Precursors and methods for producing bismuth-oxy-carbide-based photoresist
US-2024210821-A1 · Jun 27, 2024 · US
US9547240B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9547240-B2 |
| Application number | US-201414550048-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 21, 2014 |
| Priority date | Nov 26, 2013 |
| Publication date | Jan 17, 2017 |
| Grant date | Jan 17, 2017 |
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A resin comprising: a structural unit which has, at a side chain, a carbonyl group and a thiolactone ring-containing amino group where the thiolactone ring may have a substituent, and a structural unit having an acid-labile group.
Opening claim text (preview).
What is claimed is: 1. A photoresist composition comprising: a resin which comprises 6 to 60 mol % of a structural unit represented by formula (I-1): where R 1 represents a hydrogen atom, a halogen atom, or a C1-C6 alkyl group which may have a halogen atom; L 1 represents a single bond or a C1-C18 divalent saturated hydrocarbon group where a methylene group can be replaced by an oxygen atom or a carbonyl group, R 2 represents a hydrogen atom or a C1-C6 alkyl group, R 3 represents a C1-C6 alkyl group, and m represents an integer of 0 to 5, a structural unit having an acid-labile group and being represented by formula (a1-1) or (a1-2): where L a1 and L a2 each independently represent —O— or *—O—(CH 2 ) k1 —CO—O— in which k1 represents an integer of 1 to 7 and * represents a binding site to —CO—, R a4 and R a5 each independently represent a hydrogen atom or a methyl group, R a6 and a7 each independently represent a C1-C8 alkyl group, C3-C20 monovalent alicyclic hydrocarbon group, or a group formed by combining them, m1 represents an integer of 0 to 14, n1 represents an integer of 0 to 10, and n1′represents an integer of 0 to 3; and a structural unit represented by the formulae (a3-1), (a3-3) or (a3-4): where L a4 and L a6 each independently represent *—O— or *—O—(CH 2 ) k3 —CO—O— in which * represents a binding position to —CO— and k3 represents an integer of 1 to 7, R a18 and R a20 each independently represent a hydrogen atom or a methyl group, R a21 represents a C1-C4 monovalent aliphatic hydrocarbon group, R a23 is in each occurrence a carboxyl group, a cyano group or a C1-C4 monovalent aliphatic hydrocarbon group, R a24 represents a hydrogen atom, a halogen atom, or a C1-C6 alkyl group which may have a halogen atom, L a7 represents * 1 —O—, *1 —O-L a8 —O—, *1 —O-L a8 —CO—O—, *1 —O-L a8 —CO—O-L a9 -CO—O— or *1 —O-L a8 —CO—O-L 9a —O— in which L a8 and L a9 each independently represent a C1-C6 divalent alkanediyl group and *1 represents a binding position to —CO— and p1 represents an integer of 0 to 5, and r1 represents an integer of 0 to 3; an acid generator represented by formula (B1): wherein Q 1 and Q 2 respectively represent a fluorine atom or a C1-C6 perfluoroalkyl group, L b1 represents a C1-C24 saturated hydrocarbon group in which a methylene group may be replaced by —O— or —CO— and in which a hydrogen atom may be replaced by a hydroxyl group or a fluorine atom, Y represents a methyl group where a hydrogen atom may be replaced by a substituent, or a C3-C18 alicyclic hydrocarbon group where a hydrogen atom may be replaced by a substituent and where a methylene may be replaced by —O—, —SO 2 — or —CO—, and Z + represents an organic cation; and a salt which comprises an acid lower in acidity than an acid generated from the acid generator. 2. The photoresist composition according to claim 1 , wherein m is 1 to 5. 3. The photoresist composition according to claim 1 , wherein L 1 represents a single bond. 4. A process for producing a photoresist pattern comprising the following steps (1) to (5): (1) a step of applying the photoresist composition according to claim 1 on a substrate, (2) a step of forming a composition film by conducting drying, (3) a step of exposing the composition film to radiation, (4) a step of baking the exposed composition film, and (5) a step of developing the baked composition film thereby to form a photoresist pattern.
and containing other heteroatoms, e.g. 2-acrylamido-2-methylpropane sulfonic acid [AMPS] · CPC title
with perfluoro compounds, e.g. for dry lithography (G03F7/0048 takes precedence) · CPC title
with organic non-macromolecular light-sensitive compounds not otherwise provided for, e.g. dissolution inhibitors · CPC title
Non-aqueous compositions · CPC title
by a heterocyclic ring containing sulfur · CPC title
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