IP Library Granted Patent US 7,524,917
Granted Patent B2
US 7,524,917 · App. 10/562,817 · Granted Apr 28, 2009

Organosilicon compound and production process for the same, and polysiloxane and production process for the same

Assignees: Chisso Petrochemical Corporation; Chisso Corporation
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Quick Facts
Patent No.
US 7,524,917
App. No.
10/562,817
Granted
Apr 28, 2009
Kind
B2
Abstract

The present invention provides a novel organosilicon compound and polysiloxane which are useful as electronic materials, optical materials, coating materials, sealing materials and catalyst carriers and which can be used as additives for improving various physical properties such as flame retardancy, heat resistance, weatherability, light resistance, electric insulating property, a surface characteristic, hardness, a mechanical strength and a chemical resistance of a polymer material. That is, the present invention relates to an organosilicon compound represented by Formula (1) and polysiloxane comprising the above organosilicon compound as a monomer:

Claims (17)

1. Polysiloxane represented by Formula (3):

wherein R 3 is a group selected independently from hydrogen, alkyl having 1 to 45 carbon atoms, substituted or unsubstituted aryl, and arylalkyl; in which in the alkyl optional hydrogen may be replaced by fluorine and optional —CH 2 — may be replaced by —O—, —CH═CH—, cycloalkylene, or cycloalkenylene, and arylalkyl is constituted of alkylene in which optional hydrogen may be replaced by fluorine and optional —CH 2 — may be replaced by —O—, —CH═CH— or cycloalkylene, and substituted or unsubstituted aryl, and m is an integer of 2 to 1000.

2. The polysiloxane according to claim 1 , wherein m is an integer of 2 to 500.

3. The polysiloxane according to claim 1 , wherein m is an integer of 2 to 50.

4. Polysiloxane obtained by subjecting only an organosilicon compound represented by Formula (1) to polycondensation reaction:

wherein each R 1 is a group selected independently from hydrogen, alkyl having 1 to 45 carbon atoms, substituted or unsubstituted aryl, and arylalkyl; in which in the alkyl optional hydrogen may be replaced by fluorine and optional —CH 2 — may be replaced by —O—, —CH═CH—, cycloalkylene, or cycloalkenylene, and arylalkyl is constituted of alkylene in which optional hydrogen may be replaced by fluorine and optional —CH 2 — may be replaced by —O—, —CH═CH— or cycloalkylene, and substituted or unsubstituted aryl.

5. Polysiloxane obtained by reacting the organosilicon compound according to claim 4 with an organosilicon compound represented by Formula (8) having hydrolytic group

wherein R 6 to R 8 have the same meaning as that of R 1 in Formula (1), R 9 and R 10 are a hydroxyl group or a hydrolytic group, and n is an integer of 2 to 500.

6. Polysiloxane obtained by reacting the organosilicon compound according to claim 4 with an organosilicon compound represented by Formula (4), (5) or (8) having silanol

wherein, in Formula (4) and Formula (5), R 4 and R 5 are groups defined in the same manner as R 1 in Formula (1),

wherein R 6 to R 8 have the same meaning as that of R 1 in Formula (1), R 9 and R 10 are a hydroxyl group or a hydrolytic group, and n is an integer of 2 to 500.

7. The polysiloxane according to claim 5 , wherein the hydrolytic groups are alkoxysilyl groups.

8. The polysiloxane according to claim 5 , wherein the hydrolytic groups are acetoxysilyl groups.

9. The polysiloxane according to claim 5 , wherein the hydrolytic groups are halosilyl groups.

10. The polysiloxane according to claim 5 , wherein the hydrolytic groups are aminosilyl groups.

11. A production process for polysiloxane consisting of subjecting only an organosilicon compound represented by Formula (1)

wherein each R 1 is a group selected independently from hydrogen, alkyl having 1 to 45 carbon atoms, substituted or unsubstituted aryl, and arylalkyl; in which in the alkyl optional hydrogen may be replaced by fluorine and optional —CH 2 — may be replaced by —O—, —CH═CH—, cycloalkylene, or cycloalkenylene, and arylalkyl is constituted of alkylene in which optional hydrogen may be replaced by fluorine and optional —CH 2 — may be replaced by —O—, —CH═CH— or cycloalkylene, and substituted or unsubstituted aryl to polycondensation reaction.

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 Jan 27, 2006
From: OOTAKE, NOBUMASA; YOSHIDA, KAZUHIRO
To: CHISSO PETROCHEMICAL CORPORATION; CHISSO CORPORATION
Reel/Frame 017579/0480 →
Priority Claims (2)
JP 2003-186904 · Jun 30, 2003 · national
JP 2004-133045 · Apr 28, 2004 · national
Continuity (1)
Related Publication 20060155091A1 · Jul 13, 2006