IP Library › Granted Patent US 12,572,071
Granted Patent B2
US 12,572,071 · App. 17/977,157 · Granted Mar 10, 2026

Carboxylate, carboxylic acid generator, resin, resist composition and method for producing resist pattern

Inventors: Masahiko Shimada (Osaka, JP); Koji Ichikawa (Osaka, JP)
Assignee: SUMITOMO CHEMICAL COMPANY, LIMITED
G03F7/039C07C69/54C07C381/12C07D307/93C07D333/76C08F220/1808G03F7/0045G03F7/038C07C2603/74
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Quick Facts
Patent No.
US 12,572,071
App. No.
17/977,157
Granted
Mar 10, 2026
Kind
B2
Abstract

A carboxylate represented by formula (I), a resin comprising a structural unit derived from the carboxylate represented by formula (I), a resist composition comprising the carboxylate represented by formula (I) or a resin comprising a structural unit derived from the carboxylate represented by formula (I).

Claims (129)

1 . A carboxylate represented by formula (I):

wherein, in formula (I),

R 4 , R 5 , R 6 , R 7 , R 8 and R 9 each independently represent a halogen atom, a hydroxy group, a haloalkyl group having 1 to 12 carbon atoms or a hydrocarbon group having 1 to 18 carbon atoms, each of the hydrocarbon group may have a substituent, and —CH 2 — included in each of the haloalkyl group and the hydrocarbon group may be replaced by —O—, —CO—, —S— or —SO 2 —,

A 1 , A 2 and A 3 each independently represent a hydrocarbon group having 1 to 20 carbon atoms, each of the hydrocarbon group may have a substituent, and —CH 2 — included in each of the hydrocarbon group may be replaced by —O—, —CO—, —S— or —SO 2 —,

A 1 is ***—X 01 -L 01 - or ***-L01-X 01 —,

A 2 is ***—X 02 -L 02 - or ***L 02 -X 02 —,

A 3 is ***—X 03 -L 03 - or ***-L 03 -X 03 —,

X 01 , X 02 and X 03 each independently represent —O—, —CO—, —S— or —SO 2 —,

L 01 , L 02 and L 03 each independently represent a hydrocarbon group having 1 to 18 carbon atoms, and

*** represents a bonding site to the benzene ring to which S + is bonded,

m1 represents an integer of 0 to 5, and when m1 is 2 or more, a plurality of groups in parentheses may be the same or different from each other,

m2 represents an integer of 0 to 4, and when m2 is 2 or more, a plurality of groups in parentheses may be the same or different from each other,

m3 represents an integer of 0 to 4, and when m3 is 2 or more, a plurality of groups in parentheses may be the same or different from each other,

m4 represents an integer of 0 to 5, and when m4 is 2 or more, a plurality of R 4 may be the same or different from each other,

m5 represents an integer of 0 to 5, and when m5 is 2 or more, a plurality of R 5 may be the same or different from each other,

m6 represents an integer of 0 to 5, and when m6 is 2 or more, a plurality of R 6 may be the same or different from each other,

m7 represents an integer of 0 to 5, and when m7 is 2 or more, a plurality of R 7 may be the same or different from each other,

m8 represents an integer of 0 to 4, and when m8 is 2 or more, a plurality of R 8 may be the same or different from each other,

m9 represents an integer of 0 to 4, and when m9 is 2 or more, a plurality of R 9 may be the same or different from each other,

in which 0≤m1+m7≤5, 0≤m2+m8≤4, 0≤m3+m9≤4,

at least one of m1, m2 and m3 represents an integer of 1 or more,

X 4 represents a single bond, —CH 2 —, —O—, —S—, —CO—, —SO— or —SO 2 —,

X 0 represents a single bond or a hydrocarbon group having 1 to 72 carbon atoms which may have a substituent, and —CH 2 — included in the hydrocarbon group may be replaced by —O—, —S—, —CO— or —SO 2 —,

R bb1 represents a hydrogen atom, a halogen atom, or an alkyl group having 1 to 6 carbon atoms which may have a halogen atom,

X 10 represents a single bond, *—O—**, *—CO—O—**, *—O—CO—O—** or *-Ax-Ph-Ay-**,

Ph represents a phenylene group which may have a substituent,

Ax represents a single bond, an ether bond, an ester bond or a carbonic acid ester bond,

Ay represents a single bond, an ether bond, an ester bond or a carbonic acid ester bond,

* represents a bonding site to carbon atoms to which —R bb1 is bonded,

** represents a bonding site to L 10 , and

L 10 represents a single bond or a hydrocarbon group having 1 to 36 carbon atoms which may have a substituent, and —CH 2 — included in each of the hydrocarbon group may be replaced by —O—, —S—, —SO 2 — or —CO—.

2 . The carboxylate according to claim 1 , wherein X 01 , X 02 and X 03 are oxygen atoms.

3 . The carboxylate according to claim 1 , wherein L 01 , L 02 and L 03 are each independently a single bond or an alkanediyl group having 1 to 6 carbon atoms.

4 . The carboxylate according to claim 1 , wherein R 4 , R 5 and R 6 are each independently a fluorine atom, an iodine atom or a perfluoroalkyl group having 1 to 4 carbon atoms.

5 . The carboxylate according to claim 1 , wherein X 0 is an aliphatic hydrocarbon group having 1 to 72 carbon atoms which may have a substituent, and a —CH 2 — included in the aliphatic hydrocarbon group may be replaced by —O—, —S—, —CO— or —SO 2 —, or

an aromatic hydrocarbon group having 6 to 36 carbon atoms which may have a substituent.

6 . The carboxylate according to claim 5 , wherein X 0 includes an alicyclic hydrocarbon group having 3 to 36 carbon atoms which may have a fluorine atom, a perfluoroalkyl group having 1 to 4 carbon atoms or a hydroxy group, and a —CH 2 — included in the alicyclic hydrocarbon group may be replaced by —O—, —S—, —CO— or —SO 2 —,

a group obtained by combining an alicyclic hydrocarbon group having 3 to 36 carbon atoms with a chain hydrocarbon group having 1 to 18 carbon atoms, and a —CH 2 — included in the alicyclic hydrocarbon group may be replaced by —O—, —S—, —CO— or —SO 2 —, and a —CH 2 — included in the chain hydrocarbon group may be replaced by —O— or —CO—, and the alicyclic hydrocarbon group and the chain hydrocarbon group may have a fluorine atom, a perfluoroalkyl group having 1 to 4 carbon atoms or a hydroxy group, or

an aromatic hydrocarbon group having 6 to 36 carbon atoms which may have a fluorine atom, a perfluoroalkyl group having 1 to 4 carbon atoms or a hydroxy group.

7 . The carboxylate according to claim 5 , wherein X 0 includes the alicyclic hydrocarbon group, and

the alicyclic hydrocarbon group includes

a cycloalkanediyl group having 5 or 6 carbon atoms, and a —CH 2 — included in the cycloalkanediyl group may be replaced by —O— or —CO—, and the cycloalkanediyl group may be an acetal ring,

an adamandiyl group,

a norbornanediyl group,

a polycyclic alicyclic hydrocarbon group in which a cycloalkanediyl group having 5 or 6 carbon atoms and an adamantanediyl group are spiro-bonded,

a —CH 2 — included in the adamantanediyl group, the norbornanediyl group and the cycloalkanediyl group may be replaced by —O— or —CO—,

a —CH 2 —CH 2 — included in the adamantanediyl group and the norbornanediyl group may be replaced by —O—CO—,

and the cycloalkanediyl group may be an acetal ring.

8 . The carboxylate according to claim 1 , wherein X 10 is a single bond or a group represented by any one of formula (X 1 -1), formula (X 1 -2′) to formula (X 1 -7′) and formula (X 1 -8):

wherein, in formula (X 1 -1), formula (X 1 -2′) to formula (X 1 -7′) and formula (X 1 -8),

* and ** are bonding sites, and ** represents a bonding site to L10,

Rx represents a halogen atom, a hydroxy group, an alkyl fluoride group having 1 to 6 carbon atoms, an alkyl group having 1 to 18 carbon atoms or an alkoxy group having 1 to 6 carbon atoms, and

mx represents an integer of 0 to 4.

9 . The carboxylate according to claim 1 , wherein L 10 is a single bond or an alkanediyl group having 1 to 4 carbon atoms, and a —CH 2 — included in the alkanediyl group may be replaced by —O— or —CO—.

10 . The carboxylate according to claim 6 , wherein X 0 is a phenylene group which may have a substituent, and

L 10 is a single bond, and X 10 is a single bond or a group represented by formula (X 1 -1).

11 . A resin comprising a structural unit derived from the carboxylate according to claim 1 .

12 . A resin composition comprising

the carboxylate according to claim 1 or a resin including a structural unit derived from the carboxylate according to claim 1 .

13 . The resist composition according to claim 12 , further comprising

a resin including a structural unit having an acid labile group,

wherein the acid-labile group includes at least one selected from the group consisting of a structural unit represented by formula (a1-0), a structural unit represented by formula (a1-1) and a structural unit represented by formula (a1-2):

wherein, in formula (a1-0), formula (a1-1) and formula (a1-2),

L a01 , L a1 and L a2 each independently represent —O— or *—O—(CH 2 ) k1 —CO—O—, k1 represents an integer of 1 to 7, and * represents a bonding site to —CO—,

R a01 , R a4 and R a5 each independently represent a hydrogen atom, a halogen atom, or an alkyl group having 1 to 6 carbon atoms which may have a halogen atom,

R a02 , R a03 and R a04 each independently represent an alkyl group having 1 to 8 carbon atoms, an alicyclic hydrocarbon group having 3 to 18 carbon atoms, an aromatic hydrocarbon group having 6 to 18 carbon atoms, or a group obtained by combining these groups,

R a6 and R a7 each independently represent an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, an alicyclic hydrocarbon group having 3 to 18 carbon atoms, an aromatic hydrocarbon group having 6 to 18 carbon atoms, or a group formed by combining these groups,

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.

14 . The resist composition according to claim 12 , further comprising

a resin including a structural unit represented by formula (a2-A):

wherein, in formula (a2-A),

R a50 represents a hydrogen atom, a halogen atom, or an alkyl group having 1 to 6 carbon atoms which may have a halogen atom,

R a51 represents a halogen atom, a hydroxy group, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, an alkoxyalkyl group having 2 to 12 carbon atoms, an alkoxyalkoxy group having 2 to 12 carbon atoms, an alkylcarbonyl group having 2 to 4 carbon atoms, an alkylcarbonyloxy group having 2 to 4 carbon atoms, an acryloyloxy group or a methacryloyloxy group,

A a50 represents a single bond or *—X a51 -(A a52 -X a52 ) nb —, and * represents a bond to carbon atoms to which —R a50 is bonded,

A a52 represents an alkanediyl group having 1 to 6 carbon atoms,

X a51 and X a52 each independently represent —O—, —CO—O— or —O—CO—,

nb represents 0 or 1, and

mb represents an integer of 0 to 4, and when mb is an integer of 2 or more, a plurality of R a51 may be the same or different from each other.

15 . The resist composition according to claim 12 , further comprising

an acid generator including a salt represented by formula (B1):

wherein, in formula (B1),

Q b1 and Q b2 each independently represent a hydrogen atom, a fluorine atom, a perfluoroalkyl group having 1 to 6 carbon atoms or an alkyl group having 1 to 6 carbon atoms,

L b1 represents a divalent saturated hydrocarbon group having 1 to 24 carbon atoms, a —CH 2 — included in the divalent saturated hydrocarbon group may be replaced by —O— or —CO—, and a hydrogen atom included in the divalent saturated hydrocarbon group may be substituted with a fluorine atom or a hydroxy group,

Y represents a methyl group which may have a substituent or an alicyclic hydrocarbon group having 3 to 24 carbon atoms which may have a substituent, and a —CH 2 — included in the alicyclic hydrocarbon group may be replaced by —O—, —S—, —SO 2 — or —CO—, and

Z + represents an organic cation.

16 . A resist composition comprising

the carboxylate according to claim 1 and

a resin including the structural unit having an acid labile group.

17 . A resist composition comprising

a resin including a structural unit derived from the carboxylate according to claim 1 and a structural unit having an acid labile group.

18 . A resist composition comprising

the carboxylate according to claim 1 and

a resin including the structural unit derived from the carboxylate according to claim 1 .

19 . A method for producing a resist pattern, which comprises:

(1) a step of applying the resist composition according to claim 12 on a substrate,

(2) a step of drying the applied composition to form a composition layer,

(3) a step of exposing the composition layer,

(4) a step of heating the exposed composition layer, and

(5) a step of developing the heated composition layer.

20 . A carboxylate represented by formula (I):

wherein, in formula (I),

R 4 , R 5 , R 6 , R 7 , R 8 and R 9 each independently represent a halogen atom, a hydroxy group, a haloalkyl group having 1 to 12 carbon atoms or a hydrocarbon group having 1 to 18 carbon atoms, each of the hydrocarbon group may have a substituent, and —CH 2 — included in each of the haloalkyl group and the hydrocarbon group may be replaced by —O—, —CO—, —S— or —SO 2 —,

A 1 , A 2 and A 3 each independently represent a hydrocarbon group having 1 to 20 carbon atoms, each of the hydrocarbon group may have a substituent, and —CH 2 — included in each of the hydrocarbon group may be replaced by —O—, —CO—, —S— or —SO 2 —,

m1 represents an integer of 0 to 5, and when m1 is 2 or more, a plurality of groups in parentheses may be the same or different from each other,

m2 represents an integer of 0 to 4, and when m2 is 2 or more, a plurality of groups in parentheses may be the same or different from each other,

m3 represents an integer of 0 to 4, and when m3 is 2 or more, a plurality of groups in parentheses may be the same or different from each other,

m4 represents an integer of 0 to 5, and when m4 is 2 or more, a plurality of R4 may be the same or different from each other,

m5 represents an integer of 0 to 5, and when m5 is 2 or more, a plurality of R5 may be the same or different from each other,

m6 represents an integer of 0 to 5, and when m6 is 2 or more, a plurality of R6 may be the same or different from each other,

m7 represents an integer of 0 to 5, and when m7 is 2 or more, a plurality of R7 may be the same or different from each other,

m8 represents an integer of 0 to 4, and when m8 is 2 or more, a plurality of R8 may be the same or different from each other,

m9 represents an integer of 0 to 4, and when m9 is 2 or more, a plurality of R9 may be the same or different from each other,

in which 0≤m1+m7≤5, 0<m2+m8<4, 0≤m3+m9≤4,

at least one of m1 and m2 represents an integer of 1 or more,

when m1 is 1 or more, m4 is an integer of 1 or more, and at least one of the one or more R 4 represents a halogen atom or a haloalkyl group having 1 to 12 carbon atoms,

when m2 is 1 or more, m5 is an integer of 1 or more, and at least one of the one or more R 5 represents a halogen atom or a haloalkyl group having 1 to 12 carbon atoms,

when both m1 and m2 are integers of 1 or more, at least one of m4 or m5 is an integer of 1 or more, and at least one of the R 4 and at least one of the R 5 represent a halogen atom or a haloalkyl group having 1 to 12 carbon atoms,

X 4 represents a single bond, —CH 2 —, —O—, —S—, —CO—, —SO— or —SO 2 —,

X 0 represents a single bond or a hydrocarbon group having 1 to 72 carbon atoms which may have a substituent, and —CH 2 — included in the hydrocarbon group may be replaced by —O—, —S—, —CO— or —SO 2 —,

R bb1 represents a hydrogen atom, a halogen atom, or an alkyl group having 1 to 6 carbon atoms which may have a halogen atom,

X 10 represents a single bond, *—O—**, *—CO—O—**, *—O—CO—O—** or *-Ax-Ph-Ay-**,

Ph represents a phenylene group which may have a substituent,

Ax represents a single bond, an ether bond, an ester bond or a carbonic acid ester bond,

Ay represents a single bond, an ether bond, an ester bond or a carbonic acid ester bond,

* represents a bonding site to carbon atoms to which —R bb1 is bonded,

** represents a bonding site to L 10 , and

L 10 represents a single bond or a hydrocarbon group having 1 to 36 carbon atoms which may have a substituent, and —CH 2 — included in each of the hydrocarbon group may be replaced by —O—, —S—, —SO 2 — or —CO—.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 31, 2022
From: SHIMADA, MASAHIKO; ICHIKAWA, KOJI
To: SUMITOMO CHEMICAL COMPANY, LIMITED
Reel/Frame 061593/0375 →
Priority Claims (2)
JP 2021-182480 · Nov 9, 2021 · national
JP 2022-038539 · Mar 11, 2022 · national
Continuity (1)
Related Publication 20230161250A1 · May 25, 2023
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