Abstract:
Disclosed are a heterocyclic compound represented by Formula 1-1 or 1-2, wherein, in Formulae 1-1 and 1-2, X1, CY1 to CY3, R1 to R3, and a1 to a3, are the same as described in the specification. Also disclosed is an organic light-emitting device including the same.
Abstract:
A method and apparatus for generating a new chemical structure using a chemical structure generation model are provided. The method includes receiving a first descriptor of a first chemical structure, encoding the first descriptor into a latent variable using an encoder of the chemical structure generation model, generating a second descriptor by decoding the latent variable using a decoder of the chemical structure generation model, generating the second chemical structure corresponding to the second descriptor.
Abstract:
An organic light-emitting device including a first electrode, a second electrode facing the first electrode, and an organic layer disposed between the first electrode and the second electrode, wherein the organic layer includes an emission layer, and wherein the emission layer includes a fluorescent compound represented by a specific formula described in the specification.
Abstract:
Provided are a light-emitting device, a method of manufacturing the light-emitting device, and an operating method of the light-emitting device, wherein the light-emitting device includes a first conductive layer and a light-emitting group represented by Formula 1: *-A3-(A1)m1-(A2)m2. Formula 1 The detailed description of Formula 1 is the same as described in the present specification.
Abstract:
An organometallic compound represented by Formula 1: M(L1)n1(L2)n2 Formula 1 In Formula 1, M is a transition metal; L1 is a ligand represented by Formula 2 as disclosed herein; L2 is a monodentate ligand, a bidentate ligand, a tridentate ligand, or a tetradentate ligand; n1 is 1, 2, or 3, wherein, when n1 is 2 or greater, ligands L1 are identical to or different from each other; and n2 is 0, 1, 2, 3, or 4, wherein, when n2 is 2 or greater, ligands L2 are identical to or different from each other.
Abstract:
Provided are an asymmetric butadiene-based charge transporting compound represented by one of Formula (1) and (1′) as in claim 1, an electrophotographic photoreceptor including the asymmetric butadiene-based charge transporting compound, and an electrophotographic imaging apparatus. The electrophotographic photoreceptor including the organic photoconductive material as a charge transporting material may not cause a problem, such as partial crystallization during film formation and may have a high charge potential, a sufficient photoresponsive property with high sensitivity, and a high durability. Moreover, these properties may be all maintained even in the case of exposure to light as well as use in low-temperature environments or high-speed processes, thus having high reliability.