JPWO2016136481A1 - Pattern forming method, actinic ray-sensitive or radiation-sensitive resin composition, actinic ray-sensitive or radiation-sensitive film, method for producing electronic device using these, and electronic device - Google Patents

Abstract

Forming a film using an actinic ray-sensitive or radiation-sensitive resin composition, exposing the film, and developing the exposed film using a developer to form a positive pattern There is provided a pattern forming method including the step of: The actinic ray-sensitive or radiation-sensitive resin composition contains at least a repeating unit (a) represented by the following general formula (1) as a repeating unit having a group that decomposes by the action of an acid to generate a polar group. Resin (P1) is contained. [Chemical 1]

Description

  The present invention relates to a pattern forming method using a developer, an actinic ray-sensitive or radiation-sensitive resin, which is suitably used in an ultramicrolithography process such as the manufacture of VLSI and high-capacity microchips and other photofabrication processes. The present invention relates to a composition, an actinic ray-sensitive or radiation-sensitive film, a method for producing an electronic device using these, and an electronic device. More specifically, a pattern forming method using an alkaline developer, an actinic ray-sensitive or radiation-sensitive resin that can be suitably used for fine processing of a semiconductor element using electron z-rays or EUV light (wavelength: around 13 nm). The present invention relates to a composition, a resist film, an electronic device manufacturing method using these, and an electronic device.

  Conventionally, in the manufacturing process of semiconductor devices such as IC and LSI, fine processing by lithography using a photoresist composition has been performed. In recent years, with the high integration of integrated circuits, the formation of ultrafine patterns in the submicron region and the quarter micron region has been required. Along with this, there is a tendency to shorten the exposure wavelength from g-line to i-line, and further to KrF excimer laser light. Furthermore, at present, in addition to excimer laser light, lithography using electron beams, X-rays, or EUV light is being developed.

  These electron beams, X-rays, or EUV light lithography are positioned as next-generation or next-generation pattern forming techniques, and high-sensitivity and high-resolution resist compositions are desired.

  High sensitivity is an extremely important issue especially for shortening the wafer processing time. However, when high sensitivity is pursued, the resolution expressed by the pattern shape and the limit resolution line width decreases. Therefore, development of a resist composition that simultaneously satisfies these characteristics is strongly desired.

  Further, as the miniaturization of the pattern is pursued, the pattern collapse easily occurs. From the viewpoint of preventing such pattern collapse, it is required to reduce the thickness of the resist film. However, as the resist film becomes thinner as a result of pursuing miniaturization, a dilemma may occur that the resist film becomes less resistant to etching and cannot function as a resist film.

  Thus, there is a trade-off between resist pattern miniaturization and etching resistance, and it is important how to satisfy this simultaneously.

  Further, as a result of pursuing miniaturization in the pattern, the difference in exposure amount (optical contrast) between the exposed area and the unexposed area decreases, the difference in the dissolution rate with respect to the developing solution decreases, and the dissolution contrast deteriorates. There is also a problem.

  In the actinic ray-sensitive or radiation-sensitive resin composition, generally, a resin that is hardly soluble or insoluble in an alkali developer is used, and a pattern is formed by solubilizing an exposed portion in an alkali developer by exposure to radiation. There are a “positive type” and a “negative type” in which a resin is soluble in an alkali developer and a pattern is formed by making the exposed portion insoluble or insoluble in an alkali developer by radiation exposure. As various lithography techniques are developed, for example, various positive resist compositions using a resin having an acetal-type protecting group have been developed. According to these, resolution, sensitivity, and the like can be improved. Have been reported (for example, see Patent Documents 1 to 6).

  However, the conventional chemically amplified positive resist composition has the resolution, dissolution contrast, and dry etching resistance required when forming a pattern having an ultrafine (for example, several tens of nm) line width or space width at the same time. Actually, it is difficult to obtain a pattern that satisfies this condition.

JP 2010-256419 A Japanese Patent Laid-Open No. 5-279425 JP 2002-23370 A JP 2014-41329 A JP2013-129823A JP-A-2-25850

  An object of the present invention is to solve the problem of performance improvement technology in microfabrication of a semiconductor device using an electron beam or extreme ultraviolet rays (EUV light), and in particular, an ultrafine (for example, several tens of nm order) line width. Alternatively, in the formation of a pattern having a space width, a pattern forming method, an actinic ray sensitive or radiation sensitive resin composition, and an actinic ray sensitive property that simultaneously satisfy high sensitivity, high resolution, high dissolution contrast, and high dry etching resistance. Another object is to provide a radiation-sensitive film, a method for producing an electronic device using these films, and an electronic device.

In one aspect, the present invention is as follows.
[1] Actinic rays containing a resin (P1) containing at least a repeating unit (a) represented by the following general formula (1) as a repeating unit having a group that decomposes by the action of an acid to generate a polar group A film is formed using a heat-sensitive or radiation-sensitive resin composition,
Exposing the film; and
The pattern formation method including the process of developing the said film | membrane after exposure using a developing solution, and forming a positive pattern.

In general formula (1),
Y ₁ and Y ₂ each independently represent a hydrogen atom or an organic group, and may combine with each other to form an aromatic ring.
Y ₃ represents a single bond or a divalent aromatic ring group. Y ₃ may combine with Y ₁ to form a ring, and Y ₃ in this case represents a trivalent aromatic ring group.
L ₁ represents a single bond or a divalent linking group. L ₁ may combine with Y ₁ to form a ring, and in this case, L ₁ represents a trivalent linking group.
R ₁ and R ₂ each independently represents a hydrogen atom or a substituent.
M ₁ represents an organic group.
One of R ₁ and R ₂ and M ₁ may be bonded to each other to form a ring together with the oxygen atom in the formula.

However, at least one of Y ₁ , Y ₂ and Y ₃ contains an aromatic ring, or Y ₁ and Y ₂ are bonded to each other to form an aromatic ring.
When Y ₃ is an aromatic ring group and L ₁ is a single bond, at least one of R ₁ and R ₂ is an alkyl group having 6 or more carbon atoms, an aliphatic cyclic group, an aromatic ring group, a heterocyclic ring Represents a group or a halogen atom.
When Y ₃ is an aromatic ring group and L ₁ is a divalent linking group, L ₁ does not contain an aliphatic cyclic group, and _one of R ₁ and R ₂ and M ₁ are They do not combine to form a ring.

[2]
The pattern forming method according to [1], wherein the repeating unit (a) represented by the general formula (1) is a repeating unit represented by the following general formula (2).

In general formula (2),
Y ₄ and Y ₅ each independently represent a hydrogen atom or an organic group, and may combine with each other to form an aromatic ring.
L ₁₁ represents a single bond or a divalent linking group. L ₁₁ may combine with Y ₄ to form a ring, and in this case, L ₁₁ represents a trivalent linking group.
R ₃ and R ₄ each independently represents a hydrogen atom or a substituent.

M ₂ represents an organic group.
One of R ₃ and R ₄ and M ₂ may be bonded to each other to form a ring together with the oxygen atom in the formula.
However, at least one of Y ₄ and Y ₅ includes an aromatic ring, or Y ₄ and Y ₅ are bonded to each other to form an aromatic ring.

[3]
The pattern formation method according to [2], wherein R ₃ in General Formula (2) represents a hydrogen atom, and R ₄ represents a hydrogen atom, an alkyl group, an aliphatic cyclic group, or an aromatic ring group.

[4]
The pattern formation method according to [2] or [3], wherein M ₂ in the general formula (2) is an alkyl group.

[5]
The pattern formation method according to [1], wherein the repeating unit (a) represented by the general formula (1) is a repeating unit represented by the following general formula (3).

In general formula (3),
Y ₆ and Y ₇ each independently represent a hydrogen atom or a monovalent organic group.
L ₂ represents a divalent linking group having 1 atom between the aromatic ring and the carboxyl group in the formula.
R ₅ and R ₆ each independently represents a hydrogen atom, an alkyl group, an aliphatic cyclic group, a halogen atom, an aromatic ring group, or a heterocyclic group.
M ₃ represents an organic group.
One of R ₅ and R ₆ and M ₃ are not bonded to each other to form a ring.
n represents 0 or an integer of 1 or more.

[6]
At least one of R ₅ and R _{6 in} the general formula (3) is an alkyl group having 7 or more carbon atoms, an aliphatic cyclic group, a halogen atom, an aromatic ring group having 13 or more carbon atoms, or a heterocyclic group. [5] The pattern forming method according to [5].

[7]
[5] or [6] wherein M ₃ in the general formula (3) represents an alkyl group having 7 or more carbon atoms, an aliphatic cyclic group, a halogen atom, an aromatic ring group having 13 or more carbon atoms, or a heterocyclic group. ] The pattern formation method of description.

[8]
The pattern formation method according to [1], wherein the repeating unit (a) represented by the general formula (1) is a repeating unit represented by the following general formula (4).

In general formula (4),
Y ₈ and Y ₉ each independently represent a hydrogen atom or a monovalent organic group.
R ₇ represents an alkyl group having 6 or more carbon atoms, an aliphatic cyclic group, an aromatic ring group, a heterocyclic group, or a halogen atom.
R ₈ represents a hydrogen atom or a substituent.
M ₄ represents an organic group.
One of R ₇ and R ₈ and M ₄ may be bonded to each other to form a ring together with the oxygen atom in the formula.
n represents 0 or an integer of 1 or more.

[9]
The pattern formation method according to [8], wherein R ₇ in the general formula (4) represents an aliphatic cyclic group.

[10]
The pattern formation method according to any one of [1] to [9], wherein the resin (P1) further includes a repeating unit represented by the general formula (A).

In general formula (A),
Z ₁ , Z ₂ and Z ₃ each independently represent a hydrogen atom, an alkyl group, a halogen atom, a cyano group or an alkoxycarbonyl group. However, Z ₃ may combine with Ar ₂ or X ₁ to form a ring, and Z ₃ in that case represents a single bond or an alkylene group.
X ₁ represents a single bond, an alkylene group, —COO—, or —CONR ₉ —. Here, R ₉ represents a hydrogen atom or an alkyl group.
L ₃ represents a single bond, —COO—, or an alkylene group.
Ar ₂ represents an (m + 1) -valent aromatic ring group, and when bonded to Z ₃ to form a ring, represents an (m + 2) -valent aromatic ring group.
m represents an integer of 1 to 4.

[11]
Forming a film using an actinic ray-sensitive or radiation-sensitive resin composition;
A step of exposing the film, and a step of developing the exposed film using a developer to form a positive pattern,
An actinic ray-sensitive or radiation-sensitive resin composition used in a pattern forming method comprising:
An actinic ray-sensitive or sensitive material containing a resin (P1) containing at least a repeating unit (a) represented by the following general formula (1) as a repeating unit having a group that decomposes by the action of an acid to generate a polar group. Radiation resin composition.

In general formula (1),
Y ₁ and Y ₂ each independently represent a hydrogen atom or an organic group, and may combine with each other to form an aromatic ring.
Y ₃ represents a single bond or a divalent aromatic ring group. Y ₃ may combine with Y ₁ to form a ring, and Y ₃ in this case represents a trivalent aromatic ring group.
L ₁ represents a single bond or a divalent linking group. L ₁ may combine with Y ₁ to form a ring, and in this case, L ₁ represents a trivalent linking group.
R ₁ and R ₂ each independently represents a hydrogen atom or a substituent.
M ₁ represents an organic group.
One of R ₁ and R ₂ and M ₁ may be bonded to each other to form a ring together with the oxygen atom in the formula.

However, at least one of Y ₁ , Y ₂ and Y ₃ contains an aromatic ring, or Y ₁ and Y ₂ are bonded to each other to form an aromatic ring.
When Y ₃ is an aromatic ring group and L ₁ is a single bond, at least one of R ₁ and R ₂ is an alkyl group having 6 or more carbon atoms, an aliphatic cyclic group, an aromatic ring group, a heterocyclic ring Represents a group or a halogen atom.
When Y ₃ is an aromatic ring group and L ₁ is a divalent linking group, L ₁ does not contain an aliphatic cyclic group, and _one of R ₁ and R ₂ and M ₁ are They do not combine to form a ring.

[12]
The actinic ray-sensitive or radiation-sensitive resin composition according to [11], wherein the repeating unit (a) represented by the general formula (1) is a repeating unit represented by the following general formula (2).

In general formula (2),
Y ₄ and Y ₅ each independently represent a hydrogen atom or an organic group, and may combine with each other to form an aromatic ring.
L ₁₁ represents a single bond or a divalent linking group. L ₁₁ may combine with Y ₄ to form a ring, and in this case, L ₁₁ represents a trivalent linking group.
R ₃ and R ₄ each independently represents a hydrogen atom or a substituent.
M ₂ represents an organic group.
One of R ₃ and R ₄ and M ₂ may be bonded to each other to form a ring together with the oxygen atom in the formula.
However, at least one of Y ₄ and Y ₅ includes an aromatic ring, or Y ₄ and Y ₅ are bonded to each other to form an aromatic ring.

[13]
The actinic ray-sensitive or radiation-sensitive resin composition according to [11], wherein the repeating unit (a) represented by the general formula (1) is a repeating unit represented by the following general formula (3).

In general formula (3),
Y ₆ and Y ₇ each independently represent a hydrogen atom or a monovalent organic group.
L ₂ represents a divalent linking group having 1 atom between the aromatic ring and the carboxyl group in the formula.
R ₅ and R ₆ each independently represents a hydrogen atom, an alkyl group, an aliphatic cyclic group, a halogen atom, an aromatic ring group, or a heterocyclic group.
M ₃ represents an organic group.
One of R ₅ and R ₆ and M ₃ are not bonded to each other to form a ring. N represents 0 or an integer of 1 or more.

[14]
The actinic ray-sensitive or radiation-sensitive resin composition according to [11], wherein the repeating unit (a) represented by the general formula (1) is a repeating unit represented by the following general formula (4).

In general formula (4),
Y ₈ and Y ₉ each independently represent a hydrogen atom or a monovalent organic group.
R ₇ represents an alkyl group having 6 or more carbon atoms, an aliphatic cyclic group, an aromatic ring group, a heterocyclic group, or a halogen atom.
R ₈ represents a hydrogen atom or a substituent.
M ₄ represents an organic group.
One of R ₇ and R ₈ and M ₄ may be bonded to each other to form a ring together with the oxygen atom in the formula.
n represents 0 or an integer of 1 or more.

[15]
An actinic ray-sensitive or radiation-sensitive film formed using the actinic ray-sensitive or radiation-sensitive composition according to any one of [11] to [14].
[16]
The manufacturing method of an electronic device containing the pattern formation method in any one of [1]-[10].
[17]
An electronic device manufactured by the method for manufacturing an electronic device according to [16].

  According to the present invention, in an ultrafine region (for example, a region having a line width or space width on the order of several tens of nanometers), a pattern forming method and activity sensitivity that simultaneously satisfy high resolution, high dissolution contrast, and high dry etching resistance. A light-sensitive or radiation-sensitive resin composition, an actinic light-sensitive or radiation-sensitive film, an electronic device manufacturing method using these, and an electronic device can be provided.

Hereinafter, embodiments of the present invention will be described in detail.
In addition, in the description of the group (atomic group) in this specification, the description which does not specify substitution or non-substitution is both the thing which does not have a substituent, and the thing which has a substituent. To be included. For example, an “alkyl group” that does not clearly indicate substitution or unsubstituted is not only an alkyl group that does not have a substituent (unsubstituted alkyl group) but also an alkyl group that has a substituent (substituted alkyl group) Is also included.
“Actinic ray” or “radiation” in the present specification means, for example, an emission line spectrum of a mercury lamp, a far ultraviolet ray represented by an excimer laser, an extreme ultraviolet (EUV) ray, an X-ray or an electron beam (EB). Yes. In the present invention, “light” means actinic rays or radiation.

  In addition, unless otherwise specified, “exposure” in the present invention is not only exposure with far-ultraviolet rays such as mercury lamps and excimer lasers, X-rays and EUV light, but also drawing with particle beams such as electron beams and ion beams. Are also included in the exposure.

The pattern forming method of the present invention comprises:
Forming a film using an actinic ray-sensitive or radiation-sensitive resin composition;
Exposing the film,
The film after exposure is developed using a developer to form a positive pattern.

  In the following, first, the actinic ray-sensitive or radiation-sensitive resin composition (hereinafter referred to as “the composition of the present invention”) used in the pattern forming method of the present invention will be described, and then the pattern formation of the present invention will be described. Each process included in the method will be described.

<Actinic ray-sensitive or radiation-sensitive resin composition>
The actinic ray-sensitive or radiation-sensitive resin composition according to the present invention is used for positive development (development in which exposed portions are removed and unexposed portions remain as patterns). That is, the actinic ray-sensitive or radiation-sensitive resin composition according to the present invention can be an actinic ray-sensitive or radiation-sensitive resin composition for alkali development used for development using an alkali developer. Here, the term “for alkali development” means at least an application provided for a development process using an alkali developer.

  The actinic ray-sensitive or radiation-sensitive resin composition of the present invention is typically a resist composition, and it is particularly high that it is a positive resist composition (that is, a resist composition for alkali development). It is preferable because an effect can be obtained. The composition according to the present invention is typically a chemically amplified resist composition.

[1] Resin (P1)
The actinic ray-sensitive or radiation-sensitive resin composition of the present invention contains a resin (P1) containing an acid-decomposable repeating unit. Thereby, the resin (P1) is a resin whose solubility in an alkaline developer is increased by the action of an acid. Here, the acid-decomposable repeating unit is, for example, a group (hereinafter also referred to as “acid-decomposable group”) that decomposes into the main chain or side chain of the resin, or both the main chain and side chain by the action of an acid. ). The group generated by the decomposition is preferably a polar group, since the affinity with a developer containing an alkaline solution is increased and the solubilization (positiveization) proceeds.

  The resin (P1) is at least a repeating unit represented by the following general formula (1) (hereinafter also referred to as “repeating unit (a)”) as a repeating unit having a group that decomposes by the action of an acid to generate a polar group. .)including.

In general formula (1),
Y ₁ and Y ₂ each independently represent a hydrogen atom or an organic group, and may combine with each other to form an aromatic ring.

Y ₃ represents a single bond or a divalent aromatic ring group. Y ₃ may combine with Y ₁ to form a ring, and Y ₃ in this case represents a trivalent aromatic ring group.

L ₁ represents a single bond or a divalent linking group. L ₁ may combine with Y ₁ to form a ring, and in this case, L ₁ represents a trivalent linking group.

R ₁ and R ₂ each independently represents a hydrogen atom or a substituent.

M ₁ represents an organic group.

One of R ₁ and R ₂ and M ₁ may be bonded to each other to form a ring together with the oxygen atom in the formula.

However, at least one of Y ₁ , Y ₂ and Y ₃ contains an aromatic ring, or at least Y ₁ and Y ₂ are bonded to each other to form an aromatic ring.

When Y ₃ is an aromatic ring group and L ₁ is a single bond, at least one of R ₁ and R ₂ is an alkyl group having 6 or more carbon atoms, an aliphatic cyclic group, an aromatic ring group, a heterocyclic ring Represents a group or a halogen atom.

When Y ₃ is an aromatic ring group and L ₁ is a divalent linking group, L ₁ does not contain an aliphatic cyclic group, and _one of R ₁ and R ₂ and M ₁ are They do not combine to form a ring.

In the general formula (1), examples of the organic group represented by Y ₁ include an alkyl group, an aliphatic cyclic group, an aromatic ring group, and a heterocyclic group.
The alkyl group for Y ₁ preferably has 1 to 5 carbon atoms.

The aliphatic cyclic group for Y ₁ may be monocyclic or polycyclic, and is preferably an aliphatic cyclic group having 3 to 15 carbon atoms. Specific examples of the aliphatic cyclic group for Y ₁ include, for example, cyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohexyl group, cycloheptyl group, cyclooctyl group, decahydronaphthyl group, cyclodecyl group, 1-adamantyl group, A 2-adamantyl group, a 1-norbornyl group, a 2-norbornyl group and the like can be exemplified.

As the aromatic ring group for Y _1, an aromatic ring group having 6 to 18 carbon atoms (more preferably 6 to 10 carbon atoms) such as a benzene ring or a naphthalene ring, or, for example, a thiophene ring, a furan ring, a pyrrole ring, a benzo Preferred examples include aromatic ring groups including hetero rings such as thiophene ring, benzofuran ring, benzopyrrole ring, triazine ring, imidazole ring, benzimidazole ring, triazole ring, thiadiazole ring, thiazole ring, benzene ring, naphthalene A ring is more preferable, and a benzene ring group is particularly preferable.

The heterocyclic group for Y ₁ is preferably a heterocyclic group having 6 to 20 carbon atoms. Specific examples of the heterocyclic group for Y ₁ include, for example, pyridyl group, pyrazyl group, tetrahydrofuranyl group, tetrahydropyranyl group, tetrahydrothiophene group, piperidyl group, piperazyl group, furanyl group, pyranyl group, chromanyl group and the like. It is done.

The alkyl group, aliphatic cyclic group, aromatic ring group, aralkyl group and heterocyclic group as Y ₁ may further have a substituent.

Examples of the substituent that the alkyl group as Y ₁ may further have include an aliphatic cyclic group, an aryl group, an amino group, an amide group, a ureido group, a urethane group, a hydroxy group, a carboxy group, a halogen atom, and an alkoxy group. Aralkyloxy group, thioether group, acyl group, acyloxy group, alkoxycarbonyl group, cyano group and nitro group. The above substituents may be bonded to each other to form a ring, and examples of the ring when the above substituents are bonded to each other to form a ring include an aliphatic cyclic group and a phenyl group.

Examples of the substituent that the aliphatic cyclic group as Y ₁ may further have include an alkyl group and the groups described above as specific examples of the substituent that the alkyl group may further have.

Examples of the substituent that the aromatic ring group, aralkyl group and heterocyclic group as Y ₁ may further have include a halogen atom such as a nitro group and a fluorine atom, a carboxyl group, a hydroxyl group, an amino group, a cyano group, an alkyl group, Examples include an alkoxy group, an aliphatic cyclic group, an aryl group, an alkoxycarbonyl group, an acyl group, and an alkoxycarbonyloxy group.

In the general formula (1), examples of the monovalent organic group represented by Y ₂ include an alkyl group, an aliphatic cyclic group, an aromatic ring group, and a heterocyclic group.

Alkyl group Y ₂ is preferably an alkyl group having 1 to 10 carbon atoms. Specific examples of the alkyl group for Y ₂ include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a sec-butyl group, and a t-butyl group. Can do.

Specific examples and preferred examples of the aliphatic cyclic group, aromatic ring group or heterocyclic group as Y ₂ include those described for the aliphatic cyclic group, aromatic ring group or heterocyclic group as Y ₁ described above, for example. It is the same.

The alkyl group as Y _2, aliphatic cyclic group, aromatic ring group and heterocyclic group may further have a substituent group, the substituent Y ₂ may have further an alkyl of Y ₁ described above This is the same as the substituent that the group may have.

In the general formula (1), specific examples of the aromatic ring group as Y ₃ include the same specific examples as described for the aromatic ring groups as Y ₁ and Y ₂ described above, and preferable specific examples are also the same. It is.

In the general formula (1), at least one of Y ₁ , Y ₂ and Y ₃ contains an aromatic ring group, or Y ₁ and Y ₂ are bonded to each other to form an aromatic ring. The at least one aromatic ring contained in the repeating unit (a) represented by the general formula (1) is more preferably a benzene ring or a naphthalene ring, and particularly preferably a benzene ring.

In the general formula (1), the divalent linking group represented by _{L 1,} an alkylene group, aromatic ring group, a cycloalkylene _{group, -COO-L 1 '-,} - O-L 1' -, - CONH -, Groups formed by combining two or more of these, and the like. Here, L1 ′ represents an alkylene group, a cycloalkylene group, an aromatic ring group, or a group in which an alkylene group and an aromatic ring group are combined.

The alkylene group as the divalent linking group represented by L ₁ is preferably an alkylene group having 1 to 8 carbon atoms such as a methylene group, an ethylene group, a propylene group, a butylene group, a hexylene group or an octylene group. .

The cycloalkylene group as the divalent linking group represented by L ₁ is preferably a cycloalkylene group having 3 to 20 carbon atoms, such as a cyclopropylene group, a cyclobutylene group, a cyclopentylene group, and cyclohexylene. Group, cycloheptylene group, cyclooctylene group, norbornylene group or adamantylene group.

The aromatic ring group as the divalent linking group represented by L ₁ is an aromatic ring group having 6 to 18 carbon atoms such as a benzene ring or a naphthalene ring group, or a thiophene ring, furan ring, pyrrole ring, benzo Preferable examples include aromatic ring groups including heterocycles such as thiophene ring, benzofuran ring, benzopyrrole ring, triazine ring, imidazole ring, benzimidazole ring, triazole ring, thiadiazole ring, and thiazole ring.

The definitions and preferred ranges of the alkylene group, cycloalkylene group and aromatic ring group represented by L ₁ ′ are the same as those in the alkylene group, cycloalkylene group and aromatic ring group as the divalent linking group represented by L. .

The definition and preferred range of the alkylene group and aromatic ring group in the group combining the alkylene group and aromatic ring group represented by L ₁ ′ are those in the alkylene group and aromatic ring group as the divalent linking group represented by Y _3. It is the same.

In the case where Y ₃ to form a ring with Y _1, a trivalent aromatic ring group represented by Y _3, 3 pieces of arbitrarily embodiment described above aromatic ring group represented by Y ₁ The group formed by removing the hydrogen atom can be preferably mentioned.

In the case where L ₁ to form a ring with Y _1, Examples of the trivalent linking group represented by L _1, the embodiment described above of the divalent linking group represented by L ₁ 1 single Preferable examples include a group formed by removing a hydrogen atom.

In the general formula (1), the substituent represented by R ₁ and R ₂ is preferably a hydrogen atom, an alkyl group, an aliphatic cyclic group, an aryl group, an aralkyl group or a heterocyclic group.

In one embodiment of the present invention, the alkyl group of R ₁ and R ₂ is preferably an alkyl group having 1 to 15 carbon atoms, more preferably an alkyl group having 1 to 10 carbon atoms, and 1 to 1 carbon atoms. More preferably, it is an alkyl group of 6. Specific examples of the alkyl group of R ₁ and R ₂ include, for example, methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, sec-butyl group, t-butyl group, neopentyl group, hexyl group, 2 - ethylhexyl group, and a octyl group and a dodecyl group, an alkyl group of R ₁ and R ₂ are a methyl group, an ethyl group, a propyl group, and an isopropyl group or t- butyl group.

The aliphatic cyclic group for R ₁ and R ₂ may be monocyclic or polycyclic. In one embodiment of the present invention, the aliphatic cyclic group for R ₁ and R ₂ is preferably an aliphatic cyclic group having 3 to 15 carbon atoms, and is an aliphatic cyclic group having 3 to 10 carbon atoms. It is more preferable that it is a C3-C6 aliphatic cyclic group. Specific examples of the aliphatic cyclic group represented by R ₁ and R ₂ include, for example, cyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohexyl group, cycloheptyl group, cyclooctyl group, decahydronaphthyl group, cyclodecyl group, 1- Examples thereof include an adamantyl group, a 2-adamantyl group, a 1-norbornyl group, and a 2-norbornyl group. The aliphatic cyclic group for R ₁ and R ₂ is preferably a cyclopropyl group, a cyclopentyl group, or a cyclohexyl group.

The aryl group of R ₁ and R ₂ is preferably an aryl group having 6 to 15 carbon atoms, more preferably an aryl group having 6 to 12 carbon atoms, and a plurality of aromatic rings are mutually bonded via a single bond. It also includes linked structures (eg, biphenyl group, terphenyl group). Specific examples of the aryl group represented by R1 and R2 include a phenyl group, a naphthyl group, an anthranyl group, a biphenyl group, and a terphenyl group. The aryl group of R111 to R113 is preferably a phenyl group, a naphthyl group, or a biphenyl group.

The aralkyl group of R ₁ and R ₂ is preferably an aralkyl group having 6 to 20 carbon atoms, and more preferably an aralkyl group having 7 to 12 carbon atoms. Specific examples of R ₁ and R ₂ aralkyl groups include benzyl group, phenethyl group, naphthylmethyl group, naphthylethyl group, and the like.

The heterocyclic group of R ₁ and R ₂ is preferably a heterocyclic group having 6 to 20 carbon atoms, and more preferably a heterocyclic group having 6 to 12 carbon atoms. Specific examples of the heterocyclic group of R ₁ and R ₂ include, for example, pyridyl group, pyrazyl group, tetrahydrofuranyl group, tetrahydropyranyl group, tetrahydrothiophene group, piperidyl group, piperazyl group, furanyl group, pyranyl group, chromanyl group. Etc.

The alkyl group, aliphatic cyclic group, aryl group, aralkyl group and heterocyclic group as R ₁ and R ₂ may further have a substituent.

Examples of the substituent that the alkyl group as R ₁ and R ₂ may further have include an aliphatic cyclic group, an aryl group, an amino group, an amide group, a ureido group, a urethane group, a hydroxy group, a carboxy group, and a halogen atom. , Alkoxy groups, aralkyloxy groups, thioether groups, acyl groups, acyloxy groups, alkoxycarbonyl groups, cyano groups, and nitro groups. The above substituents may be bonded to each other to form a ring, and when the above substituents are bonded to each other to form a ring, the ring is an aliphatic cyclic group having 3 to 10 carbon atoms or a phenyl group. Can be mentioned.

Examples of the substituent that the aliphatic cyclic group as R ₁ and R ₂ may further include an alkyl group and the groups described above as specific examples of the substituent that the alkyl group may further have.

  In addition, the carbon number of the alkyl group and the carbon number of the substituent that the aliphatic cyclic group may further have are preferably 1 to 8, respectively.

Examples of the substituent that the aryl group, aralkyl group and heterocyclic group as R ₁ and R ₂ may further have include a halogen atom such as a nitro group and a fluorine atom, a carboxyl group, a hydroxyl group, an amino group, a cyano group, and an alkyl group. A group (preferably 1 to 15 carbon atoms), an alkoxy group (preferably 1 to 15 carbon atoms), an aliphatic cyclic group (preferably 3 to 15 carbon atoms), an aryl group (preferably 6 to 14 carbon atoms), Examples thereof include an alkoxycarbonyl group (preferably having 2 to 7 carbon atoms), an acyl group (preferably having 2 to 12 carbon atoms), an alkoxycarbonyloxy group (preferably having 2 to 7 carbon atoms), and the like.

In one embodiment of the present invention, when Y ₃ in the general formula (1) is an aromatic ring group and L ₁ is a single bond, at least one of R ₁ and R ₂ is alkyl having 6 or more carbon atoms. Represents a group, an aliphatic cyclic group, an aromatic ring group, a heterocyclic group or a halogen atom.

  These groups excluding the halogen atom may further have a substituent, and examples of the substituent that may be further included include an alkyl group, an aliphatic cyclic group, an aryl group, an amino group, an amide group, and a ureido group. , Urethane group, hydroxy group, carboxy group, halogen atom, alkoxy group, aralkyloxy group, thioether group, acyl group, acyloxy group, alkoxycarbonyl group, cyano group and nitro group.

When at least one of R ₁ and R ₂ is an alkyl group having 6 or more carbon atoms, an alkyl group having 6 to 15 carbon atoms is preferable, and an alkyl group having 6 to 10 carbon atoms is more preferable.

In one embodiment of the present invention, either _one of R ₁ and R ₂ is preferably, for example, an aliphatic cyclic group.

In the general formula (1), the organic group represented by M ₁ is preferably a group represented by * -MQ. * Represents a bond linked to the oxygen atom of the general formula (1). M represents a single bond or a divalent linking group. Q represents an alkyl group, an aliphatic cyclic group, an aryl group, or a heterocyclic group.

The divalent linking group as M is, for example, an alkylene group (preferably an alkylene group having 1 to 8 carbon atoms, such as a methylene group, an ethylene group, a propylene group, a butylene group, a hexylene group or an octylene group), a cycloalkylene group. (preferably cycloalkylene group having 3 to 15 carbon atoms, e.g., a cyclopentylene group or a cyclohexylene group), - S -, - O -, - CO -, - CS -, - SO 2 -, - N (R ₀ )-, or a combination of two or more thereof, and those having a total carbon number of 20 or less are preferred. Here, R ₀ is a hydrogen atom or an alkyl group (for example, an alkyl group having 1 to 8 carbon atoms, specifically, a methyl group, an ethyl group, a propyl group, an n-butyl group, a sec-butyl group, Hexyl group and octyl group).

M is preferably a single bond, an alkylene group, or a divalent linking group composed of a combination of an alkylene group and at least one of —O—, —CO—, —CS—, and —N (R ₀ ) —. A divalent linking group composed of a bond, an alkylene group, or a combination of an alkylene group and —O— is more preferable. Here, R ₀ has the same meaning as R ₀ described above.

  M may further have a substituent, and examples of the substituent that M may further include an aliphatic cyclic group, an aryl group, an amino group, an amide group, a ureido group, a urethane group, a hydroxy group, and a carboxy group. Group, halogen atom, alkoxy group, aralkyloxy group, thioether group, acyl group, acyloxy group, alkoxycarbonyl group, cyano group and nitro group. The above substituents may be bonded to each other to form a ring, and when the above substituents are bonded to each other to form a ring, the ring is an aliphatic cyclic group having 3 to 10 carbon atoms or a phenyl group. Can be mentioned.

  Specific examples and preferred examples of the alkyl group as Q are, for example, preferably an alkyl group having 1 to 15 carbon atoms. Specific examples of the alkyl group of Q include, for example, methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, sec-butyl group, t-butyl group, neopentyl group, hexyl group, 2-ethylhexyl group, An octyl group, a dodecyl group, etc. can be mentioned.

  The aliphatic cyclic group as Q may be monocyclic or polycyclic. Examples of the aliphatic cyclic group include a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclooctyl group, a 1-adamantyl group, a 2-adamantyl group, a 1-norbornyl group, and a 2-norbornyl group. Group, bornyl group, isobornyl group, 4-tetracyclo [6.2.13, 6.02,7] dodecyl group, 8-tricyclo [5.2.1.02,6] decyl group, 2-bicyclo [ 2.2.1] a heptyl group. Among them, a cyclopentyl group, a cyclohexyl group, a 2-adamantyl group, an 8-tricyclo [5.2.1.02,6] decyl group, and a 2-bicyclo [2.2.1] heptyl group can be mentioned.

  Specific examples and preferred examples of the aryl group as Q are preferably, for example, an aryl group having 6 to 15 carbon atoms, and have a structure in which a plurality of aromatic rings are connected to each other through a single bond (for example, a biphenyl group, Terphenyl group). Specific examples of the Q aryl group include a phenyl group, a naphthyl group, an anthranyl group, a biphenyl group, a terphenyl group, and the like. The aryl group of Q is preferably a phenyl group, a naphthyl group, or a biphenyl group.

  Specific examples and preferred examples of the heterocyclic group as Q are preferably, for example, a heterocyclic group having 6 to 20 carbon atoms. Specific examples of the heterocyclic group of Q include pyridyl group, pyrazyl group, tetrahydrofuranyl group, tetrahydropyranyl group, tetrahydrothiophene group, piperidyl group, piperazyl group, furanyl group, pyranyl group, chromanyl group and the like. .

  The alkyl group, aliphatic cyclic group, aryl group and heterocyclic group as Q may have a substituent, for example, an alkyl group, an aliphatic cyclic group, a cyano group, a halogen atom, a hydroxyl group, an alkoxy group. Group, carboxyl group and alkoxycarbonyl group.

In one embodiment of the present invention, M ₁ is preferably an alkyl group, an alkyl group substituted with an aliphatic cyclic group, an aliphatic cyclic group, an aralkyl group, an aryloxyalkyl group, or a heterocyclic group. More preferably, it is a group or an aliphatic cyclic group. The alkyl group as R _2, an aliphatic cyclic group in the "aliphatic cyclic group" and "alkyl group substituted with an aliphatic cyclic group" as R _2, and, as the group represented by M ₁ Specific examples and preferred examples of the aryl group in the “aralkyl group (arylalkyl group)” and “aryloxyalkyl group” are those described for the alkyl group, aliphatic cyclic group, and aryl group as Q, respectively. It is the same.

"Alkyl group substituted with an aliphatic cyclic group" as M _1, specific examples and preferred examples of the alkyl moiety in the "aralkyl group (aryl alkyl group)" and "aryloxyalkyl group", respectively, as a M The same as described for the alkylene group.

Specific examples and preferred examples of the heterocyclic group as M ₁ are the same as those described for the heterocyclic group as Q.

Specific examples of the organic group represented by M ₁ include a methyl group, an ethyl group, an isopropyl group, a cyclopentyl group, a cyclohexyl group, a cyclohexylethyl group, a 2-adamantyl group, and 8-tricyclo [5.2.1]. .0 ^2,6] decyl group, 2-bicyclo [2.2.1] heptyl group, a benzyl group, a 2-phenethyl group, 2-phenoxyethyl ethylene group.

When Y ₃ in the general formula (1) is an aromatic ring group and L ₁ is a single bond, the organic group represented by M ₁ is a group that does not include a ring structure in one form, Also good.

One of R ₁ and R ₂ and M ₁ may be bonded to each other to form a ring together with the oxygen atom in the formula. The oxygen-containing heterocyclic structure formed in that case may be a monocyclic, polycyclic or spiro ring, and is preferably a monocyclic oxygen-containing heterocyclic structure, preferably having a carbon number. 3 to 10, more preferably 4 or 5.

  As described above, when M is a divalent linking group, Q may be bonded to M via a single bond or another linking group to form a ring. As said another coupling group, an alkylene group (preferably C1-C3 alkylene group) is mentioned, It is preferable that the ring formed is a 5- or 6-membered ring.

In another embodiment of the present invention, when Y ₃ in the general formula (1) is an aromatic ring group and L ₁ is a divalent linking group, L ₁ includes an aliphatic cyclic group. And _one of R ₁ and R ₂ and M ₁ are not bonded to each other to form a ring.

In this case, at least one of R ₁ and R ₂ in the general formula (1) is an alkyl group having 7 or more carbon atoms, an aliphatic cyclic group, a halogen atom, an aromatic ring group having 13 or more carbon atoms, or a heterocyclic ring. It is preferably a group.

The repeating unit (a) represented by the general formula (1) is preferably a repeating unit represented by any one of the general formulas (2) to (4).
First, the repeating unit represented by the general formula (2) (hereinafter also referred to as “repeating unit (b)”) will be described.

In general formula (2),
Y ₄ and Y ₅ each independently represent a hydrogen atom or an organic group, and may combine with each other to form an aromatic ring.

L ₁₁ represents a single bond or a divalent linking group. L ₁₁ may combine with Y ₄ to form a ring, and in this case, L ₁₁ represents a trivalent linking group.

R ₃ and R ₄ each independently represents a hydrogen atom or a substituent.

M ₂ represents an organic group.

One of R ₃ and R ₄ and M ₂ may be bonded to each other to form a ring together with the oxygen atom in the formula.

However, at least one of Y ₄ and Y ₅ includes an aromatic ring, or Y ₄ and Y ₅ are bonded to each other to form an aromatic ring.

In the general formula (2), the definition and preferred range of the organic group represented by Y ₄ and Y ₅ are the same as those of the organic group represented by Y ₁ and Y ₂ in the general formula (1) described above.

In the general formula (2), the definition and preferred range of the divalent linking group represented by L ₁₁ are the same as those of the divalent linking group represented by Y ₃ in the general formula (1).

In the general formula (2), the definition and preferred range of the substituent represented by R ₃ are the same as the divalent linking group represented by R ₁ in the general formula (1). In one embodiment of the present invention, R ₃ is preferably a hydrogen atom.

In the general formula (2), the definition and preferred range of the substituent represented by R ₄ are the same as the divalent linking group represented by R ₂ in the general formula (1) described above. In one embodiment of the present invention, R ₄ is preferably a hydrogen atom, an alkyl group, an aliphatic cyclic group, or an aromatic ring group.

In the general formula (2), the definition and preferred range of the organic group represented by M ₂ are the same as the organic group represented by M ₁ in the general formula (1) described above. In one embodiment of the present invention, M ₂ is preferably an alkyl group.

In the general formula (2), at least one of Y ₄ and Y ₅ includes an aromatic ring, or Y ₄ and Y ₅ are bonded to each other to form an aromatic ring.

  That is, the repeating unit (b) represented by the general formula (2) limited the position of at least one aromatic ring included as an essential requirement with respect to the repeating unit (a) represented by the general formula (1). Is.

  The at least one aromatic ring group possessed by the general formula (2) is an aromatic ring group having 6 to 18 carbon atoms (more preferably 6 to 10 carbon atoms) such as a benzene ring or a naphthalene ring group, or, for example, thiophene Preferred examples include aromatic ring groups including hetero rings such as rings, furan rings, pyrrole rings, benzothiophene rings, benzofuran rings, benzopyrrole rings, triazine rings, imidazole rings, benzimidazole rings, triazole rings, thiadiazole rings, and thiazole rings. It is more preferable that it is a naphthalene ring, and it is particularly preferable that it is a benzene ring group.

  In addition, at least one aromatic ring group included in the general formula (2) may further have a substituent. Examples of the substituent include an alkyl group, an aliphatic cyclic group, an aryl group, and an amino group. Amide group, ureido group, urethane group, hydroxy group, carboxy group, halogen atom, alkoxy group, aralkyloxy group, thioether group, acyl group, acyloxy group, alkoxycarbonyl group, cyano group and nitro group.

In one embodiment of the present invention, in the general formula (2), the substituent represented by Y ₄ is preferably an aromatic ring group, and more preferably a benzene ring group. When Y ₄ is an aromatic ring group, Y ₅ is preferably a hydrogen atom.

  Next, the repeating unit represented by the general formula (3) (hereinafter also referred to as “repeating unit (c)”) will be described.

In general formula (3),
Y ₆ and Y ₇ each independently represent a hydrogen atom or a monovalent organic group.

L ₂ represents a divalent linking group having 1 atom between the aromatic ring and the carboxyl group in the formula.

R ₅ and R ₆ each independently represents a hydrogen atom, an alkyl group, an aliphatic cyclic group, a halogen atom, an aromatic ring group, or a heterocyclic group.

M ₃ represents an organic group.

One of R ₅ and R ₆ and M ₃ are not bonded to each other to form a ring.

  n represents 0 or an integer of 1 or more.

  The repeating unit (c) represented by the general formula (3) includes at least one aromatic ring contained as an essential requirement in the repeating unit (a) as the following aromatic ring group in the formula, and this aromatic ring group Is preferably a benzene ring or a naphthalene ring, and more preferably a benzene ring. That is, n in the general formula (3) is preferably 0 or 1, and more preferably 0.

In general formula (3), examples of the monovalent organic group represented by Y ₆ include an alkyl group, an aliphatic cyclic group, an aryl group, and a heterocyclic group.

The alkyl group as Y ₆ preferably has 1 to 5 carbon atoms, more preferably 1 to 3 carbon atoms, and still more preferably a methyl group.

The aliphatic cyclic group for Y ₆ may be monocyclic or polycyclic, and is preferably an aliphatic cyclic group having 3 to 15 carbon atoms, and has 3 to 10 carbon atoms. It is more preferably an aliphatic cyclic group, and further preferably an aliphatic cyclic group having 3 to 6 carbon atoms. Specific examples of the aliphatic cyclic group for Y6 include, for example, cyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohexyl group, cycloheptyl group, cyclooctyl group, decahydronaphthyl group, cyclodecyl group, 1-adamantyl group, 2 -Adamantyl group, 1-norbornyl group, 2-norbornyl group and the like can be mentioned.

The aryl group of Y ₆ is preferably an aryl group having 6 to 15 carbon atoms, more preferably an aryl group having 6 to 12 carbon atoms, and a plurality of aromatic rings are connected to each other via a single bond. Structures (for example, biphenyl group, terphenyl group) are also included. Specific examples of the aryl group for Y ₆ include a phenyl group, a naphthyl group, an anthranyl group, a biphenyl group, and a terphenyl group. When Y ₆ is an aryl group, it represents an (n + 1) -valent aromatic ring group. When Y ₆ is bonded to Y ₇ to form a ring, it represents an (n + 2) -valent aromatic ring group.

The heterocyclic group for Y ₆ is preferably a heterocyclic group having 6 to 20 carbon atoms, and more preferably a heterocyclic group having 6 to 12 carbon atoms. Specific examples of the heterocyclic group for Y ₆ include, for example, pyridyl group, pyrazyl group, tetrahydrofuranyl group, tetrahydropyranyl group, tetrahydrothiophene group, piperidyl group, piperazyl group, furanyl group, pyranyl group, chromanyl group and the like. It is done.

The alkyl group, aliphatic cyclic group, aryl group, aralkyl group and heterocyclic group as Y ₆ may further have a substituent.

Examples of the substituent that the alkyl group as Y ₆ may further include, for example, an aliphatic cyclic group, an aryl group, an amino group, an amide group, a ureido group, a urethane group, a hydroxy group, a carboxy group, a halogen atom, Examples thereof include an alkoxy group, an aralkyloxy group, a thioether group, an acyl group, an acyloxy group, an alkoxycarbonyl group, a cyano group, and a nitro group. The above substituents may be bonded to each other to form a ring, and when the above substituents are bonded to each other to form a ring, the ring is an aliphatic cyclic group having 3 to 10 carbon atoms or a phenyl group. Can be mentioned. In one embodiment of the present invention, when the alkyl group as Y ₆ has a substituent, the substituent is preferably a fluorine atom.

Examples of the substituent that the aliphatic cyclic group as Y ₆ may further include an alkyl group and the groups described above as specific examples of the substituent that the alkyl group may further have.

  In addition, carbon number of the said alkyl group and carbon number of the substituent which the aliphatic cyclic group may have further each are preferably 1-8.

Examples of the substituent which the aryl group, aralkyl group and heterocyclic group as Y ₆ may further have include a halogen atom such as a nitro group and a fluorine atom, a carboxyl group, a hydroxyl group, an amino group, a cyano group and an alkyl group (preferably Is an alkoxy group (preferably a carbon number of 1 to 15), an aliphatic cyclic group (preferably a carbon number of 3 to 15), an aryl group (preferably a carbon number of 6 to 14), an alkoxycarbonyl group. (Preferably having 2 to 7 carbon atoms), acyl group (preferably having 2 to 12 carbon atoms), alkoxycarbonyloxy group (preferably having 2 to 7 carbon atoms), and the like.

Y ₆ is preferably a hydrogen atom or an alkyl group having 1 to 5 carbon atoms, more preferably a hydrogen atom or an alkyl group having 1 to 3 carbon atoms, a hydrogen atom, a methyl group or ethyl. It is more preferably a group, and particularly preferably a hydrogen atom.

Examples of the monovalent organic group represented by Y ₇ in the general formula (3) include an alkyl group, an aliphatic cyclic group, an aryl group, and a heterocyclic group.

The alkyl group as Y ₇ is preferably an alkyl group having 1 to 10 carbon atoms, more preferably an alkyl group having 1 to 5 carbon atoms, and further preferably an alkyl group having 1 to 3 carbon atoms. An alkyl group having 1 or 2 carbon atoms (that is, a methyl group or an ethyl group) is preferable. Specific examples of the alkyl group for Y ₇ include, for example, methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, isobutyl group, sec-butyl group, and t-butyl group. Can do.

Specific examples and preferred examples of the aliphatic cyclic group, an aryl group or a heterocyclic group as Y ₇ are, for example, similar to that described for aliphatic cyclic group, an aryl group or a heterocyclic group as Y ₆ described above It is.

The alkyl group, aliphatic cyclic group, aryl group or heterocyclic group as Y ₇ may further have a substituent, and the substituent which these groups may further have is the alkyl as Y ₆ described above. It is the same as the substituent that the group, aliphatic cyclic group, aryl group or heterocyclic group may have.

Y ₇ is preferably a hydrogen atom or an alkyl group having 1 to 5 carbon atoms, more preferably a hydrogen atom or an alkyl group having 1 to 3 carbon atoms, a hydrogen atom, a methyl group or ethyl. It is more preferably a group, and particularly preferably a hydrogen atom.

In the general formula (3), the divalent linking group as L ₂ is, for example, a methylene group, —S—, —O—, —CO—, —CS—, —SO ₂ —, —N (R ₀ ). -Is preferable, a methylene group and -O- are more preferable, and a methylene group is particularly preferable. Here, R ₀ has the same meaning as R ₀ described above. The divalent linking group as L ₂ in the case where n in the general formula (3) is 0 can be bonded to any of the ortho, meta, and para positions, but the para position is particularly preferable. .

In General Formula (3), R ₅ and R ₆ each independently represent a hydrogen atom, an alkyl group, an aliphatic cyclic group, a halogen atom, an aromatic ring group, or a heterocyclic group.

The alkyl group for R ₅ and R ₆ preferably has 1 to 20 carbon atoms. In addition, as for carbon number of an alkyl group, 7 or more are preferable. This improves dry etching performance.

The aliphatic cyclic group of R ₅ and R ₆ may be monocyclic or polycyclic, and is preferably an aliphatic cyclic group having 3 to 15 carbon atoms, and 3 carbon atoms. Is more preferably an aliphatic cyclic group having 10 to 10 carbon atoms, and further preferably an aliphatic cyclic group having 5 to 10 carbon atoms. Specific examples of the aliphatic cyclic group represented by R ₅ and R ₆ include, for example, cyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohexyl group, cycloheptyl group, cyclooctyl group, decahydronaphthyl group, cyclodecyl group, 1- Examples thereof include an adamantyl group, a 2-adamantyl group, a 1-norbornyl group, and a 2-norbornyl group. A cyclopentyl group, a cyclohexyl group, a 1-adamantyl group, a 2-adamantyl group, a 1-norbornyl group, and 2 -A norbornyl group is preferred.

Examples of the halogen atom for R ₅ and R ₆ include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom, and a fluorine atom is particularly preferable.

The aromatic ring group of R ₅ and R ₆ is preferably an aryl group having 6 to 18 carbon atoms, and a structure in which a plurality of aromatic rings are connected to each other through a single bond (for example, biphenyl group, terphenyl group) Including. Specific examples of the aryl group of R ₅ and R ₆ include a phenyl group, a naphthyl group, an anthranyl group, a biphenyl group, a terphenyl group, and the like. The aromatic ring group preferably has 13 or more carbon atoms. This improves dry etching performance.

The heterocyclic group of R ₅ and R ₆ is preferably a heterocyclic group having 6 to 20 carbon atoms, and more preferably a heterocyclic group having 6 to 12 carbon atoms. Specific examples of the heterocyclic group of R ₅ and R ₆ include, for example, pyridyl group, pyrazyl group, tetrahydrofuranyl group, tetrahydropyranyl group, tetrahydrothiophene group, piperidyl group, piperazyl group, furanyl group, pyranyl group, chromanyl group. Etc.

The alkyl group, aliphatic cyclic group, halogen atom, aromatic ring group, or heterocyclic group as R ₅ and R ₆ may further have a substituent, and the substituent that R ₅ may further have is: is the same as the substituent which the alkyl group of the above-mentioned Y ₁ may have.

In one embodiment of the present invention, at least one of R ₅ and R ₆ is an alkyl group having 7 or more carbon atoms, an aliphatic cyclic group, a halogen atom, an aromatic ring group having 13 or more carbon atoms, or a heterocyclic group. Is preferred.

  These groups excluding the halogen atom may further have a substituent, and examples of the substituent that may be further included include an alkyl group, an aliphatic cyclic group, an aryl group, an amino group, an amide group, and a ureido group. , Urethane group, hydroxy group, carboxy group, halogen atom, alkoxy group, aralkyloxy group, thioether group, acyl group, acyloxy group, alkoxycarbonyl group, cyano group and nitro group.

When at least one of R ₅ and R ₆ is an alkyl group having 7 or more carbon atoms, it is more preferably an alkyl group having 7 to 15 carbon atoms, and further preferably an alkyl group having 7 to 10 carbon atoms.

Further, when at least one of R ₅ and R ₆ is an aromatic ring group having 13 or more carbon atoms, it is more preferably an aromatic ring group having 13 or more carbon atoms, and an aromatic ring group having 13 to 18 carbon atoms. Is more preferable.

Furthermore, in one embodiment of the present invention, at least one of R ₅ and R ₆ is preferably a hydrogen atom, an alkyl group, an aliphatic cyclic group, or an aromatic ring group.

In the general formula (3), the definition and preferred range of the organic group represented by M ₃ are the same as those of the organic group represented by M ₁ in the general formula (1) described above. However, M ₃ does not combine with one of R ₅ and R ₆ to form a ring.

In one embodiment of the present invention, M ₃ is preferably an alkyl group having 7 or more carbon atoms, an aliphatic cyclic group, a halogen atom, an aromatic ring group having 13 or more carbon atoms, or a heterocyclic group.

When M ₃ is an alkyl group having 7 or more carbon atoms, it is more preferably an alkyl group having 7 to 15 carbon atoms, and further preferably an alkyl group having 7 to 10 carbon atoms.

Further, if M ₃ is an aromatic ring group having 13 or more carbon atoms, more preferably an aromatic ring group 13 to 18 carbon atoms.

  In one embodiment of the present invention, the repeating unit (c) represented by the general formula (3) is preferably a repeating unit represented by the general formula (3c).

In General Formula (3a), Y ₆ , Y ₇ , L ₂ , R ₅ , R ₆ , and n are synonymous with each group in General Formula (3) described above.

In the general formula (3a), M and Q, in the above-mentioned general formula (1), the same meaning as M and Q in * -M-Q illustrating one embodiment of a _{M 1.}

  Next, the repeating unit represented by the general formula (4) (hereinafter also referred to as “repeating unit (d)”) will be described.

In general formula (4),
Y ₈ and Y ₉ each independently represent a hydrogen atom or a monovalent organic group.

R ₇ represents an alkyl group having 6 or more carbon atoms, an aliphatic cyclic group, an aromatic ring group, a heterocyclic group, or a halogen atom.

R ₈ represents a hydrogen atom or a substituent.

M ₄ represents an organic group.

One of R ₇ and R ₈ and M ₄ may be bonded to each other to form a ring together with the oxygen atom in the formula.

  n represents 0 or an integer of 1 or more.

  The repeating unit (d) represented by the general formula (4) includes at least one aromatic ring contained as an essential requirement in the repeating unit (a) as the following aromatic ring group in the formula, and this aromatic ring group Is preferably a benzene ring or a naphthalene ring, and more preferably a benzene ring. That is, n in the general formula (4) is preferably 0 or 1, and more preferably 0.

In General Formula (4), Y ₈ and Y ₉ have the same meanings as Y ₆ and Y ₇ in General Formula (3), respectively, and the preferred ranges are also the same.

In General Formula (4), R ₇ represents an alkyl group having 6 or more carbon atoms, an aliphatic cyclic group, a halogen atom, an aromatic ring group, or a heterocyclic group.

  These groups excluding the halogen atom may further have a substituent, and examples of the substituent that may be further included include an alkyl group, an aliphatic cyclic group, an aryl group, an amino group, an amide group, and a ureido group. , Urethane group, hydroxy group, carboxy group, halogen atom, alkoxy group, aralkyloxy group, thioether group, acyl group, acyloxy group, alkoxycarbonyl group, cyano group and nitro group.

In the alkyl group for R _7, the number of carbon atoms is preferably 6 or more from the viewpoint of dry etching performance.

R ₇ is preferably an alkyl group having 6 to 15 carbon atoms, and more preferably an alkyl group having 6 to 10 carbon atoms.

In the general formula (4), the definition and preferred range of the aliphatic cyclic group represented by R ₇ , the halogen atom, the aromatic ring group, and the heterocyclic group are the aliphatic cyclic group as R ₅ described above, This is the same as the halogen atom, aromatic ring group, and heterocyclic group. Moreover, the substituent which these groups may have is the same as the substituent which the alkyl group of Y ₁ may have.

In one embodiment of the present invention, R ₇ is preferably an aliphatic cyclic group.

The alkyl group, aliphatic cyclic group, aromatic ring group, or heterocyclic group as R ₇ may further have a substituent, and the substituent that these groups may further have is as Y ₁ described above. These are the same as the substituents that the alkyl group, aliphatic cyclic group, aromatic ring group, or heterocyclic group may have.

In the general formula (4), the organic group represented by R ₈ has the same meaning as organic groups represented by R ₁ in the general formula (1).
In one embodiment of the present invention, R ₈ is preferably a hydrogen atom, an alkyl group, an aliphatic cyclic group, or an aromatic ring group.

In the general formula (4), the definition and preferred range of the organic group represented by M ₄ are the same as those of the organic group represented by M ₁ in the above general formula (1). Further, the organic group represented by M ₄ may be a group that does not include a ring structure in one embodiment.

  Specific examples of the repeating unit (a) represented by the general formula (1) are shown below, but the present invention is not limited thereto.

  The content of the repeating unit (a) represented by the above general formula (1) in the resin (P1) (the total when plural types are contained) is 10 to 90 with respect to all the repeating units in the resin (P1). It is preferably mol%, more preferably 30 to 80 mol%, still more preferably 50 to 70 mol%.

  In one embodiment of the present invention, the resin (P1) preferably has a repeating unit represented by the following general formula (A).

In general formula (A),
R ₄₁ , R ₄₂ and R ₄₃ each independently represents a hydrogen atom, an alkyl group, a halogen atom, a cyano group or an alkoxycarbonyl group. (However, R ₄₂ may be bonded to Ar ₄ or X ₄ to form a ring, and R ₄₂ in this case represents a single bond or an alkylene group.)

X ₄ represents a single bond, an alkylene group, —COO—, or —CONR ₆₄ —. (Here, R ₆₄ represents a hydrogen atom or an alkyl group.)

L ₄ represents a single bond, —COO—, or an alkylene group.

Ar ₄ represents an (n + 1) -valent aromatic ring group, and when bonded to R ₄₂ to form a ring, represents an (n + 2) -valent aromatic ring group.

  n represents an integer of 1 to 4.

As the alkyl group for R ₄₁ , R ₄₂ and R _43, a methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, sec-butyl group, hexyl group, which may preferably have a substituent, An alkyl group having 20 or less carbon atoms such as a 2-ethylhexyl group, an octyl group, or a dodecyl group is exemplified, more preferably an alkyl group having 8 or less carbon atoms, and particularly preferably an alkyl group having 3 or less carbon atoms.

Specific examples and preferred examples of the alkyl group contained in the alkoxycarbonyl group of R _{41, R 42, R 43} are the same as those in the above-described alkyl group _{R 41,} R _{42, R 43.}

Examples of the halogen atom for R ₄₁ , R ₄₂ and R ₄₃ include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom, and a fluorine atom is particularly preferred.

Ar ₄ represents an (n + 1) -valent aromatic ring group. The divalent aromatic ring group in the case where n is 1 may have a substituent, for example, an arylene group having 6 to 18 carbon atoms such as a phenylene group, a tolylene group, a naphthylene group, and an anthracenylene group, or Examples of preferred aromatic ring groups include heterocycles such as thiophene, furan, pyrrole, benzothiophene, benzofuran, benzopyrrole, triazine, imidazole, benzimidazole, triazole, thiadiazole, thiazole.

  Specific examples of the (n + 1) -valent aromatic ring group in the case where n is an integer of 2 or more include (n-1) arbitrary hydrogen atoms removed from the above-described specific examples of the divalent aromatic ring group. The group formed can be preferably mentioned.

  The (n + 1) -valent aromatic ring group may further have a substituent.

The alkylene group for L ₄ is preferably an alkylene group having 1 to 8 carbon atoms, such as an optionally substituted methylene group, ethylene group, propylene group, butylene group, hexylene group, octylene group.

The alkylene group represented by X ₄ is the same as that in the alkylene group as the divalent linking group represented by L in formula (Ab), and the preferred range is also the same.

When R ₄₂ and Ar ₄ or X ₄ combine to form a ring, the alkylene group as R ₄₂ may be linear or branched, and has 1 to 5 carbon atoms. preferable.

The alkylene group as X ₄ when R ₄₂ and X ₄ are combined to form a ring may be linear or branched, and preferably has 1 to 5 carbon atoms.

_-CONR 64 represented by X ₄ - _{(R 64} represents a hydrogen atom, an alkyl group) The alkyl group for _{R 64 in,} the same as the alkyl group of R 41 _{to R 43.}

X ₄ is preferably a single bond, an alkylene group, —COO— or —CONH—, and more preferably a single bond or —COO—.

Ar ₄ is more preferably an aromatic ring group having 6 to 18 carbon atoms which may have a substituent, and particularly preferably a benzene ring group, a naphthalene ring group or a biphenylene ring group.

The repeating unit (b) preferably has a hydroxystyrene structure. That is, Ar ₄ is preferably a benzene ring group.

  Preferred substituents in each of the above groups include, for example, alkyl groups, cycloalkyl groups, aryl groups, amino groups, amide groups, ureido groups, urethane groups, hydroxyl groups, carboxyl groups, halogen atoms, alkoxy groups, thioether groups, acyls. Groups, acyloxy groups, alkoxycarbonyl groups, cyano groups, nitro groups and the like, and the substituent preferably has 8 or less carbon atoms.

  The repeating unit represented by the general formula (A) is preferably a repeating unit represented by the following formula (A1) or (A2). R ″ represents a hydrogen atom or a methyl group.

  As specific examples of the repeating unit (b) represented by the general formula (A), in addition to those shown below, those described in paragraphs 0226 to 0227 of JP 2014-41328 A can be used, These contents are incorporated herein.

  The resin (P1) may contain two or more types of repeating units represented by the general formula (A).

  The content of the repeating unit represented by the general formula (A) in the resin (P1) (the total when there are a plurality of types) is relative to the developer containing an organic solvent in the actinic ray-sensitive or radiation-sensitive film. From the viewpoint of improving the dissolution contrast, it is preferably 10 to 70 mol%, more preferably 15 to 55 mol%, most preferably 20 to 40 mol%, based on all repeating units in the resin (P1). is there.

  The resin (P1) may further contain a repeating unit represented by the following general formula (A5).

In formula (A5),
X is a hydrogen atom, alkyl group, hydroxyl group, alkoxy group, halogen atom, cyano group, nitro group, acyl group, acyloxy group, cycloalkyl group, aryl group, carboxyl group, alkyloxycarbonyl group, alkylcarbonyloxy group, or Represents an aralkyl group.

A ₄ represents a hydrocarbon group that is not eliminated by the action of an acid.

In the general formula (A5), examples of the hydrocarbon group that is not eliminated by the action of the acid A ₄ include hydrocarbon groups other than the acid-decomposable groups, such as an alkyl that is not eliminated by the action of the acid. A group (preferably having 1 to 15 carbon atoms), a cycloalkyl group (preferably having 3 to 15 carbon atoms) which is not eliminated by the action of an acid, an aryl group (preferably having 6 to 15 carbon atoms) which is not eliminated by the action of an acid, etc. Can be mentioned.

The hydrocarbon group that is not eliminated by the action of the acid of A ₄ may be further substituted with a hydroxyl group, an alkyl group, a cycloalkyl group, an aryl group, or the like.

  Although the specific example of the repeating unit represented by general formula (A5) below is given, it is not limited to these.

  Moreover, as an aspect of the repeating unit having an acid-decomposable group different from the repeating unit exemplified above, the resin (P1) may have a repeating unit that generates an alcoholic hydroxyl group. In this case, the repeating unit that generates an alcoholic hydroxyl group is preferably represented by at least one selected from the group consisting of the following general formulas (I-1) to (I-10). The repeating unit that generates an alcoholic hydroxyl group is more preferably represented by at least one selected from the group consisting of the following general formulas (I-1) to (I-3). More preferably, it is represented by:

Where
Each Ra independently represents a hydrogen atom, an alkyl group or a group represented by —CH ₂ —O—Ra ₂ . Here, Ra ₂ represents a hydrogen atom, an alkyl group, or an acyl group.

R ₁ represents an (n + 1) valent organic group.

R ₂ independently represents a single bond or an (n + 1) -valent organic group when m ≧ 2.

  OP each independently represents the above group which decomposes by the action of an acid to produce an alcoholic hydroxy group. When n ≧ 2 and / or m ≧ 2, two or more OPs may be bonded to each other to form a ring.

  W represents a methylene group, an oxygen atom or a sulfur atom.

n and m represent an integer of 1 or more. In general formula (I-2), (I-3) or (I-8), n is 1 when R ₂ represents a single bond.

  l represents an integer of 0 or more.

L ₁ represents a linking group represented by —COO—, —OCO—, —CONH—, —O—, —Ar—, —SO ₃ — or —SO ₂ NH—. Here, Ar represents a divalent aromatic ring group.

  Each R independently represents a hydrogen atom or an alkyl group.

R ₀ represents a hydrogen atom or an organic group.

L ₃ represents a (m + 2) -valent linking group.

R ^L each independently represents an (n + 1) -valent linking group when m ≧ 2.

R ^S each independently represents a substituent when p ≧ 2. For p ≧ 2, plural structured R ^S may be bonded to each other to form a ring.

  p represents an integer of 0 to 3.

Ra represents a hydrogen atom, an alkyl group, or a group represented by —CH ₂ —O—Ra ₂ . Ra is preferably a hydrogen atom or an alkyl group having 1 to 10 carbon atoms, and more preferably a hydrogen atom or a methyl group.

  W represents a methylene group, an oxygen atom or a sulfur atom. W is preferably a methylene group or an oxygen atom.

R ₁ represents an (n + 1) valent organic group. R ₁ is preferably a non-aromatic hydrocarbon group. In this case, R ₁ may be a chain hydrocarbon group or an alicyclic hydrocarbon group. R ₁ is more preferably an alicyclic hydrocarbon group.

R ₂ represents a single bond or an (n + 1) valent organic group. R ₂ is preferably a single bond or a non-aromatic hydrocarbon group. In this case, R ₂ may be a chain hydrocarbon group or an alicyclic hydrocarbon group.

When R ₁ and / or R ₂ is a chain hydrocarbon group, the chain hydrocarbon group may be linear or branched. The chain hydrocarbon group preferably has 1 to 8 carbon atoms. For example, when R ₁ and / or R ₂ is an alkylene group, R ₁ and / or R ₂ are methylene group, ethylene group, n-propylene group, isopropylene group, n-butylene group, isobutylene group or sec- A butylene group is preferred.

When R ₁ and / or R ₂ is an alicyclic hydrocarbon group, the alicyclic hydrocarbon group may be monocyclic or polycyclic. This alicyclic hydrocarbon group has, for example, a monocyclo, bicyclo, tricyclo or tetracyclo structure. The carbon number of this alicyclic hydrocarbon group is usually 5 or more, preferably 6 to 30, and more preferably 7 to 25.

Examples of the alicyclic hydrocarbon group include those having the partial structures listed below. Each of these partial structures may have a substituent. In each of these partial structures, the methylene group (—CH ₂ —) includes an oxygen atom (—O—), a sulfur atom (—S—), a carbonyl group [—C (═O) —], a sulfonyl group [ -S (= O) _2- ], a sulfinyl group [-S (= O)-], or an imino group [-N (R)-] (R is a hydrogen atom or an alkyl group).

For example, when R ₁ and / or R ₂ is a cycloalkylene group, R ₁ and / or R ₂ may be an adamantylene group, a noradamantylene group, a decahydronaphthylene group, a tricyclodecanylene group, a tetracyclododeca group. Nylene group, norbornylene group, cyclopentylene group, cyclohexylene group, cycloheptylene group, cyclooctylene group, cyclodecanylene group, or cyclododecanylene group are preferable, and adamantylene group, norbornylene group, cyclohexylene group, cyclopentylene It is more preferable that they are a len group, a tetracyclododecanylene group, or a tricyclodecanylene group.

The non-aromatic hydrocarbon group of R ₁ and / or R ₂ may have a substituent. Examples of the substituent include an alkyl group having 1 to 4 carbon atoms, a halogen atom, a hydroxy group, an alkoxy group having 1 to 4 carbon atoms, a carboxy group, and an alkoxycarbonyl group having 2 to 6 carbon atoms. The above alkyl group, alkoxy group and alkoxycarbonyl group may further have a substituent. As this substituent, a hydroxy group, a halogen atom, and an alkoxy group are mentioned, for example.

L ₁ represents a linking group represented by —COO—, —OCO—, —CONH—, —O—, —Ar—, —SO ₃ — or —SO ₂ NH—. Here, Ar represents a divalent aromatic ring group. L ₁ is preferably a linking group represented by —COO—, —CONH— or —Ar—, and more preferably a linking group represented by —COO— or —CONH—.

  R represents a hydrogen atom or an alkyl group. The alkyl group may be linear or branched. Carbon number of this alkyl group becomes like this. Preferably it is 1-6, More preferably, it is 1-3. R is preferably a hydrogen atom or a methyl group, and more preferably a hydrogen atom.

R ₀ represents a hydrogen atom or an organic group. Examples of the organic group include an alkyl group, a cycloalkyl group, an aryl group, an alkynyl group, and an alkenyl group. R ₀ is preferably a hydrogen atom or an alkyl group, and more preferably a hydrogen atom or a methyl group.

L ₃ represents a (m + 2) -valent linking group. That is, L ₃ represents a trivalent or higher linking group. Examples of such a linking group include corresponding groups in specific examples described later.

R ^L represents a (n + 1) -valent linking group. That is, R ^L represents a divalent or higher linking group. Examples of such a linking group include an alkylene group, a cycloalkylene group, and corresponding groups in the specific examples described below. R ^L may be bonded to each other or bonded to the following R ^S to form a ring structure.

R ^S represents a substituent. Examples of the substituent include an alkyl group, an alkenyl group, an alkynyl group, an aryl group, an alkoxy group, an acyloxy group, an alkoxycarbonyl group, and a halogen atom.

  n is an integer of 1 or more. n is preferably an integer of 1 to 3, and more preferably 1 or 2. When n is 2 or more, it is possible to further improve the dissolution contrast with respect to a developer containing an organic solvent. Accordingly, in this way, the limit resolution and roughness characteristics can be further improved.

  m is an integer of 1 or more. m is preferably an integer of 1 to 3, and more preferably 1 or 2.

  l is an integer of 0 or more. l is preferably 0 or 1.

  p is an integer of 0-3.

  The repeating unit that generates an alcoholic hydroxyl group is preferably a repeating unit that includes a group that decomposes by the action of an acid to generate an alcoholic hydroxy group.

  Specific examples of the repeating unit having a group that decomposes by the action of an acid to generate an alcoholic hydroxy group are shown below. In specific examples, Ra and OP have the same meanings as in general formulas (I-1) to (I-3). Further, when a plurality of OPs are bonded to each other to form a ring, the corresponding ring structure is represented as “OPO” for convenience.

  The group that decomposes by the action of an acid to produce an alcoholic hydroxy group is preferably represented by at least one selected from the group consisting of the following general formulas (II-1) to (II-4).

Where
R ₃ each independently represents a hydrogen atom or a monovalent organic group. R ₃ may be bonded to each other to form a ring.

R ₄ each independently represents a monovalent organic group. R ₄ may be bonded to each other to form a ring. R ₃ and R ₄ may be bonded to each other to form a ring.

R ₅ each independently represents a hydrogen atom, an alkyl group, a cycloalkyl group, an aryl group, an alkenyl group, or an alkynyl group. At least two R ₅ may be bonded to each other to form a ring. However, when one or two of the three R ₅ are hydrogen atoms, at least one of the remaining R ₅ represents an aryl group, an alkenyl group, or an alkynyl group.

  The group that decomposes by the action of an acid to produce an alcoholic hydroxy group is also preferably represented by at least one selected from the group consisting of the following general formulas (II-5) to (II-9).

Where
R ₄ has the same meaning as in general formulas (II-1) to (II-3).

R ₆ each independently represents a hydrogen atom or a monovalent organic group. R ₆ may be bonded to each other to form a ring.

  The group that decomposes by the action of an acid to produce an alcoholic hydroxy group is more preferably represented by at least one selected from the general formulas (II-1) to (II-3). More preferably, it is represented by 1) or (II-3), and particularly preferably represented by formula (II-1).

R ₃ represents a hydrogen atom or a monovalent organic group as described above. R ₃ is preferably a hydrogen atom, an alkyl group or a cycloalkyl group, more preferably a hydrogen atom or an alkyl group.

The alkyl group for R ₃ may be linear or branched. The number of carbon atoms in the alkyl group of R ₃ is preferably 1 to 10, and more preferably 1 to 3. Examples of the alkyl group for R ₃ include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, and an n-butyl group.

The cycloalkyl group for R ₃ may be monocyclic or polycyclic. The number of carbon atoms in the cycloalkyl group represented by R ₃ is preferably 3 to 10, and more preferably 4 to 8. Examples of the cycloalkyl group represented by R ₃ include a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, a norbornyl group, and an adamantyl group.

In the general formula (II-1), at least one of R ₃ is preferably a monovalent organic group. When such a configuration is employed, particularly high sensitivity can be achieved.

R ₄ represents a monovalent organic group. R ₄ is preferably an alkyl group or a cycloalkyl group, and more preferably an alkyl group. These alkyl groups and cycloalkyl groups may have a substituent.

The alkyl group represented by R ₄ preferably has no substituent, or preferably has one or more aryl groups and / or one or more silyl groups as substituents. The carbon number of the unsubstituted alkyl group is preferably 1-20. It is preferable that carbon number of the alkyl group part in the alkyl group substituted by one or more aryl groups is 1-25. It is preferable that carbon number of the alkyl group part in the alkyl group substituted by the 1 or more silyl group is 1-30. Also, if the cycloalkyl group R ₄ does not have a substituent, the carbon number thereof is preferably from 3 to 20.

R ₅ represents a hydrogen atom, an alkyl group, a cycloalkyl group, an aryl group, an alkenyl group, or an alkynyl group. However, when one or two of the three R ₅ are hydrogen atoms, at least one of the remaining R ₅ represents an aryl group, an alkenyl group, or an alkynyl group. R ₅ is preferably a hydrogen atom or an alkyl group. The alkyl group may have a substituent or may not have a substituent. When the alkyl group does not have a substituent, the carbon number is preferably 1 to 6, and preferably 1 to 3.

R ₆ represents a hydrogen atom or a monovalent organic group as described above. R ₆ is preferably a hydrogen atom, an alkyl group or a cycloalkyl group, more preferably a hydrogen atom or an alkyl group, and further preferably a hydrogen atom or an alkyl group having no substituent. R ₆ is preferably a hydrogen atom or an alkyl group having 1 to 10 carbon atoms, and more preferably a hydrogen atom or an alkyl group having 1 to 10 carbon atoms and having no substituent.

Examples of the alkyl group and cycloalkyl group of R ₄ , R _5, and R ₆ include the same as those described above for R ₃ .

  Below, the specific example of the group which decomposes | disassembles by the effect | action of an acid and produces an alcoholic hydroxy group is shown.

Specific examples of the repeating unit having a group that decomposes by the action of an acid to generate an alcoholic hydroxy group are shown below. In the following specific examples, Xa ₁ represents a hydrogen atom, CH ₃ , CF ₃ , or CH ₂ OH.

  One type of repeating unit having the acid-decomposable group may be used, or two or more types may be used in combination.

  The content of the repeating unit having an acid-decomposable group in the resin (P1) (the total when there are a plurality of types) is preferably 10 to 90 mol% with respect to all the repeating units in the resin (P1). More preferably, it is 30-80 mol%, Most preferably, it is 50-70 mol%.

  The resin (P1) may further contain a repeating unit represented by the following general formula (4).

R ⁴¹ represents a hydrogen atom or a methyl group. L ⁴¹ represents a single bond or a divalent linking group. L ⁴² represents a divalent linking group. S represents a structural site that decomposes upon irradiation with actinic rays or radiation to generate an acid in the side chain.

  Specific examples of the repeating unit represented by the general formula (4) include those described in paragraphs 0195 to 0209 of JP2014-41328A, paragraphs 0016 to 0145 of JP2013-54196A, and the like. The contents of which are incorporated herein by reference.

  The content of the repeating unit represented by the general formula (4) in the resin (P1) is preferably in the range of 1 to 40 mol%, and in the range of 2 to 30 mol% with respect to all the repeating units of the resin (P1). Is more preferable, and the range of 5 to 25 mol% is particularly preferable.

  The resin (P1) preferably contains a repeating unit (b ′) having a polar group, which is different from the repeating unit represented by the general formula (A). By including the repeating unit (b ′), for example, the sensitivity of the composition containing a resin can be improved. The repeating unit (b ′) is preferably a non-acid-decomposable repeating unit (that is, having no acid-decomposable group).

  Examples of the “polar group” that the repeating unit (b ′) may contain include the following (1) to (4). In the following, “electronegativity” means a value by Pauling.

(1) A functional group including a structure in which an oxygen atom and an atom having an electronegativity difference of 1.1 or more are bonded by a single bond. Examples of such a polar group include a hydroxy group and the like. And a group containing a structure represented by O—H.

(2) Functional group including a structure in which a nitrogen atom and an atom having a difference in electronegativity of the nitrogen atom of 0.6 or more are bonded by a single bond. Examples of such a polar group include an amino group and the like. And a group containing a structure represented by N—H.

(3) Functional group including a structure in which two atoms having electronegativity different by 0.5 or more are bonded by a double bond or a triple bond. Examples of such a polar group include C≡N, C═O, N = And a group containing a structure represented by O, S═O or C═N.

(4) Functional group having an ionic moiety Examples of such a polar group include a group having a moiety represented by N ⁺ or S ⁺ .

  Specific examples of the partial structure that can be included in the “polar group” are given below.

  The polar group that the repeating unit (b ′) may contain is a hydroxyl group, a cyano group, a lactone group, a sultone group, a carboxylic acid group, a sulfonic acid group, an amide group, a sulfonamide group, an ammonium group, a sulfonium group, a carbonate group (- O-CO-O-) (for example, cyclic carbonate structure and the like) and a group formed by combining two or more of these are preferable, and an alcoholic hydroxy group, a cyano group, a lactone group, a sultone group, or A group containing a cyanolactone structure is particularly preferred.

  When the resin further contains a repeating unit having an alcoholic hydroxy group, the exposure latitude (EL) of the composition containing the resin can be further improved.

  When the resin further contains a repeating unit having a cyano group, the sensitivity of the composition containing the resin can be further improved.

  If the resin further contains a repeating unit having a lactone group, the dissolution contrast with respect to the developer containing an organic solvent can be further improved. This also makes it possible to further improve the dry etching resistance, coating properties, and adhesion to the substrate of the resin-containing composition.

  If the resin further contains a repeating unit having a group containing a lactone structure having a cyano group, the dissolution contrast with respect to the developer containing an organic solvent can be further improved. This also makes it possible to further improve the sensitivity, dry etching resistance, applicability, and adhesion to the substrate of the composition containing the resin. In addition, this makes it possible for a single repeating unit to have a function attributable to each of the cyano group and the lactone group, thereby further increasing the degree of freedom in designing the resin.

  When the polar group of the repeating unit (b ′) is an alcoholic hydroxy group, it is preferably represented by at least one selected from the group consisting of the following general formulas (I-1H) to (I-10H). . In particular, it is more preferably represented by at least one selected from the group consisting of the following general formulas (I-1H) to (I-3H), and may be represented by the following general formula (I-1H). Further preferred.

In the formula, Ra, R ₁ , R ₂ , W, n, m, l, L ₁ , R, R ₀ , L ₃ , R ^L , R ^S and p are represented by the general formulas (I-1) to (I− It is synonymous with each of 10).

  A repeating unit having a group capable of decomposing by the action of an acid to generate an alcoholic hydroxy group, and a repeating unit represented by at least one selected from the group consisting of the above general formulas (I-1H) to (I-10H) When the unit is used in combination, for example, by suppressing acid diffusion due to an alcoholic hydroxy group and increasing sensitivity due to a group that decomposes by the action of an acid to generate an alcoholic hydroxy group, without degrading other performances, The exposure latitude (EL) can be improved.

  When it has an alcoholic hydroxy group, the content of the repeating unit is preferably from 1 to 60 mol%, more preferably from 3 to 50 mol%, still more preferably from 5 to 40 mol%, based on all repeating units in the resin (P1). It is.

  Specific examples of the repeating unit represented by any one of the general formulas (I-1H) to (I-10H) are shown below. In specific examples, Ra is as defined in general formulas (I-1H) to (I-10H).

  When the polar group of the repeating unit (b ′) is an alcoholic hydroxy group or a cyano group, one embodiment of a preferable repeating unit is a repeating unit having an alicyclic hydrocarbon structure substituted with a hydroxyl group or a cyano group. Can be mentioned. At this time, it is preferable not to have an acid-decomposable group. The alicyclic hydrocarbon structure in the alicyclic hydrocarbon structure substituted with a hydroxyl group or a cyano group is preferably an adamantyl group, a diamantyl group, or a norbornane group. As the alicyclic hydrocarbon structure substituted with a preferred hydroxyl group or cyano group, partial structures represented by the following general formulas (VIIa) to (VIIc) are preferable. This improves the substrate adhesion and developer compatibility.

In general formulas (VIIa) to (VIIc),
R ₂ c to R ₄ c each independently represents a hydrogen atom, a hydroxyl group, or a cyano group. However, at least one of R ₂ c to R ₄ c represents a hydroxyl group. Preferably, one or two of R ₂ c to R ₄ c are a hydroxyl group and the rest are hydrogen atoms. In general formula (VIIa), more preferably, _two of R ₂ c to R ₄ c are a hydroxyl group and the rest are hydrogen atoms.

  Examples of the repeating unit having a partial structure represented by the general formulas (VIIa) to (VIIc) include the repeating units represented by the following general formulas (AIIa) to (AIIc).

In the general formulas (AIIa) to (AIIc),
R ₁ c represents a hydrogen atom, a methyl group, a trifluoromethyl group, or a hydroxymethyl group.

R ₂ c to R ₄ c are in the general formula (VIIa) ~ _(VIIc), same meanings as R 2 c~R ₄ c.

  The resin (P1) may or may not contain a repeating unit having a hydroxyl group or a cyano group, but when it is contained, the content of the repeating unit having a hydroxyl group or a cyano group in the resin (P1) The total repeating unit is preferably 1 to 60 mol%, more preferably 3 to 50 mol%, still more preferably 5 to 40 mol%.

  Specific examples of the repeating unit having a hydroxyl group or a cyano group are given below, but the present invention is not limited thereto.

  The repeating unit (b ′) may be a repeating unit having a lactone structure as a polar group.

  The repeating unit having a lactone structure is more preferably a repeating unit represented by the following general formula (AII).

In general formula (AII),
Rb ₀ represents a hydrogen atom, a halogen atom or an optionally substituted alkyl group (preferably having 1 to 4 carbon atoms).

Preferable substituents that the alkyl group of Rb ₀ may have include a hydroxyl group and a halogen atom. Examples of the halogen atom for Rb ₀ include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom. Rb ₀ is preferably a hydrogen atom, a methyl group, a hydroxymethyl group or a trifluoromethyl group, and particularly preferably a hydrogen atom or a methyl group.

Ab represents a single bond, an alkylene group, a divalent linking group having a monocyclic or polycyclic cycloalkyl structure, an ether bond, an ester bond, a carbonyl group, or a divalent linking group obtained by combining these. Ab is preferably a single bond or a divalent linking group represented by —Ab ₁ —CO ₂ —.

Ab ₁ is a linear or branched alkylene group, a monocyclic or polycyclic cycloalkylene group, and preferably a methylene group, an ethylene group, a cyclohexylene group, an adamantylene group, or a norbornylene group.

  V represents a group having a lactone structure.

  As the group having a lactone structure, any group having a lactone structure can be used, but a 5- to 7-membered ring lactone structure is preferable, and a bicyclo structure or a spiro structure is added to the 5- to 7-membered ring lactone structure. Those in which other ring structures are condensed in the form to be formed are preferred. It is more preferable to have a repeating unit having a lactone structure represented by any of the following general formulas (LC1-1) to (LC1-17). The lactone structure may be directly bonded to the main chain. Preferred lactone structures are (LC1-1), (LC1-4), (LC1-5), (LC1-6), (LC1-8), (LC1-13), and (LC1-14).

The lactone structure portion may or may not have a substituent (Rb ₂ ). Preferred substituents (Rb ₂ ) include an alkyl group having 1 to 8 carbon atoms, a monovalent cycloalkyl group having 4 to 7 carbon atoms, an alkoxy group having 1 to 8 carbon atoms, and an alkoxycarbonyl group having 2 to 8 carbon atoms. , Carboxyl group, halogen atom, hydroxyl group, cyano group, acid-decomposable group and the like. More preferably, they are a C1-C4 alkyl group, a cyano group, and an acid-decomposable group. n ₂ represents an integer of 0-4. When n ₂ is 2 or more, a plurality of substituents (Rb ₂ ) may be the same or different, and a plurality of substituents (Rb ₂ ) may be bonded to form a ring. .

  The repeating unit having a lactone group 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.

  The resin (P1) may or may not contain a repeating unit having a lactone structure, but when it contains a repeating unit having a lactone structure, the content of the repeating unit having a lactone structure in the resin (P1) Is preferably in the range of 1 to 70 mol%, more preferably in the range of 3 to 65 mol%, and still more preferably in the range of 5 to 60 mol% with respect to all repeating units.

Specific examples of the repeating unit having a lactone structure in the resin (P1) are shown below, but the present invention is not limited thereto. In the formula, Rx represents H, CH ₃ , CH ₂ OH, or CF ₃ .

Moreover, as a sultone group which resin (P1) has, the following general formula (SL-1) and (SL-2) are preferable. Rb ₂ and n ₂ in the formula are synonymous with the above-described general formulas (LC1-1) to (LC1-17).

  As the repeating unit containing a sultone group that the resin (P1) has, a lactone group in the repeating unit having a lactone group described above is preferably substituted with a sultone group.

  In addition, it is also a particularly preferable aspect that the polar group that the repeating unit (b ′) may have is an acidic group. Preferred acidic groups include phenolic hydroxyl groups, carboxylic acid groups, sulfonic acid groups, fluorinated alcohol groups (eg hexafluoroisopropanol group), sulfonamide 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, A tris (alkylsulfonyl) methylene group is mentioned. Of these, the repeating unit (b) is more preferably a repeating unit having a carboxyl group. By containing the repeating unit having an acidic group, the resolution in the contact hole application is increased. The repeating unit having an acidic group includes a repeating unit in which an acidic group is directly bonded to the main chain of the resin, such as a repeating unit of acrylic acid or methacrylic acid, or an acidic group in the main chain of the resin through a linking group. It is preferable to use a polymerization initiator or a chain transfer agent having a repeating unit bonded to each other, or an acidic group, at the time of polymerization and introduce it at the end of the polymer chain. Particularly preferred are repeating units of acrylic acid or methacrylic acid.

  The acidic group that the repeating unit (b ′) may have may or may not contain an aromatic ring. When the repeating unit (b ′) has an acidic group, the content of the repeating unit having an acidic group is preferably 30 mol% or less, and 20 mol% or less with respect to all the repeating units in the resin (P1). It is more preferable that When resin (P1) contains the repeating unit which has an acidic group, content of the repeating unit which has an acidic group in resin (P1) is 1 mol% or more normally.

  Specific examples of the repeating unit having an acidic group are shown below, but the present invention is not limited thereto.

In specific examples, Rx represents H, CH ₃ , CH ₂ OH, or CF ₃ .

  The resin (P1) may have a repeating unit (c) having a plurality of aromatic rings represented by the following general formula (c1).

In general formula (c1),
R ₃ represents a hydrogen atom, an alkyl group, a halogen atom, a cyano group or a nitro group;
Y represents a single bond or a divalent linking group;
Z represents a single bond or a divalent linking group;
Ar represents an aromatic ring group;
p represents an integer of 1 or more.

  Regarding the repeating unit represented by the general formula (c1), the contents described in JP-A-2014-41328, paragraphs 0265 to 0279 can be incorporated, and these contents are incorporated in the present specification.

  The resin (P1) may or may not contain the repeating unit (c), but when it is contained, the content of the repeating unit (c) is 1 to 30 with respect to the total repeating unit of the resin (P1). It is preferably in the range of mol%, more preferably in the range of 1 to 20 mol%, and still more preferably in the range of 1 to 15 mol%. The repeating unit (c) contained in the resin (P1) may contain a combination of two or more types.

  The resin (P1) in the present invention may appropriately have a repeating unit other than the repeating units (a) to (c). As an example of such a repeating unit, it can further have a repeating unit that has an alicyclic hydrocarbon structure that does not have a polar group (for example, the above-mentioned acid group, hydroxyl group, and cyano group) and does not exhibit acid decomposability. . Thereby, the solubility of the resin can be appropriately adjusted during development using a developer containing an organic solvent. Examples of such a repeating unit include a repeating unit represented by the general formula (IV).

In general formula (IV), R ₅ represents a hydrocarbon group having at least one cyclic structure and having no polar group.

Ra represents a hydrogen atom, an alkyl group, or a —CH ₂ —O—Ra ₂ group. In the formula, Ra ₂ represents a hydrogen atom, an alkyl group, or an acyl group. Ra is preferably a hydrogen atom, a methyl group, a hydroxymethyl group or a trifluoromethyl group, particularly preferably a hydrogen atom or a methyl group.

The cyclic structure possessed by R ₅ includes a monocyclic hydrocarbon group and a polycyclic hydrocarbon group. Examples of the monocyclic hydrocarbon group include cycloalkenyl having 3 to 12 carbon atoms such as cyclopentyl group, cyclohexyl group, cycloheptyl group, cyclooctyl group and the like, and cycloalkyl groups having 3 to 12 carbon atoms and cyclohexenyl group. Groups. The preferred monocyclic hydrocarbon group is a monocyclic hydrocarbon group having 3 to 7 carbon atoms, more preferably a cyclopentyl group or a cyclohexyl group.

The polycyclic hydrocarbon group includes a ring assembly hydrocarbon group and a bridged cyclic hydrocarbon group, and examples of the ring assembly hydrocarbon group include a bicyclohexyl group and a perhydronaphthalenyl group. As the bridged cyclic hydrocarbon ring, for example, bicyclic such as pinane, bornane, norpinane, norbornane, bicyclooctane ring (bicyclo [2.2.2] octane ring, bicyclo [3.2.1] octane ring, etc.) Hydrocarbon rings and tricyclic hydrocarbon rings such as homobrendane, adamantane, tricyclo [5.2.1.0 ^2,6 ] decane, tricyclo [4.3.1.1 ^2,5 ] undecane ring, tetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] dodecane, and tetracyclic hydrocarbon rings such as perhydro-1,4-methano-5,8-methanonaphthalene ring. The bridged cyclic hydrocarbon ring includes a condensed cyclic hydrocarbon ring such as perhydronaphthalene (decalin), perhydroanthracene, perhydrophenanthrene, perhydroacenaphthene, perhydrofluorene, perhydroindene, perhydroindene. A condensed ring in which a plurality of 5- to 8-membered cycloalkane rings such as a phenalene ring are condensed is also included.

Preferred examples of the bridged cyclic hydrocarbon ring include a norbornyl group, an adamantyl group, a bicyclooctanyl group, a tricyclo [5.2.1.0 ^2,6 ] decanyl group, and the like. More preferable examples of the bridged cyclic hydrocarbon ring include a norbornyl group and an adamantyl group.

  These alicyclic hydrocarbon groups may have a substituent. Preferred examples of the substituent include a halogen atom, an alkyl group, a hydroxyl group substituted with a hydrogen atom, and an amino group substituted with a hydrogen atom. It is done. Preferred halogen atoms include bromine, chlorine and fluorine atoms, and preferred alkyl groups include methyl, ethyl, butyl and t-butyl groups. The alkyl group described above may further have a substituent, and examples of the substituent that may further include a halogen atom, an alkyl group, a hydroxyl group substituted with a hydrogen atom, and an amino group substituted with a hydrogen atom. The group can be mentioned.

  Examples of the substituent for the hydrogen atom include an alkyl group, a cycloalkyl group, an aralkyl group, a substituted methyl group, a substituted ethyl group, an alkoxycarbonyl group, and an aralkyloxycarbonyl group. Preferred alkyl groups include alkyl groups having 1 to 4 carbon atoms, preferred substituted methyl groups include methoxymethyl, methoxythiomethyl, benzyloxymethyl, t-butoxymethyl, 2-methoxyethoxymethyl groups, and preferred substituted ethyl groups. 1-ethoxyethyl, 1-methyl-1-methoxyethyl, preferred acyl groups include formyl, acetyl, propionyl, butyryl, isobutyryl, valeryl, pivaloyl groups, etc., aliphatic acyl groups having 1 to 6 carbon atoms, alkoxycarbonyl Examples of the group include an alkoxycarbonyl group having 1 to 4 carbon atoms.

  The resin (P1) has an alicyclic hydrocarbon structure having no polar group and may or may not contain a repeating unit that does not exhibit acid decomposability, but when it is contained, the content of this repeating unit is The content is preferably 1 to 20 mol%, more preferably 5 to 15 mol%, based on all repeating units in the resin (P1).

Specific examples of the repeating unit having an alicyclic hydrocarbon structure having no polar group and not exhibiting acid decomposability are shown below, but the present invention is not limited thereto. In the formula, Ra represents H, CH ₃ , CH ₂ OH, or CF ₃ .

  Further, the resin (P1) may contain the following monomer components in view of the effects such as improvement of Tg, improvement of dry edging resistance, the above-described internal filter of out-of-band light, and the like.

  Resin (P1) may contain the repeating unit represented by the following general formula (V) or the following general formula (VI).

Where
R ₆ and R ₇ are each independently a hydrogen atom, a hydroxy group, a linear, branched or cyclic alkyl group having 1 to 10 carbon atoms, an alkoxy group or an acyloxy group, a cyano group, a nitro group, an amino group, A halogen atom, an ester group (-OCOR or -COOR: R represents an alkyl group having 1 to 6 carbon atoms or a fluorinated alkyl group), or a carboxyl group.

n ₃ represents an integer of 0 to 6.
X ⁴ is a methylene group, an oxygen atom or a sulfur atom.

  Although the specific example of the repeating unit represented by general formula (V) or general formula (VI) is shown below, it is not limited to these.

  Resin (P1) may have a repeating unit having a cyclic carbonate structure.

  The repeating unit having a cyclic carbonate structure is preferably a repeating unit represented by the following general formula (A-1).

In General Formula (A-1), R _A ¹ represents a hydrogen atom or an alkyl group.

R _A ² each independently represents a substituent when n is 2 or more.

  A represents a single bond or a divalent linking group.

  Z represents an atomic group that forms a monocyclic or polycyclic structure together with a group represented by —O—C (═O) —O— in the formula.

  n represents an integer of 0 or more.

  Regarding the repeating unit represented by the general formula (A-1), the contents described in paragraphs 0293 to 0304 of JP 2014-41328 A can be used, and these contents are incorporated in the present specification. .

  In the resin (P1) used in the composition of the present invention, the content molar ratio of each repeating structural unit is the resist dry etching resistance, standard developer suitability, substrate adhesion, resist profile, and general resist requirements. It is appropriately set in order to adjust the resolution, heat resistance, sensitivity, etc., which are performance.

  Specific examples of the resin (P1) will be given below, but the present invention is not limited thereto.

  The form of the resin (P1) of the present invention may be any of random type, block type, comb type, and star type.

  Resin (P1) is compoundable by the radical, cation, or anion polymerization of the unsaturated monomer corresponding to each structure, for example. It is also possible to obtain the desired resin by conducting a polymer reaction after polymerization using an unsaturated monomer corresponding to the precursor of each structure.

  For example, as a general synthesis method, an unsaturated monomer and a polymerization initiator are dissolved in a solvent, and a batch polymerization method in which polymerization is performed by heating, a solution of an unsaturated monomer and a polymerization initiator in a heating solvent for 1 to 10 hours. The dropping polymerization method etc. which are dropped and added over are mentioned, and the dropping polymerization method is preferable.

  Examples of the solvent used for the polymerization include a solvent that can be used in preparing the actinic ray-sensitive or radiation-sensitive resin composition described below, and more preferably the composition of the present invention. Polymerization is preferably carried out using the same solvent as used in the above. Thereby, generation | occurrence | production of the particle at the time of a preservation | save 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 necessary, the polymerization may be performed in the presence of a chain transfer agent (for example, alkyl mercaptan).

The reaction concentration is 5 to 70% by mass, preferably 10 to 50% by mass. The reaction temperature is usually from 10 ° C to 150 ° C, preferably from 30 ° C to 120 ° C, more preferably from 40 ° C to 100 ° C.
The reaction time is usually 1 to 48 hours, preferably 1 to 24 hours, more preferably 1 to 12 hours.

  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 used for the precipitation or reprecipitation operation from the polymer solution (precipitation or reprecipitation solvent) may be any poor solvent for this polymer. Depending on the type of polymer, hydrocarbon, halogenated hydrocarbon, nitro 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).

  In addition, once the resin is precipitated and separated, 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 the resin solution A is dissolved again in the solvent. (Step c), and then, the resin solution A is brought into contact 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). This may be a method including precipitating a resin solid (step d) and separating the precipitated resin (step e).

  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 from 10 ° C to 150 ° C, preferably from 30 ° C to 120 ° C, more preferably from 60 ° C to 100 ° C.

  The molecular weight of the resin (P1) according to the present invention is not particularly limited, but the weight average molecular weight is preferably in the range of 1000 to 100,000, more preferably in the range of 1500 to 60000, and in the range of 2000 to 30000. It is particularly preferred. By setting the weight average molecular weight in the range of 1000 to 100,000, it is possible to prevent heat resistance and dry etching resistance from being deteriorated, and also to prevent developability from being deteriorated and the film forming property from being deteriorated due to increased viscosity. be able to. Here, the weight average molecular weight of the resin indicates a molecular weight in terms of polystyrene measured by GPC (Gel Permeation Chromatography) measurement (carrier: THF or N-methyl-2-pyrrolidone (NMP)).

  The dispersity (Mw / Mn) is preferably 1.00 to 5.00, more preferably 1.03 to 3.50, and still more preferably 1.05 to 2.50. The smaller the molecular weight distribution, the better the resolution and the resist shape, and the smoother the side wall of the resist pattern, the better the roughness.

Resin (P1) of this invention can be used individually by 1 type or in combination of 2 or more types. The content of the resin (P1) is preferably 20 to 99% by mass, more preferably 30 to 89% by mass, based on the total solid content in the actinic ray-sensitive or radiation-sensitive resin composition of the present invention. 40-79 mass% is especially preferable.
[2] Resin (B) which is different from resin (P1) and decomposes by the action of an acid to change the solubility in a developer.
The actinic ray-sensitive or radiation-sensitive resin composition of the present invention is different from the resin (P1) in that it decomposes by the action of an acid and changes its solubility in a developer (hereinafter also referred to as resin (B)). You may contain.

  The resin (B) is a resin having a structure in which a polar group is protected by a leaving group that is decomposed and eliminated by the action of an acid (hereinafter also referred to as “acid-decomposable group”).

  The resin (B) preferably has a repeating unit having an acid-decomposable group.

  Examples of the polar group include a carboxyl group, a phenolic hydroxyl group, an alcoholic hydroxyl group, a sulfonic acid group, and a thiol group.

Examples of the group capable of leaving by the action of an acid include —C (R ₃₆ ) (R ₃₇ ) (R ₃₈ ), —C (R ₃₆ ) (R ₃₇ ) (OR ₃₉ ), —C (═O) — _{O-C (R 36) (} R 37) (R 38), - C (R 01) (R 02) (OR 39), - C (R 01) (R 02) -C (= O) -O- C (R ₃₆ ) (R ₃₇ ) (R ₃₈ ) and the like can be mentioned.

In the formula, R _{36 to} R ₃₉ each independently represents an alkyl group, a cycloalkyl group, an aryl group, an aralkyl group, or an alkenyl group. R ₃₆ and R ₃₇ may be bonded to each other to form a ring. R _{01 to} R ₀₂ each independently represents a hydrogen atom, an alkyl group, a cycloalkyl group, an aryl group, an aralkyl group or an alkenyl group.

  The resin (B) can be synthesized according to a conventional method (for example, radical polymerization).

  The weight average molecular weight of the resin (B) is preferably 1,000 to 200,000, more preferably 2,000 to 20,000, and even more preferably 3,000 to 15 as a polystyrene-converted value by the GPC method. 1,000, particularly preferably 3,000 to 10,000. By setting the weight average molecular weight to 1,000 to 200,000, deterioration of heat resistance and dry etching resistance can be prevented, developability is deteriorated, and viscosity is increased, resulting in deterioration of film forming property. Can be prevented.

  The degree of dispersion (molecular weight distribution) is usually 1 to 3, preferably 1 to 2.6, more preferably 1 to 2, and particularly preferably 1.4 to 1.7. The smaller the molecular weight distribution, the better the resolution and the resist shape, and the smoother the side wall of the resist pattern, the better the roughness.

  Two or more types of resins (B) may be used in combination.

  The actinic ray-sensitive or radiation-sensitive resin composition of the present invention may or may not contain the resin (B). However, when it is contained, the amount of the resin (B) added is the actinic ray-sensitive or sensitive. It is 1-50 mass% normally with respect to the total solid of a radiation resin composition, Preferably it is 1-30 mass%, Most preferably, it is 1-15 mass%.

The resin (B) is described in paragraphs [0059] to [0169] of Japanese Patent Application Laid-Open No. 2010-217884, and described in paragraphs [0214] to [0594] of Japanese Patent Application No. 2011-2117048. Things.
[3] (B) Compound that generates acid upon irradiation with actinic ray or radiation The composition of the present invention comprises a compound that generates acid upon irradiation with actinic ray or radiation (hereinafter referred to as “acid generator” or “photoacid generation”). It is preferable to contain an agent.

  The acid generator is not particularly limited as long as it is a publicly known acid generator, but upon irradiation with actinic rays or radiation, at least any of organic acids such as sulfonic acid, bis (alkylsulfonyl) imide, and tris (alkylsulfonyl) methide. Compounds that generate such are preferred.

  The compound (B) that generates an acid upon irradiation with actinic rays or radiation may be in the form of a low molecular compound or may be incorporated in a part of the polymer. Further, the form of the low molecular compound and the form incorporated in a part of the polymer may be used in combination.

  When the compound (B) that generates an acid upon irradiation with actinic rays or radiation is in the form of a low molecular compound, the molecular weight is preferably 3000 or less, more preferably 2000 or less, and 1000 or less. Is more preferable.

  When the compound (B) that generates an acid upon irradiation with actinic rays or radiation is in the form of being incorporated in a part of the polymer, it may be incorporated in a part of the acid-decomposable resin described above. It may be incorporated in a resin different from the resin.

  More preferred examples include compounds represented by the following general formulas (ZI), (ZII), and (ZIII).

In the general formula (ZI),
R ₂₀₁ , R ₂₀₂ and R ₂₀₃ each independently represents an organic group.

The carbon number of the organic group as R ₂₀₁ , R ₂₀₂ and R ₂₀₃ is generally 1 to 30, preferably 1 to 20.

Two of R _{201 to} R ₂₀₃ may be bonded to form a ring structure, and the ring may contain an oxygen atom, a sulfur atom, an ester bond, an amide bond, or a carbonyl group. Examples of the group formed by combining two of R _{201 to} R ₂₀₃ include an alkylene group (eg, butylene group, pentylene group).

Z ⁻ represents a non-nucleophilic anion (an anion having an extremely low ability to cause a nucleophilic reaction).

  Non-nucleophilic anions include, for example, sulfonate anions (aliphatic sulfonate anions, aromatic sulfonate anions, camphor sulfonate anions, etc.), carboxylate anions (aliphatic carboxylate anions, aromatic carboxylate anions, aralkyls). Carboxylate anion, etc.), sulfonylimide anion, bis (alkylsulfonyl) imide anion, tris (alkylsulfonyl) methide anion and the like.

  The aliphatic moiety in the aliphatic sulfonate anion and the aliphatic carboxylate anion may be an alkyl group or a cycloalkyl group, preferably a linear or branched alkyl group having 1 to 30 carbon atoms and a carbon number. 3-30 cycloalkyl groups are mentioned.

  The aromatic group in the aromatic sulfonate anion and aromatic carboxylate 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 mentioned above may have a substituent. Specific examples thereof include nitro groups, halogen atoms such as fluorine atoms, carboxyl groups, hydroxyl groups, amino groups, cyano groups, alkoxy groups (preferably having 1 to 15 carbon atoms), cycloalkyl groups (preferably having 3 to 15 carbon atoms). ), An aryl group (preferably 6 to 14 carbon atoms), an alkoxycarbonyl group (preferably 2 to 7 carbon atoms), an acyl group (preferably 2 to 12 carbon atoms), an alkoxycarbonyloxy group (preferably 2 to 2 carbon atoms). 7), an alkylthio group (preferably 1 to 15 carbon atoms), an alkylsulfonyl group (preferably 1 to 15 carbon atoms), an alkyliminosulfonyl group (preferably 2 to 15 carbon atoms), an aryloxysulfonyl group (preferably carbon) Number 6-20), alkylaryloxysulfonyl group (preferably C7-20), cycloalkylary Examples thereof include an oxysulfonyl group (preferably having 10 to 20 carbon atoms), an 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.

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

  Examples of the sulfonylimide anion include saccharin anion.

  The alkyl group in the bis (alkylsulfonyl) imide anion and tris (alkylsulfonyl) methide anion is preferably an alkyl group having 1 to 5 carbon atoms. 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. A fluorine atom or an alkyl group substituted with a fluorine atom is preferred.

  The alkyl groups in the bis (alkylsulfonyl) imide anion may be bonded to each other to form a ring structure. This increases the acid strength.

Examples of other non-nucleophilic anions include fluorinated phosphorus (eg, PF ₆ ⁻ ), fluorinated boron (eg, BF ₄ ⁻ ), and fluorinated antimony (eg, SbF ₆ ⁻ ). .

  Examples of the non-nucleophilic anion include an aliphatic sulfonate anion in which at least 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 having a fluorine atom And a tris (alkylsulfonyl) methide anion in which the alkyl group is substituted with a fluorine atom. The non-nucleophilic anion is more preferably a perfluoroaliphatic sulfonate anion (more preferably 4 to 8 carbon atoms), a benzenesulfonate anion having a fluorine atom, still more preferably a nonafluorobutanesulfonate anion, or perfluorooctane. A sulfonate anion, a pentafluorobenzenesulfonate anion, and a 3,5-bis (trifluoromethyl) benzenesulfonate anion.

  From the viewpoint of acid strength, the pKa of the generated acid is preferably −1 or less in order to improve sensitivity.

  Moreover, as a non-nucleophilic anion, the anion represented with the following general formula (AN1) is also mentioned as a preferable aspect.

Where
Xf each independently represents a fluorine atom or an alkyl group substituted with at least one fluorine atom.

R ¹ and R ² each independently represent a hydrogen atom, a fluorine atom or an alkyl group, and when there are a plurality of R ¹ and R ² , they may be the same or different.

  L represents a divalent linking group, and when there are a plurality of L, L may be the same or different.

  A represents a cyclic organic group.

  x represents an integer of 1 to 20, y represents an integer of 0 to 10, and z represents an integer of 0 to 10.

  The general formula (AN1) will be described in more detail.

  The alkyl group in the alkyl group substituted with the fluorine atom of Xf preferably has 1 to 10 carbon atoms, more preferably 1 to 4 carbon atoms. The alkyl group substituted with a fluorine atom of Xf is preferably a perfluoroalkyl group.

Xf is preferably a fluorine atom or a perfluoroalkyl group having 1 to 4 carbon atoms. Specific examples of Xf include fluorine atom, CF ₃ , C ₂ F ₅ , C ₃ F ₇ , C ₄ F ₉ , CH ₂ CF ₃ , CH ₂ CH ₂ CF ₃ , CH ₂ C ₂ F ₅ , CH ₂ CH ₂ C ₂ F ₅ , CH ₂ C ₃ F ₇ , CH ₂ CH ₂ C ₃ F ₇ , CH ₂ C ₄ F ₉ , CH ₂ CH ₂ C ₄ F ₉ may be mentioned, among which a fluorine atom and CF ₃ are preferable. In particular, it is preferable that both Xf are fluorine atoms.

The alkyl group of R ¹ and R ² may have a substituent (preferably a fluorine atom), and preferably has 1 to 4 carbon atoms. More preferably, it is a C1-C4 perfluoroalkyl group. Specific examples of the alkyl group having a substituent for R ¹ and R ² include CF ₃ , C ₂ F ₅ , C ₃ F ₇ , C ₄ F ₉ , C ₅ F ₁₁ , C ₆ F ₁₃ , and C ₇ F _{15. , C 8 F 17, CH 2} CF 3, CH 2 CH 2 CF 3, CH 2 C 2 F 5, CH 2 CH 2 C 2 F 5, CH 2 C 3 F 7, CH 2 CH 2 C 3 F 7, CH ₂ C ₄ F ₉ and CH ₂ CH ₂ C ₄ F ₉ can be mentioned, among which CF ₃ is preferable.

R ¹ and R ² are preferably a fluorine atom or CF ₃ .

  x is preferably 1 to 10, and more preferably 1 to 5.

  y is preferably 0 to 4, and more preferably 0.

  z is preferably 0 to 5, and more preferably 0 to 3.

The divalent linking group of L is not particularly limited, and is —COO—, —OCO—, —CO—, —O—, —S—, —SO—, —SO ₂ —, an alkylene group, a cycloalkylene group, An alkenylene group or a linking group in which a plurality of these groups are linked can be exemplified, and a linking group having 12 or less carbon atoms is preferred. Among these, —COO—, —OCO—, —CO—, and —O— are preferable, and —COO— and —OCO— are more preferable.

  The cyclic organic group of A is not particularly limited as long as it has a cyclic structure, and is not limited to alicyclic groups, aryl groups, and heterocyclic groups (not only those having aromaticity but also aromaticity). And the like).

  The alicyclic group may be monocyclic or polycyclic, and may be a monocyclic cycloalkyl group such as a cyclopentyl group, a cyclohexyl group, or a cyclooctyl group, a norbornyl group, a tricyclodecanyl group, a tetracyclodecanyl group, or a tetracyclododecane group. A polycyclic cycloalkyl group such as a nyl group and an adamantyl group is preferred. Among them, an alicyclic group having a bulky structure having 7 or more carbon atoms such as a norbornyl group, a tricyclodecanyl group, a tetracyclodecanyl group, a tetracyclododecanyl group, an adamantyl group, or the like is present in the film in the post-exposure heating step. Diffusivity can be suppressed, which is preferable from the viewpoint of improving MEEF.

  Examples of the aryl group include a benzene ring, a naphthalene ring, a phenanthrene ring, and an anthracene ring.

  Examples of the heterocyclic group include those derived from a furan ring, a thiophene ring, a benzofuran ring, a benzothiophene ring, a dibenzofuran ring, a dibenzothiophene ring, and a pyridine ring. Of these, those derived from a furan ring, a thiophene ring and a pyridine ring are preferred.

  In addition, examples of the cyclic organic group include a lactone structure, and specific examples thereof are represented by the general formulas (LC1-1) to (LC1-17) that the above-described resin (P1) may have. Can be mentioned.

  The cyclic organic group may have a substituent, and examples of the substituent include an alkyl group (which may be linear, branched or cyclic, preferably 1 to 12 carbon atoms), cyclo Alkyl group (which may be monocyclic, polycyclic or spirocyclic, preferably 3 to 20 carbon atoms), aryl group (preferably 6 to 14 carbon atoms), hydroxy group, alkoxy group, ester group, amide Group, urethane group, ureido group, thioether group, sulfonamide group, sulfonic acid ester group and the like. The carbon constituting the cyclic organic group (carbon contributing to ring formation) may be a carbonyl carbon.

_Examples of the organic group for R ₂₀₁ , R _202, and R ₂₀₃ include an aryl group, an alkyl group, and a cycloalkyl group.

Of R ₂₀₁ , R ₂₀₂ and R ₂₀₃ , at least one is preferably an aryl group, more preferably all three are aryl groups. As the aryl group, in addition to a phenyl group, a naphthyl group, and the like, a heteroaryl group such as an indole residue and a pyrrole residue can be used. Preferred examples of the alkyl group and cycloalkyl group represented by R _{201 to} R ₂₀₃ include a linear or branched alkyl group having 1 to 10 carbon atoms and a cycloalkyl group having 3 to 10 carbon atoms. More preferable examples of the alkyl group include a methyl group, an ethyl group, an n-propyl group, an i-propyl group, and an n-butyl group. More preferable examples of the cycloalkyl group include a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, and a cycloheptyl group. These groups may further have a substituent. Examples of the substituent include halogen atoms such as nitro groups and fluorine atoms, carboxyl groups, hydroxyl groups, amino groups, cyano groups, alkoxy groups (preferably having 1 to 15 carbon atoms), cycloalkyl groups (preferably having 3 to 15 carbon atoms). ), An aryl group (preferably 6 to 14 carbon atoms), an alkoxycarbonyl group (preferably 2 to 7 carbon atoms), an acyl group (preferably 2 to 12 carbon atoms), an alkoxycarbonyloxy group (preferably 2 to 2 carbon atoms). 7) and the like, but are not limited thereto.

In _the case of forming the two members ring structure of R 201 _{to R 203,} it is preferably a structure represented by the following general formula (A1).

In general formula (A1),
R ^{1a to} R ^13a each independently represents a hydrogen atom or a substituent.

It is preferable that 1-3 are not a hydrogen atom among R ^{< 1a} > -R < ^13a >, and it is more preferable that any one of R ^{< 9a} > -R < ^13a > is not a hydrogen atom.

  Za is a single bond or a divalent linking group.

X ⁻ has the same meaning as Z ⁻ in formula (ZI).

Specific examples when R ^{1a to} R ^13a are not a hydrogen atom include a halogen atom, a linear, branched, cyclic alkyl group, alkenyl group, alkynyl group, aryl group, heterocyclic group, cyano group, nitro group, carboxyl group , Alkoxy group, aryloxy group, silyloxy group, heterocyclic oxy group, acyloxy group, carbamoyloxy group, alkoxycarbonyloxy group, aryloxycarbonyloxy group, amino group (including anilino group), ammonio group, acylamino group, amino Carbonylamino group, alkoxycarbonylamino group, aryloxycarbonylamino group, sulfamoylamino group, alkyl and arylsulfonylamino group, mercapto group, alkylthio group, arylthio group, heterocyclic thio group, sulfamoyl group, sulfo group, alkyl And arylsulfinyl groups, alkyl and arylsulfonyl groups, acyl groups, aryloxycarbonyl groups, alkoxycarbonyl groups, carbamoyl groups, aryl and heterocyclic azo groups, imide groups, phosphino groups, phosphinyl groups, phosphinyloxy groups, phosphini Ruamino group, phosphono group, silyl group, hydrazino group, ureido group, boronic acid group (—B (OH) ₂ ), phosphato group (—OPO (OH) ₂ ), sulfato group (—OSO ₃ H), other Known substituents are listed as examples.

As a case where R ^{1a to} R ^13a are not a hydrogen atom, a linear, branched or cyclic alkyl group substituted with a hydroxyl group is preferable.

Examples of the divalent linking group for Za include an alkylene group, an arylene group, a carbonyl group, a sulfonyl group, a carbonyloxy group, a carbonylamino group, a sulfonylamide group, an ether bond, a thioether bond, an amino group, a disulfide group, and — (CH _{2 ) n -CO -, - (CH} 2) n -SO 2 -, - CH = CH-, an aminocarbonylamino group, and an amino sulfonylamino group (n is an integer of 1 to 3).

In addition, as a preferable structure when at least one of R ₂₀₁ , R ₂₀₂ and R ₂₀₃ is not an aryl group, paragraphs 0047 and 0048 of JP-A No. 2004-233661, paragraphs 0040 to of JP-A No. 2003-35948 Compounds exemplified as formulas (I-1) to (I-70) in U.S. Patent Application Publication No. 2003 / 0224288A1, and formula (IA-1) in U.S. Patent Application Publication No. 2003 / 0077540A1. ) To (IA-54) and cation structures such as compounds exemplified as formulas (IB-1) to (IB-24).

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

The aryl group, alkyl group, and cycloalkyl group of R _{204 to} R ₂₀₇ are the same as the aryl group described as the aryl group, alkyl group, and cycloalkyl group of R _{201 to} R ₂₀₃ in the aforementioned compound (ZI).

The aryl group, alkyl group, and cycloalkyl group of R _{204 to} R ₂₀₇ may have a substituent. Even the substituent, an aryl group of R ₂₀₁ to R ₂₀₃ in the above compound (ZI), alkyl groups include those which may have a cycloalkyl group.

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

  Examples of the acid generator further include compounds represented by the following general formulas (ZIV), (ZV), and (ZVI).

In general formulas (ZIV) to (ZVI),
Ar ₃ and Ar ₄ each independently represents an aryl group.

R ₂₀₈ , R ₂₀₉ and R ₂₁₀ each independently represents an alkyl group, a cycloalkyl group or an aryl group.

  A represents an alkylene group, an alkenylene group or an arylene group.

Specific examples of the aryl group represented by Ar ₃ , Ar ₄ , R ₂₀₈ , R _209, and R ₂₁₀ are the same as the specific examples of the aryl group represented by R ₂₀₁ , R _202, and R ₂₀₃ in the general formula (ZI). Can be mentioned.

Specific examples of the alkyl group and cycloalkyl group represented by R ₂₀₈ , R ₂₀₉ and R ₂₁₀ include specific examples of the alkyl group and cycloalkyl group represented by R ₂₀₁ , R ₂₀₂ and R ₂₀₃ in the general formula (ZI), respectively. The same can be mentioned.

  The alkylene group of A is an alkylene group having 1 to 12 carbon atoms (for example, methylene group, ethylene group, propylene group, isopropylene group, butylene group, isobutylene group, etc.), and the alkenylene group of A is 2 carbon atoms. ˜12 alkenylene groups (for example, ethenylene group, propenylene group, butenylene group, etc.), and as the arylene group of A, C 6-10 arylene groups (for example, phenylene group, tolylene group, naphthylene group, etc.) Each can be mentioned.

  Specific examples of the acid generator include, in addition to those shown below, for example, paragraphs 0368 to 0377 of JP-A-2014-41328, paragraphs 0240 to 0262 of JP-A-2013-22868, US Patent Application Publication No. 2015 / And those described in paragraph 0339 of the specification of 004533.

  An acid generator can be used individually by 1 type or in combination of 2 or more types.

  The content of the acid generator is preferably 0.1 to 50% by mass, more preferably 0.5 to 45% by mass, and further preferably 1 to 40% by mass based on the total solid content of the composition. %.

[4] Compound that decomposes by the action of an acid to generate an acid The actinic ray-sensitive or radiation-sensitive resin composition of the present invention further includes one or two compounds that decompose by the action of an acid to generate an acid. More than one species may be included. The acid generated from the compound that decomposes by the action of the acid to generate an acid is preferably a sulfonic acid, a methide acid, or an imido acid.

  As a compound which decomposes | disassembles by the effect | action of the acid which can be used for this invention, and generate | occur | produces an acid, the thing as described in Paragraph 0379-0382 of Unexamined-Japanese-Patent No. 2014-41328 can be used, for example. Are incorporated herein.

  The compound which decomposes | disassembles by the effect | action of the acid mentioned above and generate | occur | produces an acid can be used individually by 1 type or in combination of 2 or more types.

In addition, it is preferable that content of the compound which decomposes | disassembles by the effect | action of an acid and generates an acid is 0.1-40 mass% on the basis of the total solid of actinic-ray-sensitive or radiation-sensitive resin composition. More preferably, it is 0.5-30 mass%, and it is still more preferable that it is 1.0-20 mass%.
[5] Resist solvent (coating solvent)
The solvent that can be used in preparing the composition is not particularly limited as long as it dissolves each component. For example, alkylene glycol monoalkyl ether carboxylate (propylene glycol monomethyl ether acetate (PGMEA; also known as 1-methoxy- 2-acetoxypropane)), alkylene glycol monoalkyl ether (propylene glycol monomethyl ether (PGME; also known as 1-methoxy-2-propanol)), lactate alkyl ester (ethyl lactate, methyl lactate, etc.), cyclic lactone (γ- Butyrolactone, preferably 4 to 10 carbon atoms, chain or cyclic ketone (2-heptanone, cyclohexanone, etc., preferably 4 to 10 carbon atoms), alkylene carbonate (ethylene carbonate, propylene) Such emission carbonate), alkyl carboxylic acids (alkyl acetate such as butyl acetate is preferred), an alkoxy alkyl acetates (ethyl ethoxypropionate), and the like, may be used those solvents alone or in combination.

  Other usable solvents include, for example, the solvents described in US Patent Application Publication No. 2008 / 0248425A1 after [0244].

  Of the above, alkylene glycol monoalkyl ether carboxylate and alkylene glycol monoalkyl ether are preferred.

  These solvents may be used alone or in combination of two or more. When mixing 2 or more types, it is preferable to mix the solvent which has a hydroxyl group, and the solvent which does not have a hydroxyl group. The mass ratio of the solvent having a hydroxyl group and the solvent having no hydroxyl group is from 1/99 to 99/1, preferably from 10/90 to 90/10, and more preferably from 20/80 to 60/40.

The solvent having a hydroxyl group is preferably an alkylene glycol monoalkyl ether, and the solvent having no hydroxyl group is preferably an alkylene glycol monoalkyl ether carboxylate.
[6] Basic compound The actinic ray-sensitive or radiation-sensitive resin composition according to the present invention may further contain a basic compound. The basic compound is preferably a compound having a stronger basicity than phenol. Moreover, this basic compound is preferably an organic basic compound, and more preferably a nitrogen-containing basic compound.

  Although the nitrogen-containing basic compound which can be used is not specifically limited, For example, the compound classified into the following (1)-(7) can be used.

  (1) Compound represented by general formula (BS-1)

In general formula (BS-1),
Each R independently represents a hydrogen atom or an organic group. However, at least one of the three Rs is an organic group. This organic group is a linear or branched alkyl group, a monocyclic or polycyclic cycloalkyl group, an aryl group, or an aralkyl group.

  Although carbon number of the alkyl group as R is not specifically limited, Usually, it is 1-20, Preferably it is 1-12.

  Although carbon number of the cycloalkyl group as R is not specifically limited, Usually, it is 3-20, Preferably it is 5-15.

  Although carbon number of the aryl group as R is not specifically limited, Usually, it is 6-20, Preferably it is 6-10. Specific examples include a phenyl group and a naphthyl group.

  Although carbon number of the aralkyl group as R is not specifically limited, Usually, it is 7-20, Preferably it is 7-11. Specific examples include a benzyl group.

  In the alkyl group, cycloalkyl group, aryl group and aralkyl group as R, a hydrogen atom may be substituted with a substituent. Examples of the substituent include an alkyl group, a cycloalkyl group, an aryl group, an aralkyl group, a hydroxy group, a carboxy group, an alkoxy group, an aryloxy group, an alkylcarbonyloxy group, and an alkyloxycarbonyl group.

  In the compound represented by the general formula (BS-1), it is preferable that at least two of R are organic groups.

  Specific examples of the compound represented by the general formula (BS-1) include tri-n-butylamine, tri-n-pentylamine, tri-n-octylamine, tri-n-decylamine, triisodecylamine, dicyclohexyl. Methylamine, tetradecylamine, pentadecylamine, hexadecylamine, octadecylamine, didecylamine, methyloctadecylamine, dimethylundecylamine, N, N-dimethyldodecylamine, methyldioctadecylamine, N, N-dibutylaniline, N , N-dihexylaniline, 2,6-diisopropylaniline, and 2,4,6-tri (t-butyl) aniline.

  Moreover, as a preferable basic compound represented by the general formula (BS-1), a compound in which at least one R is an alkyl group substituted with a hydroxy group can be given. Specific examples include triethanolamine and N, N-dihydroxyethylaniline.

In addition, the alkyl group as R may have an oxygen atom in the alkyl chain. That is, an oxyalkylene chain may be formed. As the oxyalkylene chain, —CH ₂ CH ₂ O— is preferable. Specifically, for example, tris (methoxyethoxyethyl) amine and compounds exemplified in the 60th and subsequent lines of column 3 of US6040112 can be mentioned.

  Among the basic compounds represented by the general formula (BS-1), examples of those having such a hydroxyl group or oxygen atom include the following.

(2) Compound having nitrogen-containing heterocyclic structure This nitrogen-containing heterocyclic ring may have aromaticity or may not have aromaticity. Moreover, you may have two or more nitrogen atoms. Furthermore, you may contain hetero atoms other than nitrogen. Specifically, for example, compounds having an imidazole structure (2-phenylbenzimidazole, 2,4,5-triphenylimidazole, etc.), compounds having a piperidine structure [N-hydroxyethylpiperidine and bis (1,2,2) , 6,6-pentamethyl-4-piperidyl) sebacate], compounds having a pyridine structure (such as 4-dimethylaminopyridine), and compounds having an antipyrine structure (such as antipyrine and hydroxyantipyrine).

  Examples of compounds having a preferred nitrogen-containing heterocyclic structure include, for example, guanidine, aminopyridine, aminoalkylpyridine, aminopyrrolidine, indazole, imidazole, pyrazole, pyrazine, pyrimidine, purine, imidazoline, pyrazoline, piperazine, aminomorpholine and Aminoalkylmorpholine is mentioned. These may further have a substituent.

  Preferred substituents include, for example, amino group, aminoalkyl group, alkylamino group, aminoaryl group, arylamino group, alkyl group, alkoxy group, acyl group, acyloxy group, aryl group, aryloxy group, nitro group, hydroxyl group And a cyano group.

  Particularly preferred basic compounds include, for example, imidazole, 2-methylimidazole, 4-methylimidazole, N-methylimidazole, 2-phenylimidazole, 4,5-diphenylimidazole, 2,4,5-triphenylimidazole, 2 -Aminopyridine, 3-aminopyridine, 4-aminopyridine, 2-dimethylaminopyridine, 4-dimethylaminopyridine, 2-diethylaminopyridine, 2- (aminomethyl) pyridine, 2-amino-3-methylpyridine, 2- Amino-4-methylpyridine, 2-amino5-methylpyridine, 2-amino-6-methylpyridine, 3-aminoethylpyridine, 4-aminoethylpyridine, 3-aminopyrrolidine, piperazine, N- (2-aminoethyl) ) Piperazine, N- (2-aminoethyl) ) Piperidine, 4-amino-2,2,6,6 tetramethylpiperidine, 4-piperidinopiperidine, 2-iminopiperidine, 1- (2-aminoethyl) pyrrolidine, pyrazole, 3-amino-5-methylpyrazole 5-amino-3-methyl-1-p-tolylpyrazole, pyrazine, 2- (aminomethyl) -5 methylpyrazine, pyrimidine, 2,4-diaminopyrimidine, 4,6-dihydroxypyrimidine, 2-pyrazoline, 3 -Pyrazolin, N-aminomorpholine and N- (2-aminoethyl) morpholine.

  A compound having two or more ring structures is also preferably used. Specific examples include 1,5-diazabicyclo [4.3.0] non-5-ene and 1,8-diazabicyclo [5.4.0] -undec-7-ene.

(3) Amine compound having a phenoxy group An amine compound having a phenoxy group is a compound having a phenoxy group at the terminal opposite to the N atom of the alkyl group contained in the amine compound. The phenoxy group is, for example, a substituent such as an alkyl group, an alkoxy group, a halogen atom, a cyano group, a nitro group, a carboxy group, a carboxylic acid ester group, a sulfonic acid ester group, an aryl group, an aralkyl group, an acyloxy group, and an aryloxy group. You may have.

This compound more preferably has at least one oxyalkylene chain between the phenoxy group and the nitrogen atom. The number of oxyalkylene chains in one molecule is preferably 3-9, more preferably 4-6. Among the oxyalkylene chains, —CH ₂ CH ₂ O— is particularly preferable.

  Specific examples include 2- [2- {2- (2,2-dimethoxy-phenoxyethoxy) ethyl} -bis- (2-methoxyethyl)]-amine, and paragraph [0066] of US2007 / 0224539A1. ] Compounds (C1-1) to (C3-3) exemplified in the above.

  The amine compound having a phenoxy group is prepared by reacting, for example, a primary or secondary amine having a phenoxy group with a haloalkyl ether, and adding an aqueous solution of a strong base such as sodium hydroxide, potassium hydroxide or tetraalkylammonium. And then extracted with an organic solvent such as ethyl acetate and chloroform. In addition, the amine compound having a phenoxy group reacts by heating a primary or secondary amine and a haloalkyl ether having a phenoxy group at the terminal, and a strong base such as sodium hydroxide, potassium hydroxide or tetraalkylammonium. It can also be obtained by adding an aqueous solution and then extracting with an organic solvent such as ethyl acetate and chloroform.

(4) Ammonium salt As the basic compound, an ammonium salt can also be used as appropriate.

  The cation of the ammonium salt is preferably a tetraalkylammonium cation substituted with an alkyl group having 1 to 18 carbon atoms, such as a tetramethylammonium cation, a tetraethylammonium cation, a tetra (n-butyl) ammonium cation, or a tetra (n-heptyl) ammonium. A cation, a tetra (n-octyl) ammonium cation, a dimethylhexadecylammonium cation, a benzyltrimethyl cation, and the like are more preferable, and a tetra (n-butyl) ammonium cation is most preferable.

  Examples of the anion of the ammonium salt include halide, sulfonate, borate, phosphate, hydroxide, and carboxylate. Of these, hydroxide or carboxylate is particularly preferred.

As the halide, 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 contained in the alkyl sulfonate may have a substituent. Examples of the substituent include a fluorine atom, a chlorine atom, a bromine atom, an alkoxy group, an acyl group, and an aryl group. 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 contained in the aryl sulfonate include a phenyl group, a naphthyl group, and an anthryl group. These aryl groups may have a substituent. As this substituent, a C1-C6 linear or branched alkyl group and a C3-C6 cycloalkyl group are preferable, for example. Specifically, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl, i-butyl, t-butyl, n-hexyl and cyclohexyl groups are preferable. 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 carboxylate may be an aliphatic carboxylate or an aromatic carboxylate, and examples thereof include acetate, lactate, birubate, trifluoroacetate, adamantane carboxylate, hydroxyadamantane carboxylate, benzoate, naphthoate, salicylate, phthalate, phenolate and the like. In particular, benzoate, naphthoate, phenolate and the like are preferable, and benzoate is most preferable.

  In this case, as the ammonium salt, tetra (n-butyl) ammonium benzoate, tetra (n-butyl) ammonium phenolate and the like are preferable.

  When the ammonium salt is a hydroxide, the ammonium salt is a tetraalkylammonium hydroxide having 1 to 8 carbon atoms (tetramethylammonium hydroxide, tetraethylammonium hydroxide, tetra- (n-butyl) ammonium hydroxide, etc. Tetraalkylammonium hydroxide is particularly preferred.

(5) A compound having a proton acceptor functional group and generating a compound which is decomposed by irradiation with actinic rays or radiation to decrease or disappear the proton acceptor property or change from proton acceptor property to acidity ( PA)
The composition according to the present invention has a proton acceptor functional group as a basic compound, and is decomposed by irradiation with actinic rays or radiation, resulting in a decrease, disappearance, or a proton acceptor property. It may further contain a compound that generates a compound that has been changed to acidity (hereinafter also referred to as compound (PA)).

  The proton acceptor functional group is a functional group having electrons or a group capable of electrostatically interacting with protons. For example, a functional group having a macrocyclic structure such as a cyclic polyether or a π-conjugated group. It means a functional group having a nitrogen atom with an unshared electron pair that does not contribute. The nitrogen atom having an unshared electron pair that does not contribute to π conjugation is, for example, a nitrogen atom having a partial structure represented by the following general formula.

  Examples of a preferable partial structure of the proton acceptor functional group include a crown ether, an azacrown ether, a primary to tertiary amine, a pyridine, an imidazole, and a pyrazine structure.

  The compound (PA) is decomposed by irradiation with an actinic ray or radiation to generate a compound in which the proton acceptor property is lowered, disappeared, or changed from proton acceptor property to acidity. Here, the decrease or disappearance of the proton acceptor property or the change from the proton acceptor property to the acid is a change in the proton acceptor property caused by the addition of a proton to the proton acceptor functional group. Specifically, when a proton adduct is formed from a compound having a proton acceptor functional group (PA) and a proton, the equilibrium constant in the chemical equilibrium is reduced.

Specific examples of the compound (PA) include the following compounds. Furthermore, as specific examples of the compound (PA), for example, those described in paragraphs 0421 to 0428 of JP2014-41328A and paragraphs 0108 to 0116 of JP2014-134686A can be used. The contents of which are incorporated herein.

  Moreover, in this invention, compounds (PA) other than the compound which generate | occur | produces the compound represented by general formula (PA-1) can also be selected suitably. For example, an ionic compound that has a proton acceptor moiety in the cation moiety may be used. More specifically, a compound represented by the following general formula (7) is exemplified.

  In the formula, A represents a sulfur atom or an iodine atom.

  m represents 1 or 2, and n represents 1 or 2. However, when A is a sulfur atom, m + n = 3, and when A is an iodine atom, m + n = 2.

  R represents an aryl group.

R _N represents an aryl group substituted with a proton acceptor functional group.

X ⁻ represents a counter anion.

Specific examples of X ⁻ include the same as Z ⁻ in the general formula (ZI) described above.

Specific examples of the aryl group of R and R _N is a phenyl group are preferably exemplified.

Specific examples of the proton acceptor functional group R _N are the same as those of the proton acceptor functional group described in the foregoing formula (PA-1).

  In the composition of the present invention, the compounding ratio of the compound (PA) in the whole composition is preferably 0.1 to 10% by mass, more preferably 1 to 8% by mass in the total solid content.

(6) Guanidine Compound The composition of the present invention may further contain a guanidine compound having a structure represented by the following formula.

  The guanidine compound exhibits strong basicity because the positive charge of the conjugate acid is dispersed and stabilized by three nitrogens.

  The basicity of the guanidine compound (A) of the present invention is preferably such that the pKa of the conjugate acid is 6.0 or more, and 7.0 to 20.0 is highly neutralizing reactivity with the acid, Since it is excellent in a roughness characteristic, it is preferable and it is more preferable that it is 8.0-16.0.

  Due to such strong basicity, it is possible to suppress acid diffusibility and contribute to the formation of an excellent pattern shape.

  Here, “pKa” means pKa in an aqueous solution, and is described in, for example, Chemical Handbook (II) (4th revised edition, 1993, edited by The Chemical Society of Japan, Maruzen Co., Ltd.). The lower the value, the higher the acid strength. Specifically, pKa in an aqueous solution can be actually measured by measuring an acid dissociation constant at 25 ° C. using an infinitely diluted aqueous solution, and using the software package 1 below, A value based on a database of constants and known literature values can also be obtained by calculation. The values of pKa described in this specification all indicate values obtained by calculation using this software package.

  Software package 1: Advanced Chemistry Development (ACD / Labs) Software V8.14 for Solaris (1994-2007 ACD / Labs).

  In the present invention, log P is a logarithmic value of n-octanol / water partition coefficient (P), and is an effective parameter that can characterize the hydrophilicity / hydrophobicity of a wide range of compounds. In general, the distribution coefficient is obtained by calculation without experimentation. In the present invention, CSChemDrawUltraVer. The value calculated by 8.0 software package (Crippen's fragmentation method) is shown.

  Moreover, it is preferable that logP of a guanidine compound (A) is 10 or less. By being below the above value, it can be contained uniformly in the resist film.

  The log P of the guanidine compound (A) in the present invention is preferably in the range of 2 to 10, more preferably in the range of 3 to 8, still more preferably in the range of 4 to 8.

  Moreover, it is preferable that the guanidine compound (A) in this invention does not have a nitrogen atom other than a guanidine structure.

  Hereinafter, although the specific example of a guanidine compound is shown, it is not limited to these.

(7) Low molecular weight compound having a nitrogen atom and having a group capable of leaving by the action of an acid The composition of the present invention comprises a low molecular weight compound having a nitrogen atom and having a group capable of leaving by the action of an acid (hereinafter referred to as “low molecular weight compound”). In this case, it is possible to contain “low molecular compound (D)” or “compound (D)”. The low molecular compound (D) preferably has basicity after the group capable of leaving by the action of an acid is eliminated.

  The group capable of leaving by the action of an acid is not particularly limited, but is preferably an acetal group, a carbonate group, a carbamate group, a tertiary ester group, a tertiary hydroxyl group, or a hemiaminal ether group, and a carbamate group or a hemiaminal ether group. It is particularly preferred.

  The molecular weight of the low molecular weight compound (D) having a group capable of leaving by the action of an acid is preferably 100 to 1000, more preferably 100 to 700, and particularly preferably 100 to 500.

  As the compound (D), an amine derivative having a group capable of leaving by the action of an acid on the nitrogen atom is preferable.

  Compound (D) may have a carbamate group having a protecting group on the nitrogen atom. The protecting group constituting the carbamate group can be represented by the following general formula (d-1).

In general formula (d-1),
R ′ each independently represents a hydrogen atom, a linear or branched alkyl group, a cycloalkyl group, an aryl group, an aralkyl group, or an alkoxyalkyl group. R ′ may be bonded to each other to form a ring.

  R ′ is preferably a linear or branched alkyl group, cycloalkyl group, or aryl group. More preferably, it is a linear or branched alkyl group or cycloalkyl group.

  The specific structure of such a group is shown below.

The compound (D) can also be constituted by arbitrarily combining the basic compound and the structure represented by the general formula (d-1).
The compound (D) particularly preferably has a structure represented by the following general formula (A).
The compound (D) may correspond to the above basic compound as long as it is a low molecular compound having a group capable of leaving by the action of an acid.

  In the general formula (A), Ra represents a hydrogen atom, an alkyl group, a cycloalkyl group, an aryl group or an aralkyl group. When n = 2, the two Ras may be the same or different, and the two Ras are bonded to each other to form a divalent heterocyclic hydrocarbon group (preferably having 20 or less carbon atoms) or a derivative thereof. May be formed.

  Rb independently represents a hydrogen atom, an alkyl group, a cycloalkyl group, an aryl group, an aralkyl group, or an alkoxyalkyl group. However, in -C (Rb) (Rb) (Rb), when one or more Rb is a hydrogen atom, at least one of the remaining Rb is a cyclopropyl group, a 1-alkoxyalkyl group or an aryl group.

At least two Rb may be bonded to form an alicyclic hydrocarbon group, an aromatic hydrocarbon group, a heterocyclic hydrocarbon group or a derivative thereof.
n represents an integer of 0 to 2, m represents an integer of 1 to 3, and n + m = 3.

  In general formula (A), the alkyl group, cycloalkyl group, aryl group and aralkyl group represented by Ra and Rb are functional groups such as hydroxyl group, cyano group, amino group, pyrrolidino group, piperidino group, morpholino group and oxo group. , An alkoxy group and a halogen atom may be substituted. The same applies to the alkoxyalkyl group represented by Rb.

An alkyl group, a cycloalkyl group, an aryl group, and an aralkyl group of Ra and / or Rb (these alkyl group, cycloalkyl group, aryl group, and aralkyl group are substituted with the above functional group, alkoxy group, or halogen atom); You may)
For example, a group derived from a linear or branched alkane such as methane, ethane, propane, butane, pentane, hexane, heptane, octane, nonane, decane, undecane, dodecane, etc., a group derived from these alkanes, for example, A group substituted with one or more cycloalkyl groups such as a cyclobutyl group, a cyclopentyl group, and a cyclohexyl group,
Groups derived from cycloalkanes such as cyclobutane, cyclopentane, cyclohexane, cycloheptane, cyclooctane, norbornane, adamantane, noradamantane, groups derived from these cycloalkanes, for example, methyl group, ethyl group, n-propyl group, a group substituted with one or more linear or branched alkyl groups such as i-propyl group, n-butyl group, 2-methylpropyl group, 1-methylpropyl group, t-butyl group and the like,
Groups derived from aromatic compounds such as benzene, naphthalene, anthracene, etc., and groups derived from these aromatic compounds are, for example, methyl group, ethyl group, n-propyl group, i-propyl group, n-butyl group, 2 A group substituted with one or more linear or branched alkyl groups such as -methylpropyl group, 1-methylpropyl group, t-butyl group, and the like;
Groups derived from heterocyclic compounds such as pyrrolidine, piperidine, morpholine, tetrahydrofuran, tetrahydropyran, indole, indoline, quinoline, perhydroquinoline, indazole, benzimidazole, and groups derived from these heterocyclic compounds are linear or branched A group substituted by one or more groups derived from an alkyl group or an aromatic compound or a group substituted by one or more, a group derived from a linear or branched alkane or a group derived from a cycloalkane, a phenyl group, a naphthyl group A group substituted with one or more groups derived from an aromatic compound such as anthracenyl group or the like, or the above-mentioned substituents are a hydroxyl group, a cyano group, an amino group, a pyrrolidino group, a piperidino group, a morpholino group, an oxo group And a group substituted with a functional group such as a group.

  Examples of the divalent heterocyclic hydrocarbon group (preferably having 1 to 20 carbon atoms) or a derivative thereof formed by bonding of Ra to each other include pyrrolidine, piperidine, morpholine, 1, 4, 5, 6-tetrahydropyrimidine, 1,2,3,4-tetrahydroquinoline, 1,2,3,6-tetrahydropyridine, homopiperazine, 4-azabenzimidazole, benzotriazole, 5-azabenzotriazole, 1H-1,2, , 3-triazole, 1,4,7-triazacyclononane, tetrazole, 7-azaindole, indazole, benzimidazole, imidazo [1,2-a] pyridine, (1S, 4S)-(+)-2, 5-diazabicyclo [2.2.1] heptane, 1,5,7-triazabicyclo [4.4.0] dec-5-ene, Groups derived from heterocyclic compounds such as dol, indoline, 1,2,3,4-tetrahydroquinoxaline, perhydroquinoline, 1,5,9-triazacyclododecane, groups derived from these heterocyclic compounds A group derived from a linear or branched alkane, a group derived from a cycloalkane, a group derived from an aromatic compound, a group derived from a heterocyclic compound, a hydroxyl group, a cyano group, an amino group, a pyrrolidino group, a piperidino And groups substituted with one or more functional groups such as a group, a morpholino group and an oxo group.

  The compound represented by the general formula (A) can be synthesized based on JP2007-298869A, JP2009-199021A, and the like.

  In the present invention, the low molecular compound (D) can be used singly or in combination of two or more.

  As specific examples of the particularly preferable compound (D) in the present invention, for example, those described in paragraphs 0468 to 0470 of JP-A-2014-41328 can be used, and the contents thereof are incorporated herein. .

(8) Ionic compound represented by general formula (I) The actinic ray-sensitive or radiation-sensitive resin composition according to the present invention may contain an ionic compound represented by the following general formula (I). Good.

In general formula (I),
A ⁻ represents an organic acid anion, L represents a single bond or a divalent linking group, X ⁺ represents a nitrogen cation or a sulfur cation, and Rx each independently represents an alkyl group or an aryl group. . A plurality of Rx may be bonded to each other to form a ring, and the formed ring may have a nitrogen atom, an oxygen atom or a sulfur atom as a ring member.

n2 represents 3 when X ⁺ is a nitrogen cation, and represents 2 when X ⁺ is a sulfur cation.

  About the ionic compound represented by general formula (I), the content of Paragraph 0167-0177 of Unexamined-Japanese-Patent No. 2014-1992273 can be used, for example, These content is integrated in this specification. .

  The composition of the present invention may or may not contain the low molecular compound (D), but when it is contained, the content of the compound (D) is the total solid of the composition combined with the basic compound described above. Based on the minutes, it is usually 0.001 to 20% by mass, preferably 0.001 to 10% by mass, and more preferably 0.01 to 5% by mass.

  When the composition of the present invention contains an acid generator, the ratio of the acid generator and the compound (D) used in the composition is: acid generator / [compound (D) + the following basic compound] (mole 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 acid generator / [compound (D) + basic compound] (molar ratio) is more preferably 5.0 to 200, and still more preferably 7.0 to 150.

  Other examples that can be used in the composition according to the present invention include compounds synthesized in Examples of JP-A No. 2002-363146, and compounds described in paragraph 0108 of JP-A No. 2007-298869. It is done.

  A photosensitive basic compound may be used as the basic compound. As the photosensitive basic compound, for example, JP-T-2003-524799 and J. Org. Photopolym. Sci & Tech. Vol. 8, P.I. 543-553 (1995) etc. can be used.

  The molecular weight of the basic compound is usually 100-1500, preferably 150-1300, and more preferably 200-1000.

  These basic compounds may be used individually by 1 type, and may be used in combination of 2 or more types.

  When the composition according to the present invention contains a basic compound, the content is preferably 0.01 to 8.0% by mass based on the total solid content of the composition, More preferably, it is 5.0 mass%, and it is especially preferable that it is 0.2-4.0 mass%.

The molar ratio of the basic compound to the photoacid generator is preferably 0.01 to 10, more preferably 0.05 to 5, and still more preferably 0.1 to 3. If this molar ratio is excessively increased, sensitivity and / or resolution may be reduced. If this molar ratio is excessively small, there is a possibility that pattern thinning occurs between exposure and heating (post-bake). More preferably, it is 0.05-5, More preferably, it is 0.1-3. The photoacid generator at the molar ratio is based on the total amount of the repeating unit (B) of the resin and the photoacid generator that the resin may further contain.
[7] Hydrophobic resin (HR)
The actinic ray-sensitive or radiation-sensitive resin composition of the present invention may have a hydrophobic resin (HR) separately from the resin (P1).

  Since the hydrophobic resin (HR) is unevenly distributed on the film surface, the hydrophobic resin (HR) preferably contains a group having a fluorine atom, a group having a silicon atom, or a hydrocarbon group having 5 or more carbon atoms. These groups may be present in the main chain of the resin or may be substituted on the side chain. Specific examples of the hydrophobic resin (HR) are shown below.

In addition, as the hydrophobic resin, those described in JP 2011-248019 A, JP 2010-175859 A, and JP 2012-032544 A can also be preferably used.
[8] Surfactant The composition according to the present invention may further contain a surfactant. By containing a surfactant, when an exposure light source having a wavelength of 250 nm or less, particularly 220 nm or less, is used, it is possible to form a pattern with less adhesion and development defects with good sensitivity and resolution. Become.

  As the surfactant, it is particularly preferable to use a fluorine-based and / or silicon-based surfactant.

  Examples of the fluorine-based and / or silicon-based surfactant include surfactants described in [0276] of US Patent Application Publication No. 2008/0248425. Also, F-top EF301 or EF303 (manufactured by Shin-Akita Kasei Co., Ltd.); Florard FC430, 431 or 4430 (manufactured by Sumitomo 3M Co., Ltd.); Megafac F171, F173, F176, F189, F113, F110, F177, F120 or R08 (manufactured by DIC Corporation); Surflon S-382, SC101, 102, 103, 104, 105 or 106 (manufactured by Asahi Glass Co., Ltd.); Troisol S-366 (manufactured by Troy Chemical Co., Ltd.); GF-300 or GF-150 (manufactured by Toa Gosei Chemical Co., Ltd.), Surflon S-393 (manufactured by Seimi Chemical Co., Ltd.); EFtop EF121, EF122A, EF122B, RF122C, EF125M, EF135M, EF351, EF352, EF801, EF802 or EF601 ( ( PF636, PF656, PF6320 or PF6520 (OMNOVA); or FTX-204G, 208G, 218G, 230G, 204D, 208D, 212D, 218D or 222D (manufactured by Neos) Good. Polysiloxane polymer KP-341 (manufactured by Shin-Etsu Chemical Co., Ltd.) can also be used as a silicon-based surfactant.

  In addition to known surfactants as described above, the surfactant is a fluoroaliphatic compound produced by a telomerization method (also referred to as a telomer method) or an oligomerization method (also referred to as an oligomer method). You may synthesize. Specifically, a polymer having a fluoroaliphatic group derived from this fluoroaliphatic compound may be used as a surfactant. This fluoroaliphatic compound can be synthesized, for example, by the method described in JP-A-2002-90991.

  The polymer having a fluoroaliphatic group is preferably a copolymer of a monomer having a fluoroaliphatic group and (poly (oxyalkylene)) acrylate or methacrylate and / or (poly (oxyalkylene)) methacrylate. Even if it distributes, block copolymerization may be sufficient.

  Examples of the poly (oxyalkylene) group include a poly (oxyethylene) group, a poly (oxypropylene) group, and a poly (oxybutylene) group. In addition, units having different chain length alkylene in the same chain, such as poly (block connection body of oxyethylene, oxypropylene, and oxyethylene) and poly (block connection body of oxyethylene and oxypropylene) Also good.

  Further, a copolymer of a monomer having a fluoroaliphatic group and (poly (oxyalkylene)) acrylate or methacrylate has a monomer having two or more different fluoroaliphatic groups and two or more different (poly (oxyalkylene). )) It may be a ternary or higher copolymer obtained by copolymerizing acrylate or methacrylate simultaneously.

Examples of commercially available surfactants include Megafac F178, F-470, F-473, F-475, F-476, and F-472 (manufactured by DIC Corporation). 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 ₆ F ₁₃ group and (poly (oxyethylene)) acrylate or methacrylate And a copolymer of (poly (oxypropylene)) acrylate or methacrylate, a copolymer of an acrylate or methacrylate having a C ₈ F ₁₇ group and (poly (oxyalkylene)) acrylate or methacrylate, and C ₈ F ₁₇ Of acrylate or methacrylate having a group with (poly (oxyethylene)) acrylate or methacrylate and (poly (oxypropylene)) acrylate or methacrylate Coalescence, and the like.

  Further, surfactants other than fluorine-based and / or silicon-based surfactants described in [0280] of US Patent Application Publication No. 2008/0248425 may be used.

  One of these surfactants may be used alone, or two or more thereof may be used in combination.

When the composition according to the present invention contains a surfactant, the content is preferably 0 to 2% by mass, more preferably 0.0001 to 2% by mass, based on the total solid content of the composition. More preferably, it is 0.0005-1 mass%.
[9] Other additives In addition to the components described above, the composition of the present invention has a molecular weight of 3000 or less as described in carboxylic acid, carboxylic acid onium salt, Proceeding of SPIE, 2724, 355 (1996), etc. A blocking compound, a dye, a plasticizer, a photosensitizer, a light absorber, an antioxidant, and the like can be appropriately contained.

  In particular, carboxylic acid is preferably used for improving the performance. As the carboxylic acid, aromatic carboxylic acids such as benzoic acid and naphthoic acid are preferable.

  The content of the carboxylic acid is preferably 0.01 to 10% by mass, more preferably 0.01 to 5% by mass, and still more preferably 0.01 to 3% by mass in the total solid content concentration of the composition.

  The actinic ray-sensitive or radiation-sensitive resin composition in the present invention is preferably used at a thickness of 10 to 250 nm, more preferably at a thickness of 20 to 200 nm, from the viewpoint of improving resolution. More preferably, it is preferably used at 30 to 100 nm. Such a film thickness can be obtained by setting the solid content concentration in the composition to an appropriate range to give an appropriate viscosity and improving the coating property and film forming property.

  The solid content concentration of the actinic ray-sensitive or radiation-sensitive resin composition in the present invention is usually 1.0 to 10% by mass, preferably 2.0 to 5.7% by mass, and more preferably 2.0. It is -5.3 mass%. By setting the solid content concentration within the above range, the resist solution can be uniformly applied on the substrate, and further, a resist pattern having excellent line width roughness can be formed. The reason for this is not clear, but perhaps the solid content concentration is 10% by mass or less, preferably 5.7% by mass or less, which suppresses aggregation of the material in the resist solution, particularly the photoacid generator. As a result, it is considered that a uniform resist film was formed.

  The solid content concentration is a weight percentage of the weight of other resist components excluding the solvent with respect to the total weight of the actinic ray-sensitive or radiation-sensitive resin composition.

In the actinic ray-sensitive or radiation-sensitive resin composition of the present invention, the above components are dissolved in a predetermined organic solvent, preferably the above mixed solvent, filtered, and then applied onto a predetermined support (substrate). Use. The pore size of the filter used for filter filtration is preferably 0.1 μm or less, more preferably 0.05 μm or less, and still more preferably 0.03 μm or less made of polytetrafluoroethylene, polyethylene, or nylon. In filter filtration, for example, as in JP-A-2002-62667, circulation filtration may be performed, or filtration may be performed by connecting a plurality of types of filters in series or in parallel. The composition may be filtered multiple times. Furthermore, you may perform a deaeration process etc. with respect to a composition before and behind filter filtration.
[Pattern formation method]
Next, the pattern forming method of the present invention will be described.
As described above, the pattern forming method of the present invention includes:
Forming a film using an actinic ray-sensitive or radiation-sensitive resin composition;
Exposing the film,
The film after exposure is developed using a developer to form a positive pattern in this order.

  According to the pattern forming method of the present invention described above, high resolution, high dissolution contrast, and high dry etching performance are simultaneously satisfied in an ultrafine region (for example, a region having a line width or space width on the order of several tens of nm). A pattern forming method, an actinic ray-sensitive or radiation-sensitive resin composition, an actinic ray-sensitive or radiation-sensitive film, a method for producing an electronic device using these, and an electronic device can be provided. The reason is not clear, but is estimated as follows.

  First, since the actinic ray-sensitive or radiation-sensitive resin composition used in the pattern forming method of the present invention contains the resin (P1) having a repeating unit represented by the general formula (1), the above sensitivity It is considered that the adhesion between the actinic ray-sensitive or radiation-sensitive film formed from the actinic ray-sensitive or radiation-sensitive resin composition and the substrate is improved.

  Thereby, when forming a line and space pattern, the fall of a pattern is suppressed and it is thought that a resolution improves as a result.

  Moreover, since the repeating unit represented by the general formula (1) has an aromatic ring group, the actinic ray-sensitive or radiation-sensitive resin composition containing the resin (P1) having the repeating unit is used. It is considered that the strength of the formed actinic ray-sensitive or radiation-sensitive film is improved and dry etching resistance is improved.

  Furthermore, when the resin (P1) contains the repeating unit represented by the general formula (1), the reactivity of the resin (P1) with respect to the acid is improved, and the polarity change accompanying the decomposition of the resin (P1) with the acid is increased. It is thought to grow.

  Thereby, it is considered that the dissolution contrast between the exposed portion and the unexposed portion with respect to the developer is improved, and the resolving power at the time of forming the line and space pattern is improved.

The above effect is considered to be particularly remarkable when a fine pattern is formed by electron beam or extreme ultraviolet exposure. (1) Film formation The actinic ray-sensitive or radiation-sensitive film of the present invention is a film formed from the actinic ray-sensitive or radiation-sensitive resin composition described above.

  More specifically, the formation of the actinic ray-sensitive or radiation-sensitive film is performed by dissolving the above-described components of the actinic ray-sensitive or radiation-sensitive resin composition in a solvent and, if necessary, filtering through a filter. It can be performed by applying to a support (substrate). The filter is preferably made of polytetrafluoroethylene, polyethylene, or nylon having a pore size of 0.5 μm or less, more preferably 0.2 μm or less, and still more preferably 0.1 μm or less.

  The composition is applied by a suitable coating method such as a spin coater on a substrate (for example, silicon, silicon dioxide coating) used for manufacturing an integrated circuit device. Thereafter, it is dried to form a photosensitive film. Heating (pre-baking) is preferably performed in the drying stage.

  Although there is no restriction | limiting in particular in a film thickness, Preferably it adjusts to the range of 10-500 nm, More preferably, it is the range of 10-200 nm, More preferably, it is adjusted to the range of 10-100 nm. When the actinic ray-sensitive or radiation-sensitive resin composition is applied by a spinner, the rotation speed is usually 500 to 3000 rpm, preferably 800 to 2000 rpm, more preferably 1000 to 1500 rpm.

  The heating (pre-baking) temperature is preferably 60 to 200 ° C, more preferably 80 to 150 ° C, and still more preferably 90 to 140 ° C.

  The time for heating (pre-baking) is not particularly limited, but is preferably 30 to 300 seconds, more preferably 30 to 180 seconds, and still more preferably 30 to 90 seconds.

  Heating can be performed by means provided in a normal exposure / developing machine, and may be performed using a hot plate or the like.

If necessary, a commercially available inorganic or organic antireflection film can be used. Further, an antireflection film can be applied to the lower layer of the actinic ray-sensitive or radiation-sensitive resin composition. 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. Further, as organic antireflection films, commercially available organic materials such as DUV30 series actinic ray-sensitive or radiation-sensitive films manufactured by Brewer Science, DUV-40 series, AR-2, AR-3, AR-5 manufactured by Shipley, etc. An antireflection film can also be used. (2) Exposure Exposure is performed with actinic rays or radiation. Examples of the actinic ray or radiation include infrared light, visible light, ultraviolet light, far ultraviolet light, X-rays, extreme ultraviolet light (EUV light), and electron beams. As these actinic rays or radiation, for example, those having a wavelength of 250 nm or less, particularly 220 nm or less are more preferable. Examples of such actinic rays or radiation include KrF excimer laser (248 nm), ArF excimer laser (193 nm), F ₂ excimer laser (157 nm), X-rays, extreme ultraviolet rays (EUV light), and electron beams. Preferable actinic rays or radiations include, for example, KrF excimer laser, electron beam, X-ray and EUV light. More preferred are electron beam, X-ray and EUV light, and still more preferred are electron beam and EUV light. (3) Baking It is preferable to perform baking (heating) after exposure and before development.

  The heating temperature is preferably 60 to 150 ° C, more preferably 80 to 150 ° C, and still more preferably 90 to 140 ° C.

  The heating time is not particularly limited, but is preferably 30 to 300 seconds, more preferably 30 to 180 seconds, and still more preferably 30 to 90 seconds.

  Heating can be performed by means provided in a normal exposure / developing machine, and may be performed using a hot plate or the like.

The reaction of the exposed part is promoted by baking, and the sensitivity and pattern profile are improved. It is also preferable to include a heating step (Post Bake) after the rinsing step. The heating temperature and heating time are as described above. The developing solution and the rinsing solution remaining between the patterns and inside the patterns are removed by baking.
(4) Development and Developer The developer used in the step of developing the actinic ray sensitivity or radiation sensitivity formed using the composition of the present invention is not particularly limited. For example, an alkali developer is used. I can do it.

Examples of the alkaline developer include inorganic alkalis such as sodium hydroxide, potassium hydroxide, sodium carbonate, sodium silicate, sodium metasilicate, and aqueous ammonia, primary amines such as ethylamine and n-propylamine, diethylamine, Secondary amines such as di-n-butylamine, tertiary amines such as triethylamine and methyldiethylamine, alcohol amines such as dimethylethanolamine and triethanolamine, tetramethylammonium hydroxide, tetraethylammonium hydroxide, tetrapropylammonium Hydroxide, tetrabutylammonium hydroxide, tetrapentylammonium hydroxide, tetrahexylammonium hydroxide, tetraoctylammonium hydroxide, ethyl Tetraalkylammonium hydroxide such as methylammonium hydroxide, butyltrimethylammonium hydroxide, methyltriamylammonium hydroxide, dibutyldipentylammonium hydroxide, trimethylphenylammonium hydroxide, trimethylbenzylammonium hydroxide, triethylbenzylammonium hydroxide, etc. Alkaline aqueous solutions such as quaternary ammonium salts, cyclic amines such as pyrrole and piperidine can be used. Furthermore, an appropriate amount of alcohol or surfactant may be added to the alkaline aqueous solution. The alkali concentration of the alkali developer is usually from 0.1 to 20% by mass. The pH of the alkali developer is usually from 10.0 to 15.0. The alkali concentration and pH of the alkali developer can be appropriately adjusted and used. The alkali developer may be used after adding a surfactant or an organic solvent.
-Surfactant A proper quantity of surfactant can be contained in a developing solution as needed.

  As the surfactant, the same surfactants as those used in the actinic ray-sensitive or radiation-sensitive resin composition described above can be used.

The amount of the surfactant used is usually 0.001 to 5% by mass, preferably 0.005 to 2% by mass, and more preferably 0.01 to 0.5% by mass with respect to the total amount of the developer.
-Basic compound The developer may contain a basic compound. Specific examples and preferred examples of the basic compound that can be contained in the developer used in the present invention are the same as those in the basic compound that can be contained in the actinic ray-sensitive or radiation-sensitive resin composition described above.
・ Development method As a development method, for example, the substrate is immersed in a tank filled with a developer for a certain period of time (dip method), and the developer is developed on the surface of the substrate by surface tension and kept stationary for a certain period of time. Method (paddle method), Method of spraying developer on the substrate surface (spray method), Method of continuously discharging developer while scanning the developer discharge nozzle at a constant speed on a substrate rotating at a constant speed (dynamic Dispensing method) can be applied.
Moreover, you may implement the process of stopping image development, after the process of developing, substituting with another solvent.

  The development time is not particularly limited as long as the resin in the unexposed area is sufficiently dissolved, and is usually 10 seconds to 300 seconds. Preferably, it is 20 seconds to 120 seconds.

The temperature of the developer is preferably from 0 ° C to 50 ° C, more preferably from 15 ° C to 35 ° C. (5) Rinse It is preferable that the pattern formation method of this invention includes a rinse process after a image development process.

  As a rinsing solution in the rinsing treatment performed after alkali development, pure water can be used, and an appropriate amount of a surfactant can be added.

As the surfactant, the same surfactant as that used in the actinic ray-sensitive or radiation-sensitive resin composition described above can be used, and the amount used is usually 0 with respect to the total amount of the rinsing liquid. 0.001 to 5 mass%, preferably 0.005 to 2 mass%, more preferably 0.01 to 0.5 mass%.
-Rinsing method In the rinsing step, the developed wafer is cleaned using the rinsing liquid.

  The method of the cleaning process is not particularly limited. For example, a method of continuously discharging the rinse liquid onto the substrate rotating at a constant speed (rotary discharge method), or immersing the substrate in a tank filled with the rinse liquid for a certain period of time. A method (dip method), a method of spraying a rinsing liquid on the substrate surface (spray method), and the like can be applied. Among these, a cleaning process is performed by a rotary discharge method, and after cleaning, the substrate is rotated at a speed of 2000 rpm to 4000 rpm. It is preferable to rotate and remove the rinse liquid from the substrate.

  The rinsing time is not particularly limited, but is usually 10 seconds to 300 seconds. It is preferably 10 seconds to 180 seconds, and most preferably 20 seconds to 120 seconds.

  The temperature of the rinse liquid is preferably 0 ° C. to 50 ° C., more preferably 15 ° C. to 35 ° C.

  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.

  Furthermore, after the development processing, the rinsing processing or the processing with the supercritical fluid, a heat processing can be performed in order to remove the solvent remaining in the pattern. The heating temperature is not particularly limited as long as a good resist pattern can be obtained, and is usually 40 ° C to 160 ° C. The heating temperature is preferably 50 ° C. or higher and 150 ° C. or lower, and most preferably 50 ° C. or higher and 110 ° C. or lower. The heating time is not particularly limited as long as a good resist pattern is obtained, but is usually 15 seconds to 300 seconds, and preferably 15 to 180 seconds.

On the other hand, at the time of EB exposure or EUV exposure, the actinic ray sensitivity or sensation of the present invention is used for the purpose of suppressing outgas, the purpose of suppressing blob defects, the deterioration of collapse due to improved reverse taper shape, and the deterioration of LWR due to surface roughness. A topcoat layer may be formed on the actinic ray-sensitive or radiation-sensitive film formed from the radiation-sensitive resin composition. Hereinafter, the topcoat composition used for forming the topcoat layer will be described.
In the top coat composition of the present invention, the solvent is preferably water or an organic solvent. More preferred is water or an alcohol solvent.
When the solvent is an organic solvent, it is preferably a solvent that does not dissolve the actinic ray-sensitive or radiation-sensitive film. As the solvent that can be used, an alcohol solvent, a fluorine solvent, or a hydrocarbon solvent is preferably used, and a non-fluorine alcohol solvent is more preferably used. The alcohol solvent is preferably a primary alcohol from the viewpoint of applicability, more preferably a primary alcohol having 4 to 8 carbon atoms. As the primary alcohol having 4 to 8 carbon atoms, linear, branched, and cyclic alcohols can be used, and linear and branched alcohols are preferable. Specific examples include 1-butanol, 1-hexanol, 1-pentanol, and 3-methyl-1-butanol.

  When the solvent of the topcoat composition in the present invention is water, an alcohol solvent or the like, it is preferable to contain a water-soluble resin. By containing a water-soluble resin, it is considered that the uniformity of solubility in a developer can be further improved. Preferred water-soluble resins include polyacrylic acid, polymethacrylic acid, polyhydroxystyrene, polyvinyl pyrrolidone, polyvinyl alcohol, polyvinyl ether, polyvinyl acetal, polyacrylimide, polyethylene glycol, polyethylene oxide, polyethyleneimine, polyester polyol and polyether polyol. , Polysaccharides, and the like. Particularly preferred are polyacrylic acid, polymethacrylic acid, polyhydroxystyrene, polyvinylpyrrolidone, and polyvinyl alcohol. The water-soluble resin is not limited to a homopolymer, and may be a copolymer. For example, it may be a copolymer having monomers corresponding to the repeating units of the homopolymers listed above and other monomer units. Specifically, acrylic acid-methacrylic acid copolymer, acrylic acid-hydroxystyrene copolymer and the like can be used in the present invention.

  Further, as the resin for the top coat composition, resins having an acidic group described in JP-A-2009-134177 and JP-A-2009-91798 can be preferably used.

  The weight average molecular weight of the water-soluble resin is not particularly limited, but is preferably from 2,000 to 1,000,000, more preferably from 5,000 to 500,000, particularly preferably from 10,000 to 100,000. Here, the weight average molecular weight of the resin indicates a molecular weight in terms of polystyrene measured by GPC (carrier: THF or N-methyl-2-pyrrolidone (NMP)).

  Although there is no restriction | limiting in particular in pH of a topcoat composition, Preferably it is 0-10, More preferably, it is 0-8, Most preferably, it is 1-7.

When the solvent of the topcoat composition is an organic solvent, the topcoat composition contains a hydrophobic resin such as the hydrophobic resin (HR) described above in the actinic ray-sensitive or radiation-sensitive resin composition section. You may do it. As the hydrophobic resin, it is also preferable to use a hydrophobic resin described in JP-A-2008-209889.
The concentration of the resin in the top coat composition is preferably 0.1 to 10% by mass, more preferably 0.2 to 5% by mass, and particularly preferably 0.3 to 3% by mass.

  The topcoat material may contain components other than the resin, but the ratio of the resin to the solid content of the topcoat composition is preferably 80 to 100% by mass, more preferably 90 to 100% by mass, and particularly preferably Is from 95 to 100% by weight.

  The solid content concentration of the top coat composition in the present invention is preferably 0.1 to 10, more preferably 0.2 to 6% by mass, and further preferably 0.3 to 5% by mass. preferable. By making solid content concentration into the said range, a topcoat composition can be uniformly apply | coated on actinic-light sensitive or radiation sensitive film | membrane.

  Examples of components other than the resin that can be added to the topcoat material include surfactants, photoacid generators, and basic compounds. Specific examples of the photoacid generator and the basic compound include compounds that generate an acid upon irradiation with actinic rays or radiation and compounds similar to the basic compound.

When using surfactant, the usage-amount of surfactant becomes like this. Preferably it is 0.0001-2 mass% with respect to the whole quantity of a topcoat composition, More preferably, it is 0.001-1 mass%.
By adding a surfactant to the topcoat composition, applicability when the topcoat composition is applied can be improved. Surfactants include nonionic, anionic, cationic and amphoteric surfactants.

  Nonionic surfactants include BALF's Plufrac series, Aoki Yushi Kogyo's ELEBASE series, Finesurf series, Braunon series, Asahi Denka Kogyo's Adekapluronic P-103, Kao Chemical's Emulgen Series, Amit series, Aminone PK-02S, Emanon CH-25, Rheodor series, Surflon S-141 from AGC Seimi Chemical Co., Neugen series from Daiichi Kogyo Seiyaku, New Calgen series from Takemoto Yushi DYNOL604 manufactured by Nissin Chemical Industry Co., Ltd., Envirogem AD01, Olphine EXP series, Surfynol series, Footage 300 manufactured by Hishie Chemical Co., etc. can be used.

  As an anionic surfactant, Kao Chemical's Emar 20T, Poise 532A, TOHO's Phosphanol ML-200, Clariant Japan's EMULSOGEN series, AGC Seimi Chemical's Surflon S-111N, Surflon S -211, Prisurf series manufactured by Daiichi Kogyo Seiyaku Co., Ltd., Pionein series manufactured by Takemoto Yushi Co., Ltd., Orphine PD-201 manufactured by Nissin Chemical Industry Co., Ltd. -3, a Lion made by Lion, etc. can be used.

As a cationic surfactant, Acetamine 24, Acetamine 86, etc. manufactured by Kao Chemical Co., Ltd. can be used.
As an amphoteric surfactant, Surflon S-131 (manufactured by AGC Seimi Chemical Co., Ltd.), Enagicol C-40H, Lipomin LA (manufactured by Kao Chemical Co., Ltd.) or the like can be used.

  These surfactants can also be mixed and used.

  In the pattern formation method of the present invention, an actinic ray-sensitive or radiation-sensitive film can be formed on the substrate using the actinic ray-sensitive or radiation-sensitive resin composition, and the actinic ray-sensitive or radiation-sensitive film is formed. A topcoat layer can be formed using the topcoat composition. The film thickness of this actinic ray-sensitive or radiation-sensitive film is preferably 10 to 100 nm, and the film thickness of the topcoat layer is preferably 10 to 200 nm, more preferably 20 to 100 nm, and particularly preferably 40 to 80 nm. It is.

  As a method of applying the actinic ray-sensitive or radiation-sensitive resin composition on the substrate, spin coating is preferable, and the rotation speed is preferably 1000 to 3000 rpm.

  For example, an actinic ray-sensitive or radiation-sensitive resin composition is applied to 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. Dry to form an actinic ray-sensitive or radiation-sensitive film. In addition, a known antireflection film can be applied in advance. Moreover, it is preferable to dry the actinic ray-sensitive or radiation-sensitive film before forming the topcoat layer.

  Next, on the obtained actinic ray-sensitive or radiation-sensitive film, a topcoat composition is applied and dried by the same means as the method for forming an actinic-ray-sensitive or radiation-sensitive film, and a topcoat layer is formed. can do.

  The actinic ray-sensitive or radiation-sensitive film having a top coat layer as an upper layer is usually irradiated with an electron beam (EB), X-ray or EUV light through a mask, and preferably baked (heated) and developed. Thereby, a good pattern can be obtained.

  The present invention also provides a resist-coated mask blank coated with the actinic ray-sensitive or radiation-sensitive composition of the present invention, that is, coated with the actinic ray-sensitive or radiation-sensitive film obtained as described above. Also related. In order to obtain such a resist-coated mask blank, when forming a resist pattern on a photomask blank for producing a photomask, examples of the transparent substrate used include transparent substrates such as quartz and calcium fluoride. it can. In general, a necessary film of a functional film such as a light shielding film, an antireflection film, a phase shift film, and additionally an etching stopper film or an etching mask film is laminated on the substrate. As a material for the functional film, a film containing a transition metal such as silicon or chromium, molybdenum, zirconium, tantalum, tungsten, titanium, niobium is laminated. In addition, as a material used for the outermost layer, silicon or a material containing oxygen and / or nitrogen in silicon as a main constituent material, and further a silicon compound material containing a transition metal-containing material as a main constituent material Or a transition metal, in particular, one or more selected from chromium, molybdenum, zirconium, tantalum, tungsten, titanium, niobium, etc., or a material further containing one or more elements selected from oxygen, nitrogen, and carbon The transition metal compound material is exemplified.

  The light shielding film may be a single layer, but more preferably has a multilayer structure in which a plurality of materials are applied. In the case of a multilayer structure, the thickness of the film per layer is not particularly limited, but is preferably 5 nm to 100 nm, and more preferably 10 nm to 80 nm. Although it does not specifically limit as thickness of the whole light shielding film, It is preferable that it is 5 nm-200 nm, and it is more preferable that it is 10 nm-150 nm.

  Of these materials, when pattern formation is performed using a negative chemically amplified resist composition on a photomask blank that generally contains a material containing oxygen or nitrogen in chromium as the outermost layer, the constriction shape is near the substrate. The so-called undercut shape is likely to be formed, but when the actinic ray-sensitive or radiation-sensitive composition of the present invention is used, the undercut problem can be improved as compared with the conventional one.

  Next, this resist-coated mask blank is exposed with an electron beam or EUV light, and preferably baked (usually 80 to 150 ° C., more preferably 90 to 130 ° C., usually 1 to 20 minutes, preferably 1 to 10 minutes). After the development, development is performed using an alkali developer. Thereby, a good pattern can be obtained. Then, using this pattern as a mask, etching processing, ion implantation, and the like are performed as appropriate to manufacture a semiconductor microcircuit, an imprint mold structure, a photomask, and the like.

  The present invention also relates to a photomask obtained by exposing and developing a resist-coated mask blank. The steps described above are applied as exposure and development. A photomask is suitably used for semiconductor manufacturing.

The photomask in the present invention may be a light transmissive mask used in an ArF excimer laser or the like, or a light reflective mask used in reflective lithography using EUV light as a light source.
[Usage]
The pattern forming method of the present invention is suitably used for the production of semiconductor microcircuits such as the production of VLSI and high-capacity microchips. When creating a semiconductor microcircuit, the actinic ray-sensitive or radiation-sensitive film having a pattern formed thereon is subjected to circuit formation or etching, and the remaining actinic ray-sensitive or radiation-sensitive film portion is finally Is removed with a solvent or the like, so that the final product such as a microchip is derived from the actinic ray-sensitive or radiation-sensitive resin composition described in the present invention, unlike so-called permanent resists used for printed boards and the like. No actinic ray-sensitive or radiation-sensitive film remains.

  The present invention also relates to an electronic device manufacturing method including the above-described pattern forming method of the present invention, and an electronic device manufactured by this manufacturing method.

  The electronic device of the present invention is suitably mounted on electrical and electronic equipment (home appliances, OA (office automation) / media related equipment, optical equipment, communication equipment, etc.).

EXAMPLES Hereinafter, although an Example demonstrates this invention in detail, the content of this invention is not limited by this.
<Reference Synthesis Example 1: Synthesis of Compound M-1-1>
(Synthesis of chloroether compound)
46.50 g of cyclohexanecarbaldehyde is dissolved in 263.5 g of n-hexane, 64.5 g of t-butanol, 46.50 g of anhydrous magnesium sulfate, 4.81 g of 10-camphorsulfonic acid are added at room temperature. Stir for 6 hours. After adding 10.49 g of triethylamine and stirring for 10 minutes, the solid was removed by filtration. 400 g of ethyl acetate was added, and the organic layer was washed 5 times with 200 g of ion-exchanged water and then dried over anhydrous magnesium sulfate. The solvent was distilled off to obtain 108.33 g of a compound (1) -containing solution.

  To 36.11 g of the compound (1) -containing solution, 12.47 g of acetyl chloride was added and stirred at 50 ° C. for 2 hours. After returning to room temperature, 34.21 g of the compound (2) -containing solution was obtained as a chloroether compound by removing unreacted acetyl chloride under reduced pressure conditions.

(Synthesis of Compound MI-1)
18.82 g of trans-cinnamic acid was dissolved in 136.8 g of dehydrated tetrahydrofuran, 23.67 g of triethylamine was added, and the mixture was stirred under a nitrogen atmosphere. The solution was cooled to 0 ° C., 34.21 g of the compound (2) -containing solution was added dropwise over 30 minutes, and the mixture was stirred for 2 hours. After returning to room temperature, 400 g of ethyl acetate was added, the organic layer was washed 5 times with 200 g of ion-exchanged water, dried over anhydrous magnesium sulfate, and the solvent was distilled off. The product was isolated and purified by column chromatography to obtain 30.41 g of compound (M-I-1).

<Reference Synthesis Example 2: Synthesis of Compound M-1-2>
11.92 g of 2- (4-vinylphenyl) acetic acid was dissolved in 61.32 g of dehydrated tetrahydrofuran, 10.64 g of triethylamine was added, and the mixture was stirred under a nitrogen atmosphere. After cooling to 0 ° C., a compound (2 ′)-containing solution synthesized by a method similar to the method for synthesizing 15.33 g of the chloroether compound (2) was added dropwise over 30 minutes and stirred for 2 hours. After returning to room temperature, 400 g of ethyl acetate was added, the organic layer was washed 5 times with 200 g of ion-exchanged water, dried over anhydrous magnesium sulfate, and the solvent was distilled off. The product was isolated and purified by column chromatography to obtain 23.55 g of compound (M-I-3).

<Reference Synthesis Example 3: Synthesis of Compound M-1-3>
18.82 g of 4-vinylbenzoic acid was dissolved in 136.8 g of dehydrated tetrahydrofuran, 23.67 g of triethylamine was added, and the mixture was stirred under a nitrogen atmosphere. The solution was cooled to 0 ° C., 34.21 g of the compound (2) -containing solution was added dropwise over 30 minutes, and the mixture was stirred for 2 hours. After returning to room temperature, 400 g of ethyl acetate was added, the organic layer was washed 5 times with 200 g of ion-exchanged water, dried over anhydrous magnesium sulfate, and the solvent was distilled off. It was isolated and purified by column chromatography to obtain 26.77 g of compound (M-I-3).

<Synthesis Example 1: Synthesis of Resin P-6>
3.61 g of a 50.00 mass% cyclohexanone solution of compound (3), 6.31 g of compound (M-I-1), and 0.35 g of a polymerization initiator V-601 (manufactured by Wako Pure Chemical Industries, Ltd.) Was dissolved in 28.07 g of cyclohexanone. 16.09 g of cyclohexanone was placed in the reaction vessel and dropped into the system at 85 ° C. over 4 hours under a nitrogen gas atmosphere. The reaction solution was heated and stirred for 2 hours, and then allowed to cool to room temperature.

  The reaction solution was added dropwise into 400 g of heptane / ethyl acetate = 9/1 (mass ratio) to precipitate a polymer and filtered. The filtered solid was washed with 200 g of heptane / ethyl acetate = 9/1 (mass ratio). Thereafter, the washed solid was subjected to vacuum drying to obtain 4.20 g of a resin (P-6).

<Synthesis Example 2: Synthesis of Resin P-15>
4.87 g of a 50.00 mass% cyclohexanone solution of compound (3), 5.68 g of compound (M-I-2), and 0.32 g of polymerization initiator V-601 (manufactured by Wako Pure Chemical Industries, Ltd.) Was dissolved in 25.26 g of cyclohexanone. 14.48 g of cyclohexanone was placed in the reaction vessel and dropped into the system at 85 ° C. over 4 hours under a nitrogen gas atmosphere. The reaction solution was heated and stirred for 2 hours, and then allowed to cool to room temperature.

  The above reaction solution was dropped into 350 g of heptane / ethyl acetate = 9/1 (mass ratio) to precipitate a polymer, followed by filtration. The filtered solid was washed with 200 g of heptane / ethyl acetate = 9/1 (mass ratio). Thereafter, the washed solid was subjected to vacuum drying to obtain 3.82 g of resin (P-15).

<Synthesis Example 3: Synthesis of Resin P-26>
4.69 g of a 50.00 mass% cyclohexanone solution of compound (3), 8.20 g of compound (MI-3), and 0.46 g of polymerization initiator V-601 (manufactured by Wako Pure Chemical Industries, Ltd.) Was dissolved in 36.49 g of cyclohexanone. 20.92 g of cyclohexanone was placed in the reaction vessel and dropped into the system at 85 ° C. over 4 hours under a nitrogen gas atmosphere. The reaction solution was heated and stirred for 2 hours, and then allowed to cool to room temperature.

  The reaction solution was added dropwise into 400 g of heptane / ethyl acetate = 9/1 (mass ratio) to precipitate a polymer and filtered. The filtered solid was washed with 200 g of heptane / ethyl acetate = 9/1 (mass ratio). Thereafter, the washed solid was subjected to reduced pressure drying to obtain 5.88 g of resin (P-26).

  Resins (P-1) to (P-40) were synthesized in the same manner as the resins (P-6), (P-15) and (P-26).

About the obtained resin, the weight average molecular weight (Mw: polystyrene conversion), the number average molecular weight (Mn: polystyrene conversion) and the dispersity (Mw / Mn, hereinafter referred to as “Pd”) by GPC (carrier: tetrahydrofuran (THF)) measurement. Was calculated. Further, the composition ratio (molar ratio) was calculated by ¹ H-NMR (Nuclear Magnetic Resonance) measurement.

  The structure of the synthesized resin is shown below together with the composition ratio (molar ratio) of repeating units, mass average molecular weight (Mw), and dispersity (Mw / Mn).

   Thereafter, resins (P′-1) to (P′-6) were synthesized in the same manner. The structure, composition ratio (molar ratio), weight average molecular weight, and dispersity of each synthesized resin are shown below.

Hereinafter, hydrophobic resins, acid generators, basic compounds, surfactants, solvents, developing solutions and rinsing solutions used in Examples and Comparative Examples are shown.
[Photoacid generator]
The photoacid generator was appropriately selected from the acid generators z1 to z30 listed above.
[Basic compounds]

  [Hydrophobic resin]

〔solvent〕
S-1: Propylene glycol monomethyl ether acetate (PGMEA) (boiling point 146 ° C.)
S-2: Propylene glycol monomethyl ether (PGME) (boiling point 120 ° C.)
S-3: Methyl lactate (boiling point 145 ° C.)
S-4: Cyclohexanone (boiling point 157 ° C.)
[Surfactant]
W-1: Megafuck R08 (manufactured by DIC Corporation; fluorine and silicon-based)
W-2: Polysiloxane polymer KP-341 (manufactured by Shin-Etsu Chemical Co., Ltd .; silicon-based)
W-3: Troisol S-366 (manufactured by Troy Chemical Co .; fluorine type)
W-4: PF6320 (manufactured by OMNOVA; fluorine-based)
[Developer / Rinse solution]
G-1: 2.38 mass% tetramethylammonium hydroxide aqueous solution G-2: pure water [Examples 1A to 40A, Comparative Examples 1A ′ to 6A ′ (electron beam (EB) exposure)]
(1) Preparation and coating of actinic ray-sensitive or radiation-sensitive resin composition coating liquid composition having a composition shown in Table 1 below and having a solid content concentration of 2.5% by mass is a membrane filter having a pore size of 0.1 μm. Was subjected to microfiltration to obtain an actinic ray-sensitive or radiation-sensitive resin composition (resist composition) solution. This actinic ray-sensitive or radiation-sensitive resin composition solution is applied onto a 6-inch Si wafer that has been previously treated with hexamethyldisilazane (HMDS) using a spin coater Mark8 manufactured by Tokyo Electron, and heated at 100 ° C. for 60 seconds. It dried on the plate and obtained the resist film with a film thickness of 50 nm.

(2) EB exposure and development The wafer coated with the resist film obtained in (1) above was subjected to pattern irradiation using an electron beam drawing apparatus (HL750 manufactured by Hitachi, Ltd., acceleration voltage 50 KeV). . At this time, drawing was performed so that a 1: 1 line and space was formed. After electron beam drawing, after heating at 100 ° C. for 60 seconds on a hot plate, paddle the alkaline developer listed in the table below and develop for 30 seconds. Except for some examples and comparative examples, After rinsing with the rinsing liquid described, the wafer was rotated at 4000 rpm for 30 seconds, and then heated at 95 ° C. for 60 seconds to obtain a 1: 1 line and space pattern resist with a line width of 100 nm. Got a pattern.

(3) Evaluation of resist pattern Using a scanning electron microscope (S-9220 manufactured by Hitachi, Ltd.), the obtained resist pattern was evaluated for resolution, dry etching resistance, and dissolution contrast by the following methods. The results are shown in Table 1 below.

(3-1) Resolution The irradiation energy when resolving a 1: 1 line and space pattern with a line width of 100 nm was defined as sensitivity (Eop). In Eop, the minimum line width of the separated line and space pattern (1: 1) was defined as the resolving power. The smaller this value, the better the performance.

(3-2) Dry Etching Resistance In the above (1) coating solution adjustment and coating of the actinic ray-sensitive or radiation-sensitive resin composition, a resist film having a thickness of 200 nm is formed, and then C ₄ F ₆ (20 mL / Min) and O ₂ (40 mL / min) were used, and plasma etching was performed for 30 seconds at a temperature of 23 ° C. Thereafter, the remaining film amount was determined, and the etching rate was calculated. And etching resistance was evaluated based on the following criteria.
(Criteria)
A: When the etching rate is less than 1 nm / sec B: When the etching rate is 1 nm / sec or more and less than 1.5 nm / sec C: When the etching rate is 1.5 nm / sec or more (3-3) Dissolution contrast In “(2) EB exposure and development”, surface exposure was performed while changing the exposure amount by 0.5 μC in the range of 0 to 25.0 μC, and baking was further performed at 100 ° C. for 90 seconds. Thereafter, using a 2.38% tetramethylammonium hydroxide aqueous solution, the dissolution rate at each exposure amount was measured to obtain a sensitivity curve. In this sensitivity curve, the exposure amount when the dissolution rate of the resist is saturated was taken as sensitivity, and the dissolution contrast (γ value) was calculated from the gradient of the linear portion of the sensitivity curve. The larger the γ value, the better the dissolution contrast.

[1B to 40B, Comparative Examples 1B ′ to 6B ′ (Extreme Ultraviolet (EUV) Exposure)]
(4) Coating solution preparation and coating of actinic ray-sensitive or radiation-sensitive resin composition 1.5% by mass of the components shown in Table 2 below are dissolved in the solvent shown in the same table in a solid content, and each has a pore size of 0.05 μm. The membrane filter was subjected to microfiltration to obtain an actinic ray-sensitive or radiation-sensitive resin composition (resist composition) solution.

  This actinic ray-sensitive or radiation-sensitive resin composition solution was applied onto a 6-inch Si wafer that had been previously treated with hexamethyldisilazane using a spin coater Mark8 manufactured by Tokyo Electron, and heated on a hot plate at 100 ° C. for 60 seconds. And dried to obtain a resist film having a thickness of 50 nm.

(5) EUV exposure and development The wafer coated with the resist film obtained in the above (4) is subjected to an EUV exposure apparatus (Micro Exposure Tool, NA 0.3, Quadrupole, outer sigma 0.68, inner sigma 0, manufactured by Exitech) .36) and pattern exposure was performed using an exposure mask (line / space = 1/1). After exposure, after heating at 100 ° C. for 90 seconds on a hot plate, paddle the alkali developer listed in the table below and develop for 30 seconds. After rinsing with a rinsing solution, the wafer is rotated at a rotation speed of 4000 rpm for 30 seconds and then baked at 95 ° C. for 60 seconds to obtain a 1: 1 line and space pattern resist pattern having a line width of 50 nm. It was.

(6) Evaluation of resist pattern Using a scanning electron microscope (S-9380II manufactured by Hitachi, Ltd.), the obtained resist pattern was evaluated for resolution, dry etching resistance, and dissolution contrast by the following methods. The results are shown in Table 2 below.

(6-1) Resolving power Irradiation energy when resolving a 1: 1 line and space pattern with a line width of 100 nm was defined as sensitivity (Eop). In Eop, the minimum line width of the separated line and space pattern (1: 1) was defined as the resolving power. The smaller this value, the better the performance.

(6-2) Dry Etching Resistance In the above (1) coating solution adjustment and coating of the actinic ray-sensitive or radiation-sensitive resin composition, a resist film having a film thickness of 200 nm is formed, and then C ₄ F ₆ (20 mL / Min) and O ₂ (40 mL / min) were used, and plasma etching was performed for 30 seconds at a temperature of 23 ° C. Thereafter, the remaining film amount was determined, and the etching rate was calculated. And etching resistance was evaluated based on the following criteria.
(Criteria)
A: When the etching rate is less than 1 nm / second B: When the etching rate is 1 nm / second or more and less than 1.5 nm / second C: When the etching rate is 1.5 nm / second or more (6-3) Dissolution contrast 5) In EUV exposure and development, surface exposure was performed while changing the exposure amount by 0.5 mJ in the range of 0 to 10.0 mJ, and baking was further performed at 100 ° C. for 90 seconds. Thereafter, using a 2.38% tetramethylammonium hydroxide aqueous solution, the dissolution rate at each exposure amount was measured to obtain a sensitivity curve. In this sensitivity curve, the exposure amount when the dissolution rate of the resist is saturated was taken as sensitivity, and the dissolution contrast (γ value) was calculated from the gradient of the linear portion of the sensitivity curve. The larger the γ value, the better the dissolution contrast.

  As can be seen from the above table, Examples 1A to 40A and Examples 1B to 40B are Comparative Examples 1A ′ to 6A ′ using a resin not having a repeating unit represented by the general formula (1) and As compared with 1B ′ to 6B ′, it is clear that high resolution, high dry etching resistance, and high dissolution contrast are satisfied at the same time.

Claims (16)

An actinic ray-sensitive or sensitive material containing a resin (P1) containing at least a repeating unit (a) represented by the following general formula (1) as a repeating unit having a group that decomposes by the action of an acid to generate a polar group. Forming a film using the radiation resin composition;
Exposing the film; and
The pattern formation method including the process of developing the said film | membrane after exposure using a developing solution, and forming a positive pattern.

In general formula (1),
Y ₁ and Y ₂ each independently represent a hydrogen atom or an organic group, and may combine with each other to form an aromatic ring.
Y ₃ represents a single bond or a divalent aromatic ring group. Y ₃ may combine with Y ₁ to form a ring, and Y ₃ in this case represents a trivalent aromatic ring group.
L ₁ represents a single bond or a divalent linking group. L ₁ may combine with Y ₁ to form a ring, and in this case, L ₁ represents a trivalent linking group.
R ₁ and R ₂ each independently represents a hydrogen atom or a substituent.
M ₁ represents an organic group.
One of R ₁ and R ₂ and M ₁ may be bonded to each other to form a ring together with the oxygen atom in the formula.
However, at least one of Y ₁ , Y ₂ and Y ₃ contains an aromatic ring, or Y ₁ and Y ₂ are bonded to each other to form an aromatic ring.
When Y ₃ is an aromatic ring group and L ₁ is a single bond, at least one of R ₁ and R ₂ is an alkyl group having 6 or more carbon atoms, an aliphatic cyclic group, an aromatic ring group, a heterocyclic ring Represents a group or a halogen atom.
When Y ₃ is an aromatic ring group and L ₁ is a divalent linking group, L ₁ does not contain an aliphatic cyclic group, and _one of R ₁ and R ₂ and M ₁ are They do not combine to form a ring. The pattern formation method according to claim 1, wherein the repeating unit (a) represented by the general formula (1) is a repeating unit represented by the following general formula (2).

In general formula (2),
Y ₄ and Y ₅ each independently represent a hydrogen atom or an organic group, and may combine with each other to form an aromatic ring.
L ₁₁ represents a single bond or a divalent linking group. L ₁₁ may combine with Y ₄ to form a ring, and in this case, L ₁₁ represents a trivalent linking group.
R ₃ and R ₄ each independently represents a hydrogen atom or a substituent.
M ₂ represents an organic group.
One of R ₃ and R ₄ and M ₂ may be bonded to each other to form a ring together with the oxygen atom in the formula.
However, at least one of Y ₄ and Y ₅ includes an aromatic ring, or Y ₄ and Y ₅ are bonded to each other to form an aromatic ring. R ₃ in the general formula (2) represents a hydrogen atom, R ₄ represents a hydrogen atom, an alkyl group, alicyclic group or an aromatic ring group, a pattern forming method according to claim 2. M ₂ in the general formula (2) is an alkyl group, a pattern forming method according to claim 2 or 3. The pattern formation method according to claim 1, wherein the repeating unit (a) represented by the general formula (1) is a repeating unit represented by the following general formula (3).

In general formula (3),
Y ₆ and Y ₇ each independently represent a hydrogen atom or a monovalent organic group.
L ₂ represents a divalent linking group having 1 atom between the aromatic ring and the carboxyl group in the formula.
R ₅ and R ₆ each independently represents a hydrogen atom, an alkyl group, an aliphatic cyclic group, a halogen atom, an aromatic ring group, or a heterocyclic group.
M ₃ represents an organic group.
One of R ₅ and R ₆ and M ₃ are not bonded to each other to form a ring.
n represents 0 or an integer of 1 or more. At least one of R ₅ and R _{6 in} the general formula (3) is an alkyl group having 7 or more carbon atoms, an aliphatic cyclic group, a halogen atom, an aromatic ring group having 13 or more carbon atoms, or a heterocyclic group. The pattern forming method according to claim 5. M ₃ in the general formula (3) is an alkyl group having 7 or more carbon atoms, an aliphatic cyclic group, a halogen atom, an aromatic ring group having 13 or more carbon atoms, or a heterocyclic group. The pattern formation method as described. The pattern formation method according to claim 1, wherein the repeating unit (a) represented by the general formula (1) is a repeating unit represented by the following general formula (4).

In general formula (4),
Y ₈ and Y ₉ each independently represent a hydrogen atom or a monovalent organic group.
R ₇ represents an alkyl group having 6 or more carbon atoms, an aliphatic cyclic group, an aromatic ring group, a heterocyclic group, or a halogen atom.
R ₈ represents a hydrogen atom or a substituent.
M ₄ represents an organic group.
One of R ₇ and R ₈ and M ₄ may be bonded to each other to form a ring together with the oxygen atom in the formula.
n represents 0 or an integer of 1 or more. The pattern formation method according to claim 8, wherein R ₇ in the general formula (4) represents an aliphatic cyclic group. The pattern formation method of any one of Claims 1-9 in which resin (P1) contains the repeating unit further shown by general formula (A).

In general formula (A),
Z ₁ , Z ₂ and Z ₃ each independently represent a hydrogen atom, an alkyl group, a halogen atom, a cyano group or an alkoxycarbonyl group. However, Z ₃ may combine with Ar ₂ or X ₁ to form a ring, and Z ₃ in that case represents a single bond or an alkylene group.
X ₁ represents a single bond, an alkylene group, —COO—, or —CONR ₉ —. Here, R ₉ represents a hydrogen atom or an alkyl group.
L ₃ represents a single bond, —COO—, or an alkylene group.
Ar ₂ represents an (m + 1) -valent aromatic ring group, and when bonded to Z ₃ to form a ring, represents an (m + 2) -valent aromatic ring group.
m represents an integer of 1 to 4. Forming a film using an actinic ray-sensitive or radiation-sensitive resin composition;
A step of exposing the film, and a step of developing the exposed film using a developer to form a positive pattern,
An actinic ray-sensitive or radiation-sensitive resin composition used in a pattern forming method comprising:
An actinic ray-sensitive or sensitive material containing a resin (P1) containing at least a repeating unit (a) represented by the following general formula (1) as a repeating unit having a group that decomposes by the action of an acid to generate a polar group. Radiation resin composition.

In general formula (1),
Y ₁ and Y ₂ each independently represent a hydrogen atom or an organic group, and may combine with each other to form an aromatic ring.
Y ₃ represents a single bond or a divalent aromatic ring group. Y ₃ may combine with Y ₁ to form a ring, and Y ₃ in this case represents a trivalent aromatic ring group.
L ₁ represents a single bond or a divalent linking group. L ₁ may combine with Y ₁ to form a ring, and in this case, L ₁ represents a trivalent linking group.
R ₁ and R ₂ each independently represents a hydrogen atom or a substituent.
M ₁ represents an organic group.
One of R ₁ and R ₂ and M ₁ may be bonded to each other to form a ring together with the oxygen atom in the formula.
However, at least one of Y ₁ , Y ₂ and Y ₃ contains an aromatic ring, or Y ₁ and Y ₂ are bonded to each other to form an aromatic ring.
When Y ₃ is an aromatic ring group and L ₁ is a single bond, at least one of R ₁ and R ₂ is an alkyl group having 6 or more carbon atoms, an aliphatic cyclic group, an aromatic ring group, a heterocyclic ring Represents a group or a halogen atom.
When Y ₃ is an aromatic ring group and L ₁ is a divalent linking group, L ₁ does not contain an aliphatic cyclic group, and _one of R ₁ and R ₂ and M ₁ are They do not combine to form a ring. The actinic ray-sensitive or radiation-sensitive resin composition according to claim 11, wherein the repeating unit (a) represented by the general formula (1) is a repeating unit represented by the following general formula (2).

In general formula (2),
Y ₄ and Y ₅ each independently represent a hydrogen atom or an organic group, and may combine with each other to form an aromatic ring.
L ₁₁ represents a single bond or a divalent linking group. L ₁₁ may combine with Y ₄ to form a ring, and in this case, L ₁₁ represents a trivalent linking group.
R ₃ and R ₄ each independently represents a hydrogen atom or a substituent.
M ₂ represents an organic group.
One of R ₃ and R ₄ and M ₂ may be bonded to each other to form a ring together with the oxygen atom in the formula.
However, at least one of Y ₄ and Y ₅ includes an aromatic ring, or Y ₄ and Y ₅ are bonded to each other to form an aromatic ring. The actinic ray-sensitive or radiation-sensitive resin composition according to claim 11, wherein the repeating unit (a) represented by the general formula (1) is a repeating unit represented by the following general formula (3).

In general formula (3),
Y ₆ and Y ₇ each independently represent a hydrogen atom or a monovalent organic group.
L ₂ represents a divalent linking group having 1 atom between the aromatic ring and the carboxyl group in the formula.
R ₅ and R ₆ each independently represents a hydrogen atom, an alkyl group, an aliphatic cyclic group, a halogen atom, an aromatic ring group, or a heterocyclic group.
M ₃ represents an organic group.
One of R ₅ and R ₆ and M ₃ are not bonded to each other to form a ring. N represents 0 or an integer of 1 or more. The actinic ray-sensitive or radiation-sensitive resin composition according to claim 11, wherein the repeating unit (a) represented by the general formula (1) is a repeating unit represented by the following general formula (4).

In general formula (4),
Y ₈ and Y ₉ each independently represent a hydrogen atom or a monovalent organic group.
R ₇ represents an alkyl group having 6 or more carbon atoms, an aliphatic cyclic group, an aromatic ring group, a heterocyclic group, or a halogen atom.
R ₈ represents a hydrogen atom or a substituent.
M ₄ represents an organic group.
One of R ₇ and R ₈ and M ₄ may be bonded to each other to form a ring together with the oxygen atom in the formula.
n represents 0 or an integer of 1 or more.   The actinic-ray-sensitive or radiation-sensitive film | membrane formed using the actinic-ray-sensitive or radiation-sensitive composition of any one of Claims 11-14.   The manufacturing method of an electronic device containing the pattern formation method of any one of Claims 1-10.