Abstract: A red phosphorescent compound includes a host material being capable of transporting an electron or a hole; and a dopant material represented by following Formula 1: wherein the is one of and each of R1 to R4 is one of the group consisting of hydrogen atom (H), C1 to C6 substituted or non-substituted alkyl group, C1 to C6 substituted or non-substituted alkoxy group, and halogen atom.

Abstract: A blue fluorescent compound includes a host material being capable of transporting an electron or a hole; and a dopant material represented by following Formula 1: [Formula 1] wherein each of the R1, the R2, the R3, the R4, and the R5 is selected from hydrogen, fluorine, C1-C6 substituted or non-substituted alkyl group, C6-C30 substituted or non-substituted aromatic group, and C6-C30 substituted or non-substituted heterocyclic group, and two of the R1, the R2, the R3, the R4 and the R5 are fluorine and wherein the R6 is selected from the C6-C30 substituted or non-substituted aromatic group, and the C6-C30 substituted or non-substituted heterocyclic group.

Abstract: The present invention relates to a blue fluorescence compound which enables to achieve high brightness, a long lifetime and high efficiency; and an organic electroluminescence device thereof.

Abstract: A red phosphorescent compound includes a host material being capable of transporting an electron or a hole; and a dopant material represented by following Formula 1: wherein the is one of and each of R1 to R4 is one of the group consisting of hydrogen atom (H), C1 to C6 substituted or non-substituted alkyl group, C1 to C6 substituted or non-substituted alkoxy group, and halogen atom.

Abstract: Disclosed herein are red phosphorescent compounds of the following formula: wherein ?includes a phenyl part and a quinoline part, each ring of the phenyl part having at least one substituent selected from hydrogen, C1-C4 alkyl groups and C1-C4 alkoxy groups and ?is selected from 2,4-pentanedione, 2,2,6,6,-tetramethylheptane-3,5-dione, 1,3 -propanedione, 1,3-butanedione, 3,5-heptanedione, 1,1,1-trifluoro-2,4-pentanedione, 1,1,1,5,5,5 -hexafluoro-2,4-pentanedione and 2,2-dimethyl-3,5-hexanedione.

Abstract: A red phosphorescent composition includes a host material being capable of transporting an electron or a hole; and a dopant material represented by the following Formula 1: wherein each of R1 to R4 is selected from the group consisting of hydrogen atom (H), C1 to C6 alkyl and C1 to C6 alkoxy, and at least one of R1 to R4 is C1 to C6 alkyl, and wherein each of R5 to R7 is selected from the group consisting of hydrogen, C1 to C6 alkyl and halogen atom, and at least one of R5 to R7 is halogen atom, and wherein each of X and Y is selected from the group consisting of H, non-substituted C1 to C6 alkyl and C1 to C6 alkyl substituted by fluorine.

Abstract: A red phosphorescent compound includes a host material being capable of transporting an electron or a hole; and a dopant material represented by following Formula 1: and each of R1 to R4 is one of the group consisting of hydrogen atom (H), C1 to C6 substituted or non-substituted alkyl group, C1 to C6 substituted or non-substituted alkoxy group, and halogen atom.

Abstract: The invention relates to a red phosphorescent compound represented by the following Formula (1) and an organic electroluminescent (EL) device using the same: wherein

Abstract: Disclosed is an organic light emitting material having the following chemical formula, for improving luminous efficiency, where R1, R2, R3 and R4 denote materials selected from an aromatic group with 6-24 carbon atoms (C6-C24), the group being independently substituted or unsubstituted, preferably, an aromatic group with 6-24 carbon atoms (C6-C24), the group consisting of trimethylsilane (TMS), CN, halogen (F, Cl, Br) alkyl groups with 1-4 carbon atoms (C1-C4).

Abstract: A blue fluorescent compound includes a host material being capable of transporting an electron or a hole; and a dopant material represented by following Formula 1: wherein at least two of the R1, the R2, the R3, and the R4 are selected from substituted or non-substituted aromatic group or substituted or non-substituted heterocyclic group, and the R5 is selected from substituted or non-substituted aromatic group or substituted or non-substituted heterocyclic group.

Abstract: Disclosed is an organic electroluminescent device comprising a structure having an anode, an emitting layer, and a cathode stacked therein, wherein a fluorescent compound represented by Formula 1 is used as a emitting material of the emitting layer or used as a dopant of the emitting layer: wherein A1 and A2 are independently selected from a substituted or unsubstituted C1-C6 aliphatic group, a C6-C20 aromatic group and a C5-C19 heterocyclic group containing N, S or O, A3 is selected from a substituted or unsubstituted C1-C6 aliphatic group, a C6-C20 aromatic group, a C5-C19 heterocyclic group containing N, S or O, and a hydrogen atom, and substituents of A1, A2 and A3 are respectively one or more and the substituent is selected from the group consisting of C1-C10 alkyl, C1-C1 alkoxy, C1-C10 alkylamino, C1-C10 alkylsilyl, a halogen atom, C6-C10 aryl, C6-C10 aryloxy, C6-C10 arylamino, C6-C10 arylsilyl and a hydrogen atom.

Abstract: A red phosphorescent compound of Formula I: wherein is and R1, R2, R3, R4 and R5 are as defined in the specification.

Abstract: Disclosed herein is a red phosphorescent compound of the following Formula 1: wherein is includes a phenyl part and a quinoline part, the quinoline part has one substituent selected from a C1-C4 alkoxy group and the phenyl part has substituents independently selected from hydrogen, C1-C4 alkyl groups and C1-C4 alkoxy groups, and is selected from 2,4-pentanedione, 2,2,6,6-tetramethylheptane-3,5-dione, 1,3-propanedione, 1,3-butanedione, 3,5-heptanedione, 1,1,1-trifluoro-2,4-pentanedione, 1,1,1,5,5,5-hexafluoro-2,4-pentanedione, and 2,2-dimethyl-3,5-hexanedione.

Abstract: An organic EL device is disclosed, which has an organic multilayer between a first electrode and a second electrode, the organic multilayer comprising a hole injection layer formed on the first electrode, and formed of a mixture of at least one selected from organic materials and at least one selected from inorganic materials; a hole transport layer having at least one layer on the hole injection layer; and an emitting layer formed on the hole transport layer.

Abstract: Disclosed herein are red phosphorescent compounds of the following one of Formulas 1 to 3 wherein Formula 1 R1 and R2 are independently a C1-C4 alkyl group, R3, R4, R5 and R6 are independently selected from hydrogen, C1-C4 alkyl groups and C1-C4 alkoxy groups, wherein Formula 2 R1, R2, R3 and R4 are independently selected from C1-C4 alkyl groups and C1-C4 alkoxy groups, wherein Formula 3 R1, R2, R3 and R4 are independently selected from hydrogen, C1-C4 alkyl groups and C1-C4 alkoxy groups, and wherein is selected from 2,4-pentanedione, 2,2,6,6,-tetramethylheptane-3,5-dione, 1,3-propanedione, 1,3-butanedione, 3,5-heptanedione, 1,1,1-trifluoro-2,4-pentanedione, 1,1,1,5,5,5-hexafluoro-2,4-pentanedione and 2,2-dimethyl-3,5-hexanedione.

Abstract: Disclosed is an organic electroluminescent device including a substrate, a first and a second electrode, and an emitting layer formed between the first electrode and the second electrode. The emitting layer includes a plurality of materials which is a blue emitting material using a following chemical formula as dopant. In this case, at least one of A1 and A2 is selected from a substituted or non-substituted aromatic group, a heterocyclic group, an aliphatic group, and hydrogen.

Abstract: A red phosphorescent compound, includes a host material being capable of transporting an electron or a hole; and a dopant material represented by the following formula 1: wherein each of R1 to R4 is selected from the group consisting of hydrogen atom (H), C1 to C6 alkyl and C1 to C6 alkoxy, and at least one of R1 to R4 is C1 to C6 alkyl, and wherein each of R5 to R7 is selected from the group consisting of hydrogen, C1 to C6 alkyl and pyrrole, and at least one of R5 to R7 is pyrrole, and wherein each of X and Y is selected from the group consisting of H, non-substituted C1 to C6 alkyl and C1 to C6 alkyl substituted by fluorine.

Abstract: The present invention relates to a blue fluorescence compound which enables to achieve high brightness, a long lifetime and high efficiency; and an organic electroluminescence device thereof.

Abstract: A blue fluorescent compound includes a host material being capable of transporting an electron or a hole; and a dopant material represented by following Formula 1: [Formula 1] wherein each of the R1, the R2, the R3, the R4, and the R5 is selected from hydrogen, fluorine, C1-C6 substituted or non-substituted alkyl group, C6-C30 substituted or non-substituted aromatic group, and C6-C30 substituted or non-substituted heterocyclic group, and two of the R1, the R2, the R3, the R4 and the R5 are fluorine and wherein the R6 is selected from the C6-C30 substituted or non-substituted aromatic group, and the C6-C30 substituted or non-substituted heterocyclic group.

Abstract: Disclosed is an organic light emitting material having the following chemical formula, for improving luminous efficiency, where R1, R2, R3 and R4 denote materials selected from an aromatic group with 6-24 carbon atoms (C6-C24), the group being independently substituted or unsubstituted, preferably, an aromatic group with 6-24 carbon atoms (C6-C24), the group consisting of trimethylsilane (TMS), CN, halogen (F, Cl, Br) alkyl groups with 1-4 carbon atoms (C1-C4).