Patent classifications
C08G2261/146
POLYMERS FOR PHOTOVOLTAIC APPLICATIONS
A method of combining different materials to produce the polymer
##STR00001##
In this polymer X.sub.1, X.sub.2, X.sub.3, and X.sub.4 are independently selected from the group consisting of: F, Cl, H, and combinations thereof. Additionally, in this polymer R.sub.15, R.sub.16, R.sub.17, and R.sub.18 are independently selected from the group consisting of: F, Cl, H, and combinations thereof. Finally, in this polymer R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.5, R.sub.6, R.sub.7, and R.sub.8 are independently selected from unsubstituted branched alkyls with 1 to 60 carbon atoms unsubstituted or substituted branched alkyls with 1 to 60 carbon atoms and unsubstituted or substituted linear alkyls with 1 to 60 carbon atoms.
PHOTOACTIVE MATERIAL
A material comprising an electron-accepting unit of formula (I): wherein Ar1 and Ar2 independently is a 5- or 6-membered aromatic or heteroaromatic ring or is absent; and each X is independently H or a substituent with the proviso that at least one X is an electron-withdrawing group and wherein X groups bound to adjacent carbon atoms may be linked to form an electron-withdrawing group. The material further comprises an electron-donating unit D comprising a fused or unfused furan or thiophene. The material may be a polymer comprising repeat units of formula (I). The material may be a non-polymeric compound. An organic photodetector may contain a bulk heterojunction layer containing an electron acceptor or an electron donor wherein at least one of the electron acceptor and electron donor contains a unit of formula (I).
##STR00001##
MODIFIED POLYMER WITH A SLIPPERY OMNIPHOBIC COVALENTLY ATTACHED LIQUID CHEMICALLY BONDED THERETO, METHOD OF MAKING THE SAME, LIQUID LENS INCORPORATING THE MODIFIED POLYMER AS AN INSULATING LAYER, AND LIQUID LENS WITH INSULATING LAYER HAVING HIGH QUALITY FACTOR USABLE UNDER DIRECT CURRENT
A liquid lens including (i) a first liquid and a second liquid disposed within a containment region, the first liquid and the second liquid forming an interface between the first liquid and the second liquid; (ii) an electrode; and (iii) an insulating layer separating the electrode from the first liquid and the second liquid, the insulating layer comprising a polymeric material and a slippery omniphobic covalently attached liquid that is chemically bonded to the polymeric material, the slippery omniphobic covalently attached liquid providing a surface contacting one or more of the first liquid and the second liquid. The polymeric material of the insulating layer can be a poly(para-xylylene). The slippery omniphobic covalently attached liquid can include units of a silicone or polyolefin, each unit individually bound to a repeating unit of the polymeric material. A liquid lens where the insulating layer has a quality factor at least 200.
ESTER-SUBSTITUTED POLYMERS FOR ORGANIC PHOTOVOLTAICS
A polymer comprising
##STR00001##
In this polymer, R, R′, and R″ are independently selected from the group consisting of: H, Cl, F, CN, alkyl, alkoxy, alkylthio, ester, ketone and aryl groups. Additionally, in this polymer X and X′ are independently selected from aryl groups. Finally, m independently ranges from 1 to 100 and n independently ranges from 0 to 99
Polymer and Organic Light-Emitting Diode Using Same
The present specification relates to a polymer and an organic light emitting device using the same, wherein the polymer is represented by the following Chemical Formula 1:
E1-[A].sub.a—[B].sub.b—[C].sub.c-E2 [Chemical Formula 1] Wherein A, B, C, E1, E2, a, b and c are described herein.
Organic semiconductors
The invention relates to novel compounds containing one or more units derived from 2,6-disubstituted-[1,5]naphthyridine or 1,6-disubstituted-1H-[1,5]naphthyridine-2-one, to methods for their preparation and educts or intermediates used therein, to mixtures and formulations containing them, to the use of the compounds, mixtures and formulations as organic semiconductors in organic electronic (OE) devices, especially in organic photovoltaic (OPV) devices and organic photodetectors (OPD), and to OE, OPV and OPD devices comprising these compounds, mixtures or formulations.
THE ORGANIC SEMICONDUCTING COMPOUND AND THE ORGANIC PHOTOELECTRIC COMPONENTS USING THE SAME
An organic semiconducting compound and an organic photoelectric component containing the same are provided. The organic semiconducting compound has a novel chemical structure to make the organic semiconducting compound have good response to the infrared light. The organic semiconducting compound can be applied to the organic photoelectric components such as organic photodetector (OPD), organic photovoltaic (OPV) cell, and organic field-effect transistor (OFET). Thus, the organic photoelectric components have better light absorption range and photoelectric response while in use.
Method of producing substrate with fine uneven pattern, resin composition, and laminate
A method of producing a substrate with a fine uneven pattern is a method of producing a substrate having a fine uneven pattern on a surface thereof, the method including a step (a) of preparing a laminate provided with a substrate and a first resin layer provided on the substrate and having a first fine uneven pattern formed on a surface thereof; and a step (b) of forming a second fine uneven pattern corresponding to the first fine uneven pattern on the surface of the substrate by etching the surface of the first fine uneven pattern using the first resin layer as a mask, in which the first resin layer is formed of a resin composition (P) including a fluorine-containing cyclic olefin polymer (A) or a cured product of the resin composition (P).
Unsymmetrical benzothiadiazole-based random copolymers
A random copolymer comprising the monomer units A, B and C. In this random copolymer A comprises ##STR00001##
B comprises ##STR00002##
and C comprises an aryl group. Additionally, R1 R2, R3 and R4 are side chains independently selected from the group consisting of: H, Cl, F, CN, alkyl, alkoxy, alkylthio, ester, ketone and aryl groups. X1 and X2 are independently selected from the group consisting of: H, Cl, F, CN, alkyl, alkoxy, ester, ketone, amide and aryl groups.
Porous compositions and related methods
Porous compositions such as flexible polymers with side chain porosity are generally provided. In some embodiments, the composition comprises a flexible polymer backbone and a plurality of rigid side chains. In some embodiments, the rigid side chains form pores. In some embodiments, the rigid side chains may comprise two or more [2.2.2] bicyclic cores (e.g., formed by a ring opening metathesis polymerization. The compounds and methods described herein may be useful in various applications including, for example, gas separation.