IP Library Granted Patent US 11,401,381
Granted Patent B2
US 11,401,381 · App. 13/980,385 · Granted Aug 2, 2022

Modified silicone compound, and thermosetting resin composition, prepreg, laminate plate and printed wiring board using same

Inventors: Tomohiko Kotake (Ibaraki, JP); Masato Miyatake (Ibaraki, JP); Shunsuke Nagai (Ibaraki, JP); Shintaro Hashimoto (Ibaraki, JP); Yasuo Inoue (Ibaraki, JP); Shin Takanezawa (Ibaraki, JP); Hikari Murai (Ibaraki, JP)
Assignee: SHOWA DENKO MATERIALS CO., LTD.
C08G73/0273C08G73/125C08G77/388C08L63/00C08L79/085C08L83/08C09D163/00C09D183/08Y10T428/31663
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Quick Facts
Patent No.
US 11,401,381
App. No.
13/980,385
Granted
Aug 2, 2022
Kind
B2
Abstract

There are provided a modified silicone compound prepared by reacting: (A) a siloxane diamine represented by the general formula (1); (B) a maleimide compound with at least two N-substituted maleimide groups in the molecular structure; and (C) an amine compound with an acidic substituent; and also provided a thermosetting resin composition, a prepreg, a laminated plate, and a printed wiring board that are formed by using this compound. The multi-layered printed wiring board produced by using the laminated plate formed by using the prepreg obtained from the modified silicone compound and the thermosetting resin composition of the present invention through laminate molding has an excellent glass transition temperature, coefficient of thermal expansion, copper foil adhesion, hygroscopicity, hygroscopic solder heat resistance, and copper-stuck solder heat resistance. Therefore, the multi-layered printed wiring board is useful as a highly integrated semiconductor package and a printed wiring board for an electronic device.

Claims (42)

1. A modified silicone compound prepared by reacting:

(A) a siloxane diamine component comprising a siloxane diamine represented by a general formula (1):

wherein a plurality of R 1 s each independently represent an alkyl group, a phenyl group, or a substituted phenyl group and may be the same as or different from each other, a plurality of R 2 s each independently represent an alkyl group, a phenyl group, or a substituted phenyl group and may be the same as or different from each other, R 3 and R 4 each independently represent an alkyl group, a phenyl group, or a substituted phenyl group, R 5 and R 6 represent C 3 H 6 , n represents an integer of 2-50, and at least one of the following conditions (i)-(iv) is met:

(i) at least one of the R 1 s represents a phenyl group or a substituted phenyl group,

(ii) at least one of the R 2 s represents a phenyl group or a substituted phenyl group,

(iii) R 3 represents a phenyl group or a substituted phenyl group, and

(iv) R 4 represents a phenyl group or a substituted phenyl group;

(B) a maleimide component comprising a maleimide compound with at least two N-substituted maleimide groups in a molecular structure, wherein an amount of the maleimide component (B) is 100-3000 parts by mass, based on 100 parts by mass of the siloxane diamine component (A);

(C) an amine component comprising an amine compound with an acidic substituent represented by a general formula (2):

wherein R 9 or a plurality of R 9 s each independently represent a hydroxyl, a carboxyl, or a sulfonic group that is an acidic substituent, R 10 or a plurality of R 10 s each independently represent a hydrogen atom, an aliphatic hydrocarbon group with 1-5 carbon atoms, or a halogen atom, x represents an integer of 1-5, y represents an integer of 0-4, and x+y=5, and

an amount of the amine compound represented by general formula (2) is 1-8.454 parts by mass, based on 100 parts by mass of the siloxane diamine represented by general formula (1); and

(D) an optional amine component comprising at least one selected from the group consisting of m-phenylenediamine, p-phenylenediamine, 1,4-bis(4-aminophenoxy)benzene, 4,4′-diaminodiphenylmethane, 3,3′-dimethyl-4,4′-diaminodiphenylmethane, 3,3′-diethyl-4,4′-diaminodiphenylmethane, 4,4′-diaminobenzophenone, 4,4′-diaminodiphenyl ether, 3,3′-diaminodiphenyl sulfone, 4,4′-diaminodiphenyl sulfone, benzidine, 4,4′-diaminodiphenyl sulfide, 4,4′-diamino-3,3′-biphenyldiol, and a guanamine.

2. A thermosetting resin composition comprising the modified silicone compound according to claim 1 .

3. The thermosetting resin composition according to claim 2 , further comprising an epoxy resin and/or a cyanate resin.

4. The thermosetting resin composition according to claim 2 , further comprising an inorganic filler.

5. A prepreg formed from the thermosetting resin composition according to claim 2 .

6. A laminated plate formed from the prepreg according to claim 5 through laminate molding.

7. A multi-layered printed wiring board produced from the laminated plate according to claim 6 .

8. The modified silicone compound according to claim 1 , wherein a ratio of C═C groups of the maleimide groups of the maleimide component (B) to total —NH 2 groups of the siloxane diamine component (A), the amine component (C) and the optional amine component (D) is 0.1≤C═C groups/total —NH 2 groups≤10.0.

9. The modified silicone compound according to claim 1 , wherein an amine equivalent of the siloxane diamine component (A) is 430-2,200.

10. The thermosetting resin composition according to claim 3 , wherein the epoxy resin includes at least one selected from the group consisting of a biphenyl aralkyl epoxy resin and a naphthalene epoxy resin, and the cyanate resin includes at least one selected from the group consisting of a novolac cyanate resin and bisphenol cyanate resin.

11. The thermosetting resin composition according to claim 10 , further comprising an imidazole curing accelerator.

12. The thermosetting resin composition according to claim 11 , further comprising at least one inorganic filler selected from the group consisting of silica and boehmite.

13. The modified silicone compound according to claim 1 , wherein

the maleimide component (B) comprises one or more of bis(4-maleimide phenyl)methane and polyphenylmethane maleimide,

the amine component (C) comprises aminophenol, and

the optional amine component (D) comprises one or more of 3,3′-diethyl-4,4′-diaminodiphenylmethane and 3,3′-diaminodiphenylsulfone.

14. A prepreg comprising a semi-cured form of the thermosetting resin composition according to claim 2 .

15. A laminated plate comprising a cured form of the prepreg according to claim 14 .

16. A multi-layered printed wiring board comprising the laminated plate according to claim 15 .

17. A modified silicone compound prepared by reacting reactants comprising:

(A) a siloxane diamine component comprising a siloxane diamine represented by a general formula (1):

wherein a plurality of R 1 s each independently represent an alkyl group, a phenyl group, or a substituted phenyl group and may be the same as or different from each other, a plurality of R 2 s each independently represent an alkyl group, a phenyl group, or a substituted phenyl group and may be the same as or different from each other, R 3 and R 4 each independently represent an alkyl group, a phenyl group, or a substituted phenyl group, R 5 and R 6 represent C 3 H 6 , n represents an integer of 2-50, and at least one of the following conditions (i)-(iv) is met:

(i) at least one of the R 1 s represents a phenyl group or a substituted phenyl group,

(ii) at least one of the R 2 s represents a phenyl group or a substituted phenyl group,

(iii) R 3 represents a phenyl group or a substituted phenyl group, and

(iv) R 4 represents a phenyl group or a substituted phenyl group;

(B) a maleimide component comprising a maleimide compound with at least two N-substituted maleimide groups in a molecular structure, wherein an amount of the maleimide component (B) is 100-3000 parts by mass, based on 100 parts by mass of the siloxane diamine component (A);

(C) an amine component comprising an amine compound with an acidic substituent represented by a general formula (2):

wherein R 9 or a plurality of R 9 s each independently represent a hydroxyl, a carboxyl, or a sulfonic group that is an acidic substituent, R 10 or a plurality of R 10 s each independently represent a hydrogen atom, an aliphatic hydrocarbon group with 1-5 carbon atoms, or a halogen atom, x represents an integer of 1-5, y represents an integer of 0-4, and x+y=5, and

an amount of the amine compound represented by general formula (2) is 1-8.454 parts by mass, based on 100 parts by mass of the siloxane diamine represented by general formula (1); and

(D) an optional amine component comprising an amine compound including at least two primary amino groups per molecule.

Assignments (4)
CHANGE OF ADDRESS Recorded Feb 14, 2024
From: RESONAC CORPORATION
To: RESONAC CORPORATION
Reel/Frame 066599/0037 →
CHANGE OF NAME Recorded Mar 8, 2023
From: SHOWA DENKO MATERIALS CO., LTD.
To: RESONAC CORPORATION
Reel/Frame 062992/0805 →
CHANGE OF NAME Recorded Apr 25, 2022
From: HITACHI CHEMICAL COMPANY, LTD.
To: SHOWA DENKO MATERIALS CO., LTD.
Reel/Frame 059790/0777 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 28, 2013
From: KOTAKE, TOMOHIKO; MIYATAKE, MASATO; NAGAI, SHUNSUKE; HASHIMOTO, SHINTARO; INOUE, YASUO; TAKANEZAWA, SHIN; MURAI, HIKARI
To: HITACHI CHEMICAL COMPANY, LTD.
Reel/Frame 031102/0375 →