A polymerizable composition according to the present invention includes a compound (A) including two or more allyloxycarbonyl groups represented by Formula (1); at least one kind of polymerization initiator (B) selected from the group consisting of a peroxyketal-based radical polymerization initiator, a peroxy monocarbonate-based radical polymerization initiator, and a peroxyester-based radical polymerization initiator; and at least one kind of photochromic compound (C) selected from a naphthopyran compound group.

Disclosed are polymerizable compositions for ophthalmic lenses. The compositions employ peroxide-based polymerization initiators with decreased capacity for dye degradation. The compositions enable the inclusion of color-balancing dyes, resulting in lenses with improved clarity and color balance.

Disclosed are polymerizable compositions for ophthalmic lenses. The compositions employ peroxide-based polymerization initiators with decreased capacity for dye degradation. The compositions enable the inclusion of color-balancing dyes, resulting in lenses with improved clarity and color balance.

The present invention relates to the use of one or more specific organic peroxides for the polymerization of an allylic monomer and/or at least one allylic copolymer.

The invention also relates to a composition comprising at least one allylic monomer and/or at least one allylic copolymer and at least one specific organic peroxide.

The invention also relates to the use of the composition as defined above for the manufacture of an organic glass, preferably an ophthalmic lens, possibly optionally being tinted by means of pigments and/or organic dyes.

An exemplary polymerizable thermosetting composition includes the reaction product of (a) allyl alcohol; (b) a cyclic polyol selected from the group consisting of a cycloaliphatic polyol having at least one secondary hydroxyl group, a heterocyclic polyol having primary and/or secondary hydroxyl groups, and mixtures thereof; (c) ethyleneglycol bischloroformate; and (d) optionally, at least one linear or branched aliphatic polyol having two to six hydroxyl groups. The allyl alcohol (a) is present in an amount of 0.4 to 1.99 equivalents of OH to 1 equivalent chloroformate, and the cyclic polyol (b) is present in an amount of 0.01 to 0.6 equivalents of OH to 1 equivalent of chloroformate. A reaction product, a polymerizate including the polymerizable thermosetting composition, and an optical article including the polymerizable thermosetting composition are also provided.

An exemplary polymerizable thermosetting composition includes the reaction product of (a) allyl alcohol; (b) a cyclic polyol selected from the group consisting of a cycloaliphatic polyol having at least one secondary hydroxyl group, a heterocyclic polyol having primary and/or secondary hydroxyl groups, and mixtures thereof; (c) ethyleneglycol bischloroformate; and (d) optionally, at least one linear or branched aliphatic polyol having two to six hydroxyl groups. The allyl alcohol (a) is present in an amount of 0.4 to 1.99 equivalents of OH to 1 equivalent chloroformate, and the cyclic polyol (b) is present in an amount of 0.01 to 0.6 equivalents of OH to 1 equivalent of chloroformate. A reaction product, a polymerizate including the polymerizable thermosetting composition, and an optical article including the polymerizable thermosetting composition are also provided.

An exemplary polymerizable composition includes the reaction product of (a) diethyleneglycol bischloroformate; (b) allyl alcohol; (c) a cyclic polyol selected from the group consisting of a cycloaliphatic polyol having at least one secondary hydroxyl group, a heterocyclic polyol having primary and/or secondary hydroxyl groups, and mixtures thereof; (d) optionally, ethyleneglycol bischloroformate; and (e) optionally, at least one linear or branched aliphatic polyol having two to six hydroxyl groups. Another exemplary polymerizable composition includes the reaction product of (a) allyl alcohol; (b) a cyclic polyol selected from the group consisting of a cycloaliphatic polyol having at least one secondary hydroxyl group, a heterocyclic polyol having primary and/or secondary hydroxyl groups, and mixtures thereof; (c) ethyleneglycol bischloroformate; and (d) optionally, at least one linear or branched aliphatic polyol having two to six hydroxyl groups is also described. A reaction product, a polymerizate including the polymerizable composition, and an optical article including the polymerizable composition are also provided.

An exemplary polymerizable composition includes the reaction product of (a) diethyleneglycol bischloroformate; (b) allyl alcohol; (c) a cyclic polyol selected from the group consisting of a cycloaliphatic polyol having at least one secondary hydroxyl group, a heterocyclic polyol having primary and/or secondary hydroxyl groups, and mixtures thereof; (d) optionally, ethyleneglycol bischloroformate; and (e) optionally, at least one linear or branched aliphatic polyol having two to six hydroxyl groups. Another exemplary polymerizable composition includes the reaction product of (a) allyl alcohol; (b) a cyclic polyol selected from the group consisting of a cycloaliphatic polyol having at least one secondary hydroxyl group, a heterocyclic polyol having primary and/or secondary hydroxyl groups, and mixtures thereof; (c) ethyleneglycol bischloroformate; and (d) optionally, at least one linear or branched aliphatic polyol having two to six hydroxyl groups is also described. A reaction product, a polymerizate including the polymerizable composition, and an optical article including the polymerizable composition are also provided.

The present invention disclose a blue-light-proof optical resin lens, comprising resin monomers, a blue light absorber and a polymerization initiator; the mass ratio of the resin monomers to the blue light absorber to the polymerization initiator is 100:0.01-2.00:1.00-4.00; the resin monomers are the mixture of allyl diglycol carbonate (ADC) and polymers thereof; the blue light absorber is a benzophenone type ultraviolet light absorber and/or indole type blue light absorber; the polymerization initiator is selected from one or two of tert-butyl peroxy-2-ethylhexyl carbonate, tert-amyl peroxy-2-ethylhexyl carbonate and 1,1-di-(tert-butylperoxy)-3,3,5-trimethylcyclohexane. A preparation method includes the following steps: weighing the resin monomers, the blue light absorber and the polymerization initiator by ratio, sealing the mixture at room temperature, uniformly stirring the mixture at vacuum, filtering the stirred mixture with a filter core, and then vacuuming; (2) immediate pouring, molding by thermocuring; (3) mold opening, washing the obtained product; (4) annealing the obtained product, and inspecting the product. The blue-light-proof optical resin lens prepared by the method has a blue light absorbency (380-500 nm) of 15%-40%.

The present invention disclose a blue-light-proof optical resin lens, comprising resin monomers, a blue light absorber and a polymerization initiator; the mass ratio of the resin monomers to the blue light absorber to the polymerization initiator is 100:0.01-2.00:1.00-4.00; the resin monomers are the mixture of allyl diglycol carbonate (ADC) and polymers thereof; the blue light absorber is a benzophenone type ultraviolet light absorber and/or indole type blue light absorber; the polymerization initiator is selected from one or two of tert-butyl peroxy-2-ethylhexyl carbonate, tert-amyl peroxy-2-ethylhexyl carbonate and 1,1-di-(tert-butylperoxy)-3,3,5-trimethylcyclohexane. A preparation method includes the following steps: weighing the resin monomers, the blue light absorber and the polymerization initiator by ratio, sealing the mixture at room temperature, uniformly stirring the mixture at vacuum, filtering the stirred mixture with a filter core, and then vacuuming; (2) immediate pouring, molding by thermocuring; (3) mold opening, washing the obtained product; (4) annealing the obtained product, and inspecting the product. The blue-light-proof optical resin lens prepared by the method has a blue light absorbency (380-500 nm) of 15%-40%.