Abstract: The present invention provides a material useful as an organic electroluminescence device material, and particularly provides: a compound having, as a substituent, a substituted aromatic heterocyclic group having a specific structure wherein any of the 1-position to 6-position or the 7-position to 10-position of fluoranthene is substituted with a nitrogen atom; a material for low-voltage organic electroluminescence devices using the compound; and an organic electroluminescence device and an electronic equipment using the material.

Abstract: A compound represented by formula (1): wherein R1 to R6, R7 to R10, R11 to R14, R15 to R18, L1, L2, Ar1, and Ar2 are as defined in the description realizes an organic electroluminescence device with long lifetime.

Abstract: A compound represented by formula (1): wherein R1 to R4, a to d, L0 to L2, and Ar are as defined in the description, is a material providing an organic electroluminescence device which can be operated at a low driving voltage and has a long lifetime.

Abstract: Anthracene derivatives each having a structure including an anthracene skeleton, a phenanthrene skeleton selected from among various phenanthrene skeletons different in bonding site which is bonded to the 9-position of the anthracene skeleton and a group selected from among various aryl groups and so on which is bonded to the 10-position of the anthracene skeleton. Organic EL devices made by using the derivatives exhibit high light emission efficiency and a long life.

Abstract: Provided are an organic EL device having a high emission efficiency, a material for organic EL devices, which is capable of realizing the same, and the like. More specifically, provided are a compound represented by the following formula (1), a material for organic electroluminescence devices, which contains the compound, an organic electroluminescence device using the compound, and an electronic equipment provided with the organic electroluminescence device: wherein Ar represents a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms, a substituted or unsubstituted heteroaryl group having 5 to 50 ring atoms, or a group formed by a combination of these groups, and W to R9 each independently represent a hydrogen atom or a substituent, provided that any pair of R2 and R3, R3 and R4, R4 and R5, R6 and R7, R7 and R8, and R8 and R9 are optionally bonded to each other to form a benzene ring.

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 (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 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 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 compound represented by the following formula (1):

Abstract: Anthracene derivatives each having a structure including an anthracene skeleton, a phenanthrene skeleton selected from among various phenanthrene skeletons different in bonding site which is bonded to the 9-position of the anthracene skeleton and a group selected from among various aryl groups and so on which is bonded to the 10-position of the anthracene skeleton. Organic EL devices made by using the derivatives exhibit high light emission efficiency and a long life.

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 fused aromatic ring derivative shown by the following formula (1): wherein Ra and Rb are independently a hydrogen atom or a substituent, p is an integer of 1 to 8 and q is an integer of 1 to 11, when p is 2 or more, plural Ras may be independently the same or different and adjacent Ras may form a ring, when q is 2 or more, plural Rbs may be independently the same or different, L1 is a single bond, or a substituted or unsubstituted divalent linking group, and Ar1 is a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms or a substituted or unsubstituted heteroaryl group having 5 to 50 ring atoms, provided that the substituent of L1, the substituent of Ar1, Ra and Rb contain no substituted or unsubstituted amino group.

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.

Abstract: An aromatic amine derivative represented by the following formula (1) wherein at least one of Ar1 to Ar4 is a heterocyclic group represented by the following formula (2) wherein X1 is an oxygen atom or a sulfur atom.

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: A compound represented by the following formula (1): wherein in the formula, L1 is a single bond or a linking group, A is a group represented by the following formula (A), B is a group represented by the following formula (B), m is an integer of 1 to 3, and n is an integer of 1 to 4.

Abstract: An organic electroluminescence device having higher performance, in particular exhibiting a better driving voltage and a better external quantum efficiency, while having an extended lifetime; and an electronic equipment provided with the organic electroluminescence device are provided. In addition, a compound for realizing the same device and 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 were provided.

Abstract: A fused fluoranthene compound which includes an indeno[3,2-b]fluoranthene skeleton having a hetero atom is a novel compound, which is useful as a material for organic electroluminescence devices for use in an organic electroluminescence device and an electronic equipment.