Silicone resin composition and an optical semiconductor device
US-2015144987-A1 · May 28, 2015 · US
US9441111B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9441111-B2 |
| Application number | US-201314653605-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 29, 2013 |
| Priority date | Dec 26, 2012 |
| Publication date | Sep 13, 2016 |
| Grant date | Sep 13, 2016 |
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Disclosed are a composition for an encapsulant that includes a first polysiloxane including a moiety represented by Chemical Formula 1 and an alkenyl group bound to silicon (Si—Vi) at the terminal end and a second polysiloxane including hydrogen bound to silicon (Si—H) at the terminal end, an encapsulant obtained by curing the composition for an encapsulant, and an electronic element including the encapsulant.
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The invention claimed is: 1. A composition for an encapsulant, the composition comprising a first polysiloxane including a moiety represented by Chemical Formula 1 and an alkenyl group bound to silicon (Si—Vi) at a terminal end thereof, and a second polysiloxane including hydrogen bound to silicon (Si—H) at a terminal end thereof: wherein, in Chemical Formula 1, A is a substituted or unsubstituted C1 to C20 alkylene group, a substituted or unsubstituted C3 to C20 cycloalkylene group, a substituted or unsubstituted C6 to C20 arylene group, a substituted or unsubstituted C2 to C20 heteroarylene group, a substituted or unsubstituted C2 to C20 alkenylene group, a substituted or unsubstituted C2 to C20 alkynylene group, or a combination thereof, and R 1 to R 4 are each independently hydrogen, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C3 to C30 cycloalkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C7 to C30 arylalkyl group, a substituted or unsubstituted C1 to C30 heteroalkyl group, a substituted or unsubstituted C2 to C30 heterocycloalkyl group, a substituted or unsubstituted C2 to C30 alkenyl group, a substituted or unsubstituted C2 to C30 alkynyl group, a substituted or unsubstituted C1 to C30 alkoxy group, a substituted or unsubstituted C1 to C30 carbonyl group, a hydroxy group, or a combination thereof. 2. The composition for an encapsulant of claim 1 , wherein A is a substituted or unsubstituted C6 to C20 arylene group. 3. The composition for an encapsulant of claim 1 , wherein the second polysiloxane is represented by Chemical Formula 2: (R 5 R 6 R 7 SiO 1/2 ) M1 (R 8 R 9 SiO 2/2 ) D1 (R 10 SiO 3/2 ) T1 (SiO 3/2 —Y 1 —SiO 3/2 ) T2 (SiO 4/2 ) Q1 [Chemical Formula 2] wherein, in Chemical Formula 2, R 5 to R 10 are each independently hydrogen, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C3 to C30 cycloalkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C7 to C30 arylalkyl group, a substituted or unsubstituted C1 to C30 heteroalkyl group, a substituted or unsubstituted C2 to C30 heterocycloalkyl group, a substituted or unsubstituted C2 to C30 alkynyl group, a substituted or unsubstituted C1 to C30 alkoxy group, a substituted or unsubstituted C1 to C30 carbonyl group, a hydroxy group, or a combination thereof, at least one of R 5 to R 10 is hydrogen, Y 1 is a single bond, a substituted or unsubstituted C1 to C20 alkylene group, a substituted or unsubstituted C3 to C20 cycloalkylene group, a substituted or unsubstituted C6 to C20 arylene group, a substituted or unsubstituted C2 to C20 heteroarylene group, a substituted or unsubstituted C2 to C20 alkenylene group, a substituted or unsubstituted C2 to C20 alkynylene group, or a combination thereof, 0<M1<1, 0<D1<1, 0<T1<1, 0<T2<1, 0<Q1<1, and M1+D1+T1+T2+Q1=1. 4. The composition for an encapsulant of claim 1 , wherein: the first polysiloxane is included in an amount of 10 to 80 wt %, based on a total weight of the composition for an encapsulant, and the second polysiloxane is included in an amount of 20 to 90 wt %, based on the total weight of the composition for an encapsulant. 5. The composition for an encapsulant of claim 1 , further comprising a third polysiloxane represented by Chemical Formula 3: (R 11 R 12 R 13 SiO 1/2 ) M2 (R 14 R 15 SiO 2/2 ) D2 (R 16 SiO 3/2 ) T3 (SiO 3/2 —Y 2 —SiO 3/2 ) T4 (SiO 4/2 ) Q2 [Chemical Formula 3] wherein, in Chemical Formula 3, R 11 to R 16 are each independently substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C3 to C30 cycloalkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C7 to C30 arylalkyl group, a substituted or unsubstituted C1 to C30 heteroalkyl group, a substituted or unsubstituted C2 to C30 heterocycloalkyl group, a substituted or unsubstituted C2 to C30 alkenyl group, a substituted or unsubstituted C2 to C30 alkynyl group, a substituted or unsubstituted C1 to C30 alkoxy group, a substituted or unsubstituted C1 to C30 carbonyl group, a hydroxy group, or a combination thereof, at least one of R 11 to R 16 is a substituted or unsubstituted C2 to C30 alkenyl group, Y 2 is a single bond, a substituted or unsubstituted C1 to C20 alkylene group, a substituted or unsubstituted C3 to C20 cycloalkylene group, a substituted or unsubstituted C6 to C20 arylene group, a substituted or unsubstituted C2 to C20 heteroarylene group, a substituted or unsubstituted C2 to C20 alkenylene group, a substituted or unsubstituted C2 to C20 alkynylene group, or a combination thereof, 0<M2<1, 0<D2<1, 0<T3<1, 0<T4<1, 0<Q2<1, and M2+D2+T3+T4+Q2=1. 6. The composition for an encapsulant of claim 5 , wherein at least one of T3 and T4 of Chemical Formula 3 is not 0. 7. The composition for an encapsulant of claim 5 , wherein: the first polysiloxane is included in an amount of 10 to 50 wt %, based on a total weight of the composition for an encapsulant, the second polysiloxane is included in an amount of 20 to 60 wt %, based on the total weight of the composition for an encapsulant, and the third polysiloxane is included in an amount of 30 to 70 wt %, based on the total weight of the composition for an encapsulant. 8. An encapsulant obtained by curing the composition for an encapsulant of claim 1 . 9. An electronic element comprising the encapsulant of claim 8 .
Organic materials comprising silicon · CPC title
characterised by their materials · CPC title
characterised by their material, e.g. epoxy or silicone resins · CPC title
characterised by their shape · CPC title
Polysiloxanes · CPC title
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