IP Library Granted Patent US 8,206,811
Granted Patent B2
US 8,206,811 · App. 12/893,218 · Granted Jun 26, 2012

Thermosetting composition

Assignee: JNC Corporation
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Quick Facts
Patent No.
US 8,206,811
App. No.
12/893,218
Granted
Jun 26, 2012
Kind
B2
Abstract

A material of cured film, a thermosetting film and a display device are provided. The thermosetting composition includes a solvent and at least one siloxane polymer selected from the group consisting of siloxane polymer (A) obtained by hydrolyzing or condensing a silane mixture containing a monofunctional silane represented by formula (1) and a trifunctional silane represented by formula (2), and siloxane polymer (B) obtained by hydrolyzing or condensing a silane mixture containing a bifunctional silane represented by formula (3) and a tetrafunctional silane represented by formula (4). R independently represents hydrogen, an alkyl group having 1 to 10 carbons whose arbitrary hydrogen can be replaced by a halogen, an aryl group having 6 to 10 carbons whose arbitrary hydrogen can be replaced by a halogen, or an alkenyl group having 2 to 10 carbons whose arbitrary hydrogen can be replaced by a halogen. R′ independently represents a hydrolyzable group.

Claims (10)

1. A thermosetting composition, comprising a solvent, a siloxane polymer (A) and a siloxane polymer (B), wherein the siloxane polymer (A) is obtained by hydrolyzing or condensing a silane mixture containing a monofunctional silane represented by formula (1) and a trifunctional silane represented by formula (2), and the siloxane polymer (B) is obtained by hydrolyzing or condensing a silane mixture containing a bifunctional silane represented by formula (3) and a tetrafunctional silane represented by formula (4):

in formulae (1) to (4), R independently represents hydrogen, an alkyl group having 1 to 10 carbons whose arbitrary hydrogen can be replaced by a halogen, an aryl group having 6 to 10 carbons whose arbitrary hydrogen can be replaced by a halogen, or an alkenyl group having 2 to 10 carbons whose arbitrary hydrogen can be replaced by a halogen, and R′ independently represents a hydrolyzable group.

2. The thermosetting composition as claimed in claim 1 , wherein in the thermosetting composition comprising the siloxane polymer (A), the siloxane polymer (B), and the solvent, in formulae (1) to (4), R independently represents hydrogen, an alkyl group having 1 to 5 carbons whose arbitrary hydrogen can be replaced by a halogen, an aryl group having 6 to 10 carbons whose arbitrary hydrogen can be replaced by a halogen, or an alkenyl group having 2 to 10 carbons whose arbitrary hydrogen can be replaced by a halogen, and R′ independently represents an alkoxyl group, a halogen, or an acetoxyl group.

3. The thermosetting composition as claimed in claim 1 , wherein the monofunctional silane represented by formula (1) is one or more monofunctional silanes selected from a group consisting of trimethylmethoxysilane and trimethylethoxysilane.

4. The thermosetting composition as claimed in claim 1 , wherein the trifunctional silane represented by formula (2) is one or more trifunctional silanes selected from a group consisting of trimethoxymethylsilane, trimethoxyphenylsilane, triethoxymethylsilane, and triethoxyphenylsilane.

5. The thermosetting composition as claimed in claim 1 , wherein the bifunctional silane represented by formula (3) is one or more bifunctional silanes selected from a group consisting of dimethyldimethoxysilane, diphenyldimethoxysilane, methylphenyldimethoxysilane, dimethyldiethoxysilane, diphenyldiethoxysilane, and methylphenyldiethoxysilane.

6. The thermosetting composition as claimed in claim 1 , wherein the tetrafunctional silane represented by formula (4) is one or more tetrafunctional silanes selected from a group consisting of tetramethoxysilane and tetraethoxysilane.

7. The thermosetting composition as claimed in claim 1 , wherein the monofunctional silane represented by formula (1) is trimethylethoxysilane, the trifunctional silane represented by formula (2) is trimethoxymethylsilane or triethoxyphenylsilane, the bifunctional silane represented by formula (3) is dimethyldiethoxysilane or methylphenyldimethoxysilane, the tetrafunctional silane represented by formula (4) is tetraethoxysilane.

8. A cured film, having crack resistance and a thickness of 10 micrometer (μm) to 200 μm, formed by a thermosetting composition as claimed in any one of claims 1 to 7 , and obtained by a curing temperature higher than 200° C.

9. A display device, having a cured film as claimed in claim 8 .

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 27, 2011
From: CHISSO CORPORATION
To: JNC CORPORATION
Reel/Frame 026187/0940 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 29, 2010
From: OKAMOTO, YUKI; KIMURA, YUUKI; ETOU, TOMOHIRO
To: CHISSO CORPORATION
Reel/Frame 025065/0474 →
Priority Claims (1)
JP 2009-238041 · Oct 15, 2009 · national
Continuity (1)
Related Publication 20110091693A1 · Apr 21, 2011