IP Library Granted Patent US 11,215,928
Granted Patent B2
US 11,215,928 · App. 16/354,344 · Granted Jan 4, 2022

Composition for resist underlayer film formation, resist underlayer film and method for forming the same, and production method of a patterned substrate

Inventors: Kazunori Takanashi (Tokyo, JP); Hiroki Nakatsu (Tokyo, JP); Kazunori Sakai (Tokyo, JP); Ichihiro Miura (Tokyo, JP)
Assignee: JSR CORPORATION
G03F7/11C07D265/16C07D413/14C09D165/00G03F7/094G03F7/162G03F7/168H01L21/0273C09D161/12H01L21/0271
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Quick Facts
Patent No.
US 11,215,928
App. No.
16/354,344
Granted
Jan 4, 2022
Kind
B2
Abstract

A composition for resist underlayer film formation contains: a first compound including at least one oxazine structure fused to an aromatic ring; and a solvent. The first compound preferably includes a partial structure represented by formula (1). In formula (1), R 2 to R 5 each independently represent a hydrogen atom or a monovalent organic group having 1 to 20 carbon atoms; Ar 1 represents a group obtained by removing (n+3) or (n+2) hydrogen atoms on the aromatic ring from an arene having 6 to 20 carbon atoms; R 6 represents a hydroxy group, a halogen atom, a nitro group or a monovalent organic group having 1 to 20 carbon atoms; and n is an integer of 0 to 9.

Claims (46)

1. A composition for resist underlayer film formation, comprising:

a resin comprising at least one oxazine structure fused to an aromatic ring; and

a solvent,

wherein the resin comprises a partial structure represented by formula (1):

wherein, in the formula (1),

R 2 to R 5 each independently represent a hydrogen atom or a monovalent organic group having 1 to 20 carbon atoms;

Ar 1 represents a group obtained by removing (n+3) or (n+2) hydrogen atoms on the aromatic ring from an arene having 6 to 20 carbon atoms;

R 6 represents a hydroxy group, a halogen atom, a nitro group or a monovalent organic group having 1 to 20 carbon atoms;

n is an integer of 0 to 9, wherein in a case in which n is no less than 2, a plurality of R 6 s are identical or different, or wherein two or more of the plurality of R 6 s taken together represent a ring structure having 4 to 20 ring atoms together with the carbon chain to which the two or more of the plurality of R 6 s bond; and

* and ** each independently denote a bonding site to a part other than the partial structure represented by the formula (1) in the resin.

2. The composition according to claim 1 , wherein the resin comprises a group represented by formula (1-1), a group represented by formula (1-2), or a combination thereof:

wherein, in the formula (1-1),

R 1A represents a monovalent organic group having 1 to 20 carbon atoms;

R 2A to R 5A each independently represent a hydrogen atom or a monovalent organic group having 1 to 20 carbon atoms;

Ar 1A represents a group obtained by removing (n1+3) or (n1+2) hydrogen atoms on the aromatic ring from an arene having 6 to 20 carbon atoms;

R 6A represents a hydroxy group, a halogen atom, a nitro group or a monovalent organic group having 1 to 20 carbon atoms;

n1 is an integer of 0 to 9, wherein in a case in which n1 is no less than 2, a plurality of R 6A s are identical or different, or wherein two or more of the plurality of R 6A s taken together represent a ring structure having 4 to 20 ring atoms together with the carbon chain to which the two or more of the plurality of R 6A s bond; and

* * denotes a bonding site to a part other than the group represented by the formula (1-1) in the resin,

wherein, in the formula (1-2),

R 2B to R 5B each independently represent a hydrogen atom or a monovalent organic group having 1 to 20 carbon atoms;

Ar 1B represents a group obtained by removing (n2+2) hydrogen atoms on the aromatic ring from an arene having 6 to 20 carbon atoms;

R 6B represents a hydroxy group, a halogen atom, a nitro group or a monovalent organic group having 1 to 20 carbon atoms;

n2 is an integer of 0 to 10, wherein in a case in which n2 is no less than 2, a plurality of R 6B s are identical or different, or wherein two or more of the plurality of R 6B s taken together represent a ring structure having 4 to 20 ring atoms together with the carbon chain to which two or more of the plurality of R 6B s bond; and

** denotes a bonding site to a part other than the group represented by the formula (1-2) in the resin.

3. The composition according to claim 2 , wherein the resin comprises a plurality of groups represented by the formula (1-1), a plurality of groups represented by the formula (1-2), or a combination thereof.

4. A production method of a patterned substrate comprising:

applying the composition for resist underlayer film formation according to claim 3 directly or indirectly on a substrate to obtain a coating film;

heating the coating film to obtain a resist underlayer film;

forming a resist pattern directly or indirectly on the resist underlayer film; and

carrying out etching with the resist pattern used as a mask.

5. A production method of a patterned substrate comprising:

applying the composition for resist underlayer film formation according to claim 2 directly or indirectly on a substrate to obtain a coating film;

heating the coating film to obtain a resist underlayer film;

forming a resist pattern directly or indirectly on the resist underlayer film; and

carrying out etching with the resist pattern used as a mask.

6. The composition according to claim 1 , wherein a content of the resin in the composition is no less than 1% by mass and no greater than 50% by mass.

7. A production method of a patterned substrate comprising:

applying the composition for resist underlayer film formation according to claim 6 directly or indirectly on a substrate to obtain a coating film;

heating the coating film to obtain a resist underlayer film;

forming a resist pattern directly or indirectly on the resist underlayer film; and

carrying out etching with the resist pattern used as a mask.

8. A production method of a patterned substrate comprising:

applying the composition for resist underlayer film formation according to claim 1 directly or indirectly on a substrate to obtain a coating film;

heating the coating film to obtain a resist underlayer film;

forming a resist pattern directly or indirectly on the resist underlayer film; and

carrying out etching with the resist pattern used as a mask.

Assignments (3)
MERGER Recorded Mar 23, 2026
From: JSR CORPORATION
To: JICC-02, CO., LTD
Reel/Frame 075191/0149 →
CHANGE OF NAME Recorded Mar 23, 2026
From: JICC-02 CO., LTD
To: JSR CORPORATION
Reel/Frame 075192/0023 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 15, 2019
From: TAKANASHI, KAZUNORI; NAKATSU, HIROKI; SAKAI, KAZUNORI; MIURA, ICHIHIRO
To: JSR CORPORATION
Reel/Frame 049186/0485 →
Priority Claims (2)
JP JP2016-181542 · Sep 16, 2016 · national
JP JP2017-054209 · Mar 21, 2017 · national
Continuity (2)
Continuation PCTJP2017032592 · Sep 8, 2017
Related Publication 20190212650A1 · Jul 11, 2019