Abstract: An organic electroluminescence device includes: an anode; a cathode opposite the anode; and an organic layer interposed between the anode and the cathode, in which the organic layer includes: an emitting layer; and a first electron transporting layer and a second electron transporting layer which are provided on a side of the emitting layer near the cathode. The first electron transporting layer includes a compound represented by a formula (1) below, and the second electron transporting layer includes a compound represented by a formula (2) below.

Abstract: A top emission organic EL device includes an anode, hole transporting zone, emitting layer, electron transporting zone, and cathode in this order. The hole transporting zone includes: a first layer interposed between the anode and the emitting layer; and a second layer interposed between the first layer and the emitting layer. The first layer contains a first compound and the second layer contains a second compound. A film thickness of the first layer and the second layer satisfies a formula (1) and (2), respectively. A hole mobility ?H1 of the first compound satisfies a formula (3) and a hole mobility ?H2 of the second compound satisfies a formula (4), 100 nm?d1?300 nm??(1) 1 nm?d2?20 nm??(2) 1.0×10?4 [cm2/Vs]??H1?1.0×10?1 [cm2/Vs]??(3) 1.0×10?10 [cm2/Vs]??H2?1.0×10?6 [cm2/Vs]??(4).

Abstract: An aromatic amine derivative represented by formula (1): wherein R1, R2, R3, L, Ar1, Ar2, k, m, and n are the same as defined in the specification, is useful as a material for an organic EL device and realizes an organic EL device with a high efficiency and a long lifetime even when driving it at a low voltage.

Abstract: An aromatic amine derivative represented by formula (1): wherein R1, R2, R3, L, Ar1, Ar2, k, m, and n are the same as defined in the specification, is useful as a material for an organic EL device and realizes an organic EL device with a high efficiency and a long lifetime even when driving it at a low voltage.

Abstract: An organic EL device includes an anode, an emitting layer, an electron transporting zone and a cathode in this sequence, in which the electron transporting zone contains an aromatic heterocyclic derivative represented by a formula (1) below. In the formula (1), X1 to X3 are a nitrogen atom or CR1, and A is represented by a formula (2) below. In the formula (2), L1 is s single bond or a linking group, and HAr is represented by a formula (3) below. In the formula (3), Y1 is an oxygen atom, a sulfur atom or the like, and one of X11 to X18 is a carbon atom bonded to L1 by a single bond and the rest of X11 to X18 are a nitrogen atom or CR13.

Abstract: An organic EL device includes an anode, an emitting layer, an electron transporting zone and a cathode in this sequence, in which the electron transporting zone contains an aromatic heterocyclic derivative represented by a formula (1) below. In the formula (1), X1 to X3 are a nitrogen atom or CR1, and A is represented by a formula (2) below. In the formula (2), L1 is s single bond or a linking group, and HAr is represented by a formula (3) below. In the formula (3), Y1 is an oxygen atom, a sulfur atom or the like, and one of X11 to X18 is a carbon atom bonded to L1 by a single bond and the rest of X11 to X18 are a nitrogen atom or CR13.

Abstract: An aromatic amine derivative represented by formula (1): wherein R1, R2, R3, L, Ar1, Ar2, k, m, and n are the same as defined in the specification, is useful as a material for an organic EL device and realizes an organic EL device with a high efficiency and a long lifetime even when driving it at a low voltage.

Abstract: An aromatic amine derivative represented by formula (1): wherein HAr1, Ar2, L1, L2, and L3 are as defined in the specification, is useful as a material for constituting an organic EL device and realizes an organic EL device having a high efficiency and a long lifetime even when driving at a low voltage.

Abstract: A top emission organic EL device includes an anode, hole transporting zone, emitting layer, electron transporting zone, and cathode in this order. The hole transporting zone includes: a first layer interposed between the anode and the emitting layer; and a second layer interposed between the first layer and the emitting layer. The first layer contains a first compound and the second layer contains a second compound. A film thickness of the first layer and the second layer satisfies a formula (1) and (2), respectively. A hole mobility ?H1 of the first compound satisfies a formula (3) and a hole mobility ?H2 of the second compound satisfies a formula (4), 100 nm?d1?300 nm??(1) 1 nm?d2?20 nm??(2) 1.0×10?4 [cm2/Vs]??H1?1.0×10?1 [cm2/Vs]??(3) 1.0×10?10 [cm2/Vs]??H2?1.0×10?6 [cm2/Vs]??(4).

Abstract: An aromatic amine derivative represented by formula (1): wherein R1, R2, R3, L, Ar1, Ar2, k, m, and n are the same as defined in the specification, is useful as a material for an organic EL device and realizes an organic EL device with a high efficiency and a long lifetime even when driving it at a low voltage.

Abstract: An aromatic amine derivative represented by formula (1): wherein R1, R2, R3, L, Ar1, Ar2, k, m, and n are the same as defined in the specification, is useful as a material for an organic EL device and realizes an organic EL device with a high efficiency and a long lifetime even when driving it at a low voltage.

Abstract: A compound is represented by a formula (1) below. In the formula (1), X1 to X8 each independently represent a carbon atom to be bonded to a group represented by the following formula (20), CRX or a nitrogen atom. At least one of X1 to X8 is a carbon atom to be bonded to the group represented by the following formula (2). RX is each independently a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, or the like.

Abstract: An organic EL device includes an anode, an emitting layer, an electron transporting zone and a cathode in this sequence, in which the electron transporting zone contains an aromatic heterocyclic derivative represented by a formula (1) below. In the formula (1), X1 to X3 are a nitrogen atom or CR1, and A is represented by a formula (2) below. In the formula (2), L1 is s single bond or a linking group, and HAr is represented by a formula (3) below. In the formula (3), Y1 is an oxygen atom, a sulfur atom or the like, and one of X11 to X18 is a carbon atom bonded to L1 by a single bond and the rest of X11 to X18 are a nitrogen atom or CR13.

Abstract: An organic EL device includes an anode, an emitting layer, an electron transporting zone and a cathode in this sequence, in which the electron transporting zone contains an aromatic heterocyclic derivative represented by a formula (1) below. In the formula (1), X1 to X3 are a nitrogen atom or CR1, and A is represented by a formula (2) below. In the formula (2), L1 is s single bond or a linking group, and HAr is represented by a formula (3) below. In the formula (3), Y1 is an oxygen atom, a sulfur atom or the like, and one of X11 to X18 is a carbon atom bonded to L1 by a single bond and the rest of X11 to X18 are a nitrogen atom or CR13.

Abstract: Provided are an organic electroluminescence device having high current efficiency and a long lifetime, and a biscarbazole derivative for realizing the device. The biscarbazole derivative has a specific substituent. The organic EL device has a plurality of organic thin-film layers including a light emitting layer between a cathode and an anode, and at least one layer of the organic thin-film layers contains the biscarbazole derivative.

Abstract: An organic EL device includes an anode, an emitting layer, an electron transporting zone and a cathode in this sequence, in which the electron transporting zone contains an aromatic heterocyclic derivative represented by a formula (1) below. In the formula (1), X1 to X3 are a nitrogen atom or CR1, and A is represented by a formula (2) below. In the formula (2), L1 is s single bond or a linking group, and HAr is represented by a formula (3) below.

Abstract: An organic EL device includes an anode, an emitting layer, an electron transporting zone and a cathode in this sequence, in which the electron transporting zone contains an aromatic heterocyclic derivative represented by a formula (1) below. In the formula (1), X1 to X3 are a nitrogen atom or CR1, and A is represented by a formula (2) below. In the formula (2), L1 is s single bond or a linking group, and HAr is represented by a formula (3) below. In the formula (3), Y1 is an oxygen atom, a sulfur atom or the like, and one of X11 to X18 is a carbon atom bonded to L1 by a single bond and the rest of X11 to X18 are a nitrogen atom or CR13.

Abstract: An aromatic amine derivative represented by formula (1): wherein R1, R2, R3, L, AR1, Ar2, k, m, and n are the same as defined in the specification, is useful as a material for an organic EL device and realizes an organic EL device with a high efficiency and a long lifetime even when driving it at a low voltage.

Abstract: An organic electroluminescence device contains an anode and a cathode facing each other, and intervening therebetween at least two hole transporting layers and a light emitting layer sequentially, and one of the hole transporting layers contains a compound having a particular structure having a fluorene structure at the center thereof, and is not adjacent to the light emitting layer. The organic electroluminescence device has a hole transporting layer having an increased thickness, is capable of being controlled in the thickness of the optical film, and has an enhanced device capability.

Abstract: An aromatic amine derivative represented by formula (1): wherein R1, R2, R3, L, Ar1, Ar2, k, m, and n are the same as defined in the specification, is useful as a material for an organic EL device and realizes an organic EL device with a high efficiency and a long lifetime even when driving it at a low voltage.