Abstract:
A compound is represented by one of formulae (11) to (13). R1 to R4 each independently represent a group represented by a formula (1-1) or the like, or a group represented by a formula (2-1), a group represented by a formula (2-2) or the like. At least one of R1 to R4 is the group represented by the formula (1-1) or the like. At least one of R1 to R4 is the group represented by the formula (2-1), (2-2) or the like. For instance, X1 represents an oxygen atom, a sulfur atom, or CR151R152, R101 to R110 and R151 and R152 each independently representing a hydrogen atom or a substituent. For instance, R161 to R168 and R171 and R180 each independently represent a hydrogen atom or a substituent. * each independently represents a bonding position to a carbon atom in a benzene ring in each of formulae (11) to (13):
Abstract:
An organic electroluminescence device includes an anode, an emitting layer, and a cathode. The emitting layer contains a first compound, a second compound, and a third compound. An ionization potential Ip1 of the first compound and an ionization potential Ip2 of the second compound satisfy a relationship represented by a numerical expression (Numerical Expression 1) below. The first compound is a delayed fluorescent compound. The second compound is a fluorescent compound. The third compound has an electron mobility of 1×10−8 cm2/(V·s) or more. 0≤Ip2−Ip1≤0.8 [eV] (Numerical Expression 1)
Abstract:
An organic electroluminescence device includes a pair of electrodes and an organic compound layer interposed therebetween. The organic compound layer includes a plurality of emitting layers at least including a first emitting layer and a second emitting layer. The first emitting layer contains a first host material and a fluorescent first luminescent material. The second emitting layer contains a second luminescent material that is different from the first luminescent material. A difference ΔST(H1) between singlet energy EgS(H1) of the first host material and an energy gap Eg77K(H1) at 77[K] of the first host material satisfies a specific relationship. One of the first luminescent material and the second luminescent material has a main peak wavelength from 400 nm to less than 500 nm and the other of the first luminescent material and the second luminescent material has a main peak wavelength from 500 nm to 700 nm.
Abstract:
An organic EL device includes a pair of electrodes and an organic compound layer between pair of electrodes. The organic compound layer includes an emitting layer including a first material and a second material. The second material is a fluorescent material. Singlet energy EgS(H) of the first material and singlet energy EgS(D) of the second material satisfy a relationship of the following formula (1). The first material satisfies a relationship of the following formula (2) in terms of a difference ΔST(H) between the singlet energy EgS(H) and an energy gap Eg77K(H) at 77K. EgS(H)>EgS(D) (1) ΔST(H)=EgS(H)−Eg77K(H)
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 compound represented by a formula (1) below and the second compound is a fluorescent compound.
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:
A biscarbazole derivative of the invention is represented by a formula (1) below. In the formula (1): A1 represents a substituted or unsubstituted nitrogen-containing heterocyclic group having 1 to 30 ring carbon atoms; A2 represents a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 ring carbon atoms, or substituted or unsubstituted nitrogen-containing heterocyclic group having 1 to 30 ring carbon atoms; X1 and X2 each are a linking group; Y1 to Y4 each represent a substituent; p and q represent an integer of 1 to 4; and r and s represent an integer of 1 to 3.
Abstract:
An organic electroluminescence device including opposite anode and cathode, and a hole-transporting region, an emitting layer and an electron-transporting region in sequential order from the anode between the anode and the cathode, wherein the emitting layer includes a red emitting portion, a green emitting portion, and a blue emitting portion; the blue emitting portion includes a host BH and a fluorescent dopant FBD; the triplet energy ETfbd of the fluorescent dopant FBD is larger than the triplet energy ETbh of the host BH; the green emitting portion includes a host GH and a phosphorescent dopant PGD; the electron-transporting region includes a common electron-transporting layer adjacent to the red emitting portion, the green emitting portion and the blue emitting portion; the common electron-transporting layer includes a material having a triplet energy ETel larger than ETbh; and the difference between the affinity of the host GH and the affinity of the material constituting the common electron-transporting layer is 0.4 eV or less.
Abstract:
A compound may include partial structures of formula (3-11B) and (31a), mutually bonded in one molecule:
R314 being a single bond bonded to * in formula (31a), R300 being independently H or a substituent, or at least one of adjacent pairs of R300 are mutually bonded to form a ring, or R300 is a single bond bonded to another atom/structure in the molecule, one or more R300 is H, at least one of H being D, Y12 to Y16 being independently N, CR31, or C bonded to another atom/structure in the molecule, 1 to 3 of Y12 to Y16 being N, and R31 independently being H or a substituent.
Abstract:
An organic electroluminescence device includes an anode, an emitting layer, and a cathode in this order. The emitting layer contains a compound, including a structure including a first partial structure of formula (3-100) and a second partial structure of formula (3-1A), mutually bonded in one molecule:
In formula (3-100), D1 to D3 are each a deuterium atom, or one of D1 to D8 is a single bond to another atom/structure in the molecule, and remaining D1 to D8 are each a deuterium atom, and R310 is a single bond bonded to the second partial structure. In formula (3-1A), one of R301 to R306 is a single bond bonded to the first partial structure, and remaining R301 to R306 not being bonded to the first partial structure are independently H, a substituent, or a single bond bonded to another atom/structure in the molecule.