JP2009251392A - Negative resist composition and pattern forming method - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a negative resist composition less liable to cause a film thickness loss and pattern collapse and a pattern forming method. <P>SOLUTION: The negative resist composition comprises: (A) an alkali-soluble resin; (B) a crosslinking agent which crosslinks an alkali-soluble resin under the action of an acid; (C1) a compound which allows a crosslinking reaction to proceed upon irradiation with actinic rays or radiation; (C2) a photoradical generator; and (D) a compound having a radical polymerizable group. The pattern forming method is also provided. <P>COPYRIGHT: (C)2010,JPO&INPIT

Description

  The present invention relates to a photoresist used in the manufacturing of semiconductor elements such as ICs, liquid crystal display devices, circuit boards such as thermal heads, and other photofabrication lithography processes. In particular, the present invention relates to a negative photoresist composition suitable for exposure with a projection exposure apparatus using a far ultraviolet ray having a wavelength of 200 nm or less as a light source, and a resist pattern forming method thereof.

  In recent years, semiconductor devices have been increasingly densely and highly integrated. Therefore, further fine pattern processing has been required. In order to satisfy this need, the operating wavelength of an exposure apparatus used for photolithography has been increasingly shortened, and now it is considered to use excimer laser light (XeCl, KrF, ArF, etc.) having a short wavelength among far ultraviolet rays. It is becoming.

The resist composition, on the other hand, uses a resin that is insoluble or insoluble in the developer and forms a pattern by solubilizing the exposed area in the developer by exposure to radiation, and is soluble in the developer. There is a “negative type” that forms a pattern by making the exposed part insoluble or insoluble in the developer by exposure to radiation, and the positive resist composition is currently in practical use. It is a thing.
In manufacturing a semiconductor element or the like, there is a demand for forming various patterns such as lines, trenches, holes, and the like. As the pattern becomes finer, higher resolution is required. To achieve this, it is desirable to use a mask that provides high optical contrast. However, in order to use a mask that provides this high optical contrast, a positive resist composition is advantageous when forming a line pattern, and a negative resist composition is advantageous when forming a trench pattern. Accordingly, development of negative resist compositions as well as positive ones is desired in order to meet various pattern formation requirements.

In the case of using 248 nm light of a KrF excimer laser as an exposure source, a resist composition using a polymer in which an acetal group or a ketal group is introduced as a protective group to a hydroxystyrene-based polymer with little light absorption at 248 nm has been proposed. Yes. These are suitable when used for KrF excimer lasers, but when used for ArF excimer lasers, there are problems such as reduced sensitivity due to strong absorption at 193 nm and degradation of resolution. Not suitable for use in
Therefore, development of a negative resist material having less light absorption at 193 nm, good sensitivity and high dry etching resistance is desired, and it is suitable for an exposure method using an ArF excimer laser and has high sensitivity. There is an urgent need to develop a resist that provides good resolution.

Therefore, resists for ArF use are proposed that use (meth) acrylic acid ester-based resins having an aliphatic group with little absorption at 193 nm, and resists into which alicyclic aliphatic groups are introduced to provide etching resistance. ing.
Patent Document 1 discloses an ArF positive resist composition containing a polymer having a naphthol structure in the side chain, and Patent Document 2 contains a polymer having a naphthol structure in the side chain and a urea-based crosslinking agent. EB negative resist compositions are known.
For ArF negative resists, for example, in Patent Documents 3 to 4, a urea-based resin is copolymerized with a repeating unit having an aliphatic group and a repeating unit having a fluorine alcohol alkali-soluble group or a carboxylic acid alkali-soluble group as an alkali-soluble group. Although a negative resist composition containing a cross-linking agent is used, it does not satisfy various performances such as resolution pattern thickness and pattern collapse prevention.
JP 2007-146142 A Japanese Patent Laid-Open No. 2004-117876 JP 2006-317803 A JP 2003-177535 A

  An object of the present invention is to solve the problem of the technology for improving the performance of microphotofabrication using far-ultraviolet light, particularly an ArF excimer laser having a wavelength of 193 nm. More specifically, the resist film is difficult to reduce. Another object of the present invention is to provide a negative resist composition that hardly resists pattern collapse and a pattern forming method.

As a result of intensive studies on the constituent materials in the chemically amplified resist, the present inventors have found that the above object can be achieved by using a specific material, and have reached the present invention.
That is, the above object is achieved by the following configuration.

(1)
(A) an alkali-soluble resin,
(B) a crosslinking agent that crosslinks the alkali-soluble resin by the action of an acid,
(C1) a compound that causes a crosslinking reaction to proceed by irradiation with actinic rays or radiation,
(C2) a photo radical generator,
(D) a compound having a radical polymerizable group,
A negative resist composition comprising:

(2)
(A) The alkali-soluble resin of the component is an alkali-soluble group, an organic group containing a fluorine-substituted alcohol structure, an organic group containing a carboxylic acid structure, an organic group containing a sulfonamide structure, an organic group containing a furfuryl alcohol structure, a carbamate structure An organic group containing a tautomeric alcohol structure, an organic group containing a thiol structure, an organic group containing a ketone oxime structure, an organic group containing a dicarbonylmethylene structure, an organic group containing an N-hydroxysuccinimide structure, The negative resist composition as described in (1) above, which has an organic group having an organic group having a triazine skeleton, an organic group having an amic acid structure, an organic group having a naphthol structure, or a sulfonic acid structure.

(3)
(A) The negative resist composition as described in (1) or (2) above, wherein the alkali-soluble resin has a monocyclic or polycyclic alicyclic structure in the side chain.

(4)
The negative resist composition according to any one of (1) to (3) above, wherein an acid having a pKa of −8 or less is generated from the component (C1) upon irradiation with actinic rays or radiation.

一般式（ＣＬＮＭ−１）に於いて、
Ｒ^ＮＭ１は、水素原子、アルキル基、シクロアルキル基又はオキソアルキル基を表す。 (5)
The negative resist composition as described in (4) above, wherein fluorinated sulfonimide acid is generated from the component (C1) upon irradiation with actinic rays or radiation.
(6)
The negative resist composition of (4) above, wherein a fluorinated sulfonemethic acid compound is generated from the component (C1) upon irradiation with actinic rays or radiation.
(7)
(D) The negative resist composition as described in any one of (1) to (6) above, wherein the compound having a radical polymerizable group is a compound having a plurality of radical polymerizable groups.
(8)
(B) The crosslinking agent of component is a compound having two or more partial structures represented by the following general formula (CLNM-1), according to any one of (1) to (7) above Negative resist composition.

In the general formula (CLNM-1),
R ^NM1 represents a hydrogen atom, an alkyl group, a cycloalkyl group or an oxoalkyl group.

一般式（ＩＩ）に於いて、
Ｒ₁及びＲ₂は、各々独立に、フッ素原子又はアルキル基を表す。Ｒ₁及びＲ₂は、互いに結合して環を形成してもよい。

一般式（ＩＩＩ）に於いて、
Ｒ₃〜Ｒ₅は、各々独立に、フッ素原子又はアルキル基を表す。Ｒ₃〜Ｒ₅の内のいずれか２つが、互いに結合して環を形成してもよい。 (9)
The negative resist composition according to (4) above, wherein the acid having a pKa of −8 or less is an acid represented by the following general formula (II) or (III).

In general formula (II):
R ₁ and R ₂ each independently represents a fluorine atom or an alkyl group. R ₁ and R ₂ may combine with each other to form a ring.

In general formula (III):
R _{3 to} R ₅ each independently represents a fluorine atom or an alkyl group. Any two of R _{3 to} R ₅ may be bonded to each other to form a ring.

(10)
A resist pattern forming method comprising: applying a negative resist composition according to any one of (1) to (9) above, exposing the resist composition, and developing the resist pattern to form a resist pattern.

  According to the present invention, there are provided a negative resist composition and a pattern forming method that are difficult to reduce a film and that do not easily collapse a pattern.

The negative resist composition in the present invention is
(A) an alkali-soluble resin,
(B) a crosslinking agent that crosslinks the alkali-soluble resin by the action of an acid,
(C1) a compound that causes a crosslinking reaction to proceed by irradiation with actinic rays or radiation,
(C2) a photo radical generator, and (D) a compound having a radical polymerizable group,
A negative resist composition characterized by comprising:
The negative resist composition of the present invention comprises (B) a compound that is crosslinked by the action of an acid by the action of an acid generated from the (C1) component and a radical generated from the (C2) component by exposure during resist pattern formation. (A) A crosslinking reaction occurs with the alkali-soluble resin, and at the same time, (D) a compound having a radical polymerizable group is polymerized, whereby the exposed portion is insoluble or hardly soluble in the alkali developer.
In some cases, (B) a cross-linking reaction may occur between the compounds cross-linked by the action of the acid, and the exposed portion may be insoluble in the alkali developer.
In this way, the exposed portion is selectively insolubilized or hardly soluble in the alkaline developer, thereby producing a dissolution contrast with the alkaline developer in the exposed portion and the unexposed portion, and a fine pattern is obtained by pattern exposure using a mask. Formation becomes possible.

  Hereinafter, each component of the negative resist composition of the present invention will be described in detail.

(A) Alkali-soluble resin The negative resist composition of the present invention contains an alkali-soluble resin (A).

The alkali-soluble resin is generally synthesized by polymerizing a monomer having a partial structure to be polymerized by radical polymerization or the like, and has a repeating unit derived from the monomer having a partial structure to be polymerized. Examples of the partial structure to be polymerized include an ethylenically polymerizable partial structure.
The repeating unit used in the alkali-soluble resin (A) is at least one selected from repeating units derived from a monomer having an ethylenically polymerizable partial structure represented by the following general formula (ASM-1) or (ASM-2). Preferably the type is used.

In general formula (ASM-1),
R ^M11 and R ^M12 each independently represent a hydrogen atom, a halogen atom, or an organic group. The plurality of R ^M12 may be the same as or different from each other.
* Represents a bond bonded to the side chain of the alkali-soluble resin.

In the formula (ASM-2),
R ^M13 each independently represents a hydrogen atom, a halogen atom, or an organic group.
Z ′ represents an atomic group for forming an alicyclic structure together with the two carbon atoms shown in the formula (ASM-2).
* Represents a bond bonded to the side chain of the alkali-soluble resin.

Examples of the organic group in R ^{M11 to} R ^M13 include an alkyl group, a halogenated alkyl group, an alkoxy group, a halogenated alkoxy group, a carboxyl group, or a cyano group, and these further have a substituent. Also good. Examples of the substituent that the organic group may further have include a halogen atom, a hydroxyl group, a cyano group, a thiol group, an alkoxy group, an alkylthio group, an alkoxycarbonyl group, an alkylcarbonyloxy group, and an alkylamide group. It is done.

R ^M11 is preferably a hydrogen atom, an alkyl group (preferably having 1 to 6 carbon atoms), an alkyl group substituted with a hydroxyl group, an alkyl group substituted with an alkoxy group, an alkyl group substituted with an alkylcarbonyloxy group, a carboxyl group Group or a halogenated alkyl group.
R ^M12 is preferably each independently a hydrogen atom, an alkyl group (preferably having 1 to 6 carbon atoms), a carboxyl group or a halogenated alkyl group.

Preferably, each of R ^M13 is independently a hydrogen atom, a halogen atom (fluorine atom, chlorine atom, bromine atom, iodine atom), an alkyl group (preferably having 1 to 6 carbon atoms), a carboxyl group (preferably having 1 carbon atom). -6), an alkyl group which may have a substituent, a halogenated alkyl group, or an alkoxy group which may have a substituent.

The alicyclic structure formed by Z ′ together with the two carbon atoms shown in the formula (ASM-2) may be substituted with a halogen atom or an organic group. Examples of the organic group which may be substituted for the alicyclic structure include an alkyl group (preferably having 1 to 6 carbon atoms), a monocyclic or polycyclic cycloalkyl group (preferably having 3 to 20 carbon atoms), and alkoxy. Group, alkylamino group, alkoxycarbonyl group, alkylsulfone group, alkylamide group, and the like.
When Z ′ forms an alicyclic structure with two carbon atoms shown in the formula (ASM-2), the alicyclic structure includes cyclopentane, cyclohexane, norbornane, tricyclodecane, tetracyclo And dodecane.

  The repeating unit including the partial structure represented by the formula (ASM-1) is preferably a repeating unit represented by the following general formula (ASM-11).

In the formula (ASM-11),
R ^M11 and R ^M12 have the same ^meaning as in formula (ASM-1).
* Represents a bond bonded to the side chain of the alkali-soluble resin.
X _he represents an oxygen atom, a sulfur atom, or -N (R ^he )-. R ^he represents a hydrogen atom or an alkyl group.

  The structure bonded with * is a group having an alicyclic hydrocarbon structure substituted with an alkaline developer, an aliphatic group, a polar group, a lactone-containing monocyclic ring or a polycyclic group, as described later. A structure such as a cycloaliphatic group is preferred.

  Specific examples of the monomer corresponding to the repeating unit represented by the formula (ASM-11) include acrylic acid, methacrylic acid, α-hydroxymethylacrylic acid, trifluoromethylacrylic acid, maleic acid, fumaric acid, itaconic acid, And their esters, amides, acid anhydrides, and the like.

  The repeating unit represented by the general formula (ASM-2) is preferably a repeating unit represented by any one of the following formulas (ASM-2a) to (ASM-2c).

In the formulas (ASM-2a) to (ASM-2c),
R ^M13 has the same meaning as ^{R M13} in formula (ASM-2).
When there are a plurality of R ^{M15 s} , each represents an organic group independently.
m represents an integer of 0 or more. 0 to 2 is preferable, and 0 or 1 is more preferable.
n ^M1 represents an integer of 0 or more. Preferably it is 0-3.
* Represents a bond bonded to the side chain of the alkali-soluble resin.

As the organic group for R ^M15 , a linear or branched alkyl group, monocyclic or polycyclic cycloalkyl group, alkoxy group, alkylamino group, alkoxycarbonyl group, which may have a substituent, An alkyl sulfone group, an alkylamide group, etc. can be mentioned.
The structure bonded with * is a group having an alicyclic hydrocarbon structure substituted with an alkaline developer, an aliphatic group, a polar group, a lactone-containing monocyclic ring or a polycyclic group, as described later. A structure such as a cycloaliphatic group is preferred.

Various structures serving as side chains of the alkali-soluble resin polymer to be described later may be directly bonded to the partial structures to be polymerized represented by the general formulas (ASM-1) and (ASM-2). (For example, a linear or branched aliphatic structure and / or a monocyclic or polycyclic aliphatic structure) to the polymerized partial structure represented by the general formula (ASM-1) or (ASM-2) It may be bonded.
As an example via a coupling group, the repeating unit represented by the following general formula (ASS-1)-(ASS-3) is mentioned, for example.

In formulas (ASS-1) to (ASS-3),
R ^M11, R ^M12, R ^M15 has the same meaning as R ^M11, R ^M12, R ^M15 in formula (ASM-1) and (ASM-2).
X _he has the same meaning as _{X he} in formula (ASM-11).
* Represents a bond bonded to the side chain of the alkali-soluble resin.
L ^s represents a single bond or an n ^F +1 valent linking group.
m represents an integer of 0 or more. Preferably 0 or 1.
n ^F represents an integer of 1 or more. Preferably it is 1.

As the n ^F +1 valent linking group of L ^S , an oxygen atom, a nitrogen atom, —N (R ^N ) —, —C (═O) —, —S (═O) ₂ —, or the following linking group group, And a combination thereof.
^RN represents a hydrogen atom or an alkyl group.

The linking group group preferably comprises a group having a linear or branched aliphatic structure, or a monocyclic or polycyclic aliphatic structure. The linear or branched aliphatic structure preferably has 1 to 30 carbon atoms, more preferably 1 to 10 carbon atoms. The monocyclic or polycyclic aliphatic structure preferably has 5 to 30 carbon atoms, and more preferably 6 to 25 carbon atoms.
Examples of the linking group group include structures represented by the following (SP1) and (SP2).

  Linking group (SP1)

  Linking group (SP2)

  These structures may further have a substituent, and a polyvalent structure obtained by removing an arbitrary number of hydrogen atoms from these aliphatic structures is also included in the linked structure. Examples of the substituent include alkyl groups, aryl groups, alkoxy groups, alkylcarbonyl groups, alkoxycarbonyl groups, alkylcarbonyloxy groups, alkylamino groups, alkylamide groups, alkylaminocarbonyl groups, alkylthio groups, alkylsulfone groups, alkylsulfonyl groups. Group, alkylsulfonylamide group, and the like.

(A) The alkali-soluble resin preferably has a monocyclic or polycyclic alicyclic structure in the side chain.
Specific examples of the alicyclic structure include monocyclic structures such as cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, norbornyl, isobornyl, tricyclodecanyl, tetracyclododecanyl, hexacycloheptadecanyl, adamantyl, Examples include polycyclic structures such as diamantyl, spirodecanyl, and spiroundecanyl. Of these, cyclohexyl, adamantyl, diamantyl and norbornyl structures are preferred.
The alicyclic structure may have a substituent, for example, may be substituted with a halogen atom or an organic group. Examples of the organic group which may be substituted for the alicyclic structure include an alkyl group (preferably having 1 to 6 carbon atoms), a monocyclic or polycyclic cycloalkyl group (preferably having 3 to 20 carbon atoms), and alkoxy. Groups, alkylamino groups, alkoxycarbonyl groups, alkylsulfone groups, alkylamide groups, and the like.

(A1) Alkali-soluble repeating unit The (A) alkali-soluble resin used in the present invention preferably has (a1) a repeating unit containing a group having solubility in an alkali developer (hereinafter also referred to as an alkali-soluble group). By having this repeating unit, the alkali-soluble resin is dissolved in the alkali-soluble resin. The alkali-soluble resin only needs to dissolve in an alkali developer when the film is formed using a resist composition, and the alkali-soluble resin alone is soluble in an alkali developer. It doesn't have to be a thing. In this case, for example, depending on the properties and contents of other components contained in the resist composition, a film formed using the resist composition often dissolves in an alkaline developer. However, also in this case, the (A) alkali-soluble resin preferably has (a1) a repeating unit containing an alkali-soluble group.

The group having solubility in an alkali developer (alkali-soluble group) includes an organic group containing a fluorine-substituted alcohol structure, an organic group containing a carboxylic acid structure, an organic group containing a sulfonamide structure, and a furfuryl alcohol structure. Organic group, organic group including carbamate structure, organic group including tautomeric alcohol structure, organic group including thiol structure, organic group including ketone oxime structure, organic group including dicarbonylmethylene structure, N-hydroxysuccinimide structure An organic group having a triazine skeleton, an organic group having an amic acid structure, an organic group having a sulfonic acid structure, and the like.
Preferably, it has an organic group containing a fluorine-substituted alcohol structure, an organic group containing a sulfonamide structure, an organic group containing a dicarbonylmethylene structure, or an organic group containing a naphthol structure.
Examples of the alkali-soluble group include the groups represented below.

In the above examples of the alkali-soluble group, * represents a bond bonded to the main chain or side chain of the alkali-soluble resin (A).
The alkali-soluble group may be directly bonded to the polymerized partial structure represented by the general formulas (ASM-1) and (ASM-2), or the general formulas (ASS-1) to (ASS-). As represented by 3), it may be bonded to the polymerizing partial structure via an organic group.

In the examples of the alkali-soluble groups,
R ^AS1 and R ^AS2 each independently represent a hydrogen atom, a fluorine atom or a fluorine-substituted alkyl group, and at least one of R ^AS1 and R ^AS2 is a fluorine atom or a fluorine-substituted alkyl group. R ^AS1 and R ^AS2 may be the same or different.
R ^AS0 represents a single bond or an n ^F +1 valent linking group, and more specifically represents the same structure as L ^S described above. R ^AS1 , R ^AS2 and R ^AS0 may be bonded to each other to form a ring structure.
Examples of the organic group containing such a fluorine-substituted alcohol structure include the following examples. In the following examples, * represents a bond bonded to the above general formula (ASM-1) or (ASM-2).

In the examples of the alkali-soluble groups, R ^AS3 and R ^AS4 are each independently an alkyl group (straight or branched), a cycloalkyl group (monocyclic or polycyclic), an aryl group, an alkylcarbonyl group, or a cycloalkyl. A carbonyl group, an alkylsulfonyl group, or a cycloalkylsulfonyl group is represented. These groups may further have a substituent. These substituents may include a hydroxyl group, an ether structure, an ester structure, an amide structure, a sulfone structure, or a sulfonyl structure. R ^AS3 and R ^AS4 are preferably linear or branched alkyl groups which may contain an ether or ester structure from the viewpoint of alkali solubility.
Examples of R ^AS3 include methyl group, ethyl group, 2-hydroxyethyl group, 2-methoxyethyl group, 2-methoxycarbonylethyl group, 2-t-butoxycarbonylethyl group, cyclopentyl group, cyclohexyl group, norbornyl group, isobornyl. Group, tricyclodecanyl group, tetracyclododecanyl group, adamantyl group, and the like.

R ^AS4 represents an alkyl group (straight or branched) which may have a substituent, a cycloalkyl group (monocyclic or polycyclic), or an aryl group. The substituent may include a hydroxyl group, an ether structure, an ester structure, an amide structure, a sulfone structure, or a sulfonyl structure. These substituents are preferably a linear or branched alkyl group which may contain an ether or ester structure from the viewpoint of alkali solubility.
Examples of R ^AS4 include methyl group, ethyl group, 2-hydroxyethyl group, 2-methoxyethyl group, 2-methoxycarbonylethyl group, 2-t-butoxycarbonylethyl group, cyclopentyl group, cyclohexyl group, norbornyl group, isobornyl. Group, tricyclodecanyl group, tetracyclododecanyl group, adamantyl group, phenyl group, naphthyl group and the like.
In the organic group containing a sulfonamide structure, a carbonyl group, an amide group, a sulfone group, an ester group, or the like may be further bonded to the sulfonamide structure.

  Examples of the organic group containing a sulfonamide structure include the following groups. In the following examples, * represents a bond bonded to the above general formula (ASM-1) or (ASM-2).

R ^AS5 and R ^AS6 each independently represent a hydrogen atom, an alkyl group (preferably having 1 to 6 carbon atoms) which may have a substituent, a cycloalkyl group (preferably having 4 to 7 carbon atoms), or an alkoxy group. (Preferably 1 to 6 carbon atoms), alkylcarbonyl group (preferably 1 to 6 carbon atoms), alkylsulfone group (preferably 1 to 6 carbon atoms), alkylamide group (preferably 1 to 6 carbon atoms) , N ^AS6 represents an integer of 0 to 5, preferably n ^AS6 is 0 to 2. When there are a plurality of R ^{AS6 s,} they may be different from each other.

R ^AS7 represents a hydrogen atom, an ^optionally substituted alkyl group (preferably having 1 to 6 carbon atoms), or an optionally substituted cycloalkyl group (preferably having 4 to 7 carbon atoms). .

R ^{AS8 to} R ^AS14 are each a hydrogen atom, an ^optionally substituted alkyl group (preferably having 1 to 6 carbon atoms), or an optionally substituted cycloalkyl group (preferably having 4 to 4 carbon atoms). 7).

R ^AS14 is preferably a hydrogen atom.
R ^AS15 is a hydrogen atom, an ^optionally substituted alkyl group (preferably having 1 to 6 carbon atoms), an optionally substituted cycloalkyl group (preferably having 4 to 7 carbon atoms), or An alkoxy group (preferably having 1 to 6 carbon atoms) which may have a substituent is represented.
R ^AS15 is preferably an alkyl group having 1 to 30 carbon atoms and a cycloalkyl group having 3 to 30 carbon atoms. For example, methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, sec -Butyl group, pentyl group, neopentyl group, hexyl group, heptyl group, octyl group, nonyl group, decyl group, undecyl group, dodecyl group, tridecyl group, tetradecyl group, pentadecyl group, hexadecyl group, heptadecyl group, octadecyl group, Nonadecyl group, eicosyl group, cyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohexyl group, adamantyl group, norbornyl group, boronyl group and the like can be mentioned.

R ^AS16 represents a hydrogen atom, an ^optionally substituted alkyl group (preferably having 1 to 6 carbon atoms) or an optionally substituted cycloalkyl group (preferably having 4 to 7 carbon atoms). .

R ^AS17 is a hydrogen atom, an alkyl group which may have a substituent (preferably 1 to 6 carbon atoms), a cycloalkyl group which may have a substituent (preferably 4 to 7 carbon atoms), or An alkylamino group (preferably having 1 to 6 carbon atoms) is represented. ^When there are a plurality of R ^{AS17 s,} they may be different from each other.
n ^AS17 is an integer of 0-2.

R ^AS18 represents an ^optionally substituted alkyl group (preferably having 1 to 6 carbon atoms) or an optionally substituted cycloalkyl group (preferably having 4 to 7 carbon atoms), and Q ^AS Represents a single bond or an alkylene group (preferably having 1 to 2 carbon atoms).

R ^AS19 is an alkyl group (preferably having 1 to 10 carbon atoms), a cycloalkyl group (preferably having 3 to 20 carbon atoms), an alkoxy group, an alkylthio group, an alkylcarbonyloxy group, an alkoxycarbonyl group, an alkylamino group, or an alkylamide. Represents a group. When a plurality of R ^AS19 are present, they may be the same or different.
n ¹⁹ represents an integer of 1-7.
n ^AS19 represents an integer of 0 to 7.

  * Represents a bond that binds to the side chain. That is, the monomer having a partial structure represented by the general formula (ASM-1) has a portion that becomes a side chain of the alkali-soluble resin.

  Among these alkali-soluble groups, an organic group containing a fluorine-substituted alcohol structure, an organic group containing a carboxylic acid structure, an organic group containing a sulfonamide structure, an organic group containing a sulfonimide structure, an organic group containing a dicarbonylmethylene structure, etc. preferable.

Examples of the repeating unit (a1) having an alkali-soluble group are shown below, but the present invention is not limited thereto. In the structural formula, R ^X represents a hydrogen atom, a methyl group, a trifluoromethyl group, or a hydroxymethyl group.

(A2) Repeating Unit Having Aliphatic Group The alkali-soluble resin component used in the present invention may contain (a2) a repeating unit having an aliphatic group. By using this repeating unit, the dissolution rate of the resist film can be adjusted and the etching resistance can be increased.
An aliphatic group represents a group having a substituted or unsubstituted linear, branched, monocyclic or polycyclic aliphatic group. However, the aliphatic group is preferably not a group having solubility in an alkali developer, but a group composed of a carbon atom and a hydrogen atom, and a polycyclic aliphatic group is preferable from the viewpoint of etching resistance.

  Examples of linear or branched aliphatic groups include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, pentyl, neopentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, Tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl, eicosyl, etc., and monocyclic aliphatic groups such as cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, etc., as polycyclic alkyl groups Includes norbornyl, isobornyl, tricyclodecanyl, tetracyclododecanyl, hexacycloheptadecanyl, adamantyl, diamantyl, spirodecanyl, spiroundecanyl and the like.

  The aliphatic group may be substituted. Examples of the substituent include various substituents such as a halogen atom, an alkyl group, an alkoxy group, an amino group, an alkoxycarbonyl group, an alkylsulfone group, a cyano group, and a hydroxyl group. As these substituents, those suitable for improving the performance of the resist film such as etching resistance and hydrophilicity / hydrophobicity can be selected and used.

Examples of the repeating unit having an aliphatic group are shown below, but the present invention is not limited thereto. In the structural formula, R ^X represents a hydrogen atom, a methyl group, a trifluoromethyl group, or a hydroxymethyl group.

  The alkali-soluble resin used in the present invention may have a repeating unit having a group having an alicyclic hydrocarbon structure substituted with a polar group. Thereby, improvement in substrate adhesion, developer compatibility, and the like can be expected. As the alicyclic hydrocarbon structure of the alicyclic hydrocarbon structure substituted with a polar group, a monocyclic or polycyclic structure can be considered, but a polycyclic structure is preferable from the viewpoint of etching resistance.

  Specific examples of the alicyclic hydrocarbon structure include cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl as the monocyclic structure, and norbornyl, isobornyl, tricyclodecanyl, tetracyclododecanyl as the polycyclic structure. Hexacycloheptadecanyl, adamantyl, diamantyl, spirodecanyl, spiroundecanyl and the like. Of these, adamantyl, diamantyl and norbornyl structures are preferred.

  Examples of the polar group include various polar groups, among which a hydroxyl group and a cyano group are preferable. The group having an alicyclic hydrocarbon structure substituted with the polar group is preferably a group represented by the following general formulas (KCA-1) to (KCA-4).

In formulas (KCA-1) to (KCA-4), R ^{CA1 to} R ^CA3 each independently represents a hydrogen atom, a hydroxyl group, or a cyano group. However, at least one of R ^{CA1 to} R ^CA3 represents a hydroxyl group or a cyano group. Preferably, one or two of R ^{CA1 to} R ^CA3 are hydroxyl groups and the rest are hydrogen atoms. In general formula (KCA-1), it is more preferable that two ^{members out} of R ^{CA1 to} R ^CA3 are hydroxyl groups and the rest are hydrogen atoms.
* Represents a bond bonded to the general formula (ASM-1) or (ASM-2).

Specific examples of the repeating unit having a group represented by formulas (KCA-1) to (KCA-4) will be given below, but the present invention is not limited thereto. R ^X represents a hydrogen atom, a methyl group, a trifluoromethyl group, or a hydroxymethyl group.

(A3-1) Repeating unit containing a group that can be cross-linked by the action of an acid (A) The alkali-soluble resin used in the present invention has (a3-1) a repeating unit containing a group that can be cross-linked by the action of an acid. By having this repeating unit, (C1) an acid generated from a compound that proceeds with a crosslinking reaction by irradiation with actinic rays or radiation upon exposure causes (B) a crosslinking reaction with a compound that is crosslinked by the action of an acid, thereby exposing the exposed portion. By forming a cross-linked structure, it becomes insoluble in an alkaline developer.

  The group that can be cross-linked by the action of the acid may be any group that reacts with the compound that cross-links by the action of the acid (B) described later by the action of the acid, and is preferably a nucleophilic group. Groups. Further, from the viewpoint of reactivity, a primary or secondary hydroxyl group, particularly a primary hydroxyl group is preferred.

  The group that reacts with the compound that crosslinks by the action of the acid (B), as represented by the general formulas (ASS-1) to (ASS-3), is converted into the polymerized partial structure via an organic group. Bonding is preferred.

Although the repeating unit containing the group which can be bridge | crosslinked by the effect | action of an acid below is illustrated, this invention is not limited to this. In the formula, R ^X represents a hydrogen atom, a methyl group, a trifluoromethyl group, or a hydroxymethyl group.

(A3-2) Repeating Unit Having Radical Polymerizable Group The (A) alkali-soluble resin used in the present invention preferably contains a repeating unit having a radical polymerizable group. The exposed portion is insolubilized in an alkali developer by a polymerization reaction between the polymerizable groups, the radical polymerizable group and a compound having a radical polymerizable group (D) described later, or a compound having a polymerizable group. I think that.

  The polymerizable group may generally be a group that causes a polymerization reaction by a radical, and preferably includes an ethylenically unsaturated bond, for example, groups represented by the following general formulas (RP1) to (RP3).

In the formula (RP1), * represents an organic group which is a bond bonded to the structure represented by the general formula (ASM-1) or (ASM-2), and R ^{RP1 to} R ^RP3 are each independently hydrogen. Represents an atom or a monovalent organic group. R ^RP1 is preferably a hydrogen atom or an alkyl group which may have a substituent, and among them, a hydrogen atom or a methyl group is preferable. R ^RP2 and R ^RP3 are each independently a hydrogen atom, a halogen atom, an amino group, a carboxyl group, an alkoxycarbonyl group, a cyano group, an alkyl group that may have a substituent, or an alkoxy that may have a substituent. Group, an alkylamino group which may have a substituent, and the like, and a hydrogen atom, a carboxyl group, an alkoxycarbonyl group, an alkyl group which may have a substituent, and the like are preferable. R ^{RP1 to} R ^RP3 may be bonded to each other to form a ring structure. Examples of the substituent that R ^{RP1 to} R ^RP3 may further include an alkyl group, an alkenyl group, an alkynyl group, an alkoxy group, a halogen atom, an amino group, an alkylamino group, a carboxyl group, an alkoxycarbonyl group, a cyano group, Etc.

Wherein (RP2), * represents an organic group which is a bond that binds to the structure represented by the general formula (ASM-1) or ^{(ASM-2), R RP4} ~R RP8 are each independently monovalent of it represents an organic group, R ^RP4 to R ^RP8 is preferably a hydrogen atom, a halogen atom, an amino group, a dialkylamino group, a carboxyl group, an alkoxycarbonyl group, a cyano group, an alkyl group which may have a substituent, Examples include an alkoxy group which may have a substituent, an alkylamino group which may have a substituent, and the like. Among these, a hydrogen atom, a carboxyl group, an alkoxycarbonyl group, and an alkyl group which may have a substituent are preferable. The ^R RP4 ^{to R RP8} may form a ring structure together. The R ^RP4 to R ^RP8 further comprising optionally substituent group is the same as the above general formula (RP1) and the like.

In the formula (RP3), * represents an organic group which is a bond bonded to the structure represented by the general formula (ASM-1) or (ASM-2), and R ^RP9 is preferably a hydrogen atom. Or the alkyl group etc. which may have a substituent are mentioned, Especially, a hydrogen atom and a methyl group are preferable. R ^RP10 and R ^RP11 each independently have a hydrogen atom, a halogen atom, an amino group, a dialkylamino group, a carboxyl group, an alkoxycarbonyl group, a cyano group, an alkyl group that may have a substituent, or a substituent. Examples thereof may include an alkoxy group which may be substituted, an alkylamino group which may have a substituent, and the like, and among them, a hydrogen atom, a carboxyl group, an alkoxycarbonyl group and an alkyl group which may have a substituent are preferable. R ^{RP9 to} R ^RP11 may be bonded to each other to form a ring structure. ^{Examples of the} substituent that R ^{RP9 to} R ^RP11 may further have include those similar to the general formula (RP1).

  In the alkali-soluble resin containing a repeating unit having a polymerizable group, for example, a free radical (a polymerization initiation radical or a growth radical in the polymerization process of a polymerizable compound) is added to the polymerizable group, and the polymerizable group (B) described later is added. Addition polymerization is carried out directly between the compounds possessed or between the resins or via the polymerization chain of the polymerizable compound, whereby a three-dimensional structure is formed in the exposed area and insolubilized in the alkaline developer. Or, atoms in a resin or (B) a compound having a polymerizable group (for example, a hydrogen atom on a carbon atom adjacent to the polymerizable structure) are extracted by free radicals to generate radicals, which are bonded to each other. As a result, the polymerization reaction proceeds between the resin molecules to form a three-dimensional structure and insolubilize in the alkaline developer.

  Although the repeating unit which has a polymeric group is illustrated below, this invention is not limited to these.

In the formula, R ^X represents a hydrogen atom, a methyl group, a hydroxymethyl group, or a trifluoromethyl group.

(A4) Lactone-containing repeating unit The (A) alkali-soluble resin component used in the present invention may contain a repeating unit having a group containing a lactone structure.
These lactone-containing structures are opened by an alkaline developer to generate carboxylic acid. The generated carboxylic acid has a function of increasing the solubility in an alkali developer. At this time, it is considered that the exposed portion forms a three-dimensional network structure by cross-linking, and the penetration of the developer is smaller than that of the unexposed portion. The lactone structure itself is also hydrophobic compared to the carboxyl group after ring opening, and the affinity with the alkaline developer in the exposed area is smaller than that in the unexposed area. By having a lactone structure by the above actions, the dissolution contrast between the unexposed area and the exposed area is further improved, or swelling of the exposed area is suppressed, and an improvement in resolution is expected.

  Any lactone structure can be used as long as it has a lactone structure, but a lactone structure having a 5- to 7-membered ring is preferable, and a bicyclo structure or a spiro structure is formed in the 5- to 7-membered lactone structure. Those in which the other ring structures are condensed are preferred. It is more preferable to have a repeating unit having a group having a lactone structure represented by any of the following general formulas (LC1-1) to (LC1-16). Further, a group having a lactone structure may be directly bonded to the main chain. Preferred lactone structures are (LC1-1), (LC1-4), (LC1-5), (LC1-6), (LC1-13), and (LC1-14), particularly preferably (LC1-4 ). By using a specific lactone structure, line edge roughness and development defects are improved.

The lactone structure moiety may or may not have a substituent (R ^LC ). Preferred substituents (R ^LC ) include an alkyl group having 1 to 8 carbon atoms, a cycloalkyl group having 4 to 7 carbon atoms, an alkoxy group having 1 to 8 carbon atoms, an alkoxycarbonyl group having 1 to 8 carbon atoms, and a carboxyl group. , Halogen atom, hydroxyl group, cyano group, acid-decomposable group and the like. More preferred are alkyl groups having 1 to 4 carbon atoms, cyano groups, and acid-decomposable groups. n ^CL represents an integer of 0 to 4. When n ^CL is 2 or more, a plurality of R ^LCs may be the same or different, and a plurality of R ^LCs may be bonded to form a ring.
* Represents a bond bonded to the general formula (ASM-1) or (ASM-2).

  The repeating unit having a lactone structure usually has an optical isomer, but any optical isomer may be used. One optical isomer may be used alone, or a plurality of optical isomers may be mixed and used. When one kind of optical isomer is mainly used, the optical purity (ee) thereof is preferably 90 or more, more preferably 95 or more.

Specific examples of the repeating unit having a group having a lactone structure are given below, but the present invention is not limited thereto. In the formula, R ^X represents a hydrogen atom, a methyl group, a trifluoromethyl group, or a hydroxymethyl group.

-Composition ratio, polymerization method, etc. The composition ratio of each component of the above repeating unit varies depending on the repeating unit used.
(A1) The repeating unit having an alkali-soluble group is generally 5 to 80 mol%, preferably 10 to 70 mol%, more preferably 15 to 60 mol%.
(A2) The repeating unit having an aliphatic group is generally 5 to 60 mol%, preferably 10 to 50 mol%, more preferably 15 to 40 mol%.
(A3-1) The repeating unit containing a group that can be cross-linked by the action of an acid is generally 5 to 30 mol%, preferably 5 to 25 mol%, more preferably 10 to 20 mol%.
(A3-2) The repeating unit containing a radically polymerizable group is generally 5 to 30 mol%, preferably 5 to 25 mol%, more preferably 5 to 20 mol%.
(A4) When a repeating unit having a lactone structure is contained, the composition ratio of the repeating unit is generally 1 to 50 mol%, preferably 5 to 45 mol%, more preferably 10 to 40 mol%.

  The resin used for the alkali-soluble resin component (A) is composed of a copolymer of the above repeating units, and the weight average molecular weight (Mw) is usually 1000 to 100,000, preferably 1000 to 20000, and more preferably 1000 to 10,000. The value obtained by dividing the weight average molecular weight by the number average molecular weight (dispersion degree Pd) is 1 to 3, preferably 1 to 2.5, and more preferably 1 to 2.0.

  As the alkali-soluble resin used in the present invention, various commercially available products can be used, or they can be synthesized according to a conventional method (for example, radical polymerization). For example, as a general synthesis method, a monomer polymerization method in which a monomer species and an initiator are dissolved in a solvent and the polymerization is performed by heating, and a solution of the monomer species and the initiator is dropped into the heating solvent over 1 to 10 hours. The dropping polymerization method is added, and the dropping polymerization method is preferable. Examples of the reaction solvent include ethers such as tetrahydrofuran, 1,4-dioxane, diisopropyl ether, ketones such as methyl ethyl ketone and methyl isobutyl ketone, ester solvents such as ethyl acetate, amide solvents such as dimethylformamide and dimethylacetamide, Furthermore, the solvent which melt | dissolves the composition of this invention like the below-mentioned propylene glycol monomethyl ether acetate, propylene glycol monomethyl ether, and cyclohexanone is mentioned. More preferably, the polymerization is performed using the same solvent as that used in the resist composition of the present invention. Thereby, the generation of particles during storage can be suppressed.

  The polymerization reaction is preferably performed in an inert gas atmosphere such as nitrogen or argon. As a polymerization initiator, a commercially available radical initiator (azo initiator, peroxide, etc.) is used to initiate the polymerization. As the radical initiator, an azo initiator is preferable, and an azo initiator having an ester group, a cyano group, or a carboxyl group is preferable. Preferred initiators include azobisisobutyronitrile, azobisdimethylvaleronitrile, dimethyl 2,2′-azobis (2-methylpropionate) and the like. If desired, an initiator is added or added in portions, and after completion of the reaction, it is put into a solvent and a desired polymer is recovered by a method such as powder or solid recovery. The concentration of the reaction is 5 to 50% by mass, preferably 10 to 30% by mass. The reaction temperature is usually 10 ° C to 150 ° C, preferably 30 ° C to 120 ° C, more preferably 60-100 ° C.

  The polymerization reaction is preferably performed in an inert gas atmosphere such as nitrogen or argon. As a polymerization initiator, a commercially available radical initiator (azo initiator, peroxide, etc.) is used to initiate the polymerization. As the radical initiator, an azo initiator is preferable, and an azo initiator having an ester group, a cyano group, or a carboxyl group is preferable. Preferred examples of the initiator include azobisisobutyronitrile, azobisdimethylvaleronitrile, dimethyl 2,2′-azobis (2-methylpropionate) and the like. In addition to the polymerization initiator, a chain transfer agent may be added to carry out the polymerization reaction. The density | concentration of a polymerization reaction is 5-50 mass%, Preferably it is 30-50 mass%. The reaction temperature is usually 10 ° C to 150 ° C, preferably 30 ° C to 120 ° C, more preferably 60-100 ° C.

  After completion of the reaction, the mixture is allowed to cool to room temperature and purified. Purification can be accomplished by a liquid-liquid extraction method that removes residual monomers and oligomer components by combining water and an appropriate solvent, and a purification method in a solution state such as ultrafiltration that extracts and removes only those having a specific molecular weight or less. , Reprecipitation method that removes residual monomer by coagulating resin in poor solvent by dripping resin solution into poor solvent and purification in solid state such as washing filtered resin slurry with poor solvent A normal method such as a method can be applied. For example, the resin is precipitated as a solid by contacting a solvent (poor solvent) in which the resin is hardly soluble or insoluble in a volume amount of 10 times or less, preferably 10 to 5 times that of the reaction solution.

  The solvent (precipitation or reprecipitation solvent) used in the precipitation or reprecipitation operation from the polymer solution may be a poor solvent for the polymer, and may be a hydrocarbon, halogenated hydrocarbon, nitro, depending on the type of polymer. A compound, ether, ketone, ester, carbonate, alcohol, carboxylic acid, water, a mixed solvent containing these solvents, and the like can be appropriately selected for use. Among these, as the precipitation or reprecipitation solvent, a solvent containing at least hydrocarbon, ether, ester, alcohol, or water is preferable.

  The amount of the precipitation or reprecipitation solvent used can be appropriately selected in consideration of efficiency, yield, and the like, but generally 100 to 10000 parts by mass, preferably 200 to 2000 parts by mass with respect to 100 parts by mass of the polymer solution, More preferably, it is 300-1000 mass parts.

  The precipitated or re-precipitated polymer is usually subjected to conventional solid-liquid separation such as filtration and centrifugation, and dried before use. Filtration is performed using a solvent-resistant filter medium, preferably under pressure. Drying is performed at a temperature of about 30 to 100 ° C., preferably about 30 to 50 ° C. under normal pressure or reduced pressure (preferably under reduced pressure).

  In addition, after depositing and separating the resin once, it may be dissolved again in a solvent, and the resin may be brought into contact with a hardly soluble or insoluble solvent. That is, after completion of the radical polymerization reaction, a solvent in which the polymer is hardly soluble or insoluble is brought into contact, the resin is precipitated (step a), the resin is separated from the solution (step b), and dissolved again in the solvent. (Step c), and then contact the resin solution A with a solvent in which the resin is hardly soluble or insoluble in a volume amount less than 10 times that of the resin solution A (preferably 5 times or less volume). This may be a method including precipitating a resin solid (step d) and separating the precipitated resin (step e).

  (A) The content of the alkali-soluble resin component in the negative resist composition is preferably from 5 to 95 mass%, more preferably from 10 to 95 mass%, still more preferably, based on the total solid content of the negative resist composition. Is 15 to 95% by mass.

(B) Crosslinking agent that crosslinks alkali-soluble resin by the action of an acid The negative resist composition of the present invention contains a crosslinking agent that crosslinks an alkali-soluble resin by the action of an acid. The crosslinking agent used in the present invention can be appropriately selected from known crosslinking agents that crosslink alkali-soluble resins by the action of acids, for example, compounds described in JP-A No. 2004-117876, JP-A No. 2002-262880, etc. However, a compound having two or more partial structures represented by the following general formula (CLNM-1) is preferable.
The crosslinking agent is more preferably a compound having 2 to 8 partial structures represented by the general formula (CLNM-1).

In the general formula (CLNM-1),
R ^NM1 represents a hydrogen atom, an alkyl group, a cycloalkyl group or an oxoalkyl group.

In general formula (CLNM-1), the alkyl group of R ^NM1 is preferably an alkyl group having 1 to 6 carbon atoms, such as methyl, ethyl, propyl, isopropyl, butyl, isobutyl, t -A butyl group, a pentyl group, a hexyl group, etc. can be mentioned.
The cycloalkyl group of R ^NM1 is preferably a cycloalkyl group having 5 to 6 carbon atoms, and examples thereof include a cyclopentyl group and a cyclohexyl group.
The oxoalkyl group of R ^NM1 is preferably an oxoalkyl group having 3 to 6 carbon atoms, and examples thereof include a β-oxopropyl group, a β-oxobutyl group, a β-oxopentyl group, and a β-oxohexyl group. it can.

  As a more preferable embodiment of the compound having two or more partial structures represented by the general formula (CLNM-1), a urea-based crosslinking agent represented by the following general formula (CLNM-2), the following general formula (CLNM-3) , A glycoluril crosslinking agent represented by the following general formula (CLNM-4), and a melamine crosslinking agent represented by the following general formula (CLNM-5).

In the general formula (CLNM-2),
, Each R ^NM1 independently, are those in formula (CLNM-1) ^at, the same as ^{R NM1.}
R ^NM2 each independently represents a hydrogen atom, an alkyl group or a cycloalkyl group.

R ^NM2 alkyl group (preferably having 1 to 6 carbon atoms), cycloalkyl group (preferably having 5 to 6 carbon atoms), more specifically, methyl group, ethyl group, propyl group, isopropyl group, butyl group, Examples thereof include an isobutyl group, a t-butyl group, a pentyl group, a cyclopentyl group, a hexyl group, and a cyclohexyl group.

  Specific examples of the urea crosslinking agent represented by the general formula (CLNM-2) include, for example, N, N-di (methoxymethyl) urea, N, N-di (ethoxymethyl) urea, N, N-di (Propoxymethyl) urea, N, N-di (isopropoxymethyl) urea, N, N-di (butoxymethyl) urea, N, N-di (t-butoxymethyl) urea, N, N-di (cyclohexyloxy) And methyl) urea, N, N-di (cyclopentyloxymethyl) urea, N, N-di (adamantyloxymethyl) urea, N, N-di (norbornyloxymethyl) urea and the like.

In the general formula (CLNM-3),
, Each R ^NM1 independently, are those in formula (CLNM-1) ^at, the same as ^{R NM1.}
R ^NM3 each independently represents a hydrogen atom, a hydroxyl group, an alkyl group, a cycloalkyl group, an oxoalkyl group, an alkoxy group or an oxoalkoxy group.
G represents a single bond, an oxygen atom, a sulfur atom, an alkylene group or a carbonyl group.

R ^NM3 alkyl group (preferably having 1 to 6 carbon atoms), cycloalkyl group (preferably having 5 to 6 carbon atoms), oxoalkyl group (preferably having 3 to 6 carbon atoms), alkoxy group (having 1 to 6 carbon atoms) Oxoalkoxy group (preferably having 2 to 6 carbon atoms), more specifically, methyl group, ethyl group, propyl group, isopropyl group, butyl group, isobutyl group, t-butyl group, pentyl group, cyclopentyl Group, hexyl group, cyclohexyl group, β-oxopropyl group, β-oxobutyl group, β-oxopentyl group, β-oxohexyl group, methoxy group, ethoxy group, propyloxy group, isopropyloxy group, butoxy group, isobutoxy group Group, t-butoxy group, pentoxy group, hexyloxy group, β-oxopropoxy group, β-oxobutoxy group, β-oxo Ntokishi group, Kishirokishi group and the like to the β- oxo.
Specific examples of the alkylene group of G (preferably having 1 to 3 carbon atoms) include a methylene group, an ethylene group, a propylene group, a 1-methylethylene group, a hydroxymethylene group, and a cyanomethylene group.

  Specific examples of the alkylene urea crosslinking agent represented by the general formula (CLNM-3) include, for example, N, N-di (methoxymethyl) -4,5-di (methoxymethyl) ethylene urea, N, N- Di (ethoxymethyl) -4,5-di (ethoxymethyl) ethyleneurea, N, N-di (propoxymethyl) -4,5-di (propoxymethyl) ethyleneurea, N, N-di (isopropoxymethyl) -4,5-di (isopropoxymethyl) ethyleneurea, N, N-di (butoxymethyl) -4,5-di (butoxymethyl) ethyleneurea, N, N-di (t-butoxymethyl) -4 5-di (t-butoxymethyl) ethyleneurea, N, N-di (cyclohexyloxymethyl) -4,5-di (cyclohexyloxymethyl) ethyleneurea, N, N-di (cyclo Nthyloxymethyl) -4,5-di (cyclopentyloxymethyl) ethyleneurea, N, N-di (adamantyloxymethyl) -4,5-di (adamantyloxymethyl) ethyleneurea, N, N-di (nor Bornyloxymethyl) -4,5-di (norbornyloxymethyl) ethyleneurea and the like.

In the general formula (CLNM-4),
, Each R ^NM1 independently, are those in formula (CLNM-1) ^at, the same as ^{R NM1.}
R ^NM4 each independently represents a hydrogen atom, a hydroxyl group, an alkyl group, a cycloalkyl group or an alkoxy group.

R ^NM4 alkyl group (preferably having 1 to 6 carbon atoms), cycloalkyl group (preferably having 5 to 6 carbon atoms), alkoxy group (preferably having 1 to 6 carbon atoms), more specifically, methyl group, Examples include an ethyl group, a butyl group, a cyclopentyl group, a cyclohexyl group, a methoxy group, an ethoxy group, and a butoxy group.

  Specific examples of the glycoluril-based crosslinking agent represented by the general formula (CLNM-4) include, for example, N, N, N, N-tetra (methoxymethyl) glycoluril, N, N, N, N-tetra ( Ethoxymethyl) glycoluril, N, N, N, N-tetra (propoxymethyl) glycoluril, N, N, N, N-tetra (isopropoxymethyl) glycoluril, N, N, N, N-tetra (butoxy) Methyl) glycoluril, N, N, N, N-tetra (t-butoxymethyl) glycoluril, N, N, N, N-tetra (cyclohexyloxymethyl) glycoluril, N, N, N, N-tetra ( Cyclopentyloxymethyl) glycoluril, N, N, N, N-tetra (adamantyloxymethyl) glycoluril, N, N, N, N- Tiger (norbornyloxymethyl) glycoluril, and the like.

In the general formula (CLNM-5),
, Each R ^NM1 independently, are those in formula (CLNM-1) ^at, the same as ^{R NM1.}
R ^NM5 each independently represents a hydrogen atom, an alkyl group, a cycloalkyl group, an aryl group, or an atomic group represented by the following general formula (CLNM-5 ′).
R ^NM6 represents a hydrogen atom, an alkyl group, a cycloalkyl group, an aryl group, or an atomic group represented by the following general formula (CLNM-5 ″).

In the general formula (CLNM-5 ′),
R ^NM1 are those in formula (CLNM-1) ^at, the same as ^{R NM1.}
In the general formula (CLNM-5 ″),
R ^NM1 of the general formula are those (CLNM-1) in ^at, the same as ^{R NM1, R NM5} are those formula (CLNM-5) in the same manner as in ^{R NM5.}

Alkyl group R ^NM5 and ^{R NM6} (1 to 6 carbon atoms is preferred), cycloalkyl groups (5 to 6 carbon atoms is preferred), an aryl group (having 6 to 10 carbon atoms is preferred), and more specifically, Examples thereof include a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, an isobutyl group, a t-butyl group, a pentyl group, a cyclopentyl group, a hexyl group, a cyclohexyl group, a phenyl group, and a naphthyl group.

  Examples of the melamine crosslinking agent represented by the general formula (CLNM-5) include N, N, N, N, N, N-hexa (methoxymethyl) melamine, N, N, N, N, N, N Hexa (ethoxymethyl) melamine, N, N, N, N, N, N-hexa (propoxymethyl) melamine, N, N, N, N, N, N-hexa (isopropoxymethyl) melamine, N, N , N, N, N, N-hexa (butoxymethyl) melamine, N, N, N, N, N, N-hexa (t-butoxymethyl) melamine, N, N, N, N, N, N-hexa (Cyclohexyloxymethyl) melamine, N, N, N, N, N, N-hexa (cyclopentyloxymethyl) melamine, N, N, N, N, N, N-hexa (adamantyloxymethyl) melamine, N, N , N, N, N, N-hexa ( Rubornyloxymethyl) melamine, N, N, N, N, N, N-hexa (methoxymethyl) acetoguanamine, N, N, N, N, N, N-hexa (ethoxymethyl) acetoguanamine, N, N, N, N, N, N-hexa (propoxymethyl) acetoguanamine, N, N, N, N, N, N-hexa (isopropoxymethyl) acetoguanamine, N, N, N, N, N, N -Hexa (butoxymethyl) acetoguanamine, N, N, N, N, N, N-hexa (t-butoxymethyl) acetoguanamine, N, N, N, N, N, N-hexa (methoxymethyl) benzoguanamine, N, N, N, N, N, N-hexa (ethoxymethyl) benzoguanamine, N, N, N, N, N, N-hexa (propoxymethyl) benzoguanamine, N, N, N, N, N, N Hexa (isopropoxymethyl) benzoguanamine, N, N, N, N, N, N-hexa (butoxymethyl) benzoguanamine, N, N, N, N, N, N-hexa (t-butoxymethyl) benzoguanamine, etc. Can be mentioned.

The groups represented by R ^{NM1 to} R ^NM6 in the general formulas (CLNM-1) to (CLNM-5) may further have a substituent. Examples of the substituent that R ^{NM1 to} R ^NM6 may have include, for example, a halogen atom, a hydroxyl group, a nitro group, a cyano group, a carboxyl group, a cycloalkyl group (preferably having 3 to 20 carbon atoms), and an aryl group (preferably 6 to 14 carbon atoms), alkoxy group (preferably 1 to 20 carbon atoms), cycloalkoxy group (preferably 3 to 20 carbon atoms), acyl group (preferably 2 to 20 carbon atoms), acyloxy group (preferably carbon 2-20) etc. can be mentioned.

  In the present invention, the cross-linking agents may be used alone or in admixture of plural kinds. Among the urea-based cross-linking agents, alkylene urea-based cross-linking agents (preferably ethylene urea-based cross-linking agents), glycoluril-based cross-linking agents. It is preferable to use one or more of these, and it is more preferable to use one or more glycoluril-based crosslinking agents. In addition, other cross-linking agents can be used in combination as appropriate.

  In the present invention, the crosslinking agent is preferably contained in the total solid content of the negative resist composition in an amount of 1 to 50 mass%, more preferably 1.5 to 40 mass%, and more preferably 2 to 30 mass%. % Content is particularly preferable. By setting the content of the cross-linking agent to 1 to 50% by mass in the total solid content, the problem that the cross-linking is not sufficient and pattern formation is not possible, the sensitivity is lowered, and other than the exposure is performed. It is possible to solve the problem that the portion is also cross-linked and the amount of resin necessary for etching resistance cannot be secured.

(C1) Compound that promotes crosslinking reaction by irradiation with actinic ray or radiation In the negative resist composition of the present invention, a compound that promotes crosslinking reaction (acid-catalyzed crosslinking reaction) by irradiation with actinic ray or radiation (hereinafter photoacid) (Also referred to as a generator).
As a photoacid generator, a photoinitiator for photocationic polymerization, a photoinitiator for photoradical polymerization, a photodecoloring agent for dyes, a photochromic agent, or an actinic ray used for a microresist or the like Known compounds that generate an acid upon irradiation with radiation and mixtures thereof can be appropriately selected and used.

  Examples thereof include diazonium salts, phosphonium salts, sulfonium salts, iodonium salts, imide sulfonates, oxime sulfonates, diazodisulfones, disulfones, and o-nitrobenzyl sulfonates.

  Preferred compounds among the photoacid generators include compounds represented by the following general formulas (ZI), (ZII), and (ZIII).

In the general formula (ZI),
R ₂₀₁ , R ₂₀₂ and R ₂₀₃ each independently represents an organic group.
The carbon number of the organic group as R ₂₀₁ , R ₂₀₂ and R ₂₀₃ is generally 1-30, preferably 1-20.

Two of R _{201 to} R ₂₀₃ may be bonded to form a ring structure, and the ring may contain an oxygen atom, a sulfur atom, an ester bond, an amide bond, or a carbonyl group. The two of the group formed by bonding of the R ₂₀₁ to R _203, there can be mentioned an alkylene group (e.g., butylene, pentylene).
Z ⁻ represents a non-nucleophilic anion.

Examples of the non-nucleophilic anion as Z ⁻ include a sulfonate anion, a carboxylate anion, a sulfonylimide anion, a bis (alkylsulfonyl) imide anion, and a tris (alkylsulfonyl) methyl anion.
A non-nucleophilic anion is an anion that has an extremely low ability to cause a nucleophilic reaction, and is an anion that can suppress degradation over time due to an intramolecular nucleophilic reaction. This improves the temporal stability of the resist.
Examples of the sulfonate anion include an aliphatic sulfonate anion, an aromatic sulfonate anion, and a camphor sulfonate anion.

  Examples of the carboxylate anion include an aliphatic carboxylate anion, an aromatic carboxylate anion, and an aralkylcarboxylate anion.

  The aliphatic moiety in the aliphatic sulfonate anion may be an alkyl group or a cycloalkyl group, preferably an alkyl group having 1 to 30 carbon atoms and a cycloalkyl group having 3 to 30 carbon atoms such as methyl. Group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, sec-butyl group, pentyl group, neopentyl group, hexyl group, heptyl group, octyl group, nonyl group, decyl group, undecyl group, dodecyl group , Tridecyl group, tetradecyl group, pentadecyl group, hexadecyl group, heptadecyl group, octadecyl group, nonadecyl group, eicosyl group, cyclopropyl group, cyclopentyl group, cyclohexyl group, adamantyl group, norbornyl group, boronyl group and the like.

  The aromatic group in the aromatic sulfonate anion is preferably an aryl group having 6 to 14 carbon atoms, such as a phenyl group, a tolyl group, and a naphthyl group.

  The alkyl group, cycloalkyl group and aryl group in the aliphatic sulfonate anion and aromatic sulfonate anion may have a substituent. Examples of the substituent of the alkyl group, cycloalkyl group, and aryl group in the aliphatic sulfonate anion and aromatic sulfonate anion include, for example, a nitro group, a halogen atom (fluorine atom, chlorine atom, bromine atom, iodine atom), carboxyl group , Hydroxyl group, amino group, cyano group, alkoxy group (preferably having 1 to 15 carbon atoms), cycloalkyl group (preferably having 3 to 15 carbon atoms), aryl group (preferably having 6 to 14 carbon atoms), alkoxycarbonyl group ( Preferably 2 to 7 carbon atoms, acyl group (preferably 2 to 12 carbon atoms), alkoxycarbonyloxy group (preferably 2 to 7 carbon atoms), alkylthio group (preferably 1 to 15 carbon atoms), alkylsulfonyl group (Preferably 1 to 15 carbon atoms), alkyliminosulfonyl group (preferably 2 to 15 carbon atoms), ant Ruoxysulfonyl group (preferably having 6 to 20 carbon atoms), alkylaryloxysulfonyl group (preferably having 7 to 20 carbon atoms), cycloalkylaryloxysulfonyl group (preferably having 10 to 20 carbon atoms), alkyloxyalkyloxy group (Preferably having 5 to 20 carbon atoms), a cycloalkylalkyloxyalkyloxy group (preferably having 8 to 20 carbon atoms), and the like. About the aryl group and ring structure which each group has, an alkyl group (preferably C1-C15) can further be mentioned as a substituent.

  Examples of the aliphatic moiety in the aliphatic carboxylate anion include the same alkyl group and cycloalkyl group as in the aliphatic sulfonate anion.

  Examples of the aromatic group in the aromatic carboxylate anion include the same aryl group as in the aromatic sulfonate anion.

  The aralkyl group in the aralkyl carboxylate anion is preferably an aralkyl group having 6 to 12 carbon atoms, such as a benzyl group, a phenethyl group, a naphthylmethyl group, a naphthylethyl group, and a naphthylmethyl group.

  The alkyl group, cycloalkyl group, aryl group and aralkyl group in the aliphatic carboxylate anion, aromatic carboxylate anion and aralkylcarboxylate anion may have a substituent. Examples of the substituent of the alkyl group, cycloalkyl group, aryl group and aralkyl group in the aliphatic carboxylate anion, aromatic carboxylate anion and aralkylcarboxylate anion include, for example, the same halogen atom and alkyl as in the aromatic sulfonate anion Group, cycloalkyl group, alkoxy group, alkylthio group and the like.

  Examples of the sulfonylimide anion include saccharin anion.

  The alkyl group in the bis (alkylsulfonyl) imide anion and tris (alkylsulfonyl) methyl anion is preferably an alkyl group having 1 to 5 carbon atoms, such as a methyl group, an ethyl group, a propyl group, an isopropyl group, an n-butyl group, An isobutyl group, a sec-butyl group, a pentyl group, a neopentyl group, and the like can be given. Examples of substituents for these alkyl groups include halogen atoms, alkyl groups substituted with halogen atoms, alkoxy groups, alkylthio groups, alkyloxysulfonyl groups, aryloxysulfonyl groups, cycloalkylaryloxysulfonyl groups, and the like. Alkyl groups substituted with fluorine atoms are preferred.

  Examples of other non-nucleophilic anions include fluorinated phosphorus, fluorinated boron, and fluorinated antimony.

Examples of the non-nucleophilic anion of Z ⁻ include an aliphatic sulfonate anion in which the α-position of the sulfonic acid is substituted with a fluorine atom, an aromatic sulfonate anion substituted with a fluorine atom or a group having a fluorine atom, and an alkyl group. A bis (alkylsulfonyl) imide anion substituted with a fluorine atom and a tris (alkylsulfonyl) methide anion wherein an alkyl group is substituted with a fluorine atom are preferred. The non-nucleophilic anion is more preferably a perfluoroaliphatic sulfonic acid anion having 4 to 8 carbon atoms, a benzenesulfonic acid anion having a fluorine atom, still more preferably a nonafluorobutanesulfonic acid anion, a perfluorooctanesulfonic acid anion, It is a pentafluorobenzenesulfonic acid anion and 3,5-bis (trifluoromethyl) benzenesulfonic acid anion.
Examples of the organic group as R ₂₀₁ , R ₂₀₂ and R ₂₀₃ include the corresponding groups in the compounds (ZI-1), (ZI-2) and (ZI-3) described later.
In addition, the compound which has two or more structures represented by general formula (ZI) may be sufficient. For example, the general formula at least one of R ₂₀₁ to R ₂₀₃ of a compound represented by (ZI) is, at least one bond with structure of R ₂₀₁ to R ₂₀₃ of another compound represented by formula (ZI) It may be a compound.

  More preferable (ZI) components include compounds (ZI-1), (ZI-2), and (ZI-3) described below.

The compound (ZI-1) is at least one of the aryl groups R ₂₀₁ to R ₂₀₃ in formula (ZI), arylsulfonium compounds, namely, compounds containing an arylsulfonium as a cation.

In the arylsulfonium compound, all of R _{201 to} R ₂₀₃ may be an aryl group, or a part of R _{201 to} R ₂₀₃ may be an aryl group with the remaining being an alkyl group or a cycloalkyl group.

Examples of the arylsulfonium compound include triarylsulfonium compounds, diarylalkylsulfonium compounds, aryldialkylsulfonium compounds, diarylcycloalkylsulfonium compounds, and aryldicycloalkylsulfonium compounds.
The aryl group of the arylsulfonium compound is preferably a phenyl group or a naphthyl group, and more preferably a phenyl group. The aryl group may be an aryl group having a heterocyclic structure having an oxygen atom, a nitrogen atom, a sulfur atom or the like. Examples of the aryl group having a heterocyclic structure include a pyrrole residue (a group formed by losing one hydrogen atom from pyrrole) and a furan residue (a group formed by losing one hydrogen atom from furan). Groups), thiophene residues (groups formed by the loss of one hydrogen atom from thiophene), indole residues (groups formed by the loss of one hydrogen atom from indole), benzofuran residues ( A group formed by losing one hydrogen atom from benzofuran), a benzothiophene residue (a group formed by losing one hydrogen atom from benzothiophene), and the like. When the arylsulfonium compound has two or more aryl groups, the two or more aryl groups may be the same or different.

  The alkyl group or cycloalkyl group that the arylsulfonium compound has as necessary is preferably a linear or branched alkyl group having 1 to 15 carbon atoms and a cycloalkyl group having 3 to 15 carbon atoms, such as a methyl group, Examples thereof include an ethyl group, a propyl group, an n-butyl group, a sec-butyl group, a t-butyl group, a cyclopropyl group, a cyclobutyl group, and a cyclohexyl group.

Aryl group, alkyl group of R ₂₀₁ to R _203, cycloalkyl group, an alkyl group (for example, 1 to 15 carbon atoms), a cycloalkyl group (for example, 3 to 15 carbon atoms), an aryl group (for example, 6 to 14 carbon atoms) , An alkoxy group (for example, having 1 to 15 carbon atoms), a halogen atom, a hydroxyl group, or a phenylthio group may be substituted. Preferred substituents are linear or branched alkyl groups having 1 to 12 carbon atoms, cycloalkyl groups having 3 to 12 carbon atoms, and linear, branched or cyclic alkoxy groups having 1 to 12 carbon atoms, more preferably carbon. These are an alkyl group having 1 to 4 carbon atoms and an alkoxy group having 1 to 4 carbon atoms. The substituent may be substituted with any one of the three R _{201 to} R ₂₀₃ , or may be substituted with all three. When R _{201 to} R ₂₀₃ are an aryl group, the substituent is preferably substituted at the p-position of the aryl group.

Next, the compound (ZI-2) will be described.
Compound (ZI-2) is a compound in which R _{201 to} R ₂₀₃ in formula (ZI) each independently represents an organic group having no aromatic ring. Here, the aromatic ring includes an aromatic ring containing a hetero atom.

The organic group having no aromatic ring as R ₂₀₁ to R ₂₀₃ generally has 1 to 30 carbon atoms, preferably 1 to 20 carbon atoms.

R _{201 to} R ₂₀₃ are each independently preferably an alkyl group, a cycloalkyl group, an allyl group, or a vinyl group, more preferably a linear or branched 2-oxoalkyl group, 2-oxocycloalkyl group, alkoxy group. A carbonylmethyl group, particularly preferably a linear or branched 2-oxoalkyl group.

The alkyl group and cycloalkyl group of R ₂₀₁ to R _203, preferably a linear or branched alkyl group having 1 to 10 carbon atoms (e.g., methyl group, ethyl group, propyl group, butyl group, pentyl group), carbon Examples thereof include cycloalkyl groups of several 3 to 10 (cyclopentyl group, cyclohexyl group, norbornyl group). More preferred examples of the alkyl group include a 2-oxoalkyl group and an alkoxycarbonylmethyl group. More preferred examples of the cycloalkyl group include a 2-oxocycloalkyl group.

The 2-oxoalkyl group may be either linear or branched, and a group having> C = O at the 2-position of the above alkyl group is preferable.
The 2-oxocycloalkyl group is preferably a group having> C═O at the 2-position of the cycloalkyl group.

  The alkoxy group in the alkoxycarbonylmethyl group is preferably an alkoxy group having 1 to 5 carbon atoms (methoxy group, ethoxy group, propoxy group, butoxy group, pentoxy group).

R _{201 to} R ₂₀₃ may be further substituted with a halogen atom, an alkoxy group (for example, having 1 to 5 carbon atoms), a hydroxyl group, a cyano group, or a nitro group.

  The compound (ZI-3) is a compound represented by the following general formula (ZI-3), and is a compound having a phenacylsulfonium salt structure.

In general formula (ZI-3),
R _{1c to} R _5c each independently represents a hydrogen atom, an alkyl group, a cycloalkyl group, an alkoxy group or a halogen atom.
R _6c and R _7c each independently represents a hydrogen atom, an alkyl group or a cycloalkyl group.
R _x and R _y each independently represents an alkyl group, a cycloalkyl group, an allyl group or a vinyl group.

Any two or more of R _{1c to} R _5c , R _6c and R _7c , and R _x and R _y may be bonded to each other to form a ring structure, and this ring structure includes an oxygen atom and a sulfur atom. , An ester bond and an amide bond may be included. Examples of the group formed by combining any two or more of R _{1c to} R _5c , R _6c and R _7c , and R _x and R _y include a butylene group and a pentylene group.

Zc ⁻ represents a non-nucleophilic anion, and examples thereof include the same non-nucleophilic anion as Z ^{− in} formula (ZI).

The alkyl group as R _{1c to} R _7c may be either linear or branched, for example, an alkyl group having 1 to 20 carbon atoms, preferably a linear or branched alkyl group having 1 to 12 carbon atoms ( Examples thereof include a methyl group, an ethyl group, a linear or branched propyl group, a linear or branched butyl group, and a linear or branched pentyl group. Examples of the cycloalkyl group include cyclohexane having 3 to 8 carbon atoms. An alkyl group (for example, a cyclopentyl group, a cyclohexyl group) can be mentioned.

The alkoxy group as R _{1c to} R _{5c may} be linear, branched or cyclic, for example, an alkoxy group having 1 to 10 carbon atoms, preferably a linear or branched alkoxy group having 1 to 5 carbon atoms. (For example, methoxy group, ethoxy group, linear or branched propoxy group, linear or branched butoxy group, linear or branched pentoxy group), C3-C8 cyclic alkoxy group (for example, cyclopentyloxy group, cyclohexyloxy group) ).

Preferably, any of R _{1c to} R _5c is a linear or branched alkyl group, a cycloalkyl group, or a linear, branched or cyclic alkoxy group, and more preferably the sum of the carbon number of R _{1c to} R _5c. Is 2-15. Thereby, solvent solubility improves more and generation | occurrence | production of a particle is suppressed at the time of a preservation | save.

_Examples of the alkyl group and cycloalkyl group as R _x and R _y include the same alkyl group and cycloalkyl group as in R _{1c to} R _7c , such as a 2-oxoalkyl group, a 2-oxocycloalkyl group, an alkoxy group. A carbonylmethyl group is more preferred.

Examples of the 2-oxoalkyl group and 2-oxocycloalkyl group include a group having> C═O at the 2-position of the alkyl group or cycloalkyl group as R _{1c to} R _7c .

Examples of the alkoxy group in the alkoxycarbonylmethyl group include the same alkoxy groups as in R _{1c to} R _5c .

R _x and R _y are preferably an alkyl group or cycloalkyl group having 4 or more carbon atoms, more preferably 6 or more, and still more preferably 8 or more alkyl groups or cycloalkyl groups.

In general formulas (ZII) and (ZIII),
R ₂₀₄ to R ₂₀₇ each independently represents an aryl group, an alkyl group or a cycloalkyl group.

Phenyl group and a naphthyl group are preferred as the aryl group of R ₂₀₄ to R _207, more preferably a phenyl group. Aryl group R ₂₀₄ to R ₂₀₇ represents an oxygen atom, a nitrogen atom, may be an aryl group having a heterocyclic structure having a sulfur atom and the like. Examples of the aryl group having a heterocyclic structure include a pyrrole residue (a group formed by losing one hydrogen atom from pyrrole) and a furan residue (a group formed by losing one hydrogen atom from furan). Groups), thiophene residues (groups formed by the loss of one hydrogen atom from thiophene), indole residues (groups formed by the loss of one hydrogen atom from indole), benzofuran residues ( A group formed by losing one hydrogen atom from benzofuran), a benzothiophene residue (a group formed by losing one hydrogen atom from benzothiophene), and the like.

The alkyl group and cycloalkyl group in R ₂₀₄ to R _207, preferably a linear or branched alkyl group having 1 to 10 carbon atoms (e.g., methyl group, ethyl group, propyl group, butyl group, pentyl group), carbon Examples thereof include cycloalkyl groups of several 3 to 10 (cyclopentyl group, cyclohexyl group, norbornyl group).

Aryl group, alkyl group of R ₂₀₄ to R _207, cycloalkyl groups may have a substituent. Aryl group, alkyl group of R ₂₀₄ to R _207, the cycloalkyl group substituent which may be possessed by, for example, an alkyl group (for example, 1 to 15 carbon atoms), a cycloalkyl group (for example, 3 to 15 carbon atoms ), An aryl group (for example, having 6 to 15 carbon atoms), an alkoxy group (for example, having 1 to 15 carbon atoms), a halogen atom, a hydroxyl group, and a phenylthio group.

Z ⁻ represents a non-nucleophilic anion, and examples thereof include the same as the non-nucleophilic anion of Z ^{− in} formula (ZI).

  Examples of the photoacid generator further include compounds represented by the following general formula (ZIV) or (ZV).

In the general formulas (ZIV) and (ZV),
Ar ₃ and Ar ₄ each independently represents an aryl group.
R ₂₀₈ represents an alkyl group, a cycloalkyl group, or an aryl group.
A represents an alkylene group, an alkenylene group or an arylene group.

Among the photoacid generators, compounds represented by the general formulas (ZI) to (ZIII) are more preferable.
Further, as the photoacid generator, a compound that generates an acid having one sulfonic acid group or imide group is preferable, more preferably a compound that generates monovalent perfluoroalkanesulfonic acid, or a monovalent fluorine atom or fluorine. A compound that generates an aromatic sulfonic acid substituted with a group containing an atom, or a compound that generates an imide acid substituted with a monovalent fluorine atom or a group containing a fluorine atom. And a sulfonium salt of fluorine-substituted benzenesulfonic acid, fluorine-substituted imide acid or fluorine-substituted methide acid. The photoacid generator that can be used is particularly preferably a fluorinated substituted alkane sulfonic acid, a fluorinated substituted benzene sulfonic acid, or a fluorinated substituted imido acid whose pKa of the generated acid is pKa = -1 or less, and the sensitivity is improved. To do.

The acid generator is preferably a compound that generates an acid having a pKa of −8 or less upon irradiation with actinic rays or radiation.
The acid generator is more preferably a compound that generates an acid having a pKa of -8 to -20 by irradiation with actinic rays or radiation, and a pKa of -10 to -20 by irradiation with actinic rays or radiation. A compound that generates an acid is even more preferable, and a compound that generates an acid having a pKa of -15 to -20 by irradiation with actinic rays or radiation is particularly preferable.
In the present invention, pKa represents the acid dissociation index pKa in an aqueous solution, and “acid dissociation index” is a logarithm of the reciprocal of the acid dissociation constant. 1993, edited by The Chemical Society of Japan, Maruzen Co., Ltd.), the lower this value, the greater the acid strength. Specifically, the acid dissociation index pKa in an aqueous solution can be actually measured by measuring an acid dissociation constant at 25 ° C. using an infinitely diluted aqueous solution, and using the following software package 1, Hammett's Values based on a substituent constant and a database of known literature values can also be obtained by calculation. The values of pKa described in this specification all indicate values obtained by calculation using this software package.
Software package 1: Advanced Chemistry Development (ACD / Labs) Software V8.14 for Solaris (1994-2007 ACD / Labs)

  Preferred compounds among the photoacid generators include compounds represented by the following general formulas (ZIa) and (ZIIa).

In the general formulas (ZIa) and (ZIIa),
R ₂₀₁ , R ₂₀₂ and R ₂₀₃ each independently represents an organic group.
The carbon number of the organic group as R ₂₀₁ , R ₂₀₂ and R ₂₀₃ is generally 1-30, preferably 1-20.
Two of R _{201 to} R ₂₀₃ may be bonded to form a ring structure, and the ring may contain an oxygen atom, a sulfur atom, an ester bond, an amide bond, or a carbonyl group. The two of the group formed by bonding of the R ₂₀₁ to R _203, there can be mentioned an alkylene group (e.g., butylene, pentylene).
R _201, R ₂₀₂ and R ₂₀₃ is in the general formula (ZI), is the same as the R _201, R ₂₀₂ and R _203.
R204 and _R205 each independently represents an aryl group, an alkyl group or a cycloalkyl group.
R ₂₀₄ and R ₂₀₅ in the general formula (ZII), is the same as the R ₂₀₄ and R _205.
Za ⁻ represents an anion of an acid having a pKa of −8 or less.

  The acid having a pKa of −8 or less is preferably a fluorinated sulfonimide acid or a fluorinated sulfonemethide acid, and more preferably represented by the following general formula (II) or (III).

In general formula (II):
R ₁ and R ₂ each independently represents a fluorine atom or an alkyl group. R ₁ and R ₂ may combine with each other to form a ring.

In general formula (III):
R _{3 to} R ₅ each independently represents a fluorine atom or an alkyl group. Any two of R _{3 to} R ₅ may be bonded to each other to form a ring.

In general formulas (II) and (III), the alkyl groups of R ₁ and R ₂ are preferably alkyl groups having 1 to 5 carbon atoms.
The alkyl group of R ₁ and R ₂ may be further substituted with a fluorine atom, a cycloalkyl group-arylene group-O—SO ₂ — group, a halogen atom —SO ₂ — group or the like.
When R ₁ and R ₂ are bonded to each other to form a ring, the group formed by combining R ₁ and R ₂ with each other is preferably an alkylene group having 1 to 5 carbon atoms, such as a fluorine atom May be substituted.
It is preferable that the alkyl group of R < ₃ > -R < ₅ > is a C1-C5 alkyl group.
The alkyl group of R _{3 to} R ₅ may be further substituted with a fluorine atom, a cycloalkyl group-arylene group-O—SO ₂ — group, a halogen atom —SO ₂ — group or the like.
When any of R _{3 to} R ₅ is bonded to each other to form a ring, the group formed by bonding any of R _{3 to} R ₅ to each other is alkylene having 1 to 5 carbon atoms. It is preferably a group, and may be substituted with a fluorine atom or the like.

  Among photoacid generators, particularly preferred examples are given below.

A photo-acid generator can be used individually by 1 type or in combination of 2 or more types.
The content of the photoacid generator in the negative resist composition is preferably 0.1 to 20% by mass, more preferably 0.5 to 10% by mass, based on the total solid content of the negative resist composition. Preferably it is 1-7 mass%.

(C2) Photoradical generator The photoradical generator contained in the negative resist composition used in the present invention is a compound that initiates a polymerization reaction upon irradiation with actinic rays or radiation (hereinafter also referred to as a photoradical polymerization initiator). is there.
The radical photopolymerization initiator is a compound that is decomposed by light and initiates and accelerates the polymerization of the compound (D) having a radical polymerizable group, and preferably has absorption in a wavelength region of 150 to 500 nm. Photo radical polymerization initiators include, for example, organic halogenated compounds, oxydiazole compounds, carbonyl compounds, ketal compounds, benzoin compounds, acridine compounds, organic peroxide compounds, azo compounds, coumarin compounds, azide compounds, metallocene compounds, hexaaryls. Examples include rubiimidazole compounds, organic boric acid compounds, disulfonic acid compounds, oxime ester compounds, onium salt compounds, and acylphosphine (oxide) compounds. These radical photopolymerization initiators can be used alone or in combination of two or more.

  Specific examples of the organic halogenated compound include Wakabayashi et al., “Bull Chem. Soc Japan” 42, 2924 (1969), US Pat. No. 3,905,815, Japanese Patent Publication No. 46-4605, JP 48-36281, JP 55-3070, JP 60-239736, JP 61-169835, JP 61-169837, JP 62-58241, JP 62 -212401, JP-A-63-70243, JP-A-63-298339, M.S. P. Hutt “Journal of Heterocyclic Chemistry” 1 (No 3), (1970) ”, and the oxazole compound and s-triazine compound substituted with a trihalomethyl group.

  More preferred examples of the s-triazine compound include s-triazine derivatives in which at least one mono, di, or trihalogen-substituted methyl group is bonded to the s-triazine ring. More specifically, for example, 2,4,6-tris (monochloromethyl) -s-triazine, 2,4,6-tris (dichloromethyl) -s-triazine, 2,4,6-tris (trichloromethyl) -S-triazine, 2-methyl-4,6-bis (trichloromethyl) -s-triazine, 2-n-propyl-4,6-bis (trichloromethyl) -s-triazine, 2- (α, α, β-trichloroethyl) -4,6-bis (trichloromethyl) -s-triazine, 2-phenyl-4,6-bis (trichloromethyl) -s-triazine, 2- (p-methoxyphenyl) -4,6 -Bis (trichloromethyl) -s-triazine, 2- (3,4-epoxyphenyl) -4,6-bis (trichloromethyl) -s-triazine, 2- (p-chlorophenyl) -4,6 Bis (trichloromethyl) -s-triazine, 2- [1- (p-methoxyphenyl) -2,4-butadienyl] -4,6-bis (trichloromethyl) -s-triazine, 2-styryl-4,6 -Bis (trichloromethyl) -s-triazine, 2- (p-methoxystyryl) -4,6-bis (trichloromethyl) -s-triazine, 2- (pi-propyloxystyryl) -4,6- Bis (trichloromethyl) -s-triazine, 2- (p-tolyl) -4,6-bis (trichloromethyl) -s-triazine, 2- (4-natoxynaphthyl) -4,6-bis (trichloromethyl)- s-triazine, 2-phenylthio-4,6-bis (trichloromethyl) -s-triazine, 2-benzylthio-4,6-bis (trichloromethyl) -s-tri Gin, 2,4,6-tris (dibromomethyl) -s-triazine, 2,4,6-tris (tribromomethyl) -s-triazine, 2-methyl-4,6-bis (tribromomethyl)- and s-triazine, 2-methoxy-4,6-bis (tribromomethyl) -s-triazine, and the like.

  Examples of the oxydiazole compound include 2-trichloromethyl-5-styryl-1,3,4-oxodiazole, 2-trichloromethyl-5- (cyanostyryl) -1,3,4-oxodiazole, 2- Examples include trichloromethyl-5- (naphth-1-yl) -1,3,4-oxodiazole, 2-trichloromethyl-5- (4-styryl) styryl-1,3,4-oxodiazole, and the like. .

  Examples of the carbonyl compound include benzophenone, Michler ketone, 2-methylbenzophenone, 3-methylbenzophenone, 4-methylbenzophenone, 2-chlorobenzophenone, 4-bromobenzophenone, 2-carboxybenzophenone and other benzophenone derivatives, 2,2-dimethoxy-2 -Phenylacetophenone, 2,2-diethoxyacetophenone, 1-hydroxycyclohexyl phenylketone, α-hydroxy-2-methylphenylpropanone, 1-hydroxy-1-methylethyl- (p-isopropylphenyl) ketone, 1-hydroxy -1- (p-dodecylphenyl) ketone, 2-methyl- (4 ′-(methylthio) phenyl) -2-morpholino-1-propanone, 1,1,1-trichloromethyl- (p-butylphenyl) , Acetophenone derivatives such as 2-benzyl-2-dimethylamino-4-morpholinobutyrophenone, thioxanthone, 2-ethylthioxanthone, 2-isopropylthioxanthone, 2-chlorothioxanthone, 2,4-dimethylthioxanthone, 2,4-diethylthioxanthone Thioxanthone derivatives such as 2,4-diisopropylthioxanthone, and benzoic acid ester derivatives such as ethyl p-dimethylaminobenzoate and ethyl p-diethylaminobenzoate.

  Examples of the ketal compound include benzyl methyl ketal and benzyl-β-methoxyethyl ethyl acetal.

  Examples of the benzoin compound include mbenzoin isopropyl ether, benzoin isobutyl ether, benzoin methyl ether, methyl o-benzoylbenzoate, and the like.

  Examples of the acridine compound include 9-phenylacridine, 1,7-bis (9-acridinyl) heptane, and the like.

  Examples of the organic peroxide compound include trimethylcyclohexanone peroxide, acetylacetone peroxide, 1,1-bis (tert-butylperoxy) -3,3,5-trimethylcyclohexane, 1,1-bis (tert-butylperoxide). Oxy) cyclohexane, 2,2-bis (tert-butylperoxy) butane, tert-butyl hydroperoxide, cumene hydroperoxide, diisopropylbenzene hydroperoxide, 2,5-dimethylhexane-2,5-dihydroper Oxide, 1,1,3,3-tetramethylbutyl hydroperoxide, tert-butylcumyl peroxide, dicumyl peroxide, 2,5-dimethyl-2,5-di (tert-butylperoxy) hexane, 2 , -Oxanoyl peroxide, succinic peroxide, benzoyl peroxide, 2,4-dichlorobenzoyl peroxide, diisopropyl peroxydicarbonate, di-2-ethylhexyl peroxydicarbonate, di-2-ethoxyethyl peroxydicarbonate , Dimethoxyisopropyl peroxycarbonate, di (3-methyl-3-methoxybutyl) peroxydicarbonate, tert-butyl peroxyacetate, tert-butyl peroxypivalate, tert-butyl peroxyneodecanoate, tert- Butyl peroxyoctanoate, tert-butyl peroxylaurate, tersyl carbonate, 3,3 ′, 4,4′-tetra- (t-butylperoxycarbonyl) benzophenone, 3,3 ′, 4 '-Tetra- (t-hexylperoxycarbonyl) benzophenone, 3,3', 4,4'-tetra- (p-isopropylcumylperoxycarbonyl) benzophenone, carbonyldi (t-butylperoxydihydrogen diphthalate) , Carbonyldi (t-hexylperoxydihydrogen diphthalate) and the like.

  Examples of the azo compound include azo compounds described in JP-A-8-108621.

  Examples of the coumarin compound include 3-methyl-5-amino-((s-triazin-2-yl) amino) -3-phenylcoumarin, 3-chloro-5-diethylamino-((s-triazin-2-yl). ) Amino) -3-phenylcoumarin, 3-butyl-5-dimethylamino-((s-triazin-2-yl) amino) -3-phenylcoumarin, and the like.

  Examples of the azide compound include organic azide compounds described in U.S. Pat. No. 2,848,328, U.S. Pat. No. 2,852,379 and U.S. Pat. No. 2,940,553, 2,6-bis (4-azidobenzylidene) -4-ethyl. And cyclohexanone (BAC-E).

  Examples of the metallocene compound include JP-A-59-152396, JP-A-61-151197, JP-A-63-41484, JP-A-2-249, JP-A-2-4705, Various titanocene compounds described in JP-A-5-83588, such as di-cyclopentadienyl-Ti-bis-phenyl, di-cyclopentadienyl-Ti-bis-2,6-difluorophen-1-yl, di -Cyclopentadienyl-Ti-bis-2,4-di-fluorophen-1-yl, di-cyclopentadienyl-Ti-bis-2,4,6-trifluorophen-1-yl, di- Cyclopentadienyl-Ti-bis-2,3,5,6-tetrafluorophen-1-yl, di-cyclopentadienyl-Ti-bis-2,3,4,5,6-pentaful Lophen-1-yl, di-methylcyclopentadienyl-Ti-bis-2,6-difluorophen-1-yl, di-methylcyclopentadienyl-Ti-bis-2,4,6-trifluoropheny -1-yl, di-methylcyclopentadienyl-Ti-bis-2,3,5,6-tetrafluorophen-1-yl, di-methylcyclopentadienyl-Ti-bis-2,3,4 , 5,6-pentafluorophen-1-yl, iron-arene complexes described in JP-A-1-304453 and JP-A-1-152109, and the like.

As the biimidazole compound, for example, a hexaarylbiimidazole compound (rophine dimer compound) is preferable.
Examples of the hexaarylbiimidazole compound include lophine dimers described in JP-B-45-37377 and JP-B-44-86516, JP-B-6-29285, U.S. Pat. No. 3,479,185, and the like. Various compounds described in each specification such as 4,311,783 and 4,622,286, specifically, 2,2′-bis (o-chlorophenyl) -4,4 ′, 5,5′-tetraphenylbiimidazole, 2,2′-bis (o-bromophenyl)) 4,4 ′, 5,5′-tetraphenylbiimidazole, 2,2′-bis (o, p-dichlorophenyl) ) -4,4 ′, 5,5′-tetraphenylbiimidazole, 2,2′-bis (o-chlorophenyl) -4,4 ′, 5,5′-tetra (m-methoxyphenyl) vididazole, 2, 2'-bis (o , O′-dichlorophenyl) -4,4 ′, 5,5′-tetraphenylbiimidazole, 2,2′-bis (o-nitrophenyl) -4,4 ′, 5,5′-tetraphenylbiimidazole, 2,2′-bis (o-methylphenyl) -4,4 ′, 5,5′-tetraphenylbiimidazole, 2,2′-bis (o-trifluorophenyl) -4,4 ′, 5,5 Examples include '-tetraphenylbiimidazole.

  Examples of the organic borate compound include JP-A-62-143044, JP-A-62-1050242, JP-A-9-188585, JP-A-9-188686, JP-A-9-188710, JP-A-2000. -131837, Japanese Patent Application Laid-Open No. 2002-107916, Japanese Patent No. 2764769, Japanese Patent Application No. 2000-310808, and Kunz, Martin “Rad Tech'98. Proceeding April 19-22, 1998, Chicago”. The organic borate described in JP-A-6-157623, JP-A-6-175564, JP-A-6-175561, or organic boron oxosulfonium complex, JP-A-6-175554 No. 6, JP-A-6-175553 The organic boron iodonium complex described in JP-A-9-188710, the organic boron phosphonium complex described in JP-A-9-188710, JP-A-6-348011, JP-A-7-128785, JP-A-7-140589, JP-A-7- Specific examples include organoboron transition metal coordination complexes such as those described in Japanese Patent No. 306527 and Japanese Patent Laid-Open No. 7-292014.

  Examples of the disulfone compound include compounds described in JP-A No. 61-166544 and Japanese Patent Application No. 2001-132318.

  Examples of oxime ester compounds include J.M. C. S. Perkin II (1979) 1653-1660), J. MoI. C. S. Perkin II (1979) 156-162, Journal of Photopolymer Science and Technology (1995) 202-232, JP-A 2000-66385, compounds described in JP-A 2000-80068, JP-T 2004-534797 Compounds and the like.

  Examples of onium salt compounds include S.I. I. Schlesinger, Photogr. Sci. Eng. 18, 387 (1974), T .; S. Bal et al, Polymer, 21, 423 (1980), diazonium salts described in U.S. Pat. No. 4,069,055, ammonium salts described in JP-A-4-365049, U.S. Pat. No. 4,069, No. 055, No. 4,069,056, phosphonium salts described in European Patent Nos. 104 and 143, U.S. Pat. Nos. 339,049 and 410,201, JP Examples include iodonium salts described in JP-A No. -150848 and JP-A-2-296514.

  The iodonium salt that can be suitably used in the present invention is a diaryl iodonium salt, and is preferably substituted with two or more electron donating groups such as an alkyl group, an alkoxy group, and an aryloxy group from the viewpoint of stability. . Further, as other preferable forms of the sulfonium salt, an iodonium salt in which one substituent of the triarylsulfonium salt has a coumarin or an anthraquinone structure is preferable.

  Examples of the sulfonium salt that can be suitably used in the present invention include European Patent Nos. 370,693, 390,214, 233,567, 297,443, 297,442, and U.S. Pat. 933,377, 161,811, 410,201, 339,049, 4,760,013, 4,734,444, 2,833,827, Germany Examples thereof include sulfonium salts described in the specifications of Patent Nos. 2,904,626, 3,604,580, and 3,604,581, and are preferably electron withdrawing groups from the viewpoint of stability. It is preferably substituted. The electron withdrawing group preferably has a Hammett value greater than zero. Preferred electron-withdrawing groups include halogen atoms and carboxylic acids.

  Moreover, as an onium salt compound, J.M. V. Crivello et al, Macromolecules, 10 (6), 1307 (1977), J. MoI. V. Crivello et al, J.A. Polymer Sci. , Polymer Chem. Ed. , 17, 1047 (1979), a selenonium salt described in C.I. S. Wen et al, Teh, Proc. Conf. Rad. Curing ASIA, p478 Tokyo, Oct (1988), and onium salts such as arsonium salts.

  Examples of the acylphosphine (oxide) compound include Irgacure 819, Darocur 4265, Darocur TPO and the like manufactured by Ciba Specialty Chemicals.

  As a radical photopolymerization initiator used in the present invention, from the viewpoint of exposure sensitivity, a trihalomethyltriazine compound, a benzyldimethyl ketal compound, an α-hydroxyketone compound, an α-aminoketone compound, an acylphosphine compound, a phosphine oxide system Compound, metallocene compound, oxime compound, triallylimidazole dimer, onium compound, benzothiazole compound, benzophenone compound, acetophenone compound and derivatives thereof, cyclopentadiene-benzene-iron complex and salt thereof, halomethyloxadiazole Compounds selected from the group consisting of compounds and 3-aryl substituted coumarin compounds are preferred. More preferred are trihalomethyltriazine compounds, α-aminoketone compounds, acylphosphine compounds, phosphine oxide compounds, oxime compounds, triallylimidazole dimers, onium compounds, benzophenone compounds, acetophenone compounds, and trihalo compounds. Particularly preferred is at least one compound selected from the group consisting of a methyltriazine compound, an α-aminoketone compound, an oxime compound, a triallylimidazole dimer, and an onium compound.

  On the other hand, when the photo radical polymerization initiator is used in a resist composition, it is necessary to develop a fine unexposed portion without residue with a curability in order to form a fine pattern with a good shape. . Further, a photo radical polymerization initiator that does not generate an out gas that may damage the exposure machine due to the possibility that the out gas generated by the decomposition of the photo radical polymerization initiator during the exposure may damage the exposure machine is preferable. In view of these points, the radical photopolymerization initiator used in the resist composition is preferably an α-aminoketone compound, an oxime compound, a triallylimidazole dimer, or an onium compound, and particularly preferably an oxime compound or onium. System compounds (sulfonium salt compounds or iodonium compounds are preferred).

The radical photopolymerization initiator contained in the resist composition of the present invention is preferably 0.1 to 50% by mass, more preferably 0.5 to 30% by mass, based on the total solid content of the resist composition. More preferably, it is 1-20 mass%.
A radical photopolymerization initiator can be used individually by 1 type or in combination of 2 or more types.

  The radical photopolymerization initiator used in the present invention is preferably an oxime compound represented by the following general formula (IO-1) or a sulfonium salt compound represented by the following general formula (IS-1).

In formula (IO-1), R ^{O1 to} R ^O3 each independently represent a hydrogen atom or an organic group, and at least one of R ^O2 to R ^O3 is preferably an organic group having an aromatic group.

R ^O1 is preferably an organic group, more preferably a group having a carbonyl group or a sulfonyl group, and the compound represented by the formula (IO-1) being a carboxylic acid ester or a sulfonic acid ester. Preferred examples of R ^O1 include an alkylcarbonyl group, a cycloalkylcarbonyl group, and an arylcarbonyl group, which may contain a hetero atom such as an oxygen atom, a sulfur atom, or a nitrogen atom in the structure. It may also have a substituent.
As an alkyl group, a C1-C20 linear or branched alkyl group is mentioned, Preferably it is C1-C10. Examples of the cycloalkyl group include monocyclic or polycyclic alkyl groups having 3 to 30 carbon atoms, and more preferably 5 to 12 carbon atoms. The aryl group is preferably an aromatic ring structure having 6 to 30 carbon atoms. Moreover, a hetero atom may be included in the ring structure.
Examples of the substituent include a halogen atom, (cyclo) alkyl group, (cyclo) alkoxy group, (cyclo) alkoxycarbonyl group, (cyclo) alkylcarbonyloxy group, (cyclo) alkylamino group, (cyclo) alkylamide group, ( A cyclo) alkylthio group, a (cyclo) alkylsulfonyl group, an aryl group, an aryloxy group, an aryloxycarbonyl group, an arylcarbonyloxy group, and the like.

R ^O2 and R ^O3 are preferably organic groups, and at least one of them is preferably an organic group having an aromatic group. The organic group may have a substituent.
As the organic group, (cyclo) alkyl group, (cyclo) alkoxy group, aryl group, cyano group, nitro group, hydroxyl group, (cyclo) alkylcarbonyl group, (cyclo) alkylcarbonyloxy group, (cyclo) alkoxycarbonyl group, (Cyclo) alkylthio group, and the like.
Substituents include halogen atoms, alkyl groups, alkoxy groups, alkoxycarbonyl groups, alkylcarbonyloxy groups, alkylamino groups, alkylamide groups, alkylthio groups, alkylsulfonyl groups, cycloalkyl groups, cycloalkoxy groups, cycloalkoxycarbonyl groups. Cycloalkylcarbonyloxy group, cycloalkylamino group, cycloalkylamide group, cycloalkylthio group, cycloalkylsulfonyl group, aryl group, aryloxy group, aryloxycarbonyl group, arylcarbonyloxy group, and the like.

In formula (IS-1), R ^{S1 to} R ^S3 each independently represents an organic group which may have a substituent, and A ^S- represents an anion.

R ^{S1 to} R ^S3 have 1 to 30 carbon atoms, preferably 1 to 20 carbon atoms. Two of R ^{S1 to} R ^S3 may be bonded to form a ring structure, and the ring structure includes an oxygen atom, a sulfur atom, a nitrogen atom, an ether bond, an ester bond, an amide bond, and a carbonyl structure. May be. Examples of the group formed by combining two of R ^{S1 to} R ^S3 include an alkylene (eg, butylene, pentylene, hexylene) group. Examples of R ^{S1 to} R ^S3 include corresponding groups in the compounds (IS-2) to (IS-4) described later.
The radical photopolymerization initiator used in the present invention may be a compound having a plurality of structures represented by the formula (IS-1). That is, for example, it may be a compound in which at least one of R ^{S1 to} R ^S3 is bonded to another structure represented by the formula (IS-1).

A preferable embodiment of the compound represented by the formula (IS-1) includes an arylsulfonium compound (IS-2) in which at least one of R ^{S1 to} R ^S3 is an aryl group. In the arylsulfonium compound (IS-2), all of R ^{S1 to} R ^S3 may be an aryl group, a part thereof may be an aryl group, and the rest may be an alkyl group or a cycloalkyl group. Examples of the arylsulfonium compound include triarylsulfonium compounds, diarylalkylsulfonium compounds, aryldialkylsulfonium compounds, diarylcycloalkylsulfonium compounds, and aryldicycloalkylsulfonium compounds. The aryl group of the arylsulfonium compound is preferably a phenyl group or a naphthyl group, and more preferably a phenyl group. The aryl group may be an aryl group having a heterocyclic structure having an oxygen atom, a nitrogen atom, a sulfur atom or the like. Examples of the aryl group having a heterocyclic structure include a pyrrole residue (a group formed by losing one hydrogen atom from pyrrole) and a furan residue (a group formed by losing one hydrogen atom from furan). Groups), thiophene residues (groups formed by the loss of one hydrogen atom from thiophene), indole residues (groups formed by the loss of one hydrogen atom from indole), benzofuran residues ( A group formed by losing one hydrogen atom from benzofuran), a benzothiophene residue (a group formed by losing one hydrogen atom from benzothiophene), and the like. When the arylsulfonium compound has two or more aryl groups, the two or more aryl groups may be the same or different.

The alkyl group or cycloalkyl group that the arylsulfonium compound has as necessary is preferably a linear or branched alkyl group having 1 to 15 carbon atoms and a cycloalkyl group having 3 to 15 carbon atoms, such as a methyl group, Examples thereof include an ethyl group, a propyl group, an n-butyl group, a sec-butyl group, a t-butyl group, a cyclopropyl group, a cyclobutyl group, and a cyclohexyl group. The aryl group, alkyl group, and cycloalkyl group of R ^{S1 to} R ^S3 are an alkyl group (for example, 1 to 15 carbon atoms), a cycloalkyl group (for example, 3 to 15 carbon atoms), an aryl group (for example, 6 to 14 carbon atoms). , An alkoxy group (for example, having 1 to 15 carbon atoms), a halogen atom, a hydroxyl group, or a phenylthio group may be substituted. Preferred substituents are linear or branched alkyl groups having 1 to 12 carbon atoms, cycloalkyl groups having 3 to 12 carbon atoms, and linear, branched or cyclic alkoxy groups having 1 to 12 carbon atoms, more preferably carbon. These are an alkyl group having 1 to 4 carbon atoms and an alkoxy group having 1 to 4 carbon atoms. The substituent may be substituted with any one of three R ^{S1 to} R ^S3 , or may be substituted with all three. When R ^{S1 to} R ^S3 are aryl groups, the substituent is preferably substituted at the p-position of the aryl group.

Another preferred embodiment of the compound represented by the formula (IS-1) is a compound (IS-3) in which R ^{S1 to} R ^S3 each independently represents an organic group having no aromatic ring. Here, the aromatic ring includes an aromatic ring containing a hetero atom. The organic group not containing an aromatic ring as R ^{S1 to} R ^S3 generally has 1 to 30 carbon atoms, preferably 1 to 20 carbon atoms.

R ^{S1 to} R ^S3 are each independently preferably an alkyl group, a cycloalkyl group, an allyl group, or a vinyl group, and more preferably a linear or branched 2-oxoalkyl group, 2-oxocycloalkyl group, alkoxy group. A carbonylmethyl group, particularly preferably a linear or branched 2-oxoalkyl group. As the alkyl group and cycloalkyl group of R ^{S1 to} R ^S3 , a linear or branched alkyl group having 1 to 10 carbon atoms (for example, methyl group, ethyl group, propyl group, butyl group, pentyl group), carbon Examples thereof include cycloalkyl groups of several 3 to 10 (cyclopentyl group, cyclohexyl group, norbornyl group). More preferred examples of the alkyl group include a 2-oxoalkyl group and an alkoxycarbonylmethyl group. More preferred examples of the cycloalkyl group include a 2-oxocycloalkyl group. The 2-oxoalkyl group may be either linear or branched, and a group having> C = O at the 2-position of the above alkyl group is preferable. The 2-oxocycloalkyl group is preferably a group having> C═O at the 2-position of the cycloalkyl group. The alkoxy group in the alkoxycarbonylmethyl group is preferably an alkoxy group having 1 to 5 carbon atoms (methoxy group, ethoxy group, propoxy group, butoxy group, pentoxy group). R ^{S1 to} R ^S3 may be further substituted with a halogen atom, an alkoxy group (for example, having 1 to 5 carbon atoms), a hydroxyl group, a cyano group, or a nitro group.

  Another preferred embodiment of the compound represented by the formula (IS-1) is a compound having a phenacylsulfonium salt structure represented by the following general formula (IS-4).

In formula (IS-4), R ^{S4 to} R ^S8 each independently represent a hydrogen atom, an alkyl group, a cycloalkyl group, an alkoxy group, or a halogen atom. R ^S9 and R ^S10 each independently represent a hydrogen atom, an alkyl group or a cycloalkyl group. R ^SX and R ^SY each independently represents an alkyl group, a cycloalkyl group, an allyl group or a vinyl group.

Any two or more of R ^{S4 to} R ^S8 , R ^S9 and R ^S10 , and R ^SX and R ^SY may be bonded to each other to form a ring structure, and this ring structure includes an oxygen atom and a sulfur atom. , An ester bond and an amide bond may be included. Examples of the group formed by combining any two or more of R ^{S4 to} R ^S8 , R ^S9 and R ^S10 , and R ^SX and R ^SY include a butylene group and a pentylene group. A ^S- represents the same anion as in formula (IS-1).

The alkyl group as R _{1c to} R _7c may be either linear or branched, for example, an alkyl group having 1 to 20 carbon atoms, preferably a linear or branched alkyl group having 1 to 12 carbon atoms ( Examples thereof include a methyl group, an ethyl group, a linear or branched propyl group, a linear or branched butyl group, and a linear or branched pentyl group. Examples of the cycloalkyl group include cyclohexane having 3 to 8 carbon atoms. An alkyl group (for example, a cyclopentyl group, a cyclohexyl group) can be mentioned.

The alkoxy group as R ^{S4 to} R ^S10 may be linear, branched or cyclic, for example, an alkoxy group having 1 to 10 carbon atoms, preferably a linear or branched alkoxy group having 1 to 5 carbon atoms. (For example, methoxy group, ethoxy group, linear or branched propoxy group, linear or branched butoxy group, linear or branched pentoxy group), C3-C8 cyclic alkoxy group (for example, cyclopentyloxy group, cyclohexyloxy group) ). Preferably, any of R ^{S4 to} R ^S8 is a linear or branched alkyl group, a cycloalkyl group, or a linear, branched or cyclic alkoxy group, and more preferably the sum of the carbon numbers of R ^{S4 to} R ^S8. Is 2-15. Thereby, solvent solubility improves more and generation | occurrence | production of a particle is suppressed at the time of a preservation | save.

^Examples of the alkyl group and cycloalkyl group as R ^SX and R ^SY include the same alkyl group and cycloalkyl group as in R ^{S4 to} R ^S8, and include a 2-oxoalkyl group, a 2-oxocycloalkyl group, an alkoxy group. A carbonylmethyl group is more preferred. Examples of the 2-oxoalkyl group and 2-oxocycloalkyl group include a group having> C═O at the 2-position of the alkyl group or cycloalkyl group as R ^{S4 to} R ^S10 . As for the alkoxy group in the alkoxycarbonylmethyl group, the same alkoxy groups as in R ^{S4 to} R ^S8 can be exemplified.

R ^SX and R ^SY are preferably an alkyl group or cycloalkyl group having 4 or more carbon atoms, more preferably 6 or more, and still more preferably 8 or more alkyl groups or cycloalkyl groups.

In formula (IS-1), A ⁻ represents an anion, and an anion that generates a Bronsted acid having a pKa of 7 or less is preferable. Further, it is preferably a non-nucleophilic anion. Examples of such anions include BF ₄ ⁻ , Cl ⁻ , ClO ₄ ⁻ , AsF ₆ ⁻ , PF ₆ ⁻ , FeCl ₄ ⁻ , ZBiCl ₄ ⁻ as inorganic anions. , SnCl ₄ ⁻ , AlF ₆ ⁻ , GaCl ₄ ⁻ , InF ₄ ⁻ , TiF ₆ ⁻ , ZrF ₆ ⁻ , SbF ₆ ^{− and the} like, and organic anions include sulfonate anion, carboxylate anion, sulfonylimide anion, bis (Alkylsulfonyl) imide anion, tris (alkylsulfonyl) methyl anion, etc. can be mentioned. A non-nucleophilic anion is an anion that has an extremely low ability to cause a nucleophilic reaction, and is an anion that can suppress degradation over time due to an intramolecular nucleophilic reaction. This improves the temporal stability of the resist. When the sulfonium salt compound is used in the present invention, it is preferably an organic anion.

  Examples of the sulfonate anion include an aliphatic sulfonate anion, an aromatic sulfonate anion, and a camphor sulfonate anion.

  Examples of the carboxylate anion include an aliphatic carboxylate anion, an aromatic carboxylate anion, and an aralkylcarboxylate anion.

  The aliphatic moiety in the aliphatic sulfonate anion may be an alkyl group or a cycloalkyl group, preferably an alkyl group having 1 to 30 carbon atoms and a cycloalkyl group having 3 to 30 carbon atoms such as methyl. Group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, sec-butyl group, pentyl group, neopentyl group, hexyl group, heptyl group, octyl group, nonyl group, decyl group, undecyl group, dodecyl group , Tridecyl group, tetradecyl group, pentadecyl group, hexadecyl group, heptadecyl group, octadecyl group, nonadecyl group, eicosyl group, cyclopropyl group, cyclopentyl group, cyclohexyl group, adamantyl group, norbornyl group, boronyl group and the like.

  The aromatic group in the aromatic sulfonate anion is preferably an aryl group having 6 to 14 carbon atoms, such as a phenyl group, a tolyl group, and a naphthyl group.

  The alkyl group, cycloalkyl group and aryl group in the aliphatic sulfonate anion and aromatic sulfonate anion may have a substituent. Examples of the substituent of the alkyl group, cycloalkyl group, and aryl group in the aliphatic sulfonate anion and aromatic sulfonate anion include, for example, a nitro group, a halogen atom (fluorine atom, chlorine atom, bromine atom, iodine atom), carboxyl group , Hydroxyl group, amino group, cyano group, alkoxy group (preferably having 1 to 15 carbon atoms), cycloalkyl group (preferably having 3 to 15 carbon atoms), aryl group (preferably having 6 to 14 carbon atoms), alkoxycarbonyl group ( Preferably 2 to 7 carbon atoms, acyl group (preferably 2 to 12 carbon atoms), alkoxycarbonyloxy group (preferably 2 to 7 carbon atoms), alkylthio group (preferably 1 to 15 carbon atoms), alkylsulfonyl group (Preferably 1 to 15 carbon atoms), alkyliminosulfonyl group (preferably 2 to 15 carbon atoms), ant Ruoxysulfonyl group (preferably having 6 to 20 carbon atoms), alkylaryloxysulfonyl group (preferably having 7 to 20 carbon atoms), cycloalkylaryloxysulfonyl group (preferably having 10 to 20 carbon atoms), alkyloxyalkyloxy group (Preferably having 5 to 20 carbon atoms), a cycloalkylalkyloxyalkyloxy group (preferably having 8 to 20 carbon atoms), and the like. About the aryl group and ring structure which each group has, an alkyl group (preferably C1-C15) can further be mentioned as a substituent.

  Examples of the aliphatic moiety in the aliphatic carboxylate anion include the same alkyl group and cycloalkyl group as in the aliphatic sulfonate anion.

  Examples of the aromatic group in the aromatic carboxylate anion include the same aryl group as in the aromatic sulfonate anion.

  The aralkyl group in the aralkyl carboxylate anion is preferably an aralkyl group having 6 to 12 carbon atoms, such as a benzyl group, a phenethyl group, a naphthylmethyl group, a naphthylethyl group, and a naphthylmethyl group.

  The alkyl group, cycloalkyl group, aryl group and aralkyl group in the aliphatic carboxylate anion, aromatic carboxylate anion and aralkylcarboxylate anion may have a substituent. Examples of the substituent of the alkyl group, cycloalkyl group, aryl group and aralkyl group in the aliphatic carboxylate anion, aromatic carboxylate anion and aralkylcarboxylate anion include, for example, the same halogen atom and alkyl as in the aromatic sulfonate anion Group, cycloalkyl group, alkoxy group, alkylthio group and the like.

  Examples of the sulfonylimide anion include saccharin anion.

  The alkyl group in the bis (alkylsulfonyl) imide anion and tris (alkylsulfonyl) methyl anion is preferably an alkyl group having 1 to 5 carbon atoms, such as a methyl group, an ethyl group, a propyl group, an isopropyl group, an n-butyl group, An isobutyl group, a sec-butyl group, a pentyl group, a neopentyl group, and the like can be given. Examples of substituents for these alkyl groups include halogen atoms, alkyl groups substituted with halogen atoms, alkoxy groups, alkylthio groups, alkyloxysulfonyl groups, aryloxysulfonyl groups, cycloalkylaryloxysulfonyl groups, and the like. Alkyl groups substituted with fluorine atoms are preferred.

Examples of the non-nucleophilic anion of Z ⁻ include an aliphatic sulfonate anion in which the α-position of the sulfonic acid is substituted with a fluorine atom, an aromatic sulfonate anion substituted with a fluorine atom or a group having a fluorine atom, and an alkyl group. A bis (alkylsulfonyl) imide anion substituted with a fluorine atom and a tris (alkylsulfonyl) methide anion wherein an alkyl group is substituted with a fluorine atom are preferred. The non-nucleophilic anion is more preferably a perfluoroaliphatic sulfonic acid anion having 4 to 8 carbon atoms, a benzenesulfonic acid anion having a fluorine atom, still more preferably a nonafluorobutanesulfonic acid anion, a perfluorooctanesulfonic acid anion, It is a pentafluorobenzenesulfonic acid anion and 3,5-bis (trifluoromethyl) benzenesulfonic acid anion.

  Examples of preferred radical photopolymerization initiators are shown below, but the present invention is not limited thereto.

  Among those exemplified as the photocationic polymerization initiator, there are those which are considered to have a function of a photoradical polymerization initiator. Some of those exemplified as the photo radical polymerization initiator are considered to function as a photo cationic polymerization initiator. However, in order to achieve the desired performance in the present invention, it is necessary to use both a photocationic polymerization initiator and a photoradical polymerization initiator. Here, an onium compound represented by general formula (ZI) or (ZII) is used as the photocationic polymerization initiator, and an oxime compound represented by general formula (IO-1) is used as the photoradical polymerization initiator. It is preferable to use it.

(D) Compound having a radical polymerizable group The compound having a radical polymerizable group used in the present invention is a compound having a polymerizable group that undergoes a polymerization reaction by radicals generated from the above-mentioned (C2) photo radical generator. A polymerization reaction is carried out between each other or the compound having the polymerizable group and (A) the alkali-soluble resin.

  The compound having a polymerizable group that can be used in the present invention only needs to contain a structure that undergoes a polymerization reaction by a radical. As a preferred example, an ethylenically unsaturated structure such as the following formulas (RM1) to (RM) The structure represented by RM3) is preferred.

Wherein (RM1), * represents an organic group which is a bond that binds to the organic group to be described later in equation ^(RM4), are each R RM1 ^{to R RM3} independently represents a hydrogen atom or a monovalent organic group. R ^RM1 is preferably a hydrogen atom or an alkyl group which may have a substituent, and among them, a hydrogen atom or a methyl group is preferable. R ^RM2 and R ^RM3 are each independently a hydrogen atom, a halogen atom, an amino group, a carboxyl group, an alkoxycarbonyl group, a cyano group, an alkyl group that may have a substituent, or an alkoxy that may have a substituent. Group, an alkylamino group which may have a substituent, and the like, and a hydrogen atom, a carboxyl group, an alkoxycarbonyl group, an alkyl group which may have a substituent, and the like are preferable. R ^{RM1 to} R ^Rm3 may be bonded to each other to form a ring structure. Examples of the substituent which may be introduced into R ^RM1 to R ^RM3, alkyl group, alkenyl group, alkynyl group, alkoxy group, a halogen atom, an amino group, an alkylamino group, a carboxyl group, an alkoxycarbonyl group, a cyano group, and the like .

In formula (RM2), * represents an organic group that is a bond bonded to the organic structure described later, and ^{RRM4 to RRM8} each independently represents a monovalent organic group, but ^{RRM4 to RRM8} are preferably , Hydrogen atom, halogen atom, amino group, dialkylamino group, carboxyl group, alkoxycarbonyl group, cyano group, alkyl group which may have a substituent, alkoxy group which may have a substituent, And an alkylamino group which may be used. Among these, a hydrogen atom, a carboxyl group, an alkoxycarbonyl group, and an alkyl group which may have a substituent are preferable. R ^{RM4 to} R ^RM8 may be bonded to each other to form a ring structure. ^{Examples of the} substituent that can be introduced into R ^{RM4 to} R ^RM8 include the same groups as those in the general formula (RM1).

In the above formula (RM3), * represents an organic group which is a bond bonded to the organic structure described later, and ^RRM9 preferably includes a hydrogen atom or an alkyl group which may have a substituent. Of these, a hydrogen atom and a methyl group are preferable. R ^RM10 and R ^RM11 each independently have a hydrogen atom, a halogen atom, an amino group, a dialkylamino group, a carboxyl group, an alkoxycarbonyl group, a cyano group, an alkyl group that may have a substituent, or a substituent. Examples thereof may include an alkoxy group which may be substituted, an alkylamino group which may have a substituent, and the like, and among them, a hydrogen atom, a carboxyl group, an alkoxycarbonyl group and an alkyl group which may have a substituent are preferable. R ^{RM9 to} R ^RM11 may be bonded to each other to form a ring structure. ^{Examples of the} substituent that can be introduced into R ^{RM9 to} R ^RM11 are the same as those in the general formula (RM1).

  Examples of the compound (D) having a radical polymerizable group include compounds represented by the following general formula (RM4).

In formula (EP2), R ^RM represents a structure represented by the general formulas (RM1) to (RM3), n ^RM represents an integer of 1 or more, preferably 2 to 10, more preferably 2 to 8. is there. ^QRM represents a single bond or an ^nRM- valent organic group. When n ^RM is 2 or more, R ^RMs may be bonded to each other to form a ring structure, and even when n ^RM is 1, R ^RM may be bonded to Q ^RM to form a ring structure. .

When Q ^RM is an n ^RM- valent organic group, a chain or cyclic saturated unit cost hydrogen structure (preferably having 2 to 20 carbon atoms) or an aromatic ring structure (preferably having 6 to 30 carbon atoms), or these structures are Examples include groups containing together with ether, ester, amide, sulfonic acid ester, sulfonic acid amide, urethane, urea and the like.

^QRM is preferably an organic group that does not absorb ArF laser (193 nm), and a chain or cyclic alkyl group and a group containing these structures together with ether, ester, amide, etc. are preferred. A cyclic alkyl group is preferable from the viewpoint of etching resistance and pattern dimension control, and a chain alkyl group is preferable from the viewpoint of high contrast. Further, ^QRM may be a group having both a chain alkyl structure and a cyclic alkyl structure, or an organic group in which these groups are bonded by ether, ester, or amide. In this case, the above performance can be balanced, which is a preferable mode.
Specific examples of the chain alkyl group include methyl, ethyl, propyl, i-propyl, butyl, s-butyl, t-butyl, pentyl, hexyl, decyl, and these groups, and ethers, esters, and amides. Groups.
Specific examples of the cyclic alkyl group include monocyclic alkanes such as cyclobutane, cyclopentane, cyclohexane, and cyclooctane, polycyclic alkanes such as norbornane, isobornane, tricyclodecane, tetracyclododecane, and adamantane, and these rings, Examples include groups containing ethers, esters, amides and the like.

When ^QRM has an aryl structure, a condensed aromatic group having a small absorption with respect to ArF laser (193 nm) and ethers, esters and amides thereof are preferable. Is preferred. Such groups include naphthalene, anthracene, phenanthrene, naphthacene, pyrene, perylene and the like. Further, ^QRM may be a group having both a condensed aromatic group and a chain or cyclic alkyl group, or an organic group in which these groups are bonded with ether, ester, or amide.

  Although the compound which has a radically polymerizable group is illustrated below, this invention is not limited to these.

  The compounds having the radical polymerizable group may be used alone or in combination.

The compound having a radical polymerizable group has a polymerization function regardless of whether it has one radical polymerizable group or a plurality of radical polymerizable groups in the molecule, but from the viewpoint of sensitivity and resolution, a plurality of radical polymerizable groups are present. The number (n ^RM ) is preferably 2 to 10, more preferably 2 to 8.

  By having a plurality of radically polymerizable groups in the compound having the radically polymerizable group, the exposed part has a more complicated three-dimensional structure and expresses high sensitivity and high dissolution contrast in an alkaline developer, Swelling is also suppressed, and high resolution is considered to be achieved.

In the case of a compound having a plurality of radically polymerizable groups, the radically polymerizable groups contained in one molecule may be the same or different. A plurality of compounds having the same radical polymerizable group may be mixed and used.
It is possible to balance sensitivity and other performances by using different functional numbers and different radical polymerizable groups in combination.

  The content of the compound having a radical polymerizable group in the present invention is 0.5 to 90% by mass, preferably 1 to 85% by mass, more preferably 2 to 80% by mass, based on the solid content of the resist composition. is there.

(E) Basic compound The resist composition of the present invention preferably contains a basic compound in order to reduce a change in performance over time from exposure to heating.
Preferred examples of the basic compound include compounds having structures represented by the following formulas (A) to (E).

In general formulas (A) to (E),
R ²⁰⁰ , R ²⁰¹ and R ²⁰² may be the same or different, and are a hydrogen atom, an alkyl group (preferably having 1 to 20 carbon atoms), a cycloalkyl group (preferably having 3 to 20 carbon atoms) or an aryl group (having a carbon number). 6-20), wherein R ²⁰¹ and R ²⁰² may combine with each other to form a ring.
About the said alkyl group, as an alkyl group which has a substituent, a C1-C20 aminoalkyl group, a C1-C20 hydroxyalkyl group, or a C1-C20 cyanoalkyl group is preferable.
R ²⁰³ , R ²⁰⁴ , R ²⁰⁵ and R ²⁰⁶ may be the same or different and each represents an alkyl group having 1 to 20 carbon atoms.
The alkyl groups in these general formulas (A) to (E) are more preferably unsubstituted.

  Preferred compounds include guanidine, aminopyrrolidine, pyrazole, pyrazoline, piperazine, aminomorpholine, aminoalkylmorpholine, piperidine and the like, and more preferred compounds include imidazole structure, diazabicyclo structure, onium hydroxide structure, onium carboxylate Examples thereof include a compound having a structure, a trialkylamine structure, an aniline structure or a pyridine structure, an alkylamine derivative having a hydroxyl group and / or an ether bond, and an aniline derivative having a hydroxyl group and / or an ether bond.

  Examples of the compound having an imidazole structure include imidazole, 2,4,5-triphenylimidazole, and benzimidazole. Examples of the compound having a diazabicyclo structure include 1,4-diazabicyclo [2,2,2] octane, 1,5-diazabicyclo [4,3,0] non-5-ene, and 1,8-diazabicyclo [5,4,0. ] Undecar 7-ene etc. are mentioned. Examples of the compound having an onium hydroxide structure include triarylsulfonium hydroxide, phenacylsulfonium hydroxide, sulfonium hydroxide having a 2-oxoalkyl group, specifically triphenylsulfonium hydroxide, tris (t-butylphenyl) sulfonium. Examples thereof include hydroxide, bis (t-butylphenyl) iodonium hydroxide, phenacylthiophenium hydroxide, and 2-oxopropylthiophenium hydroxide. As the compound having an onium carboxylate structure, an anion portion of the compound having an onium hydroxide structure is converted to a carboxylate, and examples thereof include acetate, adamantane-1-carboxylate, and perfluoroalkylcarboxylate. Examples of the compound having a trialkylamine structure include tri (n-butyl) amine and tri (n-octyl) amine. Examples of the aniline compound include 2,6-diisopropylaniline, N, N-dimethylaniline, N, N-dibutylaniline, N, N-dihexylaniline and the like. Examples of the alkylamine derivative having a hydroxyl group and / or an ether bond include ethanolamine, diethanolamine, triethanolamine, and tris (methoxyethoxyethyl) amine. Examples of aniline derivatives having a hydroxyl group and / or an ether bond include N, N-bis (hydroxyethyl) aniline.

  Further, at least one nitrogen-containing compound selected from an amine compound having a phenoxy group, an ammonium salt compound having a phenoxy group, an amine compound having a sulfonic acid ester group, and an ammonium salt compound having a sulfonic acid ester group can be exemplified. .

As the amine compound, a primary, secondary or tertiary amine compound can be used, and an amine compound in which at least one alkyl group is bonded to a nitrogen atom is preferable. The amine compound is more preferably a tertiary amine compound. As long as at least one alkyl group (preferably having 1 to 20 carbon atoms) is bonded to a nitrogen atom, the amine compound has an cycloalkyl group (preferably having 3 to 20 carbon atoms) or an aryl group (preferably having 3 to 20 carbon atoms). Preferably C6-C12) may be bonded to a nitrogen atom.
The amine compound preferably has an oxygen atom in the alkyl chain and an oxyalkylene group is formed. The number of oxyalkylene groups is one or more in the molecule, preferably 3 to 9, and more preferably 4 to 6. Among the oxyalkylene groups, an oxyethylene group (—CH ₂ CH ₂ O—) or an oxypropylene group (—CH (CH ₃ ) CH ₂ O— or —CH ₂ CH ₂ CH ₂ O—) is preferable, and more preferably oxy Ethylene group.

As the ammonium salt compound, a primary, secondary, tertiary, or quaternary ammonium salt compound can be used, and an ammonium salt compound in which at least one alkyl group is bonded to a nitrogen atom is preferable. As long as at least one alkyl group (preferably having 1 to 20 carbon atoms) is bonded to a nitrogen atom, the ammonium salt compound has a cycloalkyl group (preferably having 3 to 20 carbon atoms) or an aryl group in addition to the alkyl group. (Preferably having 6 to 12 carbon atoms) may be bonded to a nitrogen atom.
The ammonium salt compound preferably has an oxygen atom in the alkyl chain and an oxyalkylene group is formed. The number of oxyalkylene groups is one or more in the molecule, preferably 3 to 9, and more preferably 4 to 6. Among the oxyalkylene groups, an oxyethylene group (—CH ₂ CH ₂ O—) or an oxypropylene group (—CH (CH ₃ ) CH ₂ O— or —CH ₂ CH ₂ CH ₂ O—) is preferable, and more preferably oxy Ethylene group. Examples of the anion of the ammonium salt compound include halogen atoms, sulfonates, borates, and phosphates. Among them, halogen atoms and sulfonates are preferable. As the halogen atom, chloride, bromide, and iodide are particularly preferable. As the sulfonate, an organic sulfonate having 1 to 20 carbon atoms is particularly preferable. Examples of the organic sulfonate include alkyl sulfonates having 1 to 20 carbon atoms and aryl sulfonates. The alkyl group of the alkyl sulfonate may have a substituent, and examples of the substituent include fluorine, chlorine, bromine, alkoxy groups, acyl groups, and aryl groups. Specific examples of the alkyl sulfonate include methane sulfonate, ethane sulfonate, butane sulfonate, hexane sulfonate, octane sulfonate, benzyl sulfonate, trifluoromethane sulfonate, pentafluoroethane sulfonate, and nonafluorobutane sulfonate. Examples of the aryl group of the aryl sulfonate include a benzene ring, a naphthalene ring, and an anthracene ring. The benzene ring, naphthalene ring and anthracene ring may have a substituent, and the substituent is preferably a linear or branched alkyl group having 1 to 6 carbon atoms or a cycloalkyl group having 3 to 6 carbon atoms. Specific examples of the linear or branched alkyl group and cycloalkyl group include methyl, ethyl, n-propyl, isopropyl, n-butyl, i-butyl, t-butyl, n-hexyl, cyclohexyl and the like. Examples of the other substituent include an alkoxy group having 1 to 6 carbon atoms, a halogen atom, cyano, nitro, an acyl group, and an acyloxy group.

  The amine compound having a phenoxy group and the ammonium salt compound having a phenoxy group are those having a phenoxy group at the terminal opposite to the nitrogen atom of the alkyl group of the amine compound or ammonium salt compound. The phenoxy group may have a substituent. Examples of the substituent of the phenoxy group include an alkyl group, an alkoxy group, a halogen atom, a cyano group, a nitro group, a carboxyl group, a carboxylic acid ester group, a sulfonic acid ester group, an aryl group, an aralkyl group, an acyloxy group, and an aryloxy group. Etc. The substitution position of the substituent may be any of the 2-6 positions. The number of substituents may be any in the range of 1 to 5.

It is preferable to have at least one oxyalkylene group between the phenoxy group and the nitrogen atom. The number of oxyalkylene groups is one or more in the molecule, preferably 3 to 9, and more preferably 4 to 6. Among the oxyalkylene groups, an oxyethylene group (—CH ₂ CH ₂ O—) or an oxypropylene group (—CH (CH ₃ ) CH ₂ O— or —CH ₂ CH ₂ CH ₂ O—) is preferable, and more preferably oxy Ethylene group.

  In the amine compound having a sulfonic acid ester group and the ammonium salt compound having a sulfonic acid ester group, the sulfonic acid ester group may be any of alkyl sulfonic acid ester, cycloalkyl group sulfonic acid ester, and aryl sulfonic acid ester. In the case of an alkyl sulfonate ester, the alkyl group has 1 to 20 carbon atoms, in the case of a cycloalkyl sulfonate ester, the cycloalkyl group has 3 to 20 carbon atoms, and in the case of an aryl sulfonate ester, the aryl group has 6 carbon atoms. ~ 12 are preferred. Alkyl sulfonic acid ester, cycloalkyl sulfonic acid ester, and aryl sulfonic acid ester may have a substituent. Examples of the substituent include a halogen atom, a cyano group, a nitro group, a carboxyl group, a carboxylic acid ester group, and a sulfonic acid. An ester group is preferred.

It is preferable to have at least one oxyalkylene group between the sulfonate group and the nitrogen atom. The number of oxyalkylene groups is one or more in the molecule, preferably 3 to 9, and more preferably 4 to 6. Among the oxyalkylene groups, an oxyethylene group (—CH ₂ CH ₂ O—) or an oxypropylene group (—CH (CH ₃ ) CH ₂ O— or —CH ₂ CH ₂ CH ₂ O—) is preferable, and more preferably oxy Ethylene group.

The amine compound having a phenoxy group is prepared by reacting a primary or secondary amine having a phenoxy group with a haloalkyl ether by heating, and then adding an aqueous solution of a strong base such as sodium hydroxide, potassium hydroxide or tetraalkylammonium. It can be obtained by extraction with an organic solvent such as ethyl acetate or chloroform. Alternatively, after reacting by heating a primary or secondary amine and a haloalkyl ether having a phenoxy group at the end, an aqueous solution of a strong base such as sodium hydroxide, potassium hydroxide, or tetraalkylammonium is added, and then ethyl acetate, It can be obtained by extraction with an organic solvent such as chloroform.
These basic compounds are used alone or in combination of two or more.

  The usage-amount of a basic compound is 0.001-10 mass% normally based on solid content of a resist composition, Preferably it is 0.01-5 mass%.

  The proportion of the photocationic polymerization initiator and the basic compound in the composition is preferably photocationic polymerization initiator / basic compound (molar ratio) = 2 to 300. That is, the molar ratio is preferably 2 or more from the viewpoint of sensitivity and resolution, and is preferably 300 or less from the viewpoint of suppressing the reduction in resolution due to the thickening of the resist pattern over time until post-exposure heat treatment. The photocationic polymerization initiator / basic compound (molar ratio) is more preferably 3 to 200, still more preferably 5 to 150.

(F) Hydrophobic polymer Exposure (immersion exposure) may be performed by filling a liquid (immersion medium) having a higher refractive index than air between the resist film and the lens during irradiation with actinic rays or radiation. Thereby, resolution can be improved. As the immersion medium to be used, any liquid can be used as long as it has a higher refractive index than air, but pure water is preferred.

The immersion liquid used for the immersion exposure will be described below.
The immersion liquid is preferably a liquid that is transparent to the exposure wavelength and has a refractive index temperature coefficient as small as possible so as to minimize distortion of the optical image projected onto the resist film. Is an ArF excimer laser (wavelength; 193 nm), it is preferable to use water from the viewpoints of availability and ease of handling in addition to the above-mentioned viewpoints.
Further, a medium having a refractive index of 1.5 or more can be used in that the refractive index can be further improved. This medium may be an aqueous solution or an organic solvent.

  When water is used as the immersion liquid, the surface tension of the water is decreased and the surface activity is increased, so that the resist film on the wafer is not dissolved and the influence on the optical coating on the lower surface of the lens element can be ignored. An additive (liquid) may be added in a small proportion. The additive is preferably an aliphatic alcohol having a refractive index substantially equal to that of water, and specifically includes methyl alcohol, ethyl alcohol, isopropyl alcohol and the like. By adding an alcohol having a refractive index substantially equal to that of water, even if the alcohol component in water evaporates and the content concentration changes, an advantage that the change in the refractive index of the entire liquid can be made extremely small can be obtained. On the other hand, when an opaque material or impurities whose refractive index is significantly different from that of water are mixed with 193 nm light, the optical image projected on the resist film is distorted. . Further, pure water filtered through an ion exchange filter or the like may be used.

The electrical resistance of water is desirably 18.3 MQcm or more, the TOC (organic substance concentration) is desirably 20 ppb or less, and deaeration treatment is desirably performed.
Moreover, it is possible to improve lithography performance by increasing the refractive index of the immersion liquid. From such a viewpoint, an additive for increasing the refractive index may be added to water, or heavy water (D ₂ O) may be used instead of water.

  When the resist film made of the negative resist composition of the present invention is exposed through an immersion medium, a hydrophobic resin (HR) can be further added as necessary. As a result, hydrophobic resin (HR) is unevenly distributed on the surface of the resist film, and when the immersion medium is water, the receding contact angle of the resist film surface with respect to the water when the resist film is formed is improved, and the immersion water tracking is improved. Can be made. As the hydrophobic resin (HR), any resin can be used as long as the receding contact angle of the surface can be improved by addition, but a resin having at least one of fluorine atom and silicon atom is preferable. The receding contact angle of the resist film is preferably 60 ° to 90 °, more preferably 70 ° or more. The addition amount can be adjusted as appropriate so that the receding contact angle of the resist film falls within the above range, but is preferably 0.1 to 10% by mass based on the total solid content of the negative resist composition, More preferably, it is 0.1-5 mass%. Hydrophobic resin (HR) is ubiquitous at the interface as described above, but unlike a surfactant, it does not necessarily have a hydrophilic group in the molecule, and polar / nonpolar substances are mixed uniformly. There is no need to contribute.

  The fluorine atom or silicon atom in the hydrophobic resin (HR) may be contained in the main chain of the resin or may be substituted on the side chain.

The hydrophobic resin (HR) is preferably a resin having an alkyl group having a fluorine atom, a cycloalkyl group having a fluorine atom, or an aryl group having a fluorine atom as a partial structure having a fluorine atom.
The alkyl group having a fluorine atom (preferably having 1 to 10 carbon atoms, more preferably 1 to 4 carbon atoms) is a linear or branched alkyl group in which at least one hydrogen atom is substituted with a fluorine atom, It may have a substituent.
The cycloalkyl group having a fluorine atom is a monocyclic or polycyclic cycloalkyl group in which at least one hydrogen atom is substituted with a fluorine atom, and may further have another substituent.
Examples of the aryl group having a fluorine atom include those in which at least one hydrogen atom of an aryl group such as a phenyl group or a naphthyl group is substituted with a fluorine atom, and may further have another substituent.

  Preferred examples of the alkyl group having a fluorine atom, the cycloalkyl group having a fluorine atom, or the aryl group having a fluorine atom include groups represented by the following general formulas (F2) to (F4). The present invention is not limited to this.

In general formulas (F2) to (F4),
R _{57 to} R ₆₈ each independently represents a hydrogen atom, a fluorine atom or an alkyl group. However, at least one of R _{57 to} R ₆₁ , R _{62 to} R ₆₄ and R _{65 to} R ₆₈ is a fluorine atom or an alkyl group in which at least one hydrogen atom is substituted with a fluorine atom (preferably having a carbon number of 1 ~ 4). R _{57 to} R ₆₁ and R _{65 to} R ₆₇ are preferably all fluorine atoms. R ₆₂ , R ₆₃ and R ₆₈ are preferably an alkyl group (preferably having 1 to 4 carbon atoms) in which at least one hydrogen atom is substituted with a fluorine atom, and preferably a perfluoroalkyl group having 1 to 4 carbon atoms. Further preferred. R ₆₂ and R ₆₃ may be connected to each other to form a ring.

Specific examples of the group represented by the general formula (F2) include a p-fluorophenyl group, a pentafluorophenyl group, and a 3,5-di (trifluoromethyl) phenyl group.
Specific examples of the group represented by the general formula (F3) include trifluoromethyl group, pentafluoropropyl group, pentafluoroethyl group, heptafluorobutyl group, hexafluoroisopropyl group, heptafluoroisopropyl group, hexafluoro (2 -Methyl) isopropyl group, nonafluorobutyl group, octafluoroisobutyl group, nonafluorohexyl group, nonafluoro-t-butyl group, perfluoroisopentyl group, perfluorooctyl group, perfluoro (trimethyl) hexyl group, 2,2 1,3,3-tetrafluorocyclobutyl group, perfluorocyclohexyl group and the like. Hexafluoroisopropyl group, heptafluoroisopropyl group, hexafluoro (2-methyl) isopropyl group, octafluoroisobutyl group, nonafluoro-t-butyl group and perfluoroisopentyl group are preferable, and hexafluoroisopropyl group and heptafluoroisopropyl group are preferable. Further preferred.
Specific examples of the group represented by the general formula (F4) include, for example, —C (CF ₃ ) ₂ OH, —C (C ₂ F ₅ ) ₂ OH, —C (CF ₃ ) (CH ₃ ) OH, -CH (CF ₃₎ OH and the like, -C (CF _{3) 2} OH is preferred.

Hereinafter, although the specific example of the repeating unit which has a fluorine atom is shown, this invention is not limited to this.
In specific examples, X ₁ represents a hydrogen atom, —CH ₃ , —F or —CF ₃ .
X ₂ represents —F or —CF ₃ .

The hydrophobic resin (HR) is preferably a resin having an alkylsilyl structure (preferably a trialkylsilyl group) or a cyclic siloxane structure as a partial structure having a silicon atom.
Specific examples of the alkylsilyl structure or the cyclic siloxane structure include groups represented by the following general formulas (CS-1) to (CS-3).

In general formulas (CS-1) to (CS-3),
R _{12 to} R ₂₆ each independently represents a linear or branched alkyl group (preferably having 1 to 20 carbon atoms) or a cycloalkyl group (preferably having 3 to 20 carbon atoms).
L < ₃ > -L < ₅ > represents a single bond or a bivalent coupling group. As the divalent linking group, an alkylene group, a phenyl group, an ether group, a thioether group, a carbonyl group, an ester group, an amide group, a urethane group, or a urea group is used alone or in combination of two or more groups. A combination is mentioned.
n represents an integer of 1 to 5.

Hereinafter, although the specific example of the repeating unit which has a silicon atom is given, this invention is not limited to this.
In specific examples, X ₁ represents a hydrogen atom, —CH ₃ , —F or —CF ₃ .

Furthermore, the hydrophobic resin (HR) may have at least one group selected from the following groups (x) and (y).
(X) an alkali-soluble group,
(Y) A group that decomposes by the action of an alkali developer and increases the solubility in the alkali developer.

(X) Alkali-soluble groups include phenolic hydroxyl groups, carboxylic acid groups, fluorinated alcohol groups, sulfonic acid groups, sulfonamido groups, sulfonylimide groups, (alkylsulfonyl) (alkylcarbonyl) methylene groups, (alkylsulfonyl) ( Alkylcarbonyl) imide group, bis (alkylcarbonyl) methylene group, bis (alkylcarbonyl) imide group, bis (alkylsulfonyl) methylene group, bis (alkylsulfonyl) imide group, tris (alkylcarbonyl) methylene group, tris (alkylsulfonyl) And a group having a methylene group.
Preferred alkali-soluble groups include fluorinated alcohol groups (preferably hexafluoroisopropanol), sulfonimide groups, and bis (carbonyl) methylene groups.

Examples of the repeating unit having an alkali-soluble group (x) include a repeating unit in which an alkali-soluble group is directly bonded to the main chain of the resin, such as a repeating unit of acrylic acid or methacrylic acid, or a main group of the resin via a linking group. It is preferable to use a repeating unit in which an alkali-soluble group is bonded to the chain, and further introduce a polymerization initiator or chain transfer agent having an alkali-soluble group at the end of the polymer chain at the time of polymerization.
The content of the repeating unit having an alkali-soluble group (x) is preferably from 1 to 50 mol%, more preferably from 3 to 35 mol%, still more preferably from 5 to 20 mol%, based on all repeating units in the polymer.

  Specific examples of the repeating unit having an alkali-soluble group (x) are shown below, but the present invention is not limited thereto.

(Y) Examples of the group that decomposes by the action of an alkali developer and increases the solubility in the alkali developer include a group having a lactone structure, an acid anhydride, an acid imide group, and the like, and preferably a lactone group It is.
As the repeating unit having a group (y) that is decomposed by the action of an alkali developer and increases the solubility in the alkali developer, an alkali is added to the main chain of the resin, such as a repeating unit of an acrylate ester or a methacrylate ester. A polymerization initiator having a repeating unit to which a group (y) that decomposes by the action of the developer and increases the solubility in an alkali developer is bonded, or a group (y) that increases the solubility in an alkali developer And a chain transfer agent used at the time of polymerization are preferably introduced at the end of the polymer chain.
The content of the repeating unit having a group (y) whose solubility in an alkali developer is increased is preferably 1 to 40 mol%, more preferably 3 to 30 mol%, still more preferably based on all repeating units in the polymer. 5 to 15 mol%.

  Specific examples of the repeating unit having a group (y) that increases the solubility in an alkali developer include the same repeating units as those having a lactone structure exemplified for the resin of the component (A).

  The hydrophobic resin (HR) may further have a repeating unit represented by the following general formula (III).

In general formula (III):
R ₄ represents a group having an alkyl group, a cycloalkyl group, an alkenyl group, or a cycloalkenyl group.
L ₆ represents a single bond or a divalent linking group.

In general formula (III), the alkyl group represented by R ₄ is preferably a linear or branched alkyl group having 3 to 20 carbon atoms.
The cycloalkyl group is preferably a cycloalkyl group having 3 to 20 carbon atoms.
The alkenyl group is preferably an alkenyl group having 3 to 20 carbon atoms.
The cycloalkenyl group is preferably a cycloalkenyl group having 3 to 20 carbon atoms.
The divalent linking group of L ₆ is preferably an alkylene group (preferably having 1 to 5 carbon atoms) or an oxy group.

When the hydrophobic resin (HR) has a fluorine atom, the fluorine atom content is preferably 5 to 80% by mass, and 10 to 80% by mass with respect to the molecular weight of the hydrophobic resin (HR). Is more preferable. Moreover, it is preferable that the repeating unit containing a fluorine atom is 10-100 mass% in hydrophobic resin (HR), and it is more preferable that it is 30-100 mass%.
When the hydrophobic resin (HR) has a silicon atom, the content of the silicon atom is preferably 2 to 50% by mass and preferably 2 to 30% by mass with respect to the molecular weight of the hydrophobic resin (HR). Is more preferable. Moreover, it is preferable that it is 10-100 mass% in hydrophobic resin (HR), and, as for the repeating unit containing a silicon atom, it is more preferable that it is 20-100 mass%.

The weight average molecular weight of the hydrophobic resin (HR) in terms of standard polystyrene is preferably 1,000 to 100,000, more preferably 1,000 to 50,000, and even more preferably 2,000 to 15,000. is there.
The hydrophobic resin (HR), like the resin of the component (A), naturally has few impurities such as metals, and the residual monomer and oligomer components are preferably 0 to 10% by mass, more preferably. Is more preferably 0 to 5% by mass and 0 to 1% by mass. Thereby, a resist having no change over time such as foreign matter in liquid or sensitivity can be obtained. The molecular weight distribution (Mw / Mn, also referred to as dispersity) is preferably in the range of 1 to 5, more preferably 1 to 3, and still more preferably from the viewpoints of resolution, resist shape, resist pattern sidewall, roughness, and the like. It is the range of 1-2.

  As the hydrophobic resin (HR), various commercially available products can be used, or they can be synthesized according to a conventional method (for example, radical polymerization). For example, as a general synthesis method, a monomer polymerization method in which a monomer species and an initiator are dissolved in a solvent and the polymerization is performed by heating, and a solution of the monomer species and the initiator is dropped into the heating solvent over 1 to 10 hours. The dropping polymerization method is added, and the dropping polymerization method is preferable. Examples of the reaction solvent include ethers such as tetrahydrofuran, 1,4-dioxane, diisopropyl ether, ketones such as methyl ethyl ketone and methyl isobutyl ketone, ester solvents such as ethyl acetate, amide solvents such as dimethylformamide and dimethylacetamide, Furthermore, the solvent which melt | dissolves the composition of this invention like the below-mentioned propylene glycol monomethyl ether acetate, propylene glycol monomethyl ether, and cyclohexanone is mentioned. More preferably, the polymerization is performed using the same solvent as the solvent used in the negative resist composition of the present invention. Thereby, the generation of particles during storage can be suppressed.

  The polymerization reaction is preferably performed in an inert gas atmosphere such as nitrogen or argon. As a polymerization initiator, a commercially available radical initiator (azo initiator, peroxide, etc.) is used to initiate the polymerization. As the radical initiator, an azo initiator is preferable, and an azo initiator having an ester group, a cyano group, or a carboxyl group is preferable. Preferred examples of the initiator include azobisisobutyronitrile, azobisdimethylvaleronitrile, dimethyl 2,2′-azobis (2-methylpropionate) and the like. The concentration of the reaction is 5 to 50% by mass, preferably 30 to 50% by mass. The reaction temperature is usually 10 ° C to 150 ° C, preferably 30 ° C to 120 ° C, more preferably 60-100 ° C.

  After completion of the reaction, the mixture is allowed to cool to room temperature and purified. Purification can be accomplished by a liquid-liquid extraction method that removes residual monomers and oligomer components by combining water and an appropriate solvent, and a purification method in a solution state such as ultrafiltration that extracts and removes only those having a specific molecular weight or less. , Reprecipitation method that removes residual monomer by coagulating resin in poor solvent by dripping resin solution into poor solvent and purification in solid state such as washing filtered resin slurry with poor solvent A normal method such as a method can be applied. For example, the resin is precipitated as a solid by contacting a solvent (poor solvent) in which the resin is hardly soluble or insoluble in a volume amount of 10 times or less, preferably 10 to 5 times that of the reaction solution.

  The solvent (precipitation or reprecipitation solvent) used in the precipitation or reprecipitation operation from the polymer solution may be a poor solvent for the polymer, and may be a hydrocarbon, halogenated hydrocarbon, nitro, depending on the type of polymer. A compound, ether, ketone, ester, carbonate, alcohol, carboxylic acid, water, a mixed solvent containing these solvents, and the like can be appropriately selected for use. Among these, as a precipitation or reprecipitation solvent, a solvent containing at least an alcohol (particularly methanol or the like) or water is preferable.

  The amount of the precipitation or reprecipitation solvent used can be appropriately selected in consideration of efficiency, yield, and the like, but generally 100 to 10000 parts by mass, preferably 200 to 2000 parts by mass with respect to 100 parts by mass of the polymer solution, More preferably, it is 300-1000 mass parts.

  The temperature for precipitation or reprecipitation can be appropriately selected in consideration of efficiency and operability, but is usually about 0 to 50 ° C., preferably around room temperature (for example, about 20 to 35 ° C.). The precipitation or reprecipitation operation can be performed by a known method such as a batch method or a continuous method using a conventional mixing vessel such as a stirring tank.

The precipitated or re-precipitated polymer is usually subjected to conventional solid-liquid separation such as filtration and centrifugation, and dried before use. Filtration is performed using a solvent-resistant filter medium, preferably under pressure.
Drying is performed at a temperature of about 30 to 100 ° C, preferably about 30 to 50 ° C under normal pressure or reduced pressure (preferably under reduced pressure).

  The resin may be once deposited and separated, and then dissolved again in a solvent, and the resin may be brought into contact with a hardly soluble or insoluble solvent. That is, after completion of the radical polymerization reaction, a solvent in which the polymer is hardly soluble or insoluble is brought into contact, the resin is precipitated (step a), the resin is separated from the solution (step b), and dissolved again in the solvent. (Step c), and then contact the resin solution A with a solvent in which the resin is hardly soluble or insoluble in a volume amount less than 10 times that of the resin solution A (preferably 5 times or less volume). This may be a method including precipitating a resin solid (step d) and separating the precipitated resin (step e).

  Specific examples of the hydrophobic resin (HR) are shown below. Table 1 below shows the molar ratio of the repeating units in each resin (corresponding to each repeating unit in order from the left), the weight average molecular weight, and the degree of dispersion.

In order to prevent the resist film from directly contacting the immersion liquid between the resist film made of the negative resist composition of the present invention and the immersion liquid, the immersion liquid hardly soluble film (hereinafter also referred to as “top coat”). ) May be provided. The functions necessary for the top coat are suitability for application to the upper layer of the resist, transparency to radiation, particularly 193 nm, and poor immersion liquid solubility. It is preferable that the top coat is not mixed with the resist and can be uniformly applied to the resist upper layer.
From the viewpoint of 193 nm transparency, the top coat is preferably a polymer that does not contain abundant aromatics. Specifically, the polymer contains a hydrocarbon polymer, an acrylate polymer, polymethacrylic acid, polyacrylic acid, polyvinyl ether, and silicon. Examples thereof include a polymer and a fluorine-containing polymer. The aforementioned hydrophobic resin (HR) is also suitable as a top coat. From the viewpoint of contaminating the optical lens when impurities are eluted from the top coat into the immersion liquid, it is preferable that the residual monomer component of the polymer contained in the top coat is small.

When peeling the top coat, a developer may be used, or a separate release agent may be used. As the release agent, a solvent having a small penetration into the resist film is preferable. It is preferable that the peeling process can be performed with an alkali developer in that the peeling process can be performed simultaneously with the resist film development process. From the viewpoint of peeling with an alkaline developer, the topcoat is preferably acidic, but may be neutral or alkaline from the viewpoint of non-intermixability with the resist film.
The resolution is improved when there is no difference in refractive index between the top coat and the immersion liquid. In the case of using water as the immersion liquid in an ArF excimer laser (wavelength: 193 nm), the top coat for ArF immersion exposure is preferably close to the refractive index of the immersion liquid. From the viewpoint of making the refractive index close to the immersion liquid, it is preferable to have fluorine atoms in the topcoat. A thin film is more preferable from the viewpoint of transparency and refractive index.

  The top coat is preferably not mixed with the resist film and further not mixed with the immersion liquid. From this viewpoint, when the immersion liquid is water, it is preferable that the solvent used for the top coat is a slightly water-insoluble medium that is hardly soluble in the solvent used for the negative resist composition. Furthermore, when the immersion liquid is an organic solvent, the topcoat may be water-soluble or water-insoluble.

The negative resist composition of the present invention may be applied to a multilayer resist process (particularly a three-layer resist process). The multilayer resist method includes the following processes.
(a) A lower resist layer made of an organic material is formed on a substrate to be processed.
(b) On the lower resist layer, an intermediate layer and an upper resist layer made of an organic material that crosslinks or decomposes upon irradiation are sequentially laminated.
(c) After forming a predetermined pattern in the upper resist layer, the intermediate layer, the lower layer and the substrate are sequentially etched.
As the intermediate layer, organopolysiloxane (silicone resin) or SiO ₂ coating solution (SOG) is generally used. As the lower layer resist, an appropriate organic polymer film is used, but various known photoresists may be used. For example, each series of the Fuji Film Arch FH series, FHi series, or Sumitomo Chemical PFI series can be illustrated.
The film thickness of the lower resist layer is preferably 0.1 to 4.0 μm, more preferably 0.2 to 2.0 μm, and particularly preferably 0.25 to 1.5 μm. A thickness of 0.1 μm or more is preferable from the viewpoint of antireflection and dry etching resistance, and a thickness of 4.0 μm or less is preferable from the viewpoint of aspect ratio and pattern collapse of the formed fine pattern.

(G) Fluorine-based and / or silicon-based surfactant The negative resist composition of the present invention preferably further contains a surfactant, and a fluorine-based and / or silicon-based surfactant (fluorine-based surfactant). , A silicon-based surfactant, a surfactant having both a fluorine atom and a silicon atom), or two or more thereof.

When the negative resist composition of the present invention contains the above-described surfactant, a resist pattern with less adhesion and development defects can be obtained with good sensitivity and resolution when using an exposure light source of 250 nm or less, particularly 220 nm or less. It becomes possible.
Examples of the fluorine-based and / or silicon-based surfactant include, for example, JP-A No. 62-36663, JP-A No. 61-226746, JP-A No. 61-226745, JP-A No. 62-170950, JP 63-34540 A, JP 7-230165 A, JP 8-62834 A, JP 9-54432 A, JP 9-5988 A, JP 2002-277862 A, US Patent Nos. 5,405,720, 5,360,692, 5,529,881, 5,296,330, 5,436,098, 5,576,143, 5,294,511, 5,824,451 Surfactant can be mentioned, The following commercially available surfactant can also be used as it is.

  Examples of commercially available surfactants that can be used include F-top EF301, EF303 (manufactured by Shin-Akita Kasei Co., Ltd.), Florard FC430, 431, 4430 (manufactured by Sumitomo 3M Co., Ltd.), MegaFuck F171, F173, F176, F189 , F113, F110, F177, F120, R08 (Dainippon Ink Chemical Co., Ltd.), Surflon S-382, SC101, 102, 103, 104, 105, 106 (Asahi Glass Co., Ltd.), Troisol S-366 (Manufactured by Troy Chemical Co., Ltd.), GF-300, GF-150 (manufactured by Toagosei Chemical Co., Ltd.), Surflon S-393 (manufactured by Seimi Chemical Co., Ltd.), F-top EF121, EF122A, EF122B, RF122C, EF125M , EF135M, EF351, 352, EF801, EF802, EF 01 (manufactured by Gemco), PF636, PF656, PF6320, PF6520 (manufactured by OMNOVA), FTX-204D, 208G, 218G, 230G, 204D, 208D, 212D, 218, 222D (manufactured by Neos) Fluorine type surfactant or silicon type surfactant can be mentioned. Polysiloxane polymer KP-341 (manufactured by Shin-Etsu Chemical Co., Ltd.) can also be used as a silicon-based surfactant.

In addition to the known surfactants described above, the surfactant is derived from a fluoroaliphatic compound produced by a telomerization method (also called telomer method) or an oligomerization method (also called oligomer method). A surfactant using a polymer having a fluoroaliphatic group can be used. The fluoroaliphatic compound can be synthesized by the method described in JP-A-2002-90991.
As the polymer having a fluoroaliphatic group, a copolymer of a monomer having a fluoroaliphatic group and (poly (oxyalkylene)) acrylate and / or (poly (oxyalkylene)) methacrylate is preferable and distributed irregularly. Or may be block copolymerized. Examples of the poly (oxyalkylene) group include a poly (oxyethylene) group, a poly (oxypropylene) group, a poly (oxybutylene) group, and the like, and a poly (oxyethylene, oxypropylene, and oxyethylene group). A unit having different chain lengths in the same chain length, such as a block link) or poly (block link of oxyethylene and oxypropylene) may be used. Furthermore, a copolymer of a monomer having a fluoroaliphatic group and (poly (oxyalkylene)) acrylate (or methacrylate) is not only a binary copolymer but also a monomer having two or more different fluoroaliphatic groups, Further, it may be a ternary or higher copolymer obtained by simultaneously copolymerizing two or more different (poly (oxyalkylene)) acrylates (or methacrylates).

Examples of commercially available surfactants include Megafac F178, F-470, F-473, F-475, F-476, and F-472 (Dainippon Ink Chemical Co., Ltd.). Further, a copolymer of an acrylate (or methacrylate) having a C ₆ F ₁₃ group and (poly (oxyalkylene)) acrylate (or methacrylate), an acrylate (or methacrylate) having a C ₃ F ₇ group and (poly (oxy) And a copolymer of (ethylene)) acrylate (or methacrylate) and (poly (oxypropylene)) acrylate (or methacrylate).

  In the present invention, other surfactants other than fluorine-based and / or silicon-based surfactants can also be used. Specifically, polyoxyethylene lauryl ether, polyoxyethylene stearyl ether, polyoxyethylene cetyl ether, polyoxyethylene alkyl ethers such as polyoxyethylene oleyl ether, polyoxyethylene octylphenol ether, polyoxyethylene nonylphenol ether, etc. Sorbitans such as polyoxyethylene alkyl allyl ethers, polyoxyethylene / polyoxypropylene block copolymers, sorbitan monolaurate, sorbitan monopalmitate, sorbitan monostearate, sorbitan monooleate, sorbitan trioleate, sorbitan tristearate Fatty acid esters, polyoxyethylene sorbitan monolaurate, polyoxyethylene sorbitan monopal Te - DOO, polyoxyethylene sorbitan monostearate, polyoxyethylene sorbitan trioleate, may be mentioned polyoxyethylene sorbitan tristearate nonionic surfactants of polyoxyethylene sorbitan fatty acid esters such as such.

  These surfactants may be used alone or in several combinations.

  The amount of the surfactant used is preferably 0.01 to 10% by mass, more preferably 0.1 to 5% by mass, based on the total amount of the resist composition (excluding the solvent).

(H) Organic solvent The negative resist composition of the present invention is used by dissolving the above components in a predetermined organic solvent. Examples of the organic solvent that can be used include ethylene dichloride, cyclohexanone, cyclopentanone, 2-heptanone, γ-butyrolactone, methyl ethyl ketone, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, 2-methoxyethyl acetate, ethylene glycol monoethyl. Ether acetate, propylene glycol monomethyl ether, propylene glycol monomethyl ether acetate, toluene, ethyl acetate, methyl lactate, ethyl lactate, methyl methoxypropionate, ethyl ethoxypropionate, methyl pyruvate, ethyl pyruvate, propyl pyruvate, N, N -Dimethylformamide, dimethylsulfoxide, N-methylpyrrolidone, methoxybutanol, tetrahydrofuran, etc. It can be mentioned.

  In this invention, you may use the mixed solvent which mixed the solvent which has a hydroxyl group in a structure, and the solvent which does not have a hydroxyl group as an organic solvent.

  Examples of the solvent having a hydroxyl group include ethylene glycol, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, propylene glycol, propylene glycol monomethyl ether, propylene glycol monoethyl ether, ethyl lactate, and the like. Propylene glycol monomethyl ether and ethyl lactate are preferred.

Examples of the solvent having no hydroxyl group include propylene glycol monomethyl ether acetate, ethyl ethoxypropionate, 2-heptanone, γ-butyrolactone, cyclohexanone, butyl acetate, N-methylpyrrolidone, N, N-dimethylacetamide, dimethyl sulfoxide. Among these, propylene glycol monomethyl ether acetate, ethyl ethoxypropionate, 2-heptanone, γ-butyrolactone, cyclohexanone, and butyl acetate are preferable, propylene glycol monomethyl ether acetate, ethyl ethoxypropionate 2-heptanone is more preferable.
The mixing ratio (mass ratio) of the solvent having a hydroxyl group and the solvent having no hydroxyl group is preferably 1/99 to 99/1, more preferably 10/90 to 90/10, and even more preferably 20/80 to 60/40. A mixed solvent containing 50% by mass or more of a solvent having no hydroxyl group is particularly preferable from the viewpoint of coating uniformity. )

(I) Method of Use The negative resist composition of the present invention is preferably used at a film thickness of 30 to 250 nm, more preferably at a film thickness of 30 to 200 nm, from the viewpoint of improving resolution. . Such a film thickness can be obtained by setting the solid content concentration in the negative resist composition to an appropriate range to give an appropriate viscosity and improving the coating property and film forming property.

  The total solid concentration in the negative resist composition is generally 1 to 10% by mass, more preferably 1 to 8% by mass, and further preferably 1 to 6% by mass.

  The negative resist composition of the present invention is used by dissolving the above components in a predetermined organic solvent, preferably the mixed solvent, filtering the solution, and then applying the solution on a predetermined support as follows. The filter used for filter filtration is preferably made of polytetrafluoroethylene, polyethylene, or nylon of 0.1 microns or less, more preferably 0.05 microns or less, and still more preferably 0.03 microns or less.

For example, a negative resist composition is applied onto a substrate (eg, silicon / silicon dioxide coating) used for manufacturing a precision integrated circuit element by an appropriate application method such as a spinner or a coater, and dried to form a resist film. Form.
The resist film is irradiated with actinic rays or radiation through a predetermined mask, and developed and rinsed. A baking step may be added after irradiation with actinic rays or radiation. Thereby, a good pattern can be obtained.

Examples of the actinic ray or radiation include infrared light, visible light, ultraviolet light, far ultraviolet light, X-ray, electron beam, etc., preferably 250 nm or less, more preferably 220 nm or less, particularly preferably 1 to 1. Far-ultraviolet light having a wavelength of 200 nm, specifically, KrF excimer laser (248 nm), ArF excimer laser (193 nm), F ₂ excimer laser (157 nm), X-ray, electron beam, etc. ArF excimer laser, F ₂ Excimer laser, EUV (13 nm), and electron beam are preferable, and ArF excimer laser (193 nm) is particularly preferable.

  Before forming the resist film, an antireflection film may be coated on the substrate in advance.

  As the antireflection film, any of an inorganic film type such as titanium, titanium dioxide, titanium nitride, chromium oxide, carbon, and amorphous silicon, and an organic film type made of a light absorber and a polymer material can be used. In addition, as the organic antireflection film, commercially available organic antireflection films such as DUV30 series, DUV-40 series manufactured by Brewer Science, AR-2, AR-3, AR-5 manufactured by Shipley, etc. may be used. it can.

  In the development step, an alkaline developer is used as follows. Examples of the alkali developing solution for the negative resist composition include sodium hydroxide, potassium hydroxide, sodium carbonate, sodium silicate, sodium metasilicate, aqueous ammonia and other primary alkalis such as ethylamine and n-propylamine. Secondary amines such as diethylamine and di-n-butylamine, tertiary amines such as triethylamine and methyldiethylamine, alcohol amines such as dimethylethanolamine and triethanolamine, tetramethylammonium hydroxide, tetraethylammonium hydroxide Alkaline aqueous solutions of cyclic amines such as quaternary ammonium salts such as pyrrole and pihelidine can be used.

  Furthermore, alcohols and surfactants can be added in appropriate amounts to the alkaline developer.

The alkali concentration of the alkali developer is preferably from 0.1 to 20% by mass.
The pH of the alkaline developer is preferably 10.0 to 15.0.
Furthermore, alcohols and surfactants can be added in appropriate amounts to the alkaline aqueous solution.

As the rinsing liquid, pure water can be used, and an appropriate amount of a surfactant can be added.
In addition, after the developing process or the rinsing process, a process of removing the developing solution or the rinsing liquid adhering to the pattern with a supercritical fluid can be performed.

  The present invention will be described below with reference to examples, but the present invention is not limited thereto.

Synthesis Example 1 (Synthesis of the following monomers)
1,5-Dihydroxynaphthalene (30.5 g), triethylamine (38.5 g), and THF (1000 mL) were placed in a three-necked flask and cooled to 0 ° C. To this was added dropwise 23.9 g of methacrylic acid chloride over 30 minutes. After completion of the dropwise addition, the mixture was returned to room temperature and stirred for 30 minutes. To the reaction solution, 500 mL of 2M HCl aqueous solution was added, extracted with 800 mL of ethyl acetate, dried over magnesium sulfate, and then the solvent was distilled off with a rotary evaporator. The obtained reaction product was dissolved in 100 mL of acetone, and 1000 mL of hexane was added. The resulting precipitate was removed by filtration and purified by column chromatography (ethyl acetate / hexane = 20/80: volume ratio) to obtain 3.8 g of the following monomer.

Synthesis Example 2 (Synthesis of the following monomers)
29.9 g of 2-aminoethyl methacrylate hydrochloride, 36.6 g of triethylamine, and 495 mL of methylene chloride were placed in a three-necked flask and stirred for 1 hour. To this, 22.8 g of methanesulfonyl chloride was added dropwise over 1 hour. After completion of dropping, the mixture was stirred at room temperature for 2 hours. 500 mL of 2M HCl aqueous solution was added to the reaction mixture, and the mixture was extracted with 200 mL of ethyl acetate. The organic layer was dried over magnesium sulfate, and then the solvent was distilled off with a rotary evaporator. The obtained product was purified by column chromatography (ethyl acetate / hexane = 30/70: volume ratio) to obtain 37.2 g of the following monomer.

Synthesis Example 3 (Synthesis of the following monomers)
10 g of 2-aminoethyl methacrylate and 12.1 g of triethylamine were placed in a three-necked flask and stirred for 1 hour. To this was added dropwise 10.2 g of trifluoromethylmethanesulfonyl chloride over 30 minutes. After completion of the dropwise addition, the mixture was stirred for 10 hours. 150 mL of diisopropyl ether was added to the reaction mixture, and the resulting precipitate was removed by filtration. To the filtrate, 200 mL of 0.5 M HCl was added, washed with 100 mL of an aqueous sodium bicarbonate solution, dried over magnesium sulfate, and then the solvent was distilled off with a rotary evaporator. The obtained product was purified by recrystallization (chloroform / hexane = 50/50) to obtain 6.8 g of the following monomer.

Synthesis Example 4 (Synthesis of the following monomers)
34.5 g of methacrylamide, 68.3 g of triethylamine, and 65 mL of THF were placed in a three-necked flask and cooled to 0 ° C. To this, a solution prepared by dissolving 66.2 g of camphorsulfonyl chloride in 100 mL of THF was added dropwise over 1 hour. After completion of dropping, the mixture was returned to room temperature and stirred for 1 hour. 500 mL of 2M HCl aqueous solution was added to the reaction solution, extracted with 350 mL of ethyl acetate, and the solvent was distilled off with a rotary evaporator. The reaction was dissolved in 375 mL of ethyl acetate and cooled to 0 ° C. To this was added 400 mL of 2M aqueous sodium hydroxide solution, neutralized with aqueous HCl solution, and the resulting precipitate was filtered off. The solid separated by filtration was dissolved in 500 mL of ethyl acetate, washed with 250 mL of 1M HCl aqueous solution and 250 mL of pure water, dried over magnesium sulfate, and then the solvent was distilled off with a rotary evaporator to obtain 50.1 g of the following monomer.

Synthesis Example 5 (Synthesis of the following monomers)
13.0 g of 1-hydroxyethyl methacrylate, 19.3 g of triethylamine, and 450 mL of tetrahydrofuran were placed in a three-necked flask and cooled to 0 ° C. Diketene 16.0g was dripped at this over 30 minutes. After completion of dropping, the mixture was stirred at room temperature for 1 hour. 600 mL of 1M HCl aqueous solution was added to the reaction mixture, extraction was performed with 600 mL of ethyl acetate, the organic layer was dried over magnesium sulfate, and then the solvent was distilled off with a rotary evaporator. The obtained product was purified by column chromatography (ethyl acetate / hexane = 10/90: volume ratio) to obtain 10.3 g of the following monomer.

Synthesis Example 6 Synthesis of Resin (1) Under a nitrogen stream, 8.8 g of cyclohexanone was placed in a three-necked flask and heated to 80 ° C. To this, 2.6 g of hydroxyethyl methacrylate, 11.8 g of 3-hydroxyadamantyl-1-methacrylate, 2.6 g of methacrylic acid, and 13 mol% of the polymerization initiator V-60 (manufactured by Wako Pure Chemical Industries) to 79 g of cyclohexanone. The dissolved solution was added dropwise over 6 hours. After completion of the dropping, the reaction was further carried out at 80 ° C. for 2 hours. The reaction mixture was allowed to cool and then added dropwise over 20 minutes to a mixture of methanol 900 m / water 100 ml. The precipitated powder was collected by filtration and dried, yielding 15 g of Resin (1). The weight average molecular weight of the obtained resin (1) was 10,000 in terms of standard polystyrene, and the dispersity (Mw / Mn) was 1.7.

Synthesis Example 7 Synthesis of Resin 16 Under a nitrogen stream, 62.2 g of PGME (propylene glycol monomethyl ether) was placed in a three-necked flask and heated to 80 ° C. Monomer (M1) 5.3 g, monomer (M2) 2.5 g, monomer (M3) 20.8 g, monomer (M4) 2.8 g, and polymerization initiator V-601 (manufactured by Wako Pure Chemical Industries) were used as monomers. On the other hand, a solution obtained by dissolving 12 mol% in 115.6 g of PGME was added dropwise over 6 hours. After completion of the dropping, the reaction was further carried out at 80 ° C. for 2 hours. After allowing the reaction solution to cool, 4-hydroxy-2,2,6,6-tetramethylpiperidine 1-oxyl free radical (Tokyo Kasei) 17.2 mg, 1,8-diazabicyclo [5.4.0] undeca- 7-ene 26.6g was added and it stirred at room temperature for 8 hours. After completion of the reaction, the mixture was added dropwise to 1780 g of water over 20 minutes, and the precipitated powder was collected by filtration. The powder collected by filtration was redissolved in 177 g of PGME, this solution was added dropwise to a mixed solution of hexane 2700 ml / ethyl acetate 300 ml over 20 minutes, and the precipitated powder was collected by filtration and dried to obtain 23.5 g. The weight average molecular weight of the obtained resin was 5200 in terms of standard polystyrene by GPC measurement, and the dispersity (Mw / Mn) was 1.5.

Synthesis Example 8 Synthesis of Resin 17 Under a nitrogen stream, 5.9 g of monomer (M5), 7.1 g of monomer (M6), 12.4 g of monomer (M7), and 1.9 g of monomer (M8) were dissolved in 578.8 g of PGME. This was heated to 75 ° C. A polymerization initiator V-65 (manufactured by Wako Pure Chemical Industries, Ltd.) was added to the monomer in an amount of 2.0 mol% and reacted at 75 ° C. for 2 hours. The reaction solution was allowed to cool and then added dropwise to 6060 g of water over 20 minutes, and the precipitated powder was collected by filtration. The powder collected by filtration was redissolved in 600 g of PGME, this solution was dropped into 6000 g of water over 20 minutes, and the precipitated powder was collected by filtration and dried to obtain 17.2 g. The weight average molecular weight of the obtained resin was 6800 in terms of standard polystyrene by GPC measurement, and the dispersity (Mw / Mn) was 1.7.

Synthesis Example 9 Synthesis of Resin 18 Under a nitrogen stream, 62.9 g of PGME (propylene glycol monomethyl ether) was placed in a three-necked flask and heated to 80 ° C. Monomer (M9) 11.1 g, monomer (M2) 3.0 g, monomer (M10) 10.9 g, monomer (M4) 6.4 g, and polymerization initiator V-601 (manufactured by Wako Pure Chemical Industries) were used as monomers. On the other hand, a solution prepared by dissolving 13 mol% in 115.3 g of PGME was added dropwise over 6 hours. After completion of the dropping, the reaction was further carried out at 80 ° C. for 2 hours. After allowing the reaction solution to cool, 25.8 mg of 4-hydroxy-2,2,6,6-tetramethylpiperidine 1-oxyl free radical (manufactured by Tokyo Chemical Industry), 1,8-diazabicyclo [5.4.0] undeca- 7-ene 22.8g was added and it stirred at room temperature for 8 hours. After completion of the reaction, the mixture was added dropwise to 2130 g of water over 20 minutes, and the precipitated powder was collected by filtration. The powder collected by filtration was redissolved in 177 g of PGME, and this solution was dropped into a mixed solution of hexane 2700 ml / ethyl acetate 300 ml over 20 minutes. The precipitated powder was collected by filtration and dried to obtain 21.9 g. The weight average molecular weight of the obtained resin was 4400 in terms of standard polystyrene by GPC measurement, and the dispersity (Mw / Mn) was 1.4.

Synthesis Example 10 Synthesis of Resin 21 Under a nitrogen stream, 60.2 g of PGME (propylene glycol monomethyl ether) was placed in a three-necked flask and heated to 80 ° C. Monomer (M12) 10.5 g, monomer (M2) 14.4 g, monomer (M3) 4.1 g, monomer (M13) 1.4 g, and polymerization initiator V-601 (manufactured by Wako Pure Chemical Industries) were used as monomers. On the other hand, a solution prepared by dissolving 14 mol% in 111.8 g of PGME was dropped over 6 hours. After completion of the dropping, the reaction was further carried out at 80 ° C. for 2 hours. After allowing the reaction liquid to cool, 66.2 mg of 4-hydroxy-2,2,6,6-tetramethylpiperidine 1-oxyl free radical (manufactured by Tokyo Chemical Industry), 0.33 g of tetraethylammonium bromide, and 2.7 g of glycidyl methacrylate were added. , And stirred at 90 ° C. for 9 hours. After completion of the reaction, the mixture was added dropwise to 2080 g of water over 20 minutes, and the precipitated powder was collected by filtration. The powder collected by filtration was redissolved in 170 g of PGME, and this solution was dropped into a mixed solution of hexane 2700 ml / ethyl acetate 300 ml over 20 minutes. The precipitated powder was collected by filtration and dried to obtain 24.6 g. The weight average molecular weight of the obtained resin was 4200 in terms of standard polystyrene by GPC measurement, and the dispersity (Mw / Mn) was 1.6.

  Other resins were synthesized using the same method. The weight average molecular weight was adjusted by changing the amount of the polymerization initiator.

<Resist preparation>
The components shown in the following table were dissolved in a solvent, and a solution with a solid content concentration of 6% by mass was prepared for each, and this was filtered through a polyethylene filter having a pore size of 0.1 μm to prepare a negative resist solution. The prepared negative resist composition was evaluated by the following method, and the results are shown in the following table. In addition, about each component in a table | surface, ratio when using two or more is mass ratio.

Evaluation Method An organic antireflection film ARC29A (Nissan Chemical Co., Ltd.) was applied on a silicon wafer, and baked at 205 ° C. for 60 seconds to form a 78 nm antireflection film. The positive resist composition prepared thereon was applied and baked at 120 ° C. for 60 seconds to form a 200 nm resist film. The obtained wafer was exposed using an ArF excimer laser scanner (PAS5500 / 1100, manufactured by ASML, NA0.75) through a 6% halftone mask, and the wafer was heated at 100 ° C. for 60 seconds and cooled to room temperature. The mixture was cooled to room temperature, developed with an aqueous tetramethylammonium hydroxide solution (2.38 mass%) for 30 seconds, rinsed with pure water, and then spin-dried to obtain a 100 nm 1: 1 line and space resist pattern.

<Membrane loss>
The height of the resist pattern was observed with a cross section SEM S4800 manufactured by Hitachi, and the film thickness was 100 nm, and the value obtained by subtracting this value from the coating film thickness 200 nm was used as the film reduction amount.
<Dimension before collapse>
In addition, when the exposure amount was reduced to make the 100 nm 1: 1 line and space line portion thinner, the dimension at which the pattern started to collapse was defined as the dimension before collapse.
The results are shown below.

  The abbreviations listed in the table indicate the following contents.

[(D) Radical polymerizable compound]

[(C2) radical generator]

[(C1) compound]

[Crosslinking agent (B)]

[Basic compounds]
DIA: 2,6-diisopropylaniline TPA: tripentylamine PEA: N-phenyldiethanolamine TOA: trioctylamine PBI: 2-phenylbenzimidazole

[Surfactant]
W-1: MegaFuck F176 (Dainippon Ink Chemical Co., Ltd.) (Fluorine)
W-2: Megafuck R08 (Dainippon Ink Chemical Co., Ltd.) (fluorine and silicon)
W-3: Polysiloxane polymer KP-341 (manufactured by Shin-Etsu Chemical Co., Ltd.) (silicon-based)
W-4: Troisol S-366 (manufactured by Troy Chemical Co., Ltd.)
W-5: PF656 (manufactured by OMNOVA, fluorine-based)
W-6: PF6320 (manufactured by OMNOVA, fluorine-based)

〔solvent〕
A1: Propylene glycol monomethyl ether acetate A2: Cyclohexanone B1: Propylene glycol monomethyl ether B2: Ethyl lactate B3: γ-Butyrolactone

Claims (9)

(A) an alkali-soluble resin,
(B) a crosslinking agent that crosslinks the alkali-soluble resin by the action of an acid,
(C1) a compound that causes a crosslinking reaction to proceed by irradiation with actinic rays or radiation,
(C2) a photo radical generator,
(D) a compound having a radical polymerizable group,
A negative resist composition comprising:   The alkali-soluble resin of component (A) has an organic group containing a fluorine-substituted alcohol structure, an organic group containing a sulfonamide structure, an organic group containing a dicarbonylmethylene structure, or an organic group containing a naphthol structure as an alkali-soluble group. The negative resist composition according to claim 1, wherein:   (A) The negative resist composition according to claim 1 or 2, wherein the alkali-soluble resin has a monocyclic or polycyclic alicyclic structure in the side chain.   The negative resist composition according to claim 1, wherein an acid having a pKa of −8 or less is generated from the component (C1) by irradiation with actinic rays or radiation.   5. The negative resist composition according to claim 4, wherein fluorinated sulfonimide acid is generated from the component (C1) upon irradiation with actinic rays or radiation.   The negative resist composition according to claim 4, wherein a fluorinated sulfonemethic acid compound is generated from the component (C1) upon irradiation with actinic rays or radiation.   (D) The negative resist composition according to claim 1, wherein the compound having a radical polymerizable group is a compound having a plurality of radical polymerizable groups. The negative resist according to any one of claims 1 to 7, wherein the crosslinking agent of component (B) is a compound having two or more partial structures represented by the following general formula (CLNM-1). Composition.

In the general formula (CLNM-1),
R ^NM1 represents a hydrogen atom, an alkyl group, a cycloalkyl group or an oxoalkyl group.   A resist pattern forming method comprising applying the negative resist composition according to claim 1, exposing the resist composition, and developing the resist pattern to form a resist pattern.