Abstract: A fused aromatic derivative shown by the following formula (1): wherein Ra and Rb are independently a hydrogen atom or a substituent, p is an integer of 1 to 8 and q is an integer of 1 to 11, and when p and q are two or more, Ras and Rbs may be independently the same or different, and adjacent substituents Ras may form a ring, L1 is a single bond or a substituted or unsubstituted divalent linking group, and Ar1 is a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms or a substituted or unsubstituted heteroaryl group having 5 to 50 ring atoms, provided that when L1 is a single bond and at least one of Ras is not a hydrogen atom, Ar1 is not a triphenylenyl group, and provided that substituents of L1 and Ar1, and Ra and Rb contain no amino group.

Abstract: A compound represented by the following formula (1):

Abstract: A compound represented by formula (1): wherein R1 to R6, R7 to R10, R11 to R14, R15 to R18, L1, L2, Ar1, and Ar2 are as defined in the description realizes an organic electroluminescence device with long lifetime.

Abstract: A compound of general formula (I): wherein A1, A2, A3, A4, B1, B2, B3, B4, C1, C2, C3, C4, X1 and X2 have the meanings as defined in the description provides electronic devices, preferably OLEDs, which ensure good efficiencies, good operative lifetimes and a high stability to thermal stress, and a low use and operating voltage of the OLEDs.

Abstract: A compound is represented by the following formula (1). In the formula (1), Ar is a substituted or unsubstituted aryl group including 6 to 30 ring carbon atoms, Ra are independently a substituted or unsubstituted alkyl group including 1 to 15 carbon atoms, or a substituted or unsubstituted cycloalkyl group including 3 to 15 carbon atoms, Rb1 to Rb4 are independently a halogen atom, a cyano group, a substituted or unsubstituted alkyl group including 1 to 15 carbon atoms, or the like, Rc1 to Rc10 are independently a hydrogen atom, a halogen atom, a cyano group, a substituted or unsubstituted alkyl group including 1 to 15 carbon atoms, or the like, * is a bonding position at which one of Rc1 to Rc10 is bonded to either nitrogen atom, x is an integer from 0 to 3, y is an integer from 0 to 4, and z are independently an integer from 0 to 5.

Abstract: An organic light-emitting medium including a pyrene derivative represented by the following formula (1) and a phenyl-substituted anthracene derivative represented by the following formula (2): wherein Ar1 to Ar4 are independently a substituted or unsubstituted aryl group having 6 to 30 ring carbon atoms or a substituted or unsubstituted heteroaryl group having 5 to 20 ring atoms.

Abstract: Benzimidazolo[1,2-a]benzimidazole carrying benzimidazolo[1,2-a]benzimidazolylyl groups, carbazolyl groups, dibenzofurane groups, dibenzothiophene groups, fluorenyl groups or dibenzosilolyl groups, an organic electronic device, comprising said benzimidazolo[1,2-a]benzimidazole carrying groups, a charge transport layer, charge blocking layer, charge/exciton blocking layer, or an emitting layer comprising said benzimidazolo[1,2-a]benzimidazole carrying groups, an apparatus selected from the group consisting of stationary visual display units; mobile visual display units; illumination units; keyboards; items of clothing; furniture; wallpaper, comprising said organic electronic device, or said charge transport layer, said charge/exciton blocking layer, or said emitting layer, the use of said benzimidazolo[1,2-a]benzimidazole carrying groups for organic electroluminescent devices, electrophotographic photoreceptors, photoelectric converters, organic solar cells, switching elements, organic light emitting field effe

Abstract: Disclosed herein are benzimidazolo[1,2-a]benzimidazole compounds containing benzimidazolo[1,2-a]benzimidazolylyl groups, carbazolyl groups, dibenzofurane groups, dibenzothiophene groups, fluorenyl groups and/or dibenzosilolyl groups. Also disclosed herein are organic electronic devices containing the benzimidazolo[1,2-a]benzimidazole compound(s), a charge transport layer, charge blocking layer/exciton blocking layer, or an emitting layer containing the benzimidazolo[1,2-a]benzimidazole compound(s), as well as apparatuses selected from stationary visual display units, mobile visual display units, illumination units, keyboards, items of clothing, furniture, or wallpaper, containing the organic electronic device, or the charge transport layer, the charge/exciton blocking layer, or the emitting layer.

Abstract: A composition contains a mixture of at least two compounds, the at least two compounds containing a first compound represented by a formula (1) and a second compound represented by a formula (2). In the formula (1), R1 to R4, A1 and A2 include five cyclic structures in total each represented by a formula (1a) below. In the formula (2), one of A3 and A4 is a substituent represented by a formula (2a), and the other thereof is represented by a formula (2b).

Abstract: Disclosed herein are benzimidazolo[1,2-a]benzimidazole compounds containing at least one triazine group. Also disclosed herein are organic electronic devices containing the benzimidazolo[1,2-a]benzimidazole compounds, an electron transport layer, and an electron injection layer, or an emitting layer containing the benzimidazolo[1,2-a]benzimidazole compounds. Also disclosed herein are apparatuses selected from stationary visual display units, mobile visual display units, illumination units, keyboards, items of clothing, furniture, or wallpaper, containing the benzimidazolo[1,2-a]benzimidazole compounds, and use of the benzimidazolo[1,2-a]benzimidazole compounds, for organic electroluminescent devices, electrophotographic photoreceptors, photoelectric converters, organic solar cells, switching elements, organic light emitting field effect transistors, and image sensors or dye lasers. Also disclosed are processes for preparing the benzimidazolo[1,2-a]benzimidazole compounds.

Abstract: [Object] To provide a light emitting element having a configuration in which a color change depending on the current density is less likely to occur. [Solution] A light emitting element includes: a structure in which an anode 51, an organic layer 70 containing an organic material and including a light emitting layer, and a cathode 52 are stacked. The light emitting layer includes, from a side of the anode to a side of the cathode, two or more light emitting regions configured to emit different colors of light. Each light emitting region contains a host material and a dopant material. An absolute value of an ionization potential of the host material contained in a light emitting region near to the cathode is larger than an absolute value of an ionization potential of the host material contained in a light emitting region near to the anode.

Abstract: A compound represented by formula (1) provides a high performance organic electroluminescence device and a novel material for realizing such an organic electroluminescence device: wherein R1 to R6, a to f, L1 to L3, and Ar are as defined in the description.

Abstract: A compound represented by formula (1) provides an organic electroluminescence device having the performance improved: wherein R1 to R3, a to c, L1 to L3, Ar1, and Ar2 are as defined in the description.

Abstract: An organic electroluminescence device comprising an anode, a cathode and an emitting layer between the anode and the cathode, wherein the emitting layer comprises as a host material a compound represented by the following formula (1) and a compound represented by the following formula (2):

Abstract: An anthracene derivative represented by the following formula (1): wherein in the formula (1), L1 is selected from a single bond and a linking group, and the linking group is selected from a divalent arylene group, a divalent heterocyclic group, and a group formed by linking of 2 to 4 of divalent arylene groups and/or divalent heterocyclic groups. Ar1 is selected from the following formulas (2) and (3). In the formulas (2) and (3), X is selected from an oxygen atom and a sulfur atom. In the formula (2), any one of R11 to R14 is used for bonding to L1. In the formula (3), any one of R21 to R24 is used for bonding to L1. Ar2 is selected from a substituted or unsubstituted aryl group including 6 to 50 ring carbon atoms and a substituted or unsubstituted heterocyclic group including 5 to 50 ring atoms.

Abstract: An organic light-emitting medium including a pyrene derivative represented by the following formula (1) and a phenyl-substituted anthracene derivative represented by the following formula (2): wherein Ar1 to Ar4 are independently a substituted or unsubstituted aryl group having 6 to 30 ring carbon atoms or a substituted or unsubstituted heteroaryl group having 5 to 20 ring atoms.

Abstract: A heterocyclic compound wherein three five-membered rings are fused to one benzene ring and a saturated or unsaturated ring is fused to each five-membered ring. An organic electroluminescence device includes one or more organic thin film layers between an anode and a cathode. The one or more organic thin film layers include a light emitting layer. At least one layer of the one or more organic thin film layers includes the heterocyclic compound.

Abstract: An organic electroluminescence device having good emission efficiency is provided. The organic electroluminescence device includes an amine compound which includes a benzofluorene structure and an aryl group and/or a heteroaryl group, wherein the benzofluorene structure has a specific substituent at 9-position of the fluorene ring.

Abstract: A compound represented by formula (1): wherein R1 to R6, R7 to R10, R11 to R14, R15 to R18, L1, L2, Ar1, and Ar2 are as defined in the description realizes an organic electroluminescence device with long lifetime.

Abstract: Provided are an organic electroluminescence device that not only provides high efficiency but also has a long lifetime, and an aromatic amine derivative that realizes the device. The organic electroluminescence device includes an aromatic amine derivative, including at least one substituent A having dibenzofuran and at least one substituent B selected from groups each having dibenzofuran or carbazole, in a molecule thereof, in which the substituent A and the substituent B include groups different from each other, and the substituent A and the substituent B are bonded to the same nitrogen atom, or different nitrogen atoms, in the molecule. The molecules of the aromatic amine derivative hardly crystallize, which improves a yield in the production of the organic electroluminescence device.