Silicone compounds and process for producing the same
First Claim
1. A process for preparing silicone compounds in which Si—
- O—
at the end of the molecular chain of silanol-free cage and/or ladder polyphenylsilsesquioxanes represented by formula (1);
wherein n is an integer from 2 to 5000,is linked to at least one triorganosilyl group containing reactive functional group X represented by formula (2);
whereinX is selected from the group consisting of (A) CH2═
CH—
, (B) CH2═
C(R4)—
COO—
R3—
, (C) —
CH2—
O—
R3—
,(D) H2N—
R3—
, (E) HO—
R3—
, and (F) HS—
R3—
, R3 is an alkylene group containing 1 to 3 carbon atoms, and R4 is a hydrogen atom or a methyl group, said process comprising;
subjecting cage-terminated and silanol-free cage and/or ladder polyphenylsilsesquioxanes to an equilibrium reaction under heat with a disiloxane containing reactive functional groups represented by formula (3);
wherein X is the same as defined above, in an organic solvent in the presence of an alkaline rearrangement and condensation catalyst.
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Accused Products
Abstract
This invention relates to silicone compounds in which terminal SiO of cage-type and/or ladder-type polyphenylsilsesquioxanes is wholly or partly linked to a triorganosilyl group containing reactive functional group X and also relates to a process for preparing said silicone compounds by subjecting cage-terminated and silanol-free cage-type and/or ladder-type polyphenylsilsesquioxanes to an equilibrium reaction under heat with disiloxanes containing reactive functional group X of the following structural formula
in an organic solvent in the presence of an alkaline rearrangement and condensation catalyst. This invention provides silicone compounds containing terminal reactive functional groups of excellent storage stability and properties of good reproducibility such as heat resistance.
7 Citations
2 Claims
-
1. A process for preparing silicone compounds in which Si—
- O—
at the end of the molecular chain of silanol-free cage and/or ladder polyphenylsilsesquioxanes represented by formula (1);
wherein n is an integer from 2 to 5000, is linked to at least one triorganosilyl group containing reactive functional group X represented by formula (2);
wherein X is selected from the group consisting of (A) CH2═
CH—
,(B) CH2═
C(R4)—
COO—
R3—
,(C) —
CH2—
O—
R3—
,(D) H2N—
R3—
,(E) HO—
R3—
, and(F) HS—
R3—
,R3 is an alkylene group containing 1 to 3 carbon atoms, and R4 is a hydrogen atom or a methyl group, said process comprising;
subjecting cage-terminated and silanol-free cage and/or ladder polyphenylsilsesquioxanes to an equilibrium reaction under heat with a disiloxane containing reactive functional groups represented by formula (3);
wherein X is the same as defined above, in an organic solvent in the presence of an alkaline rearrangement and condensation catalyst. - View Dependent Claims (2)
- O—
Specification