Abstract: A compound represented by the following formula (1):

Abstract: An aromatic amine derivative is represented by a formula (1) below. In the formula (1), R2 to R5, R7 to R9 and R10 are each independently a hydrogen atom or a substituent. In the formula (1), R1 and R6 are represented by a formula (2) below, and L1 to L3 are each independently a single bond and the like. In the formula (2), Ar1 is a monovalent residue derived from the ring structure represented by a formula (4) below, X is an oxygen atom or a sulfur atom, and at least one of R11 to R18 is an alkyl group. In the formula (1), Ar2 represents a substituted or unsubstituted biphenyl group.

Abstract: A compound is represented by the following formula (1). In the formula (1), Ar is a substituted or unsubstituted aryl group including 6 to 30 ring carbon atoms, Ra are independently a substituted or unsubstituted alkyl group including 1 to 15 carbon atoms, or a substituted or unsubstituted cycloalkyl group including 3 to 15 carbon atoms, Rb1 to Rb4 are independently a halogen atom, a cyano group, a substituted or unsubstituted alkyl group including 1 to 15 carbon atoms, or the like, Rc1 to Rc10 are independently a hydrogen atom, a halogen atom, a cyano group, a substituted or unsubstituted alkyl group including 1 to 15 carbon atoms, or the like, * is a bonding position at which one of Rc1 to Rc10 is bonded to either nitrogen atom, x is an integer from 0 to 3, y is an integer from 0 to 4, and z are independently an integer from 0 to 5.

Abstract: An organic light-emitting medium including a pyrene derivative represented by the following formula (1) and a phenyl-substituted anthracene derivative represented by the following formula (2): wherein 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 20 ring atoms.

Abstract: An aromatic amine derivative is represented by a formula (1) below. In the formula (1), R2 to R5, R7 to R9 and R10 are each independently a hydrogen atom or a substituent. In the formula (1), R1 and R6 are represented by a formula (2) below, and L1 to L3 are each independently a single bond and the like. In the formula (2), Ar1 is a monovalent residue derived from the ring structure represented by a formula (4) below, X is an oxygen atom or a sulfur atom, and at least one of R11 to R18 is an alkyl group. In the formula (1), Ar2 is an aryl group or a monovalent residue derived from the ring structure represented by the formula (4).

Abstract: An anthracene derivative represented by the following formula (1): wherein in the formula (1), L1 is selected from a single bond and a linking group, and the linking group is selected from a divalent arylene group, a divalent heterocyclic group, and a group formed by linking of 2 to 4 of divalent arylene groups and/or divalent heterocyclic groups. Ar1 is selected from the following formulas (2) and (3). In the formulas (2) and (3), X is selected from an oxygen atom and a sulfur atom. In the formula (2), any one of R11 to R14 is used for bonding to L1. In the formula (3), any one of R21 to R24 is used for bonding to L1. Ar2 is selected from a substituted or unsubstituted aryl group including 6 to 50 ring carbon atoms and a substituted or unsubstituted heterocyclic group including 5 to 50 ring atoms.

Abstract: An organic light-emitting medium including a pyrene derivative represented by the following formula (1) and a phenyl-substituted anthracene derivative represented by the following formula (2): wherein 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 20 ring atoms.

Abstract: A material for organic electroluminescence device including a specific compound having a specific group in the central skeleton and an organic electroluminescence device including an organic thin film layer between an anode and a cathode. The organic thin film layer includes a light emitting layer and at least one layer of the organic thin film layer includes the material for organic electroluminescence device. The organic electroluminescence device has a long lifetime and the material for organic electroluminescence device realizes such a device.

Abstract: A heterocyclic compound wherein three five-membered rings are fused to one benzene ring and a saturated or unsaturated ring is fused to each five-membered ring. An organic electroluminescence device includes one or more organic thin film layers between an anode and a cathode. The one or more organic thin film layers include a light emitting layer. At least one layer of the one or more organic thin film layers includes the heterocyclic compound.

Abstract: An organic electroluminescence device having good emission efficiency is provided. The organic electroluminescence device includes an amine compound which includes a benzofluorene structure and an aryl group and/or a heteroaryl group, wherein the benzofluorene structure has a specific substituent at 9-position of the fluorene ring.

Abstract: An organic electroluminescence device includes: an anode; an emitting layer; and a cathode, the emitting layer containing a first material, a second material and a third material, the first material being a fluorescent material, the second material being a delayed fluorescent material, the third material having a singlet energy larger than a singlet energy of the second material.

Abstract: A novel carbazole derivative represented by formula (1) in which two or more groups each having a specific structure, such as a carbazolyl group, are bonded to two or more of 2-, 3- and 4-positions of the carbazole derivative is useful as a material for organic electroluminescence devices. A material for organic electroluminescence devices including the carbazole derivative, an organic electroluminescence device employing the carbazole derivative, and an electronic equipment are described. wherein at least two selected from B1 to B3 are represented by formula (2) and A, X1 to X4, L, n, Y, and R1 to R8 are as defined in claim 1.

Abstract: An anthracene derivative represented by the following formula (1): wherein in the formula (1), L1 is selected from a single bond and a linking group, and the linking group is selected from a divalent arylene group, a divalent heterocyclic group, and a group formed by linking of 2 to 4 of divalent arylene groups and/or divalent heterocyclic groups. Ar1 is selected from the following formulas (2) and (3). In the formulas (2) and (3), X is selected from an oxygen atom and a sulfur atom. In the formula (2), any one of R11 to R14 is used for bonding to L1. In the formula (3), any one of R21 to R24 is used for bonding to L1. Ar2 is selected from a substituted or unsubstituted aryl group including 6 to 50 ring carbon atoms and a substituted or unsubstituted heterocyclic group including 5 to 50 ring atoms.

Abstract: An aromatic amine derivative represented by the following formula (1): wherein at least one of R1 to R8 is a group other than a hydrogen atom, Ar1 to Ar4 are a substituted or unsubstituted aryl group having 6 to 30 ring carbon atoms.

Abstract: A compound is represented by the following formula (1). In the formula (1), Ar is a substituted or unsubstituted aryl group including 6 to 30 ring carbon atoms, Ra are independently a substituted or unsubstituted alkyl group including 1 to 15 carbon atoms, or a substituted or unsubstituted cycloalkyl group including 3 to 15 carbon atoms, Rb1 to Rb4 are independently a halogen atom, a cyano group, a substituted or unsubstituted alkyl group including 1 to 15 carbon atoms, or the like, Rc1 to Rc10 are independently a hydrogen atom, a halogen atom, a cyano group, a substituted or unsubstituted alkyl group including 1 to 15 carbon atoms, or the like, * is a bonding position at which one of Rc1 to Rc10 is bonded to either nitrogen atom, x is an integer from 0 to 3, y is an integer from 0 to 4, and z are independently an integer from 0 to 5.

Abstract: An organic electroluminescence device includes: an anode; an emitting layer; and a cathode, the emitting layer containing a first material, a second material and a third material, the first material being a fluorescent material, the second material being a delayed fluorescent material, the third material having a singlet energy larger than a singlet energy of the second material.

Abstract: A heterocyclic compound in which three 5-membered rings are fused to a benzene ring and a saturated or unsaturated ring is further fused to each of the 5-membered rings is a novel material, which is useful as a material for organic electroluminescence devices for the production of organic electroluminescence devices and electronic equipment.

Abstract: An organic electroluminescence device includes: an anode; a cathode; and an organic layer interposed between the anode and the cathode, in which the organic layer includes an emitting layer and the emitting layer includes a compound represented by a formula (1) below and a compound represented by a formula (2) below. Az1 of the formula (1) below and Az2 of the formula (2) below are each an azine ring. Cz of the formula (1) below and HAr of the formula (2) below are each a nitrogen-containing heterocyclic ring.

Abstract: An aromatic amine derivative is represented by the following formula (1). In the formula (1), R2 to R5, R7 to R9 and R10 are each independently a hydrogen atom or a substituent. R1 and R6 in the formula (1) are each represented by the following formula (2), in which L1 to L3 are each independently, for instance, a single bond. Ar1 in the formula (2) is a monovalent residue derived from a ring structure of the following formula (4), in which X is an oxygen atom or a sulfur atom and at least one of R11 to R18 is a substituted aryl group. Ar1 in the formula (1) is, for instance, an aryl group or a monovalent residue derived from the ring structure of the formula (4).

Abstract: An organic electroluminescence device 1 includes: an anode 3, a cathode 4 opposed to the anode 3 and an emitting layer 5 provided between the anode 3 and the cathode 4. The emitting layer 5 contains first and second host materials and a luminescent material. The first host material has a partial structure represented by at least one of the following formulae (1) and (2) while the second host material has a partial structure represented by the following formula (3). Az represents a substituted or unsubstituted aromatic heterocyclic group containing a nitrogen-containing six-membered ring. WCN is an aromatic hydrocarbon group substituted by at least one cyano group (CN) or an aromatic heterocyclic group substituted by at least one cyano group (CN). Ar1 is a substituted or unsubstituted aromatic hydrocarbon group or a substituted or unsubstituted aromatic heterocyclic group, but is not an aromatic heterocyclic group containing a nitrogen-containing six-membered ring.