Abstract: An additive manufacturing device comprises a lower nozzle that blows out inert gas into a chamber in a horizontal direction through a lower opening portion formed in a lower part of a first side wall constituting the chamber, and an upper nozzle that blows out the inert gas into the chamber through an upper opening portion formed in an upper part of the first side wall, wherein the upper nozzle includes a window nozzle that blows out the inert gas along an inner surface of a window portion of a top board constituting the chamber, and an oblique nozzle that blows out the inert gas obliquely downward from the upper portion of the first side wall.

Abstract: An organic electroluminescence device includes an anode, an emitting layer and a cathode, in which the emitting layer includes a first compound, a second compound and a third compound. The first compound is a compound represented by a formula (1) below. The second compound has a larger singlet energy than a singlet energy of the first compound. The third compound is a fluorescent compound.

Abstract: An organic electroluminescence device including a cathode, an anode, an emitting layer arranged between the cathode and the anode, and an electron-transporting region arranged between the emitting layer and the cathode, wherein the electron-transporting region includes one or more compounds selected from the group consisting of compounds represented by the following formulas (1) to (4) and a rare earth element, and the electron-transporting region substantially does not include an alkali metal, a compound containing an alkali metal, a metal belonging to Group 13 of the Periodic Table of the Elements, and a compound having a metal belonging to Group 13 of the Periodic Table of the Elements.

Abstract: A compound is represented by a formula (1) below. In the formula (1): R1 to R9, R101 to R108, and R111 to R118 are each independently a hydrogen atom, a substituted or unsubstituted aryl group having 6 to 20 ring carbon atoms, or the like; Ar12 is a substituted or unsubstituted aryl group having 10 to 30 ring carbon atoms or the like; p is 0 or 1; q is 0 or 1; and p+q is 1 or 2.

Abstract: A compound of the following formula (1) and others. R1 to R24, R31 to R35, A1 and A2 are as defined in the specification, n is an integer of 0 to 3, when A1 is an (n+1)-valent residue of benzene, n is an integer of 1 or more, and when n is 0, (A2)0 is a hydrogen atom.

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

Abstract: A compound is represented by a formula (1) below, in which k is an integer of 0 or more, m is an integer of 1 or more, n is an integer of 2 or more. L is a substituted or unsubstituted aromatic hydrocarbon ring having 6 to 30 ring carbon atoms, CN is a cyano group, and D1 and D2 are each independently represented by one of a formula (2), a formula (3) and formula (3x) below, D1 and D2 being optionally mutually the same or different.

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

Abstract: A compound represented by the following formula (1), wherein X1 is O or S, and two or more of Y1, Y2 and Y3 are N, provided that the case where one or both of —Ar1-Ar2 and —Ar3-Ar4 is a p-terphenyl-3-yl group is excluded.

Abstract: A compound is represented by a formula (1) below, in which k is an integer of 0 or more, m is an integer of 1 or more, n is an integer of 2 or more. L is a substituted or unsubstituted aromatic hydrocarbon ring having 6 to 30 ring carbon atoms, CN is a cyano group, and D1 and D2 are each independently represented by one of a formula (2), a formula (3) and formula (3x) below, D1 and D2 being optionally mutually the same or different.

Abstract: A compound represented by the following formula (1) (L1 is a single bond or an unsubstituted arylene group having 6 to 50 ring carbon atoms, and Ar1 is a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms).

Abstract: A compound represented by the following formula (1), wherein L1 is a single bond or an arylene group, and Ar1 and Ar2 are an unsubstituted aryl group.

Abstract: A compound that further improves the capability of an organic electroluminescent device, an organic electroluminescent device having a further improved device capability, and an electronic device including the organic electroluminescent device are provided. A compound represented by the following formula (1): wherein the symbols in the formula (1) are defined in the description, an organic electroluminescent device including the compound, and an electronic device including the organic electroluminescent device.

Abstract: A compound having anticancer activity, or a pharmaceutically acceptable salt thereof is provided. Used is a compound represented by the following formula (I) or a pharmaceutically acceptable salt thereof: (wherein, L1 and L2 are the same or different and each represents a group represented by one formula selected from the group consisting of formulas (A) to (F), and S represents a group represented by one formula selected from the group consisting of formulas (S1) to (S18)).

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: An organic electroluminescent device includes a cathode, an anode, and organic layers intervening between the cathode and the anode, where the organic layers include a light emitting layer and an electron transporting layer, where the electron transporting layer contains a compound A represented by formula (1), and the light emitting layer contains a host material B represented by formula (10):

Abstract: A compound represented by the following formula (1) and having a molecular weight of 650 or more: wherein Cz, n, Y1, Y2, Ar1, Ar2, L1, L2, L3, L4, R1, R2, R3, R4, R5, and R6 are as defined in the description, and an organic electroluminescent device which contains the compound.

Abstract: A compound represented by formula (I), a material for an organic electroluminescence device having the specific compound, an organic electroluminescence device of the specific compound, an electronic equipment having the organic electroluminescence device and the use of the compound of formula (I) in an organic electroluminescence device, where in formula (I), R1 and R1? each independently represent a C1 to C6 alkyl group; R2 represents a substituted or unsubstituted C6 to C24 aryl group, a substituted or unsubstituted heteroaryl group having 3 to 9 carbon atoms, or CN; L represents a substituted or unsubstituted C6 to C40 arylene group; m is 0 to 5; and n is 1, 2 or 3:

Abstract: A compound having anticancer activity, or a pharmaceutically acceptable salt thereof is provided. Used is a compound represented by the following formula (I) or a pharmaceutically acceptable salt thereof: (wherein, L1 and L2 are the same or different and each represents a group represented by one formula selected from the group consisting of formulas (A) to (F), and S represents a group represented by one formula selected from the group consisting of formulas (S1) to (S18)).

Abstract: A compound represented by formula (1): wherein R1 to R10, R11 to R14, L, and Ar are as defined in the description, a material for organic electroluminescence device containing the compound, an organic electroluminescence device containing the compound, and an electronic device containing the organic electroluminescence device are provided.