C08G75/045

FUNCTIONALIZED CROSS-LINKED POLYMER NETWORKS, METHODS OF MAKING SAME, AND USES THEREOF
20230231142 · 2023-07-20 ·

In various examples, a functionalized cross-linked polymer network includes a plurality of cross-linked multifunctional trione triazine groups, a plurality of disulfide groups, a plurality of cross-linked multifunctional ether groups, a plurality of cross-linked multifunctional polyether groups, or a combination thereof, a plurality of crosslinking multifunctional polyether groups, and a plurality of dangling groups, where individual cross-linked multifunctional trione triazine groups and/or cross-linked multifunctional disulfide groups and/or cross-linked multifunctional ether groups and/or cross-linked multifunctional polyether groups and individual crosslinking multifunctional polyether groups are connected by one or more covalent bond(s) and individual dangling groups may be connected to the network by a covalent bond. At least a portion of or all of the dangling groups may be halogenated. A functionalized cross-linked polymer network may be made by polymerization (e.g., Thiol-ene reach on(s)) of one or more functionalized monomer(s) and one or more multifunctional monomer(s).

FUNCTIONALIZED CROSS-LINKED POLYMER NETWORKS, METHODS OF MAKING SAME, AND USES THEREOF
20230231142 · 2023-07-20 ·

In various examples, a functionalized cross-linked polymer network includes a plurality of cross-linked multifunctional trione triazine groups, a plurality of disulfide groups, a plurality of cross-linked multifunctional ether groups, a plurality of cross-linked multifunctional polyether groups, or a combination thereof, a plurality of crosslinking multifunctional polyether groups, and a plurality of dangling groups, where individual cross-linked multifunctional trione triazine groups and/or cross-linked multifunctional disulfide groups and/or cross-linked multifunctional ether groups and/or cross-linked multifunctional polyether groups and individual crosslinking multifunctional polyether groups are connected by one or more covalent bond(s) and individual dangling groups may be connected to the network by a covalent bond. At least a portion of or all of the dangling groups may be halogenated. A functionalized cross-linked polymer network may be made by polymerization (e.g., Thiol-ene reach on(s)) of one or more functionalized monomer(s) and one or more multifunctional monomer(s).

Holographic Recording Materials and Methods of Making Same

Provided herein are compositions suitable for recording holograms containing thiol and/or thioether functionality, and optionally including additional allyl and/or propargyl functional groups. These monomers can be used to synthesize holographic poly-mers having high Lin values. Also provided herein are methods of making holographic polymers and methods recording holograms using these polymers.

Holographic Recording Materials and Methods of Making Same

Provided herein are compositions suitable for recording holograms containing thiol and/or thioether functionality, and optionally including additional allyl and/or propargyl functional groups. These monomers can be used to synthesize holographic poly-mers having high Lin values. Also provided herein are methods of making holographic polymers and methods recording holograms using these polymers.

Temporary protective lacquer optical element

A lacquer composition is provided, comprising 20%-79.9% by weight, based on the total weight of the composition, of a thiol compound having two or more thiol groups, 20%-79.9% by weight, based on the total weight of the composition, of a compound having two or more carbon-carbon double bonds and 0.1%-10% by weight, based on the total weight of the composition, of a separating agent having an alkyl radical having 4-20 carbon atoms, where the alkyl radical is unsubstituted or fluorine-substituted and the alkyl radical is bonded to a functional group. Also provided are the use of this lacquer composition as a protective lacquer on an optical surface of an optical element in the production of the optical element, and an optical element comprising the protective lacquer.

Temporary protective lacquer optical element

A lacquer composition is provided, comprising 20%-79.9% by weight, based on the total weight of the composition, of a thiol compound having two or more thiol groups, 20%-79.9% by weight, based on the total weight of the composition, of a compound having two or more carbon-carbon double bonds and 0.1%-10% by weight, based on the total weight of the composition, of a separating agent having an alkyl radical having 4-20 carbon atoms, where the alkyl radical is unsubstituted or fluorine-substituted and the alkyl radical is bonded to a functional group. Also provided are the use of this lacquer composition as a protective lacquer on an optical surface of an optical element in the production of the optical element, and an optical element comprising the protective lacquer.

Light- or heat-curing method and curable resin composition

An object of the present invention is to provide a light- or heat-curing method by which a cured product (crosslinked product or resin) can be prepared in a simple method even in a case where filler is contained in a large amount; a curable resin composition which is used in the curing method; and the like. The present invention provides a light- or heat-curing method containing a step 1 of obtaining (E) a condensate having constitutional units of Si—O—Al and/or Si—O—Si, obtained from aluminum derived from an aluminum alkoxide and a silane derived from a silane coupling agent having a mercapto group, from (A) a compound that is formed of a salt of a carboxylic acid and an amine and has a carbonyl group generating a radical and a carboxylate group generating a base through decarboxylation by irradiation with light or heating, the (B) aluminum alkoxide, the (C) silane coupling agent having a mercapto group, and (D) water, and a step 2 of performing a reaction among the (E) condensate, (H) a compound having two or more polymerizable unsaturated groups, and (I) filler under the conditions of irradiation with light or heating in the presence of the (A) compound; a curable resin composition which is used in the curing method; and the like.

Light- or heat-curing method and curable resin composition

An object of the present invention is to provide a light- or heat-curing method by which a cured product (crosslinked product or resin) can be prepared in a simple method even in a case where filler is contained in a large amount; a curable resin composition which is used in the curing method; and the like. The present invention provides a light- or heat-curing method containing a step 1 of obtaining (E) a condensate having constitutional units of Si—O—Al and/or Si—O—Si, obtained from aluminum derived from an aluminum alkoxide and a silane derived from a silane coupling agent having a mercapto group, from (A) a compound that is formed of a salt of a carboxylic acid and an amine and has a carbonyl group generating a radical and a carboxylate group generating a base through decarboxylation by irradiation with light or heating, the (B) aluminum alkoxide, the (C) silane coupling agent having a mercapto group, and (D) water, and a step 2 of performing a reaction among the (E) condensate, (H) a compound having two or more polymerizable unsaturated groups, and (I) filler under the conditions of irradiation with light or heating in the presence of the (A) compound; a curable resin composition which is used in the curing method; and the like.

Network polymers and methods of making and using same

The present invention relates to covalent adaptable networks (CANs) having exchangeable crosslinks that are able to undergo repeated covalent bond reshuffling through photo-activation at ambient temperatures. The invention provides covalent adaptable network forming compositions as well as methods of forming, remolding and recycling the CANs of the invention.

Network polymers and methods of making and using same

The present invention relates to covalent adaptable networks (CANs) having exchangeable crosslinks that are able to undergo repeated covalent bond reshuffling through photo-activation at ambient temperatures. The invention provides covalent adaptable network forming compositions as well as methods of forming, remolding and recycling the CANs of the invention.