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: 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 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: A nitrogen-containing heterocyclic derivative in which an indole structure is fused to a benzophenanthrene ring is a novel material useful as a material for organic electroluminescence devices for the production of organic electroluminescence devices and electronic equipment.

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: A compound is represented by a formula (1) below. In the formula (1), n is 1 or 2. Ar1 is represented by a formula (2) below. Ar2 represents a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 carbon atoms, or a substituted or unsubstituted heterocyclic group having 1 to 20 ring atoms. Ar3 is represented by a formula (3) below.

Abstract: A fused amine compound including a furan ring or a thiophene ring and an organic electroluminescence device employing the amine compound. The organic electroluminescence device includes a cathode, an anode, and one or more organic thin film layers which are disposed between the cathode and the anode. The organic thin film layers include a light emitting layer and at least one layer of the organic thin film layers includes at least one amine compound.

Abstract: Provided are an amine compound having a benzofluorene structure and further having a dibenzofuran structure and/or a dibenzothiophene structure, and an organic electroluminescent device containing a cathode, an anode and an organic thin film layer intervening between the cathode and anode, the organic thin film layer comprising one layer or plural layers comprising at least an emitting layer, at least one layer of the organic thin film layer comprising the aforementioned amine compound solely or as a component of a mixture.

Abstract: A fused amine compound including a furan ring or a thiophene ring and an organic electroluminescence device employing the amine compound. The organic electroluminescence device includes a cathode, an anode, and one or more organic thin film layers which are disposed between the cathode and the anode. The organic thin film layers include a light emitting layer and at least one layer of the organic thin film layers includes at least one amine compound.

Abstract: A compound is represented by a formula (1) below. In the formula (1), n is 1 or 2. Ar1 is represented by a formula (2) below. Ar2 represents a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 carbon atoms, or a substituted or unsubstituted heterocyclic group having 1 to 20 ring atoms. Ar3 is represented by a formula (3) below.

Abstract: Provided are an amine compound having a benzofluorene structure and further having a dibenzofuran structure and/or a dibenzothiophene structure, and an organic electroluminescent device containing a cathode, an anode and an organic thin film layer intervening between the cathode and anode, the organic thin film layer comprising one layer or plural layers comprising at least an emitting layer, at least one layer of the organic thin film layer comprising the aforementioned amine compound solely or as a component of a mixture.

Abstract: A compound represented by formula (1): wherein Ar is a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted aryl group having 6 to 30 ring carbon atoms, or a substituted or unsubstituted nitrogen-comprising heteroaryl group having 5 to 30 ring atoms; each of L1 and L2 is independently a single bond, a substituted or unsubstituted arylene group having 6 to 30 ring carbon atoms, a substituted or unsubstituted heteroarylene group having 5 to 30 ring atoms, or a substituted or unsubstituted divalent linking group wherein 2 to 4 groups selected from an arylene group having 6 to 30 ring carbon atoms and a heteroarylene group having 5 to 30 ring atoms are bonded to each other via a single bond; A is a monovalent group represented by formula (2); and B is a monovalent group represented by formula (5): wherein R1 to R10 and R21 to R30 are as defined in the description, enables the emission of light of a purer blue (shorter wavelength), a narrower half width (high

Abstract: A compound is represented by a formula (100) below, where X1, X2 and X3 are each independently a nitrogen atom or a carbon atom bonded with R2, Y is an oxygen atom, a sulfur atom and the like, R1, R2, R11, R21 and R22 are each a hydrogen atom or a substituent, L1 is a single bond or a linking group, and L2 is a linking group.

Abstract: A compound is represented by a formula (1). In the formula (1); Ar represents an aromatic hydrocarbon group or a heterocyclic group having 4 or more fused rings and 22 or less ring atoms; Ar optionally has a substituent; R11 is a substituted or unsubstituted aromatic hydrocarbon group; when R11 is an aromatic hydrocarbon group having a substituent, the substituent is not a heterocyclic group; X1 represents a nitrogen atom or a carbon atom bonded with R12 (CR12); R12 represents a hydrogen atom or a substituent; L1 represents a single bond or a linking group; X2 and X3 each independently represent a nitrogen atom or a carbon atom bonded with R2 (CR2); R1 and R2 each independently represent a hydrogen atom or a substituent; and L2 is a linking 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 aromatic amine derivative is represented by the following formula (1). In the formula (1), R1 to R10 each independently represent a hydrogen atom and a substituent. In the formula (1); R1 is represented by the following formula (2); any one of R2 to R5 and R7 to R10 is represented by the following formula (2); and L1 to L3 each independently represent a single bond, a divalent residue of an aryl group, or the like. In the formula (2); Ar1 is a monovalent substituent having a partial structure represented by the following formula (3); X represents an oxygen atom or a sulfur atom; and A and B represent a six-membered ring. In the formula (2), Ar2 is an aryl group, a monovalent substituent having a partial structure represented by the formula (3), and the like.

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: A high-performance organic electroluminescence device and an electronic equipment provided with the organic electroluminescence device are provided. Also, a compound for achieving the organic electroluminescence device and the electronic equipment is provided. Specifically, a compound having a specific structure having a triphenylene skeleton, an organic electroluminescence device using the compound and an electronic equipment provided with the organic electroluminescence device are provided.

Abstract: Disclosed are a compound having, as a main skeleton, a polycyclic structure represented by the following general formula (1), a material for organic electroluminescence devices including the compound, an organic electroluminescence device using the compound, and electronic equipment having the organic electroluminescence device mounted thereon. A compound capable of realizing an organic EL device with high emission efficiency, a material for organic electroluminescence devices including the compound, an organic electroluminescence device using the compound, and electronic equipment having the organic electroluminescence device mounted thereon, are provided. In the formula (1), A, L, X1 to X16, R, RA, and RB are those defined in the specification.