The use of an organocarbonate-modified prepolymer having at least an average of 1.5 carbonate, thiocarbonate, carbamate or thiocarbamate groups bonded directly to the polymer backbone each via an oxygen atom, where each of these oxygen atoms has its origin in the reaction of a primary, secondary or tertiary hydroxyl group of the polymer backbone and a reactive compound selected from the group consisting of a diorganocarbonate, a diorganothiocarbonate, a cyclic carbonate, a cyclic thiocarbonate, an N,N-diheterocyclourea derivative and an N,N-diheterocyclothiourea derivative. Also, the preparation of the alkoxysilane polymers.

A two-component curing adhesive using a curing reaction between a polyisocyanate composition (X) and a polyol composition (Y), wherein the polyisocyanate composition (X) includes a polyisocyanate (A), the polyol composition (Y) includes a polyol (B), and the polyisocyanate composition. (X) and the polyol composition (Y) each have an elongational viscosity of 0.1 to 10 Pa.Math.s.

Electro-optic assemblies and related materials (e.g., adhesive) for use therein are generally provided. The electro-optic assembly comprises a hybrid adhesive layer comprising two or more adhesive materials including a polyurethane adhesive material and a polyacrylate adhesive material. The polyurethane adhesive material includes an end-capping cyclic carbonate. In some embodiments, the adhesive layer is formed by curing the two adhesive materials under two different sets of conditions, comprising two or more curing steps.

Electro-optic assemblies and related materials (e.g., adhesive) for use therein are generally provided. The electro-optic assembly comprises a hybrid adhesive layer comprising two or more adhesive materials including a polyurethane adhesive material and a polyacrylate adhesive material. The polyurethane adhesive material includes an end-capping cyclic carbonate. In some embodiments, the adhesive layer is formed by curing the two adhesive materials under two different sets of conditions, comprising two or more curing steps.

The present disclosure provides a polymeric material including a polymerized reaction product of a polymerizable composition including components, and a thermally activatable amine curative, and has a solids content of 90% or greater. The components include a uretdione-containing material including a reaction product of a diisocyanate reacted with itself; a first hydroxyl-containing compound; and an optional second hydroxyl-containing compound having a single OH group. The first hydroxyl-containing compound has more than one OH group and the optional second hydroxyl-containing compound is a primary alcohol or a secondary alcohol. The present disclosure also provides a two-part composition, in which a polymeric material is included in the first part and the second part includes at least one liquid amine. Further, a method of adhering two substrates is provided, including obtaining a two-part composition; combining at least a portion of the first part with at least a portion of the second part to form a mixture; disposing at least a portion of the mixture on a first substrate; and contacting a second substrate with the mixture disposed on the first substrate. The disclosure also provides a polymeric material and a method of curing a two-part composition. Advantageously, two-part compositions according to the present disclosure can be used as coatings and adhesive systems having a two-step cure with handling and performance similar to existing two-part urethane systems, but with less sensitivity to water.

The present disclosure provides a polymeric material including a polymerized reaction product of a polymerizable composition including components, and a thermally activatable amine curative, and has a solids content of 90% or greater. The components include a uretdione-containing material including a reaction product of a diisocyanate reacted with itself; a first hydroxyl-containing compound; and an optional second hydroxyl-containing compound having a single OH group. The first hydroxyl-containing compound has more than one OH group and the optional second hydroxyl-containing compound is a primary alcohol or a secondary alcohol. The present disclosure also provides a two-part composition, in which a polymeric material is included in the first part and the second part includes at least one liquid amine. Further, a method of adhering two substrates is provided, including obtaining a two-part composition; combining at least a portion of the first part with at least a portion of the second part to form a mixture; disposing at least a portion of the mixture on a first substrate; and contacting a second substrate with the mixture disposed on the first substrate. The disclosure also provides a polymeric material and a method of curing a two-part composition. Advantageously, two-part compositions according to the present disclosure can be used as coatings and adhesive systems having a two-step cure with handling and performance similar to existing two-part urethane systems, but with less sensitivity to water.

A polyetherurethane polymer containing isocyanate groups and having an NCO content in the range from 1.3% to 1.9% by weight and a monomeric diisocyanate content of not more than 0.5% by weight, obtained from the reaction of at least one monomeric aromatic diisocyanate and a polyether triol having an average OH functionality in the range from 2.2 to 2.6 and an OH number in the range from 25 to 32 mg KOH/g in an NCO/OH ratio of at least 3/1 and subsequent removal of a majority of the monomeric diisocyanates by means of a suitable separation method, and to moisture-curing polyurethane compositions having a monomeric diisocyanate content of less than 0.1% by weight, comprising said polymer.

A polyetherurethane polymer containing isocyanate groups and having an NCO content in the range from 1.3% to 1.9% by weight and a monomeric diisocyanate content of not more than 0.5% by weight, obtained from the reaction of at least one monomeric aromatic diisocyanate and a polyether triol having an average OH functionality in the range from 2.2 to 2.6 and an OH number in the range from 25 to 32 mg KOH/g in an NCO/OH ratio of at least 3/1 and subsequent removal of a majority of the monomeric diisocyanates by means of a suitable separation method, and to moisture-curing polyurethane compositions having a monomeric diisocyanate content of less than 0.1% by weight, comprising said polymer.

Clickable waterborne polymers, click crosslinking of waterborne polymers, click crosslinked waterborne polymers, clickable functional compounds, and click functionalized waterborne polymers are presented. For example, the waterborne polymers have pendant groups bearing alkyne and/or azide groups and alkyne. For example, the functionalized azide-containing functional compounds such as antimicrobial or infrared-refractive compounds. The click crosslinking of clickable waterborne polymers or polymer mixtures, and the click conjugation of clickable waterborne polymers with clickable functional compounds such as clickable antimicrobial or infrared-refractive compounds, which resulted in functional waterborne polymers with antimicrobial or infrared-refractive functions, are presented. The presented polymers, including clickable waterborne polymers, click-crosslinked waterborne polymers, and functional waterborne polymers with, for example, antimicrobial or infrared-refractive functions, can be used in applications such as coating and adhesive compositions. The aqueous suspensions of waterborne polymers can also be used directly as drug delivery systems, or can be crosslinked into hydrogels or composites for biomedical applications such as drug/cell delivery, tissue engineering, and other medical device.

Clickable waterborne polymers, click crosslinking of waterborne polymers, click crosslinked waterborne polymers, clickable functional compounds, and click functionalized waterborne polymers are presented. For example, the waterborne polymers have pendant groups bearing alkyne and/or azide groups and alkyne. For example, the functionalized azide-containing functional compounds such as antimicrobial or infrared-refractive compounds. The click crosslinking of clickable waterborne polymers or polymer mixtures, and the click conjugation of clickable waterborne polymers with clickable functional compounds such as clickable antimicrobial or infrared-refractive compounds, which resulted in functional waterborne polymers with antimicrobial or infrared-refractive functions, are presented. The presented polymers, including clickable waterborne polymers, click-crosslinked waterborne polymers, and functional waterborne polymers with, for example, antimicrobial or infrared-refractive functions, can be used in applications such as coating and adhesive compositions. The aqueous suspensions of waterborne polymers can also be used directly as drug delivery systems, or can be crosslinked into hydrogels or composites for biomedical applications such as drug/cell delivery, tissue engineering, and other medical device.