Abstract: An organic electroluminescence device includes an anode, an emitting layer, and a cathode, the emitting layer including a delayed-fluorescent first compound represented by a formula (1), and a fluorescent second compound. In the formula (1), Ar1 is a substituted or unsubstituted aryl group having 6 to 30 ring carbon atoms and the like, and ArEWG is a substituted or unsubstituted heteroaryl group having 5 to 30 ring atoms and including one or more nitrogen atom in the ring, or an aryl group having 6 to 30 ring carbon atoms and substituted by one or more cyano group, at least one of Ar1 and ArX being at least one group selected from the group consisting of groups represented by a formula (1a) and the like.

Abstract: Specifically substituted ladder type compounds of formula (I) wherein A is formula (II) a material for an organic electroluminescence device comprising at least one compound of formula (I), and an organic electroluminescence device which comprises one or more organic thin film layers including an emitting layer between a cathode and an anode, wherein at least one layer of the organic thin film layers comprises at least one compound of formula (I).

Abstract: A compound represented by Formula (1): The compound can be used as insecticides.

Abstract: A compound that includes a structure including two or more structures represented by the following formula (1) in the same molecule and in which at least two of the structures represented by the formula (1) are directly bonded to each other by a single bond.

Abstract: A compound is represented by a formula (20) below.

Abstract: A compound represented by Formula (1): The compound can be used as insecticides.

Abstract: An organic electroluminescence device includes an anode, a second organic layer, a first organic layer, and a cathode in this order. The first organic layer contains a first compound and a second compound. The second organic layer contains a third compound. The first compound is a compound represented by a formula (1). The second compound is a delayed fluorescent compound. The third compound is a compound represented by a formula (3). In the formula (1), X is a nitrogen atom or a carbon atom bonded to Y, Y being a hydrogen atom or a substituent. In the formula (3), n is an integer ranging from 1 to 4, XB is a group represented by a formula (3A). In the formula (3A), Ar1 and Ar2 are each independently a monovalent or polyvalent aromatic hydrocarbon group, and Cz is a group represented by a formula (3B-1) or the like.

Abstract: An organic EL multi-color emitting device including a substrate, and a first light-emitting element and a second light-emitting element arranged on the surface of the substrate; the first light-emitting element including, between an anode and a cathode, a first organic layer, a second organic layer and a third organic layer in this sequence in a direction perpendicular to the surface of the substrate; the second light-emitting element including, between an anode and a cathode, a second organic layer and a third organic layer in this sequence in a direction perpendicular to the surface of the substrate; the first organic layer including a first light-emitting dopant; the third organic layer including a second light-emitting dopant; the second organic layer including any of (A) a compound including an arylamine site, and a furan site or a thiophene site, (B) a compound including an arylamine site and a site comprising a nitrogen-containing six-membered ring structure, (C) a compound including a carbazole site,

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 delayed-fluorescent compound represented by a formula (1) below. The second compound includes at least one of a partial structure represented by a formula (21) below and a partial structure represented by a formula (22) below in one molecule.

Abstract: An organic electroluminescence device includes an anode, an emitting layer and a cathode. The emitting layer includes a first compound and a second compound. The first compound is a delayed fluorescent compound. The second compound is a fluorescent compound. A solution of the second compound in toluene has an emission peak wavelength in a range from 430 nm to 480 nm. A molar absorbance coefficient of the second compound at an absorption peak closest to a long-wavelength side is in a range from 29,000 L/(mol·cm) to 1,000,000 L/(mol·cm). The second compound has a Stokes shift in a range from 1 nm to 20 nm.

Abstract: An organic electroluminescence device includes an anode, an emitting layer, and a cathode. The emitting layer contains a delayed fluorescent first compound, a fluorescent second compound, and a third compound represented by Cz-Az. The second compound emits light with a main peak wavelength ranging from 430 nm to 540 nm. Az is a cyclic structure selected from the group consisting of a substituted or unsubstituted pyridine ring, a substituted or unsubstituted pyrimidine ring, a substituted or unsubstituted triazine ring, and a substituted or unsubstituted pyrazine ring. Cz is represented by a formula (3B) below.

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 includes an anode, an emitting layer and a cathode, in which the emitting layer contains a first compound and a second compound, the first compound being a delayed fluorescent compound, the second compound being a compound represented by a formula (20).

Abstract: The mask of the present disclosure is adapted to be worn on a face including a main body that covers at least a portion of the face, and the main body includes a resin film having air permeability through the thickness thereof. The resin film is a non-porous film having through holes extending through the thickness of the film. The diameter of the through holes is 0.01 ?m or more and 30 ?m or less. The density of the through holes in the resin film is 10 holes/cm2 or more and 1×108 holes/cm2 or less. The mask of the present disclosure is completely different in structure from conventional masks, has high flexibility in the design of various properties such as shielding ability, air permeability, transparency, and sound permeability, and is capable, for example, of exhibiting high shielding ability, high air permeability, high transparency, and high sound permeability.

Abstract: A compound represented by the following formula (1): wherein in the formula (1), Ar1 and Ar2 are independently a substituted or unsubstituted aryl group, a substituted or unsubstituted heteroaryl group, or a substituted or unsubstituted alkyl group; X1 to X4 and X13 to X16 are independently CR1, CH or N; one of X5 to X8 is a carbon atom bonding to one of X9 to X12, and at least one of X5 to X8 that is adjacent to the carbon atom bonding to one of X9 to X12 is CR2; one of X9 to X12 is a carbon atom bonding to one of X5 to X8, and X9 to X12 that is adjacent to the carbon atom bonding to one of X5 to X8 is CH or N; and the remaining X5 to X8 and the remaining X9 to X12 are CR1, CH or N.

Abstract: A compound represented by the following formula (1). In the formula, A1 is O, S, Si(Ar1)(Ar2), P(?O)(Ar3)(Ar4), a substituted or unsubstituted arylene group including 6 to 30 ring carbon atoms, or a substituted or unsubstituted heteroarylene group including 5 to 30 ring atoms.

Abstract: An object of the present invention is to provide a compound represented by Formula (1): wherein A1, A2, A3 and A4 each represent a carbon atom, a nitrogen atom or an oxidized nitrogen atom; R1 and R2 each represent a hydrogen atom, an optionally substituted alkyl group or an optionally substituted C1-C4 alkylcarbonyl group; G1 and G2 each represent an oxygen atom or a sulfur atom; X, which may be identical or different each other, represents a hydrogen atom, a halogen atom, a C1-C3 alkyl group or a trifluoromethyl group; n is an integer of 0 to 4; and Q1 represents an optionally substituted phenyl group, an optionally substituted naphthyl group or an optionally substituted heterocyclic group; Q2 represents a phenyl group or heterocyclic group having one or more substituents, at least one of the substituent being any of a C1-C4 haloalkoxy group, a C2-C6 perfluoroalkyl group, a C1-C6 perfluoroalkylthio group, a C1-C6 perfluoroalkylsulfinyl group and a C1-C6 perfluoroalkylsulfonyl group, an insecticide com

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 compound represented by the following formula (1). In the formula (1), when Ar1 and Ar2 are the same substituents, as for all of the following pairs: Y1 and Y12, Y2 and Y11, Y3 and Y10, Y4 and Y9, Y5 and Y8, and Y6 and Y7, Y1 to Y12 of each pair are not the same as each other.

Abstract: A compound represented by Formula (1): The compound can be used as insecticides.