Functionalized polymer particles for use as toughening agent
US-2015337183-A1 · Nov 26, 2015 · US
US2019048137A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2019048137-A1 |
| Application number | US-201715826861-A |
| Country | US |
| Kind code | A1 |
| Filing date | Nov 30, 2017 |
| Priority date | Aug 10, 2017 |
| Publication date | Feb 14, 2019 |
| Grant date | — |
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A low-k, non-flammable dicyclopentdiene (DCPD)-derived polyether and a method of producing the same are introduced. Incorporation of a phosphorus group and a DCPD derivative into a low-k, non-flammable dicyclopentdiene (DCPD)-derived polyether enable the DCPD-derived polyether to not only serve as an epoxy resin curing agent but also cure itself such that the cured product not only features satisfactory thermal properties and low-k characteristics but is also non-flammable.
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What is claimed is: 1 . A dicyclopentdiene (DCPD)-derived polyether expressed by structural formula (I) below, where R is one of groups below, where n=10-100. 2 . A cured product produced by heating and curing constituents of the polyether of claim 1 . 3 . A method of producing a dicyclopentdiene (DCPD)-derived polyether expressed by structural formula (I-a), the method comprising the steps of: (1) allowing a compound expressed by structural formula (A) below to react with 4,4′-difluorobenzophenone by alkaline catalysis to obtain polymer (B) and (2) allowing polymer (B) to react with 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide (DOPO) and phenol by acid catalysis to obtain DCPD-derived polyether expressed by structural formula (I-a) below, where n=10-100. 4 . The method of claim 3 , wherein an alkali in step (1) is K 2 CO 3 . 5 . The method of claim 3 , wherein the reaction in step (1) further requires p-benzoquinone which functions as a radical inhibitor. 6 . The method of claim 3 , wherein an acid in step (2) is H 2 SO 4 . 7 . The method of claim 3 , further comprising allowing the polyether expressed by structural formula (I-a) to react with acetic anhydride by alkaline catalysis to obtain the polyether expressed by structural formula (I-b), where n=10-100. 8 . The method of claim 3 , further comprising allowing the polyether expressed by structural formula (I-a) to react with methacrylic anhydride by alkaline catalysis to obtain the polyether expressed by structural formula (I-c) below, where n=10-100. 9 . The method of claim 3 , further comprising allowing the polyether expressed by structural formula (I-a) to react with 4-vinylbenzyl chloride by alkaline catalysis to obtain the polyether expressed by structural formula (I-d) below, where n=10-100. 10 . The method of claim 7 , wherein the alkali is K 2 CO 3 . 11 . The method of claim 8 , wherein the alkali is K 2 CO 3 . 12 . The method of claim 9 , wherein the alkali is K 2 CO 3 .
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Monomer containing functional groups not involved in polymerisation · CPC title
phosphorus containing compounds · CPC title
Other compound (II) containing a ketone group, e.g. X-Ar-C(=O)-Ar-X for polyetherketones · CPC title
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