Abstract: A compound is represented by a formula (1) below, in which k is an integer of 0 or more, m is an integer of 1 or more, n is an integer of 2 or more. L is a substituted or unsubstituted aromatic hydrocarbon ring having 6 to 30 ring carbon atoms, CN is a cyano group, and D1 and D2 are each independently represented by one of a formula (2), a formula (3) and formula (3x) below, D1 and D2 being optionally mutually the same or different.

Abstract: The present invention provides a material useful as an organic electroluminescence device material, and particularly provides: a compound having, as a substituent, a substituted aromatic heterocyclic group having a specific structure wherein any of the 1-position to 6-position or the 7-position to 10-position of fluoranthene is substituted with a nitrogen atom; a material for low-voltage organic electroluminescence devices using the compound; and an organic electroluminescence device and an electronic equipment using the material.

Abstract: The present invention provides a compound having a fluoranthene skeleton represented by the formula (1); an organic electroluminescence device having plural organic thin film layers including a light-emitting layer between a cathode and an anode, wherein at least one layer of the organic thin film layers contains the compound; and an electronic equipment provided with the organic electroluminescence device. The organic electroluminescence device realizes further lower voltage driving and has high emission efficiency. [In the formula (1), X1 to X10, L, R1 to R9, and n are as stated in the description.

Abstract: A compound is represented by a formula (1) below, in which k is an integer of 0 or more, m is an integer of 1 or more, n is an integer of 2 or more. L is a substituted or unsubstituted aromatic hydrocarbon ring having 6 to 30 ring carbon atoms, CN is a cyano group, and D1 and D2 are each independently represented by one of a formula (2), a formula (3) and formula (3x) below, D1 and D2 being optionally mutually the same or different.

Abstract: A compound of formula (I), a material for an organic electroluminescence device comprising at least one compound of formula (I); an organic electroluminescence device which comprises an organic thin film layer between a cathode and an anode, wherein the organic thin film layer comprises one or more layers and comprises a light emitting layer, and at least one layer of the organic thin film layer comprises at least one compound of formula (I); an electronic equipment comprising the organic electroluminescence device; and a process for preparing the compound of formula (I).

Abstract: A compound represented by formula (1): wherein Ar is a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted aryl group having 6 to 30 ring carbon atoms, or a substituted or unsubstituted nitrogen-comprising heteroaryl group having 5 to 30 ring atoms; each of L1 and L2 is independently a single bond, a substituted or unsubstituted arylene group having 6 to 30 ring carbon atoms, a substituted or unsubstituted heteroarylene group having 5 to 30 ring atoms, or a substituted or unsubstituted divalent linking group wherein 2 to 4 groups selected from an arylene group having 6 to 30 ring carbon atoms and a heteroarylene group having 5 to 30 ring atoms are bonded to each other via a single bond; A is a monovalent group represented by formula (2); and B is a monovalent group represented by formula (5): wherein R1 to R10 and R21 to R30 are as defined in the description, enables the emission of light of a purer blue (shorter wavelength), a narrower half width (hig

Abstract: Specifically substituted ladder type compounds of formula (I) wherein A is formula (II) a material for an organic electroluminescence device comprising at least one compound of formula (I), and an organic electroluminescence device which comprises one or more organic thin film layers including an emitting layer between a cathode and an anode, wherein at least one layer of the organic thin film layers comprises at least one compound of formula (I).

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

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 EL device with high emission efficiency, an electronic equipment including the organic EL device, and a compound providing the organic EL device are provided.

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: An organic electroluminescence device including an anode, a cathode, and an emitting layer between the anode and the cathode, in which the emitting layer comprises a compound represented by the formula (1) and a compound represented by the formula (2).

Abstract: Specifically substituted benzofuro- and benzothienoquinolines and their use in electronic devices, especially electroluminescent devices. When used as charge transport material, charge blocker material and/or host material in electroluminescent devices, the specifically substituted benzofuro- and benzothienoquinolines may provide improved efficiency, stability, manufacturability, or spectral characteristics of electroluminescent devices and reduced driving voltage of electroluminescent devices.

Abstract: An organic electroluminescence device includes: an anode; a cathode; and a single- or multi-layer organic layer interposed between the anode and the cathode. The organic layer includes at least one emitting layer containing a dopant material represented by a formula below. In the formula, X1 to X5 each independently represent CR1 or a nitrogen atom, at least one of X1 to X5 is a nitrogen atom, L1 represents a divalent aromatic hydrocarbon group or a divalent heterocyclic group, A and B each independently represents a cyclic structure, at least one of the cyclic structure A and the cyclic structure B has a substituent, and R1 represents an aryl group, alkyl group or the like.

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 organic electroluminescence device includes an anode, an emitting layer, an electron-transporting region, and a cathode, the anode, the emitting layer, the electron-transporting region, and the cathode being stacked in this order, the emitting layer including a host material, and a dopant material that emits fluorescence having a main peak wavelength of 550 nm or less, the electron-transporting region including a barrier layer that is adjacent to the emitting layer, and the barrier layer including a barrier material that includes an electron-transporting structural part, and a triplet barrier structural part that includes a fused polycyclic aromatic hydrocarbon compound, and satisfies the relationship “ETb>ETh” (where, ETh is the triplet energy of the host material, and ETb is the triplet energy of the barrier material).