An organic electroluminescence device comprising: an anode, a cathode, and an emitting region between the anode and the cathode, wherein the emitting region comprises a first emitting layer and a second emitting layer, the first emitting layer and the second emitting layer are directly adjacent to each other, the first emitting layer is between the anode and the second emitting layer, and one of the first emitting layer and the second emitting layer comprises a compound having at least one deuterium atom.

The present invention is directed to a curable photochromic composition including (a) a photochromic compound; (b) a segmented polymer having active hydrogen groups, at least one first segment, and at least one second segment, wherein (i) each first segment independently includes a fluorinated polymer segment, and (ii) each second segment independently includes a segment selected from a polycarbonate segment, a polyester segment, a polyether segment, a polyurethane segment, and a segment of copolymers thereof; and (c) a curing agent having reactive functional groups that are reactive with the active hydrogen groups of the segmented polymer, wherein the curing agent includes at least one of a polyisocyanate, a polyisothiocyanate, or an aminoplast. Also provided are photochromic films and articles, including multilayer articles, which include the curable photochromic composition.

The present invention relates to compounds, which are suitable for use in electronic devices, and to electronic devices, in particular organic electroluminescent devices, containing said compounds.

The present subject matter is directed to a luminogen exhibiting aggregation induced emission, wherein T1, T2, and T3 comprise one or more polyynes as a conjugated bridge. The present subject matter is also directed to an AIEgen comprising a hydrophilic pyridium group as a strong electron-withdrawing group; a piperazine group as an electron-donating group; and a α-Cyanostilbene; wherein the AIEgen exhibits aggregation induced emission. The present subject matter is directed to a method of synthesizing an AIEgen and is further directed to a method of labeling comprising incubating a subject having cells with a conjugate formed by conjugating an AIEgen with an antibody; and selectively labeling desired cells by turn-on imaging, wherein labeling occurs when the desired cells are selectively stained by fluorescent emission of the AIEgen upon degradation of the antibody after cellular internalization of the conjugate through endocytosis.

A white light emitting material having a chemical structural formula represented by formula (I), a preparation method thereof and application thereof. The preparation method comprises subjecting tris(4-iodophenyl)amine and 4-methoxyphenylacetylene or tris(4-iodophenyl)amine and methyl 4-ethynylbenzoate to a coupling reaction under protection of a protective gas and catalysis of a Pd/Cu mixed catalyst, to obtain the white light emitting material. A novel temperature-sensitive light emitting material is synthesized through a one-step method. The material is applied to the field of diode luminescence based on the temperature-sensitive characteristic. White light luminescence can be finally realized only by reasonably controlling the temperature and duration time during heating a substrate. Compared with the existing art, the method greatly saves raw material costs and manufacturing process costs, and provides a novel idea and strategy for use of a white organic light emitting diode.

An organic molecule is disclosed having a structure of Formula I: ##STR00001##
wherein X is O or S; Y is O or S; R.sup.1 is selected from the group consisting of: hydrogen, deuterium, C.sub.1-C.sub.5-alkyl, which is optionally substituted with one or more substituents R.sup.5; C.sub.6-C.sub.60-aryl, which is optionally substituted with one or more substituents R.sup.5; and C.sub.3-C.sub.57-heteroaryl,
which is optionally substituted with one or more substituents R.sup.5.

An organic electroluminescence device of an embodiment includes a first electrode, a second electrode, and an emission layer disposed between the first electrode and the second electrode, and the emission layer includes a polycyclic compound represented by Formula 1. The organic electroluminescence device may exhibit high luminous efficiency and/or service life characteristics: ##STR00001##

An organic electroluminescence device including: an anode, a cathode, and at least one emitting layer between the cathode and the anode, wherein the emitting layer contains a first host material, a second host material, and a dopant material, the first host material is a compound having at least one deuterium atom, and the emitting layer contains the first host material in the proportion of 1% by mass or more.

Provided is an organometallic compound of Chemical Formula 1: ##STR00001## wherein, in Chemical Formula 1: X is O, S, NH, or Se; R.sub.1 is —Si(R.sub.a)(R.sub.b)(R.sub.c), where R.sub.a, R.sub.b, and R.sub.c are hydrogen, deuterium, or a substituted or unsubstituted C.sub.1-10 alkyl; R.sub.2, R.sub.3 and R.sub.4 are each independently hydrogen, deuterium, halogen, cyano, amino, a substituted or unsubstituted C.sub.1-60 alkyl, a substituted or unsubstituted C.sub.1-60 haloalkyl, a substituted or unsubstituted C.sub.1-60 alkoxy, a substituted or unsubstituted C.sub.1-60 haloalkoxy, a substituted or unsubstituted C.sub.3-60 cycloalkyl, a substituted or unsubstituted c.sub.2-60 alkenyl, a substituted or unsubstituted C.sub.6-60 aryl, a substituted or unsubstituted C.sub.6-60 aryloxy, or a substituted or unsubstituted C.sub.2-60 heterocyclic group containing one or more heteroatoms selected from the group consisting of N, O and S; a and b are each 0 and 1, or 1 and 0, respectively; and n is 1 or 2,
and an organic light emitting device including the same.

An organic electroluminescence device comprising: a cathode, an anode, and at least one organic layer disposed between the cathode and the anode, wherein at least one layer of the at least one organic layer comprises a compound represented by the following formulas (1-1) and (1-3) or a compound represented by the following formulas (1-2) and (1-3). ##STR00001##