Abstract:
An organic electroluminescent device including: an anode, a cathode, an emitting layer formed of an organic compound and interposed between the cathode and the anode, and two or more layers provided in a hole-injecting/hole-transporting region between the anode and the emitting layer; of the layers which are provided in the hole-injecting/hole-transporting region, a layer which is in contact with the emitting layer containing a compound represented by the formula (1); and of the layers which are provided in the hole-injecting/hole-transporting region, a layer which is interposed between the anode and the layer which is in contact with the emitting layer containing an amine derivative represented by the formula (2).
Abstract:
A compound of formula (7) is provided wherein L4 is a linking group selected from the group consisting of: provided that an asterisk (*) indicates the position bonding to the nitrogen atom of the carbazolyl group, R6 to R13 are independently a hydrogen atom, or a phenyl group, Ar17 is an unsubstituted phenylphenyl group, and Ar18 is a phenylphenyl group which may be substituted by a phenyl group or a naphthyl group, or a phenyl group which may be substituted by a naphthyl group.
Abstract:
Provided are: an aromatic amine derivative in which a terminal substituent such as a dibenzofuran ring or a dibenzothiophene ring is bonded to a nitrogen atom directly or through an arylene group or the like; an organic electroluminescence device including an organic thin film layer formed of one or more layers including a light emitting layer and interposed between a cathode and an anode in which a layer of the organic thin film layer contains the aromatic amine derivative by itself or as a component of a mixture, and the device has a long lifetime and high luminous efficiency; and an aromatic amine derivative for realizing the device.
Abstract:
An aromatic amine derivative represented by the following formula (1)wherein at least one of Ar1 to Ar4 is a heterocyclic group represented by the following formula (2) wherein X1 is an oxygen atom or a sulfur atom.
Abstract:
A compound represented by formula (1) provides an organic electroluminescence device having a high efficiency and a long lifetime: wherein R1 to R5, R6 to R10, and R11 to R18 are as defined in the description.
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. Also disclosed herein is the use of the benzimidazolo[1,2-a]benzimidazole compound(s) for organic electroluminescent devices, electrophotographic photoreceptors, photoelectric converters, organic solar cells, switching elements, organic light emitting field effect transistors, image sensors or dye lasers, and processes for preparing benzimidazolo[1,2-a]benzimidazole compounds.
Abstract:
An aromatic amine derivative represented by the following formula (1): wherein at least one of R1 to R8 is a group other than a hydrogen atom, Ar1 to Ar4 are a substituted or unsubstituted aryl group having 6 to 30 ring carbon atoms.
Abstract:
Anthracene derivatives each having a structure including an anthracene skeleton, a phenanthrene skeleton selected from among various phenanthrene skeletons different in bonding site which is bonded to the 9-position of the anthracene skeleton and a group selected from among various aryl groups and so on which is bonded to the 10-position of the anthracene skeleton. Organic EL devices made by using the derivatives exhibit high light emission efficiency and a long life.
Abstract:
An organic electroluminescence device having higher performance, in particular exhibiting a better driving voltage and a better external quantum efficiency, while having an extended lifetime; and an electronic equipment provided with the organic electroluminescence device are provided. In addition, a compound for realizing the same device and equipment is provided. Specifically, a compound having a specific structure having a triphenylene skeleton; an organic electroluminescence device using the compound; and an electronic equipment provided with the organic electroluminescence device were provided.