Transitions Optical, Inc.

Ramaiahgari Reddy

Anil Kumar

Meng He

Cory S Brown

Henry Nguyen

Alan M Grubb

Brad S Veldkamp

Yannian Li

David John Park

Ruisong Xu

Brian Smyth

Suvagata Tripathi

Provided is a photochromic film laminate including (a) a first polymeric film layer having a first surface and an opposing second surface; and (b) an adhesive layer over at least a portion of and in direct contact with the first surface of the first polymeric film layer (a). The adhesive layer is formed from a composition of a thermoplastic polyol having a number average molecular weight greater than or equal to 30,000 g/mol; a poly(anhydride); and a photochromic material. The thermoplastic polyol (i) is present in the composition in an amount greater than or equal to 60 percent by weight based on total combined weight of solids present in the thermoplastic polyol (i) and the poly(anhydride) (ii). Also provided is an optical article prepared with the photochromic film laminate.

Photochromic film laminate

The present invention relates to curable photochromic compositions which include an at least di-functional oxazoline functional material, an at least di-functional first carboxylic acid functional material, an optional second carboxylic acid functional material having at least three carboxylic acid groups, which optionally includes a carboxylic acid functional polymer, and a photochromic compound. The curable photochromic compositions have an equivalents ratio of oxazoline equivalents of the oxazoline functional material to a total carboxylic acid equivalents of the first and optional second carboxylic acid functional materials of from 0.5:1 to 10:1 when the second carboxylic acid functional material is not present, and from 0.5:1 to 3:1 when the second carboxylic acid functional material is present. The present invention, more particularly, relates to curable photochromic adhesive compositions, and curable photochromic coating compositions.

Curable photochromic compositions including an oxazoline functional material

The present invention relates to mesogen compounds that include a first mesogen (Mesogen-1) and a second mesogen (Mesogen-2) that are connected by a linking group (-L-), as represented by the following Formula (I): Mesogen-1, and optionally Mesogen-2, each independently include the following terminal group, where R is hydrogen, alkyl, or alkoxy. Mesogen-2 optionally includes a terminal group P—, which is selected from R, acrylate, methacrylate, trihalomethacrylate, oxirane, hydroxyl, carboxylic acid, and carboxylic acid ester. Mesogen-1 and Mesogen-2 together include a total of at least seven, or at least eight, cyclic groups. In some cases, Mesogen-1 and Mesogen-2 are the same. The present invention also relates to liquid crystal compositions that include such mesogen compounds, and to optical elements that include such mesogen compounds.

Mesogen compounds

Provided is a curable photochromic coating composition including (a) a polyol component, (b) a poly(anhydride) having at least three cyclic anhydride groups, (c) a secondary crosslinker, and (d) a photochromic material. The polyol component includes (i) a first polyol having two hydroxyl groups and a hydroxyl equivalent weight of at least 15,000 g/mol and (ii) a second polyol different from the first polyol having at least three hydroxyl groups and a hydroxyl equivalent weight of at least 300 g/mol. The secondary crosslinker is selected from a poly(carbodiimide), an oxazoline-functional material, or mixtures thereof. The present invention also provides an optical article prepared from the curable photochromic coating composition.

Photochromic composition with polyol and poly(anhydride)

The present invention relates to mesogen compounds that include first, second, and third mesogens, in which the first and second mesogens are connected by a first linking group (-L-), and the second and third mesogens are connected by a second linking group (-L-), as represented by the following Formula (I), and as graphically illustrated by Formula (Ia) of FIG.of the drawing:(Mesogen-1)-L-(Mesogen-2)-L-(Mesogen-3)&#x2003;&#x2003;(I)At least one of Mesogen-1, Mesogen-2, or Mesogen-3 include at least four cyclic groups. The linking groups -L- and -L- are each free of mesogen properties (are each non-mesogenic) and each independently have an average chain length of at least 20 bonds. The mesogen compounds are optionally polymerizable. The present invention also relates to liquid crystal compositions that include such mesogen compounds, and to optical elements that include such mesogen compounds, such as in one or more mesogen-containing layers.

The present invention relates to mesogen compounds that include a first mesogen (Mesogen-1) and a second mesogen (Mesogen-2) that are connected by a linking group (-L-), as represented by the following Formula (I): Mesogen-1, and optionally Mesogen-2, each independently include the following terminal group,

Compounds that have ultraviolet light absorbing properties, and which can also have mesogenic properties. Compositions that include one or more such compounds. Articles of manufacture that include one or more such compounds, such as optical elements that include an optical substrate and a layer that includes at least one such compound.

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Murrysville, PA, United States of America

Ramaiahgari Reddy