An example of a bottlebrush polymer has a polymer backbone and a plurality of individual brush moieties bonded to the polymer backbone. The individual brush moieties respectively include a crosslinked oxyamine moiety, a hydrophilic segment, and a surface adhesive terminal group.

To obtain a hydrophilic macromonomer mixture which is a highly polymerized hydrophilic macromonomer, has few components not bonded to the polymer chain after polymerization, and is less likely to leaching. Provided is a macromonomer mixture containing macromonomer A being a macromonomer having a group obtained by further introducing a polymerizable group into a reactive group derived from a polymerization initiator at an end thereof; and macromonomer B being a macromonomer having a group obtained by further introducing a polymerizable group into a reactive group derived from a chain transfer agent at an end thereof.

To obtain a hydrophilic macromonomer mixture which is a highly polymerized hydrophilic macromonomer, has few components not bonded to the polymer chain after polymerization, and is less likely to leaching. Provided is a macromonomer mixture containing macromonomer A being a macromonomer having a group obtained by further introducing a polymerizable group into a reactive group derived from a polymerization initiator at an end thereof; and macromonomer B being a macromonomer having a group obtained by further introducing a polymerizable group into a reactive group derived from a chain transfer agent at an end thereof.

An example of a bottlebrush polymer has a polymer backbone and a plurality of individual brush moieties bonded to the polymer backbone. The individual brush moieties respectively including a ketone, a hydrophilic segment, and a surface adhesive terminal group. The brush moieties can be functionalized and/or cross-linked.

In an aspect, a method of synthesizing a graft copolymer comprises the steps of: copolymerizing a first macromonomer and a first reactive diluent; wherein said first macromonomer comprises a first backbone precursor directly or indirectly covalently linked to a first polymer side chain group; wherein said reactive diluent is provided in the presence of the first macromonomer at an amount selected so as to result in formation said graft copolymer having a first backbone incorporating said diluent and said first macromonomer in a first polymer block characterized by a preselected first graft density or a preselected first graft distribution of said first macromonomer. In some embodiments of this aspect, said preselected first graft density is any value selected from the range of 0.05 to 0.75. In some methods, the composition and amount of said diluent is selected to provide both a first preselected first graft density and a first preselected first graft distribution.

The present invention relates to an anti-reflective film comprising: a hard coating layer and a low refractive layer which comprises a binder resin comprising a cross-linked polymer of a photopolymerizable compound, two or more kinds of fluorine-containing compounds comprising photoreactive functional groups, and polysilsesquioxane substituted by one or more reactive functional groups; and inorganic fine particles dispersed in the binder resin.

The present invention relates to an anti-reflective film comprising: a hard coating layer and a low refractive layer which comprises a binder resin comprising a cross-linked polymer of a photopolymerizable compound, two or more kinds of fluorine-containing compounds comprising photoreactive functional groups, and polysilsesquioxane substituted by one or more reactive functional groups; and inorganic fine particles dispersed in the binder resin.

Method of producing an image display device in which an image display member and light-transmitting cover member having principal surface portion and circumferential edge portion on which a light-shielding layer is formed with a step portion formed between the principal surface portion and the circumferential edge portion are laminated through light-transmitting resin layer formed from a liquid optical resin composition so a light-shielding layer formed surface of the light-transmitting cover member is arranged to face the image display member, when a resin dispenser is moved from one end of the light-shielding layer formed surface of the light-transmitting cover member toward the other end applying the liquid optical resin composition to the light-shielding layer formed surface of the light-transmitting cover member, the application amount of optical resin composition is changed on the principal surface portion of the light-shielding layer formed surface of the light-transmitting cover member and on the light-shielding layer.

The present invention pertains to a process for the manufacture of a grafted fluorinated polymer comprising at least one grafted side chain comprising one or more glycosidic recurring units [polymer (F)], said process comprising polymerizing: vinylidene fluoride (VDF), optionally, one or more other fluorinated monomers [monomers (F)], and optionally, one or more (meth)acrylic monomers [monomers (MA)],
in the presence of at least one polysaccharide derivative [derivative (P)], said polysaccharide derivative having a dynamic viscosity of less than 15 mPas, as measured according to ASTM D445 at 20 C. in an aqueous solution at a concentration of 2% by weight,
and by further providing novel polymers (F) as defined above.

The present invention pertains to a process for the manufacture of a grafted fluorinated polymer comprising at least one grafted side chain comprising one or more glycosidic recurring units [polymer (F)], said process comprising polymerizing: vinylidene fluoride (VDF), optionally, one or more other fluorinated monomers [monomers (F)], and optionally, one or more (meth)acrylic monomers [monomers (MA)],
in the presence of at least one polysaccharide derivative [derivative (P)], said polysaccharide derivative having a dynamic viscosity of less than 15 mPas, as measured according to ASTM D445 at 20 C. in an aqueous solution at a concentration of 2% by weight,
and by further providing novel polymers (F) as defined above.