if the hydrogen atom contained in the divalent saturated hydrocarbon group is substituted with a fluorine atom, a hydroxy group or an alkylcarbonyloxy group. good. _{-CH 2-} contained in the alkylcarbonyloxy group may be replaced with -O- or -CO-, and the hydrogen atom contained in the alkylcarbonyloxy group may be replaced with a hydroxy group.
L ^b26 represents a single bond or a divalent saturated hydrocarbon group having 1 to 20 carbon atoms, and the hydrogen atom contained in the divalent saturated hydrocarbon group is replaced with a fluorine atom, a hydroxy group or an alkylcarbonyloxy group. It may have been. _{The −CH 2} − contained in the alkylcarbonyloxy group may be replaced with −O− or −C (= O) −, and the hydrogen atom contained in the alkylcarbonyloxy group is substituted with a hydroxy group. May be.
^However, the total number of carbon atoms of L b24 ^{~L b26} is 21 or less. ]

In formulas (b1-9) to (b1-11), when the hydrogen atom contained in the divalent saturated hydrocarbon group is substituted with an alkylcarbonyloxy group, the carbon number of the alkylcarbonyloxy group and the ester bond Including the number of C (= O) and O in the divalent saturated hydrocarbon group, it is defined as the number of carbon atoms of the divalent saturated hydrocarbon group.

Examples of the alkylcarbonyloxy group include an acetyloxy group, a propionyloxy group, a butyryloxy group, a cyclohexylcarbonyloxy group, an adamantylcarbonyloxy group and the like.

Examples of the group represented by the formula (b1-4) include the following.

Examples of the group represented by the formula (b1-5) include the following.

Examples of the group represented by the formula (b1-6) include the following.

Examples of the group represented by the formula (b1-7) include the following.

Examples of the group represented by the formula (b1-8) include the following.

Examples of the group represented by the formula (b1-2) include the following.

Examples of the group represented by the formula (b1-9) include the following.

Examples of the group represented by the formula (b1-10) include the following.

Examples of the group represented by the formula (b1-11) include the following.

^{<Organic cation Z +} constituting salt (I)>
^{Examples of the organic cation Z +} which is a cation in the salt (I) include an organic onium cation, an organic sulfonium cation, an organic iodine cation, an organic ammonium cation, a benzothiazolium cation, and an organic phosphonium cation. Among these, an organic sulfonium cation and an organic iodonium cation are preferable, and an aryl sulfonium cation is more preferable. Specifically, the cation represented by any of the formulas (b2-1) to (b2-4) (hereinafter, may be referred to as "cation (b2-1)" or the like depending on the formula number). Can be mentioned.

［式（ｂ２−１）〜式（ｂ２−４）において、
Ｒ^b4〜Ｒ^b6は、それぞれ独立に、炭素数１〜３０の鎖式炭化水素基、炭素数３〜３６の脂環式炭化水素基又は炭素数６〜３６の芳香族炭化水素基を表し、該鎖式炭化水素基に含まれる水素原子は、ヒドロキシ基、炭素数１〜１２のアルコキシ基、炭素数３〜１２の脂環式炭化水素基又は炭素数６〜１８の芳香族炭化水素基で置換されていてもよく、該脂環式炭化水素基に含まれる水素原子は、ハロゲン原子、炭素数１〜１８の脂肪族炭化水素基、炭素数２〜４のアルキルカルボニル基又はグリシジルオキシ基で置換されていてもよく、該芳香族炭化水素基に含まれる水素原子は、ハロゲン原子、ヒドロキシ基又は炭素数１〜１２のアルコキシ基で置換されていてもよい。
Ｒ^b4とＲ^b5とは、互いに結合してそれらが結合する硫黄原子と一緒になって環を形成してもよく、該環に含まれる−ＣＨ₂−は、−Ｏ−、−Ｓ−又は−ＣＯ−に置き換わってもよい。
Ｒ^b7及びＲ^b8は、それぞれ独立に、ヒドロキシ基、炭素数１〜１２の脂肪族炭化水素基又は炭素数１〜１２のアルコキシ基を表す。
ｍ２及びｎ２は、それぞれ独立に０〜５のいずれかの整数を表す。
ｍ２が２以上のとき、複数のＲ^b7は同一でも異なってもよく、ｎ２が２以上のとき、複数のＲ^b8は同一でも異なってもよい。
Ｒ^b9及びＲ^b10は、それぞれ独立に、炭素数１〜３６の鎖式炭化水素基又は炭素数３〜３６の脂環式炭化水素基を表す。
Ｒ^b9とＲ^b10とは、互いに結合してそれらが結合する硫黄原子と一緒になって環を形成してもよく、該環に含まれる−ＣＨ₂−は、−Ｏ−、−Ｓ−又は−ＣＯ−に置き換わってもよい。
Ｒ^b11は、水素原子、炭素数１〜３６の鎖式炭化水素基、炭素数３〜３６の脂環式炭化水素基又は炭素数６〜１８の芳香族炭化水素基を表す。
Ｒ^b12は、炭素数１〜１２の鎖式炭化水素基、炭素数３〜１８の脂環式炭化水素基又は炭素数６〜１８の芳香族炭化水素基を表し、該鎖式炭化水素に含まれる水素原子は、炭素数６〜１８の芳香族炭化水素基で置換されていてもよく、該芳香族炭化水素基に含まれる水素原子は、炭素数１〜１２のアルコキシ基又は炭素数１〜１２のアルキルカルボニルオキシ基で置換されていてもよい。
Ｒ^b11とＲ^b12とは、互いに結合してそれらが結合する−ＣＨ−ＣＯ−を含めて環を形成していてもよく、該環に含まれる−ＣＨ₂−は、−Ｏ−、−Ｓ−又は−ＣＯ−に置き換わってもよい。
Ｒ^b13〜Ｒ^b18は、それぞれ独立に、ヒドロキシ基、炭素数１〜１２の脂肪族炭化水素基又は炭素数１〜１２のアルコキシ基を表す。
Ｌ^b31は、硫黄原子又は酸素原子を表す。
ｏ２、ｐ２、ｓ２、及びｔ２は、それぞれ独立に、０〜５のいずれかの整数を表す。
ｑ２及びｒ２は、それぞれ独立に、０〜４のいずれかの整数を表す。
ｕ２は０又は１を表す。
ｏ２が２以上のとき、複数のＲ^b13は同一又は相異なり、ｐ２が２以上のとき、複数のＲ^b14は同一又は相異なり、ｑ２が２以上のとき、複数のＲ^b15は同一又は相異なり、ｒ２が２以上のとき、複数のＲ^b16は同一又は相異なり、ｓ２が２以上のとき、複数のＲ^b17は同一又は相異なり、ｔ２が２以上のとき、複数のＲ^b18は同一又は相異なる。］

[In equations (b2-1) to (b2-4),
R ^{b4 to} R ^b6 independently represent a chain hydrocarbon group having 1 to 30 carbon atoms, an alicyclic hydrocarbon group having 3 to 36 carbon atoms, or an aromatic hydrocarbon group having 6 to 36 carbon atoms. The hydrogen atom contained in the chain hydrocarbon group is a hydroxy group, an alkoxy group having 1 to 12 carbon atoms, an alicyclic hydrocarbon group having 3 to 12 carbon atoms, or an aromatic hydrocarbon group having 6 to 18 carbon atoms. It may be substituted, and the hydrogen atom contained in the alicyclic hydrocarbon group is a halogen atom, an aliphatic hydrocarbon group having 1 to 18 carbon atoms, an alkylcarbonyl group having 2 to 4 carbon atoms, or a glycidyloxy group. It may be substituted, and the hydrogen atom contained in the aromatic hydrocarbon group may be substituted with a halogen atom, a hydroxy group, or an alkoxy group having 1 to 12 carbon atoms.
R ^b4 and R ^b5 may be bonded to each other to form a ring together with the sulfur atom to which they are bonded, and −CH ₂ − contained in the ring is −O−, −S− or −O−, −S− or. It may be replaced with −CO−.
R ^b7 and R ^b8 independently represent a hydroxy group, an aliphatic hydrocarbon group having 1 to 12 carbon atoms, or an alkoxy group having 1 to 12 carbon atoms.
m2 and n2 each independently represent an integer of 0 to 5.
When m2 is 2 or more, the plurality of R ^b7s may be the same or different, and when n2 is 2 or more, the plurality of R ^b8s may be the same or different.
R ^b9 and R ^b10 independently represent a chain hydrocarbon group having 1 to 36 carbon atoms or an alicyclic hydrocarbon group having 3 to 36 carbon atoms.
R ^b9 and R ^b10 may be bonded to each other to form a ring together with the sulfur atom to which they are bonded, and −CH ₂ − contained in the ring may be −O−, −S− or −O−, −S− or. It may be replaced with −CO−.
R ^b11 represents a hydrogen atom, a chain hydrocarbon group having 1 to 36 carbon atoms, an alicyclic hydrocarbon group having 3 to 36 carbon atoms, or an aromatic hydrocarbon group having 6 to 18 carbon atoms.
R ^b12 represents a chain hydrocarbon 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, and is included in the chain hydrocarbon group. The hydrogen atom may be substituted with an aromatic hydrocarbon group having 6 to 18 carbon atoms, and the hydrogen atom contained in the aromatic hydrocarbon group may be an alkoxy group having 1 to 12 carbon atoms or 1 to 12 carbon atoms. It may be substituted with 12 alkylcarbonyloxy groups.
R ^b11 and R ^b12 may form a ring including −CH—CO− to which they are bonded to each other, and −CH ₂₋ contained in the ring is −O−, −S. It may be replaced with − or −CO−.
R ^{b13 to} R ^b18 independently represent a hydroxy group, an aliphatic hydrocarbon group having 1 to 12 carbon atoms, or an alkoxy group having 1 to 12 carbon atoms.
L ^b31 represents a sulfur atom or an oxygen atom.
o2, p2, s2, and t2 each independently represent an integer of 0 to 5.
q2 and r2 each independently represent an integer of 0 to 4.
u2 represents 0 or 1.
When o2 is 2 or more, a plurality of R ^b13s are the same or different, when p2 is 2 or more, a plurality of R ^b14s are the same or different, and when q2 is 2 or more, a plurality of R ^b15s are the same or different. when r2 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 different. ]

特に、Ｒ^b9〜Ｒ^b12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。 The aliphatic hydrocarbon group represents a chain hydrocarbon group and an alicyclic hydrocarbon group.
The chain hydrocarbon group includes an alkyl group of a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, a sec-butyl group, a tert-butyl group, a pentyl group, a hexyl group, an octyl group and a 2-ethylhexyl group. Can be mentioned.
In particular, ^{the chain hydrocarbon groups of R b9 to} R ^b12 preferably have 1 to 12 carbon atoms.
The alicyclic hydrocarbon group may be either monocyclic or polycyclic, and the monocyclic alicyclic hydrocarbon group includes a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, and a cyclo. Cycloalkyl groups such as heptyl group, cyclooctyl group and cyclodecyl group can be mentioned. Examples of the polycyclic alicyclic hydrocarbon group include a decahydronaphthyl group, an adamantyl group, a norbornyl group and the following groups.

In particular, ^{the alicyclic hydrocarbon groups of R b9 to} R ^b12 preferably have 3 to 18 carbon atoms, and more preferably 4 to 12 carbon atoms.

Examples of the alicyclic hydrocarbon group in which the hydrogen atom is substituted with an aliphatic hydrocarbon group include a methylcyclohexyl group, a dimethylcyclohexyl group, a 2-methyladamantan-2-yl group, and a 2-ethyladamantan-2-yl group. , 2-Isopropyl adamantan-2-yl group, methylnorbornyl group, isobornyl group and the like. In the alicyclic hydrocarbon group in which the hydrogen atom is substituted with an aliphatic hydrocarbon group, the total number of carbon atoms of the alicyclic hydrocarbon group and the aliphatic hydrocarbon group is preferably 20 or less.

Examples of the aromatic hydrocarbon group include a phenyl group, a tolyl group, a xsilyl group, a cumenyl group, a mesityl group, a p-ethylphenyl group, a p-tert-butylphenyl group, a p-cyclohexylphenyl group and a p-adamantylphenyl group. , Biphenylyl group, naphthyl group, phenanthryl group, 2,6-diethylphenyl group, 2-methyl-6-ethylphenyl group and other aryl groups.
When the aromatic hydrocarbon group contains a chain hydrocarbon group or an alicyclic hydrocarbon group, a chain hydrocarbon group having 1 to 18 carbon atoms and an alicyclic hydrocarbon having 3 to 18 carbon atoms Groups are preferred.
Examples of the aromatic hydrocarbon group in which the hydrogen atom is substituted with an alkoxy group include a p-methoxyphenyl group.
Examples of the chain hydrocarbon group in which the hydrogen atom is substituted with an aromatic hydrocarbon group include an aralkyl group such as a benzyl group, a phenethyl group, a phenylpropyl group, a trityl group, a naphthylmethyl group and a naphthylethyl group.

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

The ^{ring formed by R b4} and R ^b5 bonding to each other and together with the sulfur atom to which they are bonded can be monocyclic, polycyclic, aromatic, non-aromatic, saturated or unsaturated. It may be a ring of. Examples of this ring include a ring having 3 to 18 carbon atoms, preferably a ring having 4 to 18 carbon atoms. Further, the ring containing a sulfur atom may be a 3-membered ring to a 12-membered ring, preferably a 3-membered ring to a 7-membered ring, and examples thereof include the following rings.

The ^{ring formed by R b9} and R ^b10 together may be any of monocyclic, polycyclic, aromatic, non-aromatic, saturated and unsaturated rings. This ring may be a 3-membered ring to a 12-membered ring, preferably a 3-membered ring to a 7-membered ring. For example, a thiolan-1-ium ring (tetrahydrothiophenium ring), a thian-1-ium ring, a 1,4-oxatian-4-ium ring and the like can be mentioned.
The ^{ring formed by R b11} and R ^b12 together may be any of monocyclic, polycyclic, aromatic, non-aromatic, saturated and unsaturated rings. This ring may be a 3-membered ring to a 12-membered ring, preferably a 3-membered ring to a 7-membered ring. Examples thereof include an oxocycloheptane ring, an oxocyclohexane ring, an oxonorbornane ring, and an oxoadamantane ring.

Among the cations (b2-1) to cations (b2-4), the cation (b2-1) is preferable.
Examples of the cation (b2-1) include the following cations.

Examples of the cation (b2-2) include the following cations.

Examples of the cation (b2-3) include the following cations.

Examples of the cation (b2-4) include the following cations.

Among them, the formulas (b2-c-1), (b2-c-10), (b2-c-12), (b2-c-14), (b2-c-27), (b2-c-30). And the cation represented by (b2-c-31) is preferable.

Of the ions constituting the salt (I), organic anions A ^- combination represented by Specific examples of combinations of ions except the following formula (I-c-1) ~ formula (I-c-18) Can be mentioned.
In the formulas (I-c-1) to (I-c-18), X ¹ is an ethylene group.
^{L b1} in the formulas (I-c-1) to (I-c-6) and formulas (I-c-13) to (I-c-18 ^{), and L b8} in the formula (b1-4). It is a group that is a single bond.
In formulas (I-c-7) to (I-c-12), L ^b1 is, and in formula (b1-7), L ^b13 is -CH _2- Ad- (Ad represents a divalent group of adamantane). ), L ^b14 and L ^b15 are single-bonded groups.
When X ¹ is an alkanediyl group, it is preferable that L ^b1 has an oxygen atom at the end on the X ¹ side thereof, and this oxygen atom is bonded to ^{X 1.}

Among them, the formula (I-c-1), the formula (I-c-2), the formula (I-c-4), the formula (I-c-5), the formula (I-c-7), and the formula (I). -C-8), the combination represented by any of the formulas (I-c-10) and (I-c-11) is preferable.

［式（Ｉ−Ａ）中、
Ｑ¹及びＱ²は、それぞれ独立に、フッ素原子又は炭素数１〜６のペルフルオロアルキル基を表す。
Ｌ^ｂｂ１は、炭素数１〜２４の２価の飽和炭化水素基を表し、該飽和炭化水素基に含まれる−ＣＨ_２−は−Ｏ−又は−Ｃ（＝Ｏ）−に置き換わっていてもよく、該飽和炭化水素基に含まれる水素原子はフッ素原子又はヒドロキシ基で置換されていてもよい。
Ｙは、置換基を有していてもよいメチル基又は置換基を有していてもよい炭素数３〜１８の１価の脂環式炭化水素基を表し、該脂環式炭化水素基に含まれる−ＣＨ_２−は、−Ｏ−、−ＳＯ_２−又は−Ｃ（＝Ｏ）−に置き換わっていてもよい。］ <Organic anions A constituting the salt (I) ^->
Examples of the organic anion A ⁻ constituting the salt (I) include a sulfonic acid anion, a sulfonylimide anion, a sulfonylmethide anion, and a carboxylic acid anion. Among these, the sulfonic acid anion is preferable, and the sulfonic acid anion represented by the formula (IA) is more preferable.

[In formula (IA),
Q ¹ and Q ² independently represent a fluorine atom or a perfluoroalkyl group having 1 to 6 carbon atoms.
L ^bb 1 represents a divalent saturated hydrocarbon group having 1 to 24 carbon atoms, and -CH _2- contained in the saturated hydrocarbon group may be replaced with -O- or -C (= O)-. , The hydrogen atom contained in the saturated hydrocarbon group may be substituted with a fluorine atom or a hydroxy group.
Y represents a methyl group which may have a substituent or a monovalent alicyclic hydrocarbon group having 3 to 18 carbon atoms which may have a substituent, and the alicyclic hydrocarbon group may be used. it is, -O - - -CH ₂ contained, - SO ₂ - or -C (= O) - may be replaced with. ]

_{In the formula (IA), when −CH 2} − contained in the saturated hydrocarbon group or the alicyclic hydrocarbon group is replaced with −O− or −C (= O) −, the number of carbon atoms before the replacement is used. Let the number of carbon atoms be the saturated hydrocarbon group and the alicyclic hydrocarbon group, respectively.

The perfluoroalkyl group having 1 to 6 carbon atoms of Q ¹ and ^{Q 2,} a trifluoromethyl group, perfluoroethyl group, perfluoropropyl group, perfluoroisopropyl group, perfluorobutyl group, a perfluoro sec- butyl group, perfluoro-tert- butyl , Perfluoropentyl group, perfluorohexyl group and the like.
It is preferable that Q ¹ and Q ² are independently fluorine atoms or trifluoromethyl groups, and it is more preferable that both are fluorine atoms.

L ^{bb 1} in the formula (IA) has the same meaning as ^{L b1 in the formula (I).} Specific examples and preferable specific examples of L ^{bb 1} in the formula (IA) are the same as those described for L bb 1 in the formula (I), and the descriptions thereof are cited. Note that * represents a bond with Y.

Examples of the monovalent alicyclic hydrocarbon group represented by Y include groups represented by formulas (Y1) to (Y11) and formulas (Y36) to (Y38).
_{When -CH 2-} contained in the monovalent alicyclic hydrocarbon group represented by Y is replaced by -O-, -SO _2- or -C (= O)-, the number may be one. It may be a plurality of two or more. Examples of such a group include groups represented by the formulas (Y12) to (Y35).

Among them, it is preferably a group represented by any one of formulas (Y1) to (Y20), formula (Y30), and formula (Y31), and more preferably formulas (Y11), formulas (Y15), and formulas (Y16). ), Formula (Y20), formula (Y30) or formula (Y31), and more preferably a group represented by formula (Y11), formula (Y15) or formula (Y30).
When Y constitutes a spiro ring of formulas (Y28) to (Y33), the alkanediyl group between the two oxygens preferably has one or more fluorine atoms. Further, among the alkanediyl groups contained in the ketal structure, those in which the fluorine atom is not substituted in the methylene group adjacent to the oxygen atom are preferable.

Examples of the substituent of the methyl group represented by Y in the formula (IA) include a halogen atom, a hydroxy group, an alicyclic hydrocarbon group having 3 to 16 carbon atoms, and an aromatic hydrocarbon having 6 to 18 carbon atoms. Group, glycidyloxy group _{or-(CH 2} ) _ja -OC (= O) -R ^b1 group (in the formula, R ^b1 is an alkyl group having 1 to 16 carbon atoms and a monovalent group having 3 to 16 carbon atoms. It represents an alicyclic hydrocarbon group or a monovalent aromatic hydrocarbon group having 6 to 18 carbon atoms. Ja represents an integer of 0 to 4) and the like.
The substituent of the monovalent alicyclic hydrocarbon group represented by Y in the formula (IA) may be an alkyl having 1 to 12 carbon atoms which may be substituted with a halogen atom, a hydroxy group or a hydroxy group. Group, alicyclic hydrocarbon group with 3 to 16 carbon atoms, alkoxy group with 1 to 12 carbon atoms, aromatic hydrocarbon group with 6 to 18 carbon atoms, aralkyl group with 7 to 21 carbon atoms, 2 to 4 carbon atoms Acyl group, glycidyloxy group _{or-(CH 2} ) _ja -OC (= O) -R ^b1 group (in the formula, R ^b1 is an alkyl group having 1 to 16 carbon atoms and 1 of 3 to 16 carbon atoms. It represents a valent alicyclic hydrocarbon group or a monovalent aromatic hydrocarbon group having 6 to 18 carbon atoms. Ja represents an integer of 0 to 4) and the like.

Examples of the halogen atom include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom.
Examples of the alicyclic hydrocarbon group include a cyclopentyl group, a cyclohexyl group, a methylcyclohexyl group, a dimethylcyclohexyl group, a cycloheptyl group, a cyclooctyl group, a norbornyl group, an adamantyl group and the like.
Examples of the aromatic hydrocarbon group include a phenyl group, a naphthyl group, an anthryl group, a p-methylphenyl group, a p-tert-butylphenyl group and a p-adamantylphenyl group; a trill group, a xsilyl group, a cumenyl group and a mesityl group. , Biphenyl group, phenanthryl group, aryl group such as 2,6-diethylphenyl group, 2-methyl-6-ethylphenyl and the like.
Examples of the alkyl group include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, a sec-butyl group, a tert-butyl group, an n-pentyl group, an n-hexyl group, a heptyl group, and 2 -Ethylhexyl group, octyl group, nonyl group, decyl group, undecyl group, dodecyl group and the like can be mentioned.
Examples of the alkyl group substituted with the hydroxy group include hydroxyalkyl groups such as a hydroxymethyl group and a hydroxyethyl group.
Examples of the alkoxy group include a methoxy group, an ethoxy group, a propoxy group, a butoxy group, a pentyloxy group, a hexyloxy group, a heptyloxy group, an octyloxy group, a decyloxy group and a dodecyloxy group.
Examples of the aralkyl group include a benzyl group, a phenethyl group, a phenylpropyl group, a naphthylmethyl group and a naphthylethyl group.
Examples of the acyl group include an acetyl group, a propionyl group, a butyryl group and the like.

Examples of the alicyclic hydrocarbon group having 1 to 18 carbon atoms which may have a substituent represented by Y in the formula (IA) include the following.

When Y is a methyl group and L ^b1 is a divalent linear or branched saturated hydrocarbon group having 1 to 24 carbon atoms, the divalent saturated hydrocarbon group at the bonding position with Y It is preferable that −CH ₂₋ is replaced with −O− or −C (= O) −.

Y is a monovalent alicyclic hydrocarbon group having 3 to 18 carbon atoms, which may preferably have a substituent, and more preferably an adamantyl group which may have a substituent. -CH ₂ constituting the cyclic hydrocarbon group or adamantyl group - is -O -, - SO ₂ - or -C (= O) - it may be replaced with. Y is more preferably an adamantyl group, a hydroxyadamantyl group, an oxoadamantyl group or a group represented by the following.

Examples of the sulfonic acid anion represented by the formula (IA) include anions represented by the formulas (B1-A-1) to (B1-A-54) [hereinafter, "anion (B1)" according to the formula number. -A-1) "etc. ] Are preferable, and formulas (B1-A-1) to (B1-A-4), formulas (B1-A-9), formulas (B1-A-10), formulas (B1-A-24) to formulas (B1-A-24) to formulas. (B1-A-33), formulas (B1-A-36) to formulas (B1-A-40), formulas (B1-A-47) to formulas (B1-A-54). Anions are more preferred.

[In the formulas (B1-A-1) to (B1-A-54),
R ^{i2 to} R ⁱ⁷ represent an alkyl group having 1 to 4 carbon atoms, and are preferably a methyl group or an ethyl group.
R ⁱ⁸ represents an aliphatic hydrocarbon group having 1 to 12 carbon atoms, preferably an alkyl group having 1 to 4 carbon atoms, a monovalent alicyclic hydrocarbon group having 5 to 12 carbon atoms, or a combination thereof. It is a group formed, more preferably a methyl group, an ethyl group, a cyclohexyl group or an adamantyl group.
^LA41 is a single bond or an alkanediyl group having 1 to 4 carbon atoms.
Q ¹ and ^{Q 2} are the same as defined above. ]

Examples of the sulfonic acid anion represented by the formula (IA) include anions represented by the formulas (B1a-1) to (B1a-30).

Of these, anions represented by any of the formulas (B1a-1) to (B1a-3), formulas (B1a-7) to formulas (B1a-19), and formulas (B1a-22) are preferable.

<Specific example of salt (I)>
Examples of the salt (I) include salts in which the above-mentioned cations and anions are arbitrarily combined. Specific examples of the salt (I) are shown in the table below.

In the table below, each reference numeral represents a reference numeral assigned to the above-mentioned structure representing an anion or cation. For example, the salt (I-1) is a salt composed of an anion represented by the formula (BIa-1) and a cation represented by the formula (I-c-1), and is a compound shown below.

Among them, the salt (I) includes salt (I-1), salt (I-2), salt (I-3), salt (I-16), salt (I-17), and salt (I-18). , Salt (I-19), Salt (I-22), Salt (I-23), Salt (I-24), Salt (I-25), Salt (I-38), Salt (I-39), Salt (I-40), salt (I-41), salt (I-44), salt (I-67), salt (I-68), salt (I-69), salt (I-82), salt (I-83), salt (I-84), salt (I-85), salt (I-88), salt (I-89), salt (I-90), salt (I-91), salt ( I-104), salt (I-105), salt (I-106), salt (I-107), salt (I-110), salt (I-133), salt (I-134), salt (I) -135), salt (I-148), salt (I-149), salt (I-150), salt (I-151), salt (I-154), salt (I-155), salt (I- 156), salt (I-157), salt (I-170), salt (I-171), salt (I-172), salt (I-173), salt (I-176), salt (I-199) ), Salt (I-200), Salt (I-201), Salt (I-214), Salt (I-215), Salt (I-216), Salt (I-217), Salt (I-220) , Salt (I-221), Salt (I-222), Salt (I-223), Salt (I-236), Salt (I-237), Salt (I-238), Salt (I-239) and Salt (I-242) is preferred.

（式中、ＬＬは、Ｌ^ｂ１から−Ｏ−を除いた基であり、
ＬＬ以外の全ての符号は、それぞれ前記と同じ意味を表す。）
溶剤としては、アセトニトリル、クロロホルム等が挙げられる。
反応は、通常１５℃〜８０℃の温度範囲で、０．５〜２４時間行われる。 <Manufacturing method of salt (I)>
When the salt (I) contains, for example, ^{—O— in which L b1} binds to X ¹ , the salt represented by the formula (Ia) and the compound represented by the formula (Ib) are used as a solvent. It can be produced by reacting in.

(In the formula, LL is a group obtained by removing -O- from ^{L b1.}
All symbols other than LL have the same meanings as described above. )
Examples of the solvent include acetonitrile, chloroform and the like.
The reaction is usually carried out in the temperature range of 15 ° C. to 80 ° C. for 0.5 to 24 hours.

Examples of the compound represented by the formula (Ib) include salts represented by the following.

（式中、全ての符号は、それぞれ前記と同じ意味を表す。）
触媒としては、安息香酸銅（ＩＩ）等が挙げられ、溶剤としては、モノクロロベンゼン等が挙げられる。
反応は、通常２０℃〜１２０℃の温度範囲で、０．５〜２４時間行われる。 In the salt represented by the formula (Ia), the salt represented by the formula (Ic) and the compound represented by the formula (Id) are reacted in a solvent in the presence of a catalyst. It can be manufactured by.

(In the formula, all the symbols have the same meanings as described above.)
Examples of the catalyst include copper (II) benzoate and the like, and examples of the solvent include monochlorobenzene and the like.
The reaction is usually carried out in the temperature range of 20 ° C. to 120 ° C. for 0.5 to 24 hours.

Examples of the salt represented by the formula (Ic) include salts represented by the following.

Examples of the compound represented by the formula (Id) include compounds represented by the following.

<Acid generator>
The acid generator of the present invention is an acid generator containing a salt (I). The acid generator of the present invention may contain two or more kinds of salts (I).
The acid generator of the present invention may contain an acid generator known in the resist field other than the salt (I) (hereinafter, may be referred to as “acid generator (B)”). The acid generator (B) will be described later.
When the salt (I) and the acid generator (B) are contained as the acid generator, the ratio of the contents of the salt (I) and the acid generator (B) (salt (I): acid generator (B). )) Are usually 1:99 to 99: 1, preferably 2:98 to 98: 2, more preferably 5:95 to 95: 5, and even more preferably 10:90 to 90:10 in terms of mass ratio.

<Resist composition>
The resist composition contains the salt (I) of the present invention and a resin having an acid unstable group (hereinafter, may be referred to as "resin (A)"). The "acid-unstable group" here is a structural unit having a leaving group, the leaving group being removed by contact with an acid, and the constituent unit having a hydrophilic group (for example, a hydroxy group or a carboxy group). Means the group that converts to.
The resist composition of the present invention may further contain an acid generator (B) in addition to the salt (I).
The resist composition preferably contains a quencher (hereinafter sometimes referred to as "quencher (C)") and preferably contains a solvent (hereinafter sometimes referred to as "solvent (E)").

<Resin (A)>
The resin (A) has a structural unit having an acid unstable group (hereinafter, may be referred to as “structural unit (a1)”). The resin (A) preferably further contains a structural unit other than the structural unit (a1). Structural units other than the structural unit (a1) include structural units having no acid-labile group (hereinafter sometimes referred to as “structural unit (s)”) and other structural units (hereinafter referred to as “structural unit (t)”). In some cases).

［式（１）中、Ｒ^a1〜Ｒ^a3は、それぞれ独立に、置換基を有していてもよい炭素数１〜８のアルキル基又は置換基を有していてもよい炭素数３〜２０の脂環式炭化水素基を表すか、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の非芳香族炭化水素環を形成する。
ｍａ及びｎａは、それぞれ独立に０又は１を表し、ｍａ及びｎａのうち少なくとも一方は１である。
＊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の複素環を形成し、該炭化水素基及び該複素環に含まれる−ＣＨ_２−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。
ｎａ’は、０又は１を表す。
＊は結合手を表す。］ <Structural unit (a1)>
The structural unit (a1) is derived from a monomer having an acid unstable group (hereinafter, may be referred to as “monomer (a1)”).
In the resin (A), the acid unstable group contained in the structural unit (a1) is preferably a group represented by the following formula (1) and / or a group represented by the formula (2).

[In the formula (1), R ^{a1 to} R ^a3 independently have an alkyl group having 1 to 8 carbon atoms which may have a substituent or an alkyl group having 3 to 20 carbon atoms which may have a substituent. R ^a1 and R ^a2 are bonded to each other to form a non-aromatic hydrocarbon ring having 3 to 20 carbon atoms together with the carbon atom to which they are bonded.
ma and na independently represent 0 or 1, respectively, and at least one of ma and na is 1.
* Represents a bond. ]

[In the 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. Representing, R ^a2'and R ^a3' are bonded to each other to form a heterocycle having 3 to 20 carbon atoms together with the carbon atom to which they are bonded, and the hydrocarbon group and −CH ₂ − contained in the heterocycle are , -O- or -S- may be replaced.
X represents an oxygen atom or a sulfur atom.
na'represents 0 or 1.
* Represents a bond. ]

置換基を有していてもよい炭素数１〜８のアルキル基の置換基としては、炭素数３〜２０の脂環式炭化水素基が挙げられる。置換基を有していてもよい炭素数３〜２０の脂環式炭化水素基の置換基としては、炭素数１〜８のアルキル基が挙げられる。より具体的には、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。
好ましくは、ｍａは０であり、ｎａは１である。 ^Examples of the alkyl group of 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, an n-octyl group and the like.
The alicyclic hydrocarbon groups of R ^{a1 to} R ^a3 may be either monocyclic or polycyclic. Examples of the monocyclic alicyclic hydrocarbon group include cycloalkyl groups such as cyclopentyl group, cyclohexyl group, cycloheptyl group and cyclooctyl group. Examples of the polycyclic alicyclic hydrocarbon group include a decahydronaphthyl group, an adamantyl group, a norbornyl group and the following groups (* indicates a bond). The alicyclic hydrocarbon groups of R ^{a1 to} R ^a3 have preferably 3 to 16 carbon atoms.

Examples of the substituent of the alkyl group having 1 to 8 carbon atoms which may have a substituent include an alicyclic hydrocarbon group having 3 to 20 carbon atoms. Examples of the substituent of the alicyclic hydrocarbon group having 3 to 20 carbon atoms which may have a substituent include an alkyl group having 1 to 8 carbon atoms. More specifically, a methylcyclohexyl group, a dimethylcyclohexyl group, a methylnorbornyl group, a cyclohexylmethyl group, an adamantylmethyl group, a norbornylethyl group and the like can be mentioned.
Preferably, ma is 0 and na is 1.

^{Examples of -C (R a1} ) (R ^a2 ) (R ^a3 ) in the case where R ^a1 and R a ² are bonded to each other to form a non-aromatic hydrocarbon ring include the following rings. The non-aromatic hydrocarbon ring preferably has 3 to 12 carbon atoms. * Represents a bond with -O-.

Specific examples of the group represented by the formula (1) include the following groups. * Represents a bond.

Ｒ^a1'及びＲ^a2'のうち、少なくとも１つは水素原子であることが好ましい。 Examples of the hydrocarbon group R ^{a1 '~R a3',} an alkyl group, an alicyclic hydrocarbon group, and a group formed by combining an aromatic hydrocarbon group and thereof.
Examples of the alkyl group and the alicyclic hydrocarbon group include the same as above.
Examples of the aromatic hydrocarbon group include a phenyl group, a naphthyl group, an anthryl group, a p-methylphenyl group, a p-tert-butylphenyl group, a p-adamantylphenyl group, a trill group, a xsilyl group, a cumenyl group, a mesityl group and a biphenyl group. Examples thereof include an aryl group such as a group, a phenanthryl group, a 2,6-diethylphenyl group and 2-methyl-6-ethylphenyl.
^{Examples of} the heterocycle in which R ^{a2'and R a3'} are bonded to each other and formed together with the carbon atom and X to which they are bonded include the following rings. * Represents a bond.

Of R ^{a1 'and} R ^a2', it is preferable that at least one is a hydrogen atom.

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

The monomer (a1) is preferably a monomer having an acid unstable group and an ethylenically unsaturated bond, and more preferably a (meth) acrylic monomer having an acid unstable group.

Among the (meth) acrylic monomers having an acid unstable group, those having an alicyclic hydrocarbon group having 5 to 20 carbon atoms are preferable. If the resin (A) having a structural unit derived from the monomer (a1) 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.

The structural unit derived from the (meth) acrylic monomer having a group represented by the formula (1) is preferably a structural unit represented by the formula (a1-0) (hereinafter referred to as a structural unit (a1-0)). In some cases, it may be referred to as a structural unit (a1-1), which is less than or equal to the structural unit represented by the formula (a1-1). ) Or a structural unit represented by the formula (a1-2) (hereinafter, may be referred to as a structural unit (a1-2)). These may be used alone or in combination of two or more.

［式（ａ１−０）中、
Ｌ^a01は、酸素原子又は^＊−Ｏ−（ＣＨ₂）_k01−Ｃ（＝Ｏ）−Ｏ−を表し、ｋ０１は１〜７のいずれかの整数を表し、＊は−Ｃ（＝Ｏ）−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 equation (a1-0),
L ^a01 represents an oxygen atom or _{^{* -O- (CH 2) k01 -C}} (= O) represents -O-, k01 represents an integer of 1-7, * is -C (= O) - Represents a bond with.
R ^a01 represents a hydrogen atom or a methyl group.
R ^a02 , R ^a03, and R ^a04 independently represent an alkyl group having 1 to 8 carbon atoms, an alicyclic hydrocarbon group having 3 to 18 carbon atoms, or a group combining these groups. ]

^La01 is preferably an oxygen atom or ^* −O− (CH ₂ ) _k01− C (= O) −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 the group combining these groups include the same groups as those mentioned in ^{R a1 to} R ^{a3 of the formula (1).}
The alkyl groups of R ^a02 , R ^a03 and R ^a04 preferably have 6 or less carbon atoms.
The alicyclic hydrocarbon groups of R ^a02 , R ^a03 and R ^a04 preferably have 3 to 8 carbon atoms, and more preferably 3 to 6 carbon atoms.
The group in which the alkyl group and the alicyclic hydrocarbon group are combined preferably has a total carbon number of 18 or less in combination with these alkyl groups and the alicyclic hydrocarbon group. Examples of such a group include a methylcyclohexyl group, a dimethylcyclohexyl group, a methylnorbornyl group and the like.
R ^a02 and R ^a03 are preferably alkyl groups having 1 to 6 carbon atoms, and more preferably methyl groups or ethyl groups.
^Ra04 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.

［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−Ｃ（＝Ｏ）−Ｏ−を表し、ｋ１は１〜７のいずれかの整数を表し、＊は−Ｃ（＝Ｏ）−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ることにより形成される基を表す。
ｍ１は、０〜１４のいずれかの整数を表す。
ｎ１は、０〜１０のいずれかの整数を表す。
ｎ１’は、０〜３のいずれかの整数を表す。］

[In the formula (a1-1) and the formula (a1-2),
L ^a1 and L ^a2 independently represent −O− or ^* −O− (CH ₂ ) _k1 −C (= O) −O−, and k1 represents an integer of any of 1 to 7, and * Represents a bond with −C (= O) −.
R ^a4 and R ^a5 independently represent a hydrogen atom or a methyl group.
R ^a6 and R ^a7 independently represent an alkyl group having 1 to 8 carbon atoms, an alicyclic hydrocarbon group having 3 to 18 carbon atoms, or a group formed by combining them.
m1 represents any integer from 0 to 14.
n1 represents any integer from 0 to 10.
n1'represents an integer of 0 to 3. ]

^La1 and ^La2 are preferably −O− or ^* −O− (CH ₂ ) _{k1 ′} −C (= O) −O−, and more preferably −O−. k1'is an integer of any of 1 to 4, preferably 1.
R ^a4 and R ^a5 are preferably methyl groups.
The alkyl groups of R ^a6 and R ^a7 include methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, sec-butyl group, tert-butyl group, n-pentyl group and n-hexyl group. Examples thereof include an n-heptyl group, a 2-ethylhexyl group and an n-octyl group.
The alicyclic hydrocarbon group of R ^a6 and R ^a7 may be either a monocyclic group or a polycyclic group, and examples of the monocyclic alicyclic hydrocarbon group include a cyclopropyl group, a cyclobutyl group and a cyclopentyl group. , Cycloalkyl group, methylcyclohexyl group, dimethylcyclohexyl group, cycloheptyl group, cyclooctyl group, cycloheptyl group, cyclodecyl group and the like. Examples of the polycyclic alicyclic hydrocarbon group include a decahydronaphthyl group, an adamantyl group, a 2-alkyladamantan-2-yl group, a 1- (adamantan-1-yl) alkyl group, a norbornyl group, and a methylnor. Examples thereof include a boronyl group and an isobornyl group.
Examples of the group formed by combining the alkyl group of R ^a6 and R ^a7 and the alicyclic hydrocarbon group include an aralkyl group, and a benzyl group, a phenethyl group and the like.
The number of carbon atoms of the alkyl groups of ^{R a6} and R ^{a7 is preferably 6 or less.}
The alicyclic hydrocarbon groups of R ^a6 and R ^a7 have preferably 3 to 8 carbon atoms, more preferably 3 to 6 carbon atoms.
m1 is preferably an integer of 0 to 3, more preferably 0 or 1.
n1 is preferably an integer of 0 to 3, and more preferably 0 or 1.
n1'is preferably 0 or 1.

As the structural unit (a1-0), for example, a structural unit represented by any of the formulas (a1-0-1) to (a1-0-12) is preferable, and the structural units (a1-0-1) to The structural unit represented by any of the formulas (a1-0-10) is more preferable.

In the above formula (a1-0-1) ~ formula (a1-0-12), structural units in which a methyl group corresponding to R ^a01 is replaced by a hydrogen atom, be mentioned as specific examples of the structural unit (a1-0) Can be done.

Examples of the structural unit (a1-1) include structural units derived from the monomers described in JP-A-2010-204646, preferably formulas (a1-1-1) to (a1-). The structural unit represented by any one of 1-8) can be mentioned, and more preferably, the structural unit represented by any of the formulas (a1-1-1) to (a1-1-4) can be mentioned.

Examples of the structural unit (a1-2) include structural units represented by any of the formulas (a1-2-1) to (a1-2-12), preferably the formula (a1-2-2). 3), the structural unit represented by the formula (a1-2-4), the formula (a1-2-9) or the formula (a1-2-10) can be mentioned, and more preferably, the formula (a1-2-3). ) Or the structural unit represented by the formula (a1-2-9).

When the resin (A) contains a structural unit (a1-0) and / or a structural unit (a1-1) and / or a structural unit (a1-2), the total content of these is the total structure of the resin (A). It is usually 10 to 95 mol%, preferably 15 to 90 mol%, more preferably 20 to 85 mol%, based on the total of the units.

［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−Ｃ（＝Ｏ）−Ｌ⁵⁴−を表し、ｈ３は１〜４のいずれかの整数を表し、＊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のいずれかの整数を表す。
ｓ１’は、０〜３のいずれかの整数を表す。 Examples of the structural unit having an acid unstable group include a structural unit represented by the formula (a1-5) (hereinafter, may be referred to as “structural unit (a1-5)”).

[In equation (a1-5),
R ^a8 represents an alkyl group having 1 to 6 carbon atoms, a hydrogen atom or a halogen atom which may have a halogen atom.
Z ^a1 represents a single bond or _{* - (CH 2) h3 -C} (= O) -L 54 - represents, h3 represents an integer of 1 to 4, * is a bond to L ⁵¹ show.
L ⁵¹ , L ⁵² , L ⁵³ and L ⁵⁴ independently represent -O- or -S-, respectively.
s1 represents an integer of 1 to 3.
s1'represents an integer of 0 to 3.

In the formula (a1-5), R ^a8 represents a hydrogen atom, a methyl group or a trifluoromethyl group.
L ⁵¹ is preferably an oxygen atom.
It is preferable that one of L ⁵² and L ⁵³ is -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- C (= O) -O-.

Examples of the structural unit (a1-5) include the structural unit described in JP-A-2010-61117. Among them, the structural units represented by the formulas (a1-5-1) to (a1-5-2) are preferable, and they are represented by the formula (a1-5-1) or the formula (a1-5-2). Structural units are more preferred.

When the resin (A) has a structural unit (a1-5), the content thereof is preferably 1 to 50 mol% with respect to the total of all the structural units of the resin (A), and 3 to 45. It is more preferably mol%, and even more preferably 5-40 mol%.

Further, as the structural unit (a1), the following groups can also be mentioned.

樹脂（Ａ）が上記構造単位を含む場合、その含有率は、樹脂（Ａ）の全構造単位に対して、１０〜９５モル％が好ましく、１５〜９０モル％がより好ましく、２０〜８５モル％がさらに好ましい。

When the resin (A) contains the above structural units, the content thereof is preferably 10 to 95 mol%, more preferably 15 to 90 mol%, and 20 to 85 mol% with respect to all the structural units of the resin (A). % Is more preferable.

<Structural unit having no acid unstable group (s)>
The structural unit (s) is derived from a monomer having no acid-labile group (hereinafter, may be referred to as “monomer (s)”). As the monomer (s) for inducing the structural unit (s), a monomer having no acid unstable group known 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 unstable group is preferable. A structure having a hydroxy group and no acid-labile group (hereinafter sometimes referred to as "structural unit (a2)") and / or a lactone ring and no acid-labile group. If a resin having a unit (hereinafter sometimes referred to as "structural unit (a3)") is used in the resist composition of the present invention, 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 a resist pattern is produced from the resist composition of the present invention, when a high-energy ray such as a KrF excimer laser (248 nm), an electron beam or EUV (ultraviolet light) is used as an exposure light source, the structural unit (a2) is used. , It is preferable to include a structural unit (a2) having a phenolic hydroxy group. When an ArF excimer laser (193 nm) or the like is used, it is preferable that the structural unit (a2) includes a structural unit (a2) having an alcoholic hydroxy group. As the structural unit (a2), one type may be contained alone, or two or more types may be included.

Examples of the structural unit (a2) having a phenolic hydroxy group include structural units derived from the monomers described in JP-A-2010-204634.

When the resin (A) contains a structural unit (a2) having a phenolic hydroxy group, the content thereof is preferably 5 to 95 mol%, preferably 10 to 80 mol%, based on the total structural units of the resin (A). % Is more preferred, and 15-80 mol% is even more preferred.

［式（ａ２−１）中、
Ｌ^a3は、−Ｏ−又は＊−Ｏ−（ＣＨ₂）_k2−Ｃ（＝Ｏ）−Ｏ−を表し、
ｋ２は、１〜７のいずれかの整数を表す。＊は−Ｃ（＝Ｏ）−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のいずれかの整数を表す。］ Examples of the structural unit (a2) having an alcoholic hydroxy group include a structural unit represented by the formula (a2-1) (hereinafter, may be referred to as “structural unit (a2-1)”).

[In equation (a2-1),
^La3 represents −O− or * −O− (CH ₂ ) _k2− C (= O) −O−.
k2 represents any integer from 1 to 7. * Represents a bond with -C (= O)-.
R ^a14 represents a hydrogen atom or a methyl group.
R ^a15 and R ^a16 independently represent a hydrogen atom, a methyl group or a hydroxy group, respectively.
o1 represents any integer from 0 to 10. ]

In the formula (a2-1), L ^a3 is preferably, -O -, - O- (CH 2) f1 -C (= O) -O- and is (wherein f1 is the one of 1 to 4 Integer), 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, and more preferably 0 or 1.

アルコール性ヒドロキシ基を有する構造単位（ａ２−１）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。 The structural unit (a2-1) is preferably a structural unit represented by any of the formulas (a2-1-1) to (a2-1-6), and the formulas (a2-1-1) to (a2). The structural unit represented by any one of -1--4) is more preferable, and the structural unit represented by the formula (a2-1-1) or the formula (a2-1-3) is further preferable.

Examples of the monomer for inducing the structural unit (a2-1) having an alcoholic hydroxy group include the monomers described in JP-A-2010-204646.

When the resin (A) contains a structural unit (a2) having an alcoholic hydroxy group, the content thereof is usually 1 to 45 mol%, preferably 1 to 45 mol%, based on the total structural units of the resin (A). It is 40 mol%, more preferably 1 to 35 mol%, still more preferably 2 to 20 mol%.

<Structural unit (a3)>
The lactone ring of the structural unit (a3) may be a monocyclic ring such as a β-propiolactone ring, a γ-butyrolactone ring, or a δ-valerolactone ring, or a fused ring of a monocyclic lactone ring and another ring. However, the lactone ring preferably includes a γ-butyrolactone ring, an adamantan lactone ring, or a crosslinked ring containing a γ-butyrolactone ring structure.

［式（ａ３−１）中、
Ｌ^ａ４は、−Ｏ−又は＊−Ｏ−（ＣＨ_２）_ｋ３−Ｃ（＝Ｏ）−Ｏ−（ｋ３は１〜７のいずれかの整数を表す。）で表される基を表す。＊は−Ｃ（＝Ｏ）−との結合手を表す。
Ｒ^ａ１８は、水素原子又はメチル基を表す。
Ｒ^ａ２１は、炭素数１〜４の脂肪族炭化水素基を表す。
ｐ１は、０〜５のいずれかの整数を表す。ｐ１が２以上のとき、複数のＲ^ａ２１は互いに同一であっても異なってもよい。
式（ａ３−２）中、
Ｌ^ａ５は、−Ｏ−又は＊−Ｏ−（ＣＨ_２）_ｋ３−Ｃ（＝Ｏ）−Ｏ−（ｋ３は１〜７のいずれかの整数を表す。）で表される基を表す。＊は−Ｃ（＝Ｏ）−との結合手を表す。
Ｒ^ａ１９は、水素原子又はメチル基を表す。
Ｒ^ａ２２は、カルボキシ基、シアノ基又は炭素数１〜４の脂肪族炭化水素基を表す。
ｑ１は、０〜３のいずれかの整数を表す。ｑ１が２以上のとき、複数のＲ^ａ２２は互いに同一であっても異なってもよい。
式（ａ３−３）中、
Ｌ^ａ６は、−Ｏ−又は＊−Ｏ−（ＣＨ_２）_ｋ３−Ｃ（＝Ｏ）−Ｏ−（ｋ３は１〜７のいずれかの整数を表す。）で表される基を表す。＊は−Ｃ（＝Ｏ）−との結合手を表す。
Ｒ^ａ２０は、水素原子又はメチル基を表す。
Ｒ^ａ２３は、カルボキシ基、シアノ基又は炭素数１〜４の脂肪族炭化水素基を表す。
ｒ１は、０〜３のいずれかの整数を表す。ｒ１が２以上のとき、複数のＲ^ａ２３は互いに同一であっても異なってもよい。
式（ａ３−４）中、
Ｒ^ａ２４は、ハロゲン原子を有していてもよい炭素数１〜６のアルキル基、水素原子又はハロゲン原子を表す。
Ｌ^ａ７は、−Ｏ−、＊−Ｏ−Ｌ^ａ８−Ｏ−、＊−Ｏ−Ｌ^ａ８−Ｃ（＝Ｏ）−Ｏ−、＊−Ｏ−Ｌ^ａ８−Ｃ（＝Ｏ）−Ｏ−Ｌ^ａ９−Ｃ（＝Ｏ）−Ｏ−又は＊−Ｏ−Ｌ^ａ８−Ｏ−Ｃ（＝Ｏ）−Ｌ^ａ９−Ｏ−を表す。
Ｒ^ａ２５は、カルボキシ基、シアノ基又は炭素数１〜４の脂肪族炭化水素基を表す。
ｗは、０〜８のいずれかの整数を表す。ｗが２以上のとき、複数のＲ^ａ２５は互いに同一であっても異なってもよい。
＊は−Ｃ（＝Ｏ）−との結合手を表す。
Ｌ^ａ８及びＬ^ａ９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。］ The structural unit (a3) is preferably a structural unit represented by the formula (a3-1), the formula (a3-2), the formula (a3-3) or the formula (a3-4). The resin (A) may contain one kind selected from these alone, or may contain two or more kinds.

[In equation (a3-1),
^La4 represents a group represented by −O− or * −O− (CH ₂ ) _k3 −C (= O) −O− (k3 represents an integer of any of 1 to 7). * Represents a bond with -C (= O)-.
R ^a18 represents a hydrogen atom or a methyl group.
Ra ²¹ represents an aliphatic hydrocarbon group having 1 to 4 carbon atoms.
p1 represents any integer from 0 to 5. When p1 is 2 or more, the plurality of Ra ^21s may be the same or different from each other.
In formula (a3-2),
^La5 represents a group represented by −O− or * −O− (CH ₂ ) _k3 −C (= O) −O− (k3 represents an integer of any of 1 to 7). * Represents a bond with -C (= O)-.
Ra ¹⁹ represents a hydrogen atom or a methyl group.
^Ra22 represents a carboxy group, a cyano group, or an aliphatic hydrocarbon group having 1 to 4 carbon atoms.
q1 represents any integer from 0 to 3. When q1 is 2 or more, the plurality of Ra ^22s may be the same or different from each other.
In formula (a3-3),
^La6 represents a group represented by −O− or * −O− (CH ₂ ) _k3 −C (= O) −O− (k3 represents an integer of any of 1 to 7). * Represents a bond with -C (= O)-.
R ^a20 represents a hydrogen atom or a methyl group.
^Ra23 represents a carboxy group, a cyano group, or an aliphatic hydrocarbon group having 1 to 4 carbon atoms.
r1 represents any integer from 0 to 3. When r1 is 2 or more, the plurality of Ra ^23s may be the same or different from each other.
In formula (a3-4),
^Ra24 represents an alkyl group having 1 to 6 carbon atoms, a hydrogen atom or a halogen atom which may have a halogen atom.
L ^{a7 is, -O -, * - O-} L a8 -O -, * - O-L a8 -C (= O) -O -, * - O-L a8 -C (= O) -O-L ^{It represents a9-} C (= O) -O- or * -OL ^a8 -OC (= O) -L ^a9- O-.
^Ra25 represents a carboxy group, a cyano group, or an aliphatic hydrocarbon group having 1 to 4 carbon atoms.
w represents any integer from 0 to 8. When w is 2 or more, the plurality of Ra ^25s may be the same or different from each other.
* Represents a bond with -C (= O)-.
^{La 8} and ^{La 9} each independently represent an alkanediyl group having 1 to 6 carbon atoms. ]

Examples of the aliphatic hydrocarbon groups of R ^a21 , R ^a22 , R ^a23 and R ^a25 include methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, sec-butyl group and tert-butyl group. Alkyl groups can be mentioned.
^{Examples of the halogen atom of Ra24} include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom.
^Examples of the alkyl group of R a24 include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, a sec-butyl group, a tert-butyl group, an n-pentyl group and an n-hexyl group. , Preferably an alkyl group having 1 to 4 carbon atoms, and more preferably a methyl group or an ethyl group.
^{Alkyl groups having a halogen atom of Ra24} include trifluoromethyl group, perfluoroethyl group, perfluoropropyl group, perfluoroisopropyl group, perfluorobutyl group, perfluorosec-butyl group, perfluorotert-butyl group, perfluoropentyl group and perfluoro. Examples thereof include a hexyl group, a trichloromethyl group, a tribromomethyl group, and a triiodomethyl group.

The ^{alkanediyl groups of La8} and ^La9 include methylene group, ethylene group, propane-1,3-diyl group, propane-1,2-diyl group, butane-1,4-diyl group and pentane-1,5. -Diyl group, hexane-1,6-diyl group, butane-1,3-diyl group, 2-methylpropane-1,3-diyl group, 2-methylpropane-1,2-diyl group, pentane-1, Examples thereof include 4-diyl group and 2-methylbutane-1,4-diyl group.

In the formula (a3-1) ~ formula ^(a3-3), L a4 ^{~L a6} are each independently preferably -O- or, k3 is a integer of 1 to 4 * -O- ( CH ₂ ) _{A group represented by k3-} C (= O) -O-, more preferably -O- and * -O-CH _2- C (= O) -O-, still more preferably an oxygen atom. ..
R ^{a18 to} R ^a21 are preferably methyl groups.
R ^a22 and R ^a23 are each independently, preferably a carboxy group, a cyano group or a methyl group.
p1, q1, r1 and w are each independently, preferably an integer of 0 to 2, and more preferably 0 or 1.

（式中、Ｒ^ａ２４、Ｌ^ａ７は、上記と同じ意味を表す。） In the formula (a3-4), R ^a24 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, more preferably a hydrogen atom or a methyl group Is.
L ^a7 is preferably -O- or * -O-L ^a8- C (= O) -O-, and more preferably -O-, * -O-CH _2- C (= O) -O-. Or * -O-C ₂ H _4- C (= O) -O-.
As for the formula (a3-4), the formula (a3-4)'is particularly preferable.

(In the formula, ^Ra24 and ^La7 have the same meanings as above.)

Examples of the monomer for inducing the structural unit (a3) include the monomer described in JP-A-2010-204646, the monomer described in JP-A-2000-122294, and the monomer described in JP-A-2012-41274. Can be mentioned. Examples of the structural unit (a3) include the following structural units. The structural unit (a3) includes formulas (a3-1-1) to (a3-1-4), formulas (a3-2-1) to formulas (a3-2-4), and formulas (a3-3-3). 1) The structural unit represented by any of the formulas (a3-3-4) and the formulas (a3-4-1) to (a3-4-12) is preferable, and the formula (a3-1-1), It is represented by any of the formulas (a3-1-2), formulas (a3-2-3) to formulas (a3-2-4) and formulas (a3-4-1) to formulas (a3-4-12). The structural unit is more preferable, and the structural unit represented by any of the formulas (a3-4-1) to (a3-4-12) is more preferable, and the structural units represented by the formulas (a3-4-1) to (a3-4-1) are more preferable. The structural unit represented by any of 4-6) is even more preferable.

In the structural unit represented by the above formula (a3-4-1) ~ formula (a3-4-12), also the compounds in which a methyl group corresponding to R ^a24 is replaced by a hydrogen atom, the structural unit (a3-4) Can be given as a specific example of.

When the resin (A) contains the structural unit (a3), the total content thereof is usually 5 to 70 mol%, preferably 10 to 65 mol%, based on all the structural units of the resin (A). , More preferably 10 to 60 mol%.
The content of each of the structural units represented by the formula (a3-1), the formula (a3-2), the formula (a3-3) and the formula (a3-4) is based on the total structural unit of the resin (A). , Usually 5-60 mol%, preferably 5-50 mol%, more preferably 10-50 mol%.

<Other structural units (t)>
The resin (A) may further contain other structural units (t). The structural unit (t) is a structural unit other than the structural unit (a2) and the structural unit (a3), and is a structural unit having a halogen atom (hereinafter, sometimes referred to as “structural unit (a4)”) and non-structural unit. Examples thereof include a structural unit having a desorbed hydrocarbon group (hereinafter, may be referred to as “structural unit (a5)”).

［式（ａ４−０）中、
Ｒ^５は、水素原子又はメチル基を表す。
Ｌ^５は、単結合又は炭素数１〜４の脂肪族飽和炭化水素基を表す。
Ｌ^３は、炭素数１〜８のペルフルオロアルカンジイル基又は炭素数５〜１２のペルフルオロシクロアルカンジイル基を表す。
Ｒ^６は、水素原子又はフッ素原子を表す。］ <Structural unit (a4)>
As the halogen atom in the structural unit (a4), a fluorine atom is preferable. Examples of the structural unit (a4) include a structural unit represented by the formula (a4-0).

[In equation (a4-0),
R ⁵ represents a hydrogen atom or a methyl group.
L ⁵ represents a single bond or an aliphatic saturated hydrocarbon group having 1 to 4 carbon atoms.
L ³ represents a perfluoroalkanediyl group having 1 to 8 carbon atoms or a perfluorocycloalkanediyl group having 5 to 12 carbon atoms.
R ⁶ represents a hydrogen atom or a fluorine atom. ]

Examples of the aliphatic saturated hydrocarbon group of L ^5, include alkanediyl group having 1 to 4 carbon atoms, e.g., methylene group, ethylene group, propane-1,3-diyl, butane-1,4-diyl group Such as linear alkanediyl group, linear alkanediyl group having an alkyl group (among others, methyl group, ethyl group, etc.) side chain, ethane-1,1-diyl group, propane-1,2 Examples thereof include branched alkanediyl groups such as −diyl group, butane-1,3-diyl group, 2-methylpropane-1,3-diyl group and 2-methylpropane-1,2-diyl group.

The perfluoro alkanediyl group L ^3, difluoromethylene group, a perfluoroalkyl ethylene group, perfluoroethyl fluoro methylene group, perfluoro-1,3-diyl group, perfluoro-1,2-diyl group, perfluoropropane-2,2 -Diyl group, perfluorobutane-1,4-diyl group, perfluorobutane-2,2-diyl group, perfluorobutane-1,2-diyl group, perfluoropentane-1,5-diyl group, perfluoropentane-2,2 -Diyl group, perfluoropentane-3,3-diyl group, perfluorohexane-1,6-diyl group, perfluorohexane-2,2-diyl group, perfluorohexane-3,3-diyl group, perfluoroheptane-1,7 -Diyl group, perfluoroheptane-2,2-diyl group, perfluoroheptane-3,4-diyl group, perfluoroheptane-4,4-diyl group, perfluorooctane-1,8-diyl group, perfluorooctane-2,2 -Diyl group, perfluorooctane-3,3-diyl group, perfluorooctane-4,4-diyl group and the like can be mentioned.
The perfluorocycloalkanes diyl group L ^3, perfluoro-cyclohexane diyl group, perfluoro cyclopentanediyl group, perfluoro cycloheptane-diyl group, a perfluoroalkyl adamantane-diyl group and the like.

L ⁵ is preferably a single bond, a methylene group or an ethylene group, and more preferably a single bond or a methylene group.
L ³ is preferably a perfluoroalkanediyl group having 1 to 6 carbon atoms, and more preferably a perfluoroalkanediyl group having 1 to 3 carbon atoms.

Examples of the structural unit (a4-0) include the following.

In the above structural unit, a structural unit in ^{which the methyl group corresponding to R 5} is replaced with a hydrogen atom can also be mentioned as a specific example of the structural unit (a4-0).

［式（ａ４−１）中、
Ｒ^ａ４１は、水素原子又はメチル基を表す。
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−Ｃ（＝Ｏ）−に置き換わっていてもよい。
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−ｇ１）で表される基を表す。ただし、Ａ^ａ４１及びＲ^ａ４２のうち少なくとも１つは、置換基としてハロゲン原子（好ましくはフッ素原子）を有する。

〔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２価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２価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−、−Ｃ（＝Ｏ）−、−Ｃ（＝Ｏ）−Ｏ−又は−Ｏ−Ｃ（＝Ｏ）−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６以下である。
＊、＊＊は結合手であり、＊が−Ｏ−Ｃ（＝Ｏ）−Ｒ^ａ４２との結合手である。〕
ただし、Ａ^a41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。］
ｓは０が好ましい。 Examples of the structural unit (a4) include a structural unit represented by the formula (a4-1).

[In equation (a4-1),
R ^a41 represents a hydrogen atom or a methyl group.
R ^a42 represents a hydrocarbon group having 1 to 20 carbon atoms which may have a substituent, and −CH ₂ − contained in the hydrocarbon group is changed to −O− or −C (= O) −. It may be replaced.
A ^a41 represents an alkanediyl group having 1 to 6 carbon atoms which may have a substituent or a group represented by the formula (ag1). However, ^{at least one of Aa41} and ^Ra42 has a halogen atom (preferably a fluorine atom) as a substituent.

[In the formula (ag1),
s represents 0 or 1.
A ^a42 and A ^a44 each independently represent a divalent aliphatic hydrocarbon group having 1 to 5 carbon atoms which may have a substituent.
A ^a43 represents a divalent aliphatic hydrocarbon group or a single bond having 1 to 5 carbon atoms which may have a substituent.
X ^a41 and X ^a42 independently represent −O−, −C (= O) −, −C (= O) −O− or −OC (= O) −.
However, the total number of carbon atoms of ^{A a42} , A ^a43 , A ^a44 , X ^a41 and X ^{a42 is 6 or less.}
* And ** are bonds, and * is a bond with ^{-OC (= O) -R a42.} ]
However, ^{at least one of A a41} and R ^a42 is a group having a halogen atom as a substituent. ]
s is preferably 0.

芳香族炭化水素基としては、例えば、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等が挙げられる。 ^Examples of the hydrocarbon group of R a42 include a chain type and a ring type aliphatic hydrocarbon group, an aromatic hydrocarbon group, and a group formed by combining these groups. Chain-type aliphatic hydrocarbon groups include methyl group, ethyl group, propyl group, butyl group, pentyl group, hexyl group, heptyl group, octyl group, decyl group, dodecyl group, hexadecyl group, pentadecyl group and hexyldecyl group. , Alkyl groups such as heptadecyl group and octadecyl group. Cyclic alicyclic aliphatic hydrocarbon groups include cycloalkyl groups such as cyclopentyl group, cyclohexyl group, cycloheptyl group and cyclooctyl group; decahydronaphthyl group, adamantyl group, norbornyl group and the following groups (*). Represents a bond.) And other polycyclic alicyclic hydrocarbon groups can be mentioned.

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.

^As the hydrocarbon group of R a42, a chain type or a ring type aliphatic hydrocarbon group and a group formed by combining these are preferable. These groups may have a carbon-carbon unsaturated bond, but chain and cyclic aliphatic saturated hydrocarbon groups and groups formed by combining them are more preferable.

［式（ａ−ｇ３）中、
Ｘ^a43は、−Ｏ−、−Ｃ（＝Ｏ）−、−Ｃ（＝Ｏ）−Ｏ−又は−Ｏ−Ｃ（＝Ｏ）−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１〜１７の脂肪族炭化水素基を表す。
＊はＲ^a42の炭化水素基との結合手を表す。］ ^Examples of the substituent of R a42 include a halogen atom and a group represented by the formula (ag3). Examples of the halogen atom include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom, and a fluorine atom is preferable.

[In the formula (ag3),
X ^a43 represents −O−, −C (= O) −, −C (= O) −O− or −OC (= O) −.
A ^a45 represents an aliphatic hydrocarbon group having 1 to 17 carbon atoms having at least one halogen atom.
* Represents a bond with the hydrocarbon group of ^Ra42. ]

Examples of the aliphatic hydrocarbon group of A ^{a45 include} the same groups as those exemplified in ^{R a42.}
R ^a42 is preferably an aliphatic hydrocarbon group which may have a halogen atom, and more preferably an alkyl group having a halogen atom and / or an aliphatic hydrocarbon group having a group represented by the formula (ag3). ..

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 further preferably having a carbon number of carbon. It is a perfluoroalkyl group of 1 to 6, and particularly preferably a perfluoroalkyl group having 1 to 3 carbon atoms. 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.

When R ^a42 is an aliphatic hydrocarbon group having a group represented by the formula (ag3), the aliphatic hydrocarbon includes the number of carbon atoms contained in the group represented by the formula (ag3). The total carbon number of the group is preferably 15 or less, more preferably 12 or less. When the group represented by the formula (ag3) is used as a substituent, the number thereof is preferably one.

［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１〜１７の脂肪族炭化水素基を表す。
Ｘ^a44は、−Ｃ（＝Ｏ）−Ｏ−又は−Ｏ−Ｃ（＝Ｏ）−を表す。
Ａ^a47は、ハロゲン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^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Ｒ^a42の炭化水素基との結合手を表す。］ The aliphatic hydrocarbon having a group represented by the formula (ag3) is more preferably a group represented by the formula (ag2).

[In the formula (ag2),
A ^a46 represents an aliphatic hydrocarbon group having 1 to 17 carbon atoms which may have a halogen atom.
X ^a44 represents −C (= O) −O− or −OC (= O) −.
A ^a47 represents an aliphatic hydrocarbon group having 1 to 17 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 the hydrocarbon group of ^Ra42. ]

The aliphatic hydrocarbon group of A ^a46 preferably has 1 to 6 carbon atoms, more preferably 1 to 3 carbon atoms.
The aliphatic hydrocarbon group of A ^a47 preferably has 4 to 15 carbon atoms, more preferably 5 to 12 carbon atoms, and even more preferably a cyclohexyl group or an adamantyl group.

Examples of the group represented by the formula (ag2) include the following groups.

The ^{alkanediyl group of A a41} includes a methylene group, an ethylene group, a propane-1,3-diyl group, a butane-1,4-diyl group, a pentane-1,5-diyl group, and a hexane-1,6-diyl group. Linear alkanediyl groups such as propane-1,2-diyl group, butane-1,3-diyl group, 2-methylpropane-1,2-diyl group, 1-methylbutane-1,4-diyl group, etc. Examples thereof include branched alkanediyl groups such as 2-methylbutane-1,4-diyl group.
^Examples of the substituent in the arcandyl 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 further preferably an ethylene group.

^{The aliphatic hydrocarbon groups of A a42} , A ^a43 and A ^{a44 in} the group represented by the formula (a-g1) (hereinafter, sometimes referred to as "group (ag1)") include a methylene group and an ethylene group. , Propane-1,3-diyl group, propane-1,2-diyl group, butane-1,4-diyl group, 1-methylpropane-1,3-diyl group, 2-methylpropane-1,3-diyl group Examples include a group, a 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 is an oxygen atom include the following groups. In the following examples, * and ** represent a bond, respectively, and ** is a bond with ^-OC (= O) -R a42.

^Examples of the group (ag1) in which X a42 is −C (= O) − include the following groups.

^Examples of the group (ag1) in which X a42 is -C (= O) -O- include the following groups.

^{Examples of the group (ag1) in} which X a42 is −OC (= O) − include the following groups.

［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), the structural unit represented by the formula (a4-2) is preferable.

[In equation (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 hydrocarbon group having 1 to 10 carbon atoms having a fluorine atom. ]

The ^{alkanediyl group of A f1} includes a methylene group, an ethylene group, a propane-1,3-diyl group, a propane-1,2-diyl group, a butane-1,4-diyl group, and a pentane-1,5-diyl group. , Hexine-1,6-diyl group and other linear alkanediyl groups; 1-methylpropane-1,3-diyl group, 2-methylpropane-1,3-diyl group, 2-methylpropane-1,2 Examples thereof include branched alkanediyl groups such as −diyl group, 1-methylbutane-1,4-diyl group and 2-methylbutane-1,4-diyl group.

The hydrocarbon group of R ^f2 includes an aliphatic hydrocarbon group and an aromatic hydrocarbon group, and the aliphatic hydrocarbon group includes a chain type, a cyclic type and a group formed by a combination thereof. As the aliphatic hydrocarbon group, an alkyl group and an alicyclic hydrocarbon group are preferable.
Alkyl groups 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-octyl group and 2 -Ethylhexyl groups can be mentioned.
The alicyclic hydrocarbon group may be either a monocyclic group or a polycyclic group, and the monocyclic alicyclic hydrocarbon group includes a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group and a methylcyclohexyl group. , Cycloalkyl groups such as dimethylcyclohexyl group, cycloheptyl group, cyclooctyl group, cycloheptyl group and cyclodecyl group. Examples of the polycyclic alicyclic hydrocarbon group include a decahydronaphthyl group, an adamantyl group, a 2-alkyladamantan-2-yl group, a 1- (adamantan-1-yl) alkane-1-yl group, and a norbornyl group. Examples thereof include a methylnorbornyl group and an isobornyl group.

Examples of the hydrocarbon group having a fluorine atom of R ^f2 include an alkyl group having a fluorine atom and an alicyclic hydrocarbon group having a fluorine atom.
Specifically, 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, and a 2,2,2-trifluoroethyl group. 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 group, 1,1,2, 2,3,3,4,5-octafluorobutyl group, perfluorobutyl group, 1,1-bis (trifluoro) methyl-2,2,2-trifluoroethyl group, 2- (perfluoropropyl) ethyl group, 1,1,2,2,3,3,4,5-octafluoropentyl group, perfluoropentyl group, 1,1,2,2,3,3,4,5,5-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, 1,1,2,2,3,3,4,5,5,6,6-dodecafluorohexyl group, perfluoropentylmethyl group and perfluorohexyl Fluoroalkyl groups such as groups can be mentioned.
Examples of the alicyclic hydrocarbon group having a fluorine atom include a cycloalkyl fluoride group such as a perfluorocyclohexyl group and a perfluoroadamantyl group.

In the formula (a4-2), A ^f1 is preferably an alkanediyl group having 2 to 4 carbon atoms, and more preferably an ethylene group.
As R ^f2 , an alkyl fluoride group having 1 to 6 carbon atoms is preferable.

Examples of the structural unit represented by the formula (a4-2) include the structural unit shown below and the structural unit in which the ^{methyl group corresponding to R f1} in the following structural unit is replaced with a hydrogen atom.

Examples of the structural unit (a4) include the structural unit shown below and the structural unit in which the ^{methyl group corresponding to R f11} in the following structural unit is replaced with a hydrogen atom.

When the resin (A) has a structural unit (a4), the content thereof is preferably 1 to 20 mol%, more preferably 2 to 15 mol%, and 3) with respect to all the structural units of the resin (A). 10 mol% is more preferable.

［式（ａ５−１）中、
Ｒ⁵¹は、水素原子又はメチル基を表す。
Ｒ⁵²は、炭素数３〜１８の脂環式炭化水素基を表し、該脂環式炭化水素基に含まれる水素原子は炭素数１〜８の脂肪族炭化水素基で置換されていてもよい。ただし、Ｌ^５５との結合位置にある炭素原子に結合する水素原子は、炭素数１〜８の脂肪族炭化水素基で置換されない。
Ｌ^５５は、単結合又は炭素数１〜１８の２価の飽和炭化水素基を表し、該飽和炭化水素基に含まれる−ＣＨ_２−は、−Ｏ−又は−Ｃ（＝Ｏ）−に置き換わっていてもよい。］ <Structural unit (a5)>
Examples of the non-desorbing hydrocarbon group contained in the structural unit (a5) include a linear, branched or cyclic hydrocarbon group, and preferably an alicyclic hydrocarbon group. Examples of the structural unit (a5) include a structural unit represented by the formula (a5-1).

[In equation (a5-1),
R ⁵¹ represents a hydrogen atom or a methyl group.
R ⁵² represents an alicyclic hydrocarbon group having 3 to 18 carbon atoms, and the hydrogen atom contained in the alicyclic hydrocarbon group may be substituted with an aliphatic hydrocarbon group having 1 to 8 carbon atoms. .. However, ^{the hydrogen atom bonded to the carbon atom at the bonding position with L 55} is not replaced by an aliphatic hydrocarbon group having 1 to 8 carbon atoms.
L ⁵⁵ represents a single bond or a divalent saturated hydrocarbon group having 1 to 18 carbon atoms, and -CH _2- contained in the saturated hydrocarbon group is replaced with -O- or -C (= O)-. May be. ]

The alicyclic hydrocarbon group of R ⁵² may be either a monocyclic or polycyclic group. Examples of the monocyclic alicyclic hydrocarbon group include a cyclopropyl group, a cyclobutyl group, a cyclopentyl group and a cyclohexyl group. Examples of the polycyclic alicyclic hydrocarbon group include an adamantyl group and a norbornyl group.
Examples of the aliphatic hydrocarbon group having 1 to 8 carbon atoms include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, a sec-butyl group, a tert-butyl group, a pentyl group and a hexyl group. , Alkyl groups such as octyl group and 2-ethylhexyl group.
Examples of the alicyclic hydrocarbon group having a substituent include a 3-methyladamantyl group.
R ⁵² is preferably an unsubstituted alicyclic hydrocarbon group having 3 to 18 carbon atoms, and more preferably an adamantyl group, a norbornyl group or a cyclohexyl group.

Examples of the divalent saturated hydrocarbon group of L ⁵⁵ include a divalent aliphatic saturated hydrocarbon group and a divalent alicyclic saturated hydrocarbon group, and a divalent aliphatic saturated hydrocarbon group is preferable. ..
Examples of the divalent aliphatic saturated hydrocarbon group include an alkanediyl group such as a methylene group, an ethylene group, a propanediyl group, a butanjiyl group and a pentandiyl group.
The divalent alicyclic saturated hydrocarbon group may be either monocyclic or polycyclic. Examples of the monocyclic alicyclic saturated hydrocarbon group include a cycloalkanediyl group such as a cyclopentanediyl group and a cyclohexanediyl group. Examples of the polycyclic divalent alicyclic saturated hydrocarbon group include an adamantandiyl group and a norbornanediyl group.

式（Ｌ１−１）中、
Ｘ^x1は、−Ｃ（＝Ｏ）−Ｏ−又は−Ｏ−Ｃ（＝Ｏ）−を表す。
Ｌ^x1は、炭素数１〜１６の２価の脂肪族飽和炭化水素基を表す。
Ｌ^x2は、単結合又は炭素数１〜１５の２価の脂肪族飽和炭化水素基を表す。
ただし、Ｌ^x1及びＬ^x2の合計炭素数は、１６以下である。
式（Ｌ１−２）中、
Ｌ^x3は、炭素数１〜１７の２価の脂肪族飽和炭化水素基を表す。
Ｌ^x4は、単結合又は炭素数１〜１６の２価の脂肪族飽和炭化水素基を表す。
ただし、Ｌ^x1及びＬ^x2の合計炭素数は、１７以下である。
式（Ｌ１−３）中、
Ｌ^x5は、炭素数１〜１５の２価の脂肪族飽和炭化水素基を表す。
Ｌ^x6及びＬ^x７は、それぞれ独立に、単結合又は炭素数１〜１４の２価の脂肪族飽和炭化水素基を表す。
ただし、Ｌ^x5、Ｌ^x6及びＬ^x7の合計炭素数は、１５以下である。
式（Ｌ１−４）中、
Ｌ^x8及びＬ^x9は、それぞれ独立に、単結合又は炭素数１〜１２の２価の脂肪族飽和炭化水素基を表す。
Ｗ^x1は、炭素数３〜１５の２価の脂環式飽和炭化水素基を表す。
ただし、Ｌ^x8、Ｌ^x9及びＷ^x1の合計炭素数は、１５以下である。 Examples of the group in which −CH ₂ − contained in the saturated hydrocarbon group is replaced by −O− or −C (= O) − are represented by the formulas (L1-1) to (L1-4). The group is mentioned. In the following formula, * represents a bond with an oxygen atom.

In formula (L1-1),
X ^x1 represents −C (= O) −O− or −OC (= O) −.
L ^x1 represents a divalent aliphatic saturated hydrocarbon group having 1 to 16 carbon atoms.
L ^x2 represents a single bond or a divalent aliphatic saturated hydrocarbon group having 1 to 15 carbon atoms.
However, the total number of carbon atoms of ^{L x1} and L ^{x2 is 16 or less.}
In formula (L1-2),
L ^x3 represents a divalent aliphatic saturated hydrocarbon group having 1 to 17 carbon atoms.
L ^x4 represents a single bond or a divalent aliphatic saturated hydrocarbon group having 1 to 16 carbon atoms.
However, the total number of carbon atoms of ^{L x1} and L ^{x2 is 17 or less.}
In formula (L1-3),
L ^x5 represents a divalent aliphatic saturated hydrocarbon group having 1 to 15 carbon atoms.
L ^x6 and L ^x7 each independently represent a single bond or a divalent aliphatic saturated hydrocarbon group having 1 to 14 carbon atoms.
However, the total number of carbon atoms of ^{L x5} , L ^x6 and L ^{x7 is 15 or less.}
In formula (L1-4),
L ^x8 and L ^x9 each independently represent a single bond or a divalent aliphatic saturated hydrocarbon group having 1 to 12 carbon atoms.
W ^{x 1} represents a divalent alicyclic saturated hydrocarbon group having 3 to 15 carbon atoms.
However, the total number of carbon atoms of ^{L x8} , L ^x9 and W ^{x1 is 15 or less.}

L ^{x 1} is preferably a divalent aliphatic saturated hydrocarbon group having 1 to 8 carbon atoms, and more preferably a methylene group or an ethylene group.
L ^x2 is preferably a single bond or a divalent aliphatic saturated hydrocarbon group having 1 to 8 carbon atoms, and more preferably a single bond.
L ^x3 is preferably a divalent aliphatic saturated hydrocarbon group having 1 to 8 carbon atoms.
L ^x4 is preferably a single bond or a divalent aliphatic saturated hydrocarbon group having 1 to 8 carbon atoms.
L ^x5 is preferably a divalent aliphatic saturated hydrocarbon group having 1 to 8 carbon atoms, and more preferably a methylene group or an ethylene group.
L ^x6 is preferably a single bond or a divalent aliphatic saturated hydrocarbon group having 1 to 8 carbon atoms, and more preferably a methylene group or an ethylene group.
L ^x7 is preferably a single bond or a divalent aliphatic saturated hydrocarbon group having 1 to 8 carbon atoms.
L ^x8 is preferably a single bond or a divalent aliphatic saturated hydrocarbon group having 1 to 8 carbon atoms, and more preferably a single bond or a methylene group.
L ^x9 is preferably a single bond or a divalent aliphatic saturated hydrocarbon group having 1 to 8 carbon atoms, and more preferably a single bond or a methylene group.
W ^{x 1} is preferably a divalent alicyclic saturated hydrocarbon group having 3 to 10 carbon atoms, and more preferably a cyclohexanediyl group or an adamantandiyl group.

Examples of the group represented by the formula (L1-1) include the following divalent groups.

Examples of the group represented by the formula (L1-2) include the following divalent groups.

Examples of the group represented by the formula (L1-3) include the divalent groups shown below.

Examples of the group represented by the formula (L1-4) include the following divalent groups.

L ⁵⁵ is preferably a single bond, a methylene group, an ethylene group or a group represented by the formula (L1-1), and more preferably a single bond or a group represented by the formula (L1-1). ..

Examples of the structural unit (a5-1) include the structural unit shown below and the structural unit in which the ^{methyl group corresponding to R 51} in the following structural unit is replaced with a hydrogen atom.

When the resin (A) has a structural unit (a5), the content thereof is preferably 1 to 30 mol%, more preferably 2 to 20 mol%, and 3) with respect to all the structural units of the resin (A). ~ 15 mol% is more preferred.

The resin (A) may have a structural unit other than the above-mentioned structural unit, and examples of such a structural unit include structural units well known in the art.

The resin (A) is preferably a resin composed of a structural unit (a1) and a structural unit (s), that is, a copolymer of a monomer (a1) and a monomer (s).
The structural unit (a1) is preferably at least one selected from the structural unit (a1-1) and the structural unit (a1-2) (preferably the structural unit having a cyclohexyl group and a cyclopentyl group), and more preferably the structural unit (a1). It is at least two kinds selected from a1-1) or a structural unit (a1-1) and a structural unit (a1-2) (preferably the structural unit having a cyclohexyl group and a cyclopentyl group).
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 a structural unit represented by the formula (a2-1).
The structural unit (a3) is preferably a structural unit represented by the formulas (a3-1-1) to (a3-1-4), and the formulas (a3-2-1) to (a3-2-4). And at least one selected from the structural units represented by the formulas (a3-4-1) to (a3-4-2).

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, a radical polymerization method) using a monomer for inducing these structural units. can do. The content of each structural unit of the resin (A) can be adjusted by adjusting the amount of the monomer used for the polymerization.
The weight average molecular weight of the resin (A) is preferably 2,000 or more (more preferably 2,500 or more, still more preferably 3,000 or more) and 50,000 or less (more preferably 30,000 or less, still more preferable. Is 15,000 or less).
In the present specification, the weight average molecular weight is a value obtained by gel permeation chromatography. Gel permeation chromatography can be measured under the analytical conditions described in the Examples.

<Resin other than resin (A)>
The resist composition of the present invention may contain a resin other than the resin (A). Examples of such a resin include a resin containing a structural unit (t) and the like.

As the resin other than the resin (A), a resin containing a structural unit having a fluorine atom is preferable, and a resin containing the structural unit (a4) (however, the structural unit (a1) is not included; hereinafter, “resin (X)”. In some cases) is more preferable. In the resin (X), the content of the structural unit (a4) is preferably 40 mol% or more, more preferably 45 mol% or more, still more preferably 50 mol% or more, based on all the structural units of the resin (X). ..
Examples of the structural unit that the resin (X) may further include include a structural unit (a2), a structural unit (a3), and a structural unit derived from other known monomers.
The weight average molecular weight of the resin (X) is preferably 8,000 or more (more preferably 10,000 or more) and 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 of the resin (A).
When the resist composition contains the resin (X), the content thereof is preferably 1 to 60 parts by mass, more preferably 1 to 50 parts by mass, and further, with respect to 100 parts by mass of the resin (A). It is preferably 1 to 40 parts by mass, and particularly preferably 2 to 30 parts by mass.

The total content of the resin (A) and the resin other than the resin (A) is preferably 80% by mass or more and 99% by mass or less with respect to the solid content of the resist composition. The solid content of the resist composition and the content of the resin relative to the solid content can be measured by a known analytical means such as liquid chromatography or gas chromatography.

<Acid generator (B)>
The acid generator (B) may be an ionic acid generator or a nonionic acid generator.
Nonionic acid generators include organic halides, sulfonate esters (eg 2-nitrobenzyl ester, aromatic sulfonate, oxime sulfonate, N-sulfonyloxyimide, sulfonyloxyketone, diazonaphthoquinone 4-sulfonate), sulfones. (For example, disulfone, ketosulfone, sulfonyldiazomethane) and the like are included. Examples of the ionic acid generator include an ionic acid generator composed of a combination of a known cation and a known anion, and an onium salt containing an onium cation (for example, a diazonium salt, a phosphonium salt, a sulfonium salt, an iodonium salt) is typical. Is the target. Examples of the onium salt anion include a sulfonic acid anion, a sulfonylimide anion, and a sulfonylmethide anion.

Examples of the acid generator (B) include Japanese Patent Application Laid-Open No. 63-26653, Japanese Patent Application Laid-Open No. 55-164824, Japanese Patent Application Laid-Open No. 62-69263, Japanese Patent Application Laid-Open No. 63-146038, Japanese Patent Application Laid-Open No. 63-163452, and Japanese Patent Application Laid-Open No. 63-163452. Kaisho 62-153853, Japanese Patent Application Laid-Open No. 63-146029, US Patent No. 3,779,778, US Patent No. 3,849,137, German Patent No. 3914407, European Patent No. 126,712, etc. The compound that generates an acid by radiation, the acid generator described in Japanese Patent Application Laid-Open No. 2013-68914, Japanese Patent Application Laid-Open No. 2013-3155, Japanese Patent Application Laid-Open No. 2013-1905, and the like can be used. Moreover, you may use the compound produced by the known method.

Examples of the acid generator (B) include organic sulfonates and the like, preferably a fluorine-containing acid generator, and more preferably an acid generator represented by the formula (B1) (hereinafter, "acid generator (B)". B1) ”) may be mentioned.

［式（Ｂ１）中、
Ｑ^１１及びＱ^１２は、それぞれ独立に、フッ素原子又は炭素数１〜６のペルフルオロアルキル基を表す。
Ｌ^Ｂ１は、炭素数１〜２４の２価の飽和炭化水素基を表し、該２価の飽和炭化水素基に含まれる−ＣＨ_２−は−Ｏ−又は−ＣＯ−に置き換わっていてもよく、該２価の飽和炭化水素基に含まれる水素原子はフッ素原子又はヒドロキシ基で置換されていてもよい。
Ｙ^Ｂ１は、置換基を有していてもよいメチル基又は置換基を有していてもよい炭素数３〜１８の脂環式炭化水素基を表し、該脂環式炭化水素基に含まれる−ＣＨ_２−は、−Ｏ−、−ＳＯ_２−又は−ＣＯ−に置き換わっていてもよい。
Ｚ１^＋は、有機カチオンを表す。］

[In equation (B1),
Q ¹¹ and ^{Q 12} each independently represent a fluorine atom or a perfluoroalkyl group having 1 to 6 carbon atoms.
L ^B1 represents a divalent saturated hydrocarbon group having 1 to 24 carbon atoms, -CH ₂ contained in a saturated hydrocarbon group of the divalent - may be replaced by -O- or -CO-, The hydrogen atom contained in the divalent saturated hydrocarbon group may be substituted with a fluorine atom or a hydroxy group.
Y ^B1 represents an alicyclic hydrocarbon group having 3 to 18 carbon atoms which may have a methyl group which may have a substituent or a substituent, and is contained in the alicyclic hydrocarbon group. -CH _2- may be replaced with -O-, -SO _{2- or -CO-.}
Z1 ⁺ represents an organic cation. ]

The perfluoroalkyl group Q ¹¹ and Q ^12, include the same groups as those listed in the perfluoroalkyl group represented by Q ¹ and Q ^2.
Q ¹¹ and Q ¹² are each independently a fluorine atom or a trifluoromethyl group are preferable, and fluorine atom is more preferable. It is more preferable that both Q ¹¹ and Q ^{12 are fluorine atoms.}

Examples of the divalent saturated hydrocarbon group represented by L ^B1, include those similar to the divalent saturated hydrocarbon group represented by L ^b1.
-CH ₂ contained in the divalent saturated hydrocarbon group represented by L ^B1 - as has been replaced by -O- or -CO- ^group, contained in the divalent saturated hydrocarbon group represented by ^{L b1} The _{same group in which −CH 2−} is replaced with −O− or −CO− can be mentioned. Specific examples thereof include groups represented by the above-mentioned formulas (b1-1) to (b1-3). In ^the case ^{L B1} is a group represented by the formula (b1-1) ~ formula (b1-3), the * in the group represented by the formula (b1-1) ~ formula (b1-3) ^{Y B1} Represents a bond with.
L ^B1 is preferably any one of groups represented by the formula (b1-1) ~ formula (b1-3), * 2-CO -O- (CH 2) t1 -, * 2- (CH ₂ ) _t2- O-CO- (t1 represents any integer from 0 to 6. t2 represents any integer from 1 to 6. * 2 represents -C (Q ¹¹ ) (Q ¹² )- It is more preferable that it represents a bond with.).

The ^{monovalent alicyclic hydrocarbon group represented by Y B1} may be a monocyclic ring, a polycyclic ring, or a spiro ring. Specific examples thereof include ^{monovalent alicyclic hydrocarbon groups represented by Y B1} (groups represented by the above formulas (Y1) to (Y38), etc.). Of the groups represented by Y ^B1 , the preferred group is the same as the preferred range of the group represented by Y.

Examples of the salt anion represented by the formula (B1) include formulas (B1-A-1) to (B1-A-55). Anions represented by the formulas (B1-A-1) to (B1-A-55) [hereinafter, may be referred to as "anions (B1-A-1)" or the like depending on the formula number. ] Are preferable, and formulas (B1-A-1) to (B1-A-4), formulas (B1-A-9), formulas (B1-A-10), formulas (B1-A-24) to formulas (B1-A-24) to formulas. (B1-A-33), formulas (B1-A-36) to formulas (B1-A-40), formulas (B1-A-47) to formulas (B1-A-55). Anions are more preferred.

Here, R ^{i2 to} R ⁱ⁷ are, for example, an alkyl group having 1 to 4 carbon atoms, preferably a methyl group or an ethyl group.
R ⁱ⁸ is, for example, an aliphatic hydrocarbon group having 1 to 12 carbon atoms, preferably an alkyl group having 1 to 4 carbon atoms, an alicyclic hydrocarbon group having 5 to 12 carbon atoms, or a combination thereof. It is a group formed, more preferably a methyl group, an ethyl group, a cyclohexyl group or an adamantyl group.
L ⁴⁴ is a single bond or an alkanediyl group having 1 to 4 carbon atoms.
Q ¹¹ and ^{Q 12} are the same as above.

Examples of the anion in the salt represented by the formula (B1) include anions represented by the formulas (Ia-1) to (Ia-34).

Among them, formulas (B1a-1) to (B1a-3) and formulas (B1a-7) to (B1a-16), formulas (B1a-18), formulas (B1a-19), and formulas (B1a-22). An anion represented by any of the formulas (B1a-34) is preferable.

Examples of the organic cation of Z1 ⁺ include the same as those exemplified for the ^{organic cation Z +} in the salt (I).

Specific examples of the acid generator (B) include salts represented by any of the formulas (B1-1) to (B1-48). Among them, those containing an arylsulfonium cation are preferable, and formulas (B1-1) to (B1-3), formulas (B1-5) to (B1-7), formulas (B1-11) to formulas (B1-14). ), Formula (B1-17), formulas (B1-20) to formulas (B1-26), formulas (B1-29), formulas (B1-31) to formulas (B1-48). Salt is more preferred.

The content of the acid generator (B) is preferably 1 to 40 parts by mass, and more preferably 3 to 35 parts by mass with respect to 100 parts by mass of the resin (A). It is more preferably 30 parts by mass or less, and even more preferably 25 parts by mass or less.
In the resist composition of the present invention, the content of the salt (I) is preferably 0.1% by mass or more and 35% by mass or less, and 0.5% by mass or more and 30% by mass or less, based on the solid content of the resist composition. The following is more preferable, and 1% by mass or more and 25% by mass or less is further preferable.
When the acid generator (B) is contained, the total content of the salt (I) and the acid generator (B) is preferably 1.5 parts by mass or more with respect to 100 parts by mass of the resin (A). (More preferably 3 parts by mass or more), preferably 40 parts by mass or less (more preferably 35 parts by mass or less). The resist composition can contain one or more acid generators (B).

In the resist composition of the present invention, the ratio of the contents of the salt (I) and the acid generator (B) (salt (I): acid generator (B)) is usually 1:99 to 100 in terms of mass ratio. : 0, preferably 1:99 to 99: 1, more preferably 2:98 to 98: 2, and even more preferably 5:95 to 95: 5.

<Solvent (E)>
The content of the solvent (E) is usually 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, based on the total mass of the resist composition. It is preferably 99% by mass or less. The content of the solvent (E) can be measured by a known analytical means such as liquid chromatography or gas chromatography.

Examples of the solvent (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 ethyl pyruvate. Esters; ketones such as acetone, methylisobutylketone, 2-heptanone and cyclohexanone; cyclic esters such as γ-butyrolactone; and the like. One type of solvent (E) may be contained alone, or two or more types may be contained.

<Quencher (C)>
Examples of the quencher (C) include a basic nitrogen-containing organic compound or a salt that generates an acid having a lower acidity than the acid generated from an acid generator. A salt that generates an acid having a lower acidity than the acid generated from the acid generator is more acidic than the acid generated from the salt (I) when only the salt (I) is contained as the acid generator. It means a salt that generates a low acid, and when it contains a salt (I) and an acid generator (B) as an acid generator, it is more acidic than the acid generated from the salt (I) and the acid generator (B). It means a salt that produces a low degree of acid.
The content of the quencher (C) is preferably about 0.01 to 5% by mass based on the solid content of the resist composition.
<Basic nitrogen-containing organic compounds>
Examples of the basic nitrogen-containing organic compound include amine and ammonium salts. Examples of amines include aliphatic amines and aromatic amines. Aliphatic amines include primary amines, secondary amines and tertiary amines.

Examples of amines include 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, trypentylamine, trihexylamine, tri Heptylamine, trioctylamine, trinonylamine, tridecylamine, methyldibutylamine, methyldipentylamine, methyldihexylamine, methyldicyclohexylamine, methyldiheptylamine, methyldioctylamine, methyldinonylamine, methyldidecylamine, 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-di) Pyridyl) ethane, 1,2-di (2-pyridyl) ethene, 1,2-di (4-pyridyl) ethane, 1,3-di (4-pyridyl) propane, 1,2-di (4-pyridyloxy) ) Ethan, di (2-pyridyl) ketone, 4,4'-dipyridyl sulfide, 4,4'-dipyridyl disulfide, 2,2'-dipyridylamine, 2,2'-dipicorylamine, bipyridine and the like. Diisopropylaniline is preferable, and 2,6-diisopropylaniline is more preferable.

Ammonium salts include 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.

<Salt that generates an acid with a lower acidity than the acid generated by an acid generator>
The acidity of a salt that produces an acid that is less acidic than the acid generated by the acid generator is indicated by the acid dissociation constant (pKa). A salt that generates an acid having a lower acidity than that generated from an acid generator is a salt having an acid dissociation constant of the acid generated from the salt usually -3 <pKa, preferably -1 <pKa <7. , More preferably 0 <pKa <5.
Examples of the salt that generates an acid having a lower acidity than the acid generated from the acid generator include salts represented by the following formulas, JP-A-2012-229206, JP-A-2012-6908, and JP-A-2012. Examples thereof include the salts described in JP-A-72109, JP-A-2011-390502, and JP-A-2011-191745.

The content of the quencher (C) is preferably 0.01 to 5% by mass, more preferably 0.01 to 3% by mass, based on the solid content of the resist composition.

<Other ingredients>
The resist composition of the present invention may contain components other than the above-mentioned components (hereinafter, may be referred to as "other components (F)"), 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), a salt (I) of the present invention, and, if necessary, a resin (X), an acid generator (B), a solvent (E), a quencher (C), and the like. And other component (F) can be prepared by mixing. The mixing order is arbitrary and is not particularly limited. The temperature at the time of mixing can be selected from 10 to 40 ° C., depending on the type of resin or the like and the solubility of the resin or the like in the solvent (E). The 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 or the like 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.

<Manufacturing method of resist pattern>
The method for producing a resist pattern of the present invention is
(1) A step of applying the resist composition of the present invention on a substrate,
(2) A step of drying the applied composition to form a composition layer,
(3) Step of exposing the composition layer,
It includes (4) a step of heating the composition layer after exposure and (5) a step of developing the composition layer after heating.

The resist composition can be applied onto the substrate by a commonly used device such as a spin coater. Examples of the substrate include an inorganic substrate such as a silicon wafer. The substrate may be washed before the resist composition is applied, 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 performed, for example, by evaporating the solvent using a heating device such as a hot plate (so-called prebaking), or by 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 at the time of vacuum drying is preferably about 1~1.0 × 10 ⁵ Pa.

The obtained composition layer is usually exposed to an exposure machine. The exposure machine may be an immersion exposure machine. The exposure light source, which emits laser light in a UV-region such as a KrF excimer laser (wavelength 248 nm), ArF excimer laser (wavelength 193 nm), _{F 2} excimer laser (wavelength 157 nm), solid-state laser source (YAG or semiconductor laser Etc.), and various ones such as those that radiate harmonic laser light in the far ultraviolet region or vacuum ultraviolet region by wavelength conversion, those that irradiate electron beams, super-ultraviolet light (EUV), etc. are used. Can be done. In addition, in this specification, irradiating these radiations may be generically referred to as "exposure". At the time of exposure, the exposure is usually performed through a mask corresponding to the required pattern. When the exposure light source is an electron beam, the exposure may be performed by drawing directly without using a mask.

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

The composition layer after heating is usually developed using a developing solution using a developing device. Examples of the developing method include a dip method, a paddle method, a spray method, and a dynamic dispense method. The developing temperature is preferably, for example, 5 to 60 ° C., and the developing time is preferably, for example, 5 to 300 seconds. 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 any alkaline aqueous solution used in this field. For example, an aqueous solution of tetramethylammonium hydroxide or (2-hydroxyethyl) trimethylammonium hydroxide (commonly known as choline) can be mentioned. The alkaline developer may contain a surfactant.
After development, it is preferable to wash the resist pattern with ultrapure water and then remove the substrate and water remaining on the pattern.

When a negative resist pattern is produced from the resist composition of the present invention, a developer containing an organic solvent (hereinafter, may be referred to as "organic developer") is used as the developer.
Examples of the organic solvent contained in the organic developing solution include a ketone solvent such as 2-hexanone and 2-heptanone; a glycol ether ester solvent such as propylene glycol monomethyl ether acetate; an ester solvent such as butyl acetate; and a glycol such as propylene glycol monomethyl ether. Examples include ether solvents; amide solvents such as N and N-dimethylacetamide; aromatic hydrocarbon solvents such as anisole.
The content of the organic solvent in the organic developer is preferably 90% by mass or more and 100% by mass or less, more preferably 95% by mass or more and 100% by mass or less, and further preferably substantially only the organic solvent.
Among them, as the organic developer, a developer containing butyl acetate and / or 2-heptanone is preferable. The total content of butyl acetate and 2-heptanone in the organic developer is preferably 50% by mass or more and 100% by mass or less, more preferably 90% by mass or more and 100% by mass or less, and substantially butyl acetate and / or 2 -It is even more preferable that it is only heptanone.
The organic developer may contain a surfactant. Further, the organic developer may contain a small amount of water.
At the time of development, the development may be stopped by substituting with a solvent of a type different from that of the organic developer.

It is preferable to wash the developed resist pattern with a rinse solution. The rinsing liquid is not particularly limited 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 cleaning, it is preferable to remove the rinse liquid remaining on the substrate and the pattern.

<Use>
The resist composition of the present invention is suitable as 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 a resist composition for EUV exposure. Yes, it is more suitable as a resist composition for ArF excimer laser exposure, and is useful for fine processing of semiconductors.

The present invention will be described in more detail with reference to examples. In the examples, "%" and "part" representing the content or the amount used are based on mass unless otherwise specified.
The weight average molecular weight is a value determined by gel permeation chromatography. The analysis conditions for gel permeation chromatography are as follows.
Column: TSKgel Multipore HXL-M x 3 + guardcolumn (manufactured by Tosoh)
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)

The structure of the compound was confirmed by measuring the molecular ion peak using mass spectrometry (LC: Agilent 1100 type, MASS: Agilent LC / MSD type). In the following examples, the value of this molecular ion peak is indicated by "MASS".

式（Ｉ−２−ａ）で表される塩２．９８部、式（Ｉ−２−ｂ）で表される化合物０．６３部及びモノクロロベンゼン２４部を反応器に仕込み、２３℃で３０分間攪拌した。得られた混合物に、式（Ｉ−２−ｃ）で表される安息香酸銅０．０３部を添加し、１００℃程度まで昇温した後、同温度で１時間攪拌した。得られた反応物を濃縮した後、得られた濃縮物に、クロロホルム４５部及びイオン交換水１５部を加え、２３℃で３０分間攪拌した。その後、静置し、分液して有機層を得た。得られた有機層に、イオン交換水１５部を加え、２３℃で３０分間攪拌した。その後、静置し、分液して有機層を得た。この水洗操作を５回繰り返した。回収された有機層をろ過した後、得られたろ液を濃縮した。得られた濃縮物に、ｔｅｒｔ−ブチルメチルエーテル２０部を加えて攪拌した。得られた上澄液を除去し、上澄液除去後の残渣をさらに濃縮した。得られた濃縮物をアセトニトリルに溶解した後、濃縮することにより、式（Ｉ−２−ｄ）で表される塩１．５９部を得た。

式（Ｉ−２−ｅ）で表される塩０．５０部、式（Ｉ−２−ｄ）で表される塩０．６３部及びアセトニトリル１０部を仕込み、２３℃で３時間攪拌した。得られた混合物を濃縮し、クロロホルム１０部及びイオン交換水５部を加えた後、分液操作により、有機層を回収した。回収された有機層をイオン交換水５部で洗浄した後、得られた有機層を濃縮して、式（Ｉ−２）で表される塩０．７２部を得た。 Example 1 [Synthesis of salt represented by formula (I-2)]

2.98 parts of the salt represented by the formula (I-2-a), 0.63 parts of the compound represented by the formula (I-2-b) and 24 parts of monochlorobenzene were charged into the reactor and 30 at 23 ° C. Stirred for minutes. 0.03 part of copper benzoate represented by the formula (I-2-c) was added to the obtained mixture, the temperature was raised to about 100 ° C., and the mixture was stirred at the same temperature for 1 hour. After concentrating the obtained reaction product, 45 parts of chloroform and 15 parts of ion-exchanged water were added to the obtained concentrate, and the mixture was stirred at 23 ° C. for 30 minutes. Then, it was allowed to stand and separated to obtain an organic layer. To the obtained organic layer, 15 parts of ion-exchanged water was added, and the mixture was stirred at 23 ° C. for 30 minutes. Then, it was allowed to stand and separated to obtain an organic layer. This washing operation was repeated 5 times. After filtering the recovered organic layer, the obtained filtrate was concentrated. To the obtained concentrate, 20 parts of tert-butyl methyl ether was added and stirred. The obtained supernatant was removed, and the residue after removing the supernatant was further concentrated. The obtained concentrate was dissolved in acetonitrile and then concentrated to obtain 1.59 parts of a salt represented by the formula (I-2-d).

0.50 parts of the salt represented by the formula (I-2-e), 0.63 parts of the salt represented by the formula (I-2-d) and 10 parts of acetonitrile were charged and stirred at 23 ° C. for 3 hours. The obtained mixture was concentrated, 10 parts of chloroform and 5 parts of ion-exchanged water were added, and then the organic layer was recovered by a liquid separation operation. The recovered organic layer was washed with 5 parts of ion-exchanged water, and then the obtained organic layer was concentrated to obtain 0.72 parts of a salt represented by the formula (I-2).

MASS (ESI (+) Spectrum): M ⁺ 263.1
MASS (ESI (-) Spectrum): M ^- 339.1
^{MASS (ESI (+) Spectrum)} : [M + M - + H] + 445.1
In the present specification, M ⁺ represents the molecular ion peak of the organic cation Z ^+. M ⁻ represents the molecular ion peak of the organic anion A ^−. [M ⁺ M ⁻ + H] ⁺ represents the molecular ion peak of the intramolecular salt obtained by removing the ^{organic cation Z +} and the organic anion A ⁻ from the salt (I). The same applies to the following examples.

式（Ｉ−２４−ｅ）で表される塩０．４７部、式（Ｉ−２−ｄ）で表される塩０．６３部及びアセトニトリル１０部を仕込み、２３℃で５時間攪拌した。得られた混合物を濃縮し、クロロホルム１０部及びイオン交換水５部を加えた後、分液操作により、有機層を回収した。回収された有機層をイオン交換水５部で洗浄した後、得られた有機層を濃縮して、式（Ｉ−２４）で表される塩０．６８部を得た。 Example 2 [Synthesis of salt represented by formula (I-24)]

0.47 parts of the salt represented by the formula (I-24-e), 0.63 parts of the salt represented by the formula (I-2-d) and 10 parts of acetonitrile were charged and stirred at 23 ° C. for 5 hours. The obtained mixture was concentrated, 10 parts of chloroform and 5 parts of ion-exchanged water were added, and then the organic layer was recovered by a liquid separation operation. The recovered organic layer was washed with 5 parts of ion-exchanged water, and then the obtained organic layer was concentrated to obtain 0.68 parts of a salt represented by the formula (I-24).

MASS (ESI (+) Spectrum): M ⁺ 237.1
MASS (ESI (-) Spectrum): M ^- 339.1
^{MASS (ESI (+) Spectrum)} : [M + M - + H] + 445.1

式（Ｉ−９０−ａ）で表される塩２．９８部、式（Ｉ−９０−ｂ）で表される化合物０．４３部及びモノクロロベンゼン２４部を反応器に仕込み、２３℃で３０分間攪拌した。得られた混合物に、式（Ｉ−９０−ｃ）で表される安息香酸銅０．０３部を添加し、１００℃程度まで昇温した後、同温度で１時間攪拌した。得られた反応物を濃縮した後、得られた濃縮物に、クロロホルム４５部及びイオン交換水１１．２５部を加え、２３℃で３０分間攪拌した。その後、静置し、分液して有機層を得た。得られた有機層に、イオン交換水１１．２５部を加え、２３℃で３０分間攪拌した。その後、静置し、分液して有機層を得た。この水洗操作をさらに５回繰り返した。回収された有機層をろ過した後、得られたろ液を濃縮した。得られた濃縮物に、ｔｅｒｔ−ブチルメチルエーテル２０．１２部を加えて攪拌した。得られた上澄液を除去し、上澄液除去後の残渣をさらに濃縮した。得られた濃縮物をアセトニトリルに溶解した後、濃縮することにより、式（Ｉ−９０−ｄ）で表される塩１．２４部を得た。

式（Ｉ−２４−ｅ）で表される塩０．４７部、式（Ｉ−９０−ｄ）で表される塩０．５８部及びアセトニトリル１０部を仕込み、２３℃で５時間攪拌した。得られた混合物を濃縮し、クロロホルム１０部及びイオン交換水５部を加えた後、分液操作により、有機層を回収した。回収された有機層をイオン交換水５部で洗浄した後、得られた有機層を濃縮して、式（Ｉ−９０）で表される塩０．６１部を得た。 Example 3 [Synthesis of salt represented by formula (I-90)]

2.98 parts of the salt represented by the formula (I-90-a), 0.43 parts of the compound represented by the formula (I-90-b) and 24 parts of monochlorobenzene were charged into the reactor and 30 at 23 ° C. Stirred for minutes. 0.03 part of copper benzoate represented by the formula (I-90-c) was added to the obtained mixture, the temperature was raised to about 100 ° C., and the mixture was stirred at the same temperature for 1 hour. After concentrating the obtained reaction product, 45 parts of chloroform and 11.25 parts of ion-exchanged water were added to the obtained concentrate, and the mixture was stirred at 23 ° C. for 30 minutes. Then, it was allowed to stand and separated to obtain an organic layer. To the obtained organic layer, 11.25 parts of ion-exchanged water was added, and the mixture was stirred at 23 ° C. for 30 minutes. Then, it was allowed to stand and separated to obtain an organic layer. This washing operation was repeated 5 more times. After filtering the recovered organic layer, the obtained filtrate was concentrated. To the obtained concentrate, 20.12 parts of tert-butyl methyl ether was added and stirred. The obtained supernatant was removed, and the residue after removing the supernatant was further concentrated. The obtained concentrate was dissolved in acetonitrile and then concentrated to obtain 1.24 parts of a salt represented by the formula (I-90-d).

0.47 parts of the salt represented by the formula (I-24-e), 0.58 parts of the salt represented by the formula (I-90-d) and 10 parts of acetonitrile were charged and stirred at 23 ° C. for 5 hours. The obtained mixture was concentrated, 10 parts of chloroform and 5 parts of ion-exchanged water were added, and then the organic layer was recovered by a liquid separation operation. The recovered organic layer was washed with 5 parts of ion-exchanged water, and then the obtained organic layer was concentrated to obtain 0.61 part of a salt represented by the formula (I-90).

MASS (ESI (+) Spectrum): M ⁺ 237.1
MASS (ESI (-) Spectrum): M ^- 339.1
^{MASS (ESI (+) Spectrum)} : [M + M - + H] + 397.1

式（Ｉ−１５６−ｅ）で表される塩０．６８部、式（Ｉ−２−ｄ）で表される塩０．６３部及びアセトニトリル１０部を仕込み、２３℃で５時間攪拌した。得られた混合物を濃縮し、クロロホルム１０部及びイオン交換水５部を加えた後、分液操作により、有機層を回収した。回収された有機層をイオン交換水５部で洗浄した後、得られた有機層を濃縮して、式（Ｉ−１５６）で表される塩０．７９部を得た。 Example 4 [Synthesis of salt represented by formula (I-156)]

0.68 parts of the salt represented by the formula (I-156-e), 0.63 parts of the salt represented by the formula (I-2-d) and 10 parts of acetonitrile were charged and stirred at 23 ° C. for 5 hours. The obtained mixture was concentrated, 10 parts of chloroform and 5 parts of ion-exchanged water were added, and then the organic layer was recovered by a liquid separation operation. The recovered organic layer was washed with 5 parts of ion-exchanged water, and then the obtained organic layer was concentrated to obtain 0.79 parts of a salt represented by the formula (I-156).

MASS (ESI (+) Spectrum): M ⁺ 237.1
MASS (ESI (-) Spectrum): M ^- 339.1
^{MASS (ESI (+) Spectrum)} : [M + M - + H] + 653.2

式（Ｉ−１５６−ｅ）で表される塩０．６８部、式（Ｉ−９０−ｄ）で表される塩０．５８部及びアセトニトリル１０部を仕込み、２３℃で５時間攪拌した。得られた混合物を濃縮し、クロロホルム１０部及びイオン交換水５部を加えた後、分液操作により、有機層を回収した。回収された有機層をイオン交換水５部で洗浄した後、得られた有機層を濃縮して、式（Ｉ−２２２）で表される塩０．６８部を得た。 Example 5 [Synthesis of salt represented by formula (I-222)]

0.68 parts of the salt represented by the formula (I-156-e), 0.58 parts of the salt represented by the formula (I-90-d) and 10 parts of acetonitrile were charged and stirred at 23 ° C. for 5 hours. The obtained mixture was concentrated, 10 parts of chloroform and 5 parts of ion-exchanged water were added, and then the organic layer was recovered by a liquid separation operation. The recovered organic layer was washed with 5 parts of ion-exchanged water, and then the obtained organic layer was concentrated to obtain 0.68 parts of a salt represented by the formula (I-222).

MASS (ESI (+) Spectrum): M ⁺ 237.1
MASS (ESI (-) Spectrum): M ^- 339.1
^{MASS (ESI (+) Spectrum)} : [M + M - + H] + 605.2

式（Ｉ−２８１−ａ）で表される塩２．４６部、式（Ｉ−２−ｂ）で表される化合物０．６３部及びモノクロロベンゼン２４部を反応器に仕込み、２３℃で３０分間攪拌した。得られた混合物に、式（Ｉ−２−ｃ）で表される安息香酸銅０．０３部を添加し、１００℃程度まで昇温した後、同温度で１時間攪拌した。得られた反応物を濃縮した後、得られた濃縮物に、クロロホルム４５部及びイオン交換水１５部を加え、２３℃で３０分間攪拌した。その後、静置し、分液して有機層を得た。得られた有機層に、イオン交換水１５部を加え、２３℃で３０分間攪拌した。その後、静置し、分液して有機層を得た。この水洗操作を５回繰り返した。回収された有機層をろ過した後、得られたろ液を濃縮した。得られた濃縮物に、ｔｅｒｔ−ブチルメチルエーテル２０部を加えて攪拌した。得られた上澄液を除去し、上澄液除去後の残渣をさらに濃縮した。得られた濃縮物をアセトニトリルに溶解した後、濃縮することにより、式（Ｉ−２８１−ｄ）で表される塩１．２８部を得た。

式（Ｉ−２−ｅ）で表される塩０．５０部、式（Ｉ−２８１−ｄ）で表される塩０．５６部及びアセトニトリル１０部を仕込み、２３℃で３時間攪拌した。得られた混合物を濃縮し、クロロホルム１０部及びイオン交換水５部を加えた後、分液操作により、有機層を回収した。回収された有機層をイオン交換水５部で洗浄した後、得られた有機層を濃縮して、式（Ｉ−２８１）で表される塩０．７２部を得た。 Example 6 [Synthesis of salt represented by formula (I-281)]

2.46 parts of the salt represented by the formula (I-281-a), 0.63 parts of the compound represented by the formula (I-2-b) and 24 parts of monochlorobenzene were charged into the reactor and 30 at 23 ° C. Stirred for minutes. 0.03 part of copper benzoate represented by the formula (I-2-c) was added to the obtained mixture, the temperature was raised to about 100 ° C., and the mixture was stirred at the same temperature for 1 hour. After concentrating the obtained reaction product, 45 parts of chloroform and 15 parts of ion-exchanged water were added to the obtained concentrate, and the mixture was stirred at 23 ° C. for 30 minutes. Then, it was allowed to stand and separated to obtain an organic layer. To the obtained organic layer, 15 parts of ion-exchanged water was added, and the mixture was stirred at 23 ° C. for 30 minutes. Then, it was allowed to stand and separated to obtain an organic layer. This washing operation was repeated 5 times. After filtering the recovered organic layer, the obtained filtrate was concentrated. To the obtained concentrate, 20 parts of tert-butyl methyl ether was added and stirred. The obtained supernatant was removed, and the residue after removing the supernatant was further concentrated. The obtained concentrate was dissolved in acetonitrile and then concentrated to obtain 1.28 parts of a salt represented by the formula (I-281-d).

0.50 parts of the salt represented by the formula (I-2-e), 0.56 parts of the salt represented by the formula (I-281-d) and 10 parts of acetonitrile were charged and stirred at 23 ° C. for 3 hours. The obtained mixture was concentrated, 10 parts of chloroform and 5 parts of ion-exchanged water were added, and then the organic layer was recovered by a liquid separation operation. The recovered organic layer was washed with 5 parts of ion-exchanged water, and then the obtained organic layer was concentrated to obtain 0.72 parts of a salt represented by the formula (I-281).

MASS (ESI (+) Spectrum): M ⁺ 263.1
MASS (ESI (-) Spectrum): M ^- 323.1
^{MASS (ESI (+) Spectrum)} : [M + M - + H] + 389.0

式（Ｉ−３−ａ）で表される塩２．９１部、式（Ｉ−２−ｂ）で表される化合物０．６３部及びモノクロロベンゼン２４部を反応器に仕込み、２３℃で３０分間攪拌した。得られた混合物に、式（Ｉ−２−ｃ）で表される安息香酸銅０．０３部を添加し、１００℃程度まで昇温した後、同温度で１時間攪拌した。得られた反応物を濃縮した後、得られた濃縮物に、クロロホルム４５部及びイオン交換水１５部を加え、２３℃で３０分間攪拌した。その後、静置し、分液して有機層を得た。得られた有機層に、イオン交換水１５部を加え、２３℃で３０分間攪拌した。その後、静置し、分液して有機層を得た。この水洗操作を５回繰り返した。回収された有機層をろ過した後、得られたろ液を濃縮した。得られた濃縮物に、ｔｅｒｔ−ブチルメチルエーテル２０部を加えて攪拌した。得られた上澄液を除去し、上澄液除去後の残渣をさらに濃縮した。得られた濃縮物をアセトニトリルに溶解した後、濃縮することにより、式（Ｉ−３−ｄ）で表される塩１．６８部を得た。

式（Ｉ−２−ｅ）で表される塩０．５０部、式（Ｉ−３−ｄ）で表される塩０．６１部及びアセトニトリル１０部を仕込み、２３℃で３時間攪拌した。得られた混合物を濃縮し、クロロホルム１０部及びイオン交換水５部を加えた後、分液操作により、有機層を回収した。回収された有機層をイオン交換水５部で洗浄した後、得られた有機層を濃縮して、式（Ｉ−３）で表される塩０．６９部を得た。 Example 7 [Synthesis of salt represented by formula (I-3)]

2.91 parts of the salt represented by the formula (I-3-a), 0.63 parts of the compound represented by the formula (I-2-b) and 24 parts of monochlorobenzene were charged into the reactor and 30 at 23 ° C. Stirred for minutes. 0.03 part of copper benzoate represented by the formula (I-2-c) was added to the obtained mixture, the temperature was raised to about 100 ° C., and the mixture was stirred at the same temperature for 1 hour. After concentrating the obtained reaction product, 45 parts of chloroform and 15 parts of ion-exchanged water were added to the obtained concentrate, and the mixture was stirred at 23 ° C. for 30 minutes. Then, it was allowed to stand and separated to obtain an organic layer. To the obtained organic layer, 15 parts of ion-exchanged water was added, and the mixture was stirred at 23 ° C. for 30 minutes. Then, it was allowed to stand and separated to obtain an organic layer. This washing operation was repeated 5 times. After filtering the recovered organic layer, the obtained filtrate was concentrated. To the obtained concentrate, 20 parts of tert-butyl methyl ether was added and stirred. The obtained supernatant was removed, and the residue after removing the supernatant was further concentrated. The obtained concentrate was dissolved in acetonitrile and then concentrated to obtain 1.68 parts of a salt represented by the formula (I-3-d).

0.50 parts of the salt represented by the formula (I-2-e), 0.61 part of the salt represented by the formula (I-3-d) and 10 parts of acetonitrile were charged and stirred at 23 ° C. for 3 hours. The obtained mixture was concentrated, 10 parts of chloroform and 5 parts of ion-exchanged water were added, and then the organic layer was recovered by a liquid separation operation. The recovered organic layer was washed with 5 parts of ion-exchanged water, and then the obtained organic layer was concentrated to obtain 0.69 parts of a salt represented by the formula (I-3).

MASS (ESI (+) Spectrum): M ⁺ 263.1
MASS (ESI (-) Spectrum): M ^- 323.0
^{MASS (ESI (+) Spectrum)} : [M + M - + H] + 445.1

式（Ｉ−２４−ｅ）で表される塩０．４７部、式（Ｉ−３−ｄ）で表される塩０．６１部及びアセトニトリル１０部を仕込み、２３℃で５時間攪拌した。得られた混合物を濃縮し、クロロホルム１０部及びイオン交換水５部を加えた後、分液操作により、有機層を回収した。回収された有機層をイオン交換水５部で洗浄した後、得られた有機層を濃縮して、式（Ｉ−２５）で表される塩０．６３部を得た。 Example 8 [Synthesis of salt represented by formula (I-25)]

0.47 parts of the salt represented by the formula (I-24-e), 0.61 part of the salt represented by the formula (I-3-d) and 10 parts of acetonitrile were charged and stirred at 23 ° C. for 5 hours. The obtained mixture was concentrated, 10 parts of chloroform and 5 parts of ion-exchanged water were added, and then the organic layer was recovered by a liquid separation operation. The recovered organic layer was washed with 5 parts of ion-exchanged water, and then the obtained organic layer was concentrated to obtain 0.63 parts of a salt represented by the formula (I-25).

MASS (ESI (+) Spectrum): M ⁺ 237.1
MASS (ESI (-) Spectrum): M ^- 323.0
^{MASS (ESI (+) Spectrum)} : [M + M - + H] + 445.1

式（Ｉ−３−ａ）で表される塩２．９１部、式（Ｉ−９０−ｂ）で表される化合物０．４３部及びモノクロロベンゼン２４部を反応器に仕込み、２３℃で３０分間攪拌した。
得られた混合物に、式（Ｉ−２−ｃ）で表される安息香酸銅０．０３部を添加し、１００℃程度まで昇温した後、同温度で１時間攪拌した。得られた反応物を濃縮した後、得られた濃縮物に、クロロホルム４５部及びイオン交換水１１．２５部を加え、２３℃で３０分間攪拌した。その後、静置し、分液して有機層を得た。得られた有機層に、イオン交換水１１．２５部を加え、２３℃で３０分間攪拌した。その後、静置し、分液して有機層を得た。この水洗操作をさらに５回繰り返した。回収された有機層をろ過した後、得られたろ液を濃縮した。得られた濃縮物に、ｔｅｒｔ−ブチルメチルエーテル２０．１２部を加えて攪拌した。得られた上澄液を除去し、上澄液除去後の残渣をさらに濃縮した。得られた濃縮物をアセトニトリルに溶解した後、濃縮することにより、式（Ｉ−９１−ｄ）で表される塩１．２２部を得た。

式（Ｉ−２４−ｅ）で表される塩０．４７部、式（Ｉ−９１−ｄ）で表される塩０．５６部及びアセトニトリル１０部を仕込み、２３℃で５時間攪拌した。得られた混合物を濃縮し、クロロホルム１０部及びイオン交換水５部を加えた後、分液操作により、有機層を回収した。回収された有機層をイオン交換水５部で洗浄した後、得られた有機層を濃縮して、式（Ｉ−９１）で表される塩０．５５部を得た。 Example 9 [Synthesis of salt represented by formula (I-91)]

2.91 parts of the salt represented by the formula (I-3-a), 0.43 parts of the compound represented by the formula (I-90-b) and 24 parts of monochlorobenzene were charged into the reactor and 30 at 23 ° C. Stirred for minutes.
0.03 part of copper benzoate represented by the formula (I-2-c) was added to the obtained mixture, the temperature was raised to about 100 ° C., and the mixture was stirred at the same temperature for 1 hour. After concentrating the obtained reaction product, 45 parts of chloroform and 11.25 parts of ion-exchanged water were added to the obtained concentrate, and the mixture was stirred at 23 ° C. for 30 minutes. Then, it was allowed to stand and separated to obtain an organic layer. To the obtained organic layer, 11.25 parts of ion-exchanged water was added, and the mixture was stirred at 23 ° C. for 30 minutes. Then, it was allowed to stand and separated to obtain an organic layer. This washing operation was repeated 5 more times. After filtering the recovered organic layer, the obtained filtrate was concentrated. To the obtained concentrate, 20.12 parts of tert-butyl methyl ether was added and stirred. The obtained supernatant was removed, and the residue after removing the supernatant was further concentrated. The obtained concentrate was dissolved in acetonitrile and then concentrated to obtain 1.22 parts of a salt represented by the formula (I-91-d).

0.47 parts of the salt represented by the formula (I-24-e), 0.56 parts of the salt represented by the formula (I-91-d) and 10 parts of acetonitrile were charged and stirred at 23 ° C. for 5 hours. The obtained mixture was concentrated, 10 parts of chloroform and 5 parts of ion-exchanged water were added, and then the organic layer was recovered by a liquid separation operation. The recovered organic layer was washed with 5 parts of ion-exchanged water, and then the obtained organic layer was concentrated to obtain 0.55 parts of a salt represented by the formula (I-91).

MASS (ESI (+) Spectrum): M ⁺ 237.1
MASS (ESI (-) Spectrum): M ^- 323.0
^{MASS (ESI (+) Spectrum)} : [M + M - + H] + 397.1

式（Ｉ−１５６−ｅ）で表される塩０．６８部、式（Ｉ−３−ｄ）で表される塩０．６１部及びアセトニトリル１０部を仕込み、２３℃で５時間攪拌した。得られた混合物を濃縮し、クロロホルム１０部及びイオン交換水５部を加えた後、分液操作により、有機層を回収した。回収された有機層をイオン交換水５部で洗浄した後、得られた有機層を濃縮して、式（Ｉ−１５７）で表される塩０．６８部を得た。 Example 10 [Synthesis of salt represented by formula (I-157)]

0.68 parts of the salt represented by the formula (I-156-e), 0.61 part of the salt represented by the formula (I-3-d) and 10 parts of acetonitrile were charged and stirred at 23 ° C. for 5 hours. The obtained mixture was concentrated, 10 parts of chloroform and 5 parts of ion-exchanged water were added, and then the organic layer was recovered by a liquid separation operation. The recovered organic layer was washed with 5 parts of ion-exchanged water, and then the obtained organic layer was concentrated to obtain 0.68 parts of a salt represented by the formula (I-157).

MASS (ESI (+) Spectrum): M ⁺ 237.1
MASS (ESI (-) Spectrum): M ^- 323.0
^{MASS (ESI (+) Spectrum)} : [M + M - + H] + 653.2

式（Ｉ−１５６−ｅ）で表される塩０．６８部、式（Ｉ−９１−ｄ）で表される塩０．５６部及びアセトニトリル１０部を仕込み、２３℃で５時間攪拌した。得られた混合物を濃縮し、クロロホルム１０部及びイオン交換水５部を加えた後、分液操作により、有機層を回収した。回収された有機層をイオン交換水５部で洗浄した後、得られた有機層を濃縮して、式（Ｉ−２２３）で表される塩０．６１部を得た。 Example 11 [Synthesis of salt represented by formula (I-223)]

0.68 parts of the salt represented by the formula (I-156-e), 0.56 parts of the salt represented by the formula (I-91-d) and 10 parts of acetonitrile were charged and stirred at 23 ° C. for 5 hours. The obtained mixture was concentrated, 10 parts of chloroform and 5 parts of ion-exchanged water were added, and then the organic layer was recovered by a liquid separation operation. The recovered organic layer was washed with 5 parts of ion-exchanged water, and then the obtained organic layer was concentrated to obtain 0.61 part of a salt represented by the formula (I-223).

MASS (ESI (+) Spectrum): M ⁺ 237.1
MASS (ESI (-) Spectrum): M ^- 323.0
^{MASS (ESI (+) Spectrum)} : [M + M - + H] + 605.2

Synthesis of Resin The compounds (monomers) used for the synthesis of resin A1, resin A2, resin X1, resin X2, and resin X1 are shown below. Hereinafter, these compounds will be referred to as "monomer (a1-1-3)" or the like according to the formula number.

Synthesis Example 1 [Synthesis of resin A1]
As the monomer, a monomer (a1-1-3), a monomer (a1-2-9), a monomer (a2-1-1) and a monomer (a3-4-2) are used, and the molar ratio [monomer (a1-1-1)] is used. -3): Monomer (a1-2-9): Monomer (a2-1-1): Monomer (a3-4-2)] are mixed so as to be 35: 15: 2.5: 47.5. A propylene glycol monomethyl ether acetate 1.5% by mass of the total amount of monomers was added to prepare a solution. To this solution, azobisisobutyronitrile and azobis (2,4-dimethylvaleronitrile) as initiators were added in an amount of 1 mol% and 3 mol%, respectively, based on the total amount of monomers, and these were heated at 75 ° C. for about 5 hours. bottom. The obtained reaction mixture was poured into a large amount of methanol / water mixed solvent to precipitate a resin, and the resin was filtered. The resulting resin was added to a methanol / water mixed solvent, after repulping, performed twice a purification operation that filtered to give the resin A1 having a weight-average molecular weight 8.0 × 10 ³ in 69% yield. This resin A1 has the following structural units.

Synthesis Example 2 [Synthesis of resin A2]
As the monomer, a monomer (a1-1-3), a monomer (a1-2-11), a monomer (a2-1-1) and a monomer (a3-4-2) are used, and the molar ratio [monomer (a1-1-1)] is used. -3): Monomer (a1-2-11): Monomer (a2-1-1): Monomer (a3-4-2)] was mixed so as to be 35: 15: 2.5: 47.5. except performs the same operation as synthesis example 1 to obtain resin A2 having a weight-average molecular weight 7.9 × 10 ³ in 65% yield. This resin A2 has the following structural units.

Synthesis Example 3 [Synthesis of resin X1]
A monomer (a4-1-7) was used as a monomer, and methyl isobutyl ketone 1.5% by mass of the total amount of the monomer was added to prepare a solution. Azobisisobutyronitrile and azobis (2,4-dimethylvaleronitrile) as initiators were added to the solution in an amount of 0.7 mol% and 2.1 mol%, respectively, based on the total amount of the monomers, and these were added at 75 ° C. It was heated for about 5 hours. The reaction mixture obtained, the resin was precipitated by pouring into a large amount of methanol / water mixed solvent, the resin was filtered, to obtain a resin X1 of weight average molecular weight 1.8 × 10 ⁴ in 77% yield. This resin X1 has the following structural units.

Synthesis Example 4 [Synthesis of resin X2]
As the monomer, a monomer (a5-1-1) and a monomer (a4-0-12) are used, and the molar ratio [monomer (a5-1-1): monomer (a4-0-12)] is 50:50. Methyl isobutyl ketone was added in an amount 1.2% by mass of the total amount of the monomers to prepare a solution. Azobis (2,4-dimethylvaleronitrile) as an initiator was added to this solution in an amount of 3 mol% based on the total amount of monomers, and the mixture was heated at 70 ° C. for about 5 hours. The reaction mixture obtained, the resin was precipitated by pouring into a large amount of methanol / water mixed solvent, the resin was filtered, the weight-average molecular weight 1.0 × 10 ⁴ of the resin X2 (copolymer) to yield 91% I got it in. This resin X2 has the following structural units.

<Preparation of resist composition>
Each of the components shown below was mixed by mass parts shown in Tables 7 and 8 and dissolved in a solvent, and filtered through a fluororesin filter having a pore size of 0.2 μm to prepare a resist composition.

<Resin>
A1, A2, X1, X2: Resin A1, Resin A2, Resin X1, Resin X2
<Salt (I)>
I-2: Salt represented by the formula (I-2) I-3: Salt represented by the formula (I-3) I-24: Salt represented by the formula (I-24) I-25: Formula Salt represented by (I-25) I-90: Salt represented by formula (I-90) I-91: Salt represented by formula (I-91) I-156: Salt represented by formula (I-156) Salt represented by I-157: Salt represented by formula (I-157) I-222: Salt represented by formula (I-222) I-223: Salt represented by formula (I-223) I-281: Salt represented by the formula (I-281)

Ｂ１−２１：式（Ｂ１−２１）で表される塩（特開２０１２−２２４６１１号公報の実施例に従って合成）
Ｂ１−２２：式（Ｂ１−２２）で表される塩（特開２０１２−２２４６１１号公報の実施例に従って合成）

<Acid generator (B)>
IX-1: Compound represented by the following formula (synthesized according to an example of US2013 / 35503)

B1-21: Salt represented by the formula (B1-21) (synthesized according to an example of JP2012-224611)
B1-22: Salt represented by the formula (B1-22) (synthesized according to an example of JP2012-224611)

<Quencher (C)>
D1: Compound represented by the following formula (D1) (manufactured by Tokyo Chemical Industry Co., Ltd.)

<Solvent>
Propylene Glycol Monomethyl Ether Acetate 265 Parts Propylene Glycol Monomethyl Ether 20 Parts 2-Heptanone 20 Parts γ-Butyrolactone 3.5 Parts

<Manufacturing of resist pattern and its evaluation>
An organic antireflection film composition (ARC-29; manufactured by Nissan Chemical Industries, Ltd.) is applied to a silicon wafer and baked at 205 ° C. for 60 seconds to produce organic reflection on the wafer with a film thickness of 78 nm. An anti-reflective film was formed. Next, the above resist composition was applied (spin coated) on the organic antireflection film so that the film thickness after drying was 85 nm. After coating, the silicon wafer was prebaked on a direct hot plate at the temperatures listed in the "PB" column of Tables 7 and 8 for 60 seconds to form a composition layer. A contact hole pattern (hole pitch 90 nm) was used on a silicon wafer on which a composition layer was formed with an ArF excimer stepper for immersion exposure (XT: 1900 Gi; manufactured by ASML, NA = 1.35, 3/4 Anal XY polarization). / Using a mask for forming a hole diameter (55 nm), the exposure amount was changed stepwise for exposure. Ultrapure water was used as the immersion medium.
After exposure, post-exposure baking was performed on a hot plate at the temperatures listed in the "PEB" column of Tables 7 and 8 for 60 seconds. Next, the composition layer on the silicon wafer was developed by the dynamic dispensing method at 23 ° C. for 20 seconds using butyl acetate (manufactured by Tokyo Chemical Industry Co., Ltd.) as a developing solution to form a negative resist pattern. Manufactured.

In the resist pattern obtained after development, the exposure amount having a hole diameter of 50 nm formed by using the mask was defined as the effective sensitivity.

<CD uniformity (CDU) evaluation>
In the effective sensitivity, the hole diameter of the pattern formed by the mask having a hole diameter of 55 nm was measured 24 times for each hole, and the average value was taken as the average hole diameter of one hole. The standard deviation was obtained by measuring the average hole diameter of a pattern formed with a mask having a hole diameter of 55 nm at 400 points on the same wafer as a population.
"A" when the standard deviation is 1.80 nm or less,
When the standard deviation was larger than 1.80 nm, it was judged as "B".
The results are shown in Table 9. The numbers in parentheses indicate the standard deviation (nm).

The resist composition containing the salt of the present invention is suitable for microfabrication of semiconductors because a resist pattern can be produced with good CD uniformity.

Claims (7)

A salt represented by the formula (I).

[In formula (I),
R ¹ represents an aromatic hydrocarbon group having 6 to 18 carbon atoms which may have a substituent.
R ² represents a hydrocarbon group having 1 to 18 carbon atoms which may have a substituent.
X ¹ represents a divalent aliphatic saturated hydrocarbon group having 1 to 12 carbon atoms, and the methylene group contained in the divalent aliphatic saturated hydrocarbon group may be replaced with an oxygen atom or a carbonyl group. ..
X ² and X ³ independently represent a fluorine atom or a perfluoroalkyl group having 1 to 6 carbon atoms.
L ^b1 represents a divalent saturated hydrocarbon group having 1 to 24 carbon atoms, and the methylene group contained in the saturated hydrocarbon group may be replaced with an oxygen atom or a carbonyl group, and the saturated hydrocarbon group may be used. The contained hydrogen atom may be substituted with a fluorine atom or a hydroxy group.
A ⁻ represents an organic anion.
Z ⁺ represents an organic cation.
The organic anion is a sulfonic acid anion represented by the formula (IA).

(In formula (IA),
Q ¹ and ^{Q 2} each independently represent a fluorine atom or a perfluoroalkyl group having 1 to 6 carbon atoms.
L ^bb 1 represents a divalent saturated hydrocarbon group having 1 to 24 carbon atoms, and -CH _2- contained in the saturated hydrocarbon group may be replaced with -O- or -C (= O)-. , The hydrogen atom contained in the saturated hydrocarbon group may be substituted with a fluorine atom or a hydroxy group.
Y represents a methyl group which may have a substituent or a monovalent alicyclic hydrocarbon group having 3 to 18 carbon atoms which may have a substituent, and the alicyclic hydrocarbon group may be used. it is, -O - - -CH ₂ contained, - SO ₂ - or -C (= O) - may be replaced with. )
The organic cation is a cation represented by any of the formulas (b2-1) to (b2-4).

(In equations (b2-1) to (b2-4),
R ^{b4 to} R ^b6 independently represent a chain hydrocarbon group having 1 to 30 carbon atoms, an alicyclic hydrocarbon group having 3 to 36 carbon atoms, or an aromatic hydrocarbon group having 6 to 36 carbon atoms. The hydrogen atom contained in the chain hydrocarbon group is a hydroxy group, an alkoxy group having 1 to 12 carbon atoms, an alicyclic hydrocarbon group having 3 to 12 carbon atoms, or an aromatic hydrocarbon group having 6 to 18 carbon atoms. It may be substituted, and the hydrogen atom contained in the alicyclic hydrocarbon group is a halogen atom, an aliphatic hydrocarbon group having 1 to 18 carbon atoms, an alkylcarbonyl group having 2 to 4 carbon atoms, or a glycidyloxy group. It may be substituted, and the hydrogen atom contained in the aromatic hydrocarbon group may be substituted with a halogen atom, a hydroxy group, or an alkoxy group having 1 to 12 carbon atoms.
R ^b4 and R ^b5 may be bonded to each other to form a ring together with the sulfur atom to which they are bonded, and -CH ₂ − contained in the ring may be -O-, -S- or. It may be replaced with −CO−.
R ^b7 and R ^b8 independently represent a hydroxy group, an aliphatic hydrocarbon group having 1 to 12 carbon atoms, or an alkoxy group having 1 to 12 carbon atoms.
m2 and n2 each independently represent an integer of 0 to 5.
When m2 is 2 or more, the plurality of R ^b7s may be the same or different, and when n2 is 2 or more, the plurality of R ^b8s may be the same or different.
R ^b9 and R ^b10 independently represent a chain hydrocarbon group having 1 to 36 carbon atoms or an alicyclic hydrocarbon group having 3 to 36 carbon atoms.
R ^b9 and R ^b10 may be bonded to each other to form a ring together with the sulfur atom to which they are bonded, and -CH ₂ − contained in the ring may be -O-, -S- or. It may be replaced with −CO−.
R ^b11 represents a hydrogen atom, a chain hydrocarbon group having 1 to 36 carbon atoms, an alicyclic hydrocarbon group having 3 to 36 carbon atoms, or an aromatic hydrocarbon group having 6 to 18 carbon atoms.
R ^b12 represents a chain hydrocarbon 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, and is included in the chain hydrocarbon group. The hydrogen atom may be substituted with an aromatic hydrocarbon group having 6 to 18 carbon atoms, and the hydrogen atom contained in the aromatic hydrocarbon group may be an alkoxy group having 1 to 12 carbon atoms or 1 to 12 carbon atoms. It may be substituted with 12 alkylcarbonyloxy groups.
R ^b11 and R ^b12 may be bonded to each other to form a ring including -CH-CO- to which they are bonded, and -CH _2- contained in the ring is -O-, -S. It may be replaced with − or −CO−.
R ^{b13 to} R ^b18 independently represent a hydroxy group, an aliphatic hydrocarbon group having 1 to 12 carbon atoms, or an alkoxy group having 1 to 12 carbon atoms.
L ^b31 represents a sulfur atom or an oxygen atom.
o2, p2, s2, and t2 each independently represent an integer of 0 to 5.
q2 and r2 each independently represent an integer of 0 to 4.
u2 represents 0 or 1.
When o2 is 2 or more, a plurality of R ^b13s are the same or different, when p2 is 2 or more, a plurality of R ^b14s are the same or different, and when q2 is 2 or more, a plurality of R ^b15s are the same or different. when r2 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 different. ) ]] The salt according to claim 1, wherein X ¹ is an alkanediyl group having 1 to 6 carbon atoms. The salt according to claim 1 or 2, wherein R ¹ and R ^{2 are phenyl groups which may independently have a substituent.} An acid generator containing the salt according to any one of claims 1 to 3. A resist composition containing the acid generator according to claim 4 and a resin containing a structural unit having an acid unstable group. The resist composition according to claim 5, further comprising a salt that generates an acid having a lower acidity than the acid generated from the acid generator. (1) A step of applying the resist composition according to claim 5 or 6 onto a substrate.
(2) A step of drying the applied composition to form a composition layer,
(3) 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.