Provided are: a composition for forming an underlayer film in an imprinting method, which includes a high-molecular-weight compound having a polymerizable functional group and a monomer having a plurality of crosslinking functional groups capable of being bonded to the polymerizable functional group, and in which a Hansen solubility parameter distance, which is a difference between a Hansen solubility parameter of the high-molecular-weight compound and a Hansen solubility parameter of the monomer, is 5.0 or less, and regarding the two crosslinking functional groups among the plurality of crosslinking functional groups, the number of atoms, which constitute a shortest atom chain mutually linking crosslinking points in the respective crosslinking functional groups, is 7 or more; a laminate including a layer formed of the composition for forming an underlayer film; and a method for manufacturing a semiconductor element, in which a semiconductor element is manufactured using a pattern obtained by a pattern producing method.

Macroparticulates may be formed through at least partial self-assembly by reacting an epoxide-containing (meth)acrylic polymer or copolymer with a compound bearing a nitrogen nucleophile, such as iminodiacetic acid or ethylenediamine. When the epoxide-containing (meth)acrylic polymer or copolymer is formed into a predetermined shape before reaction with the compound bearing the nitrogen nucleophile, a profile of the predetermined shape may be at least partially maintained and undergo expansion in the course of forming the reaction product, thereby producing macroparticulates having a larger volume than the predetermined shape itself. An internal cavity may be formed when generating the macroparticulates in this manner. Optionally, a hexasubstituted benzene or a supramolecular receptor may be adhered to a surface portion of the macroparticulates, either covalently or non-covalently. The compound bearing a nitrogen nucleophile may be further modified to form one or more functionalities capable of binding an analyte.

Macroparticulates may be formed through at least partial self-assembly by reacting an epoxide-containing (meth)acrylic polymer or copolymer with a compound bearing a nitrogen nucleophile, such as iminodiacetic acid or ethylenediamine. When the epoxide-containing (meth)acrylic polymer or copolymer is formed into a predetermined shape before reaction with the compound bearing the nitrogen nucleophile, a profile of the predetermined shape may be at least partially maintained and undergo expansion in the course of forming the reaction product, thereby producing macroparticulates having a larger volume than the predetermined shape itself. An internal cavity may be formed when generating the macroparticulates in this manner. Optionally, a hexasubstituted benzene or a supramolecular receptor may be adhered to a surface portion of the macroparticulates, either covalently or non-covalently. The compound bearing a nitrogen nucleophile may be further modified to form one or more functionalities capable of binding an analyte.

Bacteria repellant polymer composite having a reduced yellowness index prepared by melt processing a base polymer an epoxy resin and a bacteria repellant agent and methods of preparation thereof.

The present invention provides a “living” radical polymerization method for a vinyl monomer by near-infrared photothermal conversion. The method comprises irradiating a reactor with near-infrared light of 750-850 nm, wherein the reactor has a first chamber and a second chamber that are isolated from each other, the first chamber contains an organic solution of a near-infrared light responsive croconaine dye, and the second chamber is provided with a closed reaction flask containing a reaction solution, the reaction solution comprises a vinyl monomer, two or more of an ATRP initiator, an ATRP ligand, an ATRP catalyst, an RAFT reagent, a thermal initiator, and an additive, and an organic solvent; and the near-infrared light responsive dye converts the near-infrared light into heat energy, by which the reactor is heated to 50-100° C. to polymerize the monomer in the reaction solution, to obtain polymers with controlled molecular weights and molecular weight distributions.

The present invention provides a “living” radical polymerization method for a vinyl monomer by near-infrared photothermal conversion. The method comprises irradiating a reactor with near-infrared light of 750-850 nm, wherein the reactor has a first chamber and a second chamber that are isolated from each other, the first chamber contains an organic solution of a near-infrared light responsive croconaine dye, and the second chamber is provided with a closed reaction flask containing a reaction solution, the reaction solution comprises a vinyl monomer, two or more of an ATRP initiator, an ATRP ligand, an ATRP catalyst, an RAFT reagent, a thermal initiator, and an additive, and an organic solvent; and the near-infrared light responsive dye converts the near-infrared light into heat energy, by which the reactor is heated to 50-100° C. to polymerize the monomer in the reaction solution, to obtain polymers with controlled molecular weights and molecular weight distributions.

Curable compositions that undergo reaction induced phase separation of domains in cured matrix and provide beneficial physical and chemical properties and methods of use of such compositions. Curable compositions that undergo reaction induced phase separation of domains in cured matrix in response to a first set of curing conditions and the domains undergo a second reaction in response to a second set of curing conditions to improve the physical properties of the domains and the cured composition, such as improvements in glass transition temperature and thermal degradation.

Curable compositions that undergo reaction induced phase separation of domains in cured matrix and provide beneficial physical and chemical properties and methods of use of such compositions. Curable compositions that undergo reaction induced phase separation of domains in cured matrix in response to a first set of curing conditions and the domains undergo a second reaction in response to a second set of curing conditions to improve the physical properties of the domains and the cured composition, such as improvements in glass transition temperature and thermal degradation.

Provided is a laminate that includes a water absorbing layer (B), an antireflective function-imparting layer (C) and a hydrophilic layer (A) provided in this order on a substrate, wherein the hydrophilic layer (A) is formed of a crosslinked resin having an anionic, cationic or nonionic hydrophilic group, and has a gradient of hydrophilic groups (intensity of hydrophilic group on surface of the hydrophilic layer (A)/intensity of hydrophilic group at ½ of thickness of the hydrophilic layer (A)) of not less than 1.1; the water absorbing layer (B) is formed of a crosslinked resin having a water absorption rate per unit mass (g) of in the range of 5 to 500 wt %; and the refractive index of a layer forming the layer (C) satisfies a specific condition. The laminate can provide higher antifogging properties and antireflective properties.

Provided is a laminate that includes a water absorbing layer (B), an antireflective function-imparting layer (C) and a hydrophilic layer (A) provided in this order on a substrate, wherein the hydrophilic layer (A) is formed of a crosslinked resin having an anionic, cationic or nonionic hydrophilic group, and has a gradient of hydrophilic groups (intensity of hydrophilic group on surface of the hydrophilic layer (A)/intensity of hydrophilic group at ½ of thickness of the hydrophilic layer (A)) of not less than 1.1; the water absorbing layer (B) is formed of a crosslinked resin having a water absorption rate per unit mass (g) of in the range of 5 to 500 wt %; and the refractive index of a layer forming the layer (C) satisfies a specific condition. The laminate can provide higher antifogging properties and antireflective properties.