Functionalized hydrogenated interpolymer with non-hydrogenated segment
US-2024279401-A1 · Aug 22, 2024 · US
US9879110B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9879110-B2 |
| Application number | US-201414549729-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 21, 2014 |
| Priority date | Nov 21, 2014 |
| Publication date | Jan 30, 2018 |
| Grant date | Jan 30, 2018 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
An AB-type block copolymer for use in printed circuit board (PCB) fabrication is provided having a structure represented by the following formula: wherein R 1 is a silane pendant group that includes a silicon-containing moiety capable of bonding to a glass surface, and wherein R 2 is a matrix-reactive pendant group that includes at least one moiety (e.g., a vinyl-, allyl-, amine-, amide- or epoxy-containing moiety) capable of reacting with a base polymer.
Opening claim text (preview).
What is claimed is: 1. A block copolymer comprising a structure represented by the following formula: wherein R 1 is a silane pendant group that includes a silicon-containing moiety, and wherein R 2 is a matrix-reactive pendant group that includes a moiety selected from the group consisting of a vinyl-containing moiety, an allyl-containing moiety, an amine-containing moiety, an amide-containing moiety and an epoxy-containing moiety. 2. The block copolymer as recited in claim 1 , wherein the block copolymer is represented by the following formula: 3. The block copolymer as recited in claim 1 , wherein the block copolymer is represented by the following formula: 4. The block copolymer as recited in claim 1 , wherein R 1 is a silane pendant group that includes a silicon atom attached to the norbornene molecule through a linking structure and wherein R 1 is represented by the formula -L-Si(A 1 ,A 2 ,A 3 ), wherein A 1 , A 2 , and A 3 are each independently selected from the group consisting of an alkyl group of C 1 -C 10 , an alkoxy group of C 1 -C 4 , an aryl group of C 6 - C 12 , an aryl group of C 6 - C 12 substituted by an alkyl group of C 1 -C 12 , and a halogen atom, and wherein L is a linking structure selected from the group consisting of an alkyl group of C 2 -C 10 , an alkene group of C 2 -C 10 , a cycloalkyl group of C 6 -C 12 , a cycloalkane group of C 6 -C 12 , an aryl group of C 6 -C 12 , an aryl group of C 6 -C 12 substituted by an alkyl group of C 1 -C 10 , and a structure represented by any of the Linking Structures 1 to 4, represented by the following formulas: wherein x is an integer from 0 to 2, y is an integer from 0 to 3, and z is an integer from 0 to 2. 5. The block copolymer as recited in claim 1 , wherein R 1 is a silane pendant group that includes a silicon atom attached directly to the norbornene molecule and wherein R 1 is represented by the formula —Si(A 1 ,A 2 ,A 3 ), wherein A 1 , A 2 , and A 3 are each independently selected from the group consisting of an alkyl group of C 1 -C 10 , an alkoxy group of C 1 -C 4 , an aryl group of C 6 -C 12 , an aryl group of C 6 -C 12 substituted by an alkyl group of C 1 -C 12 , and a halogen atom. 6. The block copolymer as recited in claim 1 , wherein the block copolymer is synthesized by polymerizing a matrix-reactive functionalized norbornene monomer in the presence of a polynorbornene homopolymer and a multi-component catalyst system comprising a Ziegler-Natta catalyst and cocatalyst using sequential addition and Ziegler-Natta polymerization, wherein the matrix-reactive functionalized norbornene monomer is represented by the following formula: wherein R 2 is a matrix-reactive pendant group that includes a moiety selected from the group consisting of a vinyl-containing moiety, an allyl-containing moiety, an amine-containing moiety, an amide-containing moiety and an epoxy-containing moiety. 7. The block copolymer as recited in claim 6 , wherein the matrix-reactive functionalized norbornene monomer is vinyl norbornene. 8. The block copolymer as recited in claim 6 , wherein the matrix-reactive functionalized norbornene monomer is allyl norbornene. 9. The block copolymer as recited in claim 6 , wherein the matrix-reactive functionalized norbornene monomer is 5-norbornene-2-methylamine. 10. The block copolymer as recited in claim 6 , wherein the matrix-reactive functionalized norbornene monomer is 5-norbornene-2-carboxamide. 11. The block copolymer as recited in claim 6 , wherein the matrix-reactive functionalized norbornene monomer is a norbornene monomer with a terminal epoxy group represented by the following formula: wherein R 3 is a hydrogen atom or a methyl group. 12. The block copolymer as recited in claim 4 , wherein the block copolymer is synthesized by polymerizing a matrix-reactive functionalized norbornene monomer in the presence of a polynorbornene homopolymer and a multi-component catalyst system comprising a Ziegler-Natta catalyst and cocatalyst using sequential addition and Ziegler-Natta polymerization, wherein the matrix-reactive functionalized norbornene monomer is represented by the following formula: wherein R 2 is a matrix-reactive pendant group that includes a moiety selected from the group consisting of a vinyl-containing moiety, an allyl-containing moiety, an amine-containing moiety, an amide-containing moiety and an epoxy-containing moiety. 13. The block copolymer as recited in claim 12 , wherein the matrix-reactive functionalized norbornene monomer is selected from the group consisting of vinyl norbornene, allyl norbornene, 5-norbornene-2-methylamine, 5-norbornene-2-carboxamide, and a norbornene monomer with a terminal epoxy group represented by the following formula: wherein R 3 is a hydrogen atom or a methyl group. 14. The block copolymer as recited in claim 5 , wherein the block copolymer is synthesized by polymerizing a matrix-reactive functionalized norbornene monomer in the presence of a polynorbornene homopolymer and a multi-component catalyst system comprising a Ziegler-Natta catalyst and cocatalyst using sequential addition and Ziegler-Natta polymerization, wherein the matrix-reactive functionalized norbornene monomer is represented by the following formula: wherein R 2 is a matrix-reactive pendant group that includes a moiety selected from the group consisting of a vinyl-containing moiety, an allyl-containing moiety, an amine-containing moiety, an amide-containing moiety and an epoxy-containing moiety. 15. The block copolymer as recited in claim 14 , wherein the matrix-reactive functionalized norbornene monomer is selected from the group consisting of vinyl norbornene, allyl norbornene, 5-norbornene-2-methylamine, 5-norbornene-2-carboxamide, and a norbornene monomer with a terminal epoxy group represented by the following formula: wherein R 3 is a hydrogen atom or a methyl group.
Working of insulating substrates or insulating layers · CPC title
Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers · CPC title
reinforced, e.g. by fibres, fabrics (H05K1/036 takes precedence) · CPC title
Manufacturing multilayer circuits · CPC title
Crosslinking, e.g. vulcanising, of macromolecules (mechanical aspects B29C35/00; crosslinking agents C08K) · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.