Negative resist composition and pattern forming process

US9645493B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9645493-B2
Application numberUS-201615091092-A
CountryUS
Kind codeB2
Filing dateApr 5, 2016
Priority dateApr 7, 2015
Publication dateMay 9, 2017
Grant dateMay 9, 2017

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  5. First independent claim

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Abstract

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A negative resist composition is provided comprising (A) a polymer comprising recurring units having an acid-eliminatable group and recurring units capable of generating acid upon exposure and (B) a carboxylic acid onium salt. When the negative resist composition is processed by the microprocessing technology, especially EB lithography, it forms a pattern having a very high resolution and minimal LER.

First claim

Opening claim text (preview).

The invention claimed is: 1. A negative resist composition comprising (A) a polymer comprising recurring units having the general formula (1), recurring units of at least one type selected from units having the general formulae (a1), (a2), and (a3), and recurring units of at least one type selected from units having the general formulae (2) and (3): wherein A is a single bond or a C 1 -C 10 alkylene group which may contain an ethereal oxygen atom at an intermediate of the chain, R 1 is hydrogen, fluorine, methyl or trifluoromethyl, R 2 is hydrogen, halogen, an optionally halo-substituted, straight, branched or cyclic C 2 -C 8 acyloxy group, an optionally halo-substituted, straight, branched or cyclic C 1 -C 6 alkyl group, or an optionally halo-substituted, straight, branched or cyclic C 1 -C 6 alkoxy group, L is hydrogen, a monovalent, straight, branched or cyclic, aliphatic C 1 -C 10 hydrocarbon group which may contain an ethereal oxygen atom, carbonyl moiety or carbonyloxy moiety at an intermediate of the chain, or an optionally substituted monovalent aromatic group, Rx and Ry each are hydrogen, a C 1 -C 15 alkyl group which may be substituted with hydroxy or alkoxy, or an optionally substituted monovalent aromatic group, Rx and Ry may bond together to form a ring with the carbon atom to which they are attached, excluding the case where Rx and Ry are hydrogen at the same time, f is an integer of 1 to 3, s is an integer of 0 to 2, a is an integer (5+2s-f), and m is 0 or 1, wherein R 12 is each independently hydrogen or methyl, R 13 is a single bond, phenylene group, —O—R 22 —, or —C(═O)—Z 2 —R 22 —, Z 2 is oxygen or NH, R 22 is a straight, branched or cyclic C 1 -C 6 alkylene, alkenylene or phenylene group which may contain a carbonyl (—CO—), ester (—COO—), ether (—O—) or hydroxyl moiety, L′ is a single bond or —Z 3 —C(═O)—O—, Z 3 is a straight, branched or cyclic divalent C 1 -C 20 hydrocarbon group which may be substituted with a heteroatom, Z 1 is a single bond, methylene, ethylene, phenylene, fluorinated phenylene, —O—R 23 —, or —C(═O)—Z 4 —R 23 —, Z 4 is oxygen or NH, R 23 is a straight, branched or cyclic C 1 -C 6 alkylene, alkenylene or phenylene group which may contain a carbonyl, ester, ether or hydroxyl moiety, M − is a non-nucleophilic counter ion R 14 , R 15 , R 16 , R 17 , R 18 , R 19 , R 20 , and R 21 are each independently a straight C 1 -C 20 , branched or cyclic C 3 -C 20 monovalent hydrocarbon group in which at least one hydrogen atom may be replaced by a heteroatom selected from oxygen, sulfur, nitrogen and halogen, or in which a heteroatom selected from oxygen, sulfur and nitrogen may intervene, so that a hydroxyl group, cyano group, carbonyl group, ether bond, ester bond, sulfonic acid ester bond, carbonate bond, lactone ring, sultone ring, carboxylic anhydride, or haloalkyl group may form or intervene, or R 14 and R 15 may bond together to form a ring with the sulfur atom, or any two or more of R 16 , R 17 and R 18 or any two or more of R 19 , R 20 and R 21 may bond together to form a ring with the sulfur atom, wherein B and C each are a single bond or a C 1 -C 10 alkylene group which may contain an ethereal oxygen atom at an intermediate of the chain, D is a single bond or a (v+1)-valent, straight, branched or cyclic, aliphatic C 1 -C 10 hydrocarbon group which may be substituted with fluorine and which may contain an ethereal oxygen atom, carbonyl moiety or carbonyloxy moiety at an intermediate of the chain, R 1 is hydrogen, fluorine, methyl, or trifluoromethyl, R 3 and R 4 are each independently hydrogen, halogen, an optionally halo-substituted, straight, branched or cyclic C 2 -C 8 acyloxy group, an optionally halo-substituted, straight, branched or cyclic C 1 -C 6 alkyl group, or an optionally halo-substituted, straight, branched or cyclic C 1 -C 6 alkoxy group, Rf 1 and Rf 2 each are a C 1 -C 6 alkyl group having at least one fluorine, Rf 1 may bond with D to form a ring with the carbon atom to which they are attached, g is an integer of 0 to 3, h is 1 or 2, r is 0 or 1, v is 1 or 2, t and u each are an integer of 0 to 2, b is an integer (5+2t-g), c is an integer (5+2u-h), n and p are each independently 0 or 1, with the proviso that p is 1 when r is 0, (B) an acid diffusion regulator comprising a salt having the general formula (3a): R 11 —CO 2 − M +   (3a) wherein R 11 is a straight, branched or cyclic C 1 -C 20 alkyl group, C 2 -C 20 alkenyl group or C 6 -C 20 aryl group, which may contain fluorine, nitrogen, ether moiety, ester moiety, lactone ring, lactam ring, carbonyl moiety, or hydroxyl moiety, and M is a substituent-bearing counter cation selected from sulfonium, iodonium and ammonium cations, and (C) an additional polymer comprising recurring units having the general formula (1), but free of recurring units having a site capable of generating an acid upon exposure to high-energy radiation. 2. The negative resist composition of claim 1 wherein the polymer (A) further comprises recurring units of at least one type selected from units having the general formulae (4) and (5): wherein R 5 and R 6 are each independently hydrogen, halogen, an optionally halo-substituted, straight, branched or cyclic C 2 -C 8 acyloxy group, an optionally halo-substituted, straight, branched or cyclic C 1 -C 6 alkyl group, or an optionally halo-substituted, straight, branched or cyclic C 1 -C 6 alkoxy group, i and j each are an integer of 0 to 3, d is an integer of 0 to 5, and e is an integer of 0 to 3. 3. The negative resist composition of claim 1 , further comprising a compound capable of generating an acid upon exposure to high-energy radiation. 4. The negative resist composition of claim 3 wherein the compound capable of generating an acid upon exposure to high-energy radiation is a compound comprising an anion selected from the group consisting of the following formulae: 5. The negative resist composition of claim 1 wherein the acid diffusion regulator (B) consists of the salt having the general formula (3a). 6. The negative resist composition of claim 1 wherein the anion moiety in the salt of formula (3a) is selected from the group consisting of the following formulae:

Assignees

Inventors

Classifications

  • with perfluoro compounds, e.g. for dry lithography (G03F7/0048 takes precedence) · CPC title

  • G03F7/0382Primary

    the macromolecular compound being present in a chemically amplified negative photoresist composition · CPC title

  • G03F7/038Primary

    Macromolecular compounds which are rendered insoluble or differentially wettable (G03F7/075 takes precedence; macromolecular azides G03F7/012; macromolecular diazonium compounds G03F7/021) · CPC title

  • Sulfonium compounds · CPC title

  • with organic non-macromolecular light-sensitive compounds not otherwise provided for, e.g. dissolution inhibitors · CPC title

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What does patent US9645493B2 cover?
A negative resist composition is provided comprising (A) a polymer comprising recurring units having an acid-eliminatable group and recurring units capable of generating acid upon exposure and (B) a carboxylic acid onium salt. When the negative resist composition is processed by the microprocessing technology, especially EB lithography, it forms a pattern having a very high resolution and minim…
Who is the assignee on this patent?
Shinetsu Chemical Co
What technology area does this patent fall under?
Primary CPC classification G03F7/0382. Mapped technology areas include Physics.
When was this patent published?
Publication date Tue May 09 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 9 related publications on this page (citations in our corpus or others sharing the same primary CPC).