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: Compounds of formulae (2-7) or (2-9) are provided: Also provided are organic electroluminescence (EL) devices containing the compounds 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 solid up-conversion material contains a triplet sensitizer and an organic luminescent material. The triplet sensitizer and the organic luminescent material satisfy relations of a numerical formula (Numerical Formula 1) and a numerical formula (Numerical Formula 2), and the triplet sensitizer and the organic luminescent material form a solid solution crystal. T1(M1)?T1(M2)??(Numerical Formula 1) S1(M2)>S1(M1)??(Numerical Formula 2) (S1(M1) is the lowest singlet energy of the triplet sensitizer, T1(M1) is the lowest triplet energy of the triplet sensitizer, S1(M2) is the lowest singlet energy of the organic luminescent material, and T1(M2) is the lowest triplet energy of the organic luminescent material.

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: Compounds of formulae (2-7) or (2-9) are provided: Also provided are organic electroluminescence (EL) devices containing the compounds 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: 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.