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    • 专利摘要:
    PURPOSE: To solve the problems that conventionally performance enhancing technique in microfabrication of a semiconductor device using electron beams or X-rays and to provide a negative chemical amplification type resist composition for electron beams or X-rays which satisfies sensitivity, resolution and resist shape, when electron beams or X-rays are used. CONSTITUTION: The negative chemical amplification type resist composition contains a compound which generates a radical species, by irradiation with electron beams or X-rays, a water-insoluble resin insoluble but soluble in aqueous alkali solution and a specified monomer.
    公开号:KR20020008077A
    申请号:KR1020010043328
    申请日:2001-07-19
    公开日:2002-01-29
    发明作者:아오아이토시아키；아데가와유타카；야기하라모리오
    申请人:무네유키 가코우；후지 샤신 필름 가부시기가이샤；
    IPC主号:
    专利说明:

    Negative resist composition for electron beam or X-rays {NEGATIVE-WORKING RESIST COMPOSITION FOR ELECTRON RAYS OR X-RAYS}
    [1] TECHNICAL FIELD This invention relates to the negative resist composition used suitably for the ultramicrolithography process, such as manufacture of an ultra LSI and a high capacity microchip, and other photopublication processes. More specifically, the present invention relates to a negative photoresist composition capable of high-precision pattern formation using X-rays, electron beams, and the like, and particularly, may be preferably used for microfabrication of semiconductor devices using high-energy rays such as electron beams. To a negative resist composition.
    [2] Integrated circuits have increased the degree of integration even more, and in the manufacture of semiconductor substrates such as ultra-LSIs, processing of ultra-fine patterns having line widths of 1/2 micron or less has been required. In order to satisfy the necessity, the wavelength of use of the exposure apparatus used in photolithography has become shorter, and now far ultraviolet rays and excimer laser light (XeCl, KrF, ArF, etc.) have been examined. Further, finer pattern formation has been examined by electron beams or X-rays.
    [3] In particular, electron beams or X-rays occupy positions as next-generation or next-generation pattern formation technologies, and development of negative resists capable of achieving high sensitivity, high resolution, and rectangular profile shapes is desired.
    [4] In electron beam lithography, the accelerated electron beam supplies energy to a compound in the process of causing collision scattering with atoms constituting the resist material, causing the resist material to react to form an image. The use of a highly accelerated electron beam increases the straightness, reduces the influence of electron scattering, and enables the formation of a rectangular pattern at high resolution. On the other hand, the electron beam permeability increases and the sensitivity decreases. As described above, in electron beam lithography, the sensitivity and the resolution and the resist shape are in a trade-off relationship, and the problem was how to make it compatible.
    [5] As a resist material corresponding thereto, a chemically heavy-type resist mainly using an acid catalyst reaction is used for the purpose of improving the sensitivity, and as a main component corresponding to the negative resist, a chemical composed of an alkali-soluble resin, an acid generator, and an acid crosslinking agent. An amplifying composition is effectively used.
    [6] In the past, various alkali-soluble resins have been proposed for negative chemically amplified resists. For example, Patent No. 2505033, Patent Publication No. 3-170554, Patent Publication No. Hei 6-118646, Novolak-type phenol resin, Patent Publication No. Hei 7-311463, Patent Publication No. Hei 8-292559, polyvinyl phenol having a narrow molecular weight distribution. Resin, Japanese Patent Application Laid-Open No. Hei 3-87746, and Japanese Patent Application Laid-Open No. Hei 8-44061 show a phenolic resin which is converted into a partially cyclic alcohol structure by hydrogenation, Patent Publication No. Hei 7-295200, and Patent Publication No. Hei 8-152717. A resin in which a part of the OH group of vinylphenol is protected by an alkyl group, and Japanese Patent Application Laid-Open No. Hei 8-339086 disclose a polyvinylphenol resin having an inert protecting group in an acid such as an acyl group. 10-10733 discloses polyvinylphenol resins copolymerized with styrene, Patent Publication No. Hei 9-166870 discloses polyvinylphenol resins copolymerized with (meth) acrylate monomers, and Patent Publication No. Hei 8-240911. Resin is disclosed.
    [7] Regarding the acid generator, an organic halogen compound is disclosed in Japanese Patent Application Laid-Open No. Hei 8-3635, an aromatic compound substituted with Br and Cl in Japanese Patent Laid-Open No. Hei 2-52348, and Japanese Patent Laid-Open No. Hei 4-367864. Aromatic compounds having an alkyl group substituted with Br and Cl, an alkoxy group, and Japanese Patent Application Laid-Open No. Hei 2-150848; Sulfonate compounds, Patent Publication No. Hei 4-210960, Patent Publication No. Hei 4-217249 disclose Diazo disulfone compounds, or Diazosulphone compounds, Patent Publication No. Hei 4-336454 discloses Br, I substituted alkyltriazine compounds, Patent No. Hei 4-291258 discloses sulfonamides, sulfonimide compounds, and patent publications. Hei 4-291259 discloses sulfonic acid compounds of polyhydric phenols, Patent Publication Nos. Hei 4-291260, Patent Publication No. Hei 4-291261, and Patent Publication No. Hei 6-202320. No. 9-210239, naphthoquinone diazide-4-sulfonate compound. Is a disulfone compound, an N-oxyimide sulfonate compound in Japanese Patent Application Laid-open No. Hei 6-236024, a benzylsulfonate compound in US Pat.
    [8] For acid crosslinking agents, JP-A-75652, JP-A-5-181277, JP-A-7-146556, methoxymethylmelamine compounds, JP-A-4-281455, JP-A 5-232702 Japanese Patent Application Laid-Open No. Hei 6-83055 has a compound having an alkoxy methyl ether group; Patent Publication No. Hei 5-281715 has an oxazine compound, Patent Publication No. Hei 5-134412, and Patent Publication No. Hei 6-3825. In addition to the trioxane compound, an alkoxy methylluyl compound and the like described in Japanese Patent Application Laid-Open No. Hei 1-293339 are disclosed.
    [9] However, for any combination of these compounds, it is difficult to obtain sufficient high sensitivity under electron beam irradiation under high acceleration voltage conditions or under X-ray irradiation, and to make it compatible with a resist capable of satisfying sensitivity, resolution, and resist shape. It was supposed to be.
    [10] Accordingly, an object of the present invention is to solve the problem of performance improvement technology in the microfabrication of semiconductor devices using electron beams or X-rays, and satisfies the sensitivity, resolution, and resist shape characteristics with respect to the use of electron beams or X-rays. It is to provide a negative chemical amplification resist composition for electron beams or X-rays.
    [11] In addition, it is possible to cope with next-generation EB irradiation apparatus (EB block irradiator or EB stepper (annual reduction projection irradiator) for the purpose of improving throughput) suitable for mass production of semiconductor devices. It is to provide a composition.
    [12] MEANS TO SOLVE THE PROBLEM As a result of earnestly examining the various characteristics mentioned above, this inventor discovered that the objective of this invention was outstandingly achieved by using the following specific composition, and reached this invention.
    [13] That is, this invention has the following structures.
    [14] (1) (A) A compound which generates radical species by irradiation of an electron beam or X-ray,
    [15] (B) resins insoluble in water and soluble in alkaline aqueous solutions,
    [16] (C) a compound having at least one unsaturated bond polymerizable by radicals,
    [17] Negative resist composition for electron beam or X-ray containing
    [18] (2) Resin of (B) component is resin containing repeating unit represented by general formula (a1), The negative-ray composition for electron beams or X-rays as described in said (1) characterized by the above-mentioned.
    [19]
    [20] In the formula, R 1 represents an alkyl group or a haloalkyl group, which may have a hydrogen atom, a halogen atom, a cyano group, or a substituent. R 2 represents a hydrogen atom, an alkyl group, a cycloalkyl group, an aryl group, an aralkyl group, or an acyl group which may have a substituent. R <3> , R <4> may be same or different and represents an alkyl group, a cycloalkyl group, an alkenyl group, an aralkyl group, or an aryl group which may have a hydrogen atom, a halogen atom, a cyano group, or a substituent.
    [21] A may have a single bond, a substituent, an alkylene group, an alkenylene group, a cycloalkylene group, or an arylene group, or -O-, -SO 2- , -O-CO-R 5- , -CO-OR 6 -, -CO-N (R 7 ) -R 8 -is indicated.
    [22] R <5> , R <6> , R <8> may be same or different, and may be a single bond, a substituent, The alkylene group, the alkenylene group, the cycloalkylene group, or the arylene group alone, or these groups and an ether structure, ester structure, amide structure Represents a divalent group formed by combining one or more selected from the group of a urethane structure or a ureido structure.
    [23] R <7> may be same or different and represents an alkyl group, a cycloalkyl group, an aralkyl group, or an aryl group which may have a hydrogen atom and a substituent.
    [24] 1 represents the integer of 1-3. Moreover, some R <2> or R <2> and R <3> or R <4> may combine and form a ring.
    [25] (3) The negative resist composition for electron beams or X-rays according to (1) or (2), wherein the resin of component (B) is a resin having one or more unsaturated bonds polymerizable by radicals.
    [26] (4) Resin of (B) component is resin containing repeating unit of general formula (a2), The electron beam or negative resist composition for x-rays in any one of said (1)-(3) characterized by the above-mentioned.
    [27]
    [28] In formula, R <9> represents the alkyl group or haloalkyl group which may have a hydrogen atom, a halogen atom, a cyano group, and a substituent.
    [29] R 10 to R 12 represent a hydrogen atom, an alkyl group, a cycloalkyl group, an aryl group, an aralkyl group, or an acyl group which may have a substituent, any group of formula (b), (c), or (d). do.
    [30] R <13> , R <14> may be same or different and represents an alkyl group, a cycloalkyl group, an alkenyl group, an aralkyl group, or an aryl group which may have a hydrogen atom, a hydroxyl group, a halogen atom, a cyano group, or a substituent.
    [31]
    [32] In formula, R <15> -R <20> , R <24> , R <25> represents the alkyl group or haloalkyl group which may have a hydrogen atom, a halogen atom, a cyano group, and a substituent.
    [33] R <21> , R <22> represents the hydrogen atom, the halogen atom, the hydroxyl group, and the alkyl group, the alkoxy group, and the acyloxy group which may have a substituent.
    [34] R 23 represents a hydrogen atom, an alkyl group, a cycloalkyl group, an aralkyl group, or an aryl group which may have a substituent.
    [35] A 1 is a divalent alkylene group, alkenylene group, cycloalkylene group, or arylene group which may have a single bond or a substituent, or -O-, SO 2- , -O-CO-R 26- , -CO- OR 27 -represents -CO-N (R 28 ) -R 29- .
    [36] R 26 , R 27 , R 29 may be the same or different, a divalent alkylene group which may have a single bond or an ether structure, an ester structure, an amide structure, a urethane structure or a ureido structure, and may have a substituent, Alkenylene group, a cycloalkylene group, and an arylene group are shown.
    [37] R 28 represents a hydrogen atom, an alkyl group, a cycloalkyl group, an aralkyl group, or an aryl group which may have a substituent.
    [38] A 2 represents a single bond, -OR 27- , -N (R 28 ) -R 29- .
    [39] A 3 represents a single bond, -SO 2 - or alkylene may be the holding structure, it may also have a substituent represents a good, arylene.
    [40] A 4 represents a divalent alkylene group, a cycloalkylene group, an arylene group, -O-, -SO 2- , -CO-, or -CO-OR 21 -which may have a single bond or a substituent.
    [41] x, y, z represent 0 or 1, and m, n represent an integer of 0 or 1 or more.
    [42] Provided that at least one of the formulas (a2) has a group of the formulas (b), (c) or (d). In addition, two of R 10 to R 12 , or one of R 10 to R 12 , and R 13 or R 14 may combine to form a ring.
    [43] (5) The negative resist composition for electron beams or X-rays according to any one of (1) to (4), wherein the compound of component (A) is selected from a sulfonate compound of sulfonium or iodonium.
    [44] (6) The electron beam or X-ray negative resist composition according to any one of (1) to (5), wherein the electron beam is irradiated under an acceleration voltage condition of 75 KeV or more.
    [45] Hereinafter, the compound used for this invention is demonstrated in detail.
    [46] (1) Resin which is insoluble in water (B) of the present invention and soluble in alkaline aqueous solution (hereinafter referred to as alkali-soluble resin)
    [47] Alkali-soluble resins in the present invention partially protect or modify phenol novolac resins, polyvinylphenol resins, copolymers having structural units derived from vinylphenols, and polyvinylphenol resins disclosed so far as negative chemically amplified resists. In addition to the polymer which has a phenol skeleton, such as resin obtained by making it, the resin etc. which have a carboxyl group can be used widely.
    [48] Preferably, the phenol resin containing the repeating structural unit represented by the said general formula (a1) can be enumerated.
    [49] In general formula (a1), R <1> represents the alkyl group or haloalkyl group which may have a hydrogen atom, a halogen atom, a cyano group, and a substituent.
    [50] R 2 represents a hydrogen atom, an alkyl group, a cycloalkyl group, an aryl group, an aralkyl group, or an acyl group which may have a substituent.
    [51] R <3> , R <4> may be same or different and represents an alkyl group, a cycloalkyl group, an alkenyl group, an aralkyl group, or an aryl group which may have a hydrogen atom, a halogen atom, a cyano group, or a substituent.
    [52] A is a single bond may be held, substituents, a divalent alkylene group, alkenylene group, cycloalkylene group, or arylene group, or -O-, -SO 2 -, -O- CO-R 5 -, -CO- OR 6 -represents -CO-N (R 7 ) -R 8- .
    [53] R <5> , R <6> , R <8> may be same or different, and may be a single bond, a substituent, The alkylene group, the alkenylene group, the cycloalkylene group, or the arylene group alone, or these groups and an ether structure, ester structure, amide structure Represents a divalent group formed by combining one or more selected from the group of a urethane structure or a ureido structure.
    [54] R <7> may be same or different and represents an alkyl group, a cycloalkyl group, an aralkyl group, or an aryl group which may have a hydrogen atom and a substituent.
    [55] 1 represents the integer of 1-3. Moreover, some R <2> or R <2> and R <3> or R <4> may combine, and may form a ring.
    [56] (B) Alkali-soluble resin, Preferably, it is resin which is insoluble in the water which has one or more unsaturated bonds which can superpose | polymerize with a radical, and is soluble in alkaline aqueous solution, and is phenol novolak resin, polyvinyl phenol resin, and vinyl phenol origin. Of a phenol group such as a copolymer having a structural unit, a resin obtained by partially protecting or modifying a polyvinylphenol resin with a group having an unsaturated bond polymerizable by radicals, and a (meth) acrylate polymer having a phenol skeleton. Protecting or modifying some or all of the carboxyl groups of the resin having a structural unit containing a carboxyl group substituted with a group having an unsaturated bond polymerizable by radicals and a group having an unsaturated bond polymerizable with radicals. Resin obtained etc. can be used widely.
    [57] (B) As alkali-soluble resin, More preferably, the phenol resin containing the repeating structural unit represented by the said general formula (a2) can be mentioned.
    [58] In general formula (a2), R <9> represents the alkyl group or haloalkyl group which may have a hydrogen atom, a halogen atom, a cyano group, and a substituent.
    [59] R 10 to R 12 are a hydrogen atom, an alkyl group, a cycloalkyl group, an aryl group, an aralkyl group, or an acyl group which may have any of the groups and substituents of the general formulas (b), (c) or (d). Display.
    [60] R <13> , R <14> may be same or different and represents an alkyl group, a cycloalkyl group, an alkenyl group, an aralkyl group, or an aryl group which may have a hydrogen atom, a halogen atom, a cyano group, or a substituent.
    [61] R <15> -R <20> , R <24> , R <25> represents the alkyl group or haloalkyl group which may have a hydrogen atom, a halogen atom, a cyano group, and a substituent.
    [62] R <21> , R <22> represents the hydrogen atom, the halogen atom, the hydroxyl group, and the alkyl group, the alkoxy group, and the acyloxy group which may have a substituent.
    [63] R 23 represents a hydrogen atom, an alkyl group, a cycloalkyl group, an aralkyl group, or an aryl group which may have a substituent.
    [64] A 1 is a divalent alkylene group, alkenylene group, cycloalkylene group, or arylene group which may have a single bond or a substituent, or -O-, SO 2- , -O-CO-R 26- , -CO- OR 27 -represents -CO-N (R 28 ) -R 29- .
    [65] R 26 , R 27 , R 29 may be the same or different and may be a single bond or an ether group, an ester group, an amide group, a urethane group, or a ureido group, or a divalent alkylene group or egg which may have a substituent. A kenylene group, a cycloalkylene group, and an allylene group are shown.
    [66] R 28 represents a hydrogen atom, an alkyl group, a cycloalkyl group, an aralkyl group, or an aryl group which may have a substituent.
    [67] A 2 represents a single bond, -OR 27- , -N (R 28 ) -R 29- .
    [68] A 3 represents an arylene group which may have a single bond or a substituent.
    [69] A 4 represents a divalent alkylene group, a cycloalkylene group, an arylene group, -O-, -SO 2- , -CO-, or -CO-OR 27 -which may have a single bond or a substituent.
    [70] x, y, z represent 0 or 1, and m, n represent an integer of 0 or 1 or more.
    [71] Provided that at least one of the formulas (a2) has a group of the formulas (b), (c) or (d). In addition, two of R 10 to R 12 , or one of R 10 to R 12 , and R 13 or R 14 may combine to form a ring.
    [72] In addition, in said general formula, as an alkyl group of R <1> -R <4> , R <7> , R <9> -R <25> , R <28> , it is a C1-C8 alkyl group, For example, specifically, a methyl group, an ethyl group, a propyl group, n-butyl group, sec-butyl group, hexyl group, 2-ethylhexyl group, and octyl group are preferable.
    [73] The cycloalkyl group of R 2 to R 4 , R 7 , R 10 to R 14 , R 23 , and R 28 may be monocyclic or may be polycyclic.
    [74] As monocyclic type, C3-C8, for example, a cyclopropyl group, a cyclopentyl group, and a cyclohexyl group can be mentioned preferably.
    [75] As a polycyclic type, an adamantyl group, norbornyl group, isoboroyl group, dicyclopentyl group, a-pinel group, tricyclo decanyl group, etc. are mentioned preferably, for example.
    [76] As an alkenyl group of R <3> , R <4> , R <13> and R <14> , a vinyl group, an allyl group, butenyl group, and cyclohexenyl group can be mentioned specifically, as an alkenyl group of C2-C8, for example. .
    [77] As an aryl group of R <2> -R <4> , R <7> , R <10> -R <14> , R <23> and R <28> , it is a C6-C15 aryl group, specifically, a phenyl group, a tril group, a dimethylphenyl group, 2,4, 6-trimethylphenyl group, naphthyl group, anthryl group, etc. can be mentioned preferably.
    [78] As an aralkyl group of R <2> -R <4> , R <7> , R <10> -R <14> , R <23> and R <28> , it is a C7-C12 aralkyl group, For example, specifically, a benzyl group, a phenethyl group, a naphthyl methyl group, etc. May be preferably enumerated.
    [79] Examples of haloalkyl groups for R 1 , R 9 , R 15 to R 20 , R 24 , and R 25 include, for example, haloalkyl groups having 1 to 4 carbon atoms, and specifically, chloroethyl group, chloropropyl group, chlorobutyl group and bromo. Methyl group, bromoethyl group, etc. can be mentioned preferably.
    [80] As an acyl group of R <2> , R <10> -R <12> , a formyl group, an acetyl group, a propane oil group, butan oil group, a pivaloyl group, a benzoyl group etc. can be mentioned preferably, for example as an acyl group of 1-10 carbon atoms. have.
    [81] As an alkoxy group of R <21> , R <22> , a methoxy group, an ethoxy group, a propoxy group, butoxy group etc. can be mentioned preferably, for example as a C1-C8 alkoxy group. As an acyloxy group, an acetoxy group, a propanoyloxy group, a benzoyloxy group etc. can be mentioned preferably, for example as an acyloxy group of 1-10 carbon atoms.
    [82] As an alkylene group of A, R 5 , R 6 , R 8 , A 1 , A 4 , R 26 , R 27 , and R 29 , for example, an alkylene group having 1 to 8 carbon atoms, a methylene group, an ethylene group, a propylene group, Butylene group, hexylene group, octylene group, etc. can be mentioned preferably.
    [83] As an alkenylene group of A, R 5 , R 6 , R 8 , A 1 , R 26 , R 27 , and R 29 , for example, as an alkenylene group having 2 to 6 carbon atoms, an ethenylene group, a propenylene group and a butenylene group Etc. can be enumerated preferably.
    [84] As a cycloalkylene group of A, R 5 , R 6 , R 8 , A 1 , A 4 , R 26 , R 27 , and R 29 , for example, a cycloalkylene group having 5 to 8 carbon atoms, a cyclopentylene group and a cyclohexylene Group etc. can be mentioned preferably.
    [85] As an arylene group of A, R 5 , R 6 , R 8 , A 1 , A 3 , A 4 , R 26 , R 27 , and R 29 , for example, as an arylene group having 6 to 12 carbon atoms, a phenylene group, a triylene group, Xylene group, naphthylene group, etc. can be mentioned preferably.
    [86] Substituents substituted with these groups include active hydrogens such as amino groups, amide groups, ureido groups, urethane groups, hydroxyl groups and carboxyl groups, halogen atoms (fluorine atoms, chlorine atoms, bromine atoms, iodine atoms), Alkoxy group (methoxy group, ethoxy group, propoxy group, butoxy group, etc.), thioether group, acyl group (acetyl group, propaneyl group, benzoyl group, etc.), acyloxy group (acetoxy group, propaneyloxy group, benzoyl Oxy group), an alkoxycarbonyl group (methoxycarbonyl group, ethoxycarbonyl group, propoxycarbonyl group, etc.), a cyano group, a nitro group, etc. are mentioned. In particular, it is preferable to have active hydrogens, such as an amino group, a hydroxyl group, and a carboxyl group.
    [87] In addition, a plurality of R 2, or R 2 and R 3 or R 4, R 10 ~R 2 of 12, or R 10 a is a ring formed by bonding R 13 or R 14 and one 1 ~R 12, benzofuran The 4-7 membered ring containing oxygen atoms, such as a ring, a benzodioxoneol ring, and a benzopyran ring, is mentioned.
    [88] Although the resin of this invention (B) may be resin which consists only of the repeating structural unit of general formula (a1) and (a2), another polymerizable monomer may be copolymerized for the purpose of improving the performance of the negative resist of this invention. .
    [89] As a copolymerizable monomer which can be used, what is shown below is contained. For example, addition-polymerizable unsaturated bonds selected from acrylic acid esters, acrylamides, methacrylic acid esters, methacrylamides, allyl compounds, vinyl ethers, vinyl esters, styrenes, crotonic acid esters and the like other than those described above. It is a compound having one.
    [90] Specifically, for example, acrylic esters such as alkyl (preferably having 1 to 10 carbon atoms in the alkyl group) acrylate (e.g., methyl acrylate, ethyl acrylate, propyl acrylate, t-butyl acrylate, amyl acrylate, acrylic acid Cyclohexyl, ethylhexyl acrylate, octyl acrylate, t-octyl acrylate, chlorethyl acrylate, 2-hydroxyethyl acrylate, 2,2-dimethylhydroxypropyl acrylate, 5-hydroxypentyl acrylate, trimethylol Propane monoacrylate, pentaerythritol monoacrylate, glycidyl acrylate, benzyl acrylate, furfuryl acrylate, tetrahydrofurfuryl acrylate and the like) aryl acrylates (such as phenyl acrylate);
    [91] Methacrylic acid esters such as alkyl (preferably having 1 to 10 carbon atoms in the alkyl group) methacrylate (e.g., methyl methacrylate, ethyl methacrylate, propyl methacrylate, isopropyl methacrylate, t-butyl methacrylate, amyl methacrylate, hexyl methacrylate, cyclohexyl methacrylate, benzyl methacrylate, chlorbenzyl methacrylate, octyl methacrylate, 2-hydroxyethyl methacrylate, 4- Hydroxybutyl methacrylate, 5-hydroxypentyl methacrylate, 2,2-dimethyl-3-hydroxypropyl methacrylate, trimethylolpropane monomethacrylate, pentaerythritol monomethacrylate, glycy Dimethyl methacrylate, furfuryl methacrylate, tetrahydrofurfuryl methacrylate, and the like, aryl methacrylate (e.g., phenyl methacrylate, cresylmeth) Methacrylate, naphthyl methacrylate, etc.);
    [92] Acrylamides such as acrylamide and N-alkylacrylamides (as alkyl groups having from 1 to 10 carbon atoms, for example, methyl, ethyl, propyl, butyl, t-butyl, heptyl, octyl, Cyclohexyl group, benzyl group, hydroxyethyl group, benzyl group, etc.), N-arylacrylamide (Aryl group is, for example, phenyl group, trilyl group, nitrophenyl group, niphthyl group, cyanophenyl group, hydroxyphenyl group, carboxy) Phenyl group, etc.), and N, N-dialkylacrylamide (as the alkyl group, those having 1 to 10 carbon atoms, such as methyl group, ethyl group, butyl group, isobutyl group, ethylhexyl group, cyclohexyl group, etc.) N, N-diarylacrylamide (Aryl group includes, for example, a phenyl group), N-methyl-N-phenylacrylamide, N-hydroxyethyl-N-methylacrylamide, N-2- Acetoamide ethyl-N-acetylacrylamide and the like;
    [93] Methacrylamides such as methacrylamide and N-alkyl methacrylamide (as the alkyl group, those having 1 to 10 carbon atoms, for example, methyl, ethyl, t-butyl, ethylhexyl, hydroxyethyl and cyclo Hexyl group etc.), N-aryl methacrylamide (Aryl group has a phenyl group etc.), N, N- dialkyl methacrylamide (The alkyl group is an ethyl group, a propyl group, a butyl group, etc.). .) N, N-diaryl methacrylamide (Aryl group includes a phenyl group, etc.), N-hydroxyethyl-N-methylmethacrylamide, N-methyl-N-phenylmethacrylamide, N-ethyl -N-phenyl methacrylamide and the like; Allyl compounds such as allylerythritol (e.g., allyl acetate, allyl capronate, allyl caprylic acid, allyl laurate, allyl palmitate, allyl stearate, allyl benzoate, allyl acetate, allyl lactate, etc.), allyloxy Ethanol and the like;
    [94] Vinyl ethers such as alkyl vinyl ethers (eg, hexyl vinyl ether, octyl vinyl ether, decyl vinyl ether, ethylhexyl vinyl ether, methoxyethyl vinyl ether, ethoxyethyl vinyl ether, chlorethyl vinyl ether, 1-methyl-); 2,2-dimethylpropyl vinyl ether, 2-ethylbutyl vinyl ether, hydroxyethyl vinyl ether, diethylene glycol vinyl ether, dimethylaminoethyl vinyl ether, diethylaminoethyl vinyl ether, butylaminoethyl vinyl ether, benzyl vinyl ether , Tetrahydrofurfuryl vinyl ether, etc., vinyl aryl ether (e.g., vinyl phenyl ether, vinyl trityl ether, vinyl chlorphenyl ether, vinyl-2,4-dichlorophenyl ether, vinyl naphthyl ether, vinyl anthranyl ether, etc.) );
    [95] Vinyl esters, such as vinyl butyrate, vinyl isobutylate, vinyl trimethyl acetate, vinyl diethyl acetate, vinyl varate, vinyl caproate, vinyl chlor acetate, vinyl dichlor acetate, vinyl methoxy acetate, vinyl butoxy acetate , Vinyl phenyl acetate, vinyl aceto acetate, vinyl lactate, vinyl-β-phenyl butyrate, vinyl cyclohexyl carboxylate, vinyl benzoate, vinyl salicylate, chlorinated vinyl, tetrachloro benzoate, vinyl naphthoate, etc. ;
    [96] Styrene, such as styrene, alkyl styrene (e.g. methyl styrene, dimethyl styrene, trimethyl styrene, ethyl styrene, diethyl styrene, isopropyl styrene, butyl styrene, hexyl styrene, cyclohexyl styrene, decyl styrene, benzyl styrene, chlormethyl Styrene, trifluoromethylstyrene, ethoxymethylstyrene, acetoxymethylstyrene and the like), alkoxystyrene (e.g. methoxystyrene, 4-methoxy-3-methylstyrene, dimethoxystyrene, etc.), halogen styrene (e.g. Chlorstyrene, Dichlorostyrene, Trichlorstyrene, Tetrachlorstyrene, Pentachlorstyrene, Bromostyrene, Dibromostyrene, Iodine Styrene, Fluorostyrene, Trifluorostyrene, 2-Bromo-4-trifluoro Methyl styrene, 4-fluoro-3-trifluoromethyl styrene, etc.), carboxy styrene;
    [97] Crotonic acid esters such as alkyl crotonate (eg, butyl crotonate, hexyl crotonate, glycerin monocrotonate); Dialkyl itaconic acid (for example, dimethyl itaconic acid, diethyl itaconic acid, dibutyl itaconic acid, etc.); Dialkyl esters of maleic acid or fumaric acid (for example, dimethyl maleate, dibutyl maleate, etc.), maleic anhydride, maleimide, acrylonitrile, methacrylonitrile, maleylonitrile, and the like. In addition, generally, what is necessary is just the copolymerizable addition-polymerizable unsaturated compound.
    [98] Among them, monomers that improve alkali solubility, such as monomers having a carboxyl group such as carboxystyrene, N- (carboxyphenyl) acrylamide, N- (carboxyphenyl) methacrylamide, maleimide, and the like, are preferred as copolymerization components.
    [99] As content of the other polymerizable monomer in resin in this invention, 50 mol% or less is preferable with respect to all the repeating units, More preferably, it is 30 mol% or less.
    [100] Although the specific example of resin which has a repeating structural unit represented by general formula (a1) and (a2) below is shown, this invention is not limited to this.
    [101]
    [102]
    [103]
    [104]
    [105]
    [106]
    [107]
    [108]
    [109]
    [110]
    [111] N in the said specific example represents a positive integer. x, y, z represent the molar ratio of the resin composition, in the resin consisting of two components, x = 10 to 95, y = 5 to 90, preferably x = 40 to 90, y = 10 to 60 Used. In resin which consists of three components, it is used in the range of x = 10-90, y = 5-85, z = 5-85, Preferably x = 40-80, y = 10-50, z = 10-50. .
    [112]
    [113]
    [114]
    [115]
    [116]
    [117]
    [118]
    [119]
    [120]
    [121]
    [122]
    [123]
    [124] m, n, o represent the molar ratio of the resin composition, and in the resin composed of two components, m = 10 to 95, n = 5 to 90, preferably m = 40 to 90, n = 10 to 60 Used. In resin which consists of three components, it is used in the range of m = 10-90, n = 5-85, o = 5-85, Preferably m = 40-80, n = 10-50, o = 10-50. .
    [125] The preferred molecular weight of the resin (B) having a repeating structural unit represented by the general formula (a1) or (a2) is preferably 1,000 to 200,000 in the weight average, and preferably used in the range of 3,000 to 50,000. do. The molecular weight distribution is 1-10, Preferably it is 1-3, More preferably, the thing of the range of 1-1.5 is used. The smaller the molecular weight distribution is, the smoother the sidewall of the resolution, the resist shape, and the resist pattern is, and the better the roughness is.
    [126] The total content of the repeating structural unit represented by the general formula (a1) or (a2) is 5 to 100 mol%, preferably 10 to 90 mol% with respect to the total resin.
    [127] Alkali-soluble resin containing the structural unit represented by general formula (a1) or (a2) used for this invention is Macromolecules (1995), 28 (11), 3787-3789, Polym. Bull. (Berlin) (1990), 24 (4), 385-389, and the method described in Unexamined-Japanese-Patent No. 8-286375. That is, the target alkali-soluble resin can be obtained by radical polymerization or living anion polymerization method.
    [128] These resin may be used by 1 type, and may mix and use plurality.
    [129] Here, the polymerization average molecular weight is defined as the polystyrene conversion value of gel permeation chromatography.
    [130] The alkali dissolution rate of the alkali-soluble resin is preferably measured at 0.261 N tetramethylammonium hydrooxide (TMAH) (23 DEG C) and 20 Pa / sec or more. Especially preferably, it is 200 microseconds / sec or more.
    [131] Although alkali-soluble resin of this invention may be used independently, you may use other alkali-soluble resin together. The use ratio can use together alkali-soluble resin other than this invention up to 100 weight part with respect to 100 weight part of alkali-soluble resin of this invention. The alkali-soluble resin which can be used together is illustrated below.
    [132] Examples thereof include, but are not limited to, novolak resins, hydrogenated novolak resins, acetone-pyrogallol resins, styrene-maleic anhydride copolymers, carboxyl group-containing methacrylic resins, and derivatives thereof.
    [133] The addition amount of resin (B) is used in 30 to 95 weight% with respect to the total solid of a composition, Preferably it is 40 to 90 weight%, More preferably, it is 50 to 80% weight%.
    [134] (2) Compound which generates radical species by irradiation of electron beam or X-ray of this invention (A)
    [135] Any compound can be used for (A) component used for this invention as long as it is a compound which generate | occur | produces a radical species by irradiation of an electron beam or X-rays.
    [136] By irradiation of such an electron beam or X-ray, as a compound which generate | occur | produces a radical species, the photoinitiator of radical photopolymerization and its mixture can be selected suitably, and can be used.
    [137] Further, by irradiation of these electron beams or X-rays, a compound in which radical species are generated or a compound introduced into the main chain or side chain of a polymer, for example, Patent Publication No. 63-26653, Patent Publication No. 55-164824, Patent Publication The compounds described in JP-A-62-69263, JP-A-63-146038, JP-A-63-163452, JP-A-62-153853, JP-A-63-146029 and the like can be used.
    [138] In addition, well-known iodonium salts, sulfonium salts, onium salts such as selenium, organic halogen compounds, N-iminosulfonate compounds, N-imidosulfonate compounds, disulfone compounds and the like can be given.
    [139] Preferably, they are sulfonium or sulfonate compounds of iodonium, sulfonic acid ester compounds of N-hydroxyimido, or disulfone compounds.
    [140] Especially among the compounds which generate | occur | produce radical species by irradiation of the electron beam or X-ray of these invention (A), N-imidosulfonate as described in Unexamined-Japanese-Patent No. 10-7653, 11-2901 etc. is especially preferable. Although the compound and the sulfonium salt and iodonium salt represented by the following general formula (I)-(III) can be mentioned, The sulfonium salt and iodonium represented by the following general formula (I)-(III) are the most preferable.
    [141] Furthermore, the sulfonium salts and iodonium salts represented by the following general formulas (I) to (III) are compounds which generate an acid by electron beam or X-ray irradiation, but in the present invention, radical species by electron beam or X-ray irradiation It is used as an example of a compound which produces | generates.
    [142] As a compound which generate | occur | produces a radical species by irradiation of (A) electron beam or X-ray of this invention, the compound which generate | occur | produces an acid simultaneously with a radical species can also be used.
    [143]
    [144] R 1 ~R 37 in the general formula (Ⅰ) ~ formula (Ⅲ) is a group that can be represented by a hydrogen atom, an alkyl group, an alkoxy group, a hydroxy group, a halogen atom, or -SR 38.
    [145] The alkyl group represented by R 1 to R 37 may be linear, branched, or cyclic. Examples of the linear or branched alkyl group include methyl group, ethyl group, propyl group, n-butyl group, sec-butyl group, t-butyl group and the like, for example, alkyl groups having 1 to 4 carbon atoms. As a cyclic alkyl group, C3-C8 alkyl groups, such as a cyclopropyl group, a cyclopentyl group, and a cyclohexyl group, can be mentioned, for example.
    [146] The alkoxy group represented by R 1 to R 37 may be linear, may be branched, or may be a cyclic alkoxy group. Examples of the linear or branched alkoxy group include, for example, those having 1 to 8 carbon atoms, such as methoxy group, ethoxy group, hydroxyethoxy group, propoxy group, n-butoxy group, isobutoxy group, sec-butoxy group and t- Butoxy group, octyloxy group, etc. can be mentioned. Examples of the cyclic alkoxy group include a cyclopentyloxy group and a cyclohexyloxy group.
    [147] Examples of the cyclic alkoxy group include a cyclopentyloxy group and a cyclohexyloxy group.
    [148] Examples of the halogen atom represented by R 1 to R 37 include fluorine, chlorine, bromine and iodine atoms.
    [149] R 1 -SR 38 R 38 in which ~R 37 is displayed, is an alkyl group, or an aryl group. As a range of the alkyl group which R <38> represents, all the alkyl groups already listed can be mentioned as an alkyl group which R <1> -R <37> represents, for example.
    [150] Aryl groups which R 38 is displayed, and page groups, Trill group, a methoxyphenyl group, a naphthyl group, can be exemplified aryl groups having 6 to 14 carbon atoms.
    [151] Alkyl group which R <1> -R <38> represents Hereafter, to an aryl group, you may couple | bond a substituent to all one part of all groups, you may increase carbon number, and you may not have a substituent. Substituents which may be bonded to each other are preferably a C1-4 alkoxy group, a C6-10 aryl group, a C2-6 alkenyl group, and include a cyano group, a hydroxy group, a carboxyl group and an alkoxy group. Carbonyl group, nitro group, etc. can also be mentioned. In addition, a halogen atom may be sufficient. For example, a fluorine atom, a chlorine atom, and an iodine atom can be enumerated.
    [152] Two or more of those groups represented by R 1 to R 15 in General Formula (I) may be bonded to each other to form a ring. The ring may be formed by the direct bonding of the terminals of the groups represented by R 1 to R 15 . A ring may be formed by indirectly bonding through one or two or more elements selected from carbon, oxygen, sulfur, and nitrogen. As a ring structure which two or more of R <1> -R <15> combine and form, it is the same structure as ring structure shown by a furan ring, a dihydrofuran ring, a pyran ring, a trihydropyran ring, a thiophene ring, a pyrrole ring, etc. Can be enumerated. The same thing can be said about R <16> -R <27> in general formula (II). Two or more may combine directly or indirectly and may form the ring. The same applies to R 28 to R 37 in General Formula (III).
    [153] General formulas (I) to (III) have X − . X <-> which general formula (I)-(III) holds is an anion of an acid. The acid which forms an anion is organic acid whose pKa values, such as carboxylic acid and a sulfonic acid, are seven or less. Examples of the carboxylic acid include linear, branched or cyclic alkylcarboxylic acid and arylcarboxylic acid (preferably benzoic acid, naphthalenecarboxylic acid, anthracenecarboxylic acid) which may have a substituent.
    [154] Examples of sulfonic acids include linear, branched or cyclic alkylsulfonic acids and arylsulfonic acids (preferably benzenesulfonic acid, naphthalenesulfonic acid and anthracenesulfonic acid) which may have a substituent. It is preferable that at least one fluorine atom is substituted with these acids.
    [155] Or the acid is a group consisting of an alkyl group, an alkoxy group, an acyl group, an acyloxy group, a sulfonyl group, a sulfonyloxy group, a sulfonylamino group, an aryl group, an aralkyl group, and an alkoxycarbonyl group in addition to or instead of the fluorine atom. At least one organic group selected from &lt; RTI ID = 0.0 &gt; and, &lt; / RTI &gt; furthermore, the organic group further substitutes at least one fluorine atom.
    [156] The benzene sulfonic acid, naphthalene sulfonic acid, or anthracene sulfonic acid may be substituted with a halogen atom other than fluorine, a hydroxyl group, a nitro group, or the like.
    [157] The alkyl group which couple | bonds with the acid which forms the anion of X <-> is a C1-C12 alkyl group, for example. The alkyl group may be linear, branched or cyclic, and is preferably substituted with one or more fluorine atoms, preferably with 25 or less unsubstituted atoms.
    [158] Specifically, trifluoromethyl group, pentafluoroethyl group, 2,2,2-trifluoroethyl group, heptafluoropropyl group, heptafluoro isopropyl group, perfluorobutyl group, perfluorooctyl group, purple Rhododecyl groups, perfluorocyclohexyl groups, and the like. Especially, the C1-C4 perfluoroalkyl group substituted with all the fluorine is preferable.
    [159] The alkoxy group bonded to the acid which forms the anion of X <-> is a C1-C12 alkoxy group. The alkoxy group may be linear, branched or cyclic, and is preferably substituted with one or more fluorine atoms, preferably 25 or less fluorine atoms.
    [160] Specifically, trifluoromethoxy group, pentafluoroethoxy group, heptafluoroisopropyloxy group, perfluorobutoxy group, perfluorooctyloxy group, perfluoro dodecyloxy group, perfluoro cyclohexyl jade You can list when. Especially, the C1-C4 perfluoroalkoxy group substituted by the fluorine all is preferable.
    [161] It is preferable that the acyl group couple | bonded with the acid which forms the anion of X <-> is substituted by C2-C12, 1-23 fluorine atoms. Specifically, a trifluoroacetyl group, a fluoroacetyl group, a pentafluoro propionyl group, a pentafluorobenzoyl group, etc. can be mentioned.
    [162] It is preferable that the acyloxy group couple | bonded with the acid which forms the anion of X <-> is substituted by C2-C12, 1-23 fluorine atoms. Specifically, a trifluoroacetoxy group, a fluoroacetoxy group, a pentafluoro propionyloxy group, a pentafluorobenzoyloxy group, etc. are mentioned.
    [163] As a sulfonyl group which couple | bonds with the acid which forms the anion of X <-> , it is preferable that C1-C12 is substituted by 1-25 fluorine atoms. Specifically, a trichloromethane sulfonyl group, a pentafluoroethane sulfonyl group, a perfluoro butane sulfonyl group, a perfluoro octane sulfonyl group, a pentafluoro benzene sulfonyl group, 4-trifluoromethylbenzene sulfonyl group, etc. are mentioned. can do.
    [164] As said sulfonyloxy group couple | bonded with the acid which forms the anion of X <-> , it is preferable that C1-C12 and 1-25 fluorine atom are substituted. Specifically, trichloromethanesulfonyloxy, perfluorobutanesulfonyloxy group, 4-trifluoromethylbenzenesulfonyloxy group, etc. are mentioned.
    [165] As said sulfonylamino group couple | bonded with the acid which forms the anion of X <-> , it is preferable that C1-C12 is substituted by 1-25 fluorine atoms. Specifically, a trichloromethanesulfonylamino group, a perfluorobutane sulfonylamino group, a perfluorooctane sulfonylamino group, a pentafluorobenzenesulfonylamino group, etc. are mentioned.
    [166] As said aryl group couple | bonded with the acid which forms the anion of X <-> , it is preferable that C1-C14 and 1-9 fluorine atoms are substituted. Specifically, pentafluorophenyl group, 4-trifluoromethylphenyl group, heptafluoronaphthyl group, nonafluoroanthranyl group, 4-fluorophenyl group, 2,4-difluorophenyl group, etc. are mentioned.
    [167] As the aralkyl group which is bonded to an acid forming an anion of X − , it is preferable that carbon atoms are substituted with 7 to 10 and 1 to 15 fluorine atoms. Specifically, pentafluorophenylmethyl group, pentafluorophenylethyl group, perfluorobenzyl group, perfluorophenethyl group, etc. can be mentioned.
    [168] As said alkoxycarbonyl group couple | bonded with the acid which forms the anion of X < - >, it is preferable that carbon number is substituted by 2-13 and 1-25 fluorine atoms. Specific examples thereof include a trifluoromethoxycarbonyl group, pentafluoroethoxycarbonyl group, pentafluorophenoxycarbonyl group, perfluorobutoxycarbonyl group, perfluorooctyloxycarbonyl group, and the like.
    [169] Of these anions, most preferred X − is a fluorine-substituted benzenesulfonate anion, and among these, pentafluorobenzenesulfonate anion is particularly preferable.
    [170] In addition, benzene sulfonic acid, naphthalene sulfonic acid, or anthracene sulfonic acid having the fluorine-containing substituent may further be a linear, branched or cyclic alkoxy group, acyl group, acyloxy group, sulfonyl group, sulfonyloxy group, sulfonylamino group, An aryl group, an aralkyl group, an alkoxycarbonyl group (these carbon number ranges are the same as above), a halogen (except fluorine), a hydroxyl group, a nitro group, etc. may be substituted.
    [171] Although the specific example of the compound represented by these general formula (I)-(III) is shown below, it is not limited to this.
    [172]
    [173]
    [174]
    [175]
    [176]
    [177]
    [178]
    [179]
    [180]
    [181]
    [182]
    [183] The compound of general formula (I) and general formula (II) can be synthesize | combined by the following method. For example, an aryl grignard reagent such as aryl magnesium bromide is reacted with phenyl sulfoxide, and the resulting triaryl sulfonium halide is salt-exchanged with sulfonic acid. There is another way. For example, there is a method of condensation and salt exchange of an aromatic compound reacting with phenyl sulfoxide using an acid catalyst such as methanesulfonic acid / 5 diphosphate or alumina chloride. In addition, the diaryl iodonium salt and the diaryl sulfide can be synthesized by a method such as condensation and salt exchange using a catalyst such as copper acetate. In either of the above methods, the phenyl sulfoxide may have a substituent substituted with a benzene ring and may not have such a substituent.
    [184] The compound of general formula (III) can be synthesize | combined by making an aromatic compound react using a periodate.
    [185] As for content of (A) component used by this invention, 0.1-20 weight% is suitable with respect to solid content of all the negative resist compositions, Preferably it is 0.5-10 weight%, More preferably, it is 1-7 weight%. .
    [186] In the present invention, in addition to the compounds represented by the general formulas (I) to (III), or in addition to these, other compounds that decompose upon irradiation with radiation to generate radical species can be used.
    [187] When using the compound represented by general formula (I)-general formula (III), and the other compound which decomposes by irradiation of a radiation and generate | occur | produces a radical species, it is represented by said general formula (I)-general formula (III). The ratio of the compound to be displayed and other compounds that are decomposed by irradiation with radiation to generate radical species is 100/0 to 20/80, preferably 90/10 to 40/60, more preferably 80/20 in molar ratio. It is -50/50.
    [188] (3) A compound having an unsaturated bond polymerizable by the radical of the present invention (C)
    [189] As the compound having an unsaturated bond which can be polymerized by a radical generated from the compound of the present invention (A), a known monomer having a polymerizable group can be used without particular limitation.
    [190] As such a monomer, specifically, monofunctional acrylic acid ester, such as 2-ethylhexyl acrylate, 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, its derivatives, or these acrylates are methacrylylated. Compounds substituted with latex, itaconate, crotonate, maleate and the like;
    [191] Bifunctional acrylic acid esters and derivatives thereof, such as polyethylene glycol diacrylate, pentaerythritol diacrylate, bisphenol A diacrylate, and diacrylate of ε-caprolactone adduct of hydroxypivarine neopentyl glycol Compounds in which the rate is replaced by methacrylate, itaconate, crotonate, maleate, or the like;
    [192] Alternatively, polyfunctional acrylate esters and derivatives thereof such as trimethylolpropane tri (meth) acrylate, dipentaerythritol pentaacrylate, dipentaerythritol hexaacrylate, pyrogallol triacrylate, or these acrylates The compound substituted by acrylate, itaconate, a crotonate, a maleate, etc. can be mentioned. Moreover, what is called what is called a prepolymer which introduce | transduced acrylic acid or methacrylic acid into the oligomer of a suitable molecular weight, and provided photopolymerization can also be used preferably.
    [193] In addition, Korean Patent Publication Nos. 58-212994, 61-6649, 62-46688, 62-48589, 62-173295, 62-187092, 63-67189, and Patent Publication No. 1 Compounds described in -244891 and the like, and the like, and the compounds described in "11290 Chemical Goods," Japan Chemical Co., Ltd., 289-294, "UV / EB Curing Handbook (Raw Materials)", 11-65. The compound described in the above can also be used preferably.
    [194] Especially, the compound which has 2 or more acrylic group or methacryl group in a polymer is preferable in this invention, and molecular weight is 10,000 or less, More preferably, it is 5,000 or less. In the present invention, the polymerizable compound may be used in combination of two or more of the monomers and prepolymers having a polymerizable group, including those exemplified above, if the compatibility or affinity is a problem depending on the purpose.
    [195] Moreover, when (A) component is a compound which produces an acid also with a radical, even if it uses together the compound which has an unsaturated bond which can superpose | polymerize with an acid besides the compound which has an unsaturated bond which can superpose | polymerize with the radical of this invention (C), good.
    [196] The compound having an unsaturated group is used in an added amount of 2 to 50% by weight, preferably 5 to 40% by weight, more preferably 10 to 30% by weight in the total resist composition solids.
    [197] (4) Other components used in the composition of the present invention
    [198] The negative resist composition of this invention can contain another radical generating agent, an organic basic compound, dye, surfactant, etc. as needed.
    [199] (4) -1 dye
    [200] Preferred dyes include oil dyes and basic dyes. Specifically, Oil Yellow # 101, Oil Yellow # 103, Oil Pink # 312, Oil Green BG, Oryl Blue BOS, Oil Blue # 603, Oil Black BY, Oil Black BS, Oil Black T-505 (above Orient Chemical Industries, Ltd.) First), crystal violet (CI42555), methyl violet (CI42535), rhodamine B (CI45170B), marachite green (CI42000), methylene blue (CI52015) and the like.
    [201] (4) -2 organobasic compounds
    [202] As a preferable organic basic compound which can be used by this invention, it is a compound with stronger basicity than phenol. Among them, nitrogen-containing basic compounds are preferable.
    [203] As a preferable chemical environment, the structure of following formula (A)-(E) can be mentioned.
    [204]
    [205] Here, R 250 , R 251 , and R 252 may be the same or different and include a hydrogen atom, a C 1-6 alkyl group, a C 1-6 aminoalkyl group, a C 1-6 hydroxyalkyl group, or C 6-20 And substituted or unsubstituted aryl groups, wherein R 251 and R 252 may be bonded to each other alternately to form a ring.
    [206] R 253 , R 254 , R 255 and R 256 may be the same or different and represent an alkyl group having 1 to 6 carbon atoms.
    [207] Further preferred compounds are nitrogen-containing basic compounds having at least two nitrogen atoms of different chemical environments in one molecule, particularly preferably containing both substituted or unsubstituted amino groups and ring structures containing nitrogen atoms. Compound or an alkylamino group.
    [208] Preferred embodiments include substituted or unsubstituted guanidine, substituted or unsubstituted aminopyridine, substituted or unsubstituted aminoalkylpyridine, substituted or unsubstituted aminopyrrolidine, substituted or unsubstituted indazole, imidazole , Substituted or unsubstituted pyrazole, substituted or unsubstituted pyrazone, substituted or unsubstituted pyrimidine, substituted or unsubstituted pyrine, substituted or unsubstituted imidazoline, substituted or unsubstituted pyrazoline, substituted Or unsubstituted piperazine, substituted or unsubstituted aminomorpholine, substituted or unsubstituted aminoalkylmorpholine, and the like. Preferred substituents are amino group, aminoalkyl group, alkylamino group, aminoaryl group, arylamino group, alkyl group, alkoxy group, acyl group, acyloxy group, aryl group, aryloxy group, nitro group, hydroxyl group, cyano group.
    [209] Particularly preferred compounds are guanidine, 1,1-dimethylguanidine, 1,1,3,3-tetramethylguanidine, imidazole, 2-methylimidazole, 4-methylimidazole, N-methylimidazole, 2-phenylimidazole, 4,5-diphenylimidazole, 2,4,5-triphenylimidazole, 2-aminopyridine, 3-aminopyridine, 4-amizopyridine, 2-dimethylaminopyridine , 4-dimethylaminopyridine, 2-diethylaminopyridine, 2- (aminomethyl) pyridine, 2-amino-3-methylpyridine, 2-amino-4-methylpyridine, 2-amino-5-methylpyridine, 2 -Amino-6-methylpyridine, 3-aminoethylpyridine, 4-aminoethylpyridine,
    [210] 3-aminopyrrolidine, piperazine, N- (2-aminoethyl) piperazine, N- (2-aminoethyl) pyridine, 4-amino-2,2,6,6-tetramethylpiperidine , 4-piperidinopyreridine, 2-iminopiperidine, 1- (2-aminoethyl) pyrrolidine, pyrazole, 3-amino-5-methylpyrazole, 5-amino-3-methyl- 1-p-trilprazole, pyrazine, 2- (aminomethyl) -5-methylpyrazine, pyrimidine, 2,4-diaminopyrimidine, 4,6-dihydroxypyrimidine, 2-pyrazoline, 3 -Pyrazoline, N-aminomorpholine N- (2-aminoethyl) morpholine, etc. are listed, but it is not limited to this.
    [211] These nitrogen-containing basic compounds are used alone or in combination of two or more.
    [212] It is preferable that the usage ratio in the composition of a radical generator and an organic basic compound is (radical generator) / (organic basic compound) (molar ratio) = 2.5-300. If the molar ratio is less than 2.5, the resolution may decrease, and if the resolution exceeds 300, the resist pattern may become thick and the resolution may also decrease with time until the post-exposure heat treatment.
    [213] The (radical generator) / (organic basic compound) (molar ratio) is preferably 5.0 to 200, and more preferably 7.0 to 150.
    [214] (4) -3 radical generator
    [215] A radical generating agent can be used together with the negative resist composition of this invention as needed in order to accelerate reaction of the polymeric compound of (C).
    [216] As such a radical generating agent, the known radical polymerization initiator generally used for the polymer synthesis reaction by radical polymerization can be used without a restriction | limiting, 2, 2- azobisisobutyronitrile, 2, 2- azobispro Azobisnitrile compounds such as pionitrile, benzoyl peroxide, lauroyl peroxide, acetyl peroxide, perbenzoic acid-t-butyl, α-cumyl hydroperoxide, di-t-butylperoxide, diisopropylperoxydicarbonate, organic peroxides such as t-butyl peroxy isopropyl carbonate, peracids, alkyl peroxy carbamates, nitrosoaryl acylamines,
    [217] Inorganic peroxides such as potassium persulfate, ammonium persulfate, potassium perchlorate, azo or diazo compounds such as diazoaminobenzene, p-nitrobenzenediazonium, azobis substituted alkanes, diazothioethers, arylazosulfones Tetraalkylthioramsulfides such as nitrosophenyl urea and tetramethylthiolam disulfide, diaryl disulfides such as dibenzoyl disulfide, dialkyl xanthogenic acid disulfides, aryl sulfinic acids and arylalkyl sulfides Phons, 1-alkanesulfinic acids, and the like.
    [218] The activation energy for radical generation of the radical generator is preferably 30 Kcal / mol or more, and examples thereof include azobisnitrile compounds and organic peroxides. Especially, the compound which is excellent in stability at normal temperature, the decomposition rate at the time of heating, and colorless at the time of decomposition is preferable, and benzoyl peroxide, 2, 2- azobis-isobutyronitrile, etc. can be mentioned.
    [219] The radical generators may be used alone or in combination of two or more, and is used at about 0.5 to 30% by weight, preferably 2 to 10% by weight, based on the total solid of the radical polymerization layer.
    [220] (4) -4 solvents
    [221] The composition of this invention is melt | dissolved in the solvent which melt | dissolves each said component, and is apply | coated on a support body. Here, as a solvent used, ethylene dichloride, cyclohexanone, cyclopentanone, 2-heptanone, (gamma) -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-methylpyrrolidine, tetrahydrofuran and the like are preferable, and these solvents are used alone or in combination.
    [222] (5) -5 surfactants
    [223] Surfactant can be added to the said solvent. Specifically, polyoxyethylene alkyl ethers such as polyoxyethylene lauryl ether, polyoxyethylene stearyl ether, polyoxyethylene cetyl ether, polyoxyethylene oleyl ether, polyoxyethylene octyl phenol ether, polyoxyethylene nonyl Polyoxyethylene alkylallyl ethers such as phenol ethers, polyoxyethylene polyoxypropylene block copolymers, sorbitan monolaurate, sorbitan monopalmitate, sorbitan monostearate, sorbitan monooleate, sorbitan Sorbitan fatty acid esters such as trioleate and sorbitan tristearate, polyoxyethylene sorbitan monolaurate, polyoxyethylene sorbitan monopalmitate,
    [224] Nonionic surfactants, such as polyoxyethylene sorbitan fatty acid ester, such as polyoxyethylene sorbitan monostearate, polyoxyethylene sorbitan trioleate, and polyoxyethylene sorbitan tristearate, F-top EF301, EF303, EF352 (manufactured by Shin-Aki Takasei Co., Ltd.), mega pack F171, 173 (manufactured by Dainippon Inky Co., Ltd.), Florid FC430, FC431 (manufactured by Sumitomo 3M Co., Ltd.), Asahi Guide AG710, Salfron S-382 , Fluorosurfactant such as SC101, SC102, SC103, SC104, SC105, SC106 (manufactured by Asahi Glass Co., Ltd.), Troisol S-366 (manufactured by Troy Chemical Co., Ltd.), organosiloxane polymer KP341 (Shin-Etsu Chemical Co., Ltd.) No. 75, No. 95 (manufactured by Kyoeisa Yuji Chemical Co., Ltd.), etc. are mentioned.
    [225] The compounding quantity of these surfactant is 2 weight part or less normally per 100 weight part of solid content in the composition of this invention, Preferably it is 1 weight part or less.
    [226] These surfactants may be added alone, or may be added in combination.
    [227] In the fabrication of a precision integrated circuit device, the pattern forming process onto a resist film is performed by applying the negative photoresist composition of the present invention onto a substrate (e.g., a transparent substrate such as silicon / silicon dioxide coating, a glass substrate, an ITO substrate, or the like). Then, irradiation is performed using an electron beam (under accelerated voltage conditions of 75 KeV or more) or an X-ray drawing apparatus, and a good resist pattern can be formed by heating, developing, rinsing and drying.
    [228] As a developing solution of the negative photoresist composition of this invention, inorganic alkalis, such as sodium hydroxide, potassium hydroxide, sodium carbonate, sodium silicate, sodium metasilicate, ammonia water, 1st amines, such as ethylamine and n-propylamine, diethylamine , Second amines such as di-n-butylamine, third amines such as triethylamine and methyldiethylamine, alcohol amines such as dimethylethanolamine and triethanolamine, tetramethylammonium hydroxide and tetraethylammonium hydroxide Aqueous solutions of alkalis, such as quaternary ammonium salts, such as a seed and choline, and cyclic amines, such as a pyrrole and a piperidine, can be used. Moreover, alcohol, such as isopropyl alcohol, surfactant, such as nonionics, can be added and used for the said aqueous solution of alkalis.
    [229] Among these developers, quaternary ammonium salts are more preferred, tetramethylammonium hydroxide and choline.
    [230] <Example>
    [231] Hereinafter, although an Example demonstrates this invention further in detail, the content of this invention is not limited by this.
    [232] 1. Synthesis Example of Constituent Material
    [233] (1) alkali-soluble resins
    [234] Synthesis Example 1 (Synthesis of Resin Example (29))
    [235] 3.9 g (0.024 mol) of 4-acetoxy styrene and 0.8 g (0.006 mol) of 4-methoxy styrene were dissolved in 30 ml of 1-methoxy-2-propanol, and the polymerization initiator 2, 50 mg of 2-azobis (2,4-dimethylvaleronitrile) (manufactured by Hwagwang Pure Chemical Industries, Ltd .; brand name V-65), 9.1 g (0.056 mol) of 4-acetoxy styrene, 1.9 g of 4-methoxystyrene ( 0.014 mole) of a 70 ml solution of 1-methoxy-2-propanol was added dropwise over 2 hours. After 2 hours, 50 mg of the initiator was added, followed by further reaction for 2 hours. Then it heated up at 90 degreeC and stirring was continued for 1 hour. The reaction solution was left to cool and then poured into 1 L of ion-exchanged water with vigorous stirring to precipitate a white resin. The resulting resin was dried, dissolved in 100 ml of methanol, 25% tetramethylammonium hydroxide was added, the acetoxy group in the resin was hydrolyzed, and neutralized in an aqueous hydrochloric acid solution to precipitate a white resin. After washing with water with ion-exchanged water and drying under reduced pressure, 11.6 g of resin (29) of the present invention was obtained. When molecular weight was measured in GPC, it was 9,200 by weight average (Mw: polystyrene conversion) and 2.2 by dispersion degree (Mw / Mn).
    [236] Synthesis Example 2 (Synthesis of Resin Example 39)
    [237] Dissolve 12.0 g of poly (4-hydroxystyrene) (Mw = 10,500, Mw / Mn = 1.2) in 100 ml of acetone, add 2.0 g of pyridine, add 1.3 g of acetic anhydride, and react for 3 hours at 50 ° C under stirring. I was. The reaction solution was poured into 1 L of ion-exchanged water with vigorous stirring to precipitate a white resin. 12.2 g of resin (39) of this invention was obtained after drying obtained resin under reduced pressure. When molecular weight was measured in GPC, it was 11,400 in weight average (Mw: polystyrene conversion) and 1.2 in dispersion degree (Mw / Mn). Moreover, when the composition ratio was calculated by NMR measurement, it was x / y (4-hydroxystyrene / 4-acetoxy styrene) = 88/12 by molar ratio.
    [238] Synthesis Example 3 (Synthesis of Resin Example 91)
    [239] 3.8 g (0.015 mol) of 2-[(4'-hydroxyphenyl) carbonyloxy] ethyl methacrylate, 1.0 g (0.009 mol) of 2-hydroxyethyl acrylate, and 0.3 g (0.006 mol) of acrylonitrile Dissolved in 30 ml of 1-ketoxy-2-propanol, and polymerized initiator 2,2'-azobis (2,4-dimethylvaleronitrile) (manufactured by Hwagwang Pure Chemical Co., Ltd.) at 70 ° C under nitrogen stream and stirring; V-65) 50 mg, 2-[(4'-hydroxyphenyl) carbonyloxy] ethyl methacrylate 8.8 g (0.035 mol), 2-hydroxyethyl acrylate 2.4 g (0.021 mol), acrylonitrile 0.7 g (0.014 mol) of 70 ml of 1-methoxy-2-propanol solution was added dropwise over 2 hours. After 2 hours, 50 mg of the initiator was added, followed by further reaction for 2 hours. Then it heated up at 90 degreeC and stirring was continued for 1 hour. The reaction solution was left to cool and then poured into 1 L of ion-exchanged water with vigorous stirring to precipitate a white resin. After drying obtained resin under reduced pressure, 15.8g of resin (91) of this invention was obtained. When molecular weight was measured in GPC, it was 15,200 by weight average (Mw: polystyrene conversion) and 2.2 by dispersion degree (Mw / Mn).
    [240] Synthesis Example 4 (Synthesis of Resin Example 94)
    [241] 12.1 g (0.10 mol) of poly (4-hydroxystyrene) (manufactured by Nippon Sochi Co., Ltd., brand name VP-15000) was dissolved in 100 ml of THF, and 3.7 g (0.024 mol) of methacrylic anhydride was added. Furthermore, 2.4 g (0.030 mol) of pyridine was added, and it heated and refluxed for 5 hours under stirring. The reaction solution was left to cool and then poured into 1 L of ion-exchanged water with vigorous stirring to precipitate a white resin. After washing with water with ion-exchanged water, the obtained resin was dried under reduced pressure to obtain 13.1 g of resin (2) of the present invention. When the content rate of an unsaturated group was measured in NMR, the introduction amount of the methacryl group of hydroxy group of polyhydroxystyrene was 18 mol%. The molecular weight was measured in GPC and found to be 16,700 (dispersity 1.2; polystyrene standard) by weight average.
    [242] Synthesis Example 5 (Synthesis of Resin Example 96)
    [243] 12.1 g (0.10 mol) of poly (4-hydroxystyrene) (manufactured by Nippon Sochi Co., Ltd., brand name VP-8000) is dissolved in 100 ml of N, N-dimethylacetoamide, and 2-isocyanatoethyl is dissolved therein. 3.1 g (0.020 mol) of methacrylate was added, and it heated at 90 degreeC under stirring for 7 hours. The reaction solution was left to cool and then poured into 1 L of ion-exchanged water with vigorous stirring to precipitate a white resin. After washing with ion-exchanged water, the obtained resin was dried under reduced pressure to obtain 14.4 g of Resin (4) of the present invention. When the content rate of an unsaturated group was measured by NMR, the introduction amount of the methacryl group to the OH group of polyhydroxy sulfone was 16 mol%. Moreover, when molecular weight was measured in GPC, it was 9,100 (dispersion degree 1.2; polystyrene standard) by weight average.
    [244] Synthesis Example 6 (Synthesis of Resin Example (99))
    [245] 12.1 g (0.10 mol) of poly (4-hydroxystyrene) (manufactured by Nippon Sochi Co., Ltd., brand name VP-8000) was dissolved in 100 ml of THF, and 4.7 g (0.023 mol) of 4-styrenesulfonyl chloride was added. It was. In addition, a THF 20 ml solution of 0.37 g (0.003 mol) of N, N-dimethylaminopyridine / 2.1 g (0.020 mol) of triethylamine was added dropwise while stirring under cooling. Moreover, it stirred at room temperature for 5 hours. The reaction solution was filtered, and the filtrate was poured into 1 L of ion-exchanged water with vigorous stirring to precipitate a white resin. After washing with ion-exchanged water, the obtained resin was dried under reduced pressure to obtain 15.0 g of Resin (7) of the present invention. When the content rate of an unsaturated group was measured by NMR, the introduction amount of the styryl group to the OH group of polyhydroxy sulfone was 18 mol%. Moreover, when molecular weight was measured in GPC, it was 9,200 (dispersion degree 1.2; polystyrene standard) by weight average.
    [246] Synthesis Example 7 (Synthesis of Resin Example (100))
    [247] 12.1 g (0.10 mol) of poly (4-hydroxystyrene) (manufactured by Nippon Sochi Co., Ltd., brand name VP-8000) was dissolved in 100 ml of N, N-dimethylacetoamide, and 3.4 g of chloromethyl styrene was added thereto. 0.22 mole) was added. Furthermore, a 20 ml solution of 2.3 g (0.022 mol) of N, N-dimethylacetoamide in triethylamine was added dropwise while stirring at room temperature. The reaction solution was then stirred at 60 ° C. for 5 hours. The reaction solution was left to cool and poured into 1 L of ion-exchanged water with vigorous stirring to precipitate a white resin. After washing with ion-exchanged water, the obtained resin was dried under reduced pressure to obtain 13.9 g of the resin (8) of the present invention. When the content rate of an unsaturated group was measured by NMR, the introduction amount of the styryl group of hydroxy group of polyhydroxy water styrene was 17 mol%. Moreover, when molecular weight was measured in GPC, it was 9,300 (dispersion degree 1.2; polystyrene standard) by weight average.
    [248] Hereinafter, the resin of this invention (B) was synthesize | combined similarly.
    [249] (2) radical generator
    [250] 1) Synthesis of Pentafluorobenzenesulfonic Acid Tetramethylammonium Salt
    [251] 25 g of pentafluorobenzenesulfonyl chloride was dissolved in 100 ml of methanol under ice cooling, and 100 g of 25% tetramethylammonium hydroxide aqueous solution was slowly added thereto. After stirring for 3 hours at room temperature, a solution of pentafluorobenzenesulfonic acid tetramethylammonium salt was obtained. This solution was used for salt exchange with sulfonium salt and iodonium salt.
    [252] 2) Synthesis of triphenylsulfonium pentafluorobenzenesulfonate
    [253] 50 g of diphenyl sulfoxide was dissolved in 800 ml of benzene, and 200 g of aluminum chloride was added thereto, and the mixture was refluxed for 24 hours. The reaction solution was slowly poured into 2 L of ice, and 400 ml of concentrated hydrochloric acid was added thereto, followed by heating at 70 ° C for 10 minutes. The aqueous solution was washed with 500 ml of ethyl acetate, and after filtering, 200 g of ammonium iodide dissolved in 400 ml of water was added. The precipitated powder was filtered, washed with water, washed with ethyl acetate and dried to obtain 70 g of triphenylsulfonium iodine.
    [254] 30.5 g of triphenylsulfonium iodine was dissolved in 1000 ml of methanol, 19.1 g of silver oxide was added to this solution, and the mixture was stirred at room temperature for 4 hours. The solution was filtered and an excess amount of a solution of pentafluorobenzenesulfonic acid tetramethylammonium salt was added thereto. The reaction solution was concentrated, which was dissolved in 500 ml of dichloromethane, and the solution was washed with 5% aqueous tetramethylammonium hydroxide solution and water. The organic phase was dried over anhydrous sodium sulfate and concentrated to give triphenylsulfonium pentafluorobenzenesulfonate (I-1).
    [255] 3) Synthesis of di (4-t-amylphenyl) iodonium pentafluorobenzenesulfonate
    [256] 60 g of t-amylbenzene, 39.5 g of potassium iodide, 81 g of acetic anhydride, and 170 ml of dichloromethane were mixed, and 66.8 g of concentrated sulfuric acid was slowly added dropwise thereto under ice cooling. After 2 hours of stirring under ice cooling, the mixture was stirred at room temperature for 10 hours. 500 ml of water was added to the reaction liquid under ice cooling, and this was precipitated with dichloromethane, the organic phase was washed with sodium bicarbonate and water, and then concentrated to give di (4-t-amylphenyl) iodium sulfate. This sulfate was added to the solution of the excess amount of pentafluorobenzenesulfonic acid tetramethylammonium salt. 500 ml of water was added to the solution, which was precipitated with dichloromethane, the organic phase was washed with 5% aqueous tetramethylammonium hydroxide solution, and water and concentrated to give di (4-t-amylphenyl) iodiumpentafluorobenzenesulfonate. (III-1) was obtained.
    [257] Other compounds can also be synthesized using the same method as above.
    [258] 2. Example [Example, Comparative Example]
    [259] (1) application of resist
    [260] The solution of the photoresist composition of the composition shown in following Table 1 was adjusted using the compound and comparative compound which comprise this invention selected by the said synthesis example.
    [261] After filtering each sample solution with a 0.1 micrometer filter, it applied on the silicon wafer using the spin coater, and it dried at 110 degreeC and the vacuum adsorption-type hotplate for 90 second, and obtained the resist film with a film thickness of 0.3 micrometer.
    [262]
    [263] In Table 1, the composition of the resin 62 is x / y / z = 80/13/7, the composition of the resin 128 is m / n / o = 70/20/10, and the composition of the resin 139 is m / n / o = 75/15/10 and other resins were x / y or m / n = 85/15, and the weight average molecular weights were all 8,000-16,000 (dispersion degree 1.2-2.4).
    [264] In addition, PGA-1 in Example 12 was used as a radical generating agent, and in Comparative Example 1, 0.18 g of (CL-1) represented by the following structural formula was used as a crosslinking agent, without using a polymerizable monomer.
    [265]
    [266]
    [267]
    [268] As a polymerizable monomer,
    [269] RM-1: tetraethylene glycol diacrylate (manufactured by Nippon Kayaku Co., Ltd.)
    [270] RM-2: trimethylolpropane triacrylate (manufactured by Nippon Kayaku Co., Ltd.)
    [271] RM-3: dipentaerythritol hexaacrylate (manufactured by Nippon Kayaku Co., Ltd.)
    [272] Is displayed.
    [273] (2) Preparation of resist pattern
    [274] This resist film was irradiated using an electron beam drawing apparatus (acceleration voltage 50 KeV). The irradiated water was heated in a vacuum adsorption hot plate at 110 ° C. for 60 seconds, immersed in an aqueous 2.38% tetramethylammonium hydroxide (TMAH) solution for 60 seconds, rinsed with water for 30 seconds and dried. The cross-sectional shape of the obtained pattern was observed with a scanning electron microscope.
    [275] In addition, the sensitivity was made into the minimum irradiation energy at the time of resolving a 0.20 micrometer line (line: space = 1: 1), and the limit resolution (the separate resolution of a line and space) in the irradiation amount was made into the resolution. When the 0.20 µm line (line: space = 1: 1) was not resolved, the limit resolution was regarded as resolution, and the irradiation energy at that time was regarded as sensitivity.
    [276] The performance evaluation results are shown in Table 2.
    [277]
    [278] From the result of Table 2, it turns out that the negative resist composition of this invention improves a sensitivity and the resolution significantly compared with the comparative example without a polymerizable monomer.
    [279] Using the composition of Examples 1, 5, 8, and 12 and Comparative Example 1, the resist film formed in the same manner as above was irradiated with an electron beam drawing apparatus under conditions of an acceleration voltage of 100 KeV ( Examples 13-16 and Comparative Example 3). After irradiation, heating, developing, and rinsing were carried out in the same manner as in Example, and the obtained pattern was observed with a scanning electron beam microscope. The evaluation results in the same manner as in the above example are shown in Table 3.
    [280]
    [281] From the result of Table 3, it turns out that the negative resist composition of this invention shows favorable sensitivity and the resolution also with respect to the composition of a comparative example with respect to the electron beam irradiation in high acceleration voltage.
    [282] The negative resist composition for electron beam and X-ray of the present invention can provide a negative resist composition having excellent sensitivity and resolution and having a rectangular profile even under conditions of high acceleration pressure.
    权利要求:
    Claims (6)
    [1" claim-type="Currently amended] (A) A compound which generates radical species by irradiation of an electron beam or X-rays,
    (B) resins insoluble in water and soluble in alkaline aqueous solutions,
    (C) a compound having at least one unsaturated bond polymerizable by radicals,
    Negative resist composition for electron beam or X-ray containing
    [2" claim-type="Currently amended] The negative resist composition for electron beams or X-rays according to claim 1, wherein the resin of component (B) is a resin containing a repeating unit represented by the general formula (a1).

    In the formula, R 1 represents an alkyl group or a haloalkyl group, which may have a hydrogen atom, a halogen atom, a cyano group, or a substituent. R 2 represents a hydrogen atom, an alkyl group, a cycloalkyl group, an aryl group, an aralkyl group, or an acyl group which may have a substituent. R <3> , R <4> may be same or different and represents an alkyl group, a cycloalkyl group, an alkenyl group, an aralkyl group, or an aryl group which may have a hydrogen atom, a halogen atom, a cyano group, or a substituent.
    A may have a single bond, a substituent, an alkylene group, an alkenylene group, a cycloalkylene group, or an arylene group, or -O-, -SO 2- , -O-CO-R 5- , -CO-OR 6 -, -CO-N (R 7 ) -R 8 -is indicated.
    R <5> , R <6> , R <8> may be same or different, and may be a single bond, a substituent, The alkylene group, the alkenylene group, the cycloalkylene group, or the arylene group alone, or these groups and an ether structure, ester structure, amide structure Represents a divalent group formed by combining one or more selected from the group of a urethane structure or a ureido structure.
    R <7> may be same or different and represents an alkyl group, a cycloalkyl group, an aralkyl group, or an aryl group which may have a hydrogen atom and a substituent.
    1 represents the integer of 1-3. Moreover, some R <2> or R <2> and R <3> or R <4> may combine, and may form a ring.
    [3" claim-type="Currently amended] The negative resist composition for electron beams or X-rays according to claim 1 or 2, wherein the resin of component (B) is a resin having one or more unsaturated bonds polymerizable by radicals.
    [4" claim-type="Currently amended] The negative resist composition for electron beams or X-rays according to any one of claims 1 to 3, wherein the resin of component (B) is a resin containing a repeating unit of the general formula (a2).

    In formula, R <9> represents the alkyl group or haloalkyl group which may have a hydrogen atom, a halogen atom, a cyano group, and a substituent.
    R 10 to R 12 represent a hydrogen atom, an alkyl group, a cycloalkyl group, an aryl group, an aralkyl group, or an acyl group which may have a substituent, any group of formula (b), (c), or (d). do.
    R <13> , R <14> may be same or different and represents an alkyl group, a cycloalkyl group, an alkenyl group, an aralkyl group, or an aryl group which may have a hydrogen atom, a hydroxyl group, a halogen atom, a cyano group, or a substituent.

    In formula, R <15> -R <20> , R <24> , R <25> represents the alkyl group or haloalkyl group which may have a hydrogen atom, a halogen atom, a cyano group, and a substituent.
    R <21> , R <22> represents the hydrogen atom, the halogen atom, the hydroxyl group, and the alkyl group, the alkoxy group, and the acyloxy group which may have a substituent.
    R 23 represents a hydrogen atom, an alkyl group, a cycloalkyl group, an aralkyl group, or an aryl group which may have a substituent.
    A 1 is a divalent alkylene group, alkenylene group, cycloalkylene group, or arylene group which may have a single bond or a substituent, or -O-, SO 2- , -O-CO-R 26- , -CO- OR 27 -represents -CO-N (R 28 ) -R 29- .
    R 26 , R 27 , R 29 may be the same or different, a divalent alkylene group which may have a single bond or an ether structure, an ester structure, an amide structure, a urethane structure or a ureido structure, and may have a substituent, Alkenylene group, a cycloalkylene group, and an arylene group are shown.
    R 28 represents a hydrogen atom, an alkyl group, a cycloalkyl group, an aralkyl group, or an aryl group which may have a substituent.
    A 2 represents a single bond, -OR 27- , -N (R 28 ) -R 29- .
    A 3 represents a single bond, -SO 2 - or alkylene may be the holding structure, it may also have a substituent represents a good, arylene.
    A 4 represents a divalent alkylene group, a cycloalkylene group, an arylene group, -O-, -SO 2- , -CO-, or -CO-OR 21 -which may have a single bond or a substituent.
    x, y, z represent 0 or 1, and m, n represent an integer of 0 or 1 or more.
    Provided that at least one of the formulas (a2) has a group of the formulas (b), (c) or (d). In addition, two of R 10 to R 12 , or one of R 10 to R 12 , and R 13 or R 14 may combine to form a ring.
    [5" claim-type="Currently amended] The negative resist composition for electron beams or X-rays according to any one of claims 1 to 4, wherein the compound of component (A) is selected from a sulfonate compound of sulfonium or iodonium.
    [6" claim-type="Currently amended] The negative resist composition for electron beams or X-rays according to any one of claims 1 to 5, wherein the electron beam is irradiated under an acceleration voltage condition of 75 KeV or more.
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    同族专利:
    公开号 | 公开日
    KR100775453B1|2007-11-12|
    JP2002040656A|2002-02-06|
    JP4149122B2|2008-09-10|
    TW567402B|2003-12-21|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    法律状态:
    2000-07-19|Priority to JPJP-P-2000-00219253
    2000-07-19|Priority to JP2000219253A
    2001-07-19|Application filed by 무네유키 가코우, 후지 샤신 필름 가부시기가이샤
    2002-01-29|Publication of KR20020008077A
    2007-11-12|Application granted
    2007-11-12|Publication of KR100775453B1
    优先权:
    申请号 | 申请日 | 专利标题
    JPJP-P-2000-00219253|2000-07-19|
    JP2000219253A|JP4149122B2|2000-07-19|2000-07-19|Negative resist composition for electron beam or X-ray|
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