Diurethane (meth)acrylate-silane compositions and articles including the same

US10011735B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10011735-B2
Application numberUS-201314419324-A
CountryUS
Kind codeB2
Filing dateMar 1, 2013
Priority dateAug 8, 2012
Publication dateJul 3, 2018
Grant dateJul 3, 2018

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  5. First independent claim

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Abstract

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Diurethane (meth)acrylate-silane precursor compounds prepared by reacting a primary or secondary aminosilane with a cyclic carbonate to yield a hydroxylalkylene-carbamoylalkylene-alkoxysilanes (referred to as a “hydroxylcarbamoylsilane”), which is reacted with a (meth)acrylated material having isocyanate functionality, either neat or in solvent, and optionally with a catalyst, such as a tin compound. Also described are articles including a substrate, a base (co)polymer layer on a major surface of the substrate, an oxide layer on the base (co)polymer layer; and a protective (co)polymer layer on the oxide layer, the protective (co)polymer layer including the reaction product of at least one diurethane (meth)acrylate-silane precursor compound. The substrate may be a (co)polymer film or an electronic device such as an organic light emitting device, electrophoretic light emitting device, liquid crystal display, thin film transistor, or combination thereof. Methods of making the diurethane (meth)acrylate-silane and their use in composite films and electronic devices are described.

First claim

Opening claim text (preview).

The invention claimed is: 1. A composition of matter, comprising: at least one diurethane (meth)acrylate-silane compound of the formula: R A —NH—C(O)—O—C(R 12 R 13 )—C(R 14 R 15 )—[C(R 16 R 17 )] a —O—C(O)—N(R 5 )—R S , wherein: R A is a (meth)acryl group containing group of the formula R 11 -(A) n , further wherein: R 11 is a polyvalent alkylene, arylene, alkarylene, or aralkylene group, said alkylene, arylene, alkarylene, or aralkylene groups optionally containing one or more catenary oxygen atoms, A is a (meth)acryl group comprising the formula X 2 —C(O)—C(R 3 )═CH 2 , additionally wherein: X 2 is —O, —S, or —NR 3 , R 3 is independently H, or C 1 -C 4 alkyl, and n=1 to 5; each R 12 , R 13 , R 14 , R 15 , R 16 , and R 17 is independently H, a linear, branched or cyclic alkyl group of 1 to 6 carbon atoms, optionally comprising 1 to 3 catenary oxygen, sulfur, or nitrogen atoms, and optionally substituted with one or more hydroxyl groups; R S is a silane containing group of the formula —R 1 —[Si(Y p )(R 2 ) 3-p ] q , wherein: R 1 is a polyvalent alkylene, arylene, alkarylene, or aralkylene group, said alkylene, arylene, alkarylene, or aralkylene group optionally containing one or more catenary oxygen atoms, Y is a hydrolysable group, R 2 is a monovalent alkyl or aryl group, p is 1, 2, or 3, and q is independently 1 to 5; R 5 is H, C 1 to C 6 alkyl, C 3 to C 6 cycloalkyl, or R S ; and a is 0, 1, or 2. 2. A composition of matter according to claim 1 , wherein each hydrolysable group Y is independently selected from an alkoxy group, an acetate group, an aryloxy group, and a halogen. 3. A composition of matter according to claim 2 , wherein at least some of the hydrolysable groups Y are alkoxy groups. 4. An article, comprising: a substrate selected from a (co)polymeric film or an electronic device, the electronic device further comprising an organic light emitting device (OLED), an electrophoretic light emitting device, a liquid crystal display, a thin film transistor, a photovoltaic device, or a combination thereof; a base (co)polymer layer on a major surface of the substrate; an oxide layer on the base (co)polymer layer; and a protective (co)polymer layer on the oxide layer, wherein the protective (co)polymer layer comprises the reaction product of at least one diurethane (meth)acrylate-silane precursor compound of the formula: R A —NH—C(O)—O—C(R 12 R 13 )—C(R 14 R 15 )—[C(R 16 R 17 )] a —O—C(O)—N(R 5 )—R S , wherein: R A is a (meth)acryl group containing group of the formula R 11 -(A) n , further wherein: R 11 is a polyvalent alkylene, arylene, alkarylene, or aralkylene group, said alkylene, arylene, alkarylene, or aralkylene groups optionally containing one or more catenary oxygen atoms, A is a (meth)acryl group comprising the formula X 2 —C(O)—C(R 3 )═CH 2 , additionally further wherein: X 2 is —O, —S, or —NR 3 , R 3 is independently H, or C 1 -C 4 alkyl, and n=1 to 5; each R 12 , R 13 , R 14 , R 15 , R 16 , and R 17 is independently H, a linear, branched or cyclic alkyl group of 1 to 6 carbon atoms optionally comprising 1 to 3 catenary oxygen, sulfur, or nitrogen atoms, and optionally substituted with one or more hydroxyl groups; R S is a silane containing group of the formula —R 1 —[Si(Y p )(R 2 ) 3-p ] q , wherein: R 1 is a polyvalent alkylene, arylene, alkarylene, or aralkylene group, said alkylene, arylene, alkarylene, or aralkylene group optionally containing one or more catenary oxygen atoms, Y is a hydrolysable group, R 2 is a monovalent alkyl or aryl group p is 1, 2, or 3, and q is independently 1 to 5; R 5 is H, C 1 to C 6 alkyl, C 3 to C 6 cycloalkyl, or R S ; and a is 0, 1, or 2. 5. The article of claim 4 , wherein each hydrolysable group Y is independently selected from an alkoxy group, an acetate group, an aryloxy group, and a halogen. 6. The article of claim 5 , wherein at least some of the hydrolysable groups Y are alkoxy groups. 7. The article of claim 4 , further comprising a plurality of alternating layers of the oxide layer and the protective (co)polymer layer on the base (co)polymer layer. 8. The article of claim 4 , wherein the substrate comprises a flexible transparent (co)polymeric film, optionally wherein the substrate comprises polyethylene terephthalate (PET), polyethylene napthalate (PEN), heat stabilized PET, heat stabilized PEN, polyoxymethylene, polyvinylnaphthalene, polyetheretherketone, fluoro(co)polymer, polycarbonate, polymethylmethacrylate, poly α-methyl styrene, polysulfone, polyphenylene oxide, polyetherimide, polyethersulfone, polyamideimide, polyimide, polyphthalamide, or combinations thereof. 9. The article of claim 4 , wherein the base (co)polymer layer comprises an acrylate smoothing layer. 10. The article of claim 4 , wherein the oxide layer comprises oxides, nitrides, carbides or borides of atomic elements from Groups IIA, IIIA, IVA, VA, VIA, VIIA, IB, or IIB, metals of Groups IIIB, IVB, or VB, rare-earth metals, or combinations thereof. 11. The article of claim 4 , further comprising an oxide layer applied to the protective (co)polymer layer, optionally wherein the oxide layer comprises silicon aluminum oxide. 12. An electronic device incorporating the article according to claim 4 , wherein the substrate is a (co)polymer film and the electronic device is selected from a solid state lighting device, a display device, and combinations thereof. 13. A process, comprising: (a) applying a base (co)polymer layer to a major surface of a substrate selected from a (co)polymeric film or an electronic device, the electronic device further comprising an organic light emitting device (OLED), an electrophoretic light emitting device, a liquid crystal display, a thin film transistor, a photovoltaic device, or a combination thereof; (b) applying an oxide layer on the base (co)polymer layer; and (c) depositing on the oxide layer a protective (co)polymer layer, wherein the protective (co)polymer layer comprises the reaction product of at least one diurethane (meth)acrylate-silane precursor compound of the formula: R A —NH—C(O)—O—C(R 12 R 13 )—C(R 14 R 15 )—[C(R 16 R 17 )] a —O—C(O)—N(R 5 )—R S , wherein: R A is a (meth)acryl group containing group of the formula R 11 -(A) n , further wherein: R 11 is a polyvalent alkylene, arylene, alkarylene, or aralkylene group, said alkylene, arylene, alkarylene, or aralkylene groups optionally containing one or more catenary oxygen atoms, A is a (meth)acryl group comprising the formula X 2 —C(O)—C(R 3 )═CH 2 , additionally wherein: X 2 is —O, —S, or —NR 3 , and R 3 is independently H, or C 1 -C 4 alkyl, and n=1 to 5; each R 12 , R 13 , R 14 , R 15 , R 16 , and R 17 is independently H, a linear, branched or cyclic alkyl group of 1 to 6 carbon atoms, optionally comprising 1 to 3 catenary oxygen, sulfur, or nitrogen atoms, and optionally substituted with one or more hydroxyl groups; and R S is a silane containing group of the formula —R 1 —[Si(Y p )(R 2 ) 3-p ] q , wherein: R 1 is a polyvalent alkylene, arylene, alkarylene, or aralkylene group, said alkylene, arylene, alkarylene, or aralkylene group optionally containing one or more catenary oxygen atoms, Y is a hydrolysable group, R 2 is a monovalent alkyl or aryl group; p is 1, 2, or 3, and q is independently 1 to 5; R 5 is H, C 1 to C 6 alkyl, C 3 to C 6 cycloalkyl, or R S ; and a is 0, 1, or 2. 14. The process of claim 13 , wherein each hydrolysable group Y is independently selected from an alkoxy group, an acetate group, an aryloxy group, and a halogen. 15. The

Assignees

Inventors

Classifications

  • of esters containing halogen, nitrogen, sulfur or oxygen atoms in addition to the carboxy oxygen · CPC title

  • Deposition of organic layers from vapour phase (vapour phase deposition in general C23C14/00, C23C16/00) · CPC title

  • Homopolymers or copolymers of methyl methacrylate · CPC title

  • Curing or cross-linking the coating · CPC title

  • Particulate metal or metal compound-containing · CPC title

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What does patent US10011735B2 cover?
Diurethane (meth)acrylate-silane precursor compounds prepared by reacting a primary or secondary aminosilane with a cyclic carbonate to yield a hydroxylalkylene-carbamoylalkylene-alkoxysilanes (referred to as a “hydroxylcarbamoylsilane”), which is reacted with a (meth)acrylated material having isocyanate functionality, either neat or in solvent, and optionally with a catalyst, such as a tin com…
Who is the assignee on this patent?
3M Innovative Properties Co, 3M Innovative Properties Companies
What technology area does this patent fall under?
Primary CPC classification C09D143/04. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jul 03 2018 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).