JP2009258506A - Negative resist composition and resist pattern-forming method - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a negative resist composition which ensures an adequate bridge margin (that is, substantially avoids the occurrence of the defect that patterns connect with each other). <P>SOLUTION: The negative resist composition contains (A) a resin whose solubility in an alkali developer decreases by the action of an acid, (B) a cationic polymerizable compound, (C) a cationic photopolymerization initiator, and (D) a compound which generates an acid upon irradiation with actinic rays or radiation. A pattern-forming method using the composition 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 wavelength used by exposure apparatuses used in photolithography has become shorter, 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” in which a pattern is formed by making an exposed portion hardly soluble or insoluble in a developer by exposure to radiation. However, positive resist compositions are currently in practical use.
There is a demand for forming various patterns such as lines, trenches, and holes in semiconductor elements 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, when using 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 negative 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 has been proposed. Yes. These are suitable for use in a KrF excimer laser, but when used in an ArF excimer laser, there is a problem that the sensitivity decreases due to strong absorption at 193 nm and the resolution deteriorates. Not suitable.
Therefore, development of a negative resist material with less light absorption at 193 nm, good sensitivity and high dry etching resistance is desired, and it is suitable for an exposure method using ArF and has good sensitivity and solution. There is an urgent need to develop resists that provide image quality.

Therefore, resists for ArF use have been 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 have been introduced to provide etching resistance. However, sufficient resolution is not obtained.
For example, in Patent Documents 1 to 5, a negative resist in which a urea-based crosslinking agent is contained in a resin obtained by copolymerizing a repeating unit having an aliphatic group and a repeating unit having an alkali-soluble group is used. There were problems such as inability to obtain good resolution and pattern collapse.
JP 2004-317575 A JP 2003-5370 A JP 2002-139844 A Japanese Patent Laid-Open No. 11-10927 JP 2000-56459 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 bridge margin is good (ie It is an object of the present invention to provide a negative resist composition that is less prone to defects in which patterns are connected to each other.

As a result of intensive investigations of future materials that can be placed on chemically amplified resists, the present inventors have found that the above-described object can be achieved by using specific materials, and have reached the present invention.
That is, the above object is achieved by the following configuration.

[1]
(A) a resin whose solubility in an alkaline developer is reduced by the action of an acid;
(B) a cationically polymerizable compound,
(C) a photocationic polymerization initiator,
(D) A negative resist composition comprising a compound that generates an acid upon irradiation with actinic rays or radiation.
[2]
The negative resist composition as described in [1], wherein the resin (A) is a resin having an alicyclic structure.
[3]
The negative resist composition as described in [1] or [2], wherein the resin (A) is a resin having a structure in which a lactone ring is formed in the side chain by the action of an acid.
[4]
A method for forming a resist pattern, comprising: a step of forming a resist film using the resist composition according to any one of [1] to [3]; a step of exposing the resist film; and a step of developing the resist film. .

  According to the present invention, a negative resist composition having a good bridge margin and a pattern forming method using the negative resist composition can be provided.

  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.

(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 an organic group having a sulfonic acid structure, and the like.
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.
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 having 1 to 6 carbon atoms) represents an alkylcarbonyl group (preferably having 1 to 6 carbon atoms), an alkylsulfone group (preferably having 1 to 6 carbon atoms), an alkylamide group (preferably having 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 ^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 ^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 ^AS19 represents an integer of 1 to 7.
n ^RAS19 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.

  Specifically, as the alicyclic hydrocarbon structure, the monocyclic structure includes cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, and polycyclic structures such as norbornyl, isobornyl, tricyclodecanyl, tetracyclododecane. Nyl, 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) Repeating unit having polymerizable group The alkali-soluble resin used in the present invention may further contain (a3) a repeating unit having a polymerizable group. In this case, since the alkali-soluble resin contains a repeating unit having a polymerizable group, the polymerizable group and a cationic polymerizable monomer described later cause a cationic polymerization reaction, and the exposed portion involves a resin component. By forming a dimensional structure or greatly increasing the molecular weight of the resin, it is expected to obtain a high dissolution contrast in an alkali developer.
The repeating unit having a polymerizable group is preferably a repeating unit having an oxetane structure, an epoxy structure, a conjugated diene structure, or a vinyl structure.

(Repeating unit with oxetane structure)
The oxetane structure referred to here represents a cyclic skeleton formed by one oxygen atom and three carbon atoms.

  Examples of the oxetane structure include a structure represented by the following formula (1).

In Formula (1), R ^{1 to} R ⁵ each independently represents a hydrogen atom or a monovalent organic group which may have a substituent, and adjacent groups are bonded to each other to form a ring. May be. R ^{1 to} R ⁵ are each independently a hydrogen atom, a halogen atom, an amino group, or a carboxyl group. Examples thereof include an alkoxycarbonyl group, a cyano group, an alkyl group which may have a substituent, an alkoxy group which may have a substituent, and an alkylamino group which may have a substituent.

* Represents a bond bonded to the structure represented by the general formula (ASM-1) or (ASM-2). The bond may be bonded to R ^{1 to} R ⁵ to form a ring structure.

  The repeating unit having the oxetane structure may contain one or more or a plurality of the oxetane structures, and the number is preferably 1 to 4, more preferably 1 to 2.

  Examples of the repeating unit having an oxetane structure are shown below, but the present invention is not limited thereto.

(Repeating unit with epoxy structure)

  Examples of the epoxy structure include a structure represented by the following general formula (EPM1).

In the formula (EPM1),
R ^{EPM1 to} R ^EPM3 each independently represent a hydrogen atom, a halogen atom, an alkyl group, or a cycloalkyl group, and the alkyl group and the cycloalkyl group may have a substituent. R ^EPM1 and R ^EPM2 , R ^EPM2 and R ^EPM3 may be bonded to each other to form a ring structure.
* Represents a bond bonded to the structure represented by the general formula (ASM-1) or (ASM-2). The bond ^may be bonded to R ^{EPM1 to} R ^EPM3 to form a ring structure.
Examples of the substituent that the alkyl group and cycloalkyl group may have include a hydroxyl group, a cyano group, an alkoxy group, an alkylcarbonyl group, an alkoxycarbonyl group, an alkylcarbonyloxy group, an alkylthio group, an alkylsulfone group, and an alkylsulfonyl group. Groups, alkylamino groups, alkylamide groups, and the like.

  One or a plurality of the epoxy structures may be contained in the repeating unit having the epoxy structure, and the number thereof is preferably 1 to 4, more preferably 1 to 2.

Although the repeating unit which has an epoxy structure is illustrated below, this invention is not limited to these.
In the formula, R ^X represents a hydrogen atom, a methyl group, a trifluoromethyl group, or a hydroxymethyl group.

(Repeating unit having a conjugated diene structure)
The conjugated diene structure is preferably a structure represented by the following formula (2) or (3).

In formula (2), R ^{1c to} R ^5c each independently represents a hydrogen atom or an organic group. R ^{1c to} R ^5c may be linked to each other directly or via an organic group to form a ring structure. However, the benzene ring structure is excluded. * Represents a bond bonded to the structure represented by the general formula (ASM-1) or (ASM-2). The bond ^may be bonded to R ^{1c to} R ^5c to form a ring structure.

Examples of the organic group in R ^{1c to} R ^5c include a halogen atom, an amino group, an alkyl carboxyl group, an alkoxycarbonyl group, a cyano group, an alkyl group which may have a substituent, an alkoxy group, an alkylamino group, an alkylthio group, and the like. Is mentioned.

In General Formula (3), R ^{1t to} R ^5t each independently represent a hydrogen atom or an organic group. R ^{1t to} R ^5t may be linked to each other directly or via an organic group to form a ring structure. * Represents a bond bonded to the structure represented by the general formula (ASM-1) or (ASM-2). The bond may be bonded to R ^{1t to} R ^5t to form a ring structure.

In formula (3), the organic group in R ^{1t to} R ^5t is a halogen atom, an amino group, or a carboxyl group. Examples thereof include an alkoxycarbonyl group, a cyano group, an alkyl group which may have a substituent, an alkoxy group which may have a substituent, and an alkylamino group which may have a substituent.

Examples of the substituent that can be introduced into R ^{1c to} R ^5c and R ^{1t to} R ^5t 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, and a cyano group. Group, and the like.

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

R ^x represents a hydrogen atom, a methyl group, a trifluoromethyl group, or a hydroxymethyl group.

(Repeating unit with vinyl structure)
The vinyl structure here represents a structure in which a vinyl group or a hydrogen atom of the vinyl group is substituted with an organic group.

  The vinyl structure contained in the repeating unit having the vinyl structure is represented by the following general formula (MV-1).

In the general formula (MV-1), R ^{mv1 to} R ^mv3 each independently represent a hydrogen atom, a halogen atom, a hydroxyl group, or an organic group. * Represents a bond bonded to the structure represented by the general formula (ASM-1) or (ASM-2). The bond ^may be bonded to R ^{mv1 to} R ^mv3 to form a ring structure.
^Examples of the organic group in R ^{mv1 to} R ^mv3 include a cyano group, an alkyl group, an alkoxy group, an alkylcarbonyl group, an alkoxycarbonyl group, an alkylcarbonyloxy group, an alkylthio group, an alkylsulfone group, an alkylsulfonyl group, an alkylamino group, and an alkylamide. Groups.

Preferable organic groups in R ^{mv1 to} R ^mv3 include a hydrogen atom, hydroxyl group, methyl group, ethyl group, isopropyl group, n-butyl group, s-butyl group, methoxy group, ethoxy group, and the like. R ^{mv1 to} R ^mv3 may be substituted with the preferred organic group.

R ^mv1 , R ^mv2 and R ^mv3 may be bonded to each other to form a ring structure. Specific examples include an embodiment in which R ^mv1 and R ^mv2 , R ^mv1 and R ^mv3 are bonded to each other to form a ring structure. In addition, these ring structures may have a skeleton made of only carbon atoms or may contain heteroatoms such as oxygen atoms.

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

R ^x represents a hydrogen atom, a methyl group, a trifluoromethyl group, or a hydroxymethyl 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 ^LC represents an integer of 0 to 4. When n ^LC 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.

(A5) Repeating unit containing a group whose polarity is reduced by the action of an acid The alkali-soluble resin component used in the present invention contains (a5) a group whose polarity is lowered by the action of an acid.

  The group whose polarity is lowered by the action of an acid is preferably a structure that forms a lactone ring in the side chain by the action of an acid. Examples of this structure include the following general formulas (La-1) and (La-2).

In formulas (La-1) and (La-2), Rl _{1 to} Rl ₈ each independently represents a hydrogen atom, an alkyl group having 1 to 10 carbon atoms, a linking group bonded to a main chain or a side chain. However, in formula (La-1), at least one of Rl _{1 to} Rl ₆ and in formula (La-2), at least one of Rl _{1 to} Rl ₈ is a bond that binds to the main chain or side chain of the resin. It is a hand. In the formula (La-1), two or more groups selected from Rl _{1 to} Rl ₆ may be bonded to each other to form a ring structure. In the formula (La-2), Rl _{1 to} Rl Two or more groups selected from ₈ may be bonded to each other to form a ring structure. Xa represents a single bond, a linking group having a nitrogen atom or a sulfur atom, or an alkylene group having 1 to 21 carbon atoms. Z _h represents a hydrogen atom, a methyl group, an acetyl group, an acetal group.

Examples of the acetal group for Z _h include those represented by —C (H) (L) —O—Z (L and Z each independently represents an alkyl group, a cycloalkyl group, or an aralkyl group).

  Xa is preferably a single bond, a methylene group, or an ethylene group, and is selected so as to be a 5- or 6-membered ring when the structure is closed by the action of an acid to form a lactone structure. Is preferred.

Examples of the alkyl group of L and Z of the acetal group of Z _h include, for example, methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, t-butyl group, pentyl group, hexyl group, octyl group And a straight-chain or branched alkyl group having 1 to 20 carbon atoms such as a dodecyl group, and an acetal group having the following structure is preferable.

The L and Z cycloalkyl group acetal group Z _h with, for example, cyclopropyl group, cyclobutyl group, cyclopentyl group includes those having 3 to 20 carbon atoms such as a cyclohexyl group, the following structures Acetal groups are preferred.

  As a repeating unit containing a group whose polarity is reduced by the action of an acid, it is preferable to contain the structures of the formulas (La-1) and (La-2) in the side chain as compared to the linear structure. The reactivity improves by including in a side chain.

  As a repeating unit containing the structures of formulas (La-1) and (La-2) in the side chain, the polarity of which decreases by the action of an acid, for example, formula (Ls-1) can be mentioned.

In the formula (Ls-1), A represents an organic group, Y represents the formula (La-1) or (La-2), and R _m1 represents a hydrogen atom or a methyl group.

In the formula (Ls-1), examples of the organic group A include an alkylene group, a cycloalkylene group, an arylene group, an alkenylene group, and a linking group in which these groups contain a single bond, an oxygen atom, a sulfur atom, or nitrogen. And a group in which two or more are connected via each other.
The alkylene group as the organic group (A) may have a substituent, and may have an oxygen atom, a sulfur atom, or a nitrogen atom in the alkylene chain. Specifically, a methylene group, ethylene group, n-propylene group, n-butylene group, n-pentylene group, n-hexylene group, n-octylene group, n-dodecylene group, n-tetradecylene group, n-octadecylene group, etc. And a branched alkylene group such as a linear alkylene group, isopropylene group, isobutylene group, t-butylene group, neopentylene group, and 2-ethylhexylene group.
The cycloalkyl group as the organic group (A) may have a substituent, may be polycyclic, and may have an oxygen atom in the ring. Specific examples include a cyclopropylene group, a cyclopentylene group, a cyclohexylene group, a norbornylene group, and an adamantylene group.
The arylene group as the organic group (A) may have a substituent, and examples thereof include a phenylene group and a naphthylene group.

  The organic group (A) is preferably an alkylene group having a cycloalkyl group as a substituent or a cycloalkylene group. More preferably, a polycyclic cycloalkylene group is mentioned.

  Further, as a preferred form of the formula (Ls-1), the following formula (Las-1) and the like can be mentioned.

In the formula (Las-1), R _m1 represents a hydrogen atom or a methyl group.
X _{a5 to} X _a6 represent a single bond, a linking group having a nitrogen atom or a sulfur atom, or an alkylene group having 1 to 21 carbon atoms. Z _na4 represents a hydrogen atom, a methyl group, an acetyl group, or an acetal group. m _s represents an integer of 0 to 3.
X _{a5 to} X _a6 are preferably a single bond or an alkylene group having 1 to 2 carbon atoms. And when the said structure closes by the effect | action of an acid, it is preferable to select so that a 5-membered ring or a 6-membered ring may be formed.
_Examples of the acetal group of Z _na4 include the same as those described in the general formulas (La-1) and (La-2).

  Moreover, as another form preferable as an organic group (A), following formula (Las-2) or (Las-3) etc. are mentioned.

In the formulas (Las-2) and (Las-3), R _m1 represents a hydrogen atom or a methyl group.
Rl _{1 to} Rl ₂₇ each independently represents a hydrogen atom, a fluorine atom, or an organic group. _Xa7 represents a single bond, a linking group having a nitrogen atom or a sulfur atom, or an alkylene group having 1 to 21 carbon atoms. Z _na5 represents a hydrogen atom, a methyl group, an acetyl group, or an acetal group.
X _a7 is preferably a single bond or a methylene group.
_Examples of the acetal group for Z _na5 include the same as those described in the general formulas (La-1) and (La-2).

Examples of the organic group (Rl _{1 to} Rl ₂₇ ) include an alkyl group, a cycloalkyl group, an aryl group, an aralkyl group, an alkenyl group, an alkoxy group, an alkoxycarbonylamino group, and a cyano group.
Specific examples of the alkyl group of the organic group (Rl _{1 to} Rl ₂₇ ) include methyl group, ethyl group, n-propyl group, n-butyl group, n-pentyl group, n-hexyl group, n-octyl group, n Examples include linear alkyl groups such as -dodecyl group, n-tetradecyl group and n-octadecyl group, and branched alkyl groups such as isopropyl group, isobutyl group, t-butyl group, neopentyl group and 2-ethylhexyl group. These may have an atomic group having an oxygen atom, a sulfur atom, or a nitrogen atom in the chain.
The cycloalkyl group of the organic group (Rl _{1 to} Rl ₂₇ ) may be polycyclic and may have an oxygen atom in the ring. Specific examples include a cyclopropyl group, a cyclopentyl group, a cyclohexyl group, a norbornyl group, an adamantyl group, and the like.
Examples of the aryl group of the organic group (Rl _{1 to} Rl ₂₇ ) include a phenyl group and a naphthyl group.
Examples of the aralkyl group of the organic group (Rl _{1 to} Rl ₂₇ ) include those in which an alkylene group is bonded to the above-mentioned aryl group.
Examples of the alkenyl group of the organic group (Rl _{1 to} Rl ₂₇ ) include those having 2 to 10 carbon atoms such as vinyl group and allyl group.
Examples of the alkoxy group of the organic group (Rl _{1 to} Rl ₂₇ ) include those in which an oxygen atom is bonded to the above-described alkyl group.
Examples of the alkoxycarbonylamino group of the organic group (Rl _{1 to} Rl ₂₇ ) include those having 2 to 10 carbon atoms such as an ethoxycarbonylamino group.
The groups listed as the groups Rl _{1 to} Rl ₂₇ may further have a substituent. Further, examples of the substituent that may be included include an alkyl group, a cycloalkyl group, an aryl group, an aralkyl group, an alkenyl group, an alkoxy group, an alkoxycarbonylamino group, a cyano group, and a hydroxyl group.

The organic group (Rl _{1 to} Rl ₂₇ ) is preferably a hydrogen atom.

  Compounds (Lsaa-1) to (Lsaa-12) are exemplified as repeating units containing the structures of the formulas (La-1) and (La-2) whose side chains are reduced in polarity by the action of an acid. It is not limited.

-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 50 mol%, preferably 8 to 35 mol%, more preferably 10 to 30 mol%.
(A2) The repeating unit having an aliphatic group is generally 15 to 90 mol%, preferably 25 to 80 mol%, more preferably 30 to 60 mol%.
(A3) The repeat having a polymerizable group is generally 3 to 30 mol%, preferably 5 to 25 mol%, more preferably 7 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%.
(A5) The repeating unit containing a group whose polarity is lowered by the action of an acid is generally 5 to 50 mol%, preferably 8 to 35 mol%, more preferably 10 to 30 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.

  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) Polymerizable compound The negative resist composition used in the present invention contains (B) a polymerizable compound. As the polymerizable compound (B), a low molecular compound having an oxetane structure, a low molecular compound having an epoxy structure, a compound having a conjugated diene structure, a compound having a vinyl structure, or the like can be preferably used.

(Low molecular compound having oxetane structure (polymerizable monomer))
A low molecular compound (hereinafter also referred to as a polymerizable monomer) having an oxetane structure (a cyclic skeleton formed of one oxygen atom and three carbon atoms) causes a cationic polymerization reaction with an acid generated from a photocationic polymerization initiator, The low molecular weight compounds having the oxetane structure react with each other.
The low molecular weight compound having an oxetane structure is preferably a compound having a molecular weight of 2000 or less, more preferably a compound having a molecular weight of 100 to 1800, still more preferably a compound having a molecular weight of 130 to 1600, and a molecular weight of 200 to 200. Particular preference is given to 1500 compounds.

  Preferred examples of the polymerizable monomer that can be used in the present invention include a low molecular compound having an oxetane structure represented by the following general formula (1 ').

In formula (1 ′), R ^{1 to} R ⁵ each independently represents a hydrogen atom or a monovalent organic group which may have a substituent, and adjacent groups are bonded to each other to form a ring. It may be formed. R ^{1 to} R ⁵ are each independently a hydrogen atom, a halogen atom, an amino group, or a carboxyl group. Examples thereof include an alkoxycarbonyl group, a cyano group, an alkyl group which may have a substituent, an alkoxy group which may have a substituent, and an alkylamino group which may have a substituent.
Q represents a single bond or an n-valent organic group. R ^{1 to} R ⁵ may combine not only with each other but also with Q to form a ring structure.
n represents an integer greater than or equal to 2, Preferably it is 2-10, More preferably, it is 2-6.

  When Q is an n-valent organic group, a chain or cyclic alkyl structure (preferably having 2 to 20 carbon atoms) or an aryl structure (preferably having 6 to 30 carbon atoms), or an ether, ester, amide or sulfonamide thereof. Etc. are preferable.

  The polymerizable monomer has a polymerization function regardless of whether it has one or a plurality of oxetane structures in the molecule, but preferably has a plurality of oxetane structures from the viewpoint of sensitivity, preferably 2 to 10 More preferably, it is 2 to 8, more preferably 2 to 6, particularly preferably 2 to 4.

  By having multiple oxetane structures in the polymerizable monomer molecule, the exposed area has a more complicated entangled structure, high sensitivity and high dissolution contrast with alkaline developer, and suppression of swelling, high resolution. Image quality is achieved.

In the case of a polymerizable monomer having a plurality of oxetane structures in one molecule, the oxetane structures may be the same or different.
In addition, polymerizable monomers having the same oxetane structure in one molecule may be mixed with a plurality of polymerizable monomers having different oxetane structures.
By using different functional numbers and different oxetane structures together, it is possible to balance sensitivity and other performances.

  The polymerizable monomer may be in a chemical form such as, for example, a monomer, a prepolymer, that is, a dimer, a trimer and an oligomer, or a mixture thereof and a copolymer thereof. Examples of monomers and copolymers thereof include unsaturated carboxylic acids (for example, acrylic acid, methacrylic acid, itaconic acid, crotonic acid, isocrotonic acid, maleic acid, etc.), and esters and amides thereof. In this case, an ester of an unsaturated carboxylic acid and an aliphatic polyhydric alcohol compound, or an amide of an unsaturated carboxylic acid and an aliphatic polyvalent amine compound is used.

  Although the polymerizable monomer used for this invention is illustrated below, this invention is not limited to these.

  The content of the polymerizable monomer component in the present invention is preferably 0.5% to 90% by weight, more preferably 5% to 80% by weight, and still more preferably 10 to 80% by weight with respect to the alkali-soluble resin component. %, Most preferably 15 to 80% by weight.

(Low molecular compound with epoxy structure)
Examples of the epoxy compound include compounds represented by the following general formula (EP2).
The epoxy compound is preferably a compound having two or more epoxy structures in the molecule (hereinafter also referred to as an epoxy compound). The epoxy compound undergoes a cationic polymerization reaction by the action of an acid generated from the photoacid generator (C) described later, and (A) exposure is caused by causing a polymerization reaction between the epoxy moiety of the alkali-soluble resin and the epoxy compound. It is considered that a three-dimensional structure is formed in the part and the molecular weight increases. By this action, the exposed portion becomes insoluble in the alkaline developer and pattern formation becomes possible.

In formula (EP2),
R ^{EP1 to} R ^EP3 each independently represent a hydrogen atom, a halogen atom, an alkyl group or a cycloalkyl group, and the alkyl group and the cycloalkyl group may have a substituent. R ^EP1 and R ^EP2 , R ^EP2 and R ^EP3 may be bonded to each other to form a ring structure. Examples of the substituent that the alkyl group and cycloalkyl group may have include a hydroxyl group, a cyano group, an alkoxy group, an alkylcarbonyl group, an alkoxycarbonyl group, an alkylcarbonyloxy group, an alkylthio group, an alkylsulfone group, and an alkylsulfonyl group. Groups, alkylamino groups, alkylamide groups, and the like.
^QEP represents a single bond or an ^nEP- valent organic group. R ^EP1 to R ^EP3 may be combined to form a ring structure with Q ^EP not only with each other but.
n ^EP represents an integer of 2 or more, preferably 2 to 10, more preferably 2-6.

When ^QEP is an organic group having an n ^EP value, a chain or cyclic alkyl structure (preferably having 2 to 20 carbon atoms) or an aryl structure (preferably having 6 to 30 carbon atoms), or an ether, ester or amide thereof, Sulfonamide and the like are preferable.

Preferably as the Q ^EP is an organic group having no absorption with respect to ArF laser (193 nm), chain or cyclic alkyl structure and these ethers, esters, amides, sulfonamides are preferred. A cyclic alkyl structure is preferable from the viewpoint of etching resistance and pattern dimension control, and a chain alkyl structure is preferable from the viewpoint of high contrast. The Q ^EP may have a structure having both alkyl structure and cycloalkyl structure. In this case, the above performance can be balanced, which is a preferable mode.
Specific examples of the chain alkyl structure include methyl, ethyl, propyl, i-propyl, butyl, s-butyl, t-butyl, pentyl, hexyl, decyl, and ethers, esters, amides, and sulfonamides thereof. It is done.
Specific examples of the cycloalkyl structure include monocyclic alkane structures such as cyclobutane, cyclopentane, cyclohexane and cyclooctane, polycyclic alkane structures such as norbornane, isobornane, tricyclodecane, tetracyclododecane and adamantane, and ethers thereof. Examples thereof include esters, amides, and sulfonamides.

When ^QEP has an aryl structure, a condensed aromatic structure having a small absorption with respect to ArF laser (193 nm) and ethers, esters, amides and sulfonamides thereof are preferable. Is preferred. Examples of such a structure include naphthalene, anthracene, phenanthrene, naphthacene, pyrene, and perylene. Also, Q ^EP may have a structure having both condensed aromatic structures and chain or cyclic alkyl structure.

  Specific examples of the compound having an epoxy structure are illustrated below, but the present invention is not limited thereto.

  The molecular weight of an epoxy compound becomes like this. Preferably it is 100-2000, More preferably, it is 150-1500, More preferably, it is 200-1000.

  It is preferable to contain 1-80 mass% of epoxy compounds in the solid content of a resist composition, It is more preferable to contain 3-75 mass%, It is especially preferable to contain 5-70 mass%.

(Compound having conjugated diene structure (polymerizable monomer))
The conjugated diene structure is preferably a structure represented by the following general formula (2 ′) or (3 ′).
A compound having a conjugated diene structure (hereinafter also referred to as a polymerizable monomer) causes a cationic polymerization reaction with an acid generated from a photocationic polymerization initiator, and the polymerizable monomers or the polymerizable monomers and (A) an alkali-soluble resin. It has a function to polymerize with. In the case of polymerization between the polymerizable monomer and (A) the alkali-soluble resin, it can be polymerized by reacting between the repeating unit having a conjugated diene structure and (A) the alkali-soluble resin.

In general formula (2 ′), R ^{1c to} R ^5c each independently represents a hydrogen atom or an organic group. R ^{1c to} R ^5c may be bonded to each other directly or via an organic group to form a ring structure. However, the benzene ring structure is excluded.

In general formula (2 ′), as the organic group in R ^{1c to} R ^5c , a halogen atom, an amino group, an alkyl carboxyl group, an alkoxycarbonyl group, a cyano group, an alkyl group which may have a substituent, an alkoxy group, Examples thereof include an alkylamino group and an alkylthio group.
Q _1c represents a single bond or an n ^1c- valent organic group. R ^{1c to} R ^5c may combine not only with each other but also with Q _1c to form a ring structure.
n ^1c represents an integer of 2 or more, preferably 2 to 10, and more preferably 2 to 6.

When Q _1c is an n ^1c- valent organic group, a chain or cyclic alkyl structure (preferably having 2 to 20 carbon atoms) or an aryl structure (preferably having 6 to 30 carbon atoms), or an ether, ester, amide thereof, Sulfonamide and the like are preferable.

In general formula (3 ′), R ^{1t to} R ^5t each independently represents a hydrogen atom or an organic group. R ^{1t to} R ^5t may be linked to each other directly or via an organic group to form a ring structure.

In general formula (3 '), as an organic group in R ^<1t > -R < ^5t >, a halogen atom, an amino group, and a carboxyl group. Examples thereof include an alkoxycarbonyl group, a cyano group, an alkyl group which may have a substituent, an alkoxy group which may have a substituent, and an alkylamino group which may have a substituent.

Q _1t represents a single bond or an n ^1t- valent organic group. R ^{1t to} R ^5t may combine not only with each other but also with Q _1t to form a ring structure.
n ^1t represents an integer of 2 or more, preferably 2 to 10, and more preferably 2 to 6.

When Q _1t is an n ^1t valent organic group, a chain or cyclic alkyl structure (preferably having 2 to 20 carbon atoms) or an aryl structure (preferably having 6 to 30 carbon atoms), or an ether, ester, amide thereof, Sulfonamide and the like are preferable.

Examples of substituents that can be introduced into R ^{1c to} R ^5c , R ^{1t to} R ^5t , Q _1c , and Q _1t include alkyl groups, alkenyl groups, alkynyl groups, alkoxy groups, halogen atoms, amino groups, alkylamino groups, and carboxyl groups. , An alkoxycarbonyl group, a cyano group, and the like.

  The polymerizable monomer may be in a chemical form such as, for example, a monomer, a prepolymer, that is, a dimer, a trimer and an oligomer, or a mixture thereof and a copolymer thereof. Examples of monomers and copolymers thereof include unsaturated carboxylic acids (for example, acrylic acid, methacrylic acid, itaconic acid, crotonic acid, isocrotonic acid, maleic acid, etc.), and esters and amides thereof. In this case, an ester of an unsaturated carboxylic acid and an aliphatic polyhydric alcohol compound, or an amide of an unsaturated carboxylic acid and an aliphatic polyvalent amine compound is used.

  Although the polymerizable monomer used for this invention is illustrated below, this invention is not limited to these.

The molecular weight of the polymerizable monomer component is preferably 100 to 2000, more preferably 150 to 1500, and still more preferably 200 to 1000.
The content of the polymerizable monomer component in the present invention is 0.5 to 50% by weight, preferably 1 to 40% by weight, more preferably 2 to 30% by weight, based on the solid content of the resist composition.

(Compound having vinyl structure (cationically polymerizable monomer))
The compound having a vinyl structure is preferably a compound having two or more vinyl structures in the molecule. The vinyl structure is represented by the following general formula (CLV-1).
A compound having two or more vinyl structures undergoes a cationic polymerization reaction by the action of an acid generated from a photocationic polymerization initiator, which will be described later, causes a crosslinking reaction between the cationic polymerizable monomers, and has a three-dimensional crosslinked structure in the exposed area. It is thought that it is formed. By this action, the exposed portion is insoluble in the alkaline developer, and pattern formation becomes possible. By using the crosslinking system in this way, a high dissolution contrast between the exposed portion and the unexposed portion can be obtained as compared with polarity conversion, and good resolution is achieved.
Further, when (a) the alkali-soluble group in the alkali-soluble resin is a specific group such as a carboxyl group, a compound having two or more vinyl structures and (A) the (a1) in the alkali-soluble resin It is also conceivable to cause a reaction with an alkali-soluble group.

In General Formula (CLV-1), R ^{v1 to} R ^v3 each independently represent a hydrogen atom, a halogen atom, or an organic group.
Examples of the organic group in R ^{v1 to} R ^v3 include a hydroxyl group, an alkyl group, an alkoxy group, an alkylcarbonyl group, an alkoxycarbonyl group, an alkylcarbonyloxy group, an alkylthio group, an alkylsulfone group, an alkylsulfonyl group, an alkylamino group, and an alkylamide. Group.

In General Formula (CLV-1), P ^v represents a structure composed of a combination of a methylene linking group, an oxygen atom, a sulfur atom, or —N (R ^V0 ) —. R ^V0 represents a hydrogen atom or a monovalent organic group. Examples of the organic group in R ^V0 include a cyano group, an alkyl group, an alkoxy group, an alkylcarbonyl group, an alkoxycarbonyl group, an alkylcarbonyloxy group, an alkylthio group, an alkylsulfone group, an alkylsulfonyl group, an alkylamino group, and an alkylamide group. It is done.

R ^v1 , R ^v2 , R ^v3 , and P ^v may be bonded to each other to form a ring structure. Specifically, there may be mentioned embodiments in which R ^v1 and R ^v2 , R ^v3 to P ^v , R ^v1 and R ^v3 , R ^v2 and P ^v are bonded to each other to form a ring structure.

  The compound (B) having two or more vinyl structures is preferably a compound represented by the following general formula (CLV-2).

In the formula (CLV-2), R ^{v1 to} R ^v3 and P ^v have the same meaning as in the general formula (CLV-1). Q ^v represents a single bond or an n ^v- valent organic group, and n ^v represents an integer of 2 or more. However, n ^v = 2 when Q ^v is a single bond.

The n ^v-valent organic group, a chain or cyclic aliphatic group or an aromatic group and the like, chain aliphatic group may be saturated aliphatic groups be unsaturated aliphatic groups Good. Preferred embodiments of the n ^v-valent organic group, and the structure represented by the general formula (IV) or (V), n ^v-valent excluding the further n ^v -2 hydrogen atoms from these structures Structure is mentioned.

In the general formula (CLV-2), R ^{v1 to} R ^v3 have the same ^{meaning as} in the general formula (CLV-1). Preferable embodiments of R ^{v1 to} R ^v3 include a hydrogen atom, hydroxyl group, methyl group, ethyl group, isopropyl group, n-butyl group, s-butyl group, methoxy group, ethoxy group, and the like. R ^{v1 to} R ^v3 may be any combination of the preferred embodiments.

P ^{v in the} general formula (CLV-2) has the same meaning as in the general formula (CLV-1). Preferable embodiments of ^Pv include a methylene group, an ether group, a methylenecarbonyloxy group, an amino group, and the like.

R ^v1 , R ^v2 , R ^v3 , and P ^v may be bonded to each other to form a ring structure. These ring structures may be monocyclic or polycyclic. In addition, these ring structures may have a skeleton made of only carbon atoms or may contain heteroatoms such as oxygen atoms.

In the general formula (CLV-2), n ^v represents an integer of 2 or more. The preferable range of n ^v is 2 to 10, more preferably 3 to 8, and further preferably 3 to 6. When n ^v is 2 or more, the compound (B) having two or more vinyl structures has a function as a cationic polymerizable monomer and forms a cross-linked structure in which the exposed part is more complicated, and the alkali It is considered that a high dissolution contrast with respect to the developing solution is expressed, swelling is suppressed, and high resolution is achieved.

  The general formula (CLV-2) is a cationic polymerizable monomer having the same vinyl structure, but the cationic polymerizable monomer may have a plurality of different vinyl structures in the same molecule.

  In the present invention, one kind of the cationic polymerizable monomer may be used, or a plurality of different kinds may be used in combination. By using a cationic polymerizable monomer having a different number of functional groups and different vinyl structures, it is possible to balance sensitivity and other performances.

The cationically polymerizable monomer may be in a chemical form such as a monomer, a prepolymer, that is, a dimer, a trimer, and an oligomer, or a mixture thereof and a copolymer thereof. Monomers and copolymers thereof include esters of polycarboxylic acids, amides, esters of polyhydric alcohols, and ethers.
The molecular weight of the cationically polymerizable monomer in the present invention is usually 3,000 or less, preferably 1,500 to 80, more preferably 1,000 to 100.

  Examples of the cationic polymerizable monomer used in the present invention are shown below, but the present invention is not limited thereto.

The content of the cationically polymerizable monomer component in the present invention is usually 0.5 to 60% by mass, preferably 1 to 50% by mass, more preferably 5 to 40% by mass, based on the solid content of the resist composition. .
The cationically polymerizable monomer used in the present invention can be synthesized using, for example, the corresponding alcohol and vinyl bromide as described below.

(C) Photocationic polymerization initiator

The negative resist composition used in the present invention contains a compound that initiates a polymerization reaction upon irradiation with actinic rays or radiation (hereinafter also referred to as a photopolymerization initiator). The photopolymerization initiator is a compound that is decomposed by light and initiates and accelerates the polymerization of the compound (B) having a polymerizable group, and preferably has an absorption in a wavelength region of 150 to 500 nm. Photopolymerization 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, hexaarylbiphenyls. Examples include imidazole compounds, organic boric acid compounds, disulfonic acid compounds, oxime ester compounds, onium salt compounds, and acylphosphine (oxide) compounds. These photopolymerization initiators can be used alone or in combination of two or more.
The photopolymerization initiator can also serve as (D) a compound that generates an acid upon irradiation with actinic rays or radiation (photoacid generator).

  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 the 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, and a phosphine oxide compound , Metallocene compounds, oxime compounds, triallylimidazole dimers, onium compounds, benzothiazole compounds, benzophenone compounds, acetophenone compounds and derivatives thereof, cyclopentadiene-benzene-iron complexes and salts thereof, halomethyloxadiazole compounds And compounds selected from the group consisting of 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 using the said photoinitiator for a resist composition, in order to form a fine pattern with a favorable shape, it is necessary to develop a fine unexposed part with a residue without a residue. In addition, a photopolymerization initiator that does not generate an outgas that may damage the exposure machine because an outgas generated by decomposition of the photopolymerization initiator during exposure may damage the exposure machine. In view of these points, the 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 an onium compound. A compound (a sulfonium salt compound or an iodonium compound is preferred).

  The 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%.

  The 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 and R ^O3 is preferably an aryl 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 aryl 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.
In addition, the 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.

A photocationic polymerization initiator can be used individually by 1 type or in combination of 2 or more types.
The content of the cationic photopolymerization initiator 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. More preferably, it is 1-7 mass%.
(E) 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.

(F) Surfactant Fluorine-Based and / or Silicone-Surfactant The negative resist composition of the present invention preferably further contains a surfactant, and is preferably a fluorine-based and / or silicon-based surfactant (fluorine-based surfactant). It is more preferable to contain any one of surfactants, silicon surfactants, surfactants having both fluorine atoms and silicon atoms, 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 photosensitive composition (excluding the solvent).

(G) Basic compound The photosensitive composition of the present invention preferably contains a basic compound in order to reduce the 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 on the basis of solid content of a photosensitive 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) = 2.5 to 300. In other words, the molar ratio is preferably 2.5 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 5.0 to 200, and still more preferably 7.0 to 150.

(H) Hydrophobic polymer Exposure (immersion exposure) may be performed by filling a liquid (immersion medium) having a refractive index higher 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) to (z).
(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;
(Z) A group that decomposes by the action of an acid.

(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).

  In the hydrophobic resin (HR), the repeating unit having a group (z) that is decomposed by the action of an acid is a repeating unit having a group that is decomposed by the action of an acid to express an acid group (alkali-soluble group). That is. Specific examples include a repeating unit having a tertiary alkyl ester group, and more specific examples include a repeating unit represented by the following general formula (RZ-1) or (RZ-2). .

In the general formulas (RZ-1) and (RZ-2), RZ _{1 to} RZ ₃ each independently represents a linear or branched alkyl group or a cycloalkyl group, and 2 of RZ _{1 to} RZ ₃ May combine to form a ring structure. Further, these groups may further have a substituent such as an alkyl group, an alkoxy group, or a hydroxyl group.
In the hydrophobic resin (HR), the content of the repeating unit having a group (z) that is decomposed by the action of an acid is preferably 1 to 80 mol%, more preferably 10 to 10%, based on all repeating units in the polymer. 80 mol%, more preferably 20 to 60 mol%.

  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.
As for the hydrophobic resin (HR), it is preferable that the residual monomer and oligomer components are 0 to 10% by mass, more preferably, as in the resin of the component (B), there are few impurities such as metals. 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 necessary functions for the top coat are suitability for application to the upper layer of the resist, radiation, especially transparency to 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 with radiation 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.

(I) Pattern Forming Method 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. preferable. 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 having a pore size 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.

Examples of the present invention will be described below.
<Synthesis Example 1>
Synthesis of resin 1

Under a nitrogen stream, 50.0 g of 1,4-dioxane solvent was placed in a three-necked flask and heated to 80 ° C. Compound (Go-1) 6.88 g, Formula (Go-2) 8.56 g, Formula (Go-3) 2.04 g, Formula (Go-4) 1.72 g, Polymerization initiator V-601 ( Wako Pure Chemical Industries, Ltd.) was added dropwise over 7 hours with a solution of 12 mol% of the monomer dissolved in 250.0 g of 1,4-dioxane solvent. After completion of the dropping, the reaction was further carried out at 80 ° C. for 2 hours. The reaction solution was allowed to cool and then added dropwise to 2000 ml of diethyl ether over 20 minutes. The precipitated powder was collected by filtration and dried to obtain 15.2 g of Resin 1. The mass average molecular weight of the obtained resin was 8100 in terms of standard polystyrene, and the dispersity (Mw / Mn) was 2.01.

<Synthesis Example 2>
Under a nitrogen stream, 300 g of a THF solvent was placed in a three-necked flask, and a 50 g THF solution of 10.0 g of androsterone and a 10 g THF solution of 2.9 g of pyridine were successively added and cooled to 0 ° C. To this solution, a 60 g THF solution of 3.2 g of acrylic acid chloride was added dropwise. Thereafter, the mixture was further stirred at room temperature for 8 hours and then filtered. 200 g of ethyl acetate was added to the obtained filtrate, and washed with 150 g of water three times. Subsequently, anhydrous sodium sulfate was added to the obtained organic layer for drying, and the solvent was removed under reduced pressure to obtain crystals. When this was recrystallized from a mixed solvent of ethanol / tetrahydrofuran, 7.8 g of white crystals of the formula (JL1) was obtained.

  7.8 g of the obtained compound (JL1) obtained above was dissolved in 200 ml of acetic acid, 100 ml of hydrogen peroxide solution was added, and the mixture was stirred at 35 ° C. for 10 hours. After the reaction, the solvent was distilled off under reduced pressure and poured into 2000 ml of water. The precipitate was collected by filtration and dried to obtain 4.5 g of the formula (JL2).

  At room temperature, 4.5 g of (JL2) synthesized as described above was dissolved in 250 ml of tetrahydrofuran, 200 ml of 0.2N aqueous sodium hydroxide solution was added, and the mixture was stirred for 2.5 hours. Thereafter, 150 ml of 0.1N hydrochloric acid aqueous solution and 150 ml of saturated ammonium chloride solution were sequentially added. 250 ml of ethyl acetate was added to this solution and extracted twice to obtain an organic layer. Subsequently, after washing twice with 150 ml of water, the organic layer was dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure. To this, 300 ml of n-hexane was added, filtered and dried to obtain 4.4 g of the formula (JL3).

Synthesis of Resin 2 Under a nitrogen stream, PGMEA (propylene glycol monomethyl ether acetate) / PGME (propylene glycol monomethyl ether) (2/8 in mass ratio) mixed solvent 20.0 g was put into a three-necked flask, and this was brought to 80 ° C. Heated. Compound formula (Go-5) 7.56g, formula (Go-6) 6.62g, compound (JL3) 1.05g, polymerization initiator V-601 (manufactured by Wako Pure Chemical Industries, Ltd.) 8 mol% to the monomer. A solution dissolved in 180.0 g of a mixed solvent of PGMEA / PGME (2/8 in mass ratio) was dropped over 6 hours. After completion of the dropping, the reaction was further carried out at 80 ° C. for 2 hours. The reaction solution was allowed to cool and then added dropwise to a mixed solution of hexane 1400 m / ethyl acetate 600 ml over 20 minutes, and the precipitated powder was collected by filtration and dried to obtain 12.4 g of Resin 2. The weight average molecular weight of the obtained resin was 7800 in terms of standard polystyrene, and the dispersity (Mw / Mn) was 1.96.

  Resins 3 to 40 were synthesized in the same manner as described above. Tables 1 to 4 below show the structures and molar composition ratios, molecular weights, and dispersities of the resins synthesized.

<Resist preparation>
The components shown in the following table were dissolved in a solvent to prepare a solution having a solid content concentration of 4.8% by mass, and this was filtered through a 0.1 μm pore size polyethylene filter to prepare a negative resist solution. The prepared negative resist composition was evaluated by the following method, and the results are shown in Table 2 below. In addition, about each component in Table 2, the ratio at the time of using multiple is a mass ratio.

(Exposure condition (1))
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. A negative resist composition prepared thereon was applied, and baked at 105 ° C. for 60 seconds to form a 120 nm resist film. The obtained wafer was subjected to pattern exposure using an ArF excimer laser scanner (PAS5500 / 1100, manufactured by ASML, NA0.75, σo / σi = 0.85 / 0.55). Thereafter, the mixture was heated at 100 ° C. for 60 seconds, developed with an aqueous tetramethylammonium hydroxide solution (2.38 mass%) for 30 seconds, rinsed with pure water, and spin-dried to obtain a resist pattern.

(Exposure condition (2))
This condition is to form a resist pattern by an immersion exposure method using pure water.
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. A negative resist composition prepared thereon was applied, and baked at 105 ° C. for 60 seconds to form a 120 nm resist film. The obtained wafer was subjected to pattern exposure using an ArF excimer laser immersion scanner (NA 0.85). Ultra pure water was used as the immersion liquid. Thereafter, the mixture was heated at 100 ° C. for 60 seconds, developed with an aqueous tetramethylammonium hydroxide solution (2.38 mass%) for 30 seconds, rinsed with pure water, and spin-dried to obtain a resist pattern.

  Examples 1 to 25, 31 to 48, 54 to 79, 85 to 108, Comparative Examples 1 to 5 in (Exposure Conditions (1)), and Examples 26 to 30 and 49 to 53 in (Exposure Conditions (2)) 80 to 84 and 109 to 113, the bridge margins of the obtained resist patterns were evaluated.

Evaluation of Bridge Margin An exposure dose E ₀ (optimum exposure dose) for resolving the 150 nm (1: 1) line and space resist pattern obtained in Examples 1 to 24 and Comparative Examples 1 to 24 was measured with a scanning electron microscope ( S-9260) manufactured by Hitachi, Ltd. is calculated, and an exposure amount E ₁ at which a bridge is generated when the exposure amount is increased from the exposure amount E ₀ is calculated. It was used as an index.
Bridge margin (%) = (E ₁ −E ₀ ) / E ₀ × 100
The larger the value calculated above, the better the performance. The results are shown in Tables 5-8.

*: 0.05 g of hydrophobic polymer HR-22 was added and immersion exposure

[Photopolymerization initiator]

Here, all the values of pKa written in the above structure are values obtained by calculation using the following software package.
Software package 1: Advanced Chemistry Development (ACD / Labs) Software V8.14 for Solaris (1994-2007 ACD / Labs)

(Polymerizable monomer)

[Basic compounds]
HEP: N-hydroxyethylpiperidine DIA: 2,6-diisopropylaniline PEA: N-phenyldiethanolamine TOA: trioctylamine PBI: 2-phenylbenzimidazole DCMA: dicyclohexylmethylamine TPSA: triphenylsulfonium acetate DHA: N, N -Dihexylaniline HAP: Hydroxyantipyrine TBAH: Tetra-n-butylammonium hydroxide TPI: 2,4,5-triphenylimidazole TPA: Tripentylamine

[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: 2-heptanone A3: Cyclohexanone B1: Propylene glycol monomethyl ether B2: Ethyl lactate B3: Propylene carbonate

Claims (4)

(A) a resin whose solubility in an alkaline developer is reduced by the action of an acid;
(B) a cationically polymerizable compound,
(C) a photocationic polymerization initiator,
(D) A negative resist composition comprising a compound that generates an acid upon irradiation with actinic rays or radiation.   The negative resist composition according to claim 1, wherein the resin (A) is a resin having an alicyclic structure.   The negative resist composition according to claim 1, wherein the resin (A) is a resin having a structure in which a lactone ring is formed in the side chain by the action of an acid.   A resist pattern forming method, comprising: a step of forming a resist film using the resist composition according to claim 1; a step of exposing the resist film; and a step of developing the resist film.