The present invention relates to a curable resin composition comprising a curable resin mixture and at least one C.sub.2-C.sub.3-alkenyl-substituted compound of formula (I) wherein m is 1, 2 or 3; R.sup.m1, R.sup.m2, R.sup.m3 and R.sup.m4 are hydrogen or C.sub.6-C.sub.14-aryloxy, which is substituted by one or more radicals selected from C.sub.1-C.sub.24-alkyl and C.sub.6-C.sub.14-aryl-C.sub.1-C.sub.10-alkylene; R.sup.5, R.sup.6, are hydrogen or optionally substituted C.sub.6-C.sub.14-aryl, or R.sup.5 and R.sup.6 together are a diradical of the formula A; A is a diradical of the formulae A.1 or A.2 wherein R.sup.7 is C.sub.2-C.sub.3-alkenyl; R.sup.8, n are as defined in the claims and in the description. The present invention also relates to a polymer comprising in copolymerized form at least one compound of formula (I) and an organopolysiloxane and to novel compounds of formula (I).

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Provided are: an organic electronic material which can be easily multilayered and that can be used in substrates, such as resin, that cannot be processed at high temperatures; an ink composition containing the same; an organic thin film formed using said organic electronic material or said ink composition; and an organic electronic element and an organic EL element that are formed using said organic thin film and that have a superior luminous efficacy and emission lifespan than conventional elements. Specifically, provided are: an organic electronic material that is characterized by containing an oligomer or a polymer having a structure that branches into three or more directions and has at least one polymerizable substituent; an ink composition containing said organic electronic material; and an organic thin film prepared using the aforementioned organic electronic material. Further, provided are an organic electronic element and an organic electroluminescent element containing said organic thin film.

An organic compound having an excellent electron injection and transport performance is provided as a material for a low-power-consumption organic electroluminescent device. A low-power-consumption organic electroluminescent device is also provided by using the compound. The compound is a compound of general formula (1) or (2) having a substituted bipyridyl and triphenylene ring structure. The organic electroluminescent device includes a pair of electrodes, and one or more organic layers sandwiched between the pair of electrodes, and uses the compound as constituent material of at least one of the organic layers. ##STR00001##

Light harvesting luminescent multichromophores that are configured upon excitation to transfer energy to, and amplify the emission from, an acceptor signaling chromophore in energy-receiving proximity therewith are provided. Also provided are compositions for labelling a target. The labelling composition may include a donor light harvesting multichromophore and an acceptor signaling chromophore in energy-receiving proximity to the donor light harvesting multichromophore. Also provided is an aqueous composition for labelling a target, including: a donor light harvesting multichromophore; an acceptor signaling chromophore in energy-receiving proximity therewith; and a sensor biomolecule. Methods for using the subject compositions are also provided.

The present disclosure relates to an organic electroluminescent compound for near-IR light emission, an organic electroluminescent material and an organic electroluminescent device comprising the same. By comprising the organic electroluminescent compound of the present disclosure, it is possible to provide an organic electroluminescent device with near-IR light emission.

The present invention provides, among other aspects, stabilized chromophoric nanoparticles. In certain embodiments, the chromophoric nanoparticles provided herein are rationally functionalized with a pre-determined number of functional groups. In certain embodiments, the stable chromophoric nanoparticles provided herein are modified with a low density of functional groups. In yet other embodiments, the chromophoric nanoparticles provided herein are conjugated to one or more molecules. Also provided herein are methods for making rationally functionalized chromophoric nanoparticles.

Provided are transparent molded bodies for use as a scintillator for measuring the type and intensity of ionizing and non-ionizing radiation, including an organic polymer and, if desired, at least one additive which, under the influence of at least one of ionizing and non-ionizing radiation, emits scintillation radiation in the range from UV to IR light, the aim is to improve optical and mechanical properties, robustness against environmental influences and the manufacturability. This was achieved in that the organic polymer at least in part contains a polyaddition product of polyfunctional isocyanates and one or more polyfunctional hardener components.

The present disclosure provides fluorescent polyindenofluorene polymers or macromers with unique optical properties that are stable. The polymeric fluorophores are useful in various bioassays formats. The inventive polymers are useful in assays relying on fluorescence resonance energy transfer (FRET) mechanisms where two fluorophores are used.

Nanoparticle compositions comprising nanoparticles formed from -conjugated cross-linked polymers are disclosed, together with their methods of manufacture and their applications. Owing to the nature of the cross-links formed therein, the nanoparticle compositions afford a high degree of manufacturing flexibility and control, as well as being amenable to facile purification for the purpose of imaging and electronics applications.

A chromene compound having at least one indenonaphthopyran moiety which has a group forming a spiro ring together with the 13-position carbon atom and further an oligomer chain group selected from a polyalkylene oxide oligomer chain group having at least three recurring units and a polyester oligomer chain group having at least three recurring units, represented by the following formula and having reduced matrix dependence:

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wherein R.sup.1 and R.sup.2 are each a group which may have an oligomer chain group, the ring Z bonded to the 13-position carbon atom of the chromene compound is a Spiro ring group, and R.sup.3 and R.sup.4 are each an aryl group or heteroaryl group which may have an oligomer chain group.

Preferably, the chromene compound has at least one oligomer chain group in the molecule.