JP2019059713A - Compound, resin, resist composition, and method for producing resist pattern - Google Patents

Abstract

To provide a compound capable of producing a resist pattern with good line edge roughness (LER), a resin having a structural unit derived from the compound, and a resist composition containing the resin.SOLUTION: The compound is represented by formula (I) [Rand Rare each OH or a group represented by formula (R-1)-(R-3); * is a bonding position to Aror Ar; Aris an optionally substituted C6-36 aromatic hydrocarbon ring; and Aris an optionally substituted C6-36 aromatic hydrocarbon ring].SELECTED DRAWING: None

Description

  The present invention relates to a compound, a resin, a resist composition, and a method of producing a resist pattern using the resist composition.

Patent Document 1 describes a resist composition containing a resin having a structural unit derived from the following compound.

JP, 2002-201223, A

  The present invention is a structure derived from a compound capable of producing a resist pattern having better line edge roughness (LER) than a resist pattern formed from a resist composition containing a resin having a structural unit derived from the above-mentioned compound. An object of the present invention is to provide a resist composition containing a resin having a unit.

The present invention includes the following inventions.
[1] A compound represented by formula (I).
[In the formula (I),
Each of R ¹ and R ² independently represents a hydroxy group or a group represented by any of Formula (R-1) to Formula (R-3). However, at least one of R ¹ and R ² represents a group represented by any one of Formula (R-1) to Formula (R-3).
(In the formula (R-1) to the formula (R-3),
R ³ represents a hydrogen atom or a methyl group. * Represents a bonding position to Ar ¹ or Ar ² . )
Ar ¹ represents an aromatic hydrocarbon ring having 6 to 36 carbon atoms which may have a substituent.
Ar ² represents an aromatic hydrocarbon ring having 6 to 36 carbon atoms which may have a substituent. ]
[2] The compound according to [1], wherein Ar ¹ is benzene which may have a substituent or naphthalene which may have a substituent.
[3] The compound according to [1] or [2], wherein Ar ² is benzene which may have a substituent.
[4] One of R ¹ and R ² is a group represented by any one of Formula (R-1) to Formula (R-3), and the other is a hydroxy group of [1] to [3] The compound as described in any one.
[5] The compound according to any one of [1] to [3], wherein one of R ¹ and R ² is a group represented by the formula (R-1) and the other is a hydroxy group.
[6] A resin having a structural unit derived from the compound according to any one of [1] to [5].
[7] The resin according to [6], further comprising a structural unit having an acid labile group.
[8] A resist composition comprising the resin according to [6] or [7] and an acid generator.
[9] The resist composition according to [8], wherein the acid generator comprises a salt represented by Formula (B1).
[In the formula (B1),
Each of Q ^b1 and Q ^b2 independently represents a fluorine atom or a C 1 to C 6 perfluoroalkyl group.
L ^b1 represents a divalent saturated hydrocarbon group having 1 to 24 carbon atoms, and —CH ₂ — contained in the divalent saturated hydrocarbon group 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 represents a methyl group which may have a substituent or an alicyclic hydrocarbon group having 3 to 18 carbon atoms which may have a substituent, and is included in the alicyclic hydrocarbon group; CH _2- may be replaced by -O-, -S (O) ₂ -or -CO-.
Z ⁺ represents an organic cation. ]
[10] The resist composition according to [8] or [9], further comprising a salt that generates an acid having a weaker acidity than an acid generated from an acid generator.
[11] (1) A step of applying the resist composition according to any one of [8] to [10] on a substrate,
(2) drying the composition after application to form a composition layer;
(3) exposing the composition layer,
(4) A method of producing a resist pattern, comprising the steps of: heating the composition layer after exposure; and (5) developing the composition layer after heating.

  By using a resist composition using a resin having a structural unit derived from the compound of the present invention, a resist pattern can be produced with good line edge roughness (LER).

In the present specification, unless otherwise specified, “(meth) acrylate” means “at least one selected from the group consisting of acrylate and methacrylate”. Notation such as "(meth) acrylic acid" or "(meth) acryloyl" has the same meaning. When a structural unit having "CH ₂ CC (CH ₃ ) -CO-" or "CH ₂ CHCH-CO-" is exemplified, structural units having both groups are exemplified similarly. It shall be. Also, when stereoisomers exist, all stereoisomers are included.
In the present specification, “solid content of resist composition” means the total of components excluding the solvent (E) described later from the total amount of the resist composition.

[Compound represented by Formula (I)]
The present invention relates to a compound represented by the formula (I) (hereinafter sometimes referred to as "compound (I)").
In the formula (I), the aromatic hydrocarbon ring of Ar ¹ includes monocyclic, fused polycyclic and ring assembly, and, for example, aromatic carbon having 6 to 36 carbon atoms such as benzene, naphthalene, anthracene, biphenyl and the like A hydrogen ring is mentioned.
The aromatic hydrocarbon ring preferably has 6 to 24 carbon atoms, and more preferably 6 to 18 carbon atoms.
The aromatic hydrocarbon ring of Ar ² includes monocyclic, fused polycyclic and a ring assembly, and examples thereof include aromatic hydrocarbon rings having 6 to 36 carbon atoms such as benzene, naphthalene, anthracene, biphenyl and the like.
The aromatic hydrocarbon ring preferably has 6 to 24 carbon atoms, and more preferably 6 to 18 carbon atoms.

Examples of the substituent that Ar ¹ and Ar ² may have include a hydroxy group, a halogen atom, a cyano group, an alkyl group having 1 to 12 carbon atoms, an alkoxy group having 1 to 12 carbon atoms, and 2 to 13 carbon atoms An alkoxycarbonyl group, an alkylcarbonyl group having 2 to 13 carbon atoms, an alkylcarbonyloxy group having 2 to 13 carbon atoms, an alicyclic hydrocarbon group having 3 to 12 carbon atoms, or a combination of these may be mentioned.
As a halogen atom, a fluorine atom, a chlorine atom, a bromine atom and iodine are mentioned.
Examples of the alkyl group having 1 to 12 carbon atoms include methyl group, ethyl group, propyl group, butyl group, pentyl group, hexyl group, heptyl group, octyl group, nonyl group, decyl group, undecyl group and dodecyl group. .
Examples of the alkoxy group having 1 to 12 carbon atoms include methoxy, ethoxy, propoxy, butoxy, pentyloxy, hexyloxy, octyloxy, 2-ethylhexyloxy, nonyloxy, decyloxy, undecyloxy And dodecyloxy groups.
An alkoxycarbonyl group having 2 to 13 carbon atoms, an alkylcarbonyl group having 2 to 13 carbon atoms and an alkylcarbonyloxy group having 2 to 13 carbon atoms are groups in which a carbonyl group or a carbonyloxy group is bonded to the above-mentioned alkyl group or alkoxy group. Represents A methoxycarbonyl group, an ethoxycarbonyl group, a butoxycarbonyl group etc. are mentioned as a C2-C13 alkoxycarbonyl group, Acetyl group, a propionyl group, a butyryl group etc. are mentioned as a C2-C13 alkylcarbonyl group. As the alkylcarbonyloxy group having 2 to 13 carbon atoms, an acetyloxy group, a propionyloxy group, a butyryloxy group and the like can be mentioned.
The alicyclic hydrocarbon group having 3 to 12 carbon atoms may be either monocyclic or polycyclic, and examples thereof include the groups shown below. ** is a bond with an aromatic hydrocarbon group.
As a combined group in the substituent of the aromatic hydrocarbon group, a group combining a hydroxy group and an alkyl group having 1 to 12 carbon atoms, an alkoxy group having 1 to 12 carbon atoms and an alkoxy group having 1 to 12 carbon atoms And groups in which an alkyl group having 1 to 12 carbon atoms and an aromatic hydrocarbon group having 6 to 10 carbon atoms are combined.
As a group which combined the hydroxyl group and the C1-C12 alkyl group, C1-C12 hydroxyalkyl groups, such as a hydroxymethyl group and a hydroxyethyl group, etc. are mentioned.
As a group which combined the C1-C12 alkoxy group and the C1-C12 alkoxy group, C2-C24 alkoxy alkoxy groups, such as an ethoxy ethoxy group, etc. are mentioned.
As a group which combined a C1-C12 alkyl group and a C6-C10 aromatic hydrocarbon group, C7-C22 aralkyl groups, such as a benzyl group, carbon number, such as a tolyl group and xylyl group The C6-C10 aromatic hydrocarbon group which has a 1-12 alkyl group is mentioned.
As a group which combined a C3-C12 alicyclic hydrocarbon group and a C6-C10 aromatic hydrocarbon group, C3-C12 alicyclics, such as an adamantyl phenyl group and a cyclohexyl phenyl group, are mentioned. The C6-C10 aromatic hydrocarbon group etc. which have a hydrocarbon group are mentioned.

Ar ¹ is preferably benzene which may have a substituent or naphthalene which may have a substituent, and has benzene or a hydroxy group or an alkyl group which may have a hydroxy group or an alkyl group It is preferable that it may be naphthalene. In addition, when it has a substituent, although one substituent may be sufficient, two or more may be sufficient. When there are two or more substituents, they may be the same or different.
Ar ² is preferably benzene. Also in Ar ^{2, when} it has a substituent, the number of substituents may be one or two or more. When there are two or more substituents, they may be the same or different.
R ¹ and R ² are preferably a hydroxy group or a group represented by formula (R-1). However, at least one of R ¹ and R ² is a group represented by Formula (R-1). Among them, R ¹ is preferably a group represented by Formula (R-1) to Formula (R-3), and more preferably, R ¹ is a group represented by Formula (R-1) . In this case, R ² may be a group represented by any of formulas (R-1) to (R-3), but is preferably a group represented by formula (R-1), and hydroxy More preferred is a group.

Examples of the compound (I) include the following compounds.

In the compounds represented by Formula (I-1) to Formula (I-20), a compound in which a methyl group corresponding to R ³ of Formula (I) is replaced with a hydrogen atom, corresponds to R ³ of Formula (I) Compounds in which a hydrogen atom is replaced by a methyl group can also be mentioned as a specific example of the compound (I). Among them, compounds represented by Formula (I-1) to Formula (I-12) are preferable, and compounds represented by Formula (I-1) to Formula (I-8) are more preferable.

<Method for producing compound (I)>
The compound (I) is obtained by reacting the compound represented by the formula (I-b1) and / or the compound represented by the formula (I-b2) with carbonyldiimidazole in a solvent, And a compound represented by the formula (I-a).
(Wherein all symbols have the same meanings as described above)

The solvent includes chloroform and acetonitrile.
The reaction temperature is usually 15 ° C. to 80 ° C., and the reaction time is usually 0.5 hour to 24 hours.
Examples of the compound represented by the compound represented by the formula (I-b1) and the compound represented by the compound represented by the formula (I-b2) include compounds represented by the following formulas, etc. .
The compound represented by the formula (I-a) is prepared by reacting the compound represented by the formula (I-c) with the compound represented by the formula (I-d) in the presence of an acid catalyst in a solvent It can be obtained by
(Wherein all symbols have the same meanings as described above)

As an acid catalyst, p-toluenesulfonic acid etc. are mentioned.
Examples of the solvent include water and ethyl acetate.
The reaction temperature is usually 15 ° C. to 80 ° C., and the reaction time is usually 0.5 hour to 24 hours.
As a compound represented by Formula (Ic), the compound etc. which are represented by a following formula are mentioned, It can obtain easily from a market.
As a compound represented by a formula (Id), the compound etc. which are represented by a following formula are mentioned, It can obtain easily from a market.

〔resin〕
The resin of the present invention is a resin (hereinafter sometimes referred to as “resin (A)”) containing a structural unit derived from compound (I) (hereinafter sometimes referred to as “structural unit (I)”). The resin (A) may be a homopolymer of the compound (I), or may be a copolymer consisting only of the compound (I), or a polymer containing one or more structural units other than the structural unit (I) It may be. The structural unit other than the structural unit (I) is a structural unit other than a structural unit having an acid labile group (hereinafter sometimes referred to as “structural unit (a1)”) and a structural unit having an acid labile group, Structural unit having a halogen atom (hereinafter sometimes referred to as “structural unit (a4)”), structural unit not having an acid labile group (hereinafter sometimes referred to as “structural unit (s)”), non-elimination carbonization Examples include structural units having a hydrogen group (hereinafter sometimes referred to as “structural unit (a5)”) and the like. Here, the acid labile group means a group having a leaving group and leaving a leaving group upon contact with an acid to form a hydrophilic group (for example, a hydroxy group or a carboxy group).
The total content of structural units (I) is usually 1 to 90 mol%, preferably 2 to 60 mol%, more preferably 3 to 60 mol%, based on the total of all structural units in the resin (A). It is 40 mol%.

Structural Unit (a1)
The structural unit (a1) is derived from a monomer having an acid labile group (hereinafter sometimes referred to as “monomer (a1)”).
The acid labile group contained in the resin (A) is a group represented by the formula (1) (hereinafter also referred to as a group (1)) and / or a group represented by the formula (2) (hereinafter referred to as a group (2 It is preferred).
[In formula (1), R ^{a1 to} R ^a3 each independently represent an alkyl group having 1 to 8 carbon atoms, an alicyclic hydrocarbon group having 3 to 20 carbon atoms, or a combination of these, or R ^a1 and R ^a2 bond to each other to form a C3-C20 non-aromatic hydrocarbon ring together with the carbon atom to which they are bonded.
ma and na each independently represent 0 or 1, and at least one of ma and na represents 1.
* Represents a bond. ]
[In Formula (2), R ^{a1 ′} and R ^{a2 ′} each independently represent a hydrogen atom or a hydrocarbon group having 1 to 12 carbon atoms, and R ^{a3 ′} represents a hydrocarbon group having 1 to 20 carbon atoms Or R ^{a2 '} and R ^a3' combine with each other to form a C 3-20 heterocyclic ring together with the carbon atom to which they are attached and X, and the —CH ₂ contained in the hydrocarbon group and the heterocyclic ring -May be replaced by -O- or -S-.
X represents an oxygen atom or a sulfur atom.
na 'represents 0 or 1;
* Represents a bond. ]

^Examples of the alkyl group in R ^a1 , R ^a2 and R ^a3 include a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, a hexyl group, a heptyl group and an octyl group.
The alicyclic hydrocarbon group in R ^a1 , R ^a2 and R ^a3 may be monocyclic or polycyclic. Examples of monocyclic alicyclic hydrocarbon groups 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 (* represents a bond). The carbon number of the alicyclic hydrocarbon group of R ^{a1 to} R ^a3 is preferably 3 to 16.
Examples of the combination of an alkyl group and an alicyclic hydrocarbon group include a methylcyclohexyl group, a dimethylcyclohexyl group, a methyl norbornyl group, a cyclohexylmethyl group, an adamantyl methyl group, an adamantyl dimethyl group, and a norbornyl group. Ethyl group etc. are mentioned.
Preferably, ma is 0 and na is 1.
The following groups may be mentioned as -C (R ^a1 ) (R ^a2 ) (R ^a3 ) when R ^a1 and R ^a2 combine with each other to form a non-aromatic hydrocarbon ring. The non-aromatic hydrocarbon ring preferably has 3 to 12 carbon atoms. * Represents a bond with -O-.

Examples of the hydrocarbon group in R ^{a1 ′} , R ^{a2 ′} and R ^{a3 ′} include an alkyl group, an alicyclic hydrocarbon group, an aromatic hydrocarbon group, and a group combining these.
Examples of the alkyl group and the alicyclic hydrocarbon group include the same groups as the groups listed for R ^a1 , R ^a2 and R ^a3 .
Examples of the aromatic hydrocarbon group include aryl groups such as phenyl group, biphenylyl group and naphthyl group.
As the combined group, a group (for example, a cycloalkyl alkyl group) obtained by combining the above-mentioned alkyl group and an alicyclic hydrocarbon group, an aralkyl group such as a benzyl group, or an aromatic hydrocarbon group having an alkyl group (p-methyl) Phenyl group, p-tert-butylphenyl group, tolyl group, xylyl group, cumenyl group, mesityl group, 2,6-diethylphenyl group, 2-methyl-6-ethylphenyl group etc.), alicyclic hydrocarbon group Aromatic hydrocarbon groups (p-cyclohexylphenyl group, p-adamantylphenyl group etc.), aryl-cycloalkyl groups such as phenylcyclohexyl group etc. may be mentioned.
When R ^{a2 '} and R ^a3' combine with each other to form a heterocyclic ring with X and the carbon atom to which they are attached, as -C (R ^{a1 '} ) (R ^a3' ) -X-R ^{a2 '} , Groups are mentioned. * Represents a bond.
At least one of R ^{a1 ′} and R ^{a2 ′} is preferably a hydrogen atom.
na 'is preferably 0.

Examples of the group (1) include the following groups.
A group in which R ^{a1 to} R ^a3 in the formula (1) is an alkyl group, ma = 0, and na = 1. As the said group, a tert- butoxycarbonyl group is preferable.
In the formula (1), a group in which R ^a1 and R ^a2 together with the carbon atom to which they are attached form an adamantyl group, R ^a3 is an alkyl group, ma = 0, and na = 1 .
In the formula (1), a group wherein R ^a1 and R ^a2 are each independently an alkyl group, R ^a3 is an adamantyl group, ma is 0, and na is 1.
Specific examples of the group (1) include the following groups. * Represents a bond.

The following groups may be mentioned as specific examples of the group (2). * Represents a bond.

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

  Among the (meth) acrylic monomers having an acid labile group, those having an alicyclic hydrocarbon group having a carbon number of 5 to 20 are preferably mentioned. 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 for the resist composition, the resolution of the resist pattern can be improved.

As a structural unit derived from a (meth) acrylic monomer having a group (1), preferably a structural unit represented by the formula (a1-0) (hereinafter sometimes referred to as a structural unit (a1-0)) A structural unit represented by the formula (a1-1) (hereinafter sometimes referred to as structural unit (a1-1)) or a structural unit represented by the formula (a1-2) (hereinafter referred to as a structural unit (a1-) 2) may be mentioned. These may be used alone or in combination of two or more.
[In the formula (a1-0), the formula (a1-1) and the formula (a1-2),
L ^a01 , L ^a1 and L ^a2 each independently represent -O- or ^* -O- (CH ₂ ) _k1 -CO-O-, k1 represents any integer of 1 to 7, and * represents an integer Represents a bond with -CO-.
Each of R ^a01 , R ^a4 and R ^a5 independently represents a hydrogen atom or a methyl group.
Each of R ^a02 , R ^a03 and R ^a04 independently ^represents an alkyl group having 1 to 8 carbon atoms, an alicyclic hydrocarbon group having 3 to 18 carbon atoms, or a combination of these.
Each of R ^a6 and R ^a7 independently represents 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 these.
m1 represents any integer of 0-14.
n1 represents any integer of 0 to 10.
n1 'represents any integer of 0 to 3. ]

R ^a01 , R ^a4 and R ^a5 are preferably methyl groups.
L ^a01 , L ^a1 and L ^a2 are preferably an oxygen atom or * -O- (CH ₂ ) _k01 -CO-O- (provided that k01 is preferably an integer of 1 to 4 and more preferably Is 1), more preferably an oxygen atom.
As the alkyl group in R ^a02 , R ^a03 , R ^a04 , R ^a6 and R ^a7 , an alicyclic hydrocarbon group and a group combining them, the same groups as the groups mentioned in R ^{a1 to} R ^a3 of formula (1) Groups are mentioned.
The carbon number of the alkyl group in R ^a02 , R ^a03 and R ^a04 is preferably 1 to 6, more preferably a methyl group or an ethyl group, and still more preferably a methyl group.
The carbon number of the alkyl group in R ^a6 and R ^a7 is preferably 1 to 6, more preferably a methyl group, an ethyl group or an isopropyl group, and still more preferably an ethyl group or an isopropyl group.
The carbon number of the alicyclic hydrocarbon group of R ^a02 , R ^a03 , R ^a04 , R ^a6 and R ^a7 is preferably 5 to 12, more preferably 5 to 10.
In the group in which the alkyl group and the alicyclic hydrocarbon group are combined, it is preferable that the total carbon number of the combination of the alkyl group and the alicyclic hydrocarbon group is 18 or less.
R ^a02 and R ^a03 are preferably an alkyl group having 1 to 6 carbon atoms, and more preferably a methyl group or an ethyl group.
R ^a04 is preferably an alkyl group having 1 to 6 carbon atoms or an alicyclic hydrocarbon group having 5 to 12 carbon atoms, and more preferably a methyl group, an ethyl group, a cyclohexyl group or an adamantyl group.
^Each of R ^a6 and R ^a7 is preferably an alkyl group having 1 to 6 carbon atoms, more preferably a methyl group, an ethyl group or an isopropyl group, and still more preferably an ethyl group or an isopropyl group.
m1 is preferably an integer of 0 to 3, and 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, structural units represented by any one of formulas (a1-0-1) to (a1-0-12) and R ^a01 in structural unit (a1-0) can be used. The structural unit by which the corresponding methyl group replaced the hydrogen atom is mentioned, The structural unit represented by either Formula (a1-0-1)-Formula (a1-0-10) is preferable.

As a structural unit (a1-1), the structural unit derived from the monomer described in Unexamined-Japanese-Patent No. 2010-204646 is mentioned, for example. Above all, the methyl group corresponding to R ^a4 in the structural unit represented by any of the formulas (a1-1-1) to (a1-1-4) and the structural unit (a1-1) was replaced with a hydrogen atom The structural unit is preferable, and the structural unit represented by any one of Formula (a1-1-1) to Formula (a1-1-4) is more preferable.

The structural unit (a1-2) corresponds to the structural unit represented by any one of formulas (a1-2-1) to (a1-2-6) and R ^a5 in the structural unit (a1-2) The structural unit which the methyl group replaced with the hydrogen atom is mentioned, and a formula (a1-2-2), a formula (a1-2-5), and a formula (a1-2-6) are preferable.

  When the resin (A) contains the structural unit (a1-0) and / or the structural unit (a1-1) and / or the structural unit (a1-2), the total content of these is the total structure of the resin (A) The amount is usually 10 to 95 mol%, preferably 15 to 90 mol%, more preferably 20 to 85 mol%, still more preferably 25 to 70 mol%, and still more preferably, per unit. It is 30 to 70 mol%.

As a structural unit which has group (2) in structural unit (a1), the structural unit (Hereinafter, it may be called "a structural unit (a1-4).") Represented by Formula (a1-4) is mentioned. .
[In the formula (a1-4),
R ^a32 represents a hydrogen atom, a halogen atom, or an alkyl group having 1 to 6 carbon atoms which may have a halogen atom.
R ^a33 represents a halogen atom, a hydroxy group, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, an alkyl carbonyl group having 2 to 4 carbon atoms, an alkylcarbonyloxy group having 2 to 4 carbon atoms, acryloyl Represents an oxy group or a methacryloyloxy group.
la represents any integer of 0 to 4; When la is 2 or more, a plurality of R ^a33 may be the same as or different from each other.
R ^a34 and R ^a35 each independently represent a hydrogen atom or a hydrocarbon group having 1 to 12 carbon atoms, R ^a36 may represent a hydrocarbon group having 1 to 20 carbon atoms, R ^a35 and R ^a36 are bonded to each other And form a divalent hydrocarbon group having a carbon number of 2 to 20 together with -C-O- to which they are bound, and the hydrocarbon group and -CH _2- contained in the divalent hydrocarbon group are- It may be replaced by O- or -S-. ]

^Examples of the alkyl group in R ^a32 and R ^a33 include a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, a pentyl group and a hexyl group. The alkyl group is preferably an alkyl group having 1 to 4 carbon atoms, more preferably a methyl group or an ethyl group, and still more preferably a methyl group.
Examples of the halogen atom in R ^a32 and R ^a33 include a fluorine atom, a chlorine atom and a bromine atom.
Examples of the alkyl group having 1 to 6 carbon atoms which may have a halogen atom include trifluoromethyl group, difluoromethyl group, methyl group, perfluoroethyl group, 2,2,2-trifluoroethyl group, 1,1,3, 2,2-tetrafluoroethyl group, ethyl group, perfluoropropyl group, 2,2,3,3,3-pentafluoropropyl group, propyl group, perfluorobutyl group, 1,1,2,2,3,3,3 4,4-octafluorobutyl group, butyl group, perfluoropentyl group, 2,2,3,3,4,4,5,5,5-nonafluoropentyl group, pentyl group, hexyl group, perfluorohexyl group etc. It can be mentioned.
Examples of the alkoxy group include methoxy group, ethoxy group, propoxy group, butoxy group, pentyloxy group and hexyloxy group. Especially, a C1-C4 alkoxy group is preferable, a methoxy group or an ethoxy group is more preferable, and a methoxy group is further more preferable.
The alkylcarbonyl group includes an acetyl group, a propionyl group and a butyryl group.
As the alkylcarbonyloxy group, an acetyloxy group, a propionyloxy group, a butyryloxy group and the like can be mentioned.
As the hydrocarbon group for R ^a34, R ^a35 and R ^a36, an alkyl group, an alicyclic hydrocarbon group, aromatic hydrocarbon group, and include groups formed by combining these, alkyl groups and alicyclic hydrocarbon groups Examples of R ^a02 , R ^a03 , R ^a04 , R ^a6 and R ^a7 include the same groups as the alkyl group and the alicyclic hydrocarbon group.
Examples of the aromatic hydrocarbon group include aryl groups such as phenyl group, biphenylyl group and naphthyl group.
As the combined group, a group (for example, a cycloalkyl alkyl group) obtained by combining the above-mentioned alkyl group and an alicyclic hydrocarbon group, an aralkyl group such as a benzyl group, or an aromatic hydrocarbon group having an alkyl group (p-methyl) Phenyl group, p-tert-butylphenyl group, tolyl group, xylyl group, cumenyl group, mesityl group, 2,6-diethylphenyl group, 2-methyl-6-ethylphenyl group etc.), alicyclic hydrocarbon group Aromatic hydrocarbon groups (p-cyclohexylphenyl group, p-adamantylphenyl group etc.), aryl-cycloalkyl groups such as phenylcyclohexyl group etc. may be mentioned. In particular, as R ^a36 , an alkyl group having 1 to 18 carbon atoms, an alicyclic hydrocarbon group having 3 to 18 carbon atoms, an aromatic hydrocarbon group having 6 to 18 carbon atoms, or a group formed by combining these Can be mentioned.

In formula (a1-4), a hydrogen atom is preferable as R ^a32 .
As Ra ³³ , an alkoxy group having 1 to 4 carbon atoms is preferable, a methoxy group and an ethoxy group are more preferable, and a methoxy group is further preferable.
As la, 0 or 1 is preferable, and 0 is more preferable.
R ^a34 is preferably a hydrogen atom.
R ^a35 is preferably an alkyl group having 1 to 12 carbon atoms or an alicyclic hydrocarbon group, and more preferably a methyl group or an ethyl group.
The hydrocarbon group of R ^a36 is preferably an alkyl group having 1 to 18 carbon atoms, an alicyclic hydrocarbon group having 3 to 18 carbon atoms, an aromatic hydrocarbon group having 6 to 18 carbon atoms, or a combination thereof. And more preferably an alkyl group having 1 to 18 carbon atoms, an alicyclic aliphatic hydrocarbon group having 3 to 18 carbon atoms, or an aralkyl group having 7 to 18 carbon atoms. The alkyl group and alicyclic hydrocarbon group in R ^a36 are preferably unsubstituted. The aromatic hydrocarbon group in R ^a36 is preferably an aromatic ring having an aryloxy group having 6 to 10 carbon atoms.
^{-OC (R a34) (R a35} ) -O-R a36 in the structural unit (a1-4) is desorbed by contact with an acid (e.g. p- toluenesulfonic acid) to form a hydroxy group.

As a structural unit (a1-4), the structural unit derived from the monomer described in Unexamined-Japanese-Patent No. 2010-204646 is mentioned, for example. Preferably, hydrogen atom corresponding to R ^a32 in equation (a1-4-1) represented respectively to Formula (a1-4-12) structural units and structural units (a1-4) is replaced by a methyl group structure A unit is mentioned, More preferably, a structural unit represented by a formula (a 1-4-1)-a formula (a 1-4-5) and a formula (a 1-4-10) is mentioned, respectively.

  When resin (A) contains a structural unit (a1-4), it is preferable that the content rate is 10-95 mol% with respect to the sum total of all the structural units of resin (A), and 15-90. It is more preferable that it is mol%, It is further more preferable that it is 20-85 mol%, It is further more preferable that it is 20-70 mol%, It is especially preferable that it is 20-60 mol%.

As a structural unit derived from a (meth) acrylic monomer having a group (2), a structural unit represented by formula (a1-5) (hereinafter sometimes referred to as "structural unit (a1-5)") is also mentioned. Be
In formula (a1-5),
R ^a8 represents an alkyl group having 1 to 6 carbon atoms which may have a halogen atom, a hydrogen atom or a halogen atom.
Z ^a1 represents a single bond or _{* - (CH 2) h3 -CO} -L 54 - represents, h3 represents an integer of 1 to 4, * represents a bond to L ^51.
L ⁵¹ , L ⁵² , L ⁵³ and L ⁵⁴ each independently represent -O- or -S-.
s1 represents any integer of 1 to 3.
s1 'represents any integer of 0 to 3.

As a halogen atom, a fluorine atom and a chlorine atom are mentioned, and a fluorine atom is preferable.
Examples of the alkyl group having 1 to 6 carbon atoms which may have a halogen atom include methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, fluoromethyl and trifluoromethyl Groups are mentioned.
In formula (a1-5), R ^a8 is preferably a hydrogen atom, a methyl group or a trifluoromethyl group.
L ⁵¹ is preferably an oxygen atom.
It is preferable that one of L ⁵² and L ⁵³ be -O- and the other be -S-.
As s1, 1 is preferable.
s1 'is preferably an integer of 0 to 2.
Z ^a1 is preferably a single bond or * -CH ₂ -CO-O-.

As a structural unit (a1-5), the structural unit derived from the monomer described in Unexamined-Japanese-Patent No. 2010-61117 is mentioned, for example. Among them, structural units represented by Formula (a1-5-1) to Formula (a1-5-4) are preferable, and are represented by Formula (a1-5-1) or Formula (a1-5-2). Structural units are more preferred.

  When resin (A) contains a structural unit (a1-5), 1-50 mol% is preferable with respect to the total structural unit of resin (A), as for the content rate, 3-45 mol% is more preferable. 5 to 40 mol% is more preferable, and 5 to 30 mol% is even more preferable.

As a structural unit (a1), the structural unit (Hereinafter, it may be mentioned a structural unit (a1-0X).) Represented by a formula (a1-0X) is also mentioned.
[In the formula (a1-0X),
R ^x1 represents a hydrogen atom or a methyl group.
Each of R ^x2 and R ^x3 independently represents a saturated hydrocarbon group having 1 to 6 carbon atoms.
Ar ^x1 represents a C6-C36 aromatic hydrocarbon group. ]

The saturated hydrocarbon group of ^Rx2 and ^Rx3 includes an alkyl group, an alicyclic hydrocarbon group, and a group formed by combining these.
Examples of the alkyl group include methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, sec-butyl group, tert-butyl group, pentyl group and hexyl group.
The alicyclic hydrocarbon group may be monocyclic or polycyclic, and examples of the monocyclic alicyclic hydrocarbon group include a cyclopropyl group, a cyclobutyl group, a cyclopentyl group and a cyclohexyl group.
Examples of the aromatic hydrocarbon group of Ar ^x1 include aryl groups having 6 to 36 carbon atoms such as phenyl group, naphthyl group and anthryl group.
The aromatic hydrocarbon group preferably has 6 to 24 carbon atoms, more preferably 6 to 18 carbon atoms, and still more preferably a phenyl group.
Ar ^x1 is preferably an aromatic hydrocarbon group having 6 to 18 carbon atoms, more preferably a phenyl group or a naphthyl group, and still more preferably a phenyl group.
Each of R ^x1 , R ^x2 and R ^x3 is preferably independently a methyl group or an ethyl group, and more preferably a methyl group.

Examples of the structural unit (a1-0X) include structural units described below and compounds in which a methyl group corresponding to R ^x1 in the structural unit (a1-0X) is replaced with a hydrogen atom. The structural unit (a1-0X) is preferably a structural unit (a1-0X-1) to a structural unit (a1-0X-3).

When the resin (A) has a structural unit (a1-0X), the content is preferably 5 to 60 mol%, and more preferably 5 to 50 mol%, with respect to all monomers in the resin (A). And more preferably 10 to 40 mol%.
The resin (A) may contain two or more structural units (a1-0X).

Moreover, the following structural units are also mentioned as a structural unit (a1).
When resin (A) contains the said structural unit, 5-60 mol% is preferable with respect to the total structural unit of resin (A), as for the content rate, 5-50 mol% is more preferable, and 10-40 mol. % Is more preferred.

<Structural unit (s)>
As the monomer leading to the structural unit (s), monomers having no acid labile group known in the resist field can be used.
The structural unit (s) preferably has a hydroxy group or a lactone ring. Structural unit having a hydroxy group and having no acid labile group (hereinafter sometimes referred to as “structural unit (a2)”) and / or a structure having a lactone ring and having no acid labile group If a resin having a unit (hereinafter sometimes referred to as “structural unit (a3)”) is used 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 possessed by the structural unit (a2) may be either an alcoholic hydroxy group or a phenolic hydroxy group.
When a resist pattern is produced from the resist composition of the present invention, as a structural unit (a2) when using a high energy beam such as a KrF excimer laser (248 nm), an electron beam or EUV (super ultraviolet light) as an exposure light source It is preferable to use a structural unit (a2) having a phenolic hydroxy group. When using an ArF excimer laser (193 nm) or the like, a structural unit (a2) having an alcoholic hydroxy group is preferable as the structural unit (a2), and it is more preferable to use a structural unit (a2-1) described later preferable. As a structural unit (a2), 1 type may be included independently and 2 or more types may be included.

Examples of the structural unit having a phenolic hydroxy group in the structural unit (a2) include structural units represented by Formula (a2-A) (hereinafter sometimes referred to as “structural unit (a2-A)”).
[In the formula (a2-A),
R ^a50 represents a hydrogen atom, a halogen atom or an alkyl group having 1 to 6 carbon atoms which may have a halogen atom.
R ^a51 is a halogen atom, a hydroxy group, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, an alkyl carbonyl group having 2 to 4 carbon atoms, an alkylcarbonyloxy group having 2 to 4 carbon atoms, acryloyl Represents an oxy group or a methacryloyloxy group.
A ^a50 represents a single bond or ^{* -X a51 - (A a52 -X} a52) nb - represents, * represents a bond to the carbon atom to which -R ^a50 binds.
A ^a52 each independently represents a C 1 to ^C 6 alkanediyl group.
X ^a51 and X ^a52 each independently represent -O-, ^-CO -O- or -O-CO-.
nb represents 0 or 1.
mb represents any integer from 0 to 4; When mb is an integer of 2 or more, a plurality of R a ⁵¹ may be the same as or different from each other. ]

^Examples of the halogen atom in R ^a50 include a fluorine atom, a chlorine atom and a bromine atom.
^Examples of the alkyl group having 1 to 6 carbon atoms which may have a halogen atom in R ^a50 include trifluoromethyl group, difluoromethyl group, methyl group, perfluoroethyl group, 1,1,1-trifluoroethyl group, 1 1,2,2-tetrafluoroethyl group, ethyl group, perfluoropropyl group, 1,1,1,2,2-pentafluoropropyl group, propyl group, perfluorobutyl group, 1,1,2,2,3 , 3,4,4-octafluorobutyl group, butyl group, perfluoropentyl group, 1,1,1,2,2,3,3,4,4-nonafluoropentyl group, pentyl group, hexyl group and perfluorohexyl group Groups are mentioned.
R ^a50 is preferably a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, more preferably a hydrogen atom, a methyl group or an ethyl group, and still more preferably a hydrogen atom or a methyl group.
^Examples of the alkyl group in Ra ⁵¹ include 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 and a hexyl group.
^Examples of the alkoxy group in R ^a51 include a methoxy group, an ethoxy group, a propoxy group, an isopropoxy group, a butoxy group, a sec-butoxy group and a tert-butoxy group. A C1-C4 alkoxy group is preferable, a methoxy group or an ethoxy group is more preferable, and a methoxy group is further more preferable.
^Examples of the alkylcarbonyl group in R ^a51 include an acetyl group, a propionyl group and a butyryl group.
^Examples of the alkylcarbonyloxy group in R ^a51 include an acetyloxy group, a propionyloxy group and a butyryloxy group.
Ra ⁵¹ is preferably a methyl group.

^{* -Xa51-} ( ^{Aa52- Xa52} ) _nb -As ^* -O-, ^* -CO-O-, ^* -O-CO-, ^* -CO-O- ^{Aa 52} -CO-O-, ^* -O-CO-A ^a52 -O-, ^* -O-A ^a52 -CO-O-, ^* -CO-O-A ^a52 -O-CO-, ^* -O-CO-A ^a52 -O-CO -, Can be mentioned. Among them, ^* -CO-O-, ^* -CO-O- ^Aa52- CO-O- or ^* -O- ^Aa52- CO-O- is preferable.
As an alkanediyl group, a methylene group, ethylene group, propane-1,3-diyl group, propane-1,2-diyl group, butane-1,4-diyl group, 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-1,4-diyl group and 2 -Methylbutane-1,4-diyl group etc. are mentioned.
A ^a52 is preferably a methylene group or an ethylene group.
A ^a50 is preferably a single bond, ^* -CO-O- or ^* -CO-O-a ^a52- CO-O-, and a single bond, ^* -CO-O- or ^* -CO-O-CH. It is more preferable that it is _2- CO-O-, and it is further preferable that it is a single bond or ^* -CO-O-.
As mb, 0, 1 or 2 is preferable, 0 or 1 is more preferable, and 0 is particularly preferable.
The hydroxy group is preferably bonded to the o- or p-position of the benzene ring, and more preferably to the p-position.

As a structural unit (a2-A), the structural unit derived from the monomer described in Unexamined-Japanese-Patent No. 2010-204634 and 2012-12577 is mentioned.
As the structural unit (a2-A), structural units represented by formulas (a2-2-1) to (a2-2-6) and formulas (a2-2-1) to (a2-2-) The structural unit by which the methyl group corresponded to ^Ra50 in a structural unit (a2-A) in structural unit represented by 6) was ^substituted by the hydrogen atom is mentioned. The structural unit (a2-A) is a structural unit represented by the formula (a2-2-1), a structural unit represented by the formula (a2-2-3), or a structural unit represented by the formula (a2-2-6) A structural unit represented by formula (a2-2-1), a structural unit represented by formula (a2-2-3), or a structural unit represented by formula (a2-2-6) The structural unit (a2-A) is preferably a structural unit in which a methyl group corresponding to R ^a50 in the structural unit (a2-A) is replaced with a hydrogen atom.

The content of the structural unit (a2-A) in the resin (A) is preferably 5 to 80 mol%, more preferably 5 to 60 mol%, still more preferably 5 to 80 mol%, based on all structural units. It is -55 mol%, still more preferably 5 to 50 mol%.
The structural unit (a2-A) can be contained in the resin (A) by, for example, polymerization using the structural unit (a1-4) and treatment with an acid such as p-toluenesulfonic acid. In addition, the structural unit (a2-A) can be contained in the resin (A) by treating with an alkali such as tetramethyl ammonium hydroxide after polymerization using acetoxystyrene or the like.

Examples of the structural unit having an alcoholic hydroxy group in the structural unit (a2) include structural units represented by Formula (a2-1) (hereinafter sometimes referred to as “structural unit (a2-1)”).
In formula (a2-1),
L ^a3 represents -O- or ^* -O- (CH ₂ ) _k2 -CO-O-;
k2 represents any integer of 1 to 7; * Represents a bond with -CO-.
R ^a14 represents a hydrogen atom or a methyl group.
R ^a15 and R ^a16 each independently represent a hydrogen atom, a methyl group or a hydroxy group.
o1 represents any integer of 0 to 10;

In formula (a2-1), L ^a3 is preferably -O- or -O- (CH ₂ ) _f1 -CO-O- (f1 represents an integer of 1 to 4). And 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.

As a structural unit (a2-1), the structural unit derived from the monomer described in Unexamined-Japanese-Patent No. 2010-204646 is mentioned, for example. The structural unit represented by any one of Formula (a2-1-1) to Formula (a2-1-6) is preferable, and any of Formula (a2-1-1) to Formula (a2-1-4) The structural unit represented is more preferable, and the structural unit represented by Formula (a2-1-1) or Formula (a2-1-3) is more preferable.

  When the resin (A) contains a structural unit (a2-1), the content is usually 1 to 45 mol%, preferably 1 to 40 mol%, based on all structural units of the resin (A). More preferably, it is 1 to 35 mol%, more preferably 1 to 20 mol%, still more preferably 1 to 10 mol%.

Structural unit (a3)
The lactone ring possessed by the structural unit (a3) may be a monocyclic ring such as a β-propiolactone ring, a γ-butyrolactone ring, or a δ-valerolactone ring, and a fused ring of a monocyclic lactone ring and another ring May be. Preferably, a γ-butyrolactone ring, an adamantane lactone ring, or a bridged ring containing a γ-butyrolactone ring structure (for example, a structural unit represented by the following formula (a3-2)) can be mentioned.

The structural unit (a3) is preferably a structural unit represented by formula (a3-1), formula (a3-2), formula (a3-3) or formula (a3-4). One of these may be contained alone, or two or more may be contained.
[In the formula (a3-1), the formula (a3-2), the formula (a3-3) and the formula (a3-4),
L ^a4 , L ^a5 and L ^a6 are each independently represented by -O- or ^* -O- (CH ₂ ) _k3 -CO-O- (k3 represents an integer of 1 to 7). Represents a group.
^La7 is -O-, ^* -O- ^La8- O-, ^* -O- ^La8- CO-O-, ^* -O- ^La8- CO-O- ^La9- CO-O- or ^* -O- ^La8- O-CO- ^La9- O-.
Each of L ^a8 and L ^a9 independently represents an alkanediyl group having 1 to 6 carbon atoms.
* Represents a bond with a carbonyl group.
Each of R ^a18 , R ^a19 and R ^a20 independently represents a hydrogen atom or a methyl group.
R ^a24 represents an alkyl group having 1 to 6 carbon atoms which may have a halogen atom, a hydrogen atom or a halogen atom.
R ^a21 represents an aliphatic hydrocarbon group having 1 to 4 carbon atoms.
Each of R ^a22 , R ^a23 and R ^a25 independently represents a carboxy group, a cyano group or an aliphatic hydrocarbon group having 1 to 4 carbon atoms.
p1 represents any integer of 0 to 5;
q1 represents any integer of 0 to 3;
r1 represents any integer of 0 to 3;
w1 represents any integer of 0 to 8;
When p1, q1, r1 and / or w1 are 2 or more, the plurality of R ^a21 , R ^a22 , R ^a23 and / or R ^a25 may be the same as or different from each other. ]

As an aliphatic hydrocarbon group in R ^a21 , R ^a22 , R ^a23 and R ^a25 , alkyl groups such as methyl group, ethyl group, propyl group, isopropyl group, butyl group, sec-butyl group and tert-butyl group may be mentioned. Be
As a halogen atom in R ^a24 , a fluorine atom, a chlorine atom, a bromine atom and an iodine atom can be mentioned.
^Examples of the alkyl group for R ^a24 include 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 and a hexyl group. And the like, and more preferably a methyl group or an ethyl group.
Examples of the alkyl group having a halogen atom in R ^a24 include trifluoromethyl group, perfluoroethyl group, perfluoropropyl group, perfluoroisopropyl group, perfluorobutyl group, perfluorosec-butyl group, perfluorotert-butyl group, perfluoropentyl group, perfluoro Examples thereof include hexyl group, trichloromethyl group, tribromomethyl group and triiodomethyl group.
As an alkanediyl group in L ^a8 and L ^a9 , a methylene group, ethylene group, propane-1,3-diyl group, propane-1,2-diyl group, butane-1,4-diyl group, 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, 4-diyl group and 2-methyl butane-1,4-diyl group etc. are mentioned.

In formulas (a3-1) to (a3-3), each of L ^{a4 to} L ^a6 independently is preferably _{k3 in} —O— or * —O— (CH ₂ ) _k3 —CO—O—. group but is any integer of 1 to 4, more preferably -O- _{and, * - O-CH 2 -CO} -O-, more preferably an oxygen atom.
R ^{a18 to} R ^a21 are preferably methyl groups.
Each of R ^a22 and R ^a23 is preferably independently a carboxy group, a cyano group or a methyl group.
Each of p1, q1 and r1 is independently preferably an integer of 0 to 2, and more preferably 0 or 1.
In 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, and still more preferably a hydrogen atom or a methyl group It is.
Ra ²⁵ is preferably a carboxy group, a cyano group or a methyl group.
L ^a7 is preferably -O- or ^{* -O-L} a8 ^-CO-O-, more preferably an _{-O -, - O-CH 2} -CO-O- or _-O-C 2 _{H 4} - CO-O-.
w1 is preferably an integer of 0 to 2, more preferably 0 or 1.
In particular, the formula (a3-4) is preferably a formula (a3-4) ′.
(Wherein, R ^a24 and L ^a7 represent the same meaning as described above)

As the structural unit (a3), a structure described in JP-A-2010-204646, a monomer described in JP-A-2000-122294, and a structure derived from a monomer described in JP-A-2012-41274. Unit is mentioned. As the structural unit (a3), a formula (a3-1-1), a formula (a3-1-2), a formula (a3-2-1), a formula (a3-2-2) and a formula (a3-3-3) 1) The structural unit represented by any one of Formula (a3-3-2) and Formula (a3-4-1) to Formula (a3-4-12), and the structural unit represented by Formula (a3-1) A structural unit in which a methyl group corresponding to R ^a18 , R ^a19 , R ^a20 and R ^a24 in the formula (a3-4) is replaced with a hydrogen atom is preferable.

When the resin (A) contains the structural unit (a3), the total content is usually 5 to 70 mol%, preferably 5 to 65 mol%, relative to the total structural units of the resin (A). More preferably, it is 5 to 60 mol%.
Moreover, the content of the structural unit (a3-1), the structural unit (a3-2), the structural unit (a3-3) or the structural unit (a3-4) is relative to all structural units of the resin (A) 5 to 60 mol% is preferable, 5 to 50 mol% is more preferable, and 5 to 40 mol% is more preferable.

Structural unit (a4)
Examples of the structural unit (a4) include the following structural units.
[In the formula (a4),
R ⁴¹ represents a hydrogen atom or a methyl group.
R ⁴² represents a saturated hydrocarbon group having a fluorine atom of 1 to 24 carbon atoms, and —CH ₂ — contained in the saturated hydrocarbon group may be replaced by —O— or —CO. ]
Examples of the saturated hydrocarbon group represented by R ⁴² include a chain hydrocarbon group, a monocyclic or polycyclic alicyclic hydrocarbon group, and a group obtained by combining these.

As a chain hydrocarbon group, methyl group, ethyl group, propyl group, butyl group, pentyl group, hexyl group, heptyl group, octyl group, decyl group, dodecyl group, pentadecyl group, hexadecyl group, heptadecyl group and octadecyl group are mentioned. It can be mentioned. Examples of monocyclic or polycyclic alicyclic 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 Polycyclic alicyclic hydrocarbon groups such as (* represents a bond) are mentioned.
Examples of the combined group include a group in which one or more alkyl groups or one or more alkanediyl groups and one or more alicyclic hydrocarbon groups are combined, and-an alkanediyl group-an alicyclic hydrocarbon group, -Alicyclic hydrocarbon group-alkyl group,-alkanediyl group-alicyclic hydrocarbon group-alkyl group, etc. may be mentioned.

As the structural unit (a4), at least one selected from the group consisting of formula (a4-0), formula (a4-1), formula (a4-2), formula (a4-3) and formula (a4-4) The structural unit represented by 1 is mentioned.
[In the formula (a4-0),
R ⁵⁴ represents a hydrogen atom or a methyl group.
L ^4a represents a single bond or an alkanediyl group having 1 to 4 carbon atoms.
L ^3a represents a C 1 to C 8 perfluoroalkanediyl group or a C ³ to C 12 perfluorocycloalkanediyl group.
R ⁶ represents a hydrogen atom or a fluorine atom. ]

Examples of the alkanediyl group having 1 to 4 carbon atoms in L ^4a include linear alkanediyl groups such as methylene, ethylene, propane-1,3-diyl and butane-1,4-diyl, ethane-1 Branches such as 1,1-diyl, propane-1,2-diyl, butane-1,3-diyl, 2-methylpropane-1,3-diyl and 2-methylpropane-1,2-diyl Alkanediyl group is mentioned.

As a perfluoroalkanediyl group in L ^3a , a difluoromethylene group, a perfluoroethylene group, a perfluoropropane-1,1-diyl group, a perfluoropropane-1,3-diyl group, a perfluoropropane-1,2-diyl group, a perfluoropropane group -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, perfluoro ether Tan-2,2-diyl group, perfluoroheptane-3,4-diyl group, perfluoroheptane-4,4-diyl group, perfluorooctane-1,8-diyl group, perfluorooctane-2,2-diyl group, perfluorocarbon The octane-3, 3-diyl group, the perfluoro octane-4, 4-diyl group etc. are mentioned.
^Examples of the perfluorocycloalkanediyl group in L ^3a include a perfluorocyclohexanediyl group, a perfluorocyclopentanediyl group, a perfluorocycloheptanediyl group, a perfluoroadamantanediyl group and the like.
L ^4a is preferably a single bond, a methylene group or an ethylene group, more preferably a single bond or a methylene group.
L ^3a is preferably a C 1 to C 6 perfluoroalkanediyl group, more preferably a C 1 to C ³ perfluoroalkanediyl group.

The structural unit (a4-0), a methyl group corresponding to R ⁵ may be mentioned a structural unit replacing a hydrogen atom in the structural units in the structural units and the following structural units shown below (a4-0).

[In the formula (a4-1),
R ^a41 represents a hydrogen atom or a methyl group.
R ^a42 represents a saturated hydrocarbon group having 1 to 20 carbon atoms which may have a substituent, and -CH _2- contained in the saturated hydrocarbon group is replaced by -O- or -CO- May be
A ^a41 represents a alkanediyl group having 1 to 6 carbon atoms which may have a substituent or a group represented by the formula (a-g1). However, at least one of A ^a41 and R ^a42 has a halogen atom (preferably a fluorine atom) as a substituent.
[In the formula (a-g1),
s represents 0 or 1;
^Each of A ^a42 and A ^a44 independently represents a divalent aliphatic hydrocarbon group having 1 to 5 carbon atoms which may have a substituent.
A ^a43 represents a single bond or a divalent aliphatic hydrocarbon group of 1 to 5 carbon atoms which may have a substituent.
X ^a41 and X ^a42 each independently represent -O-, -CO-, ^-CO -O- or -O-CO-.
However, the total carbon number of A ^a42 , A ^a43 , A ^a44 , X ^a41 and X ^a42 is 7 or less. ]
* Is a bond, * on the right is a bond with -O-CO-Ra ⁴² . ]

^Examples of the saturated hydrocarbon group for R ^a42 include a chain hydrocarbon group, a monocyclic or polycyclic alicyclic hydrocarbon group, and a group formed by combining these.
As a chain hydrocarbon group, methyl group, ethyl group, propyl group, butyl group, pentyl group, hexyl group, heptyl group, octyl group, decyl group, dodecyl group, pentadecyl group, hexadecyl group, heptadecyl group and octadecyl group are mentioned. It can be mentioned. Examples of monocyclic or polycyclic alicyclic 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 Polycyclic alicyclic hydrocarbon groups such as (* represents a bond) are mentioned.
Examples of the group formed by the combination include a group formed by combining one or more alkyl groups or one or more alkanediyl groups and one or more alicyclic hydrocarbon groups, and -alkanediyl groups- Alicyclic hydrocarbon group, -alicyclic hydrocarbon group-alkyl group, -alkanediyl group-alicyclic hydrocarbon group-alkyl group, etc. may be mentioned.

^Examples of the substituent which may be possessed by R ^a42 include a halogen atom and a group represented by the formula (a-g3). The halogen atom includes a fluorine atom, a chlorine atom, a bromine atom and an iodine atom, preferably a fluorine atom.
[In the formula (a-g3),
X ^a43 represents * ^-O- , * ^-CO- , * ^-O -CO- or * -CO-O- (* represents a bond with R ^a42 ).
A ^a45 represents an aliphatic hydrocarbon group having 1 to 17 carbon atoms which may have a halogen atom.
* Represents a bond. ]
However, in R ^a42 -X ^a43 -A ^a45 , when R ^a42 does not have a halogen atom, A ^a45 represents a C ^1-17 aliphatic hydrocarbon group having at least one halogen atom.

^Examples of the aliphatic hydrocarbon group in A ^a45 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 decyl group, a dodecyl group, a pentadecyl group, a hexadecyl group, a heptadecyl group and Alkyl groups such as octadecyl group; monocyclic alicyclic hydrocarbon groups such as cyclopentyl group, cyclohexyl group, cycloheptyl group and cyclooctyl group; and decahydronaphthyl group, adamantyl group, norbornyl group and the following groups Polycyclic alicyclic hydrocarbon groups such as (* represents a bond) are mentioned.
R ^a42 is preferably a saturated hydrocarbon group which may have a halogen atom, more preferably an alkyl group having a halogen atom and / or a saturated hydrocarbon group having a group represented by the formula (a-g3).
When R ^a42 is a saturated hydrocarbon group having a halogen atom, it is preferably a saturated hydrocarbon group having a fluorine atom, more preferably a perfluoroalkyl group or a perfluorocycloalkyl group, and still more preferably having a carbon number of 1 to 4 It is a perfluoroalkyl group of 6, particularly preferably a perfluoroalkyl group having 1 to 3 carbon atoms. Examples of the perfluoroalkyl group include perfluoromethyl group, perfluoroethyl group, perfluoropropyl group, perfluorobutyl group, perfluoropentyl group, perfluorohexyl group, perfluoroheptyl group and perfluorooctyl group. As a perfluorocycloalkyl group, a perfluorocyclohexyl group etc. are mentioned.
When R ^a42 is a saturated hydrocarbon group having a group represented by formula (a-g3), the total carbon number of R ^a42 including the number of carbons contained in the group represented by formula (a-g3) The number is preferably 15 or less, more preferably 12 or less. When it has a group represented by formula (a-g3) as a substituent, the number is preferably one.

When R ^a42 is a saturated hydrocarbon having a group represented by formula (a-g3), R ^a42 is more preferably a group represented by formula (a-g2).
[In the formula (a-g2),
A ^a46 represents a C1- ^C17 divalent aliphatic hydrocarbon group which may have a halogen atom.
X ^a44 represents * ^-O -CO- or * -CO-O- (* represents a bond with A ^a46 ).
A ^a47 represents an aliphatic hydrocarbon group having 1 to 17 carbon atoms which may have a halogen atom.
However, the total carbon number of A ^a46 , A ^a47 and X ^a44 is 18 or less, and at least one of A ^a46 and A ^a47 has at least one halogen atom.
* Represents a bond with a carbonyl group. ]

1-6 are preferable and, as for carbon number of the aliphatic hydrocarbon group of ^Aa46 , 1-3 are more preferable.
The number of carbon atoms of the aliphatic hydrocarbon group A ^a47 is preferably 4 to 15, more preferably from 5 to 12, A ^a47 is more preferably cyclohexyl group or adamantyl group.
The preferred structure of the group represented by formula (a-g2) is the following structure (* is a bond to a carbonyl group).
As an alkanediyl group in A ^a41 , a methylene group, ethylene group, propane-1,3-diyl group, butane-1,4-diyl group, pentane-1,5-diyl group, hexane-1,6-diyl group Alkane-1, 2-diyl, butane-1, 3-diyl, 2-methylpropane-1, 2-diyl, 1-methylbutane-1, 4-diyl; Examples thereof include branched alkanediyl groups such as 2-methylbutane-1,4-diyl group.
As a substituent in the alkanediyl group which A ^a41 represents, a hydroxy group, a C1-C6 alkoxy group, etc. are mentioned.
A ^a41 is preferably an alkanediyl group having 1 to 4 carbon atoms, more preferably an alkanediyl group having 2 to 4 carbon atoms, and still more preferably an ethylene group.

^Examples of the divalent aliphatic hydrocarbon group represented by A ^a42 , A ^a43 and A ^{a44 in} the group represented by the formula (a-g1) include a linear or branched alkanediyl group and a monocyclic or polycyclic divalent And a divalent aliphatic hydrocarbon group formed by combining an alkanediyl group and a divalent alicyclic hydrocarbon group. Specifically, methylene group, ethylene group, propane-1,3-diyl group, propane-1,2-diyl group, butane-1,4-diyl group, 1-methylpropane-1,3-diyl group, Examples include 2-methylpropane-1,3-diyl group, 2-methylpropane-1,2-diyl group and the like.
As a substituent of the bivalent aliphatic hydrocarbon group which A ^a42 , A ^a43, and A ^a44 represent, a hydroxy group, a C1-C6 alkoxy group, etc. are mentioned.
s is preferably 0.

^{Examples of the} group in which X ^a42 is —O—, ^—CO— , ^—CO —O— or —O—CO— in the group represented by the formula (a-g1) include the following groups. In the following examples, * and ** each represent a bond, and ** is a bond with -O-CO-Ra ^a42 .

As the structural unit represented by the formula (a4-1), a methyl group corresponding to R ^a41 in the structural unit represented by the formula (a4-1) in the following structural units and the following structural units is a hydrogen atom The structural unit replaced is mentioned.

As a structural unit represented by Formula (a4-1), the structural unit represented by Formula (a4-2) is preferable.
[In the formula (a4-2),
R ^f5 represents a hydrogen atom or a methyl group.
L ⁴⁴ represents a C 1 to C 6 alkanediyl group, and —CH ₂ — contained in the alkanediyl group may be replaced by —O— or —CO—.
R ^f6 represents a saturated hydrocarbon group having a fluorine atom of 1 to 20 carbon atoms.
However, the upper limit of the total carbon number of L ⁴⁴ and R f ⁶ is 21. ]
Examples of the C ^1-4 alkanediyl group of L ⁴⁴ include the same groups as those exemplified for A ^a41 .
Examples of the saturated hydrocarbon group for R ^f6 include the same groups as those exemplified for R ^a42 .
The alkanediyl group having 1 to 6 carbon atoms in L ^44, preferably alkanediyl group having 2 to 4 carbon atoms, and more preferably an ethylene group.

As a structural unit represented by Formula (a4-2), the structural unit respectively represented by Formula (a4-1-1)-Formula (a4-1-11) is mentioned, for example. A structural unit in which a methyl group corresponding to R ^f5 in the structural unit (a4-2) is replaced with a hydrogen atom is also mentioned as a structural unit represented by the formula (a4-2).

[In the formula (a4-3),
R ^f7 represents a hydrogen atom or a methyl group.
And L ⁵ represents an alkanediyl group having 1 to 6 carbon atoms.
A ^f13 represents a divalent C 1 to C 18 saturated hydrocarbon group which may have a fluorine atom.
X ^f12 represents * -O-CO- or * -CO-O- (* represents a bond with A ^f13 ).
A ^f14 represents a C 1 to C 17 saturated hydrocarbon group which may have a fluorine atom.
However, at least one of A ^f13 and A ^f14 has a fluorine atom, and the upper limit of the total carbon number of L ⁵ , A ^f13 and A ^f14 is 20. ]

^Examples of the alkanediyl group for L ⁵ include the same groups as those exemplified for the alkanediyl group for A ^a41 .
As the divalent saturated hydrocarbon group which may have a fluorine atom in A ^{f13, a} divalent aliphatic saturated hydrocarbon group which may preferably have a fluorine atom and a fluorine atom are preferable. It is also a divalent alicyclic saturated hydrocarbon group, more preferably a perfluoroalkanediyl group.
Examples of the divalent aliphatic hydrocarbon group which may have a fluorine atom include alkanediyl groups such as methylene group, ethylene group, propanediyl group, butanediyl group and pentanediyl group; difluoromethylene group, perfluoroethylene group, perfluoro And perfluoroalkanediyl groups such as propanediyl group, perfluorobutanediyl group and perfluoropentanediyl group.
The divalent alicyclic hydrocarbon group which may have a fluorine atom may be either monocyclic or polycyclic. Examples of the monocyclic group include a cyclohexanediyl group and a perfluorocyclohexanediyl group. Examples of the polycyclic group include an adamantanediyl group, a norbornanediyl group, and a perfluoroadamantanediyl group.
Examples of the saturated hydrocarbon group of A ^{f14 and} the saturated hydrocarbon group which may have a fluorine atom include the same groups as those exemplified for R ^a42 . Among them, trifluoromethyl group, difluoromethyl group, methyl group, perfluoroethyl group, 2,2,2-trifluoroethyl group, 1,1,2,2-tetrafluoroethyl group, ethyl group, perfluoropropyl group, 2,2,3,3,3-pentafluoropropyl group, propyl group, perfluorobutyl group, 1,1,2,2,3,3,4,4-octafluorobutyl group, butyl group, perfluoropentyl group, Fluorination of 2,2,3,3,4,4,5,5,5-nonafluoropentyl group, pentyl group, hexyl group, perfluorohexyl group, heptyl group, perfluoroheptyl group, octyl group and perfluorooctyl group etc. Alkyl group, cyclopropylmethyl group, cyclopropyl group, cyclobutylmethyl group, cyclopentyl group, cyclohexyl group, Fluorocyclohexyl group, adamantyl group, adamantylmethyl group, adamantyl dimethyl group, norbornyl group, norbornylmethyl group, perfluoro adamantyl group, a perfluoroalkyl adamantylmethyl group and the like are preferable.

In formula (a4-3), L ⁵ is preferably an ethylene group.
The divalent saturated hydrocarbon group of A ^f13 is preferably a group containing a chain hydrocarbon group having 1 to 6 carbon atoms and an alicyclic hydrocarbon group having 3 to 12 carbon atoms, and the chain formula having 2 to 3 carbon atoms Hydrocarbon groups are more preferred.
The saturated hydrocarbon group of A ^f14 is preferably a group containing a chain hydrocarbon group having 3 to 12 carbon atoms and an alicyclic hydrocarbon group having 3 to 12 carbon atoms, and a chain hydrocarbon group having 3 to 10 carbon atoms And the group containing a C3-C10 alicyclic hydrocarbon group is further more preferable. Among them, A ^f14 is preferably a group containing an alicyclic hydrocarbon group having 3 to 12 carbon atoms, more preferably a cyclopropylmethyl group, a cyclopentyl group, a cyclohexyl group, a norbornyl group and an adamantyl group.

As a structural unit represented by Formula (a4-3), the structural unit respectively represented by Formula (a4-1-1)-Formula (a4-1-11) is mentioned, for example. A structural unit in which a methyl group corresponding to R ^f7 in the structural unit (a4-3) is replaced with a hydrogen atom is also mentioned as a structural unit represented by the formula (a4-3).

As a structural unit (a4), the structural unit represented by Formula (a4-4) is also mentioned.
[In the formula (a4-4),
R ^f21 represents a hydrogen atom or a methyl group.
A ^f21 _{is, - (CH 2) j1 -} , - (CH 2) j2 -O- (CH 2) j3 - or _{- (CH 2) j4 -CO-} O- (CH 2) j5 - represents a.
Each of j1 to j5 independently represents an integer of 1 to 6.
R ^f22 represents a C1-C10 saturated hydrocarbon group having a fluorine atom. ]

Saturated hydrocarbon groups R ^f22 include the same as the saturated hydrocarbon group represented by R ^a42. R ^{f 22} is preferably a ^C 1-10 alkyl group having a fluorine atom or a C 1-10 alicyclic hydrocarbon group having a fluorine atom, and the C 1-10 alkyl group having a fluorine atom is more preferable Preferably, a C1-C6 alkyl group having a fluorine atom is more preferable.

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

As the structural unit represented by the formula (a4-4), for example, in the structural units represented by the following structural units and the following formula, a methyl group corresponding to R ^f21 in the structural unit (a4-4) is hydrogen Structural units in which atoms are replaced can be mentioned.

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

Structural unit (a5)
As a non-elimination hydrocarbon group which a structural unit (a5) has, the group which has a linear, branched or cyclic hydrocarbon group is mentioned. Among them, the structural unit (a5) is preferably a group having an alicyclic hydrocarbon group.
As a structural unit (a5), the structural unit represented by Formula (a5-1) is mentioned, for example.
[In the formula (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 a hydrogen atom contained in the alicyclic hydrocarbon group may be substituted with 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 may be replaced by -O- or -CO- . ]

The alicyclic hydrocarbon group for R ⁵² may be monocyclic or polycyclic. As a monocyclic alicyclic hydrocarbon group, a cyclopropyl group, cyclobutyl group, a cyclopentyl group, and a cyclohexyl group are mentioned, for example. 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 methyl group, ethyl group, propyl group, isopropyl group, butyl group, sec-butyl group, tert-butyl group, pentyl group, hexyl group, octyl group and 2 And-an alkyl group such as ethylhexyl group.
As an alicyclic hydrocarbon group which has a substituent, 3-methyl adamantyl group etc. are mentioned.
R ⁵² is preferably a non-substituted alicyclic hydrocarbon group having 3 to 18 carbon atoms, more preferably an adamantyl group, a norbornyl group or a cyclohexyl group.
Examples of the divalent saturated hydrocarbon group for L ⁵⁵ include a divalent chain saturated hydrocarbon group and a divalent alicyclic saturated hydrocarbon group, preferably a divalent chain saturated hydrocarbon group .
Examples of the divalent chain saturated hydrocarbon group include alkanediyl groups such as methylene group, ethylene group, propanediyl group, butanediyl group and pentanediyl group.
The divalent alicyclic saturated hydrocarbon group may be either monocyclic or polycyclic. As a monocyclic alicyclic saturated hydrocarbon group, cycloalkane diyl groups, such as a cyclopentane diyl group and a cyclohexane diyl group, are mentioned. Examples of the polycyclic divalent alicyclic saturated hydrocarbon group include an adamantanediyl group and a norbornanediyl group.

Examples of the group in which —CH ₂ — contained in the divalent saturated hydrocarbon group represented by L ⁵⁵ is replaced by —O— or —CO— include, for example, formulas (L1-1) to (L1-4) The group represented is mentioned. In the following formula, * represents a bond with an oxygen atom.
In formula (L1-1),
X ^x1 represents * -O-CO- or * -CO-O- (* represents a bond with L ^x1 ).
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 carbon number of L ^x1 and L ^x2 is 16 or less.
In formula (L1-2),
L ^{x 3} represents a divalent aliphatic saturated hydrocarbon group having 1 to 17 carbon atoms.
L ^{x 4} represents a single bond or a divalent aliphatic saturated hydrocarbon group having 1 to 16 carbon atoms.
However, the total carbon number of L ^x3 and L ^x4 is 17 or less.
In formula (L1-3),
L ^{x 5} represents a C1-C15 divalent aliphatic saturated hydrocarbon group.
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 carbon number of L ^x5 , L ^x6 and L ^x7 is 15 or less.
In the formula (L1-4),
L ^{x 8} and L ^{x 9 each} represent a single bond or a divalent aliphatic saturated hydrocarbon group having 1 to 12 carbon atoms.
W ^x1 represents a divalent alicyclic saturated hydrocarbon group having 3 to 15 carbon atoms.
However, the total carbon number of L ^x8 , L ^x9 and W ^x1 is 15 or less.
L ^x1 is preferably a C 1 to C 8 divalent aliphatic saturated hydrocarbon group, 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, more preferably a single bond.
L ^{x 3} is preferably a divalent aliphatic saturated hydrocarbon group having 1 to 8 carbon atoms.
L ^{x 4} is preferably a single bond or a divalent aliphatic saturated hydrocarbon group having 1 to 8 carbon atoms.
L ^{x 5} is preferably a C 1 to C 8 divalent aliphatic saturated hydrocarbon group, more preferably a methylene group or an ethylene group.
L ^{x 6} is preferably a single bond or a divalent aliphatic saturated hydrocarbon group having 1 to 8 carbon atoms, more preferably a methylene group or an ethylene group.
L ^{x 7} is preferably a single bond or a divalent aliphatic saturated hydrocarbon group having 1 to 8 carbon atoms.
L ^{x 8} is preferably a single bond or a divalent aliphatic saturated hydrocarbon group having 1 to 8 carbon atoms, more preferably a single bond or a methylene group.
L ^{x 9} is preferably a single bond or a divalent aliphatic saturated hydrocarbon group having 1 to 8 carbon atoms, more preferably a single bond or a methylene group.
W ^x1 is preferably a divalent alicyclic saturated hydrocarbon group having 3 to 10 carbon atoms, more preferably a cyclohexanediyl group or an adamantanediyl group.

As a group represented by Formula (L1-1), the bivalent group shown below is mentioned, for example.

As a group represented by Formula (L1-2), the bivalent group shown below is mentioned, for example.

As a group represented by Formula (L1-3), the bivalent group shown below is mentioned, for example.

As a group represented by Formula (L1-4), the bivalent group shown below is mentioned, for example.
L ⁵⁵ is preferably a single bond or a group represented by formula (L1-1).

The structural unit (a5-1), a methyl group corresponding to R ⁵¹ may be mentioned a structural unit replacing a hydrogen atom in the structural units in the structural units and the following structural units shown below (a5-1).
When resin (A) has a structural unit (a5), 1-30 mol% is preferable with respect to the total structural unit of resin (A), and, as for the content rate, 2-20 mol% is more preferable, and 3 -15 mol% is more preferable.

<Structural unit (II)>
The resin (A) may further contain a structural unit (hereinafter, sometimes referred to as “structural unit (II)”) that is decomposed by exposure to generate an acid. As the structural unit (II), specific Structural units described in JP-A-2016-79235, structural units having a sulfonate group or carboxylate group and an organic cation in the side chain or structural units having a sulfonio group and an organic anion in the side chain. Is preferred.

The structural unit having a sulfonate group or a carboxylate group and an organic cation in the side chain is preferably a structural unit represented by the formula (II-2-A ′).
[In the formula (II-2-A '),
X ^III3 represents a divalent saturated hydrocarbon group having 1 to 18 carbon atoms, and -CH _2- contained in the saturated hydrocarbon group may be substituted by -O-, -S- or -CO- Preferably, the hydrogen atom contained in the saturated hydrocarbon group may be replaced by a halogen atom, an alkyl group having 1 to 6 carbon atoms which may have a halogen atom, or a hydroxy group.
A ^x1 represents an alkanediyl group having 1 to 8 carbon atoms, and a hydrogen atom contained in the alkanediyl group may be substituted by a fluorine atom or a perfluoroalkyl group having 1 to 6 carbon atoms.
RA ^- represents a sulfonate group or a carboxylate group.
R ^III3 represents a hydrogen atom, a halogen atom or an alkyl group having 1 to 6 carbon atoms which may have a halogen atom.
ZA ⁺ represents an organic cation. ]

Examples of the halogen atom represented by R ^III3 include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom.
As the alkyl group having 1 to 6 carbon atoms which may have a halogen atom represented by R ^III3, the alkyl group having 1 to 6 carbon atoms which may have a halogen atom represented by R ^a8 The same thing is mentioned.
Examples of the alkanediyl group having 1 to 8 carbon atoms represented by A ^x1 include a methylene group, an ethylene group, a propane-1,3-diyl group, a butane-1,4-diyl group, and a pentane-1,5-diyl group. Hexane-1,6-diyl, ethane-1,1-diyl, propane-1,1-diyl, propane-1,2-diyl, propane-2,2-diyl, pentane-2, 4-diyl group, 2-methylpropane-1,3-diyl group, 2-methylpropane-1,2-diyl group, pentane-1,4-diyl group, 2-methylbutane-1,4-diyl group, etc. It can be mentioned.
As a C1-C6 perfluoroalkyl group which may be substituted by A ^x1 , a trifluoromethyl group, a perfluoroethyl group, a perfluoropropyl group, a perfluoroisopropyl group, a perfluorobutyl group, a perfluoro sec-butyl group, a perfluorotert group -Butyl, perfluoropentyl, perfluorohexyl and the like.
As a C1-C18 bivalent saturated hydrocarbon group represented by X ^III3 , a linear or branched alkanediyl group and a monocyclic or polycyclic bivalent alicyclic saturated hydrocarbon group are mentioned. Or a combination of these.
Specifically, methylene group, ethylene group, propane-1,3-diyl group, propane-1,2-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, nonane-1,9-diyl group, decane-1,10-diyl group, undecane-1,11-diyl group , Linear alkanediyl groups such as dodecane-1,12-diyl group; butane-1,3-diyl group, 2-methylpropane-1,3-diyl group, 2-methylpropane-1,2-diyl group And branched alkanediyl groups such as pentane-1,4-diyl group and 2-methylbutane-1,4-diyl group; cyclobutane-1,3-diyl group, cyclopentane-1,3-diyl group, cyclohexane-1 , 4-diyl group, Cycloalkanediyl groups such as rooctane-1,5-diyl group; norbornane-1,4-diyl group, norbornane-2,5-diyl group, adamantane-1,5-diyl group, adamantane-2,6-diyl group And bivalent polycyclic alicyclic saturated hydrocarbon groups and the like.
As -CH _2- contained in a saturated hydrocarbon group is replaced by -O-, -S- or -CO-, for example, divalent groups represented by formula (X1) to formula (X53) It can be mentioned. However, -CH ₂ contained in a saturated hydrocarbon group - is, -O -, - number of carbon atoms before replacing with S- or -CO- is respectively 17 or less. In the following formula, * represents a bond with A ^x1 .

X ³ represents a divalent C 1-16 saturated hydrocarbon group.
X ⁴ represents a divalent C 1-15 saturated hydrocarbon group.
X ⁵ represents a divalent C 1-13 saturated hydrocarbon group.
X ⁶ represents a divalent C 1-14 saturated hydrocarbon group.
X ⁷ represents a trivalent, 1 to 14 carbon saturated hydrocarbon group.
X ⁸ represents a divalent C 1-13 saturated hydrocarbon group.

Examples of the organic cation represented by ZA ⁺ include organic onium cation, organic sulfonium cation, organic iodonium cation, organic ammonium cation, benzothiazolium cation and organic phosphonium cation. Among these, organic sulfonium cations and organic iodonium cations are preferable, and arylsulfonium cations are more preferable. Specifically, the cation represented by any one of formulas (b2-1) to (b2-4) (hereinafter, sometimes referred to as "cation (b2-1)" or the like depending on the formula number) is It can be mentioned.

In formulas (b2-1) to (b2-4),
R ^{b4 to} R ^b6 each 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 The hydrogen atom contained in the alicyclic hydrocarbon group may be a halogen atom, an aliphatic hydrocarbon group having 1 to 18 carbon atoms, an alkyl carbonyl group having 2 to 4 carbon atoms, or a glycidyloxy group. It may be substituted, and a hydrogen atom contained in the aromatic hydrocarbon group may be substituted by a halogen atom, a hydroxy group or an alkoxy group having 1 to 12 carbon atoms.
R ^b4 and R ^b5 may combine with each other to form a ring together with the sulfur atom to which they are attached, and the —CH ₂ — contained in the ring is —O—, —S— or It may replace -CO-.
R ^b7 and R ^b8 each 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 ^b7 may be the same or different, and when n2 is 2 or more, the plurality of R ^b8 may be the same or different.
R ^b9 and R ^b10 each independently represent a C1-C36 chain hydrocarbon group or a C3-C36 alicyclic hydrocarbon group.
R ^b9 and R ^b10 may be combined with each other to form a ring together with the sulfur atom to which they are attached, and -CH _2- contained in the ring is -O-, -S- or It may replace -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 The hydrogen atom to be substituted may be substituted by an aromatic hydrocarbon group having 6 to 18 carbon atoms, and the hydrogen atom contained in the aromatic hydrocarbon group is an alkoxy group having 1 to 12 carbon atoms or 1 to 1 carbon atom. It may be substituted with 12 alkylcarbonyloxy groups.
R ^b11 and R ^b12 may combine with each other to form a ring including -CH-CO- to which they are bonded, and -CH _2- contained in the ring is -O-, -S -Or -CO- may be substituted.
Each of R ^{b13 to} R ^b18 independently represents 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 any integer of 0 to 5;
Each of q2 and r2 independently represents an integer of 0 to 4.
u2 represents 0 or 1;
When o2 is 2 or more, the plurality of R ^b13 are the same or different, and when p2 is 2 or more, the plurality of R ^b14 is the same or different, and when q2 is 2 or more, the plurality of R ^b15 is the same or different , When r2 is 2 or more, the plurality of R ^b16 are the same or different, and when s2 is 2 or more, the plurality of R ^b17 is the same or different, and when t2 is 2 or more, the plurality of R ^b18 is the same or phase It is different.
The aliphatic hydrocarbon group represents a chain hydrocarbon group and an alicyclic hydrocarbon group.
As a chain hydrocarbon group, an alkyl group of methyl group, ethyl group, propyl group, isopropyl group, butyl group, sec-butyl group, tert-butyl group, pentyl group, hexyl group, octyl group and 2-ethylhexyl group is preferable. It can be mentioned.
In particular, the chain hydrocarbon group of R ^{b9 to} R ^b12 preferably has 1 to 12 carbon atoms.
The alicyclic hydrocarbon group may be either monocyclic or polycyclic, and as the monocyclic alicyclic hydrocarbon group, a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, a cyclocyclo group And cycloalkyl groups such as heptyl group, cyclooctyl group and cyclodecyl group. As a polycyclic alicyclic hydrocarbon group, a decahydronaphthyl group, an adamantyl group, a norbornyl group, the following groups, etc. are mentioned.
In particular, the alicyclic hydrocarbon group of R ^{b9 to} R ^b12 preferably has 3 to 18 carbon atoms, and more preferably 4 to 12 carbon atoms.
As an alicyclic hydrocarbon group in which a hydrogen atom is substituted with an aliphatic hydrocarbon group, a methylcyclohexyl group, a dimethylcyclohexyl group, a 2-methyladamantan-2-yl group, a 2-ethyladamantan-2-yl group And 2-isopropyladamantan-2-yl group, methyl norbornyl group, isobornyl group and the like. In an alicyclic hydrocarbon group in which a hydrogen atom is substituted with an aliphatic hydrocarbon group, the total carbon number of the alicyclic hydrocarbon group and the aliphatic hydrocarbon group is preferably 20 or less.
Examples of the aromatic hydrocarbon group include aryl groups such as phenyl group, biphenylyl group, naphthyl group and phenanthryl group.
The aromatic hydrocarbon group may have a chain hydrocarbon group or an alicyclic hydrocarbon group, and is an aromatic hydrocarbon group having a chain hydrocarbon group having 1 to 18 carbon atoms (tolyl group , Xylyl group, cumenyl group, mesityl group, p-ethylphenyl group, p-tert-butylphenyl group, 2,6-diethylphenyl group, 2-methyl-6-ethylphenyl group, etc.), and having 3 to 18 carbon atoms And aromatic hydrocarbon groups having an alicyclic hydrocarbon group (p-cyclohexylphenyl group, p-adamantylphenyl group, etc.) and the like.
As an aromatic hydrocarbon group by which the hydrogen atom was substituted by the alkoxy group, p-methoxyphenyl group etc. are mentioned.
Examples of the chain hydrocarbon group in which a hydrogen atom is substituted with an aromatic hydrocarbon group include aralkyl groups such as benzyl group, phenethyl group, phenylpropyl group, trityl group, naphthylmethyl group and naphthylethyl group.
Examples of the alkoxy group include methoxy group, ethoxy group, propoxy group, butoxy group, pentyloxy group, hexyloxy group, heptyloxy group, octyloxy group, decyloxy group and dodecyloxy group.
Examples of the alkylcarbonyl group include acetyl group, propionyl group and butyryl group.
As a halogen atom, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, etc. are mentioned.
As an alkyl carbonyloxy group, a methyl carbonyloxy group, an ethyl carbonyloxy group, a propyl carbonyloxy group, an isopropyl carbonyloxy group, a butyl carbonyloxy group, a sec-butyl carbonyloxy group, a tert-butyl carbonyloxy group, a pentyl carbonyloxy group And hexyl carbonyloxy group, octyl carbonyloxy group and 2-ethylhexyl carbonyloxy group.
The ring formed by combining R ^b4 and R ^b5 together with the sulfur atom to which they are bonded to each other is either monocyclic, polycyclic, aromatic, nonaromatic, saturated or unsaturated It may be a ring of The ring includes a ring having 3 to 18 carbon atoms, preferably a ring having 4 to 18 carbon atoms. The ring containing a sulfur atom includes a 3- to 12-membered ring, preferably a 3- to 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. The ring includes a 3- to 12-membered ring, preferably a 3- to 7-membered ring. For example, a thiolane-1-ium ring (tetrahydrothiophenium ring), a thian-1-ium ring, a 1,4-oxathiane-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. The ring includes a 3- to 12-membered ring, preferably a 3- to 7-membered ring. Examples include oxocycloheptane ring, oxocyclohexane ring, oxonorbornane ring, oxoadamantane ring and the like.

Among the cations (b2-1) to (b2-4), preferred is the cation (b2-1).
The following cations may be mentioned as the cation (b2-1).

The following cations may be mentioned as the cation (b2-2).

The following cations may be mentioned as the cation (b2-3).

The following cations may be mentioned as the cation (b2-4).

The structural unit represented by the formula (II-2-A ′) is preferably a structural unit represented by the formula (II-2-A).
[In the formula (II-2-A), R ^III3 , X ^III3 and ZA ⁺ represent the same meaning as described above.
z represents any integer of 0 to 6;
Each of R ^III2 and R ^III4 independently represents a hydrogen atom, a fluorine atom or a perfluoroalkyl group having 1 to 6 carbon atoms, and when z is 2 or more, plural R ^III2 and R ^III4 are identical to each other It may also be different.
Each of Q ^a and Q ^b independently represents a fluorine atom or a C 1 to C 6 perfluoroalkyl group. ]

^Examples of the perfluoroalkyl group having 1 to 6 carbon atoms represented by R ^III2 , R ^III4 , Q ^a and Q ^b include the same as the perfluoroalkyl group having 1 to 6 carbon atoms which is a substituent of the aforementioned A ^x 1 Be

The structural unit represented by the formula (II-2-A) is preferably a structural unit represented by the formula (II-2-A-1).
[In the formula (II-2-A-1),
R ^III2 , R ^III3 , R ^III4 , Q ^a , Q ^b , z and ZA ⁺ have the same meaning as described above.
R ^III5 represents a saturated hydrocarbon group having 1 to 12 carbon atoms.
X ^I2 represents a divalent saturated hydrocarbon group having 1 to 11 carbon atoms, and -CH _2- contained in the saturated hydrocarbon group may be replaced by -O-, -S- or -CO- Preferably, the hydrogen atom contained in the saturated hydrocarbon group may be substituted by a halogen atom or a hydroxy group. ]

As a C1- ^C12 saturated hydrocarbon group represented by R ^III5 , 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, Examples thereof include linear or branched alkyl groups such as heptyl group, octyl group, nonyl group, decyl group, undecyl group and dodecyl group.
As a bivalent saturated hydrocarbon group represented by X ^I2 , the thing similar to the bivalent saturated hydrocarbon group represented by X ^III3 is mentioned.

As a structural unit represented by Formula (II-2-A), the structural unit represented by Formula (II-2-A-2) is further more preferable.
[In the formula (II-2-A-2), R ^III3 , R ^III5 and ZA ⁺ represent the same meaning as described above.
m and n each independently represent 1 or 2; ]

Examples of the structural unit represented by the formula (II-2-A ′) include the following structural units and the structural units described in WO 2012/050015. ZA ⁺ represents an organic cation.

The structural unit having a sulfonio group and an organic anion in the side chain is preferably a structural unit represented by Formula (II-1-1).
[In the formula (II-1-1),
A ^II1 represents a single bond or a divalent linking group.
R ^II1 represents a divalent aromatic hydrocarbon group having 6 to 18 carbon atoms.
R ^II2 and R ^II3 each independently represent a hydrocarbon group having 1 to 18 carbon atoms, and R ^II2 and R ^II3 may be bonded to each other to form a ring with the sulfur atom to which they are bonded.
R ^II4 represents a hydrogen atom, a halogen atom, or an alkyl group having 1 to 6 carbon atoms which may have a halogen atom.
A ^- represents an organic anion. ]
A phenylene group, a naphthylene group, etc. are mentioned as a C6-C18 bivalent aromatic hydrocarbon group represented by R ^II1 .
Examples of the hydrocarbon group represented by R ^II2 and R ^II3 include an alkyl group, an alicyclic hydrocarbon group, an aromatic hydrocarbon group, and a group formed by combining these.
Examples of the halogen atom represented by R ^II4 include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom.
As the alkyl group having 1 to 6 carbon atoms which may have a halogen atom represented by R ^II4 is an alkyl group having 1 to 6 carbon atoms which may have a halogen atom represented by R ^a8 The same thing is mentioned.
Examples of the divalent linking group represented by A ^II1 include a divalent saturated hydrocarbon group having 1 to 18 carbon atoms, and —CH ₂ — contained in the divalent saturated hydrocarbon group is It may be replaced by -O-, -S- or -CO-. Specifically, the same thing as the C1-C18 bivalent saturated hydrocarbon group represented by X ^III3 is mentioned.

As a structural unit containing the cation in Formula (II-1-1), the structural unit etc. which are represented below are mentioned.

A ^- The organic anion represented by a sulfonic acid anion, sulfonyl imide anion, methide anion and a carboxylate anion, and the like. A ^- organic anion represented by the sulfonate anion are preferable, and as a sulfonate anion, more preferably an anion contained in the salt represented by the formula (B1) to be described later.

As a sulfonyl imide anion represented by A < ^- >, the following are mentioned.

The following are mentioned as a sulfonyl methide anion.

Examples of the carboxylate anion include the following.

As a structural unit represented by Formula (II-1-1), the structural unit etc. which are represented below are mentioned.
The content of the structural unit (II) in the case of containing the structural unit (II) in the resin (A) is preferably 1 to 20 mol% with respect to the total structural units of the resin (A). Preferably it is 2-15 mol%, More preferably, it is 3-10 mol%.

  The resin (A) may have a structural unit other than the structural units described above, and such structural units include structural units known in the art.

  The resin (A) is preferably a resin comprising the structural unit (I) and the structural unit (a1) or a resin comprising the structural unit (I), the structural unit (a1) and the structural unit (s), and more preferably Is a resin comprising the structural unit (I), the structural unit (a1) and the structural unit (s).

The structural unit (a1) is preferably a structural unit (a1-0), a structural unit (a1-0X), a structural unit (a1-1) and a structural unit (a1-2) (preferably a cyclohexyl group, and a cyclopentyl group At least one selected from the group consisting of the structural units), more preferably structural units (a1-0), structural units (a1-0X), structural units (a1-1) and structural units (a1-2) It is at least two selected from the group consisting of (the structural unit having preferably a cyclohexyl group or a cyclopentyl group).
The structural unit (s) is preferably at least one selected from the group consisting of the structural unit (a2) and the structural unit (a3). The structural unit (a2) is preferably a structural unit (a2-A) or a structural unit (a2-1). The structural unit (a3) is preferably a structural unit represented by formula (a3-1), a structural unit represented by formula (a3-2) and a group consisting of structural units represented by formula (a3-4) Or at least one selected from

Each structural unit constituting the resin (A) may be used alone or in combination of two or more, and is produced by a known polymerization method (for example, radical polymerization method) using a monomer leading to these structural units. be able to. The content rate of each structural unit which resin (A) has can be adjusted with the usage-amount of the monomer used for superposition | polymerization.
The weight average molecular weight of the resin (A) is preferably 2,000 or more (more preferably 2,500 or more, more preferably 3,000 or more), 50,000 or less (more preferably 30,000 or less, more preferably) 15,000 or less).
In the present specification, the weight average molecular weight is a value determined by gel permeation chromatography. Gel permeation chromatography can be measured by the analysis conditions described in the examples.

<Resins other than Resin (A)>
The resist composition of the present invention may contain a resin other than the resin (A). Resin other than resin (A) is resin which does not contain structural unit (I), As such resin, it has structural unit which has an acid labile group, and structural unit (I) Resin not contained (hereinafter sometimes referred to as “resin (A2)”), resin consisting only of structural unit (a4), and resin consisting of structural unit (a4) and structural unit (a5) (hereinafter structural unit (a4) And resins (X4), etc., and the like.
In the resin (X), the content of the structural unit (a4) is preferably 30 mol% or more, more preferably 40 mol% or more based on the total of all structural units of the resin (X). And 45 mol% or more. Structural units other than this can be suitably adjusted in the same manner as the range included in the resin (A) or in accordance with these ranges.
Moreover, the range of each structural unit contained in resin (A2) can also be suitably adjusted similarly to the range contained in resin (A), or according to these ranges.
Each structural unit constituting the resin (X) may be used alone or in combination of two or more, and it is produced by a known polymerization method (for example, radical polymerization method) using a monomer which derives these structural units. can do. The content rate of each structural unit which resin (X) has can be adjusted with the usage-amount of the monomer used for superposition | polymerization.
The weight average molecular weights of the resin (A2) and the resin (X) are each independently preferably 6,000 or more (more preferably 7,000 or more) and 80,000 or less (more preferably 60,000 or less) is there. The measuring means of the weight average molecular weight of resin (A2) and resin (X) is the same as that of the case of resin (A).
When the resist composition of the present invention contains the resin (A2), the content thereof is usually 1 to 2500 parts by mass (more preferably 10 to 1000 parts by mass) with respect to 100 parts by mass of the resin (A). is there.
When the resist composition contains a resin (X), the content is preferably 1 to 60 parts by mass, more preferably 1 to 50 parts by mass with respect to 100 parts by mass of the resin (A). The amount is more preferably 1 to 40 parts by mass, particularly preferably 1 to 30 parts by mass, and particularly preferably 1 to 8 parts by mass.

  The content of the resin (A) in the resist composition is preferably 80% by mass or more and 99% by mass or less, and more preferably 90% by mass to 99% by mass, with respect to the solid content of the resist composition. Moreover, when resin other than resin (A) is included, the total content rate of resin (A) and resin other than resin (A) is 80 mass% or more and 99 mass% with respect to solid content of a resist composition. It is preferable that it is the following and 90-99 mass% is more preferable. The solid content of the resist composition and the resin content relative thereto can be measured by a known analytical means such as liquid chromatography or gas chromatography.

<Acid Generator (B)>
The acid generator (B) may be either nonionic or ionic. Nonionic acid generators include sulfonate esters (eg, 2-nitrobenzyl ester, aromatic sulfonate, oxime sulfonate, N-sulfonyloxyimide, sulfonyloxy ketone, diazonaphthoquinone 4-sulfonate), sulfones (eg, disulfone, Ketosulfone, sulfonyldiazomethane) and the like. As the ionic acid generator, onium salts containing onium cations (for example, diazonium salts, phosphonium salts, sulfonium salts, iodonium salts) are representative. Examples of the anion of the onium salt include a sulfonate anion, a sulfonylimide anion, and a sulfonyl methide anion.
Examples of the acid generator (B) include JP 63-26653, JP 55-164824, JP 62-69263, JP 63-146038, JP 63-163452, and the like. JP-A-62-153853, JP-A-63-146029, U.S. Pat. No. 3,779,778, U.S. Pat. No. 3,849,137, German Patent No. 3914407, European Patent No. 126,712, etc. It is possible to use a compound which generates an acid by the radiation described in 4. Moreover, you may use the compound manufactured by the well-known method. The acid generator (B) may be used in combination of two or more.

The acid generator (B) is preferably a fluorine-containing acid generator, and more preferably a salt represented by the formula (B1) (hereinafter sometimes referred to as "acid generator (B1)").
[In the formula (B1),
Each of Q ^b1 and Q ^b2 independently represents a fluorine atom or a C 1 to C 6 perfluoroalkyl group.
L ^b1 represents a divalent saturated hydrocarbon group having 1 to 24 carbon atoms, and —CH ₂ — contained in the divalent saturated hydrocarbon group 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 represents a methyl group which may have a substituent or an alicyclic hydrocarbon group having 3 to 18 carbon atoms which may have a substituent, and is included in the alicyclic hydrocarbon group; CH _2- may be replaced by -O-, -S (O) ₂ -or -CO-.
Z ⁺ represents an organic cation. ]

The perfluoroalkyl group represented by Q ^b1 and Q ^b2 includes trifluoromethyl group, perfluoroethyl group, perfluoropropyl group, perfluoroisopropyl group, perfluorobutyl group, perfluorosec-butyl group, perfluorotert-butyl group, perfluoropentyl group and Perfluorohexyl group etc. are mentioned.
Each of Q ^b1 and Q ^b2 is preferably independently a fluorine atom or a trifluoromethyl group, and both are more preferably a fluorine atom.
Examples of the divalent saturated hydrocarbon group in L ^b1 include a linear alkanediyl group, a branched alkanediyl group, a monocyclic or polycyclic divalent alicyclic saturated hydrocarbon group, and the like. It may be a group formed by combining two or more of the 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, nonane-1,9-diyl group, decane-1,10-diyl group, undecane-1,11-diyl group, dodecane-1,12-diyl group Linear, such as tridecane-1,13-diyl group, tetradecane-1,14-diyl group, pentadecane-1,15-diyl group, hexadecane-1,16-diyl group and heptadecane-1,17-diyl group An alkanediyl group;
Ethan-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;
A 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. Cycloaliphatic 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, adamantane-2,6-diyl group and the like And the like.

Examples of the group in which —CH ₂ — contained in the divalent saturated hydrocarbon group represented by L ^b1 is replaced by —O— or —CO— include, for example, a formula (b1-1) to a formula (b1-3) Groups represented by any of the following. In the groups represented by the formulas (b1-1) to (b1-3) and the groups represented by the formulas (b1-4) to (b1-11) which are specific examples thereof, * represents- Represents a bond with Y.

[In the formula (b1-1),
L ^b2 represents a single bond or a divalent saturated hydrocarbon group having 1 to 22 carbon atoms, and a hydrogen atom contained in the saturated hydrocarbon group may be substituted by a fluorine atom.
L ^b3 represents a single bond or a divalent saturated hydrocarbon group having 1 to 22 carbon atoms, and a hydrogen atom contained in the saturated hydrocarbon group may be substituted by a fluorine atom or a hydroxy group, and the saturated The —CH ₂ — contained in the hydrocarbon group may be replaced by —O— or —CO—.
However, the total carbon number of L ^b2 and L ^b3 is 22 or less.
In formula (b1-2),
L ^b4 represents a single bond or a divalent saturated hydrocarbon group having 1 to 22 carbon atoms, and a hydrogen atom contained in the saturated hydrocarbon group may be substituted by a fluorine atom.
L ^b5 represents a single bond or a divalent saturated hydrocarbon group having 1 to 22 carbon atoms, and a hydrogen atom contained in the saturated hydrocarbon group may be substituted by a fluorine atom or a hydroxy group, and the saturated The —CH ₂ — contained in the hydrocarbon group may be replaced by —O— or —CO—.
However, the total carbon number of L ^b4 and L ^b5 is 22 or less.
In formula (b1-3),
L ^b6 represents a single bond or a divalent saturated hydrocarbon group having 1 to 23 carbon atoms, and a hydrogen atom contained in the saturated hydrocarbon group may be substituted by 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 a hydrogen atom contained in the saturated hydrocarbon group may be substituted by a fluorine atom or a hydroxy group, and the saturated The —CH ₂ — contained in the hydrocarbon group may be replaced by —O— or —CO—.
However, the total carbon number of L ^b6 and L ^b7 is 23 or less. ]
In the groups represented by Formula (b1-1) to Formula (b1-3), when -CH _2- contained in a saturated hydrocarbon group is replaced by -O- or -CO-, carbon before replacement is Let the number be the carbon number of the saturated hydrocarbon group.
As a bivalent saturated hydrocarbon group, the thing similar to the bivalent saturated hydrocarbon group of L ^b1 is mentioned.

L ^b2 is preferably a single bond.
L ^b3 is preferably a divalent C 1 to C 4 saturated hydrocarbon group.
L ^b4 is preferably a divalent saturated hydrocarbon group having 1 to 8 carbon atoms, and a hydrogen atom contained in the divalent saturated hydrocarbon group may be substituted by 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 by 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 by a fluorine atom or a hydroxy group, -CH ₂ contained in the divalent saturated hydrocarbon group - may be replaced by -O- or -CO-.
The group in which —CH ₂ — contained in the divalent saturated hydrocarbon group represented by L ^b1 is replaced by —O— or —CO— is a group represented by formula (b1-1) or formula (b1-3) Preferred groups.

As group represented by Formula (b1-1), group represented by Formula (b1-4)-Formula (b1-8) is mentioned, respectively.
[In the formula (b1-4),
L ^b8 represents a single bond or a divalent saturated hydrocarbon group having 1 to 22 carbon atoms, and a hydrogen atom contained in the saturated hydrocarbon group may be substituted by a fluorine atom or a hydroxy group.
In formula (b1-5),
L ^b9 represents a divalent C 1 to C 20 saturated hydrocarbon group.
L ^b10 represents a single bond or a divalent saturated hydrocarbon group having 1 to 19 carbon atoms, and a hydrogen atom contained in the divalent saturated hydrocarbon group may be substituted by a fluorine atom or a hydroxy group .
However, the total carbon number of L ^b9 and L ^b10 is 20 or less.
In formula (b1-6),
L ^b11 represents a bivalent 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 a hydrogen atom contained in the divalent saturated hydrocarbon group may be substituted by a fluorine atom or a hydroxy group .
However, the total carbon number of L ^b11 and L ^b12 is 21 or less.
In the formula (b1-7),
L ^b13 represents a divalent C 1-19 saturated hydrocarbon group.
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 a hydrogen atom contained in the divalent saturated hydrocarbon group may be substituted by a fluorine atom or a hydroxy group .
However, the total carbon number of L ^{b13 to} L ^b15 is 19 or less.
In formula (b1-8),
L ^b16 represents a divalent C 1 to C 18 saturated hydrocarbon group.
L ^b17 represents a divalent ^C 1 to ^C 18 saturated hydrocarbon group.
L ^b18 represents a single bond or a divalent saturated hydrocarbon group having 1 to 17 carbon atoms, and a hydrogen atom contained in the divalent saturated hydrocarbon group may be substituted by a fluorine atom or a hydroxy group .
However, the total carbon number 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 bivalent 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 C 1 to C 12 saturated hydrocarbon group.
L ^b17 is preferably a divalent C 1 to ^C 6 saturated hydrocarbon group.
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.

As group represented by Formula (b1-3), group represented by Formula (b1-9)-Formula (b1-11) is mentioned, respectively.
In formula (b1-9),
L ^b19 represents a single bond or a divalent saturated hydrocarbon group having 1 to 23 carbon atoms, and a hydrogen atom contained in the saturated hydrocarbon group may be substituted by a fluorine atom.
L ^b20 represents a single bond or a divalent saturated hydrocarbon group having 1 to 23 carbon atoms, and a hydrogen atom contained in the saturated hydrocarbon group is substituted by a fluorine atom, a hydroxy group or an alkylcarbonyloxy group It is also good. -CH _2- contained in the alkylcarbonyloxy group may be replaced by -O- or -CO-, and a hydrogen atom contained in the alkylcarbonyloxy group may be substituted by a hydroxy group.
However, the total carbon number of L ^b19 and L ^b20 is 23 or less.
In the formula (b1-10),
L ^b21 represents a single bond or a divalent saturated hydrocarbon group having 1 to ²¹ carbon atoms, and a hydrogen atom contained in the saturated hydrocarbon group may be substituted by a fluorine atom.
L ^b22 represents a single bond or a divalent saturated hydrocarbon group having 1 to 21 carbon atoms.
L ^b23 represents a single bond or a divalent saturated hydrocarbon group having 1 to ²¹ carbon atoms, and a hydrogen atom contained in the saturated hydrocarbon group is substituted by a fluorine atom, a hydroxy group or an alkylcarbonyloxy group It is also good. -CH _2- contained in the alkylcarbonyloxy group may be replaced by -O- or -CO-, and a hydrogen atom contained in the alkylcarbonyloxy group may be substituted by a hydroxy group.
However, the total carbon number of L ^b21 , L ^b22 and L ^b23 is 21 or less.
In formula (b1-11),
L ^b24 represents a single bond or a divalent saturated hydrocarbon group having 1 to 20 carbon atoms, and a hydrogen atom contained in the saturated hydrocarbon group may be substituted by a fluorine atom.
L ^b25 represents a bivalent saturated hydrocarbon group having 1 to 21 carbon atoms.
L ^b26 represents a single bond or a divalent saturated hydrocarbon group having 1 to 20 carbon atoms, and a hydrogen atom contained in the saturated hydrocarbon group is substituted by a fluorine atom, a hydroxy group or an alkylcarbonyloxy group; It is also good. -CH _2- contained in the alkylcarbonyloxy group may be replaced by -O- or -CO-, and a hydrogen atom contained in the alkylcarbonyloxy group may be substituted by a hydroxy group.
However, L ^b24, the total number of carbon atoms of L ^b25 and L ^b26 is 21 or less.

  In the group represented by the formula (b1-9) to the group represented by the formula (b1-11), when a hydrogen atom contained in a saturated hydrocarbon group is substituted by an alkylcarbonyloxy group, it is replaced Let the previous carbon number be the carbon number of the saturated hydrocarbon group.

  Examples of the alkylcarbonyloxy group include acetyloxy group, propionyloxy group, butyryloxy group, cyclohexylcarbonyloxy group, adamantyl carbonyloxy group and the like.

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

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

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

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

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

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

As an alicyclic hydrocarbon group represented by Y, group represented by Formula (Y1)-Formula (Y11), Formula (Y36)-Formula (Y38) is mentioned.
When -CH _2- contained in the alicyclic hydrocarbon group represented by Y is replaced by -O-, -S (O) ₂ -or -CO-, the number may be one or two or more. Good. As such a group, groups represented by Formula (Y12) to Formula (Y35) and Formula (Y39) to Formula (Y41) can be mentioned.
Y is preferably a group represented by any of Formula (Y1) to Formula (Y20), Formula (Y30), Formula (Y31), Formula (Y39) to Formula (Y41), and more preferably a formula (Y11), the formula (Y15), the formula (Y16), the formula (Y20), the formula (Y30), the formula (Y31), the formula (Y39) or the formula (Y40), and more preferably a group (Y11) is a group represented by the formula (Y15), the formula (Y30), the formula (Y39) or the formula (Y40).
When Y is a spiro ring such as formula (Y28) to formula (Y35), it is preferable that the alkanediyl group between two oxygen atoms have one or more fluorine atoms. Moreover, it is preferable that the fluorine atom is not substituted by the methylene group adjacent to an oxygen atom among the alkanediyl groups contained in ketal structure.

As a substituent of the methyl group represented by Y, a halogen atom, a hydroxy group, an alicyclic hydrocarbon group having 3 to 16 carbon atoms, an aromatic hydrocarbon group having 6 to 18 carbon atoms, a glycidyloxy group,-(- CH ₂ ) _ja -CO-O-R ^b1 group or-(CH ₂ ) _ja -O-CO-R ^b1 group (wherein, R ^b1 is an alkyl group having 1 to 16 carbon atoms, 3 to 16 carbon atoms Represents an alicyclic hydrocarbon group, an aromatic hydrocarbon group having 6 to 18 carbon atoms, or a combination thereof, and -CH _2- contained in the alicyclic hydrocarbon group is -O-, -SO ₂ -Or -CO- may be substituted, and a hydrogen atom contained in the alicyclic hydrocarbon group may be substituted with a hydroxy group or a fluorine atom, ja is an integer of 0 to 4 And the like.
As a substituent of the alicyclic hydrocarbon group represented by Y, a halogen atom, a hydroxy group, an alkyl group having 1 to 12 carbon atoms which may be substituted by a hydroxy group, an alicyclic group having 3 to 16 carbon atoms A hydrocarbon group, an alkoxy group having 1 to 12 carbon atoms, an aromatic hydrocarbon group having 6 to 18 carbon atoms, an aralkyl group having 7 to 21 carbon atoms, an alkylcarbonyl group having 2 to 4 carbon atoms, a glycidyloxy group,-( CH ₂ ) _ja -CO-O-R ^b1 group or-(CH ₂ ) _ja -O-CO-R ^b1 group (wherein, R ^b1 is an alkyl group having 1 to 16 carbon atoms, 3 to 16 carbon atoms Represents an alicyclic hydrocarbon group, an aromatic hydrocarbon group having 6 to 18 carbon atoms, or a combination thereof, and -CH _2- contained in the alicyclic hydrocarbon group is -O-, -SO ₂ -Or-CO-which may be substituted, the alicyclic hydrocarbon Hydrogen atoms contained in the optionally substituted hydroxy group or a fluorine atom .ja represents an integer of 0 to 4), and the like.

As a halogen atom, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, etc. are mentioned.
Examples of the alicyclic hydrocarbon group include a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclooctyl group, a norbornyl group, an adamantyl group and the like.
The alicyclic hydrocarbon group may have a chain hydrocarbon group, and examples thereof include a methylcyclohexyl group and a dimethylcyclohexyl group.
Examples of the aromatic hydrocarbon group include aryl groups such as phenyl group, biphenylyl group, naphthyl group and phenanthryl group.
The aromatic hydrocarbon group may have a chain hydrocarbon group or an alicyclic hydrocarbon group, and is an aromatic hydrocarbon group having a chain hydrocarbon group having 1 to 18 carbon atoms (tolyl group , Xylyl group, cumenyl group, mesityl group, p-ethylphenyl group, p-tert-butylphenyl group, 2,6-diethylphenyl group, 2-methyl-6-ethylphenyl group, etc.), and having 3 to 18 carbon atoms And aromatic hydrocarbon groups having an alicyclic hydrocarbon group (p-cyclohexylphenyl group, p-adamantylphenyl group, etc.) and the like.
As the alkyl group, for example, methyl group, ethyl group, propyl group, isopropyl group, butyl group, sec-butyl group, tert-butyl group, pentyl group, hexyl group, heptyl group, 2-ethylhexyl group, octyl group, nonyl group And decyl, undecyl, dodecyl and the like.
Examples of the alkyl group substituted by a hydroxy group include hydroxyalkyl groups such as hydroxymethyl group and hydroxyethyl group.
Examples of the alkoxy group include methoxy group, ethoxy group, propoxy group, butoxy group, pentyloxy group, hexyloxy group, heptyloxy group, octyloxy group, decyloxy group and dodecyloxy group.
Examples of the aralkyl group include benzyl group, phenethyl group, phenylpropyl group, naphthylmethyl group and naphthylethyl group.
As an alkyl carbonyl group, an acetyl group, a propionyl group, butyryl group etc. are mentioned, for example.

Examples of Y include the following.

Y is preferably a C3-C18 alicyclic hydrocarbon group which may have a substituent, more preferably an adamantyl group which may have a substituent, and the alicyclic carbonization The —CH ₂ — constituting the hydrogen group or the adamantyl group may be replaced by —CO—, —S (O) ₂ — or —CO—. Y is more preferably an adamantyl group, a hydroxyadamantyl group, an oxoadamantyl group or a group represented by the following.

  As a sulfonate anion in the salt represented by the formula (B1), an anion represented by the formula (B1-A-1) to the formula (B1-A-55) [hereinafter, “anion (B1 -A-1) etc. Formula (B1-A-1) to formula (B1-A-4), formula (B1-A-9), formula (B1-A-10), formula (B1-A-24) to formula (B1-A-33), formula (B1-A-36) to formula (B1-A-40), formula (B1-A-47) to formula (B1-A-55) Anion is more preferred.

Here, R ^{i2 to} R ⁱ⁷ are each independently, for example, an alkyl group having 1 to 4 carbon atoms, preferably a methyl group or an ethyl group. R ⁱ⁸ is formed by, 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 And more preferably a methyl group, an ethyl group, a cyclohexyl group or an adamantyl group. L ^A4 is a single bond or an alkanediyl group having 1 to 4 carbon atoms.
Q ^b1 and Q ^b2 represent the same meaning as described above.
Specifically as a sulfonate anion in the salt represented by Formula (B1), the anion described in Unexamined-Japanese-Patent No. 2010-204646 is mentioned.

As a sulfonate anion in the salt represented by preferable Formula (B1), the anion represented by Formula (B1a-1)-Formula (B1a-34) is mentioned, respectively.

  Among them, Formula (B1a-1) to Formula (B1a-3) and Formula (B1a-7) to Formula (B1a-16), Formula (B1a-18), Formula (B1a-19), Formula (B1a-22) The anion represented by any one of formulas (B1a-34) is preferred.

Examples of the organic cation of Z ⁺ include the same as ZA ⁺ in the structural unit represented by formula (II-2-A ′).

  The acid generator (B) is a combination of the above-mentioned sulfonate anion and the above-mentioned organic cation, and these can be optionally combined. As the acid generator (B), preferably, Formula (B1a-1) to Formula (B1a-3) and Formula (B1a-7) to Formula (B1a-16), Formula (B1a-18), and Formula (B1a-) 19) A combination of an anion represented by any of the formulas (B1a-22) to (B1a-34) and a cation (b2-1) or a cation (b2-3).

Preferred examples of the acid generator (B) include those represented by the formulas (B1-1) to (B1-48), among which those containing an arylsulfonium cation are preferred, and the formula (B1-1) Formula (B1-3), Formula (B1-5), Formula (B1-7), Formula (B1-11), Formula (B1-14), Formula (B1-20), Formula (B1-26), Those represented by Formula (B1-29), Formula (B1-31) to Formula (B1-48) are particularly preferable.

  In the resist composition of the present invention, the content of the acid generator is preferably 1 to 40 parts by mass, more preferably 3 to 35 parts by mass with respect to 100 parts by mass of the resin (A). It is. The resist composition of the present invention may contain one type of acid generator (B) alone, or may contain a plurality of types.

<Solvent (E)>
The content of the solvent (E) in the resist composition is usually 90% by mass to 99.9% by mass, preferably 92% by mass to 99% by mass, and more preferably 94% by mass to 99% by mass. % Or less. The content of the solvent (E) can be measured, for example, by a known analytical means such as liquid chromatography or gas chromatography.
As the solvent (E), 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 such as acetone, methyl isobutyl ketone, ketones such as 2-heptanone and cyclohexanone; cyclic esters such as γ-butyrolactone; and the like. One of the solvents (E) may be used alone, or two or more thereof may be used.

<Quencher (C)>
The quencher (C) includes a basic nitrogen-containing organic compound and a salt which generates an acid having a weaker acidity than the acid generated from the acid generator (B). 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 include amines and ammonium salts. The amines include aliphatic amines and aromatic amines. Aliphatic amines include primary amines, secondary amines and tertiary amines.
As the amine, 1-naphthylamine, 2-naphthylamine, aniline, diisopropylaniline, 2-, 3- or 4-methylaniline, 4-nitroaniline, N-methylaniline, N, N-dimethylaniline, diphenylamine, hexylamine, Heptylamine, Octylamine, Nonylamine, Decylamine, Dipentylamine, Dihexylamine, Diheptylamine, Dioctylamine, Dioctylamine, Didecylamine, Triethylamine, Trimethylamine, Tripropylamine, Tributylamine, Tripentylamine, Trihexylamine, Trihexylamine Heptylamine, trioctylamine, torinylamine, tridecylamine, methyldibutylamine, methyldipentylamine, methyldihexylamine, Ludicyclohexylamine, methyldiheptylamine, methyldioctylamine, methyldionylamine, methyldidecylamine, ethyl dibutylamine, ethyl dipentylamine, ethyl dihexylamine, ethyl diheptylamine, ethyl dioctylamine, ethyl dinonylamine, ethyl Didecylamine, dicyclohexylmethylamine, tris [2- (2-methoxyethoxy) ethyl] amine, triisopropanolamine, 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-methyl ester Dazole, pyridine, 4-methylpyridine, 1,2-di (2-pyridyl) ethane, 1,2-di (4-pyridyl) ethane, 1,2-di (2-pyridyl) ethene, 1,2-di (4-pyridyl) ethene, 1,3-di (4-pyridyl) propane, 1,2-di (4-pyridyloxy) ethane, di (2-pyridyl) ketone, 4,4'-dipyridyl sulfide, 4, 4'-dipyridyl disulfide, 2,2'-dipyridylamine, 2,2'-dipicolylamine, bipyridine etc. are mentioned, Preferably a diisopropyl aniline is mentioned, More preferably, a 2, 6- diisopropyl aniline is mentioned.
As an ammonium salt, tetramethyl ammonium hydroxide, tetraisopropyl ammonium hydroxide, tetrabutyl ammonium hydroxide, tetrahexyl ammonium hydroxide, tetraoctyl ammonium hydroxide, phenyltrimethyl ammonium hydroxide, 3- (trifluoromethyl) phenyltrimethyl Ammonium hydroxide, tetra-n-butylammonium salicylate, choline and the like can be mentioned.

The acidity of a salt that generates an acid having a weaker acidity than the acid generated from the acid generator (B) is represented by the acid dissociation constant (pKa). The salt which generates an acid weaker in acidity than the acid generated from the acid generator (B) is a salt having an acid dissociation constant of -3 <pKa, preferably -1 <pKa. It is a salt of pKa <7, more preferably a salt of 0 <pKa <5.
As a salt that generates an acid having a weaker acidity than the acid generated from the acid generator (B), a salt represented by the following formula, a salt represented by the formula (D) described in JP-A-2015-147926 (Hereinafter, it may be referred to as "weak acid internal salt (D)."), JP 2012-229206, JP 2012-6908, JP 2012-72109, JP 2011-39502. And salts described in JP-A No. 2011-191745. Preferred is a weak acid inner salt (D).

As the weak acid internal salt (D), the following salts may be mentioned.

  When the resist composition contains a quencher (C), the content of the quencher (C) is usually 0.01 to 5% by mass, preferably 0.01 to 5% by mass in the solid content of the resist composition. It is 3% by mass.

<Other ingredients>
The resist composition of the present invention may optionally contain components other than the components described above (hereinafter sometimes referred to as "other components (F)"). There is no particular limitation on the other component (F), and additives known in the field of resist, for example, 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 compound (I), a resin (A) and an acid generator (B), and, if necessary, a resin other than the resin (A) to be used, a solvent (E) and a quencher It can be prepared by mixing C) and other components (F). The order of mixing is arbitrary and is not particularly limited. The temperature for mixing can be selected from 10 to 40 ° C. according to the type of resin or the like, the solubility of the resin or the like in the solvent (E), and the like. The mixing time can be appropriately selected from 0.5 to 24 hours depending on the mixing temperature. The mixing means is also not particularly limited, and stirring and mixing can be used.
After mixing each component, it is preferable to filter using a filter with a pore size of about 0.003 to 0.2 μm.

<Method of manufacturing resist pattern>
The method for producing a resist pattern of the present invention is
(1) applying the resist composition of the present invention on a substrate,
(2) drying the composition after application to form a composition layer;
(3) exposing the composition layer,
(4) heating the composition layer after exposure; and (5) developing the composition layer after heating.

The resist composition can be applied onto a substrate by means of a commonly used apparatus such as a spin coater. Examples of the substrate include inorganic substrates such as silicon wafers. Before applying the resist composition, the substrate may be washed, or an antireflective film or the like may be formed on the substrate.
The solvent is removed by drying the composition after application to form a composition layer. Drying is performed, for example, by evaporating the solvent using a heating device such as a hot plate (so-called pre-baking) or using a pressure reducing device. The heating temperature is preferably 50 to 200 ° C., and the heating time is preferably 10 to 180 seconds. Moreover, it is preferable that the pressure at the time of vacuum-drying is about 1-1.0 * 10 < ⁵ > Pa.
The resulting composition layer is usually exposed using an exposure machine. The exposure device may be an immersion exposure device. 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 Use various materials such as those emitting high-frequency laser light in far ultraviolet region or vacuum ultraviolet region by converting the wavelength of laser light from etc.), electron beam, irradiation with ultra-ultraviolet light (EUV), etc. Can. In the present specification, irradiation of these radiations may be collectively 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, direct exposure may be performed without using a mask.
The composition layer after exposure is subjected to heat treatment (so-called post-exposure baking) in order to accelerate the deprotection reaction of 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. As a developing method, a dip method, a paddle method, a spray method, a dynamic dispensing method and the like can be mentioned. The development temperature is preferably 5 to 60 ° C., for example, and the development time is preferably 5 to 300 seconds, for example. A positive resist pattern or a negative resist pattern can be produced by selecting the type of developer as follows.
When a positive resist pattern is produced from the resist composition of the present invention, an alkaline developer is used as the developer. The alkaline developer may be any of various alkaline aqueous solutions used in this field. For example, an aqueous solution of tetramethyl ammonium hydroxide or (2-hydroxyethyl) trimethyl ammonium hydroxide (commonly called choline) and the like can be mentioned. The alkaline developer may contain a surfactant.
After development, the resist pattern is preferably washed with ultrapure water, and then the substrate and water remaining on the pattern are removed.
When a negative resist pattern is produced from the resist composition of the present invention, a developer containing an organic solvent (hereinafter sometimes referred to as "organic developer") is used as a developer.
Examples of organic solvents contained in the organic developer include ketone solvents such as 2-hexanone and 2-heptanone; glycol ether ester solvents such as propylene glycol monomethyl ether acetate; ester solvents such as butyl acetate; glycols such as propylene glycol monomethyl ether Ether solvents; Amide solvents such as N, N-dimethylacetamide; and Aromatic hydrocarbon solvents such as anisole.
The content of the organic solvent in the organic developer is preferably 90% by mass to 100% by mass, more preferably 95% by mass to 100% by mass, and still more 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 to 100% by mass, more preferably 90% by mass to 100% by mass, and substantially butyl acetate and / or 2 It is further preferred that only heptanone.
The organic developer may contain a surfactant. The organic developer may contain a slight amount of water.
At the time of development, development may be stopped by replacing 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 rinse solution is not particularly limited as long as it does not dissolve the resist pattern, and a solution containing a common organic solvent can be used, and is preferably an alcohol solvent or an ester solvent.
After cleaning, it is preferable to remove the rinse solution 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 It is more suitable as a resist composition for electron beam (EB) exposure or a resist composition for EUV exposure, and is useful for fine processing of semiconductors.

The present invention will be more specifically described by way of examples. In the examples, "%" and "part" representing the content or the amount used are on a mass basis unless otherwise stated.
The weight average molecular weight is a value determined by gel permeation chromatography under the following conditions.
Device: HLC-8120 GPC type (made by Tosoh Corporation)
Column: TSKgel Multipore H _XL- M x 3 + guardcolumn (made by Tosoh Corporation)
Eluent: tetrahydrofuran Flow rate: 1.0 mL / min
Detector: RI detector Column temperature: 40 ° C
Injection volume: 100 μl
Molecular weight standard: Standard polystyrene (made by Tosoh Corporation)
Further, the structure of the compound was confirmed by measuring molecular ion peaks using mass spectrometry (LC: Agilent 1100 type, MASS: Agilent LC / MSD type). In the following examples, this molecular ion peak value is indicated by "MASS". In addition, the structure of the isomer was confirmed by NMR (EX-270 type; manufactured by Nippon Denshi Co., Ltd.).

Example 1: Synthesis of Compounds Represented by Formula (I-1), Formula (I-7) and Formula (I-11)
After 22.57 parts of a compound represented by the formula (I-1-a) and 30 parts of ion exchanged water were mixed and stirred at 23 ° C. for 30 minutes, the temperature was raised to 60 ° C. To the obtained mixed solution, 30.53 parts of a compound represented by the formula (I-1-b) and 1.56 parts of p-toluenesulfonic acid are added, and the mixture is stirred at 60 ° C. for 18 hours, and then to 23 ° C. It cooled. 100 parts of ion exchanged water was added to the obtained reaction mass, and the mixture was stirred at 23 ° C. for 30 minutes and then filtered. 100 parts of ion exchanged water was added to the collected filtrate, and the mixture was stirred at 23 ° C. for 30 minutes and then filtered. This operation was performed 5 times. The collected filtrate was dried to obtain 25.04 parts of a compound represented by the formula (I-1-c).
Compound Represented by Formula (I-1-c)
¹ H-NMR (DMSO-d): δ (ppm)
5.12 (s, 1 H), 6.58 (m, 1 H), 6.66 (m, 1 H), 6.92 (m, 2 H), 6.96 (m, 1 H), 7.09 (m) , 2H), 9.40 (brs, 1H), 9.88 (brs, 1H)
After mixing 8.61 parts of a compound represented by the formula (I-1-d) and 100 parts of acetonitrile and stirring for 30 minutes at 23 ° C., 16.22 parts of carbonyldiimidazole are added, and 2 hours at 60 ° C. It stirred. 24.22 parts of compounds represented by Formula (I-1-c) were added to the obtained reaction mass, and it stirred at 60 degreeC for 2 hours. After cooling the obtained reaction mixture to 23 ° C., 200 parts of chloroform and 100 parts of ion exchanged water were added to the obtained reaction mixture, and the mixture was stirred at 23 ° C. for 30 minutes, then separated to take out the organic layer. . To the obtained organic layer, 100 parts of a 5% aqueous solution of oxalic acid was added, and the mixture was stirred at 23 ° C. for 30 minutes, and then separated to take out the organic layer. 100 parts of ion exchanged water was added to the obtained organic layer, and the mixture was stirred at 23 ° C. for 30 minutes, and then separated to take out the organic layer. This water washing operation was repeated 5 times. The obtained organic layer is concentrated, and the concentrated mass is separated into a column (silica gel 60N (spherical, neutral) 100-210 μm; manufactured by Kanto Chemical Co., Ltd., developing solvent: n-heptane / ethyl acetate = 1/1) Accordingly, 8.42 parts of the compound represented by the formula (I-1), 6.44 parts of the compound represented by the formula (I-7), and 0.46 parts of the compound represented by the formula (I-11) I got each.

Compound Represented by Formula (I-1) MASS: 311.1 [M + H] ^+
1 H-NMR (DMSO-d): δ (ppm)
2.01 (s, 3H), 5.12 (s, 1H), 5.92 (m, 1H), 6.30 (m, 1H), 6.58 (m, 1H), 6.66 (m) , 1H), 6.96 (m, 1H), 7.23 (m, 2H), 7.30 (m, 2H), 9.88 (brs, 1H)
Compound Represented by Formula (I-7) MASS: 311.1 [M + H] ^+
1 H-NMR (DMSO-d): δ (ppm)
2.01 (s, 3H), 5.12 (s, 1H), 5.92 (m, 1H), 6.30 (m, 1H), 6.92 (m, 2H), 6.95 (m) , 1 H), 7.09 (m, 3 H), 7.22 (m, 1 H), 9. 40 (brs, 1 H)
Compound Represented by Formula (I-11) MASS: 379.1 [M + H] ⁺

Example 2: Synthesis of Compounds Represented by Formula (I-2), Formula (I-6) and Formula (I-12)
After 22.57 parts of a compound represented by the formula (I-2-a) and 30 parts of ion exchanged water were mixed and stirred at 23 ° C. for 30 minutes, the temperature was raised to 60 ° C. To the obtained mixed solution, 30.53 parts of a compound represented by the formula (I-1-b) and 1.56 parts of p-toluenesulfonic acid are added, and the mixture is stirred at 60 ° C. for 18 hours, and then to 23 ° C. It cooled. 100 parts of ion exchanged water was added to the obtained reaction mass, and the mixture was stirred at 23 ° C. for 30 minutes and then filtered. 100 parts of ion exchanged water was added to the collected filtrate, and the mixture was stirred at 23 ° C. for 30 minutes and then filtered. This operation was performed 5 times. The collected filtrate was dried to obtain 26.11 parts of a compound represented by the formula (I-2-c).
Compounds Represented by Formula (I-2-c)
¹ H-NMR (DMSO-d): δ (ppm)
5.22 (s, 1 H), 6.53 (m, 1 H), 6.73 (m, 1 H), 6.93 (m, 2 H), 7.08 (m, 1 H), 7. 10 (m) , 2H), 9.39 (brs, 1H), 9.40 (brs, 1H)

After mixing 8.61 parts of a compound represented by the formula (I-1-d) and 100 parts of acetonitrile and stirring for 30 minutes at 23 ° C., 16.22 parts of carbonyldiimidazole are added, and 2 hours at 60 ° C. It stirred. To the obtained reaction mass, 24.22 parts of a compound represented by the formula (I-2-c) was added, and stirred at 60 ° C. for 2 hours. After cooling the obtained reaction mixture to 23 ° C., 200 parts of chloroform and 100 parts of ion exchanged water were added to the obtained reaction mixture, and the mixture was stirred at 23 ° C. for 30 minutes, then separated to take out the organic layer. . To the obtained organic layer, 100 parts of a 5% aqueous solution of oxalic acid was added, and the mixture was stirred at 23 ° C. for 30 minutes, and then separated to take out the organic layer. 100 parts of ion exchanged water was added to the obtained organic layer, and the mixture was stirred at 23 ° C. for 30 minutes, and then separated to take out the organic layer. This water washing operation was repeated 5 times. The obtained organic layer is concentrated, and the concentrated mass is separated into a column (silica gel 60N (spherical, neutral) 100-210 μm; manufactured by Kanto Chemical Co., Ltd., developing solvent: n-heptane / ethyl acetate = 1/1) Accordingly, 7.66 parts of the compound represented by the formula (I-2), 6.82 parts of the compound represented by the formula (I-6) and 0.33 parts of the compound represented by the formula (I-12) I got each.

Compound Represented by Formula (I-2) MASS: 311.1 [M + H] ^+
1 H-NMR (DMSO-d): δ (ppm)
2.01 (s, 3 H), 5.22 (s, 1 H), 5. 92 (m, 1 H), 6.30 (m, 1 H), 6.53 (m, 1 H), 6.73 (m) , 1H), 7.08 (m, 1H), 7.23 (m, 2H), 7.30 (m, 2H), 9.39 (brs, 1H)
Compound Represented by Formula (I-6) MASS: 311.1 [M + H] ^+
1 H-NMR (DMSO-d): δ (ppm)
2.01 (s, 3 H), 5.22 (s, 1 H), 5. 92 (m, 1 H), 6. 30 (m, 1 H), 6. 92 (m, 2 H), 7. 10 (m) , 2H), 7.21 (m, 1 H), 7.24 (m, 1 H), 7.32 (m, 1 H), 9.40 (brs, 1 H)
Compound Represented by Formula (I-12) MASS: 379.1 [M + H] ⁺

Example 3: Synthesis of a Compound Represented by Formula (I-3)
After 50.40 parts of a compound represented by the formula (I-3-a) and 30 parts of ion exchanged water were mixed and stirred at 23 ° C. for 30 minutes, the temperature was raised to 60 ° C. To the obtained mixed solution, 53.76 parts of a compound represented by the formula (I-1-b) and 3.04 parts of p-toluenesulfonic acid are added, and the mixture is stirred at 60 ° C. for 18 hours, and then to 23 ° C. It cooled. 100 parts of ion exchanged water was added to the obtained reaction mass, and the mixture was stirred at 23 ° C. for 30 minutes and then filtered. To the collected filtrate, 200 parts of ethyl acetate and 100 parts of ion-exchanged water were added, and the mixture was stirred at 23 ° C. for 30 minutes, then separated to extract an organic layer. 100 parts of ion exchanged water was added to the obtained organic layer, and the mixture was stirred at 23 ° C. for 30 minutes, and then separated to take out the organic layer. This water washing operation was performed three times. The obtained organic layer is concentrated, 130 parts of toluene is added to the concentrated mass, and after stirring for 30 minutes at 23 ° C., filtration is performed to obtain 41.68 parts of a compound represented by the formula (I-3-c) I got
After mixing 8.61 parts of a compound represented by the formula (I-1-d) and 100 parts of acetonitrile and stirring for 30 minutes at 23 ° C., 16.22 parts of carbonyldiimidazole are added, and 2 hours at 60 ° C. It stirred. To the obtained reaction mass, 25.82 parts of a compound represented by the formula (I-3-c) was added, and stirred at 60 ° C. for 2 hours. After cooling the obtained reaction mixture to 23 ° C., 200 parts of chloroform and 100 parts of ion exchanged water were added to the obtained reaction mixture, and the mixture was stirred at 23 ° C. for 30 minutes, then separated to take out the organic layer. . To the obtained organic layer, 100 parts of a 5% aqueous solution of oxalic acid was added, and the mixture was stirred at 23 ° C. for 30 minutes, and then separated to take out the organic layer. 100 parts of ion exchanged water was added to the obtained organic layer, and the mixture was stirred at 23 ° C. for 30 minutes, and then separated to take out the organic layer. This water washing operation was repeated 5 times. The obtained organic layer is concentrated, and the concentrated mass is separated into a column (silica gel 60N (spherical, neutral) 100-210 μm; manufactured by Kanto Chemical Co., Ltd., developing solvent: n-heptane / ethyl acetate = 1/1) Thus, 11.04 parts of a compound represented by the formula (I-3) was obtained.
MASS: 327.1 [M + H] ⁺

Example 4: Synthesis of a compound represented by formula (I-5)
After 25.20 parts of a compound represented by the formula (I-5-a) and 30 parts of ion exchanged water were mixed and stirred at 23 ° C. for 30 minutes, the temperature was raised to 60 ° C. To the obtained mixed solution, 26.88 parts of a compound represented by the formula (I-1-b) and 1.52 parts of p-toluenesulfonic acid are added, and the mixture is stirred at 60 ° C. for 18 hours, and then to 23 ° C. It cooled. 100 parts of ion exchanged water was added to the obtained reaction mass, and the mixture was stirred at 23 ° C. for 30 minutes and then filtered. After adding 200 parts of ethyl acetate and 80 parts of ion-exchanged water to the collected filtrate and stirring for 30 minutes at 23.degree. C., the layers were separated to take out the organic layer. To the obtained organic layer, 80 parts of ion exchanged water was added, and the mixture was stirred at 23 ° C. for 30 minutes, and then separated to take out the organic layer. This water washing operation was performed three times. The obtained organic layer is concentrated, 100 parts of toluene is added to the concentrated mass, and after stirring for 30 minutes at 23 ° C., filtration is carried out to obtain 26.57 parts of a compound represented by formula (I-5-c) I got
After mixing 8.61 parts of a compound represented by the formula (I-1-d) and 100 parts of acetonitrile and stirring for 30 minutes at 23 ° C., 16.22 parts of carbonyldiimidazole are added, and 2 hours at 60 ° C. It stirred. To the obtained reaction mass, 25.82 parts of a compound represented by the formula (I-5-c) was added, and stirred at 60 ° C. for 2 hours. After cooling the obtained reaction mixture to 23 ° C., 200 parts of chloroform and 100 parts of ion exchanged water were added to the obtained reaction mixture, and the mixture was stirred at 23 ° C. for 30 minutes, then separated to take out the organic layer. . To the obtained organic layer, 100 parts of a 5% aqueous solution of oxalic acid was added, and the mixture was stirred at 23 ° C. for 30 minutes, and then separated to take out the organic layer. 100 parts of ion exchanged water was added to the obtained organic layer, and the mixture was stirred at 23 ° C. for 30 minutes, and then separated to take out the organic layer. This water washing operation was repeated 5 times. The obtained organic layer is concentrated, and the concentrated mass is separated into a column (silica gel 60N (spherical, neutral) 100-210 μm; manufactured by Kanto Chemical Co., Ltd., developing solvent: n-heptane / ethyl acetate = 1/1) Thus, 8.92 parts of a compound represented by the formula (I-5) were obtained.
MASS: 327.1 [M + H] ⁺

Synthesis of Resin The compounds (monomers) used in the synthesis of the resin are shown below. Hereinafter, these monomers are called "monomer (a1-1-1)" etc. according to a formula number.

Example 5 [Synthesis of Resin A1]
The monomer (a1-4-2), the monomer (a1-1-3), the monomer (a1-2-6) and the monomer (I-1) are used as the monomer, and the molar ratio [monomer (a1-4-2) is used. ): Monomer (a1-1-3): Monomer (a1-2-6): Monomer (I-1)] is mixed in a ratio of 27: 25: 38: 10, and further, this monomer mixture And 1.5 mass times methyl isobutyl ketone with respect to the total mass of all the monomers. To the resulting mixture, azobisisobutyronitrile as an initiator is added so as to be 7 mol% relative to the total number of moles of all monomers, and polymerization is carried out by heating this at 83 ° C. for about 5 hours The Then, p-toluenesulfonic acid aqueous solution was added to the polymerization reaction liquid, and after stirring for 6 hours, liquid separation was carried out. The recovered organic layer was poured into a large amount of n-heptane to precipitate a resin, followed by filtration and recovery to obtain a resin A1 having a weight average molecular weight of about 5.8 × 10 ³ in a yield of 62%. This resin A1 has the following structural units.

Example 6 [Synthesis of Resin A2]
The monomer (a1-4-2), the monomer (a1-1-3), the monomer (a1-2-6) and the monomer (I-1) are used as the monomer, and the molar ratio [monomer (a1-4-2) is used. ): Monomer (a1-1-3): Monomer (a1-2-6): Monomer (I-1)] is mixed in a ratio of 17: 25: 38: 20, and further, this monomer mixture And 1.5 mass times methyl isobutyl ketone with respect to the total mass of all the monomers. To the resulting mixture, azobisisobutyronitrile as an initiator is added so as to be 7 mol% relative to the total number of moles of all monomers, and polymerization is carried out by heating this at 83 ° C. for about 5 hours The Then, p-toluenesulfonic acid aqueous solution was added to the polymerization reaction liquid, and after stirring for 6 hours, liquid separation was carried out. The recovered organic layer was poured into a large amount of n-heptane to precipitate a resin, followed by filtration and recovery to obtain a resin A2 having a weight average molecular weight of about 5.9 × 10 ³ in a yield of 60%. This resin A2 has the following structural units.

Example 7 [Synthesis of Resin A3]
The monomer (a1-4-2), the monomer (a1-1-3), the monomer (a1-2-6) and the monomer (I-1) are used as the monomer, and the molar ratio [monomer (a1-4-2) is used. ): Monomer (a1-1-3): Monomer (a1-2-6): Monomer (I-1)] is mixed in a ratio of 7: 25: 38: 30, and further, this monomer mixture And 1.5 mass times methyl isobutyl ketone with respect to the total mass of all the monomers. To the resulting mixture, azobisisobutyronitrile as an initiator is added so as to be 7 mol% relative to the total number of moles of all monomers, and polymerization is carried out by heating this at 83 ° C. for about 5 hours The Then, p-toluenesulfonic acid aqueous solution was added to the polymerization reaction liquid, and after stirring for 6 hours, liquid separation was carried out. The recovered organic layer was poured into a large amount of n-heptane to precipitate a resin, followed by filtration and recovery to obtain a resin A3 having a weight average molecular weight of about 6.1 × 10 ³ in a yield of 58%. This resin A3 has the following structural units.

Example 8 [Synthesis of Resin A4]
As a monomer, a monomer (a1-1-3), a monomer (a1-2-6) and a monomer (I-1) are used, and their molar ratio [monomer (a1-1-3): monomer (a1-2-6) ): Monomer (I-1)] is mixed in a ratio of 25:38:37, and further, to this monomer mixture, 1.5 mass times methyl isobutyl ketone based on the total mass of all the monomers. Mixed. To the resulting mixture, azobisisobutyronitrile as an initiator is added so as to be 7 mol% relative to the total number of moles of all monomers, and polymerization is carried out by heating this at 83 ° C. for about 5 hours The Thereafter, the polymerization reaction solution was poured into a large amount of n-heptane to precipitate a resin, followed by filtration and recovery to obtain a resin A4 having a weight average molecular weight of about 6.4 × 10 ³ in a yield of 58%. This resin A4 has the following structural units.

Example 9 [Synthesis of Resin A5]
The monomer (a1-4-2), the monomer (a1-1-3), the monomer (a1-2-6) and the monomer (I-2) are used as monomers, and the molar ratio [monomer (a1-4-2) is used. ): Monomer (a1-1-3): Monomer (a1-2-6): Monomer (I-2)] is mixed in a ratio of 27: 25: 38: 10, and further, this monomer mixture And 1.5 mass times methyl isobutyl ketone with respect to the total mass of all the monomers. To the resulting mixture, azobisisobutyronitrile as an initiator is added so as to be 7 mol% relative to the total number of moles of all monomers, and polymerization is carried out by heating this at 83 ° C. for about 5 hours The Then, p-toluenesulfonic acid aqueous solution was added to the polymerization reaction liquid, and after stirring for 6 hours, liquid separation was carried out. The collected organic layer was poured into a large amount of n-heptane to precipitate a resin, followed by filtration and recovery to obtain a resin A5 having a weight average molecular weight of about 5.9 × 10 ³ in a yield of 64%. This resin A5 has the following structural units.

Example 10 [Synthesis of Resin A6]
A monomer (a1-4-2), a monomer (a1-1-3), a monomer (a1-2-6) and a monomer (I-3) are used as monomers, and the molar ratio [monomer (a1-4-2) is used. ): Monomer (a1-1-3): Monomer (a1-2-6): Monomer (I-3)] is mixed in a ratio of 27: 25: 38: 10, and further, this monomer mixture And 1.5 mass times methyl isobutyl ketone with respect to the total mass of all the monomers. To the resulting mixture, azobisisobutyronitrile as an initiator is added so as to be 7 mol% relative to the total number of moles of all monomers, and polymerization is carried out by heating this at 83 ° C. for about 5 hours The Then, p-toluenesulfonic acid aqueous solution was added to the polymerization reaction liquid, and after stirring for 6 hours, liquid separation was carried out. The recovered organic layer was poured into a large amount of n-heptane to precipitate a resin, followed by filtration and recovery to obtain a resin A6 having a weight average molecular weight of about 6.2 × 10 ³ in a yield of 58%. This resin A6 has the following structural units.

Example 11 [Synthesis of Resin A7]
The monomer (a1-4-2), the monomer (a1-1-3), the monomer (a1-2-6) and the monomer (I-5) are used as the monomer, and the molar ratio [monomer (a1-4-2) is used. ): Monomer (a1-1-3): Monomer (a1-2-6): Monomer (I-5)] is mixed in a ratio of 27: 25: 38: 10, and further, this monomer mixture And 1.5 mass times methyl isobutyl ketone with respect to the total mass of all the monomers. To the resulting mixture, azobisisobutyronitrile as an initiator is added so as to be 7 mol% relative to the total number of moles of all monomers, and polymerization is carried out by heating this at 83 ° C. for about 5 hours The Then, p-toluenesulfonic acid aqueous solution was added to the polymerization reaction liquid, and after stirring for 6 hours, liquid separation was carried out. The recovered organic layer was poured into a large amount of n-heptane to precipitate a resin, followed by filtration and recovery to obtain a resin A7 having a weight average molecular weight of about 6.3 × 10 ³ in a yield of 53%. This resin A7 has the following structural units.

Example 12 [Synthesis of Resin A8]
The monomer (a1-4-2), the monomer (a1-1-3), the monomer (a1-2-6) and the monomer (I-6) are used as the monomer, and the molar ratio [monomer (a1-4-2) is used. ): Monomer (a1-1-3): Monomer (a1-2-6): Monomer (I-6)] is mixed in a ratio of 27: 25: 38: 10, and further, this monomer mixture And 1.5 mass times methyl isobutyl ketone with respect to the total mass of all the monomers. To the resulting mixture, azobisisobutyronitrile as an initiator is added so as to be 7 mol% relative to the total number of moles of all monomers, and polymerization is carried out by heating this at 83 ° C. for about 5 hours The Then, p-toluenesulfonic acid aqueous solution was added to the polymerization reaction liquid, and after stirring for 6 hours, liquid separation was carried out. The recovered organic layer was poured into a large amount of n-heptane to precipitate a resin, followed by filtration and recovery to obtain a resin A8 having a weight average molecular weight of about 5.9 × 10 ³ in a yield of 63%. This resin A8 has the following structural units.

Example 13 [Synthesis of Resin A9]
A monomer (a1-4-2), a monomer (a1-1-3), a monomer (a1-2-6) and a monomer (I-7) are used as the monomer, and the molar ratio [monomer (a1-4-2) is used. ): Monomer (a1-1-3): Monomer (a1-2-6): Monomer (I-7)] is mixed in a ratio of 27: 25: 38: 10, and further, this monomer mixture And 1.5 mass times methyl isobutyl ketone with respect to the total mass of all the monomers. To the resulting mixture, azobisisobutyronitrile as an initiator is added so as to be 7 mol% relative to the total number of moles of all monomers, and polymerization is carried out by heating this at 83 ° C. for about 5 hours The Then, p-toluenesulfonic acid aqueous solution was added to the polymerization reaction liquid, and after stirring for 6 hours, liquid separation was carried out. The recovered organic layer was poured into a large amount of n-heptane to precipitate a resin, followed by filtration and recovery to obtain a resin A9 having a weight average molecular weight of about 5.7 × 10 ³ in a yield of 62%. This resin A9 has the following structural units.

Example 14 [Synthesis of Resin A10]
As a monomer, a monomer (a1-4-2), a monomer (a1-1-3), a monomer (a1-2-6), a monomer (I-1), a monomer (I-7) and a monomer (I-11) The molar ratio [monomer (a1-4-2): monomer (a1-1-3): monomer (a1-2-6): monomer (I-1): monomer (I-7): monomer ( I-11)] is mixed in a ratio of 27: 25: 35: 5: 5: 3 and, further, to this monomer mixture, 1.5 mass times of methyl relative to the total mass of all the monomers. The isobutyl ketone was mixed. To the obtained mixture, azobisisobutyronitrile as an initiator is added so as to be 9 mol% relative to the total number of moles of all monomers, and polymerization is carried out by heating this at 83 ° C. for about 5 hours The Then, p-toluenesulfonic acid aqueous solution was added to the polymerization reaction liquid, and after stirring for 6 hours, liquid separation was carried out. The recovered organic layer was poured into a large amount of n-heptane to precipitate a resin, followed by filtration and recovery to obtain a resin A10 having a weight average molecular weight of about 6.1 × 10 ³ in a yield of 55%. This resin A10 has the following structural units.

Example 15 [Synthesis of Resin A11]
As a monomer, a monomer (a1-4-2), a monomer (a1-1-3), a monomer (a1-2-6), a monomer (I-2), a monomer (I-6) and a monomer (I-12) The molar ratio [monomer (a1-4-2): monomer (a1-1-3): monomer (a1-2-6): monomer (I-2): monomer (I-6): monomer ( I-12)] is mixed in a ratio of 27: 25: 35: 5: 5: 3 and, further, to this monomer mixture, 1.5 mass times of methyl based on the total mass of all the monomers. The isobutyl ketone was mixed. To the obtained mixture, azobisisobutyronitrile as an initiator is added so as to be 9 mol% relative to the total number of moles of all monomers, and polymerization is carried out by heating this at 83 ° C. for about 5 hours The Then, p-toluenesulfonic acid aqueous solution was added to the polymerization reaction liquid, and after stirring for 6 hours, liquid separation was carried out. The recovered organic layer was poured into a large amount of n-heptane to precipitate a resin, followed by filtration and recovery to obtain a resin A11 having a weight average molecular weight of about 6.3 × 10 ³ in a yield of 55%. This resin A11 has the following structural units.

Example 16 [Synthesis of Resin A12]
As a monomer, a monomer (a1-4-2), a monomer (a1-1-3), a monomer (a1-2-6), a monomer (a2-1-3), a monomer (a3-4-2) and a monomer The molar ratio [monomer (a1-4-2): monomer (a1-1-3): monomer (a1-2-6): monomer (a2-1-3): monomer (a3) using I-1) -4-2): Monomer (I-1)] is mixed in a ratio of 27: 20: 35: 3: 10: 5, and further, to this monomer mixture, based on the total mass of all the monomers. And 1.5 mass times of methyl isobutyl ketone were mixed. To the resulting mixture, 1.2 mol% and 3.6 mol% of azobisisobutyronitrile and azobis (2,4-dimethylvaleronitrile) as initiators, respectively, based on the total amount of monomers, are added, and 73 Heated at 5 ° C for about 5 hours. Then, p-toluenesulfonic acid aqueous solution was added to the polymerization reaction liquid, and after stirring for 12 hours, liquid separation was carried out. The recovered organic layer was poured into a large amount of n-heptane to precipitate a resin, followed by filtration and recovery to obtain a resin A12 having a weight average molecular weight of about 6.1 × 10 ³ in a yield of 61%. This resin A12 has the following structural units.

Example 17 [Synthesis of Resin A13]
As a monomer, a monomer (a1-4-2), a monomer (a1-1-3), a monomer (a1-2-6), a monomer (a2-1-3), a monomer (a3-4-2) and a monomer The molar ratio [monomer (a1-4-2): monomer (a1-1-3): monomer (a1-2-6): monomer (a2-1-3): monomer (a3) using I-2) -4-2): Monomer (I-2)] is mixed in a ratio of 27: 20: 35: 3: 10: 5, and further, to this monomer mixture, based on the total mass of all the monomers. And 1.5 mass times of methyl isobutyl ketone were mixed. To the resulting mixture, 1.2 mol% and 3.6 mol% of azobisisobutyronitrile and azobis (2,4-dimethylvaleronitrile) as initiators, respectively, based on the total amount of monomers, are added, and 73 Heated at 5 ° C for about 5 hours. Then, p-toluenesulfonic acid aqueous solution was added to the polymerization reaction liquid, and after stirring for 12 hours, liquid separation was carried out. The recovered organic layer was poured into a large amount of n-heptane to precipitate a resin, followed by filtration and recovery to obtain a resin A13 having a weight average molecular weight of about 5.9 × 10 ³ in a yield of 58%. This resin A13 has the following structural units.

Example 18 [Synthesis of Resin A14]
As a monomer, a monomer (a1-4-2), a monomer (a1-1-3), a monomer (a1-2-6), a monomer (a2-1-3), a monomer (a3-4-2) and a monomer The molar ratio [monomer (a1-4-2): monomer (a1-1-3): monomer (a1-2-6): monomer (a2-1-3): monomer (a3) using I-3) -4-2): Monomer (I-3)] is mixed in a ratio of 27: 20: 35: 3: 10: 5, and further, to this monomer mixture, based on the total mass of all the monomers. And 1.5 mass times of methyl isobutyl ketone were mixed. To the resulting mixture, 1.2 mol% and 3.6 mol% of azobisisobutyronitrile and azobis (2,4-dimethylvaleronitrile) as initiators, respectively, based on the total amount of monomers, are added, and 73 Heated at 5 ° C for about 5 hours. Then, p-toluenesulfonic acid aqueous solution was added to the polymerization reaction liquid, and after stirring for 12 hours, liquid separation was carried out. The recovered organic layer was poured into a large amount of n-heptane to precipitate a resin, followed by filtration and recovery to obtain a resin A14 having a weight average molecular weight of about 6.1 × 10 ³ in a yield of 52%. This resin A14 has the following structural units.

Example 19 [Synthesis of Resin A15]
As a monomer, a monomer (a1-4-2), a monomer (a1-1-3), a monomer (a1-2-6), a monomer (a2-1-3), a monomer (a3-4-2) and a monomer I-5), the molar ratio [monomer (a1-4-2): monomer (a1-1-3): monomer (a1-2-6): monomer (a2-1-3): monomer (a3) -4-2): Monomer (I-5)] is mixed in a ratio of 27: 20: 35: 3: 10: 5, and further, to this monomer mixture, based on the total mass of all the monomers. And 1.5 mass times of methyl isobutyl ketone were mixed. To the resulting mixture, 1.2 mol% and 3.6 mol% of azobisisobutyronitrile and azobis (2,4-dimethylvaleronitrile) as initiators, respectively, based on the total amount of monomers, are added, and 73 Heated at 5 ° C for about 5 hours. Then, p-toluenesulfonic acid aqueous solution was added to the polymerization reaction liquid, and after stirring for 12 hours, liquid separation was carried out. The recovered organic layer was poured into a large amount of n-heptane to precipitate a resin, followed by filtration and recovery to obtain a resin A15 having a weight average molecular weight of about 6.4 × 10 ³ in a yield of 54%. This resin A15 has the following structural units.

Example 20 [Synthesis of Resin A16]
As a monomer, a monomer (a1-4-2), a monomer (a1-1-3), a monomer (a1-2-6), a monomer (a2-1-3), a monomer (a3-4-2) and a monomer The molar ratio [monomer (a1-4-2): monomer (a1-1-3): monomer (a1-2-6): monomer (a2-1-3): monomer (a3) using I-6) -4-2): Monomer (I-6)] is mixed in a ratio of 27: 20: 35: 3: 10: 5, and further, to this monomer mixture, based on the total mass of all the monomers. And 1.5 mass times of methyl isobutyl ketone were mixed. To the resulting mixture, 1.2 mol% and 3.6 mol% of azobisisobutyronitrile and azobis (2,4-dimethylvaleronitrile) as initiators, respectively, based on the total amount of monomers, are added, and 73 Heated at 5 ° C for about 5 hours. Then, p-toluenesulfonic acid aqueous solution was added to the polymerization reaction liquid, and after stirring for 12 hours, liquid separation was carried out. The recovered organic layer was poured into a large amount of n-heptane to precipitate a resin, followed by filtration and recovery to obtain a resin A16 having a weight average molecular weight of about 6.3 × 10 ³ in a yield of 57%. This resin A16 has the following structural units.

Example 21 [Synthesis of Resin A17]
As a monomer, a monomer (a1-4-2), a monomer (a1-1-3), a monomer (a1-2-6), a monomer (a2-1-3), a monomer (a3-4-2) and a monomer I-7), and the molar ratio [monomer (a1-4-2): monomer (a1-1-3): monomer (a1-2-6): monomer (a2-1-3): monomer (a3) -4-2): Monomer (I-7)] is mixed in a ratio of 27: 20: 35: 3: 10: 5, and further, to this monomer mixture, based on the total mass of all monomers. And 1.5 mass times of methyl isobutyl ketone were mixed. To the resulting mixture, 1.2 mol% and 3.6 mol% of azobisisobutyronitrile and azobis (2,4-dimethylvaleronitrile) as initiators, respectively, based on the total amount of monomers, are added, and 73 Heated at 5 ° C for about 5 hours. Then, p-toluenesulfonic acid aqueous solution was added to the polymerization reaction liquid, and after stirring for 12 hours, liquid separation was carried out. The recovered organic layer was poured into a large amount of n-heptane to precipitate a resin, followed by filtration and recovery to obtain a resin A17 having a weight average molecular weight of about 5.8 × 10 ³ in a yield of 64%. This resin A17 has the following structural units.

Synthesis Example 1 [Synthesis of Resin AX1]
As a monomer, a monomer (a1-1-3), a monomer (a1-2-6) and a monomer (IX-1) are used, and their molar ratio [monomer (a1-1-3): monomer (a1-2-6) ): Monomer (IX-1)] is mixed in a ratio of 25:38:37, and further, to this monomer mixture, 1.5 mass times methyl isobutyl ketone based on the total mass of all monomers. Mixed. To the resulting mixture, azobisisobutyronitrile as an initiator is added so as to be 7 mol% relative to the total number of moles of all monomers, and polymerization is carried out by heating this at 83 ° C. for about 5 hours The Thereafter, the polymerization reaction solution was poured into a large amount of n-heptane to precipitate a resin, followed by filtration and recovery to obtain a resin AX1 having a weight average molecular weight of about 6.4 × 10 ³ in a yield of 60%. The resin AX1 has the following structural units.

Synthesis Example 2 [Synthesis of Resin AX2]
The monomer (a1-4-2), the monomer (a1-1-3), the monomer (a1-2-6) and the monomer (IX-1) are used as the monomer, and the molar ratio [monomer (a1-4-2) is used. ): Monomer (a1-1-3): Monomer (a1-2-6): Monomer (IX-1)] is mixed in a ratio of 27: 25: 38: 10, and further, this monomer mixture And 1.5 mass times methyl isobutyl ketone with respect to the total mass of all the monomers. To the resulting mixture, azobisisobutyronitrile as an initiator is added so as to be 7 mol% relative to the total number of moles of all monomers, and polymerization is carried out by heating this at 83 ° C. for about 5 hours The Then, p-toluenesulfonic acid aqueous solution was added to the polymerization reaction liquid, and after stirring for 6 hours, liquid separation was carried out. The recovered organic layer was poured into a large amount of n-heptane to precipitate a resin, followed by filtration and recovery to obtain a resin AX2 having a weight average molecular weight of about 6.1 × 10 ³ in a yield of 60%. The resin AX2 has the following structural units.

Synthesis Example 3 [Synthesis of Resin AX3]
As a monomer, a monomer (a1-4-2), a monomer (a1-1-3), a monomer (a1-2-6), a monomer (a2-1-3), a monomer (a3-4-2) and a monomer Using IX-1), the molar ratio [Monomer (a1-4-2): Monomer (a1-1-3): Monomer (a1-2-6): Monomer (a2-1-3): Monomer (a3 -4-2): Monomer (IX-1)] is mixed in a ratio of 27: 20: 35: 3: 10: 5, and further, to this monomer mixture, based on the total mass of all the monomers. And 1.5 mass times of methyl isobutyl ketone were mixed. To the resulting mixture, 1.2 mol% and 3.6 mol% of azobisisobutyronitrile and azobis (2,4-dimethylvaleronitrile) as initiators, respectively, based on the total amount of monomers, are added, and 73 Heated at 5 ° C for about 5 hours. Then, p-toluenesulfonic acid aqueous solution was added to the polymerization reaction liquid, and after stirring for 12 hours, liquid separation was carried out. The recovered organic layer was poured into a large amount of n-heptane to precipitate a resin, followed by filtration and recovery to obtain a resin AX3 having a weight average molecular weight of about 5.7 × 10 ³ in a yield of 68%. The resin AX3 has the following structural units.

<Preparation of Resist Composition>
A mixture obtained by mixing and dissolving the components shown in Table 1 and the following solvents was filtered using a fluororesin filter with a pore size of 0.2 μm to prepare a resist composition.

<Resin>
A1 to A17, AX1, AX2: resin A1 to resin A17, resin AX1, resin AX2
<Acid Generator (B)>
B 1-43: A salt represented by the formula (B 1-43) (synthesized according to an example of JP-A-2016-47815)
<Quencher (C)>
C1: synthesized by the method described in JP-A-2011-39502
<Solvent>
Propylene glycol monomethyl ether acetate 400 parts Propylene glycol monomethyl ether 150 parts γ-butyrolactone 5 parts

(Evaluation of electron beam exposure of resist composition: alkali development)
A six inch silicon wafer was treated at 90 ° C. for 60 seconds with hexamethyldisilazane on a direct hot plate. The resist composition was spin-coated on the silicon wafer such that the thickness of the composition layer was 0.04 μm. Thereafter, on a direct hot plate, the composition layer was formed by prebaking at a temperature shown in the “PB” column of Table 1 for 60 seconds. A line and space pattern was directly drawn on the composition layer formed on the wafer using an electron beam drawing machine ("HL-800D 50 keV" manufactured by Hitachi, Ltd.) and changing the exposure amount stepwise. .
After exposure, post exposure baking is performed for 60 seconds at a temperature shown in the “PEB” column of Table 1 on a hot plate, and paddle development is further performed for 60 seconds with a 2.38 mass% tetramethylammonium hydroxide aqueous solution. The resist pattern was obtained.
The obtained resist pattern (line and space pattern) was observed with a scanning electron microscope, and the exposure amount at which the line width and space width of the 60 nm line and space pattern become 1: 1 was taken as the effective sensitivity.

Line edge roughness evaluation (LER): The fluctuation width of the unevenness of the side wall surface of the resist pattern manufactured with the effective sensitivity was measured with a scanning electron microscope to obtain the line edge roughness. The results are shown in Table 2.

(Evaluation of electron beam exposure of resist composition: butyl acetate development)
A six inch silicon wafer was treated at 90 ° C. for 60 seconds with hexamethyldisilazane on a direct hot plate. The resist composition was spin-coated on the silicon wafer such that the thickness of the composition layer was 0.04 μm. Thereafter, on a direct hot plate, the composition layer was formed by prebaking at a temperature shown in the “PB” column of Table 1 for 60 seconds. A line and space pattern was directly drawn on the composition layer formed on the wafer using an electron beam drawing machine ("HL-800D 50 keV" manufactured by Hitachi, Ltd.) and changing the exposure amount stepwise. .
After exposure, post-exposure baking was performed for 60 seconds at the temperature shown in the "PEB" column of Table 1 on a hot plate. Then, a resist pattern was obtained by developing the composition layer on the silicon wafer by dynamic dispensing at 23 ° C. for 20 seconds using butyl acetate (manufactured by Tokyo Chemical Industry Co., Ltd.) as a developer. .
The obtained resist pattern (line and space pattern) was observed with a scanning electron microscope, and the exposure amount at which the line width and space width of the 60 nm line and space pattern become 1: 1 was taken as the effective sensitivity.

Line edge roughness evaluation (LER): The fluctuation width of the unevenness of the side wall surface of the resist pattern manufactured with the effective sensitivity was measured with a scanning electron microscope to obtain the line edge roughness. The results are shown in Table 3.

  A resist composition containing a resin containing a structural unit derived from the compound of the present invention is suitable for fine processing of semiconductors because it is excellent in line edge roughness (LER) of a resist pattern to be obtained, and is extremely useful industrially. .

Claims (11)

The compound represented by Formula (I).
[In the formula (I),
Each of R ¹ and R ² independently represents a hydroxy group or a group represented by any of Formula (R-1) to Formula (R-3). However, at least one of R ¹ and R ² represents a group represented by any one of Formula (R-1) to Formula (R-3).
(In the formula (R-1) to the formula (R-3),
R ³ represents a hydrogen atom or a methyl group. * Represents a bonding position to Ar ¹ or Ar ² . )
Ar ¹ represents an aromatic hydrocarbon ring having 6 to 36 carbon atoms which may have a substituent.
Ar ² represents an aromatic hydrocarbon ring having 6 to 36 carbon atoms which may have a substituent. ] The compound according to claim 1, wherein Ar ¹ is benzene which may have a substituent or naphthalene which may have a substituent. The compound according to claim 1 or 2, wherein Ar ² is benzene which may have a substituent. The group according to any one of claims 1 to 3, wherein one of R ¹ and R ² is a group represented by any one of formulas (R-1) to (R-3) and the other is a hydroxy group. Compound. The compound according to any one of claims 1 to 3, wherein one of R ¹ and R ² is a group represented by the formula (R-1), and the other is a hydroxy group.   The resin which has a structural unit derived from the compound in any one of Claims 1-5.   The resin according to claim 6, further comprising a structural unit having an acid labile group.   A resist composition comprising the resin according to claim 6 or 7 and an acid generator. The resist composition according to claim 8, wherein the acid generator comprises a salt represented by formula (B1).
[In the formula (B1),
Each of Q ^b1 and Q ^b2 independently represents a fluorine atom or a C 1 to C 6 perfluoroalkyl group.
L ^b1 represents a divalent saturated hydrocarbon group having 1 to 24 carbon atoms, and —CH ₂ — contained in the divalent saturated hydrocarbon group 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 represents a methyl group which may have a substituent or an alicyclic hydrocarbon group having 3 to 18 carbon atoms which may have a substituent, and is included in the alicyclic hydrocarbon group; CH _2- may be replaced by -O-, -S (O) ₂ -or -CO-.
Z ⁺ represents an organic cation. ]   10. The resist composition according to claim 8, further comprising a salt that generates an acid having a weaker acidity than an acid generated from an acid generator. (1) applying a resist composition according to any one of claims 8 to 10 on a substrate;
(2) drying the composition after application to form a composition layer;
(3) exposing the composition layer,
(4) heating the composition layer after exposure, and (5) developing the composition layer after heating,
A method of manufacturing a resist pattern including: