Although polyolefin elastomers are widely employed commodity polymers, there are shortcomings of this class of polymers for certain applications. For example, the rheological properties of some polyolefin elastomers may be insufficient to provide the green strength or low shear viscosity necessary to form stable foams, or to provide sufficient viscosity modification effects when present in a solvent. Cationomeric modification of polyolefin elastomers may alleviate these difficulties. Such polyolefin elastomers may feature a random cationomeric polyolefin copolymer comprising at least a first monomer and a second monomer, in which the first monomer is a neutral monomer and the second monomer has a side chain bearing a cationic moiety. The polyolefin elastomers may be present in foamed polyolefin compositions comprising a gas component and/or in liquid compositions comprising a solvent in which the polyolefin elastomer is dissolved.

Although polyolefin elastomers are widely employed commodity polymers, there are shortcomings of this class of polymers for certain applications. For example, the rheological properties of some polyolefin elastomers may be insufficient to provide the green strength or low shear viscosity necessary to form stable foams, or to provide sufficient viscosity modification effects when present in a solvent. Cationomeric modification of polyolefin elastomers may alleviate these difficulties. Such polyolefin elastomers may feature a random cationomeric polyolefin copolymer comprising at least a first monomer and a second monomer, in which the first monomer is a neutral monomer and the second monomer has a side chain bearing a cationic moiety. The polyolefin elastomers may be present in foamed polyolefin compositions comprising a gas component and/or in liquid compositions comprising a solvent in which the polyolefin elastomer is dissolved.

Methods of post-polymerization modification of a polymer are provided herein. The present methods comprise the step of reacting a polymer with at least one nucleophile in a nucleophilic substitution reaction performed without a solvent to produce a functionalized polymer. The nucleophile can be selected from the group consisting of thioacetate, phenoxide, alkoxide, carboxylate, thiolate, thiocarboxylate, dithiocarboxylate, thiourea, thiocarbamate, dithiocarbamate, xanthate, thiocyanate. Nucleophilic substitution reaction can be performed in the presence of a phase transfer catalyst. Nucleophilic substitution reaction can also be performed via a two-step in-situ reactive mixing process with the initial formation of the polymer-amine ionomer (polymer-NR.sub.3.sup.+Br) which catalyzes the subsequent nucleophilic substitution with a second nucleophile to form a bi-functional polymer.

Methods of post-polymerization modification of a polymer are provided herein. The present methods comprise the step of reacting a polymer with at least one nucleophile in a nucleophilic substitution reaction performed without a solvent to produce a functionalized polymer. The nucleophile can be selected from the group consisting of thioacetate, phenoxide, alkoxide, carboxylate, thiolate, thiocarboxylate, dithiocarboxylate, thiourea, thiocarbamate, dithiocarbamate, xanthate, thiocyanate. Nucleophilic substitution reaction can be performed in the presence of a phase transfer catalyst. Nucleophilic substitution reaction can also be performed via a two-step in-situ reactive mixing process with the initial formation of the polymer-amine ionomer (polymer-NR.sub.3.sup.+Br) which catalyzes the subsequent nucleophilic substitution with a second nucleophile to form a bi-functional polymer.

An antireflective film including: a support base, and a pattern composed of a photoresist material formed on the support base, the pattern having a larger size at a point closer to the support base. The photoresist material contains a polymer compound having an aromatic group, and the polymer compound includes at least one of: (i) a repeating unit having a cyclopentadienyl complex structure, (ii) a repeating unit having a naphthalene structure, and (iii) a repeating unit having a naphthalene structure and/or a fluorene structure. The repeating units having a naphthalene structure may include one of the following units: ##STR00001## The disclosed antireflective film shows an antireflection effect to decrease the reflection of light. A method of producing the antireflective film, and an eyeglass type display including the antireflective film are disclosed.

A porous resin used to solid phase synthesis and a preparation method therefor, specifically being a porous resin having functional groups being an amino group or a hydroxyl group and a preparation method therefor. Using an olefin compound containing two cyano groups as a modified monomer, using a high internal phase emulsion as a pore-foaming agent, and performing suspension polymerization to prepare the porous resin. And then functionalizing the porous resin to obtain the porous resin having functional groups being an amino group or a hydroxyl group. Different from the existing preparation method, the modified monomer can make the distribution of the functional groups more uniform, and make the swelling degrees of the porous resin in different solvents close. The high internal phase emulsion pore-foaming agent can make the pore size distribution of the carrier narrower. The porous resin can be used as a solid phase synthesis carrier to prepare an oligonucleotide, and the use of the carrier is beneficial for improving the yield and purity of the oligonucleotide.

A porous resin used to solid phase synthesis and a preparation method therefor, specifically being a porous resin having functional groups being an amino group or a hydroxyl group and a preparation method therefor. Using an olefin compound containing two cyano groups as a modified monomer, using a high internal phase emulsion as a pore-foaming agent, and performing suspension polymerization to prepare the porous resin. And then functionalizing the porous resin to obtain the porous resin having functional groups being an amino group or a hydroxyl group. Different from the existing preparation method, the modified monomer can make the distribution of the functional groups more uniform, and make the swelling degrees of the porous resin in different solvents close. The high internal phase emulsion pore-foaming agent can make the pore size distribution of the carrier narrower. The porous resin can be used as a solid phase synthesis carrier to prepare an oligonucleotide, and the use of the carrier is beneficial for improving the yield and purity of the oligonucleotide.

Rubber compounds that comprise rubber and propylene-a-olefin-diene (PE(D)M) polymers may be useful in tire-related articles (e.g., tire sidewalls, inner tubes, and innerliners). Such a rubber compound may comprise: about 5 phr to about 50 phr of the PE(D)M polymer that comprises about 65 wt % to about 99.5 wt % propylene, about 0.5 wt % to about 35 wt % a-olefin that is not propylene, and 0 wt % to about 20 wt % diene, said wt % based on the weight of the PE(D)M polymer, and about 50 parts per hundred parts rubber (phr) to about 95 phr of a rubber that comprises one selected from the group consisting of the halogenated isobutylene-based rubber is selected from the group consisting of: natural rubber, polyisoprene rubber, poly(styrene-co-butadiene) rubber, polybutadiene rubber, poly(isoprene-co-butadiene) rubber, styrene-isoprene-butadiene rubber, butyl rubber, star branched butyl rubber, isobutylene-isoprene rubber, poly(isobutylene-co-alkylstyrene), a halogenated isobutylene-based rubber, polychloroprene rubber, nitrile rubber, and any combination thereof.

An elastomeric composition is provided that includes from 1 to 100 parts by weight per hundred parts by weight rubber (phr) of a first propylene-α-olefin-diene (PEDM) terpolymer comprising 70 wt % to 92.5 wt % propylene, 7.5 wt % to 30 wt % a C2 or C4-C12 α-olefin, and 3.5 wt % to 20 wt % diene, said wt % based on the weight of the PEDM terpolymer. The PEDM terpolymer V may have a Mooney viscosity (ML(1+4)) of 25 MU to 100 MU. The composition may further include from 0 to 99 phr of an ethylene-based copolymer comprising 40 wt % to 95 wt % ethylene.

An elastomeric composition suitable for use in belts like transmission belts may comprise: from 5 to 100 phr of a propylene-α-olefin-diene (PEDM) terpolymer comprising 80 wt % to 97.5 wt % propylene, 2.5 wt % to 20 wt % a-olefin, and 0.5 wt % to 10 wt % diene, said wt % based on the weight of the PEDM terpolymer, and wherein the PEDM terpolymer has (a) Mooney viscosity (ML(1+4)) of 1 MU to 60 MU, (b) melt flow rate of 0.5 g/min to 100 g/min, and (c) a weight average molecular weight to n-average molecular weight (Mw/Mn) ratio of 1.5 to 3.0; and from 60 to 95 phr of an ethylene-based copolymer comprising 0 wt % to 95 wt % ethylene, 0 wt % to 10 wt % of one or more dienes, and 5 wt % to 60 wt % C3 to C12 α-olefin, said wt % based on the total weight of the ethylene-based copolymer.