Patent classifications
C08F267/04
Ester polymer, preparation method therefor and use thereof
An ester polymer has a structure represented by the following formula (I): ##STR00001##
T represents the backbone of the ester polymer; the group B is each independently selected from O or S; the group R each independently represents C.sub.1-10 hydrocarbylene group; the group A is each independently selected from O, S or NR″; the group R′ each independently represents C.sub.1-10 hydrocarbylene group; the group N.sub.b is each independently selected from H or —R″′—B′H, wherein at least one of the two N.sub.b on the same nitrogen atom is —R″′—B′H; the group R″ is each independently selected from H or C.sub.1-10 hydrocarbyl group; the group R″′ each independently represents C.sub.1-10 hydrocarbylene group; the group B′ is each independently selected from O or S; each y independently represents an integer between 1 and 6; and m is an integer between 1 and 10.
COMPOSITION FOR FORMING HARD COAT, METHOD FOR PRODUCING ARTICLE HAVING HARD COAT, HARD COAT, HARD-COATED ARTICLE, AND SILANE-MODIFIED ALICYCLIC COMPOUND
A composition that makes it easy to form a hard coat having both high hardness and high transparency regardless of the surface hardness level of the article to be hard-coated; a method for producing an article having a hard coat using such a composition; a hard coat including a cured product of such a composition; a hard-coated article having such a hard coat; and a silane-modified alicyclic compound suitable for use as a component of such a composition. The composition includes a silane-modified alicyclic compound that is a mixture of products of reaction of an alicyclic tetracarboxylic dianhydride with an aminosilane compound having a specific structure with a hydrolyzable silyl group.
COMPOSITION FOR FORMING HARD COAT, METHOD FOR PRODUCING ARTICLE HAVING HARD COAT, HARD COAT, HARD-COATED ARTICLE, AND SILANE-MODIFIED ALICYCLIC COMPOUND
A composition that makes it easy to form a hard coat having both high hardness and high transparency regardless of the surface hardness level of the article to be hard-coated; a method for producing an article having a hard coat using such a composition; a hard coat including a cured product of such a composition; a hard-coated article having such a hard coat; and a silane-modified alicyclic compound suitable for use as a component of such a composition. The composition includes a silane-modified alicyclic compound that is a mixture of products of reaction of an alicyclic tetracarboxylic dianhydride with an aminosilane compound having a specific structure with a hydrolyzable silyl group.
RADICALLY POLYMERIZABLE COMPOSITIONS
Polymerizable compositions comprising a radically polymerizable resin can be polymerized in the absence of a peroxide initiator and other undesirable components. The polymerizable compositions and methods employ a manganese- or iron-containing salt or organic complex and a 1,3-dioxo compound with one or more other components. The polymerizable compositions have better storage stability and reduced gel time-drift.
RADICALLY POLYMERIZABLE COMPOSITIONS
Polymerizable compositions comprising a radically polymerizable resin can be polymerized in the absence of a peroxide initiator and other undesirable components. The polymerizable compositions and methods employ a manganese- or iron-containing salt or organic complex and a 1,3-dioxo compound with one or more other components. The polymerizable compositions have better storage stability and reduced gel time-drift.
ESTER POLYMER, PREPARATION METHOD THEREFOR AND USE THEREOF
An ester polymer according to the present application has a structure represented by the following formula (I):
##STR00001##
represents the backbone of the ester polymer; the group B is each independently selected from O or S; the group R each independently represents C.sub.1-10 hydrocarbylene group; the group A is each independently selected from O, S or NR; the group R each independently represents C.sub.1-10 hydrocarbylene group; the group N.sub.b is each independently selected from H or RBH, wherein at least one of the two N.sub.b on the same nitrogen atom is RBH; the group R is each independently selected from H or C.sub.1-10 hydrocarbyl group; the group R each independently represents C.sub.1-10 hydrocarbylene group; the group B is each independently selected from O or S; each y independently represents an integer between 1 and 6; and m is an integer between 1 and 10.
PHOTOSENSITIVE ADHESIVE COMPOSITION, PHOTOSENSITIVE CONDUCTIVE ADHESIVE COMPOSITION, AND ELECTRONIC DEVICE CONTAINING PHOTOSENSITIVE CONDUCTIVE ADHESIVE COMPOSITION
The disclosure provides a photosensitive adhesive composition including 10 parts by weight to 90 parts by weight of a monomer having a vinyl ether functional group, 10 parts by weight to 90 parts by weight of a tertiary amine polymer, and 0.5 parts by weight to 10 parts by weight of a photoacid initiator. The weight-average molecular weight of the tertiary amine polymer is between 2000 and 20000. The disclosure also provides a photosensitive conductive adhesive composition and an electronic device containing the photosensitive conductive adhesive composition.
PHOTOSENSITIVE ADHESIVE COMPOSITION, PHOTOSENSITIVE CONDUCTIVE ADHESIVE COMPOSITION, AND ELECTRONIC DEVICE CONTAINING PHOTOSENSITIVE CONDUCTIVE ADHESIVE COMPOSITION
The disclosure provides a photosensitive adhesive composition including 10 parts by weight to 90 parts by weight of a monomer having a vinyl ether functional group, 10 parts by weight to 90 parts by weight of a tertiary amine polymer, and 0.5 parts by weight to 10 parts by weight of a photoacid initiator. The weight-average molecular weight of the tertiary amine polymer is between 2000 and 20000. The disclosure also provides a photosensitive conductive adhesive composition and an electronic device containing the photosensitive conductive adhesive composition.
REVERSIBLE CROSSLINKING REACTANT COMPOSITION
A reversible crosslinking reactant composition is provided. The composition includes at least one furan-group-containing oligomer having a structure represented by Formula (I) and a bismaleimide compound having a structure represented by
##STR00001##
Formula (II), wherein the equivalent ratio of the furan group of the furan-group-containing oligomer having a structure represented by Formula (I) to the maleimide group of the bismaleimide compound having a structure represented by Formula (II) is from 0.5:1 to 1:0.5.
REVERSIBLE CROSSLINKING REACTANT COMPOSITION
A reversible crosslinking reactant composition is provided. The composition includes at least one furan-group-containing oligomer having a structure represented by Formula (I) and a bismaleimide compound having a structure represented by
##STR00001##
Formula (II), wherein the equivalent ratio of the furan group of the furan-group-containing oligomer having a structure represented by Formula (I) to the maleimide group of the bismaleimide compound having a structure represented by Formula (II) is from 0.5:1 to 1:0.5.