Coating composition for use with an overcoated photoresist

US11567408B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11567408-B2
Application numberUS-201916653659-A
CountryUS
Kind codeB2
Filing dateOct 15, 2019
Priority dateOct 15, 2019
Publication dateJan 31, 2023
Grant dateJan 31, 2023

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

A method for forming a photoresist relief image including applying a layer of a coating composition on a substrate; and disposing a layer of a photoresist composition on the layer of the coating composition, wherein the coating composition comprises an amine-containing polymer comprising a hydrocarbon-substituted amino group and having nitrogen atoms in an amount from 3 to 47 weight percent, based on a total weight of the amine-containing polymer.

First claim

Opening claim text (preview).

The invention claimed is: 1. A method for forming a photoresist relief image, the method comprising: applying a layer of a coating composition on a substrate; and disposing a layer of a photoresist composition on the layer of the coating composition, wherein the coating composition comprises an amine-containing polymer comprising a hydrocarbon-substituted amino group and having nitrogen atoms in an amount from 3 to 47 weight percent, based on a total weight of the amine-containing polymer, wherein the amine-containing polymer comprises a repeating structural unit represented by at least one of Formulae (1) or (2): wherein, in Formulae (1) and (2), R 1 to R 3 are each independently hydrogen, a substituted or unsubstituted C 1-10 alkyl group, a substituted or unsubstituted C 3-10 cycloalkyl group, or a substituted or unsubstituted C 6-20 aryl group; L 1 is a substituted or unsubstituted C 1-30 alkylene group, a substituted or unsubstituted C 2-30 alkenylene group, a substituted or unsubstituted C 1-30 heteroalkene group, a substituted or unsubstituted C 3-7 heterocycloalkylene group, a substituted or unsubstituted C 6-30 arylene group, a substituted or unsubstituted C 3-30 heteroarylene group, —O—, —C(═O)O—, —O(C═O)—, —CONR b —, or —OC(═O)NR b —; L 2 is a single bond, a substituted or unsubstituted C 1-30 alkylene group, a substituted or unsubstituted C 2-30 alkenylene group, a substituted or unsubstituted C 1-30 heteroalkene group, a substituted or unsubstituted C 3-7 heterocycloalkylene group, a substituted or unsubstituted C 6-30 arylene group, a substituted or unsubstituted C 3-30 heteroarylene group, —(C(R c )═N—(C 2-3 )alkylene) n -, —(NR b —(C 2-3 )alkylene) n —, or —(O—(C 2-3 alkylene) n -; X 1 is —N(R b ) 2 or a substituted or unsubstituted nitrogen-containing monocyclic, polycyclic, or fused polycyclic C 2-7 heterocycloalkyl group or C 3-30 heteroaryl group; X 2 is —C(R c )═NR b , —N═C(R c ) 2 , —(NR b —(C 2-3 )alkylene) n -N(R b ) 2 , —(O—(C 2-3 )alkylene) n -N(R b ) 2 , or a substituted or unsubstituted nitrogen-containing monocyclic, polycyclic, or fused polycyclic C 2-7 heterocycloalkyl group or C 3-30 heteroaryl group; each R b is independently hydrogen, a substituted or unsubstituted C 1-30 alkyl group, a substituted or unsubstituted polycyclic or monocyclic C 3-30 cycloalkyl group, or a substituted or unsubstituted polycyclic or monocyclic C 6-30 aryl group; each R c is independently hydrogen, a halogen, a cyano group, a nitro group, an amino group, a substituted or unsubstituted C 1-30 alkyl group, a substituted or unsubstituted C 2-30 alkenyl group, a substituted or unsubstituted C 2-30 alkynyl group, a substituted or unsubstituted C 1-30 alkoxy group, a substituted or unsubstituted C 3-30 cycloalkyl group, a substituted or unsubstituted C 3-30 cycloalkenyl group, a substituted or unsubstituted C 6-30 aryl group, a substituted or unsubstituted C 6-30 aryloxy group, a substituted or unsubstituted C 6-30 arylthio group, or a substituted or unsubstituted C 7-30 arylalkyl group; and each n is independently an integer from 1 to 20. 2. The method of claim 1 , further comprising disposing an additional layer directly on the layer of the coating composition; and disposing the layer of the photoresist composition directly on the additional layer, wherein the additional layer comprises at least one of a hardmask layer, a silicon-containing layer, or organic layer. 3. The method of claim 1 , wherein in Formulae (1) and (2), R 1 to R 3 are hydrogen; L 1 is a C 6-30 arylene group, —C(═O)O—, or —CONR b —; L 2 is single bond, a C 1-10 alkylene group, a C 2-10 alkenylene group, a C 1-20 heteroalkene group, a C 3-7 heterocycloalkylene group, a C 6-12 arylene group, a C 3-12 heteroarylene group, —(C(R c )═N—(C 2-3 )alkylene) n -, —(NR b —(C 2-3 )alkylene) n -, or —(O—(C 2-3 )alkylene) n -; X 1 is a substituted or unsubstituted nitrogen-containing monocyclic C 2-7 heterocycloalkyl group or C 3-30 heteroaryl group; X 2 is —C(R c )═NR b , —N═C(R c ) 2 , —(NR b —(C 2-3 )alkylene) n -N(R b ) 2 , —(O—(C 2-3 )alkylene n -N(R b ) 2 , or a substituted or unsubstituted nitrogen-containing monocyclic C 2-7 heterocycloalkyl group or C 3-30 heteroaryl group; each R b is independently hydrogen, a substituted or unsubstituted C 1-10 alkyl group, a substituted or unsubstituted polycyclic or monocyclic C 3-10 cycloalkyl group, or a substituted or unsubstituted polycyclic or monocyclic C 6-12 aryl group; each R c is independently hydrogen, a halogen, a substituted or unsubstituted C 1-10 alkyl group, a substituted or unsubstituted C 2-10 alkenyl group, a substituted or unsubstituted C 2-10 alkynyl group, a substituted or unsubstituted C 1-10 alkoxy group, a substituted or unsubstituted C 3-10 cycloalkyl group, a substituted or unsubstituted C 3-10 cycloalkenyl group, a substituted or unsubstituted C 6-12 aryl group, a substituted or unsubstituted C 6-12 aryloxy group, a substituted or unsubstituted C 6-12 arylthio group, or a substituted or unsubstituted C 7-10 arylalkyl group; and each n is independently an integer from 1 to 5. 4. The method of claim 1 , wherein the amine-containing polymer has a weight average molecular weight from 1,000 to 100,000 grams per mole, as determined by gel permeation chromatography. 5. The method of claim 1 , wherein the coating composition further comprises a crosslinking agent. 6. The method of claim 1 , wherein the coating composition further comprises a thermal acid generator or a thermal base generator. 7. A method for forming a photoresist relief image, the method comprising: applying a layer of a coating composition on a substrate; and disposing a layer of a photoresist composition on the layer of the coating composition, wherein the coating composition comprises an amine-containing polymer comprising a hydrocarbon-substituted amino group and having nitrogen atoms in an amount from 3 to 47 weight percent, based on a total weight of the amine-containing polymer, wherein the amine-containing polymer comprises a repeating structural unit represented by at least one of Formulae (3) or (4): wherein, in Formulae (3) and (4), R 1 and R 2 are each independently hydrogen, a substituted or unsubstituted C 1-10 alkyl group, a substituted or unsubstituted C 3-10 cycloalkyl group, or a substituted or unsubstituted C 6-20 aryl group; Q 2 is a substituted or unsubstituted aliphatic group, a substituted or unsubstituted cycloaliphatic group, a substituted or unsubstituted aromatic group, a substituted or unsubstituted heteroaromatic group, and combinations thereof, optionally with one or more linking moiety chosen from —O—, —N(R b )—, —COO—, —CONR b —, —CONR b —, and —OCONR b —, and wherein Q 2 is optionally a branching group connected to at least two repeat units represented by Formula (3); Ar is a substituted or unsubstituted C 6-18 arylene group or a substituted or unsubstituted C 3-18 heteroarylene group; X 3 is a substituted or unsubstituted nitrogen-containing monocyclic, polycyclic, or fused polycyclic C 2-7 heterocycloalkyl group or C 3-30 heteroaryl group; R a is hydrogen or a substituted or unsubstituted C 1-30 alkyl group; and each R b is independently hydrogen, a substituted or unsubstituted C 1-30 alkyl group, a substituted or unsubstituted polycyclic or monocyclic C 3-30 cycloalkyl group, or a substituted or unsu

Assignees

Inventors

Classifications

  • Anti-reflective coatings · CPC title

  • Polyamines · CPC title

  • Homopolymers or copolymers of vinyl-pyridine · CPC title

  • of esters containing halogen, nitrogen, sulfur or oxygen atoms in addition to the carboxy oxygen · CPC title

  • G03F7/091Primary

    characterised by antireflection means or light filtering or absorbing means, e.g. anti-halation, contrast enhancement · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US11567408B2 cover?
A method for forming a photoresist relief image including applying a layer of a coating composition on a substrate; and disposing a layer of a photoresist composition on the layer of the coating composition, wherein the coating composition comprises an amine-containing polymer comprising a hydrocarbon-substituted amino group and having nitrogen atoms in an amount from 3 to 47 weight percent, ba…
Who is the assignee on this patent?
Rohm & Haas Elect Materials Korea Ltd, Rohm & Haas Elect Mat
What technology area does this patent fall under?
Primary CPC classification G03F7/091. Mapped technology areas include Physics.
When was this patent published?
Publication date Tue Jan 31 2023 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 12 related publications on this page (citations in our corpus or others sharing the same primary CPC).