Abstract: Discussed is a space-through charge transfer compound including a paracyclophane core, an electron donor moiety selected from the group consisting of carbazole and diphenyl amine, and an electron acceptor moiety selected from the group consisting of pyrimidine, diphenyltriazine, and triazole. The electron donor moiety and the electron acceptor moiety are indirectly or directly combined to the paracyclophane core with or without a linker, respectively.

Abstract: Embodiments relate to a delayed fluorescence compound of Formula 1: or Formula 2: The excitons in the triplet state are engaged in emission such that the emitting efficiency of the delayed fluorescent compound is increased. Embodiments also relate to a display device with an organic light emitting diode (OLED) that includes the delayed fluorescence compound.

Abstract: Embodiments relate to an organic compound of Formula 1: The excitons in the triplet state are engaged in emission such that the emitting efficiency of the organic compound is increased. Embodiments also relate to an organic light emitting display device with an organic light emitting diode that includes the organic compound.

Abstract: An organic compound is represented by the Formula below, and an organic light-emitting diode and an organic light-emitting diode display device include the organic compound.

Abstract: The present invention provides an organic compound of following formula and an organic light emitting diode and an OLED device including the organic compound.

Abstract: Embodiments relate to a delayed fluorescence compound of Formula 1: or Formula 2: The excitons in the triplet state are engaged in emission such that the emitting efficiency of the delayed fluorescent compound is increased. Embodiments also relate to a display device with an organic light emitting diode (OLED) that includes the delayed fluorescence compound.

Abstract: An organic light emitting diode includes an emitting material layer including first and second layers; a first electrode on a side of the emitting material layer; and a second electrode on the other side of the light emitting material layer and facing the first electrode, wherein the first layer includes a first compound, and the second layer includes a second compound, wherein the first compound has a difference, between a singlet energy and a triplet energy, less than 0.3 eV, and wherein the singlet energy of the first compound is greater than a singlet energy of the second compound.

Abstract: Discussed is a delayed fluorescence compound including a first electron donor moiety of indolo-[3,2,1-j,k]carbazole; a second electron donor moiety selected from indolo-[3,2,1-j,k]carbazole, carbazole, or triphenylamine; and an electron acceptor moiety selected from dibenzothiophene sulfone or diphenyl sulfone, wherein the first and second electron donor moieties are combined to the electron acceptor moiety, and the electron acceptor moiety is combined to a third position or a sixth position of the first electron donor moiety.

Abstract: Embodiments relate to a delayed fluorescence compound and a display device including the delayed fluorescence compound. The delayed fluorescence compound includes an electron acceptor moiety of benzo[4,5]thieno[2,3-b]quinoxaline and at least one electron donor moiety covalently bonded to the electron acceptor moiety. The at least one electron donor moiety is covalently bonded to a benzene ring of benzo[4,5]thieno[2,3-b]quinoxaline and is selected from carbazole, phenylcarbazole, acridine, and phenylacridine. The effective charge transfer in the delayed fluorescence compound results in improved emitting efficiency of the compound.

Abstract: Discussed is a delayed fluorescence compound of Formula 1: wherein n is 1 or 0, and A is selected from Formula 2: wherein D is selected from Formula 3: and each of “L1” and “L2” is independently selected from Formula 4: wherein R1 in the Formula 2 is selected from hydrogen or phenyl, and each of X, Y, and Z is independently selected from carbon and nitrogen, and wherein at least two selected from X, Y, and Z are nitrogen, and R2 in the Formula 4 is selected from one of hydrogen and C1 alkyl through C10 alkyl.

Abstract: An organic light emitting diode (OLED) device includes a first electrode; a second electrode facing the first electrode; an emitting material layer disposed between the first and second electrodes and a horizontally oriented liquid crystal type emitting material.

Abstract: Embodiments relate to a delayed fluorescence compound and a display device including the delayed fluorescence compound. The delayed fluorescence compound includes an electron acceptor moiety of benzo[4,5]thieno[2,3-b]quinoxaline and at least one electron donor moiety covalently bonded to the electron acceptor moiety. The at least one electron donor moiety is covalently bonded to a benzene ring of benzo[4,5]thieno[2,3-b]quinoxaline and is selected from carbazole, phenylcarbazole, acridine, and phenylacridine. The effective charge transfer in the delayed fluorescence compound results in improved emitting efficiency of the compound.

Abstract: Discussed is a space-through charge transfer compound including a paracyclophane core, an electron donor moiety selected from the group consisting of carbazole and diphenyl amine, and an electron acceptor moiety selected from the group consisting of pyrimidine, diphenyltriazine, and triazole. The electron donor moiety and the electron acceptor moiety are indirectly or directly combined to the paracyclophane core with or without a linker, respectively.

Abstract: Embodiments relate to a delayed fluorescence compound of Formula 1: or Formula 2: The excitons in the triplet state are engaged in emission such that the emitting efficiency of the delayed fluorescent compound is increased. Embodiments also relate to a display device with an organic light emitting diode (OLED) that includes the delayed fluorescence compound.

Abstract: Discussed is a delayed fluorescence compound of Formula 1: wherein n is 1 or 0, and A is selected from Formula 2: wherein D is selected from Formula 3: and each of “L1” and “L2” is independently selected from Formula 4: wherein R1 in the Formula 2 is selected from hydrogen or phenyl, and each of X, Y, and Z is independently selected from carbon and nitrogen, and wherein at least two selected from X, Y, and Z are nitrogen, and R2 in the Formula 4 is selected from one of hydrogen and C1 alkyl through C10 alkyl.

Abstract: Discussed is a delayed fluorescence compound including a first electron donor moiety of indolo-[3,2,1-j,k]carbazole; a second electron donor moiety selected from indolo-[3,2,1-j,k]carbazole, carbazole, or triphenylamine; and an electron acceptor moiety selected from dibenzothiophene sulfone or diphenyl sulfone, wherein the first and second electron donor moieties are combined to the electron acceptor moiety, and the electron acceptor moiety is combined to a third position or a sixth position of the first electron donor moiety.

Abstract: Discussed is a space-through charge transfer compound including a naphthalene core; an electron donor moiety selected from carbazole and phenylcarbazole; and an electron acceptor moiety selected from pyridine, diazine, triazole, and phenyl benzodiazole, wherein the electron donor moiety and the electron acceptor moiety are combined to first and eighth positions of the naphthalene core with a benzene linker, respectively.

Abstract: The present invention provides an organic light emitting diode (OLED) device including a first electrode; a second electrode facing the first electrode; an emitting material layer disposed between the first and second electrodes and including a liquid crystal type emitting material being horizontally oriented.

Abstract: Disclosed are a blue phosphorescent compound with a high color purity and a high efficiency, and an organic electroluminescent device using the same. The blue phosphorescent compound is represented by the following Formula: wherein R1 to R5 are each independently hydrogen (H), fluorine (F), chlorine (Cl), bromine (Br), a cyano group, a C1 to C6 alkyl group, a C1 to C6 alkoxy group, a C6 to C20 substituted or unsubstituted aromatic group, a C5 to C20 substituted or unsubstituted heterocyclic group, a C1 to C6 amine group, a C6 to C20 aromatic-substituted amine group, or a C5 to C20 heterocycle-substituted amine group, X is selected from nitrogen (N), oxygen (O), phosphorous (P) and sulfur (S) atoms, at least one of A1, A2, A3 and A4 is nitrogen (N), and the remaining are selected from hydrogen (H)-substituted carbon, and alkyl or alkoxy-substituted carbon, L is a monodentate or bidentate ligand and n is 1 to 3.