Abstract: 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.

Abstract: A method of producing a five-carbon ring derivative-containing polyurethane involves introducing a DCPD-derived 5-carbon cyclic compound into a polyurethane material and effectuating polymerization in the presence of a solvent of a low boiling point and low toxicity to produce a five-carbon ring derivative-containing polyurethane of a high molecular weight.

Abstract: A method of producing a five-carbon ring derivative-containing polyurethane involves introducing a DCPD-derived 5-carbon cyclic compound into a polyurethane material and effectuating polymerization in the presence of a solvent of a low boiling point and low toxicity to produce a five-carbon ring derivative-containing polyurethane of a high molecular weight.

Abstract: 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.

Abstract: Epoxy/MMT composite material and a crosslinking method for epoxy/MMT composite material with second order nonlinear optical properties are introduced. Chromophore-containing intercalating agents are applied to modify montmorillonites (MMTs) to form organoclays by an ion-exchange process, wherein the chrmophores are neatly packed on exfoliated epoxy/organoclay nanocomposites. As a result, optical nonlinearity, i.e. the Pockels effect is observed for the nanocomposites without resorting to the poling process due to self-assembly process. Furthermore, a series of epoxy/MMT nanocomposites comprising thermally reversible furan-norbornene Diels-Alder adducts are prepared to establish a crosslinking feature. Self-alignment behavior, electro-optical (EO) coefficient and temporal stability of the epoxy/MMT nanocomposites are improved by the Diels-Alders crosslinking.

Abstract: Epoxy/MMT composite material and a crosslinking method for epoxy/MMT composite material with second order nonlinear optical properties are introduced. Chromophore-containing intercalating agents are applied to modify montmorillonites (MMTs) to form organoclays by an ion-exchange process, wherein the chrmophores are neatly packed on exfoliated epoxy/organoclay nanocomposites. As a result, optical nonlinearity, i.e. the Pockels effect is observed for the nanocomposites without resorting to the poling process due to self-assembly process. Furthermore, a series of epoxy/MMT nanocomposites comprising thermally reversible furan-norbornene Diels-Alder adducts are prepared to establish a crosslinking feature. Self-alignment behavior, electro-optical (EO) coefficient and temporal stability of the epoxy/MMT nanocomposites are improved by the Diels-Alders crosslinking.

Abstract: A polymeric benzoxazine resin structure with an adamantane-containing main chain produces materials of low dielectric characteristics when cured.

Abstract: A copolymer of DCPD-containing benzoxazine (DCPDBz) and cyanate ester resin forms a low-dielectric thermosetting polymeric material for making electronic components. A method of manufacturing the copolymer is also introduced. The method includes allowing DCPD-phenol oligomer, aniline, and paraformaldehyde to react at 110° C. for 6-12 hours before being extracted and baked to obtain DCPDBz; and mixing cyanate ester and the DCPDBz at 150° C.; heating the mixture up to 220° C.

Abstract: A copolymer of DCPD-containing benzoxazine (DCPDBz) and cyanate ester resin forms a low-dielectric thermosetting polymeric material for making electronic components. A method of manufacturing the copolymer is also introduced. The method includes allowing DCPD-phenol oligomer, aniline, and paraformaldehyde to react at 110° C. for 6-12 hours before being extracted and baked to obtain DCPDBz; and mixing cyanate ester and the DCPDBz at 150° C.; heating the mixture up to 220° C.

Abstract: A crosslinkable polysiloxane molecule is in the form of a polysiloxane polymeric chain with a pendant group, that is, a benzoxazine group, and thus is capable of undergoing a cross-linking reaction spontaneously to produce a crosslinkable polysiloxane polymeric material. The benzoxazine group enhances the compatibility between a polysiloxane polymer and a conventional organic polymeric material, functions as a polymer flame retardant or reaction-oriented additive, and widens the application of a polysiloxane polymer to organic polymeric materials in property adjustment and the applicability of the organic polymeric materials.

Abstract: A method for forming an aqueous polyurethane dispersion including providing an isocyanate (NCO)-terminated prepolymer with a side-chain reactive functional group by admixing (i) at least one diisocyanate, (ii) at least one difunctional polyol, (iii) a short-chain diol monomer having a side-chain reactive functional group or a modified clay thereof, (iv) at least one hydroxy carboxylic acid compound and (v) a hydrophilic cosolvent; neutralizing the NCO-terminated prepolymer with a tertiary amine; dispersing the NCO-terminated prepolymer in water; and admixing the NCO-terminated prepolymer with at least one chain extending agent comprising a hydrophilic diamine; wherein the short-chain diol monomer (iii) is expressed by structural formula (I): wherein, A is an azetidine-2,4-dione functional group or a malonamide-linked alkyl group and B is a nitrogen-linked di-hydroxy terminal group or tertiary amine-linked di-hydroxy terminal group wherein IDD was synthesized by methylenedi-p-phenyl dii

Abstract: A benzoxazine-bridged compound is provided. The compound has a low dielectric constant, a high mechanic strength and a high glass transition temperature. The compound has a highly cross-linked structure with a yellow-light photoluminescent emission. Characterization of the present disclosure has been conducted with Fourier transform infrared, nuclear magnetic resonance, molecular mass and elemental analysis.

Abstract: A facile synthesis of amphiphilic hyperbranched polymers consisting of poly(amic acid) and polyimide was developed via “A2+B3” approach from difunctional anhydride and trifunctional hydrophilic poly(oxyalkylene)triamine. Various amphiphilic hyperbranched poly(amic acid)s (HBPAAs) with terminal amine functionalities and amic acid structures were prepared through ring-opening polyaddition at room temperature, followed by thermal imidization process for the formation of hyperbranched polyimides (HBPIs), accordingly. The resulting HBPIs were analyzed by GPC, indicating the molecule weights of 5000˜7000 g/mol with a distribution of polydispersity between 2.0 and 3.8. The amine titration for HBPIs indicated the peripheral total-amine contents to be 8.32˜18.32 mequiv/g dependent on compositions.

Abstract: A method prepares high-yield adamantane in the presence of an ionic liquid catalyst formed by mixing an aluminum bromide-containing or aluminum iodide-containing catalyst and an ionic liquid. Given the method, isomerization of tetrahydrodicyclopentadiene (THDCPD) takes place in the presence of the ionic liquid catalyst to produce adamantane of high reactant conversion, high selectivity, and high yield and cut costs.

Abstract: A method disclosed for making a side-chain dendrimer vesicle. The method includes the steps of: At first, there is provided a random copolymer with a narrow distribution of molecular weights by active polymerization and chemical modification. Then, chemical modification is executed to graft various generations of dendrimers to the random copolymer to provide a side-chain dendritic random copolymer with various generations. Two steps of emulsification are taken to induce macromolecular self-assembling of the side-chain dendritic random copolymer solution to form the macromolecular vesicle. The side-chain dendrimer includes C10˜C18 hydrophobic alkyl chains.

Abstract: A method for forming an aqueous polyurethane dispersion including providing an isocyanate (NCO)-terminated prepolymer with a side-chain reactive functional group by admixing (i) at least one diisocyanate, (ii) at least one difunctional polyol, (iii) a short-chain diol monomer having a side-chain reactive functional group or a modified clay thereof, (iv) at least one hydroxy carboxylic acid compound and (v) a hydrophilic cosolvent; neutralizing the NCO-terminated prepolymer with a tertiary amine; dispersing the NCO-terminated prepolymer in water; and admixing the NCO-terminated prepolymer with at least one chain extending agent comprising a hydrophilic diamine; wherein the short-chain diol monomer (iii) is expressed by structural formula (I): wherein, A is an azetidine-2,4-dione functional group or a malonamide-linked alkyl group and B is a nitrogen-linked di-hydroxy terminal group or tertiary amine-linked di-hydroxy terminal group wherein IDD was synthesized by methylenedi-p-phenyl diisocy

Abstract: A series of curing agents are provided. The curing agents are multi-functional and phosphorus-containing. The curing agents have excellent processability to be used as an epoxy resin curing agent. The curing agents can be cured to obtain a phosphorus-containing epoxy thermoset with flame retardancy characteristic. The epoxy thermosets are very fit for circuit board substrate having high glass transition temperature; semiconductor packaging material; and related materials.

Abstract: The present invention provides benzoxazine containing propargyl group as formula (I): wherein and The present invention provides a method of preparing a compound of formula (I). The present invention also provides a flame resistant resin.

Abstract: A facile synthesis of amphiphilic hyperbranched polymers consisting of poly(amic acid) and polyimide was developed via “A2+B3” approach from difunctional anhydride and trifunctional hydrophilic poly(oxyalkylene)triamine. Various amphiphilic hyperbranched poly(amic acid)s (HBPAAs) with terminal amine functionalities and amic acid structures were prepared through ring-opening polyaddition at room temperature, followed by thermal imidization process for the formation of hyperbranched polyimides (HBPIs), accordingly. The resulting HBPIs were analyzed by GPC, indicating the molecule weights of 5000˜7000 g/mol with a distribution of polydispersity between 2.0 and 3.8. The amine titration for HBPIs indicated the peripheral total-amine contents to be 8.32˜18.32 mequiv/g dependent on compositions.

Abstract: A method disclosed for making a side-chain dendrimer vesicle. The method includes the steps of: At first, there is provided a random copolymer with a narrow distribution of molecular weights by active polymerization and chemical modification. Then, chemical modification is executed to graft various generations of dendrimers to the random copolymer to provide a side-chain dendritic random copolymer with various generations. Two steps of emulsification are taken to induce macromolecular self-assembling of the side-chain dendritic random copolymer solution to form the macromolecular vesicle. The side-chain dendrimer includes C10˜C18 hydrophobic alkyl chains.