A polyol polymer is obtained from reactants including: a) a non-aromatic epoxy functional compound that includes at least 30 weight % of the total solids weight of the reactants; and b) an aromatic mono-carboxylic acid functional compound, or anhydride thereof, that is substantially free of non-aromatic ethylenic unsaturation. The polyol polymer has ester linkages and hydroxyl functional groups. Further, if the reactants further include an aromatic polycarboxylic acid, the aromatic polycarboxylic acid makes up less than 15 weight % of the total solids weight of the reactants. A coating composition is also prepared with the polyol polymer.

A method of making a functionalized fluorinated monomer for use in making oligomers and polymers that can be used to improve surface properties of polymer-derived systems, such as coatings. The method of making a functionalized fluorinated monomer includes reacting at least one fluorinated nucleophilic reactant, such as a fluorinated alcohol, with at least one compound containing at least one epoxide group. Other methods include reaction of a fluorinated alcohol with a cyclic carboxylic anhydride. In another embodiment, a method includes reacting a fluorinated mesylate, tosylate or triflate with an amine, alkoxide or phenoxide. In other embodiments, the method includes reacting a fluorinated alcohol with an alkyl halide, or reacting a fluorinated alkyl halide with an amine. The functionalized fluorinated monomers may be used as intermediates and reacted to modify the functional groups thereon. Further, the functionalized fluorinated monomers may be reacted to form polymers or oligomers, or with polymers or oligomers having functional groups to modify the polymer or oligomer through the functional group thereon.

A method of making a functionalized fluorinated monomer for use in making oligomers and polymers that can be used to improve surface properties of polymer-derived systems, such as coatings. The method of making a functionalized fluorinated monomer includes reacting at least one fluorinated nucleophilic reactant, such as a fluorinated alcohol, with at least one compound containing at least one epoxide group. Other methods include reaction of a fluorinated alcohol with a cyclic carboxylic anhydride. In another embodiment, a method includes reacting a fluorinated mesylate, tosylate or triflate with an amine, alkoxide or phenoxide. In other embodiments, the method includes reacting a fluorinated alcohol with an alkyl halide, or reacting a fluorinated alkyl halide with an amine. The functionalized fluorinated monomers may be used as intermediates and reacted to modify the functional groups thereon. Further, the functionalized fluorinated monomers may be reacted to form polymers or oligomers, or with polymers or oligomers having functional groups to modify the polymer or oligomer through the functional group thereon.

Provided are catalysts, methods of making catalysts, methods of using catalysts, and copolymers made utilizing the catalysts. The catalyst has a metal salen complex group, a bridging group, and one or more co-catalyst groups. The metal salen complex group is attached to the bridging group and the bridging group is attached to the co-catalyst group. The copolymers made utilizing the catalysts are polyesters or polycarbonates.

Provided are catalysts, methods of making catalysts, methods of using catalysts, and copolymers made utilizing the catalysts. The catalyst has a metal salen complex group, a bridging group, and one or more co-catalyst groups. The metal salen complex group is attached to the bridging group and the bridging group is attached to the co-catalyst group. The copolymers made utilizing the catalysts are polyesters or polycarbonates.

The present disclosure relates to a process for preparing polyester. The process for preparing the polyester essentially involves the preparation of the isosorbide oligomer and the isosorbide polymer from the isosorbide oligomer. The isosorbide oligomer or isosorbide polymer is then co-polymerized with the polyester. The copolymerization isosorbide oligomer or isosorbide polymer may be carried out at any stage of the preparation of the polyester. The polyester obtained in accordance with the process of the present disclosure can be used in packaging applications such as preparing packaging materials or containers. The material or container obtained from the polyester of the present disclosure is capable of withstanding a temperature of 60 to 90° C. without undergoing any deformation and shrinkage. Further, the material or container obtained from the polyester of the present disclosure is transparent or has lower color b* value.

The present disclosure relates to a process for preparing polyester. The process for preparing the polyester essentially involves the preparation of the isosorbide oligomer and the isosorbide polymer from the isosorbide oligomer. The isosorbide oligomer or isosorbide polymer is then co-polymerized with the polyester. The copolymerization isosorbide oligomer or isosorbide polymer may be carried out at any stage of the preparation of the polyester. The polyester obtained in accordance with the process of the present disclosure can be used in packaging applications such as preparing packaging materials or containers. The material or container obtained from the polyester of the present disclosure is capable of withstanding a temperature of 60 to 90° C. without undergoing any deformation and shrinkage. Further, the material or container obtained from the polyester of the present disclosure is transparent or has lower color b* value.

A polyol polymer is obtained from reactants including: a) a non-aromatic epoxy functional compound that includes at least 30 weight % of the total solids weight of the reactants; and b) an aromatic mono-carboxylic acid functional compound, or anhydride thereof, that is substantially free of non-aromatic ethyl enic unsaturation. The polyol polymer has ester linkages and hydroxyl functional groups, Further, if the reactants further include an aromatic polycarboxylic acid, the aromatic polycarboxylic acid makes up less than 15 weight % of the total solids weight of the reactants. A coating composition is also prepared with the polyol polymer.

A polyol polymer is obtained from reactants including: a) a non-aromatic epoxy functional compound that includes at least 30 weight % of the total solids weight of the reactants; and b) an aromatic mono-carboxylic acid functional compound, or anhydride thereof, that is substantially free of non-aromatic ethyl enic unsaturation. The polyol polymer has ester linkages and hydroxyl functional groups, Further, if the reactants further include an aromatic polycarboxylic acid, the aromatic polycarboxylic acid makes up less than 15 weight % of the total solids weight of the reactants. A coating composition is also prepared with the polyol polymer.

The present invention provides a multi-block copolymer comprising at least blocks A-B-A or B-A-B, wherein block A comprises a polyester formed by polymerisation of a lactone and/or a lactide; and block B comprises a copolyester formed by polymerisation of an epoxide and an anhydride, or a polycarbonate formed by polymerisation of an epoxide and carbon dioxide, and methods of production thereof.