Abstract: Light emitting polymers can include a plurality of arylene monomeric units and a plurality of soft segment units independently selected from soft segment end caps; soft segment side chains coupled to a portion, but not all, of the arylene monomeric units; internal soft segment monomeric units; and combinations thereof. These light emitting polymers can be used in forming electroluminescent devices or other articles.

Abstract: The invention provides a cholesteric liquid crystal composition that includes at least one cholesteric liquid crystal precursor, and at least one non-liquid crystalline additive that is a non-liquid crystalline compound of formula I The invention also provides cholesteric liquid crystal films and optical bodies formed from cholesteric liquid crystal compositions of the invention. The invention further provides an optical display that includes a display medium, and a reflective polarizer including a cholesteric liquid crystal composition in accordance with the invention.

Abstract: A process is provided for preparing a pressure sensitive adhesive hydrogel, comprising: (A) providing an oligomeric precursor, the oligomeric precursor comprising a polyether moiety endcapped with ethylenic unsaturation, the oligomeric precursor being associated with methacrylic acid; (B) providing an ethylenically unsaturated crosslinking agent selected from the group consisting of difunctional ethylenically unsaturated monomer, trifunctional ethylenically unsaturated monomer and combinations of the foregoing; (C) free radically curing the oligomeric precursor and the ethylenically unsaturated crosslinking agent in water at a pH between about 3.5 and about 9 to provide the pressure sensitive adhesive hydrogel.

Abstract: Methods of making an optical body are disclosed. A method includes the steps of coating a mixture including a first cholesteric liquid crystal polymer, a second cholesteric liquid crystal monomer, a second cholesteric liquid crystal polymer formed from a portion of the second cholesteric liquid crystal monomer, and a solvent on a substrate. The first cholesteric liquid crystal polymer is different than the second cholesteric liquid crystal polymer. Then, forming from the mixture an optical body including a first layer, a second layer, and a third layer disposed between the first and second layer. The first layer includes a majority of the first cholesteric liquid crystal polymer. The second layer includes a majority of a second cholesteric liquid crystal monomer. The third layer includes the second cholesteric liquid crystal polymer.

Abstract: A cholesteric liquid crystal composition includes a) a cholesteric liquid crystal compound or a cholesteric liquid crystal precursor; and b) a compound of formula (I), formula (II) or formula (III): R—R1—R2?R3R4?nR5—R6??(I) R—R7—R2?R3R4?nR5—R8??(II) R9??R4R3?mR2—R10—R)2??(III) where, n is 1, 2, 3, or 4; m is 1, 2, or 3; R is an acrylate, methacrylate, acrylamide, isocyanate, epoxy, or silane; R1 is a (C3-C8) alkylene, (C3-C8) alkenylene, or (C3-C8) alkylyne; R2 is a bond, —O—, —C(O)O—, —O(O)C—, —OC(O)O—, —C(O)N—, —CH?N—, —N?CH—, or —NC(O)—; R3 is a cycloalkylene, cycloalkenylene, heterocyclylene, arylene, or hetroarylene; R4 is a bond, (C1-C8) alkylene, (C2-C8) alkenylene, (C2-C8) alkylyne, carbonyl, —O—, —C(O)O—, —O(O)C—, —OC(O)O—, —C(O)N—, —CH?N—, —N?CH—, or —NC(O)—; R5 is a bond, cycloalkylene, cycloalkenylene, hetrocyclylene, arylene, or hetroarylene; R6 is hydrogen, cyano, halo, (C1-C8) alkoxy, (C1-C8) alkyl, nitro, amino, carboxy, mercapto, (C1-C4)thioalkyl, COCH3, CF3, OCF3, or SCF3; R7 is a (C1