A resist topcoat composition and a method of forming patterns using the resist topcoat composition. The resist topcoat composition includes an acrylic copolymer including a first structural unit represented by Chemical Formula M-1, and a second structural unit represented by Chemical Formula M-2; an acid compound; and a solvent

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The invention relates to a hydroxyl-functional polyester containing a perfluoropolyether block prepared by a method comprising the following steps: a) subjecting a carboxyl-terminated perfluoropolyether C to a reaction with an epoxy-functional compound D, and b) subjecting the reaction product of step a) to a reaction with a lactone E. The polyester thus prepared can be used in a coating composition, comprising further (b) an OH-functional or epoxy-functional resin, and (c) a hardener comprising groups reactive to the OH or epoxy-functional groups of resin (b).

A polymer blend is provided of a fluoropolymer and a liquid crystal polymer. The blend is achieved using a compatibilizer composition that contains a copolymer having a fluorine-containing monomer and a liquid crystal monomer.

Halogenated cyclic diesters, halogenated polymers derived from the cyclic diesters, and methods for making the halogenated cyclic diesters and related halogenated polymers.

Methods of functionalizing α-halogenated hydroxy acid-based polymers and coupling α-halogenated hydroxy acid-based polymers are provided. Suitable α-halogenated hydroxy acid-based polymers include α-halogenated polyesters and α-halogenated acrylate-based inimers. Methods include coupling α-halogenated polyesters and functionalizing α-halogenated polyesters without polymer cleavage. Certain α-halogenated hydroxy acid-based polymers may be functionalized, crosslinked or, intiate polymerization by inducing the α-halogenated hydroxy acid-based polymers to make a dioxolenium ion intermediate. The α-halogenated hydroxy acid-based polymers may also be functionalized using a radical trap.

Polyester compositions are disclosed herein, as well as methods of making and using such polyesters. In some embodiments, the polyesters are formed from monomers derived from natural oils. In some embodiments, the polyesters are highly branched polymers, such as highly branched polymers that have low viscosity at higher molecular weights.

Disclosed herein are novel copolymers of poly(ε-caprolactone) (PCL) and polydopamine (PDA), optionally further comprising a PEG chain, methods for making them as well as their use in pharmaceutical preparations, especially implants or in situ gelling depots, for the treatment of ocular disorders or eye diseases.

A method of preparing a fluorinated polycaprolactone membrane includes the following steps: (1) reacting a polycaprolactone with an aminoalcohol compound to prepare a hydroxyl-terminated polycaprolactone; (2) reacting the hydroxyl-terminated polycaprolactone with an anhydride to prepare a carboxyl-terminated polycaprolactone; (3) reacting an ethylene glycol bromoisobutyrate with a fluorinated acrylate to prepare a hydroxyl-terminated fluoro-acrylate polymer; (4) reacting the carboxyl-terminated polycaprolactone with the hydroxyl-terminated fluoro-acrylate polymer to prepare a fluorinated polycaprolactone; (5) at room temperature, dissolving the fluorinated polycaprolactone in an organic solvent to prepare a solution; then naturally drying the solution at room temperature to prepare the fluorinated polycaprolactone membrane.

A process of forming a flame retardant polylactide includes forming a flame retardant lactide monomer. The process also includes forming a lactide feedstock that includes at least the flame retardant lactide monomer. The process further includes polymerizing the lactide feedstock to form a flame retardant polylactide.

A method of preparing a fluorinated polycaprolactone membrane includes the following steps: (1) reacting a polycaprolactone with an aminoalcohol compound to prepare a hydroxyl-terminated polycaprolactone; (2) reacting the hydroxyl-terminated polycaprolactone with an anhydride to prepare a carboxyl-terminated polycaprolactone; (3) reacting an ethylene glycol bromoisobutyrate with a fluorinated acrylate to prepare a hydroxyl-terminated fluoro-acrylate polymer; (4) reacting the carboxyl-terminated polycaprolactone with the hydroxyl-terminated fluoro-acrylate polymer to prepare a fluorinated polycaprolactone; (5) at room temperature, dissolving the fluorinated polycaprolactone in an organic solvent to prepare a solution; then naturally drying the solution at room temperature to prepare the fluorinated polycaprolactone membrane.