JP2013033262A - Resist material and pattern forming method - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a resist material using a polymeric compound derived from a fluorine-containing monomer useful as a monomer of an additive polymer that has high repellency and high water slipping property and can achieve immersion lithography, a chemically amplified resist material in particular, and a pattern formation method using the material.SOLUTION: The resist material contains: (A) a polymeric compound having an acrylic repeating unit having a hexafluoropropyl acid ester group in a side chain; (B) a polymeric compound as a base resin, which includes having a skeleton derived from a lactone ring and/or a skeleton having a hydroxyl group and/or a skeleton derived from maleic acid anhydride, and which is converted into soluble with an alkali developing solution by an action of an acid; (C) a compound generating an acid by exposure to high-energy rays; and (D) an organic solvent. The material can achieve a resist film having high water repellency and high water slipping property durable against high-speed scanning without using a resist protective film. Further, the surface of a resist film can be modified into hydrophilic after development by the hydrolysis of a polymer in the resist material with an alkali developing solution, thereby significantly reducing blob defects.

Description

  The present invention relates to a photoresist material comprising a polymer (polymer compound) having a repeating unit derived from a fluorine-containing monomer (monomer, that is, a polymerizable compound) useful as a raw material for functional materials, pharmaceuticals, agricultural chemicals, etc., In particular, it relates to a chemically amplified positive resist material. This fluorine-containing monomer uses photolithography for fine processing in a manufacturing process of a semiconductor device or the like, for example, an ArF excimer laser having a wavelength of 193 nm as a light source, and a liquid (for example, water) is inserted between the projection lens and the substrate. In immersion photolithography in which exposure is performed in this manner, it is very useful as a raw material monomer for producing a resin for an additive of a radiation sensitive resist material having excellent transparency and excellent development characteristics.

  Furthermore, the present invention relates to a pattern forming method using this photoresist material.

In recent years, along with higher integration and higher speed of LSI, pattern rule miniaturization is progressing rapidly. The background of this is the shortening of the wavelength of the exposure light source. For example, a 64 Mbit DRAM (dynamic size of 0.25 μm or less) DRAM (dynamic Random access memory) is now available for mass production. Furthermore, in order to realize DRAM manufacturing with an integration degree of 256M and 1G or more, lithography using an ArF excimer laser (193 nm) has been studied in earnest, and 65 nm by combining with a high NA lens (NA ≧ 0.9). Node devices are being studied. Postponed its Although the use of F ₂ laser having a wavelength of 157nm to device fabrication of the next 45nm node is a candidate. In addition to the disadvantage in cost, is applied by a number of the problems typified by poor performance of the resist It was done. Then, ArF immersion lithography has been proposed as an alternative to F ₂ lithography (see Non-Patent Document 1: Proc. SPIE. Vol. 4690, xxix (2002)).

  In ArF immersion lithography, water is impregnated between a projection lens and a wafer, and ArF excimer laser is irradiated through the water. Since the refractive index of water at 193 nm is 1.44, it is possible to form a pattern using a lens having an NA of 1.0 or more, and theoretically the NA can be increased to 1.44. The resolving power is improved by the improvement of NA, and miniaturization of 45 nm or less is possible by combining a lens with NA of 1.2 or more and strong super-resolution technology (Non-patent Document 2: Proc. SPIE. Vol. 5040). P724 (2003)).

  In ArF immersion exposure, water-soluble components in the resist film may be eluted into the immersion water during exposure. That is, the acid generated during exposure and the basic compound added to the resist material may elute into the immersion water (reaching), and as a result, the pattern shape may change or the pattern may collapse. . It has also been pointed out that when the resist film has insufficient water repellency, a small amount of water droplets remaining after the scan permeates into the resist film, which may induce defects. For this reason, in ArF immersion lithography, a method (top coat process) is proposed in which a protective film is provided between the resist film and water to suppress elution of the resist components and water permeation into the resist film (Non-Patent Document 3). : 2nd Immersion Work Shop: See Resist and Cover Material Investigation for Immersion Lithography (2003)).

  When a top coat is used in ArF immersion exposure, the use of a protective film material that is soluble in an alkaline developer eliminates the need for a protective film removal step, and has great cost and process advantages. Therefore, development of a water-insoluble resist protective film material using a resin having an alkali-soluble unit (for example, a fluorine-containing alcohol, a carboxyl group, a sulfo group, etc.) has been energetically advanced (Patent Documents 1 to 5: International publication 2005/42453 pamphlet, international publication 2005/69676 pamphlet, Unexamined-Japanese-Patent No. 2005-264131, Unexamined-Japanese-Patent No. 2006-133716, Unexamined-Japanese-Patent No. 2006-91798).

  On the other hand, a method (top coatless process) for suppressing elution of resist components and water permeation into the resist film without using a protective film material has also been developed (Patent Documents 6 to 8: JP 2006-48029 A). JP, 2006-309245, A, JP, 2007-187887, A). In the top coat-less process, an alkali-soluble hydrophobic polymer compound is added to the resist as a surfactant, and the hydrophobic compound is localized on the resist surface during resist film formation. Similar effects can be expected. This method is advantageous in terms of cost in that a process for forming and removing the resist protective film is not necessary.

  In any of the topcoat / topcoatless processes, a scanning speed of about 300 to 700 (mm / s) is required in ArF immersion exposure to increase the throughput. When performing such high-speed scanning, if the water repellency of the resist film or the protective film is insufficient, water droplets remain on the film surface after scanning, which may induce defects. In order to eliminate such defects, it is necessary to improve the water repellency and water slidability of the coating film, and in particular, a material design that increases the receding contact angle is required (Non-Patent Document 4: 2nd International Symposium on Immersion Lithography, -15 / Sept., 2005, Detectivity data take with a full-field immersion exposure tool, Nakano et al.). In such polymer design, it is reported that introduction of fluorine into the resin is effective for improving water repellency, and formation of a microdomain structure by combining different water repellency groups is effective for improving water slidability. (See Non-Patent Documents 5 and 6: XXIV FATIPEC Congress Book, Vol. B, p15 (1997), Progress in Organic Coatings, 31, p97 (1997)).

Specific examples of materials excellent in water repellency and water slidability include a copolymer of α-trifluoromethyl acrylate and a norbornene derivative (Non-patent Document 7: Proc. SPIE. Vol. 4690, p18 (2002). )). This resin was developed as an F ₂ resist material and is characterized in that a highly water-repellent α-trifluoromethyl acrylate ester and a norbornene derivative are regularly arranged in a ratio of 2 to 1. In general, when a water molecule interacts with a methyl group or a trifluoromethyl group, the orientation distance between the water and the methyl group tends to be longer. Therefore, in the resin in which both substituents are regularly arranged, the orientation distance of water becomes long, and as a result, the water sliding performance of the resin is improved. In fact, it has been reported that when this polymer is used as a base polymer for a liquid immersion protective film, the water slidability is drastically improved (see Patent Document 9: JP 2007-140446 A). A fluorine-containing ring-closing polymer having a hexafluoroalcohol unit in the side chain also exhibits excellent water repellency and water slidability (see Non-Patent Document 8: Proc. SPIE. Vol. 6519, p651905 (2007)). This polymer further improves the water sliding performance by protecting the hydroxyl group of the side chain with an acid labile group.

  The introduction of fluorine into the resin is effective in improving water repellency and water slidability, but excessive introduction induces a new defect called a blob defect. This defect occurs during spin drying after development, and is likely to occur when the surface contact angle after development is high. For this reason, blob defects can be suppressed by introducing a highly hydrophilic substituent (for example, carboxyl group or sulfo group) into the resin and reducing the surface contact angle after development. Since it reduces the water slidability, it cannot be applied to the high-speed scanning as described above. Therefore, development of a material capable of suppressing blob defects while maintaining high water repellency and water slidability during immersion exposure is desired.

  The materials described above are not limited to ArF immersion lithography, and are expected to be applied to resist materials for mask blanks. Mask blanks are exposed for a long time in a vacuum, and it has been pointed out that the amine component in the resist may be adsorbed on the resist film surface and cause sensitivity fluctuations or shape changes. In view of this, a method has been proposed in which the surface of the resist film is modified by adding a compound having a surface-active effect so that amine is not adsorbed on the resist film.

International Publication No. 2005/42453 Pamphlet International Publication No. 2005/69676 Pamphlet JP 2005-264131 A JP 2006-133716 A JP 2006-91798 A JP 2006-48029 A JP 2006-309245 A Japanese Patent Laid-Open No. 2007-187887 JP 2007-140446 A

Proc. SPIE. Vol. 4690, xxix (2002) Proc. SPIE. Vol. 5040, p724 (2003) 2nd Immersion Work Shop: Resist and Cover Material Investigation for Immersion Lithography (2003) 2nd International Symposium on Immersion Lithography, 12-15 / Sept. , 2005, Detectivity data take with a full-field immersion exposure tool, Nakano et al. XXIV FATIPEC Congress Book, Vol. B, p15 (1997) Progress in Organic Coatings, 31, p97 (1997) Proc. SPIE. Vol. 4690, p18 (2002) Proc. SPIE. Vol. 6519, p651905 (2007)

  The present invention has been made in view of the above-described problems, and is useful as a monomer for a polymer compound for additives that can realize immersion lithography with excellent water repellency and water slidability and few development defects. Another object of the present invention is to provide a resist material using a polymer compound obtained from such a fluorine-containing monomer, particularly a chemically amplified positive resist material, and a pattern forming method using this material. The additive used in the present invention has excellent transparency with respect to radiation having a wavelength of 200 nm or less, and adjustment of various performances such as water repellency, water slidability, fat solubility, acid decomposability, hydrolyzability by selection of the resin structure Can be produced from raw materials that are easy to obtain and handle.

  As a result of intensive studies to achieve the above object, the present inventors use a resist protective film when a polymer compound having a plurality of fluorine-containing alkylcarbonyloxy groups in a repeating unit is used as a resist additive. The present inventors have found that a highly water-repellent and highly lubricious resist film that can withstand high-speed scanning is realized. Furthermore, the present invention has been completed by finding that the resist film surface after development is modified to be hydrophilic by hydrolysis of the polymer with an alkali developer, and as a result, blob defects can be significantly suppressed.

（式中、Ｒ¹は水素原子、フッ素原子、メチル基又はトリフルオロメチル基を示す。Ｒ²はハロゲン原子又は酸素原子を有していてもよい炭素数１〜１５の直鎖状、分岐状又は環状の１価炭化水素基を示す。Ａは炭素数１〜６の直鎖状、分岐状又は環状の２価炭化水素基を示す。ｋ¹は０〜２の整数である。）
請求項２：
（Ａ）請求項１に記載の一般式（１ａ）で表される繰り返し単位に加えて、下記一般式（２ａ）〜（２ｇ）で表される繰り返し単位のうちの１つ又は２つ以上を有する高分子化合物、（Ｂ）ベース樹脂として、ラクトン環由来の骨格及び／又は水酸基を有する骨格及び／又は無水マレイン酸由来の骨格を有し、酸の作用によりアルカリ現像液に可溶となる高分子化合物、（Ｃ）高エネルギー線の露光により酸を発生する化合物、（Ｄ）有機溶剤を含有することを特徴とする請求項１に記載のレジスト材料。

（式中、Ｒ¹は上記と同様である。Ｒ^4a及びＲ^4bは水素原子、又は炭素数１〜１５の直鎖状、分岐状又は環状の１価炭化水素基であり、Ｒ^4aとＲ^4bは互いに結合してこれらが結合する炭素原子と共に炭素数３〜８の非芳香環を形成することもできる。Ｒ^5aは水素原子、又は炭素数１〜１５の直鎖状、分岐状又は環状の１価炭化水素基又はフッ素化１価炭化水素基、又は酸不安定基を示し、１価炭化水素基の場合、構成する−ＣＨ₂−が−Ｏ−又は−Ｃ（＝Ｏ）−に置換されていてもよい。Ｒ^6a、Ｒ^6b、及びＲ^6cは水素原子、又は炭素数１〜１５の直鎖状、分岐状又は環状の１価炭化水素基であり、Ｒ^6aとＲ^6b、Ｒ^6aとＲ^6c、Ｒ^6bとＲ^6cは互いに結合してこれらが結合する炭素原子と共に炭素数３〜８の非芳香環を形成することもできる。Ｒ^7aは水素原子、又は炭素数１〜１５の直鎖状、分岐状又は環状の１価炭化水素基である。Ｒ^7bは炭素数１〜１５の直鎖状、分岐状又は環状の１価炭化水素基であり、Ｒ^7aとＲ^7bは互いに結合してこれらが結合する炭素原子と共に炭素数３〜８の非芳香環を形成することもできる。Ｒ^8aは炭素数１〜１５の直鎖状、分岐状又は環状のフッ素化１価炭化水素基である。ｋ²は０又は１を示す。）
請求項３：
（Ｂ）成分の高分子化合物が、（メタ）アクリル酸エステル重合体、（α−トリフルオロメチル）アクリル酸エステル−無水マレイン酸共重合体、シクロオレフィン−無水マレイン酸共重合体、ポリノルボルネン、シクロオレフィンの開環メタセシス反応により得られる高分子化合物、シクロオレフィンの開環メタセシス反応により得られる重合体を水素添加して得られる高分子化合物、ヒドロキシスチレンと（メタ）アクリル酸エステル誘導体、スチレン、ビニルナフタレン、ビニルアントラセン、ビニルピレン、ヒドロキシビニルナフタレン、ヒドロキシビニルアントラセン、インデン、ヒドロキシインデン、アセナフチレン、ノルボルナジエン類を共重合した高分子化合物の中から選択されることを特徴とする請求項１又は２に記載のレジスト材料。
請求項４：
（Ｂ）成分の高分子化合物が、下記一般式（２Ａ）〜（２Ｄ）で示される繰り返し単位のいずれか１種以上を含有することを特徴とする請求項１又は２に記載のレジスト材料。

（式中、Ｒ^1Aは水素原子、フッ素原子、メチル基又はトリフルオロメチル基を示す。ＸＡは酸不安定基を示す。ＸＢ、ＸＣはそれぞれ独立に単結合又は炭素数１〜４の直鎖状又は分岐状の２価の炭化水素基を示す。ＹＡはラクトン構造を有する置換基を示す。ＺＡは水素原子、又は炭素数１〜１５のフルオロアルキル基又は炭素数１〜１５のフルオロアルコール含有置換基を示す。ｋ^1Aは１〜３の整数を示す。）
請求項５：
高分子化合物（Ｂ）１００質量部に対して、一般式（１ａ）で表される繰り返し単位を含む高分子化合物（Ａ）の添加量が０．１〜５０質量部であることを特徴とする請求項１乃至４のいずれか１項に記載のレジスト材料。
請求項６：
更に、（Ｅ）塩基性化合物を含有することを特徴とする請求項１乃至５のいずれか１項に記載のレジスト材料。
請求項７：
更に、（Ｆ）溶解制御剤を含有することを特徴とする請求項１乃至６のいずれか１項に記載のレジスト材料。
請求項８：
（１）請求項１乃至７のいずれか１項に記載のレジスト材料を基板上に塗布する工程と、（２）加熱処理後、フォトマスクを介して高エネルギー線で露光する工程と、（３）現像液を用いて現像する工程を含むことを特徴とするパターン形成方法。
請求項９：
（１）請求項１乃至７のいずれか１項に記載のレジスト材料を基板上に塗布する工程と、（２）加熱処理後、投影レンズとウエハーの間に液体を挿入させ、フォトマスクを介して高エネルギー線で露光する工程と、（３）現像液を用いて現像する工程を含むことを特徴とするパターン形成方法。
請求項１０：
（１）請求項１乃至７のいずれか１項に記載のレジスト材料を基板上に塗布する工程と、（２）フォトレジスト膜の上に保護膜層を形成する工程と、（３）加熱処理後、投影レンズとウエハーの間に液体を挿入させ、フォトマスクを介して高エネルギー線で露光する工程と、（４）現像液を用いて現像する工程を含むことを特徴とするパターン形成方法。
請求項１１：
前記露光工程において、投影レンズと基板の間に挿入する液体が水であることを特徴とする請求項９又は１０に記載のパターン形成方法。
請求項１２：
露光光源として波長１８０〜２５０ｎｍの範囲の高エネルギー線を用いることを特徴とする請求項８乃至１１のいずれか１項に記載のパターン形成方法。
請求項１３：
（１）請求項１乃至７のいずれか１項に記載のレジスト材料をマスクブランクス上に塗布する工程と、（２）加熱処理後、真空中電子ビームで露光する工程と、（３）現像液を用いて現像する工程を含むことを特徴とするパターン形成方法。
また、本発明は、以下の含フッ素単量体及び含フッ素高分子化合物が関連する。
［１］下記一般式（１）で示される含フッ素単量体。

（式中、Ｒ¹は水素原子、フッ素原子、メチル基又はトリフルオロメチル基を示す。Ｒ²はハロゲン原子又は酸素原子を有していてもよい炭素数１〜１５の直鎖状、分岐状又は環状の１価炭化水素基を示す。Ａは炭素数１〜６の直鎖状、分岐状又は環状の２価炭化水素基を示す。ｋ¹は０〜２の整数である。）
［２］下記一般式（１ａ）で示される繰り返し単位を含有することを特徴とする高分子化合物。

（式中、Ｒ¹は水素原子、フッ素原子、メチル基又はトリフルオロメチル基を示す。Ｒ²はハロゲン原子又は酸素原子を有していてもよい炭素数１〜１５の直鎖状、分岐状又は環状の１価炭化水素基を示す。Ａは炭素数１〜６の直鎖状、分岐状又は環状の２価炭化水素基を示す。ｋ¹は０〜２の整数である。） That is, the present invention provides the following resist material and pattern forming method.
Claim 1:
(A) a polymer compound having a repeating unit represented by the following general formula (1a), (B) as a base resin, a lactone ring-derived skeleton and / or a hydroxyl group-containing skeleton and / or a maleic anhydride-derived skeleton And a high molecular compound that is soluble in an alkali developer by the action of an acid, (C) a compound that generates an acid upon exposure to high energy rays, and (D) an organic solvent.

(In the formula, R ¹ represents a hydrogen atom, a fluorine atom, a methyl group, or a trifluoromethyl group. R ² is a linear or branched chain having 1 to 15 carbon atoms which may have a halogen atom or an oxygen atom. Or a cyclic monovalent hydrocarbon group, A represents a linear, branched or cyclic divalent hydrocarbon group having 1 to 6 carbon atoms, and k ¹ is an integer of 0 to 2.)
Claim 2:
(A) In addition to the repeating unit represented by the general formula (1a) according to claim 1, one or more of the repeating units represented by the following general formulas (2a) to (2g) The polymer compound having (B) the base resin has a lactone ring-derived skeleton and / or a hydroxyl group-containing skeleton and / or a maleic anhydride-derived skeleton, and is highly soluble in an alkaline developer by the action of an acid. 2. The resist material according to claim 1, comprising a molecular compound, (C) a compound that generates an acid upon exposure to high energy rays, and (D) an organic solvent.

(Wherein, R ¹ is the a is the same .R ^4a and R ^4b are hydrogen atoms, or of the straight, a monovalent hydrocarbon group branched or cyclic, R ^4a and R ^4b can be bonded to each other to form a non-aromatic ring having 3 to 8 carbon atoms together with the carbon atom to which they are bonded, R ^5a is a hydrogen atom, or a straight, branched or cyclic group having 1 to 15 carbon atoms. A monovalent hydrocarbon group, a fluorinated monovalent hydrocarbon group, or an acid labile group, and in the case of a monovalent hydrocarbon group, the constituent —CH ₂ — is —O— or —C (═O) —. R ^6a , R ^6b , and R ^6c are each a hydrogen atom or a linear, branched, or cyclic monovalent hydrocarbon group having 1 to 15 carbon atoms, and R ^6a and R ^6b , R ^6a and R ^6c , R ^6b and R ^6c may be bonded to each other to form a non-aromatic ring having 3 to 8 carbon atoms together with the carbon atom to which they are bonded. ^7a is hydrogen, or of the straight, a monovalent hydrocarbon group branched or cyclic .R ^7b is a C1-15 straight, monovalent branched or cyclic hydrocarbon It is a hydrogen group, and R ^7a and R ^7b can be bonded to each other to form a non-aromatic ring having 3 to 8 carbon atoms together with the carbon atom to which they are bonded, and R ^8a is a straight chain having 1 to 15 carbon atoms. A branched or cyclic fluorinated monovalent hydrocarbon group, k ² represents 0 or 1.)
Claim 3:
The polymer compound of component (B) is a (meth) acrylic acid ester polymer, (α-trifluoromethyl) acrylic acid ester-maleic anhydride copolymer, cycloolefin-maleic anhydride copolymer, polynorbornene, A polymer compound obtained by ring-opening metathesis reaction of cycloolefin, a polymer compound obtained by hydrogenating a polymer obtained by ring-opening metathesis reaction of cycloolefin, hydroxystyrene and a (meth) acrylate derivative, styrene, 3. The polymer according to claim 1, wherein the polymer is selected from polymer compounds obtained by copolymerizing vinylnaphthalene, vinylanthracene, vinylpyrene, hydroxyvinylnaphthalene, hydroxyvinylanthracene, indene, hydroxyindene, acenaphthylene, and norbornadiene. of Resist material.
Claim 4:
The resist material according to claim 1 or 2, wherein the polymer compound of component (B) contains any one or more of repeating units represented by the following general formulas (2A) to (2D).

(In the formula, R ^1A represents a hydrogen atom, a fluorine atom, a methyl group or a trifluoromethyl group. XA represents an acid labile group. XB and XC are each independently a single bond or a straight chain having 1 to 4 carbon atoms. YA represents a substituent having a lactone structure, ZA represents a hydrogen atom, a fluoroalkyl group having 1 to 15 carbon atoms, or a fluoroalcohol having 1 to 15 carbon atoms. Represents a substituent, k ^1A represents an integer of ¹ to 3)
Claim 5:
The addition amount of the polymer compound (A) containing the repeating unit represented by the general formula (1a) is 0.1 to 50 parts by mass with respect to 100 parts by mass of the polymer compound (B). The resist material according to claim 1.
Claim 6:
The resist material according to any one of claims 1 to 5, further comprising (E) a basic compound.
Claim 7:
The resist material according to claim 1, further comprising (F) a dissolution control agent.
Claim 8:
(1) a step of applying the resist material according to any one of claims 1 to 7 on a substrate; (2) a step of exposing to high energy rays through a photomask after heat treatment; ) A pattern forming method comprising a step of developing using a developer.
Claim 9:
(1) a step of applying the resist material according to any one of claims 1 to 7 on the substrate; and (2) after the heat treatment, a liquid is inserted between the projection lens and the wafer, and the photomask is interposed. A pattern forming method comprising: a step of exposing with a high energy beam; and (3) a step of developing using a developer.
Claim 10:
(1) a step of applying the resist material according to any one of claims 1 to 7 on a substrate; (2) a step of forming a protective film layer on the photoresist film; and (3) a heat treatment. Thereafter, a pattern forming method comprising a step of inserting a liquid between the projection lens and the wafer and exposing with a high energy beam through a photomask, and (4) developing with a developer.
Claim 11:
The pattern forming method according to claim 9 or 10, wherein in the exposure step, the liquid inserted between the projection lens and the substrate is water.
Claim 12:
The pattern forming method according to claim 8, wherein high-energy rays having a wavelength in the range of 180 to 250 nm are used as the exposure light source.
Claim 13:
(1) A step of applying the resist material according to any one of claims 1 to 7 on a mask blank, (2) a step of exposing to an electron beam in a vacuum after heat treatment, and (3) a developer. The pattern formation method characterized by including the process developed using this.
The present invention also relates to the following fluorine-containing monomers and fluorine-containing polymer compounds.
[1] A fluorine-containing monomer represented by the following general formula (1).

(In the formula, R ¹ represents a hydrogen atom, a fluorine atom, a methyl group, or a trifluoromethyl group. R ² is a linear or branched chain having 1 to 15 carbon atoms which may have a halogen atom or an oxygen atom. Or a cyclic monovalent hydrocarbon group, A represents a linear, branched or cyclic divalent hydrocarbon group having 1 to 6 carbon atoms, and k ¹ is an integer of 0 to 2.)
[2] A polymer compound comprising a repeating unit represented by the following general formula (1a).

(In the formula, R ¹ represents a hydrogen atom, a fluorine atom, a methyl group, or a trifluoromethyl group. R ² is a linear or branched chain having 1 to 15 carbon atoms which may have a halogen atom or an oxygen atom. Or a cyclic monovalent hydrocarbon group, A represents a linear, branched or cyclic divalent hydrocarbon group having 1 to 6 carbon atoms, and k ¹ is an integer of 0 to 2.)

  The fluorine-containing monomer related to the present invention is useful as a raw material for functional materials, pharmaceuticals, agricultural chemicals and the like, and has excellent transparency with respect to radiation having a wavelength of 500 nm or less, particularly a wavelength of 300 nm or less. It is very useful as a monomer for producing an additive resin for a radiation sensitive resist material with very few defects. In addition, the polymer compound related to the present invention can be adjusted for various performances such as water repellency, water slidability, fat solubility, acid decomposability, hydrolyzability, etc. by selecting the resin structure, and is easily available and handled. Can be manufactured from various raw materials.

  Hereinafter, the present invention will be described in detail. In addition, in the following chemical formulas, there are many enantiomers or diastereoisomers that may exist due to the chemical structure, but in any case, these chemical formulas are the same unless otherwise specified. All stereoisomers shall be represented as representatives. In addition, these stereoisomers may be used alone or as a mixture.

（式中、Ｒ¹は水素原子、フッ素原子、メチル基又はトリフルオロメチル基を示す。Ｒ²はハロゲン原子又は酸素原子を有していてもよい炭素数１〜１５の直鎖状、分岐状又は環状の１価炭化水素基を示す。Ａは炭素数１〜６の直鎖状、分岐状又は環状の２価炭化水素基を示す。ｋ¹は０〜２の整数である。） [Fluoromonomer]
The fluorine-containing monomer used in the present invention is represented by the following general formula (1).

(In the formula, R ¹ represents a hydrogen atom, a fluorine atom, a methyl group, or a trifluoromethyl group. R ² is a linear or branched chain having 1 to 15 carbon atoms which may have a halogen atom or an oxygen atom. Or a cyclic monovalent hydrocarbon group, A represents a linear, branched or cyclic divalent hydrocarbon group having 1 to 6 carbon atoms, and k ¹ is an integer of 0 to 2.)

ここで、破線は結合手を示す（以下、同様）。 Specific examples of the linear, branched or cyclic monovalent hydrocarbon group having 1 to 15 carbon atoms of R ² include a methyl group, an ethyl group, a propyl group, an isopropyl group, an n-butyl group, and a sec-butyl group. Tert-butyl group, tert-amyl group, n-pentyl group, n-hexyl group, n-octyl group, n-nonyl group, n-decyl group, cyclopentyl group, cyclohexyl group, cyclopentylmethyl group, cyclopentylethyl group, Linear, branched such as cyclopentylbutyl, cyclohexylmethyl, cyclohexylethyl, cyclohexylbutyl, norbornyl, oxanorbornyl, tricyclo [5.2.1.0 ^2,6 ] decanyl, adamantyl Or cyclic alkyl groups, and some of these hydrogen atoms are fluorine atoms, hydroxyl groups, alkoxy groups, carboxy groups, alcohols Examples include those substituted with a xoxycarbonyl group, an oxo group, and the like.
Specific examples of the linear, branched, or cyclic monovalent hydrocarbon group having 1 to 15 carbon atoms that may have a halogen atom include the following groups.

Here, a broken line shows a bond (hereinafter the same).

Specific examples of the linear, branched or cyclic divalent hydrocarbon group having 1 to 6 carbon atoms of A include the following groups.

（式中、Ｒ¹は上記と同様である。） Specific examples of the compound represented by the general formula (1) include the following.

(In the formula, R ¹ is the same as above.)

（式中、Ｒ¹は上記と同様である。）

(In the formula, R ¹ is the same as above.)

（式中、Ｒ¹は上記と同様である。）

(In the formula, R ¹ is the same as above.)

（式中、Ｒ¹、Ｒ²、Ａ及びｋ¹は、上記と同様である。Ｒ³はハロゲン原子、水酸基又は−ＯＲ⁶を示す。Ｒ⁶はメチル基、エチル基又は下記式（８）

を示す。Ｒ⁴はハロゲン原子を示す。Ｒ⁵はハロゲン原子、水酸基又は−ＯＲ⁷を示す。Ｒ⁷はメチル基、エチル基又は下記式（９）

を示す。Ｍ^aはＬｉ、Ｎａ、Ｋ、Ｍｇ_1/2、Ｃａ_1/2又は置換もしくは未置換のアンモニウムを示す。Ｍｅはメチル基を示す。） The fluorine-containing monomer represented by the general formula (1) used in the present invention can be obtained by, for example, steps i) to iv) shown in the following reaction formula, but is not limited thereto.

(Wherein R ¹ , R ² , A and k ¹ are the same as described above. R ³ represents a halogen atom, a hydroxyl group or —OR ^6. R ⁶ represents a methyl group, an ethyl group or the following formula (8):

Indicates. R ⁴ represents a halogen atom. R ⁵ represents a halogen atom, a hydroxyl group or —OR ⁷ . R ⁷ is a methyl group, an ethyl group, or the following formula (9)

Indicates. M ^a represents _{Li, Na, K, Mg 1/2} , the ammonium Ca _1/2, or substituted or unsubstituted. Me represents a methyl group. )

  The methyl 3,3,3-trifluoro-2-trifluoromethyl-2-hydroxypropionate represented by the general formula (2) is, for example, octafluoroisobutylene produced as a by-product when synthesizing hexafluoropropene, for example. However, since the supply source is a by-product of the industrial product, it is a fluorine compound that can be obtained in large quantities at a relatively low cost.

Step i) is a step leading to the alcohol compound (3) by an ester exchange reaction between the alcohol compound R ² OH and the ester compound (2) in the presence of a catalyst.

  The reaction can be carried out without solvent, but a solvent can be used as an auxiliary. In this case, examples of the solvent include ethers such as tetrahydrofuran, diethyl ether, di-n-butyl ether and 1,4-dioxane, and hydrocarbons such as n-hexane, n-heptane, benzene, toluene, xylene and cumene. These can be used alone or in combination. Catalysts include metal alkoxides such as sodium methoxide, sodium ethoxide, potassium tert-butoxide, magnesium ethoxide, titanium (IV) methoxide, titanium (IV) ethoxide, titanium (IV) isopropoxide, triethylamine, N , N-dimethylaminopyridine, organic amines such as 1,8-diazabicyclo [5.4.0] -7-undecene, inorganic bases such as sodium hydroxide, potassium carbonate, sodium carbonate, etc. These can be used alone or in combination. The usage-amount of a catalyst is 0.001-5.0 mol with respect to ester compound (2), and especially 0.001-0.1 mol is preferable. Although reaction temperature changes with reaction conditions, 50-200 degreeC is preferable and it is good to carry out, distilling off the methanol produced by reaction. The reaction time is preferably about 0.5 to 20 hours, although it is desirable in terms of yield to follow the reaction by gas chromatography (GC) or silica gel thin layer chromatography (TLC) to complete the reaction. The target alcohol compound (3) can be obtained from the reaction mixture by ordinary aqueous work-up, and if necessary, it can be purified according to conventional methods such as distillation and chromatography.

  Step ii) is a step of leading to the fluorine-containing monomer (1) by the reaction of the esterifying agent (4) and the alcohol compound (3).

Although the reaction proceeds easily by a known method, the esterifying agent (4) may be an acid chloride {when R ³ is a chlorine atom in formula (4)} or a carboxylic acid {in formula (4), R ³ Is a hydroxyl group} is preferred. In the case of using acid chloride, the corresponding acid chloride such as alcohol compound (3), methacryloyloxyacetic acid chloride, triethylamine, pyridine, 4-dimethylaminopyridine, etc. without solvent or in a solvent such as methylene chloride, acetonitrile, toluene, hexane, etc. These bases may be added sequentially or simultaneously, and cooled or heated as necessary. In the case of using a carboxylic acid, the alcohol compound (3) and the corresponding carboxylic acid such as methacryloyloxyacetic acid are heated in the presence of an acid catalyst in a solvent such as toluene or hexane, and water generated as necessary is removed from the system. It is better to remove it. Examples of the acid catalyst to be used include inorganic acids such as hydrochloric acid, sulfuric acid, nitric acid and perchloric acid, and organic acids such as p-toluenesulfonic acid and benzenesulfonic acid.

  Step iii) is a step leading to the haloester compound (6) by the reaction of the esterifying agent (5) and the alcohol compound (3).

The reaction proceeds easily by a known method. As the esterifying agent (5), an acid chloride {when R ³ is a chlorine atom in formula (5)} or a carboxylic acid {in formula (5), R ³ Is a hydroxyl group} is preferred. When acid chloride is used, alcohol compound (3) and 2-chloroacetic acid chloride, 4-chlorobutyric acid chloride, etc. are used in the absence of solvent or in a solvent such as methylene chloride, toluene, hexane, diethyl ether, tetrahydrofuran, and acetonitrile. A base such as acid chloride, triethylamine, pyridine, 4-dimethylaminopyridine and the like may be added sequentially or simultaneously, and may be cooled or heated as necessary. In the case of using carboxylic acid, the alcohol compound (3) and the corresponding carboxylic acid such as 2-chloroacetic acid and 4-chlorobutyric acid are heated in the presence of an acid catalyst in a solvent such as toluene and hexane. It is recommended to remove the water generated from the system. Examples of the acid catalyst to be used include inorganic acids such as hydrochloric acid, sulfuric acid, nitric acid and perchloric acid, and organic acids such as p-toluenesulfonic acid and benzenesulfonic acid.

Step iv) is a step of leading to the fluorine-containing monomer (1) by the reaction of the haloester compound (6) and the carboxylate compound (7).
The reaction can be carried out according to a conventional method. As the carboxylate compound (7), commercially available carboxylate compounds such as various carboxylic acid metal salts may be used as they are, or carboxylic acids and bases such as methacrylic acid and acrylic acid are used in the reaction system. An acid salt compound may be prepared and used. The amount of the carboxylate compound (7) used is preferably 0.5 to 10 mol, particularly preferably 1.0 to 3.0 mol, per 1 mol of the haloester compound (6) as a raw material. If the amount used is less than 0.5 mol, a large amount of raw material remains, so the yield may be significantly reduced. If the amount is more than 10 mol, the cost may be disadvantageous due to an increase in raw material cost, a decrease in the yield of the kettle, etc. There is a case. Examples of bases that can be used when preparing a carboxylate compound from the corresponding carboxylic acid and base in the reaction system include amines such as ammonia, triethylamine, pyridine, lutidine, collidine, and N, N-dimethylaniline. Hydroxides such as sodium hydroxide, potassium hydroxide and tetramethylammonium hydroxide; carbonates such as potassium carbonate and sodium hydrogen carbonate; metals such as sodium; metal hydrides such as sodium hydride; sodium methoxide Selected from metal alkoxides such as potassium-t-butoxide; organometals such as butyl lithium and ethyl magnesium bromide; metal amides such as lithium diisopropylamide, or a mixture of two or more thereof. . The amount of the base used is preferably 0.2 to 10 mol, particularly 0.5 to 2.0 mol, per 1 mol of the corresponding carboxylic acid. If the amount is less than 0.2 mol, a large amount of carboxylic acid is wasted, which may be disadvantageous in terms of cost. If the amount is more than 10 mol, the yield may be significantly reduced due to an increase in side reactions.

  Solvents used in the reaction shown in the above step iv) include hydrocarbons such as toluene, xylene, hexane and heptane; chlorinated solvents such as methylene chloride, chloroform and dichloroethane; ethers such as diethyl ether, tetrahydrofuran and dibutyl ether Ketones such as acetone and 2-butanone; esters such as ethyl acetate and butyl acetate; nitriles such as acetonitrile; alcohols such as methanol and ethanol; N, N-dimethylformamide, N, N-dimethylacetamide and dimethyl An aprotic polar solvent such as sulfoxide; selected from water and used alone or in admixture of two or more. In the reaction, a phase transfer catalyst such as tetrabutylammonium hydrogen sulfate may be added as a catalyst. In this case, the addition amount of the phase transfer catalyst is preferably 0.0001 to 1.0 mol, particularly preferably 0.001 to 0.5 mol, relative to 1 mol of the alcohol compound as a raw material. If the amount is less than 0.0001 mol, the effect of addition may not be obtained. If the amount exceeds 1.0 mol, the cost may be disadvantageous due to an increase in raw material costs.

  The reaction temperature of the esterification reaction is preferably from about -70 ° C to the boiling point of the solvent used, and an appropriate reaction temperature can be selected depending on the reaction conditions, but usually from about 0 ° C to the boiling point of the solvent used is particularly preferred. Since side reactions may become prominent as the reaction temperature increases, it is important to carry out the reaction at as low a temperature as possible so that the reaction proceeds at a realistic rate in order to achieve a high yield. The reaction time of the above reaction is preferably determined by tracking the progress of the reaction by thin layer chromatography, gas chromatography or the like in order to improve the yield, but is usually about 30 minutes to 40 hours. The fluorine-containing monomer (1) can be obtained from the reaction mixture by ordinary aqueous work-up, and if necessary, can be purified according to conventional methods such as distillation, recrystallization, and chromatography. .

[Configuration of polymer compound for resist additive]
The polymer compound for resist additives used in the present invention is characterized by containing a repeating unit represented by the following general formula (1a). Hereinafter, the polymer compound containing the repeating unit represented by the general formula (1a) is referred to as a polymer compound (P1).

（式中、Ｒ¹、Ｒ²、Ａ及びｋ¹は上記と同様である。）

(In the formula, R ¹ , R ² , A and k ¹ are the same as above.)

  The polymer compound (P1) contains a plurality of fluorine atoms in the repeating unit represented by the general formula (1a). Therefore, when the polymer compound (P1) is added to the resist material, the polymer itself functions as a surfactant, and the polymer compound (P1) is localized and distributed on the resist film surface simultaneously with the film formation.

  In general, fluorine-containing polymers exhibit excellent performance in water repellency and water slidability. Therefore, when the polymer compound (P1) is used as a resist additive, the resist film surface is excellent in water repellency and water slidability simultaneously with the film formation of the resist. Thus, the same effect as when a resist protective film material is used can be expected. This method is advantageous in terms of cost in that a process for forming and removing the resist protective film is not necessary.

（式中、Ｒ¹、Ｒ²、Ａ及びｋ¹は上記と同様である。） Since the repeating unit represented by the general formula (1a) contains a fluorinated ester that is susceptible to alkali hydrolysis, it is easily hydrolyzed by an alkali developer, and as shown in the following reaction formula, the carboxylic acid unit (1aa) and (1ab) is generated. Therefore, when the polymer compound (P1) is used as a resist additive, the hydrophilicity of the resist film surface after alkali development is increased, and the surface contact angle after development can be greatly reduced. As a result, the occurrence of blob defects can be suppressed.

(In the formula, R ¹ , R ² , A and k ¹ are the same as above.)

（式中、Ｒ¹は上記と同様である。Ｒ^4a及びＲ^4bは水素原子、又は炭素数１〜１５の直鎖状、分岐状又は環状の１価炭化水素基であり、Ｒ^4aとＲ^4bは互いに結合してこれらが結合する炭素原子と共に炭素数３〜８の非芳香環を形成することもできる。Ｒ^5aは水素原子、又は炭素数１〜１５の直鎖状、分岐状又は環状の１価炭化水素基又はフッ素化１価炭化水素基、又は酸不安定基を示し、１価炭化水素基の場合、構成する−ＣＨ₂−が−Ｏ−又は−Ｃ（＝Ｏ）−に置換されていてもよい。Ｒ^6a、Ｒ^6b、及びＲ^6cは水素原子、又は炭素数１〜１５の直鎖状、分岐状又は環状の１価炭化水素基であり、Ｒ^6aとＲ^6b、Ｒ^6aとＲ^6c、Ｒ^6bとＲ^6cは互いに結合してこれらが結合する炭素原子と共に炭素数３〜８の非芳香環を形成することもできる。Ｒ^7aは水素原子、又は炭素数１〜１５の直鎖状、分岐状又は環状の１価炭化水素基である。Ｒ^7bは炭素数１〜１５の直鎖状、分岐状又は環状の１価炭化水素基であり、Ｒ^7aとＲ^7bは互いに結合してこれらが結合する炭素原子と共に炭素数３〜８の非芳香環を形成することもできる。Ｒ^8aは炭素数１〜１５の直鎖状、分岐状又は環状のフッ素化１価炭化水素基である。ｋ²は０又は１を示す。） In the polymer compound (P1) used in the present invention, in addition to the repeating unit represented by the general formula (1a), one or more repeating units of the following general formulas (2a) to (2g) are allowed to coexist. As a result, a polymer compound having further excellent water repellency, water slidability, alkali solubility, and contact angle after development can be realized.

(Wherein, R ¹ is the a is the same .R ^4a and R ^4b are hydrogen atoms, or of the straight, a monovalent hydrocarbon group branched or cyclic, R ^4a and R ^4b can be bonded to each other to form a non-aromatic ring having 3 to 8 carbon atoms together with the carbon atom to which they are bonded, R ^5a is a hydrogen atom, or a straight, branched or cyclic group having 1 to 15 carbon atoms. A monovalent hydrocarbon group, a fluorinated monovalent hydrocarbon group, or an acid labile group, and in the case of a monovalent hydrocarbon group, the constituent —CH ₂ — is —O— or —C (═O) —. R ^6a , R ^6b , and R ^6c are each a hydrogen atom or a linear, branched, or cyclic monovalent hydrocarbon group having 1 to 15 carbon atoms, and R ^6a and R ^6b , R ^6a and R ^6c , R ^6b and R ^6c may be bonded to each other to form a non-aromatic ring having 3 to 8 carbon atoms together with the carbon atom to which they are bonded. ^7a is hydrogen, or of the straight, a monovalent hydrocarbon group branched or cyclic .R ^7b is a C1-15 straight, monovalent branched or cyclic hydrocarbon It is a hydrogen group, and R ^7a and R ^7b can be bonded to each other to form a non-aromatic ring having 3 to 8 carbon atoms together with the carbon atom to which they are bonded, and R ^8a is a straight chain having 1 to 15 carbon atoms. A branched or cyclic fluorinated monovalent hydrocarbon group, k ² represents 0 or 1.)

Specific examples of linear, branched and cyclic alkyl groups having 1 to 15 carbon atoms in R ^4a , R ^4b , R ^5a , R ^6a , R ^6b , R ^6c , R ^7a , R ^7b and R ^8a , Methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, sec-butyl group, tert-butyl group, tert-amyl group, n-pentyl group, n-hexyl group, n-heptyl group, n-octyl group, n-nonyl group, n-decyl group, cyclopentyl group, cyclohexyl group, cyclopentylmethyl group, cyclopentylethyl group, cyclopentylbutyl group, cyclohexylmethyl group, cyclohexylethyl group, cyclohexylbutyl group, adamantyl group, etc. are used. It is done. R ^4a and R ^4b , R ^6a and R ^6b , R ^6a and R ^6c , R ^6b and R ^6c , R ^7a and R ^7b are bonded to each other and together with the carbon atom to which they are bonded, a non-aromatic ring having 3 to 8 carbon atoms In this case, these groups are alkylene groups, and those having a form in which one hydrogen atom in the alkyl group exemplified above is extracted are used. Specific examples of the ring include , Cyclopentyl group, cyclohexyl group and the like.

In R ^5a and R ^8a , as specific examples of the linear, branched, and cyclic fluorinated alkyl groups having 1 to 15 carbon atoms, some or all of the hydrogen atoms of the above alkyl groups are substituted with fluorine atoms. For example, trifluoromethyl group, 2,2,2-trifluoroethyl group, 3,3,3-trifluoro-1-propyl group, 3,3,3-trifluoro- 2-propyl group, 2,2,3,3-tetrafluoropropyl group, 1,1,1,3,3,3-hexafluoroisopropyl group, 2,2,3,3,4,4,4-hepta Fluorobutyl group, 2,2,3,3,4,4,5,5-octafluoropentyl group, 2,2,3,3,4,4,5,5,6,6,7,7-dodeca Fluoroheptyl group, 2- (perfluorobutyl) ethyl group, 2- (perfluoro Hexyl) ethyl group, 2- (perfluorooctyl) ethyl group, 2- (perfluorodecyl) ethyl group, 3,3,4,4,5,5,6,6,6-nonafluorohexyl group it can. In addition, for the linear, branched, and cyclic fluorinated alkyl groups having 1 to 10 carbon atoms of R ^8a , trifluoromethyl group, 2,2,2-trifluoroethyl group, 3,3,3-trimethyl, Fluoro-1-propyl group, 3,3,3-trifluoro-2-propyl group, 2,2,3,3-tetrafluoropropyl group, 1,1,1,3,3,3-hexafluoroisopropyl group 2,2,3,3,4,4,4-heptafluorobutyl group, 2,2,3,3,4,4,5,5-octafluoropentyl group, 2,2,3,3,4 , 4,5,5,6,6,7,7-dodecafluoroheptyl group, 2- (perfluorobutyl) ethyl group, 2- (perfluorohexyl) ethyl group, 2- (perfluorooctyl) ethyl group, 3,3,4,4,5,5,6,6,6-nonafluorohexyl Etc. groups can be exemplified.

（式中、Ｒ^L01及びＲ^L02は水素原子又は炭素数１〜１８、好ましくは１〜１０の直鎖状、分岐状又は環状のアルキル基を示す。Ｒ^L03は炭素数１〜１８、好ましくは炭素数１〜１０の酸素原子等のヘテロ原子を有してもよい１価の炭化水素基を示し、直鎖状、分岐状又は環状のアルキル基、これらの水素原子の一部が水酸基、アルコキシ基、オキソ基、アミノ基、アルキルアミノ基等に置換されたものを挙げることができる。Ｒ^L04は炭素数４〜２０、好ましくは炭素数４〜１５の三級アルキル基、各アルキル基がそれぞれ炭素数１〜６のトリアルキルシリル基、炭素数４〜２０のオキソアルキル基又は上記一般式（Ｌ１）で示される基を示す。Ｒ^L05は炭素数１〜１０の置換されていてもよい直鎖状、分岐状又は環状のアルキル基又は炭素数６〜２０の置換されていてもよいアリール基を示す。Ｒ^L06は炭素数１〜１０の置換されていてもよい直鎖状、分岐状又は環状のアルキル基又は炭素数６〜２０の置換されていてもよいアリール基である。Ｒ^L07〜Ｒ^L16はそれぞれ独立に水素原子又は炭素数１〜１５の１価の非置換又は置換炭化水素基を示す。ｙは０〜６の整数である。ｍは０又は１、ｎは０〜３の整数であり、２ｍ＋ｎ＝２又は３である。なお、破線は結合手を示す。） Next, the acid labile group of R ^5a will be described. Although various groups can be used as the acid labile group, specifically, a group represented by the following general formulas (L1) to (L4), a tertiary alkyl having 4 to 20 carbon atoms, preferably 4 to 15 carbon atoms. Groups, each alkyl group may be a trialkylsilyl group having 1 to 6 carbon atoms, an oxoalkyl group having 4 to 20 carbon atoms, and the like.

(In the formula, R ^L01 and R ^L02 represent a hydrogen atom or a linear, branched or cyclic alkyl group having 1 to 18 carbon atoms, preferably 1 to 10. R ^L03 represents 1 to 18 carbon atoms, preferably A monovalent hydrocarbon group which may have a hetero atom such as an oxygen atom having 1 to 10 carbon atoms, a linear, branched or cyclic alkyl group, a part of these hydrogen atoms being a hydroxyl group, an alkoxy group Group, oxo group, amino group, alkylamino group, etc. R ^L04 is a tertiary alkyl group having 4 to 20 carbon atoms, preferably 4 to 15 carbon atoms, and each alkyl group is A trialkylsilyl group having 1 to 6 carbon atoms, an oxoalkyl group having 4 to 20 carbon atoms, or a group represented by the above general formula (L1), R ^L05 is an ^optionally substituted one having 1 to 10 carbon atoms; Chain, branched or cyclic alkyl group or 6 carbon atoms .R ^L06 showing a an optionally substituted aryl group 20 have been substituted 6-20 alkyl group carbon atoms or a substituted or unsubstituted, linear, branched or cyclic C1-10 R ^{L07 to} R ^L16 each independently represent a hydrogen atom or a monovalent unsubstituted or substituted hydrocarbon group having 1 to 15 carbon atoms, y is an integer of 0 to 6. m is 0 or 1, n is an integer of 0 to 3, and 2m + n = 2 or 3. The broken line indicates a bond.)

In the formula (L1), specific examples of R ^L01 and R ^L02 include methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, sec-butyl group, tert-butyl group, cyclopentyl group, cyclohexyl group, Examples include 2-ethylhexyl group, n-octyl group, adamantyl group and the like.

R ^L03 represents a monovalent hydrocarbon group which may have a hetero atom such as an oxygen atom having 1 to 18 carbon atoms, preferably 1 to 10 carbon atoms, and is a linear, branched or cyclic alkyl group, Examples in which a part of these hydrogen atoms are substituted with a hydroxyl group, an alkoxy group, an oxo group, an amino group, an alkylamino group, and the like can be given. Specifically, a linear, branched or cyclic alkyl group Examples thereof include those similar to R ^L01 and R ^L02 above, and examples of the substituted alkyl group include the following groups.

R ^L01 and R ^L02 , R ^L01 and R ^L03 , R ^L02 and R ^L03 may be bonded to each other to form a ring together with the carbon atom or oxygen atom to which they are bonded. R ^L01 , R ^L02 and R ^L03 involved in the formation each represent a linear or branched alkylene group having 1 to 18 carbon atoms, preferably 1 to 10 carbon atoms.

In the formula (L2), specific examples of the tertiary alkyl group of R ^L04 include tert-butyl group, tert-amyl group, 1,1-diethylpropyl group, 2-cyclopentylpropan-2-yl group, and 2-cyclohexyl. Propan-2-yl group, 2- (bicyclo [2.2.1] heptan-2-yl) propan-2-yl group, 2- (adamantan-1-yl) propan-2-yl group, 1-ethyl Cyclopentyl group, 1-butylcyclopentyl group, 1-ethylcyclohexyl group, 1-butylcyclohexyl group, 1-ethyl-2-cyclopentenyl group, 1-ethyl-2-cyclohexenyl group, 2-methyl-2-adamantyl group, Examples thereof include a 2-ethyl-2-adamantyl group. Specific examples of the trialkylsilyl group include trimethylsilyl group, triethylsilyl group, dimethyl-tert-butylsilyl group and the like. Specific examples of the oxoalkyl group include 3-oxocyclohexyl group, 4-methyl-2 Examples thereof include -oxooxan-4-yl group and 5-methyl-2-oxooxolan-5-yl group.

In the formula (L3), specific examples of the linear, branched or cyclic alkyl group having 1 to 10 carbon atoms which may be substituted in R ^L05 include a methyl group, an ethyl group, a propyl group, an isopropyl group, Straight chain such as n-butyl group, sec-butyl group, tert-butyl group, tert-amyl group, n-pentyl group, n-hexyl group, cyclopentyl group, cyclohexyl group, bicyclo [2.2.1] heptyl group , Branched or cyclic alkyl groups, some of these hydrogen atoms are hydroxyl, alkoxy, carboxy, alkoxycarbonyl, oxo, amino, alkylamino, cyano, mercapto, alkylthio, sulfo Examples thereof include those substituted with a group or the like, or those wherein a part of these methylene groups is substituted with an oxygen atom or a sulfur atom. Specific examples of the optionally substituted aryl group having 6 to 20 carbon atoms include a phenyl group, a methylphenyl group, a naphthyl group, an anthryl group, a phenanthryl group, and a pyrenyl group.

Specific examples of the linear, branched, or cyclic alkyl group having 1 to 10 carbon atoms that may be substituted or an aryl group having 6 to 20 carbon atoms that may be substituted in R ^L06 in formula (L4) Examples thereof include those similar to R ^L05 .

In R ^{L07 to} R ^L16 , specific examples of the monovalent hydrocarbon group having 1 to 15 carbon atoms include methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, tert- Butyl group, tert-amyl group, n-pentyl group, n-hexyl group, n-octyl group, n-nonyl group, n-decyl group, cyclopentyl group, cyclohexyl group, cyclopentylmethyl group, cyclopentylethyl group, cyclopentylbutyl group A linear, branched or cyclic alkyl group such as a cyclohexylmethyl group, a cyclohexylethyl group, and a cyclohexylbutyl group, and some of these hydrogen atoms are a hydroxyl group, an alkoxy group, a carboxy group, an alkoxycarbonyl group, an oxo group, an amino group, Group, alkylamino group, cyano group, mercapto group, alkylthio group, sulfo group, etc. Or the like can be exemplified those.

R ^{L07 to} R ^L16 may be bonded to each other to form a ring together with the carbon atoms to which they are bonded (for example, R ^L07 and R ^L08 , R ^L07 and R ^L09 , R ^L08 and R ^L10 , R ^L09 and R ^L10 , R ^L11 and R ^L12 , R ^L13 and R ^L14, etc.), in which case the group involved in ring formation represents a divalent hydrocarbon group such as an alkylene group having 1 to 15 carbon atoms, specifically Can be exemplified by those obtained by removing one hydrogen atom from those exemplified above for the monovalent hydrocarbon group. R ^{L07 to} R ^L16 may be bonded to each other adjacent to each other to form a double bond (for example, R ^L07 and R ^L09 , R ^L09 and R ^L15 , R ^L13 and R ^L15 etc.).

Of the acid labile groups represented by the formula (L1), specific examples of the linear or branched ones include the following groups.

  Among the acid labile groups represented by the above formula (L1), specific examples of cyclic groups include tetrahydrofuran-2-yl group, 2-methyltetrahydrofuran-2-yl group, tetrahydropyran-2-yl group, 2 -A methyltetrahydropyran-2-yl group etc. can be illustrated.

  Specific examples of the acid labile group of the above formula (L2) include tert-butoxycarbonyl group, tert-butoxycarbonylmethyl group, tert-amyloxycarbonyl group, tert-amyloxycarbonylmethyl group, 1,1-diethyl. Propyloxycarbonyl group, 1,1-diethylpropyloxycarbonylmethyl group, 1-ethylcyclopentyloxycarbonyl group, 1-ethylcyclopentyloxycarbonylmethyl group, 1-ethyl-2-cyclopentenyloxycarbonyl group, 1-ethyl-2 Examples include -cyclopentenyloxycarbonylmethyl group, 1-ethoxyethoxycarbonylmethyl group, 2-tetrahydropyranyloxycarbonylmethyl group, 2-tetrahydrofuranyloxycarbonylmethyl group and the like.

  Specific examples of the acid labile group of the above formula (L3) include 1-methylcyclopentyl, 1-ethylcyclopentyl, 1-n-propylcyclopentyl, 1-isopropylcyclopentyl, 1-n-butylcyclopentyl, 1-sec- Butylcyclopentyl, 1-cyclohexylcyclopentyl, 1- (4-methoxy-n-butyl) cyclopentyl, 1- (bicyclo [2.2.1] heptan-2-yl) cyclopentyl, 1- (7-oxabicyclo [2. 2.1] heptan-2-yl) cyclopentyl, 1-methylcyclohexyl, 1-ethylcyclohexyl, 3-methyl-1-cyclopenten-3-yl, 3-ethyl-1-cyclopenten-3-yl, 3-methyl- 1-cyclohexen-3-yl, 3-ethyl-1-cyclohexen-3-yl, etc. It can be exemplified.

（式中、Ｒ^L41はそれぞれ独立に炭素数１〜１０の直鎖状、分岐状又は環状のアルキル基等の１価炭化水素基を示す。破線は結合位置及び結合方向を示す。） As the acid labile group of the above formula (L4), groups represented by the following formulas (L4-1) to (L4-4) are particularly preferable.

(In the formula, R ^L41 each independently represents a monovalent hydrocarbon group such as a linear, branched or cyclic alkyl group having 1 to 10 carbon atoms. The broken lines indicate the bonding position and bonding direction.)

In the above formulas (L4-1) to (L4-4), specific examples of the monovalent hydrocarbon group of R ^L41 include methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, sec-butyl group. Tert-butyl group, tert-amyl group, n-pentyl group, n-hexyl group, cyclopentyl group, cyclohexyl group and the like.

  In the general formulas (L4-1) to (L4-4), enantiomers and diastereomers may exist, but the general formulas (L4-1) to (L4-4) may exist. ) Represents all of these stereoisomers. These stereoisomers may be used alone or as a mixture.

（式中、Ｒ^L41は前述と同様である。） For example, the general formula (L4-3) represents one or a mixture of two selected from the groups represented by the following general formulas (L4-3-1) and (L4-3-2). To do.

(In the formula, R ^L41 is the same as described above.)

（式中、Ｒ^L41は前述と同様である。） The general formula (L4-4) represents one or a mixture of two or more selected from groups represented by the following general formulas (L4-4-1) to (L4-4-4). And

(In the formula, R ^L41 is the same as described above.)

  The general formulas (L4-1) to (L4-4), (L4-3-1), (L4-3-2), and formulas (L4-4-1) to (L4-4-4) are Their enantiomers and enantiomeric mixtures are also shown representatively.

  In addition, the coupling | bonding of Formula (L4-1)-(L4-4), (L4-3-1), (L4-3-2), and Formula (L4-4-1)-(L4-4-4) High reactivity in the acid-catalyzed elimination reaction is realized by the fact that each direction is on the exo side with respect to the bicyclo [2.2.1] heptane ring (see JP 2000-336121 A). In the production of a monomer having a tertiary exo-alkyl group having a bicyclo [2.2.1] heptane skeleton as a substituent, the following general formulas (L4-1-endo) to (L4-4-endo) are used. In some cases, a monomer substituted with the indicated endo-alkyl group may be included, but in order to achieve good reactivity, the exo ratio is preferably 50% or more, and the exo ratio is 80% or more. More preferably.

（式中、Ｒ^L41は前述と同様である。）

(In the formula, R ^L41 is the same as described above.)

Specific examples of the acid labile group of the above formula (L4) include the following groups.

Further, tertiary alkyl groups having 4 to 20 carbon atoms, trialkylsilyl groups each having 1 to 6 carbon atoms, and oxoalkyl groups having 4 to 20 carbon atoms are specifically exemplified as ^RL04 . The thing similar to a thing etc. can be illustrated.

（式中、Ｒ¹は前述と同様である。） Specific examples of the repeating units of the above formulas (2a) to (2g) include the following, but are not limited thereto.

(Wherein R ¹ is the same as described above.)

  The polymer compound (P1) of the present invention can exhibit sufficient performance only by the combination of the repeating units represented by the general formulas (1a) and (2a) to (2g). The following general formulas (3a) to (3e), (4a) to (4e), (5a) to (5c), (6a) to (6c) It is also possible to configure by combining one or two or more repeating units represented by:

（式中、Ｒ¹¹は炭素数１〜１５の１価炭化水素基又はフッ素化１価炭化水素基である。Ｒ¹²は密着性基である。Ｒ¹³は酸不安定基である。Ｒ¹⁴は単結合又は炭素数１〜１５の２価の有機基である。Ｒ¹⁵及びＲ¹⁶は水素原子、メチル基又はトリフルオロメチル基である。）

(In the formula, R ¹¹ is a monovalent hydrocarbon group having 1 to 15 carbon atoms or a fluorinated monovalent hydrocarbon group. R ¹² is an adhesive group. R ¹³ is an acid labile group. R ¹⁴ Is a single bond or a divalent organic group having 1 to 15 carbon atoms, and R ¹⁵ and R ¹⁶ are a hydrogen atom, a methyl group or a trifluoromethyl group.)

As the monovalent hydrocarbon group having 1 to 15 carbon atoms or the fluorinated monovalent hydrocarbon group of R ¹¹ , those similar to R ^5a and R ^8a are used.

The adhesive group for R ¹² is variously selected, and is particularly preferably a group exemplified by the following formula.

（上記式中、破線は結合手を示す。）

(In the above formula, a broken line indicates a bond.)

As the acid labile group for R ¹³ , those described for R ^5a can be used.

As the divalent organic group having 1 to 15 carbon atoms of R ¹⁴ , those of the type in which one hydrogen atom in the aforementioned monovalent hydrocarbon group is extracted (for example, methylene group or ethylene group) are used. In addition, groups exemplified by the following formula can also be used.

（上記式中、破線は結合手を示す。）

(In the above formula, a broken line indicates a bond.)

[Synthesis of polymer compounds]
When synthesizing the polymer compound (P1), radical polymerization using an initiator such as 2,2′-azobisisobutyronitrile (hereinafter abbreviated as AIBN), ionic polymerization (anionic polymerization) using alkyllithium, etc. These general polymerization techniques can be used, and these polymerizations can be carried out in accordance with conventional methods. Of these, the synthesis of the polymer compound (P1) is preferably carried out by radical polymerization. In this case, the polymerization conditions are governed by the type and addition amount of the initiator, temperature, pressure, concentration, solvent, additive and the like.

  The radical polymerization initiator is not particularly limited, but examples include AIBN, 2,2′-azobis (4-methoxy-2,4-dimethylvaleronitrile), 2,2′-azobis (2,4- Dimethylvaleronitrile), 2,2′-azobis (2,4,4-trimethylpentane), azo compounds such as 2,2′-azobis (isobutyric acid) dimethyl, tert-butyl peroxypivalate, lauroyl peroxide Peroxide compounds such as benzoyl peroxide and tert-butyl peroxylaurate, water-soluble polymerization initiators such as potassium persulfate, and peroxides such as potassium persulfate and hydrogen peroxide and sodium sulfite. Examples thereof include a redox initiator composed of a combination of such reducing agents. The amount of the polymerization initiator used can be appropriately changed according to the type and polymerization conditions, but is usually 0.001 to 10 mol%, particularly 0.01 to 6 mol%, based on the total amount of monomers to be polymerized. Is adopted.

  When synthesizing the polymer compound (P1), a known chain transfer agent such as dodecyl mercaptan or 2-mercaptoethanol may be used in combination for adjusting the molecular weight. In that case, it is preferable that the addition amount of these chain transfer agents is 0.01-10 mol% with respect to the total number of moles of the monomer to polymerize.

  When synthesizing the polymer compound (P1), the general formulas (1a), (2a) to (2g), (3a) to (3e), (4a) to (4e), (5a) to (5c), ( A polymerizable monomer corresponding to the repeating unit represented by 6a) to (6c) is mixed, and polymerization is performed by adding the above-described initiator or chain transfer agent.

In the polymer compound (P1),
The total number of moles of the monomer corresponding to the unit of the general formula (1a) is U1,
U2 represents the total number of moles of monomers corresponding to the units of the general formulas (2a) to (2g),
The total number of moles of monomers corresponding to the units of the general formulas (3a) to (3e), (4a) to (4e), (5a) to (5c), (6a) to (6c) is U3,
U1 + U2 + U3 = U (= 100 mol%)
If
0 <U1 / U <1, more preferably 0.1 ≦ U1 / U ≦ 0.8, still more preferably 0.1 ≦ U1 / U ≦ 0.7,
0 ≦ U2 / U <1, more preferably 0.1 ≦ U2 / U ≦ 0.8, still more preferably 0.2 ≦ U2 / U ≦ 0.8,
0 ≦ U3 / U <1, more preferably 0 ≦ U3 / U ≦ 0.4, still more preferably 0 ≦ U3 / U ≦ 0.2
It is.

  When performing the polymerization, a solvent may be used as necessary. As the polymerization solvent, those that do not inhibit the polymerization reaction are preferable, and typical examples include esters such as ethyl acetate, n-butyl acetate, and γ-butyrolactone, ketones such as acetone, methyl ethyl ketone, and methyl isobutyl ketone, toluene, Aliphatic or aromatic hydrocarbons such as xylene and cyclohexane, alcohols such as isopropyl alcohol and ethylene glycol monomethyl ether, and ether solvents such as diethyl ether, dioxane and tetrahydrofuran can be used. These solvents may be used alone or in combination of two or more. The amount of the polymerization solvent used can be appropriately changed according to the polymerization conditions such as the target degree of polymerization (molecular weight), the amount of initiator added, and the polymerization temperature. Usually, the concentration of the monomer to be polymerized is 0.1. A solvent is added so that it may be -95 mass%, especially 5-90 mass%.

  The reaction temperature of the polymerization reaction is appropriately changed depending on the kind of the polymerization initiator or the boiling point of the solvent, but is usually preferably 20 to 200 ° C, particularly preferably 50 to 140 ° C. The reaction vessel used for such a polymerization reaction is not particularly limited.

  Any known method can be used as a method for removing the organic solvent or water as a medium from the polymer solution or dispersion thus obtained. For example, reprecipitation filtration or reduced pressure can be used. There are methods such as heating distilling at

  In the case of the polymer compound (P1), if the weight average molecular weight (Mw) is too small, dissolution in water tends to occur. However, if the weight average molecular weight is too large, the alkali solubility decreases and causes of coating defects during spin coating. Is likely to be. From that viewpoint, the polystyrene-reduced weight average molecular weight by gel permeation chromatography (GPC) is 1,000 to 500,000, preferably 2,000 to 30,000.

（式中、Ｒ^5a及びＲ¹³は前記と同様である。Ｘは塩素原子、臭素原子、ヨウ素原子である。） In the polymer compound (P1), R ^5a in the general formulas (2a), (2b), and (2f) and R ^{13 in} the general formulas (3c) and (4c) can be introduced by a post-protection reaction. It is. That is, advance R ^5a and R ¹³ by polymerizing a monomer of the hydrogen after the synthesis of the polymer compound, a part or all of the hydroxyl groups of the polymer obtained by the protection reaction after as shown in the following formula R ^5a and R Replace with ¹³ .

(In the formula, R ^5a and R ¹³ are the same as described above. X is a chlorine atom, a bromine atom, or an iodine atom.)

In the post-protection reaction, after 1 to 2 equivalents of the base is reacted with the polymer compound with respect to the target value of the substitution rate of the hydroxyl group, the base is reacted with 1 to 2 equivalents of R ^5a -X or R ¹³ -X. Thus, the desired post-protected polymer compound can be obtained.

  The solvent used in the post-protection reaction is selected from hydrocarbons such as benzene and toluene, ethers such as dibutyl ether, diethylene glycol diethyl ether, diethylene glycol dimethyl ether, tetrahydrofuran, and 1,4-dioxane alone or 2 A mixture of seeds or more can be used. Examples of the base include, but are not limited to, sodium hydride, n-butyllithium, lithium diisopropylamide, triethylamine, pyridine and the like.

  When adding the high molecular compound (P1) used by this invention to a resist material, the total mass of the high molecular compound (P1) to add is 0.1-50 with respect to 100 mass parts of base resin (B) of a resist material. Part by mass, preferably 0.5 to 10 parts by mass is preferred. If the addition amount is 0.1 parts by mass or more, the receding contact angle between the resist film surface and water is sufficiently improved, and if it is 50 parts by mass or less, the dissolution rate of the resist film in the alkaline developer is small and formed. The height of the fine pattern is sufficiently maintained.

[Composition of resist material]
In the resist material of the present invention, the polymer compound (P1) is used by blending with the base resin (B) described later. Since the polymer compound (P1) contains a plurality of fluorine atoms, the entire polymer functions as a surfactant, and the polymer compound (P1) is localized in the upper layer of the resist film during spin coating. As a result, the water repellency and water slidability of the resist surface can be improved, and the leaching of the water-soluble compound in the resist material can be suppressed. Further, as described above, since the polymer compound (P1) includes a structure that is susceptible to alkaline hydrolysis, it is possible to increase the hydrophilicity of the resist film surface after development, and as a result, the occurrence of blob defects is suppressed. be able to.

  The resist material of the present invention has a lactone ring-derived skeleton and / or a hydroxyl group-containing skeleton and / or a maleic anhydride-derived skeleton as the base resin, and is soluble in an alkaline developer by the action of an acid. A polymer compound (base resin). The polymer compound constituting the base resin (B) includes (meth) acrylic acid ester polymer, (α-trifluoromethyl) acrylic acid ester-maleic anhydride copolymer, cycloolefin-maleic anhydride copolymer. , Polynorbornene, polymer compound obtained by ring-opening metathesis reaction of cycloolefin, polymer compound obtained by hydrogenating polymer obtained by ring-opening metathesis reaction of cycloolefin, hydroxystyrene and (meth) acrylic acid ester Derivatives, styrene, vinyl naphthalene, vinyl anthracene, vinyl pyrene, hydroxy vinyl naphthalene, hydroxy vinyl anthracene, indene, hydroxy indene, acenaphthylene, polymer compounds copolymerized with norbornadiene, and novolac can be selected. That. Specific examples thereof are described in paragraphs [0072] to [0120] of JP-A-2008-111103. In addition, the high molecular compound which comprises the said base resin (B) is not restricted to 1 type, 2 or more types can be added. The performance of the resist material can be adjusted by using a plurality of types of polymer compounds.

（式中、Ｒ^1Aは水素原子、フッ素原子、メチル基又はトリフルオロメチル基を示す。ＸＡは酸不安定基を示す。ＸＢ、ＸＣはそれぞれ独立に単結合又は炭素数１〜４の直鎖状又は分岐状のアルキレン基等の２価の炭化水素基を示す。ＹＡはラクトン構造を有する置換基を示す。ＺＡは水素原子、又は炭素数１〜１５のフルオロアルキル基又は炭素数１〜１５のフルオロアルコール含有置換基を示す。ｋ^1Aは１〜３の整数を示す。） Moreover, the base resin (B) used in the resist material of the present invention can contain any one or more repeating units represented by the following general formulas (2A) to (2D).

(In the formula, R ^1A represents a hydrogen atom, a fluorine atom, a methyl group or a trifluoromethyl group. XA represents an acid labile group. XB and XC are each independently a single bond or a straight chain having 1 to 4 carbon atoms. A divalent hydrocarbon group such as a linear or branched alkylene group, YA represents a substituent having a lactone structure, ZA represents a hydrogen atom, a fluoroalkyl group having 1 to 15 carbon atoms or a C1 to 15 carbon atoms; And k ^1A represents an integer of 1 to 3.)

The polymer containing the repeating unit represented by the general formula (2A) is decomposed by the action of an acid to generate a carboxylic acid to give a polymer that becomes alkali-soluble. The acid labile group XA can be variously used, and specific examples thereof include those similar to those exemplified in the description of R ^{5a in} the general formulas (2a) to (2g).

  Specific examples of the repeating unit represented by the general formula (2A) include the following, but are not limited thereto.

Specific examples of the repeating unit represented by the general formula (2B) include the following.

Specific examples of the repeating unit represented by the general formula (2C) include the following.

Specific examples of the repeating unit represented by the general formula (2D) include the following.

  Since the resist material of the present invention functions as a chemically amplified positive resist material, it may contain (C) a compound that generates an acid (photo acid generator) upon exposure to high energy rays. As the component of the photoacid generator, any compound can be used as long as it generates an acid upon irradiation with high energy rays, but suitable photoacid generators include sulfonium salts, iodonium salts, sulfonyldiazomethane, N-sulfonyloxyimide. Oxime-O-sulfonate type acid generators and the like, and specific examples thereof are described in paragraphs [0123] to [0138] of JP-A-2008-111103.

（式中、Ｒ⁴⁰⁵、Ｒ⁴⁰⁶、Ｒ⁴⁰⁷はそれぞれ独立に水素原子、又はヘテロ原子を含んでもよい炭素数１〜２０の直鎖状、分岐状又は環状の１価の炭化水素基、特にアルキル基又はアルコキシ基を示す。Ｒ⁴⁰⁸はヘテロ原子を含んでもよい炭素数７〜３０の直鎖状、分岐状又は環状の１価の炭化水素基を示す。） Especially as a photo-acid generator, what is shown by the following general formula (C) -1 is used suitably.

(Wherein R ⁴⁰⁵ , R ⁴⁰⁶ and R ⁴⁰⁷ are each independently a hydrogen atom or a C 1-20 linear, branched or cyclic monovalent hydrocarbon group which may contain a hetero atom, particularly an alkyl group. R ⁴⁰⁸ represents a C7-30 linear, branched or cyclic monovalent hydrocarbon group which may contain a hetero atom.

Specific examples of the hydrocarbon group which may contain a hetero atom of R ⁴⁰⁵ , R ⁴⁰⁶ and R ⁴⁰⁷ include a methyl group, an ethyl group, a propyl group, an isopropyl group, an n-butyl group, a sec-butyl group, and a tert-butyl group. Tert-amyl group, n-pentyl group, n-hexyl group, cyclopentyl group, cyclohexyl group, ethylcyclopentyl group, butylcyclopentyl group, ethylcyclohexyl group, butylcyclohexyl group, adamantyl group, ethyladamantyl group, butyladamantyl group, and Between any carbon-carbon bonds of these groups, —O—, —S—, —SO—, —SO ₂ —, —NH—, —C (═O) —, —C (═O) O—, -C (= O) NH- group hetero atom group is inserted such that any hydrogen atom replaced -OH, -NH _2, -CHO, the functional group such as -CO ₂ H It can be exemplified. R ⁴⁰⁸ represents a linear, branched or cyclic monovalent hydrocarbon group having 7 to 30 carbon atoms which may contain a hetero atom, and specific examples thereof include, but are not limited to, the following. It is not a thing.

Specific examples of the acid generator represented by (C) -1 include the following, but are not limited thereto.

  When two or more photoacid generators are used in combination, and one of the photoacid generators is an onium salt that generates a so-called weak acid, a function of acid diffusion control can be provided. That is, when a photoacid generator that generates a strong acid (for example, fluorine-substituted sulfonic acid) and an onium salt that generates a weak acid (for example, a sulfonic acid or carboxylic acid that is not fluorine-substituted) are mixed and used, When a strong acid generated from a photoacid generator upon irradiation collides with an onium salt having an unreacted weak acid anion, a weak acid is released by salt exchange to produce an onium salt having a strong acid anion. In this process, the strong acid is exchanged with a weak acid having a lower catalytic ability, so that the acid is apparently deactivated and the acid diffusion can be controlled.

  Here, when the photoacid generator that generates strong acid is an onium salt, the strong acid generated by irradiation with high energy rays can be exchanged for weak acid as described above, but the weak acid generated by irradiation with high energy rays is not yet. The salt exchange cannot be performed by colliding with an onium salt that generates a strong acid of reaction. These are due to the phenomenon that the onium cation is more likely to form an ion pair with the anion of the strong acid.

  The addition amount of a photo-acid generator is 0.1-30 mass parts with respect to 100 mass parts of base resin (B) in a resist material, Preferably it is 0.1-20 mass parts. When the photoacid generator is 30 parts by mass or less, the transmittance of the resist film is sufficiently large, and there is little possibility that the resolution performance is deteriorated. The photoacid generators can be used alone or in combination of two or more. Further, a photoacid generator having a low transmittance at the exposure wavelength can be used, and the transmittance in the resist film can be controlled by the addition amount.

  The resist material of the present invention further contains any one or more of (D) an organic solvent, (E) a basic compound, (F) a dissolution controller, (G) a surfactant, and (H) an acetylene alcohol derivative. can do.

  The organic solvent (D) used in the resist material of the present invention is an organic solvent that can dissolve the polymer compound (P1), the resist base resin (B), the acid generator (C), other additives, and the like. Any of these may be used, and a specific example is described in paragraph [0144] of JP-A-2008-111103. The organic solvents can be used alone or in admixture of two or more. The amount of the organic solvent used is preferably 200 to 10,000 parts by mass, particularly 400 to 7,000 parts by mass with respect to 100 parts by mass of the base resin (B) in the resist material. In the present invention, diethylene glycol dimethyl ether, 1-ethoxy-2-propanol, propylene glycol monomethyl ether acetate and mixed solvents thereof, which are most excellent in solubility of the acid generator in the resist component, are preferably used.

  The (E) basic compound used in the resist material of the present invention is preferably a nitrogen-containing organic compound, and can be used by blending one or more nitrogen-containing organic compounds. As the nitrogen-containing organic compound, a compound capable of suppressing the diffusion rate when the acid generated from the acid generator diffuses into the resist film is suitable. Incorporation of nitrogen-containing organic compounds suppresses the acid diffusion rate in the resist film, improves resolution, suppresses sensitivity changes after exposure, reduces substrate and environmental dependence, and reduces exposure margins and patterns. Profiles and the like can be improved.

  Such nitrogen-containing organic compounds include primary, secondary and tertiary aliphatic amines, hybrid amines, aromatic amines, heterocyclic amines, nitrogen-containing compounds having a carboxy group, sulfonyl Nitrogen-containing compounds having a group, nitrogen-containing compounds having a hydroxyl group, nitrogen-containing compounds having a hydroxyphenyl group, amides, imides, carbamates and the like. Specific examples thereof include those described in JP-A-2008-111103. It is described in paragraphs [0149] to [0163]. The amount of the basic compound used is preferably 0.001 to 2 parts by mass, particularly 0.01 to 1 part by mass with respect to 100 parts by mass of the base resin (B). If the amount is 0.001 part by mass or more, a sufficient blending effect is obtained, and if it is 2 parts by mass or less, the sensitivity is less likely to decrease.

  Particularly preferred basic compounds are tertiary amines, specifically, tri-n-butylamine, tri-n-pentylamine, tri-n-hexylamine, tri-n-octylamine, N, N- Dimethylaniline, triethanolamine, triisopropanolamine, tris (2-methoxymethoxyethyl) amine, tris (2-methoxyethoxyethyl) amine, tris {2- (2-methoxyethoxy) ethyl} amine, tris {2- ( 2-methoxyethoxymethoxy) ethyl} amine, tris {2- (1-methoxyethoxy) ethyl} amine, tris {2- (1-ethoxyethoxy) ethyl} amine, tris {2- (1-ethoxypropoxy) ethyl} Amine, tris [2- {2- (2-hydroxyethoxy) ethoxy} ethyl] a 4,7,13,16,21,24-hexaoxa-1,10-diazabicyclo [8.8.8] hexacosane, 4,7,13,18-tetraoxa-1,10-diazabicyclo [8.5. 5] Eicosane, 1,4,10,13-tetraoxa-7,16-diazabicyclooctadecane, 1-aza-12-crown-4, 1-aza-15-crown-5, 1-aza-18-crown -6, tris (2-formyloxyethyl) amine, tris (2-acetoxyethyl) amine, tris (2-propionyloxyethyl) amine, tris (2-butyryloxyethyl) amine, tris (2-isobutyryl) Oxyethyl) amine, tris (2-valeryloxyethyl) amine, tris (2-pivaloyloxyethyl) amine, N, N-bis (2 Acetoxyethyl) 2- (acetoxyacetoxy) ethylamine, tris (2-methoxycarbonyloxyethyl) amine, tris (2-tert-butoxycarbonyloxyethyl) amine, tris [2- (2-oxopropoxy) ethyl] amine, tris [2- (methoxycarbonylmethyl) oxyethyl] amine, tris [2- (tert-butoxycarbonylmethyloxy) ethyl] amine, tris [2- (cyclohexyloxycarbonylmethyloxy) ethyl] amine, tris (2-methoxycarbonylethyl) ) Amine, tris (2-ethoxycarbonylethyl) amine, tris (2-benzoyloxyethyl) amine, tris [2- (4-methoxybenzoyloxy) ethyl] amine, N, N-bis (2-hydroxyethyl) 2- (methoxycarbonyl) ethylamine, N, N-bis (2-acetoxyethyl) 2- (methoxycarbonyl) ethylamine, N, N-bis (2-hydroxyethyl) 2- (ethoxycarbonyl) ethylamine, N, N- Bis (2-acetoxyethyl) 2- (ethoxycarbonyl) ethylamine, N, N-bis (2-hydroxyethyl) 2- (2-methoxyethoxycarbonyl) ethylamine, N, N-bis (2-acetoxyethyl) 2- (2-methoxyethoxycarbonyl) ethylamine, N, N-bis (2-hydroxyethyl) 2- (2-hydroxyethoxycarbonyl) ethylamine, N, N-bis (2-acetoxyethyl) 2- (2-acetoxyethoxycarbonyl) ) Ethylamine, N, N-bis (2-hydroxyethyl) 2- [ Methoxycarbonyl) methoxycarbonyl] ethylamine, N, N-bis (2-acetoxyethyl) 2-[(methoxycarbonyl) methoxycarbonyl] ethylamine, N, N-bis (2-hydroxyethyl) 2- (2-oxopropoxycarbonyl) ) Ethylamine, N, N-bis (2-acetoxyethyl) 2- (2-oxopropoxycarbonyl) ethylamine, N, N-bis (2-hydroxyethyl) 2- (tetrahydrofurfuryloxycarbonyl) ethylamine, N, N -Bis (2-acetoxyethyl) 2- (tetrahydrofurfuryloxycarbonyl) ethylamine, N, N-bis (2-hydroxyethyl) 2-[(2-oxotetrahydrofuran-3-yl) oxycarbonyl] ethylamine, N, N-bis (2-acetoxy Til) 2-[(2-oxotetrahydrofuran-3-yl) oxycarbonyl] ethylamine, N, N-bis (2-hydroxyethyl) 2- (4-hydroxybutoxycarbonyl) ethylamine, N, N-bis (2- Formyloxyethyl) 2- (4-formyloxybutoxycarbonyl) ethylamine, N, N-bis (2-formyloxyethyl) 2- (2-formyloxyethoxycarbonyl) ethylamine, N, N-bis (2-methoxyethyl) ) 2- (methoxycarbonyl) ethylamine, N- (2-hydroxyethyl) bis [2- (methoxycarbonyl) ethyl] amine, N- (2-acetoxyethyl) bis [2- (methoxycarbonyl) ethyl] amine, N -(2-hydroxyethyl) bis [2- (ethoxycarbonyl) ethyl] Amine, N- (2-acetoxyethyl) bis [2- (ethoxycarbonyl) ethyl] amine, N- (3-hydroxy-1-propyl) bis [2- (methoxycarbonyl) ethyl] amine, N- (3- Acetoxy-1-propyl) bis [2- (methoxycarbonyl) ethyl] amine, N- (2-methoxyethyl) bis [2- (methoxycarbonyl) ethyl] amine, N-butylbis [2- (methoxycarbonyl) ethyl] Amine, N-butylbis [2- (2-methoxyethoxycarbonyl) ethyl] amine, N-methylbis (2-acetoxyethyl) amine, N-ethylbis (2-acetoxyethyl) amine, N-methylbis (2-pivaloyl) Oxyethyl) amine, N-ethylbis [2- (methoxycarbonyloxy) ethyl] amine, N- Tilbis [2- (tert-butoxycarbonyloxy) ethyl] amine, tris (methoxycarbonylmethyl) amine, tris (ethoxycarbonylmethyl) amine, N-butylbis (methoxycarbonylmethyl) amine, N-hexylbis (methoxycarbonylmethyl) amine , Β- (diethylamino) -δ-valerolactone is exemplified.

  Furthermore, 1- [2- (methoxymethoxy) ethyl] pyrrolidine, 1- [2- (methoxymethoxy) ethyl] piperidine, 4- [2- (methoxymethoxy) ethyl] morpholine, 1- [2- (methoxymethoxy) Ethyl] imidazole, 1- [2- (methoxymethoxy) ethyl] benzimidazole, 1- [2- (methoxymethoxy) ethyl] -2-phenylbenzimidazole, 1- [2-[(2-methoxyethoxy) methoxy] Ethyl] pyrrolidine, 1- [2-[(2-methoxyethoxy) methoxy] ethyl] piperidine, 4- [2-[(2-methoxyethoxy) methoxy] ethyl] morpholine, 1- [2-[(2-methoxy Ethoxy) methoxy] ethyl] imidazole, 1- [2-[(2-methoxyethoxy) methoxy] ethyl] benzi Dazole, 1- [2-[(2-methoxyethoxy) methoxy] ethyl] -2-phenylbenzimidazole, 1- [2- [2- (2-methoxyethoxy) ethoxy] ethyl] pyrrolidine, 1- [2- [2- (2-methoxyethoxy) ethoxy] ethyl] piperidine, 4- [2- [2- (2-methoxyethoxy) ethoxy] ethyl] morpholine, 1- [2- [2- (2-methoxyethoxy) ethoxy ] Ethyl] imidazole, 1- [2- [2- (2-methoxyethoxy) ethoxy] ethyl] benzimidazole, 1- [2- [2- (2-methoxyethoxy) ethoxy] ethyl] -2-phenylbenzimidazole 1- [2- [2- (2-butoxyethoxy) ethoxy] ethyl] pyrrolidine, 1- [2- [2- (2-butoxyethoxy) eth Ci] ethyl] piperidine, 4- [2- [2- (2-butoxyethoxy) ethoxy] ethyl] morpholine, 1- [2- [2- (2-butoxyethoxy) ethoxy] ethyl] imidazole, 1- [2 -[2- (2-butoxyethoxy) ethoxy] ethyl] benzimidazole, 1- [2- [2- (2-butoxyethoxy) ethoxy] ethyl] -2-phenylbenzimidazole, 1- [2- [2- [2- (2-methoxyethoxy) ethoxy] ethoxy] ethyl] pyrrolidine, 1- [2- [2- [2- (2-methoxyethoxy) ethoxy] ethoxy] ethyl] piperidine, 4- [2- [2- [2- (2-methoxyethoxy) ethoxy] ethoxy] ethyl] morpholine, 1- [2- [2- [2- (2-methoxyethoxy) ethoxy] ethoxy] ethyl ] Imidazole, 1- [2- [2- [2- (2-methoxyethoxy) ethoxy] ethoxy] ethyl] benzimidazole, 1- [2- [2- [2- (2-methoxyethoxy) ethoxy] ethoxy] Ethyl] -2-phenylbenzimidazole, 4- [2- {2- [2- (2-butoxyethoxy) ethoxy] ethoxy} ethyl] morpholine, 2- (1-pyrrolidinyl) ethyl acetate, 2-piperidinoethyl acetate, acetic acid 2-morpholinoethyl, 2- (1-imidazolyl) ethyl acetate, 2- (1-benzimidazolyl) ethyl acetate, 2- (2-phenyl-1-benzimidazolyl) ethyl acetate, 2-methoxyethyl morpholinoacetate, 2- 2- (1-pyrrolidinyl) ethyl methoxyacetate, 2-piperidinoethyl 2-methoxyacetate, 2-methoxyacetate 2- Rufolinoethyl, 2- (1-imidazolyl) ethyl 2-methoxyacetate, 2- (1-benzimidazolyl) ethyl 2-methoxyacetate, 2- (2-phenyl-1-benzimidazolyl) ethyl 2-methoxyacetate, 2- ( 2-methoxyethoxy) acetic acid 2- (1-pyrrolidinyl) ethyl, 2- (2-methoxyethoxy) acetic acid 2-piperidinoethyl, 2- (2-methoxyethoxy) acetic acid 2-morpholinoethyl, 2- (2-methoxyethoxy) 2- (1-imidazolyl) ethyl acetate, 2- (2-methoxyethoxy) acetic acid 2- (1-benzimidazolyl) ethyl, 2- (2-methoxyethoxy) acetic acid 2- (2-phenyl-1-benzimidazolyl) Ethyl, 2- [2- (2-methoxyethoxy) ethoxy] acetic acid 2- (1-pyrrolidinyl) ethyl, 2- [2 (2-Methoxyethoxy) ethoxy] 2-piperidinoethyl acetate, 2- [2- (2-methoxyethoxy) ethoxy] acetate 2-morpholinoethyl, 2- [2- (2-methoxyethoxy) ethoxy] acetate 2- (1 -Imidazolyl) ethyl, 2- [2- (2-methoxyethoxy) ethoxy] acetic acid 2- (1-benzimidazolyl) ethyl, 2- [2- (2-methoxyethoxy) ethoxy] acetic acid 2- (2-phenyl- 1-benzimidazolyl) ethyl, 2-morpholinoethyl butyrate, 2-morpholinoethyl hexanoate, 2-morpholinoethyl octoate, 2-morpholinoethyl decanoate, 2-morpholinoethyl laurate, 2-morpholinoethyl myristic acid, palmitic acid 2-morpholinoethyl, 2-morpholinoethyl stearate, 2-mol behenate Pholinoethyl, 2-morpholinoethyl cholic acid, 2-morpholinoethyl tris (O-acetyl) cholic acid, 2-morpholinoethyl tris (O-formyl) cholic acid, 2-morpholinoethyl dehydrocholic acid, 2-morpholino cyclopentanecarboxylic acid Ethyl, 2-morpholinoethyl cyclohexanecarboxylic acid, 2- (1-pyrrolidinyl) ethyl 7-oxanorbornane-2-carboxylate, 2-piperidinoethyl 7-oxanorbornane-2-carboxylic acid, 7-oxanorbornane-2-carboxylic acid 2-morpholinoethyl, 2- (1-imidazolyl) ethyl 7-oxanorbornane-2-carboxylate, 2- (1-benzimidazolyl) ethyl 7-oxanorbornane-2-carboxylate, 7-oxanorbornane-2-carboxylic acid Acid 2- (2-Fe 1-benzimidazolyl) ethyl, 2-morpholinoethyl adamantanecarboxylate, 2- (1-pyrrolidinyl) ethyl formate, 2-piperidinoethyl propionate, 2-morpholinoethyl acetoxyacetate, 2- (1-pyrrolidinyl) ethyl methoxyacetate 2- (1-pyrrolidinyl) ethyl benzoate, 2-piperidinoethyl benzoate, 2-morpholinoethyl benzoate, 2- (1-imidazolyl) ethyl benzoate, 2- (1-benzimidazolyl) ethyl benzoate, benzoic acid 2- (2-phenyl-1-benzimidazolyl) ethyl, 2- (1-pyrrolidinyl) ethyl 4-methoxybenzoate, 2-piperidinoethyl 4-methoxybenzoate, 2-morpholinoethyl 4-methoxybenzoate, 4-methoxy 2- (1-imidazolyl) ethyl benzoate, 2- (1-Benzimidazolyl) ethyl 4-methoxybenzoate, 2- (2-phenyl-1-benzimidazolyl) ethyl 4-methoxybenzoate, 2- (1-pyrrolidinyl) ethyl 4-phenylbenzoate, 4-phenyl 2-piperidinoethyl benzoate, 2-morpholinoethyl 4-phenylbenzoate, 2- (1-imidazolyl) ethyl 4-phenylbenzoate, 2- (1-benzimidazolyl) ethyl 4-phenylbenzoate, 4-phenylbenzoic acid 2- (2-phenyl-1-benzimidazolyl) ethyl, 2- (1-pyrrolidinyl) ethyl 1-naphthalenecarboxylate, 2-piperidinoethyl 1-naphthalenecarboxylate, 2-morpholinoethyl 1-naphthalenecarboxylate, 1-naphthalene 2- (1-imidazolyl) ethyl carboxylate, 1-naphthalene 2- (1-benzimidazolyl) ethyl rubonate, 2- (2-phenyl-1-benzimidazolyl) ethyl 1-naphthalenecarboxylate, 2- (1-pyrrolidinyl) ethyl 2-naphthalenecarboxylate, 2-naphthalenecarboxylic acid 2-piperidinoethyl, 2-morpholinoethyl 2-naphthalenecarboxylate, 2- (1-imidazolyl) ethyl 2-naphthalenecarboxylate, 2- (1-benzimidazolyl) ethyl 2-naphthalenecarboxylate, 2-naphthalenecarboxylic acid 2- (2-Phenyl-1-benzimidazolyl) ethyl, 4- [2- (methoxycarbonyloxy) ethyl] morpholine, 1- [2- (t-butoxycarbonyloxy) ethyl] piperidine, 4- [2- (2- Methoxyethoxycarbonyloxy) ethyl] morpholine, 3- (1-pi Lysinyl) methyl propionate, methyl 3-piperidinopropionate, methyl 3-morpholinopropionate, methyl 3- (thiomorpholino) propionate, methyl 2-methyl-3- (1-pyrrolidinyl) propionate, 3-morpholino Ethyl propionate, methoxycarbonylmethyl 3-piperidinopropionate, 2-hydroxyethyl 3- (1-pyrrolidinyl) propionate, 2-acetoxyethyl 3-morpholinopropionate, 2- (1-pyrrolidinyl) propionate 2- Oxotetrahydrofuran-3-yl, tetrahydrofurfuryl 3-morpholinopropionate, glycidyl 3-piperidinopropionate, 2-methoxyethyl 3-morpholinopropionate, 2- (2-methoxy-2-propyridinyl) propionate Ethoxy) , 3-morpholinopropionate butyl, 3-piperidinopropionate cyclohexyl, α- (1-pyrrolidinyl) methyl-γ-butyrolactone, β-piperidino-γ-butyrolactone, β-morpholino-δ-valerolactone, 1- Examples include methyl pyrrolidinyl acetate, methyl piperidinoacetate, methyl morpholinoacetate, methyl thiomorpholinoacetate, and ethyl 1-pyrrolidinyl acetate.

  The (F) dissolution controller used in the resist material of the present invention is a compound in which a phenolic hydroxyl group of a compound having two or more phenolic hydroxyl groups in the molecule is protected with an acid labile group, or a carboxy group in the molecule. A compound in which the carboxy group of the compound is protected with an acid labile group is used, and specific examples thereof are described in paragraphs [0155] to [0178] of JP-A-2008-122932.

  In addition to the above components, a surfactant (G) that is conventionally used for improving the coating property can be added to the resist material of the present invention. Specific examples of the (G) surfactant are described in paragraph [0166] of JP-A-2008-111103.

  (H) Acetylene alcohol derivative may be added as an optional component to the resist material of the present invention as necessary. Specific examples of (H) acetylene alcohol derivatives are described in paragraphs [0180] to [0181] of JP-A-2008-122932.

  If necessary, (I) a fluorine-containing alcohol may be added to the resist material of the present invention. In the resist material of the present invention, when the basic compound (E) is used, the fluorine-containing ester in the repeating unit (1a) in the polymer compound (P1) is gradually hydrolyzed during the preservation of the resist material. In addition, there is a possibility that the water repellency performance and the water sliding performance at the time of immersion exposure may be lowered. In such a case, when (I) fluorine-containing alcohol is added to the resist material, (E) hydrolysis by the basic compound can be suppressed, and storage stability can be improved.

  (I) Specific examples of the fluorine-containing alcohol include 2,2,2-trifluoroethanol, 2,2,3,3-tetrafluoro-1-propanol, 1,3-difluoro-2-propanol, 1,1 , 1,3,3,3-hexafluoro-2-propanol, 1,1,1,3,3,3-hexafluoro-2-trifluoromethyl-2-propanol, 2,2,3,4,4 , 4-hexafluoro-1-butanol, 2,2,2,2 ′, 2 ′, 2′-hexafluorocumyl alcohol, 2,2,3,3,4,4,5,5-octafluoro- Although 1-pentanol etc. can be illustrated, it is not limited to these.

  (I) The usage-amount of fluorine-containing alcohol is 0.01-10 mass parts with respect to 1 mass part of (E) basic compounds, Especially 0.01-5 mass parts is suitable.

[Pattern formation method]
Next, a pattern forming method using the resist material of the present invention will be described. In the pattern forming method of the present invention, a known lithography technique can be used, but it includes at least a step of forming a resist film on a substrate, a step of exposing high energy rays, and a step of developing using a developer. Is preferred.

  When a resist film is formed on a substrate such as a silicon wafer, for example, a resist material is applied so as to have a film thickness of 0.01 to 2.0 μm by a technique such as spin coating, and this is applied on a hot plate for 60 to 60 μm. A resist film is formed by prebaking at 150 ° C. for 1 to 10 minutes, preferably 80 to 140 ° C. for 1 to 5 minutes. In addition, when the resist solution is applied in a state where the substrate surface is preliminarily wetted with a resist solvent or a solution mixed with the resist solvent at the time of spin coating, the dispensing amount of the resist material can be reduced (see JP-A-9-246173).

In the exposure step, a mask for forming a target pattern is placed over the resist film, and a high energy beam such as deep ultraviolet light, excimer laser, or X-ray, or an electron beam is applied in an exposure amount of 1 to 200 mJ / cm ² , preferably Irradiation is performed so as to be 10 to 100 mJ / cm ² . The high energy ray used at this time is preferably in the wavelength range of 180 to 250 nm.

  In addition to dry exposure in air or in a nitrogen atmosphere, exposure may be performed by an immersion method in which the projection lens and the resist film are immersed in a liquid such as water. In addition to water, a liquid having a refractive index of 1 or more such as alkane and having a high transparency for the exposure wavelength is used. Further, exposure in a vacuum such as EB or EUV may be used.

  The resist film formed using the resist material of the present invention has a good barrier performance against water and suppresses the elution of the resist material into water, so that no protective film is required in immersion lithography, and the protective film is formed. The cost required for such as In addition, since the resist film has a high receding contact angle with respect to water, it is difficult for droplets to remain on the resist film surface after immersion exposure, thereby reducing pattern formation defects induced by droplets remaining on the film surface. be able to.

  On the other hand, it is also possible to perform immersion exposure by providing a protective film on the resist film. The resist protective film includes a solvent peeling type and a developer soluble type, and a developer soluble type that can be peeled off at the time of development like the resist material of the present invention is preferred. Specific examples of the resist protective film include acidic units such as 1,1,1,3,3,3-hexafluoro-2-hydroxy-2-propyl group, carboxyl group, and sulfo group, and are insoluble in water. A polymer compound dissolved in an alkali developer is used as a base resin, and an alcohol solvent having 4 or more carbon atoms, an ether solvent having 8 to 12 carbon atoms, and a material dissolved in a mixed solvent thereof are preferably used. These are not limited.

  As a method of forming a resist protective film, a topcoat solution is spin-coated on a pre-baked resist film, and is applied on a hot plate at 50 to 150 ° C. for 1 to 10 minutes, preferably 70 to 140 ° C. for 1 to 5 minutes. Pre-bake to form a protective film. The film thickness is preferably in the range of 10 to 500 nm. As in the case of the resist material, the amount of dispensed protective film material can be reduced by applying the resist protective film after the resist film surface is wetted with a solvent in advance during spin coating of the resist protective film.

  After exposure through a photomask using the above-mentioned high-energy rays, post exposure on a hot plate at 60 to 150 ° C. for 1 to 5 minutes, preferably 80 to 140 ° C. for 1 to 3 minutes Bake (PEB).

  When using a resist protective film, if PEB is performed with water remaining on the protective film, water may pass through the protective film in the PEB. As a result, it is necessary to completely remove the water on the protective film before PEB in order to avoid that the acid in the resist is sucked out and the pattern cannot be formed. Examples of the method include a spin dry method, a method of purging a protective film surface with dry air or nitrogen, a shape of a water recovery nozzle on the stage, and optimization of a water recovery process.

  After exposure, an aqueous alkali solution such as tetramethylammonium hydroxide (TMAH) is used, and development is performed by a conventional method such as a dip method, a paddle method, or a spray method. Form a pattern. The concentration of the developer is preferably 0.1 to 5% by mass, more preferably 2 to 3% by mass, and particularly a 2.38% by mass aqueous tetramethylammonium hydroxide solution is preferably used. The development time is preferably 10 to 300 seconds, more preferably 0.5 to 2 minutes.

When the polymer compound (P1) of the present invention is used as an additive for a mask blank resist material, a polymer solution (P1) is added to a base resin to prepare a resist solution, and then SiO ₂ , Cr, CrO, CrN, A resist is applied on a mask blank substrate such as MoSi. A three-layer structure may be formed by forming an SOG film and an organic underlayer film between a resist and a blank substrate.

  Novolac and hydroxystyrene are mainly used as the base resin for the mask blank resist. Those in which an alkali-soluble hydroxyl group in these resins is substituted with an acid labile group are used as a positive type, and those obtained by adding a crosslinking agent are used as a negative type. Specifically, a polymer compound obtained by copolymerizing hydroxystyrene and a (meth) acryl derivative, styrene, vinylnaphthalene, vinylanthracene, vinylpyrene, hydroxyvinylnaphthalene, hydroxyvinylanthracene, indene, hydroxyindene, acenaphthylene, norbornadiene is preferable. Used.

  After forming the resist film, exposure is performed with an electron beam in a vacuum using an electron beam drawing machine. After exposure, post-exposure baking (PEB) is performed, and development is performed with an alkali developer for 10 to 300 seconds to form a pattern.

  EXAMPLES Hereinafter, although a synthesis example, an Example, and a comparative example are shown and this invention is demonstrated concretely, this invention is not restrict | limited to the following Example. In the following examples, Me represents a methyl group, Et represents an ethyl group, and t-Bu represents a tertiary butyl group.

２−ヒドロキシ−３，３，３−トリフルオロ−２−トリフルオロメチルプロピオン酸メチル１１３ｇ、トリエチルアミン７５．９ｇ、アセトニトリル２５０ｍｌの溶液にメタクリル酸クロリド６７．９ｇ、アセトニトリル３．３ｇの混合物を２０℃以下にて滴下した。室温にて５時間撹拌した後、氷冷下水２０ｇを滴下して反応を停止した。通常の後処理操作を行い、減圧蒸留により目的物１２５ｇを得た（収率８５％）。
沸点：６３℃／１．６ｋＰａ。
ＩＲ（Ｄ−ＡＴＲ）：ν＝１７７８、１７５９、１６３８、１４５８、１４４０、１２６１、１２３７、１１２３、１０４７、１００２、９５３ｃｍ^-1。
¹Ｈ−ＮＭＲ（６００ＭＨｚ ｉｎ ＤＭＳＯ−ｄ₆）：δ＝１．９４（３Ｈ，ｓ）、３．９３（３Ｈ，ｓ）、６．０６（１Ｈ，ｓ）、６．２６（１Ｈ，ｓ）ｐｐｍ。
¹⁹Ｆ−ＮＭＲ（５６５ＭＨｚ ｉｎ ＤＭＳＯ−ｄ₆ トリフルオロ酢酸標準）：δ＝−７１．２８（６Ｆ，ｓ）ｐｐｍ。 The fluorine-containing monomer of the present invention was synthesized according to the following formulation.
[Synthesis Example 1-1] Synthesis of Monomer 1

A mixture of 113 g of methyl 2-hydroxy-3,3,3-trifluoro-2-trifluoromethylpropionate, 75.9 g of triethylamine and 250 ml of acetonitrile was mixed with a mixture of 67.9 g of methacrylic acid chloride and 3.3 g of acetonitrile at 20 ° C. or lower. It was dripped at. After stirring at room temperature for 5 hours, 20 g of water was added dropwise under ice cooling to stop the reaction. A usual post-treatment operation was performed, and 125 g of the desired product was obtained by distillation under reduced pressure (yield 85%).
Boiling point: 63 ° C./1.6 kPa.
IR (D-ATR): ν = 1778, 1759, 1638, 1458, 1440, 1261, 1237, 1123, 1047, 1002, 953 cm ⁻¹ .
¹ H-NMR (600 MHz in DMSO-d ₆ ): δ = 1.94 (3H, s), 3.93 (3H, s), 6.06 (1H, s), 6.26 (1H, s) ppm.
¹⁹ F-NMR (565 MHz in DMSO-d ₆ trifluoroacetic acid standard): δ = −71.28 (6F, s) ppm.

[Synthesis Example 1-2] Synthesis of Monomer 2 Monomer 2 was obtained in the same manner as in [Synthesis Example 1-1] except that acrylic acid chloride was used instead of methacrylic acid chloride (yield 87%).

[Synthesis Example 1-3] Synthesis of Monomer 3 Monomer 3 was obtained in the same manner as in [Synthesis Example 1-1] except that α-trifluoromethylacrylic acid chloride was used instead of methacrylic acid chloride (yield). 73%).

[Synthesis Example 1-4] Synthesis of Monomer 4

Synthesis Example 1-4-1 Synthesis of Alcohol 1 A mixture of 148 g of isobutyl alcohol, 226 g of methyl 2-hydroxy-3,3,3-trifluoro-2-trifluoromethylpropionate, 800 ml of benzene, and 5 g of sodium methoxide. The mixture was heated to reflux for 10 hours while gradually distilling off the methanol produced by the reaction. After cooling, 200 g of 5% by mass hydrochloric acid was added dropwise under ice cooling to stop the reaction. Normal post-treatment operation was performed, and 171 g of the desired product was obtained by atmospheric distillation (yield 64%).
Boiling point: 150 ° C./normal pressure.
IR (D-ATR): ν = 3469, 2973, 2883, 1755, 1473, 1401, 1382, 1328, 1240, 1163, 1012, 979, 939 cm ⁻¹ .
¹ H-NMR (600 MHz in DMSO-d ₆ ): δ = 0.89 (6H, d), 1.95 (1H, sept), 4.14 (2H, d), 9.11 (1H, s) ppm.
¹⁹ F-NMR (565 MHz in DMSO-d ₆ trifluoroacetic acid standard): δ = −71.28 (6F, s) ppm.

[Synthesis Example 1-4-2] Synthesis of Monomer 4 [Synthesis Example 1-1] except that alcohol 1 was used instead of methyl 2-hydroxy-3,3,3-trifluoro-2-trifluoromethylpropionate The monomer 4 was obtained in the same manner as in the above (yield 83%).
Boiling point: 75-76 ° C./600 Pa.
IR (D-ATR): v = 2969, 2937, 2881, 1774, 1759, 1638, 1472, 1439, 1398, 1381, 1259, 1235, 1123, 1041, 999, 952 cm ⁻¹ .
¹ H-NMR (600 MHz in DMSO-d ₆ ): δ = 0.86 (6H, d), 1.92 (1H, sept), 1.93 (3H, s), 4.14 (2H, d) 6.06 (1H, s), 6.26 (1H, s) ppm.
¹⁹ F-NMR (565 MHz in DMSO-d ₆ trifluoroacetic acid standard): δ = −71.23 (6F, s) ppm.

[Synthesis Example 1-5] Synthesis of Monomer 5

[Synthesis Example 1-5-1] Synthesis of Alcohol 2 Alcohol 2 was obtained in the same manner as in [Synthesis Example 1-4-1] except that isoamyl alcohol was used instead of isobutyl alcohol (yield 82%). .
Boiling point: 115-116 ° C./19 kPa.
IR (D-ATR): ν = 3466, 2965, 2877, 1752, 1467, 1372, 1390, 1324, 1220, 1157, 1010, 977, 929 cm ⁻¹ .
¹ H-NMR (600 MHz in DMSO-d ₆ ): δ = 0.87 (6H, d), 1.52 (2H, q), 1.64 (1H, sept), 4.36 (2H, t) 9.10 (1H, s) ppm.
¹⁹ F-NMR (565 MHz in DMSO-d ₆ trifluoroacetic acid standard): δ = −75.06 (6F, s) ppm.

[Synthesis Example 1-5-2] Synthesis of Monomer 5 [Synthesis Example 1-1] except that alcohol 2 was used instead of methyl 2-hydroxy-3,3,3-trifluoro-2-trifluoromethylpropionate The monomer 5 was obtained in the same manner as in the above (yield 84%).
Boiling point: 67-68 ° C / 253Pa.
IR (D-ATR): ν = 2963, 2875, 1773, 1757, 1638, 1464, 1389, 1256, 1230, 1167, 1118, 1036, 995, 951 cm ⁻¹ .
¹ H-NMR (600 MHz in DMSO-d ₆ ): δ = 0.86 (6H, d), 1.49 (1H, q), 1.59 (1H, sept), 1.93 (3H, s) 4.36 (2H, t), 6.06 (1 H, s), 6.25 (1 H, s) ppm.
¹⁹ F-NMR (565 MHz in DMSO-d ₆ trifluoroacetic acid standard): δ = −71.23 (6F, s) ppm.

[Synthesis Example 1-6] Synthesis of Monomer 6

[Synthesis Example 1-6-1] Synthesis of Alcohol 3 2,2,3,3,4,4,5,5-octafluoropentanol 100 g, 2-hydroxy-3,3,3-trifluoro-2- 487 g of methyl trifluoromethylpropionate was dissolved in 50 g of benzene and subjected to azeotropic dehydration. After cooling to room temperature, 9.0 g of potassium tert-butoxide was added, and the mixture was heated to reflux for 30 hours while gradually distilling off the methanol produced by the reaction. After cooling, 60 g of 5 mass% hydrochloric acid and 440 g of water were added dropwise at room temperature or lower to stop the reaction. A usual post-treatment operation was performed, and 104 g of the desired product was obtained by distillation under reduced pressure (yield 58%).
Boiling point: 133 ° C./20 kPa.
IR (D-ATR): ν = 3511, 1778, 1402, 1362, 1326, 1233, 1164, 1135, 1086, 1054, 1030, 979, 960, 902, 864, 804, 749, 749, 668 ⁻¹ .
¹ H-NMR (600 MHz in DMSO-d ₆ ): δ = 5.20 (2H, t), 7.05 (1H, tt), 9.58 (1H, s) ppm.
¹⁹ F-NMR (565 MHz in DMSO-d ₆ trifluoroacetic acid standard): δ = −139.96 (1F), −139.87 (1F), −131.06 (2F), −126.02 (2F) , -120.46 (2F), -75.20 (6F) ppm.
GC-MS (CI: Methane): (m / z) ⁺ = 69, 95, 113, 145, 167, 193, 213, 233, 259, 287, 309, 341, 359, 379, 407, 427 (M + H) ⁺ , 467, 489.

[Synthesis Example 1-6-2] Synthesis of Monomer 6 [Synthesis Example 1-1] except that alcohol 3 was used instead of methyl 2-hydroxy-3,3,3-trifluoro-2-trifluoromethylpropionate The monomer 6 was obtained in the same manner as in the above (yield 79%).
Boiling point: 78 ° C./270 Pa.
IR (D-ATR): ν = 1791, 1759, 1457, 1443, 1405, 1385, 1259, 1240, 1175, 1123, 1086, 1066, 1008, 993, 971, 957, 904, 852, 805, 748, 731 , 703, 656 cm ⁻¹ .
¹ H-NMR (600 MHz in DMSO-d ₆ ): δ = 1.93 (3H, s), 5.22 (2H, t), 6.09 (1H, m), 6.27 (1H, m) 7.00 (1H, tt) ppm.
¹⁹ F-NMR (565 MHz in DMSO-d ₆ trifluoroacetic acid standard): δ = -140.00 (1F), −139.91 (1F), −131.08 (2F), −125.94 (2F) -12.42 (2F), -71.66 (6F) ppm.
GC-MS (CI: Methane): (m / z) ⁺ = 69, 89, 109, 145, 175, 213, 233, 263, 299, 328, 349, 371, 391, 427, 451, 475, 495 ( M + H) ⁺ , 522, 545.

[Synthesis Example 1-7] Synthesis of Monomer 7 Monomer 7 was obtained in the same manner as in [Synthesis Example 1-1] except that methacryloyloxyacetic acid chloride was used instead of methacrylic acid chloride (yield 87%).
Boiling point: 68-69 ° C./13 Pa.
IR (D-ATR): ν = 1809, 1777, 1733, 1639, 1455, 1440, 1420, 1387, 1263, 1239, 1170, 1121, 1048, 1004, 949 cm ⁻¹ .
¹ H-NMR (600 MHz in DMSO-d ₆ ): δ = 1.90 (3H, s), 3.91 (3H, s), 5.12 (2H, s), 5.81 (1H, d-like) ), 6.13 (1H, d-like) ppm.
¹⁹ F-NMR (565 MHz in DMSO-d ₆ trifluoroacetic acid standard): δ = −71.44 (6F, d-like) ppm.

[Synthesis Example 1-8] Synthesis of Monomer 8 Methacryloyloxyacetic acid chloride was substituted for methacrylic acid chloride, and alcohol 1 was substituted for methyl 2-hydroxy-3,3,3-trifluoro-2-trifluoromethylpropionate. Monomer 8 was obtained in the same manner as in [Synthesis Example 1-1] except that it was used (yield 86%).

[Synthesis Example 1-9] Synthesis of Monomer 9 Methacryloyloxyacetic acid chloride was substituted for methacrylic acid chloride, and alcohol 2 was substituted for methyl 2-hydroxy-3,3,3-trifluoro-2-trifluoromethylpropionate. Monomer 9 was obtained in the same manner as in [Synthesis Example 1-1] except that it was used (yield 84%).
Boiling point: 78-79 ° C./20 Pa.
IR (D-ATR): ν = 2964, 2935, 2875, 1813, 1773, 1737, 1639, 1466, 1419, 1387, 1261, 1236, 1170, 1122, 1046, 999, 946 cm ⁻¹ .
¹ H-NMR (600 MHz in DMSO-d ₆ ): δ = 0.88 (6H, d), 1.51 (2H, q), 1.61 (1H, sept), 4.36 (2H, t) 5.81 (1H, s), 6.12 (1H, s) ppm.

[Synthesis Example 1-10] Synthesis of Monomer 10 Methacryloyloxyacetic acid chloride was used instead of methacrylic acid chloride, and alcohol 3 was used instead of methyl 2-hydroxy-3,3,3-trifluoro-2-trifluoromethylpropionate. Monomer 10 was obtained in the same manner as in [Synthesis Example 1-1] except that it was used (yield 77%).
Boiling point: 78 ° C / 9Pa
IR (D-ATR): ν = 1792, 1737, 1639, 1455, 1420, 1405, 1388, 1256, 1242, 1174, 1124, 1064, 1011, 973, 954, 903, 812, 759, 748, 692, 653 cm ^-1 .
¹ H-NMR (600 MHz in DMSO-d ₆ ): δ = 1.90 (3H, s), 5.13 (2H, s), 5.24 (2H, t), 5.81 (1H, m) 6.13 (1H, m), 7.05 (1H, tt) ppm.
¹⁹ F-NMR (565 MHz in DMSO-d ₆ trifluoroacetic acid standard): δ = −139.96 (1F), −139.87 (1F), −131.03 (2F), −125.94 (2F) -12.42 (2F), -71.46 (6F) ppm.

[Synthesis Example 1-11] Synthesis of Monomer 11

[Synthesis Example 1-11-1] Synthesis of alcohol 4 3,3,4,4,5,5,6 instead of 2,2,3,3,4,4,5,5-octafluoropentanol Alcohol 4 was obtained in the same manner as in [Synthesis Example 1-6-1] except that 6,6-nonafluorohexanol was used (yield 79%).
Boiling point: 133-134 ° C./19.4 kPa.
IR (D-ATR): [nu] = 3481, 1762, 1470, 1429, 1328, 1225, 1164, 1135, 1076, 1019, 980 cm < ^-1 >.
¹ H-NMR (600 MHz in DMSO-d ₆ ): δ = 2.72 (2H, dt), 4.63 (2H, t), 9.18 (1H, s) ppm.
¹⁹ F-NMR (565 MHz in DMSO-d ₆ trifluoroacetic acid standard): δ = −127.22 (2F), −125.75 (2F), −114.84 (2F), −82.27 (3F) -75.38 (6F) ppm.

Synthesis Example 1-11-2 Synthesis of Monomer 11 Methacryloyloxyacetic acid chloride was used instead of methacrylic acid chloride, and alcohol was used instead of methyl 2-hydroxy-3,3,3-trifluoro-2-trifluoromethylpropionate. 4 was obtained in the same manner as in [Synthesis Example 1-1] except that pyridine was used instead of triethylamine (yield 81%).
Boiling point: 80-81 ° C / 16Pa
IR (D-ATR): ν = 1780, 1734, 1639, 1456, 1421, 1386, 1236, 1172, 1134, 1053, 1004, 950, 879 cm ⁻¹ .
¹ H-NMR (600 MHz in DMSO-d ₆ ): δ = 1.90 (3H, s), 2.74 (2H, dt), 4.61 (2H, t), 5.09 (2H, s) 5.80 (1H, s), 6.11 (1H, s) ppm.
¹⁹ F-NMR (565 MHz in DMSO-d ₆ trifluoroacetic acid standard): δ = −127.22 (2F), −125.74 (2F), −114.82 (2F), −82.15 (3F) -71.60 (6F) ppm.

Structural formulas of monomers 1 to 11 obtained in the above synthesis examples are shown below.

The polymer compound of the present invention was synthesized according to the formulation shown below. In the examples, “GPC” refers to gel permeation chromatography, and the weight average molecular weight (Mw) and number average molecular weight (Mn) of the obtained polymer compound are measured by GPC as polystyrene conversion values. did.
Synthesis Example 2-1 Synthesis of Polymer 1 In a flask under nitrogen atmosphere, 9.63 g of monomer 7 and 5.37 g of methacrylic acid 4,4,4-trifluoro-3-hydroxy-2-methyl-3-tri A monomer solution was prepared by adding fluoromethylbutan-2-yl, 0.53 g of 2,2′-azobis (isobutyrate) dimethyl, and 15.0 g of methyl ethyl ketone, and the solution temperature was set to 20 to 25 ° C. . 7.50 g of methyl ethyl ketone was put into another flask under a nitrogen atmosphere and heated to 80 ° C. with stirring, and then the monomer solution was added dropwise over 4 hours. After completion of the dropping, stirring was continued for 2 hours while maintaining the temperature of the polymerization solution at 80 ° C., and after completion of the aging, the solution was cooled to room temperature. The polymerization solution was transferred to an eggplant flask and concentrated by an evaporator. Next, toluene was added to the flask, and finally adjusted to be a 40% by mass solution of toluene / methyl ethyl ketone (mixing ratio 9/1), and then dropped into 150 g of hexane. The precipitated copolymer was separated by filtration and washed with 90 g of hexane to separate a white solid. The white solid was vacuum dried at 50 ° C. for 20 hours to obtain a white powder solid polymer compound represented by the following formula polymer 1. The yield was 12.7 g, and the yield was 80%.

[Synthesis Examples 2-2 to 17, Comparative Synthesis Examples 1-1 to 3] Synthesis of Polymers 2 to 20 The same as [Synthesis Example 2-1] except that the types and blending ratios of the monomers were changed. The polymer compounds shown in Table 1 were produced by the procedure. Table 2 shows the structure of each unit in Table 1. The introduction ratio is a molar ratio.

[Examples 1-1 to 17, Comparative Examples 1-1 to 4] Resist evaluation 5 g of the following resist polymer, 0.25 g of the above polymers 1 to 20, 0.25 g of PAG1, and 0.05 g of Quencher 1 were used. It was dissolved in 75 g of propylene glycol monoethyl ether acetate (PGMEA) and filtered through a 0.2 μm size polypropylene filter to prepare a resist solution. Moreover, the resist solution which does not add the said polymers 1-20 as Comparative Example 1-4 was also prepared.

  After forming an antireflection film ARC-29A (Nissan Chemical Industry Co., Ltd.) on a silicon substrate (film thickness: 87 nm), the resist solution is applied thereon and baked at 120 ° C. for 60 seconds to obtain a film thickness. A 150 nm resist film was prepared.

A wafer on which a resist film is formed by the above method is kept horizontal, 50 μL of pure water is dropped on the wafer to form polka dots, and then a tilt contact angle meter Drop Master 500 (manufactured by Kyowa Interface Science Co., Ltd.) is used. The wafer was tilted gradually, and the wafer angle (falling angle) and receding contact angle at which the polka dots began to fall were determined. The results are shown in Table 3.
In Table 3, the lower the falling angle, the easier the water on the resist film flows, and the higher the receding contact angle, the less likely the droplets remain even during high-speed scanning exposure. It can be confirmed that the resist film formed from the resist solution containing the polymer compound of the present invention can remarkably improve the receding contact angle as compared with the resist film not containing it, and does not deteriorate the sliding angle. It was.

Further, the wafer on which the resist film was formed by the above method was irradiated with energy of 50 mJ / cm ^{2 with} an open frame using an ArF scanner S305B (manufactured by Nikon Corporation). Next, a perfectly circular Teflon (registered trademark) ring having an inner diameter of 10 cm was placed on the resist film, 10 ml of pure water was carefully poured therein, and the resist film and pure water were contacted at room temperature for 60 seconds. Then, pure water was collect | recovered and the anion component density | concentration of the photo-acid generator (PAG1) in pure water was measured with LC-MS analyzer (Agilent Technology Co., Ltd. product). The results are shown in Table 3.
As is apparent from Table 3, the resist film formed from the resist solution containing the polymer compound according to the present invention was found to have an effect of suppressing elution of the photoacid generator component from the resist film into water.

Next, the wafer on which the resist film is formed by the above method is exposed with an ArF scanner S307E (Nikon Corporation, NA 0.85, σ 0.93, 4/5 annular illumination, 6% halftone phase shift mask). Then, rinsing was performed for 5 minutes while applying pure water, post-exposure baking (PEB) was performed at 110 ° C. for 60 seconds, and development was performed with a 2.38 mass% TMAH aqueous solution for 60 seconds. The obtained wafer was cleaved, and the pattern shape and sensitivity of 75 nm line and space were compared. The results are shown in Table 3.
From the results shown in Table 3, when pure water rinsing was performed after exposure, the pattern shape became a T-top shape in the resist solution not containing the polymer compound of the present invention. On the other hand, it was found that when a resist solution containing the polymer compound of the present invention was used, a rectangular shape was obtained.

[Examples 2-1 to 3 and Comparative Examples 2-1 to 3] Evaluation of development defects The resist solution used in the patterning experiment was microfiltered with a high density polyethylene filter of 0.02 μm size. A resist solution is applied on an antireflection film ARC-29A (Nissan Chemical Industry Co., Ltd., film thickness: 87 nm) prepared on an 8-inch Si substrate, and baked at 120 ° C. for 60 seconds to have a film thickness of 150 nm. A resist film was prepared. A checkered flag that alternately exposes the exposed and unexposed portions of the open frame with an area of 20 mm square on the entire surface of the wafer using an ArF scanner S307E (manufactured by Nikon Corporation, NA: 0.85, σ: 0.93, Cr mask). After exposure, post-exposure bake (PEB) was performed, and development was performed for 60 seconds with a 2.38 mass% TMAH aqueous solution. The number of blob defects in the unexposed portion of the checker flag was measured at a pixel size of 0.125 μm using a defect inspection device WinWin-50-1200 (manufactured by Tokyo Seimitsu Co., Ltd.). The results are shown in Table 4.

  From the results of Table 4, it can be seen that many development defects are observed after immersion exposure in the resist solution not containing the polymer compound of the present invention. This defect could not be improved by adding polymer 18 or polymer 20, but the defect could be suppressed by using a resist solution containing the polymer compound of the present invention (polymers 1, 5, 10).

Claims (13)

(A) a polymer compound having a repeating unit represented by the following general formula (1a), (B) as a base resin, a lactone ring-derived skeleton and / or a hydroxyl group-containing skeleton and / or a maleic anhydride-derived skeleton And a high molecular compound that is soluble in an alkali developer by the action of an acid, (C) a compound that generates an acid upon exposure to high energy rays, and (D) an organic solvent.

(In the formula, R ¹ represents a hydrogen atom, a fluorine atom, a methyl group, or a trifluoromethyl group. R ² is a linear or branched chain having 1 to 15 carbon atoms which may have a halogen atom or an oxygen atom. Or a cyclic monovalent hydrocarbon group, A represents a linear, branched or cyclic divalent hydrocarbon group having 1 to 6 carbon atoms, and k ¹ is an integer of 0 to 2.) (A) In addition to the repeating unit represented by the general formula (1a) according to claim 1, one or more of the repeating units represented by the following general formulas (2a) to (2g) The polymer compound having (B) the base resin has a lactone ring-derived skeleton and / or a hydroxyl group-containing skeleton and / or a maleic anhydride-derived skeleton, and is highly soluble in an alkaline developer by the action of an acid. 2. The resist material according to claim 1, comprising a molecular compound, (C) a compound that generates an acid upon exposure to high energy rays, and (D) an organic solvent.

(Wherein, R ¹ is the a is the same .R ^4a and R ^4b are hydrogen atoms, or of the straight, a monovalent hydrocarbon group branched or cyclic, R ^4a and R ^4b can be bonded to each other to form a non-aromatic ring having 3 to 8 carbon atoms together with the carbon atom to which they are bonded, R ^5a is a hydrogen atom, or a straight, branched or cyclic group having 1 to 15 carbon atoms. A monovalent hydrocarbon group, a fluorinated monovalent hydrocarbon group, or an acid labile group, and in the case of a monovalent hydrocarbon group, the constituent —CH ₂ — is —O— or —C (═O) —. R ^6a , R ^6b , and R ^6c are each a hydrogen atom or a linear, branched, or cyclic monovalent hydrocarbon group having 1 to 15 carbon atoms, and R ^6a and R ^6b , R ^6a and R ^6c , R ^6b and R ^6c may be bonded to each other to form a non-aromatic ring having 3 to 8 carbon atoms together with the carbon atom to which they are bonded. ^7a is hydrogen, or of the straight, a monovalent hydrocarbon group branched or cyclic .R ^7b is a C1-15 straight, monovalent branched or cyclic hydrocarbon It is a hydrogen group, and R ^7a and R ^7b can be bonded to each other to form a non-aromatic ring having 3 to 8 carbon atoms together with the carbon atom to which they are bonded, and R ^8a is a straight chain having 1 to 15 carbon atoms. A branched or cyclic fluorinated monovalent hydrocarbon group, k ² represents 0 or 1.)   The polymer compound of component (B) is a (meth) acrylic acid ester polymer, (α-trifluoromethyl) acrylic acid ester-maleic anhydride copolymer, cycloolefin-maleic anhydride copolymer, polynorbornene, A polymer compound obtained by ring-opening metathesis reaction of cycloolefin, a polymer compound obtained by hydrogenating a polymer obtained by ring-opening metathesis reaction of cycloolefin, hydroxystyrene and a (meth) acrylate derivative, styrene, 3. The polymer compound according to claim 1, wherein the polymer compound is selected from polymer compounds obtained by copolymerization of vinylnaphthalene, vinylanthracene, vinylpyrene, hydroxyvinylnaphthalene, hydroxyvinylanthracene, indene, hydroxyindene, acenaphthylene, and norbornadiene. of Resist material. The resist material according to claim 1 or 2, wherein the polymer compound of component (B) contains any one or more of repeating units represented by the following general formulas (2A) to (2D).

(In the formula, R ^1A represents a hydrogen atom, a fluorine atom, a methyl group or a trifluoromethyl group. XA represents an acid labile group. XB and XC are each independently a single bond or a straight chain having 1 to 4 carbon atoms. YA represents a substituent having a lactone structure, ZA represents a hydrogen atom, a fluoroalkyl group having 1 to 15 carbon atoms, or a fluoroalcohol having 1 to 15 carbon atoms. Represents a substituent, k ^1A represents an integer of ¹ to 3)   The addition amount of the polymer compound (A) containing the repeating unit represented by the general formula (1a) is 0.1 to 50 parts by mass with respect to 100 parts by mass of the polymer compound (B). The resist material according to claim 1.   The resist material according to any one of claims 1 to 5, further comprising (E) a basic compound.   The resist material according to claim 1, further comprising (F) a dissolution control agent.   (1) a step of applying the resist material according to any one of claims 1 to 7 on a substrate; (2) a step of exposing to high energy rays through a photomask after heat treatment; ) A pattern forming method comprising a step of developing using a developer.   (1) a step of applying the resist material according to any one of claims 1 to 7 on the substrate; and (2) after the heat treatment, a liquid is inserted between the projection lens and the wafer, and the photomask is interposed. A pattern forming method comprising: a step of exposing with a high energy beam; and (3) a step of developing using a developer.   (1) a step of applying the resist material according to any one of claims 1 to 7 on a substrate; (2) a step of forming a protective film layer on the photoresist film; and (3) a heat treatment. Thereafter, a pattern forming method comprising a step of inserting a liquid between the projection lens and the wafer and exposing with a high energy beam through a photomask, and (4) developing with a developer.   The pattern forming method according to claim 9 or 10, wherein in the exposure step, the liquid inserted between the projection lens and the substrate is water.   The pattern forming method according to claim 8, wherein a high energy ray having a wavelength of 180 to 250 nm is used as an exposure light source.   (1) A step of applying the resist material according to any one of claims 1 to 7 on a mask blank, (2) a step of exposing to an electron beam in a vacuum after heat treatment, and (3) a developer. The pattern formation method characterized by including the process developed using this.