JP2007327062A - Polymer for resist, resist composition, pattern forming method and starting compound for resist polymer - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a polymer for resist generating little line edge roughness and forming little defect in DUV excimer laser lithography, etc. <P>SOLUTION: The acrylic polymer for resist contains an acid-decomposable unit having a structure expressed by formula (3) and a unit having a hydrophilic group as constitution units. In the formula (3), K<SP>1</SP>and K<SP>2</SP>are each independently one or more groups selected from alkylene, cycloalkylene, oxyalkylene and arylene; L<SP>1</SP>and L<SP>2</SP>are each independently one or more groups selected from -C(O)- and -OC(O)-; M<SP>2</SP>groups are one or more groups selected from alkylene, cycloalkylene and oxyalkylene; and Y<SP>1</SP>and Y<SP>2</SP>are each independently an acid-decomposable bond containing a group having specific ether structure or a group having a specific cyclic ether. <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

  The present invention relates to a resist polymer, a resist composition, and a pattern manufacturing method, and more particularly to a chemically amplified resist composition suitable for fine processing using an excimer laser, an electron beam, and an X-ray. The present invention also relates to a novel raw material compound for producing a resist polymer.

  In recent years, in the field of microfabrication in the manufacture of semiconductor elements and liquid crystal elements, miniaturization has rapidly progressed due to advances in lithography technology. As a method for miniaturization, generally, a shorter wavelength of irradiation light is used. Specifically, from conventional ultraviolet rays typified by g-line (wavelength: 438 nm) and i-line (wavelength: 365 nm) to DUV ( The irradiation light is changing to Deep Ultra Violet.

At present, KrF excimer laser (wavelength: 248 nm) lithography technology is introduced into the market, and ArF excimer laser (wavelength: 193 nm) lithography technology for further shortening the wavelength is about to be introduced. Further, as a next-generation technique, an F ₂ excimer laser (wavelength: 157 nm) lithography technique has been studied. Also, as a slightly different type of lithography technology, electron beam lithography technology and EUV lithography technology using extreme ultraviolet light (Extreme Ultra Violet light: EUV light) in the vicinity of 13.5 nm have been energetically studied. .

  As a high-resolution resist for such short-wavelength irradiation light or electron beam, a “chemically amplified resist” containing a photoacid generator has been proposed. At present, improvements and development of this chemically amplified resist are energetically active. It is being advanced.

  As a resist resin used in ArF excimer laser lithography, an acrylic resin that is transparent with respect to light having a wavelength of 193 nm has attracted attention. As such an acrylic resin, for example, Patent Document 1 discloses a chemically amplified resist composition containing a polymer whose side chain is decomposed to show alkali solubility.

  However, when these polymers are used in a resist composition for ArF excimer laser lithography, there is a problem in solubility in a developing solution, and there is a problem that defects occur. There is also a problem that the line edge roughness is large.

  On the other hand, in KrF excimer laser lithography, Patent Document 2 describes a resist composition having high resolution and excellent etching resistance. In this document, a hydroxystyrene resin obtained by copolymerizing a crosslinking agent having a tertiary ester structure that decomposes with an acid is used as a raw material.

  However, since the resin described in Patent Document 2 is a styrene resin, it cannot be used for ArF excimer laser lithography. Therefore, it is conceivable to use an acrylic resin obtained by copolymerizing a crosslinking agent having a tertiary ester structure described in Patent Document 2, but a crosslinking agent having a tertiary ester structure that decomposes with an acid is simply an acrylic resin. Even when copolymerized with a resin, the line edge roughness and defects cannot be sufficiently improved.

JP 2003-122007 A Japanese Patent Laid-Open No. 2002-62656

  The present invention relates to a resist polymer, a resist composition, and a pattern manufacturing method using the resist composition, which have low line edge roughness and little defect generation when used in DUV excimer laser lithography or electron beam lithography. An object of the present invention is to provide a compound which is one of raw materials for producing this resist polymer.

  The first gist of the present invention relates to a resist polymer containing an acid-decomposable unit having a structure represented by the following formula (1) or (2) as a constituent unit.

(In the formula (1) and the formula (2), n represents an integer of 2 to 24. When n = 2, J may have a single bond or a substituent and / or a hetero atom. Represents a valent hydrocarbon group, and when n ≧ 3, it represents an n-valent hydrocarbon group which may have a substituent and / or a hetero atom, and E represents a polymerization terminator, a chain transfer agent, or a polymerization initiator. And each of K ¹ and K ² independently represents at least one selected from the group consisting of alkylene, cycloalkylene, oxyalkylene, arylene, divalent thiazoline ring, divalent oxazoline ring, and divalent imidazoline ring. L ¹ and L ² each independently represent at least one of the group consisting of —C (O) O—, —C (O) —, and —OC (O) —, and M ¹ , M ² , M ³ are each independently alkylene or cycloal Represents at least one member selected from the group consisting of xylene, oxyalkylene, and arylene, and Y, Y ¹ , and Y ² each independently represents an acid-decomposable bond, and k1, k2, l1, l2, m1, m2, And m3 each represent the number of K ¹ , K ² , L ¹ , L ² , M ¹ , M ² , and M ^{3 and} are independently 0 or 1. R ¹ represents a hydrogen atom or a methyl group. And S represents a sulfur atom.)

  The second gist of the present invention relates to an acrylic polymer for resists containing an acid-decomposable unit having a structure represented by the following formula (3) and a unit having a hydrophilic group as constituent units. .

(In Formula (3), K ¹ and K ² are each independently at least one selected from the group consisting of alkylene, cycloalkylene, oxyalkylene, arylene, divalent thiazoline ring, divalent oxazoline ring, and divalent imidazoline ring. L ¹ and L ² each independently represent at least one of the group consisting of —C (O) O—, —C (O) —, and —OC (O) —, and M ¹ , M ² , M ³ each independently represents at least one member selected from the group consisting of alkylene, cycloalkylene, oxyalkylene, and arylene, and Y ¹ and Y ² each independently represents an acid-decomposable bond, k1, k2, l1, l2, m1, m2, respectively m3 and ^{n1 K 1, K 2, L} 1, L 2, M 1, M 2, M 3, and represents the number of Y ^2, independently 0 or 1. the , R ² and R ³ Respectively independently represents a hydrogen atom or a methyl group.)

  The third gist of the present invention relates to a resist composition containing the resist polymer according to the first or second gist of the present invention described above.

  According to a fourth aspect of the present invention, there is provided a step of applying a composition containing a resist composition and a photoacid generator according to the third aspect of the present invention on a substrate to be processed, and exposing the applied product. The present invention relates to a pattern manufacturing method including a step and a step of developing the exposed product using a developer.

  The fifth gist of the present invention relates to a compound represented by the following formula (6) used in producing the resist polymer as the first gist of the present invention described above.

(In formula (6), n represents an integer of 2 to 24. J is a divalent hydrocarbon group which may have a single bond or a substituent and / or a hetero atom when n = 2. When n ≧ 3, it represents an n-valent hydrocarbon group which may have a substituent and / or a hetero atom, and E ¹ represents a functional group having a polymerization termination ability or a chain transfer ability. ¹ and K ² each independently represents an alkylene, cycloalkylene, oxyalkylene, arylene, a divalent thiazoline ring, a divalent oxazoline ring, and at least one of the group consisting of divalent imidazoline ring, L ¹ and L ² represents each independently at least one of the group consisting of —C (O) O—, —C (O) —, and —OC (O) —, and M ¹ and M ² are each independently alkylene, Cycloalkylene, oxyalkylene, And represents at least one of the group consisting of arylene, Y represents an acid-decomposable bond. Further, k1, k2, l1, l2 , m1, and m2, respectively ^{K 1, K 2, L 1} , L 2, M 1 And represents the number of M ² and is independently 0 or 1.)

  When used as a resist resin in DUV excimer laser lithography or electron beam lithography, the resist polymer of the present invention can be developed without losing high sensitivity and resolution as compared with conventional resist polymers. The solubility in the liquid is improved, the generation of defects is suppressed, and the line edge roughness is small.

  The present invention will be described below. Note that “(meth) acrylic acid” means “acrylic acid or methacrylic acid”, and “(meth) acrylonitrile” means “acrylonitrile or methacrylonitrile”.

  In the present invention, the acid-decomposable unit refers to a unit in which a repeating unit itself is decomposed by the bond of the repeating unit of the polymer being cleaved by the action of an acid. The unit having an acid leaving group refers to a unit having a group that is cleaved and removed by bonding of a portion other than the bond of the repeating unit of the polymer by the action of an acid.

  The resist polymer of the present invention contains an acid-decomposable unit as a constituent unit. The acid-decomposable unit is at least one of structural units represented by the following formulas (1) to (3).

In the formulas (1) to (3), R ^{1 to} R ³ each independently represent a hydrogen atom or a methyl group, and S represents a sulfur atom. N represents an integer of 2 to 24.

In formulas (1) to (3), K ¹ and K ² are each independently an alkylene, cycloalkylene, oxyalkylene, arylene, divalent thiazoline ring, divalent oxazoline ring, or divalent imidazoline ring. L ¹ and L ² each independently represent at least one of the group consisting of —C (O) O—, —C (O) —, and —OC (O) —, and M 1 ¹ to M ³ each independently represent at least one of the group consisting of alkylene, cycloalkylene, oxyalkylene, and arylene.

In the formulas (1) to (2), K ¹ and K ² are preferably alkylene, cycloalkylene, and arylene, and L ¹ and L ² are preferably —C (O) O— or OC (O) — ^{1 to} M ³ are preferably alkylene, cycloalkylene, or arylene.

K1, k2, l1, l2, m1, m2, and m3 represent the numbers of K ¹ , K ² , L ¹ , L ² , M ¹ , M ² , and M ³ , respectively, and are independently 0 or 1 It is.

In formulas (1) to (3), Y, Y ¹ and Y ² each independently represent an acid-decomposable bond.

  Here, the acid-decomposable bond is not particularly limited, and examples thereof include the following formulas (23-1) to (23-4).

(In the formulas (23-1) to (23-4), R ⁷⁰¹ , R ⁷⁰² , R ⁷⁰³ and R ⁷⁰⁴ are each independently a linear, branched or cyclic alkyl group or alkenyl group having 1 to 18 carbon atoms. Or an aryl group, or R ⁷⁰¹ , R ⁷⁰² , R ⁷⁰³ , and R ⁷⁰⁴ represent a cyclic hydrocarbon group together with the carbon atom to which they are bonded.

R ⁷⁰⁵ and R ⁷⁰⁶ each independently represents a hydrogen atom, a linear or branched alkyl group having 1 to 18 carbon atoms, an alkenyl group, or an aryl group.

^R707 represents a hydrogen atom, a linear or branched alkyl group having 1 to 4 carbon atoms, an alkenyl group, or an aryl group. Moreover, v1 is an integer of 1-5. )

  The action of the acid-decomposable bond will be described with reference to the above formulas (23-1) to (23-4). In the bond represented by the formula (23-1), an ester bond is decomposed by an acid to form a carboxy group and a residue. Moreover, as for the bond represented by the formula (23-2), a carbonate ester bond is decomposed by an acid by decarboxylation. The bonds represented by the formulas (23-3) and (23-4) are decomposed into acetal or ketal by an acid to form a hydroxyl group and a residue. Among them, the above formula (23-1) or (23-3) is preferable because of high acid decomposability.

  A polymer containing an acid-decomposable unit becomes soluble in an alkali developer or the like by being decomposed by the action of an acid. In the conventional resist polymer, the side chain of the structural unit having an acid leaving group was decomposed or eliminated and the polarity at the end of the side chain was increased, so that it was alkali-solubilized. There was no change. On the other hand, the polymer of the present invention is significantly reduced in molecular weight due to the decomposition of the polymer by the action of an acid, and the solubility in a developing solution is remarkably increased as compared with a conventional product. For this reason, such a polymer can be suitably used as a resist composition having a small line edge roughness and less defects.

  In the formula (1), J represents a single bond or a divalent hydrocarbon group which may have a substituent and / or a hetero atom when n = 2, and a substituent when n ≧ 3 And / or an n-valent hydrocarbon group which may have a hetero atom.

  In the formula (1), the structure represented by J binds a branch containing an acid-decomposable bond and a functional group having a polymerization termination ability or a chain transfer ability, or a vinyl ether group.

  In the formula (1), the substituents possessed by J itself include a thiol group, a hydroxy group, a carboxy group, an acyl group having 1 to 6 carbon atoms, a carboxy group esterified with an alcohol having 1 to 6 carbon atoms, and carbon. A straight chain having 1 to 6 carbon atoms which may have one or more groups selected from the group consisting of a carboxy group, a cyano group, an amino group, a halogen, and a nitroxy group thioesterified with a thiol having 1 to 6 A branched or cyclic alkyl group, a thiol group, a hydroxy group, a carboxy group, an acyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, a carboxy group esterified with an alcohol having 1 to 6 carbon atoms, carbon Examples thereof include a carboxy group, a cyano group, an amino group, a halogen or a nitroxy group thioesterified with a thiol having a number of 1 to 6. Moreover, as a hetero atom contained in J, a sulfur atom, a nitrogen atom, an oxygen atom, and a phosphorus atom are mentioned. At this time, the bond coming out of the heteroatom varies depending on the valence of the heteroatom.

  Examples of J include structures represented by the following formulas (24-1) to (24-198).

  Especially, what is represented by said Formula (24-1), (24-61), (24-179), (24-190)-(24-198) is preferable.

  Moreover, in Formula (1), E represents the residue of a polymerization terminator, a chain transfer agent, or a polymerization initiator.

In the formula (1), as the ^{E, -B 11 -, - S} -, - O -, - NB 12 -O- or -NB ¹² -B ¹¹ - represents, B ¹¹ is 1 to 6 carbon atoms A linear, branched or cyclic divalent hydrocarbon having 1 to 20 carbon atoms which may have at least one group selected from the group consisting of carboxy group, cyano group and amino group esterified with alcohol And B ¹¹ may have a hetero atom in its main skeleton, and B ¹² is a hydrogen atom, a linear, branched or cyclic alkyl group having 1 to 10 carbon atoms.

  In particular, in the formula (1), when n = 2 and E is -S-, the formula (1) has a structure represented by the following formula (4).

In formula (4), S represents a sulfur atom. Further, K ¹ , K ² , L ¹ , L ² , M ¹ , M ² , M ³ , Y ¹ , Y ² , k ¹ , k ² , l ¹ , l ² , m 1, m 2, m 3, and n 1 are represented by the formula (1 ).

  The resist polymer of the present invention contains the acid-decomposable units represented by the above formulas (1) to (3) as constituent units, whereby the resist defect and line edge roughness are improved.

  In particular, when the resist polymer contains an acid-decomposable unit represented by the above formulas (1) to (3) and a unit having a hydrophilic group, it exhibits a synergistic effect, and resist defects and line edge roughness. Is preferable because it tends to be good.

  In particular, in the case of the acid-decomposable unit represented by the formula (3), since this synergistic effect is great, it is preferably used in combination with a unit having a hydrophilic group.

  The resist polymer containing the acid-decomposable unit represented by the formula (3) and the unit having a hydrophilic group is preferably an acrylic polymer. Here, the acrylic polymer means a polymer containing 50 mol% or more of a structural unit of the following formula (25).

  In formula (25), R represents a hydrogen atom or a methyl group, and D represents an arbitrary group constituting a hydrophilic group or containing a hydrophilic group.

Here, the hydrophilic group means any one of —C (CF ₃ ) ₂ —OH, a hydroxy group, a cyano group, a methoxy group, a carboxy group, and an amino group.

  As a unit having the above hydrophilic group, D in the above formula (25) is a hydrogen atom, a linear or branched alkyl group having 1 to 6 carbon atoms, having at least the above hydrophilic group as a substituent, and 4 to 4 carbon atoms. It is preferably an 8 cyclic hydrocarbon group, a bridged cyclic hydrocarbon group having 4 to 16 carbon atoms, or a lactone group. Specifically, at least one selected from the group consisting of the following formulas (26-1) to (26-7) is preferable from the viewpoint of high dry etching resistance required for the resist. It is not limited to.

(In the above formula, R ⁵¹ , R ⁵² , R ⁵³ , R ⁵⁴ , R ⁵⁵ , R ⁵⁶ , R ⁵⁷ each independently represents a hydrogen atom or a methyl group, and R ⁵⁰¹ , R ⁵⁰² , R ⁵⁰³ , R ⁵⁰⁶ are each Independently represents a hydrogen atom or an alkyl group having 1 to 3 carbon atoms, R ⁵⁰⁴ and R ⁵⁰⁵ each independently represents an alkyl group having 1 to 3 carbon atoms, and R ⁵³¹ , R ⁵³² , R ⁵³³ , R ⁵³⁴ , R ⁵³⁵ , R ⁵³⁶ independently represents a hydrogen atom or a linear or branched alkyl group having 1 to 6 carbon atoms, R ⁵⁷¹ and R ⁵⁷² represent a bridged cyclic hydrocarbon group having 4 to 16 carbon atoms, or 4 to 4 carbon atoms, A straight chain or branched alkyl group having 1 to 6 carbon atoms having 16 bridged cyclic hydrocarbon groups, and a bridged cyclic carbonization having 4 to 16 carbon atoms together with the carbon atom to which R ⁵⁷¹ and R ⁵⁷² are bonded A hydrogen group may be formed, and W ¹ , W ² , and W ³ are each independently —O—, —S—, -NH- or a methylene chain having a chain length of 1 to 6 [-(CH ₂ ) _t- (t represents an integer of 1 to 6)], X ⁵¹ , X ⁵² , X ⁵³ , X ⁵⁴ , X ⁵⁵ , to X ^56, X ⁵⁷ are each independently, -C a substituent (CF _{3) 2} -OH, hydroxy group, a cyano group, a carboxy group, an acyl group having 1 to 6 carbon atoms, an ester with an alcohol having 1 to 6 carbon atoms A linear or branched alkyl group having 1 to 6 carbon atoms, which may have at least one group selected from the group consisting of a carboxy group and an amino group, —C (CF ₃ ) ₂ —OH, a hydroxy group , A cyano group, a carboxy group, an acyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, a carboxy group or an amino group esterified with an alcohol having 1 to 6 carbon atoms, n51, n52, n53 , N54, n55, and n56 represent an integer of 1 to 4. q1, q2 represents 0 or 1. Incidentally, n51, n52, n53, n54 , n55, when n56 is 2 or ^{more, X 51, X 52, X} 53, X 54, X 55, X 56 are each It includes having a plurality of different groups.

Here, the alkyl group of R ⁵⁷¹ and R ⁵⁷² and the bridged cyclic hydrocarbon group may have a linear or branched alkyl group having 1 to 6 carbon atoms, and further, a hydroxy group of R ⁵⁷¹ and R ⁵⁷² , You may have a carboxyl group esterified with a carboxy group, a C2-C6 acyl group, or a C1-C6 alcohol. )

R ⁵⁰¹ in formula (26-1), R ⁵⁰² in formula (26-3), R ⁵⁰³ in formula (26-4), R ⁵⁰⁶ in formula (26-6) is, in terms of sensitivity and resolution Is preferably a methyl group, an ethyl group, or an isopropyl group, and is preferably a hydrogen atom from the viewpoint of good solubility in an organic solvent.

  In formulas (26-1) to (26-6), n51, n52, n53, n54, n55, and n56 are preferably 1 from the viewpoint of high dry etching resistance.

X ⁵¹ , X ⁵² , X ⁵³ , X ⁵⁴ , X ⁵⁵ , and X ⁵⁶ in the formulas (26-1) to (26-6) are —C (CF ₃ ) ₂ —OH, A hydroxy group, a cyano group and a methoxy group are preferred. X ⁵⁷ in formula (26-7) represents —CH ₂ —C (CF ₃ ) ₂ —OH, —CH ₂ —OH group, —CH ₂ —CN group, —CH ₂ from the viewpoint of good pattern shape. It is preferably a —O—CH ₃ group or a — (CH ₂ ) ₂ —O—CH ₃ group.

W ^1, W ² in the formula (26-3), W ³ in the formula (26-6), from the viewpoint high dry etching _{resistance, -CH 2 -, - CH 2} CH 2 - is preferably a .

R ⁵³¹ , R ⁵³² , R ⁵³³ , and R ⁵³⁴ in formula (26-3) and R ⁵³⁵ and R ^{536 in} formula (26-6) are each independently from the viewpoint of high solubility in an organic solvent. And preferably a hydrogen atom, a methyl group, an ethyl group, or an isopropyl group.

  Q1 in Formula (26-3) and q2 in Formula (26-6) are preferably 1 from the viewpoint of high dry etching resistance, and 0 from the viewpoint of good solubility in organic solvents. It is preferable that

  R1 in the formula (26-4) is preferably 1 from the viewpoint of high dry etching resistance, and preferably 0 from the viewpoint of good solubility in an organic solvent.

R ⁵⁰⁴ and R ^{505 in} formula (26-5) are each independently preferably a methyl group, an ethyl group, or an isopropyl group from the viewpoint of sensitivity and resolution.

R ⁵⁷¹ and R ⁵⁷² in the formula (26-7) are such that, from the viewpoint of high dry etching resistance, R ⁵⁷¹ and R ⁵⁷² are combined together to form a carbon atom having 4 to 16 carbon atoms together with the carbon atom to which each is bonded. A structure in which a crosslinked cyclic hydrocarbon group is formed is preferable. From the standpoint of excellent heat resistance and stability, R ⁵⁷¹ and R ⁵⁷² are combined together to form a ring contained in a bridged cyclic hydrocarbon group formed together with the carbon atom to which each is bonded. It preferably has a ring, an adamantane ring, a norbornane ring, a pinane ring, a bicyclo [2.2.2] octane ring, a tetracyclododecane ring, a tricyclodecane ring, or a decahydronaphthalene ring.

In the formulas (26-1) to (26-6), the position substituted with X ⁵¹ , X ⁵² , X ⁵³ , X ⁵⁴ , X ⁵⁵ and X ⁵⁶ may be any position in the cyclic structure. .

  The structural unit which has a hydrophilic group can be used 1 type or in combination of 2 or more type as needed.

  Specific examples of the monomer that is a raw material for forming the structural unit having a hydrophilic group include monomers represented by the following formulas (27-1) to (27-103). In formulas (27-1) to (27-103), R represents a hydrogen atom or a methyl group.

  Among these, from the viewpoint of good solubility in a resist solvent, the above formulas (27-1) to (27-4), the above formulas (27-9) to (27-13), and the above formula (27-21). To (27-24), the above formulas (27-33) to (27-36), the above formulas (27-42) to (27-46), the above formulas (27-53) to (27-59), the above Formulas (27-78) to (27-79), Formulas (27-82) to (27-83), Formulas (27-88) to (27-89), Formulas (27-94) to ( 27-97), monomers represented by the above formula (27-100), geometric isomers thereof, and optical isomers thereof are more preferable, and in terms of high dry etching resistance, Formulas (27-37) to (27-42), Formulas (27-60) to (27-77), Formula (27-8) ) To (27-85), the above formulas (27-90) to (27-91), the above formula (27-99), the monomers represented by the above formulas (27-101) to (27-103). And geometrical isomers and optical isomers thereof are more preferable. From the viewpoint of sensitivity and resolution, the above formulas (27-5) to (27-8) and the above formulas (27-17) to ( 27-20), the above formulas (27-29) to (27-32), the above formulas (27-49) to (27-52), the above formulas (27-62) to (27-63), the above formula ( 27-68) to (27-69), the above formulas (27-74) to (27-75), the above formulas (27-80) to (27-81), the above formulas (27-86) to (27- 87), monomers represented by the above formulas (27-92) to (27-93), and geometric isomers thereof, and These optical isomers are more preferred.

  When the acid-decomposable unit is a structure represented by the formula (3), the structure represented by the formula (3) is preferably a structure represented by the following formula (5). When the structure represented by the formula (3) is the following formula (5), the defect of the resist tends to be particularly good.

In the formula (5), A represents an alkylene group having 1 to 18 carbon atoms, a cycloalkylene group, an oxyalkylene group, or a group obtained by arbitrarily combining these. R ^{2 to} R ⁵ each independently represents a hydrogen atom or a methyl group. When R ⁴ and / or R ⁵ is a methyl group, it tends to be excellent in decomposability, and when it is a hydrogen atom, it tends to be excellent in thermal stability and storage stability of the polymer.

  For example, in the structural unit containing an acid-decomposable acetal group represented by the following formula (28-1), an acetal bond is decomposed by an acid to become a carboxyl group and a vinyl ether.

  As decomposition examples of decomposition products, decomposition example 1, decomposition example 2, and decomposition example 3 are shown below.

  The resist polymer of the present invention may contain a unit having an acid-eliminable group as a constituent unit in addition to the aforementioned acid-decomposable unit and unit having a hydrophilic group.

  The structural unit having an acid leaving group is at least one selected from the group consisting of the following formulas (29-1) to (29-8) from the viewpoint of high dry etching resistance required for a resist. It is preferable.

(Wherein R ³¹ , R ³² , R ³³ , R ³⁴ , R ³⁵ , R ³⁶ , R ³⁷ , R ³⁸ represent a hydrogen atom or a methyl group, and R ²⁹¹ , R ²⁹² , R ²⁹³ , R ²⁹⁴ , R ²⁹⁵ Represents an alkyl group having 1 to 3 carbon atoms, X ¹ , X ² , X ³ , X ⁴ , X ⁵ and X ⁶ represent a linear or branched alkyl group having 1 to ⁶ carbon atoms, and n1, n2, n3 , N4, n5, n6 represent an integer of 0 to ^{4. When} n1, n2, n3, n4, n5, n6 is 2 or more, X ¹ , X ² , X ³ , X ⁴ , X ⁵ , Including a plurality of different groups as X ^6. R ³³¹ , R ³³² , R ³³³ , R ³³⁴ , R ³⁵¹ , R ³⁵² , R ³⁵³ , R ³⁵⁴ , R ³⁶¹ , R ³⁶² , R ³⁶³ , R ³⁶⁴ are each Independently represents a hydrogen atom, a linear or branched alkyl group having 1 to 6 carbon atoms, and Z ³ , Z ⁴ , Z ⁵ , Z ⁶ , Z ⁷ and Z ⁸ are each independently —O—, —S—, — NH- Methylene chain with a chain length _{1~6 [- (CH 2) u1} - (u1 represents an integer of 1 to 6)] represents, q, q3, q4 is 0 or 1, r is 0 to 2 integer Represents.

In formula (29-5), R ³⁵⁵ , R ³⁵⁶ and R ³⁵⁷ are each independently a monovalent alicyclic hydrocarbon group having 4 to 20 carbon atoms or a derivative thereof, or a linear or branched group having 1 to 4 carbon atoms. And at least one of R ³⁵⁵ , R ³⁵⁶ and R ³⁵⁷ is the alicyclic hydrocarbon group or a derivative thereof, or any two of R ³⁵⁵ , R ³⁵⁶ and R ³⁵⁷ are Bonded to each other to form an alicyclic hydrocarbon group having 4 to 20 carbon atoms or a derivative thereof together with the carbon atoms to which they are bonded, and was not involved in bonding among R ³⁵⁵ , R ³⁵⁶ , and R ³⁵⁷ . The remaining one represents a linear or branched alkyl group having 1 to 4 carbon atoms, a monovalent alicyclic hydrocarbon group having 4 to 20 carbon atoms, or a derivative thereof.

In the formula (29-6), R ³⁶⁷ represents a monovalent alicyclic hydrocarbon group having 4 to 20 carbon atoms or a derivative thereof, or a linear or branched alkyl group having 1 to 4 carbon atoms, and R ³⁶⁵ , R ³⁶⁶ represents a hydrogen atom, or R ³⁶⁵ and R ³⁶⁷ or R ³⁶⁶ and R ³⁶⁷ are bonded to each other, and together with the carbon atom to which each is bonded, an alicyclic ring having 4 to 20 carbon atoms The remaining one of the R ³⁶⁵ and R ³⁶⁶ that did not participate in the bond represents a hydrogen atom.

In the formula (29-7), R ³⁷³ represents a monovalent alicyclic hydrocarbon group having 4 to 20 carbon atoms or a derivative thereof, or a linear or branched alkyl group having 1 to 4 carbon atoms, and R ³⁷¹ , R ³⁷² each represents a hydrogen atom, or R ³⁷¹ and R ³⁷³ or R ³⁷² and R ³⁷³ are bonded to each other, and together with the carbon atom to which each is bonded, an alicyclic ring having 4 to 20 carbon atoms The remaining one of R ³⁷¹ and R ³⁷² that formed the formula hydrocarbon group or derivative thereof and did not participate in the bond represents a hydrogen atom.

In formula (29-8), R ³⁸¹ , R ³⁸² and R ³⁸³ each independently represents a linear or branched alkyl group having 1 to 4 carbon atoms. )

R ²⁹¹ in formula (29-1), R ²⁹² and R ^{293 in} formula (29-2), R ²⁹⁴ in formula (29-3), R ^{295 in} formula (29-4) are sensitivity and From the viewpoint of resolution, a methyl group, an ethyl group, or an isopropyl group is preferable.

  N1, n2, n3, n4, n5, and n6 in the formulas (29-1) to (29-6) are preferably 0 from the viewpoint of high dry etching resistance.

Z ³ and Z ^{4 in} formula (29-3), Z ⁵ and Z ^{6 in} formula (29-5), and Z ⁷ and Z ^{8 in} formula (29-6) have high dry etching resistance. And each independently preferably —CH ₂ — or —CH ₂ CH ₂ —.

R ³³¹ , R ³³² , R ³³³ and R ³³⁴ in formula (29-3), R ³⁵¹ , R ³⁵² , R ³⁵³ and R ³⁵⁴ in formula (29-5), R ^{361 in} formula (29-6) , R ³⁶² , R ³⁶³ and R ³⁶⁴ are each independently preferably a hydrogen atom, a methyl group, an ethyl group or an isopropyl group from the viewpoint of high solubility in an organic solvent.

  Q in the formula (29-3), q3 in the formula (29-5), and q4 in the formula (29-6) are preferably 1 in view of high dry etching resistance. From the viewpoint of good solubility, 0 is preferable.

  R in the formula (29-4) is preferably 1 from the viewpoint of high dry etching resistance, and preferably 0 from the viewpoint of good solubility in an organic solvent.

-C (R ³⁵⁵ ) (R ³⁵⁶ ) (R ³⁵⁷ ) in the formula (29-5) is represented by the following formulas (K-1) to (K-6) from the viewpoint of excellent line edge roughness. In view of high dry etching resistance, structures represented by the following formulas (K-7) to (K-17) are preferable.

-C (R ³⁶⁵ ) (R ³⁶⁶ ) -O-R ³⁶⁷ in the formula (29-6) is represented by the following formulas (J-1) to (J-24) in that it has excellent line edge roughness. The structure represented by following formula (J-25)-(J-52) is preferable at the point with high dry etching tolerance.

-C (R ³⁷¹ ) (R ³⁷² ) -O-R ³⁷³ in the formula (29-7) is represented by the above formulas (J-1) to (J-24) in that it has excellent line edge roughness. The structure represented by said Formula (J-25)-(J-52) is preferable at the point with the high dry etching tolerance.

  The structural unit which has an acid leaving group can be used 1 type or in combination of 2 or more type as needed.

  Specific examples of the monomer that is a raw material for forming the structural unit having an acid leaving group include monomers represented by the following formulas (30-1) to (30-196). In formulas (30-1) to (30-196), R and R ′ each independently represents a hydrogen atom or a methyl group.

  Among these, from the points of sensitivity and resolution, the above formulas (30-1) to (30-3), the above formula (30-5), the above formula (30-16), the above formula (30-19), the above formula (30), 30-20), the above formula (30-22), the above formula (30-23), the above formulas (30-25) to (30-28), the above formula (30-30), and the above formula (30-31). The monomers represented by the above formula (30-33), the above formula (30-34), the above formulas (30-102) to (30-129), and their geometrical isomers and optical isomers. Preferably, the above formula (30-1), the above formula (30-2), the above formula (30-16), the above formula (30-20), the above formula (30-23), the above formula (30-28), Formula (30-31), Formula (30-34), Formula (30-109), Formula (30-111), Top Equation (30-114) - (30-117), the formula (30-125), the formula (30-128) and a monomer represented by the formula (30-129) are particularly preferred.

  Moreover, from the point which is excellent in line edge roughness, it represents with the monomer represented by said Formula (30-35)-(30-40), said Formula (30-52)-(30-62). Monomer, monomers represented by the above formulas (30-76) to (30-88), monomers represented by the above formulas (30-130) to (30-135), the above formula (30 -147) to (30-157), monomers represented by the above formulas (30-171) to (30-183), and geometrical isomers and optical isomers thereof. preferable.

  Moreover, from the point which is excellent in dry etching tolerance, it represents with the monomer represented by said Formula (30-41)-(30-51), said Formula (30-63)-(30-75). Monomer, monomers represented by the above formulas (30-89) to (30-101), monomers represented by the above formulas (30-136) to (30-146), the above formula (30 -158) to (30-170), monomers represented by the above formulas (30-184) to (30-196), and geometrical and optical isomers thereof are more preferable.

  The resist polymer of the present invention can contain a structural unit having a lactone skeleton in addition to the structural unit described above because of its excellent adhesion to the substrate.

  The structural unit having a lactone skeleton is preferably at least one selected from the group consisting of the following formulas (31-1) to (31-5) from the viewpoint of sensitivity or dry etching resistance.

(In the ^{formula, R 41, R 42, R} 43, R 44, R 311, R 312 and R ³¹³ are each independently represent a hydrogen atom or a methyl ^{group, R 401, R 402, R} 201, R 202, R ²⁰³ , R ²⁰⁴ , R ⁹¹ , R ⁹² , R ⁹³ , R ⁹⁴ , A ¹ , A ² , A ³ , A ⁴ are each independently a hydrogen atom, a linear or branched alkyl group having 1 to 6 carbon atoms, a hydroxy group Represents a carboxy group or a carboxy group esterified with an alcohol having 1 to 6 carbon atoms, and X ⁴¹ , X ⁴² , X ⁴³ and X ⁴⁴ are each a hydroxy group, a carboxy group, or an acyl having 1 to 6 carbon atoms as a substituent. A carbon number which may have at least one group selected from the group consisting of a group, an alkoxy group having 1 to 6 carbon atoms, a carboxy group esterified with an alcohol having 1 to 6 carbon atoms, a cyano group and an amino group 1-6 linear or branched alkyl groups, hydro A carboxy group, an carboxy group, an acyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, a carboxy group esterified with an alcohol having 1 to 6 carbon atoms, or an amino group; n41, n42, n43 N44 represents an integer of 0 to 4. In the case where n41, n42, n43, and n44 are 2 or more, X ⁴¹ , X ⁴² , X ⁴³ , and X ⁴⁴ each include a plurality of different groups. ¹¹ , Y ¹² and Y ¹³ each independently represent —CH ₂ — or —CO—O—, of which at least one represents —CO—O—, i represents 0 or 1, m30 and m31 represent 1 Or R ⁴⁰¹ and R ⁴⁰² (when i = 1), R ⁹¹ and R ⁹² (when m31 = 1) are taken together to form a methylene chain having 2 to 6 carbon atoms [— (CH ₂ ) _j - (j represents an integer of 2-6)], or -O -, - S -, - NH- Methylene chain having 1 to 6 carbon atoms containing _{[- (CH 2) k -} (k represents an integer of 1 to 6) may form a (in the case of m1 = 2) R ⁹¹ s or R ⁹² together , A ¹ and A ² , A ³ and A ⁴ together may contain —O—, —S—, or —NH—, a C 1-6 methylene chain [— (CH ₂ ) _l -(L represents an integer of 1 to 6)] or -O-, -S-, -NH- may be formed.

  In these formulas, the linear or branched alkyl group having 1 to 6 carbon atoms includes methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, isobutyl group, t-butyl group, n- Pentyl group, neo-pentyl group, 1,1-dimethylpropyl group, 1,2-dimethylpropyl group, 1,1-dimethylbutyl group, 2,2-dimethylbutyl group, n-hexyl group, 1-methylpentyl group , 2-methylpentyl group, 3-methylpentyl group and the like.

  N41, n42, n43, and n44 in the formulas (31-1) to (31-4) are preferably 0 from the viewpoint of high dry etching resistance.

  M30 in the formula (31-1) is preferably 1 in terms of sensitivity and resolution.

A ¹ and A ² in the formula (31-2), A ³ and A ⁴ in the formula (31-3), from the viewpoint high dry etching resistance is -CH together ₂ -, - CH ₂ CH ₂ — is preferable, and from the viewpoint of high solubility in an organic solvent, it is preferable to form —O— together.

R ²⁰¹ and R ²⁰² in the formula (31-2) and R ²⁰³ and R ²⁰⁴ in the formula (31-3) are each independently a hydrogen atom, a methyl group, from the viewpoint of high solubility in an organic solvent, It is preferably an ethyl group or an isopropyl group.

R ³¹¹ , R ³¹² and R ^{313 in} formula (31-4) are preferably a hydrogen atom from the viewpoint of high solubility in an organic solvent.

Y ¹¹ , Y ¹² and Y ¹³ in the formula (31-4) are one of —CO—O— and the remaining two are —CH ₂ — from the viewpoint of high adhesion to the substrate surface and the like. It is preferable.

In formula (31-5), R ⁹¹ , R ⁹² , R ⁹³ and R ⁹⁴ are each independently preferably a hydrogen atom or a methyl group from the viewpoint of high solubility in an organic solvent.

  M31 in Formula (31-5) is preferably 1 from the viewpoints of sensitivity and resolution.

  The structural unit having a lactone skeleton may be one type or two or more types.

  Specific examples of the monomer that is a raw material for forming the structural unit having a lactone skeleton include monomers represented by the following formulas (32-1) to (32-26). In formulas (32-1) to (32-26), R represents a hydrogen atom or a methyl group.

  Among these, from the viewpoint of sensitivity, the monomers represented by the above formulas (32-1) to (32-3) and the above formula (32-5), and geometric isomers and optical isomers thereof are more preferable. From the point of dry etching resistance, the above formulas (32-7), (32-9), (32-10), (32-12), (32-14), (32-24) to (32-26) ), And geometric isomers and optical isomers thereof are more preferable. From the viewpoint of solubility in a resist solvent, the above formulas (32-8), (32-13), and Monomers represented by (32-16) to (32-23), and geometric isomers and optical isomers thereof are more preferable.

  The resist polymer of the present invention is excellent in the dry etching resistance required for the resist in addition to the structural units described above, and therefore has an alicyclic skeleton having no acid-eliminable group and no hydrophilic group. The structural unit which has (nonpolar alicyclic skeleton) can be contained.

Here, the alicyclic skeleton is a skeleton having one or more cyclic saturated hydrocarbon groups.
The structural unit having the nonpolar alicyclic skeleton may be one type or two or more types.
As the structural unit having the nonpolar alicyclic skeleton, structural units represented by the following formulas (33-1) to (33-4) are preferable from the viewpoint of high dry etching resistance required for a resist. .

(In the formula, R ³⁰¹ , R ³⁰² , R ³⁰³ and R ³⁰⁴ each independently represent a hydrogen atom or a methyl group, and X ³⁰¹ , X ³⁰² , X ³⁰³ and X ³⁰⁴ are each independently a straight chain having 1 to 6 carbon atoms. Alternatively, it represents a branched alkyl group, and n301, n302, n303, and n304 each independently represents an integer of 0 to 4. When n301, n302, n303, and n304 are 2 or more, X ³⁰¹ , X ³⁰² , X ³⁰³ , X ^{304 includes} a plurality of different groups, and p and p1 each independently represents an integer of 0 to 2.)

In the equation (33-1) - (33-4), the position X ^301, X ^302, X ³⁰³ and X ³⁰⁴ are attached can be anywhere cyclic structure.

  N301, n302, n303, and n304 in the formulas (33-1) to (33-4) are preferably 0 from the viewpoint of high dry etching resistance.

  P in formula (33-3) and p1 in formula (33-4) are preferably 0 from the viewpoint of high solubility in organic solvents, and are 1 from the viewpoint of high dry etching resistance. It is preferable.

  In order to introduce such a structural unit into the polymer, a monomer having a nonpolar alicyclic skeleton may be copolymerized. Monomers having a nonpolar alicyclic skeleton can be used alone or in combination of two or more as required.

  Examples of the monomer having a nonpolar alicyclic skeleton include cyclohexyl (meth) acrylate, isobornyl (meth) acrylate, norbornyl (meth) acrylate, adamantyl (meth) acrylate, and (meth) acrylate tri Cyclodecanyl, dicyclopentadienyl (meth) acrylate, and derivatives having a linear or branched alkyl group having 1 to 6 carbon atoms on the alicyclic skeleton of these compounds are preferred.

  Specific examples of the monomer having a nonpolar alicyclic skeleton include monomers represented by the following formulas (34-1) to (34-5). In formulas (34-1) to (34-5), R represents a hydrogen atom or a methyl group.

  The resist polymer of the present invention may further contain structural units other than those described above.

  Examples of the monomer that is a raw material for forming the structural unit include, for example, methyl (meth) acrylate, ethyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, n-propyl (meth) acrylate, ( (Meth) acrylic acid isopropyl, (meth) butyl acrylate, (meth) acrylic acid isobutyl, (meth) acrylic acid tert-butyl, (meth) acrylic acid methoxymethyl, (meth) acrylic acid n-propoxyethyl, (meth) Iso-propoxyethyl acrylate, n-butoxyethyl (meth) acrylate, iso-butoxyethyl (meth) acrylate, tert-butoxyethyl (meth) acrylate, 2-hydroxyethyl (meth) acrylate, (meth) 3-hydroxypropyl acrylate, 2-hydroxy- (n-propyl) (meth) acrylate Pill, 4-hydroxy-n-butyl (meth) acrylate, 2-ethoxyethyl (meth) acrylate, 1-ethoxyethyl (meth) acrylate, 2,2,2-trifluoroethyl (meth) acrylate, (Meth) acrylic acid 2,2,3,3-tetrafluoro-n-propyl, (meth) acrylic acid 2,2,3,3,3-pentafluoro-n-propyl, α- (tri) fluoromethylacrylic Acid methyl, α- (tri) fluoromethyl acrylate ethyl, α- (tri) fluoromethyl acrylate 2-ethylhexyl, α- (tri) fluoromethyl acrylate n-propyl, α- (tri) fluoromethyl acrylate iso -Propyl, α- (tri) fluoromethyl acrylate n-butyl, α- (tri) fluoromethyl acrylate iso-butyl, α- (tri) fluoromethyl Tert-butyl acrylate, methoxymethyl α- (tri) fluoromethyl acrylate, ethoxyethyl α- (tri) fluoromethyl acrylate, n-propoxyethyl α- (tri) fluoromethyl acrylate, α- (tri) fluoro Iso-propoxyethyl methyl acrylate, n-butoxyethyl α- (tri) fluoromethyl acrylate, iso-butoxyethyl α- (tri) fluoromethyl acrylate, tert-butoxyethyl α- (tri) fluoromethyl acrylate, etc. (Meth) acrylic acid ester having a linear or branched structure of

  Styrene, α-methylstyrene, vinyltoluene, p-hydroxystyrene, p-tert-butoxycarbonylhydroxystyrene, 3,5-di-tert-butyl-4-hydroxystyrene, 3,5-dimethyl-4-hydroxystyrene, aromatic alkenyl compounds such as p-tert-perfluorobutylstyrene and p- (2-hydroxy-iso-propyl) styrene;

  Unsaturated carboxylic acids and carboxylic anhydrides such as (meth) acrylic acid, maleic acid, maleic anhydride, itaconic acid, itaconic anhydride;

  Examples thereof include ethylene, propylene, norbornene, tetrafluoroethylene, acrylamide, N-methylacrylamide, N, N-dimethylacrylamide, vinyl chloride, vinyl fluoride, vinylidene fluoride, and vinylpyrrolidone. These monomers can be used alone or in combination of two or more as required.

  Usually, the sum of the structural units other than the structural unit having a hydrophilic group, the structural unit having an acid-eliminable group, and the structural unit having a lactone skeleton has a range of 20 mol% or less based on the entire polymer. preferable.

  The mass average molecular weight of the resist polymer of the present invention is not particularly limited, but is preferably 1,000 or more, more preferably 2,000 or more, from the viewpoint of dry etching resistance and resist pattern shape. Of 5,000 or more, more preferably 5,000 or more. Further, the mass average molecular weight of the resist polymer of the present invention is preferably 100,000 or less, more preferably 50,000 or less, and more preferably 30,000, from the viewpoints of solubility in a resist solution and resolution. The following is particularly preferable, and from the viewpoint of line edge roughness and skirting, 15,000 or less is more preferable.

  Next, a method for producing the resist polymer of the present invention will be described.

  A resist polymer containing an acid-decomposable unit having a structure represented by the formula (1) as a constituent unit is polymerized using a polymerization initiator and a compound represented by the following formula (6). Can be manufactured.

In the formula (6), E ¹ represents a functional group having a polymerization termination ability or a chain transfer ability. J, K ¹ , K ² , L ¹ , L ² , M ¹ , M ² , M ³ , Y ¹ , Y ² , k1, k2, l1, l2, m1, m2, m3, n1, and n are Each is synonymous with Formula (1).
Examples of the functional group E ¹ having a polymerization termination ability or chain transfer ability include radical groups such as a hydroxyl group substituted with a halogen atom such as bromine or a halogen group such as a hydroxy group or a thiol group, or a radical group such as a nitroxy radical. Can be mentioned.

In particular, in Formula (6), when n = 2 and E ¹ is a thiol group, Formula (6) has a structure represented by Formula (7) below.

In formula (7), S represents a sulfur atom. Further, K ¹ , K ² , L ¹ , L ² , M ¹ , M ² , M ³ , Y ¹ , Y ² , k ¹ , k ² , l ¹ , l ² , m 1, m 2, m 3, and n 1 are represented by the formula (1 ).

  Specific examples of the compounds represented by the formulas (6) and (7) include the following formulas (35-1) to (35-80). Among these, the following formula (35-3), the following formula (35-25), and the following formula (35-26) are preferable.

  0.1-30 mol% is preferable and, as for the ratio of the structural unit derived from the compound which has an acid-decomposable bond in a polymer, 0.1-15 mol% is more preferable.

  The production method of the resist polymer of the present invention is not limited, but is preferably obtained by radical polymerization of the monomer composition in the presence of a polymerization initiator. Polymerization by radical polymerization can be produced at low cost, and the resulting polymer has few foreign substances and high transparency.

  A mechanism for producing the polymer of the present invention by radical polymerization will be described.

  In radical polymerization, first, a polymerization initiator is decomposed by heat or the like to generate a radical, and monomer chain polymerization proceeds from this radical as a starting point. Thereafter, a polymer having a radical at the growth end is generated, but when a functional group having chain transfer capability (chain transfer functional group) is used, the radical at the growth end extracts hydrogen of the chain transfer functional group, and the growth end Becomes a deactivated polymer. On the other hand, the chain transfer functional group from which hydrogen is extracted becomes a structure having a radical, that is, a radical body, and the monomer is chain-polymerized again starting from the radical body. When a chain transfer functional group having a plurality of functional groups is used, polymerization proceeds from each functional group, and an acid-decomposable bond is incorporated into the main chain of the obtained polymer.

  Even in an anionic polymerization reaction, it is possible to incorporate an acid-decomposable bond into a polymer by adding a compound having a functional group having a polymerization termination ability among the compounds having an acid-decomposable bond at the end of polymerization. is there.

  As the polymerization initiator used in the production of the resist polymer of the present invention, those that generate radicals efficiently by heat are preferable. Examples of such a polymerization initiator include 2,2′-azobisisobutyronitrile, dimethyl-2,2′-azobisisobutyrate, 2,2′-azobis [2- (2-imidazoline- Azo compounds such as 2-yl) propane; and organic peroxides such as 2,5-dimethyl-2,5-bis (tert-butylperoxy) hexane. In addition, when producing a resist polymer used in ArF excimer laser (wavelength: 193 nm) lithography, the light transmittance of the resulting resist polymer (transmittance for light with a wavelength of 193 nm) is not reduced as much as possible. As the polymerization initiator to be used, those having no aromatic ring in the molecular structure are preferable. Furthermore, in consideration of safety during polymerization, the polymerization initiator used preferably has a 10-hour half-life temperature of 60 ° C. or higher.

  When producing the resist polymer of the present invention, a chain transfer agent (chain transfer agent B) other than the acid-decomposable chain transfer agent may be used.

  Suitable examples of the chain transfer agent B include 1-butanethiol, 2-butanethiol, 1-octanethiol, 1-decanethiol, 1-tetradecanethiol, cyclohexanethiol, 2-methyl-1-propanethiol, 2 -Thiols such as mercaptoethanol, 1-thioglycerol, mercaptoacetic acid and the like.

  When producing a resist polymer used in ArF excimer laser (wavelength: 193 nm) lithography, the chain used is that the light transmittance (transmittance with respect to light having a wavelength of 193 nm) of the resulting resist polymer is not lowered as much as possible. As the transfer agent, those having no aromatic ring are preferable.

  The amount of the polymerization initiator used is not particularly limited, but is preferably 0.3 mol% or more with respect to the total amount of monomers used for copolymerization, and 1 mol% is preferable in terms of increasing the yield of the copolymer. More preferably, from the viewpoint of narrowing the molecular weight distribution of the copolymer, it is preferably 30 mol% or less based on the total amount of monomers used for the copolymerization.

  Although the usage-amount of the compound which has the said acid-decomposable bond is not specifically limited, 0.01-30 mol% is preferable with respect to the monomer whole quantity used for copolymerization, and 0.1-15 mol% is more preferable. . The compound having an acid-decomposable bond used is almost quantitatively incorporated into the polymer.

  The method for producing the polymer of the present invention is not particularly limited, but solution polymerization is generally preferred. Among them, from the viewpoint that a polymer having a narrow composition distribution and / or molecular weight distribution can be easily obtained, a monomer that becomes a constituent unit of a target polymer by polymerization (even if only a monomer is used, The polymer of the present invention is preferably produced by a polymerization method called dropping polymerization in which the polymerization is carried out while dropping the solution in an organic solvent.

  Although the polymerization temperature in the dropping polymerization method is not particularly limited, it is usually preferably in the range of 50 to 150 ° C.

  As the organic solvent used in the dropping polymerization method, a solvent that can dissolve any of the monomers used in the polymerization, such as the monomer to be used, the polymerization initiator and the resulting polymer, and the compound having an acid-decomposable bond, is preferable. Examples of such an organic solvent include 1,4-dioxane, isopropyl alcohol, acetone, tetrahydrofuran (hereinafter also referred to as “THF”), methyl ethyl ketone (hereinafter also referred to as “MEK”), methyl isobutyl ketone (hereinafter referred to as “MIBK”). And γ-butyrolactone, propylene glycol monomethyl ether acetate (hereinafter also referred to as “PGMEA”), ethyl lactate, and the like.

  The monomer concentration of the monomer solution dropped into the organic solvent is not particularly limited, but is preferably in the range of 5 to 50% by mass.

  The amount of the organic solvent charged into the polymerization vessel is not particularly limited and may be determined as appropriate. Usually, 30 to 700% by mass is preferable with respect to the total amount of monomers used for copolymerization.

  The polymer solution produced by a method such as solution polymerization can be prepared with a good solvent viscosity such as 1,4-dioxane, acetone, THF, MEK, MIBK, γ-butyrolactone, PGMEA, and ethyl lactate as necessary. Then, it is dropped into a large amount of poor solvent such as methanol or water to precipitate the polymer. This process is generally called reprecipitation and is very effective for removing unreacted monomers, polymerization initiators, etc. remaining in the polymerization solution. If these unreacted substances remain as they are, there is a possibility of adversely affecting the resist performance. Therefore, it is preferable to remove them as much as possible. The reprecipitation step may be unnecessary in some cases. Thereafter, the precipitate is filtered off and sufficiently dried to obtain the polymer of the present invention. Moreover, after filtering off, it can also be used with a wet powder, without drying.

  Further, the produced copolymer solution can be used as a resist composition as it is or after being diluted with an appropriate solvent. At that time, additives such as a storage stabilizer may be appropriately added.

  Moreover, the resist polymer containing an acid-decomposable unit having a structure represented by the formula (1) as a constituent unit has the following formula (8-1) at the end of at least one molecular chain, in addition to the method described above. ) To (8-4) can be produced by reacting a polymer precursor (P) having at least one structure selected from the group consisting of (8-4) and a vinyl ether compound represented by the following formula (9).

In formulas (8-1) to (8-4), B ¹ has at least one group selected from the group consisting of a carboxy group esterified with an alcohol having 1 to 6 carbon atoms, a cyano group, and an amino group. Represents a linear, branched or cyclic divalent hydrocarbon group having 1 to 20 carbon atoms, and B ² is a hydrogen atom, a linear or branched alkyl group having 1 to 10 carbon atoms, or a cyclic group. Represents an alkyl group.

Moreover, in Formula (9), n represents the integer of 2-24. J represents a single bond or a divalent hydrocarbon group which may have a substituent and / or a hetero atom when n = 2, and a substituent and / or a hetero atom when n ≧ 3. It represents an n-valent hydrocarbon group that may have. X represents a single bond or ^{-B 11 -, - S-B} 11 -, - O-B 11 -, - O-NB 12 -, - NB 12 -B 11 - or ^{-O-Si (B 13) (} B 14 )-, And B ¹¹ may have at least one group selected from the group consisting of a carboxy group esterified with an alcohol having 1 to 6 carbon atoms, a cyano group, and an amino group. 20 represents a straight chain, branched or cyclic divalent hydrocarbon group, and B ¹¹ may have a hetero atom in its main skeleton, B ¹² represents a hydrogen atom, a straight chain of 1 to 10 carbon atoms, B ¹³ and B ¹⁴ each independently represent a hydrogen atom, a linear or branched alkyl group having 1 to 10 carbon atoms, or a cyclic alkyl group. )

  The polymer precursor (P) of the present invention is at least one selected from the group consisting of the above formulas (8-1) to (8-4) at least one of the molecular terminals. That is, for at least one molecular chain in the polymer, at least one of the molecular chain terminals may be at least one selected from the group consisting of the formulas (8-1) to (8-4). The molecular chain terminal is preferably contained in an average of 0.2 to 2, more preferably 0.4 to 1, more preferably 0.5 to 1 per molecule. A large amount is effective for reducing defects and improving line edge roughness, and a small amount is difficult to cause gelation.

For example, when the polymer precursor (P) contains a molecular chain terminal represented by the formula (8-2), ³³ S-NMR is measured, and -SH or -S- This can be confirmed by changing S- to -S-. The molecular chain terminal concentration can be quantified by measuring the sulfur atom content by fluorescent X-ray analysis.

  Among the molecular ends, the molecular ends represented by formula (8-1) and formula (8-2) are preferable.

Examples of the linear, branched or cyclic divalent hydrocarbon group having 1 to 20 carbon atoms contained in B ¹ include, for example, a methylene group, an ethylene group, a propylene group, a tetramethylene group, a 1,2-butylene group, 1 Alkylene groups such as 1,3-butylene groups; alkylidene groups such as ethylidene groups and propylidene groups; cycloalkylene groups such as 1,2-cyclopentylene groups and 1,2-cyclohexylene groups; 1,2-phenylene groups, 2 , 3-tolylene groups, 1,4-naphthylene groups, and the like; aralkylene groups such as xylylene groups, and the like. These are substituted with at least one group selected from the group consisting of a carboxy group (for example, methoxycarbonyl group, ethoxycarbonyl group, etc.) esterified with an alcohol having 1 to 6 carbon atoms, a cyano group, and an amino group. May be.

B ¹ is preferably a linear or branched alkylene group having 1 to 5 carbon atoms, a linear or branched alkylene group having 1 to 5 carbon atoms having a cyano group, a cyclopentylene group, or a cyclohexylene group.

  The polymer precursor (P) having a molecular chain terminal represented by the formulas (8-1) to (8-4) has a specific polymerization initiator and / or a specific chain transfer agent as shown below. Can be obtained by performing radical polymerization, anionic polymerization, group transfer polymerization (GTP) and reversible addition-fragmentation chain transfer (RAFT) type living radical polymerization in the presence of The polymer precursor (P) having a molecular chain terminal represented by the formulas (8-1) to (8-4) is added with a specific polymerization terminator during radical polymerization, anionic polymerization and group transfer polymerization. It can also be obtained by the method of Specific examples include the following methods (a) to (f).

However, in the following methods (a) to (d), M means an arbitrary monomer giving a structural unit, M ^* means a structural unit derived from the monomer M, and n0 is M and M. ^An integer representing the number of ^* .

(A) Reaction example of a method of performing radical polymerization in the presence of a polymerization initiator having a molecular chain terminal represented by the above formulas (8-1) to (8-4):
A reaction example of this method is shown in the following formula.

  Specific examples of these radical polymerization initiators include 4,4'-azobis (4-cyanovaleric acid) and the like.

  The polymer precursor (P) of the present invention is preferably a polymerization initiator having a molecular chain terminal represented by the above formulas (8-1) to (8-4) (hereinafter referred to as polymerization initiator A). In the presence, one or more monomers having an acid leaving group, one or more monomers having a lactone skeleton, and one or more monomers having an alicyclic structure having a hydrophilic group are included. It is obtained by copolymerizing the monomer composition. A polymerization initiator other than the polymerization initiator A (hereinafter referred to as polymerization initiator B) can be used in combination. Examples of the polymerization initiator B include 2,2′-azobisisobutyronitrile, dimethyl-2,2′-azobisisobutyrate, 2,2′-azobis [2- (2-imidazoline-2- Yl) propane] and the like; organic peroxides such as 2,5-dimethyl-2,5-bis (tert-butylperoxy) hexane and the like. Moreover, when producing a polymer precursor (P) used in ArF excimer laser (wavelength: 193 nm) lithography, the light transmittance (transmittance for light with a wavelength of 193 nm) of the resulting resist polymer is not reduced as much as possible. In view of this, the polymerization initiator B preferably has no aromatic ring in the molecular structure. Furthermore, in consideration of safety during polymerization, the polymerization initiator B preferably has a 10-hour half-life temperature of 60 ° C. or higher.

  The total amount of polymerization initiator A and polymerization initiator B used is not particularly limited, but from the viewpoint of increasing the yield of the polymer, the total amount of polymerization initiator is 0 with respect to the total amount of monomers used for copolymerization. 0.1 mol% or more is preferable, and from the viewpoint of narrowing the molecular weight distribution of the polymer, 30 mol% or less is preferable with respect to the total amount of monomers used for copolymerization. Furthermore, the amount of the polymerization initiator used is more preferably 0.3 mol% or more, particularly preferably 1 mol% or more, based on the total amount of monomers used for copolymerization.

(B) Reaction example of a method of performing radical polymerization in the presence of a chain transfer agent having a molecular chain terminal represented by the above formulas (8-1) to (8-4):
A reaction example of this method is shown in the following formula. In the formula, E ⁰ represents an initiator residue.

  Specific examples of these chain transfer agents include, for example, mercaptoacetic acid, thiosalicylic acid, dithiodiglycolic acid, 3,3′-dithiodipropionic acid, 2,2′-dithiodibenzene acid, DL-2-mercaptomethyl. -3-guanidinoethylthiopropanoic acid, 2-mercapto-4-methyl-5-thiazoleacetic acid, p-mercaptophenol, 2-mercaptopropionic acid, 3-mercaptopropionic acid, thiomalic acid, (5-mercapto-1,3 , 4-thiadiazol-2-ylthio) acetic acid, 2- (5-mercapto-1,3,4-thiadiazol-2-ylthio) propionic acid, 3- (5-mercapto-1,3,4-thiadiazole-2- Ylthio) propionic acid, 2- (5-mercapto-1,3,4-thiadiazol-2-ylthio) succinic acid, etc. It is below.

  When producing the polymer precursor (P) of the present invention, a chain transfer agent having a molecular chain terminal represented by the above formulas (8-1) to (8-4) (hereinafter referred to as chain transfer agent A). ) Other than the chain transfer agent (hereinafter referred to as chain transfer agent B). By using the chain transfer agent B, the molecular weight distribution of the obtained polymer can be reduced. The narrow molecular weight distribution is attributed to the reduced production of high molecular weight polymers, which further improves solubility in resist solvents when used in resists, and the generation of microgels and defects. Is preferable because of a decrease. Examples of such chain transfer agent B include 1-butanethiol, 2-butanethiol, 1-octanethiol, 1-decanethiol, 1-tetradecanethiol, cyclohexanethiol, 2-methyl-1-propanethiol, and the like. Can be mentioned.

  ArF excimer laser (wavelength: 193 nm) When producing a polymer precursor (P) used in lithography, the light transmittance (transmittance to light with a wavelength of 193 nm) of the resulting polymer precursor (P) is reduced as much as possible. From the viewpoint of preventing the chain transfer agent B, the chain transfer agent B preferably has no aromatic ring.

  The total amount of the chain transfer agent A and the chain transfer agent B used is not particularly limited, but from the point of narrowing the molecular weight distribution of the polymer, the total amount of chain transfer agent is 0 with respect to the total amount of monomers used for copolymerization. 0.001 to 30 mol% is preferable. The amount of the chain transfer agent used in the production of the resist polymer of the present invention is more preferably 5 mol% or less, particularly preferably 2 mol% or less, based on the total amount of monomers used for copolymerization.

  (C) Reaction example of a method of adding a terminator having a molecular chain terminal represented by the above formulas (8-1) to (8-4) during radical polymerization:

A reaction example of this method is shown in the following formula. Hal represents a halogen atom, and E ⁰ represents an initiator residue.

  Specific examples of these terminators include, for example, bromoacetic acid, 2-bromobenzoic acid, 3-bromobenzoic acid, 4-bromobenzoic acid, 2-bromobutyric acid, 3-bromobutyric acid, 4-bromobutyric acid, chloroacetic acid. 2-chlorobenzoic acid, 3-chlorobenzoic acid, 4-chlorobenzoic acid, 2-bromobutyric acid, 3-bromobutyric acid, 4-bromobutyric acid, iodoacetic acid, 2-iodobenzoic acid, 3-iodobenzoic acid, 4 -Iodobenzoic acid, 2-iodobutyric acid, 3-iodobutyric acid, 4-iodobutyric acid and the like.

  (D) A molecular chain represented by the above formulas (8-1) to (8-4) by using a reversible addition-cleavage chain transfer complex (T) in the presence of a polymerization initiator and conducting living radical polymerization. Reaction example of a method of modifying a terminal by adding a radical initiator having a terminal:

A reaction example of this method is shown in the following formula. In the formula, E ⁰ represents an initiator residue.
In the following formula (T) which is a reversible addition-cleavage chain transfer complex, S represents a sulfur atom. R ^A represents a C 1-15 alkyl group, an aryl group or an aralkyl group which may contain a hydroxy group, an ester group, an ether group, an amino group, an amide group, etc., and L represents a single bond, an oxygen atom, sulfur Represents an atom or —N (R ^A ′) — group (R ^A ′ represents a hydrogen atom or R ^A ), and R ^B contains a hydroxy group, an ester group, an ether group, an amino group, a cyano group, or the like; Or an alkyl group having 1 to 15 carbon atoms, an aryl group or an aralkyl group.

In the above formula (T), as R ^A , specific examples of those particularly preferred when L is a single bond, oxygen atom or sulfur atom include methyl, ethyl, propyl, butyl, cyclohexyl, norbornyl, tri Examples thereof include a cyclodecanyl group, a tetracyclododecanyl group, an adamantyl group, a phenyl group, a benzyl group, a hydroxymethyl group, a hydroxyethyl group, and a hydroxycyclohexyl group.

L is -N (R ^A ') - For group, R ^A-L-is in the above formula R ^A -NH- or (R ^A) (R ^A) N-and becomes, the R ^A at that time Specific examples of particularly preferred are independently methyl, ethyl, propyl, butyl, cyclohexyl, norbornyl, tricyclodecanyl, tetracyclododecanyl, adamantyl, phenyl, benzyl, acetyl Group, hydroxymethyl group, hydroxyethyl group, hydroxycyclohexyl group and the like. R ^A may be bonded to each other to form a ring, and in this case, groups represented by formula (T-1) and formula (T-2) are exemplified.

Further, a particularly specific example of preferred R ^B, include groups represented by the formula (T-4) ~ formula (T-8).

  More specific examples of the above formula (T) include pyrazole-1-dithiocarboxylic acid cyanodimethylmethyl ester.

  Other specific reaction examples are omitted, but there are also the following methods.

  (E) A method in which living polymerization is performed in the presence of a bifunctional polymerization initiator and a terminator having a molecular chain terminal represented by the above formulas (8-1) to (8-4) is added.

  (F) A method in which living polymerization is performed in the presence of a monofunctional polymerization initiator and a terminator having a molecular chain terminal represented by the above formulas (8-1) to (8-4) is added.

  Moreover, in order to obtain the resist polymer of this invention, the said polymerization initiator A, the said chain transfer agent A, and the terminator which has the molecular chain terminal represented by said Formula (8-1)-(8-4). It is also possible to use together.

  The method for producing the polymer precursor (P) of the present invention is not particularly limited, but a polymerization method called drop polymerization, which is generally performed by solution polymerization and a monomer is dropped into a polymerization vessel, is preferable. Among these, from the viewpoint that a polymer precursor (P) having a narrow composition distribution and / or molecular weight distribution can be easily obtained, a monomer that becomes a constituent unit of the target polymer by polymerization (only monomer is used). The polymer precursor (P) of the present invention is produced by a polymerization method called dropping polymerization in which polymerization is performed while dropping a monomer in an organic solvent into a polymerization vessel. It is preferable to do.

  In the drop polymerization method, for example, an organic solvent is previously charged in a polymerization vessel and heated to a predetermined polymerization temperature, and then a monomer, a polymerization initiator, and a chain transfer agent dissolved in an organic solvent if necessary The body solution is dropped into the organic solvent in the polymerization vessel. The monomer may be dropped without being dissolved in the organic solvent. In that case, a solution in which the polymerization initiator and, if necessary, the chain transfer agent are dissolved in the monomer is dropped into the organic solvent. Further, the monomer may be dropped into the polymerization vessel without previously charging the organic solvent into the polymerization vessel.

  Moreover, a monomer, a polymerization initiator, and a chain transfer agent can each be dripped individually or in arbitrary combinations.

  Although the polymerization temperature in the dropping polymerization method is not particularly limited, it is usually preferably in the range of 50 to 150 ° C.

  Examples of the organic solvent used in the dropping polymerization method include a monomer that can be used, a polymerization initiator and a polymer precursor (P) to be obtained, and a solvent that can dissolve both the chain transfer agent when a chain transfer agent is used. Is preferred. Examples of such an organic solvent include 1,4-dioxane, isopropyl alcohol, acetone, tetrahydrofuran (hereinafter also referred to as “THF”), methyl ethyl ketone (hereinafter also referred to as “MEK”), methyl isobutyl ketone (hereinafter referred to as “MIBK”). And γ-butyrolactone, propylene glycol monomethyl ether acetate (hereinafter also referred to as “PGMEA”), ethyl lactate, dimethylacetamide (hereinafter also referred to as “DMAc”), dimethyl sulfoxide, and the like.

  The monomer concentration of the monomer solution dropped into the organic solvent is not particularly limited, but is preferably in the range of 5 to 50% by mass.

  The amount of the organic solvent charged into the polymerization vessel is not particularly limited and may be determined as appropriate. Usually, it uses within the range of 30-700 mass% with respect to the monomer whole quantity used for copolymerization.

  The polymer precursor (P) solution produced by a method such as solution polymerization is a good solvent such as 1,4-dioxane, acetone, THF, MEK, MIBK, γ-butyrolactone, PGMEA, and ethyl lactate, if necessary. After diluting to an appropriate solution viscosity, the polymer is dropped by dripping into a large amount of poor solvent such as methanol or water. This process is generally called reprecipitation and is very effective for removing unreacted monomers, polymerization initiators, etc. remaining in the polymerization solution. If these unreacted substances remain as they are, there is a possibility of adversely affecting the resist performance. Therefore, it is preferable to remove them as much as possible. The reprecipitation step may be unnecessary in some cases. Thereafter, the precipitate is filtered off and sufficiently dried to obtain the polymer precursor (P) of the present invention. Moreover, after filtering off, it can also be used with a wet powder, without drying.

  Further, the produced polymer precursor (P) solution can be used as it is or diluted with an appropriate solvent as a raw material for the reaction step with polyfunctional vinyl ether described later. At that time, additives such as a storage stabilizer may be appropriately added.

  The mass average molecular weight of the polymer precursor (P) of the present invention is not particularly limited, but is preferably 1,000 or more and more preferably 1,500 or more from the viewpoint of dry etching resistance and resist pattern shape. It is preferably 2,000 or more, more preferably 2,500 or more. Further, the mass average molecular weight of the polymer precursor (P) of the present invention is preferably 20,000 or less, more preferably 15,000 or less from the viewpoint of resolution, and line edge roughness and tailing. From this point, it is particularly preferably 13,000 or less, and further preferably 10,000 or less.

  Next, the polyfunctional vinyl ether compound represented by the formula (9) will be described.

In the formula (9), X represents a single bond or ^{-B 11 -, - S-B} 11 -, - O-B 11 -, - O-NB 12 -, - NB 12 -B 11 - or -O-Si (B ¹³ ) (B ¹⁴ ) —, wherein B ¹¹ has at least one group selected from the group consisting of a carboxy group esterified with an alcohol having 1 to 6 carbon atoms, a cyano group, and an amino group. Represents a linear, branched or cyclic divalent hydrocarbon group having 1 to 20 carbon atoms, B ¹¹ may have a hetero atom in its main skeleton, and B ¹² represents a hydrogen atom or a carbon number. 1 to 10 linear, branched or cyclic alkyl groups, each of B ¹³ and B ¹⁴ independently represents a hydrogen atom, a linear or branched alkyl group having 1 to 10 carbon atoms, or a cyclic alkyl group; To express.

Examples of the linear, branched or cyclic divalent hydrocarbon group having 1 to 20 carbon atoms of B ¹¹ include the following formulas (B-1) to (B-21).

Moreover, as a hetero atom which these may have in a main skeleton, a sulfur atom, a nitrogen atom, an oxygen atom, and a phosphorus atom are mentioned. Examples of B ¹¹ having a hetero atom in these main skeletons include the following formulas (B1-1) to (B1-21).

Examples of the linear, branched or cyclic alkyl group having 1 to 10 carbon atoms of B ¹² , B ¹³ and B ¹⁴ include a methyl group, an ethyl group, a propyl group, an iso-propyl group, a butyl group, a t-butyl group, and pentyl. Group, neo-pentyl group, octyl group, nonyl group, decyl group, cyclopentyl group, cyclohexyl group and the like.

X is preferably a single bond or —B ¹¹ —.

  In the formula (9), the substituents possessed by J itself include a thiol group, a hydroxy group, a carboxy group, an acyl group having 1 to 6 carbon atoms, a carboxy group esterified with an alcohol having 1 to 6 carbon atoms, and carbon. A straight chain having 1 to 6 carbon atoms which may have one or more groups selected from the group consisting of a carboxy group, a cyano group, an amino group, a halogen, and a nitroxy group thioesterified with a thiol having 1 to 6 A branched or cyclic alkyl group, a thiol group, a hydroxy group, a carboxy group, an acyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, a carboxy group esterified with an alcohol having 1 to 6 carbon atoms, carbon Examples thereof include a carboxy group, a cyano group, an amino group, a halogen or a nitroxy group thioesterified with a thiol having a number of 1 to 6. Moreover, as a hetero atom contained in J, a sulfur atom, a nitrogen atom, an oxygen atom, and a phosphorus atom are mentioned. At this time, the bond coming out of the heteroatom varies depending on the valence of the heteroatom.

  The basic structure of J is synonymous with J in the formula (1).

  Specific examples of the compound represented by the formula (9) include the following formulas (36-1) to (36-21). Among these, the following formulas (36-1) to (36-5) and the following formula (36-9) are preferable.

  Next, the process of reacting the polymer precursor (P) with the polyfunctional vinyl ether compound represented by the formula (9) will be described.

  The step of reacting the polymer precursor (P) with the polyfunctional vinyl ether compound represented by the formula (9) is a known method of reacting a vinyl ether compound with a phenolic hydroxyl group with respect to poly-p-hydroxystyrene. The catalyst may be used in the same manner as in the method, and is not particularly limited. For example, as the catalyst used in the above reaction, p-toluenesulfonic acid and its hydrate, methanesulfonic acid, trifluoromethanesulfonic acid, camphorsulfonic acid, oxalic acid Organic acids such as 1,1,1-fluoroacetic acid; inorganic acids such as sulfuric acid and hydrochloric acid; or p-toluenesulfonic acid pyridinium salt, p-toluenesulfonic acid ammonium salt, p-toluenesulfonic acid 4-methylpyridinium salt Such salts can be mentioned.

  The above reaction can be carried out by dissolving an organic solvent that can dissolve both the polymer precursor (P) and the polyfunctional vinyl ether compound represented by the formula (9), such as 1,4-dioxane, PGMEA, ethyl acetate, MEK, γ- It is preferable to carry out in butyrolactone or the like. The reaction temperature is preferably 15 to 60 ° C, more preferably 20 to 50 ° C. The reaction time varies depending on the polyfunctional vinyl ether compound to be used, the type of catalyst, the reaction temperature, and the like, but may be, for example, 0.1 to 24 hours. After completion of the reaction, for example, post-treatment can be performed as follows. After neutralizing the reaction mixture with concentrated aqueous ammonia, triethylamine, etc., in order to remove unreacted polyfunctional vinyl ether compound and catalyst remaining in the reaction solution, it is dropped into a large amount of poor solvent such as methanol, water, etc. To precipitate the polymer. Moreover, this reprecipitation process may become unnecessary depending on the case. Thereafter, the precipitate is filtered off and sufficiently dried to obtain the resist polymer of the present invention. Moreover, after filtering off, it can also be used with a wet powder, without drying.

  The reaction solution can be used as a resist composition as it is or after diluting with an appropriate solvent. At that time, additives such as a storage stabilizer may be appropriately added.

  In addition, the resist polymer containing the acid-decomposable unit having the structure represented by the formula (1) as a constituent unit can be produced in addition to the two production methods described above. It is not limited.

  The resist polymer of the present invention produced by the above reaction has, for example, a structure schematically represented by the following formulas (37-1) to (37-9).

  In the formula, a chain line represents a polymer chain composed of structural units described below, and J represents J in the formula (1). Note that the number of dots in the chain line between JJ and the number of bonds (repetition number) of the structural units of the polymer are irrelevant.

  The mass average molecular weight of the resist polymer of the present invention is not particularly limited, but is preferably 1,000 or more, more preferably 2,000 or more, from the viewpoint of dry etching resistance and pattern shape, 000 or more is particularly preferable. Further, the mass average molecular weight of the resist polymer of the present invention is preferably 100,000 or less, more preferably 50,000 or less, and more preferably 30,000, from the viewpoints of solubility in a resist solution and resolution. It is particularly preferred that

  The resist polymer containing an acid-decomposable unit having a structure represented by the formula (2) as a constituent unit polymerizes at least a monomer containing a monomer represented by the following formula (10). Can be manufactured.

In formula (10), R ¹ represents a hydrogen atom or a methyl group, and S represents a sulfur atom. Further, K ¹ , K ² , L ¹ , L ² , M ¹ , M ² , M ³ , Y ¹ , Y ² , k ¹ , k ² , l ¹ , l ² , m 1, m 2, m 3, and n 1 are represented by the formula (1 ).

In the above formula (10), K ¹ and K ² are preferably alkylene or cycloalkylene, and L ¹ and L ² are preferably —C (O) O— or —OC (O) —, and M ¹ , M ² , M ³ is preferably alkylene, cycloalkylene, or arylene.

  Among these, a (meth) acrylic acid ester represented by the following formula (38) is preferable from the viewpoint of excellent copolymerizability with other resist acrylic monomers.

In formula (38), K ² , L ² , M ¹ , M ² , M ³ , Y ¹ , Y ² , k ² , l ² , m 1, m 2, m 3 and n 1 have the same meanings as in formula (1), respectively.

  Specific examples of the monomer represented by the above formula (38) include monomers represented by the following formulas (39-1) to (39-24). In the formula, R represents a hydrogen atom or a methyl group.

  Among these, monomers having the above formulas (39-1), (39-5), (39-8), and (39-13) are preferable because of high acid decomposability, and the above formula (39-1) is preferable. ) Is particularly preferred.

  A mechanism for generating the structure represented by Formula (2) will be described. In the polymerization step, first, radicals derived from a polymerization initiator or the like are generated in the reaction solution, and monomer chain polymerization proceeds from this radical.

The radical form is present at the growth end, and the vinyl end of the (meth) acrylic acid ester represented by the formula (38) and the hydrogen atom of —SH are pulled out to become a polymer in which the growth end is deactivated. On the other hand, the vinyl group or —SH from which hydrogen is extracted becomes a structure having a radical, that is, a radical body, and the monomer is chain-polymerized again starting from this radical body. In this way, the structure represented by the formula (2) is generated. It can be confirmed that the polymer contains the structure represented by the formula (2) by measuring ³³ S-NMR and changing -SH to -S-.

  Among the (meth) acrylic acid esters represented by the above formula (38), for example, a methacrylic acid ester in which R in the above formula (39-1) is a methyl group can be synthesized by the following steps. Other (meth) acrylic acid esters represented by the above formula (38) can also be synthesized in a similar process.

  The resist polymer containing the acid-decomposable unit having the structure represented by the formula (2) as a constituent unit is not limited to the production method described above.

  The acrylic polymer for resists containing, as constituent units, an acid-decomposable unit having a structure represented by the formula (3) and a unit having a hydrophilic group is at least a single unit represented by the following formula (11). It can be produced by polymerizing a monomer, a monomer represented by the following formula (12), and a monomer represented by the following formula (13).

In the formula (11), R ⁶ represents a hydrogen atom or a methyl group, R ⁷ represents a linear or branched alkyl group having 1 to 6 carbon atoms, a cyclic hydrocarbon group having 4 to 8 carbon atoms, or 4 to 16 carbon atoms. Represents a bridged cyclic hydrocarbon group or a lactone group which does not have a hydrophilic group. Here, the alkyl group, cyclic hydrocarbon group, bridged cyclic hydrocarbon group, and lactone group may have a substituent.

In the formula (12), R ⁸ represents a hydrogen atom or a methyl group, R ⁹ represents a hydrogen atom, a linear or branched alkyl group having 1 to 6 carbon atoms, a cyclic hydrocarbon group having 4 to 8 carbon atoms, Or it is a C4-C16 bridged cyclic hydrocarbon group, Comprising: The group which has a hydrophilic group as a substituent is represented.

In formula (13), R ² and R ³ each independently represent a hydrogen atom or a methyl group. Further, K ¹ , K ² , L ¹ , L ² , M ¹ , M ² , M ³ , Y ¹ , Y ² , k ¹ , k ² , l ¹ , l ² , m 1, m 2, m 3, and n 1 are represented by the formula (1 ).

  Preferable examples of the monomer represented by the formula (13) include a monomer represented by the following formula (40).

(In formula (40), R ² and R ³ have the same meanings as in formula (2), R ^{411 to} R ⁴¹⁴ each independently represents an alkyl group having 1 to 4 carbon atoms, Y ² represents an alkylene group, cyclo Represents an alkylene group or an arylene group, and m40 represents the number of methylenes substituted with R ⁴¹³ and R ⁴¹⁴ and is 0 or 1.)

  Specific examples of the formula (40) include the following formulas (40-1) and (40-2).

  The ratio of the cross-linked structural unit in the polymer is preferably from 0.1 to 10 mol%, more preferably from 0.1 to 5 mol%, based on all monomer units. In the vicinity of this ratio, the larger the ratio, the better the soaking, and the smaller the ratio, the higher the solubility in the resist solvent.

  The 2-methyl-2,4-butanediol dimethacrylate represented by the above formula (40-1) can be produced, for example, by the following steps.

  Commercially available products can be used as 2-methyl-2,4-butanediol as a raw material.

  The esterification reaction of 2-methyl-2,4-butanediol proceeds easily by a known method. For example, it can be reacted with methacrylic acid chloride in the presence of triethylamine. The reaction is preferably carried out without solvent or in a polar solvent such as tetrahydrofuran.

  In the present invention, the product of the above reaction can be used in the polymerization reaction without being purified, but it is preferable to purify by simple distillation, thin film distillation, column chromatography or the like.

  More preferable examples of the monomer represented by the formula (13) include a monomer represented by the following formula (41).

(R ^{2 to} R ⁵ and A in Formula (41) have the same meanings as in Formula (5).)

  Specific examples of the monomer containing an acid-decomposable acetal group represented by the formula (41) include formulas (41-1) to (41-17). The monomer of the formula (41) that can be used in the present invention is not limited to these.

  Synthesis examples of these compounds are shown below. For example, the compound represented by the formula (41-3) can be synthesized by any one of the following schemes 1 to 3, for example.

  In Scheme 1, a cross-linking agent having a target acid-decomposable acetal structure can be obtained by allowing (meth) acrylic acid to act on a di-chloromethyl ether. It is preferable to use 1.0-fold mole to 10-fold mole of vinyl (meth) acrylate with respect to the diol. For example, by reacting in the presence of an alkali such as pyridine or trimethylamine, the reaction time can be shortened and the yield can be obtained.

  In Scheme 2, a cross-linking agent having a target acid-decomposable acetal structure can be obtained by allowing vinyl (meth) acrylate to act on the diol body. It is preferable to use 1.0-fold mole to 10-fold mole of vinyl (meth) acrylate with respect to the diol. The reaction time can be shortened by reacting in the presence of a Lewis acid.

  That is, in Scheme 3, a cross-linking agent having a target acid-decomposable acetal structure can be obtained by allowing (meth) acrylic acid to act on divinyl ether. It is preferable to use (meth) acrylic acid in an amount of 1.0 times to 10 times the amount of divinyl ether. The reaction time can be shortened by reacting in the presence of a Lewis acid.

  Specific examples of the formula (11) include the following formulas (29A-1) to (29A-8) as monomers having an acid leaving group.

In the above formula, R ³¹ , R ³² , R ³³ , R ³⁴ , R ³⁵ , R ³⁶ , R ³⁷ , R ³⁸ , R ²⁹¹ , R ²⁹² , R ²⁹³ , R ²⁹⁴ , R ²⁹⁵ , X ¹ , X ² , X ³ , X ⁴ , X ⁵ , X ⁶ , n 1, n 2, n 3, n 4, n 5, n 6, R ³³¹ , R ³³² , R ³³³ , R ³³⁴ , R ³⁵¹ , R ³⁵² , R ³⁵³ , R ³⁵⁴ , R ³⁵⁵ , ^{R 356, R 357, R 361} , R 362, R 363, R 364, R 365, R 366, R 367, R 371, R 372, R 373, R 381, R 382, R 383, Z 3, Z 4 , Z ⁵ , Z ⁶ , Z ⁷ and Z ⁸ have the same meanings as those in the above formulas (29-1) to (29-8).

R ²⁹¹ in formula (29A-1), R ²⁹² and R ²⁹³ in formula (29A-2), R ²⁹⁴ in formula (29A-3), R ²⁹⁵ in formula (29A-4) are the sensitivity and From the viewpoint of resolution, a methyl group, an ethyl group, or an isopropyl group is preferable.

  N1, n2, n3, n4, n5, and n6 in the formulas (29A-1) to (29A-6) are preferably 0 from the viewpoint of high dry etching resistance.

Z ³ and Z ⁴ in formula (29A-3), Z ⁵ and Z ⁶ in formula (29A-5), and Z ⁷ and Z ⁸ in formula (29A-6) have high dry etching resistance. And each independently preferably —CH ₂ — or —CH ₂ CH ₂ —.

R ³³¹ , R ³³² , R ³³³ and R ³³⁴ in formula (29A-3), R ³⁵¹ , R ³⁵² , R ³⁵³ and R ³⁵⁴ in formula (29A-5), R ^{361 in} formula (29A-6) , R ³⁶² , R ³⁶³ and R ³⁶⁴ are each independently preferably a hydrogen atom, a methyl group, an ethyl group or an isopropyl group from the viewpoint of high solubility in an organic solvent.

  Q in the formula (29A-3), q3 in the formula (29A-5), and q4 in the formula (29A-6) are preferably 1 from the viewpoint of high dry etching resistance. From the viewpoint of good solubility, 0 is preferable.

  In formula (29A-4), r is preferably 1 from the viewpoint of high dry etching resistance, and preferably 0 from the viewpoint of good solubility in an organic solvent.

-C (R ³⁵⁵ ) (R ³⁵⁶ ) (R ³⁵⁷ ) in the formula (29A-5) is represented by the above formulas (K-1) to (K-6) in that the line edge roughness is excellent. The structure represented by the formulas (K-7) to (K-17) is preferable from the viewpoint of high dry etching resistance.

-C (R ³⁶⁵ ) (R ³⁶⁶ ) -O-R ³⁶⁷ in the formula (29A-6) is represented by the formulas (J-1) to (J-24) in that it has excellent line edge roughness. The structure represented by said Formula (J-25)-(J-52) is preferable at the point with the high dry etching tolerance.

-C (R ³⁷¹ ) (R ³⁷² ) -O-R ³⁷³ in the formula (29A-7) is represented by the above formulas (J-1) to (J-24) in that it has excellent line edge roughness. The structure represented by said Formula (J-25)-(J-52) is preferable at the point with the high dry etching tolerance.

  Monomers having an acid leaving group can be used alone or in combination of two or more as required.

  More specifically, examples of the monomer having an acid leaving group include monomers represented by the formulas (30-1) to (30-196).

  Among these, from the points of sensitivity and resolution, the formulas (30-1) to (30-3), the formula (30-5), the formula (30-16), the formula (30-19), the formula (30-19), 30-20), Formula (30-22), Formula (30-23), Formula (30-25) to (30-28), Formula (30-30), Formula (30-31) The monomers represented by the formula (30-33), the formula (30-34) and the formulas (30-102) to (30-129), and their geometrical isomers and optical isomers. Preferably, the formula (30-1), the formula (30-2), the formula (30-16), the formula (30-20), the formula (30-23), the formula (30-28), Formula (30-31), Formula (30-34), Formula (30-109), Formula (30-111), Previous Equation (30-114) - (30-117), the formula (30-125), the formula (30-128) and a monomer represented by the formula (30-129) are particularly preferred.

  Moreover, from the point which is excellent in line edge roughness, it represents with the monomer represented by said Formula (30-35)-(30-40), said Formula (30-52)-(30-62). A monomer, a monomer represented by the formulas (30-76) to (30-88), a monomer represented by the formulas (30-130) to (30-135), and the formula (30 -147) to (30-157), monomers represented by the above formulas (30-171) to (30-183), and geometric isomers and optical isomers thereof. preferable.

  Moreover, from the point which is excellent in dry etching tolerance, it represents with the monomer represented by said Formula (30-41)-(30-51), said Formula (30-63)-(30-75). A monomer, a monomer represented by the formulas (30-89) to (30-101), a monomer represented by the formulas (30-136) to (30-146), and the formula (30 -158) to (30-170), monomers represented by the above formulas (30-184) to (30-196), and geometric isomers and optical isomers thereof preferable.

  Moreover, as said formula (11), the following formula (31A-1)-(31A-5) are specifically mentioned as a monomer which has a lactone skeleton.

(In the above formula, R ⁴¹ , R ⁴² , R ⁴³ , R ⁴⁴ , R ³¹¹ , R ³¹² , R ³¹³ , R ⁴⁰¹ , R ⁴⁰² , R ²⁰¹ , R ²⁰² , R ²⁰³ , R ²⁰⁴ , R ⁹¹ , R ⁹² , ^{R 93, R 94, A 1} , A 2, A 3, A 4, X 41, X 42, X 43, X 44, n41, n42, n43, n44, Y 11, Y 12, Y 13, i, m30 M31 is synonymous with the above formulas (31-1) to (31-5).

  In these formulas, the linear or branched alkyl group having 1 to 6 carbon atoms includes methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, isobutyl group, t-butyl group, n- Pentyl group, neo-pentyl group, 1,1-dimethylpropyl group, 1,2-dimethylpropyl group, 1,1-dimethylbutyl group, 2,2-dimethylbutyl group, n-hexyl group, 1-methylpentyl group , 2-methylpentyl group, 3-methylpentyl group and the like.

  N41, n42, n43, and n44 in the formulas (31A-1) to (31A-4) are preferably 0 from the viewpoint of high dry etching resistance.

  M30 in Formula (31A-1) is preferably 1 from the viewpoints of sensitivity and resolution.

A ¹ and A ^{2 in} the formula (31A-2) and A ³ and A ⁴ in the formula (31A-3) are combined together from the viewpoint of high dry etching resistance, —CH ₂ —, —CH _2. CH ₂ — is preferable, and from the viewpoint of high solubility in an organic solvent, it is preferable to form —O— together.

R ²⁰¹ and R ^{202 in} the formula (31A-2) and R ²⁰³ and R ²⁰⁴ in the formula (31A-3) are each independently a hydrogen atom, a methyl group, from the viewpoint of high solubility in an organic solvent, It is preferably an ethyl group or an isopropyl group.

R ³¹¹ , R ³¹² and R ^{313 in} formula (31A-4) are preferably a hydrogen atom from the viewpoint of high solubility in an organic solvent.

Y ¹¹ , Y ^12, and Y ^{13 in} formula (31A-4) are each one of —CO—O— and the remaining two are —CH ₂ — in view of high adhesion to the substrate surface and the like. It is preferable.

In formula (31A-5), R ⁹¹ , R ⁹² , R ⁹³ and R ⁹⁴ are each independently preferably a hydrogen atom or a methyl group from the viewpoint of high solubility in an organic solvent.

  M31 in Formula (31A-5) is preferably 1 from the viewpoints of sensitivity and resolution.

  The monomers having a lactone skeleton can be used alone or in combination of two or more.

  More specifically, examples of the monomer having a lactone skeleton include monomers represented by the formulas (32-1) to (32-24).

  Among these, from the viewpoint of sensitivity, the monomers represented by the above formulas (32-1) to (32-3) and the above formula (32-5), and geometric isomers and optical isomers thereof are more preferable. From the point of dry etching resistance, the above formulas (32-7), (32-9), (32-10), (32-12), (32-14), (32-24) to (32-26) ), And geometrical isomers and optical isomers thereof are more preferable. From the viewpoint of solubility in a resist solvent, the above formulas (32-8), (32-13), and Monomers represented by (32-16) to (32-23), and geometric isomers and optical isomers thereof are more preferable.

  Furthermore, as said Formula (11), the following formula (33A-1)-(33A-4) is specifically mentioned as a monomer which has a nonpolar alicyclic skeleton.

(In the above formula, R ³⁰¹ , R ³⁰² , R ³⁰³ , R ³⁰⁴ , X ³⁰¹ , X ³⁰² , X ³⁰³ , X ³⁰⁴ , n ³⁰¹ , n ³⁰² , n ³⁰³ , n ³⁰⁴ , p, p 1 are the same as those in the above formula (33-1) to (It is synonymous with (33-4).)

In the formulas (33A-1) to (33A-4), the position where X ³⁰¹ , X ³⁰² , X ³⁰³ and X ³⁰⁴ are bonded may be anywhere in the cyclic structure.

  N301, n302, n303, and n304 in formulas (33A-1) to (33A-4) are preferably 0 from the viewpoint of high dry etching resistance.

  P in formula (33A-3) and p1 in formula (33A-4) are preferably 0 from the viewpoint of high solubility in organic solvents, and are 1 from the viewpoint of high dry etching resistance. It is preferable.

  In order to introduce such a structural unit into the polymer, a monomer having a nonpolar alicyclic skeleton may be copolymerized. Monomers having a nonpolar alicyclic skeleton can be used alone or in combination of two or more as required.

  Examples of the monomer having a nonpolar alicyclic skeleton include cyclohexyl (meth) acrylate, isobornyl (meth) acrylate, norbornyl (meth) acrylate, adamantyl (meth) acrylate, and (meth) acrylate tri Cyclodecanyl, dicyclopentadienyl (meth) acrylate, and derivatives having a linear or branched alkyl group having 1 to 6 carbon atoms on the alicyclic skeleton of these compounds are preferred.

  Specific examples of the monomer having a nonpolar alicyclic skeleton include monomers represented by the above formulas (34-1) to (34-5).

  Specifically as said Formula (12), what is at least 1 sort (s) chosen from the group which consists of following formula (26A-1)-(26A-7) is preferable.

(In the ^{formula, R 51, R 52, R} 53, R 54, R 55, R 56, R 57, R 501, R 502, R 503, R 504, R 505, R 506, R 531, R 532, R ⁵³³ , R ⁵³⁴ , R ⁵³⁵ , R ⁵³⁶ , R ⁵⁷¹ , R ⁵⁷² , W ¹ , W ² , W ³ , X ⁵¹ , X ⁵² , X ⁵³ , X ⁵⁴ , X ⁵⁵ , X ⁵⁶ , X ⁵⁷ , n51, (n52, n53, n54, n55, n56, q1, and q2 are synonymous with the above formulas (26-1) to (26-7).)

R ⁵⁰¹ in formula (26A-1), R ⁵⁰² in formula (26A-3), R ⁵⁰³ in formula (26A-4), and R ⁵⁰⁶ in formula (26A-6) are points of sensitivity and resolution. Is preferably a methyl group, an ethyl group, or an isopropyl group, and is preferably a hydrogen atom from the viewpoint of good solubility in an organic solvent.

  In formulas (26A-1) to (26A-6), n51, n52, n53, n54, n55, and n56 are preferably 1 from the viewpoint of high dry etching resistance.

X ⁵¹ , X ⁵² , X ⁵³ , X ⁵⁴ , X ⁵⁵ , and X ⁵⁶ in formulas (26A-1) to (26A-6) are —C (CF ₃ ) ₂ —OH, It is preferably a hydroxy group, a cyano group, or a methoxy group. X ^{57 in} formula (26A-7) represents —CH ₂ —C (CF ₃ ) ₂ —OH, —CH ₂ —OH group, —CH ₂ —CN group, —CH ₂ from the viewpoint of good pattern shape. It is preferably a —O—CH ₃ group or a — (CH ₂ ) ₂ —O—CH ₃ group.

W ¹ and W ² in formula (26A- ³ ) and W ³ in formula (26A-6) are preferably —CH ₂ — and —CH ₂ CH ₂ — from the viewpoint of high dry etching resistance. .

R ⁵³¹ , R ⁵³² , R ⁵³³ , and R ⁵³⁴ in formula (26A-3) and R ⁵³⁵ and R ⁵³⁶ in formula (26A-6) are each independently from the viewpoint of high solubility in an organic solvent. And preferably a hydrogen atom, a methyl group, an ethyl group, or an isopropyl group.

  Q1 in formula (26A-3) and q2 in formula (26A-6) are preferably 1 from the viewpoint of high dry etching resistance, and 0 from the viewpoint of good solubility in organic solvents. It is preferable that

  R1 in Formula (26A-4) is preferably 1 from the viewpoint of high dry etching resistance, and preferably 0 from the viewpoint of good solubility in an organic solvent.

In the formula (26A-5), R ⁵⁰⁴ and R ⁵⁰⁵ are preferably each independently a methyl group, an ethyl group, or an isopropyl group from the viewpoint of sensitivity and resolution.

R ⁵⁷¹ and R ⁵⁷² in the formula (26A-7) are, together with the carbon atom to which R ⁵⁷¹ and R ⁵⁷² are combined, each having 4 to 16 carbon atoms from the viewpoint of high dry etching resistance. A structure in which a crosslinked cyclic hydrocarbon group is formed is preferable. From the standpoint of excellent heat resistance and stability, R ⁵⁷¹ and R ⁵⁷² are combined together to form a ring contained in a bridged cyclic hydrocarbon group formed together with the carbon atom to which each is bonded. It preferably has a ring, an adamantane ring, a norbornane ring, a pinane ring, a bicyclo [2.2.2] octane ring, a tetracyclododecane ring, a tricyclodecane ring, or a decahydronaphthalene ring.

In the formulas (26A-1) to (26A-6), the position substituted with X ⁵¹ , X ⁵² , X ⁵³ , X ⁵⁴ , X ⁵⁵ and X ⁵⁶ may be any position in the cyclic structure. .

  The structural unit which has a hydrophilic group can be used 1 type or in combination of 2 or more type as needed.

  More specifically, examples of the formula (12) include monomers represented by the formulas (27-1) to (27-103).

  Among these, from the viewpoint of good solubility in a resist solvent, the above formulas (27-1) to (27-4), the above formulas (27-9) to (27-13), and the above formula (27-21). To (27-24), the above formulas (27-33) to (27-36), the above formulas (27-42) to (27-46), the above formulas (27-53) to (27-59), the above Formulas (27-78) to (27-79), Formulas (27-82) to (27-83), Formulas (27-88) to (27-89), Formulas (27-94) to ( 27-97), monomers represented by the above formula (27-100), geometric isomers thereof, and optical isomers thereof are more preferable, and in terms of high dry etching resistance, Formulas (27-37) to (27-42), Formulas (27-60) to (27-77), Formula (27-8) ) To (27-85), the above formulas (27-90) to (27-91), the above formula (27-99), the monomers represented by the above formulas (27-101) to (27-103). And geometrical isomers and optical isomers thereof are more preferable. From the viewpoint of sensitivity and resolution, the above formulas (27-5) to (27-8) and the above formulas (27-17) to ( 27-20), the above formulas (27-29) to (27-32), the above formulas (27-49) to (27-52), the above formulas (27-62) to (27-63), the above formula ( 27-68) to (27-69), the above formulas (27-74) to (27-75), the above formulas (27-80) to (27-81), the above formulas (27-86) to (27- 87), monomers represented by the above formulas (27-92) to (27-93), and geometric isomers thereof, and These optical isomers are more preferred.

  Next, the resist composition of the present invention will be described.

  The resist composition of the present invention is obtained by dissolving the resist polymer of the present invention in a solvent. The chemically amplified resist composition of the present invention is obtained by dissolving the resist polymer of the present invention and a photoacid generator in a solvent. The resist polymer of the present invention may be used alone or in combination of two or more. In addition, without separating the polymer from the polymer solution obtained by solution polymerization or the like, the polymer solution is used as it is for the resist composition, or the polymer solution is diluted with an appropriate solvent, or It can also be concentrated and used in a resist composition.

  Examples of the solvent include linear or branched ketones such as methyl ethyl ketone, methyl isobutyl ketone, 2-pentanone and 2-hexanone; cyclic ketones such as cyclopentanone and cyclohexanone; propylene glycol monomethyl ether acetate, propylene glycol monoethyl Propylene glycol monoalkyl acetates such as ether acetate; Ethylene glycol monoalkyl ether acetates such as ethylene glycol monomethyl ether acetate and ethylene glycol monoethyl ether acetate; Propylene glycol monoalkyl ethers such as propylene glycol monomethyl ether and propylene glycol monoethyl ether Class: ethylene glycol monomethyl ether, ethylene glycol monoe Ethylene glycol monoalkyl ethers such as ether; diethylene glycol alkyl ethers such as diethylene glycol dimethyl ether and diethylene glycol monomethyl ether; esters such as ethyl acetate and ethyl lactate; n-propyl alcohol, isopropyl alcohol, n-butyl alcohol, cyclohexanol, 1 -Alcohols such as octanol; 1,4-dioxane, ethylene carbonate, γ-butyrolactone and the like. These solvents may be used alone or in combination of two or more.

  The content of the solvent is usually 200 to 5000 parts by mass and more preferably 300 to 2000 parts by mass with respect to 100 parts by mass of the resist polymer (the polymer of the present invention).

  When the resist polymer of the present invention is used for a chemically amplified resist, it is necessary to use a photoacid generator.

  The photoacid generator contained in the chemically amplified resist composition of the present invention can be arbitrarily selected from those that can be used as the acid generator of the chemically amplified resist composition. A photo-acid generator may use 1 type or may use 2 or more types together.

  Examples of such a photoacid generator include onium salt compounds, sulfonimide compounds, sulfone compounds, sulfonic acid ester compounds, quinonediazide compounds, diazomethane compounds, and the like. As the photoacid generator, among them, onium salt compounds such as sulfonium salts, iodonium salts, phosphonium salts, diazonium salts, pyridinium salts are preferable, specifically, triphenylsulfonium triflate, triphenylsulfonium hexafluoroantimonate, Triphenylsulfonium naphthalenesulfonate, (hydroxyphenyl) benzylmethylsulfonium toluenesulfonate, diphenyliodonium triflate, diphenyliodonium pyrenesulfonate, diphenyliodonium dodecylbenzenesulfonate, diphenyliodonium hexafluoroantimonate, p-methylphenyldiphenylsulfonium nonafluorobutanesulfonate, Tri (tert-butylphenyl) sulfonium trifluor B methanesulfonate, and the like.

  The content of the photoacid generator is appropriately determined depending on the type of the photoacid generator selected, but is usually 0.1 parts by mass or more with respect to 100 parts by mass of the resist polymer (the polymer of the present invention). Yes, and more preferably 0.5 parts by mass or more. By setting the content of the photoacid generator within this range, a chemical reaction due to the catalytic action of the acid generated by exposure can be sufficiently caused. Moreover, content of a photo-acid generator is 20 mass parts or less normally with respect to 100 mass parts of polymers for resists (polymer of this invention), and it is more preferable that it is 10 mass parts or less. By setting the content of the photoacid generator within this range, the stability of the resist composition is improved, and the occurrence of uneven coating during application of the composition and scum during development is sufficiently reduced.

  Furthermore, a nitrogen-containing compound can also be mix | blended with the chemically amplified resist composition of this invention. By containing a nitrogen-containing compound, the resist pattern shape, the stability over time, and the like are further improved. In other words, the cross-sectional shape of the resist pattern is closer to a rectangle, and the resist film is exposed, post-exposure baked (PEB), and left for several hours before the next development process. However, the deterioration of the cross-sectional shape of the resist pattern is further suppressed when such leaving (aging) is performed.

  As the nitrogen-containing compound, any known compounds can be used, but amines are preferable, and among them, secondary lower aliphatic amines and tertiary lower aliphatic amines are more preferable.

  Here, the “lower aliphatic amine” refers to an alkyl or alkyl alcohol amine having 5 or less carbon atoms.

  Examples of the secondary lower aliphatic amine and tertiary lower aliphatic amine include trimethylamine, diethylamine, triethylamine, di-n-propylamine, tri-n-propylamine, tripentylamine, diethanolamine, triethanolamine and the like. Is mentioned. Among these nitrogen-containing compounds, tertiary alkanolamines such as triethanolamine are more preferable.

  The nitrogen-containing compound may be used alone or in combination of two or more.

  The content of the nitrogen-containing compound is appropriately determined depending on the type of the selected nitrogen-containing compound, but is usually 0.01 parts by mass or more with respect to 100 parts by mass of the resist polymer (the polymer of the present invention). It is preferable. By setting the content of the nitrogen-containing compound within this range, the resist pattern shape can be made more rectangular. Moreover, it is preferable that content of a nitrogen-containing compound is 2 mass parts or less normally with respect to 100 mass parts of polymers for resists (polymer of this invention). By setting the content of the nitrogen-containing compound within this range, it is possible to reduce the sensitivity deterioration.

  In addition, the chemically amplified resist composition of the present invention may contain an organic carboxylic acid, a phosphorus oxo acid, or a derivative thereof. By containing these compounds, it is possible to prevent sensitivity deterioration due to the compounding of the nitrogen-containing compound, and further improve the resist pattern shape, the stability with time of standing, and the like.

  As the organic carboxylic acid, for example, malonic acid, citric acid, malic acid, succinic acid, benzoic acid, salicylic acid and the like are preferable.

  Phosphorus oxoacids or derivatives thereof include, for example, phosphoric acid, phosphoric acid di-n-butyl ester, phosphoric acid diphenyl ester and other phosphoric acid and derivatives thereof; phosphonic acid, phosphonic acid dimethyl ester Phosphonic acids such as phosphonic acid di-n-butyl ester, phenylphosphonic acid, phosphonic acid diphenyl ester, phosphonic acid dibenzyl ester and the like; derivatives such as phosphinic acid, phenylphosphinic acid and the like Examples thereof include derivatives such as esters, and among them, phosphonic acid is preferable.

  These compounds (organic carboxylic acid, phosphorus oxo acid, or derivatives thereof) may be used alone or in combination of two or more.

  The content of these compounds (organic carboxylic acid, phosphorus oxo acid, or derivative thereof) is appropriately determined depending on the type of the selected compound, etc., but is usually a resist polymer (the polymer of the present invention) 100. It is preferable that it is 0.01 mass part or more with respect to a mass part. By setting the content of these compounds within this range, the resist pattern shape can be made more rectangular. In addition, the content of these compounds (organic carboxylic acid, phosphorus oxo acid or derivative thereof) is usually 5 parts by mass or less with respect to 100 parts by mass of the resist polymer (the polymer of the present invention). It is preferable. By reducing the content of these compounds within this range, the film loss of the resist pattern can be reduced.

  Note that both the nitrogen-containing compound and the organic carboxylic acid, phosphorus oxoacid, or a derivative thereof can be contained in the chemically amplified resist composition of the present invention, or only one of them can be contained. .

  Furthermore, the resist composition of the present invention may contain various additives such as surfactants, other quenchers, sensitizers, antihalation agents, storage stabilizers, and antifoaming agents as necessary. it can. Any of these additives can be used as long as it is known in the art. Moreover, the compounding quantity of these additives is not specifically limited, What is necessary is just to determine suitably.

  The resist polymer of the present invention may be used as a resist composition for metal etching, photofabrication, plate making, hologram, color filter, retardation film and the like.

  Next, an example of the pattern manufacturing method of the present invention will be described.

  First, the resist composition of the present invention is applied to the surface of a substrate to be processed such as a silicon wafer for producing a pattern by spin coating or the like. And the to-be-processed board | substrate with which this resist composition was apply | coated is dried by baking processing (prebaking) etc., and a resist film is manufactured on a board | substrate.

Next, the resist film thus obtained is irradiated with light having a wavelength of 250 nm or less through a photomask (exposure). The light used for exposure is preferably a KrF excimer laser, an ArF excimer laser, or an F ₂ excimer laser, and particularly preferably an ArF excimer laser. It is also preferable to expose with an electron beam.

  After exposure, heat treatment is appropriately performed (post-exposure baking, PEB), the substrate is immersed in an alkaline developer, and the exposed portion is dissolved and removed in the developer (development). Any known alkaline developer may be used. Then, after development, the substrate is appropriately rinsed with pure water or the like. In this way, a resist pattern is manufactured on the substrate to be processed.

  Usually, a substrate to be processed on which a resist pattern has been manufactured is appropriately heat-treated (post-baked) to strengthen the resist and selectively etch portions without the resist. After etching, the resist is usually removed using a release agent.

  Finally, the compound represented by the following formula (6), which is one of raw materials for producing the resist polymer of the present invention, will be described.

In the formula (6), E ¹ represents a functional group having a polymerization termination ability or a chain transfer ability. J, K ¹ , K ² , L ¹ , L ² , M ¹ , M ² , M ³ , Y ¹ , Y ² , k1, k2, l1, l2, m1, m2, m3, n1, and n are Each is synonymous with Formula (1).

In particular, in the formula (6), when n = 2 and E ¹ is a thiol group, the formula (6) has a structure represented by the following formula (7). Then, a resist polymer having a structure represented by the formula (4) is obtained.

In formula (7), S represents a sulfur atom. Further, K ¹ , K ² , L ¹ , L ² , M ¹ , M ² , M ³ , Y ¹ , Y ² , k ¹ , k ² , l ¹ , l ² , m 1, m 2, m 3, and n 1 are represented by the formula (1 ).

  The compound represented by the above formula (7) is a compound obtained by the following methods (a) to (c).

(A) A method in which a compound represented by the following formula (15) is added to a compound represented by the following formula (14) and converted into a compound represented by the following formula (16), followed by dithiolation.

(M ^{2 in} Formula (14) and Formula (16) represents alkylene, cycloalkylene, oxyalkylene, or arylene, m2 represents 0 or 1, and R ¹⁰ and R ¹¹ each independently have 1 to 18 carbon atoms. Represents a linear, branched or cyclic alkyl group, alkenyl group or aryl group, wherein R ¹² and R ¹³ each independently represents a hydrogen atom or a methyl group, and are represented by formulas (15) and (16) S represents a sulfur atom, and Z represents an acyl group or an alkali metal.)

(B) A method of dithiolating the following formula (19) obtained by coupling a diol represented by the following formula (17) and a carboxylic acid chloride having a sulfur atom represented by the following formula (18).

(M ^{2 in} Formula (17) and Formula (19) represents alkylene, cycloalkylene, oxyalkylene, or arylene, m2 represents 0 or 1, and R ¹⁰ and R ¹¹ each independently have 1 to 18 carbon atoms. In the formula (18), Cl represents a chlorine atom, and S in the formula (18) and the formula (19) is S. Represents a sulfur atom, Z ² represents an acyl group, and K ¹ represents at least one selected from the group consisting of alkylene, cycloalkylene, oxyalkylene, arylene, divalent thiazoline ring, divalent oxazoline ring, and divalent imidazoline ring. Represents.)

(C) A method of dithiolating the following formula (22) obtained by adding a carboxylic acid having a sulfur atom represented by the following formula (21) to the divinyl ether represented by the following formula (20).

(M ^{2 in} Formula (20) and Formula (22) represents alkylene, cycloalkylene, oxyalkylene, or arylene, and m2 represents 0 or 1. In addition, S in Formula (21) and Formula (22) Represents a sulfur atom, Z ² represents an acyl group, and K ¹ represents at least one selected from the group consisting of alkylene, cycloalkylene, oxyalkylene, arylene, divalent thiazoline ring, divalent oxazoline ring, and divalent imidazoline ring. Represents a kind.)

  Of the above formula (6), for example, the compounds represented by the above formula (35-23) can be synthesized by the following scheme, respectively.

  Next, a method for producing the compound represented by the above formula (7) will be described.

(A) A compound represented by the above formula (15) is added to the compound represented by the above formula (14) to convert it to a compound represented by the above formula (16), followed by dithiolation to obtain the above formula. How to get (7)

First, examples of the compound represented by the formula (14) include the following. In the formula, R ¹⁰ , R ¹¹ , R ¹⁴ , and R ¹⁵ each independently represent a linear, branched, or cyclic alkyl group, alkenyl group, or aryl group having 1 to 18 carbon atoms. R ¹² and R ¹³ each independently represents a hydrogen atom or a methyl group.

Specific examples of R ¹⁰ , R ¹¹ , R ¹⁴ and R ¹⁵ include a methyl group, an ethyl group, a propyl group, a pentyl group, an octyl group, and an isopropyl group. A methyl group and an ethyl group are preferable from the viewpoint of acid decomposability. In particular, R ¹⁰ , R ¹¹ , R ¹⁴ and R ^{15 are} all preferably methyl groups.

  Moreover, as a compound which has a sulfur atom represented by the said Formula (15), hydrogen sulfide, NaSH, KSH, and the following can be mentioned, for example.

  In the production method of the present invention, first, a compound represented by formula (15) is added to a compound represented by formula (14) to obtain a compound represented by formula (16). In this addition step, it is preferable to add the compound represented by the formula (15) to the compound represented by the formula (14) by 2 times to 6 times by mole with respect to the compound represented by the formula (14). The reaction proceeds at room temperature, but the reaction proceeds faster as the reaction temperature is increased. The reaction temperature at this time is preferably usually -30 to 100 ° C. The reaction may be performed in a solvent or without a solvent.

  Next, the chain transfer agent of Formula (7) is obtained by dithiolating the compound represented by Formula (16). The dithiolation step is performed in the presence of an aqueous alkaline solution. Examples of the alkaline aqueous solution include a sodium hydroxide aqueous solution, a potassium hydroxide aqueous solution, a potassium carbonate aqueous solution, a sodium carbonate aqueous solution, a sodium hydrogen carbonate aqueous solution, a potassium hydrogen carbonate aqueous solution, and an ammonia aqueous solution. In order to suppress decomposition of the ester bond of the formula (16) and to remove only Z, a weak base such as an aqueous sodium hydrogen carbonate solution, an aqueous potassium hydrogen carbonate solution, or an aqueous ammonia solution is preferable. By adding an organic solvent such as methanol to the reaction solution, the reaction system becomes uniform and the progress of the reaction can be accelerated. In general, the reaction temperature is preferably in the range of −30 ° C. to 80 ° C., and by setting it to −30 ° C. or higher, the progress of dithiolation can be accelerated. The target product can be obtained with good yield. The obtained reaction product is preferably purified by extraction, distillation, column chromatography, and recrystallization.

(B) The above formula (19) obtained by coupling the diol body represented by the formula (17) and the carboxylic acid chloride having a sulfur atom represented by the formula (18) is dithiolated to form the above Method for obtaining equation (7)

In this production method, first, the diol represented by the formula (17) and the carboxylic acid chloride represented by the formula (18) are coupled. The following can be mentioned as an example as a diol body represented by said Formula (17). In the formula, each of R ¹⁰ , R ¹¹ , R ¹⁴ and R ¹⁵ independently represents a linear, branched or cyclic alkyl group, alkenyl group or aryl group having 1 to 18 carbon atoms. Particularly preferred are those wherein R ¹⁰ , R ¹¹ , R ¹⁴ and R ¹⁵ are methyl groups.

  Examples of the carboxylic acid chloride represented by the formula (18) include the following.

  The coupling of the diol of formula (17) and the carboxylic acid chloride of formula (18) is generally reacted in the presence of an alkali. Examples of the alkali include sodium hydrogen carbonate, pyridine, triethylamine, dimethylaminopyridine and the like. It is preferable to add the carboxylic acid chloride of the formula (18) and the alkali to the diol body of the formula (17) in an amount of 2 to 30 moles, respectively. When the amount is 2 times or more, the reaction time can be shortened, and when the amount is 30 times or less, by-products are suppressed and the yield can be improved.

  This reaction proceeds at room temperature, but the reaction proceeds faster as the reaction temperature increases. The reaction temperature at this time is usually preferably -50 ° C to 80 ° C. When the temperature is set to −50 ° C. or higher, the reaction time can be shortened, and by setting the temperature to 80 ° C. or lower, byproducts can be suppressed and the yield can be improved. The reaction may be performed in a solvent or without a solvent.

  A compound represented by the formula (19) can be obtained by coupling the diol body of the formula (17) and the carboxylic acid chloride of the formula (18). A chain transfer agent of the formula (7) is obtained by dithiolation of the compound represented by the formula (19). The step of dithiolation may be performed in the same manner as the dithiolation of the compound represented by the formula (16).

(C) The above formula (22) obtained by adding a carboxylic acid having a sulfur atom represented by the above formula (21) to the divinyl ether represented by the above formula (20) is dithiolated to form the above formula ( 7) How to get

  In this production method, first, the carboxylic acid represented by the formula (21) is added to the divinyl ether represented by the formula (20). Examples of the divinyl ether represented by the formula (20) include the following.

  Examples of the carboxylic acid represented by the formula (21) include the following.

  In the step of adding the carboxylic acid represented by the formula (21) to the divinyl ether represented by the formula (20), it is preferable to react the latter in a range of 2 to 8 moles relative to the former. . If the molar ratio is 2 times or more, the reaction can proceed completely. Although the reaction proceeds at room temperature, the reaction proceeds faster as the reaction temperature is higher, and the compound represented by the formula (22) can be obtained. The reaction temperature at this time is preferably usually −30 ° C. to 100 ° C. By making it -30 degrees C or less, reaction time can be shortened, and it can be advanced efficiently by making it 100 degrees C or less. The reaction may be performed in a solvent or without a solvent. The compound represented by the formula (22) can be obtained by adding the carboxylic acid represented by the formula (21) to the divinyl ether represented by the formula (20). A chain transfer agent of formula (7) is obtained by dithiolation of the compound represented by formula (22). The step of dithiolation may be performed in the same manner as the dithiolation of the compound represented by the formula (16).

  Hereinafter, the present invention will be specifically described by way of examples, but the present invention is not limited thereto. In addition, “part” in each example and comparative example means “part by mass” unless otherwise specified.

  In the examples and comparative examples, the resist polymer and the resist composition were evaluated by the following methods.

1. Evaluation of resist polymer <mass average molecular weight of resist polymer>
About 20 mg of the resist polymer is dissolved in 5 mL of THF, filtered through a 0.5 μm membrane filter to prepare a sample solution, and this sample solution is measured using Tosoh gel permeation chromatography (GPC). did. For this measurement, a separation column was manufactured by Showa Denko Co., Ltd., and Shodex GPC K-805L (trade name) was used in series, the solvent was THF, the flow rate was 1.0 mL / min, the detector was a differential refractometer, measurement Measurements were made using polystyrene as the standard polymer at a temperature of 40 ° C. and an injection volume of 0.1 mL.

<Average copolymer composition ratio of resist polymer (mol%)>
^It calculated | required by the measurement of < ¹ > H-NMR. This measurement is performed using JSX Corporation GSX-400 type FT-NMR (trade name), deuterated chloroform, deuterated acetone or deuterated about 5 mass% resist polymer sample. The dimethyl sulfoxide solution was put in a test tube having a diameter of 5 mmφ, and the measurement was carried out 64 times in a single pulse mode at a measurement temperature of 40 ° C., an observation frequency of 400 MHz.

2. Evaluation of Resist Composition Using a resist polymer, a resist composition was prepared as follows, a resist pattern was produced, and performance was evaluated.

<Preparation of resist composition>
100 parts of the produced resist polymer, 2 parts of triphenylsulfonium triflate as a photoacid generator, and 700 parts of PGMEA as a solvent were mixed to form a uniform solution, and then filtered through a membrane filter having a pore size of 0.1 μm. Then, a resist composition solution was prepared.

<Manufacture of resist pattern>
The prepared resist composition solution was spin-coated on a silicon wafer (diameter: 200 mm), and prebaked at 120 ° C. for 60 seconds using a hot plate to form a resist film having a thickness of 0.4 μm. Subsequently, after exposing using an ArF excimer laser exposure machine (wavelength: 193 nm) and a mask, post-exposure baking was performed using a hot plate at 120 ° C. for 60 seconds. Subsequently, it developed at room temperature using the 2.38 mass% tetramethylammonium hydroxide aqueous solution, wash | cleaned with the pure water, and dried and formed the resist pattern.

<Sensitivity>
The exposure amount (mJ / cm ² ) at which a 0.16 μm line-and-space pattern mask was transferred to a line width of 0.16 μm was measured as sensitivity.

<Resolution>
The minimum dimension (μm) of the resist pattern resolved when exposed at the exposure amount was defined as the resolution.

<Line edge roughness>
JSM-6340F type field emission scanning electron microscope manufactured by JEOL Ltd. with respect to the range of 5 μm on the side edge in the longitudinal direction of the 0.20 μm resist pattern obtained by the minimum exposure amount reproducing the 0.20 μm resist pattern on the mask Based on (product name), the distance from the reference line where the pattern side edge should be was measured at 50 points, the standard deviation was obtained, and 3σ was calculated as an index of line edge roughness. A smaller value indicates better performance.

<Travel>
The cross section in the vertical direction of the above 0.20 μm resist pattern was observed at a magnification of 30,000 times with a JSM-6340F field emission scanning electron microscope (trade name) manufactured by JEOL. The case where no skirt was seen was evaluated as ◯, and the case where skirt was seen was evaluated as ×.

<Defect amount>
For the resist pattern, the number of development defects was measured with a surface defect observation apparatus KLA2132 (trade name) manufactured by KLA Tencor.

<Resist pattern collapse>
Regarding the resist pattern, a pattern without pattern collapse was marked with ◎, a pattern with slight pattern collapse was marked with ◯, and a pattern with many pattern collapses was marked with x.

<Example 1>
Under a nitrogen atmosphere, 34.9 parts of PGMEA was placed in a flask equipped with a nitrogen inlet, a stirrer, a condenser, and a thermometer, and the temperature of the hot water bath was raised to 80 ° C. while stirring.

1-part α-methacryloyloxy-γ-butyrolactone represented by the following formula (101) (hereinafter referred to as GBLMA) 13.3 parts 2-methacryloyloxy-2-methyladamantyl represented by the following formula (102) Called MAdMA.) 19.2 parts,
9.4 parts of 1-methacryloyloxy-3-hydroxyadamantyl (hereinafter referred to as HAdMA) represented by the following formula (103);
Chain transfer agent represented by the formula (35-3) (hereinafter referred to as CTA-1) 0.20 part (0.4 mol% based on the total monomers),

From a dropping apparatus containing a monomer solution in which 62.8 parts of PGMEA and 1.31 parts of 2,2′-azobisisobutyronitrile (hereinafter referred to as AIBN) were mixed, the flask was stirred at a constant rate for 6 hours. It was dripped in. Then, the temperature of 80 degreeC was hold | maintained for 1 hour. Next, the obtained reaction solution was added dropwise to about 10 times amount of methanol with stirring to obtain a white precipitate (polymer A-1). The resulting precipitate was filtered off and dried under reduced pressure at 60 ° C. for about 40 hours. The fact that the polymer A-1 contains a structure derived from the chain transfer agent (CTA-1) of the formula (35-3) is determined by measuring ³³ S-NMR and changing -SH to -S-. confirmed. That is, the obtained polymer A-1 contains the structure of the formula (104), and Table 1 shows the results of measuring the physical properties of this polymer.

<Example 2>
In a device similar to Example 1, 31.2 parts of PGMEA was placed under a nitrogen atmosphere, and the temperature of the hot water bath was raised to 80 ° C. while stirring.

13.6 parts GBLMA,
15.7 parts of 2-ethylcyclohexyl methacrylate (hereinafter referred to as ECHMA) represented by the following formula (105);
8.2 parts of a mixture of 2- and 3-cyano-5-norbornyl methacrylate represented by the following formula (106) (hereinafter referred to as CNNNMA),
1.42 parts of chain transfer agent (hereinafter referred to as CTA-2) represented by the above formula (35-25) (2.2 mol% based on the total monomers),

From a dropping device containing a monomer solution in which 56.2 parts of PGMEA and 1.84 parts of dimethyl-2,2′-azobisisobutyrate were mixed, it was dropped into the flask at a constant rate over 6 hours. Then, the temperature of 80 degreeC was hold | maintained for 1 hour. Subsequently, the obtained reaction solution was dropped into about 10 times amount of methanol with stirring to obtain a white precipitate (polymer A-2). The resulting precipitate was filtered off and dried under reduced pressure at 60 ° C. for about 40 hours. In the same manner as in Example 1, it was confirmed that the obtained polymer A-2 contained a structure of the formula (107) which is a structure derived from the chain transfer agent (CTA-2) of the formula (35-25). The results of measuring the physical properties of this polymer are shown in Table 1.

<Example 3>
31.2 parts of PGMEA was put in the same apparatus as in Example 1 under a nitrogen atmosphere, and the temperature of the hot water bath was raised to 80 ° C. while stirring.

A mixture of 8- and 9-acryloyloxy-4-oxatricyclo [5.2.1.0 ^2,6 ] decan-3-one represented by the following formula (108) (hereinafter referred to as OTDA) 13 .6 parts,
15.7 parts of ECHMA,
8.2 parts of 1-acryloyloxy-3-hydroxyadamantyl (hereinafter referred to as HAdA) represented by the following formula (109);
1.42 parts of chain transfer agent (hereinafter referred to as CTA-3) represented by the following formula (110) (1.3 mol% based on the total monomers),

From a dropping device containing a monomer solution in which 56.2 parts of PGMEA and 1.84 parts of AIBN were mixed, it was dropped into the flask at a constant rate over 6 hours. Then, the temperature of 80 degreeC was hold | maintained for 1 hour. Next, the obtained reaction solution was added dropwise to about 10 times amount of methanol with stirring to obtain a white precipitate (polymer A-3). The resulting precipitate was filtered off and dried under reduced pressure at 60 ° C. for about 40 hours. In the same manner as in Example 1, it was confirmed that the polymer contained a structure derived from the chain transfer agent (CTA-3) of the formula (110). Table 1 shows the results obtained by measuring the physical properties of the obtained polymer A-3.

<Example 4>
In the same apparatus as in Example 1, 30.6 parts of PGMEA was placed under a nitrogen atmosphere, and the temperature of the hot water bath was raised to 80 ° C. while stirring.

GBLMA 16.0 parts, ECHMA 20.8 parts, CTA-2 2.13 parts (3.3 mol% based on the total monomers), PGMEA 55.1 parts and AIBN 0.16 parts It dropped from the dripping apparatus which entered into the flask over 6 hours at a constant speed. Then, the temperature of 80 degreeC was hold | maintained for 1 hour. Next, the obtained reaction solution was added dropwise to about 10 times amount of methanol with stirring to obtain a white precipitate (polymer A-4). The resulting precipitate was filtered off and dried under reduced pressure at 60 ° C. for about 40 hours. In the same manner as in Example 1, it was confirmed that the polymer contained the structure of the formula (107), which was a structure derived from the chain transfer agent (CTA-2) of the formula (35-25). Table 1 shows a result obtained by measuring physical properties of the obtained polymer A-4.

<Comparative Example 1>
Polymer B-1 was obtained in the same manner as in Example 1 except that the chain transfer agent used was changed to CTA-1 and 0.06 part of n-octyl mercaptan (hereinafter referred to as nOM). . Table 1 shows the results obtained by measuring the physical properties of the obtained polymer B-1.

  A resist composition using a resist polymer produced using the formulas (6) and (7) of the present invention and containing an acid-decomposable unit of the formula (1) as a constituent unit is sufficient. In addition to having sensitivity, the resolution was high, the line edge roughness was small, and the generation of defects was small (Examples 1 to 4). In Example 4, although there was a slight collapse of the resist pattern, it was within a range that is practically acceptable.

  On the other hand, a resist composition using a polymer not containing the structure represented by the formula (1), produced by performing polymerization using only nOM as a chain transfer agent, has a large line edge roughness, Many defects were also confirmed (Comparative Example 1).

<Synthesis Example 1>
In the same apparatus as in Example 1, 35.3 parts of dimethylacetamide (hereinafter referred to as DMAc) was placed in a nitrogen atmosphere, and the temperature of the hot water bath was raised to 80 ° C. while stirring.

GBLMA 11.9 parts, MAdMA 21.1 parts, HAdMA 9.4 parts, DMAc 63.6 parts, 4,4′-azobis (4-cyanovaleric acid) (hereinafter referred to as ACVA) 2.24 parts and 3-mercaptopropion From a dropping device containing a monomer solution mixed with 0.85 parts of acid, the solution was dropped into the flask at a constant rate over 6 hours. Then, the temperature of 80 degreeC was hold | maintained for 1 hour. Subsequently, the obtained reaction solution was dropped into about 10 times amount of methanol / water = 9/1 (volume ratio; 25 ° C.) with stirring to precipitate a white precipitate (polymer precursor P-1). Obtained. The resulting precipitate was filtered off and dried under reduced pressure at 60 ° C. for about 40 hours. The fact that the ACVA residue is bonded to the molecular chain terminal of the polymer precursor P-1 is measured by ¹³ C-NMR, and the quaternary carbon bonded to the azo group = N— C (CH ₃ ) (CN) - is _{- C (CH 3) (CN} ) - and it was confirmed by changes. Similarly, the binding of 3-mercaptopropionic acid residue was determined by measuring ³³ S-NMR and changing -SH to -S-. The obtained polymer precursor P-1 contains the structures of the formulas (111) and (112). Table 2 shows the results of measuring the physical properties of the polymer.

<Synthesis Example 2>
In the same apparatus as in Example 1, 34.6 parts of DMAc was placed under a nitrogen atmosphere, and the temperature of the hot water bath was raised to 80 ° C. while stirring.

OTDA 17.8 parts, ECHMA 17.6 parts, CNNNMA 6.2 parts, DMAc 62.3 parts, dimethyl-2,2′-azobisisobutyrate (hereinafter referred to as DAIB) 1.84 parts and mercaptoacetic acid 0.64 From the dropping device containing the monomer solution mixed with the part, it was dropped into the flask at a constant rate over 6 hours. Then, the temperature of 80 degreeC was hold | maintained for 1 hour. Next, the obtained reaction solution was added dropwise to about 10 times amount of methanol with stirring to obtain a white precipitate (polymer precursor P-2). The resulting precipitate was filtered off and dried under reduced pressure at 60 ° C. for about 40 hours. And it carried out similarly to the synthesis example 1, and confirmed that the obtained polymer precursor contains the structure of Formula (113). The results of measuring the physical properties of this polymer are shown in Table 2.

<Synthesis Example 3>
A polymer precursor P-3 was obtained in the same manner as in Synthesis Example 1 except that 1.84 parts of DAIB was used instead of 2.24 parts of the polymerization initiator ACVA and the chain transfer agent 3-mercaptopropionic acid was not used. . The results of measuring the physical properties of this polymer are shown in Table 2.

<Example 5>
20 g of the polymer precursor P-1 obtained in Synthesis Example 1 was dissolved in 100 g of PGMEA. After a catalytic amount of camphorsulfonic acid was added to this solution, the remaining water was distilled off under reduced pressure together with PGMEA to prepare a solid content concentration of 20% by mass. Next, 1.6 g of the bifunctional divinyl ether compound of the above formula (36-1) was added to this solution, reacted at 25 ° C. for 12 hours with stirring, and then neutralized with triethylamine. And the reprecipitation operation similar to the synthesis example 1 was performed, and polymer A-5 was obtained. Table 3 shows the results of measuring the physical properties of this polymer.

<Example 6>
A polymer A-6 was obtained in the same manner as in Example 5 except that the polymer precursor P-2 obtained in Synthesis Example 2 was used in place of the polymer precursor P-1. Table 3 shows the results of measuring the physical properties of this polymer.

<Example 7>
In the same manner as in Example 5, except that 1.6 g of the bifunctional divinyl ether compound of the formula (36-4) was used instead of 1.6 g of the bifunctional divinyl ether compound of the formula (36-1), Polymer A-7 was obtained. Table 3 shows the results of measuring the physical properties of this polymer.

<Example 8>
In the same manner as in Example 6, except that 2.2 g of the trifunctional divinyl ether compound of the formula (36-9) was used instead of 1.6 g of the bifunctional divinyl ether compound of the formula (36-1), Polymer A-8 was obtained. Table 3 shows the results of measuring the physical properties of this polymer.

<Comparative example 2>
Using the polymer precursor P-3 obtained in Synthesis Example 3 as it was, a resist composition was prepared, and each physical property was measured. The results are shown in Table 3.

  A polymer precursor (P) having at least one molecular chain terminal having at least one structure selected from the group consisting of the above formulas (8-1) to (8-4) of the present invention, and the above formula (9) A resist composition using a resist polymer containing the acid-decomposable unit of the formula (1) as a constituent unit, which is produced by reacting with a vinyl ether compound represented by formula (1), has sufficient sensitivity. Furthermore, the resolution was high, the line edge roughness was small, and the generation of defects was small (Examples 5 to 8).

  On the other hand, the resist composition using the polymer not containing the structure represented by the formula (1) has large line edge roughness and many defects (Comparative Example 2).

<Example 9>
In a device similar to Example 1, 175.8 parts of PGMEA was placed under a nitrogen atmosphere, and the temperature of the hot water bath was raised to 80 ° C. while stirring. CNNNMA 41.0 parts, GBLMA 68.0 parts, MAdMA 93.6 parts, 2-methyl-2,4-butanediol dimethacrylate (hereinafter referred to as MBDMA) 8.4 parts represented by the formula (40-1). , PGMEA 316.5 parts, AIBN 6.56 parts and nOM 5.11 parts monomer solution was dropped into the flask over 6 hours at a constant rate using a dropping device, and then kept at 80 ° C. for 1 hour did. Next, the obtained reaction solution was added dropwise to about 30 times amount of methanol with stirring to obtain a white precipitate (polymer A-9). In order to remove the monomer remaining in the precipitate, the obtained precipitate was separated by filtration, and the precipitate was washed in about 30 times as much methanol as the monomer used for the polymerization. The precipitate was filtered off and dried at 50 ° C. under reduced pressure for about 40 hours. Table 4 shows the results obtained by measuring properties of the obtained polymer A-9.

<Example 10>
In a device similar to Example 1, 180.0 parts of PGMEA was placed under a nitrogen atmosphere, and the temperature of the hot water bath was raised to 80 ° C. while stirring. A monomer solution in which 47.2 parts of HAdMA, 93.6 parts of MAdMA, 68.0 parts of GBLMA, 7.2 parts of MBDMA, 324.0 parts of PGMEA, 6.56 parts of AIBN and 4.38 parts of nOM were mixed at a constant speed Was dropped into the flask over 6 hours, and then kept at 80 ° C. for 1 hour. Next, the obtained reaction solution was added dropwise to about 30 times amount of methanol with stirring to obtain a white precipitate (polymer A-10). Thereafter, the same operations as conducted in Example 9 were carried out, so as to obtain a polymer A-10. Table 4 shows the results obtained by measuring properties of the obtained polymer A-10.

<Example 11>
In the same apparatus as in Example 1, 168.3 parts of PGMEA was placed under a nitrogen atmosphere, and the temperature of the hot water bath was raised to 80 ° C. while stirring. MAdMA 117.0 parts, GBLMA 85.0 parts, 2,5-dimethyl-2,5-hexanediol diacrylate (hereinafter referred to as DMHDA) represented by the following formula (40-2) 0.3 parts, PGMEA 303. A monomer solution in which 0 part, 6.56 parts of AIBN and 1.46 parts of nOM were mixed was dropped into the flask over 6 hours at a constant rate using a dropping device, and then kept at 80 ° C. for 1 hour. Next, the obtained reaction solution was added dropwise to about 30 times amount of methanol with stirring to obtain a white precipitate (Polymer A-11). Thereafter, the same operations as conducted in Example 9 were carried out, so as to obtain a polymer A-11. Table 4 shows the results obtained by measuring physical properties of the obtained polymer A-11.

<Example 12>
In a device similar to Example 1, 176.2 parts of PGMEA was placed under a nitrogen atmosphere, and the temperature of the hot water bath was raised to 80 ° C. while stirring. A monomer solution in which 41.0 parts of CNNNMA, 93.6 parts of MAdMA, 68.0 parts of GBLMA, 8.9 parts of DMHDA, 317.2 parts of PGMEA, 6.56 parts of AIBN and 5.11 parts of nOM were mixed at a constant speed Was dropped into the flask over 6 hours, and then kept at 80 ° C. for 1 hour. Next, the obtained reaction solution was added dropwise to about 30 times amount of methanol with stirring to obtain a white precipitate (polymer A-12). Thereafter, the same operations as conducted in Example 9 were carried out, so as to obtain a polymer A-12. Table 4 shows the results obtained by measuring properties of the obtained polymer A-12.

<Example 13>
180.4 parts of PGMEA was put into the apparatus similar to Example 1 under nitrogen atmosphere, and the temperature of the hot water bath was raised to 80 degreeC, stirring. A monomer solution in which 47.2 parts of HAdMA, 93.6 parts of MAdMA, 68.0 parts of GBLMA, 7.6 parts of DMHDA, 324.6 parts of PGMEA, 6.56 parts of AIBN and 4.38 parts of nOM were mixed at a constant speed Was dropped into the flask over 6 hours, and then kept at 80 ° C. for 1 hour. Next, the obtained reaction solution was added dropwise to about 30 times the amount of methanol with stirring to obtain a white precipitate (polymer A-13). Thereafter, the same operations as conducted in Example 9 were carried out, so as to obtain a polymer A-13. Table 4 shows the results obtained by measuring properties of the obtained polymer A-13.

<Example 14>
In a device similar to Example 1, 39.0 parts of PGMEA was placed under a nitrogen atmosphere, and the temperature of the hot water bath was raised to 80 ° C. while stirring.

From a dropping apparatus containing a monomer solution in which 13.3 parts of GBLMA, 19.2 parts of MAdMA, 9.4 parts of HAdMA, 5.1 parts of DMHDA, 68.8 parts of PGMEA, and 6.56 parts of AIBN were mixed at a constant speed over 6 hours. And dropped into the flask. Then, the temperature of 80 degreeC was hold | maintained for 1 hour. Subsequently, the obtained reaction solution was added dropwise to about 10 times amount of methanol with stirring to obtain a white precipitate (polymer A-14). The resulting precipitate was filtered off and dried under reduced pressure at 60 ° C. for about 40 hours. Table 4 shows a result obtained by measuring properties of the obtained polymer A-14.

<Example 15>
The polymer A-15 obtained in the same manner as in Example 14 except that DMHDA was changed to 6.3 parts of a crosslinking agent (hereinafter referred to as BDADMA) represented by the following formula (115). The results of measuring the physical properties of this polymer are shown in Table 5.

<Example 16>
In the same apparatus as in Example 1, 35.4 parts of PGMEA was placed under a nitrogen atmosphere, and the temperature of the hot water bath was raised to 80 ° C. while stirring.

GDRMA 13.6 parts, ECHMA 15.7 parts, BDADMA 6.3 parts, CNNMA 8.2 parts, PGMEA 62.5 parts and DAIB 11.50 parts from a dropping apparatus containing a monomer solution, it was taken at a constant speed for 6 hours. And dropped into the flask. Then, the temperature of 80 degreeC was hold | maintained for 1 hour. Next, the obtained reaction solution was added dropwise to about 10 times amount of methanol with stirring to obtain a white precipitate (polymer A-16). The resulting precipitate was filtered off and dried under reduced pressure at 60 ° C. for about 40 hours. Obtained polymer A-16 contains the structure of Formula (116), The result of having measured each physical property of this polymer was shown in Table 5.

<Example 17>
In the same apparatus as in Example 1, 35.9 parts of PGMEA was placed under a nitrogen atmosphere, and the temperature of the hot water bath was raised to 80 ° C. while stirring.

GBLMA 15.6 parts, MAdMA 21.2 parts, BDADMA 6.3 parts, PGMEA 64.6 parts and AIBN 3.94 parts mixed from a dropping apparatus containing a monomer solution into a flask at a constant rate over 6 hours did. Then, the temperature of 80 degreeC was hold | maintained for 1 hour. Next, the obtained reaction solution was added dropwise to about 10 times amount of methanol with stirring to obtain a white precipitate (polymer A-16). The resulting precipitate was filtered off and dried under reduced pressure at 60 ° C. for about 40 hours. Obtained polymer A-16 contains the structure of Formula (116), The result of having measured each physical property of this polymer was shown in Table 5.

<Comparative Example 3>
The polymerization reaction operation was performed in the same manner as in Example 11 except that DMHDA was changed to 38.0 parts. However, since the contents of the flask gelled during the polymerization, the polymer could not be obtained.

<Comparative example 4>
In a device similar to Example 9, 168.8 parts of PGMEA was placed under a nitrogen atmosphere, and the temperature of the hot water bath was raised to 80 ° C. while stirring. A monomer solution in which 41.0 parts of CNNNMA, 93.6 parts of MAdMA, 68.0 parts of GBLMA, 303.9 parts of PGMEA, 6.56 parts of AIBN and 1.75 parts of nOM were mixed with a dropping device at a constant rate over 6 hours. The solution was dropped into the flask and then kept at 80 ° C. for 1 hour. Next, the obtained reaction solution was added dropwise to about 30 times amount of methanol with stirring to obtain a white precipitate (polymer B-4). Thereafter, the same operations as conducted in Example 9 were carried out, so as to obtain a polymer B-4. Table 6 shows the results obtained by measuring properties of the obtained polymer B-4.

<Comparative Example 5>
In a device similar to Example 9, 174.0 parts of PGMEA was placed under a nitrogen atmosphere, and the temperature of the hot water bath was raised to 80 ° C. while stirring. A monomer solution in which 47.2 parts of HAdMA, 93.6 parts of MAdMA, 68.0 parts of GBLMA, 313.2 parts of PGMEA, 6.56 parts of AIBN and 0.58 parts of nOM were mixed with a dropping device at a constant rate over 6 hours. The solution was dropped into the flask and then kept at 80 ° C. for 1 hour. Next, the obtained reaction solution was added dropwise to about 30 times the amount of methanol with stirring to obtain a white precipitate (polymer B-5). Thereafter, the same operations as conducted in Example 9 were carried out, so as to obtain a polymer B-5. Table 6 shows the results obtained by measuring properties of the obtained polymer B-5.

  Resist compositions (Examples 9 to 17) using a resist polymer produced using the formula (13) of the present invention and containing the acid-decomposable unit of the formula (3) as a constituent unit are as follows. In addition to sufficient sensitivity and resolution, the line edge roughness was small. Moreover, there was little defect generation and no skirting was observed.

  Among them, resist compositions (Examples 9, 10, 12, and 13) using a resist polymer containing a structural unit as the acid-decomposable unit of the formula (3) and a structural unit further having a hydrophilic group are as follows. The line edge roughness was smaller. Also, fewer defects were generated.

  And, the acid-decomposable unit of the formula (3) is the formula (5), and a resist composition using a resist polymer containing a structural unit having a hydrophilic group (Examples 14 and 15), The line edge roughness was even smaller. In addition, there were fewer defects generated.

  On the other hand, the resist composition (Comparative Examples 4 and 5) using a polymer that does not contain the structure represented by the formula (3) has a large line edge roughness, many defects, and skirting. It was.

  Moreover, when there was much usage-amount of said Formula (13), it could not be used as a polymer for a resist because a polymer gelatinized. (Comparative Example 3)

<Example 18> Synthesis of chain transfer agent (CTA-2) In an argon atmosphere, 12.716 g (50 mmol) of diacrylate represented by the following formula (120) was charged into a 100 mL flask, and the temperature of the system was 25 ° C. Then, 5.0 mL of toluene was added and stirred until dissolved. Further, 16.31 g (150 mmol) of thioacetic acid was added, and aging was performed at 25 ° C. for 8 hours. Next, the reaction solution was concentrated to obtain 20.3 g of a concentrate. Among these, 5.0 g of the concentrate was weighed into a 500 mL eggplant flask, and 50 mL of methanol was added. Thereafter, 50 mL of saturated aqueous sodium bicarbonate was added dropwise over 30 minutes while cooling in an ice bath. 4 hours after the completion of dropping, 100 mL of pure water and 100 mL of ethyl acetate were added and stirred. The oil layer of this reaction solution was concentrated. The concentrate was recrystallized from hexane to obtain 2.91 g (yield 75%) of CTA-2 as shown below.

<Example 19> Synthesis of chain transfer agent (CTA-1) In a 500 mL eggplant flask, 4.17 g (40 mmol) of 3-methyl-1,3-butanediol and 20.0 mL of tetrahydrofuran (THF) were weighed. Was stirred at a temperature of 25 ° C. After adding 18.98 g (240 mmol) of pyridine, 36.6 g (240 mmol) of S-acetylmercaptoacetic chloride was added dropwise over 30 minutes. After dropping, aging was carried out at 25 ° C. for 5 hours. Subsequently, 20 mL of toluene and 20 mL of pure water were added and stirred, and the oil layer was concentrated. 35.0 g of the concentrate was weighed into a 500 mL eggplant flask and 100 mL of methanol was added. Thereafter, 200 mL of saturated aqueous sodium bicarbonate was added dropwise over 30 minutes while cooling in an ice bath. Four hours after the completion of dropping, 50 mL of pure water and 100 mL of ethyl acetate were added and stirred. The oil layer of this reaction solution was concentrated. The concentrate was recrystallized using hexane to obtain 5.04 g (yield 50%) of CTA-1 as shown below.

<Example 20> Synthesis of chain transfer agent (CTA-4) 7.10 g (50 mmol) of butyl divinyl ether was charged into a 500 mL eggplant flask, and the temperature of the system was 25 ° C and stirred. After adding 20.1 g (150 mmol) of S-acetylmercaptoacetic acid, aging was performed at 70 ° C. for 6 hours. Subsequently, 136 mL of saturated sodium bicarbonate water and 50 mL of toluene were added, and the toluene layer was concentrated to obtain 10.1 g of a concentrate. 10.1 g of this concentrate was weighed into a 500 mL eggplant flask, and 100 mL of saturated aqueous sodium bicarbonate was added dropwise over 60 minutes while cooling in an ice bath. 4 hours after the completion of dropping, 100 mL of pure water and 100 mL of ethyl acetate were added and stirred, and the oil layer was concentrated. The concentrate was recrystallized using hexane to obtain 1.14 g (yield 70%) of CTA-4 as shown below.

Claims (5)

The acrylic polymer for resists which contains the acid-decomposable unit which has a structure represented by following formula (3), and the unit which has a hydrophilic group as a structural unit.
(In Formula (3), K ¹ and K ² each independently represent at least one of the group consisting of alkylene, cycloalkylene, oxyalkylene, and arylene, and L ¹ and L ² each independently represent —C (O )-And -OC (O)-, M ² represents at least one group selected from the group consisting of alkylene, cycloalkylene and oxyalkylene, and Y ¹ and Y ² each independently represent the following formula (23-3) or (23-4) represents any one of the acid-decomposable bonds, and k1, k2, l1, l2, m2, and n1 are K ¹ , K ² , L ¹ , L ² , M ² , And Y ² and independently represent 0 or 1. R ² and R ³ each independently represent a hydrogen atom or a methyl group.)
(In Formula (23-3), R ⁷⁰⁵ and R ⁷⁰⁶ each independently represent a hydrogen atom, a linear or branched alkyl group having 1 to 18 carbon atoms, an alkenyl group, or an aryl group.
In Formula (23-4), ^R707 represents a hydrogen atom, a linear or branched alkyl group having 1 to 4 carbon atoms, an alkenyl group, or an aryl group. Moreover, v1 is an integer of 1-5. ) In formula (3), k1 and k2 are both 0, n2, m2, l1, and l2 are all 1, L ¹ and L ² are both —C (O) —, and M ² Is A, Y ¹ and Y ² are both represented by formula (23-2), R ⁷⁰⁵ is a hydrogen atom, and R ⁷⁰⁶ is R ⁴ and R ⁵ , respectively, in the following formula (5) The acrylic polymer for resists according to claim 1, wherein
(R ^{2 to} R ⁵ in Formula (5) each independently represent a hydrogen atom or a methyl group. A represents an alkylene group having 1 to 18 carbon atoms, a cycloalkylalkylene group, or an oxyalkylene group. ) Claims produced by polymerizing at least a monomer represented by the following formula (11), a monomer represented by the following formula (12), and a monomer represented by the following formula (13). 1. Acrylic polymer for resist according to 1.
(In the formula (11), R ⁶ represents a hydrogen atom or a methyl group, R ⁷ represents a linear or branched alkyl group having 1 to 6 carbon atoms, a cyclic hydrocarbon group having 4 to 8 carbon atoms, or 4 to 4 carbon atoms. 16 represents a bridged cyclic hydrocarbon group or a lactone group that does not have a hydrophilic group, wherein the alkyl group, cyclic hydrocarbon group, bridged cyclic hydrocarbon group, and lactone The group may have a substituent.)
(In the formula (12), R ⁸ represents a hydrogen atom or a methyl group, R ⁹ represents a hydrogen atom, a linear or branched alkyl group having 1 to 6 carbon atoms, a cyclic hydrocarbon group having 4 to 8 carbon atoms, or (It is a bridged cyclic hydrocarbon group having 4 to 16 carbon atoms and represents a group having a hydrophilic group as a substituent.)
(In formula (13), K ¹ and K ² each independently represent at least one of the group consisting of alkylene, cycloalkylene, oxyalkylene, and arylene, and L ¹ and L ² each independently represent —C (O )-And -OC (O)-, M ² represents at least one group selected from the group consisting of alkylene, cycloalkylene and oxyalkylene, and Y ¹ and Y ² each independently represent the following formula It represents any one of the acid-decomposable bonds of (23-3) or (23-3), k1, k2, l1, l2, m2, and n1 are K ¹ , K ² , L ¹ , L ² , M ² represents the number of Y ² and is independently 0 or 1. R ² and R ³ each independently represent a hydrogen atom or a methyl group.)
(In the formula (23-3), R ⁷⁰⁵ and R ⁷⁰⁶ each independently represents a hydrogen atom, a linear or branched alkyl group having 1 to 18 carbon atoms, an alkenyl group, or an aryl group. R ⁷⁰⁷ represents a hydrogen atom, a linear or branched alkyl group having 1 to 4 carbon atoms, an alkenyl group or an aryl group, and v1 is an integer of 1 to 5.)   A resist composition comprising the resist polymer according to claim 1.   The process of apply | coating the composition containing the resist composition of Claim 4 and a photo-acid generator on a to-be-processed substrate, the process of exposing this coating material, and developing this exposed material using a developing solution. Pattern manufacturing method having a process