JP2006063016A - New compound, polymer and radiation-sensitive resin composition - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a radiation-sensitive resin composition which has high transparency for radiations, has excellent resist fundamental physical properties such as sensitivity, resolution, dry etching resistance, and pattern formation, and has high resolution performance and small pattern line edge roughness, to provide a polymer capable of being used for the composition, and to provide a new compound used for synthesizing the polymer. <P>SOLUTION: This radiation-sensitive resin composition comprising an acid-dissociable group-containing resin which is alkali-insoluble or slightly alkali-soluble and becomes easily alkali-soluble by the action of an acid, and a radiation-sensitive acid-generating agent is characterized in that the acid-dissociable group-containing resin contains groups represented by formula (2) at the molecular ends and has a polystyrene-converted weight-average mol.wt. of 2,000 to 100,000 measured by gel permeation chromatography (GPC). <P>COPYRIGHT: (C)2006,JPO&NCIPI

Description

  The present invention relates to a novel compound, a polymer and a radiation sensitive resin composition, and in particular, various radiations such as deep ultraviolet rays such as KrF excimer laser or ArF excimer laser, X-rays such as synchrotron radiation, and charged particle beams such as electron beams. The present invention relates to a radiation-sensitive resin composition that can be suitably used as a chemically amplified resist useful for microfabrication using a polymer, a polymer that can be used in the composition, and a novel compound that is used in the synthesis of the polymer.

In the field of microfabrication represented by the manufacture of integrated circuit elements, in order to obtain a higher degree of integration, recently, an ArF excimer laser (wavelength 193 nm), an F ₂ excimer laser (wavelength 157 nm) or the like has been used. There is a need for a lithography technique capable of microfabrication at the same level. As a radiation-sensitive resin composition suitable for irradiation with such an excimer laser, a chemical utilizing the chemical amplification effect by the component having an acid-dissociable functional group and the acid generator which is a component generating an acid by irradiation with radiation. Many amplified radiation-sensitive compositions have been proposed. For example, as a resin component, a polymer compound for a photoresist having a specific structure including a monomer unit having a norbornane ring derivative as a resin component is known (Patent Documents 1 and 2).
JP 2002-201232 A JP 2002-145955 A

  The resin component is synthesized by radical polymerization, and a chain transfer agent may be used to control the degree of polymerization. Known chain transfer agents include trimethylolpropane tris (3-mercaptopropionate), pentaerythritol tetrakis (3-mercaptopropionate), and the like.

  However, when a higher degree of integration is required in the semiconductor field, a radiation-sensitive resin composition that is a resist is required to have better resolution. At the same time, as the miniaturization progresses, the demand for reducing the line edge roughness of the pattern has increased. In addition, with the miniaturization, a reduction in margin for process conditions has been demanded. With the progress of miniaturization in the semiconductor industry, there is an urgent need to develop a radiation-sensitive resin composition that satisfies such conditions as excellent resolution, low pattern line edge roughness, and low pattern density dependency.

  The present invention is a radiation-sensitive resin composition having high transparency to radiation, excellent basic properties as a resist such as sensitivity, resolution, dry etching resistance, pattern shape, etc., high resolution performance, and low pattern line edge roughness. It is an object of the present invention to provide a polymer, a polymer that can be used in the composition, and a novel compound used in the synthesis of the polymer.

式（１）において、Ａは２価の有機基を、ｐは１〜３の整数をそれぞれ表す。
また、上記式（１）で表される新規化合物が連鎖移動剤であることを特徴とする。 The novel compound of the present invention is represented by the following formula (1).

In Formula (1), A represents a divalent organic group, and p represents an integer of 1 to 3, respectively.
The novel compound represented by the above formula (1) is a chain transfer agent.

式（２）において、Ａおよびｐは式（１）におけるＡおよびｐと同一である。
また、上記重合体は酸解離性基を有する繰返し単位を含有することを特徴とする。 The polymer of the present invention comprises a group represented by the following formula (2), and has a polystyrene-reduced weight average molecular weight measured by gel permeation chromatography (GPC) of 2,000 to 100,000. To do.

In the formula (2), A and p are the same as A and p in the formula (1).
The polymer contains a repeating unit having an acid dissociable group.

  The radiation-sensitive resin composition of the present invention is a radiation-sensitive material containing an acid-dissociable group-containing resin that is insoluble or hardly soluble in alkali and easily soluble in alkali by the action of an acid, and a radiation-sensitive acid generator. A resin composition, wherein the acid-dissociable group-containing resin is the polymer of the present invention.

  The radiation-sensitive resin composition of the present invention is a chemically amplified resist that is sensitive to actinic radiation, particularly far ultraviolet rays represented by ArF excimer laser (wavelength 193 nm), and has high transparency to radiation, dry etching resistance, and pattern shape. In addition to having basic performance as a good resist, firstly, it is possible to improve resolution performance, and secondly, it is possible to reduce pattern line edge roughness after development. . In particular, by using a polymer containing a group represented by the formula (2) as a resin component, the above effect is further improved.

  The present invention is represented by the formula (2) introduced by the chain transfer mechanism by using the novel compound represented by the formula (1) as a chain transfer agent for radical polymerization in a larger amount than a normal chain transfer agent amount. A radiation-sensitive resin composition having excellent basic physical properties as a resist, high resolution performance, and low pattern line edge roughness. This is based on the knowledge that products can be obtained.

In Formula (1) and Formula (2), A represents a divalent organic group. Examples of the divalent organic group include a substituted or unsubstituted divalent hydrocarbon group and a divalent group having a hetero atom in the main chain.
Examples of the unsubstituted divalent hydrocarbon group include a methylene group; 1,1-ethylene group, 1,2-ethylene group, propylene group, trimethylene group, tetramethylene group, pentamethylene group, hexamethylene group, and the like. An alkylene group having 2 to 8 carbon atoms; a cycloalkylene group having 3 to 10 carbon atoms such as a 1,3-cyclopentylene group, a 1,3-cyclohexylene group and a 1,4-cyclohexylene group; Examples thereof include arylene groups having 6 to 14 carbon atoms such as phenylene group, 1,4-phenylene group, methyl-1,4-phenylene group and 1,4-phenylenemethylene group.

  Among the substituents for the divalent hydrocarbon group represented by A, those for the methylene group and alkylene group include, for example, a hydroxyl group, a carboxyl group, a cyano group, and an alkoxyl group having 1 to 4 carbon atoms (for example, methoxy group). Group, ethoxy group, n-propoxy group, i-propoxy group, n-butoxy group, 2-methylpropoxy group, 1-methylpropoxy group, t-butoxy group, etc.), alkylcarbonyloxy group having 2 to 5 carbon atoms ( For example, a methylcarbonyloxy group, an ethylcarbonyloxy group, a t-butylcarbonyloxy group, etc.), an alkoxycarbonyl group having 2 to 5 carbon atoms (for example, a methoxycarbonyl group, an ethoxycarbonyl group, a t-butoxycarbonyl group, etc.), carbon A number 3 to 6 alkoxycarbonylalkoxy group (for example, methoxycarbonylmeth) Shi group, ethoxycarbonylmethoxy group, t-butoxycarbonyl methoxy group), a halogen atom (e.g., fluorine atom, may be mentioned one or more types of chlorine atoms, etc.) or the like.

  Among the substituents for the divalent hydrocarbon group represented by A, examples of the substituent for the cycloalkylene group and the arylene group include a hydroxyl group, a carboxyl group, an oxo group (= O), and an alkyl having 1 to 4 carbon atoms. Group (for example, methyl group, ethyl group, n-propyl group, i-propyl group, n-butyl group, t-butyl group, etc.), C1-C4 hydroxyalkyl group (for example, hydroxymethyl group, 1- Hydroxyethyl group, 2-hydroxyethyl group, 1-hydroxypropyl group, 2-hydroxypropyl group, 3-hydroxypropyl group, 1-hydroxybutyl group, 2-hydroxybutyl group, 3-hydroxybutyl group, 4-hydroxybutyl Group), an alkoxyl group having 1 to 4 carbon atoms (for example, methoxy group, ethoxy group, n-propoxy group, i-propoxy group). Group, n-butoxy group, 2-methylpropoxy group, 1-methylpropoxy group, t-butoxy group, etc.), cyano group, cyanoalkyl group having 2 to 5 carbon atoms (for example, cyanomethyl group, 2-cyanoethyl group, 3 -Cyanopropyl group, 4-cyanobutyl group, etc.), C2-C5 alkylcarbonyloxy group (for example, methylcarbonyloxy group, ethylcarbonyloxy group, t-butylcarbonyloxy group, etc.), C2-C5 Alkoxycarbonyl groups (for example, methoxycarbonyl group, ethoxycarbonyl group, t-butoxycarbonyl group, etc.), C3-C6 alkoxycarbonylalkoxy groups (for example, methoxycarbonylmethoxy group, ethoxycarbonylmethoxy group, t-butoxycarbonylmethoxy) Group), halogen atom (for example, fluorine atom, Atom, etc.), fluoroalkyl group having 1 to 4 carbon atoms (e.g., fluoromethyl group, trifluoromethyl group, and a number of one or more types of pentafluoroethyl group) or the like.

Examples of the divalent group having a hetero atom in the main chain represented by A include, for example, a group in which one bond of the above substituted or unsubstituted divalent hydrocarbon group is bonded to —O—, the above substituted or A group in which one bond of an unsubstituted divalent hydrocarbon group is bonded to —S—, a group in which both bonds of the above substituted or unsubstituted divalent hydrocarbon group are bonded to —O—, A group in which both bonds of a substituted or unsubstituted divalent hydrocarbon group are bonded to -S-, one bond of the above substituted or unsubstituted divalent hydrocarbon group is -O-, A group in which a bond is bonded to —S—, —O—, —S—, —SO ₂ —, —SO—, —SO ₂ O—, —CO—, —COO—, —OCOO—, —NR—; _{, -NRCO -, - OCH 2 CONR} -, - O (CH 2) 2 CONR -, - SCH 2 CONR -, - S (CH 2) ₂ CONR- and the like. However, each R bonded to the nitrogen atom is independently a substituted or unsubstituted linear or branched alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted monovalent group having 3 to 20 carbon atoms. An alicyclic hydrocarbon group or a linear or branched alkenyl group having 2 to 20 carbon atoms is shown.

  The number of carbon atoms of the unsubstituted linear or branched alkyl group having 1 to 20 carbon atoms represented by R is preferably 1 to 18, more preferably 1 to 15, particularly preferably 1 to 12, The carbon number of the unsubstituted monovalent alicyclic hydrocarbon group of R is preferably 3 to 18, more preferably 3 to 12, particularly preferably 3 to 8, and the carbon number of the alkenyl group of R is Preferably it is 2-18, More preferably, it is 2-15, Most preferably, it is 2-12.

  Examples of the unsubstituted linear or branched alkyl group having 1 to 20 carbon atoms represented by R include, for example, methyl group, ethyl group, n-propyl group, i-propyl group, n-butyl group, 2 -Methylpropyl group, 1-methylpropyl group, t-butyl group, n-pentyl group, n-hexyl group, n-heptyl group, n-octyl group, n-nonyl group, n-decyl group, n-undecyl group N-dodecyl group, t-dodecyl group, n-tridecyl group, n-tetradecyl group, n-pentadecyl group, n-hexadecyl group, n-heptadecyl group, n-octadecyl group, n-nonadecyl group, n-eicosyl group Etc.

  Examples of the substituent for the alkyl group of R include a hydroxyl group, a carboxyl group, a cyano group, and an alkoxyl group having 1 to 4 carbon atoms (for example, a methoxy group, an ethoxy group, an n-propoxy group, an i-propoxy group, n -Butoxy group, 2-methylpropoxy group, 1-methylpropoxy group, t-butoxy group, etc.), alkylcarbonyloxy group having 2 to 5 carbon atoms (for example, methylcarbonyloxy group, ethylcarbonyloxy group, t-butylcarbonyl) Oxy group etc.), C2-C5 alkoxycarbonyl group (e.g. methoxycarbonyl group, ethoxycarbonyl group, t-butoxycarbonyl group etc.), C3-C6 alkoxycarbonylalkoxy group (e.g. methoxycarbonylmethoxy group). , Ethoxycarbonylmethoxy group, t-butoxycarbonyl Methoxy group), a halogen atom (e.g., fluorine atom, may be mentioned one or more types of chlorine atoms, etc.) or the like.

Examples of the unsubstituted C 3-20 monovalent alicyclic hydrocarbon group represented by R include, for example, a cycloalkyl group such as a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, and a cyclohexyl group; a norbornyl group And a bridged alicyclic hydrocarbon group such as tricyclodecanyl group, tetracyclododecyl group, adamantyl group, methyladamantyl group, ethyladamantyl group and n-butyladamantyl group.
Furthermore, examples of the linear or branched alkenyl group having 2 to 20 carbon atoms of R include a vinyl group, an isopropenyl group, a 1-propenyl group, and a 2-propenyl group.

  Examples of the substituent for R in the alicyclic hydrocarbon group include a hydroxyl group, a carboxyl group, an oxo group (═O), and an alkyl group having 1 to 4 carbon atoms (for example, a methyl group, an ethyl group, and n-propyl). Group, i-propyl group, n-butyl group, t-butyl group, etc.), C1-C4 hydroxyalkyl group (for example, hydroxymethyl group, 1-hydroxyethyl group, 2-hydroxyethyl group, 1-hydroxy group) Propyl group, 2-hydroxypropyl group, 3-hydroxypropyl group, 1-hydroxybutyl group, 2-hydroxybutyl group, 3-hydroxybutyl group, 4-hydroxybutyl group, etc.), an alkoxyl group having 1 to 4 carbon atoms ( For example, methoxy group, ethoxy group, n-propoxy group, i-propoxy group, n-butoxy group, 2-methylpropoxy group, 1-methylpropoxy group Xy group, t-butoxy group, etc.), cyano group, C2-C5 cyanoalkyl group (e.g., cyanomethyl group, 2-cyanoethyl group, 3-cyanopropyl group, 4-cyanobutyl group, etc.), C2-C2 5 alkylcarbonyloxy groups (for example, methylcarbonyloxy group, ethylcarbonyloxy group, t-butylcarbonyloxy group, etc.), C2-C5 alkoxycarbonyl groups (for example, methoxycarbonyl group, ethoxycarbonyl group, t- Butoxycarbonyl group etc.), C3-C6 alkoxycarbonylalkoxy group (eg methoxycarbonylmethoxy group, ethoxycarbonylmethoxy group, t-butoxycarbonylmethoxy group etc.), halogen atom (eg fluorine atom, chlorine atom etc.) , A fluoroalkyl group having 1 to 4 carbon atoms (for example, full Romechiru group, a trifluoromethyl group, and a number of one or more types of pentafluoroethyl group) or the like.

In Formula (1), specific examples of preferable A include a methylene group, 1,2-ethylene group, trimethylene group, tetramethylene group, pentamethylene group, hexamethylene group, difluoromethylene group, 1,4-cyclohexylene group. 1,4-phenylene group, 1,4-phenylenemethylene group, fluoro-1,4-phenylene group, 1,1,2,2-tetrafluoropentamethylene group, —CH ₂ O—, — (CH ₂ ) ₂ O—, — (CH ₂ ) ₃ O—, — (CH ₂ ) ₄ O—, — (CH ₂ ) ₅ O—, 1,4-cyclohexyleneoxy group, 1,4-phenyleneoxy group, —CH _{2 CO -, - (CH 2} ) 2 CO -, - (CH 2) 3) CO -, - CH 2 COO -, - (CH 2) 2 COO -, - (CH 2) 3 COO -, - OCH 2 _{COO -, - O (CH 2} ) 2 COO -, - O (C H ₂ ) ₃ COO—, —CH ₂ SO ₂ —, — (CH ₂ ) ₂ SO ₂ —, — (CH ₂ ) ₃ SO ₂ —, —OCH ₂ SO ₂ —, —O (CH ₂ ) ₂ SO _{2 -, - O (CH 2)} 3 SO 2 -, - CH 2 S -, - (CH 2) 2 S -, - (CH 2) 3 S -, - (CH 2) 4 S -, - (CH 2 ) ₅ S-, 1,4-cyclohexylene thio group, 1,4 Fenirenchio _{group, -OCH 2 CONR -, - O} (CH 2) 2 CONR -, - given the S (CH _{2) 2} CONR- like be able to.
In the formula (1), p is an integer of 1 to 3, but it is preferable that p is 1 from the raw material supply surface and the like.

Preferable examples of the novel compound represented by formula (1) include compounds (1-1) to (1-3).

As shown in the following reaction formula, the novel compound represented by the formula (1) synthesizes the corresponding precursor thioester compound (1c) by reacting the olefin compound (1a) with thioacetic acid (1b). Furthermore, it can be synthesized by treating the precursor with a base. The olefin compound (1a), which is a precursor of (1-1) to (1-3), can be synthesized by, for example, a Diels-Alder reaction between formula (1-4) and cyclopentadiene, furan, or thiophene. it can.

In the above reaction, the molar ratio of the olefin compound (1a) to the thioacetic acid (1b) is usually 1 to 100, preferably 1.0 to 10.
This reaction is usually carried out under solvent-free conditions.
The reaction temperature is usually −40 to + 50 ° C., preferably −20 to + 30 ° C., and the reaction time is usually 0.1 to 72 hours, preferably 0.5 to 3 hours.

In the above reaction, the molar ratio of the precursor thioester compound (1c) to the base is usually 1 to 100, preferably 1.0 to 10.
This reaction is usually carried out in an organic solvent such as toluene, tetrahydrofuran, methylene chloride, pyridine, dimethylformamide, dimethyl sulfoxide, methanol, ethanol or the like, preferably in methanol or ethanol.
The reaction temperature is usually −40 to + 50 ° C., preferably −20 to + 30 ° C., and the reaction time is usually 0.1 to 72 hours, preferably 0.5 to 3 hours.
Examples of the base used in the reaction include triethylamine, pyridine, potassium hydroxide, sodium hydroxide, sodium hydrogen carbonate, potassium hydrogen carbonate, and the like, preferably triethylamine, pyridine and the like.

The polymer of the present invention is a polymer containing a group represented by the formula (2) at the molecular end, and this polymer uses a novel compound represented by the formula (1) as a chain transfer agent for radical polymerization. Is obtained. Moreover, it is preferable that the polymer of this invention contains the repeating unit which has an acid dissociable group.
The acid dissociable group is a group in which a hydrogen atom in an acidic functional group such as a phenolic hydroxyl group, a carboxyl group, or a sulfonic acid group is substituted, and means a group that dissociates in the presence of an acid.
Examples of such an acid dissociable group include a substituted methyl group, a 1-substituted ethyl group, a 1-substituted n-propyl group, a 1-branched alkyl group, an alkoxycarbonyl group, and a cyclic acid dissociable group. be able to.

Examples of the substituted methyl group include methoxymethyl group, cyclopropylmethyl group, methoxycarbonylmethyl group, t-butoxycarbonylmethyl group and the like. Examples of the 1-substituted ethyl group include 1-methoxyethyl group, 1-cyclopropyloxyethyl group, 1-cyclohexyloxyethyl group, 1-t-butoxycarbonylethyl group and the like.
Examples of the 1-substituted-n-propyl group include 1-methoxy-n-propyl group and 1-ethoxy-n-propyl group.
Examples of the 1-branched alkyl group include a t-butyl group and a 1,1-dimethylpropyl group.
Examples of the alkoxycarbonyl group include a t-butoxycarbonyl group.
Examples of the cyclic acid dissociable group include a cyclopropyl group, a cyclopentyl group, a cyclohexyl group, a cyclohexenyl group, and a 4-methoxycyclohexyl group.

  Among the acid dissociable groups, benzyl group, t-butoxycarbonylmethyl group, 1-methoxyethyl group, 1-ethoxyethyl group, 1-cyclohexyloxyethyl group, 1-ethoxy-n-propyl group, t-butyl group 1,1-dimethylpropyl group, t-butoxycarbonyl group, tetrahydropyranyl group, tetrahydrofuranyl group, tetrahydrothiopyranyl group, tetrahydrothiofuranyl group and the like are preferable.

式（３）において、Ｒ¹は相互に独立に炭素数１〜４の直鎖状もしくは分岐状のアルキル基または炭素数４〜２０の１価の脂環式炭化水素基もしくはその置換誘導体を表すか、あるいは何れか２つのＲ¹が相互に結合して、それぞれが結合している炭素原子とともに炭素数４〜２０の２価の脂環式炭化水素基もしくはその置換誘導体を形成し、残りの１つのＲ¹が炭素数１〜４の直鎖状もしくは分岐状のアルキル基または炭素数４〜２０の１価の脂環式炭化水素基もしくはその置換誘導体を表す。 Moreover, the group represented by Formula (3) can be used as an acid dissociable group.

In Formula (3), R ¹ independently represents a linear or branched alkyl group having 1 to 4 carbon atoms, a monovalent alicyclic hydrocarbon group having 4 to 20 carbon atoms, or a substituted derivative thereof. Or any two R ¹ 's bonded to each other to form a divalent alicyclic hydrocarbon group having 4 to 20 carbon atoms or a substituted derivative thereof together with the carbon atoms to which each is bonded, One R ¹ represents a linear or branched alkyl group having 1 to 4 carbon atoms, a monovalent alicyclic hydrocarbon group having 4 to 20 carbon atoms, or a substituted derivative thereof.

Examples of the linear or branched alkyl group having 1 to 4 carbon atoms of R ¹ include a methyl group, an ethyl group, an n-propyl group, an i-propyl group, an n-butyl group, a 2-methylpropyl group, Examples thereof include 1-methylpropyl group and t-butyl group. Of these alkyl groups, a methyl group, an ethyl group, and the like are preferable.
In addition, a monovalent alicyclic hydrocarbon group having 4 to 20 carbon atoms of R ¹ and any two R ¹ 's bonded to each other to form a carbon atom having 4 to 20 carbon atoms. Examples of the divalent alicyclic hydrocarbon group include groups derived from cycloalkanes such as cyclobutane, cyclopentane, cyclohexane, cycloheptane, and cyclooctane; adamantane, bicyclo [2.2.1] heptane, and tricyclo [ 5.2.1.0 ^2,6 ] decane, tetracyclo [6.2.1.1 ^3,6 . [0 ^2,7 ] groups derived from bridged hydrocarbons such as dodecane.
Of these monovalent alicyclic hydrocarbon groups and divalent alicyclic hydrocarbon groups, groups derived from cyclopentane, cyclohexane, adamantane, bicyclo [2.2.1] heptane and the like are preferable.
Examples of the substituent in the substituted derivative of the monovalent or divalent alicyclic hydrocarbon group include, for example, the divalent linear or branched hydrocarbon group of R ¹ and a divalent alicyclic group. The substituent similar to what was illustrated about the substituent with respect to a hydrocarbon can be mentioned.
Of these substituents, a hydroxyl group, a carboxyl group, a hydroxymethyl group, a cyano group, a cyanomethyl group, and the like are preferable. One or more or one or more of these substituents may be present in each substituted derivative.

In the formula (3), examples of the structure corresponding to —C (R ¹ ) ₃ include, for example, a t-butyl group, a 2-methyl-2-butyl group, a 2-ethyl-2-butyl group, and 3-methyl-3. -Trialkylmethyl groups such as butyl group, 3-ethyl-3-butyl group, 3-methyl-3-pentyl group;
1-alkylcyclopentyl group, 1-ethylcyclopentyl group, 1-n-propylcyclopentyl group, 1-alkylcyclohexyl group such as 1-methylcyclohexyl group, 1-ethylcyclohexyl group, 1-n-propylcyclohexyl group;
2-methyladamantan-2-yl group, 2-methyl-3-hydroxyadamantan-2-yl group, 2-ethyladamantan-2-yl group, 2-ethyl-3-hydroxyadamantan-2-yl group, 2- n-propyladamantan-2-yl group, 2-n-butyladamantan-2-yl group, 2-methoxymethyladamantan-2-yl group, 2-methoxymethyl-3-hydroxyadamantan-2-yl group, 2- Ethoxymethyladamantan-2-yl group, 2-n-propoxymethyladamantan-2-yl group, 2-methylbicyclo [2.2.1] heptan-2-yl group, 2-methyl-5-hydroxybicyclo [2] 2.1] heptan-2-yl group, 2-methyl-6-hydroxybicyclo [2.2.1] heptan-2-yl group, 2-methyl-5- Anobicyclo [2.2.1] heptan-2-yl group, 2-methyl-6-cyanobicyclo [2.2.1] heptan-2-yl group, 2-ethylbicyclo [2.2.1] heptane- 2-yl group, 2-ethyl-5-hydroxybicyclo [2.2.1] heptan-2-yl group, 2-ethyl-6-hydroxybicyclo [2.2.1] heptan-2-yl group, 4 -Methyltetracyclo [6.2.1.1 ^3,6 . 0 ^2,7 ] -4-yl group, 4-methyl-9-hydroxytetracyclo [6.2.1.1 ^3,6 . 0 ^2,7 ] dodecan-4-yl group, 4-methyl-10-hydroxytetracyclo [6.2.1.1 ^3,6 . 0 ^2,7 ] dodecan-4-yl group, 4-methyl-9-cyanotetracyclo [6.2.1.1 ^3,6 . 0 ^2,7 ] dodecan-4-yl group, 4-methyl-10-cyanotetracyclo [6.2.1.1 ^3,6 . 0 ^2,7 ] dodecan-4-yl group, 4-ethyltetracyclo [6.2.1.1 ^3,6 . 0 ^2,7 ] dodecan-4-yl group, 4-ethyl-9-hydroxytetracyclo [6.2.1.1 ^3,6 . 0 ^2,7 ] dodecan-4-yl group, 4-ethyl-10-hydroxytetracyclo [6.2.1.1 ^3,6 . 0 ^2,7 ] dodecan-4-yl group, 8-methyltricyclo [5.2.1.0 ^2,6 ] decan-8-yl group, 8-methyl-4-hydroxytricyclo [5.2. 1.0 ^2,6 ] decan-8-yl group, 8-methyl-4-cyanotricyclo [5.2.1.0 ^2,6 ] decan-8-yl group, 8-ethyltricyclo [5. 2.1.0 ^2,6 ] Decan-8-yl group, 8-ethyl-4-hydroxytricyclo [5.2.1.0 ^2,6 ] decan-8-yl group, etc. A hydrocarbon group;

1-methyl-1-cyclopentylethyl group, 1-methyl-1- (2-hydroxycyclopentyl) ethyl group, 1-methyl-1- (3-hydroxycyclopentyl) ethyl group, 1-methyl-1-cyclohexylethyl group, 1-methyl-1- (3-hydroxycyclohexyl) ethyl group, 1-methyl-1- (4-hydroxycyclohexyl) ethyl group, 1-methyl-1-cycloheptylethyl group, 1-methyl-1- (3- Dialkyl-cycloalkylmethyl groups such as hydroxycycloheptyl) ethyl group, 1-methyl-1- (4-hydroxycycloheptyl) ethyl group;
1-methyl-1- (adamantan-1-yl) ethyl group, 1-methyl-1- (3-hydroxyadamantan-1-yl) ethyl group, 1-methyl-1- (bicyclo [2.2.1] Heptan-2-yl) ethyl group, 1-methyl-1- (5-hydroxybicyclo [2.2.1] heptan-2-yl) ethyl group, 1-methyl-1- (6-hydroxybicyclo [2. 2.1] Heptan-2-yl) ethyl group, 1-methyl-1- (tetracyclo [6.2.1.1 ^3,6 .0 ^2,7 ] dodecan-4-yl) ethyl group, 1-methyl -1- (9-hydroxy tetracyclo [6.2.1.1 ^3,6 .0 ^2,7] dodecane-4-yl) ethyl group, 1-methyl-1- (10-hydroxy-tetracyclo [6. 2.1.1 ^3,6 .0 ^2,7] dodecane-4-yl) ethyl group, 1-methyl-1 (Tricyclo [5.2.1.0 ^2,6] decan-8-yl) ethyl group, 1-methyl-1- (4-hydroxy-tricyclo [5.2.1.0 ^{2, 6]} decane -8 -Yl) alkyl-substituted / bridged hydrocarbon group-substituted methyl group such as ethyl group;
1,1-dicyclopentylethyl group, 1,1-di (2-hydroxycyclopentyl) ethyl group, 1,1-di (3-hydroxycyclopentyl) ethyl group, 1,1-dicyclohexylethyl group, 1,1-di (3-hydroxycyclohexyl) ethyl group, 1,1-di (4-hydroxycyclohexyl) ethyl group, 1,1-dicycloheptylethyl group, 1,1-di (3-hydroxycycloheptyl) ethyl group, 1, Alkyl / dicycloalkylmethyl groups such as 1-di (4-hydroxycycloheptyl) ethyl group;
1,1-di (adamantan-1-yl) ethyl group, 1,1-di (3-hydroxyadamantan-1-yl) ethyl group, 1,1-di (bicyclo [2.2.1] heptane-2 -Yl) ethyl group, 1,1-di (5-hydroxybicyclo [2.2.1] heptan-2-yl) ethyl group, 1,1-di (6-hydroxybicyclo [2.2.1] heptane -2-yl) ethyl group, 1,1-di (tetracyclo [6.2.1.1 ^3,6 .0 ^2,7 ] dodecan-4-yl) ethyl group, 1,1-di (9-hydroxy) Tetracyclo [6.2.1.1 ^3,6 .0 ^2,7 ] dodecan-4-yl) ethyl group, 1,1-di (10-hydroxytetracyclo [6.2.1.1 ^3,6] .0 ^2,7] dodecane-4-yl) ethyl group, 1,1-di (tricyclo [5.2.1.0 ^2,6] decan-8-yl) Butyl group, 1,1-di (4-hydroxy-tricyclo [5.2.1.0 ^2,6] decan-8-yl) alkyl-substituted di (bridged hydrocarbon group) such as an ethyl group-substituted methyl Groups and the like.

Among these structures corresponding to —C (R ¹ ) ₃ , in particular, t-butyl group, 1-methylcyclopentyl group, 1-ethylcyclopentyl group, 1-methylcyclohexyl group, 1-ethylcyclohexyl group, 2-methyl Adamantane-2-yl group, 2-ethyladamantan-2-yl group, 2-methylbicyclo [2.2.1] heptan-2-yl group, 2-ethylbicyclo [2.2.1] heptane-2- An yl group, a 1-methyl-1- (adamantan-1-yl) ethyl group, a 1-methyl-1- (bicyclo [2.2.1] heptan-2-yl) ethyl group and the like are preferable.

上記各式においてＲは、水素原子、メチル基、またはトリフルオロメチル基を表す。 The repeating unit having an acid dissociable group in the polymer of the present invention can be introduced into the polymer by polymerizing the acrylic acid derivative having the acid dissociable group in the side chain as a monomer.
Monomers suitable for the present invention are exemplified below as formulas (3-1) to (3-5).

In the above formulas, R represents a hydrogen atom, a methyl group, or a trifluoromethyl group.

上記式においてＲ’は、水素原子、メチル基、またはトリフルオロメチル基を表し、Ｒ²は置換基を表す。
ラクトン骨格として５−オキソ−４−オキサトリシクロ［４．２．１．０^3,7］ノナンを有する脂環式炭化水素基を側鎖の一部に有する。またこのラクトン骨格は、Ｒ²で表される、炭素数１〜４の直鎖状または分岐状のアルキル基、アルコキシ基、またはフッ素化アルキル基で置換されていてもよい。
炭素数１〜４の直鎖状または分岐状のアルキル基としては、例えば、メチル基、エチル基、ｎ−プロピル基、ｉ−プロピル基、ｎ−ブチル基、２−メチルプロピル基、１−メチルプロピル基、ｔ−ブチル基等が挙げられ、炭素数１〜４の直鎖状または分岐状のアルコキシ基としては、メトキシ基、エトキシ基、ｎ−プロポキシ基、ｉ−プロポキシ基、ｎ−ブトキシ基、２−メチルプロポキシ基、１−メチルプロポキシ基、ｔ−ブトキシ基等が挙げられる。炭素数１〜４の直鎖状あるいは分岐状のフッ素化アルキル基としては、上記アルキル基の水素の一部または全部をフッ素原子で置換した基が挙げられる。
上記ラクトンユニット含有繰り返し単位は、該クトンユニットを側鎖に有するアクリル酸誘導体を単量体として用いて重合させることにより重合体中に導入できる。 The polymer of this invention can contain the lactone unit containing repeating unit represented by following formula (4) with the repeating unit which has an acid dissociable group.

In the above formula, R ′ represents a hydrogen atom, a methyl group, or a trifluoromethyl group, and R ² represents a substituent.
It has an alicyclic hydrocarbon group having 5-oxo-4-oxatricyclo [4.2.1.0 ^3,7 ] nonane as a lactone skeleton in a part of the side chain. The lactone skeleton is represented by R ^2, a linear or branched alkyl group having 1 to 4 carbon atoms, may be substituted with an alkoxy group or a fluorinated alkyl group.
Examples of the linear or branched alkyl group having 1 to 4 carbon atoms include a methyl group, an ethyl group, an n-propyl group, an i-propyl group, an n-butyl group, a 2-methylpropyl group, and a 1-methyl group. Examples thereof include a propyl group and a t-butyl group. Examples of the linear or branched alkoxy group having 1 to 4 carbon atoms include a methoxy group, an ethoxy group, an n-propoxy group, an i-propoxy group, and an n-butoxy group. , 2-methylpropoxy group, 1-methylpropoxy group, t-butoxy group and the like. Examples of the linear or branched fluorinated alkyl group having 1 to 4 carbon atoms include groups in which part or all of the hydrogen atoms in the alkyl group have been substituted with fluorine atoms.
The lactone unit-containing repeating unit can be introduced into a polymer by polymerizing the lactone unit-containing acrylic acid derivative as a monomer.

上記式においてＲ''は、水素原子、メチル基、またはトリフルオロメチル基を表し、Ｘは１価の有機基を表す。
１価の有機基としては、炭素数７〜２０の極性基を含まない炭素および水素のみからなる多環型脂環式炭化水素基が好ましく、このような多環型脂環式炭化水素基としては、例えば、ビシクロ［２．２．１］ヘプタン、ビシクロ［２．２．２］オクタン、トリシクロ［５．２．１．０^2,6］デカン、テトラシクロ［４．４．０．１^2,6．１^7,10］ドデカン、テトラシクロ［６．２．１．１^3,6．０^2,7］ドデカン等のシクロアルカン類に由来する脂環族環からなる炭化水素基が挙げられる。
また、これらのシクロアルカン由来の脂環族環は、置換基を有していてもよく、例えば、メチル基、エチル基、ｎ−プロピル基、ｉ−プロピル基、ｎ−ブチル基、２−メチルプロピル基、１−メチルプロピル基、ｔ−ブチル基等の炭素数１〜４の直鎖状、分岐状または環状のアルキル基の１種以上あるいは１個以上で置換した骨格等が挙げられる。これらは単独でも、２種以上を混合して用いることができる。
式（５）で表される繰り返し単位は、Ｘを側鎖に有するアクリル酸誘導体を単量体として用いて重合させることにより重合体中に導入できる。 The polymer of this invention can contain the repeating unit represented by Formula (5) with the repeating unit which has an acid dissociable group, and the lactone unit containing repeating unit.

In the above formula, R ″ represents a hydrogen atom, a methyl group, or a trifluoromethyl group, and X represents a monovalent organic group.
As the monovalent organic group, a polycyclic alicyclic hydrocarbon group consisting only of carbon and hydrogen not containing a polar group having 7 to 20 carbon atoms is preferable, and as such a polycyclic alicyclic hydrocarbon group, Are, for example, bicyclo [2.2.1] heptane, bicyclo [2.2.2] octane, tricyclo [5.2.1.0 ^2,6 ] decane, tetracyclo [4.4.0.1 ^{2, 6} ． 1 ^7,10 ] dodecane, tetracyclo [6.2.1.1 ^3,6 . ^0,7 ] hydrocarbon groups composed of alicyclic rings derived from cycloalkanes such as dodecane.
In addition, these cycloalkane-derived alicyclic rings may have a substituent, for example, methyl group, ethyl group, n-propyl group, i-propyl group, n-butyl group, 2-methyl group. Examples thereof include skeletons substituted with one or more linear, branched or cyclic alkyl groups having 1 to 4 carbon atoms such as propyl group, 1-methylpropyl group and t-butyl group. These can be used alone or in admixture of two or more.
The repeating unit represented by the formula (5) can be introduced into the polymer by polymerizing using an acrylic acid derivative having X as a side chain as a monomer.

The polymer of the present invention comprises a repeating unit having an acid dissociable group (hereinafter referred to as repeating unit I), a lactone unit-containing repeating unit (hereinafter referred to as repeating unit II), and a repeating unit represented by formula (5) (hereinafter referred to as “repeating unit”). The repeating unit III is preferably 5 to 80 mol%, preferably 10 to 70 mol%, and 5 to 60 mol% of the repeating unit II, based on the whole polymer. The repeating unit III is preferably 0 to 50 mol%, preferably 5 to 40 mol%.
When the repeating unit I is less than 5 mol%, the resolution is insufficient, and when it exceeds 80 mol%, the etching resistance is insufficient. If the repeating unit II is less than 5 mol%, the resolution is insufficient, and if it exceeds 60 mol%, the solubility in the solvent decreases. When the repeating unit III exceeds 50 mol%, the resolution is insufficient.

The polymer of this invention can be variously selected according to the kind of radiation to be used. For example, the polymer containing the repeating unit I, the repeating unit II, and the repeating unit III can be used as an acid-dissociable group-containing resin suitable for a radiation-sensitive resin composition using an ArF excimer laser. The resin may be suitably used in KrF excimer laser, F ₂ excimer laser radiation-sensitive resin composition using other radiation such as electron beams.
On the other hand, as an acid-dissociable group-containing resin particularly suitable for a radiation-sensitive resin composition using a KrF excimer laser, for example, a part of hydrogen atoms of a phenolic hydroxyl group in poly (p-hydroxystyrene) or a derivative thereof or Resin having all substituted with acid-dissociable groups, hydrogen atom and / or carboxyl group of phenolic hydroxyl group in copolymer of p-hydroxystyrene and / or p-hydroxy-α-methylstyrene and (meth) acrylic acid A resin in which some or all of the hydrogen atoms are substituted with an acid dissociable group can be preferably used. Incidentally, the resin, ArF excimer laser, F ₂ excimer laser can also be suitably used in radiation-sensitive resin compositions using other radiation such as electron beams.

The polymer of the present invention can usually be produced by radical polymerization. In addition to the radical polymerization initiator, the polymer represented by the formula (1) is used as a chain transfer agent to carry out radical polymerization at the end of the molecular chain. A polymer having the group (2) is obtained. Since the group represented by the formula (2) is added by a chain transfer mechanism, it is often added to one end of the molecular chain.
The polymer having the group of formula (2) at the molecular chain terminal is preferably 30 to 70% of the total number of polymers. If it is less than 30%, no effect is observed, and if it exceeds 70%, the degree of polymerization becomes low.
The molar ratio between the radical polymerization initiator amount and the chain transfer agent amount is (1: 1) to (0.005: 1). Preferably, it is (1: 1) to (0.1: 1).

The chain transfer agent used in the present invention can be used in combination with a radical polymerization initiator.
Examples of the radical polymerization initiator that can be used in the present invention include a thermal polymerization initiator, a redox polymerization initiator, and a photopolymerization initiator. Examples thereof include polymerization initiators such as peroxides and azo compounds. Although not particularly limited, specific radical polymerization initiators include t-butyl hydroperoxide, t-butyl perbenzoate, benzoyl peroxide, 2,2′-azobis (2,4-dimethylvaleronitrile), 2, Examples include 2′-azobisisobutyronitrile (AIBN), 1,1′-azobis (cyclohexanecarbonitrile), dimethyl-2,2′-azobisisobutyrate (MAIB), and the like.

The polymerization operation can be synthesized by a usual method such as batch polymerization or dropping polymerization. For example, an acid dissociable group-containing polymer can be obtained by dissolving a necessary monomer amount in an organic solvent and polymerizing in the presence of a radical polymerization initiator and a chain transfer agent.
As the polymerization solvent, an organic solvent capable of dissolving the monomer, the radical polymerization initiator, and the chain transfer agent is used. Examples of the organic solvent include ketone solvents, ether solvents, aprotic polar solvents, ester solvents, aromatic solvents, and linear or cyclic aliphatic solvents. Examples of the ketone solvent include methyl ethyl ketone and acetone. Examples of ether solvents include alkoxyalkyl ethers such as methoxymethyl ether, ethyl ether, tetrahydrofuran, and 1,4-dioxane. Examples of the aprotic polar solvent include dimethylformamide and dimethyl sulfoxide. Examples of ester solvents include alkyl acetates such as ethyl acetate and methyl acetate. Aromatic solvents include alkylaryl solvents such as toluene, xylene, and halogenated aromatic solvents such as chlorobenzene. Examples of the aliphatic solvent include hexane and cyclohexane.
The polymerization temperature is 20 to 120 ° C, preferably 50 to 110 ° C, more preferably 60 to 100 ° C. Although polymerization may be performed even in a normal air atmosphere, polymerization in an inert gas atmosphere such as nitrogen or argon is preferable. The molecular weight of the polymer can be adjusted by controlling the ratio between the monomer amount and the chain transfer agent amount.
The polymerization time is generally 0.5 to 144 hours, preferably 1 to 72 hours, more preferably 2 to 24 hours.

The polymer of the present invention has a polystyrene-reduced weight average molecular weight (hereinafter also referred to as “Mw”) measured by gel permeation chromatography (GPC) of 2,000 to 100,000, preferably 2,000 to 60,000. Especially preferably, it is 2,000-40,000. The ratio (Mw / Mn) between Mw and the polystyrene-equivalent number average molecular weight (hereinafter also referred to as “Mn”) measured by GPC is usually 1 to 5.
The polymer of the present invention can be used as an acid-dissociable group-containing resin which is alkali-insoluble or hardly alkali-soluble and becomes alkali-soluble by the action of an acid.

上記式（６）において、Ｒ⁴は１価の有機基を表し、Ｒ³は２価の有機基を表す。
１価の有機基としては、置換もしくは非置換の直鎖または分岐アルキル基、置換もしくは非置換の環式アルキル基、置換もしくは非置換のアリール基、パーフルオロアルキル基等が、２価の有機基としては、置換もしくは非置換のアルキレン基、置換もしくは非置換のアルケニレン基、置換もしくは非置換のフェニレン基等が挙げられる。 Examples of the radiation-sensitive acid generator (hereinafter referred to as “acid generator”) that can be used with the acid-dissociable group-containing resin include sulfonimide compounds and onium salt compounds.
As a sulfonimide compound, it represents with following formula (6), for example.

In the above formula (6), R ⁴ represents a monovalent organic group, and R ³ represents a divalent organic group.
Examples of the monovalent organic group include a divalent organic group such as a substituted or unsubstituted linear or branched alkyl group, a substituted or unsubstituted cyclic alkyl group, a substituted or unsubstituted aryl group, and a perfluoroalkyl group. Examples thereof include a substituted or unsubstituted alkylene group, a substituted or unsubstituted alkenylene group, a substituted or unsubstituted phenylene group, and the like.

  Specific examples of the sulfonimide compound include N- (trifluoromethylsulfonyloxy) succinimide, N- (trifluoromethylsulfonyloxy) bicyclo [2.2.1] hept-5-ene-2,3-dicarboximide. N- (10-camphorsulfonyloxy) succinimide, N- (10-camphorsulfonyloxy) bicyclo [2.2.1] hept-5-ene-2,3-dicarboximide, N- (10-camphorsulfonyl) Oxy) -7-oxabicyclo [2.2.1] hept-5-ene-2,3-dicarboximide, N- (p-toluenesulfonyloxy) succinimide, N- (p-toluenesulfonyloxy) bicyclo [ 2.2.1] Hept-5-ene-2,3-dicarboximide, N- (4-trifluoromethylbenzene) Sulfonyloxy) succinimide, N- (4-trifluoromethylbenzenesulfonyloxy) bicyclo [2.2.1] hept-5-ene-2,3-dicarboximide, N- (perfluorobenzenesulfonyloxy) succinimide, N -(Perfluorobenzenesulfonyloxy) bicyclo [2.2.1] hept-5-ene-2,3-dicarboximide, N- (nonafluorobutylsulfonyloxy) succinimide, N- (nonafluorobutylsulfonyloxy) Bicyclo [2.2.1] hept-5-ene-2,3-dicarboximide, N- (perfluorooctanesulfonyloxy) succinimide, N- (perfluorooctanesulfonyloxy) bicyclo [2.2.1] Hept-5-ene-2,3-dicarboximide, N- (benzene Sulfonyloxy) succinimide, N- (benzenesulfonyloxy) bicyclo [2.2.1] hept-5-ene-2,3-dicarboximide, N- (benzenesulfonyloxy) -7-oxabicyclo [2.2. 1] hept-5-ene-2,3-dicarboximide, N-{(5-methyl-5-carboxymethanebicyclo [2.2.1] hept-2-yl) sulfonyloxy} succinimide and the like. .

  Among the sulfonamides, N- (trifluoromethylsulfonyloxy) bicyclo [2.2.1] hept-5-ene-2,3-dicarboximide, N- (10-camphorsulfonyloxy) succinimide, N -(P-toluenesulfonyloxy) succinimide, N- (nonafluorobutylsulfonyloxy) bicyclo [2.2.1] hept-5-ene-2,3-dicarboximide, N- (benzenesulfonyloxy) bicyclo [ 2.2.1] Hept-5-ene-2,3-dicarboximide, N-{(5-methyl-5-carboxymethanebicyclo [2.2.1] hept-2-yl) sulfonyloxy} succinimide Is preferred.

Examples of the onium salt compounds include iodonium salts, sulfonium salts, phosphonium salts, diazonium salts, ammonium salts, pyridinium salts, and the like.
Examples of the onium salt compound include bis (4-t-butylphenyl) iodonium nonafluorobutanesulfonate, bis (4-t-butylphenyl) iodonium trifluoromethanesulfonate, bis (4-t-butylphenyl) iodonium perfluorooctanesulfonate, Bis (4-t-butylphenyl) iodonium p-toluenesulfonate, bis (4-t-butylphenyl) iodonium 10-camphorsulfonate, 4-trifluoromethylbenzenesulfonate, bis (4-t-butylphenyl) iodonium perfluoro Benzene sulfonate, diphenyliodonium nonafluorobutanesulfonate, diphenyliodonium trifluoromethanesulfonate, diphenyliodonium perfluorooctanesulfone Diphenyliodonium p-toluenesulfonate, diphenyliodoniumbenzenesulfonate, diphenyliodonium10-camphorsulfonate, diphenyliodonium4-trifluoromethylbenzenesulfonate, diphenyliodonium perfluorobenzenesulfonate, bis (p-fluorophenyl) iodonium trifluoromethanesulfonate Bis (p-fluorophenyl) iodonium nonafluoromethanesulfonate, bis (p-fluorophenyl) iodonium camphorsulfonate, (p-fluorophenyl) (phenyl) iodonium trifluoromethanesulfonate,

  Triphenylsulfonium nonafluorobutanesulfonate, triphenylsulfonium trifluoromethanesulfonate, triphenylsulfonium perfluorooctanesulfonate, triphenylsulfonium p-toluenesulfonate, triphenylsulfoniumbenzenesulfonate, triphenylsulfonium 10-camphorsulfonate, triphenylsulfonium 4- Trifluoromethylbenzenesulfonate, triphenylsulfonium perfluorobenzenesulfonate, 4-hydroxyphenyl diphenylsulfonium trifluoromethanesulfonate, tri (p-methoxyphenyl) sulfonium nonafluorobutanesulfonate, tri (p-methoxyphenyl) sulfonium trifluoromethanesulfonate Tri (p-methoxyphenyl) sulfonium perfluorooctane sulfonate, tri (p-methoxyphenyl) sulfonium p-toluenesulfonate, tri (p-methoxyphenyl) sulfonium benzenesulfonate, tri (p-methoxyphenyl) sulfonium 10-camphorsulfonate, Examples include tris (p-fluorophenyl) sulfonium trifluoromethanesulfonate, tris (p-fluorophenyl) sulfonium p-toluenesulfonate, (p-fluorophenyl) diphenylsulfonium trifluoromethanesulfonate, and the like.

  In this invention, the usage-amount of an acid generator becomes like this. Preferably it is 0.1-20 weight part with respect to 100 weight part of resin components, More preferably, it is 0.5-15 weight part. In the present invention, two or more acid generators can be mixed and used.

式中、Ｒ⁵は、相互に同一でも異なってもよく、水素原子、アルキル基、アリール基またはアラルキル基を表す（アルキル基、アリール基、アラルキル基等の水素原子が、例えば、ヒドロキシ基など、官能基で置換されている場合を含む）。 The radiation-sensitive resin composition of the present invention can contain an acid diffusion controller and other additives.
The acid diffusion control agent controls the diffusion phenomenon in the resist film of the acid generated from the acid generator by exposure, and has an action of suppressing an undesirable chemical reaction in the non-exposed region. By using such an acid diffusion control agent, the storage stability of the composition is improved, the resolution of the resist is improved, and the change of the line width of the resist pattern due to the fluctuation of PED can be suppressed, thereby stabilizing the process. It is extremely excellent in properties.
As the acid diffusion controller, a nitrogen-containing organic compound whose basicity is not changed by exposure or heat treatment in the resist pattern forming step is preferable.
Examples of such nitrogen-containing organic compounds include compounds represented by the following formula (7) (hereinafter referred to as “nitrogen-containing compound (I)”), amide group-containing compounds, nitrogen-containing heterocyclic compounds, and the like. It is done.

In the formula, R ⁵ may be the same as or different from each other, and represents a hydrogen atom, an alkyl group, an aryl group or an aralkyl group (wherein a hydrogen atom such as an alkyl group, an aryl group, an aralkyl group, Including the case where it is substituted with a functional group).

  Examples of the nitrogen-containing compound (I) include monoalkylamines such as n-hexylamine, n-heptylamine, n-octylamine, n-nonylamine, n-decylamine; di-n-butylamine, di-n- Dialkylamines such as pentylamine, di-n-hexylamine, di-n-heptylamine, di-n-octylamine, di-n-nonylamine, di-n-decylamine; triethylamine, tri-n-propylamine, Trialkylamines such as tri-n-butylamine, tri-n-pentylamine, tri-n-hexylamine, tri-n-heptylamine, tri-n-octylamine, tri-n-nonylamine, tri-n-decylamine Aniline, N-methylaniline, N, N-dimethylaniline, 2-methylaniline, 3-methyl Examples thereof include aromatic amines such as ruaniline, 4-methylaniline, 4-nitroaniline, diphenylamine, triphenylamine, and 1-naphthylamine.

Examples of the amide group-containing compound include formamide, N-methylformamide, N, N-dimethylformamide, acetamide, N-methylacetamide, N, N-dimethylacetamide, propionamide, benzamide, pyrrolidone, N-methylpyrrolidone and the like. Can be mentioned.
Examples of the nitrogen-containing heterocyclic compound include imidazoles such as imidazole, benzimidazole, 4-methylimidazole, 4-methyl-2-phenylimidazole, 2-phenylbenzimidazole; pyridine, 2-methylpyridine, 4-methylpyridine. Pyridine such as 2-ethylpyridine, 4-ethylpyridine, 2-phenylpyridine, 4-phenylpyridine, N-methyl-4-phenylpyridine, nicotine, nicotinic acid, nicotinamide, quinoline, 8-oxyquinoline, acridine In addition to the above, pyrazine, pyrazole, pyridazine, quinosaline, purine, pyrrolidine, piperidine, morpholine, 4-methylmorpholine, piperazine, 1,4-dimethylpiperazine, 1,4-diazabicyclo [2.2.2] octane, etc. It is done.

  A base precursor having an acid dissociable group can also be used as the acid diffusion controller. Specifically, N- (t-butoxycarbonyl) piperidine, N- (t-butoxycarbonyl) imidazole, N- (t-butoxycarbonyl) benzimidazole, N- (t-butoxycarbonyl) 2-phenylbenzimidazole, N -(T-Butoxycarbonyl) dioctylamine, N- (t-butoxycarbonyl) diethanolamine, N- (t-butoxycarbonyl) dicyclohexylamine, N- (t-butoxycarbonyl) diphenylamine and the like can be mentioned.

Of these nitrogen-containing organic compounds, nitrogen-containing compounds (I) and nitrogen-containing heterocyclic compounds are preferred. Further, among the nitrogen-containing compounds (I), trialkylamines are particularly preferable, and among the nitrogen-containing heterocyclic compounds, imidazoles are particularly preferable.
The acid diffusion control agents can be used alone or in admixture of two or more.
The compounding amount of the acid diffusion controller is 15 parts by weight or less, preferably 0.001 to 10 parts by weight, and more preferably 0.005 to 5 parts by weight with respect to 100 parts by weight of the resin. In this case, when the compounding amount of the acid diffusion controller exceeds 15 parts by weight, the sensitivity as a resist and the developability of the exposed part tend to be lowered. If the blending amount of the acid diffusion controller is less than 0.001 part by weight, the pattern shape and dimensional fidelity as a resist may be lowered depending on the process conditions.

In the radiation sensitive resin composition of the present invention, a surfactant exhibiting an effect of improving the coating property and striation of the composition, the developing property as a resist, and the like can be blended.
Examples of such surfactants include polyoxyethylene lauryl ether, polyoxyethylene stearyl ether, polyoxyethylene oleyl ether, polyoxyethylene octylphenol ether, polyoxyethylene nonylphenol ether, polyethylene glycol dilaurate, and polyethylene glycol distearate. Examples of commercially available products include F-top EF301, EF303, EF352 (manufactured by Tochem Products), Megafax F171, F173 (manufactured by Dainippon Ink & Chemicals, Inc.), Florard FC430, FC431 ( Manufactured by Sumitomo 3M Limited), Asahi Guard AG710, Surflon S-382, SC101, SC102, SC103, SC104, SC105, SC106 (Asahi Glass Co., Ltd.), KP341 (Shin-Etsu Chemical Co., Ltd.), Polyflow No. 75, No. 95 (Kyoeisha Chemical Co., Ltd.) and the like.
The compounding amount of the surfactant is preferably 2 parts by weight or less with respect to 100 parts by weight of the acid dissociable group-containing resin.
Further, other sensitizers can be blended. Examples of preferred sensitizers include carbazoles, benzophenones, rose bengals, anthracenes and the like.
The blending amount of the sensitizer is preferably 50 parts by weight or less with respect to 100 parts by weight of the acid dissociable group-containing resin.

When the radiation-sensitive resin composition of the present invention is used, the total solid content is, for example, 0. It is prepared as a composition solution by uniformly dissolving in a solvent so as to be ˜50 wt%, preferably 1 to 40 wt%, and then filtering through a filter having a pore size of about 200 nm, for example.
Examples of the solvent used for the preparation of the composition solution include ethylene glycol monomethyl ether acetate, ethylene glycol monoethyl ether acetate, ethylene glycol mono-n-propyl ether acetate, ethylene glycol mono-n-butyl ether acetate and the like. Glycol monoalkyl ether acetates; propylene glycol monoalkyl ethers such as propylene glycol monomethyl ether, propylene glycol monoethyl ether, propylene glycol mono-n-propyl ether, propylene glycol mono-n-butyl ether; propylene glycol dimethyl ether, propylene glycol diethyl Ether, propylene glycol di-n-propyl ether, propylene Propylene glycol dialkyl ethers such as recall di-n-butyl ether; propylene glycol monoalkyl such as propylene glycol monomethyl ether acetate, propylene glycol monoethyl ether acetate, propylene glycol mono-n-propyl ether acetate, propylene glycol mono-n-butyl ether acetate Ether acetates; lactate esters such as methyl lactate, ethyl lactate, n-propyl lactate, i-propyl lactate; n-amyl formate, i-amyl formate, ethyl acetate, n-propyl acetate, i-propyl acetate, Aliphatic carboxylates such as n-butyl acetate, i-butyl acetate, n-amyl acetate, i-amyl acetate, i-propyl propionate, n-butyl propionate and i-butyl propionate Ethyl hydroxyacetate, ethyl 2-hydroxy-2-methylpropionate, methyl 2-hydroxy-3-methylbutyrate, ethyl methoxyacetate, ethyl ethoxyacetate, methyl 3-methoxypropionate, ethyl 3-methoxypropionate, Methyl 3-ethoxypropionate, ethyl 3-ethoxypropionate, 3-methoxybutyl acetate, 3-methyl-3-methoxybutyl acetate, 3-methyl-3-methoxybutylpropionate, 3-methyl-3-methoxybutyl Other esters such as butyrate, methyl acetoacetate, ethyl acetoacetate, methyl pyruvate, ethyl pyruvate; aromatic hydrocarbons such as toluene, xylene; methyl ethyl ketone, methyl propyl ketone, methyl butyl ketone, 2-heptanone, 3-heptanone, 4 Ketones such as heptanone and cyclohexanone; amides such as N-methylformamide, N, N-dimethylformamide, N-methylacetamide, N, N-dimethylacetamide and N-methylpyrrolidone; lactones such as γ-butyrolacun Can be mentioned.

Among these solvents, propylene glycol monoalkyl ether acetates, 2-heptanone, lactic acid esters, 2-hydroxypropionic acid esters, 3-alkoxypropionic acid esters, etc. have good in-plane uniformity during coating. Is preferable in that.
These solvents can be used alone or in admixture of two or more.

When forming a resist pattern from the radiation-sensitive resin composition of the present invention, the composition solution prepared as described above is applied by appropriate coating means such as spin coating, cast coating, roll coating, etc. A resist film is formed by coating on a substrate such as a silicon wafer or a wafer coated with aluminum, and a heat treatment (hereinafter referred to as “PB”) is performed at a temperature of about 70 ° C. to 160 ° C. in some cases. After that, exposure is performed through a predetermined mask pattern. The radiation used in this case depends on the type of the acid generator, for example, far ultraviolet rays such as F ₂ excimer laser (wavelength 157 nm), ArF excimer laser (wavelength 193 nm), KrF excimer laser (wavelength 248 nm), and synchrotron. X-rays such as radiation, and charged particle beams such as electron beams are appropriately selected and used. Moreover, exposure conditions, such as exposure amount, are suitably selected according to the compounding composition of a radiation sensitive resin composition, the kind of each additive, etc. In the present invention, far ultraviolet rays such as KrF excimer laser (wavelength 248 nm) are preferably used.

In the present invention, in order to stably form a high-precision fine pattern, it is preferable to perform heat treatment (hereinafter referred to as “PEB”) for 30 seconds or more at a temperature of 70 ° C. to 160 ° C. after exposure. In this case, if the post-exposure baking temperature is less than 70 ° C., there is a possibility that the variation in sensitivity depending on the type of the substrate will spread.
Thereafter, development is performed with an alkali developer at 10 ° C. to 50 ° C., 10 seconds to 200 seconds, preferably 15 ° C. to 30 ° C., 15 seconds to 100 seconds, particularly preferably 20 ° C. to 25 ° C., 15 seconds to 90 seconds. As a result, a predetermined resist pattern is formed.
As the alkaline developer, for example, an alkaline compound such as tetraalkylammonium hydroxide is usually used at a concentration of 1% by weight to 10% by weight, preferably 1% by weight to 5% by weight, particularly preferably 1 to 3% by weight. An alkaline aqueous solution dissolved so as to be used is used.
In addition, a water-soluble organic solvent such as methanol or ethanol or a surfactant can be appropriately added to the developer composed of the alkaline aqueous solution. In forming the resist pattern, a protective film can be provided on the resist film in order to prevent the influence of basic impurities contained in the environmental atmosphere.

Example 1
120 g of 2-bicyclo [2.2.1] -5-hepten-2-ylmethyl-1,1,1,3,3,3-hexafluoro-2-propanol was placed in a 1 liter eggplant flask and 10 ° C. Then, 35 g of thioacetic acid was slowly added dropwise. After dropping, the temperature was raised to 40 ° C. and stirred for 1 hour. Thereafter, the product was dissolved in 300 ml of chloroform and washed with 100 g of 5% aqueous sodium hydrogen carbonate solution three times. Then, chloroform was removed and the intermediate body 1 was obtained. The intermediate 1 was dissolved in 500 ml of methanol, a methanol solution (100 ml) of 36 g of sodium ethoxide was added, and the mixture was stirred at room temperature for 3 hours. After completion of the reaction, 100 ml of water was added, 2N hydrochloric acid was added to the aqueous solution from which methanol had been removed until acidic, and then extracted with MIBK. Thereafter, MIBK was removed, and 1,1,1,3,3,3-hexafluoro-2- (6-mercapto-bicyclo [2.2.1] -2-heptyl was obtained by distillation under reduced pressure (120 ° C., 6 mmHg). 80 g of methyl) -propanol (hereinafter referred to as α-1) was obtained.

The obtained α-1 was subjected to molecular weight analysis under the following conditions using a “JMS-AX505W type mass spectrometer” manufactured by JEOL Ltd. The result obtained is a parent ion peak of 308, 1,1,1,3,3,3-hexafluoro-2- (6-mercaptobicyclo [2.2.1] -2-heptylmethyl)- It was confirmed to be propanol.
Emitter current: 5 mA (used gas: Xe)
Acceleration voltage: 3.0 kV
10N MULTI: 1.3
Ionization method: Fast atom bombardment method (FAB)
Detection ion: Cation (+)
Measurement mass range: 20-1500 m / z
Scan: 30 sec
Resolution: 1500
Matrix: 3-nitrobenzyl alcohol Further, α-1 was obtained as a result of ¹ H-NMR analysis (measuring solvent: deuterated chloroform) using “JNM-EX270” manufactured by JEOL Ltd. The chemical shifts were 0.62-2.16 (8H, m), 2.65-2.98 (2H, m), 3.11-3.21 (2H, m), 1,1,1 , 3,3,3-hexafluoro-2- (6-mercaptobicyclo [2.2.1] -2-heptylmethyl) -propanol.

Example 2
120 g of 1,1,1-trifluoro-2-trifluoro-3-buten-2-ol was placed in a 1 liter eggplant flask, cooled to 10 ° C., and 46 g of thioacetic acid was slowly added dropwise. After dropping, the temperature was raised to 40 ° C. and stirred for 1 hour. Thereafter, the product was dissolved in 300 ml of chloroform and washed with 100 g of 5% aqueous sodium hydrogen carbonate solution three times. Then, chloroform was removed and the intermediate body 2 was obtained. The intermediate 2 was dissolved in 500 ml of methanol, a methanol solution (100 ml) of 47 g of sodium ethoxide was added, and the mixture was stirred at room temperature for 3 hours. After completion of the reaction, 100 ml of water was added, 2N hydrochloric acid was added to the aqueous solution from which methanol had been removed until acidic, and then extracted with MIBK. Thereafter, MIBK was removed, and 80 g of 1,1,1-trifluoro-4-mercapto-2-trifluoromethyl-2-butanol (hereinafter referred to as α-2) was obtained by distillation under reduced pressure (79 ° C., 21 mmHg). .
With respect to the obtained α-2, the molecular weight analysis result was the parent ion of 242 under the same conditions as in Example 1. As a result of ¹ H-NMR analysis, the obtained chemical shift was 1.37-1. 43 (1H, t, J = 8.4 Hz, SH), 1.81-1.92 (2H, m, CH2), 2.03 to 2.09 (2H, m, CH2), 2.53-2 .61 (2H, m, CH2), 3.12 (1H, br, OH), confirmed to be 1,1,1-trifluoro-4-mercapto-2-trifluoromethyl-2-butanol It was done.

化合物（Ｅ１−１）５３．９２ｇ（５０モル％）、化合物（Ｅ１−２）１０．６９ｇ（１０モル％）、化合物（Ｅ１−３）３５．３８ｇ（４０モル％）を２−ブタノン１８７ｇに溶かし、さらにジメチル２，２'−アゾビス（２−メチルプロピオネート）２．２４ｇ、（α―１）５．９８ｇを投入した単量体溶液を準備し、１００ｇの２−ブタノンを投入した１０００ｍｌの三口フラスコを３０分窒素パージする。窒素パージの後、反応釜を攪拌しながら８０℃に加熱し、事前に準備した上記単量体溶液を滴下漏斗を用いて３時間かけて滴下した。滴下開始を重合開始時間とし、重合反応を６時間実施した。重合終了後、重合溶液は水冷することにより３０℃以下に冷却し、２０００ｇのメタノールへ投入し、析出した白色粉末をろ別する。
ろ別された白色粉末を２度４００ｇのメタノールにてスラリー上で洗浄した後、ろ別し、５０℃にて１７時間乾燥し、白色粉末の重合体を得た（７２ｇ、収率７２％）。この重合体はＭｗが７，４００であり、¹³Ｃ-ＮＭＲ分析の結果、化合物（Ｅ１−１）、化合物（Ｅ１−２）、化合物（Ｅ１−３）で表される繰り返し単位、各繰り返し単位の含有率が５２．２：８．６：３９．２（モル％）の共重合体であった。この重合体を重合体（Ａ−１）とする。ＩＲ測定を行なった結果、３３００ｃｍ^-1吸収が確認されたことから式（２）で表される基は分子末端に付加していると考えられる。 Example 3

Compound (E1-1) 53.92 g (50 mol%), compound (E1-2) 10.69 g (10 mol%), compound (E1-3) 35.38 g (40 mol%) into 2-butanone 187 g A monomer solution containing 2.24 g of dimethyl 2,2′-azobis (2-methylpropionate) and 5.98 g of (α-1) was prepared, and 1000 ml of 100 g of 2-butanone was added. The three-neck flask is purged with nitrogen for 30 minutes. After purging with nitrogen, the reaction kettle was heated to 80 ° C. with stirring, and the monomer solution prepared in advance was added dropwise using a dropping funnel over 3 hours. The polymerization start was carried out for 6 hours with the start of dropping as the polymerization start time. After completion of the polymerization, the polymerization solution is cooled with water to 30 ° C. or less, put into 2000 g of methanol, and the precipitated white powder is filtered off.
The filtered white powder was washed twice with 400 g of methanol on the slurry, filtered, and dried at 50 ° C. for 17 hours to obtain a white powder polymer (72 g, yield 72%). . This polymer has Mw of 7,400, and as a result of ¹³ C-NMR analysis, the repeating unit represented by compound (E1-1), compound (E1-2), compound (E1-3), and each repeating unit Was a copolymer having a content of 52.2: 8.6: 39.2 (mol%). This polymer is referred to as “polymer (A-1)”. As a result of IR measurement, 3300 cm ⁻¹ absorption was confirmed, and therefore the group represented by the formula (2) is considered to be added to the molecular end.

化合物（Ｅ２−１）２４．３１ｇ（５０モル％）、化合物（Ｅ２−２）７．７５ｇ（１５モル％）、化合物（Ｅ２−３）１７．９４ｇ（３５モル％）を２−ブタノン１５０ｇに溶かし、さらにジメチル２，２'−アゾビス（２−メチルプロピオネート）１．０１ｇ、（α―１）２．７０ｇを投入した単量体溶液を準備し、１００ｇの２−ブタノンを投入した１０００ｍｌの三口フラスコを３０分窒素パージする。窒素パージの後、反応釜を攪拌しながら８０℃に加熱し、事前に準備した上記単量体溶液を滴下漏斗を用いて３時間かけて滴下した。滴下開始を重合開始時間とし、重合反応を６時間実施した。重合終了後、重合溶液は水冷することにより３０℃以下に冷却し、２０００ｇのメタノールへ投入し、析出した白色粉末をろ別する。
ろ別された白色粉末を２度４００ｇのメタノールにてスラリー上で洗浄した後、ろ別し、５０℃にて１７時間乾燥し、白色粉末の重合体を得た（３８ｇ、収率８８％）。この重合体はＭｗが７，２００であり、¹³Ｃ-ＮＭＲ分析の結果、化合物（Ｅ２−１）、化合物（Ｅ２−２）、化合物（Ｅ２−３）で表される繰り返し単位、各繰り返し単位の含有率が５２．１：１３．６：３４．３（モル％）の共重合体であった。この重合体を重合体（Ａ−２）とする。ＩＲ測定を行なった結果、３３００ｃｍ^-1吸収が確認されたことから式（２）で表される基は分子末端に付加していると考えられる。 Example 4

Compound (E2-1) 24.31 g (50 mol%), compound (E2-2) 7.75 g (15 mol%), compound (E2-3) 17.94 g (35 mol%) into 2-butanone 150 g A monomer solution containing 1.01 g of dimethyl 2,2′-azobis (2-methylpropionate) and 2.70 g of (α-1) was prepared, and 1000 ml of 100 g of 2-butanone was added. The three-neck flask is purged with nitrogen for 30 minutes. After purging with nitrogen, the reaction kettle was heated to 80 ° C. with stirring, and the monomer solution prepared in advance was added dropwise using a dropping funnel over 3 hours. The polymerization start was carried out for 6 hours with the start of dropping as the polymerization start time. After completion of the polymerization, the polymerization solution is cooled with water to 30 ° C. or less, put into 2000 g of methanol, and the precipitated white powder is filtered off.
The filtered white powder was washed twice with 400 g of methanol on the slurry, filtered, and dried at 50 ° C. for 17 hours to obtain a white powder polymer (38 g, yield 88%). . This polymer has Mw of 7,200, and as a result of ¹³ C-NMR analysis, the repeating unit represented by compound (E2-1), compound (E2-2), compound (E2-3), and each repeating unit Was a copolymer having a content of 52.1: 13.6: 34.3 (mol%). This polymer is referred to as “polymer (A-2)”. As a result of IR measurement, 3300 cm ⁻¹ absorption was confirmed, and therefore the group represented by the formula (2) is considered to be added to the molecular end.

化合物（Ｅ３−１）２４．６２ｇ（５０モル％）、化合物（Ｅ３−２）５．７７ｇ（３７モル％）、化合物（Ｅ３−３）１９．６１ｇ（１３モル％）を２−ブタノン１５０ｇに溶かし、さらにジメチル２，２'−アゾビス（２−メチルプロピオネート）１．０４ｇ、（α−１）２．７９ｇを投入した単量体溶液を準備し、１００ｇの２−ブタノンを投入した１０００ｍｌの三口フラスコを３０分窒素パージする。窒素パージの後、反応釜を攪拌しながら８０℃に加熱し、事前に準備した上記単量体溶液を滴下漏斗を用いて３時間かけて滴下した。滴下開始を重合開始時間とし、重合反応を６時間実施した。重合終了後、重合溶液は水冷することにより３０℃以下に冷却し、２０００ｇのメタノールへ投入し、析出した白色粉末をろ別する。
ろ別された白色粉末を２度２０００ｇのイソプロピルアルコールにてスラリー上で洗浄した後、ろ別し、６０℃にて１７時間乾燥し、白色粉末の重合体を得た（８５ｇ、収率８５％）。この重合体はＭｗが６，２００であり、¹³Ｃ-ＮＭＲ分析の結果、化合物（Ｅ３−１）、化合物（Ｅ３−２）、化合物（Ｅ３−３）で表される繰り返し単位、各繰り返し単位の含有率が５４．１：３１．９：１３．９（モル％）の共重合体であった。この重合体を重合体（Ａ−３）とする。ＩＲ測定を行なった結果、３３００ｃｍ^-1吸収が確認されたことから式（２）で表される基は分子末端に付加していると考えられる。 Example 5

Compound (E3-1) 24.62g (50mol%), compound (E3-2) 5.77g (37mol%), compound (E3-3) 19.61g (13mol%) to 2-butanone 150g A monomer solution was prepared by dissolving 1.04 g of dimethyl 2,2′-azobis (2-methylpropionate) and 2.79 g of (α-1), and 1000 ml of 100 g of 2-butanone. The three-neck flask is purged with nitrogen for 30 minutes. After purging with nitrogen, the reaction kettle was heated to 80 ° C. with stirring, and the monomer solution prepared in advance was added dropwise using a dropping funnel over 3 hours. The polymerization start was carried out for 6 hours with the start of dropping as the polymerization start time. After completion of the polymerization, the polymerization solution is cooled with water to 30 ° C. or less, put into 2000 g of methanol, and the precipitated white powder is filtered off.
The filtered white powder was washed twice with 2000 g of isopropyl alcohol on the slurry, filtered, and dried at 60 ° C. for 17 hours to obtain a white powder polymer (85 g, 85% yield). ). This polymer has Mw of 6,200, and as a result of ¹³ C-NMR analysis, the repeating unit represented by compound (E3-1), compound (E3-2), compound (E3-3), and each repeating unit Was a copolymer having a content of 54.1: 31.9: 13.9 (mol%). This polymer is referred to as “polymer (A-3)”. As a result of IR measurement, 3300 cm ⁻¹ absorption was confirmed, and therefore the group represented by the formula (2) is considered to be added to the molecular end.

化合物（Ｅ１−１）２６．９６ｇ（５０モル％）、化合物（Ｅ１−２）５．３５ｇ（１０モル％）、化合物（Ｅ１−３）１７．６９ｇ（４０モル％）を２−ブタノン１５０ｇに溶かし、さらにジメチル２，２'−アゾビス（２−メチルプロピオネート）１．１２ｇ、（α−２）２．３５ｇを投入した単量体溶液を準備し、１００ｇの２−ブタノンを投入した１０００ｍｌの三口フラスコを３０分窒素パージする。窒素パージの後、反応釜を攪拌しながら８０℃に加熱し、事前に準備した上記単量体溶液を滴下漏斗を用いて３時間かけて滴下した。滴下開始を重合開始時間とし、重合反応を６時間実施した。重合終了後、重合溶液は水冷することにより３０℃以下に冷却し、２０００ｇのメタノールへ投入し、析出した白色粉末をろ別する。
ろ別された白色粉末を２度４００ｇのメタノールにてスラリー上で洗浄した後、ろ別し、５０℃にて１７時間乾燥し、白色粉末の重合体を得た（４１ｇ、収率８２％）。この重合体はＭｗが６，８００であり、¹³Ｃ-ＮＭＲ分析の結果、化合物（Ｅ１−１）、化合物（Ｅ１−２）、化合物（Ｅ１−３）で表される繰り返し単位、各繰り返し単位の含有率が５２．２：９．１：３８．７（モル％）の共重合体であった。この重合体を重合体（Ａ−４）とする。ＩＲ測定を行なった結果、３３００ｃｍ^-1吸収が確認されたことから式（２）で表される基は分子末端に付加していると考えられる。 Example 6

Compound (E1-1) 26.96 g (50 mol%), compound (E1-2) 5.35 g (10 mol%), compound (E1-3) 17.69 g (40 mol%) into 2-butanone 150 g A monomer solution containing 1.12 g of dimethyl 2,2′-azobis (2-methylpropionate) and 2.35 g of (α-2) was prepared, and 1000 ml of 100 g of 2-butanone was added. The three-neck flask is purged with nitrogen for 30 minutes. After purging with nitrogen, the reaction kettle was heated to 80 ° C. with stirring, and the monomer solution prepared in advance was added dropwise using a dropping funnel over 3 hours. The polymerization start was carried out for 6 hours with the start of dropping as the polymerization start time. After completion of the polymerization, the polymerization solution is cooled with water to 30 ° C. or less, put into 2000 g of methanol, and the precipitated white powder is filtered off.
The filtered white powder was washed twice with 400 g of methanol on the slurry, filtered, and dried at 50 ° C. for 17 hours to obtain a white powder polymer (41 g, yield 82%). . This polymer has Mw of 6,800, and as a result of ¹³ C-NMR analysis, the repeating unit represented by compound (E1-1), compound (E1-2), compound (E1-3), and each repeating unit Was a copolymer having a content of 52.2: 9.1: 38.7 (mol%). This polymer is referred to as “polymer (A-4)”. As a result of IR measurement, 3300 cm ⁻¹ absorption was confirmed, and therefore the group represented by the formula (2) is considered to be added to the molecular end.

化合物（Ｅ２−１）２４．３１ｇ（５０モル％）、化合物（Ｅ２−２）７．７５ｇ（１５モル％）、化合物（Ｅ２−３）１７．９４ｇ（３５モル％）を２−ブタノン１５０ｇに溶かし、さらにジメチル２，２'−アゾビス（２−メチルプロピオネート）１．０１ｇ、（α−２）２．１２ｇを投入した単量体溶液を準備し、１００ｇの２−ブタノンを投入した１０００ｍｌの三口フラスコを３０分窒素パージする。窒素パージの後、反応釜を攪拌しながら８０℃に加熱し、事前に準備した上記単量体溶液を滴下漏斗を用いて３時間かけて滴下した。滴下開始を重合開始時間とし、重合反応を６時間実施した。重合終了後、重合溶液は水冷することにより３０℃以下に冷却し、２０００ｇのメタノールへ投入し、析出した白色粉末をろ別する。
ろ別された白色粉末を２度４００ｇのメタノールにてスラリー上で洗浄した後、ろ別し、５０℃にて１７時間乾燥し、白色粉末の重合体を得た（３８ｇ、収率８８％）。この重合体はＭｗが６，８００であり、¹³Ｃ-ＮＭＲ分析の結果、化合物（Ｅ２−１）、化合物（Ｅ２−２）、化合物（Ｅ２−３）で表される繰り返し単位、各繰り返し単位の含有率が５２．１：１４．１：３３．８（モル％）の共重合体であった。この重合体を重合体（Ａ−５）とする。 Example 7

Compound (E2-1) 24.31 g (50 mol%), compound (E2-2) 7.75 g (15 mol%), compound (E2-3) 17.94 g (35 mol%) into 2-butanone 150 g Dissolve and prepare a monomer solution containing 1.01 g of dimethyl 2,2′-azobis (2-methylpropionate) and 2.12 g of (α-2), and 1000 ml of 100 g of 2-butanone. The three-neck flask is purged with nitrogen for 30 minutes. After purging with nitrogen, the reaction kettle was heated to 80 ° C. with stirring, and the monomer solution prepared in advance was added dropwise using a dropping funnel over 3 hours. The polymerization start was carried out for 6 hours with the start of dropping as the polymerization start time. After completion of the polymerization, the polymerization solution is cooled with water to 30 ° C. or less, put into 2000 g of methanol, and the precipitated white powder is filtered off.
The filtered white powder was washed twice with 400 g of methanol on the slurry, filtered, and dried at 50 ° C. for 17 hours to obtain a white powder polymer (38 g, yield 88%). . This polymer has Mw of 6,800, and as a result of ¹³ C-NMR analysis, the repeating unit represented by compound (E2-1), compound (E2-2), compound (E2-3), and each repeating unit Was a copolymer having a content of 52.1: 14.1: 33.8 (mol%). This polymer is referred to as “polymer (A-5)”.

化合物（Ｅ３−１）２４．６２ｇ（５０モル％）、化合物（Ｅ３−２）５．７７ｇ（３７モル％）、化合物（Ｅ３−３）１９．６１ｇ（１３モル％）を２−ブタノン１５０ｇに溶かし、さらにジメチル２，２'−アゾビス（２−メチルプロピオネート）１．０４ｇ、（α−２）２．１９ｇを投入した単量体溶液を準備し、１００ｇの２−ブタノンを投入した１０００ｍｌの三口フラスコを３０分窒素パージする。窒素パージの後、反応釜を攪拌しながら８０℃に加熱し、事前に準備した上記単量体溶液を滴下漏斗を用いて３時間かけて滴下した。滴下開始を重合開始時間とし、重合反応を６時間実施した。重合終了後、重合溶液は水冷することにより３０℃以下に冷却し、２０００ｇのメタノールへ投入し、析出した白色粉末をろ別する。
ろ別された白色粉末を２度２０００ｇのイソプロピルアルコールにてスラリー上で洗浄した後、ろ別し、６０℃にて１７時間乾燥し、白色粉末の重合体を得た（８５ｇ、収率８５％）。この重合体はＭｗが６，４００であり、¹³Ｃ-ＮＭＲ分析の結果、化合物（Ｅ３−１）、化合物（Ｅ３−２）、化合物（Ｅ３−３）で表される繰り返し単位、各繰り返し単位の含有率が５３．８：３１．９：１４．２（モル％）の共重合体であった。この重合体を重合体（Ａ−６）とする。ＩＲ測定を行なった結果、３３００ｃｍ^-1吸収が確認されたことから式（２）で表される基は分子末端に付加していると考えられる。 Example 8

Compound (E3-1) 24.62g (50mol%), compound (E3-2) 5.77g (37mol%), compound (E3-3) 19.61g (13mol%) to 2-butanone 150g Dissolve and prepare a monomer solution containing 1.04 g of dimethyl 2,2′-azobis (2-methylpropionate) and 2.19 g of (α-2), and 1000 ml of 100 g of 2-butanone. The three-neck flask is purged with nitrogen for 30 minutes. After purging with nitrogen, the reaction kettle was heated to 80 ° C. with stirring, and the monomer solution prepared in advance was added dropwise using a dropping funnel over 3 hours. The polymerization start was carried out for 6 hours with the start of dropping as the polymerization start time. After completion of the polymerization, the polymerization solution is cooled with water to 30 ° C. or less, put into 2000 g of methanol, and the precipitated white powder is filtered off.
The filtered white powder was washed twice with 2000 g of isopropyl alcohol on the slurry, filtered, and dried at 60 ° C. for 17 hours to obtain a white powder polymer (85 g, 85% yield). ). This polymer has Mw of 6,400, and as a result of ¹³ C-NMR analysis, the repeating unit represented by compound (E3-1), compound (E3-2), compound (E3-3), and each repeating unit Was a copolymer having a content of 53.8: 31.9: 14.2 (mol%). This polymer is referred to as “polymer (A-6)”. As a result of IR measurement, 3300 cm ⁻¹ absorption was confirmed, and therefore the group represented by the formula (2) is considered to be added to the molecular end.

化合物（Ｅ１−１）５３．９２ｇ（５０モル％）、化合物（Ｅ１−２）１０．６９ｇ（１０モル％）、化合物（Ｅ１−３）３５．３８ｇ（４０モル％）を２−ブタノン１８７ｇに溶かし、さらにジメチル２，２'−アゾビス（２−メチルプロピオネート）２．２４ｇを投入した単量体溶液を準備し、１００ｇの２−ブタノンを投入した１０００ｍｌの三口フラスコを３０分窒素パージする。窒素パージの後、反応釜を攪拌しながら８０℃に加熱し、事前に準備した上記単量体溶液を滴下漏斗を用いて３時間かけて滴下した。滴下開始を重合開始時間とし、重合反応を６時間実施した。重合終了後、重合溶液は水冷することにより３０℃以下に冷却し、２０００ｇのメタノールへ投入し、析出した白色粉末をろ別する。
ろ別された白色粉末を２度４００ｇのメタノールにてスラリー上で洗浄した後、ろ別し、５０℃にて１７時間乾燥し、白色粉末の重合体を得た（７２ｇ、収率７２％）。この重合体はＭｗが８，５００であり、¹³Ｃ-ＮＭＲ分析の結果、化合物（Ｅ１−１）、化合物（Ｅ１−２）、化合物（Ｅ１−３）で表される繰り返し単位、各繰り返し単位の含有率が５２．２：８．０：３９．８（モル％）の共重合体であった。この重合体を重合体（Ａ'−１）とする。 Comparative Example 1

Compound (E1-1) 53.92 g (50 mol%), compound (E1-2) 10.69 g (10 mol%), compound (E1-3) 35.38 g (40 mol%) into 2-butanone 187 g Dissolve and prepare a monomer solution charged with 2.24 g of dimethyl 2,2′-azobis (2-methylpropionate), and purge a 1000 ml three-necked flask charged with 100 g of 2-butanone with nitrogen for 30 minutes. . After purging with nitrogen, the reaction kettle was heated to 80 ° C. with stirring, and the monomer solution prepared in advance was added dropwise using a dropping funnel over 3 hours. The polymerization start was carried out for 6 hours with the start of dropping as the polymerization start time. After completion of the polymerization, the polymerization solution is cooled with water to 30 ° C. or less, put into 2000 g of methanol, and the precipitated white powder is filtered off.
The filtered white powder was washed twice with 400 g of methanol on the slurry, filtered, and dried at 50 ° C. for 17 hours to obtain a white powder polymer (72 g, yield 72%). . This polymer has Mw of 8,500, and as a result of ¹³ C-NMR analysis, the repeating unit represented by compound (E1-1), compound (E1-2), compound (E1-3), and each repeating unit Was a copolymer having a content of 52.2: 8.0: 39.8 (mol%). This polymer is referred to as “polymer (A′-1)”.

化合物（Ｅ２−１）２４．３１ｇ（５０モル％）、化合物（Ｅ２−２）７．７５ｇ（１５モル％）、化合物（Ｅ２−３）１７．９４ｇ（３５モル％）を２−ブタノン１５０ｇに溶かし、さらにジメチル２，２'−アゾビス（２−メチルプロピオネート）１．０１ｇ単量体溶液を準備し、１００ｇの２−ブタノンを投入した１０００ｍｌの三口フラスコを３０分窒素パージする。窒素パージの後、反応釜を攪拌しながら８０℃に加熱し、事前に準備した上記単量体溶液を滴下漏斗を用いて３時間かけて滴下した。滴下開始を重合開始時間とし、重合反応を６時間実施した。重合終了後、重合溶液は水冷することにより３０℃以下に冷却し、２０００ｇのメタノールへ投入し、析出した白色粉末をろ別する。
ろ別された白色粉末を２度４００ｇのメタノールにてスラリー上で洗浄した後、ろ別し、５０℃にて１７時間乾燥し、白色粉末の重合体を得た（３８ｇ、収率８８％）。この重合体はＭｗが８，２００であり、¹³Ｃ-ＮＭＲ分析の結果、化合物（Ｅ２−１）、化合物（Ｅ２−２）、化合物（Ｅ２−３）で表される繰り返し単位、各繰り返し単位の含有率が５２．１：１３．６：３４．３（モル％）の共重合体であった。この重合体を重合体（Ａ'−２）とする。 Comparative Example 2

Compound (E2-1) 24.31 g (50 mol%), compound (E2-2) 7.75 g (15 mol%), compound (E2-3) 17.94 g (35 mol%) into 2-butanone 150 g Dissolve and prepare a 1.01 g monomer solution of dimethyl 2,2′-azobis (2-methylpropionate), and purge a 1000 ml three-necked flask charged with 100 g of 2-butanone with nitrogen for 30 minutes. After purging with nitrogen, the reaction kettle was heated to 80 ° C. with stirring, and the monomer solution prepared in advance was added dropwise using a dropping funnel over 3 hours. The polymerization start was carried out for 6 hours with the start of dropping as the polymerization start time. After completion of the polymerization, the polymerization solution is cooled with water to 30 ° C. or less, put into 2000 g of methanol, and the precipitated white powder is filtered off.
The filtered white powder was washed twice with 400 g of methanol on the slurry, filtered, and dried at 50 ° C. for 17 hours to obtain a white powder polymer (38 g, yield 88%). . This polymer has Mw of 8,200, and as a result of ¹³ C-NMR analysis, the repeating unit represented by compound (E2-1), compound (E2-2), compound (E2-3), and each repeating unit Was a copolymer having a content of 52.1: 13.6: 34.3 (mol%). This polymer is referred to as “polymer (A′-2)”.

化合物（Ｅ３−１）２４．６２ｇ（５０モル％）、化合物（Ｅ３−２）５．７７ｇ（３７モル％）、化合物（Ｅ３−３）１９．６１ｇ（１３モル％）を２−ブタノン１５０ｇに溶解させ、さらにジメチル２，２'−アゾビス（２−メチルプロピオネート）１．０４ｇを投入した単量体溶液を準備し、１００ｇの２−ブタノンを投入した１０００ｍｌの三口フラスコを３０分窒素パージする。窒素パージの後、反応釜を攪拌しながら８０℃に加熱し、事前に準備した上記単量体溶液を滴下漏斗を用いて３時間かけて滴下した。滴下開始を重合開始時間とし、重合反応を６時間実施した。重合終了後、重合溶液は水冷することにより３０℃以下に冷却し、２０００ｇのメタノールへ投入し、析出した白色粉末をろ別する。
ろ別された白色粉末を２度２０００ｇのイソプロピルアルコールにてスラリー上で洗浄した後、ろ別し、６０℃にて１７時間乾燥し、白色粉末の重合体を得た（８５ｇ、収率８５％）。この重合体はＭｗが６，１００であり、¹³Ｃ-ＮＭＲ分析の結果、化合物（Ｅ３−１）、化合物（Ｅ３−２）、化合物（Ｅ３−３）で表される繰り返し単位、各繰り返し単位の含有率が５４．１：３２．３：１３．６（モル％）の共重合体であった。この重合体を重合体（Ａ'−３）とする。 Comparative Example 3

Compound (E3-1) 24.62g (50mol%), compound (E3-2) 5.77g (37mol%), compound (E3-3) 19.61g (13mol%) to 2-butanone 150g Dissolve and prepare a monomer solution charged with 1.04 g of dimethyl 2,2′-azobis (2-methylpropionate), and purge a 1000 ml three-necked flask charged with 100 g of 2-butanone with nitrogen for 30 minutes. To do. After purging with nitrogen, the reaction kettle was heated to 80 ° C. with stirring, and the monomer solution prepared in advance was added dropwise using a dropping funnel over 3 hours. The polymerization start was carried out for 6 hours with the start of dropping as the polymerization start time. After completion of the polymerization, the polymerization solution is cooled with water to 30 ° C. or less, put into 2000 g of methanol, and the precipitated white powder is filtered off.
The filtered white powder was washed twice with 2000 g of isopropyl alcohol on the slurry, filtered, and dried at 60 ° C. for 17 hours to obtain a white powder polymer (85 g, 85% yield). ). This polymer has Mw of 6,100, and as a result of ¹³ C-NMR analysis, the repeating unit represented by compound (E3-1), compound (E3-2), compound (E3-3), and each repeating unit Was a copolymer having a content ratio of 54.1: 32.3: 13.6 (mol%). This polymer is referred to as “polymer (A′-3)”.

Example 9 to Example 14, Comparative Example 4 to Comparative Example 6
Each polymer obtained in Examples 3 to 8 and Comparative Examples 1 to 3, the acid generator shown below, and other components were mixed in the ratios shown in Table 1 to obtain a uniform solution. Then, it filtered with the membrane filter with a hole diameter of 200 nm, and obtained each radiation sensitive resin composition solution.
The obtained radiation-sensitive resin composition solution was exposed under the conditions shown in Table 2 and subjected to various evaluations. The evaluation results are shown in Table 2. Here, the part is based on weight unless otherwise specified.
Acid generator (B)
(B-1): Triphenylsulfonium / nonafluoro-n-butanesulfonate acid diffusion controller (C)
(C-1): 2-Phenylbenzimidazole solvent (D)
(D-1): Propylene glycol monomethyl ether acetate (D-2): Cyclohexanone

Here, each resist was evaluated in the following manner.
(1) Sensitivity:
When performing exposure using an ArF light source, a silicon wafer (ARC29) having an ARC29 film (manufactured by Brewer Science) with a film thickness of 770 angstroms formed on the wafer surface is used, and each composition solution is spin-coated on the substrate. A Nikon ArF excimer laser exposure apparatus (numerical aperture 0.75) is applied to a resist film having a film thickness of 250 nm formed by applying and PB on a hot plate under the conditions shown in Table 1 through a mask pattern. And exposed. Thereafter, PEB is performed under the conditions shown in Table 1, and then developed with a 2.38 wt% tetramethylammonium hydroxide aqueous solution at 25 ° C. for 60 seconds, washed with water, and dried to form a positive resist pattern. did. At this time, the exposure amount for forming a line-and-space pattern (1L1S) having a line width of 110 nm in a one-to-one line width was defined as the optimum exposure amount, and this optimum exposure amount was defined as the sensitivity.
(2) Resolution:
The dimension of the smallest line and space pattern that can be resolved at the optimum exposure dose was taken as the resolution.
(3) Pattern profile:
The bottom side dimension L1 and the top and bottom side dimension L2 of the rectangular cross section of the line and space pattern (1L1S) having a line width of 160 nm are measured with a scanning electron microscope, and 0.85 ≦ L2 / L1 ≦ 1 is satisfied, and The case where the pattern profile did not have a tail was regarded as “good”.
(4) Line edge roughness (LER):
A line pattern of a line and space pattern (1L1S) having a design line width of 110 nm was observed with a scanning electron microscope. FIG. 1 shows a schematic diagram of the pattern (unevenness is exaggerated more than actual). 1A is a plan view, and FIG. 1B is a cross-sectional view of a pattern 2 formed on the silicon wafer 1.
For the shapes observed in each of the examples and comparative examples, the difference ΔCD between the line width and the design line width 110 nm at the most conspicuous portion of the irregularities generated along the lateral surface 2a of the line pattern was measured. The measurement was performed at n = 10, and the measurement variation was evaluated at 3σ.

  As shown in each example of Table 2, a radiation sensitive resin composition excellent in resolution, pattern file, and line edge roughness (LER) characteristics, which are basic resist performances, can be obtained.

  Since the radiation-sensitive resin composition of the present invention is excellent in line edge roughness (LER) characteristics, it is extremely useful as a chemically amplified resist for semiconductor device production, which is expected to be further refined from now on.

It is a schematic diagram of the line pattern for LER measurement.

Explanation of symbols

1 Substrate 2 Resist pattern

Claims (5)

A novel compound represented by the following formula (1).

(In Formula (1), A represents a divalent organic group, and p represents an integer of 1 to 3, respectively.) A polymer containing a group represented by the following formula (2) and having a polystyrene-reduced weight average molecular weight of 2,000 to 100,000 as measured by gel permeation chromatography (GPC).

(In Formula (2), A represents a divalent organic group, and p represents an integer of 1 to 3, respectively.)   The polymer according to claim 2, wherein the polymer contains a repeating unit having an acid dissociable group.   A radiation-sensitive resin composition comprising an acid-dissociable group-containing resin that is insoluble in alkali or hardly soluble in alkali and easily soluble in alkali by the action of an acid, and a radiation-sensitive acid generator. A radiation-sensitive resin composition, wherein the group-containing resin is the polymer according to claim 3. A chain transfer agent represented by the following formula (1).

(In Formula (1), A represents a divalent organic group, and p represents an integer of 1 to 3, respectively.)

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