The present invention provides multifunctional monomers, including, but not limited to include multifunctional methylene malonate and methylene beta-ketoester monomers; methods for producing the same; and compositions and products formed therefrom. The multifunctional monomers of the invention may be produced by transesterification or by direct synthesis from monofunctional methylene malonate monomers or methylene beta-ketoester monomers. The present invention further compositions and products formed from methylene beta-ketoester monomers of the invention, including monomer-based products (e.g., inks, adhesives, coatings, sealants or reactive molding) and polymer-based products (e.g., fibers, films, sheets, medical polymers, composite polymers and surfactants).

The present invention provides multifunctional monomers, including, but not limited to include multifunctional methylene malonate and methylene beta-ketoester monomers; methods for producing the same; and compositions and products formed therefrom. The multifunctional monomers of the invention may be produced by transesterification or by direct synthesis from monofunctional methylene malonate monomers or methylene beta-ketoester monomers. The present invention further compositions and products formed from methylene beta-ketoester monomers of the invention, including monomer-based products (e.g., inks, adhesives, coatings, sealants or reactive molding) and polymer-based products (e.g., fibers, films, sheets, medical polymers, composite polymers and surfactants).

The present invention provides multifunctional monomers, including, but not limited to include multifunctional methylene malonate and methylene beta-ketoester monomers; methods for producing the same; and compositions and products formed therefrom. The multifunctional monomers of the invention may be produced by transesterification or by direct synthesis from monofunctional methylene malonate monomers or methylene beta-ketoester monomers. The present invention further compositions and products formed from methylene beta-ketoester monomers of the invention, including monomer-based products (e.g., inks, adhesives, coatings, sealants or reactive molding) and polymer-based products (e.g., fibers, films, sheets, medical polymers, composite polymers and surfactants).

Polymer compositions for UV curable primer formulations, as described herein. The primer formulations contain a modifier selected from the following: at least one modifier selected from a) through d) below: a) R1R2CCR3-(CO)Z (Formula A), as described herein, b) an acrylate-containing oligomer that has a Mn1500 g/mol, and an acid value from 50 to 500 mg KOH/g; c) a random terpolymer comprising, in polymerized form, vinyl chloride, vinyl acetate, and at least one of the following: a hydroxyl-containing alkyl acrylate, a hydroxyl-containing alkyl meth-acrylate, or a combination thereof or d) any combination of a) through c). Such primer formulations are useful for the binding of olefin-based polymer foams.

Polymer compositions for UV curable primer formulations, as described herein. The primer formulations contain a modifier selected from the following: at least one modifier selected from a) through d) below: a) R1R2CCR3-(CO)Z (Formula A), as described herein, b) an acrylate-containing oligomer that has a Mn1500 g/mol, and an acid value from 50 to 500 mg KOH/g; c) a random terpolymer comprising, in polymerized form, vinyl chloride, vinyl acetate, and at least one of the following: a hydroxyl-containing alkyl acrylate, a hydroxyl-containing alkyl meth-acrylate, or a combination thereof or d) any combination of a) through c). Such primer formulations are useful for the binding of olefin-based polymer foams.

The present teachings are directed at 1,1-di substituted alkene monomers (e.g., methylene beta-ketoester monomers), methods for producing the same, polymerizable compositions including a methylene beta-ketoester monomer, and polymers, compositions and products formed therefrom. The monomer preferably is a high purity monomer. In the method for producing the methylene beta-ketoesters of the invention, a beta-ketoester may be reacted with a source of formaldehyde. The methylene beta-ketoester monomers may be used in monomer-based products (e.g., inks, adhesives, coatings, sealants or reactive molding) and polymer-based products (e.g., fibers, films, sheets, medical polymers, composite polymers and surfactants).

The present teachings are directed at 1,1-di substituted alkene monomers (e.g., methylene beta-ketoester monomers), methods for producing the same, polymerizable compositions including a methylene beta-ketoester monomer, and polymers, compositions and products formed therefrom. The monomer preferably is a high purity monomer. In the method for producing the methylene beta-ketoesters of the invention, a beta-ketoester may be reacted with a source of formaldehyde. The methylene beta-ketoester monomers may be used in monomer-based products (e.g., inks, adhesives, coatings, sealants or reactive molding) and polymer-based products (e.g., fibers, films, sheets, medical polymers, composite polymers and surfactants).

A resist composition which generates an acid by exposure and whose solubility in a developing solution changes by the action of an acid. The resist composition contains a high-molecular-weight compound having a constitutional unit represented by General Formula (a0-1), and a high-molecular-weight compound having a constitutional unit represented by General Formula (f01-1) and a constitutional unit including an acid-dissociable group represented by General Formula (f02-r-1). In the formulas, R represents a hydrogen atom or the like; Va.sup.01 represents a divalent linking group; n.sub.a01 represents an integer of 0 to 2; Ra.sup.01 is a lactone-containing cyclic group having a cyano group or the like; Vf.sup.01 represents a divalent linking group; Rf.sup.011 and Rf.sup.012 each represents a trifluoromethyl group or the like; Rf.sup.021 and Rf.sup.022 each represents an alkyl group having 1 to 3 carbon atoms; and Rf.sup.023 represents a polycyclic aliphatic hydrocarbon group ##STR00001##

Described herein is a pressure sensitive adhesive is comprising: (a) a high molecular weight (meth)acrylate polymer wherein the high molecular weight (meth)acrylate polymer is derived from (i) a C4 to C24 (meth)acrylate ester monomer; and (ii) 0 to less than 10 wt % of a polar comonomer based on the weight of the high molecular weight (meth)acrylate polymer; and (b) 10 to 100 parts of a low molecular weight fluorinated polymer per 100 parts of the high molecular weight (meth)acrylate polymer, wherein the low molecular weight fluorinated polymer has a glass transition temperature (Tg) of less than 40 C. The low molecular weight fluorinated polymer is preferably derived from fluorinated (meth)acrylate, fluorinated (meth)acrylate comprising a sulfonylamide group, fluorinated vinyl monomers, fluorinated vinyl ethers, or fluorinated styrene.

Described herein is a pressure sensitive adhesive is comprising: (a) a high molecular weight (meth)acrylate polymer wherein the high molecular weight (meth)acrylate polymer is derived from (i) a C4 to C24 (meth)acrylate ester monomer; and (ii) 0 to less than 10 wt % of a polar comonomer based on the weight of the high molecular weight (meth)acrylate polymer; and (b) 10 to 100 parts of a low molecular weight fluorinated polymer per 100 parts of the high molecular weight (meth)acrylate polymer, wherein the low molecular weight fluorinated polymer has a glass transition temperature (Tg) of less than 40 C. The low molecular weight fluorinated polymer is preferably derived from fluorinated (meth)acrylate, fluorinated (meth)acrylate comprising a sulfonylamide group, fluorinated vinyl monomers, fluorinated vinyl ethers, or fluorinated styrene.