Abstract: Provided are an aromatic compound represented by Chemical Formula 1 and an electroluminescent device including the same. In Chemical Formula 1, R1, R2, R3, Ar1, and Ar2 are the same as described in the detailed description.

Abstract: The present disclosure relates to a boron-containing compound including a structure of Formula (I), and the use of the compound as a dopant in an emitting layer of an organic light emitting diode. The present disclosure also relates to an emitting layer of an organic light emitting diode and an organic light emitting diode device.

Abstract: A method for preparing a multi-substituted acrylic acid compound includes steps as follow. A reaction solution is provided, wherein the reaction solution includes an organometallic reagent, a nickel-containing metal catalyst, a catalyst ligand, a first solvent, and the organometallic reagent is a Grignard reagent or a Gilman reagent. An addition step is conducted, wherein an alkyne compound is mixed with the reaction solution so as to undergo an addition reaction, thus an intermediate solution is obtained. A substitution step is conducted, wherein a carbon dioxide is introduced into the intermediate solution so as to obtain the multi-substituted acrylic acid compound.

Abstract: A phenanthroimidazole compound represented by chemical formula 1 and an organic light-emitting diode including the same are provided. In chemical formula 1, R1, R2, and m are the same as described in the specification.

Abstract: The present disclosure relates to a boron-containing compound including a structure of Formula (I), and the use of the compound as a dopant in an emitting layer of an organic light emitting diode. The present disclosure also relates to an emitting layer of an organic light emitting diode and an organic light emitting diode device.

Abstract: The present disclosure relates to a compound including a structure of Formula (I), and the use of the compound as a dopant in an emitting layer of an organic light emitting diode. The present disclosure also relates to an emitting layer of an organic light emitting diode and an organic light emitting diode device.

Abstract: The present disclosure relates to a compound including a structure of Formula (I), and the use of the compound as a dopant in an emitting layer of an organic light emitting diode. The present disclosure also relates to an emitting layer of an organic light emitting diode and an organic light emitting diode device.

Abstract: An aromatic compound represented by chemical formula 1 and an organic light-emitting diode including the same are provided. In chemical formula 1, A, Ar2, R1, R2, and m are as described in the embodiments.

Abstract: A carrier generation material is provided, which has a chemical structure of: wherein R1 is hydrogen or alkyl group; each of R2 is independently hydrogen, halogen, —CN, —CF3, —NO2, or alkyl group; each of R3 is independently hydrogen, halogen, —CN, —CF3, —NO2, or alkyl group; R4 is hydrogen, halogen, —CN, —CF3, —NO2, or alkyl group; R5 is hydrogen, halogen, —CN, —CF3, —NO2, or alkyl group; R6 is ?O, ?NH, or malononitrile group, and R7 is hydrogen, halogen, —CN, —CF3, —NO2, or alkyl group.

Abstract: A 1,9-diazaphenalene derivative is represented by where R, R1, R2, R3, Y1, and Y2 are as defined in the specification and claims. The 1,9-diazaphenalene derivative may emit fluorescence after being excited, and is thus suitable for use as a fluorescent material for an organic light emitting diode. A method for preparing the 1,9-diazaphenalene derivative is also disclosed.

Abstract: Triptycene derivatives having symmetric or asymmetric substituents are provided. The triptycene derivatives of the present invention may be applied in phosphorescent lighting devices ranging from deep blue to red and may be applied as a host material, an electron transporting material or a hole transporting material. An OLED device is also herein disclosed.

Abstract: A carrier generation material is provided, which has a chemical structure of: wherein R1 is hydrogen or alkyl group; each of R2 is independently hydrogen, halogen, —CN, —CF3, —NO2, or alkyl group; each of R3 is independently hydrogen, halogen, —CN, —CF3, —NO2, or alkyl group; R4 is hydrogen, halogen, —CN, —CF3, —NO2, or alkyl group; R5 is hydrogen, halogen, —CN, —CF3, —NO2, or alkyl group; R6 is ?O, ?NH, or malononitrile group, and R7 is hydrogen, halogen, —CN, —CF3, —NO2, or alkyl group.

Abstract: This invention provides a transition metal carbene complexes and the electroluminescent application thereof. Through employing different N?N heteroleptic ligand, the transition metal carbene complex can display wide-range color tuning ability from deep blue to red. The mentioned transition metal carbene complex can be applied in luminescent device, and the luminescent device can display wide-range color tuning ability with high luminescent efficiency while employing different N?N heteroleptic ligand in the transition metal carbene comlex.

Abstract: This invention provides transition metal carbene complexes and the electroluminescent application thereof. Through employing different N^N heteroleptic ligand, as the following, the transition metal carbene complex can display wide-range color tuning ability from deep blue to red. The mentioned transition metal carbene complex can be applied in luminescent device, and the luminescent device can display wide-range color tuning ability with high luminescent efficiency while employing different N^N heteroleptic ligand in the transition metal carbene complex.

Abstract: Organic compounds and organic electroluminescence devices employing the same are provided. The organic compound has a chemical structure as represented as follows: wherein, R1 is independently the same or different C1-6 alkyl, and R2 is independently the same or different hydrogen, halogen, cyano, hydroxy, C1-8 alkyl group, C1-8 alkoxy group, C5-10 aryl, or C2-8 heteroaryl group.

Abstract: Aromatic derivatives having an electron donating group and an electron accepting group at each end are provided. The aromatic derivatives of the present invention can emit blue or green light and may function as a host material or a dopant material. An OLED device using the aromatic derivatives is also herein disclosed.

Abstract: A 1,9-diazaphenalene derivative is represented by where R, R1, R2, R3, Y1, and Y2 are as defined in the specification and claims. The 1,9-diazaphenalene derivative may emit fluorescence after being excited, and is thus suitable for use as a fluorescent material for an organic light emitting diode. A method for preparing the 1,9-diazaphenalene derivative is also disclosed.

Abstract: An aminoferrocene derivative is represented by the formula (I): wherein Ar1 and Ar2 independently represent a substituted or unsubstituted C6-C10 aryl group. The aminoferrocene derivative is useful for forming a p-type carrier generation layer of a tandem OLED so that the tandem OLED has superior luminous efficiencies in terms of maximum luminance, maximum external quantum efficiency, maximum current efficiency, etc.

Abstract: A 6H-indeno[2,1-b]quinoline derivative has a structure of formula (I). Each of Ar1 and Ar2 is a member selected from the group consisting of a substituted or non-substituted aryl group and a substituted or non-substituted heteroaryl group and R1 to R9 are substituents. The 6H-indeno[2,1-b]quinoline derivative of the present invention is provided with thermal stability. Chemical compounds of the present invention are adequate for the materials of the light-emitting layer of an OLED device with high device performance.

Abstract: Organic compounds and organic electroluminescence devices employing the same are provided. The organic compound has a chemical structure represented below: wherein, R1 are independently a hydrogen, or C1-8 alkyl; and R2 is a hydrogen, hydroxy, or C1-8 alkoxy. The organic compounds have a high triplet energy (tEg) gap and apt to transmit the energy to a guest emitter.