JP2012025762A - Compound used for photosensitive composition - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a novel compound used for a photosensitive composition forming a good-profile pattern improved in pattern collapse even in formation of a fine pattern of ≤100 nm.SOLUTION: The compound is an arylsulfonium salt represented by formula (I) (wherein Xand Xeach independently denote an aryl group or the like; Ardenotes an aryl group; Ydenotes a single bond or a divalent linking group; Ydenotes a polycyclic hydrocarbon group; mand mdenote an integer of 0 to 2; mdenotes 1 or 2; here, m+m+m=3; mdenotes an integer of 1 to 3; and X- denotes a counter anion).

Description

  The present invention relates to a photosensitive composition used in a semiconductor manufacturing process such as IC, circuit boards such as liquid crystal and thermal head, and other photofabrication processes, a compound used in the photosensitive composition, and the photosensitive composition. The present invention relates to a pattern forming method using a conductive composition. More specifically, a photosensitive composition suitable for use as an exposure light source such as far ultraviolet rays of 250 nm or less, preferably 220 nm or less, and an irradiation source by an electron beam, the compound used in the photosensitive composition, and the photosensitive composition The present invention relates to a pattern forming method using an object.

  The chemically amplified photosensitive composition generates an acid in the exposed area by irradiation with radiation such as far ultraviolet light, and the acid-catalyzed reaction causes the solubility of the active radiation irradiated area and non-irradiated area in the developer. This is a pattern forming material for changing the pattern to form a pattern on the substrate.

  When a KrF excimer laser is used as an exposure light source, a resin having a basic skeleton of poly (hydroxystyrene) having a small absorption mainly in the 248 nm region is used as a main component. A pattern is formed, which is a better system than the conventional naphthoquinone diazide / novolak resin system.

On the other hand, when a further short wavelength light source, for example, ArF excimer laser (193 nm) is used as the exposure light source, the compound having an aromatic group essentially shows a large absorption in the 193 nm region. It wasn't.
For this reason, an ArF excimer laser resist containing a resin having an alicyclic hydrocarbon structure has been developed. Various compounds have also been developed for photoacid generators that generate an acid in an exposed area by irradiation with radiation such as far ultraviolet light. For example, sulfonium salt compounds having specific substituents are disclosed. (WO 00/08525 pamphlet, JP 2000-47387).
However, from the viewpoint of overall performance as a resist, it is actually difficult to find an appropriate combination of resin, photoacid generator, additive, solvent, etc. to be used, and the line width is 100 nm or less. When forming such a fine pattern, even if the resolution performance is excellent, the formed line pattern collapses, resulting in a pattern collapse problem that causes defects during device manufacturing, and dense and isolated patterns The difference in performance, particularly the reduction of the film of the isolated pattern, was not sufficient.

International Publication No. 00/08525 JP 2000-47387 A

  Accordingly, an object of the present invention is to provide a compound used for a photosensitive composition which can improve pattern collapse and form a pattern with a good profile even in the formation of a fine pattern of 100 nm or less.

一般式（Ｉ）に於いて、
Ｘ₁及びＸ₂は、それぞれ独立に、アルキル基、シクロアルキル基、アリール基又はアラルキル基を表す。Ｘ₁とＸ₂がアルキル基である場合は、Ｘ₁とＸ₂とが結合して環構造を形成するものに限る。
Ａｒ₁は、アリール基を表す。
Ｙ₁は、単結合又は２価の連結基を表す。
Ｙ₂は、多環環状炭化水素基を表す。
ｍ₁は、０〜２を表す。
ｍ₂は、０〜２を表す。
ｍ₃は、１又は２を表す。
但し、ｍ₁＋ｍ₂＋ｍ₃＝３である。
ｍ₄は、１〜３を表す。
Ｘ^-は、対アニオンを表す。
＜２＞ 一般式（Ｉ）に於いて、ｍ₃＝１である、上記＜１＞に記載の化合物。
＜３＞ 下記一般式（Ｉ−ａ）又は（Ｉ−ｂ）で表される上記＜１＞に記載の化合物。

一般式（Ｉ−ａ）及び（Ｉ−ｂ）に於いて、Ａｒ_１、Ｙ_１、Ｙ_２、ｍ_１、ｍ_２、ｍ_３、ｍ_４及びＸ⁻は、一般式（Ｉ）に於ける、Ａｒ₁、Ｙ₁、Ｙ_２、ｍ_１、ｍ_２、ｍ_３、ｍ_４及びＸ⁻と同義である。Ａｒ_２及びＡｒ_３は、アリール基を表す。
＜４＞ 一般式（Ｉ）、（Ｉ−ａ）、及び（Ｉ−ｂ）に於いて、Ｙ_２が、アダマンタン構造を有する多環環状炭化水素基である、上記＜１＞〜＜３＞のいずれか一項に記載の化合物。
＜５＞ 一般式（Ｉ）、（Ｉ−ａ）、及び（Ｉ−ｂ）に於いて、Ｘ⁻が、下記一般式（ＡＮ１）で表される有機アニオンである、上記＜１＞〜＜４＞のいずれか一項に記載の化合物。
Ｒ_ｃ１−ＳＯ_３ ⁻ （ＡＮ１）
一般式（ＡＮ１）に於いて、Ｒｃ_１は、有機基を表す。
＜６＞ 一般式（ＡＮ１）に於いて、Ｒｃ_１が、１位がフッ素原子もしくはフロロアルキル基で置換されたアルキル基、又は、フッ素原子もしくはフロロアルキル基で置換されたフェニル基である、上記＜５＞に記載の化合物。
＜７＞ 一般式（Ｉ）、（Ｉ−ａ）及び（Ｉ−ｂ）に於いて、Ｙ_１が、アルキレン基、アリーレン基、-Ｏ-、-Ｓ-、-Ｃ（＝Ｏ）-Ｏ-、-ＳＯ_２-、-ＳＯ_３-、-Ｃ（＝Ｏ）ＮＲｄ-、-ＳＯ_２ＮＲｄ-、又は、これらの複数が組み合わさった２価の連結基である、上記＜１＞〜＜６＞のいずれか一項に記載の化合物。
本発明は上記＜１＞〜＜７＞に記載の発明であるが、以下、他の事項も含めて記載している。 The present invention is as follows.
<1> A compound represented by the following general formula (I):

In general formula (I),
X ₁ and X ₂ each independently represents an alkyl group, a cycloalkyl group, an aryl group or an aralkyl group. When X ₁ and X ₂ are alkyl groups, they are limited to those in which X ₁ and X ₂ are bonded to form a ring structure.
Ar ₁ represents an aryl group.
Y ₁ represents a single bond or a divalent linking group.
Y ₂ represents a polycyclic hydrocarbon group.
m ₁ represents 0 to 2.
m ₂ represents 0-2.
m ₃ represents 1 or 2.
However, m ₁ + m ₂ + m ₃ = 3.
m ₄ is an integer of 1 to 3.
X ⁻ represents a counter anion.
<2> The compound according to <1>, wherein m ₃ = 1 in the general formula (I).
<3> The compound according to <1>, which is represented by the following general formula (Ia) or (Ib).

In the general formulas (Ia) and (Ib), Ar ₁ , Y ₁ , Y ₂ , m ₁ , m ₂ , m ₃ , m ₄ and X ⁻ are in the general formula (I). , Ar ₁ , Y ₁ , Y ₂ , m ₁ , m ₂ , m ₃ , m ₄ and X ⁻ . Ar ₂ and Ar ₃ represent an aryl group.
<4> In the general formulas (I), (Ia), and (Ib), the above <1> to <3>, wherein Y ₂ is a polycyclic hydrocarbon group having an adamantane structure. The compound as described in any one of these.
<5> formula (I), In (I-a), and (I-b), X ^- is an organic anion represented by the following general formula (AN1), the <1> to < The compound as described in any one of 4>.
R _c1 —SO ₃ ^— (AN1)
In the general formula (AN1), Rc ₁ represents an organic group.
<6> In the general formula (AN1), Rc ₁ is an alkyl group substituted at the 1-position with a fluorine atom or a fluoroalkyl group, or a phenyl group substituted with a fluorine atom or a fluoroalkyl group, The compound as described in <5>.
<7> In the general formulas (I), (Ia), and (Ib), Y ₁ is an alkylene group, an arylene group, —O—, —S—, —C (═O) —O. _{-, - SO 2 -, -} SO 3 -, - C (= O) NRd -, - SO 2 NRd-, or a divalent linking group the plurality are combined, the <1> to < The compound as described in any one of 6>.
The present invention is the invention described in <1> to <7> above, but is described below including other matters.

(1) A photosensitive composition comprising (A) an arylsulfonium salt compound having a polycyclic hydrocarbon structure in the cation moiety.

(2) characterized in that it contains (A) an arylsulfonium salt compound having a polycyclic hydrocarbon structure in the cation moiety and (B) a resin that decomposes by the action of an acid and increases the solubility in an alkali developer. A positive photosensitive composition.

  (3) An arylsulfonium salt compound having a polycyclic hydrocarbon structure in the cation moiety.

  (4) A compound represented by the following general formula (I):

In general formula (I),
X ₁ and X ₂ each independently represents an alkyl group, a cycloalkyl group, an aryl group or an aralkyl group. X ₁ and X ₂ may combine to form a ring structure.
Ar ₁ represents an aryl group.
Y ₁ represents a single bond or a divalent linking group.
Y ₂ represents a polycyclic hydrocarbon group.
m ₁ represents 0 to 2.
m ₂ represents 0-2.
m ₃ is an integer of 1 to 3.
However, m ₁ + m ₂ + m ₃ = 3.
m ₄ is an integer of 1 to 3.
X ⁻ represents a counter anion.

(5) A pattern forming method comprising a step of forming a photosensitive film from the photosensitive composition according to (1) or (2), and exposing and developing the photosensitive film.
(6) The positive photosensitive composition as described in (2), wherein the resin as the component (B) is a resin having a hydroxystyrene repeating unit.
(7) The positive photosensitive composition as described in (2), wherein the resin as the component (B) is a resin having a monocyclic or polycyclic alicyclic hydrocarbon structure.
(8) The positive photosensitive composition as described in (2), wherein the resin as the component (B) is a resin having a silicon atom.
(9) The positive photosensitive composition as described in (2), wherein the resin as the component (B) is a resin having a repeating unit having a lactone structure.

  INDUSTRIAL APPLICABILITY According to the present invention, it is possible to provide a photosensitive composition in which pattern collapse is improved even when a fine pattern of 100 nm or less is formed and a pattern with a good profile is formed, and a pattern forming method using the photosensitive composition. .

It is the schematic of a two-beam interference exposure experiment apparatus.

Hereinafter, the best mode for carrying out the present invention will be described.
In addition, in the description of the group (atomic group) in this specification, the description which does not describe substitution and non-substitution includes what does not have a substituent and what has a substituent. . For example, the “alkyl group” includes not only an alkyl group having no substituent (unsubstituted alkyl group) but also an alkyl group having a substituent (substituted alkyl group).

(A) Arylsulfonium Salt Compound Having Polycyclic Cyclic Hydrocarbon Structure in Cation Part The photosensitive composition of the present invention comprises an arylsulfonium salt compound having a polycyclic cyclic hydrocarbon structure in the cation part (hereinafter referred to as “component (A)”. Also referred to as “compounds of”.
An arylsulfonium salt compound having a polycyclic hydrocarbon structure in the cation moiety is a compound that generates an acid upon irradiation with actinic rays or radiation.
The arylsulfonium salt compound having a polycyclic hydrocarbon structure in the cation part is an arylsulfonium salt in which an aryl group is bonded to a sulfur cation and has a polycyclic hydrocarbon structure in the cation part. But it can also be used. As the arylsulfonium salt, all substituents bonded to the sulfur atom may be aryl groups, or some of the substituents bonded to the sulfur atom may be aryl groups, and the rest may be alkyl groups, cycloalkyl groups, or aralkyl groups. . The polycyclic hydrocarbon structure may be provided in any of an aryl group, an alkyl group, a cycloalkyl group, and an aralkyl group, but is preferably provided in an aryl group.

Examples of arylsulfonium compounds include triarylsulfonium compounds, diarylalkylsulfonium compounds, aryldialkylsulfonium compounds, diarylcycloalkylsulfonium compounds, aryldicycloalkylsulfonium compounds, diarylaralkylsulfonium compounds, aryldiaralkylsulfonium compounds, and the like. Can do.
The aryl group in the arylsulfonium compound is preferably an aryl group having 6 to 20 carbon atoms, for example, a heteroaryl containing a heteroatom such as a hydrocarbon aryl group such as a phenyl group, a naphthyl group or an anthranyl group, a pyrrole group or an indole group. An aryl group is mentioned.
As an alkyl group, a C1-C20 alkyl group is preferable, for example, a methyl group, an ethyl group, etc. can be mentioned.
The cycloalkyl group is preferably a cycloalkyl group having 3 to 20 carbon atoms, and examples thereof include a cyclopropyl group, a cyclohexyl group, a norbornane group, and an adamantyl group.
As the aralkyl group, an aralkyl group having 7 to 20 carbon atoms is preferable, and examples thereof include a benzyl group and a phenethyl group.

  As the arylsulfonium salt compound having a polycyclic hydrocarbon structure in the cation part, a compound represented by the following general formula (I) is preferable.

In general formula (I),
X ₁ and X ₂ each independently represents an alkyl group, a cycloalkyl group, an aryl group or an aralkyl group. X ₁ and X ₂ may combine to form a ring structure.
Ar ₁ represents an aryl group.
Y ₁ represents a single bond or a divalent linking group.
Y ₂ represents a polycyclic hydrocarbon group.
m ₁ represents 0 to 2.
m ₂ represents 0-2.
m ₃ is an integer of 1 to 3.
However, m ₁ + m ₂ + m ₃ = 3.
m ₄ is an integer of 1 to 3.
X ⁻ represents a counter anion.

As the aryl group in the general formula (I), X ₁ , X ₂ and Ar ₁ , an aryl group having 6 to 20 carbon atoms is preferable, for example, a hydrocarbon aryl group such as a phenyl group, a naphthyl group, an anthranyl group, Examples include heteroaryl groups containing heteroatoms such as a pyrrole group and an indole group, and more preferred are a phenyl group, a naphthyl group, and an indole group.
The alkyl group in X ₁ and X ₂ is preferably an alkyl group having 1 to 20 carbon atoms, and examples thereof include a methyl group and an ethyl group.
The cycloalkyl group in X ₁ and X ₂ is preferably a cycloalkyl group having 3 to 20 carbon atoms, and examples thereof include a cyclopropyl group, a cyclohexyl group, a norbornane group, and an adamantyl group.
The aralkyl group in X ₁ and X ₂ is preferably an aralkyl group having 7 to 20 carbon atoms, and examples thereof include a benzyl group and a phenethyl group.
X ₁ and X ₂ are preferably such that both X ₁ and X ₂ are phenyl groups, or X ₁ and X ₂ are bonded to form an alkylene group (preferably having 4 to 6 carbon atoms).
Examples of the divalent linking group for Y ₁ include an alkylene group, an arylene group, —O—, —S—, —C (═O) —, —C (═O) —O—, —SO ₂ —, —SO ₃ —, —C (═O) NRd—, —SO ₂ NRd—, or a divalent linking group formed by combining a plurality of these can be given. In the formula, Rd represents a hydrogen atom or an alkyl group.
The polycyclic hydrocarbon group for Y ₂ is a polycyclic hydrocarbon group having two or more rings, and preferably an adamantyl group, a norbornane group, a bicyclo [2.2.2] octane group, a tetracyclododecanyl group, A tricyclodecanyl group, a diamantyl group, etc. are mentioned. An adamantyl group is preferred.
Examples of counter anions of X ⁻ include sulfonate anions, carboxylate anions, bissulfonylimide anions, organic anions having carbon atoms such as trissulfonylmethide anions, BF ₄₋ , PF ₆ ⁻ , AsF ₆ ⁻ , ClO ₄ ^−. Inorganic anions such as organic anions are preferable.

  Preferred organic anions include organic anions represented by the following general formulas (AN1) to (AN4).

In general formulas (AN1) to (AN2),
Rc ₁ represents an organic group.
Examples of the organic group in Rc ₁ include those having 1 to 30 carbon atoms, and preferably an alkyl group, an aryl group, or a plurality of which may be substituted is a single bond, —O—, —CO ₂ —, _{-S -, - SO 3 -,} - SO 2 N (Rd 1) - can be exemplified linked group a linking group such as. Rd ₁ represents a hydrogen atom or an alkyl group, and may form a ring structure with the bonded alkyl group or aryl group.
More preferred as the organic group for Rc ₁ is an alkyl group substituted at the 1-position with a fluorine atom or a fluoroalkyl group, or a phenyl group substituted with a fluorine atom or a fluoroalkyl group. By having a fluorine atom or a fluoroalkyl group, the acidity of the acid generated by light irradiation is increased and the sensitivity is improved. When Rc ₁ has 5 or more carbon atoms, it is preferable that at least one carbon atom is not substituted for all hydrogen atoms by fluorine atoms, and more preferably, the number of hydrogen atoms is larger than that of fluorine atoms. By not having a perfluoroalkyl group having 5 or more carbon atoms, ecotoxicity is reduced.

A particularly preferred embodiment of Rc ₁ is a group represented by the following general formula.

Where
Rc ₆ is substituted with a perfluoroalkylene group having 3 or less carbon atoms, more preferably 2 to 4 carbon atoms, more preferably 2 to 3 carbon atoms, 3 to 4 fluorine atoms and / or 1 to 3 fluoroalkyl groups. Represents a phenylene group.
Ax represents a single bond or a divalent linking group (preferably —O—, —CO ₂ —, —S—, —SO ₃ —, —SO ₂ N (Rd ₁ ) —). Rd ₁ represents a hydrogen atom or an alkyl group, and may combine with Rc ₇ to form a ring structure.
Rc ₇ represents a hydrogen atom, a fluorine atom, a linear or branched alkyl group which may be substituted, a monocyclic or polycyclic cycloalkyl group or an aryl group which may be substituted. The optionally substituted alkyl group, cycloalkyl group and aryl group preferably do not contain a fluorine atom as a substituent.

In general formulas (AN3) to (AN4),
Rc ₃ , Rc ₄ and Rc ₅ each independently represents an organic group.
Preferred examples of the organic group for Rc ₃ , Rc ₄ and Rc ₅ include the same organic groups as those for Rc ₁ .
Rc ₃ and Rc ₄ may combine to form a ring. Examples of the group formed by combining Rc ₃ and Rc ₄ include an alkylene group and an arylene group. Preferably, it is a C2-C4 perfluoroalkylene group. Rc ₃ and Rc ₄ are preferably bonded to form a ring, so that the acidity of the acid generated by light irradiation is increased and the sensitivity is improved, which is preferable.

  The arylsulfonium salt compound having a polycyclic hydrocarbon structure in the cation moiety is more preferably a compound represented by the following general formula (Ia) or (Ib).

In the general formulas (Ia) and (Ib),
_{Ar 1, Y 1, Y 2} , m 1, m 2, m 3, m 4 and X ^- is in the general formula _{(I), Ar 1, Y} 1, Y 2, m 1, m 2, m ₃ , m _4, and X ⁻ are synonymous.
Ar ₂ and Ar ₃ represent an aryl group.

In the general formulas (Ia) and (Ib), the substituents that Ar ₁ , Ar ₂ , Ar ₃ and Y ₂ may have are preferably an alkyl group, an alkoxy group, a hydroxyl group, A cyano group, a halogen atom, an alkoxycarbonyl group, etc. are mentioned.

  Specific examples of preferred sulfonium cations in the compound of component (A) are shown below, but the present invention is not limited thereto.

  Specific examples of preferred counter anions in the compound of component (A) are shown below, but the present invention is not limited thereto.

The compound of the component (A) is preferably an arbitrary combination of the above-mentioned preferable sulfonium cation and a preferable counter anion.
Although the compound of the (A) component especially preferable is shown below, this invention is not limited to this. I-3 is a reference example.

The compound of component (A) is a novel compound.
The compound of component (A) can be synthesized, for example, by forming a cation moiety by reacting an aryl compound having a polycyclic hydrocarbon group with a sulfoxide compound and exchanging it with a desired counter anion by salt exchange. .

  The content of the compound (A) in the composition is preferably 0.1 to 20% by mass, more preferably 0.5 to 10% by mass, and still more preferably based on the total solid content of the photosensitive composition. It is 1-7 mass%, Most preferably, it is 3-7 weight%.

The photosensitive composition of this invention may use together the compound which generate | occur | produces an acid by irradiation of actinic rays or radiation other than the aryl sulfonium salt compound which has a polycyclic hydrocarbon structure in a cation part.
Examples of such an acid generator include a photoinitiator for photocationic polymerization, a photoinitiator for photoradical polymerization, a photodecolorant for dyes, a photochromic agent, or an actinic ray or radiation used for a microresist. A known compound that generates an acid by irradiation and a mixture thereof can be appropriately selected and used.

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

  Further, a group that generates an acid upon irradiation with these actinic rays or radiation, or a compound in which a compound is introduced into the main chain or side chain of the polymer, for example, US Pat. No. 3,849,137, German Patent No. 3914407. JP, 63-26653, JP, 55-164824, JP, 62-69263, JP, 63-146038, JP, 63-163452, JP, 62-153853, The compounds described in JP-A 63-146029 can be used.

  Furthermore, compounds capable of generating an acid by light described in US Pat. No. 3,779,778, European Patent 126,712 and the like can also be used.

  Among the compounds that generate an acid upon irradiation with actinic rays or radiation that may be used in combination, compounds represented by the following general formulas (ZI), (ZII), and (ZIII) can be exemplified.

In general formula (ZI):
R ₂₀₁ , R ₂₀₂ and R ₂₀₃ each independently represents an organic group.
X ⁻ represents a counter anion and is the same as the counter anion of X ⁻ in formula (I).

In formula (ZI), the carbon number of the organic group as R _201, R ₂₀₂ and R ₂₀₃ is generally from 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. The two of the group formed by bonding of the R ₂₀₁ to R _203, there can be mentioned an alkylene group (e.g., butylene, pentylene).
Specific examples of the organic group as R ₂₀₁ , R ₂₀₂ and R ₂₀₃ include corresponding groups in the compounds (ZI-1), (ZI-2) and (ZI-3) described later.

In addition, the compound which has two or more structures represented by general formula (ZI) may be sufficient. For example, the general formula at least one of R ₂₀₁ to R ₂₀₃ of a compound represented by (ZI) is, at least one bond with structure of R ₂₀₁ to R ₂₀₃ of another compound represented by formula (ZI) It may be a compound.

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

The compound (ZI-1) is at least one of the aryl groups R ₂₀₁ to R ₂₀₃ in formula (ZI), arylsulfonium compound, i.e., a compound having arylsulfonium as a cation.
In the arylsulfonium compound, all of R _{201 to} R ₂₀₃ may be an aryl group, or a part of R _{201 to} R ₂₀₃ may be an aryl group, and the rest may be an alkyl group or a cycloalkyl group.
Examples of the arylsulfonium compound include triarylsulfonium compounds, diarylalkylsulfonium compounds, aryldialkylsulfonium compounds, diarylcycloalkylsulfonium compounds, and aryldicycloalkylsulfonium compounds.
The aryl group of the arylsulfonium compound is preferably an aryl group such as a phenyl group or a naphthyl group, or a heteroaryl group such as an indole residue or a pyrrole residue, more preferably a phenyl group or an indole residue. When the arylsulfonium compound has two or more aryl groups, the two or more aryl groups may be the same or different.
The alkyl group that the arylsulfonium compound has as necessary is preferably a linear or branched alkyl group having 1 to 15 carbon atoms, such as a methyl group, an ethyl group, a propyl group, an n-butyl group, sec- Examples thereof include a butyl group and a t-butyl group.
The cycloalkyl group that the arylsulfonium compound has as necessary is preferably a cycloalkyl group having 3 to 15 carbon atoms, and examples thereof include a cyclopropyl group, a cyclobutyl group, and a cyclohexyl group.
The aryl group, alkyl group, and cycloalkyl group of R _{201 to} R ₂₀₃ are an alkyl group (for example, having 1 to 15 carbon atoms), a cycloalkyl group (for example, having 3 to 15 carbon atoms), an aryl group (for example, having 6 to 14 carbon atoms). ), An alkoxy group (for example, having 1 to 15 carbon atoms), a halogen atom, a hydroxyl group, or a phenylthio group as a substituent. Preferred substituents are linear or branched alkyl groups having 1 to 12 carbon atoms, cycloalkyl groups having 3 to 12 carbon atoms, and linear, branched or cyclic alkoxy groups having 1 to 12 carbon atoms, particularly preferably. They are a C1-C4 alkyl group and a C1-C4 alkoxy group. The substituent may be substituted with any one of the three R _{201 to} R ₂₀₃ , or may be substituted with all three. When R _{201 to} R ₂₀₃ are an aryl group, the substituent is preferably substituted at the p-position of the aryl group.

Next, the compound (ZI-2) will be described.
Compound (ZI-2) is a compound in the case where R _{201 to} R ₂₀₃ in formula (ZI) each independently represents an organic group containing no aromatic ring. Here, the aromatic ring includes an aromatic ring containing a hetero atom.
The organic group having no aromatic ring as R ₂₀₁ to R ₂₀₃ generally has 1 to 30 carbon atoms, preferably 1 to 20 carbon atoms.
R _{201 to} R ₂₀₃ are each independently preferably an alkyl group, a cycloalkyl group, an allyl group, or a vinyl group, more preferably a linear, branched, cyclic 2-oxoalkyl group, or an alkoxycarbonylmethyl group, particularly preferably Is a linear, branched 2-oxoalkyl group.

The alkyl group as R ₂₀₁ to R ₂₀₃ is preferably include a linear or branched alkyl group having 1 to 10 carbon atoms (e.g., methyl group, ethyl group, propyl group, butyl group, pentyl group) . The alkyl group as R ₂₀₁ to R ₂₀₃ may be linear, branched 2-oxoalkyl group, more preferably an alkoxymethyl group.
The cycloalkyl group as R ₂₀₁ to R ₂₀₃ is preferably, and a cycloalkyl group having 3 to 10 carbon atoms (e.g., cyclopentyl, cyclohexyl, norbornyl).
The cycloalkyl group as R ₂₀₁ to R ₂₀₃ is more preferably a cyclic 2-oxoalkyl group.
Linear as R ₂₀₁ to R _203, branched or cyclic 2-oxoalkyl group may preferably be a group having a 2-position> C = O in the above-described alkyl or cycloalkyl group.
The alkoxy group in the alkoxycarbonylmethyl group as R ₂₀₁ to R _203, preferably may be mentioned alkoxy groups having 1 to 5 carbon atoms (a methoxy group, an ethoxy group, a propoxy group, a butoxy group, a pentoxy group).
R _{201 to} R ₂₀₃ may be further substituted with a halogen atom, an alkoxy group (eg, having 1 to 5 carbon atoms), a hydroxyl group, a cyano group, a nitro group, or the like.

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

In general formula (ZI-3),
R _{1c to} R _5c each independently represents a hydrogen atom, an alkyl group, a cycloalkyl group, an alkoxy group or a halogen atom.
R _6c and R _7c each independently represents a hydrogen atom, an alkyl group or a cycloalkyl group.
Rx and Ry each independently represents an alkyl group, a cycloalkyl group, an allyl group or a vinyl group.
Any two or more of R _1c to R _7c, and R _x and R _y may be bonded to each other to form a ring structure, the ring structure may contain an oxygen atom, a sulfur atom, an ester bond, an amide bond May be included. Examples of the group formed by combining any two or more of R _{1c to} R _7c and R _x and R _y include a butylene group and a pentylene group.
X ⁻ represents a counter anion, and examples thereof include the same as the counter anion of X ^{− in} the general formula (I).

The alkyl group as R _{1c to} R _7c is, for example, a linear or branched alkyl group having 1 to 20 carbon atoms, preferably a linear or branched alkyl group having 1 to 12 carbon atoms (for example, a methyl group). , Ethyl group, linear or branched propyl group, linear or branched butyl group, linear or branched pentyl group).
Preferable examples of the cycloalkyl group as R _{1c to} R _7c include a cycloalkyl group having 3 to 8 carbon atoms (for example, a cyclopentyl group and a cyclohexyl group).
The alkoxy group as R _{1c to} R _{5c may} be linear, branched or cyclic, for example, an alkoxy group having 1 to 10 carbon atoms, preferably a linear or branched alkoxy group having 1 to 5 carbon atoms. (For example, methoxy group, ethoxy group, linear or branched propoxy group, linear or branched butoxy group, linear or branched pentoxy group), C3-C8 cyclic alkoxy group (for example, cyclopentyloxy group, cyclohexyloxy group) ).
Preferably any one of R _{1c to} R _5c is a linear or branched alkyl group, a cycloalkyl group, or a linear, branched or cyclic alkoxy group, and more preferably the sum of the carbon number of R _{1c to} R _5c is 2-15. Thereby, solvent solubility improves more and generation | occurrence | production of a particle is suppressed at the time of a preservation | save.

_Examples of the alkyl group as R _x and R _y include the same alkyl groups as R _{1c to} R _7c . The alkyl group as R _x and R _y is more preferably a linear or branched 2-oxoalkyl group or an alkoxymethyl group.
The cycloalkyl group as R _x and R _y may be the same as the cycloalkyl group as R _1c to R _7c. The cycloalkyl group as R _x and R _y is more preferably a cyclic 2-oxoalkyl group.
Examples of the linear or branched 2-oxoalkyl group and cyclic 2-oxoalkyl group include a group having> C═O at the 2-position of the alkyl group or cycloalkyl group as R _{1c to} R _7c .
Examples of the alkoxy group in the alkoxycarbonylmethyl group include the same alkoxy groups as R _{1c to} R _5c .
R _x and R _y are preferably an alkyl group having 4 or more carbon atoms, more preferably 6 or more, and still more preferably 8 or more.

In the 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 of R ₂₀₄ to R _207, a phenyl group, a naphthyl group, more preferably a phenyl group.
The alkyl group as R ₂₀₄ to R ₂₀₇ may preferably be mentioned a linear or branched alkyl group having 1 to 10 carbon atoms (e.g., methyl group, ethyl group, propyl group, butyl group, pentyl group).
The cycloalkyl group as R ₂₀₄ to R ₂₀₇ is preferably, and a cycloalkyl group having 3 to 10 carbon atoms (e.g., cyclopentyl, cyclohexyl, norbornyl).
R ₂₀₄ to R ₂₀₇ may have a substituent. The R ₂₀₄ to R ₂₀₇ are substituents which may have, for example, an alkyl group (for example, 1 to 15 carbon atoms), a cycloalkyl group (for example, 3 to 15 carbon atoms), an aryl group (e.g., 6 carbon atoms 15), alkoxy groups (for example, having 1 to 15 carbon atoms), halogen atoms, hydroxyl groups, phenylthio groups and the like.
X ⁻ represents a counter anion, and examples thereof include the same as the counter anion of X ^{− in} formula (I).

  Among the compounds that generate an acid upon irradiation with actinic rays or radiation that may be used in combination, compounds represented by the following general formulas (ZIV), (ZV), and (ZVI) can be exemplified. .

In the general formulas (ZIV) to (ZVI),
Ar ₃ and Ar ₄ each independently represents an aryl group.
R ₂₀₆ represents an alkyl group, a cycloalkyl group or an aryl group.
R ₂₀₇ and R ₂₀₈ each independently represents an alkyl group, a cycloalkyl group, an aryl group, or an electron-withdrawing group. R ₂₀₇ is preferably an aryl group. R ₂₀₈ is preferably an electron-withdrawing group, more preferably a cyano group or a fluoroalkyl group.
A represents an alkylene group, an alkenylene group or an arylene group.

  Of the compounds that generate an acid upon irradiation with actinic rays or radiation, more preferred are compounds represented by general formulas (ZI) to (ZIII), and even more preferred are compounds represented by general formula (ZI). And particularly preferred are compounds represented by the general formulas (ZI-1) to (ZI-3).

  Furthermore, the compound which generate | occur | produces the acid represented by the following general formula (AC1)-(AC3) by irradiation of actinic light or a radiation is preferable.

In formula (AC1) ~ (AC3), Rc 1, Rc 3 ~Rc 5 , it said in the general formula (AN1) ~ (AN4), the same meanings as Rc _1, Rc ₃ ~Rc _5.

A particularly preferable embodiment of the acid generator is a compound in which, in the structure of the general formula (ZI), X ⁻ is a counter anion selected from the above (AN1), (AN3), and (AN4).

  Of the compounds that generate an acid upon irradiation with actinic rays or radiation that may be used in combination, examples of particularly preferable compounds are listed below.

The acid generator that may be used in combination may be used alone or in combination of two or more. When two or more types are used in combination, it is preferable to combine two types of compounds that generate two types of organic acids that differ in the total number of atoms excluding hydrogen atoms by two or more.
The total content of the compound (A) and the acid generator that may be used in combination is preferably 0.1 to 20% by mass, more preferably 0, based on the total solid content of the resist composition. 0.5 to 10% by mass, more preferably 1 to 7% by mass, and particularly preferably 3 to 7% by mass.

(A) The photosensitive composition containing the compound of a component can take the aspect of a positive photosensitive composition and a negative photosensitive composition.
The photosensitive composition containing a resin that decomposes by the action of the compound (A) and (B) acid and increases the solubility in an alkaline developer is a positive photosensitive composition, and the photosensitive film When formed, irradiated with actinic rays or radiation, and developed with an alkali developer, the exposed portion is dissolved and removed, and a pattern is formed.
The photosensitive composition containing the compound (A), a resin soluble in an alkali developer, and an acid crosslinking agent that crosslinks a resin soluble in an alkali developer by the action of an acid is a negative photosensitive composition. Yes, when a photosensitive film is formed, irradiated with actinic rays or radiation, and developed with an alkali developer, unexposed portions are dissolved and removed, and a pattern is formed.

(B) Resin that is decomposed by the action of an acid and has increased solubility in an alkaline developer The resin that is used in the positive photosensitive composition of the present invention to be decomposed by an acid and has increased solubility in an alkaline developer (Hereinafter also referred to as “resin of component (B)”) is a group capable of decomposing with an acid (hereinafter referred to as “acid-decomposable group”) on the main chain or side chain of the resin, or both of the main chain and side chain. Resin). Among these, a resin having a group capable of decomposing with an acid in the side chain is more preferable.

A group preferable as a group that can be decomposed by an acid is a group in which a hydrogen atom of a —COOH group or —OH group is substituted with a group capable of leaving with an acid.
Examples of the group capable of leaving with 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.
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 and} R ₀₂ each independently represents a hydrogen atom, an alkyl group, a cycloalkyl group, an aryl group, an aralkyl group or an alkenyl group.
In the present invention, the acid-decomposable group is preferably an acetal group or a tertiary ester group.

  The base resin in the case where these acid-decomposable groups are bonded as side chains is an alkali-soluble resin having —OH or —COOH groups in the side chains. For example, the alkali-soluble resin mentioned later can be mentioned.

  The alkali dissolution rate of these alkali-soluble resins is preferably 170 A / second or more as measured with 0.261 N tetramethylammonium hydroxide (TMAH) (23 ° C.). Particularly preferably, it is 330 Å / second or more.

  From this point of view, particularly preferred alkali-soluble resins are o-, m-, p-poly (hydroxystyrene) and copolymers thereof, hydrogenated poly (hydroxystyrene), halogen or alkyl-substituted poly (hydroxystyrene). Hydroxystyrene structural units such as a part of poly (hydroxystyrene), O-alkylated or O-acylated product, styrene-hydroxystyrene copolymer, α-methylstyrene-hydroxystyrene copolymer, hydrogenated novolak resin, etc. An alkali-soluble resin containing a repeating unit having a carboxyl group such as (meth) acrylic acid or norbornenecarboxylic acid.

  Preferred examples of the repeating unit having an acid-decomposable group in the present invention include t-butoxycarbonyloxystyrene, 1-alkoxyethoxystyrene, (meth) acrylic acid tertiary alkyl ester, and the like. Alkyl-2-adamantyl (meth) acrylate and dialkyl (1-adamantyl) methyl (meth) acrylate are more preferred.

  The resin of component (B) used in the present invention is an acid soluble in an alkali-soluble resin as disclosed in European Patent No. 254853, JP-A-2-25850, JP-A-3-223860, JP-A-4-251259, and the like. It can be obtained by reacting a precursor of a group capable of decomposing with an acid, or copolymerizing an alkali-soluble resin monomer having a group capable of decomposing with an acid with various monomers.

  When the positive photosensitive composition of the present invention is irradiated with a KrF excimer laser beam, an electron beam, an X-ray, or a high energy beam having a wavelength of 50 nm or less (preferably EUV, etc.), It preferably has a styrene repeating unit. More preferably, a copolymer containing a hydroxystyrene repeating unit / hydroxystyrene repeating unit protected with an acid-decomposable group, and a copolymer containing a hydroxystyrene repeating unit / (meth) acrylate repeating unit protected with an acid-decomposing group. Polymers are preferred.

  Specific examples of the component (B) resin used in the present invention are shown below, but the present invention is not limited thereto.

  In the above specific example, tBu represents a t-butyl group.

The content of the group that can be decomposed by an acid is determined by the number of groups (B) that can be decomposed by an acid in the resin and the number of alkali-soluble groups that are not protected by a group capable of leaving by an acid (S). B + S).
The content is preferably 0.01 to 0.7, more preferably 0.05 to 0.50, and still more preferably 0.05 to 0.40.

  When the positive photosensitive composition of the present invention is irradiated with ArF excimer laser light, the resin of component (B) has a monocyclic or polycyclic alicyclic hydrocarbon structure and is decomposed by the action of an acid. It is preferable that the resin has increased solubility in an alkaline developer.

  Resin that has a monocyclic or polycyclic alicyclic hydrocarbon structure, decomposes by the action of an acid, and increases solubility in an alkali developer (hereinafter also referred to as “alicyclic hydrocarbon-based acid-decomposable resin”) Is selected from the group consisting of repeating units having a partial structure containing an alicyclic hydrocarbon represented by the following general formula (pI) to general formula (pV) and repeating units represented by the following general formula (II-AB). It is preferable that the resin contains at least one kind.

In the general formulas (pI) to (pV),
R ₁₁ represents a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, or a sec-butyl group.
Z represents an atomic group necessary for forming a cycloalkyl group together with a carbon atom.
R _{12 to} R ₁₆ each independently represents a linear or branched alkyl group or cycloalkyl group having 1 to 4 carbon atoms. However, at least one of R _{12 to} R ₁₄ , or any of R ₁₅ and R ₁₆ represents a cycloalkyl group.
R _{17 to} R ₂₁ each independently represents a hydrogen atom, a linear or branched alkyl group having 1 to 4 carbon atoms, or a cycloalkyl group. However, at least one of R _{17 to} R ₂₁ represents a cycloalkyl group. Further, either R ₁₉ or R ₂₁ represents a linear or branched alkyl group or cycloalkyl group having 1 to 4 carbon atoms.
R _{22 to} R ₂₅ each independently represents a hydrogen atom, a linear or branched alkyl group having 1 to 4 carbon atoms, or a cycloalkyl group. However, at least one of R _{22 to} R ₂₅ represents a cycloalkyl group. R ₂₃ and R ₂₄ may be bonded to each other to form a ring.

In general formula (II-AB):
R ₁₁ ′ and R ₁₂ ′ each independently represents a hydrogen atom, a cyano group, a halogen atom or an alkyl group.
Z ′ represents an atomic group for forming an alicyclic structure containing two bonded carbon atoms (C—C).

  The general formula (II-AB) is more preferably the following general formula (II-AB1) or general formula (II-AB2).

In the general formulas (II-AB1) and (II-AB2),
R ₁₃ ′ to R ₁₆ ′ each independently represents a hydrogen atom, a halogen atom, a cyano group, —COOH, —COOR ₅ , a group that decomposes by the action of an acid, —C (═O) —XA′—R. ₁₇ ′ represents an alkyl group or a cycloalkyl group. At least two of R ₁₃ ′ to R ₁₆ ′ may combine to form a ring.
Here, R ₅ represents an alkyl group, a cycloalkyl group, or a group having a lactone structure.
X represents an oxygen atom, a sulfur atom, -NH -, - NHSO ₂ - or an -NHSO ₂ NH-.
A ′ represents a single bond or a divalent linking group.
R ₁₇ ′ represents —COOH, —COOR ₅ , —CN, a hydroxyl group, an alkoxy group, —CO—NH—R ₆ , —CO—NH—SO ₂ —R ₆ or a group having a lactone structure.
R ₆ represents an alkyl group or a cycloalkyl group.
n represents 0 or 1.

In the general formulas (pI) to (pV), examples of the linear or branched alkyl group having 1 to 4 carbon atoms in R _{12 to} R ₂₅ include a methyl group and an ethyl group.

The cycloalkyl group represented by R _{12 to} R ₂₅ or the cycloalkyl group formed by Z and the carbon atom may be monocyclic or polycyclic. Specific examples include groups having a monocyclo, bicyclo, tricyclo, tetracyclo structure or the like having 5 or more carbon atoms. The carbon number is preferably 6-30, and particularly preferably 7-25.

  Preferred cycloalkyl groups include adamantyl group, noradamantyl group, decalin residue, tricyclodecanyl group, tetracyclododecanyl group, norbornyl group, cedrol group, cyclopentyl group, cyclohexyl group, cycloheptyl group, cyclooctyl group, A cyclodecanyl group and a cyclododecanyl group can be mentioned. More preferable examples include an adamantyl group, norbornyl group, cyclohexyl group, cyclopentyl group, tetracyclododecanyl group, and tricyclodecanyl group.

  As further substituents of these alkyl groups and cycloalkyl groups, alkyl groups (1 to 4 carbon atoms), halogen atoms, hydroxyl groups, alkoxy groups (1 to 4 carbon atoms), carboxyl groups, alkoxycarbonyl groups (carbon numbers) 2-6). Examples of the substituent that the alkyl group, alkoxy group, alkoxycarbonyl group and the like may further have include a hydroxyl group, a halogen atom, and an alkoxy group.

  The structures represented by the general formulas (pI) to (pV) in the resin can be used for protecting alkali-soluble groups. Examples of the alkali-soluble group include various groups known in this technical field.

  Specific examples include a structure in which a hydrogen atom of a carboxylic acid group, a sulfonic acid group, a phenol group, or a thiol group is substituted with a structure represented by the general formulas (pI) to (PV), preferably a carboxylic acid Group, a hydrogen atom of a sulfonic acid group is substituted with a structure represented by general formulas (pI) to (pV).

  As the repeating unit having an alkali-soluble group protected by the structure represented by the general formulas (pI) to (pV), a repeating unit represented by the following general formula (PA) is preferable.

Here, R represents a hydrogen atom, a halogen atom, or a linear or branched alkyl group having 1 to 4 carbon atoms. A plurality of R may be the same or different.
A represents a single bond, an alkylene group, an ether group, a thioether group, a carbonyl group, an ester group, an amide group, a sulfonamide group, a urethane group, or a urea group, or a combination of two or more groups. Represents. A single bond and —COO—CH ₂ — are preferable.
Rp ₁ represents any group of the above formulas (pI) to (pV).

  The repeating unit represented by the general formula (PA) is most preferably a repeating unit of 2-alkyl-2-adamantyl (meth) acrylate and dialkyl (1-adamantyl) methyl (meth) acrylate.

  Hereinafter, although the specific example of the repeating unit shown by general formula (PA) is shown, this invention is not limited to this.

In the formula, Rx represents H, CH ₃ , CF ₃ or CH ₂ OH, and Rxa and Rxa each independently represents an alkyl group having 1 to 4 carbon atoms.

Examples of the halogen atom in the general formula (II-AB), R ₁₁ ′, and R ₁₂ ′ include a chlorine atom, a bromine atom, a fluorine atom, and an iodine atom.
Examples of the alkyl group for R ₁₁ ′ and R ₁₂ ′ include linear or branched alkyl groups having 1 to 10 carbon atoms.

The atomic group for forming the alicyclic structure of Z ′ is an atomic group that forms a repeating unit of an alicyclic hydrocarbon which may have a substituent in the resin, and in particular, a bridged alicyclic ring An atomic group for forming a bridged alicyclic structure forming a repeating unit of the formula hydrocarbon is preferred.
Examples of the skeleton of the alicyclic hydrocarbon formed include the same alicyclic hydrocarbon groups as R _{12 to} R _{25 in} the general formulas (pI) to (pV).
The alicyclic hydrocarbon skeleton may have a substituent. Examples of such a substituent include R ₁₃ ′ to R ₁₆ ′ in the general formula (II-AB1) or (II-AB2).

In the alicyclic hydrocarbon-based acid-decomposable resin according to the present invention, the group decomposed by the action of an acid has a partial structure containing the alicyclic hydrocarbon represented by the general formula (pI) to the general formula (pV). It can be contained in at least one kind of repeating unit among the repeating unit having, the repeating unit represented by formula (II-AB), and the repeating unit of the copolymerization component described later.
One acid-decomposable repeating unit may be used, but it is preferable to use two or more acid-decomposable repeating units having different numbers of carbon atoms in the acid leaving group. Thereby, the balance between the resolution and the exposure latitude is improved.

Various substituents of R ₁₃ ′ to R ₁₆ ′ in the general formula (II-AB1) or the general formula (II-AB2) are atomic groups for forming the alicyclic structure in the general formula (II-AB). It can also be a substituent of the atomic group Z for forming a bridged alicyclic structure.

  Specific examples of the repeating unit represented by the general formula (II-AB1) or (II-AB2) include the following specific examples, but the present invention is not limited to these specific examples.

  The alicyclic hydrocarbon-based acid-decomposable resin of the present invention preferably has a lactone group. As the lactone group, any group can be used as long as it contains a lactone structure, but a group containing a 5- to 7-membered ring lactone structure is preferable, and a polycyclic structure is added to the 5- to 7-membered ring lactone structure. In addition, it is preferable that another ring structure is condensed in a form that forms a spiro structure. It is more preferable to have a repeating unit having a group having a lactone structure represented by any of the following general formulas (LC1-1) to (LC1-16). Further, a group having a lactone structure may be directly bonded to the main chain. Preferred lactone structures are (LC1-1), (LC1-4), (LC1-5), (LC1-6), (LC1-13), (LC1-14), and a specific lactone structure is used. This improves line edge roughness and development defects.

The lactone structure moiety may or may not have a substituent (Rb ₂ ). Preferred substituents (Rb ₂ ) include an alkyl group having 1 to 8 carbon atoms, a cycloalkyl group having 4 to 7 carbon atoms, an alkoxy group having 1 to 8 carbon atoms, an alkoxycarbonyl group having 1 to 8 carbon atoms, and a carboxyl group. , Halogen atom, hydroxyl group, cyano group, acid-decomposable group and the like. n2 represents an integer of 0 to 4. When n2 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.

As the repeating unit having a group having a lactone structure represented by any of the general formulas (LC1-1) to (LC1-16), R _{13 in the} general formula (II-AB1) or (II-AB2) may be used. Wherein at least one of 'to R ₁₆ ' has a group represented by the general formulas (LC1-1) to (LC1-16) (for example, R _{5 of} -COOR ₅ is represented by the general formulas (LC1-1) to (LC1) -16) or a repeating unit represented by the following general formula (AI).

In general formula (AI),
Rb ₀ represents a hydrogen atom, a halogen atom, or an alkyl group having 1 to 4 carbon atoms.
Preferred substituents that the alkyl group represented by 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 or a methyl group.
Ab represents a single bond, an alkylene group, a divalent linking group having a monocyclic or polycyclic alicyclic hydrocarbon structure, an ether group, an ester group, a carbonyl group, a carboxyl group, or a divalent group obtained by combining these. To express.
Ab is preferably a single bond or a linking group represented by —Ab ₁ —CO ₂ —. Ab ₁ is a linear, branched alkylene group, monocyclic or polycyclic cycloalkylene group, preferably a methylene group, an ethylene group, a cyclohexyl group, an adamantyl group, or a norbornyl group.
V represents a group represented by any one of the general formulas (LC1-1) to (LC1-16).

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

  The content of the repeating unit having a lactone structure is preferably from 15 to 60 mol%, more preferably from 20 to 50 mol%, still more preferably from 30 to 50 mol%, based on all repeating units in the polymer.

Preferred repeating units having a lactone group include the following repeating units.
By selecting the optimum lactone structure, the pattern profile and the density dependence become good.

  The alicyclic hydrocarbon-based acid-decomposable resin of the present invention preferably has a repeating unit having an alicyclic hydrocarbon structure substituted with a polar group. This improves the substrate adhesion and developer compatibility. The alicyclic hydrocarbon structure of the alicyclic hydrocarbon structure substituted with a polar group is preferably an adamantyl group, a diamantyl group, or a norbornane group. The polar group is preferably a hydroxyl group or a cyano group. As the alicyclic hydrocarbon structure substituted with a preferable polar group, partial structures represented by the following (VIIa) to (VIId) are preferable.

In general formulas (VIIa) to (VIIc),
R _{2c to} R _4c each independently represents a hydrogen atom, a hydroxyl group or a cyano group. However, at least one of R _{2c to} R _4c represents a hydroxyl group or a cyano group. Preferably, one or two of R _{2c to} R _4c are a hydroxyl group and the rest are hydrogen atoms. In general formula (VIIa), it is more preferable that two of R _{2c to} R _4c are a hydroxyl group and the remaining is a hydrogen atom.

As the repeating unit having a group represented by general formulas (VIIa) to (VIId), at least one of R ₁₃ ′ to R ₁₆ ′ in general formula (II-AB1) or (II-AB2) is generally Those having a group represented by formulas (VIIa) to (VIId) (for example, R _{5 in} —COOR ₅ represents a group represented by general formula (VIIa) to (VIId)), or the following general formula (AIIa) The repeating unit represented by-(AIId) can be exemplified.

In general formulas (AIIa) to (AIId),
R _1c represents a hydrogen atom, a methyl group, a trifluoromethyl group or a hydroxymethyl group.
R _2c to R _4c are in the general formula (VIIa) ~ (VIIc), same meanings as R _2c to R _4c.

  The content of the repeating unit having an alicyclic hydrocarbon structure substituted with a polar group is preferably 5 to 40 mol%, more preferably 5 to 30 mol%, still more preferably 10 to 25 mol based on all repeating units in the polymer. %.

  Specific examples of the repeating units represented by the general formulas (AIIa) to (AIId) are given below, but the present invention is not limited thereto.

  The alicyclic hydrocarbon-based acid-decomposable resin of the present invention may have a repeating unit represented by the following general formula (VIII).

In general formula (VIII):
Z ₂ represents —O— or —N (R ₄₁ ) —. R ₄₁ represents a hydrogen atom, a hydroxyl group, an alkyl group, or —OSO ₂ —R ₄₂ . R ₄₂ represents an alkyl group, a cycloalkyl group or a camphor residue. The alkyl group of R ₄₁ and R ₄₂ may be substituted with a halogen atom (preferably a fluorine atom) or the like.

  Examples of the repeating unit represented by the general formula (VIII) include the following specific examples, but the present invention is not limited thereto.

  The alicyclic hydrocarbon-based acid-decomposable resin of the present invention preferably has a repeating unit having an alkali-soluble group. As an alkali-soluble group, a carboxyl group, a sulfonamide group, a sulfonylimide group, a bisulsulfonylimide group, an aliphatic alcohol substituted with an electron-attracting group at the α-position (preferably a structure represented by the following general formula (F1)) It is more preferable to have a repeating unit having a carboxyl group.

In general formula (F1),
R _{50 to} R ₅₅ each independently represents a hydrogen atom, a fluorine atom or an alkyl group. However, at least one of R _{50 to} R ₅₅ represents a fluorine atom or an alkyl group in which at least one hydrogen atom is substituted with a fluorine atom, and all of R _{50 to} R ₅₅ are preferably fluorine atoms. .

  By containing the repeating unit having an alkali-soluble group, the resolution in contact hole applications is increased. The repeating unit having an alkali-soluble group includes a repeating unit in which an alkali-soluble group is directly bonded to the main chain of the resin, such as a repeating unit of acrylic acid or methacrylic acid, or an alkali in the main chain of the resin through a linking group. Either a repeating unit to which a soluble group is bonded, or a polymerization initiator or chain transfer agent having an alkali-soluble group is used at the time of polymerization and introduced at the end of the polymer chain, and the linking group is monocyclic or polycyclic. It may have a cyclic hydrocarbon structure. Most preferred is a repeating unit of acrylic acid or methacrylic acid.

  As for content of the repeating unit which has an alkali-soluble group, 1-20 mol% is preferable with respect to all the repeating units in a polymer, More preferably, it is 3-15 mol%, More preferably, it is 5-10 mol%.

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

  The alicyclic hydrocarbon-based acid-decomposable resin of the present invention may further have a repeating unit having an alicyclic hydrocarbon structure and not exhibiting acid decomposability. This can reduce the elution of low molecular components from the resist film to the immersion liquid during immersion exposure. Examples of such a repeating unit include 1-adamantyl (meth) acrylate, tricyclodecanyl (meth) acrylate, and cyclohexyl (meth) acrylate.

  In addition to the above repeating structural units, the alicyclic hydrocarbon-based acid-decomposable resin of the present invention has a dry etching resistance, standard developer suitability, substrate adhesion, resist profile, and resolving power that is a general necessary characteristic of a resist. Various repeating structural units can be contained for the purpose of adjusting heat resistance, sensitivity, and the like.

  In addition, any addition-polymerizable unsaturated compound that can be copolymerized with monomers corresponding to the above various repeating structural units may be copolymerized.

  In alicyclic hydrocarbon-based acid-decomposable resins, the molar ratio of each repeating structural unit is the resist's dry etching resistance, standard developer suitability, substrate adhesion, resist profile, and resolution that is a general required performance of resists. In order to adjust heat resistance, sensitivity, etc., it is set appropriately.

  In the alicyclic hydrocarbon-based acid-decomposable resin, the content of the repeating unit having an acid-decomposable group is preferably 10 to 60 mol%, more preferably 20 to 50 mol%, still more preferably 25 in all repeating structural units. -40 mol%.

  In the alicyclic hydrocarbon-based acid-decomposable resin, the content of the repeating unit having a partial structure containing the alicyclic hydrocarbon represented by the general formulas (pI) to (pV) is 20 to 70 in all the repeating structural units. The mol% is preferable, more preferably 20 to 50 mol%, still more preferably 25 to 40 mol%.

  In the alicyclic hydrocarbon-based acid-decomposable resin, the content of the repeating unit represented by the general formula (II-AB) is preferably 10 to 60 mol%, more preferably 15 to 55 mol% in all repeating structural units. More preferably, it is 20-50 mol%.

  When the photosensitive composition of the present invention is for ArF exposure, the resin preferably does not have an aromatic group from the viewpoint of transparency to ArF light.

  The alicyclic hydrocarbon-based acid-decomposable resin used in the present invention is preferably one in which all of the repeating units are composed of (meth) acrylate-based repeating units. In this case, all of the repeating units may be methacrylate-based, all of the repeating units may be acrylate-based, or methacrylate / acrylate-based mixed, but the acrylate-based repeating unit is 50 mol% or less of the total repeating units. It is preferable. More preferably, 20 to 50% of repeating units having a partial structure containing an alicyclic hydrocarbon represented by general formulas (pI) to (pV), 20 to 50% of repeating units having a lactone structure, and a polar group are substituted. A copolymer having 5 to 30% of repeating units having an alicyclic hydrocarbon structure, or a copolymer having 0 to 20% of other repeating units.

Particularly preferable resins include 20 to 50 mol% of repeating units having an acid-decomposable group represented by the following general formulas (ARA-1) to (ARA-5), and general formulas (ARL-1) to (ARL-7). ) Having a lactone group represented by general formula (ARH-1) to (ARH-3) and having a alicyclic hydrocarbon structure substituted with a polar group represented by formula (ARH-1) to (ARH-3) 5 Resin containing ˜30 mol%, or further a repeating unit containing a carboxyl group or a structure represented by the general formula (F1), a repeating unit having an alicyclic hydrocarbon structure and not exhibiting acid decomposability It is a resin containing ˜20 mol%.
(In the formula, Rxy ₁ represents a hydrogen atom or a methyl group, and Rxa ₁ and Rxb ₁ each independently represents a methyl group or an ethyl group.)

  When the photosensitive composition of the present invention is used as an upper layer resist of a multilayer resist, the resin as the component (B) preferably has a silicon atom.

As the resin having a silicon atom and decomposing by the action of an acid to increase the solubility in an alkaline developer, a resin having a silicon atom in at least one of a main chain and a side chain can be used. Examples of the resin having a siloxane structure in the side chain of the resin include, for example, an olefin monomer having a silicon atom in the side chain, maleic anhydride and a (meth) acrylic acid monomer having an acid-decomposable group in the side chain. Mention may be made of copolymers.
As the resin having a silicon atom, a resin having a trialkylsilyl structure or a monocyclic or polycyclic siloxane structure is preferable, and a resin having a structure represented by the following general formulas (SS-1) to (SS-4) is used. The (meth) acrylic acid ester-based repeating unit, vinyl-based repeating unit or allyl-based repeating unit having a structure represented by the general formulas (SS-1) to (SS-4) is more preferable.

In general formulas (SS-1) to (SS-4),
Rs represents an alkyl group having 1 to 5 carbon atoms, preferably a methyl group or an ethyl group.

  The resin having a silicon atom preferably has a repeating unit having two or more different types of silicon atoms, more preferably (Sa) a repeating unit having 1 to 4 silicon atoms and (Sb) 5 to 10 silicon atoms. A resin having both of the repeating units, and more preferably, at least one repeating unit having a structure represented by formulas (SS-1) to (SS-3) and formula (SS-4). It is resin which has a repeating unit which has the structure represented by these.

  Although the following (SI-1)-(SI-5) is mentioned as a specific example of resin which has a preferable silicon atom, This invention is not limited to this.

The resin of component (B) can be synthesized according to a conventional method (for example, radical polymerization). For example, as a general synthesis method, a monomer polymerization method in which a monomer species and an initiator are dissolved in a solvent and the polymerization is performed by heating, and a solution of the monomer species and the initiator is dropped into the heating solvent over 1 to 10 hours. The dropping polymerization method is added, and the dropping polymerization method is preferable. Examples of the reaction solvent include ethers such as tetrahydrofuran, 1,4-dioxane, diisopropyl ether, ketones such as methyl ethyl ketone and methyl isobutyl ketone, ester solvents such as ethyl acetate, amide solvents such as dimethylformamide and dimethylacetamide, Furthermore, the solvent which melt | dissolves the composition of this invention like the below-mentioned propylene glycol monomethyl ether acetate, propylene glycol monomethyl ether, and cyclohexanone is mentioned. More preferably, the polymerization is performed using the same solvent as that used in the resist composition of the present invention. Thereby, 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 examples of the initiator include azobisisobutyronitrile, azobisdimethylvaleronitrile, dimethyl 2,2′-azobis (2-methylpropionate) and the like. A chain transfer agent such as a thiol compound may be used in combination with the polymerization initiator. If desired, an initiator is added or added in portions, and after completion of the reaction, it is put into a solvent and a desired polymer is recovered by a method such as powder or solid recovery. The concentration of the reaction is 5 to 50% by mass, preferably 10 to 30% by mass. The reaction temperature is usually 10 ° C to 150 ° C, preferably 30 ° C to 120 ° C, more preferably 60-100 ° C.

The weight average molecular weight of the resin of component (B) is preferably 1,000 to 200,000, more preferably 3,000 to 20,000, and most preferably 5,000 to as a polystyrene equivalent value by GPC method. 15,000. 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 molecular weight distribution (dispersity) of the component (B) resin is usually 1 to 5, preferably 1 to 2, more preferably 1.3 to 2. 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.

In the photosensitive composition of the present invention, the blending amount of all the resins according to the present invention in the entire composition is preferably 60 to 99% by mass, more preferably 80 to 98% by mass in the total solid content.
In the present invention, the resins may be used alone or in combination.

Solubility control compound having a molecular weight of 3000 or less having at least one selected from an alkali-soluble group, a hydrophilic group, and an acid-decomposable group. The photosensitive composition of the present invention includes an alkali-soluble group, a hydrophilic group, and an acid-decomposable group. A dissolution controlling compound having a molecular weight of 3000 or less (hereinafter also referred to as “solubility controlling compound”) having at least one may be added.
Examples of the dissolution control compound include a carboxyl group, a sulfonylimide group, a compound having an alkali-soluble group such as a hydroxyl group substituted at the α-position with a fluoroalkyl group, a hydroxyl group, a lactone group, a cyano group, an amide group, a pyrrolidone group, a sulfone group. A compound having a hydrophilic group such as an amide group or a compound containing a group capable of decomposing by the action of an acid to release an alkali-soluble group or a hydrophilic group is preferable. The group capable of decomposing by the action of an acid to release an alkali-soluble group or a hydrophilic group is preferably a group in which a carboxyl group or a hydroxyl group is protected with an acid-decomposable group. In order not to lower the permeability of 220 nm or less as the dissolution control compound, it is preferable to use a compound that does not contain an aromatic ring, or to use a compound having an aromatic ring in an amount of 20 wt% or less based on the solid content of the composition.
Preferred dissolution control compounds include carboxylic acid compounds having an alicyclic hydrocarbon structure such as adamantane (di) carboxylic acid, norbornane carboxylic acid, cholic acid, or the like, compounds in which the carboxylic acid is protected with an acid-decomposable group, saccharides, and the like. A polyol or a compound obtained by protecting the hydroxyl group with an acid-decomposable group is preferred.

  The molecular weight of the dissolution controlling compound in the present invention is 3000 or less, preferably 300 to 3000, and more preferably 500 to 2500.

  The addition amount of the dissolution control compound is preferably 3 to 40% by mass, more preferably 5 to 20% by mass, based on the solid content of the photosensitive composition.

  Specific examples of the dissolution control compound are shown below, but the present invention is not limited thereto.

Resin soluble in alkaline developer The alkali dissolution rate of a resin soluble in an alkaline developer (hereinafter also referred to as “alkali-soluble resin”) used in the negative photosensitive composition is 0.261 N tetramethylammonium. Those measured at 23 ° C. with a hydroxide (TMAH) are preferably 20 kg / sec or more.
Particularly preferred is 200 liters / second or more.

  Examples of the alkali-soluble resin used in the present invention include novolak resin, hydrogenated novolak resin, acetone-pyrogalol resin, o-polyhydroxystyrene, m-polyhydroxystyrene, p-polyhydroxystyrene, hydrogenated polyhydroxystyrene, Halogen- or alkyl-substituted polyhydroxystyrene, hydroxystyrene-N-substituted maleimide copolymer, o / p- and m / p-hydroxystyrene copolymer, partially O-alkylated product of hydroxyl group of polyhydroxystyrene (for example, 5 ˜30 mol% O-methylated product, O- (1-methoxy) ethylated product, O- (1-ethoxy) ethylated product, O-2-tetrahydropyranylated product, O- (t-butoxycarbonyl) methylated product, etc. ) Or an O-acylated product (for example, 5 to 30 mol) % O-acetylated product, O- (t-butoxy) carbonylated product, etc.), styrene-maleic anhydride copolymer, styrene-hydroxystyrene copolymer, α-methylstyrene-hydroxystyrene copolymer, carboxyl group-containing Examples thereof include, but are not limited to, methacrylic resins and derivatives thereof, and polyvinyl alcohol derivatives.

  Particularly preferred alkali-soluble resins are novolak resins and o-polyhydroxystyrene, m-polyhydroxystyrene, p-polyhydroxystyrene and copolymers thereof, alkyl-substituted polyhydroxystyrene, partially O-alkylated polyhydroxystyrene. Or an O-acylated product, a styrene-hydroxystyrene copolymer, and an α-methylstyrene-hydroxystyrene copolymer.

  The novolak resin is obtained by subjecting a predetermined monomer as a main component to addition condensation with aldehydes in the presence of an acidic catalyst.

  The weight average molecular weight of alkali-soluble resin is 2000 or more, Preferably it is 5000-200000, More preferably, it is 5000-100000.

  Here, the weight average molecular weight is defined as a polystyrene equivalent value of gel permeation chromatography.

  These alkali-soluble resins in the present invention may be used in combination of two or more.

  The usage-amount of alkali-soluble resin is 40-97 mass% normally with respect to solid content of the whole composition of a photosensitive composition, Preferably it is 60-90 mass%.

Acid cross-linking agent that crosslinks with alkali-soluble resin by the action of acid An acid cross-linking agent that cross-links with alkali-soluble resin by the action of acid (hereinafter also referred to as “crosslinking agent”) is used in the negative photosensitive composition of the present invention. Is done.

As the crosslinking agent, any compound that crosslinks with an alkali-soluble resin by the action of an acid can be used, but the following (1) to (3) are preferable.
(1) Hydroxymethyl, alkoxymethyl, and acyloxymethyl forms of phenol derivatives.
(2) A compound having an N-hydroxymethyl group, an N-alkoxymethyl group, or an N-acyloxymethyl group.
(3) A compound having an epoxy group.

  The alkoxymethyl group preferably has 6 or less carbon atoms, and the acyloxymethyl group preferably has 6 or less carbon atoms.

  Among these crosslinking agents, particularly preferable ones are listed below, but the present invention is not limited to these.

In the formula, L _{1 to} L ₈ may be the same or different and each represents a hydrogen atom, a hydroxymethyl group, a methoxymethyl group, an ethoxymethyl group, or an alkyl group having 1 to 6 carbon atoms.

  The crosslinking agent is used in an amount of usually 3 to 70% by mass, preferably 5 to 50% by mass, in the solid content of the negative photosensitive composition.

Basic Compound The photosensitive composition of the present invention preferably contains a basic compound in order to reduce the change in performance over time from exposure to heating or to control the diffusibility of the acid generated by exposure in the film. .

Examples of basic compounds include nitrogen-containing basic compounds and onium salt compounds.
Preferred examples of the structure of the nitrogen-containing basic compound include compounds having partial structures represented by the following general formulas (A) to (E).

In general formula (A),
R ^250, R ²⁵¹ and R ²⁵² are each independently a hydrogen atom, an alkyl having 1 to 20 carbon atoms, a cycloalkyl group or an aryl group having 6 to 20 carbon atoms having 3 to 20 carbon atoms, R ²⁵⁰ and R ²⁵¹ may be bonded to each other to form a ring. These may have a substituent. Examples of the alkyl group and cycloalkyl group having a substituent include an aminoalkyl group having 1 to 20 carbon atoms, an aminocycloalkyl group having 3 to 20 carbon atoms, and 1 to 1 carbon atoms. A 20 hydroxyalkyl group or a C 3-20 hydroxycycloalkyl group is preferred.
These may contain an oxygen atom, a sulfur atom, or a nitrogen atom in the alkyl chain.

In general formula (E),
R ²⁵³ , R ²⁵⁴ , R ²⁵⁵ and R ²⁵⁶ each independently represent an alkyl group having 1 to 6 carbon atoms or a cycloalkyl group having 3 to 6 carbon atoms.

  Preferable compounds include guanidine, aminopyrrolidine, pyrazole, pyrazoline, piperazine, aminomorpholine, aminoalkylmorpholine, and piperidine, and may have a substituent. More preferable compounds include compounds having an imidazole structure, a diazabicyclo structure, an onium hydroxide structure, an onium carboxylate structure, a trialkylamine structure, an aniline structure or a pyridine structure, an alkylamine derivative having a hydroxyl group and / or an ether bond, a hydroxyl group and / or Or the aniline derivative which has an ether bond etc. can be mentioned.

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

These basic compounds are used alone or in combination of two or more.
The usage-amount of a basic compound is 0.001-10 mass% normally on the basis of solid content of a photosensitive composition, Preferably it is 0.01-5 mass%. In order to obtain a sufficient addition effect, 0.001% by mass or more is preferable, and 10% by mass or less is preferable in terms of sensitivity and developability of the non-exposed area.

Fluorine and / or silicon-based surfactant The photosensitive composition of the present invention further comprises a fluorine-based and / or silicon-based surfactant (fluorine-based surfactant and silicon-based surfactant, both fluorine atom and silicon atom). It is preferable to contain any one or two or more kinds of surfactants.

  When the photosensitive composition of the present invention contains fluorine and / or a silicon-based surfactant, adhesion and development defects can be obtained with good sensitivity and resolution when using an exposure light source of 250 nm or less, particularly 220 nm or less. A small resist pattern can be provided.

  Examples of these fluorine and / or silicon surfactants include, for example, JP-A No. 62-36663, JP-A No. 61-226746, JP-A No. 61-226745, JP-A No. 62-170950, JP 63-34540 A, JP 7-230165 A, JP 8-62834 A, JP 9-54432 A, JP 9-5988 A, JP 2002-277862 A, US Patent Nos. 5,405,720, 5,360,692, 5,529,881, 5,296,330, 5,436,098, 5,576,143, 5,294,511, 5,824,451 Surfactant can be mentioned, The following commercially available surfactant can also be used as it is.

  Examples of commercially available surfactants that can be used include F-top EF301, EF303 (manufactured by Shin-Akita Kasei Co., Ltd.), Florard FC430, 431 (manufactured by Sumitomo 3M Co., Ltd.), MegaFuck F171, F173, F176, F189, R08 (Dainippon Ink Chemical Co., Ltd.), Surflon S-382, SC101, 102, 103, 104, 105, 106 (Asahi Glass Co., Ltd.), Troisol S-366 (Troy Chemical Co., Ltd.), etc. Fluorine type surfactant or silicon type surfactant can be mentioned. Polysiloxane polymer KP-341 (manufactured by Shin-Etsu Chemical Co., Ltd.) can also be used as a silicon-based surfactant.

  In addition to the known surfactants described above, surfactants are derived from fluoroaliphatic compounds produced by the telomerization method (also referred to as the telomer method) or the oligomerization method (also referred to as the oligomer method). A surfactant using a polymer having a fluoroaliphatic group can be used. The fluoroaliphatic compound can be synthesized by the method described in JP-A-2002-90991.

  As the polymer having a fluoroaliphatic group, a copolymer of a monomer having a fluoroaliphatic group and (poly (oxyalkylene)) acrylate and / or (poly (oxyalkylene)) methacrylate is preferable and distributed irregularly. It may be block copolymerized. Examples of the poly (oxyalkylene) group include a poly (oxyethylene) group, a poly (oxypropylene) group, a poly (oxybutylene) group, and the like, and a poly (oxyethylene, oxypropylene, and oxyethylene group). A unit having different chain lengths in the same chain length, such as a block link) or poly (block link of oxyethylene and oxypropylene) may be used. Furthermore, a copolymer of a monomer having a fluoroaliphatic group and (poly (oxyalkylene)) acrylate (or methacrylate) is not only a binary copolymer but also a monomer having two or more different fluoroaliphatic groups, Further, it may be a ternary or higher copolymer obtained by simultaneously copolymerizing two or more different (poly (oxyalkylene)) acrylates (or methacrylates).

Examples of commercially available surfactants include Megafac F178, F-470, F-473, F-475, F-476, and F-472 (Dainippon Ink Chemical Co., Ltd.). Further, a copolymer of an acrylate (or methacrylate) having a C ₆ F ₁₃ group and (poly (oxyalkylene)) acrylate (or methacrylate), an acrylate (or methacrylate) having a C ₆ F ₁₃ group and (poly (oxy) (Ethylene)) acrylate (or methacrylate) and (poly (oxypropylene)) acrylate (or methacrylate) copolymer, acrylate (or methacrylate) and (poly (oxyalkylene)) acrylate having C ₈ F ₁₇ groups (or Copolymer of acrylate (or methacrylate), (poly (oxyethylene)) acrylate (or methacrylate), and (poly (oxypropylene)) acrylate (or methacrylate) having a C ₈ F ₁₇ group Coalesce, etc. Can.

  The amount of fluorine and / or silicon surfactant used is preferably 0.0001 to 2% by mass, more preferably 0.001 to 1% by mass, based on the total amount of the photosensitive composition (excluding the solvent). is there.

Surface Hydrophobic Resin When a photosensitive film made of the photosensitive composition of the present invention is exposed through immersion water, a surface hydrophobic resin can be further added to the photosensitive composition part t as necessary. . Thereby, the receding contact angle on the resist film surface can be improved and the immersion water followability can be improved.
As the surface hydrophobizing resin, any resin can be used as long as the receding contact angle of the surface can be improved by addition, but a resin having at least one of fluorine atom and silicon atom is preferable. The addition amount can be adjusted as appropriate so that the receding contact angle of the resist film is 60 ° to 80 °, but preferably 0.1 to 5% by mass.

Organic Solvent The photosensitive composition of the present invention is used by dissolving the above components in a predetermined organic solvent.

  Examples of the organic solvent that can be used include ethylene dichloride, cyclohexanone, cyclopentanone, 2-heptanone, γ-butyrolactone, methyl ethyl ketone, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, 2-methoxyethyl acetate, ethylene glycol monoethyl. Ether acetate, propylene glycol monomethyl ether, propylene glycol monomethyl ether acetate, toluene, ethyl acetate, methyl lactate, ethyl lactate, methyl methoxypropionate, ethyl ethoxypropionate, methyl pyruvate, ethyl pyruvate, propyl pyruvate, N, N -Dimethylformamide, dimethyl sulfoxide, N-methylpyrrolidone, tetrahydrofuran, etc.

In the present invention, the organic solvent may be used alone or in combination, but it is preferable to use a mixed solvent containing two or more solvents having different functional groups. As a result, the solubility of the material is increased, and not only the generation of particles over time can be suppressed, but also a good pattern profile can be obtained. The mixed solvent containing two or more solvents having different functional groups is at least selected from a solvent containing a hydroxyl group, a solvent having an ester structure, a solvent having a ketone structure, a solvent having a lactone structure, and a solvent having a carbonate structure. A mixed solvent containing two kinds is preferred.
As the mixed solvent containing two or more kinds of solvents having different functional groups, the following mixed solvents (S1) to (S6) are preferable. (S1) At least a solvent containing a hydroxyl group and a solvent not containing a hydroxyl group Mixed solvent containing,
(S2) a mixed solvent containing at least a solvent having an ester structure and a solvent having a ketone structure;
(S3) a mixed solvent containing at least a solvent having an ester structure and a solvent having a lactone structure;
(S4) a mixed solvent containing at least a solvent having an ester structure, a solvent having a lactone structure, and a solvent having a hydroxyl group;
(S5) a mixed solvent containing at least a solvent having an ester structure, a solvent having a carbonate structure, and a solvent having a hydroxyl group;
(S6) A mixed solvent containing at least a solvent having an ester structure, a solvent having a ketone structure, and a solvent having a lactone structure.
As a result, the generation of particles during storage of the resist solution can be reduced, and the generation of defects during application can be suppressed.

Examples of the solvent containing a hydroxyl group include ethylene glycol, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, propylene glycol, propylene glycol monomethyl ether, propylene glycol monoethyl ether, ethyl lactate, and the like. And propylene glycol monomethyl ether and ethyl lactate are more preferred.
Examples of the solvent not containing a hydroxyl group include propylene glycol monomethyl ether acetate, ethyl ethoxypropionate, 2-heptanone, γ-butyrolactone, cyclohexanone, butyl acetate, N-methylpyrrolidone, N, N-dimethylacetamide, dimethyl sulfoxide and the like. Among these, propylene glycol monomethyl ether acetate, ethyl ethoxypropionate, 2-heptanone, γ-butyrolactone, cyclohexanone, and butyl acetate are more preferable, and propylene glycol monomethyl ether acetate, ethyl ethoxypropionate. 2-heptanone and cyclohexanone are particularly preferred.
Examples of the solvent having a ketone structure include cyclohexanone and 2-heptanone, and 2-heptanone is preferable.
Examples of the solvent having an ester structure include propylene glycol monomethyl ether acetate, ethyl ethoxypropionate, and butyl acetate, and propylene glycol monomethyl ether acetate is preferable.
Examples of the solvent having a lactone structure include γ-butyrolactone.
Examples of the solvent having a carbonate structure include propylene carbonate and ethylene carbonate, and propylene carbonate is preferred.

In (S1), the mixing ratio (mass) of the solvent containing a hydroxyl group and the solvent not containing a hydroxyl group is 1/99 to 99/1, preferably 10/90 to 90/10, more preferably 20/80 to. 60/40. A mixed solvent containing 50% by mass or more of a solvent not containing a hydroxyl group is particularly preferred from the viewpoint of coating uniformity.
The mixing ratio (mass) of the solvent having an ester structure and the solvent having a ketone structure in (S2) is 1/99 to 99/1, preferably 10/90 to 90/10, more preferably 40/60 to 80/20. A mixed solvent containing 50% by mass or more of a solvent having an ester structure is particularly preferable from the viewpoint of coating uniformity.
In (S3), the mixing ratio (mass) of the solvent having an ester structure and the solvent having a lactone structure is 70/30 to 99/1, preferably 80/20 to 99/1, more preferably 90/10 to 10. 99/1. A mixed solvent containing 70% by mass or more of a solvent having an ester structure is particularly preferable from the viewpoint of stability over time.
When mixing the solvent having an ester structure, the solvent having a lactone structure, and the solvent containing a hydroxyl group in (S4), the solvent having an ester structure is 30 to 80% by weight, and the solvent having a lactone structure is 1 to 20% by weight. %, Preferably containing 10 to 60% by weight of a solvent containing a hydroxyl group.
In (S5), when mixing the solvent having an ester structure, the solvent having a carbonate structure, and the solvent containing a hydroxyl group, the solvent having an ester structure is 30 to 80% by weight, and the solvent having a carbonate structure is 1 to 20% by weight. %, Preferably containing 10 to 60% by weight of a solvent containing a hydroxyl group.
In (S6), when mixing the solvent having an ester structure, the solvent having a ketone structure, and the solvent containing a lactone structure, 30 to 80% by weight of the solvent having an ester structure and 10 to 60% of the solvent having a ketone structure. It is preferable to contain 1 to 20% by weight of a solvent containing a lactone structure.

<Other additives>
The photosensitive composition of the present invention further promotes solubility in dyes, plasticizers, surfactants other than the fluorine and / or silicon surfactants, photosensitizers, and developers as necessary. A compound etc. can be contained.

  The compound that promotes the solubility in the developer that can be used in the present invention is a low molecular weight compound having a molecular weight of 1,000 or less and having two or more phenolic OH groups or one or more carboxy groups. When it has a carboxy group, an alicyclic or aliphatic compound is preferable.

  A preferable addition amount of these dissolution promoting compounds is 2 to 50% by mass, and more preferably 5 to 30% by mass with respect to the resin of component (B). 50 mass% or less is preferable at the point of development residue suppression and the pattern deformation prevention at the time of image development.

  Such phenolic compounds having a molecular weight of 1000 or less can be obtained by referring to methods described in, for example, JP-A-4-1222938, JP-A-2-28531, U.S. Pat. No. 4,916,210, European Patent 219294, and the like. Can be easily synthesized.

  Specific examples of alicyclic or aliphatic compounds having a carboxyl group include carboxylic acid derivatives having a steroid structure such as cholic acid, deoxycholic acid, lithocholic acid, adamantane carboxylic acid derivatives, adamantane dicarboxylic acid, cyclohexane carboxylic acid, cyclohexane Examples thereof include, but are not limited to, dicarboxylic acids.

  In the present invention, a surfactant other than the fluorine-based and / or silicon-based surfactant may be added. Specifically, nonionic interfaces such as polyoxyethylene alkyl ethers, polyoxyethylene alkyl allyl ethers, polyoxyethylene / polyoxypropylene block copolymers, sorbitan aliphatic esters, polyoxyethylene sorbitan aliphatic esters, etc. Mention may be made of activators.

  These surfactants may be added alone or in some combination.

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

  For example, an arbitrary thickness (usually 50 to 500 nm) is applied by a suitable coating method such as a spinner or a coater on a substrate (eg, silicon / silicon dioxide coating) on which a photosensitive composition is used for manufacturing a precision integrated circuit device. Apply with. After application, the resist film is formed by drying by spinning or baking. The bake temperature can be set as appropriate, but is usually 60 to 150 ° C, and preferably 90 to 130 ° C.

Next, exposure is performed through a mask or the like for pattern formation.
Although an exposure amount can be set suitably, it is 1-100 mJ / cm < ² > normally. After exposure, preferably, spinning or / and baking is performed, development and rinsing are performed to obtain a pattern.

  Exposure (immersion exposure) may be performed by filling a liquid (immersion medium) having a higher refractive index than air between the photosensitive film and the lens during irradiation with actinic rays or radiation. Thereby, resolution can be improved. As the immersion medium to be used, any liquid can be used as long as it has a higher refractive index than air, but pure water is preferred. Further, an overcoat layer may be further provided on the photosensitive film so that the immersion medium and the photosensitive film do not come into direct contact with each other during the immersion exposure. Thereby, the elution of the composition from the photosensitive film to the immersion medium is suppressed, and development defects are reduced.

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

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

In the development step, an alkaline developer is used as follows. As an alkaline developer of the resist composition, inorganic hydroxides such as sodium hydroxide, potassium hydroxide, sodium carbonate, sodium silicate, sodium metasilicate, and aqueous ammonia, primary amines such as ethylamine and n-propylamine, Secondary amines such as diethylamine and di-n-butylamine, tertiary amines such as triethylamine and methyldiethylamine, alcohol amines such as dimethylethanolamine and triethanolamine, tetramethylammonium hydroxide, tetraethylammonium hydroxide and the like Alkaline aqueous solutions such as quaternary ammonium salts, cyclic amines such as pyrrole and pihelidine can be used.
Furthermore, alcohols and surfactants can be added in appropriate amounts to the alkaline developer.
The alkali concentration of the alkali developer is usually from 0.1 to 20% by mass.
The pH of the alkali developer is usually from 10.0 to 14.0.

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

Examples of the present invention will be described below, but the present invention is not limited thereto.
In the following, Compound I-3 and Example 3 using the compound I-3 are reference examples.

Synthesis Example 1 (Synthesis of Compound (I-1))
5 g of silver trifluoromethanesulfonate and 50 ml of benzene were mixed, and 4.2 g of 1-bromoadamantane dissolved in 50 ml of benzene was added to this over 30 minutes. Stir in the dark for 12 hours. The reaction solution was poured into 300 ml of water and extracted with hexane, and the organic phase was washed with water and saturated brine, dried and concentrated to obtain a crude product. When this was purified by column chromatography, 1.7 g of 1-phenyladamantane was obtained.
1.6 g of 1-phenyladamantane and 1.5 g of diphenyl sulfoxide were mixed with 10 ml of dichloromethane, and 10 g of trifluoroacetic anhydride was added thereto. At −30 ° C., 2.4 g of nonafluorobutanesulfonic acid was added and reacted for 2 hours. After raising the temperature to room temperature and stirring for another 1 hour, the reaction solution was poured onto ice. This was extracted with chloroform, and the organic phase was washed with saturated NaHCO 3 aqueous solution and water and concentrated. Purification by column chromatography gave 2.9 g of compound (I-1).
¹ H-NMR (CDCl ₃ )
δ 1.6 to 2.2 (m, 15H), δ 7.6 to 7.8 (m, 14H)

Synthesis Example 2 (Synthesis of Compound (I-2))
2 g of 4- (1-adamantylmethoxymethyl) phenyldiphenylsulfonium bromide was dissolved in 30 ml of methanol, and 1.36 g of potassium nonafluorobutanesulfonate dissolved in a water / methanol mixture was added thereto. The reaction solution was extracted with chloroform, and the organic phase was washed with water and concentrated to obtain a crude product. When diisopropyl ether was added to this and stirred, powder precipitated. This was collected by filtration and dried, yielding 1.2 g of compound (I-2).
¹ H-NMR (CDCl ₃ )
δ 1.6 to 1.8 (m, 12 H), δ 2.0 (bs, 3H), δ 3.1 (s, 2H), δ 4.6 (s, 2H), δ 7.6 to 7.8 (m, 14H)

  The other compounds (A) were synthesized using the same method.

Synthesis Example 3 (Synthesis of resin (RA-1))
Under a nitrogen stream, 8.4 g of cyclohexanone was placed in a three-necked flask and heated to 80 ° C. To this was added 6.8 g of γ-butyrolactone methacrylate, 4.7 g of 3-hydroxyadamantyl-1-methacrylate, 9.4 g of 2-methyl-2-adamantyl methacrylate, and 13 mol of polymerization initiator V-60 (manufactured by Wako Pure Chemical Industries) with respect to the monomer. % Was dissolved in 75 g of cyclohexanone dropwise over 6 hours. After completion of dropping, the reaction was further carried out at 80 ° C. for 2 hours. The reaction solution was allowed to cool and then added dropwise over 20 minutes to a mixed solution of methanol 900 m / water 100 ml. The precipitated powder was collected by filtration and dried to obtain 178 g of Resin (RA-1). The weight average molecular weight of the obtained resin was 6300 in terms of standard polystyrene, and the dispersity (Mw / Mn) was 1.60.

  Resins (RA-2) to (RA-12) were synthesized using the same method. The weight average molecular weight was adjusted by changing the amount of initiator.

  Hereinafter, the structures of the resins (RA-1) to (RA-12) are shown.

Examples 1-13 and Comparative Examples 1-2
<Resist preparation>
The components shown in Table 1 below were dissolved in a solvent to prepare a solution having a solid content concentration of 7% by mass, and this was filtered through a 0.03 micron polyethylene filter to prepare a positive resist solution. The prepared positive resist solution was evaluated by the following method, and the results are also shown in Table 1.
<Resist evaluation>
An anti-reflective coating DUV-42 manufactured by Brewer Science Co., Ltd. was uniformly applied to 600 angstroms on a silicon substrate subjected to hexamethyldisilazane treatment with a spin coater, dried on a hot plate at 100 ° C. for 90 seconds, and then at 190 ° C. Heat drying was performed for 240 seconds. Thereafter, each positive resist solution was applied by a spin coater and dried at 120 ° C. for 60 seconds to form a 160 nm resist film.
The resist film was exposed with an ArF excimer laser stepper (NA = 0.75, dipole manufactured by ASML) through a mask, and heated on a hot plate at 120 ° C. for 60 seconds immediately after the exposure. Further, the resist film was developed with an aqueous 2.38 mass% tetramethylammonium hydroxide solution at 23 ° C. for 60 seconds, rinsed with pure water for 30 seconds, and then dried to obtain a line pattern.
Pattern collapse evaluation method:
When the exposure amount that reproduces the mask pattern of 75 nm line / 75 nm space is the optimum exposure amount, and the line width of the line pattern formed by further increasing the exposure amount from the optimum exposure amount is reduced, the pattern does not collapse It was defined as the line width that resolves to. The smaller the value, the finer pattern is resolved without falling, and the pattern collapse is less likely to occur and the resolution is higher.
Evaluation method for film loss:
The pattern profile of 90 nm line / 900 nm space (isolated pattern) at the exposure amount for reproducing the mask pattern of 75 nm line / 75 nm space was evaluated.
A rectangle was marked with ◯, a film with a slight film loss was marked with Δ, and a film with a large film loss was marked with x.

    The abbreviations in Table 1 are shown below.

  [Acid generator]

[Basic compounds]
TPSA: triphenylsulfonium acetate DIA: 2,6-diisopropylaniline TEA: triethanolamine PBI: 2-phenylbenzimidazole TMEA: tris (methoxyethoxyethyl) amine PEA: N-phenyldiethanolamine [surfactant]
W-1: MegaFuck F176 (Dainippon Ink Chemical Co., Ltd.) (Fluorine)
W-2: Megafuck R08 (Dainippon Ink Chemical Co., Ltd.) (fluorine and silicon)
W-3: Polysiloxane polymer KP-341 (manufactured by Shin-Etsu Chemical Co., Ltd.) (silicon-based)
W-4: Troisol S-366 (manufactured by Troy Chemical Co., Ltd.) (silicon-based)
〔solvent〕
S1: Propylene glycol methyl ether acetate S2: 2-heptanone S3: Cyclohexanone S4: γ-Butyrolactone S5: Propylene glycol methyl ether S6: Ethyl lactate S7: Propylene carbonate

  From Table 1, it is clear that the photosensitive composition of the present invention has improved pattern collapse performance and good profile.

(Immersion exposure)
<Resist preparation>
The components of Examples 1 to 13 and Comparative Examples 1 and 2 in Table 1 were dissolved in a solvent to prepare a solution having a solid content concentration of 5% by mass, and this was filtered through a 0.03 μm polyethylene filter to obtain a positive resist solution. It was adjusted. The adjusted positive resist solution was evaluated by the following method.
<Resolution evaluation>
An organic antireflection film ARC29A (Nissan Chemical Co., Ltd.) was applied onto a silicon wafer and baked at 205 ° C. for 60 seconds to form a 78 nm antireflection film. A positive resist solution prepared thereon was applied and baked at 115 ° C. for 60 seconds to form a 140 nm resist film.
The wafer thus obtained was subjected to two-beam interference exposure (wet exposure) using pure water as the immersion liquid. In the two-beam interference exposure (wet), as shown in FIG. 1, a laser 1, an aperture 2, a shutter 3, three reflecting mirrors 4, 5, 6 and a condenser lens 7 are used, and a prism 8, liquid The wafer 10 having an antireflection film and a resist film was exposed through an immersion liquid (pure water) 9. The wavelength of the laser 1 was 193 nm, and the prism 8 forming a 65 nm line and space pattern was used. Immediately after the exposure, the resist pattern obtained by heating at 115 ° C. for 90 seconds, developing with an aqueous tetramethylammonium hydroxide solution (2.38%) for 60 seconds, rinsing with pure water, and spin drying is then applied to a scanning electron microscope. (Hitachi S-9260) was used for observation. When the positive resist solutions of Examples 1 to 13 were used, the 65 nm line and space pattern was resolved without causing pattern collapse. When the positive resist solutions of Comparative Examples 1 and 2 were used, pattern collapse was observed in some patterns although the 65 nm line and space pattern was resolved.
It is apparent that the photosensitive composition of the present invention has a good image forming ability even in an exposure method through an immersion liquid.

Example 14 and Comparative Example 3
(1) Formation of lower resist layer FHi-028DD resist (resist for i-line made by Fuji Film Orin Co., Ltd.) was applied to a silicon wafer using a spin coater, baked at 90 ° C. for 90 seconds, and a uniform thickness of 0.55 μm A membrane was obtained.
This was further heated at 200 ° C. for 3 minutes to form a lower resist layer having a thickness of 0.40 μm.
(2) Formation of the upper resist layer The components shown in Table 2 below are dissolved in a solvent to prepare a solution having a solid content of 8% by mass, and the solution is precisely filtered through a membrane filter having a caliber of 0.03 μm to prepare an upper resist composition. did.
An upper resist composition was applied on the lower resist layer in the same manner as the lower layer, and heated at 130 ° C. for 90 seconds to form an upper resist layer having a thickness of 0.20 μm.
(3) Resist evaluation The wafer thus obtained was exposed with an ArF excimer laser stepper (NAML = 0.75 manufactured by ASML) through a mask, and immediately after exposure, heated on a hot plate at 120 ° C. for 90 seconds. Further, the resist film was developed with an aqueous 2.38 mass% tetramethylammonium hydroxide solution at 23 ° C. for 60 seconds, rinsed with pure water for 30 seconds, and then dried to obtain a line pattern.

Pattern collapse evaluation method:
The exposure amount that reproduces a line-and-space mask pattern with a line width of 90 nm was set as the optimal exposure amount, the exposure amount was increased from the optimal exposure amount, and the line width at which the pattern collapsed when the line pattern was thinned was observed. . The smaller the value is, the more pattern can be formed without causing pattern collapse, and the pattern collapse performance is better.
Evaluation method for film loss:
The pattern profile of 100 nm line / 1000 nm space (isolated pattern) at the exposure amount for reproducing the mask pattern of 90 nm line / 90 nm space was evaluated. A rectangle was marked with ◯, a film with a slight film loss was marked with Δ, and a film with a large film loss was marked with x.
The evaluation results are shown in Table 2.

  Hereinafter, the structure of the resin (SI-3) in Table 2 is shown.

  From Table 2, it is clear that the photosensitive composition of the present invention has improved pattern collapse performance and good profile.

Examples 15 to 16 and Comparative Example 4
<Resist preparation>
The components shown in Table 3 below were dissolved in a solvent and filtered through a 0.05 μm polytetrafluoroethylene filter to prepare a positive resist solution having a solid content concentration of 14% by mass.
<Resist evaluation>
The prepared positive resist solution is uniformly coated on a silicon substrate subjected to hexamethyldisilazane treatment using a spin coater, and is heated and dried on a hot plate at 120 ° C. for 90 seconds to obtain a 0.4 μm resist. A film was formed.
The resist film was subjected to pattern exposure using a line and space mask using a KrF excimer laser stepper (NA = 0.63), and heated on a hot plate at 110 ° C. for 90 seconds immediately after the exposure. Further, the resist film was developed with an aqueous 2.38 mass% tetramethylammonium hydroxide solution at 23 ° C. for 60 seconds, rinsed with pure water for 30 seconds, and then dried to form a line pattern.
Method for evaluating the line width at which film loss occurs:
The exposure amount for reproducing an isolated pattern having a line width of 130 nm was set as the optimal exposure amount, and the exposure amount was increased from the optimal exposure amount, and the line width at which film reduction occurred when the line pattern was thinned was observed. The smaller the value, the better the performance because a thinner pattern can be formed without causing film loss.

  Hereinafter, the structures of the resins (R-8) and (R-13) in Table 3 are shown.

  From Table 3, it is clear that the photosensitive composition of the present invention has good film loss generation line width performance.

Examples 17-18 and Comparative Example 5
<Resist preparation>
The components shown in Table 3 were dissolved in a solvent and filtered through a 0.05 μm polytetrafluoroethylene filter to prepare a positive resist solution having a solid content concentration of 11% by mass.
<Resist evaluation>
The prepared positive resist solution is uniformly coated on a silicon substrate subjected to hexamethyldisilazane treatment using a spin coater, and is heated and dried on a hot plate at 120 ° C. for 60 seconds to form a 250 nm resist film. Formed.
This resist film was irradiated with a pattern with an electron beam direct drawing device (acceleration voltage 50 keV), and immediately after irradiation, heated on a hot plate at 120 ° C. for 90 seconds. Further, development was performed at 23 ° C. for 60 seconds using an aqueous tetramethylammonium hydroxide solution having a concentration of 2.38% by mass, rinsed with pure water for 30 seconds, and then dried to form a line and space pattern.
Pattern collapse:
The irradiation dose that reproduces a line-and-space mask pattern with a line width of 120 nm was set as the optimal dose, and the line width at which the pattern collapsed when the line pattern was thinned was increased by increasing the dose from the optimal dose. . The smaller the value is, the more pattern can be formed without causing pattern collapse, and the pattern collapse performance is better.
The evaluation results are shown in Table 4.

  From Table 4, it is clear that the photosensitive composition of the present invention has improved pattern collapse performance.

DESCRIPTION OF SYMBOLS 1 Laser 2 Aperture 3 Shutter 4, 5, 6 Reflection mirror 7 Condensing lens 8 Prism 9 Immersion liquid 10 Wafer having antireflection film and resist film 11 Wafer stage

Claims (7)

A compound represented by the following general formula (I):

In general formula (I),
X ₁ and X ₂ each independently represents an alkyl group, a cycloalkyl group, an aryl group or an aralkyl group. When X ₁ and X ₂ are alkyl groups, they are limited to those in which X ₁ and X ₂ are bonded to form a ring structure.
Ar ₁ represents an aryl group.
Y ₁ represents a single bond or a divalent linking group.
Y ₂ represents a polycyclic hydrocarbon group.
m ₁ represents 0 to 2.
m ₂ represents 0-2.
m ₃ represents 1 or 2.
However, m ₁ + m ₂ + m ₃ = 3.
m ₄ is an integer of 1 to 3.
X ⁻ represents a counter anion. The compound according to claim 1, wherein in the general formula (I), m ₃ = 1. The compound of Claim 1 represented by the following general formula (Ia) or (Ib).

In the general formulas (Ia) and (Ib), Ar ₁ , Y ₁ , Y ₂ , m ₁ , m ₂ , m ₃ , m ₄ and X ⁻ are in the general formula (I). , Ar ₁ , Y ₁ , Y ₂ , m ₁ , m ₂ , m ₃ , m ₄ and X ⁻ . Ar ₂ and Ar ₃ represent an aryl group. In the general formulas (I), (Ia), and (Ib), Y ₂ is a polycyclic hydrocarbon group having an adamantane structure. The described compound. In general formula (I), (Ia), and (Ib), X < ^- > is an organic anion represented by the following general formula (AN1). The compound according to item.
R _c1 —SO ₃ ^— (AN1)
In the general formula (AN1), Rc ₁ represents an organic group. In the general formula (AN1), Rc ₁ is an alkyl group substituted at the 1-position with a fluorine atom or a fluoroalkyl group, or a phenyl group substituted with a fluorine atom or a fluoroalkyl group. The described compound. In the general formulas (I), (Ia) and (Ib), Y ₁ represents an alkylene group, an arylene group, —O—, —S—, —C (═O) —O—, — The SO _2- , -SO _3- , -C (= O) NRd-, -SO ₂ NRd-, or a divalent linking group in which a plurality of these are combined is any one of claims 1 to 6. The compound according to item.

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