KR20140001795A - Positive-type photoresist composition for thick film, method for producing thick film resist pattern, and method for producing connection terminal - Google Patents

Abstract

Provided are a positive-type photoresist composition for a thick film, a method for producing a thick film resist pattern using the same, and a method for producing a connection terminal. The positive-type photoresist composition used for forming the thick film resist pattern on a supporter includes a resin component (A) in which the solubility for a developer is changed by actions of the acid; and an acid generator component (B) which generates acid by light exposure. The acid generator component (B) includes an acid generator (B1) which includes a compound represented by general formula (b1-1). [In the formula, Y^1 is a bivalent coupler; W is S, Se or I; R1 is a hydrocarbon having a substituent; R2 is an alkyl group with 1-5 hydrocarbons or alkoxy groups; if W=I, m+n=2; if W=S or Se, m+n=3, and m>=1, n>=0; p is 0-5; and X^- is double anion].

Description

Positive type resist composition for thick film, manufacturing method of thick film resist pattern, manufacturing method of connection terminal {POSITIVE-TYPE PHOTORESIST COMPOSITION FOR THICK FILM, METHOD FOR PRODUCING THICK FILM RESIST PATTERN, AND METHOD FOR PRODUCING CONNECTION TERMINAL}

The present invention provides a positive resist composition for a thick film containing an acid generator containing a compound useful for acid generation in a positive resist composition for a thick film, a method for producing a resist pattern and a connection terminal using the positive resist composition for a thick film. It relates to a method for producing.

Photo production is now the mainstream of precision micromachining technology. Photo production is applied to the surface of the workpiece by applying a photosensitive resin composition to form a coating film, and the coating film is patterned by photolithography technology, and the electrochemical mainly using chemical etching, electrolytic etching, or electroplating using the patterned coating film as a mask. It is a general term of the technology which manufactures various precision components, such as a semiconductor package by performing electroforming and the like.

In addition, with the recent downsizing of electronic devices, high-density packaging technology for semiconductor packages has been advanced, and package-based multi-pin thin film packaging, package size miniaturization, flip chip method, two-dimensional mounting technology, and three-dimensional mounting technology The improvement of the density is aimed at. In such a high-density mounting technique, as a connection terminal, for example, a protruding electrode (mounting terminal) such as a bump protruding on a package, a metal post connecting the redistribution line extending from a peripheral terminal on a wafer and the mounting terminal, etc. It is placed on the substrate with high accuracy.

Although resist is used for photo preparation as mentioned above, the resist composition containing an acid generator is known as a resist used for photo preparation (for example, refer patent document 1, 2). The resist generates an acid from an acid generator by irradiation (exposure), promotes diffusion of the acid by heat treatment, causes an acid catalyzed reaction with the base resin in the resin composition, and changes its alkali solubility.

Moreover, there exists a thick film resist as a resist used for photo production as mentioned above. The thick film resist is used, for example, for forming bumps or metal posts by a plating process. For example, a thick film resist layer having a thickness of about 20 μm is formed on a support, and a resist pattern is formed by selectively removing (peeling) a portion forming a bump or a metal post by exposing and developing through a predetermined mask pattern. do. Then, after the conductor (such as copper) is embedded in the removed portion (non-resist portion) by plating, bumps and metal posts can be formed by removing the resist pattern around it.

Japanese Patent Application Laid-Open No. 9-176112 Japanese Patent Application Laid-Open No. 11-52562 Japanese Patent Laid-Open No. 6-184170

As semiconductor packages become denser in the future, further densification of the protruding electrodes or metal posts is required. For this reason, when using a resist composition as a resist for thick films, in order to realize the further high density of a protruding electrode and a metal post, the resist composition for thick films which has high sensitivity of mask with high sensitivity is calculated | required.

However, when a conventional acid generator or a structural unit having an acid generating ability is used, there is still room for improvement in sensitivity and the like.

The present invention has been made in view of the above circumstances, and a positive resist composition for a thick film containing an acid generator useful for acid generation in a positive resist composition for thick films, a resist pattern forming method using the positive resist composition for thick films, and It is a subject to provide a manufacturing method of a connection terminal.

In order to solve the said subject, this invention employ | adopted the following structures.

That is, the first aspect of the present invention is a positive resist composition used for forming a thick film resist pattern on a support, wherein the resin component (A) in which the solubility in a developer changes due to the action of an acid and acid is exposed by exposure. Containing the acid generator component (B) to be generated,

The said acid generator component (B) contains the acid generator (B1) containing the compound represented by following General formula (b1-1), It is a positive resist composition for thick films.

[Wherein, Y ¹ is a divalent linking group, W is S, Se or I, R ¹ is a hydrocarbon group which may have a substituent, and R ² is a C1-C5 alkyl or alkoxy group. M + n = 2 for W = I, m + n = 3 for W = S and Se, and m ≧ 1 and n ≧ 0. p is 0-5. X ^- is a dianion.]

According to a second aspect of the present invention, there is provided a lamination step of laminating a thick film resist layer containing the positive resist composition for thick films on a support, an exposure step of selectively irradiating active light or radiation to the thick film resist layer, and the exposure step. It is a manufacturing method of the thick film resist pattern containing the developing process of developing the said thick film resist layer exposed at the process and obtaining a thick film resist pattern.

The 3rd aspect of this invention is a manufacturing method of the connection terminal including the process of forming the connection terminal which consists of a conductor in the non-resist part of the thick film resist pattern obtained using the manufacturing method of the said thick film resist pattern.

According to the present invention, a positive resist composition for a thick film containing an acid generator useful for acid generation in a positive resist composition for a thick film, a resist pattern forming method using the positive resist composition for a thick film, and a manufacturing method of a connection terminal Can be provided.

In the present specification and the claims, "aliphatic" is defined as a relative concept with respect to aromatic, meaning a group, a compound, or the like having no aromaticity.

"Alkyl group" shall contain a linear, branched, and cyclic monovalent saturated hydrocarbon group unless there is particular notice.

"Alkylene group" shall contain a linear, branched, and cyclic divalent saturated hydrocarbon group unless there is particular notice. The alkyl group in an alkoxy group is the same.

The "halogenated alkyl group" is a group in which a part or all of the hydrogen atoms of the alkyl group are substituted with halogen atoms, and examples of the halogen atom include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom.

The " fluorinated alkyl group " or " fluorinated alkylene group " refers to a group in which a part or all of the hydrogen atoms of the alkyl group or alkylene group are substituted with fluorine atoms.

A "structural unit" means the monomeric unit (monomer unit) which comprises a high molecular compound (resin, a polymer, a copolymer).

The term "structural unit derived from an acrylate ester" means a structural unit in which an ethylenic double bond of an acrylate ester is cleaved and constituted.

"Acrylic acid ester" is a compound in which the hydrogen atom at the carboxyl terminal end of acrylic acid (CH ₂ ═CH-COOH) is substituted with an organic group.

The acrylic acid ester may have a hydrogen atom bonded to the carbon atom at the? -Position thereof substituted with a substituent. The substituent (R ^α ) for substituting a hydrogen atom bonded to a carbon atom at the α position is an atom or group other than a hydrogen atom, and for example, an alkyl group having 1 to 5 carbon atoms, a halogenated alkyl group having 1 to 5 carbon atoms, a hydroxyalkyl group, or the like. Can be mentioned. In addition, the carbon atom of the (alpha) position of an acrylic acid ester is a carbon atom which the carbonyl group couple | bonds unless there is particular notice.

Hereinafter, the acrylic ester in which the hydrogen atom couple | bonded with the carbon atom of the (alpha) position was substituted by the substituent may be called (alpha) substituted acrylic ester. In some cases, an acrylic acid ester and an? -Substituted acrylic acid ester are referred to as "(? -Substituted) acrylic acid ester".

The term "structural unit derived from hydroxystyrene or hydroxystyrene derivative" means a structural unit in which an ethylenic double bond of hydroxystyrene or hydroxystyrene derivative is cleaved and constituted.

"Hydroxystyrene derivative" is taken as the concept containing the thing substituted by the other substituents, such as an alkyl group and a halogenated alkyl group, in the hydrogen position of the hydroxystyrene in the (alpha) position, and these derivatives. Examples of these derivatives include those obtained by substituting the hydrogen atom of the hydroxyl group of the hydroxystyrene which may be substituted with a hydrogen atom at the α-position with an organic group, with the benzene ring of the hydroxystyrene where the hydrogen atom at the α- , And the like. The? Position (carbon atom at?) Refers to a carbon atom to which a benzene ring is bonded unless otherwise specified.

As a substituent which substitutes the hydrogen atom of the (alpha) position of hydroxy styrene, the thing similar to what was mentioned as a substituent of the (alpha) position in the said (substituted) acrylic acid ester is mentioned.

The "structural unit derived from a vinylbenzoic acid or a vinylbenzoic acid derivative" means a structural unit in which an ethylenic double bond of a vinylbenzoic acid or a vinylbenzoic acid derivative is cleaved and constituted.

A "vinyl benzoic acid derivative" is taken as the concept containing the thing substituted by the other substituents, such as an alkyl group and a halogenated alkyl group, in the hydrogen position of the alpha position of vinyl benzoic acid, and these derivatives. As these derivatives, the hydrogen atom of the carboxy group of vinyl benzoic acid in which the hydrogen atom in the α position may be substituted with an organic group, and the hydroxyl group in the benzene ring of the vinyl benzoic acid in which the hydrogen atom in the α position may be substituted with the substituent other than the hydroxyl group and the carboxyl group The thing which the substituent of couple | bonded together etc. are mentioned. The? Position (carbon atom at?) Refers to a carbon atom to which a benzene ring is bonded unless otherwise specified.

The term " styrene " includes the concept that hydrogen atoms at the [alpha] -position of styrene and styrene are substituted with other substituents such as an alkyl group and a halogenated alkyl group.

"Constituent unit derived from styrene" and "constituent unit derived from styrene derivative" refer to a constituent unit in which an ethylene double bond of styrene or styrene derivative is formed by cleavage.

The alkyl group as the substituent at the? -Position is preferably a linear or branched alkyl group, and more specifically, an alkyl group having 1 to 5 carbon atoms such as a methyl group, an ethyl group, a propyl group, an isopropyl group, -Butyl group, pentyl group, isopentyl group, neopentyl group).

Moreover, the halogenated alkyl group as a substituent of the (alpha) position specifically, mention | raise | lifted the group which substituted one part or all the hydrogen atoms of the said "alkyl group as a substituent of the (alpha) position" by the halogen atom. Examples of the halogen atom include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom, and a fluorine atom is particularly preferable.

Moreover, the hydroxyalkyl group as a substituent of an alpha position can mention the group which substituted one part or all of the hydrogen atom of the "alkyl group as a substituent of alpha position" with a hydroxyl group specifically ,. 1-5 are preferable and, as for the number of the hydroxyl groups in this hydroxyalkyl group, 1 is the most preferable.

When it described as "which may have a substituent", and a methylene group (-CH ₂ -) When substituting the hydrogen atom (-H) groups substituted monovalent When the divalent group includes both.

&Quot; Exposure " is a concept including the entire irradiation of radiation.

The positive resist composition for thick films of this invention contains the resin component (A) which changes the solubility to a developing solution by the action of an acid, and the acid generator component (B) which generate | occur | produces an acid by exposure, The said acid It is a positive resist composition for thick films which a generator component (B) contains the acid generator (B1) containing the compound represented by following General formula (b1-1).

[Wherein, Y ¹ is a divalent linking group, W is S, Se or I, R ¹ is a hydrocarbon group which may have a substituent, and R ² is a C1-C5 alkyl or alkoxy group. M + n = 2 for W = I, m + n = 3 for W = S and Se, and m ≧ 1 and n ≧ 0. p is 0-5. X ^- is a dianion.]

≪ Resin component (A) >

It does not specifically limit as a resin component (A) which changes the solubility to alkali by the action of an acid, Any resin which changes solubility to an alkali by the action of an acid can be used. Among them, it is preferable to contain at least one resin selected from the group consisting of a novolac resin (Anv1), a polyhydroxystyrene resin (Aphs1) and an acrylic resin (Aac1).

The resin component (A) includes an acid-decomposable group whose polarity changes by the action of an acid.

An "acid-decomposable group" is a group having an acid-decomposable property that at least part of the bonds in the structure of the acid-decomposable group can cleave by the action of an acid.

As an acid-decomposable group in which polarity increases by the action of an acid, the group which decomposes by the action of an acid and produces | generates a polar group is mentioned, for example.

Examples of the polar group include a carboxy group, a hydroxyl group, an amino group, and a sulfo group (-SO ₃ H). Among these, a polar group (hereinafter sometimes referred to as an "OH-containing polar group") in the structure is preferable, a carboxyl group or a hydroxyl group is preferable, and a carboxyl group is particularly preferable.

As an acid-decomposable group, the group by which the said polar group was protected by the acid dissociable group (for example, the group which protected the hydrogen atom of the OH containing polar group by the acid dissociable group) is mentioned.

The term " acid dissociable group "

(i) a group having an acid-dissociable property by which the bond between the acid dissociable group and an atom adjacent to the acid dissociable group can be cleaved by the action of an acid, or

(ii) refers to both the groups capable of cleaving the bond between the acid dissociable group and an atom adjacent to the acid dissociable group by cleaving a portion of the bond by the action of the acid, and then further decarbonizing reaction. .

The acid dissociable group constituting the acid-decomposable group is required to be a group having a lower polarity than the polar group produced by dissociation of the acid dissociable group, whereby when the acid dissociable group dissociates due to the action of the acid, A polar group having a polarity higher than that of a dissociative group is generated to increase the polarity. As a result, the polarity of the entire component (A1) increases. As the polarity increases, the solubility in the developer relatively changes. When the developer is an alkaline developer, the solubility increases. When the developer is an organic developer, the solubility decreases.

It does not specifically limit as an acid dissociable group, The thing currently proposed as an acid dissociable group of the base resin for chemically amplified resist can be used.

As an acid dissociable group which protects a carboxyl group or a hydroxyl group among the said polar groups, the acid dissociable group represented by the following general formula (a1-r-1) (hereinafter, may be called "acetal type acid dissociable group"). ).

[Wherein, Ra ^'1, Ra' ² is a hydrogen atom or an alkyl group, Ra ^'3 is a hydrocarbon group Ra' is ³ to form a ring in combination with any one of ^{Ra '1, Ra' 2.} ]

In formula (a1-r-1), at least one of Ra ' ¹ and Ra' ² is preferably a hydrogen atom, and more preferably both are hydrogen atoms.

When Ra ' ¹ or Ra' ² is an alkyl group, examples of the alkyl group include the same alkyl groups as the substituents which may be bonded to a carbon atom in the α-position in the description of the α-substituted acrylic acid ester, and each having 1 to 5 carbon atoms. Alkyl groups are preferred. Specifically, straight chain or branched chain alkyl groups such as methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, tert-butyl, pentyl, isopentyl and neopentyl groups And a methyl group or an ethyl group is preferable, and a methyl group is particularly preferable.

In formula (a1-r-1), a hydrocarbon group of Ra ' ³ includes a linear, branched or cyclic alkyl group. The straight-chain alkyl group preferably has 1 to 5 carbon atoms, more preferably 1 to 4 carbon atoms, and even more preferably 1 or 2 carbon atoms. Specific examples include methyl, ethyl, n-propyl, n-butyl and n-pentyl. Among them, a methyl group, an ethyl group or an n-butyl group is preferable, and a methyl group or an ethyl group is more preferable.

The branched alkyl group preferably has 3 to 10 carbon atoms, more preferably 3 to 5 carbon atoms. Specifically, isopropyl, isobutyl, tert-butyl, isopentyl, neopentyl and the like are preferable, and an isopropyl group is most preferable.

The cyclic alkyl group preferably has 3 to 20 carbon atoms, more preferably 4 to 12 carbon atoms. Specifically, monocycloalkane such as cyclopentane, cyclohexane, etc., or a group excluding at least one hydrogen atom from a polycycloalkane such as adamantane, norbornane, isoborane, tricyclodecane, or tetracyclododecane, . A part of the carbon atoms constituting the ring of the cyclic alkyl group may be substituted with an etheric oxygen atom (-O-).

When Ra ' ³ is bonded to any one of Ra' ¹ and Ra ' ² to form a ring, the ring is preferably a 4- to 7-membered ring, and more preferably a 4- to 6-membered ring. Specific examples of the cyclic group include a tetrahydropyranyl group, a tetrahydrofuranyl group, and the like.

Examples of the acid dissociable group for protecting the carboxyl group among the polar groups include an acid dissociable group represented by the following general formula (a1-r-2) (acid dissociation represented by the following formula (a1-r-2) Among these groups, those constituted by an alkyl group are hereinafter referred to as " tertiary alkyl ester-type acid-dissociable group " for convenience).

[Wherein, Ra ' ⁴ to Ra' ⁶ are each a hydrocarbon group, and Ra ' ⁵ and Ra' ⁶ may be bonded to each other to form a ring.]

Examples of the hydrocarbon group of Ra ' ⁴ to Ra' ⁶ include the same groups as those of Ra ' ³ above.

Ra ' ⁴ is preferably an alkyl group having 1 to 5 carbon atoms. When Ra ' ⁵ and Ra' ⁶ are bonded to each other to form a ring, the group represented by the following general formula (a1-r2-1) may be mentioned. On the other hand, when Ra ' ⁴ to Ra' ⁶ do not bond with each other and are independent hydrocarbon groups, groups represented by the following general formula (a1-r2-2) are mentioned.

[Wherein, Ra represents a hydrocarbon group, each is ¹² ~ Ra ^'14' group, Ra to form an aliphatic cyclic group together with the carbon atom of ¹⁰ combines' ¹⁰ is an alkyl group, Ra of 1 to 10 carbon atoms, ¹¹ is Ra independently .]

Equation (a1-r2-1) of, Ra 'group having a carbon number of alkyl group of from 1 to 10 of ¹⁰ the formula (a1-r-1) Ra of the "preferred is either a straight chain or branched chain alkyl of ³ . Equation (a1-r2-1) of, Ra 'cycloaliphatic group to the ¹¹ configurations of Ra in the formula (a1-r-1)' is preferably an alkyl group as any of the ^three annular.

In formula (a1-r2-2), Ra ^'12 and Ra' ¹⁴ are each independently an alkyl group having 1 to 10 carbon atoms, and the alkyl group is selected from Ra ' ³ in formula (a1-r-1). The group mentioned as a linear or branched alkyl group is more preferable, It is still more preferable that it is a C1-C5 linear alkyl group, It is especially preferable that it is a methyl group or an ethyl group.

In the formula (a1-r2-2), Ra is preferably a ^"13 expression (a1-r-1) Ra of the" alkyl group having a straight chain, branched chain or cyclic hydrocarbon group exemplified as the group of ^three. Among them, it is more preferable that the group is a group which is used as a cyclic alkyl group of Ra ' ³ .

Specific examples of the formula (a1-r2-1) are shown below.

Specific examples of the formula (a1-r2-2) are shown below.

Examples of the acid dissociable group for protecting the hydroxyl group in the polar group include an acid dissociable group represented by the following general formula (a1-r-3) (hereinafter referred to as " tertiary alkyloxycarbonyl acid dissociable group &Quot;).

Wherein Ra ' ⁷ to Ra' ⁹ each represent an alkyl group.

In the formula (a1-r-3), the Ra ' ⁷ to Ra' ⁹ groups are preferably an alkyl group having 1 to 5 carbon atoms, more preferably 1 to 3.

The total number of carbon atoms of each alkyl group is preferably from 3 to 7, more preferably from 3 to 5, and most preferably from 3 to 4.

[Acrylic resin (Aac1)]

As the acrylic resin (Aac1), resins containing the structural units represented by the following general formulas (a1-1) to (a1-2) can be used.

[In formula, R is a hydrogen atom, a C1-C5 alkyl group, or a C1-C5 halogenated alkyl group. Va ¹ is a divalent hydrocarbon group which may have an ether bond, a urethane bond, or an amide bond, n _a1 is each independently 0 to 2, and Ra ¹ is the formulas (a1-r-1) to (a1-r). It is an acid dissociable group represented by -2). Wa ¹ is an n _a2 + monovalent hydrocarbon group, n _a2 is 1-3, and Ra ² is an acid dissociable group represented by the formula (a1-r-1) or (a1-r-3).]

In the formula (a1-1), the alkyl group having 1 to 5 carbon atoms is preferably a linear or branched alkyl group, and specifically, a methyl group, an ethyl group, a propyl group, an isopropyl group, Butyl group, pentyl group, isopentyl group, neopentyl group and the like. The halogenated alkyl group having 1 to 5 carbon atoms is a group in which a part or all of the hydrogen atoms of the alkyl group having 1 to 5 carbon atoms is substituted with a halogen atom. Examples of the halogen atom include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom, and a fluorine atom is particularly preferable.

R is preferably a hydrogen atom, an alkyl group having 1 to 5 carbon atoms or a fluorinated alkyl group having 1 to 5 carbon atoms, and most preferably a hydrogen atom or a methyl group because of industrial availability.

The divalent hydrocarbon group of Va ^{1 may be} an aliphatic hydrocarbon group or an aromatic hydrocarbon group. An aliphatic hydrocarbon group means a hydrocarbon group having no aromaticity. The aliphatic hydrocarbon group as the divalent hydrocarbon group in Va ¹ may be saturated or unsaturated, and is preferably saturated.

More specific examples of the aliphatic hydrocarbon group include a linear or branched aliphatic hydrocarbon group or an aliphatic hydrocarbon group containing a ring in its structure.

The roneun Va ¹ may be mentioned groups wherein the divalent hydrocarbon group bonded via an ether bond, a urethane bond, or amide bond.

The straight-chain or branched-chain aliphatic hydrocarbon group preferably has 1 to 10 carbon atoms, more preferably 1 to 6 carbon atoms, further preferably 1 to 4 carbon atoms, and most preferably 1 to 3 carbon atoms.

The aliphatic hydrocarbon group in a straight chain is preferably an alkylene group of a straight chain, particularly a methylene group [-CH ₂ -], an ethylene group _{[- (CH 2) 2 -} ], a trimethylene group [- (CH _{2) 3} -], tetramethylene group [- (CH ₂ ) ₄ -], pentamethylene group [- (CH ₂ ) ₅ -] and the like.

As the branched aliphatic hydrocarbon group, a branched alkylene group is preferable, and specifically -CH (CH ₃ )-, -CH (CH ₂ CH ₃ )-, -C (CH ₃ ) _2- , -C (CH Alkyl methylene groups such as ₃ ) (CH ₂ CH ₃ )-, -C (CH ₃ ) (CH ₂ CH ₂ CH ₃ )-, and -C (CH ₂ CH ₃ ) ₂ -;-CH (CH ₃ ) CH ₂ -, -CH (CH ₃ ) CH (CH ₃ )-, -C (CH ₃ ) ₂ CH _2- , -CH (CH ₂ CH ₃ ) CH _2- , -C (CH ₂ CH ₃ ) ₂ -CH ₂ Alkyl ethylene groups such as -CH (CH ₃ ) CH ₂ CH _2- , alkyltrimethylene groups such as -CH ₂ CH (CH ₃ ) CH ₂ -;-CH (CH ₃ ) CH ₂ CH ₂ CH _2- And alkylalkylene groups such as alkyltetramethylene groups such as -CH ₂ CH (CH ₃ ) CH ₂ CH ₂ -and the like. As an alkyl group in an alkylalkylene group, a C1-C5 linear alkyl group is preferable.

The aliphatic hydrocarbon group containing a ring in the above structure includes an alicyclic hydrocarbon group (a group excluding two hydrogen atoms from an aliphatic hydrocarbon ring), and an alicyclic hydrocarbon group bonded to an end of an aliphatic hydrocarbon group which is linear or branched, or alicyclic The group etc. which the hydrocarbon group interposes in the middle of the linear or branched aliphatic hydrocarbon group are mentioned. Examples of the straight chain or branched chain aliphatic hydrocarbon group include the same ones as described above.

The alicyclic hydrocarbon group preferably has 3 to 20 carbon atoms, more preferably 3 to 12 carbon atoms.

The alicyclic hydrocarbon group may be polycyclic or monocyclic. The monocyclic alicyclic hydrocarbon group is preferably a group in which two hydrogen atoms are removed from the monocycloalkane. The monocycloalkane preferably has 3 to 6 carbon atoms, and specific examples thereof include cyclopentane, cyclohexane, and the like. As a polycyclic alicyclic hydrocarbon group, the group remove | excluding two hydrogen atoms from polycycloalkane is preferable, The thing of C7-12 is preferable as this polycycloalkane, Specifically, adamantane, norbornane, and isobornane , Tricyclodecane, tetracyclododecane and the like.

The aromatic hydrocarbon group is a hydrocarbon group having an aromatic ring.

The aromatic hydrocarbon group as the divalent hydrocarbon group in Va ¹ preferably has 3 to 30 carbon atoms, more preferably 5 to 30 carbon atoms, still more preferably 5 to 20 carbon atoms, particularly preferably 6 to 15 carbon atoms, 10 is most preferable. However, this carbon number shall not contain carbon number in a substituent.

As an aromatic ring which an aromatic hydrocarbon group has, Specifically, Aromatic hydrocarbon ring, such as benzene, biphenyl, fluorene, naphthalene, anthracene, phenanthrene; The aromatic heterocycle in which some carbon atoms which comprise the said aromatic hydrocarbon ring were substituted by the hetero atom; Etc. can be mentioned. Examples of the heteroatom in the aromatic heterocycle include an oxygen atom, a sulfur atom and a nitrogen atom.

Specifically as an aromatic hydrocarbon group, group which removed two hydrogen atoms from the said aromatic hydrocarbon ring (arylene group); One of the hydrogen atoms of the group (aryl group) which removed one hydrogen atom from the said aromatic hydrocarbon ring is substituted by the alkylene group A hydrogen atom is selected from an aryl group in an arylalkyl group such as a group (for example, a benzyl group, a phenethyl group, a 1-naphthylmethyl group, a 2-naphthylmethyl group, a 1-naphthylethyl group, or a 2-naphthylethyl group). The group which removed 2 more; The group which removed two hydrogen atoms from the aromatic compound (for example, biphenyl, fluorene, etc.) containing two or more aromatic rings; etc. are mentioned. The number of carbon atoms of the alkylene group (alkyl chain in the arylalkyl group) is preferably 1 to 4, more preferably 1 to 2, and particularly preferably 1.

In the formula (a1-2), the n _a2 + monovalent hydrocarbon group in Wa ^{1 may} be an aliphatic hydrocarbon group or an aromatic hydrocarbon group. This aliphatic hydrocarbon group means a hydrocarbon group having no aromaticity, may be saturated or unsaturated, and is preferably saturated. Examples of the aliphatic hydrocarbon group include a straight chain or branched chain aliphatic hydrocarbon group, an aliphatic hydrocarbon group containing a ring in the structure, or a combination of a straight chain or branched aliphatic hydrocarbon group and an aliphatic hydrocarbon group containing a ring in the structure , Specifically, the same group as Va ¹ in the above-mentioned formula (a1-1).

The n _a2 + 1 is preferably 2 to 4, more preferably 2 or 3.

As the formula (a1-2), a constituent unit represented by the following general formula (a1-2-01) is particularly preferable.

In the formulas (a1-2-01), Ra ² is an acid-dissociable group represented by the formula (a1-r-1) or (a1-r-3). n _a2 is an integer of 1 to 3, preferably 1 or 2, more preferably 1. c is an integer of 0 to 3, preferably 0 or 1, more preferably 1. R is the same as above.

Specific examples of the formula (a1-1) are shown below. In each of the following formulae, R ^alpha is a hydrogen atom, a methyl group or a trifluoromethyl group.

Specific examples of the formula (a1-2) are shown below.

In addition, the acrylic resin (Aac1) consists of a copolymer containing the structural unit derived from the polymeric compound which has an ether bond further with respect to the structural unit represented by the said General Formula (a1-1)-(a1-2). It is preferable that it is resin.

Examples of the polymerizable compound having an ether bond include radical polymerizable compounds such as a (meth) acrylic acid derivative having an ether bond and an ester bond, and specific examples thereof include 2-methoxyethyl (meth) acrylate and 2- Ethoxyethyl (meth) acrylate, methoxytriethylene glycol (meth) acrylate, 3-methoxybutyl (meth) acrylate, ethylcarbitol (meth) acrylate, phenoxy polyethylene glycol (meth) acrylate, Methoxy polypropylene glycol (meth) acrylate, tetrahydrofurfuryl (meth) acrylate, and the like. Moreover, the polymeric compound which has the said ether bond becomes like this. Preferably it is 2-methoxyethyl (meth) acrylate, 2-ethoxyethyl (meth) acrylate, and methoxy triethylene glycol (meth) acrylate. These polymerizable compounds may be used independently or may be used in combination of 2 or more type.

The acrylic resin (Aac1) may contain another polymerizable compound as a constituent unit for the purpose of appropriately controlling the physical and chemical properties. Examples of such a polymerizable compound include a known radical polymerizable compound and an anionic polymerizable compound. Examples of such a polymerizable compound include monocarboxylic acids such as acrylic acid, methacrylic acid and crotonic acid, dicarboxylic acids such as maleic acid, fumaric acid and itaconic acid, and 2-methacryloyloxyethylsuccinic acid , Methacrylic acid derivatives having a carboxyl group and an ester bond such as 2-methacryloyloxyethyl maleic acid, 2-methacryloyloxyethyl phthalic acid and 2-methacryloyloxyethyl hexahydrophthalic acid, methyl methacrylate (Meth) acrylates such as 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate and the like; (Meth) acrylic acid hydroxyalkyl esters, (meth) acrylic acid aryl esters such as phenyl (meth) acrylate and benzyl (meth) acrylate, dicarboxylic acid diesters such as diethyl maleate and dibutyl fumarate, Tere; vinyl group-containing aromatic compounds such as styrene, α-methylstyrene, chlorostyrene, chloromethylstyrene, vinyltoluene, hydroxystyrene, α-methylhydroxystyrene and α-ethylhydroxystyrene; vinyl acetate Vinyl group-containing aliphatic compounds; conjugated diolefins such as butadiene and isoprene; nitrile group-containing polymerizable compounds such as acrylonitrile and methacrylonitrile; chlorine-containing polymerizable compounds such as vinyl chloride and vinylidene chloride; acryl Amide bond containing polymeric compounds, such as an amide and methacrylamide; These etc. are mentioned.

(Constituent unit (a4))

The acrylic resin (Aac1) may further have a structural unit (a4) containing an acid non-ring cyclic group as necessary. (Aac1) has the structural unit (a4), it is considered that the dry etching resistance of the formed resist pattern is improved.

The "acid non-labile cyclic group" in a structural unit (a4) is a cyclic group which remains in the said structural unit as it is, without dissociating even if this acid acts when an acid generate | occur | produces from (B) component by exposure.

As the structural unit (a4), for example, a structural unit derived from an acrylate ester containing an acid-labile aliphatic cyclic group is preferable. This cyclic group can illustrate the same thing as what was illustrated in the case of said acrylic resin (Aac1), for example, and many things conventionally known as being used for the resin component of a resist composition can be used.

Especially at least 1 sort (s) chosen from a tricyclodecyl group, an adamantyl group, a tetracyclo dodecyl group, an isobonyl group, and a norbornyl group is preferable at the point of being easy to obtain industrially. These polycyclic groups may have a linear or branched alkyl group having 1 to 5 carbon atoms as a substituent.

Specific examples of the acrylic resin (Aac1) include those having the structures represented by the following general formulas (a4-1) to (a4-7).

[Wherein R ^? Is as defined above].

The number of the structural units (a4) contained in the resin component (A1) may be one or two or more.

When the constituent unit (a4) is contained in the resin component (A1), the proportion of the constituent unit (a4) is preferably from 1 to 30 mol%, more preferably from 10 to 10 mol% based on the total constituent units constituting the component (A1) By mole to 20% by mole.

It is preferable to use acrylic resin (Aac1) among the said resin component (A). Among such acrylic resins (Aac1), structural units represented by the general formula (a1-1), structural units derived from (meth) acrylic acid, structural units derived from (meth) acrylic acid alkyl esters, and (meth) acrylic acid aryl It is preferable that it is a copolymer which has a structural unit derived from esters.

Such a copolymer is preferably a copolymer represented by the following general formula (a8).

In said general formula (a8), Ra <^30> represents a hydrogen atom or a methyl group, Ra <^31> represents a C2-C4 linear or branched alkyl group, and Xa is a C5-C20 compound with the carbon atom to which it is couple | bonded. A hydrocarbon ring is formed, Ra ³² represents a linear or branched alkyl group having 1 to 6 carbon atoms or an alkoxy alkyl group having 1 to 6 carbon atoms, and Ra ³³ represents an aryl group having 6 to 12 carbon atoms.

And X &lt; a &gt; together with the carbon atoms to which they are attached form an aliphatic cyclic group having 5 to 20 carbon atoms. Specific examples of such aliphatic cyclic groups include groups in which at least one hydrogen atom is removed from a polycycloalkane such as a monocycloalkane, bicycloalkane, tricycloalkane, or tetracycloalkane. Specific examples include monocycloalkanes such as cyclopentane, cyclohexane, cycloheptane, and cyclooctane, and polycycloalkanes such as adamantane, norbornane, isoborane, tricyclodecane, and tetracyclododecane, And a group excluding an atom. In particular, group (you may further have a substituent) remove | excluding one or more hydrogen atoms from cyclohexane and adamantane is preferable.

When the aliphatic cyclic group of Xa has a substituent on the ring skeleton, examples of the substituent include a polar group such as a hydroxyl group, a carboxy group, a cyano group and an oxygen atom (= O), a straight chain or branched chain having 1 to 4 carbon atoms Lt; / RTI &gt; As the polar group, an oxygen atom (= O) is particularly preferable.

In addition, in the copolymer represented by the said general formula (a8), s, t, u, v represent the molar ratio of each structural unit, s is 8-45 mol%, t is 10-65 mol%, u is 3-25 mol%, v is 6-25 mol%.

[Novolac resin (Anv1)]

As the novolak resin (Anv1), a resin containing a constituent unit represented by the following formula (anv1) may be used.

[Wherein Ra ¹¹ is an acid dissociable group, and Ra ¹² and Ra ¹³ are each independently a hydrogen atom or an alkyl group having 1 to 6 carbon atoms.]

Wherein the general formula (anv1), Ra ¹¹ represents an acid dissociable, Ra ^12, Ra ¹³ represents a hydrogen atom or an alkyl group having 1 to 6 carbon atoms independently. Ra ¹¹ is a group represented by general formula (a1-r-1) or (a1-r-3), a linear, branched, or cyclic alkyl group having 1 to 6 carbon atoms, tetrahydropyranyl group, tetrafuranyl group, Or a trialkylsilyl group.

The said C1-C6 alkyl group is a C1-C6 linear, branched, or cyclic alkyl group, for example. Examples of the linear or branched alkyl group include methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, tert-butyl, pentyl, , Examples of the alkyl group include a cyclopentyl group and a cyclohexyl group.

[Polyhydroxystyrene resin (Aphs1)]

As the polyhydroxystyrene resin (Aphs1), a resin containing a constitutional unit represented by the following formula (aphs1) can be used.

Wherein Ra ¹⁸ is a hydrogen atom or an alkyl group having 1 to 6 carbon atoms, and Ra ¹⁹ is an acid dissociable group.

Wherein the general formula (aphs1), Ra ¹⁸ represents a hydrogen atom or an alkyl group having a carbon number of 1 ~ 6, Ra ¹⁹ represents an acid dissociable, dissolution inhibiting group.

In the above general formula (aphs1), Ra ¹⁹ and Ra may be the same groups ¹¹ in the formula (anv1).

The said C1-C6 alkyl group is a C1-C6 linear, branched, or cyclic alkyl group, for example. Examples of the linear or branched alkyl group include methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, tert-butyl, pentyl, , Examples of the alkyl group include a cyclopentyl group and a cyclohexyl group.

In addition, the polyhydroxystyrene resin (Aphs1) may contain other polymerizable compounds as structural units for the purpose of appropriately controlling physical and chemical properties. Examples of such a polymerizable compound include a known radical polymerizable compound and an anionic polymerizable compound. Moreover, as such a polymeric compound, For example, monocarboxylic acids, such as acrylic acid, methacrylic acid, and crotonic acid; Dicarboxylic acids, such as maleic acid, a fumaric acid, and itaconic acid; 2-methacryloyloxy ethyl succinic acid; Methacrylic acid derivatives having a carboxyl group and an ester bond such as 2-methacryloyloxyethyl maleic acid, 2-methacryloyloxyethyl phthalic acid and 2-methacryloyloxyethylhexahydrophthalic acid; methyl (meta (Meth) acrylic acid alkyl esters such as) acrylate, ethyl (meth) acrylate, and butyl (meth) acrylate; 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, and the like. (Meth) acrylic acid hydroxyalkyl esters; (meth) acrylic acid aryl esters such as phenyl (meth) acrylate and benzyl (meth) acrylate; dicarboxylic acid diesters such as diethyl maleate and dibutyl fumarate Vinyl group-containing aromatic compounds such as styrene, α-methylstyrene, chlorostyrene, chloromethylstyrene, vinyltoluene, hydroxystyrene, α-methylhydroxystyrene and α-ethylhydroxystyrene; vinyl such as vinyl acetate Group-containing aliphatic compounds; conjugated diolefins such as butadiene and isoprene; nitrile group-containing polymerizable compounds such as acrylonitrile and methacrylonitrile; chlorine-containing polymerizable compounds such as vinyl chloride and vinylidene chloride; acrylamide And amide bond-containing polymerizable compounds such as methacrylamide; and the like.

As the resin component (A), a novolak resin (Anv1) and a polyhydroxystyrene resin (Aphs1) may be used in combination with an acrylic resin (Aac1). In this case, the proportion of the acrylic resin in the total of these resins is 5 to 100. It is preferable that it is mass%, It is more preferable that it is 50-100 mass%, It is still more preferable that it is 100 mass%.

The mass average molecular weight of the resin component (A) in terms of polystyrene is preferably 5,000 to 300,000, more preferably 7,000 to 200,000, and still more preferably 10,000 to 200,000. By setting it as such a mass average molecular weight, sufficient intensity | strength of a thick film resist layer can be maintained without peeling property with a support body, and expansion of a profile and the generation of a crack at the time of plating can be prevented.

The resin component (A) is preferably a resin having a degree of dispersion of 1.05 or more. Here, a dispersion degree is the value which divided | diluted the mass mean molecular weight by the number average molecular weight. By such a dispersion, it is possible to avoid the stress tolerance against the desired plating and the problem that the metal layer obtained by the plating treatment is liable to expand.

It is preferable that content of a resin component (A) is 5-60 mass% with respect to the total mass of the resist composition which concerns on this invention, More preferably, it is 20-60 mass%, More preferably, it is 30-50 mass%.

&Lt; Alkali-soluble resin (C) &gt;

It is preferable that the positive type resist composition for thick films of this invention contains alkali-soluble resin (C) further in order to improve crack resistance. Here, with alkali-soluble resin, the resin film of 1 micrometer in thickness is formed on the board | substrate with the resin solution (solvent: propylene glycol monomethyl ether acetate) of 20 mass% of resin concentration, and it is immersed for 1 minute in 2.38 mass% TMAH aqueous solution. When it says, it melt | dissolves 0.01 micrometer or more. The alkali-soluble resin (C) is preferably at least one resin selected from the group consisting of a novolak resin (Cnv1), a polyhydroxystyrene resin (Cphs1) and an acrylic resin (Cac1).

[Novolac resin (Cnv1)]

Novolak resin (Cnv1) is obtained by addition condensation of, for example, an aromatic compound having a phenolic hydroxyl group (hereinafter simply referred to as "phenols") and aldehydes under an acid catalyst.

Examples of the phenols include phenol, o-cresol, m-cresol, p-cresol, o-ethylphenol, m-ethylphenol, p-ethylphenol, o-butylphenol, m-butylphenol and p-butyl Phenol, 2,3-xylenol, 2,4-xylenol, 2,5-xylenol, 2,6-xylenol, 3,4-xylenol, 3,5-xylenol, 2,3,5-trimethylphenol, 3,4,5-trimethylphenol, p-phenylphenol, resorcinol, hydroquinone, hydroquinone monomethyl ether, pyrogarol, proroglycinol, hydroxydiphenyl, bisphenol A, gallic acid, a gallic acid ester, (alpha)-naphthol, (beta) -naphthol, etc. are mentioned.

The aldehydes include, for example, formaldehyde, furfural, benzaldehyde, nitrobenzaldehyde, acetaldehyde and the like.

Although the catalyst at the time of addition condensation reaction is not specifically limited, For example, hydrochloric acid, nitric acid, sulfuric acid, formic acid, oxalic acid, acetic acid etc. are used as an acid catalyst.

In addition, by using o-cresol, it is possible to further improve the flexibility of the novolak resin by substituting a hydrogen atom of the hydroxyl group in the resin with another substituent or by using bulky aldehydes.

The novolak resin (Cnv1) preferably has a mass average molecular weight of 1,000 to 50,000.

[Polyhydroxystyrene resin (Cphs1)]

P-hydroxy styrene, (alpha) -methylhydroxy styrene, (alpha)-ethylhydroxy styrene etc. are mentioned as a hydroxy styrene type compound which comprises polyhydroxy styrene resin (Cphs1).

Moreover, it is preferable to make polyhydroxy styrene resin (Cphs1) into a copolymer with a styrene resin. Examples of the styrene compounds constituting such styrene resins include styrene, chlorostyrene, chloromethylstyrene, vinyltoluene, and α-methylstyrene.

The weight average molecular weight of the polyhydroxystyrene resin (Cphs1) is preferably 1,000 to 50,000.

[Acrylic resin (Cac1)]

The acrylic resin (Cac1) preferably contains a constituent unit derived from a polymerizable compound having an ether bond and a constituent unit derived from a polymerizable compound having a carboxyl group.

Examples of the polymerizable compound having an ether bond include 2-methoxyethyl (meth) acrylate, methoxy triethylene glycol (meth) acrylate, 3-methoxybutyl (meth) acrylate, ethylcarbitol (Meth) acrylic acid derivatives having an ether bond and an ester bond such as phenoxypolyethylene glycol (meth) acrylate, methoxypolypropylene glycol (meth) acrylate, tetrahydrofurfuryl (meth) acrylate and the like . The polymerizable compound having an ether bond is preferably 2-methoxyethyl acrylate, methoxy triethylene glycol acrylate. These polymerizable compounds may be used independently or may be used in combination of 2 or more type.

Examples of the polymerizable compound having a carboxyl group include monocarboxylic acids such as acrylic acid, methacrylic acid and crotonic acid; dicarboxylic acids such as maleic acid, fumaric acid and itaconic acid; 2-methacryloyloxyethyl succinic acid and 2-metha; The compound which has carboxyl groups and ester bonds, such as a chryloyl oxyethyl maleic acid, 2-methacryloyl oxyethyl phthalic acid, and 2-methacryloyl oxyethyl hexahydrophthalic acid; etc. can be illustrated. The polymerizable compound having a carboxyl group is preferably acrylic acid or methacrylic acid. These polymerizable compounds may be used independently or may be used in combination of 2 or more type.

The mass average molecular weight of the acrylic resin (Cac1) is preferably 50,000 to 800,000.

The content of the alkali-soluble resin (C) is preferably 5 to 200 parts by mass, more preferably 10 to 180 parts by mass, per 100 parts by mass of the resin component (A). When the content of the alkali-soluble resin (C) is 5 parts by mass or more with respect to 100 parts by mass of the resin component (A), the crack resistance can be improved. When the content is 200 parts by mass or less, have.

In addition, when using alkali-soluble resin (C), it is preferable to use novolak resin (Cnv1) and polyhydroxy styrene resin (Cphs1) in combination with the said acrylic resin (Aac1). In this case, the proportion of the acrylic resin in the total of these resins is preferably 5 to 80 mass%, more preferably 10 to 70 mass%, and even more preferably 10 to 40 mass%. The proportion of the novolac resin is preferably 5 to 80 mass%, more preferably 20 to 70 mass%, still more preferably 45 to 65 mass%. The proportion of the polyhydroxystyrene resin is preferably 5 to 60 mass%, more preferably 5 to 35 mass%, and still more preferably 5 to 30 mass%. By setting the ratio to the above range, the acid generator can be more uniformly dispersed in the thick film resist layer.

&Lt; Acid Generator Component: Component (B) &gt;

The positive resist composition for thick films of this invention contains the acid generator component (B) (henceforth (B) component) which generate | occur | produces an acid by exposure. In addition, an acid generator component (B) contains the acid generator (B1) containing the compound represented by the following general formula (b1-1).

[Wherein, Y ¹ is a divalent linking group, W is S, Se or I, R ¹ is a hydrocarbon group which may have a substituent, and R ² is a C1-C5 alkyl or alkoxy group. In the case of W = I, m + n = 2, in the case of W = S and Se, m + n = 3, and m≥1 and n≥0. p is 0-5. X ^- is a dianion.]

In General Formula (b1-1), Y ¹ is a divalent linking group. Although it does not specifically limit as a bivalent coupling group of Y <^1> , The bivalent hydrocarbon group which may have a substituent, the bivalent coupling group containing a hetero atom, etc. are mentioned.

(Bivalent hydrocarbon group which may have a substituent)

The hydrocarbon group as a divalent linking group may be an aliphatic hydrocarbon group or an aromatic hydrocarbon group.

The aliphatic hydrocarbon group means a hydrocarbon group having no aromaticity. This aliphatic hydrocarbon group may be saturated or unsaturated, and it is preferable that it is normally saturated.

The aliphatic hydrocarbon group and the like aliphatic hydrocarbon group containing a ring in the structure of the aliphatic hydrocarbon group or straight-chain or branched-chain, specifically exemplified by Va ¹ in the above-described formula (a1-1) a group Can be mentioned.

The straight chain or branched chain aliphatic hydrocarbon group may or may not have a substituent. Examples of the substituent include a fluorine atom, a fluorinated alkyl group having 1 to 5 carbon atoms substituted with a fluorine atom, and a carbonyl group.

The aliphatic hydrocarbon group containing a ring in the above structure includes a cyclic aliphatic hydrocarbon group (group excluding two hydrogen atoms from the aliphatic hydrocarbon ring) which may include a substituent containing a hetero atom in the ring structure, and the cyclic aliphatic hydrocarbon group is directly The group couple | bonded with the terminal of a linear or branched aliphatic hydrocarbon group, the group which the said cyclic aliphatic hydrocarbon group interposes in the middle of a linear or branched aliphatic hydrocarbon group, etc. are mentioned. Examples of the straight chain or branched chain aliphatic hydrocarbon group include the same ones as described above.

The cyclic aliphatic hydrocarbon group preferably has 3 to 20 carbon atoms, more preferably 3 to 12 carbon atoms.

Specific examples of the cyclic aliphatic hydrocarbon group include groups exemplified by Va ¹ in formula (a1-1) described above.

The cyclic aliphatic hydrocarbon group may or may not have a substituent. Examples of the substituent include an alkyl group, an alkoxy group, a halogen atom, a halogenated alkyl group, a hydroxyl group, and a carbonyl group.

The alkyl group as the substituent is preferably an alkyl group having 1 to 5 carbon atoms, and most preferably a methyl group, an ethyl group, a propyl group, an n-butyl group or a tert-butyl group.

The alkoxy group as the substituent is preferably an alkoxy group having 1 to 5 carbon atoms, more preferably a methoxy group, an ethoxy group, an n-propoxy group, an isopropoxy group, a n-butoxy group or a tert- The ethoxy group is most preferred.

Examples of the halogen atom as the substituent include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom, and a fluorine atom is preferable.

Examples of the halogenated alkyl group as the substituent include groups in which a part or all of the hydrogen atoms of the alkyl group are substituted with the halogen atom.

The cyclic aliphatic hydrocarbon group may be substituted with a substituent in which part of the carbon atoms constituting the ring structure contains a hetero atom. The substituent containing the hetero atom is preferably -O-, -C (= O) -O-, -S-, -S (= O) _2- or -S (= O) ₂ -O-.

An aromatic hydrocarbon group as the divalent hydrocarbon group is specifically exemplified by Va may be the group ¹ in the above-described formula (a1-1).

The hydrogen atom which the said aromatic hydrocarbon group has may be substituted by the said aromatic hydrocarbon group by the substituent. For example, the hydrogen atom bonded to the aromatic ring in the aromatic hydrocarbon group may be substituted with a substituent.

Examples of the substituent include an alkyl group, an alkoxy group, a halogen atom, a halogenated alkyl group, and a hydroxyl group.

The alkyl group as the substituent is preferably an alkyl group having 1 to 5 carbon atoms, and most preferably a methyl group, an ethyl group, a propyl group, an n-butyl group or a tert-butyl group.

Examples of the alkoxy group, halogen atom and halogenated alkyl group as the substituent include those exemplified as substituents for substituting the hydrogen atom of the cyclic aliphatic hydrocarbon group.

(A divalent linking group containing a hetero atom)

The hetero atom in the divalent linking group containing a hetero atom is an atom other than a carbon atom and a hydrogen atom, and examples thereof include an oxygen atom, a nitrogen atom, a sulfur atom and a halogen atom.

When Ya ²¹ is a divalent linking group containing a hetero atom, preferred as this linking group are -O-, -C (= 0) -O-, -C (= 0)-, -OC (= 0) -O-. , -C (= O) -NH-, -NH-, -NH-C (= NH)-(H may be substituted with a substituent such as an alkyl group, acyl group), -S-, -S (= O ) _2- , -S (= O) ₂ -O-, general formula -Y ²¹ -OY ^22- , -Y ²¹ -O-, -Y ²¹ -C (= O) -O-,-(Y ^21- C (= O) -O] _{m '} -Y ²² -or -Y ²¹ -OC (= O) -Y ²² -in the group represented by Y ²¹ and Y ²² may each independently have a substituent 2 It is a hydrocarbon group, O is an oxygen atom, m 'is an integer of 0-3.] Etc. are mentioned.

When the divalent linking group containing the hetero atom is -C (= O) -NH-, -NH-, -NH-C (= NH)-, the H may be substituted with a substituent such as an alkyl group or acyl. . The substituent (alkyl group, acyl group, etc.) preferably has 1 to 10 carbon atoms, more preferably 1 to 8 carbon atoms, and particularly preferably 1 to 5 carbon atoms.

Formula -Y ²¹ -OY ^22- , -Y ²¹ -O-, -Y ²¹ -C (= O) -O-,-[Y ²¹ -C (= O) -O] _{m '} -Y ²² -or- Y <^21> -OC (= O) -Y <^22> -Y <^21> and Y <^22> are the bivalent hydrocarbon groups which may each independently have a substituent. As this bivalent hydrocarbon group, the thing similar to the "divalent hydrocarbon group which may have a substituent" mentioned in the description as said bivalent coupling group is mentioned.

Y ²¹ is preferably a straight-chain aliphatic hydrocarbon group, more preferably a straight-chain alkylene group, more preferably a straight-chain alkylene group having 1 to 5 carbon atoms, particularly preferably a methylene group or an ethylene group.

Y ²² is preferably a linear or branched aliphatic hydrocarbon group, more preferably a methylene group, an ethylene group or an alkylmethylene group. The alkyl group in this alkylmethylene group is preferably a linear alkyl group having 1 to 5 carbon atoms, preferably a linear alkyl group having 1 to 3 carbon atoms, and most preferably a methyl group.

In the group represented by the formula - [Y ²¹ -C (═O) -O] _{m '} -Y ²² -, m' is an integer of 0 to 3, preferably an integer of 0 to 2, more preferably 0 or 1 And 1 is particularly preferable. That is, the group represented by the formula - [Y ²¹ -C (═O) -O] _{m '} -Y ²² - is particularly preferably a group represented by the formula -Y ²¹ -C (═O) -OY ²² -. Among them, a group represented by the formula - (CH ₂ ) _{a '} -C (═O) -O- (CH ₂ ) _b' - is preferable. In this formula, a 'is an integer of 1 to 10, preferably an integer of 1 to 8, more preferably an integer of 1 to 5, more preferably 1 or 2, and most preferably 1. b 'is an integer of 1 to 10, preferably an integer of 1 to 8, more preferably an integer of 1 to 5, more preferably 1 or 2, and most preferably 1.

Among the above general formulas (b1-1), as the divalent linking group for Y ¹ , a linking group represented by general formulas (Y-lg-1) to (Y-lg-14) shown below is preferable. In the following general formulas (Y-lg-1) to (Y-lg-14), * represents a bonding hand. It is assumed that the left hand bond is bonded to SO ₂ in General Formula (b1-1), and the right hand bond is bonded to W ⁺ in General Formula (b1-1).

[Wherein, V ′ ¹ to V ′ ³ are a divalent hydrocarbon group which may have a substituent, V ′ ⁴ is a divalent hydrocarbon group having a fluorine atom, and R ′ ¹ is a hydrogen atom or an alkyl group having 1 to 5 carbon atoms. to be.]

In the formulas (Y-lg-1) to (Y-lg-14), V ′ ¹ to V ′ ³ are a divalent hydrocarbon group which may have a substituent.

The hydrocarbon group as a divalent linking group may be an aliphatic hydrocarbon group or an aromatic hydrocarbon group.

The aliphatic hydrocarbon group means a hydrocarbon group having no aromaticity. This aliphatic hydrocarbon group may be saturated or unsaturated, and it is preferable that it is normally saturated.

Examples of the aliphatic hydrocarbon group include linear or branched aliphatic hydrocarbon groups or aliphatic hydrocarbon groups containing a ring in the structure.

Specific examples of the linear or branched aliphatic hydrocarbon group include groups exemplified by Va ¹ in General Formula (a1-1).

The straight chain or branched chain aliphatic hydrocarbon group may or may not have a substituent. Examples of the substituent include a fluorine atom, a fluorinated alkyl group having 1 to 5 carbon atoms substituted with a fluorine atom, and a carbonyl group.

The aliphatic hydrocarbon group containing a ring in the above structure includes a cyclic aliphatic hydrocarbon group (group excluding two hydrogen atoms from the aliphatic hydrocarbon ring) which may include a substituent containing a hetero atom in the ring structure, and the cyclic aliphatic hydrocarbon group is directly The group couple | bonded with the terminal of a linear or branched aliphatic hydrocarbon group, the group in which the said cyclic aliphatic hydrocarbon group is interposed in the middle of a linear or branched aliphatic hydrocarbon group, etc. are mentioned. Examples of the straight chain or branched chain aliphatic hydrocarbon group include the same ones as described above.

The cyclic aliphatic hydrocarbon group preferably has 3 to 20 carbon atoms, more preferably 3 to 12 carbon atoms.

Specific examples of the cyclic aliphatic hydrocarbon group include groups exemplified by Va ¹ in General Formula (a1-1).

The cyclic aliphatic hydrocarbon group may or may not have a substituent. Examples of the substituent include an alkyl group, an alkoxy group, a halogen atom, a halogenated alkyl group, a hydroxyl group, and a carbonyl group.

The alkyl group as the substituent is preferably an alkyl group having 1 to 5 carbon atoms, and most preferably a methyl group, an ethyl group, a propyl group, an n-butyl group or a tert-butyl group.

The alkoxy group as the substituent is preferably an alkoxy group having 1 to 5 carbon atoms, more preferably a methoxy group, an ethoxy group, an n-propoxy group, an isopropoxy group, a n-butoxy group or a tert- The ethoxy group is most preferred.

Examples of the halogen atom as the substituent include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom, and a fluorine atom is preferable.

Examples of the halogenated alkyl group as the substituent include groups in which a part or all of the hydrogen atoms of the alkyl group are substituted with the halogen atom.

The cyclic aliphatic hydrocarbon group may be substituted with a substituent in which part of the carbon atoms constituting the ring structure contains a hetero atom. The substituent containing the hetero atom is preferably -O-, -C (= O) -O-, -S-, -S (= O) _2- or -S (= O) ₂ -O-.

Specific examples of the aromatic hydrocarbon group as the divalent hydrocarbon group include groups exemplified by Va ¹ in the general formula (a1-1).

The hydrogen atom which the said aromatic hydrocarbon group has may be substituted by the said aromatic hydrocarbon group by the substituent. For example, the hydrogen atom couple | bonded with the aromatic ring in the said aromatic hydrocarbon group may be substituted by the substituent. Examples of the substituent include an alkyl group, an alkoxy group, a halogen atom, a halogenated alkyl group, and a hydroxyl group.

The alkyl group as the substituent is preferably an alkyl group having 1 to 5 carbon atoms, and most preferably a methyl group, an ethyl group, a propyl group, an n-butyl group or a tert-butyl group.

Examples of the alkoxy group, halogen atom and halogenated alkyl group as the substituent include those exemplified as substituents for substituting the hydrogen atom of the cyclic aliphatic hydrocarbon group.

In General Formulas (Y-lg-1) to (Y-lg-14), V ′ ¹ is preferably a divalent aromatic hydrocarbon group which may have a substituent, and particularly preferably an arylene group and an aralkylene group.

In the general formulas (Y-lg-1) to (Y-lg-14), V ′ ² to V ′ ³ are preferably an alkylene group which may have a substituent, and in particular, a chain alkylene group which may have a substituent is preferable. Do.

In General Formulas (Y-lg-1) to (Y-lg-14), V ′ ⁴ is a divalent hydrocarbon group having a fluorine atom.

V '2-valent hydrocarbon group having a fluorine atom in the ⁴ in the formula (Y-lg-1) ~ (Y-lg-14), V' is exemplified as the divalent hydrocarbon group of ¹ ~ V ^'3 It is preferable that it is a C1-C5 alkylene group, and it is still more preferable that it is a methylene group or ethylene group. A part or all of the hydrogen atoms of the hydrocarbon group constituting the V ^'4 are replaced by fluorine atoms, is 30 to 100% of the hydrogen atoms of the hydrocarbon group is more preferable, which is substituted with a fluorine atom. In particular, the V ^'1 ~ V' some or all of the fluorine atoms of the hydrogen atoms of the alkylene groups exemplified as the divalent hydrocarbon group of ^{3-substituted} by alkyl (per) fluoro-alkylene group it is in particular preferred.

Examples of the alkyl group having 1 to 5 carbon atoms for R ′ ¹ in the general formulas (Y-lg-1) to (Y-lg-14) include methyl group, ethyl group, propyl group, isopropyl group, n-butyl group and isobutyl group. and tert-butyl group, pentyl group, isopentyl group and neopentyl group.

In said general formula (b1-1), R <^1> is a hydrocarbon group which may have a substituent, For example, the cyclic group which may have a substituent, the chain alkyl group which may have a substituent, or the chain which may have a substituent Alkenyl group is mentioned.

(A cyclic group which may have a substituent)

It is preferable that the said cyclic group is a cyclic hydrocarbon group, and this cyclic hydrocarbon group may be an aromatic hydrocarbon group, or an aliphatic hydrocarbon group may be sufficient as it.

The aromatic hydrocarbon group in R ¹ includes an aryl group excluding one hydrogen atom from an aromatic hydrocarbon ring contained in a divalent aromatic hydrocarbon group in Va ¹ of the formula (a1-1), or an aromatic compound containing two or more aromatic rings. A phenyl group and a naphthyl group are preferable.

The cyclic aliphatic hydrocarbon group in R ¹ includes a group in which one hydrogen atom is removed from a monocycloalkane or polycycloalkane contained in the divalent aliphatic hydrocarbon group in Va ¹ of the formula (a1-1), and an adamantyl group And norbornyl group is preferable.

Moreover, the cyclic hydrocarbon group in R <^1> may contain a hetero atom like a heterocyclic ring, Specifically, the lactone containing cyclic group represented by the following general formula (a2-r-1) (a2-r-7), the following formula (a5-r-1) ~ -SO 2 each represent a (a5-r-4) - may be a cyclic group containing, heterocyclic favorite More or less.

[Wherein, Ra ^'21 each independently represent a hydrogen atom, an alkyl group, an alkoxy group, a halogen atom, a halogenated alkyl group, a hydroxyl group, -COOR ", -OC (= O ) R", a hydroxyalkyl group or a cyano group; R " Is an alkylene group, an oxygen atom or a sulfur atom having 1 to 5 carbon atoms which may contain an oxygen atom or a sulfur atom, n 'is an integer of 0 to 2, m' is 0 or 1, 1.]

In the general formulas (a2-r-1) to (a2-r-7), A "represents an alkylene group having 1 to 5 carbon atoms which may contain an oxygen atom (-O-) , An oxygen atom or a sulfur atom. The alkylene group having 1 to 5 carbon atoms in A "is preferably a linear or branched alkylene group, and a methylene group, an ethylene group, an n-propylene group, . When the alkylene group containing an oxygen atom or a sulfur atom, and specific examples there may be mentioned a group which is -O- or -S-, or interposed between the terminal carbon atoms of the alkylene group, such as -O-CH ₂ -, -CH ₂ -O-CH _2- , -S-CH _2- , -CH ₂ -S-CH ₂ -and the like. A ″ is preferably an alkylene group having 1 to 5 carbon atoms or —O—, more preferably an alkylene group having 1 to 5 carbon atoms, and most preferably a methylene group. Alkyl group, alkoxy group, halogen atom, halogenated at Ra ′ ²¹ alkyl group, -COOR ", -OC (= O ) R", hydroxy-alkyl group is in the -SO ₂ respectively contain as a substituent which may have cyclic groups any alkyl, alkoxy, halogenated alkyl group, -COOR ", -OC (= O) R "and the same thing as a hydroxyalkyl group are mentioned.

Specific examples of the group represented by the general formulas (a2-r-1) to (a2-r-7) are given below.

As a lactone containing cyclic group, group represented by the said general formula (a2-r-1) is preferable among the above, and the group of any of the said general formula (r-lc-1-1)-(r-lc-1-7) is More preferably, group represented by the said general formula (r-lc-1-1) is still more preferable.

[Wherein, Ra ^'51 each independently represent a hydrogen atom, an alkyl group, an alkoxy group, a halogen atom, a halogenated alkyl group, a hydroxyl group, -COOR ", -OC (= O ) R", a hydroxyalkyl group or a cyano group; R " Is an alkylene group, an oxygen atom or a sulfur atom having 1 to 5 carbon atoms which may contain an oxygen atom or a sulfur atom, and n 'is an integer of 0 to 2.]

In the general formulas (a5-r-1) to (a5-r-4), A "is the same as A" in the general formulas (a2-r-1) to (a2-r-7). (A2-r-1) to (a2-r-1) in the above Ra ^'51 are ^exemplified by an alkyl group, an alkoxy group, a halogen atom, a halogenated alkyl group, -COOR " 7) the same as those of Ra ^'21.

Specific examples of the groups represented by the general formulas (a5-r-1) to (a5-r-4) are described below. "Ac" in a formula represents an acetyl group.

-SO ₂ - containing polycyclic group is Among the above, represented by the above-mentioned formula (a5-r-1) group is preferably represented by the above formula (r-sl-1-1) or (r-sl-1-18) Group is more preferable.

As a substituent in the cyclic hydrocarbon group of R <^1> , an alkyl group, an alkoxy group, a halogen atom, a halogenated alkyl group, a hydroxyl group, a carbonyl group, a nitro group, etc. are mentioned, for example.

The alkyl group as a substituent is preferably an alkyl group having 1 to 5 carbon atoms, and most preferably a methyl group, an ethyl group, a propyl group, an n-butyl group or a tert-butyl group.

The alkoxy group as a substituent is preferably an alkoxy group having 1 to 5 carbon atoms, more preferably a methoxy group, an ethoxy group, an n-propoxy group, an iso- propoxy group, a n-butoxy group or a tert- The ethoxy group is most preferred.

As a halogen atom as a substituent, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, etc. are mentioned, A fluorine atom is preferable.

Examples of the halogenated alkyl group as a substituent include an alkyl group having 1 to 5 carbon atoms such as a group in which a part or all of hydrogen atoms such as methyl, ethyl, propyl, n-butyl and tert-butyl groups are substituted with the halogen atom .

(A linear alkyl group which may have a substituent)

The linear alkyl group of R ¹ may be either linear or branched.

The straight-chain alkyl group preferably has 1 to 20 carbon atoms, more preferably 1 to 15, and most preferably 1 to 10 carbon atoms. Specifically, for example, methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decanyl, undecyl, dodecyl, tridecyl, isotridecyl, Tetradecyl group, pentadecyl group, hexadecyl group, isohexadecyl group, heptadecyl group, octadecyl group, nonadecyl group, eicosyl group, a hentai group, a docosyl group, etc. are mentioned.

The branched alkyl group preferably has 3 to 20 carbon atoms, more preferably 3 to 15 carbon atoms, and most preferably 3 to 10 carbon atoms. Specific examples thereof include 1-methylethyl, 1-methylpropyl, 2-methylpropyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, Ethylbutyl group, 1-methylpentyl group, 2-methylpentyl group, 3-methylpentyl group and 4-methylpentyl group.

(A straight chain alkenyl group which may have a substituent)

The linear alkenyl group of R ¹ may be either linear or branched, preferably 2 to 10 carbon atoms, more preferably 2 to 5, still more preferably 2 to 4, and particularly preferably 3 Do. Examples of the straight chain alkenyl group include a vinyl group, a propenyl group (allyl group), and a butyryl group. As the branched-chain alkenyl group, for example, 1-methylpropenyl group, 2-methylpropenyl group and the like can be given.

Among the above-mentioned alkenyl groups, a propenyl group is especially preferable.

Examples of the substituents on the chain in the alkyl or alkenyl groups of R ¹ are, for example, there may be mentioned an alkoxy group, a halogen atom, a halogenated alkyl group, a hydroxyl group, a carbonyl group, a nitro group, an amino group, a cyclic group etc. in the R ^101.

Especially, R <^1> is preferable and the cyclic group which may have a substituent is more preferable that it is a cyclic hydrocarbon group which may have a substituent. More specifically, a lactone-containing cyclic group represented by each of the above-mentioned formulas (a2-r-1) to (a2-r-7), a cyclic group containing a lactone- -SO ₂ -containing cyclic groups represented by (a5-r-1) to (a5-r-4), respectively.

As a hydrocarbon group which may have a substituent in R <^1> , Preferably, they are the aryl group which may have a substituent, the alkyl group which may have a substituent, and the alkenyl group which may have a substituent.

As an aryl group in R <^1> , a C6-C20 unsubstituted aryl group is mentioned, A phenyl group and a naphthyl group are preferable.

As an alkyl group in R <^1> , a C1-C30 thing is preferable as a linear or cyclic alkyl group.

As an alkenyl group in R <^1> , it is preferable that carbon number is 2-10.

Examples of the substituent that R ¹ may have include an alkyl group, a halogen atom, a halogenated alkyl group, a carbonyl group, a cyano group, an amino group, an aryl group, an arylthio group, and the following formulas (ca-r-1) to (ca-r- Groups represented by 7) are mentioned, respectively.

As an aryl group in the arylthio group as a substituent, a phenylthio group or a biphenylthio group is mentioned specifically ,.

Wherein each of R ' ²⁰¹ independently represents a hydrogen atom, a cyclic group which may have a substituent, a straight chain alkyl group, or a straight chain alkenyl group.

R 'ring which may have a substituent, ^201. Tableware, alkyl chain which may be substituted, or alkenyl chain which may have a substituent group other that will be exemplified by the same as R ¹ in the formula (b1-1) As the cyclic group which may have a substituent or the chain alkyl group which may have a substituent, the same thing as the acid dissociable group shown by said formula (a1-r-2) is mentioned.

As a substituent which R <^1> may have, an alkyl group, an aryl group, and an arylthio group are especially preferable.

In said general formula (b1-1), R <^2> is a C1-C5 alkyl group or an alkoxy group. Examples of the alkyl group having 1 to 5 carbon atoms include methyl group, ethyl group, propyl group, n-butyl group and tert-butyl group. It is preferable that a C1-C5 alkoxy group in R <^2> is linear or branched form. The group couple | bonded with the oxygen atom (-O-) can be mentioned specifically, the alkyl group mentioned as the alkyl group as said substituent.

P is 0-5 in the said General formula (b1-1). In General Formula (b1-1), p is preferably 0 to 3, more preferably 0 to 1, and particularly preferably 0.

In the general formula (b1-1), the position where the sulfonyl group is bonded to the naphthoquinone diazide structure is preferably 4th, 5th, or 6th, more preferably 4th or 5th, and 4th is Most preferred.

The specific example of the cation part of a compound represented by the said general formula (b1-1) is given below.

In General Formula (b1-1), X ⁻ is a dianion.

As an anion of X <^-> , anions, such as a sulfonic acid anion, a carboxylic acid anion, an imide anion, a meted anion, a carbo anion, a borate anion, a halogen anion, a phosphate anion, an antimonic acid anion, a arsenic acid anion, are mentioned.

For example, the anion represented by general formula (b-1)-(b-3) mentioned later and the anion represented by the following general formula (b-an1) may be sufficient.

[Wherein, R ¹¹ to R ¹⁴ are each independently a fluorine atom, an alkyl group which may have a substituent, or an aryl group.]

The general formula (b-an1) of, R ¹¹ ~ R in an alkyl group from ¹⁴ is preferably of 1 to 20 carbon atoms alkyl, and the formula (a1-r-1) of the Ra ^'3 and the alkyl group of the same chain or cyclic Can be mentioned.

As an aryl group in R <^11> -R <^14> , a phenyl group or a naphthyl group is preferable.

As a substituent which you may have when R <^11> -R <^14> is an alkyl group or an aryl group, a halogen atom, a halogenated alkyl group, an alkyl group, an alkoxy group, an alkylthio group, a hydroxyl group, a carbonyl group, etc. are mentioned. Examples of these substituents include groups represented by the general formulas (a2-r-1) to (a2-r-7). Moreover, a C1-C4 thing is mentioned as an alkylthio group. Especially, a halogen atom, a halogenated alkyl group, an alkyl group, an alkoxy group, and an alkylthio group are preferable.

It is a group represented by the general formula (b-an1) of, R ¹¹ ~ R ¹⁴ preferably a fluorine atom, a fluorinated alkyl group, or the following general formula (b-an1 ') for being preferred.

[Wherein, R ^'11 ~ R' ¹⁵ are each independently a hydrogen atom, a fluorine atom, trifluoromethyl, alkyl, alkoxy or alkylthio group having from 1 to 4 carbon atoms.]

In said general formula, a C1-C4 alkyl group specifically, can mention methyl group, an ethyl group, n-propyl group, n-butyl group, etc. Among them, a methyl group, an ethyl group or an n-butyl group is preferable, and a methyl group or an ethyl group is more preferable.

In said general formula, a C1-C4 alkoxy group specifically, has a methoxy group, an ethoxy group, n-propoxy group, iso-propoxy group, n-butoxy group, tert-butoxy group, and a methoxy group and an ethoxy group are preferable. The timing is more preferable.

In the general formula, as the alkylthio group having 1 to 4 carbon atoms, methylthio group, ethylthio group, n-propylthio group, iso-propylthio group, n-butylthio group, tert-butylthio group are preferable, and methyl thi Ogi and ethylthio group are more preferable.

Preferable specific examples of the anion moiety represented by general formula (b-an1) include tetrakis (pentafluorophenyl) borate ([B (C ₆ F ₅ ) ₄ ] ^- ), tetrakis [(trifluoromethyl) phenyl] Borate ([B (C ₆ H ₄ CF ₃ ) ₄ ] ^- ), difluorobis (pentafluorophenyl) borate ([(C ₆ F ₅ ) ₂ BF ₂ ] ^- ), trifluoro (pentafluoro Phenyl) borate ([(C ₆ F ₅ ) BF ₃ ] ^- ), tetrakis (difluorophenyl) borate ([B (C ₆ H ₃ F ₂ ) ₄ ] ^- ), and the like. Among them, tetrakis (pentafluorophenyl) borate ([B (C ₆ F ₅ ) ₄ ] ^- ) is particularly preferable.

The anion of X ⁻ may be a halogen anion, a phosphate anion, an antimony acid anion (SbF ₆ ⁻ ), or a non ^- acidic anion (AsF ₆ ⁻ ). Examples of the halogen anion include chlorine and bromine, and the phosphate anion includes PF ₆ ^- and the anion represented by the following general formula (b-an2).

Wherein each R &lt; ¹⁵ &gt; is independently a fluorinated alkyl group having 1 to 8 carbon atoms. q is 1 to 6.]

Specific examples of the fluorinated alkyl group having 1 to 8 carbon atoms in the general formula (b-an2) include CF ₃ , CF ₃ CF ₂ , (CF ₃ ) ₂ CF, CF ₃ CF ₂ CF ₂ , CF ₃ CF ₂ CF ₂ CF _2, (CF ₃₎ there may be mentioned _{2 CFCF 2, CF 3 CF 2} (CF 3) CF, C (CF 3) 3.

Wherein R ¹⁰¹ and R ¹⁰⁴ to R ¹⁰⁸ are each independently a cyclic group which may have a substituent, a chain alkyl group which may have a substituent, or a straight chain alkenyl group which may have a substituent. R ¹⁰⁴ and R ¹⁰⁵ may combine with each other to form a ring. Any two of R ¹⁰⁶ to R ¹⁰⁷ may be bonded to each other to form a ring. R ¹⁰² is a fluorine atom or a fluorinated alkyl group having 1 to 5 carbon atoms. Y ¹⁰¹ is a single bond or a divalent linking group containing an oxygen atom. V ¹⁰¹ to V ¹⁰³ each independently represent a single bond, an alkylene group, or a fluorinated alkylene group. L ¹⁰¹ to L ¹⁰² each independently represent a single bond or an oxygen atom. L ¹⁰³ to L ¹⁰⁵ each independently represents a single bond, -CO- or -SO ₂ -.

{Negative ion part}

The negative ion part of the component (b-1)

In formula (b-1), R ¹⁰¹ is a cyclic group which may have a substituent, a chain alkyl group which may have a substituent, or a straight chain alkenyl group which may have a substituent.

(A cyclic group which may have a substituent)

It is preferable that the said cyclic group is a cyclic hydrocarbon group, and this cyclic hydrocarbon group may be an aromatic hydrocarbon group, or an aliphatic hydrocarbon group may be sufficient as it.

The aromatic hydrocarbon group in R ¹⁰¹ includes an aryl group excluding one hydrogen atom from an aromatic hydrocarbon ring contained in a divalent aromatic hydrocarbon group in Va ¹ of Formula (a1-1) or an aromatic compound containing two or more aromatic rings. A phenyl group and a naphthyl group are preferable.

The cyclic aliphatic hydrocarbon group for R ¹⁰¹ includes a group in which one hydrogen atom is removed from monocycloalkane or polycycloalkane contained in the divalent aliphatic hydrocarbon group in Va ¹ of formula (a1-1), and an adamantyl group And norbornyl group is preferable.

Moreover, the cyclic hydrocarbon group in R <^101> may contain a hetero atom like a heterocyclic ring, Specifically, the lactone containing cyclic group represented by said general formula (a2-r-1)-(a2-r-7), respectively, can be given either containing heterocyclic group as R ¹ in the cyclic group, the formula (b1-1) - the general formula (a5-r-1) ~ (a5-r-4) each represent a -SO _2.

As a substituent in the cyclic hydrocarbon group of R <^101> , an alkyl group, an alkoxy group, a halogen atom, a halogenated alkyl group, a hydroxyl group, a carbonyl group, a nitro group, etc. are mentioned, for example.

The alkyl group as a substituent is preferably an alkyl group having 1 to 5 carbon atoms, and most preferably a methyl group, an ethyl group, a propyl group, an n-butyl group or a tert-butyl group.

The alkoxy group as a substituent is preferably an alkoxy group having 1 to 5 carbon atoms, more preferably a methoxy group, an ethoxy group, an n-propoxy group, an iso- propoxy group, a n-butoxy group or a tert- The ethoxy group is most preferred.

As a halogen atom as a substituent, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, etc. are mentioned, A fluorine atom is preferable.

Examples of the halogenated alkyl group as a substituent include an alkyl group having 1 to 5 carbon atoms such as a group in which a part or all of hydrogen atoms such as methyl, ethyl, propyl, n-butyl and tert-butyl groups are substituted with the halogen atom .

(A linear alkyl group which may have a substituent)

The linear alkyl group of R ¹⁰¹ may be either linear or branched.

The straight-chain alkyl group preferably has 1 to 20 carbon atoms, more preferably 1 to 15, and most preferably 1 to 10 carbon atoms. Specifically, for example, methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decanyl, undecyl, dodecyl, tridecyl, isotridecyl, Tetradecyl group, pentadecyl group, hexadecyl group, isohexadecyl group, heptadecyl group, octadecyl group, nonadecyl group, eicosyl group, a hentai group, a docosyl group, etc. are mentioned.

The branched alkyl group preferably has 3 to 20 carbon atoms, more preferably 3 to 15 carbon atoms, and most preferably 3 to 10 carbon atoms. Specific examples thereof include 1-methylethyl, 1-methylpropyl, 2-methylpropyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, Ethylbutyl group, 1-methylpentyl group, 2-methylpentyl group, 3-methylpentyl group and 4-methylpentyl group.

(A straight chain alkenyl group which may have a substituent)

The linear alkenyl group of R ¹⁰¹ may be either linear or branched, preferably 2 to 10 carbon atoms, more preferably 2 to 5, still more preferably 2 to 4, and particularly preferably 3 Do. Examples of the straight chain alkenyl group include a vinyl group, a propenyl group (allyl group), and a butyryl group. As the branched-chain alkenyl group, for example, 1-methylpropenyl group, 2-methylpropenyl group and the like can be given.

As the chain alkenyl group, a propenyl group is particularly preferable.

Examples of the substituent in the alkyl group or the alkenyl group on the chain of R ¹⁰¹ include an alkoxy group, a halogen atom, a halogenated alkyl group, a hydroxyl group, a carbonyl group, a nitro group, an amino group and a cyclic group in the R ¹⁰¹ .

Among them, R ¹⁰¹ is preferably a cyclic group which may have a substituent, more preferably a cyclic hydrocarbon group which may have a substituent. More specifically, a lactone-containing cyclic group represented by each of the above-mentioned formulas (a2-r-1) to (a2-r-7), a cyclic group containing a lactone- -SO ₂ -containing cyclic groups represented by (a5-r-1) to (a5-r-4), respectively.

In the formula (b-1), Y ¹⁰¹ is a divalent linking group containing a single bond or an oxygen atom.

¹⁰¹ If Y is a divalent connecting group containing an oxygen atom, the Y ¹⁰¹ is may contain atoms other than oxygen atoms. Reactors other than oxygen atoms include, for example, carbon atoms, hydrogen atoms, sulfur atoms, and nitrogen atoms.

As a bivalent coupling group containing an oxygen atom, an oxygen atom (ether bond: -O-), an ester bond (-C (= O) -O-), an oxycarbonyl group (-OC (= O)-), for example Hydrogen atom-containing oxygen atom-containing linking groups such as amide bond (-C (= O) -NH-), carbonyl group (-C (= O)-) and carbonate bond (-OC (= O) -O-); The combination of this non-hydrocarbon type | system | group oxygen atom containing coupling group and alkylene group, etc. are mentioned. In addition to the above combination, a sulfonyl group (-SO ₂ -) may be connected. Examples of the combination include a linking group represented by the following formulas (y-al-1) to (y-al-7).

[Wherein, V ′ ¹⁰¹ is a single bond or an alkylene group having 1 to 5 carbon atoms, and V ′ ¹⁰² is a divalent saturated hydrocarbon group having 1 to 30 carbon atoms.]

It is preferable that the divalent saturated hydrocarbon group in V ' ¹⁰² is a C1-C30 alkylene group.

The alkylene group at V ' ¹⁰¹ and V' ¹⁰² may be a straight chain alkylene group, a branched chain alkylene group or a straight chain alkylene group.

Specific examples of the alkylene group at V ′ ¹⁰¹ and V ′ ¹⁰² include methylene group [—CH ₂ —]; —CH (CH ₃ ) —, —CH (CH ₂ CH ₃ ) —, and —C (CH ₃ ) ₂ − Alkyl methylene groups such as -C (CH ₃ ) (CH ₂ CH ₃ )-, -C (CH ₃ ) (CH ₂ CH ₂ CH ₃ )-, and -C (CH ₂ CH ₃ ) _2- ; -CH ₂ CH _2- ]; -CH (CH ₃ ) CH _2- , -CH (CH ₃ ) CH (CH ₃ )-, -C (CH ₃ ) ₂ CH _2- , -CH (CH ₂ CH ₃ ) Alkyl ethylene groups such as CH _2- ; trimethylene group (n-propylene group) [-CH ₂ CH ₂ CH _2- ]; -CH (CH ₃ ) CH ₂ CH _2- , -CH ₂ CH (CH ₃ ) CH Alkyltrimethylene groups such as _2- ; tetramethylene group [-CH ₂ CH ₂ CH ₂ CH _2- ]; -CH (CH ₃ ) CH ₂ CH ₂ CH _2- , -CH ₂ CH (CH ₃ ) CH ₂ CH _2-alkyl groups, such as tetramethylene; pentamethylene group _{[-CH 2 CH 2 CH 2 CH} 2 CH 2 -] and the like.

In addition, V part of the methylene in the alkyl group in the ^'101 or V' ¹⁰² groups are optionally substituted by a divalent aliphatic cyclic group with a carbon number of 5-10. The aliphatic cyclic group is preferably a divalent group excluding one hydrogen atom from the cyclic aliphatic hydrocarbon group of Ra ′ ³ in the formula (a1-r-1), and a cyclohexylene group and 1,5-adamantyl A benzene group or a 2,6-adamantylene group is more preferable.

Y ¹⁰¹ is preferably a divalent linking group including an ester linkage or an ether linkage, and a linking group represented by the above formulas (y-al-1) to (y-al-5) is preferable.

In formula (b-1), V ¹⁰¹ is a single bond, an alkylene group, or a fluorinated alkylene group. The alkylene group and fluorinated alkylene group in V ¹⁰¹ preferably have 1 to 4 carbon atoms. ^Examples of the fluorinated alkylene group in V ¹⁰¹ include groups in which a part or all of the hydrogen atoms of the alkylene group in V ¹⁰¹ are substituted with fluorine atoms. Among them, V ¹⁰¹ is preferably a single bond or a fluorinated alkylene group having 1 to 4 carbon atoms.

In the formula (b-1), R ¹⁰² is a fluorine atom or a fluorinated alkyl group having 1 to 5 carbon atoms. R ¹⁰² is preferably a fluorine atom or a perfluoroalkyl group having 1 to 5 carbon atoms, more preferably a fluorine atom.

Specific examples of the anion moiety of the component (b-1) include, for example,

When Y ¹⁰¹ becomes a single bond, fluorinated alkylsulfonate anions such as trifluoromethanesulfonate anion and perfluorobutanesulfonate anion may be mentioned; when Y ¹⁰¹ is a divalent linking group containing an oxygen atom, The anion represented by either of following formula (an-1)-(an-3) is mentioned.

[Wherein, R ″ ¹⁰¹ is an aliphatic cyclic group which may have a substituent, a group represented by the formulas (r-hr-1) to (r-hr-6), or a chain alkyl group which may have a substituent; R " ¹⁰² is an aliphatic cyclic group which may have a substituent, the lactone containing cyclic groups represented by said formula (a2-r-1)-(a2-r-7), respectively, or the said general formula (a5-r-1)- (a5-r-4) each represent a -SO ₂ - containing cyclic group and; R ^"103 is an alkenyl chain of which may have an aliphatic cyclic group, or a substituent which may have an aromatic ring group, substituents may have a substituent A Nyl group; V " ¹⁰¹ is a fluorinated alkylene group; L" ¹⁰¹ is -C (= O)-or -SO _2- ; and v "are each independently an integer of 0-3, q" is each independently 1 Is an integer of -20 and n "is 0 or 1.]

R ^"101, R" ¹⁰² and R "aliphatic ring which may have a ¹⁰³ substituents of the dish is preferably a group exemplified as the cyclic aliphatic hydrocarbon group in the R ^101. As the substituent of the cyclic in R ¹⁰¹ an aliphatic May be the same as the substituent which may be substituted with a hydrocarbon group.

R "aromatic ring group which may have a substituent in ¹⁰³ is preferably a group exemplified as the aromatic hydrocarbon group in the cyclic hydrocarbon group in the R ^101. As the substituent may be substituted with an aromatic hydrocarbon in R ¹⁰¹ The same thing as the substituent to be mentioned is mentioned.

R alkenyl chain which may have a substituent in "the alkyl group of the chain which may have a substituent in ¹⁰¹ is caused, it is preferable. R exemplified as the alkyl group of the chain in the R ^{101" 103} groups in the R ¹⁰¹ Is preferably a group exemplified as a chain alkenyl group.

V " ¹⁰¹ is preferably a fluorinated alkylene group having 1 to 3 carbon atoms, particularly preferably -CF ₂ -, -CF ₂ CF ₂ -, -CHFCF ₂ -, -CF (CF ₃ ) CF ₂ -, -CH (CF ₃₎ CF ₂ - a.

Specific examples of the anion represented by the above general formula (an-1) are given below. However, the present invention is not limited to this.

Specific examples of the anion represented by the above general formula (an-2) are given below. However, the present invention is not limited to this.

Specific examples of the anion represented by the above general formula (an-3) are given below. However, the present invention is not limited to this.

The negative ion part of component (b-2)

In formula (b-2), R <^104> , R <^105> is respectively independently the cyclic group which may have a substituent, the chain alkyl group which may have a substituent, or the chain alkenyl group which may have a substituent, respectively, Formula (b The same thing as R <^101> in -1) is mentioned. However, R ¹⁰⁴ and R ¹⁰⁵ may be bonded to each other to form a ring.

R ¹⁰⁴ and R ¹⁰⁵ are preferably a linear alkyl group which may have a substituent, more preferably a linear or branched alkyl group or a linear or branched fluorinated alkyl group.

The alkyl group of this chain preferably has 1 to 10 carbon atoms, more preferably 1 to 7 carbon atoms, and still more preferably 1 to 3 carbon atoms. Carbon number of the linear alkyl group of R <^104> , R <^105> is in the range of the said carbon number, and it is so preferable that it is so small that it is good in solubility to a resist solvent. In the chain alkyl groups of R ¹⁰⁴ and R ^105, the higher the number of hydrogen atoms substituted with fluorine atoms, the stronger the strength of the acid, and the higher the transparency to high energy light and electron beam of 200 nm or less are preferable. The ratio of the fluorine atoms in the alkyl group on the chain, that is, the fluoride ratio is preferably 70 to 100%, more preferably 90 to 100%, and most preferably all the hydrogen atoms are fluorine-substituted perfluoroalkyl groups.

In the formula (b-2), V ¹⁰² and V ¹⁰³ are each independently a single bond, an alkylene group or a fluorinated alkylene group, and the same groups as those of V ¹⁰¹ in the formula (b-1)

In the formula (b-2), L ¹⁰¹ to L ¹⁰² each independently represent a single bond or an oxygen atom.

Specific examples of the anions represented by the above general formula (b-2) are given below. However, the present invention is not limited to this.

The anion portion of the component (b-3)

In formula (b-3), R ¹⁰⁶ to R ¹⁰⁸ are each independently a cyclic group which may have a substituent, a chain alkyl group which may have a substituent, or a chain alkenyl group which may have a substituent, respectively. The same thing as R <^101> in -1) is mentioned.

L ¹⁰³ to L ¹⁰⁵ each independently represent a single bond, -CO- or -SO ₂ -.

Specific examples of the anion represented by the above general formula (b-3) are given below. However, the present invention is not limited to this.

An acid generator (B1) may be used independently and may be used in combination of 2 or more type. The content of the acid generator (B1) is preferably 0.1 to 10% by mass, more preferably 0.5 to 5% by mass, and more preferably 0.5 to 3% by mass relative to the total mass of the resist composition of the present invention Is more preferable.

As the acid generator (B), other acid generators than those described above may be used in combination.

The first embodiment in other acid generators includes 2,4-bis (trichloromethyl) -6-piperonyl-1,3,5-triazine, 2,4-bis (trichloromethyl) (2-furyl) ethenyl] -s-triazine, 2,4-bis (trichloromethyl) -6- [2- , 2,4-bis (trichloromethyl) -6- [2- (5-ethyl-2-furyl) ethenyl] -S-triazine, 2,4-bis (trichloromethyl) -6- [2- (3,5-dimethoxyphenyl) ethenyl] -s- (Trichloromethyl) -6- [2- (3,5-diethoxyphenyl) ethenyl] -s-triazine, 2,4-bis (2,4-bis (trichloromethyl) -6- [2- (3-methoxy-5-ethoxyphenyl) (Trichloromethyl) -6- [2- (3-methoxy-5-propoxyphenyl) ethenyl] -s-triazine, 2,4- Bis (trichloromethyl) -6- [2- (3,4-methylenedioxyphenyl) ether (Trichloromethyl) -6- (3,4-methylenedioxyphenyl) -s-triazine, 2,4-bis-trichloromethyl-6- Methoxy) phenyl-s-triazine, 2,4-bis-trichloromethyl-6- (2-bromo- (2-bromo-4-methoxy) styrylphenyl-s-triazine, 2,4-bis-trichloromethyl-6- Methoxyphenyl) -4,6-bis (trichloromethyl) -1,3,5-triazine, 2- (4-methoxynaphthyl) ) -4,6-bis (trichloromethyl) -1,3,5-triazine, 2- [2- (2-furyl) ethenyl] , 5-triazine, 2- [2- (5-methyl-2-furyl) ethenyl] -4,6-bis (trichloromethyl) 3,6-bis (trichloromethyl) -1,3,5-triazine, 2- [2- (3,4-dimethoxyphenyl) ethenyl] 4,6-bis (trichloromethyl) -1,3,5-triazine, 2- (3,4-methylenedioxyphenyl) -4 , 6-bis (trichloromethyl) -1,3,5-triazine, tris (1,3-dibromopropyl) -1,3,5-triazine, tris (2,3-dibromopropyl ) -1,3,5-triazine and halogen-containing triazine compounds represented by the following general formula (b3), such as tris (2,3-dibromopropyl) isocyanurate, .

In the above general formula ^{(b3), Rb 9, Rb} 10, Rb 11 represents a halogenated alkyl group each independently.

Moreover, as 2nd aspect in another acid generator, (alpha)-(p-toluenesulfonyloxyimino) -phenylacetonitrile, (alpha)-(benzenesulfonyloxyimino) -2,4- dichlorophenyl acetonitrile, (alpha)- (Benzenesulfonyloxyimino) -2,6-dichlorophenylacetonitrile, α- (2-chlorobenzenesulfonyloxyimino) -4-methoxyphenylacetonitrile, α- (ethylsulfonyloxyimino) -1- The compound represented by the following general formula (b4) containing cyclopentenyl acetonitrile and an oxime sulfonate group is mentioned.

In Formula (b4), Rb ¹² represents a monovalent, divalent, or trivalent organic group, Rb ¹³ represents a substituted or unsubstituted saturated hydrocarbon group, unsaturated hydrocarbon group, or aromatic compound group, and n represents parentheses. The number of repeat units in the inner structure is shown.

In the general formula (b4), the aromatic compound group represents a group of a compound that exhibits physical and chemical properties peculiar to an aromatic compound, and includes, for example, aryl groups such as phenyl group and naphthyl group, heteroaryl groups such as furyl group and thienyl group . These may have at least one substituent suitable for the cyclic structure, for example, a halogen atom, an alkyl group, an alkoxy group, and a nitro group. Rb ¹³ is particularly preferably an alkyl group having 1 to 6 carbon atoms, and examples thereof include a methyl group, an ethyl group, a propyl group and a butyl group. Particularly preferred are compounds wherein Rb ¹² is an aromatic compound group and Rb ¹³ is an alkyl group having 1 to 4 carbon atoms.

Acid generator represented by the above general formula (b4) is when n = 1, and Rb ¹² are a phenyl group, any one of phenyl group, a methoxyphenyl group, Rb ¹³ The compounds of the methyl group, specifically, α- (methylsulfonyl Oxyimino) -1-phenylacetonitrile, α- (methylsulfonyloxyimino) -1- (p-methylphenyl) acetonitrile, α- (methylsulfonyloxyimino) -1- (p-methoxyphenyl) aceto Nitrile, [2- (propylsulfonyloxyimino) -2,3-dihydroxythiophen-3-ylidene] (o-tolyl) acetonitrile, and the like. When n = 2, the acid generator represented by the general formula (b4) specifically includes an acid generator represented by the following formula.

Moreover, onium salt which has a naphthalene ring as a cation part in a 3rd aspect in another acid generator is mentioned. This "having a naphthalene ring" means having a structure derived from naphthalene, and means that at least two ring structures and their aromaticity are maintained. The naphthalene ring may have a substituent such as a linear or branched alkyl group having 1 to 6 carbon atoms, a hydroxyl group, a linear or branched alkoxy group having 1 to 6 carbon atoms, and the like. Although the structure derived from a naphthalene ring may be monovalent (one free valence is 1) or divalent (two free valences) may be sufficient, it is preferable that it is monovalent (except the part couple | bonded with the said substituent at this time) The free valence is counted). The number of naphthalene rings is preferably 1 to 3.

As a cation part of the onium salt which has a naphthalene ring in such a cation part, the structure represented by following General formula (b5) is preferable.

In General Formula (b5), Rb ¹⁴ , Rb ¹⁵ , Rb ¹⁶ At least 1 represents group represented by the following general formula (b6), and the remainder is a C1-C6 linear or branched alkyl group, the phenyl group which may have a substituent, a hydroxyl group, or a C1-C6 linear or branched form An alkoxy group is shown. Or one of Rb ¹⁴ , Rb ¹⁵ , and Rb ¹⁶ is a group represented by the following General Formula (b6), and the other two are each independently a linear or branched alkylene group having 1 to 6 carbon atoms, and these terminals are bonded to each other. It may be an illusion.

Wherein the general formula ^{(b6), Rb 17, Rb} 18 are each independently a hydroxyl group, represents a straight-chain or alkyl groups on the branches of a carbon number of 1 to 6 linear or branched alkoxy group, or a group having 1 to 6 carbon atoms on the a, Rb ¹⁹ are The C1-C6 linear or branched alkylene group which may have a single bond or a substituent is shown. 1 and m respectively independently represent the integer of 0-2, and l + m is 3 or less. However, if Rb ¹⁷ are a plurality is present, they may be the same or different from each other. When a plurality of Rb ¹⁸ exist, they may be the same or different.

The number of groups represented by the general formula (b6) in the Rb ¹⁴ , Rb ¹⁵ , and Rb ¹⁶ is preferably one from the viewpoint of the stability of the compound, and the remainder is a linear or branched alkylene group having 1 to 6 carbon atoms, These terminals may be bonded to form a ring. In this case, the two alkylene groups constitute a 3- to 9-membered ring including a sulfur atom. The number of atoms (including sulfur atoms) constituting the ring is preferably 5 to 6.

Examples of the substituent which the alkylene group may have include an oxygen atom (in this case, forming a carbonyl group together with a carbon atom constituting the alkylene group), and a hydroxyl group.

Examples of the substituent which the phenyl group may have include a hydroxyl group, a linear or branched alkoxy group having 1 to 6 carbon atoms, and a linear or branched alkyl group having 1 to 6 carbon atoms.

Preferable examples of these cationic moieties include those represented by the following formulas (b7) and (b8), and particularly preferably a structure represented by the following formula (b8).

Although such a cation part may be an iodonium salt or a sulfonium salt, sulfonium salt is preferable from an acid generation efficiency point.

Therefore, as an anion part of the onium salt which has a naphthalene ring in a cation part, the anion which can form a sulfonium salt is preferable.

The anion portion of such an acid generator is a fluoroalkyl sulfonic acid ion or an aryl sulfonic acid ion in which part or all of hydrogen atoms are fluorinated.

The alkyl group in the fluoroalkylsulfonic acid ion may be linear, branched or cyclic, having 1 to 20 carbon atoms, and preferably 1 to 10 carbon atoms from the volume size of the generated acid and its diffusion distance. Particularly, it is preferable to use a branched or annular one because the diffusion distance is short. Moreover, a methyl group, an ethyl group, a propyl group, a butyl group, an octyl group etc. are mentioned as a preferable thing from the point which can be synthesize | combined cheaply.

The aryl group in an aryl sulfonic acid ion is a C6-C20 aryl group, The phenyl group and naphthyl group which may not be substituted by the alkyl group and a halogen atom are mentioned. In particular, a C6-C10 aryl group is preferable at the point which can be synthesize | combined cheaply. Preferable specific examples include phenyl group, toluenesulfonyl group, ethylphenyl group, naphthyl group, methylnaphthyl group and the like.

In the fluoroalkyl sulfonic acid ion or the aryl sulfonic acid ion, the fluorination rate in the case where some or all of the hydrogen atoms are fluorinated is preferably 10 to 100%, more preferably 50 to 100%, particularly hydrogen It is preferable to replace all the atoms with fluorine atoms because the strength of the acid becomes stronger. Specific examples of the same are trifluoromethane sulfonate, perfluorobutane sulfonate, perfluorooctane sulfonate, perfluorobenzene sulfonate, and the like.

Among these, preferable anion moieties include those represented by the following general formula (b9).

Wherein in the formula (b9), ²⁰ Rb is a group represented by the formula (b12) group or represented by the formula (b10), (b11).

In the general formula (b10), x represents an integer of 1 to 4. Further, in the general formula (b11), Rb ²¹ is an alkoxy group on the hydrogen, hydroxyl, straight-chain or alkyl groups on the branches of 1 to 6 carbon atoms, or 1 to 6 carbon atoms straight chain or branched, y is 1 to 3 Represents an integer. Among them, trifluoromethanesulfonate and perfluorobutanesulfonate are preferable from the viewpoint of safety.

Moreover, it is preferable to use what contains nitrogen represented by following General formula (b13) and (b14) as an anion part.

In the general formula (a13), Xb represents a linear or branched alkylene group in which at least one hydrogen atom is substituted with a fluorine atom, and the number of carbon atoms of the alkylene group is 2 to 6, preferably 3 to 5, Is 3 carbon atoms. In the general formula (a14), Yb and Zb each independently represent a straight-chain or branched alkyl group in which at least one hydrogen atom is substituted with a fluorine atom, and the alkyl group of the alkyl group has 1 to 10 carbon atoms, 7, and more preferably 1 to 3.

The smaller the carbon number of the alkylene group of Xb or the carbon number of the alkyl group of Yb and Zb, the better the solubility in the organic solvent is preferable.

In the alkylene group of Xb or the alkyl group of Yb and Zb, the larger the number of hydrogen atoms substituted with a fluorine atom is, the stronger the strength of the acid is. The ratio of the fluorine atom in the alkylene group or alkyl group, that is, the fluorine-containing group, is preferably 70 to 100%, more preferably 90 to 100%, and most preferably the perfluoroalkylene group in which all hydrogen atoms are substituted with fluorine atoms A perfluoroalkyl group.

As a preferable onium salt which has a naphthalene ring in such a cation part, the compound represented by following formula (b15) and (b16) is mentioned.

As the fourth embodiment of the other acid generator, bis (p-toluenesulfonyl) diazomethane, bis (1,1-dimethylethylsulfonyl) diazomethane, bis (cyclohexylsulfonyl) diazomethane , And bis (2,4-dimethylphenylsulfonyl) diazomethane; p-toluenesulfonic acid 2-nitrobenzyl, p-toluenesulfonic acid 2,6-dinitrobenzyl, nitrobenzyl Nitrobenzyl derivatives such as tolylate, dinitrobenzyltosylate, nitrobenzylsulfonate, nitrobenzyl carbonate, dinitrobenzyl carbonate, etc .; nitrobenzyl derivatives such as pyroglutamylate, pyrogalloltritosylate, benzyltosylate, Sulfonic acid esters such as benzyl sulfonate, N-methylsulfonyloxysuccinimide, N-trichloromethylsulfonyloxysuccinimide, N-phenylsulfonyloxymaleimide and N-methylsulfonyloxyphthalimide ; Triflur such as N-hydroxyphthalimide and N-hydroxynaphthalimide; Romethane sulfonic acid esters; diphenyl iodonium hexafluorophosphate, (4-methoxyphenyl) phenyl iodonium trifluoromethanesulfonate, bis (p-tert-butylphenyl) iodonium trifluoromethanesulfonate, Onium salts such as triphenylsulfonium hexafluorophosphate, (4-methoxyphenyl) diphenylsulfonium trifluoromethanesulfonate, and (p-tert-butylphenyl) diphenylsulfonium trifluoromethanesulfonate Benzointosylates such as benzointosylate and α-methylbenzointosylate; other diphenylyodonium salts, triphenylsulfonium salts, phenyldiazonium salts, benzyl carbonates, and the like.

As the other acid generator, preferably, the value of the preferred n is a compound represented by the formula (b4) is 2, Further, preferred Rb ¹² are a substituted divalent group having 1 to 8 carbon atoms or unsubstituted alkylene ring, or a substituted or Although it is an unsubstituted aromatic group, Preferable Rb ¹³ is a C1-C8 substituted or unsubstituted alkyl group or a substituted or unsubstituted aryl group, However, It is not limited to this.

The use ratio in the case where such another acid generator is used in combination is not particularly limited as long as the effect of the present invention is not impaired. Generally, with respect to 100 parts by mass of the acid generator containing the cation portion represented by the general formula (b5) and the anion portion represented by the general formula (b-an1), the other acid generator is preferably used in an amount of 1 to 300 parts by mass, 10 to 100 parts by mass.

An acid generator (B) may be used independently and may be used in combination of 2 or more type. The content of the acid generator (B) is preferably 0.1 to 10% by mass, more preferably 0.5 to 3% by mass based on the total mass of the resist composition of the present invention.

<Optional ingredients>

[Basic compound component: (D) component]

In addition to the component (A), the resist composition of the present invention may further contain a basic compound component (hereinafter also referred to as "component (D)").

(Component (D))

The component (D) is a compound that is relatively basic to the component (B), and acts as an acid acid control agent, and is not particularly limited as long as the component does not correspond to the component (D). do. Of these, aliphatic amines, especially secondary aliphatic amines and tertiary aliphatic amines are preferred.

The aliphatic amine is an amine having at least one aliphatic group, and the aliphatic group preferably has 1 to 12 carbon atoms.

Examples of the aliphatic amines include amines (alkylamines or alkylalcoholamines) or cyclic amines in which at least one hydrogen atom of ammonia NH ₃ is substituted with an alkyl group having 12 or less carbon atoms or a hydroxyalkyl group.

Specific examples of alkylamines and alkylalcoholamines include monoalkylamines such as n-hexylamine, n-heptylamine, n-octylamine, n-nonylamine and n-decylamine; , Dialkylamines such as di-n-heptylamine, di-n-octylamine and dicyclohexylamine; aliphatic amines such as trimethylamine, triethylamine, tri-n-propylamine, Trialkylamines such as triethylamine, triethylamine, triethylamine, n-hexylamine, triethylamine, triethylamine, And alkyl alcohol amines such as diethanolamine, triethanolamine, diisopropanolamine, triisopropanolamine, di-n-octanolamine and tri-n-octanolamine. Of these, trialkylamines having 5 to 10 carbon atoms are more preferred, and tri-n-pentylamine or tri-n-octylamine is particularly preferred.

The cyclic amine includes, for example, a heterocyclic compound containing a nitrogen atom as a hetero atom. The heterocyclic compound may be monocyclic (aliphatic monocyclic amine) or polycyclic (aliphatic polycyclic amine).

Specific examples of the aliphatic monocyclic amines include piperidine and piperazine.

As the aliphatic polycyclic amine, one having 6 to 10 carbon atoms is preferable, and specifically 1,5-diazabicyclo [4.3.0] -5-nonene and 1,8-diazabicyclo [5.4.0] -7 -Undecene, hexamethylenetetramine, 1,4-diazabicyclo [2.2.2] octane, etc. are mentioned.

Other aliphatic amines include tris (2-methoxymethoxyethyl) amine, tris {2- (2-methoxyethoxy) ethyl} amine, tris {2- (2-methoxyethoxymethoxy) ethyl} Amine, tris {2- (1-methoxyethoxy) ethyl} amine, tris {2- (1-ethoxyethoxy) ethyl} amine, tris {2- (1-ethoxypropoxy) ethyl} amine, Tris [2- {2- (2-hydroxyethoxy) ethoxy} ethyl] amine, triethanolamine triacetate, and the like, and triethanolamine triacetate is preferable.

Moreover, you may use aromatic amine as (D2) component.

Examples of the aromatic amine include aniline, pyridine, 4-dimethylaminopyridine, pyrrole, indole, pyrazole, imidazole or a derivative thereof, diphenylamine, triphenylamine, tribenzylamine, 2,6-diisopropylaniline, N -tet-butoxycarbonylpyrrolidine and the like.

(D) component may be used independently and may be used in combination of 2 or more type.

(D) component is normally used in 0.01-5.0 mass part with respect to 100 mass parts of resin solid content (the sum total of (A) component and (C) component). By setting the concentration in the above range, the shape of the resist pattern, the stability over time, and the like are improved.

<Optional ingredients>

[Component (E)] [

The resist composition of the present invention includes at least one compound selected from the group consisting of organic carboxylic acids and oxo acids of phosphorus and derivatives thereof as arbitrary components for the purpose of preventing sensitivity deterioration, improving the resist pattern shape, atmospheric stability over time, and the like. (E) (henceforth (E) component) can be contained.

Examples of the organic carboxylic acid include acetic acid, malonic acid, citric acid, malic acid, succinic acid, benzoic acid, salicylic acid and the like. Phosphoric acid, phosphonic acid and phosphinic acid are examples of the phosphoric acid, and phosphonic acid is particularly preferable among them.

As a derivative of the oxo acid of phosphorus, the ester etc. which substituted the hydrogen atom of the said oxo acid with a hydrocarbon group, etc. are mentioned, for example, A C1-C5 alkyl group, a C6-C15 aryl group, etc. are mentioned, for example. Can be.

Examples of the phosphoric acid derivative include phosphoric acid esters such as di-n-butyl phosphate and diphenyl phosphate.

Examples of the derivatives of phosphonic acid include phosphonic acid esters such as phosphonic acid dimethyl ester, phosphonic acid di-n-butyl ester, phenylphosphonic acid, phosphonic acid diphenyl ester and phosphonic acid dibenzyl ester.

Examples of phosphinic acid derivatives include phosphinic acid esters and phenylphosphinic acid.

The component (E) may be used alone or in combination of two or more.

(E) component is normally used in 0.01-5.0 mass part with respect to 100 mass parts of resin solid content (the sum total of (A) component and (C) component).

[Other additives]

The resist composition of the present invention may further contain miscible additives such as an additive resin for improving the performance of the resist film, a dissolution inhibitor, a plasticizer, a stabilizer, a colorant, a halation inhibitor, .

[Component (S)] [

The resist composition of the present invention can be produced by dissolving the material in an organic solvent (hereinafter sometimes referred to as component (S)).

What is necessary is just to be able to melt | dissolve each component to be used as a (S) component, and to make it a uniform solution, and can use suitably the 1 type (s) or 2 or more types from a well-known thing as a solvent of the conventional chemically amplified resist, and can use.

For example, lactones, such as (gamma) -butyrolactone (GBL); Ketones, such as acetone, methyl ethyl ketone (MEK), cyclohexanone, methyl-n-pentyl ketone, methyl isopentyl ketone, and 2-heptanone; Polyhydric alcohols such as ethylene glycol, diethylene glycol, propylene glycol, dipropylene glycol; compounds having ester bonds such as ethylene glycol monoacetate, diethylene glycol monoacetate, propylene glycol monoacetate, or dipropylene glycol monoacetate; Derivatives of polyhydric alcohols such as polyhydric alcohols or compounds having ether bonds such as monoalkyl ethers such as monomethyl ether, monoethyl ether, monopropyl ether and monobutyl ether or monophenyl ethers of the compounds having ester bonds [ Among these, propylene glycol monomethyl ether acetate (PGMEA) and propylene glycol monomethyl PGME is preferred]; cyclic ethers such as dioxane, methyl lactate, ethyl lactate (EL), methyl acetate, ethyl acetate, butyl acetate, methyl pyruvate, ethyl pyruvate, methyl methoxypropionate and ethyl ethoxypropionate. Esters such as anisole, ethyl benzyl ether, cresyl methyl ether, diphenyl ether, dibenzyl ether, phentol, butyl phenyl ether, ethyl benzene, diethyl benzene, pentyl benzene, isopropyl benzene, toluene, xylene, Aromatic organic solvents, such as cymene and mesitylene, dimethyl sulfoxide (DMSO), etc. are mentioned.

Moreover, an organic solvent can be mix | blended suitably for the viscosity adjustment to the positive photoresist composition for thick films which concerns on this invention. Specific examples of the organic solvent include ketones such as methyl isoamyl ketone; ethylene glycol, ethylene glycol monoacetate, diethylene glycol, diethylene glycol monoacetate, propylene glycol, propylene glycol monoacetate, dipropylene glycol and dipropylene glycol monoacetate. Polyhydric alcohols and derivatives thereof such as monomethyl ether, monoethyl ether, monopropyl ether, monobutyl ether, or monophenyl ether; cyclic ethers such as dioxane; methyl acetate, ethyl acetate, ethyl pyruvate, Ethyl oxyacetic acid, methyl 2-hydroxypropionate, ethyl 2-hydroxypropionate, ethyl 2-hydroxy-2-methylpropionate, methyl 2-hydroxy-3-methylbutanoic acid, 3-methoxybutyl acetate, 3- Esters such as methyl-3-methoxybutyl acetate; aromatic hydrocarbons such as toluene and xylene It may be a flow. These may be used independently, or may mix and use 2 or more types.

These organic solvents may be used alone or in combination of two or more.

Especially, PGMEA and 3-methoxybutyl acetate are preferable.

The amount of the component (S) to be used is not particularly limited and is appropriately set in accordance with the coating film thickness at a concentration that can be applied to a substrate or the like. Generally, it is preferable that it is the range whose solid content concentration of a resist composition becomes 30 mass%-65 mass%. If the solid content concentration is less than 30% by mass, it is difficult to obtain a thick film of 5 µm or more, more preferably 10 µm or more, which is preferable for the manufacture of the connection terminal. In the spin coat method, a uniform resist film is hardly obtained.

"etc"

In order to improve reversibility, the positive photoresist composition for thick film according to the present invention may further contain polyvinyl resin. The polyvinyl resin preferably has a mass average molecular weight of 10,000 to 200,000, more preferably 50,000 to 100,000.

Such polyvinyl resin is poly (vinyl lower alkyl ether), and consists of a polymer or copolymer obtained by superposing | polymerizing single or 2 or more types of vinyl lower alkyl ethers represented by the following general formula (Vi-1).

In the general formula (Vi-1), Rvi ¹ represents a linear or branched alkyl group having 1 to 6 carbon atoms.

Such a polyvinyl resin is a polymer obtained from a vinyl compound. Specific examples of such polyvinyl resins include polyvinyl chloride, polystyrene, polyhydroxystyrene, polyvinyl acetate, polyvinylbenzoic acid, polyvinylmethyl ether, polyvinylethyl ether, polyvinyl alcohol, polyvinylpyrrolidone, poly Vinylphenols and copolymers thereof. The polyvinyl resin is preferably polyvinyl methyl ether from the low glass transition point.

Moreover, in order to improve adhesiveness with a board | substrate, the positive type photoresist composition for thick films which concerns on this invention can also be further contained. As the adhesive aid to be used, a functional silane coupling agent is preferred. Examples of the functional silane coupling agent include silane coupling agents having reactive substituents such as a carboxyl group, a methacryloyl group, an isocyanate group, and an epoxy group. In addition, specific examples of the functional silane coupling agent include trimethoxysilylbenzoic acid, γ-methacryloxypropyltrimethoxysilane, vinyltriacetoxysilane, vinyltrimethoxysilane, and γ-glycidoxypropyltrimethoxysilane and β- (3,4-epoxycyclohexyl) ethyltrimethoxysilane. The content of the adhesive aid is preferably 20 parts by mass or less based on 100 parts by mass of the total mass of the resin (A) and the alkali-soluble resin (C).

Moreover, in order to improve applicability | paintability, antifoaming property, leveling property, etc., the positive photoresist composition for thick films which concerns on this invention can also contain surfactant. Examples of the surfactant include BM-1000, BM-1100 (all manufactured by BM Chemi Corporation), Megapack F142D, Megapack F172, Megapack F173, Megapack F183 (all manufactured by Nippon Ink Chemical Co., Ltd.), Fluoride FC-135 Fluoride FC-170C, Fluoride FC-430, Fluoride FC-431 (all made by Sumitomo 3M), Supron S-112, Supron S-113, Supron S-131, Supron S-141, Commercially available fluorine-based surfactants such as SUPRON S-145 (all manufactured by Asahi Glass Co., Ltd.), SH-28PA, SH-190, SH-193, SZ-6032, SF-8428 (all manufactured by Toray Silicone Co., Ltd.). However, it is not limited to these.

In addition, the positive photoresist composition for thick film according to the present invention may further contain an acid, an acid anhydride, or a high boiling point solvent in order to perform fine adjustment of solubility in an alkaline developer.

Examples of acids and acid anhydrides include monocarboxylic acids such as acetic acid, propionic acid, n-butyric acid, isobutyric acid, n-valeric acid, isovaleric acid, benzoic acid, cinnamic acid; lactic acid, 2-hydroxybutyric acid, 3-hydroxybutyric acid, Hydroxy monocarboxylic acids, such as salicylic acid, m-hydroxy benzoic acid, p-hydroxy benzoic acid, 2-hydroxycinnamic acid, 3-hydroxycinnamic acid, 4-hydroxycinnamic acid, 5-hydroxyisophthalic acid, and cyringic acid Oxalic acid, succinic acid, glutaric acid, adipic acid, maleic acid, itaconic acid, hexahydrophthalic acid, phthalic acid, isophthalic acid, terephthalic acid, 1,2-cyclohexanedicarboxylic acid, 1,2,4-cyclohexanetricarboxyl Polyhydric carboxylic acids such as acid, butanetetracarboxylic acid, trimellitic acid, pyromellitic acid, cyclopentanetetracarboxylic acid, butanetetracarboxylic acid, 1,2,5,8-naphthalenetetracarboxylic acid; itaconic anhydride, succinic anhydride, citraconic anhydride , Nothing Dodecenyl succinic acid, tricarbanic anhydride, maleic anhydride, hexahydrophthalic anhydride, methyltetrahydrophthalic anhydride, hymic anhydride, 1,2,3,4-butanetetracarboxylic anhydride, cyclopentanetetracarboxylic dianhydride, And acid anhydrides such as phthalic anhydride, pyromellitic anhydride, trimellitic anhydride, benzophenone tetracarboxylic acid, ethylene glycol bis trimellitate anhydride, and glycerin tris anhydride.

In addition, examples of the high boiling point solvent include N-methylformamide, N, N-dimethylformamide, N-methylformanilide, N-methylacetamide, N, N-dimethylacetamide, N-methylpyrrolidone, and dimethyl. Sulfoxide, benzyl ethyl ether, dihexyl ether, acetyl acetone, isophorone, caproic acid, capuric acid, 1-octanol, 1-nonanol, benzyl alcohol, benzyl acetate, ethyl benzoate, diethyl oxalate, di maleic acid Ethyl, gamma -butyrolactone, ethylene carbonate, propylene carbonate, phenylcellosolve acetate, and the like.

The amount of the compound used for fine-adjusting the solubility in the alkaline developer as described above can be adjusted depending on the use and the coating method, and is not particularly limited as long as the composition can be uniformly mixed. It is 60 mass% or less, Preferably you may be 40 mass% or less.

Preparation of the positive type photoresist composition for thick films which concerns on this invention only mixes and stirs each said component by a conventional method, For example, it is necessary, such as a resolver, a homogenizer, and three roll mills. You may disperse and mix using a disperser. Moreover, after mixing, you may filter using a mesh, a membrane filter, etc. further.

The positive type photoresist composition for thick films according to the present invention comprises a thick film photoresist layer having a film thickness of about 5 to about 200 µm, preferably about 10 to about 120 µm, and more preferably about 10 to about 100 µm. Suitable for forming on

It does not specifically limit as a support body, A conventionally well-known thing can be used, For example, the board | substrate for electronic components, the thing in which predetermined wiring pattern was formed, etc. can be illustrated. Examples of the substrate include metal substrates such as silicon, silicon nitride, titanium, tantalum, palladium, titanium tungsten, copper, chromium, iron, and aluminum, and glass substrates. In particular, the thick film chemically amplified positive photoresist composition of the present embodiment can form a resist pattern even on a copper substrate. As a material of a wiring pattern, copper, a hander, chromium, aluminum, nickel, gold, etc. are used, for example.

<< manufacturing method of a thick film resist pattern >>

A thick film resist pattern can be manufactured as follows, for example. That is, the coating film (thick film photoresist layer) is formed by apply | coating the solution of the positive photoresist composition for thick films prepared as mentioned above on a support body, and removing a solvent by heating. As a coating method on a support body, methods, such as a spin coat method, the slit coat method, the roll coat method, the screen printing method, the applicator method, can be employ | adopted. Prebaking conditions of the coating film containing the composition of this embodiment differ with the kind of each component in a composition, a compounding ratio, coating film thickness, etc., but are usually 70-150 degreeC, Preferably it is 80-140 degreeC, and 2 ~ 60 minutes or so.

The thickness of the thick resist layer is preferably in the range of about 5 to about 200 占 퐉, preferably about 10 to about 120 占 퐉, more preferably about 10 to about 100 占 퐉.

Then, the obtained thick film resist layer is selectively irradiated (exposed) with radiation including electromagnetic waves or particle rays, for example, ultraviolet rays or visible rays having a wavelength of 300 to 500 nm through a mask of a predetermined pattern.

As a source of radiation, a low pressure mercury lamp, a high pressure mercury lamp, an ultra high pressure mercury lamp, a metal halide lamp, an argon gas laser, or the like can be used. The radiation includes microwaves, infrared rays, visible rays, ultraviolet rays, X rays,? Rays, electron rays, proton rays, neutron rays, and ion rays. The radiation dose varies depending on the type of each component in the composition, the compounding amount, the film thickness of the coating film, and the like, but is, for example, 100 to 10,000 mJ / cm 2 in the case of using an ultrahigh pressure mercury lamp. In addition, the radiation includes a light beam that activates the acid generator to generate an acid.

After exposure, the acid diffusion is promoted by heating using a known method to change the alkali solubility of the thick film photoresist layer of the exposed portion. Next, for example, a predetermined alkaline aqueous solution is used as a developing solution to dissolve and remove unnecessary portions to obtain a predetermined thick film resist pattern.

As a developing solution, for example, sodium hydroxide, potassium hydroxide, sodium carbonate, sodium silicate, sodium metasilicate, aqueous ammonia, ethylamine, n-propylamine, diethylamine, di-n-propylamine, triethylamine, methyldiethyl Amine, dimethylethanolamine, triethanolamine, tetramethylammonium hydroxide, tetraethylammonium hydroxide, pyrrole, piperidine, 1,8-diazabicyclo [5,4,0] -7-undecene, 1 An aqueous solution of alkalis, such as a 5-5-diazabicyclo [4,3,0] -5-nonane, can be used. An aqueous solution in which an appropriate amount of a water-soluble organic solvent such as methanol or ethanol or a surfactant is added to the aqueous alkaline solution may be used as a developer.

The development time varies depending on the type of each component of the composition, the blending ratio, and the dry film thickness of the composition, but is usually 1 to 30 minutes, and the development method is a liquid method, a dipping method, a paddle method, a spray development The law may be anything. After image development, washing with running water is performed for 30 to 90 seconds and dried using an air gun or an oven.

In addition, connection terminals such as metal posts and bumps can be formed by embedding conductors such as metal in the non-resist portions (parts removed by the alkaline developer) of the resist pattern thus obtained. In addition, the plating treatment method is not particularly limited and conventionally known various methods can be adopted. Especially as a plating liquid, hander plating, copper plating, gold plating, and a nickel plating liquid are used suitably.

The remaining resist pattern is finally removed using a stripping solution or the like according to a conventional method.

Since the positive photoresist composition for thick films of this invention contains an acid generator component (B1), it is excellent in lithography characteristics, such as a sensitivity, in pattern formation of the resist film using this resist composition. Although the reason is not clear, it is inferred as follows.

The naphthoquinone diazide structure contained in the acid generator component (B1) can be changed from hydrophobic to hydrophilic by decomposing upon exposure to generate carboxylic acid. By changing to hydrophilicity, it is inferred that the difference (dissolution contrast) of the solubility with respect to the developing solution of a non-exposure range and an exposure range improves and lithography characteristic improves.

In addition, since the naphthoquinone diazide structure has a wide absorption band, an acid generator having a naphthoquinone diazide structure has g-ray (436 nm), h-ray (405 nm), i-ray (365 nm), and KrF. (248 nm) and ArF (193 nm), it is thought that it is possible to use with good sensitivity even in a wide wavelength range.

Example

Hereinafter, the present invention will be described in more detail with reference to Examples, but the present invention is not limited to the following Examples.

Synthesis Example of Compound 1

PAG-A (4.0 g), 1,2-naphthoquinone diazide-4-sulfonyl chloride (3.2 g), and dichloromethane (29 g) were added, and it stirred at room temperature. Triethylamine (TEA) (1.3 g) was slowly added thereto and stirred at room temperature for 4 hours. Thereafter, the dichloromethane phase was washed with soft hydrochloric acid, and further washed three times with pure water, followed by distilling off the solvent under reduced pressure to obtain 3.6 g of Compound 1.

Obtained compound 1 measured the NMR and identified the structure from the following results.

¹ H-NMR (400 MHz, DMSO-d 6): δ (ppm) = 8.57 (1H, ArH), 8.34 (2H, ArH), 7.71-7.99 (14H, ArH), 2.21 (6H, CH ₃ ).

In the same manner as in compound 1, compound 2 was synthesized. The obtained compound performed NMR measurement and identified the structure from the following results.

Compound 2: ¹ H-NMR (400 MHz, DMSO-d6): δ (ppm) = 8.56, (1H, ArH), 8.46 (1H, ArH), 8.10 (1H, ArH), 7.86 (1H, ArH), 7.71 -7.89 (11H, ArH), 7.59 (2H, ArH), 2.30 (6H, CH ₃ ).

The compounds 1-2 were salt-exchanged with a predetermined anion, leading to the following compounds BQ-1 to BQ-4.

[Preparation of positive resist composition for thick film]

The positive type resist composition (Examples 1-4, Comparative Examples 1-2) for thick films which mix | blended each component by the compounding ratio shown in Table 1 was prepared.

And these were melt | dissolved uniformly and filtered through the membrane filter of 1 micrometer of pore diameters, and the positive resist composition for thick films of 30-60 mass% of solid content mass concentration was obtained.

In Table 1, each symbol has the following meanings, and the numerical value in [] is the compounding amount (parts by mass).

(A) -1; 12.5 mass parts of compounds represented by following formula (1) (l / m / n / o = 45/35/10/10) (molecular weight 200,000), and following formula (2) (l / m) 25 parts by mass of a mixed resin represented by (n / o / p = 25/20/5/10/40) (molecular weight 50,000)

(C) -1; 52.5 parts by mass of novolak resin (2/88 novolak resin molecular weight obtained by addition condensation in the presence of m / p-cresol = 6/4 and formaldehyde and acid catalyst), polyhydroxystyrene resin 10 parts by mass of VPS-2515 (made in Japan procurement company)

(BQ) -1 to (BQ) -4; the compounds BQ-1 to BQ-4 synthesized above, respectively.

B-1 to B-2; the following compounds B-1 to B-2, respectively.

(3); The compound represented by following formula (3).

(D) -1; triamylamine.

(E) -1; salicylic acid.

(S) -1; mixed solvent of PGMEA / 3-methoxybutyl acetate (mass ratio 40/60).

(Formation of thick film resist pattern)

(Examples 1-4 and Comparative Examples 1-2)

The positive photoresist compositions for thick films of each of the examples and the comparative examples obtained as described above were applied onto an 8 inch copper substrate using a spinner, and the applied photoresist composition was dried to have a film thickness of about 50 μm. A thick film photoresist layer was obtained. Next, this thick film resist layer was placed on a hot plate and prebaked at 140 ° C. for 5 minutes.

After prebaking, it exposed using exposure apparatus NSR-i14E (made by Nikon Corporation, NA: 0.54, (sigma): 0.59). Then, the wafer was placed on a hot plate and post-exposure baking (PEB) was performed at 85 캜 for 3 minutes. Then, the 2.38% tetramethylammonium hydroxide (TMAH) aqueous solution was dripped at the thick film photoresist layer, it was left to stand at 23 degreeC for 60 second, and this was repeated 4 times and developed. Thereafter, the resultant was washed with running water and blown with nitrogen to obtain a thick film resist pattern having a line and space pattern of 100 µm and a large area (10000 µm ² ) pattern.

The minimum amount of exposure in which a resist film with a large area pattern was absent was measured as Eth (mJ / cm 2). The results are shown in Table 2.

From the above results, it was confirmed that the positive resist composition for thick films of Examples 1 to 4 had better sensitivity than the positive resist composition for thick films of Comparative Examples 1-2.

Claims (6)

A positive resist composition used for forming a thick film resist pattern on a support, comprising: a resin component (A) in which solubility in a developer changes due to the action of an acid and an acid generator component (B) which generates an acid upon exposure And an acid generator (B1) containing the compound represented by the following general formula (b1-1), wherein said acid generator component (B) contains a positive type resist composition for thick films.

[Wherein, Y ¹ is a divalent linking group, W is S, Se or I, R ¹ is a hydrocarbon group which may have a substituent, and R ² is a C1-C5 alkyl or alkoxy group. M + n = 2 for W = I, m + n = 3 for W = S and Se, and m ≧ 1 and n ≧ 0. p is 0-5. X ^- is a dianion.] The method according to claim 1,
The said resin component (A) is a positive resist composition for thick films containing at least 1 sort (s) of resin chosen from the group which consists of novolak resin, a polyhydroxy styrene resin, and an acrylic resin. The method according to claim 1 or 2,
The positive resist composition for thick films whose solid content concentration is 30 mass% or more. A lamination step of laminating a thick film resist layer containing the positive resist composition for thick films according to any one of claims 1 to 3 on a support;
An exposure step of selectively irradiating an active ray or a radiation to the thick film resist layer;
And developing the exposed thick film resist layer in the exposing step to obtain a thick film resist pattern. The method of claim 4,
Wherein the thickness of the thick film resist layer is 10 占 퐉 or more. The manufacturing method of the connection terminal containing the process of forming the connection terminal which consists of a conductor in the non-resist part of the thick film resist pattern obtained using the manufacturing method of the thick film resist pattern of Claim 4 or 5.