Abstract: An organic electroluminescence device including at least an anode, an emitting layer, an electron-transporting region and a cathode in sequential order, wherein the emitting layer contains a host and a dopant which gives fluorescent emission of which the main peak wavelength is 550 nm or less; the affinity Ad of the dopant is equal to or larger than the affinity Ah of the host; the triplet energy ETd of the dopant is larger than the triplet energy ETh of the host; and a blocking layer is provided within the electron-transporting region such that it is adjacent to the emitting layer, and the triplet energy ETb of the blocking layer is larger than ETh.

Abstract: A composition for an organic electroluminescent device is a composition for forming an organic light emitting layer of an organic electroluminescent device by wet coating process. The composition contains a phosphorescent material, a charge transport material, and a solvent, in which the phosphorescent material and the charge transport material are each an unpolymerized organic compound, and the first oxidation potential of the phosphorescent material ED+, the first reduction potential of the phosphorescent material ED?, the first oxidation potential of the charge transporting material ET+, and the first reduction potential of the charge transporting material ET? satisfy the following condition: ET?+0.1?ED?<ET+?ED+?0.1 or ED?+0.1?ET?<ED+?ET+?0.1.

Abstract: An organic electroluminescence device sequentially includes an anode, an emitting layer, an electron-transporting region, and a cathode, the electron-transporting region including an electron-transporting material that includes a cyano group and an aromatic ring group.

Abstract: An oxygen-containing fused ring derivative represented by the following formula (1) wherein Ar1 is an m-valent fused ring group in which four or more rings including one or more rings selected from a furan ring and a pyran ring are fused and HAr is any of the nitrogen-containing heterocyclic group represented by the following formulas (2) to (5):

Abstract: An organic electroluminescence device includes an anode, an emitting layer and a cathode, in which the emitting layer includes a first compound, a second compound and a third compound. The first compound is a delayed fluorescent compound. The first compound has an energy gap T77K at 77 [K] larger than an energy gap T77K at 77 [K] of the second compound. The third compound has an energy gap T77K at 77 [K] larger than the energy gap T77K at 77 [K] of the second compound. The second compound has a fused ring structure represented by a formula (2) below and has eight or less rings in total.

Abstract: An organic electroluminescence device that includes an anode, an emitting layer that includes a host and a fluorescent dopant, an electron transporting zone, a cathode, a blocking layer adjacent to the emitting layer in the electron transporting zone where the blocking layer includes an aromatic heterocyclic derivative with an azine ring and where the triplet energy ETb (eV) of the aromatic heterocyclic derivative is larger than a triplet energy ETh (eV) of the host.

Abstract: A composition for an organic electroluminescent device is a composition for forming an organic light emitting layer of an organic electroluminescent device by wet coating process. The composition contains a phosphorescent material, a charge transport material, and a solvent, in which the phosphorescent material and the charge transport material are each an unpolymerized organic compound, and the first oxidation potential of the phosphorescent material ED+, the first reduction potential of the phosphorescent material ED?, the first oxidation potential of the charge transporting material ET+, and the first reduction potential of the charge transporting material ET? satisfy the following condition: ET?+0.1?ED?<ET+?ED+?0.1 or ED?+0.1?ET?<ED+?ET+?0.1.

Abstract: An organic electroluminescence device includes an anode, an emitting layer and a cathode, in which the emitting layer includes a first compound and a second compound. The first compound is a delayed-fluorescent compound. The second compound is represented by a formula (2) below, in which X is a nitrogen atom or a carbon atom bonded to Y; R21 to R26 are each independently a hydrogen atom or a substituent; Z21 and Z22 are each independently selected from the group consisting of a halogen atom, a substituted or unsubstituted aryl group, a substituted or unsubstituted alkoxy group, and a substituted or unsubstituted aryloxy group.

Abstract: An object of the invention is to provide a high-performance organic electroluminescence device and an electronic device including the organic electroluminescence device. 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, the first compound is a delayed fluorescent compound, and the second compound is represented by a formula (2) below.

Abstract: A composition for an organic electroluminescent device is a composition for forming an organic light emitting layer of an organic electroluminescent device by wet coating process. The composition contains a phosphorescent material, a charge transport material, and a solvent, in which the phosphorescent material and the charge transport material are each an unpolymerized organic compound, and the first oxidation potential of the phosphorescent material ED+, the first reduction potential of the phosphorescent material ED?, the first oxidation potential of the charge transporting material ET+, and the first reduction potential of the charge transporting material ET? satisfy the following condition: ET?+0.1?ED?<ET+?ED+?0.1 or ED?+0.1?ET?<ED+?ET+?0.1.

Abstract: An organic electroluminescence device includes a pair of electrodes and an organic compound layer therebetween. The organic compound layer includes an emitting layer. The emitting layer includes a pyrene derivative represented by formula (1), such that a content of the pyrene derivative in the emitting layer is 50 to 100 wt %. Ar1 and Ar2 are independently a substituted or unsubstituted aryl group having 6 to 30 ring carbon atoms. X1 and X3 to X8 are a hydrogen atom. X2 is a substituted or unsubstituted aryl group having 6 to 30 ring carbon atoms, provided that Ar1 or Ar2 is different from X2. In a case where any of Ar1, Ar2, and X2 is the aryl group having a substituent, the substituent is independently an alkyl group, a cycloalkyl group, an aryl group, a silyl group, or a cyano group.

Abstract: An organic electroluminescence device that includes an anode, an emitting layer that includes a host and a fluorescent dopant, an electron transporting zone, a cathode, a blocking layer adjacent to the emitting layer in the electron transporting zone where the blocking layer includes an aromatic heterocyclic derivative with an azine ring and where the triplet energy ETb (eV) of the aromatic heterocyclic derivative is larger than a triplet energy ETh (eV) of the host.

Abstract: A benzo[k]fluoranthene derivative represented by the following formula (1): wherein R1 to R12 are as defined in the specification. The benzo[k]fluoranthene derivative represented by the formula (1) reduces a driving voltage of an organic electroluminescence device and makes it possible to realize light emission with high efficiency and long lifetime.

Abstract: A compound is shown by the following formula (1). wherein l, m, and n are independently an integer from 1 to 3, Ar1 to Ar4 are independently a substituted or unsubstituted aryl group having 6 to 30 ring carbon atoms, or a substituted or unsubstituted heteroaryl group having 5 to 30 ring atoms, Ar5, Ar6, and Ar7 are independently a substituted or unsubstituted arylene group having 6 to 30 ring carbon atoms, or a substituted or unsubstituted heteroarylene group having 5 to 30 ring atoms, and p is an integer from 0 to 2, and Ar6 and N are bonded via a single bond when p is 0, provided that at least one of Ar1 to Ar4 is substituted with a substituted silyl group, a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, or a substituted or unsubstituted cycloalkyl group having 3 to 10 carbon atoms, and at least one of Ar1 to Ar4 is substituted with a cyano group.

Abstract: A fluorene-containing aromatic compound represented by a formula (1) below. In the formula (1): Nr1 represents a substituted or unsubstituted monocyclic nitrogen-containing aromatic ring having 2 to 5 ring carbon atoms, or a bicyclic nitrogen-containing aromatic ring having 2 to 9 ring carbon atoms; Ar represents an aromatic ring and the like; Fl1 and Fl2 represent a fluorenyl group; and Cz1 and Cz2 represent a carbazolyl group. A compound represented by a formula (2) below is omitted from the fluorene-containing aromatic compound represented by the formula (1).

Abstract: An organic electroluminescence device including: an anode (10), a cathode (70), an emitting layer (40) including an organic compound, which is between the anode (10) and the cathode (70), two or more layers arranged in a hole injection and transport region which is between the anode (10) and the emitting layer (40), and one or more layers arranged in an electron injection and transport region which is between the emitting layer (40) and the cathode (70), wherein a layer in the hole injection and transport region, which is in contact with the emitting layer (40), includes an aromatic amine derivative having a carbazole skeleton, one of the layers other than the layer in contact with the emitting layer (40) in the hole injection and transport region includes one or more materials selected from the group consisting of thiophene derivatives, tricyclic or more cyclic fused aromatic derivatives, amine derivatives excluding the compound represented by the following formula (A), conductive polymers, CFx, CuPc, transi

Abstract: A pyrene derivative represented by the following formula (1); wherein R1 to R10 are independently a hydrogen atom, a substituted or unsubstituted aryl group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted cycloalkyl group or a group represented by the following formula (2), at least one of R1 to R10 is a group represented by the following formula (2) and at least two of R1 to R10 are substituted or unsubstituted aryl group. Provided that in the case where only one of R1 to R10 is a group represented by the following formula (2), at least one of the substituted or unsubstituted aryl groups is an aryl group having 10 to 50 carbon atoms.

Abstract: An organic electroluminescence device including an anode, an emitting layer, a blocking layer, an electron-injecting layer and a cathode in sequential order; wherein the emitting layer contains a host and a dopant which gives fluorescent emission of which the main peak wavelength is 550 nm or less; the affinity Ad of the dopant is smaller than the affinity Ah of the host; the triplet energy ETd of the dopant is larger than the triplet energy ETh of the host; the triplet energy ETb of the blocking layer is larger than ETh; and the blocking layer includes an aromatic hydrocarbon compound.

Abstract: A nitrogen-containing heterocyclic derivative represented by the following formula (1): wherein any “12-a” groups of R1 to R12 are independently a hydrogen atom, a fluorine atom, a substituted or unsubstituted aryl group having 6 to 30 ring carbon atoms or a substituted or unsubstituted heterocyclic group having 5 to 30 ring atoms; any “a” groups of R1 to R12 are independently a single bond which is bonded to L1; L1 is a single bond, a “b+1” valent substituted or unsubstituted hydrocarbon ring group having 6 to 30 ring carbon atoms or a “b+1” valent substituted or unsubstituted heterocyclic group having 5 to 30 ring atoms; HAr is a substituted or unsubstituted nitrogen-containing heterocyclic group; and “a” and “b” are independently an integer of 1 to 4, and at least one of “a” and “b” is 1.

Abstract: An organic electroluminescence device that includes an anode, an emitting layer that includes a host and a dopant, a blocking layer, an electron injecting layer, and a cathode where the blocking layer includes an aromatic heterocyclic derivative, the triplet energy ETb (eV) of the blocking layer is larger than a triplet energy ETh (eV) of the host, and the affinity Ab (eV) of the blocking layer and an affinity Ae (eV) of the electron injecting layer satisfy a relationship of Ae?Ab<0.2.