Abstract: An organic electroluminescence device includes a first emitting unit, a first charge generating layer, a second emitting unit, a second charge generating layer, and a third emitting unit provided between an anode and a cathode in this order from the anode, in which the second charge generating layer includes an N layer close to the anode and a P layer close to the cathode, the third emitting layer contains a blue fluorescent compound, at least one of the first or second emitting layer contains a blue fluorescent compound, the third emitting unit includes a hole transporting zone between the second charge generating layer and the third emitting layer, the hole transporting zone is in contact with the second charge generating layer, and a thickness of the hole transporting zone is in a range from 5 nm to 40 nm and smaller than a thickness of the N layer.

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 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 compound represented by formula (1): wherein A, B, R1, and R2 are as defined in the description, provides organic electroluminescence (EL) devices having a high emission efficiency when operated at low voltage and a long lifetime and electronic devices including such organic EL devices.

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 compound represented by formula (1): wherein A, B, R1, and R2 are as defined in the description, provides organic electroluminescence (EL) devices having a high emission efficiency when operated at low voltage and a long lifetime and electronic devices including such organic EL devices.

Abstract: An organic electroluminescence device includes a first emitting unit, a first charge generating layer, a second emitting unit, a second charge generating layer, and a third emitting unit provided between an anode and a cathode in this order from the anode, in which the second charge generating layer includes an N layer close to the anode and a P layer close to the cathode, the third emitting layer contains a blue fluorescent compound, at least one of the first or second emitting layer contains a blue fluorescent compound, the third emitting unit includes a hole transporting zone between the second charge generating layer and the third emitting layer, the hole transporting zone is in contact with the second charge generating layer, and a thickness of the hole transporting zone is in a range from 5 nm to 40 nm and smaller than a thickness of the N layer.

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 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 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: 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 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 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: 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: An organic electroluminescence device includes an anode, a cathode and an emitting layer, in which the emitting layer includes a first compound and a second compound and each of the first compound and the second compound is a compound emitting thermally activated delayed fluorescence.

Abstract: The compound represented by formula (1): wherein A, B, R1, and R2 are as defined in the description, provides organic electroluminescence (EL) devices having a high emission efficiency when operated at low voltage and a long lifetime and electronic devices including such organic EL devices.

Abstract: An organic electroluminescence device includes an anode, a cathode and an emitting layer, in which the emitting layer includes a first compound and a second compound and each of the first compound and the second compound is a compound emitting thermally activated delayed fluorescence.

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: An organic electroluminescence device includes a cathode, an anode, a charge generating layer provided between the cathode and the anode, a first emitting unit provided between the charge generating layer and the cathode, and a second emitting unit provided between the charge generating layer and the anode. The first emitting unit includes a blue emitting layer containing a first compound represented by a formula and a second compound emitting a blue light, in which Z1 is represented by a formula and a cyclic structure represented by a formula or is fused to Z1, and X1 and X2 are each an oxygen atom or a sulfur atom.

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).