Thiol containing compositions for preparing a composite, polymeric composites prepared therefrom, and articles including the same

US9701901B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9701901-B2
Application numberUS-201615184011-A
CountryUS
Kind codeB2
Filing dateJun 16, 2016
Priority dateJul 1, 2010
Publication dateJul 11, 2017
Grant dateJul 11, 2017

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  1. Title

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  2. Abstract

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  4. Key dates

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  5. First independent claim

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Abstract

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A composition comprising: a first monomer comprising at least three thiol groups, each located at a terminal end of the first monomer, wherein the first monomer is represented by the following Chemical Formula 1-1: a second monomer comprising at least two unsaturated carbon-carbon bonds, each located at a terminal end of the second monomer, wherein the second monomer is represented by the following Chemical Formula 2: wherein in Chemical Formulae 1 and 2 groups R 2 , R a to R d , Y a to Y d , L 1 ′ and L 2 , X and variables k3 and k4 are the same as described in the specification, and a first light emitting particle, wherein the first light emitting particle consists of a semiconductor nanocrystal comprising a Group II-VI compound, a Group III-V compound, a Group IV-VI compound, or a combination thereof, wherein the first light emitting particle has a core/shell structure having a first semiconductor nanocrystal being surrounded by a second semiconductor nanocrystal, and the first semiconductor nanocrystal being different from the second semiconductor nanocrystal.

First claim

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What is claimed is: 1. A composition comprising: a first monomer including at least three thiol groups, each located at a terminal end of the first monomer, wherein the first monomer is represented by the following Chemical Formula 1-1: wherein, in Chemical Formula 1-1, L 1 ′ is carbon, a substituted or unsubstituted C6 to C30 arylene group, a substituted or a unsubstituted C3 to C30 heteroarylene group, a substituted or unsubstituted C3 to C30 cycloalkylene group, or a substituted or unsubstituted C3 to C30 heterocycloalkylene group; each of Y a to Y d is independently a direct bond, a substituted or unsubstituted C1 to C30 alkylene group; a substituted or unsubstituted C2 to C30 alkenylene group; or a C1 to C30 alkylene group or a C2 to C30 alkenylene group wherein at least one methylene group is replaced by sulfonyl, carbonyl, ether, sulfide, sulfoxide, ester, amide of formula —C(═O)NR— wherein R is hydrogen or a C1 to C10 alkyl group, imine of formula —NR— wherein R is hydrogen or a C1 to C10 alkyl group, or a combination thereof; and R a to R d are R 1 or —SH, provided that at least three of R a to R d are —SH and R 1 is hydrogen, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C3 to C30 heteroaryl group, a substituted or unsubstituted C3 to C30 cycloalkyl group, a substituted or unsubstituted C3 to C30 heterocycloalkyl group, a hydroxyl group, —NH 2 , a substituted or unsubstituted C1 to C30 amine group of formula —NRR′ wherein R and R′ are each independently hydrogen or a C1 to C30 alkyl group, an isocyanate group, an isocyanurate group, a (meth)acrylate group, a halogen, —ROR′ wherein R is a substituted or unsubstituted C1 to C20 alkylene group and R′ is hydrogen or a C1 to C20 alkyl group, an acyl halide of formula —RC(O)X wherein R is a substituted or unsubstituted alkylene group and X is a halogen, —C(═O)OR′ wherein R′ is hydrogen or a C1 to C20 alkyl group, —CN, or —C(═O)ONRR′ wherein R and R′ are each independently hydrogen or a C1 to C20 alkyl group; a second monomer including at least two unsaturated carbon-carbon bonds, each located at a terminal end of the second monomer, wherein the second monomer is represented by the following Chemical Formula 2: wherein, in Chemical Formula 2, X is an acrylate group, a methacrylate group, a C2 to C30 alkenyl group, a C2 to C30 alkynyl group, a substituted or unsubstituted C3 to C30 alicyclic group including a ring having a double bond or a triple bond in the ring, a substituted or unsubstituted C3 to C30 heterocycloalkyl group including a ring having a double bond or a triple bond in the ring, a C3 to C30 alicyclic group substituted with a C2 to C30 alkenyl group or a C2 to C30 alkynyl group, a C3 to C30 heterocycloalkyl group substituted with a C2 to C30 alkenyl group or a C2 to C30 alkynyl group, or a combination thereof; R 2 is hydrogen, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C3 to C30 heteroaryl group, a substituted or unsubstituted C3 to C30 cycloalkyl group, a substituted or unsubstituted C3 to C30 heterocycloalkyl group, a hydroxy group, —NH 2 , a substituted or unsubstituted C1 to C30 amine group of formula —NRR′ wherein R and R′ are each independently hydrogen or a C1 to C30 alkyl group, an isocyanate group, an isocyanurate group, a (meth)acrylate group, a halogen, —ROR′ wherein R is a substituted or unsubstituted C1 to C20 alkylene group and R′ is hydrogen or a C1 to C20 alkyl group, an acyl halide of formula —RC(O)X wherein R is a substituted or unsubstituted alkylene group and X is a halogen, —C(═O)OR′ wherein R′ is hydrogen or a C1 to C20 alkyl group, —CN, or —C(═O)ONRR′ wherein R and R′ are each independently hydrogen or a C1 to C20 alkyl group; L 2 is a single bond, a substituted or unsubstituted C1 to C30 alkylene group, a substituted or unsubstituted C6 to C30 arylene group, or a substituted or unsubstituted C3 to C30 heteroarylene group; Y 2 is a single bond; or a substituted or unsubstituted C1 to C30 alkylene group; or a C1 to C30 alkylene group wherein at least one methylene group is replaced by a sulfonyl, a carbonyl, an ether, a sulfide, a sulfoxide, an ester, an amide of formula —C(═O)NR— wherein R is hydrogen or a C1 to C10 alkyl group, an imine of formula —NR— wherein R is hydrogen or a C1 to C10 alkyl group, or a combination thereof; n is an integer of 1 or more; k3 is an integer of 0 or 1 or more; k4 is an integer of 1 or more; the sum of n and k4 is an integer of 3 or more; n does not exceed the valance of Y 2 ; and k3 and k4 does not exceed the valence of the L 2 ; and a light emitting particle, wherein the light emitting particle consists of a semiconductor nanocrystal comprising a Group II-VI compound, a Group III-V compound, or a combination thereof, wherein the light emitting particle has a core/shell structure having a first semiconductor nanocrystal being surrounded by a second semiconductor nanocrystal, and the first semiconductor nanocrystal being different from the second semiconductor nanocrystal, wherein the Group II-VI compound comprises a binary compound selected from CdSe, CdTe, ZnS, ZnSe, ZnTe, HgS, HgSe, HgTe, MgSe, MgS, and a combination thereof, or a ternary compound selected from CdSeS, CdSeTe, CdSTe, ZnSeS, ZnSeTe, ZnSTe, HgSeS, HgSeTe, HgSTe, CdZnS, CdZnSe, CdZnTe, CdHgS, CdHgSe, CdHgTe, HgZnS, HgZnSe, HgZnTe, MgZnSe, MgZnS, and a combination thereof, or wherein the Group III-V compound comprises a binary compound selected from GaN, GaP, GaAs, GaSb, AlN, AlP, AlAs, AlSb, InN, InP, InAs, InSb, and a combination thereof, or a ternary compound selected from GaNP, GaNAs, GaNSb, GaPAs, GaPSb, AlNP, AlNAs, AlNSb, AlPAs, AlPSb, InNP, InZnP, InNAs, InNSb, InPAs, InPSb, and a combination thereof. 2. The composition of claim 1 , wherein the first monomer of the above Chemical Formula 1 comprises the compounds of the following Chemical Formulas 1-2 to 1-5: 3. The composition of claim 1 , wherein in Chemical Formula 2, X is an acrylate group, a methacrylate group, or a C2 to C30 alkenyl group. 4. The composition of claim 1 , wherein in Chemical Formula 2, L 2 is a pyrrolidine group, a tetrahydrofuran group, a pyridine group, a pyrimidine group, a piperidine group, a triazine group, or an isocyanurate group. 5. The composition of claim 1 , wherein the second monomer of the above Chemical Formula 2 comprises the compounds of the following Chemical Formula 2-1 and Chemical Formula 2-2: wherein, in Chemical Formulas 2-1 and 2-2, Z 1 to Z 3 are the same or different, and correspond to —[Y 2 —X n ] of Chemical Formula 2. 6. The composition of claim 1 , wherein the second monomer comprises the compounds of the following Chemical Formulas 2-3 to 2-5: 7. The composition claim 1 , wherein the first monomer and the second monomer are present in combination in an amount of about 80 to about 99.9 weight percent, based on the total weight of the composition for a light emitti

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What does patent US9701901B2 cover?
A composition comprising: a first monomer comprising at least three thiol groups, each located at a terminal end of the first monomer, wherein the first monomer is represented by the following Chemical Formula 1-1: a second monomer comprising at least two unsaturated carbon-carbon bonds, each located at a terminal end of the second monomer, wherein the second monomer …
Who is the assignee on this patent?
Samsung Electronics Co Ltd
What technology area does this patent fall under?
Primary CPC classification C09K11/883. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jul 11 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).