An adhesive composition having excellent adhesiveness to a cycloolefin resin or the like. The adhesive composition of the present invention includes a polymer having a repeating unit derived from a polymerizable compound represented by formula (I): Y—N(Ar)(R) Formula (I), in which Ar represents an unsubstituted or substituted C6 to C14 aryl group or an unsubstituted or substituted C6 to C10 aryl C1 to C3 alkyl group; R represents an unsubstituted or substituted C1 to C6 alkyl group, an unsubstituted or substituted C3 to C6 cycloalkyl group, an unsubstituted or substituted C6 to C14 aryl group, or an unsubstituted or substituted C6 to C10 aryl C1 to C3 alkyl group; and Y represents a polymerizable functional group. In Formula (I), a substituent on Ar and a substituent on R can bond to form a divalent organic group.

An adhesive composition having excellent adhesiveness to a cycloolefin resin or the like. The adhesive composition of the present invention includes a polymer having a repeating unit derived from a polymerizable compound represented by formula (I): YN(Ar)(R) Formula (I), in which Ar represents an unsubstituted or substituted C6 to C14 aryl group or an unsubstituted or substituted C6 to C10 aryl C1 to C3 alkyl group; R represents an unsubstituted or substituted C1 to C6 alkyl group, an unsubstituted or substituted C3 to C6 cycloalkyl group, an unsubstituted or substituted C6 to C14 aryl group, or an unsubstituted or substituted C6 to C10 aryl C1 to C3 alkyl group; and Y represents a polymerizable functional group. In Formula (I), a substituent on Ar and a substituent on R can bond to form a divalent organic group.

An adhesive composition having excellent adhesiveness to a cycloolefin resin or the like. The adhesive composition of the present invention includes a polymer having a repeating unit derived from a polymerizable compound represented by formula (I): YN(Ar)(R) Formula (I), in which Ar represents an unsubstituted or substituted C6 to C14 aryl group or an unsubstituted or substituted C6 to C10 aryl C1 to C3 alkyl group; R represents an unsubstituted or substituted C1 to C6 alkyl group, an unsubstituted or substituted C3 to C6 cycloalkyl group, an unsubstituted or substituted C6 to C14 aryl group, or an unsubstituted or substituted C6 to C10 aryl C1 to C3 alkyl group; and Y represents a polymerizable functional group. In Formula (I), a substituent on Ar and a substituent on R can bond to form a divalent organic group.

An active energy ray curable composition contains an acrylamide compound A1 represented by the following Chemical formula 1 or the following Chemical formula 2; a multi-functional polymerizable compound B1 having an SI value of 3 or less in a skin sensitivity test; a polymerization initiator C1 having no maximum absorption peak in a wavelength range of from 365 to 405 nm; and a hydrogen donor D,

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An active energy ray curable composition contains an acrylamide compound A1 represented by the following Chemical formula 1 or the following Chemical formula 2; a multi-functional polymerizable compound B1 having an SI value of 3 or less in a skin sensitivity test; a polymerization initiator C1 having no maximum absorption peak in a wavelength range of from 365 to 405 nm; and a hydrogen donor D,

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The present, invention provides a liquid crystal display device that can exhibit excellent retardation stability against heat and that can prevent reduction in contrast ratio due to scattering even when the liquid crystal display device includes a retardation layer formed by polymerization of a reactive monomer, and a method for producing a liquid crystal display device suitable for production of the liquid crystal display device. The liquid crystal display device of the present invention includes paired substrates and a liquid crystal layer provided between the paired substrates. At least one of the paired substrates includes a retardation layer formed from a polymer of at least one type of monomer. The at least one type of monomer includes a photo-aligning monomer that is to be aligned by polarized light.

The present, invention provides a liquid crystal display device that can exhibit excellent retardation stability against heat and that can prevent reduction in contrast ratio due to scattering even when the liquid crystal display device includes a retardation layer formed by polymerization of a reactive monomer, and a method for producing a liquid crystal display device suitable for production of the liquid crystal display device. The liquid crystal display device of the present invention includes paired substrates and a liquid crystal layer provided between the paired substrates. At least one of the paired substrates includes a retardation layer formed from a polymer of at least one type of monomer. The at least one type of monomer includes a photo-aligning monomer that is to be aligned by polarized light.

The invention is related to a class of hydrophilic poly(meth)acrylamide-based copolymer comprising dangling (i.e., pendant) phosphorylcholine groups and dangling (i.e., pendant) reactive groups or chains each of which comprises one carboxyl group, one thiol group, or one primary or secondary amino group. The hydrophilic copolymers have a relatively high affinity to a base coating of a polyanionic polymer on a medical device or contact lens and are reactive towards azetidinium groups of an azetidinium-containing polymer upon heating. They can find particular use in producing water-soluble highly-branched hydrophilic polymeric material and in producing water gradient contact lenses.

The invention is related to a class of hydrophilic poly(meth)acrylamide-based copolymer comprising dangling (i.e., pendant) phosphorylcholine groups and dangling (i.e., pendant) reactive groups or chains each of which comprises one carboxyl group, one thiol group, or one primary or secondary amino group. The hydrophilic copolymers have a relatively high affinity to a base coating of a polyanionic polymer on a medical device or contact lens and are reactive towards azetidinium groups of an azetidinium-containing polymer upon heating. They can find particular use in producing water-soluble highly-branched hydrophilic polymeric material and in producing water gradient contact lenses.

A transparent polyimide film manufacturing method includes following steps: producing a polyimide film having a tensile modulus of elasticity greater than 5.4 GPa ((N/m.sup.2)109), a light transmittance greater than 85%, and a chromaticity b* less than 2; providing an ether-free dianhydride and a diamine to form an ether-free polyamic acid; reacting the ether-free polyamic acid with an aromatic cyclic dianhydride to form a copolymerized polyamic acid; and chemically cyclizing the copolymerized polyamic acid to form a transparent polyimide film.