Abstract: An organic compound denoted by formula (1) below. In formula (1), each of R1 to R8 is selected from the group consisting of a hydrogen atom, an alkyl group, and the like. A represents a structure denoted by A above, * represents a position where bonding is performed. In A, B is selected from structures denoted by (B-1) and the like above, * represents a position where bonding is performed. In (B-1) and the like, each of R9 to R17 is selected from a hydrogen atom, an alkyl group, and the like. X represents an oxygen atom or a sulfur atom.

Abstract: The present disclosure provides an organic compound represented by general formula [1] below. In formula [1], Ar1 and Ar2 each represent an alkyl group having 1 to 8 carbon atoms, an aromatic hydrocarbon group having 6 to 18 carbon atoms, or a heteroaromatic group having 3 to 17 carbon atoms. Ar1 and Ar2 may be the same or different. Ar3 and Ar4 are each a substituent having a carbazolyl group. Ar3 and Ar4 may be the same or different. Ar1 to Ar4 may be substituted. At least one of Ar1 to Ar4 has a tert-butyl group. The total number of tert-butyl groups in one molecule of the organic compound is 2 or more.

Abstract: An organic compound represented by the following general formula [1] is provided. In the following general formula [1] IrLmL?n, where L and L? denote different bidentate ligands, the partial structure IrL denotes a partial structure represented by the general formula [A-1] or [A-2], and the partial structure IrL? denotes a partial structure represented by the general formula [B-1] or [B-2].

Abstract: An organic compound represented by general formula [1]: where in formula [1], R1 to R14 are each independently selected from, for example, a hydrogen atom and an alkyl group, provided that at least one of R1 to R14 is a tertiary alkyl group, m is an integer of 1 or more and 3 or less, and n is an integer of 0 or more and 2 or less, provided that m+n is 3, X is a bidentate ligand, and a partial structure IrX is any of structures represented by general formulae [2] and [3], where in formulae [2] and [3], R21 to R23, and R31 to R38 are each independently selected from, for example, a hydrogen atom and an alkyl group, and adjacent groups of R35 to R38 are optionally taken together to form a ring.

Abstract: An organic compound is represented by formula [1]. In formula [1], L and L? are bidentate ligands different from each other, a partial structure IrLm is a partial structure represented by formula [2], and a partial structure IrL?n is a partial structure represented by formula [3-1] or formula [3-2].

Abstract: An organic light-emitting device includes first and second electrodes and a light-emitting layer disposed between the first and second electrodes. The light-emitting layer contains first and second compounds. The first compound is represented by formula [1] or [2]. The second compound is a hydrocarbon compound. In formulae [1] and [2], R1 to R12 and R21 to R32 are each independently selected from a hydrogen atom, alkyl groups, and other groups. Each m is an integer of 1 or more and 3 or less, and each n is an integer of 0 or more and 2 or less, provided that m+n is 3. Each X is a bidentate ligand. Each partial structure IrX is any of the structures illustrated in formulae [3] to [5]. In formulae [3] to [5], R41 to R55 are each independently selected from a hydrogen atom, alkyl groups, and other groups.

Abstract: A organic light-emitting element including a positive electrode, a light-emitting layer, and a negative electrode in this order, wherein the light-emitting layer contains a dopant material, a host material, and an assist material, the dopant material is a compound represented by the following general formula [1], the host material is a hydrocarbon compound, and the assist material has a lower LUMO level than the host material. In the formula [1], R1 to R10 denote a hydrogen atom, an alkyl group, or the like. X denotes O or S. m denotes an integer in the range of 1 to 3, and n denotes an integer in the range of 0 to 2, provided that m+n is 3. The partial structure IrLn is any one of structures represented by the following formulae [2] and [3], wherein R11 to R21 denote a hydrogen atom, an alkyl group, or the like.

Abstract: The present disclosure provides an organic compound represented by general formula [1] below. In formula [1], Ar1 and Ar2 each represent an alkyl group having 1 to 8 carbon atoms, an aromatic hydrocarbon group having 6 to 18 carbon atoms, or a heteroaromatic group having 3 to 17 carbon atoms. Ar1 and Ar2 may be the same or different. Ar3 and Ar4 are each a substituent having a carbazolyl group. Ar3 and Ar4 may be the same or different. Ar1 to Ar4 may be substituted. At least one of Ar1 to Ar4 has a tert-butyl group. The total number of tert-butyl groups in one molecule of the organic compound is 2 or more.

Abstract: An organic compound represented by the following general formula [1] is excellent in thermal stability. In the general formula [1], R1 to R12 are each independently selected from the group consisting of a hydrogen atom and a substituent. Symbol A is selected from the group consisting of a divalent residue of naphthalene, phenanthrene, fluorene, benzofluorene, dibenzofluorene or spirofluorene, and a heteroarylene group having 4 to 12 carbon atoms. Symbol B is selected from the group consisting of an arylene group having 6 to 25 carbon atoms and a heteroarylene group having 4 to 12 carbon atoms. Symbol n is an integer of 0 to 3.

Abstract: The present disclosure provides an organic light emitting element which has a pair of electrodes and an organic compound layer disposed therebetween and in which the organic compound layer contains an organic compound represented by the following general formula [1], wherein in the formula [1], Ar1 and Ar2 each independently represent an aromatic hydrocarbon group or a heteroaromatic ring group, R1 to R4 are each independently selected from a hydrogen atom or a substituent, R1 and R2 and R3 and R4 each may form a benzene ring, wherein the benzene ring may have at least one substituent.

Abstract: An organic compound represented by formula [1], where in formula [1], R1 to R8 are each independently selected from the group consisting of a hydrogen atom, a halogen atom, an alkyl group, and other substituents, and X1 is oxygen, sulfur, selenium, tellurium, or a CR9R10 group, in which R9 and R10 are each independently selected from the group consisting of a hydrogen atom, a halogen atom, an alkyl group, and other substituents, and at least one of R1 to R8 is a group represented by formula [2].

Abstract: The present disclosure provides an organic compound that has a mother skeleton with a fused-ring structure, an electron-withdrawing group bonded to the mother skeleton, and an electron-donating group bonded to the mother skeleton, wherein the electron-withdrawing group is bonded at a position satisfying the following relationship in the mother skeleton.

Abstract: An organic compound represented by formula [1]: where R1 to R14 are each independently selected from the group consisting of a hydrogen atom and substituents, wherein at least one of R1 to R4 and R8 to R11 is an amino group or an amino group-containing group, and X is oxygen, sulfur, selenium, tellurium, or a CR15R16 group, wherein R15 and R16 are each independently selected from the group consisting of a hydrogen atom and substituents.

Abstract: An organic compound, represented by formula [1] or [2], suitably used for a thermally activated delayed fluorescent device: where X1 to X18 and X21 to X38 are each independently selected from the group consisting of a hydrogen atom, and substituents, Y is oxygen, sulfur, selenium, tellurium, a CR1R2 group, or a carbonyl group, where R1 and R2 are each independently selected from the group consisting of a hydrogen atom, and substituents, and Z is an alkyl group, an aryl group, or a heterocyclic group.

Abstract: An organic light emitting element includes, in sequence, an anode, a first light emitting layer, a second light emitting layer, and a cathode. The first light emitting layer includes a first compound and a first light emitting material. The second light emitting layer includes a second compound and a second light emitting material having an energy gap different from an energy gap of the first light emitting material. The organic light emitting element satisfies relations (a) to (c). LUMO(H1)>LUMO(D1)??(a) LUMO(H2)>LUMO(D2)??(b) LUMO(H2)?LUMO(D2)>LUMO(H1)?LUMO(D1)??(c) Where LUMO (H1), LUMO (D1), LUMO (H2), and LUMO (D2) represent a LUMO level of the first compound, a LUMO level of the first light emitting material, a LUMO level of the second compound, and a LUMO level of the second light emitting material, respectively.

Abstract: An organic light-emitting element including a first electrode, a second electrode, and a light-emitting layer located between the first electrode and the second electrode. The light-emitting layer contains a first organic compound material, a second organic compound that is a delayed fluorescent material, and a third organic compound that is a light-emitting material. In the second organic compound, an electron is transferred from a plurality of occupied molecular orbitals (OMO) to a lowest unoccupied molecular orbital (LUMO) in a second excited triplet state.

Abstract: An organic compound is represented by general formula [1-1]. In general formula [1-1], X is an oxygen atom, a sulfur atom, a selenium atom, or a tellurium atom, and R1 to R18 are each independently selected from the group consisting of a hydrogen atom, a halogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkoxy group, a substituted or unsubstituted amino group, a substituted or unsubstituted aromatic hydrocarbon group, a substituted or unsubstituted heterocyclic group, a substituted or unsubstituted aryloxy group, a substituted or unsubstituted silyl group, and a cyano group.

Abstract: An organic compound that emits red light having a long wavelength is represented by formula (1). In formula (1), R1 to R24 are each independently selected from the group consisting of a hydrogen atom, a halogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkoxy group, a substituted or unsubstituted amino group, a substituted or unsubstituted aryl group, a substituted or unsubstituted heterocyclic group, a substituted or unsubstituted aryloxy group, a silyl group, and a cyano group.

Abstract: An organic compound represented by formula [1]: where in formula [1], R1 to R6 are each independently selected from the group consisting of a hydrogen atom, a hydrocarbon group, and other substituents having a substituted or unsubstituted alkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted heterocyclic group, at least one of R1 to R6 is one of the other substituents, at least any one of R1 and R2 is a hydrogen atom or a hydrocarbon group, at least any one of R3 and R4 is a hydrogen atom or a hydrocarbon group, and at least any one of R5 and R6 is a hydrogen atom.

Abstract: There is provided an organic compound represented by formula [1-1] or [1-2]: where R1 to R20 are each independently selected from a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, an amino group, an aromatic hydrocarbon group, a heterocyclic group, an aryloxy group, a silyl group, and a cyano group, in which at least one of R1 to R4 and R6 to R9 and at least one of R11 to R14 and R16 to R19 are amino groups; and X1 to X4 are each oxygen, sulfur, selenium, or tellurium and are optionally the same or different.