Abstract:
Embodiments relate to a delayed fluorescence compound of 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 an organic compound having a benzofluorenocarbazole core and an aromatic or hetero aromatic groups bonded to a specific positions of the benzofluorenocarbazole core, and an organic light emitting diode and an organic light emitting device including the compound. The organic compound has a narrow Stokes Shift between an absorption spectrum peak and an emission spectrum peak, it has a broad spectral overlapping area between its absorption wavelength range and an emission wavelength range of another luminous material. Therefore, it can emit light having high color purity and exhibit excellent luminous efficiency.
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:
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.