Provided are a composition capable of forming a cured product with excellent hardness, scratch resistance, chemical resistance, and flexibility; and a polyisocyanate compound that can be used as a curing agent for the composition. The polyisocyanate compound is represented by Formula (1), wherein R.sup.1 to R.sup.3 are identical or different and are a group represented by Formula (1a), wherein L.sup.1 and L.sup.2 are identical or different and represent an alkylene group having from 1 to 10 carbons, m represents a number of 0 or greater, L.sup.3 represents a divalent hydrocarbon group having from 4 to 18 carbons, and X represents an isocyanate group or a blocked isocyanate group blocked with a blocking agent, where m is not simultaneously 0 for R.sup.1 to R.sup.3, and the bond with the wavy line bonds to a nitrogen atom in Formula (1). In addition, the composition contains a polyisocyanate compound and a polyacrylic polyol.

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The present disclosure provides a photocurable composition, which has excellent coatability and is capable of providing a coating layer having excellent surface quality and thickness uniformity, a coating layer including a cured product of the photocurable composition, and a substrate for a semiconductor process including the coating layer.

A composition, a film, a display device and article prepared therefrom, and a method of preparing the article, the composition including: a compound having a fluorine-containing (poly)ether group represented by Formula 1; and a heteroatom-containing cyclic silane compound represented by Formula 2 or 3: ##STR00001## wherein, in Formulas 1 to 3, Rf is a fluorine-containing (poly)ether group, and L1, Q1, p1, q1, q2, q3, A1, A2, A3, R.sub.a, R.sub.b, R.sub.i, R.sub.j, R.sub.c, R.sub.d, R.sub.e, R.sub.f, R.sub.g, R.sub.h, R.sub.k, R.sub.l, R.sub.m, R.sub.n, R.sub.o, R.sub.p, R.sub.q, R.sub.r, R.sub.s, and R.sub.t are as described in the detailed description.

The invention relates to a fluorinated, alkoxysilyl-functional polymer, obtainable by a method comprising the steps of: a) reacting an OH-functional (per)fluoropolyether (PFPE) with a polyisocyanate A under urethane formation reaction conditions, to obtain an isocyanate-functional intermediate B, b) reacting intermediate B with a secondary, alkoxysilyl-functional monoamine C, to obtain the alkoxysilyl-functional polymer. The polymer can be used as an additive in preparation of a coating with easy-clean, anti-stain and anti-scratch properties, which can advantageously be used for coating various substrates in consumer electronics or automotive applications such as glass, metal, metal alloy, anodized substrates, plastics, composite etc.

A room-temperature-curable organopolysiloxane composition comprising (A) an organopolysiloxane resin which contains silanol groups in a specified amount and has a specified molecular weight and a specified three-dimensional net-like structure, (B) a hydrolyzable organosilane compound containing an organooxymethyl group and/or a partial hydrolysis-condensation product thereof, (C) a linear diorganopolysiloxane of which each molecule chain terminal is capped with a silanol group, and (D) a hydrolyzable to organosilane containing an amino group and/or a partial hydrolysis-condensation product thereof at specified content ratios can be produced easily and at low cost, and can be formed into a high-hardness cured article or coating film even when a metal compound that can serve as a condensation catalyst is not contained.

The present application provides a storage-stable polyisocyanate composition and a preparation method. The polyisocyanate composition is obtained by selecting one or more diisocyanate from aliphatic diisocyanates and alicyclic diisocyanates, and reacting same with an alcohol compound; the polyisocyanate composition contains an isocyanurate group, a uretdione group, a carbamate group, and an allophanate group; within the polyisocyanate composition, the molar ratio of the carbamate group/(uretdione group+isocyanurate group) is 0.01-0.2, and preferably 0.01-0.1. Compared to existing techniques, the present application has the advantage of a noticeable increase in system viscosity of uretdione polyisocyanate during storage. With the present application, by means of controlling the ratio of the carbamate group/(uretdione group+isocyanurate group) within the system, the increase in viscosity of a product during storage is inhibited, thereby improving the storage stability of the product.

The present application relates to aziridine functional compounds with reduced genotoxicity and good crosslinking efficiency, for use in the preparation of, for example, coatings.

##STR00001##

The invention relates to an alkoxysilane functional polyurethane-urea that can be used to prepare an adhesive or coating composition. The polyurethane-urea is obtainable by polymerization of reaction components comprising: (a) an alkoxysilane functional thioether diol; (b) a polyisocyanate; and (c) an alkoxysilane functional aspartate ester, wherein the alkoxysilane functional aspartate ester (c) is a Michael addition product of an amino-functional silane and an unsaturated diester. The polyurethane-urea has a low viscosity and can be used in solvent- and water-free adhesives or coatings. The adhesive or coating can be applied to various substrates such as wood, wood-containing composite, metal, plastics, paper, stone, glass or concrete.

The invention relates to compositions containing A) at least one component having at least one uretdione group, B) at least one component having at least one hydroxyl group, C1) of at least one catalyst, containing a structural element of the general formula (I) and/or (II), wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5 and R.sup.6 independently of each other represent the same or different radicals meaning saturated or unsaturated, linear or branched, aliphatic, cycloaliphatic, araliphatic or aromatic organic radicals with 1 to 18 carbon atoms that are substituted or unsubstituted and/or have heteroatoms in the chain, the radicals being capable of forming, even when combined with each other and optionally together with an additional heteroatom, rings with 3 to 8 carbon atoms that can optionally be further substituted, wherein R.sup.3, R.sup.4, R.sup.5 and R.sup.6 independently of each other can also represent hydrogen, and R.sup.7 represents hydrogen or a carboxylate anion (COO−), and C2) at least one catalyst containing at least one N,N,N′-trisubstituted amidine structure and having an amidine group content (calculated as CN2; molecular weight=40) of 12.0 to 47.0 wt.-%.

The present invention relates to a multi-aziridine crosslinker composition, characterized in that the multi-aziridine crosslinker composition is an aqueous dispersion having a pH ranging from 8 to 14 and comprises a multi-aziridine compound in dispersed form, wherein said multi-aziridine compound has: a. from 2 to 6 of the following structural units A: whereby R.sub.1 is H, R.sub.2 and R.sub.4 are independently chosen from H or an aliphatic hydrocarbon group containing from 1 to 4 carbon atoms, R a is an aliphatic hydrocarbon group containing from 1 to 4 carbon atoms, m is 1, b. one or more linking chains wherein each one of these linking chains links two of the structural units A; and c. a molecular weight in the range from 500 to 10000 Daltons wherein the molecular weight is determined using MALDI-TOF mass spectrometry according to the description.

##STR00001##