IP Library Granted Patent US 11,243,468
Granted Patent B2
US 11,243,468 · App. 16/564,499 · Granted Feb 8, 2022

Composition for resist underlayer film formation, resist underlayer film and formation method thereof, and patterned substrate production method

Inventors: Naoya Nosaka (Tokyo, JP); Goji Wakamatsu (Tokyo, JP); Tsubasa Abe (Tokyo, JP); Ichihiro Miura (Tokyo, JP); Kengo Ehara (Tokyo, JP); Hiroki Nakatsu (Tokyo, JP); Hiroki Nakagawa (Tokyo, JP)
Assignee: JSR CORPORATION
G03F7/0395C08G61/04C08G61/124G03F7/094G03F7/20
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Quick Facts
Patent No.
US 11,243,468
App. No.
16/564,499
Granted
Feb 8, 2022
Kind
B2
Abstract

A composition for resist underlayer film formation contains: a compound having a partial structure represented by the following formula (1); and a solvent. In the formula (1): X represents a group represented by formula (i), (ii), (iii) or (iv). In the formula (i): R 1 and R 2 each independently represent a hydrogen atom, a substituted or unsubstituted monovalent aliphatic hydrocarbon group having 1 to 20 carbon atoms, or a substituted or unsubstituted aralkyl group having 7 to 20 carbon atoms provided that at least one of R 1 and R 2 represents the substituted or unsubstituted monovalent aliphatic hydrocarbon group having 1 to 20 carbon atoms or the substituted or unsubstituted aralkyl group having 7 to 20 carbon atoms; or R 1 and R 2 taken together represent a part of a ring structure having 3 to 20 ring atoms together with the carbon atom to which R 1 and R 2 bond.

Claims (44)

1. A patterned substrate production method comprising:

applying a composition for resist underlayer film formation directly or indirectly on an upper face side of a substrate to obtain a coating film;

heating the coating film to form a resist underlayer film;

forming a resist pattern on an upper face side of the resist underlayer film; and

carrying out etching using the resist pattern as a mask,

wherein

the composition for resist underlayer film formation, comprising:

a compound represented by formula (2-1); and

a solvent:

R B Z) m   (2-1)

wherein in the formula (2-1):

Z represents a partial structure represented by formula (1);

R B represents a group obtained by removing m hydrogen atoms from a substituted or unsubstituted arene having 6 to 20 carbon atoms, the arene being benzene, naphthalene, anthracene, phenanthrene, tetracene, pyrene, triphenylene, or perylene, or a group obtained by removing m hydrogen atoms from a substituted or unsubstituted heteroarene having 5 to 20 ring atoms, the heteroarene being pyridine, pyrazine, pyrimidine, pyridazine, triazine, quinoline, isoquinoline, quinazoline, cinnoline, phthalazine, quinoxaline, pyrrole, indole, furan, benzofuran, thiophene, benzothiophene, pyrazole, imidazole, benzimidazole, triazole, oxazole, benzoxazole, thiazole, benzothiazole, isothiazole, benzisothiazole, thiadiazole, isoxazole, or benzisoxazole; and

m is an integer of 2 to 20,

wherein in a case in which m is no less than 2, a plurality of Zs are identical or different,

wherein, in the formula (1):

X represents a group represented by formula (i), (ii), (iii) or (iv);

n1 and n2 are each independently an integer of 0 to 2;

Y and Y′ each independently represent a monovalent organic group having 1 to 20 carbon atoms;

n3 and n4 are each independently an integer of 0 to 8;

* and ** each denote a bonding site to R B in the formula (2-1); and

n5 is 1 and n6 is 0, or n5 is 0 and n6 is 1,

wherein in a case in which n3 is no less than 2, a plurality of Ys are identical or different, and in a case in which n4 is no less than 2, a plurality of Y's are identical or different,

and wherein n3+n5 is no greater than 8, and n4+n6 is no greater than 8,

wherein, in the formula (i): R 1 and R 2 each independently represent a hydrogen atom, a hydroxy group, a substituted or unsubstituted monovalent aliphatic hydrocarbon group having 1 to 20 carbon atoms, or a substituted or unsubstituted aralkyl group having 7 to 20 carbon atoms provided that at least one of R 1 and R 2 represents the substituted or unsubstituted monovalent aliphatic hydrocarbon group having 1 to 20 carbon atoms or the substituted or unsubstituted aralkyl group having 7 to 20 carbon atoms; or R 1 and R 2 taken together represent a part of a ring structure having 3 to 20 ring atoms together with the carbon atom to which R 1 and R 2 bond,

in the formula (ii): R 3 and R 4 each independently represent a hydrogen atom, a hydroxy group or a monovalent organic group having 1 to 20 carbon atoms; or R 3 and R 4 taken together represent a part of a ring structure having 3 to 20 ring atoms together with the carbon atom to which R 3 and R 4 bond,

in the formula (iii), R 5 represents a hydrogen atom, a hydroxy group or a monovalent organic group having 1 to 20 carbon atoms, and

in the formula (iv), R 6 represents a substituted or unsubstituted monovalent aliphatic hydrocarbon group, or a substituted or unsubstituted aralkyl group having 7 to 20 carbon atoms.

2. The patterned substrate production method according to claim 1 , wherein, in the formula (i): R 1 and R 2 each independently represent a hydrogen atom, a substituted or unsubstituted monovalent aliphatic hydrocarbon group having 1 to 20 carbon atoms, or a substituted or unsubstituted aralkyl group having 7 to 20 carbon atoms; or R 1 and R 2 taken together represent a part of a ring structure having 3 to 20 ring atoms together with the carbon atom to which R 1 and R 2 bond.

3. The patterned substrate production method according to claim 1 , wherein the composition for resist underlayer film formation further comprises a crosslinkable compound other than the compound represented by the formula (2-1).

4. The patterned substrate production method according to claim 1 , wherein in the formula (2-1), m is an integer of 3 to 6.

5. The patterned substrate production method according to claim 1 , wherein in the formula (2-1), m is an integer of 3.

6. The patterned substrate production method according to claim 1 , wherein in the formula (1), n1 is 0, and n2 is 0.

7. The patterned substrate production method according to claim 1 , wherein R B represents a group obtained by removing m hydrogen atoms from a substituted or unsubstituted arene having 6 to 20 carbon atoms, and the arene is benzene or naphthalene.

8. The patterned substrate production method according to claim 1 , wherein R B represents a group obtained by removing m hydrogen atoms from a substituted or unsubstituted arene having 6 to 20 carbon atoms, and the arene is benzene.

9. The patterned substrate production method according to claim 1 , wherein R B represents a group obtained by removing m hydrogen atoms from a substituted or unsubstituted heteroarene having 5 to 20 ring atoms, and the heteroarene is triazine.

10. The patterned substrate production method according to claim 1 , wherein a content of the compound represented by the formula (2-1) with respect to a total solid content in the composition for resist underlayer film formation is from 70% to 100% by mass.

11. The patterned substrate production method according to claim 1 , wherein a content of the compound represented by the formula (2-1) with respect to a total solid content in the composition for resist underlayer film formation is from 85% to 100% by mass.

12. The patterned substrate production method according to claim 1 , wherein a content of the compound represented by the formula (2-1) in the composition for resist underlayer film formation is from 1% to 50% by mass.

13. The patterned substrate production method according to claim 1 , wherein a content of the compound represented by the formula (2-1) in the composition for resist underlayer film formation is from 3% to 30% by mass.

14. The patterned substrate production method according to claim 1 , wherein a content of the compound represented by the formula (2-1) in the composition for resist underlayer film formation is from 5% to 15% by mass.

15. The patterned substrate production method according to claim 1 , wherein the solvent is at least one selected from the group consisting of an alcohol solvent, a ketone solvent, an ether solvent, an ester solvent, and a nitrogen-containing solvent.

16. The patterned substrate production method according to claim 1 , wherein the composition for resist underlayer film formation further comprises an acid generating agent.

17. The patterned substrate production method according to claim 16 , an amount of the acid generating agent in the composition for resist underlayer film formation is 3 to 10 parts by mass with respect to 100 parts by mass of the compound represented by the formula (2-1).

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 Oct 9, 2019
From: NOSAKA, NAOYA; WAKAMATSU, GOJI; ABE, TSUBASA; MIURA, ICHIHIRO; EHARA, KENGO; NAKATSU, HIROKI; NAKAGAWA, HIROKI
To: JSR CORPORATION
Reel/Frame 050666/0885 →
Priority Claims (1)
JP JP2017-046092 · Mar 10, 2017 · national
Continuity (2)
Continuation PCTJP2018009257 · Mar 9, 2018
Related Publication 20200012193A1 · Jan 9, 2020
Cited By (1)
US 12,517,433